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Early neonatal vitamin A supplementation and infant mortality: an individual participant data meta-analysis of
Insights
Neonatal vitamin A supplementation (NVAS) did not reduce overall infant mortality but showed benefits in South Asia where vitamin A deficiency is common. In Africa, NVAS had no effect and may have increased infant mortality.
Area of Science:
- Public Health and Nutrition
- Maternal and Child Health
- Epidemiology
Background:
- Biannual vitamin A supplementation is effective for older children but misses opportunities to prevent early infant deaths.
- Neonatal vitamin A supplementation (NVAS) trials have yielded inconsistent results regarding impact on under-6-month mortality in low/middle-income countries.
Purpose of the Study:
- To reanalyze and pool data from randomized placebo-controlled NVAS trials to assess impact on infant mortality through 6 and 12 months of age.
- To investigate variations in NVAS effectiveness based on study population characteristics and geographical context.
Main Methods:
- Pooled analysis of primary mortality outcomes from 11 published randomized placebo-controlled NVAS trials (n=163,567 children).
- Utilized random effects models and meta-regression to analyze mortality through 6 and 12 months of age.
- Data reanalysis followed an agreed plan, with one investigator withdrawing but allowing data use.
Main Results:
- Overall, NVAS showed no significant effect on infant survival through 6 months (RR 0.97) or 12 months (RR 1.00).
- NVAS significantly reduced 6-month mortality in Southern Asia, contexts with moderate/severe vitamin A deficiency, high early infant mortality, and lower maternal education.
- NVAS did not reduce mortality in Africa, where vitamin A deficiency and infant mortality were lower; a suggestion of increased infant mortality was observed (RR 1.07).
Conclusions:
- Neonatal vitamin A supplementation is beneficial for reducing infant mortality in South Asia, particularly in areas with moderate to severe maternal vitamin A deficiency and high early infant mortality.
- NVAS demonstrated no benefit and potentially increased infant mortality in African contexts characterized by lower maternal vitamin A deficiency prevalence and lower early infant mortality rates.
- The effectiveness of NVAS is context-dependent, highlighting the importance of regional nutritional status and baseline mortality rates in determining intervention impact.
Background:
Biannual vitamin A supplementation is a well-established survival tool for preschool children 6 months and older in vitamin A deficient populations but this schedule misses the opportunity to intervene on most young infant deaths. Randomised trials of neonatal vitamin A supplementation (NVAS) in the first few days of life to assess its impact on under 6-month mortality in low/middle-income countries have had varying results.
Methods:
Investigators of 11 published randomised placebo-controlled NVAS trials (n=163 567 children) reanalysed their data according to an agreed plan and pooled the primary outcomes of mortality from supplementation through 6 and 12 months of age using random effects models and meta-regression. One investigator withdrew but allowed use of the data.
Findings:
Overall there was no effect of NVAS on infant survival through 6 (risk ratio (RR) 0.97; 95% CI 0.89 to 1.06) or 12 months of age (RR 1.00; 95% CI 0.93 to 1.08) but results varied by study population characteristics.NVAS significantly reduced 6-month mortality among the trials conducted in Southern Asia (RR 0.87; 95% CI 0.77 to 0.98), in contexts with moderate or severe vitamin A deficiency (defined as 10% or higher proportion of women with serum retinol <0.7 µmol/L or 5% or more women with night blindness) (RR 0.87; 95% CI 0.80 to 0.94), early infant mortality was 30 or more per 1000 live births (RR 0.91; 95% CI 0.85 to 0.98), 75% or more of infant mortality occurred in the first 6 months of life (RR 0.92; 95% CI 0.84 to 1.01), or where >32% mothers had no schooling (RR 0.88; 95% CI 0.80 to 0.96). NVAS did not reduce mortality in the first 6 months of life in trials conducted in Africa, in contexts characterised by a low prevalence of vitamin A deficiency, lower rates of infant mortality and where maternal education was more prevalent. There was a suggestion of increased infant mortality in trials conducted in Africa (RR 1.07; 95% CI 1.00 to 1.15).Individual-level characteristics such as sex, birth weight, gestational age and size, age at dosing, parity, time of breast feeding initiation, maternal education and maternal vitamin A supplementation did not modify the impact of NVAS.
Conclusion:
NVAS reduced infant mortality in South Asia, in contexts where the prevalence of maternal vitamin A deficiency is moderate to severe and early infant mortality is high; but it had no beneficial effect on infant survival in Africa, in contexts where the prevalence of maternal vitamin A deficiency is lower, early infant mortality is low.
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