Assessment of Nail Content in the American Academy of Dermatology Patient Education Website

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To the Editor:

Patients with skin, hair, or nail concerns often utilize online resources to self-diagnose or learn more about physician-diagnosed conditions. The American Academy of Dermatology (AAD) website offers the public access to informational pages categorized by disease or treatment (https://www.aad.org/public). We sought to evaluate the nail content by searching the Patients and Public section of the AAD website to qualitatively and quantitatively describe mentions of nail conditions. Psoriasis, psoriatic arthritis, atopic dermatitis, and ringworm content also were analyzed and compared to nail content. The analysis was performed on September 7, 2019.

Of the 73 topics listed in the Diseases and Treatments section of the site, 17 (23%) specifically mentioned nail symptoms or pathology (Table). Three additional topics—atopic dermatitis, cellulitis, and neurodermatitis—recommended keeping nails short to prevent injury from scratching. There was 1 mention of obtaining fungal cultures, 2 of nail scraping microscopy, 2 of nail clippings, and 2 of nail-related cancers. There were no mentions of nail biopsies. The total number of unique clinical images across all sections was 300, with 12 of nails. The video library contained 84 videos, of which 6 focused on nail health.



Several sections were reviewed for overall content to understand the typical number of images and videos included for other common conditions. The general psoriasis section included 6 images and 3 videos detailing disease etiology, symptoms, and treatments, without depictions of nails. The psoriatic arthritis section included 8 images and 1 video as well as 1 image of nail pitting. The atopic dermatitis section included 6 images and 6 videos on disease etiology, symptoms, and treatment. The ringworm section, which collectively included all tinea infections, contained 11 images and 1 video on symptoms. In contrast, the only nail-specific section—nail fungus—contained only 2 images and 1 video.

Our study demonstrated that nail content is underrepresented in the public education section of the AAD website. If patients are unable to find nail disease material on the AAD website, they may seek alternative sources that are unreliable. Prior studies have shown that patient Internet resources for subungual melanoma and onychomycosis often are inadequate in quality and readability.1,2

Representative photographs and key information on common nail diseases could be added to improve patient education. The atopic dermatitis section should include text on related nail changes with accompanying images. We also recommend including paronychia information and images as either a separate topic or in the cellulitis section. The contact dermatitis section mentions nail cosmetics as causative factors, but an image of roller-coaster onycholysis may be more helpful.3 Although the alopecia areata section mentions nail changes, this information should be added to the general hair loss section of the site, as many patients may initially seek out the latter category. Herpes simplex may affect nails, and an image showing these changes would be instructive. In addition, pyogenic granulomas and paronychia occur with isotretinoin use.4



Many of the included images were not representative of common clinical findings. The nail lichen planus image showed pitting instead of more typical findings of nail plate atrophy and pterygium. The nail melanoma image showed thickened yellow toenails and the fifth toenail with a thin gray-brown band instead of an isolated wide black band. The nail fungus section included images of superficial onychomycosis and severe onychodystrophy instead of showing more common changes such as distal onycholysis with subungual hyperkeratosis, which is typical of the most common subtype, distal lateral subungual onychomycosis.5 Onychomycosis was referenced again in the ringworm section with 1 image repeated from the nail fungus section and another image that appeared to be a subungual hematoma.

The AAD website offers important patient education resources; however, nail content is underrepresented on this platform. Dermatologists are experts on nail disease, and increased efforts are needed to educate the public about frequently encountered nail signs and symptoms that could signify a serious underlying condition.

After our original search and analysis, new nail topics, images, and videos have been added; therefore, there has been a positive trend toward new nail content being added to site, which will greatly benefit patients.

References
  1. Kang R, Lipner S. Assessment of internet sources on subungual melanoma [published online August 30, 2018]. Melanoma Res. doi:10.1097/CMR.0000000000000508.
  2. Kang R, Lipner S. Evaluation of onychomycosis information on the internet. J Drugs Dermatol. 2019;18:484-487.
  3. Rieder EA, Tosti A. Cosmetically induced disorders of the nail with update on contemporary nail manicures. J Clin Aesthet Dermatol. 2016;9:39-44.
  4. Arias-Santiago S, Husein-ElAhmed H, Aneiros-Cachaza J, et al. Uncommon side effects of isotretinoin therapy: paronychia and pyogenic granuloma. J Am Acad Dermatol. 2011;64:AB37.
  5. Lipner SR, Scher RK. Onychomycosis: clinical overview and diagnosis. J Am Acad Dermatol. 2019;80:835-851.
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Dr. Zusstone is from MedStar Washington Hospital Center, Washington, DC. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

Dr. Zusstone reports no conflict of interest. Dr. Lipner is Deputy Chair of the American Academy of Dermatology Public Education Committee.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Dr. Zusstone is from MedStar Washington Hospital Center, Washington, DC. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

Dr. Zusstone reports no conflict of interest. Dr. Lipner is Deputy Chair of the American Academy of Dermatology Public Education Committee.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

Author and Disclosure Information

Dr. Zusstone is from MedStar Washington Hospital Center, Washington, DC. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

Dr. Zusstone reports no conflict of interest. Dr. Lipner is Deputy Chair of the American Academy of Dermatology Public Education Committee.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

Article PDF
Article PDF

To the Editor:

Patients with skin, hair, or nail concerns often utilize online resources to self-diagnose or learn more about physician-diagnosed conditions. The American Academy of Dermatology (AAD) website offers the public access to informational pages categorized by disease or treatment (https://www.aad.org/public). We sought to evaluate the nail content by searching the Patients and Public section of the AAD website to qualitatively and quantitatively describe mentions of nail conditions. Psoriasis, psoriatic arthritis, atopic dermatitis, and ringworm content also were analyzed and compared to nail content. The analysis was performed on September 7, 2019.

Of the 73 topics listed in the Diseases and Treatments section of the site, 17 (23%) specifically mentioned nail symptoms or pathology (Table). Three additional topics—atopic dermatitis, cellulitis, and neurodermatitis—recommended keeping nails short to prevent injury from scratching. There was 1 mention of obtaining fungal cultures, 2 of nail scraping microscopy, 2 of nail clippings, and 2 of nail-related cancers. There were no mentions of nail biopsies. The total number of unique clinical images across all sections was 300, with 12 of nails. The video library contained 84 videos, of which 6 focused on nail health.



Several sections were reviewed for overall content to understand the typical number of images and videos included for other common conditions. The general psoriasis section included 6 images and 3 videos detailing disease etiology, symptoms, and treatments, without depictions of nails. The psoriatic arthritis section included 8 images and 1 video as well as 1 image of nail pitting. The atopic dermatitis section included 6 images and 6 videos on disease etiology, symptoms, and treatment. The ringworm section, which collectively included all tinea infections, contained 11 images and 1 video on symptoms. In contrast, the only nail-specific section—nail fungus—contained only 2 images and 1 video.

Our study demonstrated that nail content is underrepresented in the public education section of the AAD website. If patients are unable to find nail disease material on the AAD website, they may seek alternative sources that are unreliable. Prior studies have shown that patient Internet resources for subungual melanoma and onychomycosis often are inadequate in quality and readability.1,2

Representative photographs and key information on common nail diseases could be added to improve patient education. The atopic dermatitis section should include text on related nail changes with accompanying images. We also recommend including paronychia information and images as either a separate topic or in the cellulitis section. The contact dermatitis section mentions nail cosmetics as causative factors, but an image of roller-coaster onycholysis may be more helpful.3 Although the alopecia areata section mentions nail changes, this information should be added to the general hair loss section of the site, as many patients may initially seek out the latter category. Herpes simplex may affect nails, and an image showing these changes would be instructive. In addition, pyogenic granulomas and paronychia occur with isotretinoin use.4



Many of the included images were not representative of common clinical findings. The nail lichen planus image showed pitting instead of more typical findings of nail plate atrophy and pterygium. The nail melanoma image showed thickened yellow toenails and the fifth toenail with a thin gray-brown band instead of an isolated wide black band. The nail fungus section included images of superficial onychomycosis and severe onychodystrophy instead of showing more common changes such as distal onycholysis with subungual hyperkeratosis, which is typical of the most common subtype, distal lateral subungual onychomycosis.5 Onychomycosis was referenced again in the ringworm section with 1 image repeated from the nail fungus section and another image that appeared to be a subungual hematoma.

The AAD website offers important patient education resources; however, nail content is underrepresented on this platform. Dermatologists are experts on nail disease, and increased efforts are needed to educate the public about frequently encountered nail signs and symptoms that could signify a serious underlying condition.

After our original search and analysis, new nail topics, images, and videos have been added; therefore, there has been a positive trend toward new nail content being added to site, which will greatly benefit patients.

To the Editor:

Patients with skin, hair, or nail concerns often utilize online resources to self-diagnose or learn more about physician-diagnosed conditions. The American Academy of Dermatology (AAD) website offers the public access to informational pages categorized by disease or treatment (https://www.aad.org/public). We sought to evaluate the nail content by searching the Patients and Public section of the AAD website to qualitatively and quantitatively describe mentions of nail conditions. Psoriasis, psoriatic arthritis, atopic dermatitis, and ringworm content also were analyzed and compared to nail content. The analysis was performed on September 7, 2019.

Of the 73 topics listed in the Diseases and Treatments section of the site, 17 (23%) specifically mentioned nail symptoms or pathology (Table). Three additional topics—atopic dermatitis, cellulitis, and neurodermatitis—recommended keeping nails short to prevent injury from scratching. There was 1 mention of obtaining fungal cultures, 2 of nail scraping microscopy, 2 of nail clippings, and 2 of nail-related cancers. There were no mentions of nail biopsies. The total number of unique clinical images across all sections was 300, with 12 of nails. The video library contained 84 videos, of which 6 focused on nail health.



Several sections were reviewed for overall content to understand the typical number of images and videos included for other common conditions. The general psoriasis section included 6 images and 3 videos detailing disease etiology, symptoms, and treatments, without depictions of nails. The psoriatic arthritis section included 8 images and 1 video as well as 1 image of nail pitting. The atopic dermatitis section included 6 images and 6 videos on disease etiology, symptoms, and treatment. The ringworm section, which collectively included all tinea infections, contained 11 images and 1 video on symptoms. In contrast, the only nail-specific section—nail fungus—contained only 2 images and 1 video.

Our study demonstrated that nail content is underrepresented in the public education section of the AAD website. If patients are unable to find nail disease material on the AAD website, they may seek alternative sources that are unreliable. Prior studies have shown that patient Internet resources for subungual melanoma and onychomycosis often are inadequate in quality and readability.1,2

Representative photographs and key information on common nail diseases could be added to improve patient education. The atopic dermatitis section should include text on related nail changes with accompanying images. We also recommend including paronychia information and images as either a separate topic or in the cellulitis section. The contact dermatitis section mentions nail cosmetics as causative factors, but an image of roller-coaster onycholysis may be more helpful.3 Although the alopecia areata section mentions nail changes, this information should be added to the general hair loss section of the site, as many patients may initially seek out the latter category. Herpes simplex may affect nails, and an image showing these changes would be instructive. In addition, pyogenic granulomas and paronychia occur with isotretinoin use.4



Many of the included images were not representative of common clinical findings. The nail lichen planus image showed pitting instead of more typical findings of nail plate atrophy and pterygium. The nail melanoma image showed thickened yellow toenails and the fifth toenail with a thin gray-brown band instead of an isolated wide black band. The nail fungus section included images of superficial onychomycosis and severe onychodystrophy instead of showing more common changes such as distal onycholysis with subungual hyperkeratosis, which is typical of the most common subtype, distal lateral subungual onychomycosis.5 Onychomycosis was referenced again in the ringworm section with 1 image repeated from the nail fungus section and another image that appeared to be a subungual hematoma.

The AAD website offers important patient education resources; however, nail content is underrepresented on this platform. Dermatologists are experts on nail disease, and increased efforts are needed to educate the public about frequently encountered nail signs and symptoms that could signify a serious underlying condition.

After our original search and analysis, new nail topics, images, and videos have been added; therefore, there has been a positive trend toward new nail content being added to site, which will greatly benefit patients.

References
  1. Kang R, Lipner S. Assessment of internet sources on subungual melanoma [published online August 30, 2018]. Melanoma Res. doi:10.1097/CMR.0000000000000508.
  2. Kang R, Lipner S. Evaluation of onychomycosis information on the internet. J Drugs Dermatol. 2019;18:484-487.
  3. Rieder EA, Tosti A. Cosmetically induced disorders of the nail with update on contemporary nail manicures. J Clin Aesthet Dermatol. 2016;9:39-44.
  4. Arias-Santiago S, Husein-ElAhmed H, Aneiros-Cachaza J, et al. Uncommon side effects of isotretinoin therapy: paronychia and pyogenic granuloma. J Am Acad Dermatol. 2011;64:AB37.
  5. Lipner SR, Scher RK. Onychomycosis: clinical overview and diagnosis. J Am Acad Dermatol. 2019;80:835-851.
References
  1. Kang R, Lipner S. Assessment of internet sources on subungual melanoma [published online August 30, 2018]. Melanoma Res. doi:10.1097/CMR.0000000000000508.
  2. Kang R, Lipner S. Evaluation of onychomycosis information on the internet. J Drugs Dermatol. 2019;18:484-487.
  3. Rieder EA, Tosti A. Cosmetically induced disorders of the nail with update on contemporary nail manicures. J Clin Aesthet Dermatol. 2016;9:39-44.
  4. Arias-Santiago S, Husein-ElAhmed H, Aneiros-Cachaza J, et al. Uncommon side effects of isotretinoin therapy: paronychia and pyogenic granuloma. J Am Acad Dermatol. 2011;64:AB37.
  5. Lipner SR, Scher RK. Onychomycosis: clinical overview and diagnosis. J Am Acad Dermatol. 2019;80:835-851.
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  • Patients often utilize online resources to research skin, hair, and nail conditions.
  • Nail signs and symptoms may represent a serious underlying condition, and nail content is underrepresented on the American Academy of Dermatology (AAD) Patients and Public section of the website.
  • There is a need for more information on nail conditions on the AAD website, offering patients a more comprehensive online dermatology resource. Subsequently, there has been a positive trend toward new nail content being added to the site.
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New Insights Into the Dermatology Residency Application Process Amid the COVID-19 Pandemic

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Tue, 11/03/2020 - 13:48

Residency application is an arduous experience for many medical students. The National Resident Matching Program reported that US medical school seniors who matched into dermatology applied to a median of 90 programs and attended 9 interviews in 2019.1 High application and interview travel costs are a disadvantage for applicants from lower socioeconomic backgrounds. We propose that the coronavirus disease 2019 (COVID-19) pandemic should serve as a call to action for dermatology to update and promote a more equitable, time-effective, and cost-efficient residency interview process.

In light of COVID-19, dermatology residency program directors have recommended a holistic application review process, taking into consideration “disparities in strength of applications due to lack of opportunity for students with smaller home programs or in areas more affected by this crisis.”2 However, in a 2018 survey of 180 dermatology faculty members, 80% stated that time spent reviewing residency applications was already excessive.3 The Association of American Medical Colleges reported that for medical student applicants with US Medical Licensing Examination Step 1 scores lower than 237 or higher than 251, the value added by submitting one additional application beyond means of 43 (95% confidence interval [CI], 34-53) and 34 (95% CI, 28-41), respectively, is reduced relative to the value added by each application before reaching the point of diminishing returns.4 Therefore, we suggest limiting the number of applications per applicant to the upper bounds of the CI for the lower US Medical Licensing Examination Step 1 score (53), facilitating a more detailed review of fewer applications by each program and limiting student expenses.

On May 7, 2020, the Association of American Medical Colleges made a statement strongly encouraging medical school and teaching hospital faculty to conduct interviews through videoconferencing.5 Videoconferencing interviews (VCIs) minimize travel-associated health risks, providing a more equitable structure for applicants and programs in areas disproportionately impacted by the pandemic. In the 2018 survey of dermatology faculty members, only 11% believed that applicants interviewing virtually received equal consideration to those interviewing in person; a solution to this problem would be to mandate that all applicants use VCIs during the COVID-19 pandemic.3 This coming year, residency programs may elect to replace in-person interviews with VCIs, or they may utilize VCIs as screening tools to narrow down the applicant pool and for students to rank their preferred programs prior to an in-person interview. By inviting fewer applicants for in-person interviews, travel-associated health risks, financial costs, and missed educational activities would be minimized. Given that many medical students have had academic activities cancelled or postponed due to COVID-19, student opportunities for live clinical experiences should be maximized.

As programs plan for future application cycles beyond COVID-19, they must work to balance competing interests. Videoconferencing interviews allow for improved access to interviewing for applicants of lower socioeconomic classes, improved geographic mobility of applicants, and increased flexibility in accommodating faculty schedules with reduced time away from patient care and research; however, with VCIs one may lose the personal element that comes from the in-person interview, including interactions among applicants, faculty, current residents, and staff on the day of interview, as well as the departmental tour. Additionally, the quality of VCIs may be diminished by technical difficulties and the possibility of distractions, making standardization of the interview experience for applicants challenging.



The COVID-19 pandemic will surely leave its mark on the residency application cycle. We must take time now to collaborate and brainstorm creative solutions to maximize the equity and efficiency of the application process for both residency programs and students. We welcome reader feedback on these ideas and other possible solutions in the form of Letters to the Editor.

References
  1. National Resident Matching Program. Results of the 2019 NRMP Applicant Survey by Preferred Specialty and Applicant Type. Washington, DC: National Resident Matching Program; 2019. https://mk0nrmp3oyqui6wqfm.kinstacdn.com/wp-content/uploads/2019/06/Applicant-Survey-Report-2019.pdf. Accessed June 22, 2020.
  2. Association of American Medical Colleges. Specialty response to COVID-19: dermatology residency program director consensus statement on 2020-21 application cycle. https://aamc-orange.global.ssl.fastly.net/production/media/filer_
    public/0f/7b/0f7b547e-65b5-4d93-8247-951206e7f726/updated_dermatology_program_director_
    statement_on_2020-21_application_cycle_.pdf. Updated June 1, 2020. Accessed June 24, 2020.
  3. Rojek NW, Shinkai K, Fett N. Dermatology faculty and residents’ perspectives on the dermatology residency application process: a nationwide survey. J Am Acad Dermatol. 2018;79:157-159.
  4. Association of American Medical Colleges. Apply smart: data to consider when applying to residency. https://www.students-residents.aamc.org/applying-residency/filteredresult/apply-smart-data-consider-when-applying-residency/. Accessed June 22, 2020.
  5. Association of American Medical Colleges. Conducting interviews during the coronavirus pandemic. https://www.aamc.org/what-we-do/mission-areas/medical-education/conducting-interviews-during-coronavirus-pandemic/. Published May 7, 2020. Accessed June 22, 2020.
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From the Department of Dermatology, Weill Cornell Medical College, New York, New York.

The authors report no conflict of interest.

Correspondence: Shari R. Lipner, MD, PhD, Department of Dermatology, Weill Cornell Medicine, 1305 York Ave, 9th Floor, New York, NY 10021 (shl9032@med.cornell.edu).

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From the Department of Dermatology, Weill Cornell Medical College, New York, New York.

The authors report no conflict of interest.

Correspondence: Shari R. Lipner, MD, PhD, Department of Dermatology, Weill Cornell Medicine, 1305 York Ave, 9th Floor, New York, NY 10021 (shl9032@med.cornell.edu).

Author and Disclosure Information

From the Department of Dermatology, Weill Cornell Medical College, New York, New York.

The authors report no conflict of interest.

