Can earlier BCG-Japan and OPV vaccination reduce early infant mortality? A cluster-randomised trial in Guinea-Bissau

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  • Sanne Marie Thysen
  • Igualdino da Silva Borges
  • Jailson Martins
  • Alexander Dahl Stjernholm
  • Jesper Sloth Hansen
  • Leontino Manuel Vieira da Silva
  • Justiniano Sebastião Durga Martins
  • Jensen, Aksel Karl Georg
  • Amabelia Rodrigues
  • Peter Aaby
  • Christine Stabell Benn
  • Ane Baerent Fisker
Objective To assess the effect of providing BCG and oral polio vaccine (OPV) at an early home visit after delivery.

Design Cluster-randomised trial, randomising 92 geographically defined clusters 1:1 to intervention/control arms.

Setting Bandim Health Project Health and Demographic Surveillance System, Guinea-Bissau.

Participants 2226 newborns enrolled between July 2016 and August 2019.

Interventions In both arms, newborns received a home visit within 72 hours after birth. In intervention clusters (n=46), BCG and OPV were provided at the home visit.

Main outcome measure Rates of non-accidental mortality were compared in Cox proportional hazards models from (last of) day 1 or enrolment, until (first of) day 60 or registration of non-trial vaccines.

Results A total of 35 deaths (intervention: 7, control: 28) were registered during the trial. Providing BCG and OPV reduced non-accidental early infant mortality by 59% (8–82%). The intervention also reduced non-accidental hospital admissions. The intervention had little impact on growth and BCG scarring and tended to increase the risk of consultations.

Conclusions The trial was stopped early due to lower-than-expected enrolment and event rates when 33% of the planned number of newborns had been enrolled. Despite the small size of the trial, the results support that early BCG and OPV vaccinations are beneficial and reduce early child mortality and morbidity.
OriginalsprogEngelsk
TidsskriftBMJ Global Health
Vol/bind9
Udgave nummer2
Antal sider12
ISSN2059-7908
DOI
StatusUdgivet - 2024

Bibliografisk note

© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

ID: 383334888