Abstract
Background: Bleach bathing is frequently recommended to treat atopic dermatitis (AD), but its efficacy and safety are uncertain. Objective: To systematically synthesize randomized controlled trials (RCTs) addressing bleach baths for AD. Methods: We searched MEDLINE, EMBASE, CENTRAL, and GREAT from inception to December 29, 2021, for RCTs assigning patients with AD to bleach vs no bleach baths. Paired reviewers independently and in duplicate screened records, extracted data, and assessed risk of bias (Cochrane version 2) and GRADE quality of evidence. We obtained unpublished data, harmonized individual patient data and did Frequentist and Bayesian random-effects meta-analyses. Results: There were 10 RCTs that enrolled 307 participants (median of mean age 7.2 years, Eczema Area Severity Index baseline mean of means 27.57 [median SD, 10.74]) for a median of 6 weeks (range, 4-10). We confirmed that other trials registered globally were terminated. Bleach baths probably improve AD severity (22% vs 32% improved Eczema Area Severity Index by 50% [ratio of means 0.78, 95% credible interval 0.59-0.99]; moderate certainty) and may slightly reduce skin Staphylococcal aureus colonization (risk ratio, 0.89 [95% confidence interval, 0.73-1.09]; low certainty). Adverse events, mostly dry skin and irritation, along with itch, patient-reported disease severity, sleep quality, quality of life, and risk of AD flares were not clearly different between groups and of low to very low certainty. Conclusion: In patients with moderate-to-severe AD, bleach baths probably improve clinician-reported severity by a relative 22%. One in 10 will likely improve severity by 50%. Changes in other patient-important outcomes are uncertain. These findings support optimal eczema care and the need for additional large clinical trials. Trial Registration: PROSPERO Identifier: CRD42021238486.
Original language | English (US) |
---|---|
Pages (from-to) | 660-668.e9 |
Journal | Annals of Allergy, Asthma and Immunology |
Volume | 128 |
Issue number | 6 |
DOIs | |
State | Published - Jun 2022 |
ASJC Scopus subject areas
- Pulmonary and Respiratory Medicine
- Immunology and Allergy
- Immunology
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In: Annals of Allergy, Asthma and Immunology, Vol. 128, No. 6, 06.2022, p. 660-668.e9.
Research output: Contribution to journal › Article › peer-review
TY - JOUR
T1 - Bleach baths for atopic dermatitis
T2 - A systematic review and meta-analysis including unpublished data, Bayesian interpretation, and GRADE
AU - Bakaa, Layla
AU - Pernica, Jeffrey M.
AU - Couban, Rachel J.
AU - Tackett, Kelly Jo
AU - Burkhart, Craig N.
AU - Leins, Liz
AU - Smart, Joanne
AU - Garcia-Romero, Maria Teresa
AU - Elizalde-Jiménez, Itzel Guadalupe
AU - Herd, Michael
AU - Asiniwasis, Rachel Netahe
AU - Boguniewicz, Mark
AU - De Benedetto, Anna
AU - Chen, Lina
AU - Ellison, Kathy
AU - Frazier, Winfred
AU - Greenhawt, Matthew
AU - Huynh, Joey
AU - LeBovidge, Jennifer
AU - Lind, Mary Laura
AU - Lio, Peter
AU - O'Brien, Monica
AU - Ong, Peck Y.
AU - Silverberg, Jonathan I.
AU - Spergel, Jonathan M.
AU - Wang, Julie
AU - Begolka, Wendy Smith
AU - Schneider, Lynda
AU - Chu, Derek K.