Correspondence: Shari R. Lipner, MD, PhD, Department of Dermatology, Weill Cornell Medicine, 1305 York Ave, 9th Floor, New York, NY 10021 (shl9032@med.cornell.edu).

Article PDF
Article PDF

Residency application is an arduous experience for many medical students. The National Resident Matching Program reported that US medical school seniors who matched into dermatology applied to a median of 90 programs and attended 9 interviews in 2019.1 High application and interview travel costs are a disadvantage for applicants from lower socioeconomic backgrounds. We propose that the coronavirus disease 2019 (COVID-19) pandemic should serve as a call to action for dermatology to update and promote a more equitable, time-effective, and cost-efficient residency interview process.

In light of COVID-19, dermatology residency program directors have recommended a holistic application review process, taking into consideration “disparities in strength of applications due to lack of opportunity for students with smaller home programs or in areas more affected by this crisis.”2 However, in a 2018 survey of 180 dermatology faculty members, 80% stated that time spent reviewing residency applications was already excessive.3 The Association of American Medical Colleges reported that for medical student applicants with US Medical Licensing Examination Step 1 scores lower than 237 or higher than 251, the value added by submitting one additional application beyond means of 43 (95% confidence interval [CI], 34-53) and 34 (95% CI, 28-41), respectively, is reduced relative to the value added by each application before reaching the point of diminishing returns.4 Therefore, we suggest limiting the number of applications per applicant to the upper bounds of the CI for the lower US Medical Licensing Examination Step 1 score (53), facilitating a more detailed review of fewer applications by each program and limiting student expenses.

On May 7, 2020, the Association of American Medical Colleges made a statement strongly encouraging medical school and teaching hospital faculty to conduct interviews through videoconferencing.5 Videoconferencing interviews (VCIs) minimize travel-associated health risks, providing a more equitable structure for applicants and programs in areas disproportionately impacted by the pandemic. In the 2018 survey of dermatology faculty members, only 11% believed that applicants interviewing virtually received equal consideration to those interviewing in person; a solution to this problem would be to mandate that all applicants use VCIs during the COVID-19 pandemic.3 This coming year, residency programs may elect to replace in-person interviews with VCIs, or they may utilize VCIs as screening tools to narrow down the applicant pool and for students to rank their preferred programs prior to an in-person interview. By inviting fewer applicants for in-person interviews, travel-associated health risks, financial costs, and missed educational activities would be minimized. Given that many medical students have had academic activities cancelled or postponed due to COVID-19, student opportunities for live clinical experiences should be maximized.

As programs plan for future application cycles beyond COVID-19, they must work to balance competing interests. Videoconferencing interviews allow for improved access to interviewing for applicants of lower socioeconomic classes, improved geographic mobility of applicants, and increased flexibility in accommodating faculty schedules with reduced time away from patient care and research; however, with VCIs one may lose the personal element that comes from the in-person interview, including interactions among applicants, faculty, current residents, and staff on the day of interview, as well as the departmental tour. Additionally, the quality of VCIs may be diminished by technical difficulties and the possibility of distractions, making standardization of the interview experience for applicants challenging.



The COVID-19 pandemic will surely leave its mark on the residency application cycle. We must take time now to collaborate and brainstorm creative solutions to maximize the equity and efficiency of the application process for both residency programs and students. We welcome reader feedback on these ideas and other possible solutions in the form of Letters to the Editor.

Residency application is an arduous experience for many medical students. The National Resident Matching Program reported that US medical school seniors who matched into dermatology applied to a median of 90 programs and attended 9 interviews in 2019.1 High application and interview travel costs are a disadvantage for applicants from lower socioeconomic backgrounds. We propose that the coronavirus disease 2019 (COVID-19) pandemic should serve as a call to action for dermatology to update and promote a more equitable, time-effective, and cost-efficient residency interview process.

In light of COVID-19, dermatology residency program directors have recommended a holistic application review process, taking into consideration “disparities in strength of applications due to lack of opportunity for students with smaller home programs or in areas more affected by this crisis.”2 However, in a 2018 survey of 180 dermatology faculty members, 80% stated that time spent reviewing residency applications was already excessive.3 The Association of American Medical Colleges reported that for medical student applicants with US Medical Licensing Examination Step 1 scores lower than 237 or higher than 251, the value added by submitting one additional application beyond means of 43 (95% confidence interval [CI], 34-53) and 34 (95% CI, 28-41), respectively, is reduced relative to the value added by each application before reaching the point of diminishing returns.4 Therefore, we suggest limiting the number of applications per applicant to the upper bounds of the CI for the lower US Medical Licensing Examination Step 1 score (53), facilitating a more detailed review of fewer applications by each program and limiting student expenses.

On May 7, 2020, the Association of American Medical Colleges made a statement strongly encouraging medical school and teaching hospital faculty to conduct interviews through videoconferencing.5 Videoconferencing interviews (VCIs) minimize travel-associated health risks, providing a more equitable structure for applicants and programs in areas disproportionately impacted by the pandemic. In the 2018 survey of dermatology faculty members, only 11% believed that applicants interviewing virtually received equal consideration to those interviewing in person; a solution to this problem would be to mandate that all applicants use VCIs during the COVID-19 pandemic.3 This coming year, residency programs may elect to replace in-person interviews with VCIs, or they may utilize VCIs as screening tools to narrow down the applicant pool and for students to rank their preferred programs prior to an in-person interview. By inviting fewer applicants for in-person interviews, travel-associated health risks, financial costs, and missed educational activities would be minimized. Given that many medical students have had academic activities cancelled or postponed due to COVID-19, student opportunities for live clinical experiences should be maximized.

As programs plan for future application cycles beyond COVID-19, they must work to balance competing interests. Videoconferencing interviews allow for improved access to interviewing for applicants of lower socioeconomic classes, improved geographic mobility of applicants, and increased flexibility in accommodating faculty schedules with reduced time away from patient care and research; however, with VCIs one may lose the personal element that comes from the in-person interview, including interactions among applicants, faculty, current residents, and staff on the day of interview, as well as the departmental tour. Additionally, the quality of VCIs may be diminished by technical difficulties and the possibility of distractions, making standardization of the interview experience for applicants challenging.



The COVID-19 pandemic will surely leave its mark on the residency application cycle. We must take time now to collaborate and brainstorm creative solutions to maximize the equity and efficiency of the application process for both residency programs and students. We welcome reader feedback on these ideas and other possible solutions in the form of Letters to the Editor.

References
  1. National Resident Matching Program. Results of the 2019 NRMP Applicant Survey by Preferred Specialty and Applicant Type. Washington, DC: National Resident Matching Program; 2019. https://mk0nrmp3oyqui6wqfm.kinstacdn.com/wp-content/uploads/2019/06/Applicant-Survey-Report-2019.pdf. Accessed June 22, 2020.
  2. Association of American Medical Colleges. Specialty response to COVID-19: dermatology residency program director consensus statement on 2020-21 application cycle. https://aamc-orange.global.ssl.fastly.net/production/media/filer_
    public/0f/7b/0f7b547e-65b5-4d93-8247-951206e7f726/updated_dermatology_program_director_
    statement_on_2020-21_application_cycle_.pdf. Updated June 1, 2020. Accessed June 24, 2020.
  3. Rojek NW, Shinkai K, Fett N. Dermatology faculty and residents’ perspectives on the dermatology residency application process: a nationwide survey. J Am Acad Dermatol. 2018;79:157-159.
  4. Association of American Medical Colleges. Apply smart: data to consider when applying to residency. https://www.students-residents.aamc.org/applying-residency/filteredresult/apply-smart-data-consider-when-applying-residency/. Accessed June 22, 2020.
  5. Association of American Medical Colleges. Conducting interviews during the coronavirus pandemic. https://www.aamc.org/what-we-do/mission-areas/medical-education/conducting-interviews-during-coronavirus-pandemic/. Published May 7, 2020. Accessed June 22, 2020.
References
  1. National Resident Matching Program. Results of the 2019 NRMP Applicant Survey by Preferred Specialty and Applicant Type. Washington, DC: National Resident Matching Program; 2019. https://mk0nrmp3oyqui6wqfm.kinstacdn.com/wp-content/uploads/2019/06/Applicant-Survey-Report-2019.pdf. Accessed June 22, 2020.
  2. Association of American Medical Colleges. Specialty response to COVID-19: dermatology residency program director consensus statement on 2020-21 application cycle. https://aamc-orange.global.ssl.fastly.net/production/media/filer_
    public/0f/7b/0f7b547e-65b5-4d93-8247-951206e7f726/updated_dermatology_program_director_
    statement_on_2020-21_application_cycle_.pdf. Updated June 1, 2020. Accessed June 24, 2020.
  3. Rojek NW, Shinkai K, Fett N. Dermatology faculty and residents’ perspectives on the dermatology residency application process: a nationwide survey. J Am Acad Dermatol. 2018;79:157-159.
  4. Association of American Medical Colleges. Apply smart: data to consider when applying to residency. https://www.students-residents.aamc.org/applying-residency/filteredresult/apply-smart-data-consider-when-applying-residency/. Accessed June 22, 2020.
  5. Association of American Medical Colleges. Conducting interviews during the coronavirus pandemic. https://www.aamc.org/what-we-do/mission-areas/medical-education/conducting-interviews-during-coronavirus-pandemic/. Published May 7, 2020. Accessed June 22, 2020.
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  • We propose that the coronavirus disease 2019 pandemic should serve as a call to action for dermatology to update and promote a more equitable, time-effective, and cost-efficient residency interview process.
  • A limitation on the number of applications per candidate may lower expenses and allow for a more holistic review process by residency programs.
  • The benefits and challenges of videoconferencing interviews must be weighed as residency programs decide on their continued use beyond this application cycle.
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Brilliant Green Staining of the Fingernails

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Case Report

A 92-year-old Eastern European woman presented to our nail clinic with a history of onychodystrophy and arthralgia of the digits of several months’ duration. Her dermatologic history was notable for irritant hand dermatitis. A prior nail plate clipping with histopathologic examination was negative for fungal elements. Physical examination revealed onychorrhexis of all fingernails as well as onycholysis and subungual hyperkeratosis of the right fourth fingernail. Blue-green staining was incidentally noted on the right second and third fingernails and nail folds (Figure 1). Contact dermoscopy using ultrasound gel revealed translucent areas with sparse pigment, though denser areas had a fine branching pattern (Figure 2). When questioned, the patient reported use of “zelyonka,” a brilliant green solution, to self-treat the nails. Histopathology on repeat nail clippings showed parakeratosis and serum, which was most consistent with her known history of irritant hand dermatitis. Radiographs of the hands revealed osteoarthritis that was most prominent at the distal interphalangeal joints.

Figure 1. Blue-green staining on the right second and third fingernails and nail folds from use of brilliant green to self-treat onychodystrophy.
Figure 2. Contact dermoscopy showed translucent areas with sparse pigment and denser areas with a fine branching pattern.

Comment

Brilliant green is a triphenylmethane dye commonly used in Eastern Europe and other regions for the treatment of superficial skin infections and onychomycosis.1 Its use as an antiseptic and wound healing agent has been investigated in the scientific literature since at least the early 20th century.2 Brilliant green typically is applied in a 0.1% to 2% ethanol solution.1 The dye has bactericidal activity against gram-positive organisms, particularly staphylococci and streptococci.2,3 It has been used for the treatment of fungal skin and nail infections since at least the early 20th century, with anecdotal success.4 Although there have been no studies investigating use of brilliant green alone for the treatment of onychomycosis, it is sometimes used in combination with conventional oral agents for this purpose.5 Because of its availability, safety, ease of use, and low cost, brilliant green has been promoted as an antiseptic in resource-poor settings.3 The revival of brilliant green and other antiseptic dyes in these settings has been suggested as an alternative to oral antibiotic agents, to which resistance is rising, and as a potential cancer therapy.6,7 Although brilliant green’s mechanism of action in treating skin infections is unclear, it has been shown to form covalent adducts with thioredoxin reductase 2, a protein conserved from bacteria to humans with an essential function for cellular activity.7

Early case studies suggested that brilliant green was beneficial in treating wounds2; however, this indication is controversial. In a guinea pig study, brilliant green was shown to inhibit wound healing and the formation of granulation tissue.8 It also should be noted that when used topically, brilliant green may cause skin sensitization, necrotic skin reactions, and permanent staining of clothing. It has no known anti-inflammatory properties and also may cause skin irritation.8 Brilliant green may cause blindness if it comes in contact with the eyes.1

Brilliant green has other potential dermatologic indications. For example, a combination of brilliant green and gentian violet, a related dye, has demonstrated efficacy in the treatment of cutaneous hemangiomas in mouse models by blocking expression of angiopoietin-2.7

Dermatologists should be familiar with brilliant green and its common uses as well as adverse effects. Brilliant green is commercially available for a low cost ($5 to $20) in specialty pharmacies or online (eg, Amazon). It is sold alone or in combination with gentian violet and proflavine hemisulfate, and a prescription is not required. Due to its low cost and accessibility, patients may use brilliant green to self-treat dermatologic conditions. Green nails due to staining with brilliant green dye must be distinguished from other etiologies causing green nail discoloration, such as infection with Pseudomonas aeruginosa or Aspergillus, bullous disorders, jaundice, “old” hematomas, nail polish, and other exogenous pigments.

References
  1. Balabanova M, Popova L, Tchipeva R. Dyes in dermatology. Clin Dermatol. 2003;21:2-6.
  2. Browning CH, Gulbransen R, Kennaway EL, et al. Flavine and brilliant green, powerful antiseptics with low toxicity to the tissues: their use in the treatment of infected wounds. Br Med J. 1917;1:73-78.
  3. Bakker P, Doorne H, Gooskens V, et al. Activity of gentian violet and brilliant green against some microorganisms associated with skin infections. Int J Dermatol. 1992;31:210-213.
  4. Montgomery RM, Casper EA. Cutaneous manifestations of the fungi causing dermatophytosis and onychomycosis and their treatment. J Am Med Assoc. 1945;128:77-83.
  5. Tchernev G, Cardoso JC, Ali MM, et al. Primary onychomycosis with granulomatous Tinea faciei. Braz J Infect Dis. 2010;14:546-547.
  6. Berrios RL, Arbiser JL. Effectiveness of gentian violet and similar products commonly used to treat pyodermas. Dermatol Clin. 2011;29:69-73.
  7. Maley AM, Arbiser JL. Gentian violet: a 19th century drug re-emerges in the 21st century. Exp Dermatol. 2013;22:775-80.
  8. Niedner R, Schöpf E. Inhibition of wound healing by antiseptics. Br J Dermatol. 1986;115:41-44
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The authors report no conflict of interest.

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Case Report

A 92-year-old Eastern European woman presented to our nail clinic with a history of onychodystrophy and arthralgia of the digits of several months’ duration. Her dermatologic history was notable for irritant hand dermatitis. A prior nail plate clipping with histopathologic examination was negative for fungal elements. Physical examination revealed onychorrhexis of all fingernails as well as onycholysis and subungual hyperkeratosis of the right fourth fingernail. Blue-green staining was incidentally noted on the right second and third fingernails and nail folds (Figure 1). Contact dermoscopy using ultrasound gel revealed translucent areas with sparse pigment, though denser areas had a fine branching pattern (Figure 2). When questioned, the patient reported use of “zelyonka,” a brilliant green solution, to self-treat the nails. Histopathology on repeat nail clippings showed parakeratosis and serum, which was most consistent with her known history of irritant hand dermatitis. Radiographs of the hands revealed osteoarthritis that was most prominent at the distal interphalangeal joints.

Figure 1. Blue-green staining on the right second and third fingernails and nail folds from use of brilliant green to self-treat onychodystrophy.
Figure 2. Contact dermoscopy showed translucent areas with sparse pigment and denser areas with a fine branching pattern.

Comment

Brilliant green is a triphenylmethane dye commonly used in Eastern Europe and other regions for the treatment of superficial skin infections and onychomycosis.1 Its use as an antiseptic and wound healing agent has been investigated in the scientific literature since at least the early 20th century.2 Brilliant green typically is applied in a 0.1% to 2% ethanol solution.1 The dye has bactericidal activity against gram-positive organisms, particularly staphylococci and streptococci.2,3 It has been used for the treatment of fungal skin and nail infections since at least the early 20th century, with anecdotal success.4 Although there have been no studies investigating use of brilliant green alone for the treatment of onychomycosis, it is sometimes used in combination with conventional oral agents for this purpose.5 Because of its availability, safety, ease of use, and low cost, brilliant green has been promoted as an antiseptic in resource-poor settings.3 The revival of brilliant green and other antiseptic dyes in these settings has been suggested as an alternative to oral antibiotic agents, to which resistance is rising, and as a potential cancer therapy.6,7 Although brilliant green’s mechanism of action in treating skin infections is unclear, it has been shown to form covalent adducts with thioredoxin reductase 2, a protein conserved from bacteria to humans with an essential function for cellular activity.7

Early case studies suggested that brilliant green was beneficial in treating wounds2; however, this indication is controversial. In a guinea pig study, brilliant green was shown to inhibit wound healing and the formation of granulation tissue.8 It also should be noted that when used topically, brilliant green may cause skin sensitization, necrotic skin reactions, and permanent staining of clothing. It has no known anti-inflammatory properties and also may cause skin irritation.8 Brilliant green may cause blindness if it comes in contact with the eyes.1

Brilliant green has other potential dermatologic indications. For example, a combination of brilliant green and gentian violet, a related dye, has demonstrated efficacy in the treatment of cutaneous hemangiomas in mouse models by blocking expression of angiopoietin-2.7

Dermatologists should be familiar with brilliant green and its common uses as well as adverse effects. Brilliant green is commercially available for a low cost ($5 to $20) in specialty pharmacies or online (eg, Amazon). It is sold alone or in combination with gentian violet and proflavine hemisulfate, and a prescription is not required. Due to its low cost and accessibility, patients may use brilliant green to self-treat dermatologic conditions. Green nails due to staining with brilliant green dye must be distinguished from other etiologies causing green nail discoloration, such as infection with Pseudomonas aeruginosa or Aspergillus, bullous disorders, jaundice, “old” hematomas, nail polish, and other exogenous pigments.

Case Report

A 92-year-old Eastern European woman presented to our nail clinic with a history of onychodystrophy and arthralgia of the digits of several months’ duration. Her dermatologic history was notable for irritant hand dermatitis. A prior nail plate clipping with histopathologic examination was negative for fungal elements. Physical examination revealed onychorrhexis of all fingernails as well as onycholysis and subungual hyperkeratosis of the right fourth fingernail. Blue-green staining was incidentally noted on the right second and third fingernails and nail folds (Figure 1). Contact dermoscopy using ultrasound gel revealed translucent areas with sparse pigment, though denser areas had a fine branching pattern (Figure 2). When questioned, the patient reported use of “zelyonka,” a brilliant green solution, to self-treat the nails. Histopathology on repeat nail clippings showed parakeratosis and serum, which was most consistent with her known history of irritant hand dermatitis. Radiographs of the hands revealed osteoarthritis that was most prominent at the distal interphalangeal joints.

Figure 1. Blue-green staining on the right second and third fingernails and nail folds from use of brilliant green to self-treat onychodystrophy.
Figure 2. Contact dermoscopy showed translucent areas with sparse pigment and denser areas with a fine branching pattern.

