Randomized, double-blind, placebo-controlled clinical trial of the efficacy of treatment with zinc or vitamin A in infants and young children with severe acute lower respiratory infection123

https://doi.org/10.1093/ajcn/79.3.430Get rights and content
Under an Elsevier user license
open archive

ABSTRACT

Background

Acute lower respiratory infection (ALRI) is a leading cause of childhood death. Zinc supplementation prevents ALRI. Vitamin A supplementation reduces childhood mortality, but its benefit concerning ALRI-specific mortality is unproven.

Objective

The objective was to evaluate the effect of zinc and vitamin A on the clinical recovery of children with severe ALRI.

Design

In a controlled trial with a factorial design, 153 children aged 2-24 mo who were hospitalized with severe ALRI were randomly assigned to receive 10 mg zinc as acetate (twice daily for 5 d) plus vitamin A placebo, 10 000 μg retinol equivalents vitamin A (twice daily for 4 d) plus zinc placebo, zinc plus vitamin A, or zinc and vitamin A placebos. The main outcome variable was the time for resolution of very ill status; other outcomes were resolution of fever, tachypnea, and feeding difficulty.

Results

Recovery rates from very ill status and from fever in zinc-treated boys were 2.6 times (P = 0.004) and 3 times (P = 0.003) those in non-zinc-treated children; feeding difficulty and tachypnea were not significantly different between groups after an adjusted analysis. Recovery rates were not significantly different between groups on the basis of vitamin A treatment. At discharge, serum zinc was 6.06 μmol/L higher (P = 0.001) in the zinc-treated children, and serum retinol was 0.387 μmol/L higher (P = 0.001) in the vitamin A-treated children.

Conclusion

Zinc treatment significantly reduces duration of fever and very ill status in boys, but not in girls, with severe ALRI. Vitamin A treatment of children with severe ALRI had no significant beneficial effect.

Key Words

Zinc
vitamin A
acute lower respiratory infection
ALRI
therapy
sex effect
clinical trial

Cited by (0)

1

From the Society for Applied Studies, Kolkata, India (DM and SG); the BC Roy Memorial Hospital for Children, Kolkata, India (ML, DP, and AG); the ICDDR-B, Dhaka, Bangladesh (MAW); and the University of Alabama at Birmingham (MAK).

2

Supported by a research grant from Nutricia Research Foundation, The Hague.

3

Reprints not available. Address correspondence to D Mahalanabis, Society for Applied Studies, 108 Manicktala Main Road, Flat-3/21, Kolkata 700054, India. E-mail: [email protected].