Abstract
To the Editor: Teledermatology may serve as a platform for the education of dermatology residents.1–3 Few studies have measured diagnostic1–2 and management1 concordance between residents evaluating patients in-person and attending dermatologists supervising residents via teledermatology. We report diagnostic and management concordance between resident and attending dermatologists responding to store-and-forward teledermatology consults submitted by primary care providers and discuss implications for resident education.
Keywords: teledermatology, mobile, store-and-forward, outpatient dermatology consultation, telemedicine, resident education, technology
We performed a prospective study between January and November 2013 with inclusion of 84 consults encompassing 90 dermatologic conditions. This study received approval from the Philadelphia Field Initiating Group of Human Immunodeficiency Virus Trials, Philadelphia Department of Public Health, and University of Pennsylvania institutional review boards. Verbal informed consent and Health Insurance Portability and Accountability Act authorization were obtained from patients; written informed consent was obtained from providers.
Consults were submitted to the University of Pennsylvania by 25 primary care providers at the Jonathan Lax Center, the Dr. Bernett L. Johnson, Jr. Sayre Health Center, and eight Philadelphia Department of Public Health centers using the AccessDerm (Vignet Corporation, Fairfax, VA) mobile platform.4 Diagnoses and management plans, initially drafted by dermatology residents, were reviewed, edited, and submitted by attending dermatologists. Nine residents and nine attending dermatologists responded to consults. For each dermatologic condition, two investigators (CAN, JT) independently determined the concordance of differential diagnoses and management plans between resident and attending dermatologists. Cohen’s κ assessing inter-rater reliability (95% confidence interval) for diagnostic and management concordance between the two investigators were 0.94 (0.91–0.98) and 0.87 (0.78–0.90), respectively. Statistical analyses were performed in Stata 12.1 (StatCorp LP, College Station, TX).
Each resident responded to a median (interquartile range) of 9 (4–15) consults. The number of responses stratified by dermatology training year was: 10 (12%) first, 29 (34%) second, and 45 (54%) third year residents. Based on the leading diagnosis of the attending dermatologist or definitive diagnosis when available, dermatologic conditions were classified into the following categories: 24 (27%) eczematous conditions, 13 (14%) infectious diseases, 7 (8%) benign tumors or proliferations, 6 (7%) papulosquamous conditions, 5 (6%) pigmented disorders, 4 (4%) acneiform or follicular occlusion disorders, 4 (4%) premalignant or malignant lesions, 23 (26%) other, and 4 (4%) indeterminate.
Diagnoses and management plans between resident and attending dermatologists were fully concordant for 53% and 65% of dermatologic conditions, respectively (Figure 1). Table I categorizes the changes made by attending dermatologists for those conditions with at least partial management discordance (adapted from Lamel et al5). Most changes were consistent with recommendation for education or observation (53%) and medication initiation or discontinuation (50%). Recommendation for in-person evaluation was concordant in 93% of consults.
Figure 1.
Diagnostic and management concordance between resident and attending dermatologists.
* Designation of “concordant” required complete agreement in diagnoses or management plan between resident and attending dermatologist.
† Designation of “partially concordant” was defined by agreement in at least one but not all diagnoses or partial agreement in management plan with one or more of the following categories of change between resident and attending dermatologist: recommendation for education or observation, medication initiation or discontinuation, recommendation for laboratory testing, change in medication dosage or vehicle, recommendation for procedural intervention.
†† Designation of “discordant” was defined by no agreement in diagnoses or management plan between resident and attending dermatologist.
Table I.
Categories of change in management
| Category, No. (%) | N = 32 |
|---|---|
| Recommendation for education or observation | 17 (53) |
| Medication initiation or discontinuation | 16 (50) |
| Recommendation for laboratory testing | 5 (16) |
| Change in medication dosage or vehicle* | 2 (6) |
| Recommendation for procedural intervention † | 1 (3) |
One change in medication dosage or vehicle pertained to oral antihistamines and the other pertained to a topical steroid.
The recommendation for procedural intervention pertained to a biopsy.
With the development of sustainable teledermatology programs, it is important for dermatologists to become familiar with the strengths and limitations of this practice model. Our data revealed at least partial diagnostic and management discordance between resident and attending dermatologists for 47% and 35% of dermatologic conditions, respectively. Although limited by small sample size, this study suggests that teledermatology provides residents an opportunity for practice-based learning. Further research is required to evaluate educational outcome measures.
Acknowledgements
We thank the physicians, administrators, and patients who participated in the teledermatology consult service and research study. In particular, we acknowledge the support of Dr. Kent Bream at the Dr. Bernett L. Johnson, Jr. Sayre Health Center, Dr. Helen Koenig at the Jonathan Lax Center, and Dr. Kalpana Vaidya at the Philadelphia Department of Public Health. We also express our gratitude to participating resident and attending dermatologists at the University of Pennsylvania. We appreciate the contributions of Praduman Jain, Gagan Jindal, Dave Klein, and other individuals at the Vignet Corporation as well as Kristina Finney, Alison Shippy, Scott Weinberg, and the Telemedicine Task Force of the American Academy of Dermatology.
The Philadelphia Field Initiating Group of Human Immunodeficiency Virus Trials, Philadelphia Department of Public Health, and University of Pennsylvania institutional review boards approved this study.
Funding sources:
Bertha Dagan Berman Award for a FOCUS Medical Student Fellowship in Women’s Health Dermatology Research Training Grant, National Institute Of Arthritis And Musculoskeletal And Skin Diseases of the National Institutes of Health, Award Number T32AR007465 Penn Medicine CAREs Foundation Grant
Role of the sponsors: Funding sources had no role in the design and conduct of the study; in the collection, analysis, and interpretation of data; or in the preparation, review, or approval of the manuscript.
Disclaimer: Research reported in this publication was supported by the National Institute Of Arthritis And Musculoskeletal And Skin Diseases of the National Institutes of Health under Award Number T32AR007465. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.
The American Academy of Dermatology’s AccessDerm program (accessderm.aad.org) and this research study is made possible by the Vignet (www.vignetcorp.com) teledermatology technology platform. The Vignet Corporation provided the AccessDerm software and assistance with technical support.
Footnotes
Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
Disclosure: Drs Nelson, Wanat, James, Kovarik, and Takeshita were involved in the creation of the mobile platform, however, have no institutional or corporate affiliations or any associations that might pose a conflict of interest, and have no other conflicts of interest to declare. Dr Roth had no role in the creation of the mobile platform and has no conflicts of interest to declare.
This work was presented at the Semiannual Meeting of the Dermatology Teachers Exchange Group on March 24, 2014 in Denver, CO USA. This work has not been previously published.
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