Comment

Brilliant green is a triphenylmethane dye commonly used in Eastern Europe and other regions for the treatment of superficial skin infections and onychomycosis.1 Its use as an antiseptic and wound healing agent has been investigated in the scientific literature since at least the early 20th century.2 Brilliant green typically is applied in a 0.1% to 2% ethanol solution.1 The dye has bactericidal activity against gram-positive organisms, particularly staphylococci and streptococci.2,3 It has been used for the treatment of fungal skin and nail infections since at least the early 20th century, with anecdotal success.4 Although there have been no studies investigating use of brilliant green alone for the treatment of onychomycosis, it is sometimes used in combination with conventional oral agents for this purpose.5 Because of its availability, safety, ease of use, and low cost, brilliant green has been promoted as an antiseptic in resource-poor settings.3 The revival of brilliant green and other antiseptic dyes in these settings has been suggested as an alternative to oral antibiotic agents, to which resistance is rising, and as a potential cancer therapy.6,7 Although brilliant green’s mechanism of action in treating skin infections is unclear, it has been shown to form covalent adducts with thioredoxin reductase 2, a protein conserved from bacteria to humans with an essential function for cellular activity.7

Early case studies suggested that brilliant green was beneficial in treating wounds2; however, this indication is controversial. In a guinea pig study, brilliant green was shown to inhibit wound healing and the formation of granulation tissue.8 It also should be noted that when used topically, brilliant green may cause skin sensitization, necrotic skin reactions, and permanent staining of clothing. It has no known anti-inflammatory properties and also may cause skin irritation.8 Brilliant green may cause blindness if it comes in contact with the eyes.1

Brilliant green has other potential dermatologic indications. For example, a combination of brilliant green and gentian violet, a related dye, has demonstrated efficacy in the treatment of cutaneous hemangiomas in mouse models by blocking expression of angiopoietin-2.7

Dermatologists should be familiar with brilliant green and its common uses as well as adverse effects. Brilliant green is commercially available for a low cost ($5 to $20) in specialty pharmacies or online (eg, Amazon). It is sold alone or in combination with gentian violet and proflavine hemisulfate, and a prescription is not required. Due to its low cost and accessibility, patients may use brilliant green to self-treat dermatologic conditions. Green nails due to staining with brilliant green dye must be distinguished from other etiologies causing green nail discoloration, such as infection with Pseudomonas aeruginosa or Aspergillus, bullous disorders, jaundice, “old” hematomas, nail polish, and other exogenous pigments.

References
  1. Balabanova M, Popova L, Tchipeva R. Dyes in dermatology. Clin Dermatol. 2003;21:2-6.
  2. Browning CH, Gulbransen R, Kennaway EL, et al. Flavine and brilliant green, powerful antiseptics with low toxicity to the tissues: their use in the treatment of infected wounds. Br Med J. 1917;1:73-78.
  3. Bakker P, Doorne H, Gooskens V, et al. Activity of gentian violet and brilliant green against some microorganisms associated with skin infections. Int J Dermatol. 1992;31:210-213.
  4. Montgomery RM, Casper EA. Cutaneous manifestations of the fungi causing dermatophytosis and onychomycosis and their treatment. J Am Med Assoc. 1945;128:77-83.
  5. Tchernev G, Cardoso JC, Ali MM, et al. Primary onychomycosis with granulomatous Tinea faciei. Braz J Infect Dis. 2010;14:546-547.
  6. Berrios RL, Arbiser JL. Effectiveness of gentian violet and similar products commonly used to treat pyodermas. Dermatol Clin. 2011;29:69-73.
  7. Maley AM, Arbiser JL. Gentian violet: a 19th century drug re-emerges in the 21st century. Exp Dermatol. 2013;22:775-80.
  8. Niedner R, Schöpf E. Inhibition of wound healing by antiseptics. Br J Dermatol. 1986;115:41-44
References
  1. Balabanova M, Popova L, Tchipeva R. Dyes in dermatology. Clin Dermatol. 2003;21:2-6.
  2. Browning CH, Gulbransen R, Kennaway EL, et al. Flavine and brilliant green, powerful antiseptics with low toxicity to the tissues: their use in the treatment of infected wounds. Br Med J. 1917;1:73-78.
  3. Bakker P, Doorne H, Gooskens V, et al. Activity of gentian violet and brilliant green against some microorganisms associated with skin infections. Int J Dermatol. 1992;31:210-213.
  4. Montgomery RM, Casper EA. Cutaneous manifestations of the fungi causing dermatophytosis and onychomycosis and their treatment. J Am Med Assoc. 1945;128:77-83.
  5. Tchernev G, Cardoso JC, Ali MM, et al. Primary onychomycosis with granulomatous Tinea faciei. Braz J Infect Dis. 2010;14:546-547.
  6. Berrios RL, Arbiser JL. Effectiveness of gentian violet and similar products commonly used to treat pyodermas. Dermatol Clin. 2011;29:69-73.
  7. Maley AM, Arbiser JL. Gentian violet: a 19th century drug re-emerges in the 21st century. Exp Dermatol. 2013;22:775-80.
  8. Niedner R, Schöpf E. Inhibition of wound healing by antiseptics. Br J Dermatol. 1986;115:41-44
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  • Chloronychia, or green nail syndrome, is due to Pseudomonas aeruginosaPalatino LT Std infection and is a common etiology of green nail discoloration. Green nail discoloration also may be secondary to use of the antiseptic dye brilliant green.
  • Brilliant green is bactericidal but has no known antifungal or anti-inflammatory activity; it should be considered in the differential diagnosis of green nail discoloration and also may cause blindness with eye contact.
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Utilization of a Stress Ball to Diminish Anxiety During Nail Surgery

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Utilization of a Stress Ball to Diminish Anxiety During Nail Surgery

Practice Gap

Anxiety is common in patients undergoing surgery with general anesthesia and may be exacerbated in patients undergoing dermatologic surgery with local anesthesia. Apprehension might be worse for nail surgery patients because the nail unit is highly innervated and vascular. Many patients fear the anesthetic injections, and there often is pain postoperatively. Perioperative anxiety correlates with increased postoperative pain,1 analgesic use,2 and delayed recovery.3 Several alternatives have been proposed to decrease perioperative anxiety, including nonpharmacologic interventions such as using educational videos, personalized music, hand holding, art activities, and virtual reality, as well as pharmacologic interventions such as benzodiazepines. However, these techniques have not been well studied for nail surgery.

The Technique

Patients generally are anxious about nail surgery secondary to the pain associated with the local anesthetic infiltration; hence, it is crucial to decrease anxiety during this initial step. In our practice, we provide patients with a palm-sized stress ball made of closed-cell polyurethane foam rubber before surgery. Patients are then instructed to hold the stress ball with the free hand and squeeze it whenever they feel anxious or when they feel any discomfort related to the procedure (Figure). A variety of balls can be bought for less than $1 each, thus making it a cost-effective option.

A patient holding a stress ball with the free hand while the nail surgeon is infiltrating the affected nail unit with the local anesthetic agent.

Practice Implications

Holding a stress ball has been found to reduce both pain and anxiety in patients undergoing conscious surgery.4 Furthermore, squeezing a stress ball perioperatively may increase feelings of empowerment, given that patients have direct control over the object, which in turn may have a positive effect on anxiety and patient satisfaction without interfering with the surgical procedure.5 Holding a stress ball is a safe, widely accessible, and inexpensive technique that may aid in decreasing patients’ anxiety related to nail surgery. Nonetheless, controlled clinical trials assessing the efficacy of this method in reducing anxiety related to nail surgery are needed to determine its benefit compared to other methods.

References
  1. Carr EC, Nicky Thomas V, Wilson-Barnet J. Patient experiences of anxiety, depression and acute pain after surgery: a longitudinal perspective. Int J Nurs Stud. 2005;42:521-530.
  2. Powell R, Johnston M, Smith WC, et al. Psychological risk factors for chronic post-surgical pain after inguinal hernia repair surgery: a prospective cohort study. Eur J Pain. 2012;16:600-610.
  3. Mavros MN, Athanasiou S, Gkegkes ID, et al. Do psychological variables affect early surgical recovery? PLoS One. 2011;6:e20306.
  4. Hudson BF, Ogden J, Whiteley MS. Randomized controlled trial to compare the effect of simple distraction interventions on pain and anxiety experienced during conscious surgery. Eur J Pain. 2015;19:1447-1455.
  5. Foy CR, Timmins F. Improving communication in day surgery settings. Nurs Stand. 2004;19:37-42.
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The authors report no conflict of interest.

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Practice Gap

Anxiety is common in patients undergoing surgery with general anesthesia and may be exacerbated in patients undergoing dermatologic surgery with local anesthesia. Apprehension might be worse for nail surgery patients because the nail unit is highly innervated and vascular. Many patients fear the anesthetic injections, and there often is pain postoperatively. Perioperative anxiety correlates with increased postoperative pain,1 analgesic use,2 and delayed recovery.3 Several alternatives have been proposed to decrease perioperative anxiety, including nonpharmacologic interventions such as using educational videos, personalized music, hand holding, art activities, and virtual reality, as well as pharmacologic interventions such as benzodiazepines. However, these techniques have not been well studied for nail surgery.

The Technique

Patients generally are anxious about nail surgery secondary to the pain associated with the local anesthetic infiltration; hence, it is crucial to decrease anxiety during this initial step. In our practice, we provide patients with a palm-sized stress ball made of closed-cell polyurethane foam rubber before surgery. Patients are then instructed to hold the stress ball with the free hand and squeeze it whenever they feel anxious or when they feel any discomfort related to the procedure (Figure). A variety of balls can be bought for less than $1 each, thus making it a cost-effective option.

A patient holding a stress ball with the free hand while the nail surgeon is infiltrating the affected nail unit with the local anesthetic agent.

Practice Implications

Holding a stress ball has been found to reduce both pain and anxiety in patients undergoing conscious surgery.4 Furthermore, squeezing a stress ball perioperatively may increase feelings of empowerment, given that patients have direct control over the object, which in turn may have a positive effect on anxiety and patient satisfaction without interfering with the surgical procedure.5 Holding a stress ball is a safe, widely accessible, and inexpensive technique that may aid in decreasing patients’ anxiety related to nail surgery. Nonetheless, controlled clinical trials assessing the efficacy of this method in reducing anxiety related to nail surgery are needed to determine its benefit compared to other methods.

Practice Gap

Anxiety is common in patients undergoing surgery with general anesthesia and may be exacerbated in patients undergoing dermatologic surgery with local anesthesia. Apprehension might be worse for nail surgery patients because the nail unit is highly innervated and vascular. Many patients fear the anesthetic injections, and there often is pain postoperatively. Perioperative anxiety correlates with increased postoperative pain,1 analgesic use,2 and delayed recovery.3 Several alternatives have been proposed to decrease perioperative anxiety, including nonpharmacologic interventions such as using educational videos, personalized music, hand holding, art activities, and virtual reality, as well as pharmacologic interventions such as benzodiazepines. However, these techniques have not been well studied for nail surgery.

The Technique

Patients generally are anxious about nail surgery secondary to the pain associated with the local anesthetic infiltration; hence, it is crucial to decrease anxiety during this initial step. In our practice, we provide patients with a palm-sized stress ball made of closed-cell polyurethane foam rubber before surgery. Patients are then instructed to hold the stress ball with the free hand and squeeze it whenever they feel anxious or when they feel any discomfort related to the procedure (Figure). A variety of balls can be bought for less than $1 each, thus making it a cost-effective option.

A patient holding a stress ball with the free hand while the nail surgeon is infiltrating the affected nail unit with the local anesthetic agent.

Practice Implications

Holding a stress ball has been found to reduce both pain and anxiety in patients undergoing conscious surgery.4 Furthermore, squeezing a stress ball perioperatively may increase feelings of empowerment, given that patients have direct control over the object, which in turn may have a positive effect on anxiety and patient satisfaction without interfering with the surgical procedure.5 Holding a stress ball is a safe, widely accessible, and inexpensive technique that may aid in decreasing patients’ anxiety related to nail surgery. Nonetheless, controlled clinical trials assessing the efficacy of this method in reducing anxiety related to nail surgery are needed to determine its benefit compared to other methods.

References
  1. Carr EC, Nicky Thomas V, Wilson-Barnet J. Patient experiences of anxiety, depression and acute pain after surgery: a longitudinal perspective. Int J Nurs Stud. 2005;42:521-530.
  2. Powell R, Johnston M, Smith WC, et al. Psychological risk factors for chronic post-surgical pain after inguinal hernia repair surgery: a prospective cohort study. Eur J Pain. 2012;16:600-610.
  3. Mavros MN, Athanasiou S, Gkegkes ID, et al. Do psychological variables affect early surgical recovery? PLoS One. 2011;6:e20306.
  4. Hudson BF, Ogden J, Whiteley MS. Randomized controlled trial to compare the effect of simple distraction interventions on pain and anxiety experienced during conscious surgery. Eur J Pain. 2015;19:1447-1455.
  5. Foy CR, Timmins F. Improving communication in day surgery settings. Nurs Stand. 2004;19:37-42.
References
  1. Carr EC, Nicky Thomas V, Wilson-Barnet J. Patient experiences of anxiety, depression and acute pain after surgery: a longitudinal perspective. Int J Nurs Stud. 2005;42:521-530.
  2. Powell R, Johnston M, Smith WC, et al. Psychological risk factors for chronic post-surgical pain after inguinal hernia repair surgery: a prospective cohort study. Eur J Pain. 2012;16:600-610.
  3. Mavros MN, Athanasiou S, Gkegkes ID, et al. Do psychological variables affect early surgical recovery? PLoS One. 2011;6:e20306.
  4. Hudson BF, Ogden J, Whiteley MS. Randomized controlled trial to compare the effect of simple distraction interventions on pain and anxiety experienced during conscious surgery. Eur J Pain. 2015;19:1447-1455.
  5. Foy CR, Timmins F. Improving communication in day surgery settings. Nurs Stand. 2004;19:37-42.
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Hand Hygiene in Preventing COVID-19 Transmission

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Hand Hygiene in Preventing COVID-19 Transmission

 

Handwashing with antimicrobial soaps or alcohol-based sanitizers is an effective measure in preventing microbial disease transmission. In the context of coronavirus disease 2019 (COVID-19) prevention, the World Health Organization and Centers for Disease Control and Prevention have recommended handwashing with soap and water after coughing/sneezing, visiting a public place, touching surfaces outside the home, and taking care of a sick person(s), as well as before and after eating. When soap and water are not available, alcohol-based sanitizers may be used.1,2

Irritant contact dermatitis (ICD) is most commonly associated with wet work and is frequently seen in health care workers in relation to hand hygiene, with survey-based studies reporting 25% to 55% of nurses affected.3-5 In a prospective study (N=102), health care workers who washed their hands more than 10 times per day were55% more likely to develop hand dermatitis.6 Frequent ICD of the hands has been reported in Chinese health care workers in association with COVID-19.7 Handwashing and/or glove wearing may be newly prioritized by workers who handle frequently touched goods and surfaces, such as flight attendants (Figure). Patients with obsessive-compulsive disorder may be another vulnerable population.8

A 62-year-old flight attendant with irritant contact hand dermatitis who reported frequent use of hand wipes due to fear of contracting coronavirus disease 2019. A skin fissure was noted on the right thumb.


Alcohol-based sanitizers and detergents or antimicrobials in soaps may cause ICD of the hands by denaturation of stratum corneum proteins, depletion of intercellular lipids, and decreased corneocyte cohesion. These agents alter the skin flora, with increased colonization by staphylococci and gram-negative bacilli.9 Clinical findings include xerosis, scaling, fissuring, and bleeding. Physicians may evaluate severity of ICD of the hands using the hand eczema severity index, with scores ranging from 0 to 360 based on involvement in 5 different hand zones.10

Cleansing the hands with alcohol-based sanitizers has consistently shown equivalent or greater efficacy than antimicrobial soaps for eradication of most microbes, with exception of bacterial spores and protozoan oocysts.11 In an in vivo experiment, 70% ethanol solution was more effective in eradicating rotavirus from the fingerpads of adults than 10% povidone-iodine solution, nonmedicated soaps, and soaps containing chloroxylenol 4.8% or chlorhexidine gluconate 4%.12 Coronavirus disease 2019 is a lipophilic enveloped virus. The lipid-dissolving effects of alcohol-based sanitizers is especially effective against these kinds of viruses. An in vitro experiment showed that alcohol solutions are effective against enveloped viruses including severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus.13 There are limited data for the virucidal efficacy of non–alcohol-based sanitizers containing quaternary ammonium compounds (most commonly benzalkonium chloride) and therefore they are not recommended for protection against COVID-19. Handwashing is preferred over alcohol-based solutions when hands are visibly dirty.

Alcohol-based sanitizers typically are less likely to cause ICD than handwashing with detergent-based or antimicrobial soaps. Antimicrobial ingredients in soaps such as chlorhexidine, chloroxylenol, and triclosan are frequent culprits.11 Detergents in soap such as sodium laureth sulfate cause more skin irritation and transepidermal water loss than alcohol14; however, among health care workers, alcohol-based sanitizers often are perceived as more damaging to the skin.15 During the 2014 Ebola outbreak, use of alcohol-based sanitizers vs handwashing resulted in lower hand eczema severity index scores (n=108).16



Propensity for ICD is a limiting factor in hand hygiene adherence.17 In a double-blind randomized trial (N=54), scheduled use of an oil-containing lotion was shown to increase compliance with hand hygiene protocols in health care workers by preventing cracks, scaling, and pain.18 Using sanitizers containing humectants (eg, aloe vera gel) or moisturizers with petrolatum, liquid paraffin, glycerin, or mineral oil have all been shown to decrease the incidence of ICD in frequent handwashers.19,20 Thorough hand drying also is important in preventing dermatitis. Drying with disposable paper towels is preferred over automated air dryers to prevent aerosolization of microbes.21 Because latex has been implicated in development of ICD, use of latex-free gloves is recommended.22

Alcohol-based sanitizer is not only an effective virucidal agent but also is less likely to cause ICD, therefore promoting hand hygiene adherence. Handwashing with soap still is necessary when hands are visibly dirty but should be performed less frequently if feasible. Hand hygiene and emollient usage education is important for physicians and patients alike, particularly during the COVID-19 crisis.

