Development and Assessment of an Artificial Intelligence-Based Tool for Skin Condition Diagnosis by Primary Care Physicians and Nurse Practitioners in Teledermatology Practices.

Importance: Most dermatologic cases are initially evaluated by nondermatologists such as primary care physicians (PCPs) or nurse practitioners (NPs). Objective: To evaluate an artificial intelligence (AI)-based tool that assists with diagnoses of dermatologic conditions. Design, Setting, and Participants: This multiple-reader, multiple-case diagnostic study developed an AI-based tool and evaluated its utility. Primary care physicians and NPs retrospectively reviewed an enriched set of cases representing 120 different skin conditions. Randomization was used to ensure each clinician reviewed each case either with or without AI assistance; each clinician alternated between batches of 50 cases in each modality. The reviews occurred from February 21 to April 28, 2020. Data were analyzed from May 26, 2020, to January 27, 2021. Exposures: An AI-based assistive tool for interpreting clinical images and associated medical history. Main Outcomes and Measures: The primary analysis evaluated agreement with reference diagnoses provided by a panel of 3 dermatologists for PCPs and NPs. Secondary analyses included diagnostic accuracy for biopsy-confirmed cases, biopsy and referral rates, review time, and diagnostic confidence.
Results: Forty board-certified clinicians, including 20 PCPs (14 women [70.0%]; mean experience, 11.3 [range, 2-32] years) and 20 NPs (18 women [90.0%]; mean experience, 13.1 [range, 2-34] years) reviewed 1048 retrospective cases (672 female [64.2%]; median age, 43 [interquartile range, 30-56] years; 41 920 total reviews) from a teledermatology practice serving 11 sites and provided 0 to 5 differential diagnoses per case (mean [SD], 1.6 [0.7]). The PCPs were located across 12 states, and the NPs practiced in primary care without physician supervision across 9 states. The NPs had a mean of 13.1 (range, 2-34) years of experience and practiced in primary care without physician supervision across 9 states. Artificial intelligence assistance was significantly associated with higher agreement with reference diagnoses. For PCPs, the increase in diagnostic agreement was 10% (95% CI, 8%-11%; P < .001), from 48% to 58%; for NPs, the increase was 12% (95% CI, 10%-14%; P < .001), from 46% to 58%. In secondary analyses, agreement with biopsy-obtained diagnosis categories of maglignant, precancerous, or benign increased by 3% (95% CI, -1% to 7%) for PCPs and by 8% (95% CI, 3%-13%) for NPs. Rates of desire for biopsies decreased by 1% (95% CI, 0-3%) for PCPs and 2% (95% CI, 1%-3%) for NPs; the rate of desire for referrals decreased by 3% (95% CI, 1%-4%) for PCPs and NPs. Diagnostic agreement on cases not indicated for a dermatologist referral increased by 10% (95% CI, 8%-12%) for PCPs and 12% (95% CI, 10%-14%) for NPs, and median review time increased slightly by 5 (95% CI, 0-8) seconds for PCPs and 7 (95% CI, 5-10) seconds for NPs per case. Conclusions and Relevance: Artificial intelligence assistance was associated with improved diagnoses by PCPs and NPs for 1 in every 8 to 10 cases, indicating potential for improving the quality of dermatologic care.

Introduction

With 2 billion people affected globally,[1] skin conditions are a leading cause of morbidity. The examination of some skin conditions by dermatologists results in significantly higher diagnostic accuracy[2,3,4] and is associated with better clinical outcomes[5] than nondermatologist examination. However, owing to lack of access to dermatologists, only 28% of skin cases are seen by a specialist[6]; therefore, nonspecialists play a pivotal role in the assessment of skin lesions and initiation of clinical management and referrals.[7] The diagnostic accuracy of nonspecialists is reportedly only 24% to 70%,[4,8,9,10] suggesting that currently available resources, such as dermatology textbooks, medical information portals, and online image search engines, remain insufficient to guide nonspecialists.

Several algorithms incorporating artificial intelligence (AI) have been developed to help interpret both clinical[11,12,13,14,15] and dermoscopic[16,17,18,19,20,21,22,23] images for a variety of skin conditions, and the effect of AI-based support on dermoscopic images has been studied.[15,24] However, an open question remains as to whether AI assistance can help primary care physicians (PCPs) and nurse practitioners (NPs) diagnose skin conditions from clinical images (ie, taken without specialized equipment).