N1 - Funding Information: Disclosures: Dr. De Benedetto is an investigator for Dermira, Kiniksa, Novartis, and Pfizer and a consultant for dMed Biopharmaceutical Co, Ltd. Dr. Boguniewicz conducts research at Regeneron and Incyte; and is part of advisory boards and consults for AbbVie, Janssen, LEO Pharma, Lilly, Pfizer, Regeneron, and Sanofi Genzyme. Ms. Begolka declares receiving research grants from Pfizer; is on the advisory board for Incyte and Pfizer; received honoraria from Incyte and Pfizer; and is a principal investigator for Pfizer. Dr. Greenhawt is a consultant for Aquestive; a member of physician and medical advisory boards for DBV Technologies, Sanofi/Regeneron, Genentech, Nutricia, Novartis, Acquestive, Allergy Therapeutics, Pfizer, US World Meds, Allergenis, Aravax, and Prota; a member of the Scientific Advisory Council for the National Peanut Board; the senior associate editor for the Annals of Allergy, Asthma & Immunology; a member of the Joint Taskforce on Allergy Practice Parameters; and has received honorarium for lectures from ImSci, the Allergy and Asthma Foundation of America, and the MedLearningGroup. Dr. Garcia-Romero has received honoraria as a speaker from Pierre Fabre and Sanofi; and has served on an advisory board for Pfizer. Dr. Lind is the co-founder of Sequitur Health Corporation. Dr. Lio reports receiving research grants/funding from the National Eczema Association, AOBiome, Regeneron/Sanofi Genzyme, and AbbVie; is on the speaker's bureau for Regeneron/Sanofi Genzyme, Pfizer, Incyte, Eli Lilly, LEO, Galderma, and L'Oreal; reports serving on the consulting/advisory boards for Almirall, ASLAN Pharmaceuticals, Concerto Biosciences, Dermavant, Regeneron/Sanofi Genzyme, Pfizer, LEO Pharmaceuticals, AbbVie, Eli Lilly, Micreos, L'Oreal, Pierre-Fabre, Johnson & Johnson, Level Ex, KPAway, Unilever, Menlo Therapeutics, Theraplex, IntraDerm, Exeltis, AOBiome, Realm Therapeutics, Altus Labs, Galderma, Verrica, Arbonne, Amyris, Bodewell, Burt's Bees, My-Or Diagnostics, and Kimberly-Clark; has a patent pending for a Theraplex product with royalties paid; is a board member and scientific advisory committee member of the National Eczema Association; an investor at LearnSkin; and has stock options with Micreos, Altus Labs, Boston Skin Science, and Concerto Biosciences. Dr. Ong is a consultant for Regeneron, Sanofi, Janssen, Incyte, and AbbVie. Dr. Pernica reports receiving a grant from MedImmune. Dr. Spergel declares receiving grants or contracts from Novartis, Abbott, Regeneron, Sanofi, and the National Institutes of Health; receiving royalties or licenses from UpToDate; receiving consulting fees from Regeneron, Sanofi, Novartis, Takeda, Allakos, and Alladapt; receiving payment or honoraria for lectures, presentations, speakers’ bureaus, manuscript writing, or educational events from Medscape and Rockpointe; and being on the Safety Monitoring Board or Advisory Board of the National Institute of Allergy and Infectious Disease and of Syneos. Dr. Schneider is on the Medical Advisory Board for Food Allergy Research and Education and the Data and Safety Monitoring Board for Alladapt; and an investigator for DBV Technologies and Regeneron. Dr. Wang reports receiving institutional research funding from Regeneron, DBV, and Aimmune; consultancy fees from DBV, ALK Abello, and Genentech; being an UpToDate author; and being a member of Joint Task Force on Practice Parameters. All other authors declare no conflict of interest. Funding: This work receives funding from the American Academy of Allergy, Asthma & Immunology and the American College of Allergy, Asthma and Immunology. Role of the Funding Source: The American College of Allergy, Asthma & Immunology and the American Academy of Allergy, Asthma & Immunology commissioned this review through the Joint Task Force on Practice Parameters to inform upcoming guidance on management of atopic dermatitis. The funder contributed to defining the scope of the review but otherwise had no role in study design and data collection. After agreeing to the initial scope of the project, the funder did not have any input in the interpretation of