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


Journal

Clinical and experimental dermatology
ISSN: 1365-2230
Titre abrégé: Clin Exp Dermatol
Pays: England
ID NLM: 7606847

Informations de publication

Date de publication:
Dec 2020
Historique:
accepted: 21 04 2020
pubmed: 28 8 2020
medline: 29 7 2021
entrez: 28 8 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 32852805
doi: 10.1111/ced.14303
pmc: PMC7692938
doi:

Substances chimiques

Fatty Acids 0
Janus Kinase Inhibitors 0
Narcotic Antagonists 0
Skin Lightening Preparations 0
Steroids 0
Whey Proteins 0
Vitamin D 1406-16-2
Naltrexone 5S6W795CQM

Types de publication

Comparative Study Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

974-979

Subventions

Organisme : Programme Grants for Applied Research
ID : RP-PG-0216-20007

Informations de copyright

© 2020 The Authors. Clinical and Experimental Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.

Références

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pubmed: 30552987
Am J Clin Dermatol. 2019 Jun;20(3):367-377
pubmed: 30465329
Dermatol Ther (Heidelb). 2018 Sep;8(3):339-347
pubmed: 29790104
J Am Acad Dermatol. 2018 Sep;79(3):535-544
pubmed: 29673776
Int Arch Allergy Immunol. 2018;177(2):123-134
pubmed: 30001534
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pubmed: 29894408
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pubmed: 29055852
Allergy. 2018 Jan;73(1):37-49
pubmed: 28675776
J Clin Aesthet Dermatol. 2018 Dec;11(12):42-47
pubmed: 30666279
Cochrane Database Syst Rev. 2018 Oct 19;10:CD003664
pubmed: 30338526
JAMA Dermatol. 2019 Feb 1;155(2):229-236
pubmed: 30484835
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pubmed: 29762205
Horm Res Paediatr. 2018;89(6):389-396
pubmed: 29898449
Nutrients. 2018 Sep 18;10(9):
pubmed: 30231505
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World Allergy Organ J. 2015 Jan 27;8(1):4
pubmed: 25628773

Auteurs

F Tasker (F)

Guy's and St Thomas' Hospitals NHS Foundation Trust, London, UK.

A Brown (A)

University Hospital Plymouth NHS Trust, Devon, UK.

D J C Grindlay (DJC)

Centre of Evidence Based Dermatology, University of Nottingham, King's Meadow Campus, Nottingham, UK.

N K Rogers (NK)

Centre of Evidence Based Dermatology, University of Nottingham, King's Meadow Campus, Nottingham, UK.

K E Harman (KE)

Centre of Evidence Based Dermatology, University of Nottingham, King's Meadow Campus, Nottingham, UK.

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Classifications MeSH