Europe PMC

This website requires cookies, and the limited processing of your personal data in order to function. By using the site you are agreeing to this as outlined in our privacy notice and cookie policy.

Abstract 


Background

Bleach baths have been proposed as a treatment for decreasing the severity of atopic dermatitis (AD). However, conflicting results have been found regarding their efficacy.

Objective

To determine the efficacy of bleach vs water baths at decreasing AD severity.

Methods

We performed a systematic review of all studies evaluating the efficacy of bleach baths for AD. Cochrane, EMBASE, GREAT, LILACS, MEDLINE, and Scopus were searched. Two authors independently performed study selection and data extraction.

Results

Five studies were included in the review. Four studies reported significantly decreased AD severity in patients treated with bleach on at least 1 time point. However, of 4 studies comparing bleach with water baths, only 2 found significantly greater decreases in AD severity with bleach baths, 1 found greater decreases with water baths, and 1 found no significant differences. In pooled analyses, there were no significant differences observed between bleach vs water baths at 4 weeks vs baseline for the Eczema Area and Severity Index (I2 = 98%; random effect regression model, P = .16) or body surface area (I2 = 96%; P = .36).

Conclusion

Although bleach baths are effective in decreasing AD severity, they do not appear to be more effective than water baths alone. Future larger-scale, well-designed randomized controlled trials are needed.

Free full text 


Logo of hhspaLink to Publisher's site
Ann Allergy Asthma Immunol. Author manuscript; available in PMC 2018 Nov 1.
Published in final edited form as:
PMCID: PMC5726436
NIHMSID: NIHMS904119
PMID: 29150071

Efficacy of bleach baths in reducing severity of atopic dermatitis: A systematic review and meta-analysis

Rishi Chopra, MS,1 Paras P. Vakharia, PharmD,1 Ryan Sacotte, BS,1 and Jonathan I. Silverberg, MD, PhD, MPH2,3

Introduction

Atopic dermatitis (AD) is a chronic, relapsing inflammatory skin disorder affecting 15–20% of children and 1–10% of adults in the United States and worldwide14. Deficiencies in the epidermal barrier and dysfunction of the immune system contribute to AD pathogenesis, resulting in the characteristic signs and symptoms of AD (e.g. xerosis and pruritus) and predisposing patients to cutaneous infections. AD is associated with a higher prevalence of epidermal S. aureus colonization compared with healthy controls (>70% vs. 10–20%)5, 6. In particular, AD severity is correlated with epidermal S. aureus density; AD flares are associated with cutaneous S. aureus infection, and AD exacerbations may be induced by S. aureus overgrowth even without frank infection5, 7, 8. Given the importance of S. aureus colonization and microbiome in AD, anti-bacterial treatments have been considered for managing AD9. However, the prolonged use of traditional topical and/or systemic antibiotics to suppress recolonization may be impractical given potential concerns about increased antibiotic resistance from long-term antibiotic use10, 11.

Bleach (sodium hypochlorite, NaOCl) baths are an inexpensive, widely accessible, alternative antibiotic treatment that may not worsen antibiotic resistance12. Bleach baths demonstrate in vitro and in vivo antibacterial and anti-biofilm properties13, 14, are associated with few adverse events, demonstrate no harmful effects on stratum corneum hydration, transepidermal water loss (TEWL), and epidermal pH15, and do not appear to cause antibiotic resistance12. As such, dilute bleach baths have been proposed to suppress epidermal S. aureus load and ultimately reduce AD severity. Huang et al.9 first conducted a randomized controlled trial (RCT) of bleach baths as a treatment for moderate-to-severe AD with promising results. However, subsequent RCT yielded conflicting results. Nevertheless, bleach baths are recommended in multiple clinical practice guidelines1619. We performed a systematic review in order to determine the whether bleach baths are consistently effective in improving the severity of AD.

Methods

Literature search

This study was exempt from Institutional Review Board approval at Northwestern University Feinberg School of Medicine as data were gathered from published literature. The following databases were searched for articles prior to June 5, 2017: Cochrane Library, MEDLINE, EMBASE, Global Resource of EczemA Trials (GREAT), Latin American and Caribbean Health Sciences (LILACS) and Scopus.