the data, drafting of the manuscript, and submission of the report. The funder received a copy of the manuscript at time of submission. The review team had the ability, but not obligation, to consider the funder's feedback. The first and corresponding authors had full access to all data in the study and had final responsibility for the decision to submit for publication. Funding Information: Disclosures: Dr. De Benedetto is an investigator for Dermira, Kiniksa, Novartis, and Pfizer and a consultant for dMed Biopharmaceutical Co, Ltd. Dr. Boguniewicz conducts research at Regeneron and Incyte; and is part of advisory boards and consults for AbbVie, Janssen, LEO Pharma, Lilly, Pfizer, Regeneron, and Sanofi Genzyme. Ms. Begolka declares receiving research grants from Pfizer; is on the advisory board for Incyte and Pfizer; received honoraria from Incyte and Pfizer; and is a principal investigator for Pfizer. Dr. Greenhawt is a consultant for Aquestive; a member of physician and medical advisory boards for DBV Technologies, Sanofi/Regeneron, Genentech, Nutricia, Novartis, Acquestive, Allergy Therapeutics, Pfizer, US World Meds, Allergenis, Aravax, and Prota; a member of the Scientific Advisory Council for the National Peanut Board; the senior associate editor for the Annals of Allergy, Asthma & Immunology; a member of the Joint Taskforce on Allergy Practice Parameters; and has received honorarium for lectures from ImSci, the Allergy and Asthma Foundation of America, and the MedLearningGroup. Dr. Garcia-Romero has received honoraria as a speaker from Pierre Fabre and Sanofi; and has served on an advisory board for Pfizer. Dr. Lind is the co-founder of Sequitur Health Corporation. Dr. Lio reports receiving research grants/funding from the National Eczema Association, AOBiome, Regeneron/Sanofi Genzyme, and AbbVie; is on the speaker's bureau for Regeneron/Sanofi Genzyme, Pfizer, Incyte, Eli Lilly, LEO, Galderma, and L'Oreal; reports serving on the consulting/advisory boards for Almirall, ASLAN Pharmaceuticals, Concerto Biosciences, Dermavant, Regeneron/Sanofi Genzyme, Pfizer, LEO Pharmaceuticals, AbbVie, Eli Lilly, Micreos, L'Oreal, Pierre-Fabre, Johnson & Johnson, Level Ex, KPAway, Unilever, Menlo Therapeutics, Theraplex, IntraDerm, Exeltis, AOBiome, Realm Therapeutics, Altus Labs, Galderma, Verrica, Arbonne, Amyris, Bodewell, Burt's Bees, My-Or Diagnostics, and Kimberly-Clark; has a patent pending for a Theraplex product with royalties paid; is a board member and scientific advisory committee member of the National Eczema Association; an investor at LearnSkin; and has stock options with Micreos, Altus Labs, Boston Skin Science, and Concerto Biosciences. Dr. Ong is a consultant for Regeneron, Sanofi, Janssen, Incyte, and AbbVie. Dr. Pernica reports receiving a grant from MedImmune. Dr. Spergel declares receiving grants or contracts from Novartis, Abbott, Regeneron, Sanofi, and the National Institutes of Health; receiving royalties or licenses from UpToDate; receiving consulting fees from Regeneron, Sanofi, Novartis, Takeda, Allakos, and Alladapt; receiving payment or honoraria for lectures, presentations, speakers’ bureaus, manuscript writing, or educational events from Medscape and Rockpointe; and being on the Safety Monitoring Board or Advisory Board of the National Institute of Allergy and Infectious Disease and of Syneos. Dr. Schneider is on the Medical Advisory Board for Food Allergy Research and Education and the Data and Safety Monitoring Board for Alladapt; and an investigator for DBV Technologies and Regeneron. Dr. Wang reports receiving institutional research funding from Regeneron, DBV, and Aimmune; consultancy fees from DBV, ALK Abello, and Genentech; being an UpToDate author; and being a member of Joint Task Force on Practice Parameters. All other authors declare no conflict of interest. Funding Information: Funding: This work receives funding from the American Academy of Allergy, Asthma & Immunology and the American College of Allergy, Asthma and Immunology. Publisher Copyright: © 2022 American College of Allergy, Asthma & Immunology
PY - 2022/6
Y1 - 2022/6
