Evidence map›Paper›PMID 35275399›Full record

SynthesisThe Cochrane database of systematic reviews2022

Strategies for using topical corticosteroids in children and adults with eczema.

Stephanie J Lax, Jane Harvey, Emma Axon, Laura Howells, Miriam Santer, Matthew J Ridd, Sandra Lawton, Sinéad Langan, Amanda Roberts, Amina Ahmed and 8 more

Open access · bronzeAbstract readSystematic Review
In one paragraph

Synthesis in The Cochrane database of systematic reviews, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed, 4 pooled it
7.4field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

41 citing papers in PubMed, 4 syntheses or guidelines pooled it, 38 citations in OpenAlex.

  1. Topical Anti-Inflammatory Treatments for Eczema: A Cochrane Systematic Review and Network Meta-Analysis.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2024
    Pooled it
  2. Topical anti-inflammatory treatments for eczema: network meta-analysis.The Cochrane database of systematic reviews · 2024
    Pooled it
  3. Pooled it
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  5. Trial
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  8. Recommended Quantities of Emollients and Topical Corticosteroids for Eczema Management: A Comprehensive UK Survey of Hospital Guidance.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
  9. Real-World Use of Topical Treatments for Atopic Eczema in Children and Young People: Systematic Review.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
  10. Article
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  15. Review
  16. Review
  17. Fatty Acid-Rich Fraction ofPlants (Basel, Switzerland) · 2025
    Article
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  19. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 10 institutions in 4 countries.

Stephanie J Lax *Centre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Jane Harvey *Centre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Emma AxonCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Laura HowellsCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Miriam SanterDepartment of Primary Care and Population Sciences, University of Southampton, Southampton, UK.
Matthew J RiddUniversity of Bristol, Bristol, UK.
Sandra LawtonDepartment of Dermatology, Rotherham NHS Foundation Trust, Rotherham, UK.
Sinéad LanganLondon School of Hygiene and Tropical Medicine, London, UK.
Amanda RobertsNottingham Support Group for Carers of Children with Eczema, Nottingham, UK.
Amina Ahmedc/o Cochrane Skin Group, University of Nottingham, Nottingham, UK.
Ingrid MullerDepartment of Primary Care and Population Sciences, University of Southampton, Southampton, UK.
Long Chiau MingPAPRSB Institute of Health Sciences, Universiti Brunei Darussalam, Gadong, Brunei Darussalam.
Saumya PandaDepartment of Dermatology, KPC Medical College and Hospital, Kolkata, India.
Pavel ChernyshovDepartment of Dermatology and Venereology, National Medical University, Kiev, Ukraine.
Ben CarterBiostatistics and Health Informatics, King's College London; Institute of Psychiatry, Psychology & Neuroscience, London, UK.
Hywel C WilliamsCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Kim S ThomasCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
Joanne R ChalmersCentre of Evidence Based Dermatology, University of Nottingham, Nottingham, UK.
University of Nottingham · GBUniversity of Southampton · GBCochrane · GBKing's College London · GBKPC Medical College and Hospital · INLondon School of Hygiene & Tropical Medicine · GBOdessa National Medical University · UAThe Rotherham NHS Foundation Trust · GBUniversiti Brunei Darussalam · BNUniversity of Bristol · GB

Funding

Wellcome Trust 205039/Z/16/Z
6 · The paper itself

Abstract

backgroundEczema is a common skin condition. Although topical corticosteroids have been a first-line treatment for eczema for decades, there are uncertainties over their optimal use.

objectivesTo establish the effectiveness and safety of different ways of using topical corticosteroids for treating eczema. SEARCH

methodsWe searched databases to January 2021 (Cochrane Skin Specialised Register; CENTRAL; MEDLINE; Embase; GREAT) and five clinical trials registers. We checked bibliographies from included trials to identify further trials. SELECTION CRITERIA: Randomised controlled trials in adults and children with eczema that compared at least two strategies of topical corticosteroid use. We excluded placebo comparisons, other than for trials that evaluated proactive versus reactive treatment. DATA COLLECTION AND ANALYSIS: We used standard Cochrane methods, with GRADE certainty of evidence for key findings. Primary outcomes were changes in clinician-reported signs and relevant local adverse events. Secondary outcomes were patient-reported symptoms and relevant systemic adverse events. For local adverse events, we prioritised abnormal skin thinning as a key area of concern for healthcare professionals and patients. MAIN