We developed an AI-based tool and conducted a multiple-reader, multiple-case diagnostic study in which PCPs and independently practicing NPs retrospectively reviewed skin cases from a teledermatology service, representing 120 different skin conditions. We used randomization to ensure readers reviewed each case only once, either with or without AI assistance. Our primary objective was to measure the AI assistance–associated changes in diagnostic accuracy of PCPs and NPs without specialist training in dermatology.

Methods

This study was approved by the Quorum Institutional Review Board, Seattle, Washington, and deemed exempt from informed consent because all data and images were deidentified. The Standards for Reporting of Diagnostic Accuracy (STARD)[25] reporting guideline was followed for this study.

The AI Tool

Liu et al[26] previously described an AI algorithm that provides a differential diagnosis given clinical photographs of skin conditions and the medical history (eTable 1 in the Supplement). Their AI model was developed using 16 114 cases and used a convolutional neural network to output prediction scores across 419 skin conditions. In the present study, we created a web-based tool using the AI model described by Liu et al by incorporating user experience insights (Figure 1).

Figure 1.

User Interface of the Artificial Intelligence (AI)–Based Assistive Tool and the Study Design

The AI assistant shows as many as 5 top predictions of skin conditions, with the confidence in each prediction shown as colored dots and additional information (eg, sample images from an atlas) available with a click. More details are available in eFigure 1 in the Supplement. The study was designed as a multiple-reader, multiple-case (MRMC) study comprising 1048 cases. Two groups of clinicians (primary care physicians [PCPs] and nurse practitioners [NPs]) reviewed each case with or without AI assistance. The modality alternated every 50 cases. For every case, each clinician was instructed to rank as many as 3 differential diagnoses using a search-as-you-type interface and selecting matching skin conditions from a list of 3961 conditions. If their desired skin condition was not present, clinicians could provide free-text entries. All skin conditions were mapped to a list of 419 conditions. SCC indicates squamous cell carcinoma; SCCIS, SCC in situ.

The tool provides information about the case, including demographic information, history of present illness, and other elements of the patient’s medical history. For each case, 1 to 6 images were available for review (median, 4), and readers could toggle between or zoom in on images. Primary care physicians and NPs reviewed these cases using a laptop and could consult additional resources as they would in clinical practice.

The AI assistance component of the web-based tool was only available during the assisted mode of the study (described below). At the top of the panel, the interface displayed the skin conditions that were output by the AI, sorted in order of the AI’s predicted likelihood scores. Artificial intelligence predictions with low scores (<0.05) were removed, and the list was limited to 5 skin conditions to avoid presenting extraneous information. Each condition could be clicked on to display additional information (Figure 1 and eFigure 1 and the AI Tool Interface section in the eMethods in the Supplement).

Study Design

To evaluate whether this tool could assist primary care clinicians in diagnosing skin conditions, we conducted a multiple-reader, multiple-case diagnostic study with 20 PCPs and 20 NPs (Figure 1). The characteristics of the clinicians are described in the Reader Characteristics section of the eMethods and eFigures 2 and 3 in the Supplement. Before reviewing the study cases, each reader was presented with materials describing how to use the AI assistant and given the opportunity to practice using the AI assistant with 2 sample cases (independent of the study cases). Additional details of this training[27] can be found in the Onboarding Process section in the eMethods in the Supplement.

The study used cases from 2 retrospective data sets from California and Hawaii previously used to validate the AI algorithm.[26] Specifically, the prior study used a validation set A and a subset (validation set B) enriched for rarer conditions via random sampling stratified by condition. Validation set B (963 cases) was included in its entirety. From validation set A, all 85 cases for which biopsy results were available were also included to yield a total of 1048 cases (Table). None of the PCPs or NPs in this study previously reviewed these cases, and the AI algorithm used was identical to the one used in the previous study.[26]

Table.