References
  1. Centers for Disease Control and Prevention. Coronavirus disease 2019. how to protect yourself & others. https://www.cdc.gov/coronavirus/2019-ncov/prepare/prevention.html. Updated April 13, 2020. Accessed April 21, 2020.
  2. World Health Organization. Coronavirus disease (COVID-19) advice for the public. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/advice-for-public. Updated March 31, 2020. Accessed April 21, 2020.
  3. Carøe TK, Ebbehøj NE, Bonde JPE, et al. Hand eczema and wet work: dose-response relationship and effect of leaving the profession. Contact Dermatitis. 2018;78:341-347.
  4. Larson E, Friedman C, Cohran J, et al. Prevalence and correlates of skin damage on the hands of nurses. Heart Lung. 1997;26:404-412.
  5. Lampel HP, Patel N, Boyse K, et al. Prevalence of hand dermatitis in inpatient nurses at a United States hospital. Dermatitis. 2007;18:140-142.
  6. Callahan A, Baron E, Fekedulegn D, et al. Winter season, frequent hand washing, and irritant patch test reactions to detergents are associated with hand dermatitis in health care workers. Dermatitis. 2013;24:170-175.
  7. Lan J, Song Z, Miao X, et al. Skin damage among healthcare workers managing coronavirus disease-2019 [published online March 18, 2020]. J Am Acad Dermatol. 2020;82:1215-1216.
  8. Katz RJ, Landau P, DeVeaugh-Geiss J, et al. Pharmacological responsiveness of dermatitis secondary to compulsive washing. Psychiatry Res. 1990;34:223-226.
  9. Larson EL, Hughes CA, Pyrek JD, et al. Changes in bacterial flora associated with skin damage on hands of health care personnel. Am J Infect Control. 1998;26:513-521.
  10. Held E, Skoet R, Johansen JD, et al. The hand eczema severity index (HECSI): a scoring system for clinical assessment of hand eczema. a study of inter- and intraobserver reliability. Br J Dermatol. 2005;152:302-307.
  11. Boyce JM, Pittet D, Healthcare Infection Control Practices Advisory Committee, et al. Guideline for Hand Hygiene in Health-Care Settings. Recommendations of the Healthcare Infection Control Practices Advisory Committee and the HIPAC/SHEA/APIC/IDSA Hand Hygiene Task Force. Am J Infect Control. 2002;30:S1-S46.
  12. Ansari SA, Sattar SA, Springthorpe VS, et al. Invivo protocol for testing efficacy of hand-washing agents against viruses and bacteria—experiments with rotavirus and Escherichi coli. Appl Environ Microbiol. 1989;55:3113-3118.
  13. Siddharta A, Pfaender S, Vielle NJ, et al. virucidal activity of world health organization-recommended formulations against enveloped viruses, including Zika, Ebola, and emerging coronaviruses. J Infect Dis. 2017;215:902-906.
  14. Pedersen LK, Held E, Johansen JD, et al. Less skin irritation from alcohol-based disinfectant than from detergent used for hand disinfection. Br J Dermatol. 2005;153:1142-1146.
  15. Stutz N, Becker D, Jappe U, et al. Nurses’ perceptions of the benefits and adverse effects of hand disinfection: alcohol-based hand rubs vs. hygienic handwashing: a multicentre questionnaire study with additional patch testing by the German Contact Dermatitis Research Group. Br J Dermatol. 2009;160:565-572.
  16. Wolfe MK, Wells E, Mitro B, et al. Seeking clearer recommendations for hand hygiene in communities facing Ebola: a randomized trial investigating the impact of six handwashing methods on skin irritation and dermatitis. PLoS One. 2016;11:e0167378.
  17. Pittet D, Allegranzi B, Storr J. The WHO Clean Care is Safer Care programme: field-testing to enhance sustainability and spread of hand hygiene improvements. J Infect Public Health. 2008;1:4-10.
  18. McCormick RD, Buchman TL, Maki DG. Double-blind, randomized trial of scheduled use of a novel barrier cream and an oil-containing lotion for protecting the hands of health care workers. Am J Infect Control. 2000;28:302-310.
  19. Berndt U, Wigger-Alberti W, Gabard B, et al. Efficacy of a barrier cream and its vehicle as protective measures against occupational irritant contact dermatitis. Contact Dermatitis. 2000;42:77-80.
  20. Kampf G, Ennen J. Regular use of a hand cream can attenuate skin dryness and roughness caused by frequent hand washing. BMC Dermatol. 2006;6:1.
  21. Gammon J, Hunt J. The neglected element of hand hygiene - significance of hand drying, efficiency of different methods, and clinical implication: a review. J Infect Prev. 2019;20:66-74.
  22. Elston DM. Letter from the editor: occupational skin disease among healthcare workers during the coronavirus (COVID-19) epidemic [published online March 18, 2020]. J Am Acad Dermatol. 2020;82:1085-1086.
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Mr. Gupta is from SUNY Downstate College of Medicine, Brooklyn. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

The authors report no conflict of interest.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Mr. Gupta is from SUNY Downstate College of Medicine, Brooklyn. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

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Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Handwashing with antimicrobial soaps or alcohol-based sanitizers is an effective measure in preventing microbial disease transmission. In the context of coronavirus disease 2019 (COVID-19) prevention, the World Health Organization and Centers for Disease Control and Prevention have recommended handwashing with soap and water after coughing/sneezing, visiting a public place, touching surfaces outside the home, and taking care of a sick person(s), as well as before and after eating. When soap and water are not available, alcohol-based sanitizers may be used.1,2

Irritant contact dermatitis (ICD) is most commonly associated with wet work and is frequently seen in health care workers in relation to hand hygiene, with survey-based studies reporting 25% to 55% of nurses affected.3-5 In a prospective study (N=102), health care workers who washed their hands more than 10 times per day were55% more likely to develop hand dermatitis.6 Frequent ICD of the hands has been reported in Chinese health care workers in association with COVID-19.7 Handwashing and/or glove wearing may be newly prioritized by workers who handle frequently touched goods and surfaces, such as flight attendants (Figure). Patients with obsessive-compulsive disorder may be another vulnerable population.8

A 62-year-old flight attendant with irritant contact hand dermatitis who reported frequent use of hand wipes due to fear of contracting coronavirus disease 2019. A skin fissure was noted on the right thumb.


Alcohol-based sanitizers and detergents or antimicrobials in soaps may cause ICD of the hands by denaturation of stratum corneum proteins, depletion of intercellular lipids, and decreased corneocyte cohesion. These agents alter the skin flora, with increased colonization by staphylococci and gram-negative bacilli.9 Clinical findings include xerosis, scaling, fissuring, and bleeding. Physicians may evaluate severity of ICD of the hands using the hand eczema severity index, with scores ranging from 0 to 360 based on involvement in 5 different hand zones.10

Cleansing the hands with alcohol-based sanitizers has consistently shown equivalent or greater efficacy than antimicrobial soaps for eradication of most microbes, with exception of bacterial spores and protozoan oocysts.11 In an in vivo experiment, 70% ethanol solution was more effective in eradicating rotavirus from the fingerpads of adults than 10% povidone-iodine solution, nonmedicated soaps, and soaps containing chloroxylenol 4.8% or chlorhexidine gluconate 4%.12 Coronavirus disease 2019 is a lipophilic enveloped virus. The lipid-dissolving effects of alcohol-based sanitizers is especially effective against these kinds of viruses. An in vitro experiment showed that alcohol solutions are effective against enveloped viruses including severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus.13 There are limited data for the virucidal efficacy of non–alcohol-based sanitizers containing quaternary ammonium compounds (most commonly benzalkonium chloride) and therefore they are not recommended for protection against COVID-19. Handwashing is preferred over alcohol-based solutions when hands are visibly dirty.

Alcohol-based sanitizers typically are less likely to cause ICD than handwashing with detergent-based or antimicrobial soaps. Antimicrobial ingredients in soaps such as chlorhexidine, chloroxylenol, and triclosan are frequent culprits.11 Detergents in soap such as sodium laureth sulfate cause more skin irritation and transepidermal water loss than alcohol14; however, among health care workers, alcohol-based sanitizers often are perceived as more damaging to the skin.15 During the 2014 Ebola outbreak, use of alcohol-based sanitizers vs handwashing resulted in lower hand eczema severity index scores (n=108).16



Propensity for ICD is a limiting factor in hand hygiene adherence.17 In a double-blind randomized trial (N=54), scheduled use of an oil-containing lotion was shown to increase compliance with hand hygiene protocols in health care workers by preventing cracks, scaling, and pain.18 Using sanitizers containing humectants (eg, aloe vera gel) or moisturizers with petrolatum, liquid paraffin, glycerin, or mineral oil have all been shown to decrease the incidence of ICD in frequent handwashers.19,20 Thorough hand drying also is important in preventing dermatitis. Drying with disposable paper towels is preferred over automated air dryers to prevent aerosolization of microbes.21 Because latex has been implicated in development of ICD, use of latex-free gloves is recommended.22

Alcohol-based sanitizer is not only an effective virucidal agent but also is less likely to cause ICD, therefore promoting hand hygiene adherence. Handwashing with soap still is necessary when hands are visibly dirty but should be performed less frequently if feasible. Hand hygiene and emollient usage education is important for physicians and patients alike, particularly during the COVID-19 crisis.

 

Handwashing with antimicrobial soaps or alcohol-based sanitizers is an effective measure in preventing microbial disease transmission. In the context of coronavirus disease 2019 (COVID-19) prevention, the World Health Organization and Centers for Disease Control and Prevention have recommended handwashing with soap and water after coughing/sneezing, visiting a public place, touching surfaces outside the home, and taking care of a sick person(s), as well as before and after eating. When soap and water are not available, alcohol-based sanitizers may be used.1,2

Irritant contact dermatitis (ICD) is most commonly associated with wet work and is frequently seen in health care workers in relation to hand hygiene, with survey-based studies reporting 25% to 55% of nurses affected.3-5 In a prospective study (N=102), health care workers who washed their hands more than 10 times per day were55% more likely to develop hand dermatitis.6 Frequent ICD of the hands has been reported in Chinese health care workers in association with COVID-19.7 Handwashing and/or glove wearing may be newly prioritized by workers who handle frequently touched goods and surfaces, such as flight attendants (Figure). Patients with obsessive-compulsive disorder may be another vulnerable population.8

A 62-year-old flight attendant with irritant contact hand dermatitis who reported frequent use of hand wipes due to fear of contracting coronavirus disease 2019. A skin fissure was noted on the right thumb.


Alcohol-based sanitizers and detergents or antimicrobials in soaps may cause ICD of the hands by denaturation of stratum corneum proteins, depletion of intercellular lipids, and decreased corneocyte cohesion. These agents alter the skin flora, with increased colonization by staphylococci and gram-negative bacilli.9 Clinical findings include xerosis, scaling, fissuring, and bleeding. Physicians may evaluate severity of ICD of the hands using the hand eczema severity index, with scores ranging from 0 to 360 based on involvement in 5 different hand zones.10

Cleansing the hands with alcohol-based sanitizers has consistently shown equivalent or greater efficacy than antimicrobial soaps for eradication of most microbes, with exception of bacterial spores and protozoan oocysts.11 In an in vivo experiment, 70% ethanol solution was more effective in eradicating rotavirus from the fingerpads of adults than 10% povidone-iodine solution, nonmedicated soaps, and soaps containing chloroxylenol 4.8% or chlorhexidine gluconate 4%.12 Coronavirus disease 2019 is a lipophilic enveloped virus. The lipid-dissolving effects of alcohol-based sanitizers is especially effective against these kinds of viruses. An in vitro experiment showed that alcohol solutions are effective against enveloped viruses including severe acute respiratory syndrome coronavirus, Ebola virus, and Zika virus.13 There are limited data for the virucidal efficacy of non–alcohol-based sanitizers containing quaternary ammonium compounds (most commonly benzalkonium chloride) and therefore they are not recommended for protection against COVID-19. Handwashing is preferred over alcohol-based solutions when hands are visibly dirty.

Alcohol-based sanitizers typically are less likely to cause ICD than handwashing with detergent-based or antimicrobial soaps. Antimicrobial ingredients in soaps such as chlorhexidine, chloroxylenol, and triclosan are frequent culprits.11 Detergents in soap such as sodium laureth sulfate cause more skin irritation and transepidermal water loss than alcohol14; however, among health care workers, alcohol-based sanitizers often are perceived as more damaging to the skin.15 During the 2014 Ebola outbreak, use of alcohol-based sanitizers vs handwashing resulted in lower hand eczema severity index scores (n=108).16



Propensity for ICD is a limiting factor in hand hygiene adherence.17 In a double-blind randomized trial (N=54), scheduled use of an oil-containing lotion was shown to increase compliance with hand hygiene protocols in health care workers by preventing cracks, scaling, and pain.18 Using sanitizers containing humectants (eg, aloe vera gel) or moisturizers with petrolatum, liquid paraffin, glycerin, or mineral oil have all been shown to decrease the incidence of ICD in frequent handwashers.19,20 Thorough hand drying also is important in preventing dermatitis. Drying with disposable paper towels is preferred over automated air dryers to prevent aerosolization of microbes.21 Because latex has been implicated in development of ICD, use of latex-free gloves is recommended.22

Alcohol-based sanitizer is not only an effective virucidal agent but also is less likely to cause ICD, therefore promoting hand hygiene adherence. Handwashing with soap still is necessary when hands are visibly dirty but should be performed less frequently if feasible. Hand hygiene and emollient usage education is important for physicians and patients alike, particularly during the COVID-19 crisis.

References
  1. Centers for Disease Control and Prevention. Coronavirus disease 2019. how to protect yourself & others. https://www.cdc.gov/coronavirus/2019-ncov/prepare/prevention.html. Updated April 13, 2020. Accessed April 21, 2020.
  2. World Health Organization. Coronavirus disease (COVID-19) advice for the public. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/advice-for-public. Updated March 31, 2020. Accessed April 21, 2020.
  3. Carøe TK, Ebbehøj NE, Bonde JPE, et al. Hand eczema and wet work: dose-response relationship and effect of leaving the profession. Contact Dermatitis. 2018;78:341-347.
  4. Larson E, Friedman C, Cohran J, et al. Prevalence and correlates of skin damage on the hands of nurses. Heart Lung. 1997;26:404-412.
  5. Lampel HP, Patel N, Boyse K, et al. Prevalence of hand dermatitis in inpatient nurses at a United States hospital. Dermatitis. 2007;18:140-142.
  6. Callahan A, Baron E, Fekedulegn D, et al. Winter season, frequent hand washing, and irritant patch test reactions to detergents are associated with hand dermatitis in health care workers. Dermatitis. 2013;24:170-175.
  7. Lan J, Song Z, Miao X, et al. Skin damage among healthcare workers managing coronavirus disease-2019 [published online March 18, 2020]. J Am Acad Dermatol. 2020;82:1215-1216.
  8. Katz RJ, Landau P, DeVeaugh-Geiss J, et al. Pharmacological responsiveness of dermatitis secondary to compulsive washing. Psychiatry Res. 1990;34:223-226.
  9. Larson EL, Hughes CA, Pyrek JD, et al. Changes in bacterial flora associated with skin damage on hands of health care personnel. Am J Infect Control. 1998;26:513-521.
  10. Held E, Skoet R, Johansen JD, et al. The hand eczema severity index (HECSI): a scoring system for clinical assessment of hand eczema. a study of inter- and intraobserver reliability. Br J Dermatol. 2005;152:302-307.
  11. Boyce JM, Pittet D, Healthcare Infection Control Practices Advisory Committee, et al. Guideline for Hand Hygiene in Health-Care Settings. Recommendations of the Healthcare Infection Control Practices Advisory Committee and the HIPAC/SHEA/APIC/IDSA Hand Hygiene Task Force. Am J Infect Control. 2002;30:S1-S46.
  12. Ansari SA, Sattar SA, Springthorpe VS, et al. Invivo protocol for testing efficacy of hand-washing agents against viruses and bacteria—experiments with rotavirus and Escherichi coli. Appl Environ Microbiol. 1989;55:3113-3118.
  13. Siddharta A, Pfaender S, Vielle NJ, et al. virucidal activity of world health organization-recommended formulations against enveloped viruses, including Zika, Ebola, and emerging coronaviruses. J Infect Dis. 2017;215:902-906.
  14. Pedersen LK, Held E, Johansen JD, et al. Less skin irritation from alcohol-based disinfectant than from detergent used for hand disinfection. Br J Dermatol. 2005;153:1142-1146.
  15. Stutz N, Becker D, Jappe U, et al. Nurses’ perceptions of the benefits and adverse effects of hand disinfection: alcohol-based hand rubs vs. hygienic handwashing: a multicentre questionnaire study with additional patch testing by the German Contact Dermatitis Research Group. Br J Dermatol. 2009;160:565-572.
  16. Wolfe MK, Wells E, Mitro B, et al. Seeking clearer recommendations for hand hygiene in communities facing Ebola: a randomized trial investigating the impact of six handwashing methods on skin irritation and dermatitis. PLoS One. 2016;11:e0167378.
  17. Pittet D, Allegranzi B, Storr J. The WHO Clean Care is Safer Care programme: field-testing to enhance sustainability and spread of hand hygiene improvements. J Infect Public Health. 2008;1:4-10.
  18. McCormick RD, Buchman TL, Maki DG. Double-blind, randomized trial of scheduled use of a novel barrier cream and an oil-containing lotion for protecting the hands of health care workers. Am J Infect Control. 2000;28:302-310.
  19. Berndt U, Wigger-Alberti W, Gabard B, et al. Efficacy of a barrier cream and its vehicle as protective measures against occupational irritant contact dermatitis. Contact Dermatitis. 2000;42:77-80.
  20. Kampf G, Ennen J. Regular use of a hand cream can attenuate skin dryness and roughness caused by frequent hand washing. BMC Dermatol. 2006;6:1.
  21. Gammon J, Hunt J. The neglected element of hand hygiene - significance of hand drying, efficiency of different methods, and clinical implication: a review. J Infect Prev. 2019;20:66-74.
  22. Elston DM. Letter from the editor: occupational skin disease among healthcare workers during the coronavirus (COVID-19) epidemic [published online March 18, 2020]. J Am Acad Dermatol. 2020;82:1085-1086.
References
  1. Centers for Disease Control and Prevention. Coronavirus disease 2019. how to protect yourself & others. https://www.cdc.gov/coronavirus/2019-ncov/prepare/prevention.html. Updated April 13, 2020. Accessed April 21, 2020.
  2. World Health Organization. Coronavirus disease (COVID-19) advice for the public. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/advice-for-public. Updated March 31, 2020. Accessed April 21, 2020.
  3. Carøe TK, Ebbehøj NE, Bonde JPE, et al. Hand eczema and wet work: dose-response relationship and effect of leaving the profession. Contact Dermatitis. 2018;78:341-347.
  4. Larson E, Friedman C, Cohran J, et al. Prevalence and correlates of skin damage on the hands of nurses. Heart Lung. 1997;26:404-412.
  5. Lampel HP, Patel N, Boyse K, et al. Prevalence of hand dermatitis in inpatient nurses at a United States hospital. Dermatitis. 2007;18:140-142.
  6. Callahan A, Baron E, Fekedulegn D, et al. Winter season, frequent hand washing, and irritant patch test reactions to detergents are associated with hand dermatitis in health care workers. Dermatitis. 2013;24:170-175.
  7. Lan J, Song Z, Miao X, et al. Skin damage among healthcare workers managing coronavirus disease-2019 [published online March 18, 2020]. J Am Acad Dermatol. 2020;82:1215-1216.
  8. Katz RJ, Landau P, DeVeaugh-Geiss J, et al. Pharmacological responsiveness of dermatitis secondary to compulsive washing. Psychiatry Res. 1990;34:223-226.
  9. Larson EL, Hughes CA, Pyrek JD, et al. Changes in bacterial flora associated with skin damage on hands of health care personnel. Am J Infect Control. 1998;26:513-521.
  10. Held E, Skoet R, Johansen JD, et al. The hand eczema severity index (HECSI): a scoring system for clinical assessment of hand eczema. a study of inter- and intraobserver reliability. Br J Dermatol. 2005;152:302-307.
  11. Boyce JM, Pittet D, Healthcare Infection Control Practices Advisory Committee, et al. Guideline for Hand Hygiene in Health-Care Settings. Recommendations of the Healthcare Infection Control Practices Advisory Committee and the HIPAC/SHEA/APIC/IDSA Hand Hygiene Task Force. Am J Infect Control. 2002;30:S1-S46.
  12. Ansari SA, Sattar SA, Springthorpe VS, et al. Invivo protocol for testing efficacy of hand-washing agents against viruses and bacteria—experiments with rotavirus and Escherichi coli. Appl Environ Microbiol. 1989;55:3113-3118.
  13. Siddharta A, Pfaender S, Vielle NJ, et al. virucidal activity of world health organization-recommended formulations against enveloped viruses, including Zika, Ebola, and emerging coronaviruses. J Infect Dis. 2017;215:902-906.
  14. Pedersen LK, Held E, Johansen JD, et al. Less skin irritation from alcohol-based disinfectant than from detergent used for hand disinfection. Br J Dermatol. 2005;153:1142-1146.
  15. Stutz N, Becker D, Jappe U, et al. Nurses’ perceptions of the benefits and adverse effects of hand disinfection: alcohol-based hand rubs vs. hygienic handwashing: a multicentre questionnaire study with additional patch testing by the German Contact Dermatitis Research Group. Br J Dermatol. 2009;160:565-572.
  16. Wolfe MK, Wells E, Mitro B, et al. Seeking clearer recommendations for hand hygiene in communities facing Ebola: a randomized trial investigating the impact of six handwashing methods on skin irritation and dermatitis. PLoS One. 2016;11:e0167378.
  17. Pittet D, Allegranzi B, Storr J. The WHO Clean Care is Safer Care programme: field-testing to enhance sustainability and spread of hand hygiene improvements. J Infect Public Health. 2008;1:4-10.
  18. McCormick RD, Buchman TL, Maki DG. Double-blind, randomized trial of scheduled use of a novel barrier cream and an oil-containing lotion for protecting the hands of health care workers. Am J Infect Control. 2000;28:302-310.
  19. Berndt U, Wigger-Alberti W, Gabard B, et al. Efficacy of a barrier cream and its vehicle as protective measures against occupational irritant contact dermatitis. Contact Dermatitis. 2000;42:77-80.
  20. Kampf G, Ennen J. Regular use of a hand cream can attenuate skin dryness and roughness caused by frequent hand washing. BMC Dermatol. 2006;6:1.
  21. Gammon J, Hunt J. The neglected element of hand hygiene - significance of hand drying, efficiency of different methods, and clinical implication: a review. J Infect Prev. 2019;20:66-74.
  22. Elston DM. Letter from the editor: occupational skin disease among healthcare workers during the coronavirus (COVID-19) epidemic [published online March 18, 2020]. J Am Acad Dermatol. 2020;82:1085-1086.
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  • Alcohol-based sanitizers are as or even more effective as handwashing with soap and water for preventing disease transmission of enveloped viruses such as severe acute respiratory syndrome coronavirus.
  • Although perceived as more irritating, alcohol-based sanitizers are less likely to cause irritant contact dermatitis of the hands than handwashing with soap and water.
  • Use of humectants, moisturizers, and/or emollients in combination with alcohol-based sanitizers allows for effective hand hygiene without irritating the skin.
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Analysis of Education on Nail Conditions at the American Academy of Dermatology Annual Meetings

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Analysis of Education on Nail Conditions at the American Academy of Dermatology Annual Meetings

 

To the Editor:

The diagnosis and treatment of nail conditions are necessary competencies for board-certified dermatologists, but appropriate education often is lacking.1 The American Academy of Dermatology (AAD) annual meeting is one of the largest and most highly attended dermatology educational conferences worldwide. We sought to determine the number of hours dedicated to nail-related topics at the AAD annual meetings from 2013 to 2019.

We accessed programs from the AAD annual meetings archive online (https://www.aad.org/meetings/previous-meetings-archive), and we used hair and psoriasis content for comparison. Event titles and descriptions were searched for nail-related content (using search terms nail, onychia, and onycho), hair-related content (hair, alopecia, trichosis, hirsutism), and psoriasis content (psoriasis). Data acquired for each event included the date, hours, title, and event type (eg, forum, course, focus session, symposium, discussion group, workshop, plenary session).

The number of hours dedicated to nail education consistently lagged behind those related to hair and psoriasis content during the study period (Figure 1). According to the AAD, the conference runs Friday to Tuesday with higher attendance Friday to Sunday (Tim Moses, personal communication, July 9, 2019). Lectures during the weekend are likely to have a broader reach than lectures on Monday and Tuesday. The proportion of nail content during weekend prime time slots was similar to that of hair and psoriasis (Figure 2). Plenary sessions often are presented by renowned experts on hot topics in dermatology. Notably, hair (2014-2015) and psoriasis (2015-2017) content were represented in the plenary sessions during the study period, while nail content was not featured.

Figure 1. Comparison of the number of hours dedicated to nails, hair, and psoriasis events at the American Academy of Dermatology annual meetings (2013-2019).

Figure 2. Comparison of the proportion of time Friday to Sunday for nails, hair, and psoriasis events at the American Academy of Dermatology annual meetings (2013-2019).

Our study shows that nail-related education was underrepresented at the AAD annual meetings from 2013 to 2019 compared to hair- and psoriasis-related content. Educational gaps in the diagnosis of fignail conditions previously have been delineated, and prioritization of instruction on nail disease pathology and diagnostic procedures has been recommended to improve patient care.1 The majority of nail unit melanomas are diagnosed at late stages, which has been attributed to deficiencies in clinical knowledge and failure to perform or inadequate biopsy techniques.2 Notably, a survey of third-year dermatology residents (N=240) assessing experience in procedural dermatology showed that 58% performed 10 or fewer nail procedures and 30% did not feel competent in performing nail surgery.3 Furthermore, a survey examining the management of longitudinal melanonychia among attending and resident dermatologists (N=402) found that 62% of residents and 28% of total respondents were not confident in managing melanonychia.4

A limitation of this study was the lack of online data available for AAD annual meetings before 2013, so we were unable to characterize any long-term trends. Furthermore, we were unable to assess the educational reach of these sessions, as data on attendance are lacking.

This study demonstrates a paucity of nail-related content at the AAD annual meetings. The introduction of the “Hands-on: Nail Surgery” in 2015 is an important step forward to diminish the knowledge gap in the diagnosis of various nail diseases and malignancies. We recommend increasing the number of hours and overall content of didactic nail sessions at the AAD annual meeting to further the knowledge and procedural skills of dermatologists in caring for patients with nail disorders.

References
  1. Hare AQ, R ich P. Clinical and educational gaps in diagnosis of nail disorders. Dermatol Clin. 2016;34:269-273.
  2. Tan KB, Moncrieff M, Thompson JF, et al. Subungual melanoma: a study of 124 cases highlighting features of early lesions, potential pitfalls in diagnosis, and guidelines for histologic reporting. Am J Surg Pathol. 2007;31:1902-1912.
  3. Lee EH, Nehal KS, Dusza SW, et al. Procedural dermatology training during dermatology residency: a survey of third-year dermatology residents. J Am Acad Dermatol. 2011;64:475-483.
  4. Halteh P, Scher R, Artis A, et al. A survey-based study of management of longitudinal melanonychia amongst attending and resident dermatologists. J Am Acad Dermatol. 2017;76:994-996.
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Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, 9th Floor, New York, NY 10021 (shl9032@med.cornell.edu).

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From Weill Cornell Medicine, New York, New York. Dr. Lipner is from the Department of Dermatology.

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To the Editor:

The diagnosis and treatment of nail conditions are necessary competencies for board-certified dermatologists, but appropriate education often is lacking.1 The American Academy of Dermatology (AAD) annual meeting is one of the largest and most highly attended dermatology educational conferences worldwide. We sought to determine the number of hours dedicated to nail-related topics at the AAD annual meetings from 2013 to 2019.

We accessed programs from the AAD annual meetings archive online (https://www.aad.org/meetings/previous-meetings-archive), and we used hair and psoriasis content for comparison. Event titles and descriptions were searched for nail-related content (using search terms nail, onychia, and onycho), hair-related content (hair, alopecia, trichosis, hirsutism), and psoriasis content (psoriasis). Data acquired for each event included the date, hours, title, and event type (eg, forum, course, focus session, symposium, discussion group, workshop, plenary session).

The number of hours dedicated to nail education consistently lagged behind those related to hair and psoriasis content during the study period (Figure 1). According to the AAD, the conference runs Friday to Tuesday with higher attendance Friday to Sunday (Tim Moses, personal communication, July 9, 2019). Lectures during the weekend are likely to have a broader reach than lectures on Monday and Tuesday. The proportion of nail content during weekend prime time slots was similar to that of hair and psoriasis (Figure 2). Plenary sessions often are presented by renowned experts on hot topics in dermatology. Notably, hair (2014-2015) and psoriasis (2015-2017) content were represented in the plenary sessions during the study period, while nail content was not featured.

Figure 1. Comparison of the number of hours dedicated to nails, hair, and psoriasis events at the American Academy of Dermatology annual meetings (2013-2019).

Figure 2. Comparison of the proportion of time Friday to Sunday for nails, hair, and psoriasis events at the American Academy of Dermatology annual meetings (2013-2019).

Our study shows that nail-related education was underrepresented at the AAD annual meetings from 2013 to 2019 compared to hair- and psoriasis-related content. Educational gaps in the diagnosis of fignail conditions previously have been delineated, and prioritization of instruction on nail disease pathology and diagnostic procedures has been recommended to improve patient care.1 The majority of nail unit melanomas are diagnosed at late stages, which has been attributed to deficiencies in clinical knowledge and failure to perform or inadequate biopsy techniques.2 Notably, a survey of third-year dermatology residents (N=240) assessing experience in procedural dermatology showed that 58% performed 10 or fewer nail procedures and 30% did not feel competent in performing nail surgery.3 Furthermore, a survey examining the management of longitudinal melanonychia among attending and resident dermatologists (N=402) found that 62% of residents and 28% of total respondents were not confident in managing melanonychia.4

A limitation of this study was the lack of online data available for AAD annual meetings before 2013, so we were unable to characterize any long-term trends. Furthermore, we were unable to assess the educational reach of these sessions, as data on attendance are lacking.

This study demonstrates a paucity of nail-related content at the AAD annual meetings. The introduction of the “Hands-on: Nail Surgery” in 2015 is an important step forward to diminish the knowledge gap in the diagnosis of various nail diseases and malignancies. We recommend increasing the number of hours and overall content of didactic nail sessions at the AAD annual meeting to further the knowledge and procedural skills of dermatologists in caring for patients with nail disorders.

 

To the Editor:

The diagnosis and treatment of nail conditions are necessary competencies for board-certified dermatologists, but appropriate education often is lacking.1 The American Academy of Dermatology (AAD) annual meeting is one of the largest and most highly attended dermatology educational conferences worldwide. We sought to determine the number of hours dedicated to nail-related topics at the AAD annual meetings from 2013 to 2019.

We accessed programs from the AAD annual meetings archive online (https://www.aad.org/meetings/previous-meetings-archive), and we used hair and psoriasis content for comparison. Event titles and descriptions were searched for nail-related content (using search terms nail, onychia, and onycho), hair-related content (hair, alopecia, trichosis, hirsutism), and psoriasis content (psoriasis). Data acquired for each event included the date, hours, title, and event type (eg, forum, course, focus session, symposium, discussion group, workshop, plenary session).

The number of hours dedicated to nail education consistently lagged behind those related to hair and psoriasis content during the study period (Figure 1). According to the AAD, the conference runs Friday to Tuesday with higher attendance Friday to Sunday (Tim Moses, personal communication, July 9, 2019). Lectures during the weekend are likely to have a broader reach than lectures on Monday and Tuesday. The proportion of nail content during weekend prime time slots was similar to that of hair and psoriasis (Figure 2). Plenary sessions often are presented by renowned experts on hot topics in dermatology. Notably, hair (2014-2015) and psoriasis (2015-2017) content were represented in the plenary sessions during the study period, while nail content was not featured.

Figure 1. Comparison of the number of hours dedicated to nails, hair, and psoriasis events at the American Academy of Dermatology annual meetings (2013-2019).

Figure 2. Comparison of the proportion of time Friday to Sunday for nails, hair, and psoriasis events at the American Academy of Dermatology annual meetings (2013-2019).

Our study shows that nail-related education was underrepresented at the AAD annual meetings from 2013 to 2019 compared to hair- and psoriasis-related content. Educational gaps in the diagnosis of fignail conditions previously have been delineated, and prioritization of instruction on nail disease pathology and diagnostic procedures has been recommended to improve patient care.1 The majority of nail unit melanomas are diagnosed at late stages, which has been attributed to deficiencies in clinical knowledge and failure to perform or inadequate biopsy techniques.2 Notably, a survey of third-year dermatology residents (N=240) assessing experience in procedural dermatology showed that 58% performed 10 or fewer nail procedures and 30% did not feel competent in performing nail surgery.3 Furthermore, a survey examining the management of longitudinal melanonychia among attending and resident dermatologists (N=402) found that 62% of residents and 28% of total respondents were not confident in managing melanonychia.4

A limitation of this study was the lack of online data available for AAD annual meetings before 2013, so we were unable to characterize any long-term trends. Furthermore, we were unable to assess the educational reach of these sessions, as data on attendance are lacking.

This study demonstrates a paucity of nail-related content at the AAD annual meetings. The introduction of the “Hands-on: Nail Surgery” in 2015 is an important step forward to diminish the knowledge gap in the diagnosis of various nail diseases and malignancies. We recommend increasing the number of hours and overall content of didactic nail sessions at the AAD annual meeting to further the knowledge and procedural skills of dermatologists in caring for patients with nail disorders.

References
  1. Hare AQ, R ich P. Clinical and educational gaps in diagnosis of nail disorders. Dermatol Clin. 2016;34:269-273.
  2. Tan KB, Moncrieff M, Thompson JF, et al. Subungual melanoma: a study of 124 cases highlighting features of early lesions, potential pitfalls in diagnosis, and guidelines for histologic reporting. Am J Surg Pathol. 2007;31:1902-1912.
  3. Lee EH, Nehal KS, Dusza SW, et al. Procedural dermatology training during dermatology residency: a survey of third-year dermatology residents. J Am Acad Dermatol. 2011;64:475-483.
  4. Halteh P, Scher R, Artis A, et al. A survey-based study of management of longitudinal melanonychia amongst attending and resident dermatologists. J Am Acad Dermatol. 2017;76:994-996.
References
  1. Hare AQ, R ich P. Clinical and educational gaps in diagnosis of nail disorders. Dermatol Clin. 2016;34:269-273.
  2. Tan KB, Moncrieff M, Thompson JF, et al. Subungual melanoma: a study of 124 cases highlighting features of early lesions, potential pitfalls in diagnosis, and guidelines for histologic reporting. Am J Surg Pathol. 2007;31:1902-1912.
  3. Lee EH, Nehal KS, Dusza SW, et al. Procedural dermatology training during dermatology residency: a survey of third-year dermatology residents. J Am Acad Dermatol. 2011;64:475-483.
  4. Halteh P, Scher R, Artis A, et al. A survey-based study of management of longitudinal melanonychia amongst attending and resident dermatologists. J Am Acad Dermatol. 2017;76:994-996.
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  • Diagnosis and treatment of nail conditions are necessary competencies for board-certified dermatologists, but appropriate education often is lacking.
  • We recommend increasing the number of hours and overall content of didactic nail sessions at the American Academy of Dermatology annual meeting to further the knowledge and procedural skills of dermatologists caring for patients with nail disorders.
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Evaluating the Impact and Educational Value of YouTube Videos on Nail Biopsy Procedures

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Evaluating the Impact and Educational Value of YouTube Videos on Nail Biopsy Procedures

To the Editor:

Nail biopsy is an important surgical procedure for diagnosis of nail pathology. YouTube has become a potential instrument for physicians and patients to learn about medical procedures.1,2 However, the sources, content, and quality of the information available have not been fully studied or characterized. Our objective was to analyze the efficiency of information and quality of YouTube videos on nail biopsies. We hypothesized that the quality of patient education and physician training videos would be unrepresentative on YouTube.

The term nail biopsy was searched on January 29, 2019, and filtered by relevance and rating using the default YouTube algorithm. Data were collected from the top 40 hits for the search term and filter coupling. All videos were viewed and sorted for nail biopsy procedures, and then those videos were categorized as being produced by a physician or other health care provider. The US medical board status of each physician videographer was determined using the American Board of Medical Specialties database.3 DISCERN criteria for assessing consumer health care information4 were used to interpret the videos by researchers (S.I. and S.R.L.) in this study.

From the queried search term collection, only 10 videos (1,023,423 combined views) were analyzed in this study (eTable). Although the other resulting videos were tagged as nail biopsy, they were excluded due to irrelevant content (eg, patient blogs, PowerPoints, nail avulsions). The mean age of the videos was 4 years (range, 4 days to 11 years), with a mean video length of 3.30 minutes (range, 49 seconds to 9.03 minutes). Four of 10 videos were performed for longitudinal melanonychia, and 5 of 10 videos were performed for melanonychia, clinically consistent with subungual hematoma. Dermatologists, plastic surgeons, and podiatrists produced the majority of the nail biopsy videos. The overall mean DISCERN rating was 1.60/5.00 (range, 1–3), meaning that the quality of content on nail biopsies was poor. This low DISCERN score signifies poor consumer health information. Video 2 (published in 2015) received a DISCERN score of 2 and received almost 1 million views, which is likely because the specific channel has a well-established subscriber pool (4.9 million subscribers). The highest DISCERN score of 3, demonstrating a tangential shave biopsy, was given to video 4 (published in 2010) and only received about 17,400 views (56 subscribers). Additionally, many videos lacked important information about the procedure. For instance, only 3 of 10 videos demonstrated the anesthetic technique and only 5 videos showed repair methods.



YouTube is an electronic learning source for general information; however, the content and quality of information on nail biopsy is not updated, reliable, or abundant. Patients undergoing nail biopsies are unlikely to find reliable and comprehensible information on YouTube; thus, there is a strong need for patient education in this area. In addition, physicians who did not learn to perform a nail biopsy during training are unlikely to learn this procedure from YouTube. Therefore, there is an unmet need for an outlet that will provide updated reliable content on nail biopsies geared toward both patients and physicians.

References
  1. Kwok TM, Singla AA, Phang K, et al. YouTube as a source of patient information for varicose vein treatment options. J Vasc Surg Venous Lymphat Disord. 2017;5:238-243.
  2. Ward B, Ward M, Nicheporuck A, et al. Assessment of YouTube as an informative resource on facial plastic surgery procedures. JAMA Facial Plastic Surgery. 2019;21:75-76.
  3. American Board of Medical Specialties. Certification Matters. https://www.certificationmatters.org. Accessed February 7, 2020.
  4. The DISCERN Instrument. DISCERN Online. http://www.discern.org.uk/discern_instrument.php. Published October 1999. Accessed February 7, 2020.
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Dr. Ishack is from New York University School of Medicine, New York. Dr. Lipner is from Department of Dermatology, Weill Cornell Medicine, New York.

The authors report no conflict of interest.

The eTable is available in the Appendix online at www.mdedge.com/dermatology.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Dr. Ishack is from New York University School of Medicine, New York. Dr. Lipner is from Department of Dermatology, Weill Cornell Medicine, New York.

The authors report no conflict of interest.

The eTable is available in the Appendix online at www.mdedge.com/dermatology.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

Author and Disclosure Information

Dr. Ishack is from New York University School of Medicine, New York. Dr. Lipner is from Department of Dermatology, Weill Cornell Medicine, New York.

The authors report no conflict of interest.

The eTable is available in the Appendix online at www.mdedge.com/dermatology.

Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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To the Editor:

Nail biopsy is an important surgical procedure for diagnosis of nail pathology. YouTube has become a potential instrument for physicians and patients to learn about medical procedures.1,2 However, the sources, content, and quality of the information available have not been fully studied or characterized. Our objective was to analyze the efficiency of information and quality of YouTube videos on nail biopsies. We hypothesized that the quality of patient education and physician training videos would be unrepresentative on YouTube.

The term nail biopsy was searched on January 29, 2019, and filtered by relevance and rating using the default YouTube algorithm. Data were collected from the top 40 hits for the search term and filter coupling. All videos were viewed and sorted for nail biopsy procedures, and then those videos were categorized as being produced by a physician or other health care provider. The US medical board status of each physician videographer was determined using the American Board of Medical Specialties database.3 DISCERN criteria for assessing consumer health care information4 were used to interpret the videos by researchers (S.I. and S.R.L.) in this study.

