HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Protective efficacy of co-trimoxazole prophylaxis against malaria in HIV exposed children in rural Uganda: a randomised clinical trial.

AbstractOBJECTIVE:
To evaluate the protective efficacy of co-trimoxazole prophylaxis against malaria in HIV exposed children (uninfected children born to HIV infected mothers) in Africa.
DESIGN:
Non-blinded randomised control trial
SETTING:
Tororo district, rural Uganda, an area of high malaria transmission intensity
PARTICIPANTS:
203 breastfeeding HIV exposed infants enrolled between 6 weeks and 9 months of age
INTERVENTION:
Co-trimoxazole prophylaxis from enrollment until cessation of breast feeding and confirmation of negative HIV status. All children who remained HIV uninfected (n = 185) were then randomised to stop co-trimoxazole prophylaxis immediately or continue co-trimoxazole until 2 years old.
MAIN OUTCOME MEASURE:
Incidence of malaria, calculated as the number of antimalarial treatments per person year.
RESULTS:
The incidence of malaria and prevalence of genotypic mutations associated with antifolate resistance were high throughout the study. Among the 98 infants randomised to continue co-trimoxazole, 299 malaria cases occurred in 92.28 person years (incidence 3.24 cases/person year). Among the 87 infants randomised to stop co-trimoxazole, 400 malaria cases occurred in 71.81 person years (5.57 cases/person year). Co-trimoxazole prophylaxis yielded a 39% reduction in malaria incidence, after adjustment for age at randomisation (incidence rate ratio 0.61 (95% CI 0.46 to 0.81), P = 0.001). There were no significant differences in the incidence of complicated malaria, diarrhoea, pneumonia, hospitalisations, or deaths between the two treatment arms.
CONCLUSIONS:
Co-trimoxazole prophylaxis was moderately protective against malaria in HIV exposed infants when continued beyond the period of HIV exposure despite the high prevalence of Plasmodium genotypes associated with antifolate resistance. Trial registration Clinical Trials NCT00527800.
AuthorsTaylor G Sandison, Jaco Homsy, Emmanuel Arinaitwe, Humphrey Wanzira, Abel Kakuru, Victor Bigira, Julius Kalamya, Neil Vora, James Kublin, Moses R Kamya, Grant Dorsey, Jordan W Tappero
JournalBMJ (Clinical research ed.) (BMJ) Vol. 342 Pg. d1617 (Mar 31 2011) ISSN: 1756-1833 [Electronic] England
PMID21454456 (Publication Type: Journal Article, Randomized Controlled Trial, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antimalarials
  • Trimethoprim, Sulfamethoxazole Drug Combination
Topics
  • Antimalarials (therapeutic use)
  • Breast Feeding (epidemiology)
  • Diarrhea, Infantile (prevention & control)
  • Female
  • HIV Infections
  • HIV Seronegativity
  • Humans
  • Incidence
  • Infant
  • Malaria (epidemiology, prevention & control)
  • Pregnancy
  • Pregnancy Complications, Infectious
  • Respiratory Tract Infections (prevention & control)
  • Rural Health
  • Treatment Outcome
  • Trimethoprim, Sulfamethoxazole Drug Combination (therapeutic use)
  • Uganda (epidemiology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: