Topical treatments for atopic dermatitis (eczema): Systematic review and network meta-analysis of randomized trials
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Date
2023-12-31Author
Derek K., ChuChu, Alexandro W.L.
Rayner, Daniel G.
Guyatt, Gordon H.
Yepes-Nuñez, Juan José
Gomez-Escobar, Luis
Pérez-Herrera, Lucia C.
Díaz Martinez, Juan Pablo
Brignardello-Petersen, Romina
Sadeghirad, Behnam
Wong, Melanie M.
Ceccacci, Renata
Zhao, Irene X.
Basmaji, John
MacDonald, Margaret
Chu, Xiajing
Islam, Nazmul
Gao, Ya
Izcovich, Ariel
Asiniwasis, Rachel N.
Boguniewicz, Mark
De Benedetto, Anna
Capozza, Korey
Chen, Lina
Ellison, Kathy
Frazier, Winfred T.
Greenhawt, Matthew
Huynh, Joey
LeBovidge, Jennifer
Lio, Peter A.
Martin, Stephen A.
O’Brien, Monica
Ong, Peck Y.
Silverberg, Jonathan I.
Spergel, Jonathan M.
Smith Begolka, Wendy
Wang, Julie
Wheeler, Kathryn E.
Gardner, Donna D.
Schneider, Lynda
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BackgroundAtopic dermatitis (AD) is a common skin condition with multiple topical treatment options, but uncertain comparative effects. ObjectiveWe sought to systematically synthesize the benefits and harms of AD prescription topical treatments. MethodsFor the 2023 American Academy of Allergy, Asthma & Immunology and American College of Allergy, Asthma, and Immunology Joint Task Force on Practice Parameters AD guidelines, we searched MEDLINE, EMBASE, CENTRAL, CINAHL, LILACS, ICTRP, and GREAT databases to September 5, 2022, for randomized trials addressing AD topical treatments. Paired reviewers independently screened records, extracted data, and assessed risk of bias. Random-effects network meta-analyses addressed AD severity, itch, sleep, AD-related quality of life, flares, and harms. The Grading of Recommendations Assessment, Development and Evaluation approach informed certainty of evidence ratings. We classified topical corticosteroids (TCS) using 7 groups—group 1 being most potent. This review is registered in the Open Science Framework (https://osf.io/q5m6s). ResultsThe 219 included trials (43,123 patients) evaluated 68 interventions. With high-certainty evidence, pimecrolimus improved 6 of 7 outcomes—among the best for 2; high-dose tacrolimus (0.1%) improved 5—among the best for 2; low-dose tacrolimus (0.03%) improved 5—among the best for 1. With moderate- to high-certainty evidence, group 5 TCS improved 6—among the best for 3; group 4 TCS and delgocitinib improved 4—among the best for 2; ruxolitinib improved 4—among the best for 1; group 1 TCS improved 3—among the best for 2. These interventions did not increase harm. Crisaborole and difamilast were intermediately effective, but with uncertain harm. Topical antibiotics alone or in combination may be among the least effective. To maintain AD control, group 5 TCS were among the most effective, followed by tacrolimus and pimecrolimus. ConclusionsFor individuals with AD, pimecrolimus, tacrolimus, and moderate-potency TCS are among the most effective in improving and maintaining multiple AD outcomes. Topical antibiotics may be among the least effective.
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