Patient Characteristics in the Original Data Set and Final Enriched Data Set

Characteristic	Data set
	Full study (n = 1048)a	Cases with diagnoses from histologic findings (n = 152)b
Years	2017-2018	2017-2018
No. of sites	11	10
No. of images included in study	3935	413
No. of patients included in study	1016	152
Age, median (IQR), ya	43 (30-56)	49 (35-59)
Sex, No. (%)
Female	672 (64.2)	99 (65.1)
Male	375 (35.8)	53 (34.9)
Race and ethnicity, No. (%)
American Indian or Alaska Native	9 (0.9)	0
Asian	102 (9.7)	5 (3.3)
Black or African American	66 (6.3)	5 (3.3)
Hispanic or Latino	447 (42.7)	59 (38.8)
Native Hawaiian or Pacific Islander	20 (1.9)	2 (1.3)
White	365 (34.9)	80 (52.6)
Not specified	38 (3.6)	1 (0.7)
Fitzpatrick skin type (6 types), No. (%)
I	2 (0.2)	2 (1.3)
II	109 (10.4)	17 (11.2)
III	668 (63.8)	111 (73.0)
IV	205 (19.6)	14 (9.2)
V	25 (2.4)	1 (0.7)
VI	0	0
Unknown	38 (3.6)	7 (4.6)
Skin conditions based on primary diagnosis, No. (%)c
Acne	40 (3.8)	NA
Actinic keratosis	39 (3.7)	1 (0.7)
Allergic contact dermatitis	25 (2.4)	NA
Alopecia areata	37 (3.5)	NA
Androgenetic alopecia	32 (3.1)	NA
Basal cell carcinoma	36 (3.4)	32 (21.1)
Cyst	32 (3.1)	1 (0.7)
Eczema	53 (5.1)	NA
Folliculitis	32 (3.1)	3 (2.0)
Hidradenitis	34 (3.2)	NA
Lentigo	32 (3.1)	3 (2.0)
Melanocytic nevus	61 (5.8)	28 (18.4)
Melanoma	20 (1.9)	6 (3.9)
Postinflammatory hyperpigmentation	28 (2.7)	NA
Psoriasis	40 (3.8)	NA
SCC/SCCIS	34 (3.2)	14 (9.2)
SK/ISK	52 (5.0)	13 (8.6)
Scar condition	34 (3.2)	2 (1.3)
Seborrheic dermatitis	37 (3.5)	NA
Skin tag	36 (3.4)	3 (2.0)
Stasis dermatitis	25 (2.4)	NA
Tinea	31 (3.0)	1 (0.7)
Tinea versicolor	34 (3.2)	NA
Urticaria	33 (3.2)	NA
Verruca vulgaris	37 (3.5)	8 (5.3)
Vitiligo	36 (3.4)	NA
Otherd	116 (11.1)	65 (42.8)

Abbreviations: IQR, interquartile range; NA, not applicable; SCC/SCCIS, squamous cell carcinoma/squamous cell carcinoma in situ; SK/ISK, seborrheic keratosis/irritated seborrheic keratosis.

One case was removed from the study for logistical reasons.

Of 165 cases, 13 had equivocal biopsy results and were excluded from the biopsy analysis. A total of 141 cases had growths and 53 were malignant.

Enrichment was performed to avoid skew toward common conditions (eg, acne and eczema) as described previously and additionally to include all available cases with biopsy confirmation.

Conditions with fewer than 10 cases each.

Each reader was randomly assigned to 1 of 2 reader cohorts. The 2 reader cohorts read the same cases but with the opposite assistance modalities (ie, unassisted vs AI assisted) for each case. To reduce effects associated with switching modalities, the 1048 cases were divided into batches of 50 cases (except the last 48 cases, which were divided into 2 batches of 24 cases), and the assistance modality switched after each batch of cases. For the first batch of 50 cases, reader cohort 1 reviewed these cases with AI assistance, whereas reader cohort 2 reviewed the same cases unassisted. The next batch of cases were reviewed in the opposite modality (Figure 1). By ensuring each reader reviewed each case only once in either the assisted or unassisted modality, this design eliminated any memory effect associated with a crossover study (where memorable cases may inflate the diagnostic performance when reviewed a second time by the same readers).[28,29]

During the case reviews, the readers either provided their top differential diagnoses or indicated that they were unable to diagnose a case. They also answered a few questions on their intended clinical next steps for each case (see the Study End Points section below). Reviews were performed without time constraint. These reviews occurred from February 21 to April 28, 2020.

