Coverage and Timeliness of Birth Dose Vaccination in Sub-Saharan Africa: A Systematic Review and Meta-Analysis

Oumar Bassoum1,2, Moe Kimura3,4, Anta Tal Dia1,2

  • 1Faculté de Médecine, de Pharmacie et d'Odontologie, Université Cheikh Anta Diop de Dakar, Dakar-Fann 5005, Sénégal.

Vaccines
|June 18, 2020
PubMed

Insights

Birth vaccination coverage in sub-Saharan Africa is critically low, especially for Bacille Calmette-Guerin (BCG) and Hepatitis B (HepB-BD) vaccines within the first 24 hours. Further research is needed to improve timely vaccine administration and reduce vaccine-preventable diseases.

Area of Science:

  • Public Health
  • Epidemiology
  • Vaccinology

Background:

  • The World Health Organization (WHO) recommends three essential vaccines (BCG, OPV0, HepB-BD) for administration immediately after birth.
  • Sub-Saharan Africa faces challenges in timely birth vaccination due to a high proportion of deliveries occurring outside healthcare facilities.
  • Low coverage of these critical early vaccines can increase the incidence of vaccine-preventable diseases.

Purpose of the Study:

  • To systematically review and meta-analyze the coverage rates of WHO-recommended birth vaccines in neonates in sub-Saharan Africa.
  • To assess vaccine coverage at specific time points within 28 days after birth.
  • To identify potential disparities in coverage based on place of birth.

Main Methods:

  • Systematic review and meta-analysis of studies published up to March 31, 2017, from PubMed, Embase, CINAHL, and Web of Science.
  • Inclusion criteria: studies conducted in sub-Saharan Africa reporting birth vaccine coverage within 28 days of birth.
  • Data extraction and analysis performed by two independent investigators; study registered in PROSPERO (CRD42017071269).

Main Results:

  • Pooled coverage rates at 0-1 day post-birth were low: 14.2% for BCG and 1.3% for HepB-BD; no data available for OPV0.
  • Coverage by day 28 improved: 71.7% for BCG, 60.8% for HepB-BD, and 76.1% for OPV0.
  • No significant difference in vaccine coverage was found between infants born inside versus outside healthcare facilities.

Conclusions:

  • Immediate postnatal coverage for BCG and HepB-BD vaccines in sub-Saharan Africa is alarmingly low.
  • A significant data gap exists for oral polio vaccine (OPV0) coverage in the immediate postnatal period.
  • Further research is crucial to understand barriers and facilitators for timely birth vaccination to mitigate disease burden.

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