Inclusion criteria were: any retrospective or prospective study, use of bleach bath or topical bleach agent interventions, evaluation of AD severity, patients with AD of any age, published online, in print, or in press, in any language before June 5, 2017. Title and abstract review were performed independently by three reviewers (R.C, P.V, and R.S.) with conflicts resolved by discussion. Studies were excluded based on the title and/or abstract if there was no clear indication they evaluated the efficacy of bleach therapy in AD patients. The remaining articles underwent full-text review for inclusion.

Data extraction

The following data were collected: first author; year of publication; study design; comparison/control arm; geographical region; type of intervention; number of patients enrolled in study; number of patients completed study; age; gender; level of blinding; baseline severity instruments and means; target population; severity scale used for inclusion and whether thresholds were provided; inclusion and exclusion criteria; AD diagnostic criteria; permitted and prohibited medications; bathing protocol; bleach concentration; duration and frequency of baths; bath aftercare; non-adherence criteria; length of study; follow-up intervals; severity scores; S. aureus colonization; epidermal S. aureus density; and frequency of adverse events. Study authors were contacted in order to obtain any values unspecified or incorrectly documented in the manuscripts.

Statistical analysis

Statistical analyses were performed in SAS version 9.4 (SAS Institute; Cary, NC). Comparable outcomes across at least 3 studies were combined and pooled means were estimated. Pooled mean and standard deviations were estimated and plotted. Cohen’s D and 95% confidence intervals (CI) were used to measure effect size. Significant heterogeneity of results was detected across studies as judged by an I2 statistic >50%. Therefore, random-effect models were performed in order to generate more accurate estimates of standard error between studies. A 2-sided P-value of 0.05 was taken as significant.

Results

Study selection

We identified 124 non-duplicate citations via our initial search strategy. The title and abstract review excluded 116 citations, while the full-text review excluded an additional 3 citations. We included 5 studies9, 2023 in this systematic review as outlined in the Preferred Reporting Items for Systematic Reviews and Meta-Analyses24 flow diagram (Fig. 1).

An external file that holds a picture, illustration, etc.
Object name is nihms904119f1.jpg
Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) diagram

Study characteristics

Study characteristics are described in Table 1. Among the 5 studies, 3 were RCT, one was a randomized crossover trial, and one was a single-arm pilot study. Two studies were double-blinded, two were single-blinded, and one was unblinded. Four studies were prospective and one was partially prospective and retrospective. Date of publication ranged from 2009–2016. Three studies were conducted in North America and 2 in Asia.

Table 1

Characteristics of bleach bath randomized controlled trials.

