|
|
||||||||||||||
|
|
|||||||||||||||
Design
Randomised (unclear allocation concealment*), blinded (clinicians, patients, and outcome assessors),*) controlled trial with 2 years of follow up.
Setting
Antenatal clinics in Turku, Finland.
Patients
159 pregnant women who had atopic disease, or
1 first-degree relative (mother, father, or older sibling), or partner with atopic eczema, allergic rhinitis, or asthma. 132 women (83%) and 132 children completed follow up.
Intervention
Mothers were allocated to LGG (1 x 1010 colony-forming units [Valio Limited, Helsinki, Finland]) (n=77) or to placebo (microcrystalline cellulose) (n=82). The capsules were taken daily for 2 to 4 weeks before expected delivery. After delivery, breastfeeding mothers continued to take the capsules, or the children received the contents mixed with water by spoon. The capsules were taken postnatally for 6 months.
Main outcome measures
A diagnosis of atopic eczema, the main outcome measure, required pruritis or facial or extensor involvement, or both, and a chronic relapsing course (eczema for
1 mo at the
Hywel C Williams, MSc, PhD
Centre of Evidence-Based Dermatology Queen's Medical Centre Nottingham, UK
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS | REGISTER |