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. 2022 Mar 7;87(5):1186–1189. doi: 10.1016/j.jaad.2022.03.004

Telemedicine management of systemic therapy with isotretinoin of patients with moderate-to-severe acne during the COVID-19 pandemic: A longitudinal prospective feasibility study

David Moreno-Ramírez a,, Miguel A Duarte-Ferreras a, Teresa Ojeda-Vila a, Irene García-Morales a, Maria D Conejo-Mir a, Almudena Fernández-Orland a, Ana I Sánchez-del-Campo a, Noemí Eiris a, Ana M Carrizosa a, Andrés Ruiz-de-Casas a, Jose M de-la-Torre a, Juan M Herrerías-Esteban b, Lara Ferrándiz a
PMCID: PMC8901237  PMID: 35271937

To the Editor: Moderate-to-severe acne bears a high risk of scarring, which makes timely therapy a mainstay for successful management. A prospective longitudinal study was conducted at the Dermatology Digital Center of the University Hospital Virgen Macarena (Seville, Spain), an academic public hospital covering an area of 550,000 inhabitants, between September 1, 2020, and December 31, 2020, to assess the feasibility of store-and-forward teledermatology to manage patients with acne suitable for treatment with oral isotretinoin.1 Family physicians captured clinical pictures using mobile phones (Fig 1 ).1 The Dermatology Digital Center responded with a report with the diagnosis and recommended treatment (oral isotretinoin), additional information sheets, and instructions. Acne severity was assessed using the Global Acne Grading System (GAGS) and the Investigator Global Assessment of acne.2

Fig 1.

Fig 1

Teledermatology-based acne management procedure: (1) the family physician captures pictures using a smartphone and a specific app that uploads the pictures to the teledermatology web platform of the Andalusian Health Service; (2) the teleconsultation is assessed by the dermatologist of the Dermatology Digital Center; (3) in patients suitable for treatment with oral isotretinoin, a teleconsultation report is submitted to the family physician with the following attached documents: an information sheet about expected benefits and potential adverse effects of isotretinoin, instructions about isotretinoin intake, a template to collect additional information (eg, weight, current medication intake, major medical conditions), instructions about oral contraception according to local protocols, a consent form to be signed in case they agree to participate, and basal blood tests request (eg, complete blood cell count, serum lipid profile, liver function tests, and a pregnancy test); (4) if the patient agrees to start treatment with isotretinoin, blood tests are taken at the primary care center and are available for the dermatologist through the electronic records; (5) isotretinoin is then prescribed by the dermatologist through the electronic prescription platform and is available to be picked up by the patients at their community pharmacy using their health care electronic card. A further teleconsultation report with treatment and follow-up instructions is also submitted to the family physician. Follow-up of these patients is supported by the dermatologist at the digital center through teleconsultations as scheduled in the report or on request in case of any drug reaction or other events. Follow-up teleconsultations and blood tests are scheduled, if no unexpected event occurs, for 2 months after the start and after the end of the treatment. TD, Teledermatology.

During the study period, the Dermatology Digital Center received 4394 teleconsultations with an average response time of 33.03 hours (range, 0.7-164.00 hours) and 284 of those (6.46%) involving patients with acne. Oral isotretinoin was offered to 60 patients (21.13%) with moderate-to-severe acne. Six of them (9.38%) refused isotretinoin. Fifty-three patients composed the intention-to-treat sample, and 46 (86.79%) patients completed the treatment as per protocol (Table I ). Oral corticosteroids were prescribed before isotretinoin for 8 patients (15.09%), and 11 women (52.38%) started receiving oral contraceptives.

Table I.