VariablesHuang, 2009Wong, 2013Gonzales, 2015Hon, 2016
Study designRCTRCTRCTRCT (crossover design)
N completed study22361840
Completion rate (Treatment/Placebo)60.0/81.385.7/85.790.0/81.8100.0/100.0
Age (min-max months)8.4–207.636–3603–60145.2*
Diagnostic criteriaNot documentedH&REichenfield modificationH&R
Inclusion criteria; definitions providedModerate-to-severe (IGA); YesModerate-to-severe (R-L); NoModerate-to-severe (IGA); YesModerate-to-severe (oSCORAD); Yes
Signs of cutaneous infection required for inclusionYesNoNoYes
InterventionsCephalexin (2 weeks) and intranasal mupirocin and bleach baths vs. cephalexin and intranasal petrolatum and water bathBleach baths vs. water bathsBleach baths and TCS BID vs. water baths and TCS BIDBleach baths vs. water baths
BlindingSingleDoubleSingleDouble
Blinding protocolMupirocin and petrolatum ointment were dispensed in identical white jars. Bleach and water were dispensed in identical bleach bottles with identical brand-name labels. Patients and/or family members were able to distinguish bleach from water based on odor, but were directed not to reveal their treatment to investigators. Bathing in bleach did not result in lasting odor so investigators were not able to differentiate between study arms.Bleach and distilled water were dispensed in identical bottles.Plain white bottles were filled with bleach or water.Bleach and water were dispensed in identical opaque, brown bottles with identical brand-name labels. Investigators were blinded to the contents of the bottles. Patients and investigators were blinded to study arm. The bleach and water dilution was pretested so that the color and odor were similar. Patients and/or family members were able to distinguish bleach from water based on odor, but were directed not to reveal their treatment to investigators. Bathing in bleach did not result in lasting odor so investigators were not able to differentiate between study arms.
Bathing instructions provided to patient0.5 cup of 6% bleach or water was added to a full bathtub of water (40 gallons). Amount of bleach or water was adjusted by the family on the basis of the bathtub size and height of bathtub water.Clear oral and written instructions were provided. 100 mL of sodium hypochlorite 5% or 100 mL of distilled water was added to 100 L of water (e.g. half a bathtub). For children <12 years old, 50 mL was added to a ¼ tub of water (50 L). Patients instructed to soak neck down.Instruction handout was provided. ¼ cup of household bleach (6.15% sodium hypochlorite) was added to half-full bathtub, or a ½ cup in a full bathtub (40 gallons), or ½ teaspoon per gallon of water if they were using a baby tub.83 ml of 6% bleach from a prepared bottle or water to 100 L of water. Amount was adjusted by the family on the basis of the bathtub size and estimated height of bathtub water.
Bath frequency and durationBIW; 5–10 minutesBIW; 10 minutesBIW; Not documentedBIW-TIW; 10 minutes
Bath aftercareNot documentedPatients should rinse off with normal tap water.Not documentedNot documented
Standardization of TCSNot documentedNot documentedBID but unrelated to bath scheduleNot permitted
Other interventions prohibitedtopical or systemic antibioticssystemic antibiotics or oral steroidstopical or systemic antibioticsSystemic antibiotics, topical steroids, or antihistamines
Other interventions permittedstable regimen of topical anti-inflammatories and emollientsstable regimen of topical anti-inflammatories and emollientspreviously used emollientsstable regimen of emollients
Adherence definedYesNoYesYes
Study duration (days)84562828
Outcomes assessedTotal EASI, IGA, BSATotal EASI, BSA, VAS-itch, PROIGA, Total EASI, local EASISCORAD, oSCORAD, BSA, CDLQI, TEWL, SH
Follow-up assessment schedule (days)28, 8414, 28, 562828
Bleach baths cause significant reduction in severityYesYesYesNot documented
Water baths cause significant reduction in severityYesNot documentedYesNot documented
Bleach or water baths more effective1 month=Bleach (EASI, BSA, IGA); 3 months=Bleach (EASI, BSA), No difference (IGA)1 month=No difference (total EASI, BSA, VAS itch, PRO); 2 months=Bleach (EASI, BSA), No difference (VAS itch, PRO)1 month= No difference (IGA, total EASI, local EASI)1 month (ITT)= No difference (oSCORAD, pruritus, sleep loss, SCORAD intensity, CDLQI), Bleach (BSA and [oSCORAD per protocol approach])
Changes in S. aureus colonization
Absence/Presence CFU or quantitative PCRNo significant differenceNot documentedNot documentedNot documented
Not documentedNo significant differenceNo significant differenceNo significant difference
Adverse eventsNot documentedNo significant differenceNo significant differenceNo significant difference
*Mean age not documented

BIW=twice weekly; TIW=thrice weekly; BID=twice daily; RCT=randomized controlled trial; DC=diagnostic criteria; IGA=Investigator Global Assessment; HR=Hanifin & Rajka criteria; R-L=Rajka and Langeland; oSCORAD=objective Scoring Atopic Dermatitis; TCS=topical corticosteroid; PRO=undefined patient reported outcome (patient overall assessment of treatment response); CFU=colony forming units; PCR=polymerase chain reaction; SH=skin hydration (unspecified methodology); TEWL=transepidermal water loss; VAS=visual analog scale; BSA=body surface area;

Four trials were included children and one included both children and adults (mean: 13.7–145.2 months; range: 3–360 months). Study populations ranged from 18 to 40 patients. AD was diagnosed by the Hanifin & Rajka (H&R) criteria in 2 studies, and Eichenfield modification of H&R criteria in one study; diagnostic criteria were not documented in 2 studies. All 5 studies recruited patients with moderate-severe AD, as judged by Investigator Global Assessments (IGA) (n=3), objective SCORing AD (oSCORAD) (n=1), or Rajka & Langeland (R-L) (n=1). Washout and concomitant treatment regimen are presented in Table 1.

