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Vitamin A supplements are well tolerated with the pentavalent vaccine
Sam Newton1, Seth Owusu-Agyei, Suzanne Filteau
1Kintampo Health Research Centre, Ghana. samkofinewton@yahoo.com
Insights
Administering high-dose vitamin A with routine infant immunisations showed fewer illnesses but a concerning, though not statistically significant, increase in infant mortality. Caution is advised for this combined intervention in developing countries.
Area of Science:
- Public Health
- Pediatric Medicine
- Nutritional Science
Background:
- The Expanded Programme on Immunisation (EPI) offers a platform for vitamin A supplementation to enhance infant vitamin A status.
- Safety concerns exist regarding high-dose vitamin A supplementation in infants under six months in developing nations.
Purpose of the Study:
- To evaluate the safety and immunogenicity of co-administering 15 mg retinol equivalent (RE) of vitamin A with the pentavalent vaccine.
- To assess adverse events and infant health outcomes following combined administration at 6, 10, and 14 weeks of age.
Main Methods:
- A randomized controlled trial was conducted by the Kintampo Health Research Centre.
- Infants received vitamin A alongside the pentavalent vaccine (diphtheria-polio-tetanus-Haemophilus influenzae b-hepatitis B) at 6, 10, and 14 weeks.
- Mothers were interviewed regarding infant side effects and adverse events 24 hours post-vaccination and over the preceding four weeks.
Main Results:
- Infants receiving vitamin A showed significantly fewer reported illnesses and fevers compared to the control group.
- The pentavalent vaccine was well-tolerated when given with vitamin A according to the WHO/EPI schedule.
- Six infant deaths occurred: five in the vitamin A intervention group and one in the control group (RR 4.65, p=0.12).
Conclusions:
- While co-administration with the pentavalent vaccine appeared safe and reduced illness, the observed higher mortality rate in the intervention group warrants caution.
- Further investigation is recommended before widespread implementation of high-dose vitamin A supplementation alongside infant immunisation in resource-limited settings.
Abstract:
The Expanded Programme on Immunisation provides an opportunity to deliver vitamin A supplements to young infants in order to improve their vitamin A status. However, concerns have been raised about the safety of administering high dose vitamin A supplements to infants less than 6 months of age in developing countries. A randomized controlled trial was carried out by the Kintampo Health Research Centre to assess the safety and immunogenicity of administering 15 mg retinol equivalent (RE)1 vitamin A alongside the pentavalent "diphtheria-polio-tetanus-Haemophilus influenzae b-hepatitis B vaccine" at 6, 10 and 14 weeks of age. All mothers received a post-partum supplement of 120 mg RE vitamin A as per national policy. Mothers of infants who had been vaccinated were visited 24 h after vaccination to assess the side effects of the vaccine. They were also interviewed about adverse events which may have occurred in the past 4 weeks since the child was vaccinated. There were significantly fewer reports of illnesses and fever in infants who had been given vitamin A compared to infants in the control group. The pentavalent vaccine was found to be tolerable when administered with vitamin A according to the WHO/EPI schedule for infant immunisation at 6, 10 and 14 weeks. There were few complaints made by the mothers of the children which were not thought to be related to giving vitamin A with the vaccines. There were six deaths in the trial, five in the intervention group and one in the control RR 4.65 (0.55-39.5), p = 0.12. Due to the high point estimate of 4.65, we wish to urge caution in administering high doses of vitamin A to young infants with the pentavalent vaccine at 6, 10 and 14 weeks of age.
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