N2 - Background: Bleach bathing is frequently recommended to treat atopic dermatitis (AD), but its efficacy and safety are uncertain. Objective: To systematically synthesize randomized controlled trials (RCTs) addressing bleach baths for AD. Methods: We searched MEDLINE, EMBASE, CENTRAL, and GREAT from inception to December 29, 2021, for RCTs assigning patients with AD to bleach vs no bleach baths. Paired reviewers independently and in duplicate screened records, extracted data, and assessed risk of bias (Cochrane version 2) and GRADE quality of evidence. We obtained unpublished data, harmonized individual patient data and did Frequentist and Bayesian random-effects meta-analyses. Results: There were 10 RCTs that enrolled 307 participants (median of mean age 7.2 years, Eczema Area Severity Index baseline mean of means 27.57 [median SD, 10.74]) for a median of 6 weeks (range, 4-10). We confirmed that other trials registered globally were terminated. Bleach baths probably improve AD severity (22% vs 32% improved Eczema Area Severity Index by 50% [ratio of means 0.78, 95% credible interval 0.59-0.99]; moderate certainty) and may slightly reduce skin Staphylococcal aureus colonization (risk ratio, 0.89 [95% confidence interval, 0.73-1.09]; low certainty). Adverse events, mostly dry skin and irritation, along with itch, patient-reported disease severity, sleep quality, quality of life, and risk of AD flares were not clearly different between groups and of low to very low certainty. Conclusion: In patients with moderate-to-severe AD, bleach baths probably improve clinician-reported severity by a relative 22%. One in 10 will likely improve severity by 50%. Changes in other patient-important outcomes are uncertain. These findings support optimal eczema care and the need for additional large clinical trials. Trial Registration: PROSPERO Identifier: CRD42021238486.
AB - Background: Bleach bathing is frequently recommended to treat atopic dermatitis (AD), but its efficacy and safety are uncertain. Objective: To systematically synthesize randomized controlled trials (RCTs) addressing bleach baths for AD. Methods: We searched MEDLINE, EMBASE, CENTRAL, and GREAT from inception to December 29, 2021, for RCTs assigning patients with AD to bleach vs no bleach baths. Paired reviewers independently and in duplicate screened records, extracted data, and assessed risk of bias (Cochrane version 2) and GRADE quality of evidence. We obtained unpublished data, harmonized individual patient data and did Frequentist and Bayesian random-effects meta-analyses. Results: There were 10 RCTs that enrolled 307 participants (median of mean age 7.2 years, Eczema Area Severity Index baseline mean of means 27.57 [median SD, 10.74]) for a median of 6 weeks (range, 4-10). We confirmed that other trials registered globally were terminated. Bleach baths probably improve AD severity (22% vs 32% improved Eczema Area Severity Index by 50% [ratio of means 0.78, 95% credible interval 0.59-0.99]; moderate certainty) and may slightly reduce skin Staphylococcal aureus colonization (risk ratio, 0.89 [95% confidence interval, 0.73-1.09]; low certainty). Adverse events, mostly dry skin and irritation, along with itch, patient-reported disease severity, sleep quality, quality of life, and risk of AD flares were not clearly different between groups and of low to very low certainty. Conclusion: In patients with moderate-to-severe AD, bleach baths probably improve clinician-reported severity by a relative 22%. One in 10 will likely improve severity by 50%. Changes in other patient-important outcomes are uncertain. These findings support optimal eczema care and the need for additional large clinical trials. Trial Registration: PROSPERO Identifier: CRD42021238486.
UR - http://www.scopus.com/inward/record.url?scp=85130588627&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85130588627&partnerID=8YFLogxK
U2 - 10.1016/j.anai.2022.03.024
DO - 10.1016/j.anai.2022.03.024
M3 - Article
C2 - 35367346
AN - SCOPUS:85130588627
SN - 1081-1206
VL - 128
SP - 660-668.e9
JO - Annals of Allergy, Asthma and Immunology
JF - Annals of Allergy, Asthma and Immunology
IS - 6
ER -