What's new in atopic eczema? An analysis of systematic reviews published in 2018. Part 1: prevention and topical therapies.
Administration, Topical
Animals
Breast Feeding
/ statistics & numerical data
Complementary Therapies
/ adverse effects
Dermatitis, Atopic
/ diagnosis
Eczema
/ drug therapy
Fatty Acids
/ administration & dosage
Female
Humans
Hypothalamo-Hypophyseal System
/ drug effects
Infant Formula
/ adverse effects
Infant, Newborn
Janus Kinase Inhibitors
/ administration & dosage
Lacticaseibacillus rhamnosus
/ immunology
Milk
/ adverse effects
Naltrexone
/ administration & dosage
Narcotic Antagonists
/ administration & dosage
Pituitary-Adrenal System
/ drug effects
Pregnancy
Probiotics
/ therapeutic use
Skin Lightening Preparations
/ adverse effects
Steroids
/ administration & dosage
Vitamin D
/ therapeutic use
Whey Proteins
/ administration & dosage
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
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
974-979Subventions
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.
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