Basal and final characteristics of the study patients

Characteristic Basal End of study
Age (y) 18.89
95% CI, 11.11-20.66
Range, 13-38
Sex
 Male 60.38% (n = 32)
 Female 39.62% (n = 21)
Initial dose
 20 mg/d 5.66% (n = 3)
 30 mg/d 58.49% (n = 31)
 40 mg/d 33.96% (n = 18)
 50 mg/d 1.89% (n = 1)
Cumulative dose (mg/kg, mean) 123.1
95% CI, 118.18-128.04
Range, 160.00-62.07
Treatment time (d) 240.10
95% CI, 229.87-250.33
Range, 120-300
Teleconsultations (n) 175
Average number of teleconsultations per patient 3.57
95% CI, 3.31-3.84
IGA 0 58.49% n = 31
IGA 1 22.64% n = 12
IGA 2 5.66% n = 3
IGA 3§ 77.36% n = 41 5.66% n = 3
IGA 4װ 22.64% n = 12 0
GAGS 20.81
18.64-22.99
2.51
1.17-3.85
<0.001
Mean GAGS reduction 87.94%

GAGS, Global Acne Grading System; IGA, Investigator Global Assessment.

IGA 0: “clear skin”—residual hyperpigmentation and erythema may be present.

IGA 1: “almost clear”—a few scattered comedones and a few small papules.

IGA 2: “mild”—easily recognizable, less than half the face is involved, some comedones and some papules and pustules.

§

IGA 3: “moderate”—more than half the face is involved, many comedones, papules and pustules, 1 nodule may be present.

װ

IGA 4: “severe”—entire face is involved, covered with comedones, numerous papules and pustules, and few nodules and cysts.

In the intention-to-treat analysis, 42 patients (79.25%) achieved an 80% reduction in the basal GAGS score, with 31 patients (58.49%) achieving a 100% reduction in the basal GAGS score (Investigator Global Assessment score, 0). At the end of the study, the GAGS score showed an 87.94% reduction (Table I). The per-protocol analysis yielded GAGS80 and GAGS100 rates of 91.30% (n = 42) and 67.39% (n = 31), respectively (Table I).

After exclusion of mucocutaneous effects, the most common adverse effects were hyperlipidemia (13.04%), myalgia (10.87%), and hypertransaminasemia (6.52%), followed by creatine-phosphokinase increase (6.52%), headache (4.30%), arthralgia (4.30%), effluvium (4.30%), keloids (2.17%), and hand eczema (2.17%). All these toxic events were mild and led to isotretinoin discontinuation in only 1 patient, who showed a 3-fold increase in liver enzyme levels.

This study was conducted during the second wave of the COVID-19 pandemic in Spain. Primary care services had still not been restored to normal, and hospital services were avoiding in-person care as much as possible. In these settings, teledermatology-based acne management has yielded remarkable therapeutic response, with a refusal rate (9.38%) similar to the rate reported with face-to-face visits (13.3%)3 and an early termination percentage (13.21%) much lower than that reported by the iPLEDGE REMS (Risk Evaluation and Mitigation Strategy) program (36.8%).4

Limitations of this study are related to the sample size, consequence of the innovative approach, GAGS score underestimation due to the lack of pictures from some anatomic areas in 15.43% of teleconsultations, and the more difficult assessment of nodules (score, 4).

Store-and-forward teledermatology is feasible for the management of patients with moderate-to-severe acne who need oral isotretinoin in situations of health care delivery restrictions, such as those stemming from the COVID-19 pandemic. This pilot experience may also support the use of this procedure beyond the pandemic, particularly in health care services not capable of offering timely care to patients with moderate-to-severe acne.

Conflicts of interest

None disclosed.

Acknowledgments

This study has been possible thanks to the efforts and interest of the family physicians and staff nurses of the North Seville and Seville Primary Care Areas who have cared for patients with acne jointly with the dermatologists of the Dermatology Digital Center of the University Hospital Virgen Macarena.

Footnotes

Funding sources: The Dermatology Digital Center takes part in the Digital Hospital for Managing First Access to Care Project funded by a competitive grant obtained from the Health Council of the Regional Government of Andalusia, Spain (PIN-0187-2018).

IRB approval status: Reviewed and approved by the local investigation board of the University Hospital Virgen Macarena for the project proposal PIN-0187-2018.

Reprints not available from the authors.

References

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