From the queried search term collection, only 10 videos (1,023,423 combined views) were analyzed in this study (eTable). Although the other resulting videos were tagged as nail biopsy, they were excluded due to irrelevant content (eg, patient blogs, PowerPoints, nail avulsions). The mean age of the videos was 4 years (range, 4 days to 11 years), with a mean video length of 3.30 minutes (range, 49 seconds to 9.03 minutes). Four of 10 videos were performed for longitudinal melanonychia, and 5 of 10 videos were performed for melanonychia, clinically consistent with subungual hematoma. Dermatologists, plastic surgeons, and podiatrists produced the majority of the nail biopsy videos. The overall mean DISCERN rating was 1.60/5.00 (range, 1–3), meaning that the quality of content on nail biopsies was poor. This low DISCERN score signifies poor consumer health information. Video 2 (published in 2015) received a DISCERN score of 2 and received almost 1 million views, which is likely because the specific channel has a well-established subscriber pool (4.9 million subscribers). The highest DISCERN score of 3, demonstrating a tangential shave biopsy, was given to video 4 (published in 2010) and only received about 17,400 views (56 subscribers). Additionally, many videos lacked important information about the procedure. For instance, only 3 of 10 videos demonstrated the anesthetic technique and only 5 videos showed repair methods.



YouTube is an electronic learning source for general information; however, the content and quality of information on nail biopsy is not updated, reliable, or abundant. Patients undergoing nail biopsies are unlikely to find reliable and comprehensible information on YouTube; thus, there is a strong need for patient education in this area. In addition, physicians who did not learn to perform a nail biopsy during training are unlikely to learn this procedure from YouTube. Therefore, there is an unmet need for an outlet that will provide updated reliable content on nail biopsies geared toward both patients and physicians.

To the Editor:

Nail biopsy is an important surgical procedure for diagnosis of nail pathology. YouTube has become a potential instrument for physicians and patients to learn about medical procedures.1,2 However, the sources, content, and quality of the information available have not been fully studied or characterized. Our objective was to analyze the efficiency of information and quality of YouTube videos on nail biopsies. We hypothesized that the quality of patient education and physician training videos would be unrepresentative on YouTube.

The term nail biopsy was searched on January 29, 2019, and filtered by relevance and rating using the default YouTube algorithm. Data were collected from the top 40 hits for the search term and filter coupling. All videos were viewed and sorted for nail biopsy procedures, and then those videos were categorized as being produced by a physician or other health care provider. The US medical board status of each physician videographer was determined using the American Board of Medical Specialties database.3 DISCERN criteria for assessing consumer health care information4 were used to interpret the videos by researchers (S.I. and S.R.L.) in this study.

From the queried search term collection, only 10 videos (1,023,423 combined views) were analyzed in this study (eTable). Although the other resulting videos were tagged as nail biopsy, they were excluded due to irrelevant content (eg, patient blogs, PowerPoints, nail avulsions). The mean age of the videos was 4 years (range, 4 days to 11 years), with a mean video length of 3.30 minutes (range, 49 seconds to 9.03 minutes). Four of 10 videos were performed for longitudinal melanonychia, and 5 of 10 videos were performed for melanonychia, clinically consistent with subungual hematoma. Dermatologists, plastic surgeons, and podiatrists produced the majority of the nail biopsy videos. The overall mean DISCERN rating was 1.60/5.00 (range, 1–3), meaning that the quality of content on nail biopsies was poor. This low DISCERN score signifies poor consumer health information. Video 2 (published in 2015) received a DISCERN score of 2 and received almost 1 million views, which is likely because the specific channel has a well-established subscriber pool (4.9 million subscribers). The highest DISCERN score of 3, demonstrating a tangential shave biopsy, was given to video 4 (published in 2010) and only received about 17,400 views (56 subscribers). Additionally, many videos lacked important information about the procedure. For instance, only 3 of 10 videos demonstrated the anesthetic technique and only 5 videos showed repair methods.



YouTube is an electronic learning source for general information; however, the content and quality of information on nail biopsy is not updated, reliable, or abundant. Patients undergoing nail biopsies are unlikely to find reliable and comprehensible information on YouTube; thus, there is a strong need for patient education in this area. In addition, physicians who did not learn to perform a nail biopsy during training are unlikely to learn this procedure from YouTube. Therefore, there is an unmet need for an outlet that will provide updated reliable content on nail biopsies geared toward both patients and physicians.

References
  1. Kwok TM, Singla AA, Phang K, et al. YouTube as a source of patient information for varicose vein treatment options. J Vasc Surg Venous Lymphat Disord. 2017;5:238-243.
  2. Ward B, Ward M, Nicheporuck A, et al. Assessment of YouTube as an informative resource on facial plastic surgery procedures. JAMA Facial Plastic Surgery. 2019;21:75-76.
  3. American Board of Medical Specialties. Certification Matters. https://www.certificationmatters.org. Accessed February 7, 2020.
  4. The DISCERN Instrument. DISCERN Online. http://www.discern.org.uk/discern_instrument.php. Published October 1999. Accessed February 7, 2020.
References
  1. Kwok TM, Singla AA, Phang K, et al. YouTube as a source of patient information for varicose vein treatment options. J Vasc Surg Venous Lymphat Disord. 2017;5:238-243.
  2. Ward B, Ward M, Nicheporuck A, et al. Assessment of YouTube as an informative resource on facial plastic surgery procedures. JAMA Facial Plastic Surgery. 2019;21:75-76.
  3. American Board of Medical Specialties. Certification Matters. https://www.certificationmatters.org. Accessed February 7, 2020.
  4. The DISCERN Instrument. DISCERN Online. http://www.discern.org.uk/discern_instrument.php. Published October 1999. Accessed February 7, 2020.
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  • A nail biopsy is sometimes necessary for histopathologic confirmation of a clinical diagnosis.
  • YouTube has become a potential educational platform for physicians and patients to learn about nail biopsy procedures.
  • Physicians and patients interested in learning more about nail biopsies are unlikely to find reliable and comprehensible information on YouTube; therefore, there is a need for updated reliable video content on nail biopsies geared toward both physicians and patients.
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Concurrent Beau Lines, Onychomadesis, and Retronychia Following Scurvy

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Concurrent Beau Lines, Onychomadesis, and Retronychia Following Scurvy

Beau lines are palpable transverse depressions on the dorsal aspect of the nail plate that result from a temporary slowing of nail plate production by the proximal nail matrix. Onychomadesis is a separation of the proximal nail plate from the distal nail plate leading to shedding of the nail. It occurs due to a complete growth arrest in the nail matrix and is thought to be on a continuum with Beau lines. The etiologies of these 2 conditions overlap and include trauma, inflammatory diseases, systemic illnesses, hereditary conditions, and infections.1-5 In almost all cases of both conditions, normal nail plate production ensues upon identification and removal of the inciting agent or recuperation from the causal illness.3,4,6 Beau lines will move distally as the nail grows out and can be clipped. In onychomadesis, the affected nails will be shed with time. Resolution of these nail defects can be estimated from average nail growth rates (1 mm/mo for fingernails and 2–3 mm/mo for toenails).7

Retronychia is defined as a proximal ingrowing of the nail plate into the ventral surface of the proximal nail fold.4,6 It is thought to occur via vertical progression of the nail plate into the proximal nail fold, repetitive nail matrix trauma, or shearing forces, resulting in inflammation that leads to nail plate stacking.8,9 Although conservative treatment using topical corticosteroids may be attempted, proximal nail plate avulsion typically is required for treatment.10

Braswell et al1 suggested a unifying hypothesis for a common pathophysiologic basis for these 3 conditions; that is, nail matrix injury results in slowing and/or cessation of nail plate production, followed by recommencement of nail plate production by the nail matrix after removal of the insult. We report a case of a patient presenting with concurrent Beau lines, onychomadesis, and retronychia following scurvy, thus supporting the hypothesis that these 3 nail conditions lie on a continuum.

Case Report

A 41-year-old woman with a history of thyroiditis, gastroesophageal reflux disease, endometriosis, osteoarthritis, gastric ulcer, pancreatitis, fatty liver, and polycystic ovarian syndrome presented with lines on the toenails and no growth of the right second toenail of several months’ duration. She denied any pain or prior trauma to the nails, participation in sports activities, or wearing tight or high-heeled shoes. She had presented 6 months prior for evaluation of perifollicular erythema on the posterior thighs, legs, and abdomen, as well as gingival bleeding.11 At that time, one of the authors (S.R.L.) found that she was vitamin C deficient, and a diagnosis of scurvy was made. The rash and gingival bleeding resolved with vitamin C supplementation.11

At the current presentation, physical examination revealed transverse grooves involving several fingernails but most evident on the left thumbnail (Figure, A). The grooves did not span the entire breadth of the nail, which was consistent with Beau lines. Several toenails had parallel transverse grooves spanning the entire width of the nail plate such that the proximal nail plate was discontinuous with the distal nail plate, which was consistent with onychomadesis (Figure, B). The right second toenail was yellow and thickened with layered nail plates, indicative of retronychia (Figure, B). Histopathology of a nail plate clipping from the right second toenail was negative for fungal hyphae, and a radiograph was negative for bony changes or exostosis.

A, Beau lines on the thumbnails presented as transverse depressions that did not span the width of the nail plate. B, Transverse lines spanning the width of the nail plate were noted on the right first, third, fourth, and fifth toenails, representing onychomadesis. Layered nail plates on the right second toenail were indicative of retronychia.

Comment

The nail matrix is responsible for nail plate production, and the newly formed nail plate then moves outward over the nail bed. It is hypothesized that the pathophysiologic basis for Beau lines, onychomadesis, and retronychia lies on a continuum such that all 3 conditions are caused by an insult to the nail matrix that results in slowing and/or halting of nail plate growth. Beau lines result from slowing or disruption in cell growth from the nail matrix, whereas onychomadesis is associated with a complete halt in nail plate production.1,3 In retronychia, the new nail growing from the matrix pushes the old one upward, interrupting the longitudinal growth of the nail and leading to nail plate stacking.10

Our patient presented with concurrent Beau lines, onychomadesis, and retronychia. Although Beau lines and onychomadesis have been reported together in some instances,12-14 retronychia is not commonly reported with either of these conditions. The exact incidence of each condition has not been studied, but Beau lines are relatively common, onychomadesis is less common, and retronychia is seen infrequently; therefore, the concurrent presentation of these 3 conditions in the same patient is exceedingly rare. Thus, it was most likely that one etiology accounted for all 3 nail findings.



Because the patient had been diagnosed with scurvy 6 months prior to presentation, we hypothesized that the associated vitamin C deficiency caused a systemic insult to the nail matrix, which resulted in cessation of nail growth. The mechanism of nail matrix arrest in the setting of systemic disease is thought to be due to inhibition of cellular proliferation or a change in the quality of the newly manufactured nail plate, which becomes thinner and more dystrophic.15 Vitamin C (ascorbic acid) deficiency causes scurvy, which is characterized by cutaneous signs such as perifollicular hemorrhage and purpura, corkscrew hairs, bruising, gingivitis, arthralgia, and impaired wound healing.16 These clinical manifestations are due to impaired collagen synthesis and disordered connective tissue. Ascorbic acid also is involved in fatty acid transport, neurotransmitter synthesis, prostaglandin metabolism, and nitric oxide synthesis.17 Ascorbic acid has not been studied for its role in nail plate synthesis18; however, given the role that ascorbic acid plays in a myriad of biologic processes, the deficiency associated with scurvy likely had a considerable systemic effect in our patient that halted nail plate synthesis and resulted in the concurrent presentation of Beau lines, onychomadesis, and retronychia.

References
  1. Braswell MA, Daniel CR III, Brodell RT. Beau lines, onychomadesis, and retronychia: a unifying hypothesis. J Am Acad Dermatol. 2015;73:849-855.
  2. Lipner SR. Onychomadesis following a fish pedicure. JAMA Dermatol. 2018;154:1091-1092.
  3. Bettoli V, Zauli S, Toni G, et al. Onychomadesis following hand, foot, and mouth disease: a case report from Italy and review of the literature. Int J Dermatol. 2013;52:728-730.
  4. Lawry M, Daniel CR III. Nails in systemic disease. In: Scher RK, Daniel CR III, eds. Nails: Diagnosis, Therapy, Surgery. 3rd ed. Oxford, England: Elsevier Saunders; 2005:147-176.
  5. Lipner SR, Scher RK. Evaluation of nail lines: color and shape hold clues. Cleve Clin J Med. 2016;83:385.
  6. Rich P. Nail signs and symptoms. In: Scher RK, Daniel CR III, eds. Nails: Diagnosis, Therapy, Surgery. 3rd ed. Oxford, England: Elsevier Saunders; 2005:1-6.
  7. Lipner SR, Scher RK. Nail growth evaluation and factors affecting nail growth. In: Humbert P, Fanian F, Maibach H, et al, eds. Agache’s Measuring the Skin. Cham, Switzerland: Springer; 2017:1-15.
  8. de Berker DA, Richert B, Duhard E, et al. Retronychia: proximal ingrowing of the nail plate. J Am Acad Dermatol. 2008;58:978-983.
  9. Wortsman X, Wortsman J, Guerrero R, et al. Anatomical changes in retronychia and onychomadesis detected using ultrasound. Dermatol Surg. 2010;36:1615-1620.
  10. Piraccini BM, Richert B, de Berker DA, et al. Retronychia in children, adolescents, and young adults: a case series. J Am Acad Dermatol. 2014;70:388-390.
  11. Lipner S. A classic case of scurvy. Lancet. 2018;392:431.
  12. Jacobsen L, Zimmerman S, Lohr J. Nail findings in hand-foot-and-mouth disease. Pediatr Infect Dis J. 2015;34:449-450.
  13. Damevska K, Gocev G, Pollozhani N, et al. Onychomadesis following cutaneous vasculitis. Acta Dermatovenerol Croat. 2017;25:77-79.
  14. Clementz GC, Mancini AJ. Nail matrix arrest following hand‐foot‐mouth disease: a report of five children. Pediatr Dermatol. 2000;17:7-11.
  15. Weismann K. J.H.S Beau and his descriptions of transverse depressions on nails. Br J Dermatol. 1977;97:571-572.
  16. Abdullah M, Jamil RT, Attia FN. Vitamin C (ascorbic acid). Treasure Island, FL: StatPearls Publishing; 2019. https://www.ncbi.nlm.nih.gov/books/NBK499877/. Updated October 21, 2019. Accessed February 24, 2020.
  17. Pazirandeh S, Burns DL. Overview of water-soluble vitamins. UpToDate. https://www.uptodate.com/contents/overview-of-water-soluble-vitamins. Updated January 29, 2020. Accessed February 24, 2020.
  18. Scheinfeld N, Dahdah MJ, Scher RK. Vitamins and minerals: their role in nail health and disease. J Drugs Dermatol. 2007;6:782-787.
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Ms. Ko is from Duke University School of Medicine, Durham, North Carolina. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

The authors report no conflict of interest.

Correspondence: Shari R. Lipner, MD, PhD, Weill Cornell Medicine, Department of Dermatology, 1305 York Ave, 9th Floor, New York, NY 10021 (shl9032@med.cornell.edu).

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Ms. Ko is from Duke University School of Medicine, Durham, North Carolina. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

The authors report no conflict of interest.

Correspondence: Shari R. Lipner, MD, PhD, Weill Cornell Medicine, Department of Dermatology, 1305 York Ave, 9th Floor, New York, NY 10021 (shl9032@med.cornell.edu).

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Beau lines are palpable transverse depressions on the dorsal aspect of the nail plate that result from a temporary slowing of nail plate production by the proximal nail matrix. Onychomadesis is a separation of the proximal nail plate from the distal nail plate leading to shedding of the nail. It occurs due to a complete growth arrest in the nail matrix and is thought to be on a continuum with Beau lines. The etiologies of these 2 conditions overlap and include trauma, inflammatory diseases, systemic illnesses, hereditary conditions, and infections.1-5 In almost all cases of both conditions, normal nail plate production ensues upon identification and removal of the inciting agent or recuperation from the causal illness.3,4,6 Beau lines will move distally as the nail grows out and can be clipped. In onychomadesis, the affected nails will be shed with time. Resolution of these nail defects can be estimated from average nail growth rates (1 mm/mo for fingernails and 2–3 mm/mo for toenails).7

Retronychia is defined as a proximal ingrowing of the nail plate into the ventral surface of the proximal nail fold.4,6 It is thought to occur via vertical progression of the nail plate into the proximal nail fold, repetitive nail matrix trauma, or shearing forces, resulting in inflammation that leads to nail plate stacking.8,9 Although conservative treatment using topical corticosteroids may be attempted, proximal nail plate avulsion typically is required for treatment.10

Braswell et al1 suggested a unifying hypothesis for a common pathophysiologic basis for these 3 conditions; that is, nail matrix injury results in slowing and/or cessation of nail plate production, followed by recommencement of nail plate production by the nail matrix after removal of the insult. We report a case of a patient presenting with concurrent Beau lines, onychomadesis, and retronychia following scurvy, thus supporting the hypothesis that these 3 nail conditions lie on a continuum.

Case Report

A 41-year-old woman with a history of thyroiditis, gastroesophageal reflux disease, endometriosis, osteoarthritis, gastric ulcer, pancreatitis, fatty liver, and polycystic ovarian syndrome presented with lines on the toenails and no growth of the right second toenail of several months’ duration. She denied any pain or prior trauma to the nails, participation in sports activities, or wearing tight or high-heeled shoes. She had presented 6 months prior for evaluation of perifollicular erythema on the posterior thighs, legs, and abdomen, as well as gingival bleeding.11 At that time, one of the authors (S.R.L.) found that she was vitamin C deficient, and a diagnosis of scurvy was made. The rash and gingival bleeding resolved with vitamin C supplementation.11

At the current presentation, physical examination revealed transverse grooves involving several fingernails but most evident on the left thumbnail (Figure, A). The grooves did not span the entire breadth of the nail, which was consistent with Beau lines. Several toenails had parallel transverse grooves spanning the entire width of the nail plate such that the proximal nail plate was discontinuous with the distal nail plate, which was consistent with onychomadesis (Figure, B). The right second toenail was yellow and thickened with layered nail plates, indicative of retronychia (Figure, B). Histopathology of a nail plate clipping from the right second toenail was negative for fungal hyphae, and a radiograph was negative for bony changes or exostosis.

A, Beau lines on the thumbnails presented as transverse depressions that did not span the width of the nail plate. B, Transverse lines spanning the width of the nail plate were noted on the right first, third, fourth, and fifth toenails, representing onychomadesis. Layered nail plates on the right second toenail were indicative of retronychia.

Comment

The nail matrix is responsible for nail plate production, and the newly formed nail plate then moves outward over the nail bed. It is hypothesized that the pathophysiologic basis for Beau lines, onychomadesis, and retronychia lies on a continuum such that all 3 conditions are caused by an insult to the nail matrix that results in slowing and/or halting of nail plate growth. Beau lines result from slowing or disruption in cell growth from the nail matrix, whereas onychomadesis is associated with a complete halt in nail plate production.1,3 In retronychia, the new nail growing from the matrix pushes the old one upward, interrupting the longitudinal growth of the nail and leading to nail plate stacking.10

Our patient presented with concurrent Beau lines, onychomadesis, and retronychia. Although Beau lines and onychomadesis have been reported together in some instances,12-14 retronychia is not commonly reported with either of these conditions. The exact incidence of each condition has not been studied, but Beau lines are relatively common, onychomadesis is less common, and retronychia is seen infrequently; therefore, the concurrent presentation of these 3 conditions in the same patient is exceedingly rare. Thus, it was most likely that one etiology accounted for all 3 nail findings.