Four studies evaluated the efficacy of 0.005% bleach baths, and one study evaluated a 0.0061% cleanser containing bleach. Lengths of baths ranged from 5–10 minutes with one study not documenting whether bathing times were standardized. Patients were instructed to bathe in bleach baths or use the bleach cleanser biweekly (n=3), biweekly or triweekly (n=1), and triweekly or more frequently (n=1). Allowance for additional regular water baths were not restricted (n=1) or not documented (n=4).

Study follow-up assessments ranged from 2 (n=1), 4 (n=5), 8 (n=2), and 12 weeks (n=2). Outcome measures included body surface area (BSA; n=4), eczema area and severity index (EASI; n=3), IGA (n=3), local-EASI (n=1), SCORAD/oSCORAD (n=1), children’s dermatology life quality index (CDLQI; n=1), visual analog scale (VAS)-itch (n=1), TEWL (n=1) and skin hydration using an unspecified methodology (n=1). Four studies assessed different bacteriologic parameters.

Efficacy

Four studies documented whether bleach baths or cleansers caused significant reductions in AD severity. All 4 demonstrated significant reductions in the bleach group in at least one time point. However, among 4 studies comparing bleach to water baths, only 2 found significantly greater reductions in AD severity with bleach baths, 1 with water baths, and 1 found no significant differences.

At 4 weeks, one study found a significant reduction in AD severity compared to controls (EASI, BSA, IGA), two found no significant differences (EASI [n=2], IGA [n=1], local-EASI [n=1], BSA [n=1], VAS-itch [n=1], and patient self-assessment [n=1]), and one showed mixed results. In other words, out of the aggregated 15 severity assessment evaluations, only 3 assessments demonstrated that bleach baths were more effective than water baths, 11 revealed no difference, and 1 demonstrated regular water baths to be more effective.

In one study at 8-weeks, bleach baths caused significant reductions in EASI and BSA assessments, but not VAS-itch or the patient’s self-assessment. In one study at 12-weeks, bleach baths caused significant reductions in EASI and BSA, but not IGA. Across all five studies at all follow-up periods, there were no significant differences in patient-reported outcomes (PRO) between both treatment arms.

Pooled analysis of efficacy

EASI and BSA assessments at 4-weeks were the only end-points and time-points in common across at least 3 studies (Fig. 2A, B). In pooled analyses, the mean ± std. dev. EASI and BSA decreased at 4 weeks vs. baseline in both the bleach (EASI: 11.0±7.8 vs. 24.9±25.3; BSA: 42.8%±12.7% vs. 49.8%±18.1%) and water bath (EASI: 14.2±7.7 vs. 25.2±12.3; BSA: 41.1%±18.1% vs. 45.6%±17.9%) groups, respectively (Fig. 2C, D). There were no significant differences observed between bleach vs. water baths at 4 weeks vs. baseline for EASI (I2=98%; random effect regression model, P=0.16) or BSA (I2=96%; P=0.36).a

An external file that holds a picture, illustration, etc.
Object name is nihms904119f2.jpg
EASI and BSA for bleach vs. water baths at 4 weeks compared with baseline

Mean (A) EASI and (B) BSA of bleach baths (solid lines) and water baths (dashed lines) are presented for individual studies. Pooled mean ± std. dev. (C) EASI and (D) BSA of bleach baths (solid lines) and water baths (dashed lines) are presented for 3 combined studies.

Bacteriologic assessments

All 5 studies evaluated the effect of bleach baths or cleansers on S. aureus status, but only 4 were able to reliably assess bacteriologic parameters. One study found no reduction in the proportion of patients colonized in both groups. Three of 3 studies found reductions in S. aureus density after both bleach and normal baths, but with no significant differences between groups. Two studies found no significant differences of antibiotic resistance between groups.

Safety, tolerability, and adherence

Adverse events (AE) of bleach baths and cleansers were documented in 4 of 5 studies. AE included stinging/burning (6/56; 11%), itch (6/57; 0.5%), xerosis (4/38; 10.5%), erythema (2/29; 6.9%), urticaria (1/20; 5%), oozing (1/20; 5%). There were no differences of AE between bleach and water baths.

