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    Topical treatments for atopic dermatitis (eczema): Systematic review and network meta-analysis of randomized trials

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    1-s2.0-S0091674923011132-main.pdf (1.371Mb)
    Date
    2023-12-31
    Author
    Derek K., Chu
    Chu, 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
    ...show more authors ...show less authors
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    Abstract
    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.
    URI
    https://www.sciencedirect.com/science/article/pii/S0091674923011132
    DOI/handle
    http://dx.doi.org/10.1016/j.jaci.2023.08.030
    http://hdl.handle.net/10576/50632
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