Reference Diagnoses

Reference diagnoses were provided by a panel of dermatologists.[26] Briefly, 3 US board-certified dermatologists (from a pool of 12) independently reviewed each case. The dermatologists participated in the study via Advanced Clinical, Deerfield, Illinois; had 5 to 13 years of experience (mean [SD], 7.2 [2.7] years); and practiced in multiple states, including Colorado, Hawaii, Iowa, Maryland, New York, South Carolina, Tennessee, and Texas. Reference diagnoses were obtained using a previously described collective intelligence approach, which results in more reproducible diagnoses than diagnoses obtained by individual dermatologist review (eTable 2 in the Supplement).[26,30] This approach assigns a vote to each diagnosis based on its ranking: the first diagnosis in a dermatologist’s differential was given a weight of 1/1 = 1; the secondary diagnosis was given a weight of 1/2 = 0.5. The votes for each diagnosis were summed across the 3 dermatologists, and the top-voted diagnosis was considered the primary diagnosis of the panel.

Agreement was also assessed against biopsy-confirmed diagnoses when available. Diagnoses were extracted from pathology reports by the teledermatology service before transfer to study investigators. These diagnoses were then mapped to skin conditions by US board-certified dermatologists (including K.K. and S.J.H.). The case distribution across these diagnoses (both clinical and histologic) are presented in the Table; of 152 cases with available biopsy results, the diagnosis of 141 cases was growths.

Study End Points

Our study was designed to evaluate 2 prespecified primary end points: (1) the agreement rate of the primary differential diagnosis of the PCPs with the reference diagnosis and (2) the agreement rate of the primary differential diagnosis of the NPs with the reference diagnosis. Based on the relative frequencies of conditions in this data set, the chance agreement is 3.77%.

Several secondary analyses were planned. First, for cases with biopsy results, diagnoses were classified as malignant, precancerous, or benign and were evaluated against biopsy-determined diagnoses. Clinicians were also asked to report whether they would have recommended a biopsy or referred the case to a dermatologist. For the subset of reads in which clinicians reported they would not opt for a referral, we assessed the diagnostic agreement rate. We also analyzed the time taken to review cases and self-reported diagnostic confidence.

Finally, 2 additional metrics (top-3 agreement and average overlap)[31] were used for more comprehensive evaluation of cases in which additional follow-up may be needed to arrive at a definitive diagnosis (Additional Evaluation Metrics section in the eMethods in the Supplement). An exploratory analysis also measured the effect of AI assistance on dermatologist agreement with reference diagnoses.

Statistical Analysis

Data were analyzed from May 26, 2020, to January 27, 2021. To compare clinicians reviewing cases with AI assistance and reviewing cases without, we used a permutation test[32] with 1000 iterations. In each iteration, we permuted the assignment of whether reads were assisted or unassisted (ie, one-half of the full set of assisted and unassisted reads per case were selected to be assisted and the other half unassisted). Sensitivity analysis using a permutation test that preserved the reader cohorts’ structure and another statistical analysis via a generalized linear mixed model produced similar results (see the Alternative Statistical Analyses section in the eMethods in the Supplement). Because this study had 2 prespecified primary end points (both 1-tailed superiority tests), we applied the Bonferroni correction, and P < .0125 was considered statistically significant (halved from α = 0.05 owing to 1-tailed tests and halved again owing to having 2 primary end points). Confidence intervals were computed by bootstrapping across both cases and readers for each sampled case (1000 iterations; sampling both cases and reader with replacement in each iteration). Hypothesis tests were conducted in Python, version 3.6.7 (Python Software Foundation).

Results

This study involved the participation of 40 board-certified clinicians, including 20 PCPs (14 women [70.0%] and 6 men [30.0%]; mean experience, 11.3 [range, 2-32] years) who were located across 12 states and 20 NPs (18 women [90.0%] and 2 men [10.0%]; mean experience, 13.1 [range, 2-34] years) who practiced in primary care without physician supervision across 9 states. These clinicians reviewed 1048 teledermatology cases (672 women [64.2%] and 375 men [35.8%], with 1 missing; median age, 43 [interquartile range, 30-56] years) from 11 sites (Table) and provided 0 to 5 differential diagnoses per case (mean [SD], 1.6 [0.7]), for a total of 41 920 case reviews. Every PCP and NP reviewed each case only once, either with or without AI assistance (Figure 1).