Adherence was assessed in 3 studies, but was measured differently across all studies (completion of cephalexin therapy, frequency and concentration of bleach baths, frequency and duration of intranasal mupirocin application, whether patients bathed <2 times per week, delayed follow-up, or using oral antibiotics during the study). There were no significant differences in adherence between patients in both treatment arms.

Discussion

This systematic review found that bleach baths/cleansers and water baths alone significantly reduced AD severity. However, water baths were as effective as bleach baths at 4 weeks in pooled analyses, with only one study of efficacy at later time-points. There were no differences of S. aureus density in patients treated with bleach vs. water baths. Together, the results suggest that much of the efficacy of bleach baths at reducing AD severity is attributable to water baths and less the bleach per se.

Bleach baths are compound interventions with multiple steps: water bath, exposure to bleach during the bath, and application of emollients and/or topical anti-inflammatory agents after the bath. Each of these 3 steps may be effective at reducing AD severity. Water baths alone may hydrate and sooth the skin, and can wash away scale and serum-crust. The bleach may have anti-staphylococcal and other disinfecting properties. Although, the results of the present study indicate that water baths were similarly effective as bleach baths at disinfecting the skin. Application of emollients and/or topical anti-inflammatories after the bath (referred to as prehydration, “soak and seal”, or “soak and smear”) may seal moisture in the stratum corneum, increased permeability, and enhance drug absorption25, 26. Previous studies showed good efficacy for soak and smears2729, though a recent RCT found no greater efficacy than TCS on dry skin30. Water bath alone or the soak and smear regimen may be effective without the addition of bleach.

Bleach baths are commonly recommended because they are inexpensive, relatively safe and easily accessible. Upon reviewing the results of this study, clinicians might wonder what difference does it make whether bleach baths or water baths alone should be recommended? However, there are several important considerations. Exposure to dilute bleach can result in stinging, burning and transient worsening of itch. Ocular exposure to bleach can be particularly uncomfortable and hinders prehydration of the face. There is additional cost and time spent acquiring bleach, albeit fairly minimal. Bleach may stain towels, linens and/or clothing. Bleach baths emit caustic fumes. One of the authors (JS) had two patients with reported asthma exacerbations due to inhalation of fumes from bleach baths. It is important to recognize that water baths alone might accomplish similar efficacy as bleach baths without these additional concerns.

Comparison of study results is hindered by differences of inclusion criteria, patient phenotype, interventions, and outcome measures across studies. Different diagnostic criteria and severity assessments were used to recruit patients, which may result in study populations with differing phenotype31, 32. Active cutaneous infections were used as inclusion criteria in half of studies and exclusion criteria in the other half. Blinding protocols and success varied across studies. Only half of RCT exclusively compared bleach to water baths without other concurrent interventions. One study concurrently administered mupirocin and cephalexin, which may be confounding factors9. Different severity measures were used to evaluate efficacy outcomes across studies, showing inconsistent efficacy between studies and within individual studies. Differences in bathing protocol may have impacted study results. Bathing is a multicomponent process comprised of soap, water and bleach exposure factors (e.g. duration, frequency, temperature, etc.), and aftercare such as drying, emollients and topical medications. There was no documented efforts to standardize most of these variables, except frequency and duration of baths in all studies and soap-use in one study. Only one study standardized TCS use, and no studies coordinated the use of TCS and emollient with bath regimens. As the principal intervention of interest, bathing protocol should be thoroughly documented, standardized, and isolated from the effect of confounding factors such as additional concurrent interventions. Future studies are needed that properly address these concerns.

Current primary care provider recommendations advocate for infrequent bathing in AD33. However, the results of this systematic review indicate that regular bathing and emollient use is an effective treatment for AD and better than infrequent bathing. These results provide evidence to support the AAD guidelines’ recommendation for regular bathing in the care of AD34. The AAD guidelines also recommend use of dilute bleach baths in patients with frequent bacterial infections34. Interestingly, bleach baths were not more effective than water baths in studies that recruited patients with clinically infected AD. It may be that water baths alone can reduce risk of bacterial infection in AD patients and future studies are needed to elucidate this point.

