Evidence map›Paper›PMID 32852805›Full record

SynthesisClinical and experimental dermatology2020

What's new in atopic eczema? An analysis of systematic reviews published in 2018. Part 1: prevention and topical therapies.

F Tasker, A Brown, D J C Grindlay, N K Rogers, K E Harman

Open access · hybridAbstract readComparative StudySystematic Review
In one paragraph

Synthesis in Clinical and experimental dermatology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 1 pooled it
0.3field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Skin care interventions in infants for preventing eczema and food allergy.The Cochrane database of systematic reviews · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

F TaskerGuy's and St Thomas' Hospitals NHS Foundation Trust, London, UK.
A BrownUniversity Hospital Plymouth NHS Trust, Devon, UK.ORCID https://orcid.org/0000-0003-2707-968X
D J C GrindlayCentre of Evidence Based Dermatology, University of Nottingham, King's Meadow Campus, Nottingham, UK.ORCID https://orcid.org/0000-0002-0992-7182
N K RogersCentre of Evidence Based Dermatology, University of Nottingham, King's Meadow Campus, Nottingham, UK.ORCID https://orcid.org/0000-0001-9076-129X
K E HarmanCentre of Evidence Based Dermatology, University of Nottingham, King's Meadow Campus, Nottingham, UK.
University of Nottingham · GBSt Thomas' Hospital · GBUniversity Hospitals Plymouth NHS Trust · GB

Funding

Programme Grants for Applied Research RP-PG-0216-20007
6 · The paper itself

Abstract

This review is part of a series of annual updates that summarize the evidence base for atopic eczema (AE). The aim is to provide a succinct guide for clinicians on the key findings from 14 systematic reviews on the prevention and topical treatment of AE published or indexed in 2018. Various supplements, including long-chain polyunsaturated fatty acids, vitamin D and the probiotic Lactobacillus rhamnosus GG, given prenatally and postnatally, have not been shown to prevent AE in infants, although mixed strains of probiotics may decrease the risk of AE if given to the mother during pregnancy and to the infant for the first 6 months of life. In the postnatal period, there is no evidence that hydrolysed formula, compared with cow's milk formula (CMF), reduces the risk of AE in partially breastfed infants. However, weak evidence suggests that a specific partially hydrolysed whey formula decreases the risk of AE compared with CMF. No specific skin practices can be recommended to reduce the eczema risk in healthy term babies. There is weak evidence of a low risk of reversible hypothalamic-pituitary-adrenal axis suppression following 2-4 weeks of treatment with low-potency topical steroids, and conflicting evidence as to whether bleach bathing affects skin flora or AE severity. A single study demonstrated that the topical Janus kinase inhibitor tofacitinib at 2% significantly reduces the Eczema Area and Severity Index compared with vehicle. Topical naltrexone cream 1% improves pruritus (measured using a visual analogue scale) by 30% more than placebo. There is weak evidence that topical alternative therapies, including antioxidants, micronutrients and some herbal medicines, may improve AE.

Indexed as

Administration, TopicalAnimalsBreast FeedingComplementary TherapiesDermatitis, AtopicEczemaFatty AcidsFemaleHumansHypothalamo-Hypophyseal SystemInfant FormulaInfant, NewbornJanus Kinase InhibitorsLacticaseibacillus rhamnosusMilkNaltrexoneFatty AcidsJanus Kinase InhibitorsNaltrexoneNarcotic AntagonistsSkin Lightening PreparationsSteroidsVitamin DWhey Proteins

Identifiers

PMID32852805
PMCPMC7692938
OpenAlexW3081345402

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.