Artificial intelligence assistance was associated with significantly higher top-1 agreement with the reference diagnosis (Figure 2A and eTable 3 in the Supplement). For PCPs, the increase in diagnostic agreement was 10% (95% CI, 8%-11%; P < .001), from 48% to 58%; for NPs, the improvement was 12% (95% CI, 10%-14%; P < .001), from 46% to 58%. Assistance was associated with improvements for all 40 readers, although the magnitude varied by reader (range, 2%-22%; median, 10%) (Figure 2B). Similar improvements were observed beyond the primary diagnosis based on the top-3 agreement, average overlap, per-condition sensitivity, and κ value (eFigures 4 and 5 and eTable 3 in the Supplement). In an exploratory analysis, 2 dermatologists’ agreement with the reference diagnosis remained largely unchanged with AI assistance, increasing by 2% (95% CI, −1% to 5%), from 63% to 66% (eFigures 4 and 5 in the Supplement).[26]

Figure 2.

Comparison of Clinicians’ Diagnostic Agreement Rate With Dermatologists When Assisted by Artificial Intelligence (AI) vs Unassisted

Every clinician (primary care physicians [PCPs] or nurse practitioners [NPs]) provided their differential diagnosis (several rank-ordered conditions), which were then mapped to 419 skin conditions. Only agreement in the top differential diagnosis (how often the clinicians’ primary diagnosis agreed with the top diagnosis of a panel of dermatologists [top-1 agreement]) is considered, with additional details in eFigures 4 and 5 in the Supplement. Panels A and B cover all 1048 cases, whereas panels C and D cover 141 cases with growths and biopsy confirmation. A, Top-1 agreement increased with AI assistance (P < .001 for both PCPs and NPs). B, For top-1 agreement for unassisted vs assisted modalities for each individual clinician, a value above the diagonal indicates that the clinician had a higher agreement with dermatologists when assisted by AI. C and D, A similar analysis evaluated diagnostic accuracy for growths with biopsy confirmation on the 3-way classification of malignant, precancerous, and benign. Error bars represent 95% CIs. Additional analysis of assistance stratified by AI agreement with the reference diagnoses is presented in eFigures 6 and 7 in the Supplement.

For cases with available biopsy diagnoses (n = 141), the readers’ accuracy at classifying lesions as malignant, precancerous, or benign trended upward by 3% for PCPs (95% CI, −1% to 7%) from 64% to 67% and by 8% for NPs (95% CI, 3%-13%) from 60% to 68% (Figure 2C-D). Subgroup analysis further found that sensitivity for malignant lesions, precancerous lesions, infectious skin diseases, and categories of hair loss trended upward or remained similar with assistance for both NPs and PCPs, with improvements ranging from −1% to 36% (eTable 4 in the Supplement).

On the subset of cases in which the top prediction of AI was accurate (63% of cases), the use of assistance was associated with an increased top-1 agreement with reference diagnosis of 18% (95% CI, 16%-20%) for PCPs and 21% (95% CI, 19%-23%) for NPs. On the contrary, when none of the AI tool’s predictions was correct (13% of cases), the agreement was 8% lower (95% CI, 5%-12%) for PCPs and 9% lower (95% CI, 6%-12%) for NPs. The effects were intermediate when the correct diagnosis was in the second or third position instead of the first (see the Impact of AI Accuracy on Assistance section of eMethods and eFigures 6 and 7 in the Supplement). An exploratory analysis also suggested that assistance was particularly beneficial for less ambiguous cases. For example, in the subset of cases in which the dermatologist panel had unanimous agreement, the use of AI assistance was associated with a top-1 agreement increase of 13% (95% CI, 10%-15%) for PCPs and of 16% (95% CI, 14%-19%) for NPs (eFigure 8 in the Supplement). Subanalyses also indicated that assistance-associated benefits were consistent during the study and across several skin types (eFigures 9 and 10 in the Supplement).

