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Published on: August 30, 2014
Zinc for severe pneumonia in very young children: double-blind placebo-controlled trial
W Abdullah Brooks1, M Yunus, Mathuram Santosham
1Centre for Health and Population Research, International Centre for Diarrhoeal Disease Research, Bangladesh, GPO Box 128 Mohakhali, Dhaka 1000, Bangladesh. abrooks@icddrb.org
Insights
Zinc supplementation significantly reduces the duration of severe pneumonia in children. This intervention also shortens hospital stays, offering a cost-effective treatment for pediatric pneumonia.
Area of Science:
- Pediatric Infectious Diseases
- Nutritional Science
- Public Health
Background:
- Pneumonia is a major cause of childhood illness and death globally.
- Early symptom resolution in severe pneumonia improves patient outcomes.
- Zinc's role as an acute phase reactant suggests potential therapeutic benefits.
Purpose of the Study:
- To investigate if zinc supplementation shortens the duration of severe pneumonia in children.
- To determine the effect of zinc on hospital stay length for pediatric pneumonia patients.
- To evaluate zinc as an adjuvant therapy for severe pneumonia.
Main Methods:
- A double-blind, placebo-controlled trial involving 270 children aged 2-23 months.
- Participants received either 20 mg of elemental zinc daily or a placebo, alongside standard antimicrobial treatment.
- Outcomes measured included time to resolution of severe pneumonia signs and hospital discharge duration.
Main Results:
- Zinc supplementation significantly reduced the duration of severe pneumonia (RH=0.70).
- The treatment also shortened overall hospital stay duration (RH=0.75), averaging one day less.
- Effects were more pronounced when children with wheezing were excluded from analysis.
Conclusions:
- Daily 20 mg zinc accelerates recovery in children with severe pneumonia.
- Zinc may reduce antibiotic resistance by decreasing exposure to multiple antibiotics.
- This intervention could lessen complications and mortality in resource-limited settings.
Background:
Pneumonia is a leading cause of morbidity and mortality in young children. Early reversal of severity signs--chest indrawing, hypoxia, and tachypnoea--improves outcome. We postulated that zinc, an acute phase reactant, would shorten duration of severe pneumonia and time in hospital.
Methods:
In a double-blind placebo-controlled clinical trial in Matlab Hospital, Bangladesh, 270 children aged 2-23 months were randomised to receive elemental zinc (20 mg per day) or placebo, plus the hospital's standard antimicrobial management, until discharge. The outcomes were time to cessation of severe pneumonia (no chest indrawing, respiratory rate 50 per min or less, oxygen saturation at least 95% on room air) and discharge from hospital. Discharge was allowed when respiratory rate was 40 per minute or less for 24 consecutive hours while patients were maintained only on oral antibiotics.
Findings:
The group receiving zinc had reduced duration of severe pneumonia (relative hazard [RH]=0.70, 95% CI 0.51-0.98), including duration of chest indrawing (0.80, 0.61-1.05), respiratory rate more than 50 per min (0.74, 0.57-0.98), and hypoxia (0.79, 0.61-1.04), and overall hospital duration (0.75, 0.57-0.99). The mean reduction is equivalent to 1 hospital day for both severe pneumonia and time in hospital. All effects were greater when children with wheezing were omitted from the analysis.
Interpretation:
Adjuvant treatment with 20 mg zinc per day accelerates recovery from severe pneumonia in children, and could help reduce antimicrobial resistance by decreasing multiple antibiotic exposures, and lessen complications and deaths where second line drugs are unavailable.
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