resultsWe included 104 trials (8443 participants). Most trials were conducted in high-income countries (81/104), most likely in outpatient or other hospital settings. We judged only one trial to be low risk of bias across all domains. Fifty-five trials had high risk of bias in at least one domain, mostly due to lack of blinding or missing outcome data. Stronger-potency versus weaker-potency topical corticosteroids Sixty-three trials compared different potencies of topical corticosteroids: 12 moderate versus mild, 22 potent versus mild, 25 potent versus moderate, and 6 very potent versus potent. Trials were usually in children with moderate or severe eczema, where specified, lasting one to five weeks. The most reported outcome was Investigator Global Assessment (IGA) of clinician-reported signs of eczema. We pooled four trials that compared moderate- versus mild-potency topical corticosteroids (420 participants). Moderate-potency topical corticosteroids probably result in more participants achieving treatment success, defined as cleared or marked improvement on IGA (52% versus 34%; odds ratio (OR) 2.07, 95% confidence interval (CI) 1.41 to 3.04; moderate-certainty evidence). We pooled nine trials that compared potent versus mild-potency topical corticosteroids (392 participants). Potent topical corticosteroids probably result in a large increase in number achieving treatment success (70% versus 39%; OR 3.71, 95% CI 2.04 to 6.72; moderate-certainty evidence). We pooled 15 trials that compared potent versus moderate-potency topical corticosteroids (1053 participants). There was insufficient evidence of a benefit of potent topical corticosteroids compared to moderate topical corticosteroids (OR 1.33, 95% CI 0.93 to 1.89; moderate-certainty evidence). We pooled three trials that compared very potent versus potent topical corticosteroids (216 participants). The evidence is uncertain with a wide confidence interval (OR 0.53, 95% CI 0.13 to 2.09; low-certainty evidence). Twice daily or more versus once daily application We pooled 15 of 25 trials in this comparison (1821 participants, all reported IGA). The trials usually assessed adults and children with moderate or severe eczema, where specified, using potent topical corticosteroids, lasting two to six weeks. Applying potent topical corticosteroids only once a day probably does not decrease the number achieving treatment success compared to twice daily application (OR 0.97, 95% CI 0.68 to 1.38; 15 trials, 1821 participants; moderate-certainty evidence). Local adverse events Within the trials that tested 'treating eczema flare-up' strategies, we identified only 26 cases of abnormal skin thinning from 2266 participants (1% across 22 trials). Most cases were from the use of higher-potency topical corticosteroids (16 with very potent, 6 with potent, 2 with moderate and 2 with mild). We assessed this evidence as low certainty, except for very potent versus potent topical corticosteroids, which was very low-certainty evidence.  Longer versus shorter-term duration of application for induction of remission No trials were identified. Twice weekly application (weekend, or 'proactive therapy') to prevent relapse (flare-ups) versus no topical corticosteroids/reactive application Nine trials assessed this comparison, generally lasting 16 to 20 weeks. We pooled seven trials that compared weekend (proactive) topical corticosteroids therapy versus no topical corticosteroids (1179 participants, children and adults with a range of eczema severities, though mainly moderate or severe). Weekend (proactive) therapy probably results in a large decrease in likelihood of a relapse from 58% to 25% (risk ratio (RR) 0.43, 95% CI 0.32 to 0.57; 7 trials, 1149 participants; moderate-certainty evidence). Local adverse events We did not identify any cases of abnormal skin thinning in seven trials that assessed skin thinning (1050 participants) at the end of treatment. We assessed this evidence as low certainty. Other comparisons  Other comparisons included newer versus older preparations of topical corticosteroids (15 trials), cream versus ointment (7 trials), topical corticosteroids with wet wrap versus no wet wrap (6 trials), number of days per week applied (4 trials), different concentrations of the same topical corticosteroids (2 trials), time of day applied (2 trials), topical corticosteroids alternating with topical calcineurin inhibitors versus topical corticosteroids alone (1 trial), application to wet versus dry skin (1 trial) and application before versus after emollient (1 trial). No trials compared branded versus generic topical corticosteroids and time between application of emollient and topical corticosteroids. AUTHORS'

conclusionsPotent and moderate topical corticosteroids are probably more effective than mild topical corticosteroids, primarily in moderate or severe eczema; however, there is uncertain evidence to support any advantage of very potent over potent topical corticosteroids. Effectiveness is similar between once daily and twice daily (or more) frequent use of potent topical corticosteroids to treat eczema flare-ups, and topical corticosteroids weekend (proactive) therapy is probably better than no topical corticosteroids/reactive use to prevent eczema relapse (flare-ups). Adverse events were not well reported and came largely from low- or very low-certainty, short-term trials. In trials that reported abnormal skin thinning, frequency was low overall and increased with increasing potency. We found no trials on the optimum duration of treatment of a flare, branded versus generic topical corticosteroids, and time to leave between application of topical corticosteroids and emollient. There is a need for longer-term trials, in people with mild eczema.

Indexed as

Dermatologic AgentsEczemaAdrenal Cortex HormonesAdultChildEmollientsGlucocorticoidsHumansImmunoglobulin ARecurrenceAdrenal Cortex HormonesDermatologic AgentsEmollientsGlucocorticoidsImmunoglobulin A

Identifiers

PMID35275399
PMCPMC8916090
OpenAlexW4221063702

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.