Artificial intelligence assistance was also associated with changes in several simulated clinical decisions (Figure 3A-B). The rates of indicating a need for biopsy were 1% lower (95% CI, 0%-3%) for PCPs and 2% lower (95% CI, 1%-3%) for NPs; the rate of desire was 3% lower (95% CI, 1%-4%) for both PCPs and NPs (eTable 5 in the Supplement). For cases in which readers indicated referrals were unnecessary, their top-1 agreement rate with dermatologists was higher by 10% for PCPs (95% CI, 8%-12%), from 51% to 61%, and by 12% for NPs (95% CI, 10%-14%), from 47% to 59%, with a similar effect on referred cases (Figure 3C-D and eFigure 11 in the Supplement). In related findings, self-reported diagnostic confidence was substantially higher with AI assistance for both reader cohorts (Figure 4A). The top-1 agreement of cases that were rated with more than 90% confidence was substantially higher (73% vs 64% for PCPs and 68% vs 58% for NPs) (eFigure 12 in the Supplement).

Figure 3.

Comparing Simulated Clinical Decisions by Clinicians When Assisted by Artificial Intelligence vs Unassisted

A, Rate of biopsy for all cases. B, Rate of referrals for all cases. C, Diagnostic accuracy among nonreferred cases. D, Diagnostic accuracy among referred cases. Top-3 agreement rates for cases for whom the primary care physicians (PCPs) and nurse practitioners (NPs) did and did not indicate a referral are presented in eFigure 11 in the Supplement. Error bars represent 95% CIs.

Figure 4.

Comparing Clinicians’ Confidence and Case Review Time When Assisted by Artificial Intelligence vs Unassisted

A, Confidence of the primary care physicians (PCPs) and nurse practitioners (NPs) as a stacked bar plot. NA indicates cases for which the clinician could not provide a diagnosis. B, Comparison of the differences in case review time for the full set of 1048 cases as a box plot. The box edges represent quartiles, whereas the whiskers extend to the last observed points that fall within 1.5 times the interquartile range from the quartiles. Outliers beyond the whiskers are indicated with dots; a total of 182 (0.4% of the reads) outliers beyond 900 seconds are excluded from the 4 box plots for ease of visualization. The median time for diagnosis increased from 89 to 94 seconds for PCPs and from 77 to 84 seconds for NPs.

In terms of review time per case, AI assistance was associated with a slightly increased median review time. A difference of 5 (95% CI, 0-8) seconds, from 89 to 94 seconds, was observed for PCPs and a difference of 7 (95% CI, 5-10) seconds, from 77 to 84 seconds, was observed for NPs (Figure 4B and eFigure 9D in the Supplement). We also present representative examples of cases in which AI assistance was associated with the largest increases or decreases in agreement with reference diagnoses (eFigures 13 and 14 in the Supplement) and results of follow-up surveys investigating the usefulness of various AI assistant features (eFigures 15-17 in the Supplement).

Discussion

In this study, 40 clinicians each reviewed 1048 teledermatology cases, with AI assistance for a random half of the cases and without AI assistance for the remaining half. Artificial intelligence assistance was associated with a higher agreement rate with dermatologists’ reference diagnoses for both PCPs and NPs. The absolute effect size of 10% and 12% corresponds to an improved diagnosis for 1 in every 8 to 10 cases.

For both PCPs and NPs, AI assistance was also associated with lower rates of recommending a biopsy or specialist referral, marked increase in self-reported diagnostic confidence, and higher diagnostic agreement rates (with dermatologists) in nonreferred cases. These observations suggest that AI assistance improved skin condition diagnosis and diagnostic confidence of nonspecialists without incurring a reflexive increased use of referrals or biopsies. These improvements came at a modest cost of only a median of 5 to 7 additional seconds per case.

Our observations suggest that AI has the potential to augment the ability of PCPs and NPs independently practicing primary care to diagnose and triage skin conditions more effectively. Cutaneous disease is the chief complaint in 12% to 21% of primary care visits,[33,34,35,36] and access to dermatologists is limited. Nonspecialists have suboptimal diagnostic accuracy and have been shown to perform more biopsies while diagnosing fewer malignant neoplasms than dermatologists.[37] Therefore, improving the diagnostic accuracy of nonreferred cases while reducing unnecessary referrals and biopsies could have enormous implications for health care systems.