Because the patient had been diagnosed with scurvy 6 months prior to presentation, we hypothesized that the associated vitamin C deficiency caused a systemic insult to the nail matrix, which resulted in cessation of nail growth. The mechanism of nail matrix arrest in the setting of systemic disease is thought to be due to inhibition of cellular proliferation or a change in the quality of the newly manufactured nail plate, which becomes thinner and more dystrophic.15 Vitamin C (ascorbic acid) deficiency causes scurvy, which is characterized by cutaneous signs such as perifollicular hemorrhage and purpura, corkscrew hairs, bruising, gingivitis, arthralgia, and impaired wound healing.16 These clinical manifestations are due to impaired collagen synthesis and disordered connective tissue. Ascorbic acid also is involved in fatty acid transport, neurotransmitter synthesis, prostaglandin metabolism, and nitric oxide synthesis.17 Ascorbic acid has not been studied for its role in nail plate synthesis18; however, given the role that ascorbic acid plays in a myriad of biologic processes, the deficiency associated with scurvy likely had a considerable systemic effect in our patient that halted nail plate synthesis and resulted in the concurrent presentation of Beau lines, onychomadesis, and retronychia.

Beau lines are palpable transverse depressions on the dorsal aspect of the nail plate that result from a temporary slowing of nail plate production by the proximal nail matrix. Onychomadesis is a separation of the proximal nail plate from the distal nail plate leading to shedding of the nail. It occurs due to a complete growth arrest in the nail matrix and is thought to be on a continuum with Beau lines. The etiologies of these 2 conditions overlap and include trauma, inflammatory diseases, systemic illnesses, hereditary conditions, and infections.1-5 In almost all cases of both conditions, normal nail plate production ensues upon identification and removal of the inciting agent or recuperation from the causal illness.3,4,6 Beau lines will move distally as the nail grows out and can be clipped. In onychomadesis, the affected nails will be shed with time. Resolution of these nail defects can be estimated from average nail growth rates (1 mm/mo for fingernails and 2–3 mm/mo for toenails).7

Retronychia is defined as a proximal ingrowing of the nail plate into the ventral surface of the proximal nail fold.4,6 It is thought to occur via vertical progression of the nail plate into the proximal nail fold, repetitive nail matrix trauma, or shearing forces, resulting in inflammation that leads to nail plate stacking.8,9 Although conservative treatment using topical corticosteroids may be attempted, proximal nail plate avulsion typically is required for treatment.10

Braswell et al1 suggested a unifying hypothesis for a common pathophysiologic basis for these 3 conditions; that is, nail matrix injury results in slowing and/or cessation of nail plate production, followed by recommencement of nail plate production by the nail matrix after removal of the insult. We report a case of a patient presenting with concurrent Beau lines, onychomadesis, and retronychia following scurvy, thus supporting the hypothesis that these 3 nail conditions lie on a continuum.

Case Report

A 41-year-old woman with a history of thyroiditis, gastroesophageal reflux disease, endometriosis, osteoarthritis, gastric ulcer, pancreatitis, fatty liver, and polycystic ovarian syndrome presented with lines on the toenails and no growth of the right second toenail of several months’ duration. She denied any pain or prior trauma to the nails, participation in sports activities, or wearing tight or high-heeled shoes. She had presented 6 months prior for evaluation of perifollicular erythema on the posterior thighs, legs, and abdomen, as well as gingival bleeding.11 At that time, one of the authors (S.R.L.) found that she was vitamin C deficient, and a diagnosis of scurvy was made. The rash and gingival bleeding resolved with vitamin C supplementation.11

At the current presentation, physical examination revealed transverse grooves involving several fingernails but most evident on the left thumbnail (Figure, A). The grooves did not span the entire breadth of the nail, which was consistent with Beau lines. Several toenails had parallel transverse grooves spanning the entire width of the nail plate such that the proximal nail plate was discontinuous with the distal nail plate, which was consistent with onychomadesis (Figure, B). The right second toenail was yellow and thickened with layered nail plates, indicative of retronychia (Figure, B). Histopathology of a nail plate clipping from the right second toenail was negative for fungal hyphae, and a radiograph was negative for bony changes or exostosis.

A, Beau lines on the thumbnails presented as transverse depressions that did not span the width of the nail plate. B, Transverse lines spanning the width of the nail plate were noted on the right first, third, fourth, and fifth toenails, representing onychomadesis. Layered nail plates on the right second toenail were indicative of retronychia.

Comment

The nail matrix is responsible for nail plate production, and the newly formed nail plate then moves outward over the nail bed. It is hypothesized that the pathophysiologic basis for Beau lines, onychomadesis, and retronychia lies on a continuum such that all 3 conditions are caused by an insult to the nail matrix that results in slowing and/or halting of nail plate growth. Beau lines result from slowing or disruption in cell growth from the nail matrix, whereas onychomadesis is associated with a complete halt in nail plate production.1,3 In retronychia, the new nail growing from the matrix pushes the old one upward, interrupting the longitudinal growth of the nail and leading to nail plate stacking.10

Our patient presented with concurrent Beau lines, onychomadesis, and retronychia. Although Beau lines and onychomadesis have been reported together in some instances,12-14 retronychia is not commonly reported with either of these conditions. The exact incidence of each condition has not been studied, but Beau lines are relatively common, onychomadesis is less common, and retronychia is seen infrequently; therefore, the concurrent presentation of these 3 conditions in the same patient is exceedingly rare. Thus, it was most likely that one etiology accounted for all 3 nail findings.



Because the patient had been diagnosed with scurvy 6 months prior to presentation, we hypothesized that the associated vitamin C deficiency caused a systemic insult to the nail matrix, which resulted in cessation of nail growth. The mechanism of nail matrix arrest in the setting of systemic disease is thought to be due to inhibition of cellular proliferation or a change in the quality of the newly manufactured nail plate, which becomes thinner and more dystrophic.15 Vitamin C (ascorbic acid) deficiency causes scurvy, which is characterized by cutaneous signs such as perifollicular hemorrhage and purpura, corkscrew hairs, bruising, gingivitis, arthralgia, and impaired wound healing.16 These clinical manifestations are due to impaired collagen synthesis and disordered connective tissue. Ascorbic acid also is involved in fatty acid transport, neurotransmitter synthesis, prostaglandin metabolism, and nitric oxide synthesis.17 Ascorbic acid has not been studied for its role in nail plate synthesis18; however, given the role that ascorbic acid plays in a myriad of biologic processes, the deficiency associated with scurvy likely had a considerable systemic effect in our patient that halted nail plate synthesis and resulted in the concurrent presentation of Beau lines, onychomadesis, and retronychia.

References
  1. Braswell MA, Daniel CR III, Brodell RT. Beau lines, onychomadesis, and retronychia: a unifying hypothesis. J Am Acad Dermatol. 2015;73:849-855.
  2. Lipner SR. Onychomadesis following a fish pedicure. JAMA Dermatol. 2018;154:1091-1092.
  3. Bettoli V, Zauli S, Toni G, et al. Onychomadesis following hand, foot, and mouth disease: a case report from Italy and review of the literature. Int J Dermatol. 2013;52:728-730.
  4. Lawry M, Daniel CR III. Nails in systemic disease. In: Scher RK, Daniel CR III, eds. Nails: Diagnosis, Therapy, Surgery. 3rd ed. Oxford, England: Elsevier Saunders; 2005:147-176.
  5. Lipner SR, Scher RK. Evaluation of nail lines: color and shape hold clues. Cleve Clin J Med. 2016;83:385.
  6. Rich P. Nail signs and symptoms. In: Scher RK, Daniel CR III, eds. Nails: Diagnosis, Therapy, Surgery. 3rd ed. Oxford, England: Elsevier Saunders; 2005:1-6.
  7. Lipner SR, Scher RK. Nail growth evaluation and factors affecting nail growth. In: Humbert P, Fanian F, Maibach H, et al, eds. Agache’s Measuring the Skin. Cham, Switzerland: Springer; 2017:1-15.
  8. de Berker DA, Richert B, Duhard E, et al. Retronychia: proximal ingrowing of the nail plate. J Am Acad Dermatol. 2008;58:978-983.
  9. Wortsman X, Wortsman J, Guerrero R, et al. Anatomical changes in retronychia and onychomadesis detected using ultrasound. Dermatol Surg. 2010;36:1615-1620.
  10. Piraccini BM, Richert B, de Berker DA, et al. Retronychia in children, adolescents, and young adults: a case series. J Am Acad Dermatol. 2014;70:388-390.
  11. Lipner S. A classic case of scurvy. Lancet. 2018;392:431.
  12. Jacobsen L, Zimmerman S, Lohr J. Nail findings in hand-foot-and-mouth disease. Pediatr Infect Dis J. 2015;34:449-450.
  13. Damevska K, Gocev G, Pollozhani N, et al. Onychomadesis following cutaneous vasculitis. Acta Dermatovenerol Croat. 2017;25:77-79.
  14. Clementz GC, Mancini AJ. Nail matrix arrest following hand‐foot‐mouth disease: a report of five children. Pediatr Dermatol. 2000;17:7-11.
  15. Weismann K. J.H.S Beau and his descriptions of transverse depressions on nails. Br J Dermatol. 1977;97:571-572.
  16. Abdullah M, Jamil RT, Attia FN. Vitamin C (ascorbic acid). Treasure Island, FL: StatPearls Publishing; 2019. https://www.ncbi.nlm.nih.gov/books/NBK499877/. Updated October 21, 2019. Accessed February 24, 2020.
  17. Pazirandeh S, Burns DL. Overview of water-soluble vitamins. UpToDate. https://www.uptodate.com/contents/overview-of-water-soluble-vitamins. Updated January 29, 2020. Accessed February 24, 2020.
  18. Scheinfeld N, Dahdah MJ, Scher RK. Vitamins and minerals: their role in nail health and disease. J Drugs Dermatol. 2007;6:782-787.
References
  1. Braswell MA, Daniel CR III, Brodell RT. Beau lines, onychomadesis, and retronychia: a unifying hypothesis. J Am Acad Dermatol. 2015;73:849-855.
  2. Lipner SR. Onychomadesis following a fish pedicure. JAMA Dermatol. 2018;154:1091-1092.
  3. Bettoli V, Zauli S, Toni G, et al. Onychomadesis following hand, foot, and mouth disease: a case report from Italy and review of the literature. Int J Dermatol. 2013;52:728-730.
  4. Lawry M, Daniel CR III. Nails in systemic disease. In: Scher RK, Daniel CR III, eds. Nails: Diagnosis, Therapy, Surgery. 3rd ed. Oxford, England: Elsevier Saunders; 2005:147-176.
  5. Lipner SR, Scher RK. Evaluation of nail lines: color and shape hold clues. Cleve Clin J Med. 2016;83:385.
  6. Rich P. Nail signs and symptoms. In: Scher RK, Daniel CR III, eds. Nails: Diagnosis, Therapy, Surgery. 3rd ed. Oxford, England: Elsevier Saunders; 2005:1-6.
  7. Lipner SR, Scher RK. Nail growth evaluation and factors affecting nail growth. In: Humbert P, Fanian F, Maibach H, et al, eds. Agache’s Measuring the Skin. Cham, Switzerland: Springer; 2017:1-15.
  8. de Berker DA, Richert B, Duhard E, et al. Retronychia: proximal ingrowing of the nail plate. J Am Acad Dermatol. 2008;58:978-983.
  9. Wortsman X, Wortsman J, Guerrero R, et al. Anatomical changes in retronychia and onychomadesis detected using ultrasound. Dermatol Surg. 2010;36:1615-1620.
  10. Piraccini BM, Richert B, de Berker DA, et al. Retronychia in children, adolescents, and young adults: a case series. J Am Acad Dermatol. 2014;70:388-390.
  11. Lipner S. A classic case of scurvy. Lancet. 2018;392:431.
  12. Jacobsen L, Zimmerman S, Lohr J. Nail findings in hand-foot-and-mouth disease. Pediatr Infect Dis J. 2015;34:449-450.
  13. Damevska K, Gocev G, Pollozhani N, et al. Onychomadesis following cutaneous vasculitis. Acta Dermatovenerol Croat. 2017;25:77-79.
  14. Clementz GC, Mancini AJ. Nail matrix arrest following hand‐foot‐mouth disease: a report of five children. Pediatr Dermatol. 2000;17:7-11.
  15. Weismann K. J.H.S Beau and his descriptions of transverse depressions on nails. Br J Dermatol. 1977;97:571-572.
  16. Abdullah M, Jamil RT, Attia FN. Vitamin C (ascorbic acid). Treasure Island, FL: StatPearls Publishing; 2019. https://www.ncbi.nlm.nih.gov/books/NBK499877/. Updated October 21, 2019. Accessed February 24, 2020.
  17. Pazirandeh S, Burns DL. Overview of water-soluble vitamins. UpToDate. https://www.uptodate.com/contents/overview-of-water-soluble-vitamins. Updated January 29, 2020. Accessed February 24, 2020.
  18. Scheinfeld N, Dahdah MJ, Scher RK. Vitamins and minerals: their role in nail health and disease. J Drugs Dermatol. 2007;6:782-787.
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Concurrent Beau Lines, Onychomadesis, and Retronychia Following Scurvy
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Practice Points

  • Beau lines, onychomadesis, and retronychia are nail conditions with distinct clinical findings.
  • Beau lines and onychomadesis may be seen concurrently following trauma, inflammatory diseases, systemic illnesses, hereditary conditions, and infections.
  • Retronychia shares a common pathophysiology with Beau lines and onychomadesis, and all reflect slowing or cessation of nail plate production.
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Transillumination for Improved Diagnosis of Digital Myxoid Cysts

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Transillumination for Improved Diagnosis of Digital Myxoid Cysts

 

Practice Gap

Myxoid cysts are among the most common space-occupying lesions involving the nail unit. Their etiology has not been fully elucidated, but these cysts likely form due to leakage of synovial fluid following trauma or chronic wear and tear. They are highly associated with osteoarthritis and typically are found in close proximity to the distal interphalangeal joints.1 Myxoid cysts often extend into the eponychium, where mechanical stress on the nail matrix may lead to nail dystrophy, most commonly resulting in a longitudinal groove in the nail plate (Figure, A). The presence of multiple myxoid cysts is not uncommon. Differentiation of this lesion from other nodules of the digits, including epidermoid cysts, acquired digital fibrokeratomas, and giant cell tendon sheath tumors often is challenging without a biopsy.

A, A translucent compressible nodule of the proximal nail fold and longitudinal groove in the nail plate of the right thumb. B, Transillumination using a dermatoscope to project light from the dorsal digit through the nail unit demonstrated a central nodule in the proximal nail fold as well as a second cyst radially.

Technique

The normal nail unit transmits light to some extent, and masses may be identified by how easily they transmit light relative to the adjacent skin. Solid tumors of the nail unit, such as acquired digital fibrokeratomas and giant cell tendon sheath tumors, will not transmit light, while myxoid cysts transmit light easily. A dermatoscope can be used to project light from the dorsal digit through the nail unit. The area occupied by the myxoid cyst will appear bright compared to the surrounding skin (Figure, B). Drainage of the lesion using an 18-gauge needle yielded a clear jellylike fluid that was consistent with a myxoid cyst. This technique aids in localizing and characterizing the myxoid cyst for treatment or drainage. Physician assessment of transillumination has been shown to demonstrate clinical accuracy and high intraobserver reliability in differentiating between cystic and solid tumors.2

Practice Implications

Transillumination is a valuable technique that may aid dermatologists in both the diagnosis and subsequent treatment of myxoid cysts. Location is important to consider when choosing a treatment option. Although lower recurrence rates are achieved with nail surgery, permanent nail dystrophy is likely when cysts are in close proximity to the nail matrix.3 When multiple cysts are present, only the largest may be apparent. Transillumination can guide the physician in achieving more accurate and thorough drainage of the cyst contents, negating the need for more costly imaging modalities. Dermatologists may utilize transillumination as a rapid and economical diagnostic method for space-occupying lesions involving the nail unit.

References
  1. Lin YC, Wu YH, Scher RK. Nail changes and association of osteoarthritis in digital myxoid cyst. Dermatol Surg. 2008;34:364-369.
  2. Erne HC, Gardner TR, Strauch RJ. Transillumination of hand tumors: a cadaver study to evaluate accuracy and intraobserver reliability. Hand (N Y). 2011;6:390-393.
  3. Fritz GR, Stern PJ, Dickey M. Complications following mucous cyst excision. J Hand Surg Br. 1997;22:222-225.
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Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Mr. Gupta is from State University of New York Downstate College of Medicine, Brooklyn. Dr. Lipner is from Weill Cornell Medicine, Department of Dermatology, New York, New York.

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Correspondence: Shari R. Lipner, MD, PhD, 1305 York Ave, New York, NY 10021 (shl9032@med.cornell.edu).

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Practice Gap

Myxoid cysts are among the most common space-occupying lesions involving the nail unit. Their etiology has not been fully elucidated, but these cysts likely form due to leakage of synovial fluid following trauma or chronic wear and tear. They are highly associated with osteoarthritis and typically are found in close proximity to the distal interphalangeal joints.1 Myxoid cysts often extend into the eponychium, where mechanical stress on the nail matrix may lead to nail dystrophy, most commonly resulting in a longitudinal groove in the nail plate (Figure, A). The presence of multiple myxoid cysts is not uncommon. Differentiation of this lesion from other nodules of the digits, including epidermoid cysts, acquired digital fibrokeratomas, and giant cell tendon sheath tumors often is challenging without a biopsy.

A, A translucent compressible nodule of the proximal nail fold and longitudinal groove in the nail plate of the right thumb. B, Transillumination using a dermatoscope to project light from the dorsal digit through the nail unit demonstrated a central nodule in the proximal nail fold as well as a second cyst radially.

Technique

The normal nail unit transmits light to some extent, and masses may be identified by how easily they transmit light relative to the adjacent skin. Solid tumors of the nail unit, such as acquired digital fibrokeratomas and giant cell tendon sheath tumors, will not transmit light, while myxoid cysts transmit light easily. A dermatoscope can be used to project light from the dorsal digit through the nail unit. The area occupied by the myxoid cyst will appear bright compared to the surrounding skin (Figure, B). Drainage of the lesion using an 18-gauge needle yielded a clear jellylike fluid that was consistent with a myxoid cyst. This technique aids in localizing and characterizing the myxoid cyst for treatment or drainage. Physician assessment of transillumination has been shown to demonstrate clinical accuracy and high intraobserver reliability in differentiating between cystic and solid tumors.2

Practice Implications

Transillumination is a valuable technique that may aid dermatologists in both the diagnosis and subsequent treatment of myxoid cysts. Location is important to consider when choosing a treatment option. Although lower recurrence rates are achieved with nail surgery, permanent nail dystrophy is likely when cysts are in close proximity to the nail matrix.3 When multiple cysts are present, only the largest may be apparent. Transillumination can guide the physician in achieving more accurate and thorough drainage of the cyst contents, negating the need for more costly imaging modalities. Dermatologists may utilize transillumination as a rapid and economical diagnostic method for space-occupying lesions involving the nail unit.

