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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.
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.
Abstract:
Background: Depending on the epidemiological context of each country, three vaccines are recommended by the World Health Organization (WHO) to be administered as soon as possible after birth (birth vaccines); namely, BCG, zero dose of oral polio vaccine (OPV0), and birth dose of hepatitis B vaccine (HepB-BD). The timely administration of these vaccines immediately after birth might pose significant challenges in sub-Saharan Africa, where about half of childbirths occur outside health facilities. We therefore conducted a systematic review and meta-analysis to estimate the coverage rate of these vaccines at a specific timing in neonates in sub-Saharan Africa. Methods: We searched PubMed, Embase, CINAHL, and Web of Science for studies conducted in sub-Saharan Africa and published up to March 31, 2017, which provided a coverage rate of the birth vaccines at any specific time points within 28 days after birth. Two investigators independently screened the titles and abstracts and extracted data from the eligible full-text articles. This study was registered in PROSPERO (CRD42017071269). Results: Of 7283 articles identified, we finally included 31 studies with 204,111 infants in the meta-analysis. The pooled coverage rates at day 0-1 after birth were 14.2% (95% CI: 10.1-18.9) for BCG and 1.3% (0.0-4.5) for HepB-BD. No data were available for OPV0 at day 0-1. The coverage at day 28 was 71.7% (63.7-79.2) for BCG, 60.8% (45.8-74.7) for HepB-BD, and 76.1% (67.1-84.0) for OPV0. No significant difference in the vaccine coverage was observed between infants born in healthcare facilities and those born outside facilities. Conclusions: The rates of vaccine coverage immediately after birth were very low for BCG and HepB-BD, and no data for OPV0. We need additional data to better define barriers and facilitators for the timely administration of the birth vaccines in sub-Saharan Africa, since the delay in its provision may increase the burden of these vaccine-preventable diseases.
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