According to the American Academy of Dermatology,[38] the estimated direct health care cost of skin disease in the US is $75 billion, including $46 billion in medical costs (office visits, procedures, and tests), with an additional $11 billion of indirect opportunity costs from missed work or decreased productivity for patients and their caregivers. Appropriate diagnosis of dermatologic conditions at the point of care in primary care settings could translate to fewer delays in diagnosis and management and increased capacity for dermatology offices. Artificial intelligence also has the potential to enhance triage by improving the quality of information in referrals and enable dermatology offices to better prioritize the urgency of referrals. The clinical impact of this tool would need to be determined in prospective studies.

This AI tool uses as input images of the skin condition as well as a structured medical history. These images were taken using consumer-grade point-and-shoot cameras and mobile devices without specialized hardware. The interface used in this study was designed for store-and-forward teledermatology; however, extension to live, interactive teledermatology is in principle straightforward. In either case, the telemedicine format could be particularly useful in the COVID-19 era[39] for populations at high risk of complications in the event of infection due to in-person care. The AI tool could also be used in an in-person clinic setting because AI interpretation of images is feasible within seconds on modern smartphones. Such use could enable physicians to conduct follow-up tests (eg, potassium hydroxide test to confirm fundal infection), ask clarifying questions about the medical history, or conduct a closer physical examination to realize greater improvements in diagnostic ability.

More generally, and consistent with the consensus statements from both the American Medical Association[40] and the American Academy of Dermatology,[41] this tool was specifically designed to augment clinicians’ diagnostic ability. To improve trust and empower readers to evaluate suggestion reliability, the tool provides a measure of its confidence and canonical examples of each suggested diagnosis. For skin conditions from which the AI algorithm had limited data to learn, suggestions are accompanied by a limited data warning. These features were designed to enable nonspecialists to diagnose cases more accurately and with greater confidence.

Other studies have explored the potential of AI-based dermatology tools. Han et al[15] found a 7% increase in diagnostic accuracy when 2 dermatologists and 2 residents reviewed 2201 cases a second time with AI assistance. Assistance-associated improvements were also seen for 21 dermatologists and 26 residents on 240 images for detection of malignant neoplasms.[15] Tschandl et al[24] highlighted the importance of effective human/computer interaction for AI tools for interpreting dermoscopic images, with improvements in showing multiclass prediction probabilities by skin condition but not for binary predictions of malignant neoplasms or AI-based retrieval of similar images. Our study complements these prior works. First, we evaluated images from nonspecialized, widely available devices. Second, we specifically examined the effect of AI assistance on PCPs and NPs, who perform most skin condition assessments. In addition, we assessed 2 pivotal clinical decisions: biopsy and referral. Finally, our randomized study design avoids any potential memory effects of reviewing the same case more than once.

Limitations

This study has some limitations. First, these were teledermatology cases that were a mix of cases that were referred from primary care and other cases that were submitted at the patient’s request. The potentially increased case difficulty and case enrichment may have affected clinician diagnostic performance. Second, in terms of Fitzpatrick skin types[42] (which categorize skin tone and propensity to tan), types I and V are underrepresented, and type VI is absent in this data set.[26] Because disease can present differently across skin types, the further study of additional skin types is warranted. Third, AI-associated improvements for malignant neoplasms were lower than those across all cases, and future work is needed to further improve the AI tool for malignant neoplasms. Our randomized study design of 1 modality per case/reader pair precludes inferences about any specific case and reader. Alternative study designs such as sequential reading (unassisted followed by assisted) or fully crossed setups could be explored, although biases from anticipation of AI assistance or incomplete washout will need to be averted.[28] Finally, the “store-and-forward” nature of these cases restricted the ability of the clinicians to ask follow-up questions and perform tests. As such, the insights here are more directly relevant to a store-and-forward setting than in-person clinics or live interactive telemedicine visits.

Conclusions

Our AI tool was significantly associated with improved PCP and NP diagnostic agreement with dermatologists on skin condition cases from a teledermatology service. Prospective studies are warranted to study the impact of its use in both telemedicine settings and in-person primary care visits.