 

Practice Gap

Myxoid cysts are among the most common space-occupying lesions involving the nail unit. Their etiology has not been fully elucidated, but these cysts likely form due to leakage of synovial fluid following trauma or chronic wear and tear. They are highly associated with osteoarthritis and typically are found in close proximity to the distal interphalangeal joints.1 Myxoid cysts often extend into the eponychium, where mechanical stress on the nail matrix may lead to nail dystrophy, most commonly resulting in a longitudinal groove in the nail plate (Figure, A). The presence of multiple myxoid cysts is not uncommon. Differentiation of this lesion from other nodules of the digits, including epidermoid cysts, acquired digital fibrokeratomas, and giant cell tendon sheath tumors often is challenging without a biopsy.

A, A translucent compressible nodule of the proximal nail fold and longitudinal groove in the nail plate of the right thumb. B, Transillumination using a dermatoscope to project light from the dorsal digit through the nail unit demonstrated a central nodule in the proximal nail fold as well as a second cyst radially.

Technique

The normal nail unit transmits light to some extent, and masses may be identified by how easily they transmit light relative to the adjacent skin. Solid tumors of the nail unit, such as acquired digital fibrokeratomas and giant cell tendon sheath tumors, will not transmit light, while myxoid cysts transmit light easily. A dermatoscope can be used to project light from the dorsal digit through the nail unit. The area occupied by the myxoid cyst will appear bright compared to the surrounding skin (Figure, B). Drainage of the lesion using an 18-gauge needle yielded a clear jellylike fluid that was consistent with a myxoid cyst. This technique aids in localizing and characterizing the myxoid cyst for treatment or drainage. Physician assessment of transillumination has been shown to demonstrate clinical accuracy and high intraobserver reliability in differentiating between cystic and solid tumors.2

Practice Implications

Transillumination is a valuable technique that may aid dermatologists in both the diagnosis and subsequent treatment of myxoid cysts. Location is important to consider when choosing a treatment option. Although lower recurrence rates are achieved with nail surgery, permanent nail dystrophy is likely when cysts are in close proximity to the nail matrix.3 When multiple cysts are present, only the largest may be apparent. Transillumination can guide the physician in achieving more accurate and thorough drainage of the cyst contents, negating the need for more costly imaging modalities. Dermatologists may utilize transillumination as a rapid and economical diagnostic method for space-occupying lesions involving the nail unit.

References
  1. Lin YC, Wu YH, Scher RK. Nail changes and association of osteoarthritis in digital myxoid cyst. Dermatol Surg. 2008;34:364-369.
  2. Erne HC, Gardner TR, Strauch RJ. Transillumination of hand tumors: a cadaver study to evaluate accuracy and intraobserver reliability. Hand (N Y). 2011;6:390-393.
  3. Fritz GR, Stern PJ, Dickey M. Complications following mucous cyst excision. J Hand Surg Br. 1997;22:222-225.
References
  1. Lin YC, Wu YH, Scher RK. Nail changes and association of osteoarthritis in digital myxoid cyst. Dermatol Surg. 2008;34:364-369.
  2. Erne HC, Gardner TR, Strauch RJ. Transillumination of hand tumors: a cadaver study to evaluate accuracy and intraobserver reliability. Hand (N Y). 2011;6:390-393.
  3. Fritz GR, Stern PJ, Dickey M. Complications following mucous cyst excision. J Hand Surg Br. 1997;22:222-225.
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Comment on “Intraoperative Electrosurgical Smoke During Outpatient Surgery: A Survey of Dermatologic Surgeon and Staff Preferences”

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To the Editor:

We read with great interest the recent Cutis article by Golda et al,1 “Intraoperative Electrosurgical Smoke During Outpatient Surgery: A Survey of Dermatologic Surgeon and Staff Preferences.” We applaud the growing interest in the topic of dermatologist safety, as there are currently no established guidelines for precautions while performing surgical procedures. In 2018 we conducted a comprehensive review2 to characterize the specific risks, hazard reduction strategies available, and current use of surgical smoke safety techniques during surgery among dermatologists, and ultimately recommend guidance based on the current available evidence. To conduct this review, we collected data from 45 manuscripts in the dermatology, surgery, infectious disease, obstetrics, and cancer biology literature. Herein, we summarize key findings.2

Dermatologic surgeons, residents, staff, and patients are exposed to many infectious, inhalational, chemical, and mutagenic hazards when performing procedures that liberate smoke and plume. These risks are commonplace; however, they are particularly notable during ablative laser and laser hair removal procedures, which produce a heavy plume (averaging >100,000 particles/cm3). Brief periods of heavy plume exposure also are commonplace during electrosurgery.

Infectious particles in surgical plume have been extensively studied, and viral transmission has been demonstrated in animal studies. Human papillomavirus transmission appears to be the most prevalent risk. Surgical smoke has been shown to cause acute and chronic inhalational injury in rat and sheep studies.3-6

Additionally, chemicals with carcinogenic potential are present in surgical smoke and have been described.7,8 Chemicals in the greatest quantity include hydrocarbons, nitriles, fatty acids, and phenols. Although there have been no human studies on smoke carcinogenesis to date, surgical smoke has been shown to have carcinogenic properties in vitro.



Given these risks—both evidence based and theoretical—we believe that diligent hazard reduction strategies should be employed whenever possible. Surgical masks and high-efficiency particulate air respirators, such as N95 respirator masks, have been well studied and do provide smoke protection. High-efficiency particulate air masks can be worn when possible, especially during procedures that produce heavy plume, though surgical masks are capable of filtering most of the noxious chemicals in surgical smoke. It should be noted that proper fit with minimal air leak is the most important aspect of overall performance.

Smoke evacuators provide another level of protection. The physician should consider the evacuator’s filtration efficiency, capture velocity, and suction strength when evaluating overall performance. Furthermore, the smoke collection tip should be within 2 in of the surgical field to maximize efficacy. Maintenance for smoke evacuation systems should include regular (as defined by manufacturer instructions) flushing of the smoke evacuator lines.

Despite the risks of surgical smoke and the available options of minimizing these risks, the hazards of surgical smoke and the importance of protection are likely underemphasized. Many dermatologic surgeons do not use surgical masks or smoke evacuators in routine practice, according to several survey studies.9-11

It is important for the dermatologic community to consider effective ways of spreading awareness. We propose that surgical smoke safety be taught early in residency training. Additionally, smoke safety can be implemented into certification examinations. Access to masks and smoke evacuation devices are an important part of dermatology training. Accreditation Council for Graduate Medical Education funds should be appropriated to provide for such resources.



Finally, and perhaps most importantly, continued awareness should be established in the dermatology community via standardized guidelines and periodic updates in the dermatology literature and lectures at local and national conferences. Not until these strategies are implemented will surgical smoke protection be viewed as a necessary and important component of routine practice when performing dermatologic surgical procedures.

References
  1. Golda N, Merrill B, Neill B. Intraoperative electrosurgical smoke during outpatient surgery: a survey of dermatologic surgeon and staff preferences. Cutis. 2019;104:120-124.
  2. Georgesen C, Lipner SR. Surgical smoke: risk assessment and mitigation strategies. J Am Acad Dermatol. 2018;79:746-755.
  3. Wenig BL, Stenson KM, Wenig BM, et al. Effects of plume produced by the Nd:YAG laser and electrocautery on the respiratory system. Lasers Surg Med. 1993;13:242-245.
  4. Baggish MS, Elbakry M. The effects of laser smoke on the lungs of rats. Am J Obstet Gynecol. 1987;156:1260-1265.
  5. Baggish MS, Baltoyannis P, Sze E. Protection of the rat lung from the harmful effects of laser smoke. Lasers Surg Med. 1988;8:248-253.
  6. Freitag L, Chapman GA, Sielczak M, et al. Laser smoke effect on the bronchial system. Lasers Surg Med. 1987;7:283-288.
  7. Barrett WL, Garber SM. Surgical smoke: a review of the literature. Is this just a lot of hot air? Surg Endosc. 2003;17:979-987.
  8. Hensman C, Baty D, Willis RG, et al. Chemical composition of smoke produced by high-frequency electrosurgery in a closed gaseous environment. Surg Endosc. 1998;12:1017-1019.
  9. Edwards BE, Reiman RE. Results of a survey on current surgical smoke control practices. AORN J. 2008;87:739-749.
  10. Oganesyan G, Eimpunth S, Kim SS, et al. Surgical smoke in dermatologic surgery. Dermatol Surg. 2014;40:1373-1377.
  11. Chapman LW, Korta DZ, Lee PK, et al. Awareness of surgical smoke risks and assessment of safety practices during electrosurgery among US dermatology residents. JAMA Dermatol. 2017;153:467-468.
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Dr. Georgesen is from the Department of Dermatology, University of Pittsburgh Medical Center, Pennsylvania. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

The authors report no conflict of interest.

Correspondence: Corey Georgesen, MD, UPMC Dermatology, 9000 Brooktree Rd, Ste 200, Wexford, PA 15090 (corey.georgesen@gmail.com).

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Dr. Georgesen is from the Department of Dermatology, University of Pittsburgh Medical Center, Pennsylvania. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

The authors report no conflict of interest.

Correspondence: Corey Georgesen, MD, UPMC Dermatology, 9000 Brooktree Rd, Ste 200, Wexford, PA 15090 (corey.georgesen@gmail.com).

Author and Disclosure Information

Dr. Georgesen is from the Department of Dermatology, University of Pittsburgh Medical Center, Pennsylvania. Dr. Lipner is from the Department of Dermatology, Weill Cornell Medicine, New York, New York.

The authors report no conflict of interest.

Correspondence: Corey Georgesen, MD, UPMC Dermatology, 9000 Brooktree Rd, Ste 200, Wexford, PA 15090 (corey.georgesen@gmail.com).

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To the Editor:

We read with great interest the recent Cutis article by Golda et al,1 “Intraoperative Electrosurgical Smoke During Outpatient Surgery: A Survey of Dermatologic Surgeon and Staff Preferences.” We applaud the growing interest in the topic of dermatologist safety, as there are currently no established guidelines for precautions while performing surgical procedures. In 2018 we conducted a comprehensive review2 to characterize the specific risks, hazard reduction strategies available, and current use of surgical smoke safety techniques during surgery among dermatologists, and ultimately recommend guidance based on the current available evidence. To conduct this review, we collected data from 45 manuscripts in the dermatology, surgery, infectious disease, obstetrics, and cancer biology literature. Herein, we summarize key findings.2

Dermatologic surgeons, residents, staff, and patients are exposed to many infectious, inhalational, chemical, and mutagenic hazards when performing procedures that liberate smoke and plume. These risks are commonplace; however, they are particularly notable during ablative laser and laser hair removal procedures, which produce a heavy plume (averaging >100,000 particles/cm3). Brief periods of heavy plume exposure also are commonplace during electrosurgery.

Infectious particles in surgical plume have been extensively studied, and viral transmission has been demonstrated in animal studies. Human papillomavirus transmission appears to be the most prevalent risk. Surgical smoke has been shown to cause acute and chronic inhalational injury in rat and sheep studies.3-6

Additionally, chemicals with carcinogenic potential are present in surgical smoke and have been described.7,8 Chemicals in the greatest quantity include hydrocarbons, nitriles, fatty acids, and phenols. Although there have been no human studies on smoke carcinogenesis to date, surgical smoke has been shown to have carcinogenic properties in vitro.



Given these risks—both evidence based and theoretical—we believe that diligent hazard reduction strategies should be employed whenever possible. Surgical masks and high-efficiency particulate air respirators, such as N95 respirator masks, have been well studied and do provide smoke protection. High-efficiency particulate air masks can be worn when possible, especially during procedures that produce heavy plume, though surgical masks are capable of filtering most of the noxious chemicals in surgical smoke. It should be noted that proper fit with minimal air leak is the most important aspect of overall performance.

Smoke evacuators provide another level of protection. The physician should consider the evacuator’s filtration efficiency, capture velocity, and suction strength when evaluating overall performance. Furthermore, the smoke collection tip should be within 2 in of the surgical field to maximize efficacy. Maintenance for smoke evacuation systems should include regular (as defined by manufacturer instructions) flushing of the smoke evacuator lines.

Despite the risks of surgical smoke and the available options of minimizing these risks, the hazards of surgical smoke and the importance of protection are likely underemphasized. Many dermatologic surgeons do not use surgical masks or smoke evacuators in routine practice, according to several survey studies.9-11

It is important for the dermatologic community to consider effective ways of spreading awareness. We propose that surgical smoke safety be taught early in residency training. Additionally, smoke safety can be implemented into certification examinations. Access to masks and smoke evacuation devices are an important part of dermatology training. Accreditation Council for Graduate Medical Education funds should be appropriated to provide for such resources.



Finally, and perhaps most importantly, continued awareness should be established in the dermatology community via standardized guidelines and periodic updates in the dermatology literature and lectures at local and national conferences. Not until these strategies are implemented will surgical smoke protection be viewed as a necessary and important component of routine practice when performing dermatologic surgical procedures.

To the Editor:

We read with great interest the recent Cutis article by Golda et al,1 “Intraoperative Electrosurgical Smoke During Outpatient Surgery: A Survey of Dermatologic Surgeon and Staff Preferences.” We applaud the growing interest in the topic of dermatologist safety, as there are currently no established guidelines for precautions while performing surgical procedures. In 2018 we conducted a comprehensive review2 to characterize the specific risks, hazard reduction strategies available, and current use of surgical smoke safety techniques during surgery among dermatologists, and ultimately recommend guidance based on the current available evidence. To conduct this review, we collected data from 45 manuscripts in the dermatology, surgery, infectious disease, obstetrics, and cancer biology literature. Herein, we summarize key findings.2

Dermatologic surgeons, residents, staff, and patients are exposed to many infectious, inhalational, chemical, and mutagenic hazards when performing procedures that liberate smoke and plume. These risks are commonplace; however, they are particularly notable during ablative laser and laser hair removal procedures, which produce a heavy plume (averaging >100,000 particles/cm3). Brief periods of heavy plume exposure also are commonplace during electrosurgery.

Infectious particles in surgical plume have been extensively studied, and viral transmission has been demonstrated in animal studies. Human papillomavirus transmission appears to be the most prevalent risk. Surgical smoke has been shown to cause acute and chronic inhalational injury in rat and sheep studies.3-6

Additionally, chemicals with carcinogenic potential are present in surgical smoke and have been described.7,8 Chemicals in the greatest quantity include hydrocarbons, nitriles, fatty acids, and phenols. Although there have been no human studies on smoke carcinogenesis to date, surgical smoke has been shown to have carcinogenic properties in vitro.



Given these risks—both evidence based and theoretical—we believe that diligent hazard reduction strategies should be employed whenever possible. Surgical masks and high-efficiency particulate air respirators, such as N95 respirator masks, have been well studied and do provide smoke protection. High-efficiency particulate air masks can be worn when possible, especially during procedures that produce heavy plume, though surgical masks are capable of filtering most of the noxious chemicals in surgical smoke. It should be noted that proper fit with minimal air leak is the most important aspect of overall performance.

Smoke evacuators provide another level of protection. The physician should consider the evacuator’s filtration efficiency, capture velocity, and suction strength when evaluating overall performance. Furthermore, the smoke collection tip should be within 2 in of the surgical field to maximize efficacy. Maintenance for smoke evacuation systems should include regular (as defined by manufacturer instructions) flushing of the smoke evacuator lines.

Despite the risks of surgical smoke and the available options of minimizing these risks, the hazards of surgical smoke and the importance of protection are likely underemphasized. Many dermatologic surgeons do not use surgical masks or smoke evacuators in routine practice, according to several survey studies.9-11

It is important for the dermatologic community to consider effective ways of spreading awareness. We propose that surgical smoke safety be taught early in residency training. Additionally, smoke safety can be implemented into certification examinations. Access to masks and smoke evacuation devices are an important part of dermatology training. Accreditation Council for Graduate Medical Education funds should be appropriated to provide for such resources.



Finally, and perhaps most importantly, continued awareness should be established in the dermatology community via standardized guidelines and periodic updates in the dermatology literature and lectures at local and national conferences. Not until these strategies are implemented will surgical smoke protection be viewed as a necessary and important component of routine practice when performing dermatologic surgical procedures.

References
  1. Golda N, Merrill B, Neill B. Intraoperative electrosurgical smoke during outpatient surgery: a survey of dermatologic surgeon and staff preferences. Cutis. 2019;104:120-124.
  2. Georgesen C, Lipner SR. Surgical smoke: risk assessment and mitigation strategies. J Am Acad Dermatol. 2018;79:746-755.
  3. Wenig BL, Stenson KM, Wenig BM, et al. Effects of plume produced by the Nd:YAG laser and electrocautery on the respiratory system. Lasers Surg Med. 1993;13:242-245.
  4. Baggish MS, Elbakry M. The effects of laser smoke on the lungs of rats. Am J Obstet Gynecol. 1987;156:1260-1265.
  5. Baggish MS, Baltoyannis P, Sze E. Protection of the rat lung from the harmful effects of laser smoke. Lasers Surg Med. 1988;8:248-253.
  6. Freitag L, Chapman GA, Sielczak M, et al. Laser smoke effect on the bronchial system. Lasers Surg Med. 1987;7:283-288.
  7. Barrett WL, Garber SM. Surgical smoke: a review of the literature. Is this just a lot of hot air? Surg Endosc. 2003;17:979-987.
  8. Hensman C, Baty D, Willis RG, et al. Chemical composition of smoke produced by high-frequency electrosurgery in a closed gaseous environment. Surg Endosc. 1998;12:1017-1019.
  9. Edwards BE, Reiman RE. Results of a survey on current surgical smoke control practices. AORN J. 2008;87:739-749.
  10. Oganesyan G, Eimpunth S, Kim SS, et al. Surgical smoke in dermatologic surgery. Dermatol Surg. 2014;40:1373-1377.
  11. Chapman LW, Korta DZ, Lee PK, et al. Awareness of surgical smoke risks and assessment of safety practices during electrosurgery among US dermatology residents. JAMA Dermatol. 2017;153:467-468.
References
  1. Golda N, Merrill B, Neill B. Intraoperative electrosurgical smoke during outpatient surgery: a survey of dermatologic surgeon and staff preferences. Cutis. 2019;104:120-124.
  2. Georgesen C, Lipner SR. Surgical smoke: risk assessment and mitigation strategies. J Am Acad Dermatol. 2018;79:746-755.
  3. Wenig BL, Stenson KM, Wenig BM, et al. Effects of plume produced by the Nd:YAG laser and electrocautery on the respiratory system. Lasers Surg Med. 1993;13:242-245.
  4. Baggish MS, Elbakry M. The effects of laser smoke on the lungs of rats. Am J Obstet Gynecol. 1987;156:1260-1265.
  5. Baggish MS, Baltoyannis P, Sze E. Protection of the rat lung from the harmful effects of laser smoke. Lasers Surg Med. 1988;8:248-253.
  6. Freitag L, Chapman GA, Sielczak M, et al. Laser smoke effect on the bronchial system. Lasers Surg Med. 1987;7:283-288.
  7. Barrett WL, Garber SM. Surgical smoke: a review of the literature. Is this just a lot of hot air? Surg Endosc. 2003;17:979-987.
  8. Hensman C, Baty D, Willis RG, et al. Chemical composition of smoke produced by high-frequency electrosurgery in a closed gaseous environment. Surg Endosc. 1998;12:1017-1019.
  9. Edwards BE, Reiman RE. Results of a survey on current surgical smoke control practices. AORN J. 2008;87:739-749.
  10. Oganesyan G, Eimpunth S, Kim SS, et al. Surgical smoke in dermatologic surgery. Dermatol Surg. 2014;40:1373-1377.
  11. Chapman LW, Korta DZ, Lee PK, et al. Awareness of surgical smoke risks and assessment of safety practices during electrosurgery among US dermatology residents. JAMA Dermatol. 2017;153:467-468.
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