The studies included in this systematic review showed no significant difference between bleach and water bath interventions in reducing S. aureus epidermal colonization or density. These findings are unexpected as AD exacerbations are correlated with epidermal S. aureus density and bleach baths are hypothesized to improve AD severity via their antibacterial properties14, 35. In contrast, bleach baths and mupirocin were found to eradicate S. aureus colonization in an RCT of non-AD patients with community acquired staphylococcal skin/soft tissue infections compared to controls at 1 and 4 months (63% vs. 38% and 71% vs. 48%, respectively)36. A recent Cochrane review concluded there are no discernable benefits of anti-staphylococcal interventions in reducing S. aureus density in AD patients compared to anti-inflammatory medications37, which is consistent with the results of our study.

Our study has several strengths including the use of a comprehensive search strategy and examination of studies from all countries and languages. Pooled analysis was performed at 4 weeks using random-effects regression models to address issues of heterogeneity. This pooled analysis provided novel insight by demonstrating that water baths were also effective at reducing AD severity. However, there are several limitations to our study, including a small number of studies, small study populations, short follow-up durations, and each were conducted at a single center. Moreover, there was a lack of uniformity with respect to AD diagnostic and inclusion criteria, demographics, study interventions, and outcome measures across studies, which require cautious interpretation.

In conclusion, while bleach baths are effective in reducing AD severity, they do not appear to be more effective than water bath alone. However, there are a number of limitations with the currently available studies. Future, larger-scale RCT are needed that address these limitations.

Abbreviations used

ADatopic dermatitis
RCTrandomized controlled trial
SCORAD indexScoring Atopic Dermatitis index
EASIEczema Area and Severity Index
IGAInvestigator’s Global Assessment

Footnotes

Publisher's Disclaimer: This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final citable form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.

JI Silverberg had full access to all the data in the study and takes responsibility for the integrity of the data and accuracy of the data analysis.

Study concept and design: JI Silverberg

Acquisition of Data: P Vakharia, R Chopra R Sacotte

Analysis and interpretation of data: JI Silverberg, P Vakharia, R Chopra, R Sacotte, Drafting of the manuscript: JI Silverberg, P Vakharia, R Chopra, R Sacotte

Critical revision of the manuscript for important intellectual content: JI Silverberg, P Vakharia, R Chopra, R Sacotte

Statistical analysis: R Chopra, J Silverberg

Obtained funding: JI Silverberg

Administrative technical or material support: None

Study supervision: None

Financial disclosures: None

Funding Support: This publication was made possible with support from the Agency for Healthcare Research and Quality (AHRQ), grant number K12 HS023011, and the Dermatology Foundation.

Design and conduct of the study? No

Collection, management, analysis and interpretation of data? No

Preparation, review, or approval of the manuscript? No

Decision to submit the manuscript for publication? No

Conflicts of interest: There are no conflicts of interest to declare for JI Silverberg, PP Vakharia, R Chopra, or R Sacotte.

