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    Allergen immunotherapy for atopic dermatitis: Systematic review and meta-analysis of benefits and harms

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    1-s2.0-S0091674922013227-main.pdf (650.0Kb)
    Date
    2023-01-31
    Author
    Juan José, Yepes-Nuñez
    Guyatt, Gordon H.
    Gómez-Escobar, Luis Guillermo
    Pérez-Herrera, Lucia C.
    Chu, Alexandro W.L.
    Ceccaci, Renata
    Acosta-Madiedo, Ana Sofía
    Wen, Aaron
    Moreno-López, Sergio
    MacDonald, Margaret
    Barrios, Mónica
    Chu, Xiajing
    Islam, Nazmul
    Gao, Ya
    Wong, Melanie M.
    Couban, Rachel
    Garcia, Elizabeth
    Chapman, Edgardo
    Oykhman, Paul
    Chen, Lina
    Winders, Tonya
    Asiniwasis, Rachel Netahe
    Boguniewicz, Mark
    De Benedetto, Anna
    Ellison, Kathy
    Frazier, Winfred T.
    Greenhawt, Matthew
    Huynh, Joey
    Kim, Elaine
    LeBovidge, Jennifer
    Lind, Mary Laura
    Lio, Peter
    Martin, Stephen A.
    O’Brien, Monica
    Ong, Peck Y.
    Silverberg, Jonathan I.
    Spergel, Jonathan
    Wang, Julie
    Wheeler, Kathryn E.
    Schneider, Lynda
    Chu, Derek K.
    ...show more authors ...show less authors
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    Abstract
    BackgroundAtopic dermatitis (AD, eczema) is driven by a combination of skin barrier defects, immune dysregulation, and extrinsic stimuli such as allergens, irritants, and microbes. The role of environmental allergens (aeroallergens) in triggering AD remains unclear. ObjectiveWe systematically synthesized evidence regarding the benefits and harms of allergen immunotherapy (AIT) for AD. MethodsAs part of the 2022 American Academy of Allergy, Asthma & Immunology/American College of Allergy, Asthma and Immunology Joint Task Force on Practice Parameters AD Guideline update, we searched the MEDLINE, EMBASE, CENTRAL, CINAHL, LILACS, Global Resource for Eczema Trials, and Web of Science databases from inception to December 2021 for randomized controlled trials comparing subcutaneous immunotherapy (SCIT), sublingual immunotherapy (SLIT), and/or no AIT (placebo or standard care) for guideline panel–defined patient-important outcomes: AD severity, itch, AD-related quality of life (QoL), flares, and adverse events. Raters independently screened, extracted data, and assessed risk of bias in duplicate. We synthesized intervention effects using frequentist and Bayesian random-effects models. The GRADE approach determined the quality of evidence. ResultsTwenty-three randomized controlled trials including 1957 adult and pediatric patients sensitized primarily to house dust mite showed that add-on SCIT and SLIT have similar relative and absolute effects and likely result in important improvements in AD severity, defined as a 50% reduction in SCORing Atopic Dermatitis (risk ratio [95% confidence interval] 1.53 [1.31-1.78]; 26% vs 40%, absolute difference 14%) and QoL, defined as an improvement in Dermatology Life Quality Index by 4 points or more (risk ratio [95% confidence interval] 1.44 [1.03-2.01]; 39% vs 56%, absolute difference 17%; both outcomes moderate certainty). Both routes of AIT increased adverse events (risk ratio [95% confidence interval] 1.61 [1.44-1.79]; 66% with SCIT vs 41% with placebo; 13% with SLIT vs 8% with placebo; high certainty). AIT’s effect on sleep disturbance and eczema flares was very uncertain. Subgroup and sensitivity analyses were consistent with the main findings. ConclusionsSCIT and SLIT to aeroallergens, particularly house dust mite, can similarly and importantly improve AD severity and QoL. SCIT increases adverse effects more than SLIT. These findings support a multidisciplinary and shared decision-making approach to optimally managing AD.
    URI
    https://www.sciencedirect.com/science/article/pii/S0091674922013227
    DOI/handle
    http://dx.doi.org/10.1016/j.jaci.2022.09.020
    http://hdl.handle.net/10576/44628
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