Daily Zinc Supplementation for Infection Prevention in Children With Sickle Cell Anemia: The ZIPS-2 Randomized Clinical Trial
- Journal
- JAMA (Q1)
- Published
- 19 August 2026
- Study design
- Randomized controlled trial
- Evidence level
- Level 1, High (CEBM 1b)
- Authors
- Ruth Namazzi, Kagan A Mellencamp, Irene Bagala, Andrea L Conroy, Charles Kato, Isaac Birungi, et al.
- PMID
- 42616536
- DOI
- 10.1001/jama.2026.14190
Why clinicians should know about it
- Picked for Breast and Endocrine Surgery (top studies of the week, 23 August 2026): Zinc supplementation in sickle cell, unrelated
- Picked for Bariatric and Metabolic Surgery (top studies of the week, 23 August 2026): High-quality evidence in a top journal
- Picked for Pediatrics and Child Health (top studies of the week, 23 August 2026): Zinc reduces infection rate in children with sickle cell anemia
Abstract
IMPORTANCE: Despite existing prevention strategies, infections remain a major cause of morbidity and mortality in children in Africa with sickle cell anemia. OBJECTIVE: To determine the safety and effectiveness of daily zinc supplementation to prevent all-cause infection in children with sickle cell anemia in Uganda. DESIGN, SETTING, AND PARTICIPANTS: A randomized, double-blind, placebo-controlled trial of children aged 1.00 to 4.99 years with sickle cell anemia at Jinja Regional Referral Hospital in Jinja, Uganda, from February 10, 2025, to April 30, 2025, with 6 months of follow-up through November 7, 2025. INTERVENTIONS: Participants received zinc sulfate at 20 mg daily or placebo daily for 6 months. MAIN OUTCOMES AND MEASURES: The primary outcome was all-cause infections per 100 person-years, using standardized clinical criteria to define infections. RESULTS: Among 118 children screened for eligibility, 100 were randomly assigned to receive zinc supplementation (n = 50) or placebo (n = 50) (mean [SD] age, 36.0 [13.2] months; 45 female [45%]). At enrollment, 45 participants (45%) were receiving hydroxyurea therapy. All participants initiated or continued receiving hydroxyurea after enrollment. During the 6-month follow-up, there was complete ascertainment for all participants and no loss to follow-up. There were 80 all-cause infections in the zinc group and 124 in the placebo group, corresponding to a significantly lower infection rate in the zinc group than the placebo group (305.7 [95% CI, 242.4-380.4] infections per 100 person-years vs 480.7 [95% CI, 399.8-573.1] infections per 100 person-years; rate difference, -176.0 [95% CI, -300.8 to -51.3]; incidence rate ratio after adjustment for baseline age, sex, and hydroxyurea use, 0.62 [95% CI, 0.45-0.86]). No adverse events requiring discontinuation of the study intervention were observed in either group. CONCLUSIONS AND RELEVANCE: Zinc supplementation at 20 mg per day reduced all-cause infection in children with sickle cell anemia younger than 5 years in Uganda. Multisite clinical trials are needed to validate these findings and to assess effectiveness in older children. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT06561061.
Abstract as published, via PubMed.
For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.