What's new in atopic eczema? An analysis of systematic reviews published in 2018. Part 1: prevention and topical therapies
- PMID: 32852805
- PMCID: PMC7692938
- DOI: 10.1111/ced.14303
What's new in atopic eczema? An analysis of systematic reviews published in 2018. Part 1: prevention and topical therapies
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.
© 2020 The Authors. Clinical and Experimental Dermatology published by John Wiley & Sons Ltd on behalf of British Association of Dermatologists.
Conflict of interest statement
There is no evidence that long chain polyunsaturated fatty acids, vitamin D and the probiotic L In the postnatal period, there is no evidence for the use of hydrolysed formula compared with CMF for the prevention of eczema in infants who are not exclusively breastfed. There is conflicting evidence as to whether bleach baths, compared with water baths, have any effect on the skin flora and severity of AE. Topical tofacitinib 2% (a JAKi) improves the severity of AE compared with vehicle. There is weak evidence for the use of topical alternative therapies to improve AE, including antioxidants, micronutrients and
References
-
- Vahdaninia M, Mackenzie H, Dean T, Helps S. Omega‐3 LCPUFA supplementation during pregnancy and risk of allergic outcomes or sensitization in offspring: a systematic review and meta‐analysis. Ann Allergy Asthma Immunol 2019; 122: 302–13.e2. - PubMed
-
- Li L, Han Z, Niu X et al Probiotic supplementation for prevention of atopic dermatitis in infants and children: a systematic review and meta‐analysis. Am J Clin Dermatol 2019; 20: 367–77. - PubMed
-
- Yepes‐Nunez JJ, Brozek JL, Fiocchi A et al Vitamin D supplementation in primary allergy prevention: systematic review of randomized and non‐randomized studies. Allergy 2018; 73: 37–49. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Medical