Trial registration: Not applicable

References

1. Eichenfield LF. Consensus guidelines in diagnosis and treatment of atopic dermatitis. Allergy. 2004;59(Suppl 78):86–92. [Abstract] [Google Scholar]
2. Garg N, Silverberg JI. Epidemiology of childhood atopic dermatitis. Clin Dermatol. 2015;33:281–288. [Abstract] [Google Scholar]
3. Silverberg JI, Garg NK, Paller AS, Fishbein AB, Zee PC. Sleep disturbances in adults with eczema are associated with impaired overall health: a US population-based study. The Journal of investigative dermatology. 2015;135:56–66. [Abstract] [Google Scholar]
4. Silverberg JI, Hanifin JM. Adult eczema prevalence and associations with asthma and other health and demographic factors: a US population-based study. The Journal of allergy and clinical immunology. 2013;132:1132–1138. [Abstract] [Google Scholar]
5. Clausen ML, Edslev SM, Andersen PS, Clemmensen K, Krogfelt KA, Agner T. Staphylococcus aureus colonization in atopic eczema and its association with filaggrin gene mutations. The British journal of dermatology. 2017 [Abstract] [Google Scholar]
6. Totte JE, van der Feltz WT, Hennekam M, van Belkum A, van Zuuren EJ, Pasmans SG. Prevalence and odds of Staphylococcus aureus carriage in atopic dermatitis: a systematic review and meta-analysis. The British journal of dermatology. 2016;175:687–695. [Abstract] [Google Scholar]
7. Guzik TJ, Bzowska M, Kasprowicz A, et al. Persistent skin colonization with Staphylococcus aureus in atopic dermatitis: relationship to clinical and immunological parameters. Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 2005;35:448–455. [Abstract] [Google Scholar]
8. Hauser C. The role of Staphylococcus aureus in atopic dermatitis. International journal of dermatology. 1986;25:573–574. [Abstract] [Google Scholar]
9. Huang JT, Abrams M, Tlougan B, Rademaker A, Paller AS. Treatment of Staphylococcus aureus colonization in atopic dermatitis decreases disease severity. Pediatrics. 2009;123:e808–814. [Abstract] [Google Scholar]
10. Jung MY, Chung JY, Lee HY, Park J, Lee DY, Yang JM. Antibiotic Susceptibility of Staphylococcus aureus in Atopic Dermatitis: Current Prevalence of Methicillin-Resistant Staphylococcus aureus in Korea and Treatment Strategies. Ann Dermatol. 2015;27:398–403. [Europe PMC free article] [Abstract] [Google Scholar]
11. Chaptini C, Quinn S, Marshman G. Methicillin-resistant Staphylococcus aureus in children with atopic dermatitis from 1999 to 2014: A longitudinal study. Australas J Dermatol. 2016;57:122–127. [Abstract] [Google Scholar]
12. Barnes TM, Greive KA. Use of bleach baths for the treatment of infected atopic eczema. Australas J Dermatol. 2013;54:251–258. [Abstract] [Google Scholar]
13. Fisher RG, Chain RL, Hair PS, Cunnion KM. Hypochlorite killing of community-associated methicillin-resistant Staphylococcus aureus. Pediatr Infect Dis J. 2008;27:934–935. [Abstract] [Google Scholar]
14. Eriksson S, van der Plas MJ, Morgelin M, Sonesson A. Antibacterial and anti-biofilm effects of sodium hypochlorite against Staphylococcus aureus isolates derived from patients with atopic dermatitis. The British journal of dermatology. 2017 [Abstract] [Google Scholar]
15. Shi VY, Foolad N, Ornelas JN, et al. Comparing the effect of bleach and water baths on skin barrier function in atopic dermatitis: a split-body randomized controlled trial. The British journal of dermatology. 2016;175:212–214. [Abstract] [Google Scholar]
16. Weitz NA, Brody E, Lauren CT, et al. Management of Infectious Aspects of Atopic Dermatitis in Primary Care: A Resident Survey. Clin Pediatr (Phila) 2016 [Abstract] [Google Scholar]
17. Chong M, Fonacier L. Treatment of Eczema: Corticosteroids and Beyond. Clinical reviews in allergy & immunology. 2016;51:249–262. [Abstract] [Google Scholar]
18. Mohan GC, Lio PA. Comparison of Dermatology and Allergy Guidelines for Atopic Dermatitis Management. JAMA dermatology. 2015;151:1009–1013. [Abstract] [Google Scholar]
19. Ophir D, Elad Y, Dolev Z, Geller-Bernstein C. Effects of inhaled humidified warm air on nasal patency and nasal symptoms in allergic rhinitis. Annals of allergy. 1988;60:239–242. [Abstract] [Google Scholar]
20. Hon KL, Tsang YC, Lee VW, et al. Efficacy of sodium hypochlorite (bleach) baths to reduce Staphylococcus aureus colonization in childhood onset moderate-to-severe eczema: A randomized, placebo-controlled cross-over trial. The Journal of dermatological treatment. 2016;27:156–162. [Abstract] [Google Scholar]
21. Wong SM, Ng TG, Baba R. Efficacy and safety of sodium hypochlorite (bleach) baths in patients with moderate to severe atopic dermatitis in Malaysia. The Journal of dermatology. 2013;40:874–880. [Abstract] [Google Scholar]
22. Ryan C, Shaw RE, Cockerell CJ, Hand S, Ghali FE. Novel sodium hypochlorite cleanser shows clinical response and excellent acceptability in the treatment of atopic dermatitis. Pediatric dermatology. 2013;30:308–315. [Europe PMC free article] [Abstract] [Google Scholar]
23. Gonzalez ME, Schaffer JV, Orlow SJ, et al. Cutaneous microbiome effects of fluticasone propionate cream and adjunctive bleach baths in childhood atopic dermatitis. Journal of the American Academy of Dermatology. 2016;75:481–493. e488. [Europe PMC free article] [Abstract] [Google Scholar]
24. Liberati A, Altman DG, Tetzlaff J, et al. The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. PLoS Med. 2009;6:e1000100. [Europe PMC free article] [Abstract] [Google Scholar]
25. Schaefer H, Zesch A, Stüttgen Gn. Skin permeability. Berlin ; New York: Springer-Verlag; 1982. [Google Scholar]
26. Rothman S. Physiology and biochemistry of the skin. Chicago: Univ. of Chicago Press; 1954. [Google Scholar]
27. Hajar T, Hanifin JM, Tofte SJ, Simpson EL. Prehydration is effective for rapid control of recalcitrant atopic dermatitis. Dermatitis : contact, atopic, occupational, drug : official journal of the American Contact Dermatitis Society, North American Contact Dermatitis Group. 2014;25:56–59. [Europe PMC free article] [Abstract] [Google Scholar]
28. Rustad K, Henning S. Direct observed "soak and smear" therapy for severe eczematous dermatitis in the combat setting. Dermatitis : contact, atopic, occupational, drug : official journal of the American Contact Dermatitis Society, North American Contact Dermatitis Group. 2009;20:275–277. [Abstract] [Google Scholar]
29. Gutman AB, Kligman AM, Sciacca J, James WD. Soak and smear: a standard technique revisited. Archives of dermatology. 2005;141:1556–1559. [Abstract] [Google Scholar]
30. Kohn LL, Kang Y, Antaya RJ. A randomized, controlled trial comparing topical steroid application to wet versus dry skin in children with atopic dermatitis (AD) Journal of the American Academy of Dermatology. 2016;75:306–311. [Abstract] [Google Scholar]
31. Vakharia PP, Chopra R, Silverberg JI. Systematic Review of Diagnostic Criteria Used in Atopic Dermatitis Randomized Controlled Trials. American journal of clinical dermatology. 2017 [Abstract] [Google Scholar]
32. Chopra RVP, Simpson E, Paller A, Silverberg JI. Severity assessments used for inclusion criteria and baseline severity evaluation in atopic dermatitis clinical trials: a systematic review. JEADV. 2017 [Abstract] [Google Scholar]
33. Cardona ID, Kempe E, Hatzenbeuhler JR, Antaya RJ, Cohen B, Jain N. Bathing Frequency Recommendations for Children with Atopic Dermatitis: Results of Three Observational Pilot Surveys. Pediatric dermatology. 2015;32:e194–196. [Abstract] [Google Scholar]
34. Eichenfield LF, Tom WL, Berger TG, et al. Guidelines of care for the management of atopic dermatitis: section 2. Management and treatment of atopic dermatitis with topical therapies. Journal of the American Academy of Dermatology. 2014;71:116–132. [Europe PMC free article] [Abstract] [Google Scholar]
35. Alsterholm M, Strombeck L, Ljung A, et al. Variation in Staphylococcus aureus Colonization in Relation to Disease Severity in Adults with Atopic Dermatitis during av Five-month Follow-up. Acta dermato-venereologica. 2017 [Abstract] [Google Scholar]
36. Fritz SA, Camins BC, Eisenstein KA, et al. Effectiveness of measures to eradicate Staphylococcus aureus carriage in patients with community-associated skin and soft-tissue infections: a randomized trial. Infect Control Hosp Epidemiol. 2011;32:872–880. [Europe PMC free article] [Abstract] [Google Scholar]
37. Bath-Hextall FJ, Birnie AJ, Ravenscroft JC, Williams HC. Interventions to reduce Staphylococcus aureus in the management of atopic eczema: an updated Cochrane review. The British journal of dermatology. 2010;163:12–26. [Abstract] [Google Scholar]

Citations & impact 


Impact metrics

Jump to Citations

Citations of article over time

Alternative metrics

Altmetric item for https://www.altmetric.com/details/28969053
Altmetric
Discover the attention surrounding your research
https://www.altmetric.com/details/28969053

Article citations


Go to all (35) article citations

Funding 


Funders who supported this work.

AHRQ HHS (1)