Publications des scientifiques de l'IRD

Denoeud Ndam Lise, Zannou D. M., Fourcade C., Taron-Brocard C., Porcher R., Atadokpede F., Komongui D. G., Dossou-Gbete L., Afangnihoun A., Tuikue Ndam Nicaise, Girard P. M., Cot Michel. (2014). Cotrimoxazole prophylaxis versus mefloquine intermittent preventive treatment to prevent malaria in HIV-infected pregnant women : wo randomized controlled trials. Jaids.Journal of Acquired Immune Deficiency Syndromes, 65 (2), p. 198-206. ISSN 1525-4135.

Titre du document
Cotrimoxazole prophylaxis versus mefloquine intermittent preventive treatment to prevent malaria in HIV-infected pregnant women : wo randomized controlled trials
Année de publication
2014
Type de document
Article référencé dans le Web of Science WOS:000335650300023
Auteurs
Denoeud Ndam Lise, Zannou D. M., Fourcade C., Taron-Brocard C., Porcher R., Atadokpede F., Komongui D. G., Dossou-Gbete L., Afangnihoun A., Tuikue Ndam Nicaise, Girard P. M., Cot Michel
Source
Jaids.Journal of Acquired Immune Deficiency Syndromes, 2014, 65 (2), p. 198-206 ISSN 1525-4135
Background: Malaria during pregnancy has serious consequences that are worsened by HIV infection. Malaria preventive measures for HIV-infected pregnant women include cotrimoxazole (CTX) prophylaxis given to prevent HIV-related opportunistic infections and also protective against malaria, or intermittent preventive treatment (IPTp) with an antimalarial drug. Here, we present the first study evaluating CTX efficacy versus mefloquine (MQ)-IPTp, alone and in combination, in HIV-infected pregnant women. Methods: We conducted 2 randomized, open-label, noninferiority trials in Benin. In the CTX-mandatory trial, HIV-infected women with CD4 counts of <350 per cubic millimeter received CTX either alone or with MQ-IPTp (N = 292). In the CTX-not-mandatory trial (CD4 count >350/mm(3)), CTX was compared with MQ-IPTp (N = 140). In both the trials, the primary end point was microscopic placental parasitemia. Results: At delivery, 1 woman in each CTX-alone treatment group exhibited placental parasitemia, versus no women in the groups receiving MQ. CTX alone demonstrated noninferiority in the CTX-mandatory trial. However, polymerase chain reaction-detected placental parasitemia was markedly reduced in the CTX + MQ group compared with CTX alone (0/105 vs. 5/103, P = 0.03). Because of insufficient recruitment in the CTX-not-mandatory trial, noninferiority could not be conclusively assessed. Dizziness and vomiting of moderate intensity were reported by 34%-37% of women receiving MQ in both the trials, versus 0%-3% in CTX groups (P < 0.0001). No serious adverse events related to these drugs were found. Conclusions: CTX alone provided adequate protection against malaria in HIV-infected pregnant women, although MQ-IPTp showed higher efficacy against placental infection. Although more frequently associated with dizziness and vomiting, MQ-IPTp may be an effective alternative given concerns about parasite resistance to CTX.
Plan de classement
Santé : généralités [050] ; Entomologie médicale / Parasitologie / Virologie [052]
Localisation
Fonds IRD [F B010062046]
Identifiant IRD
fdi:010062046
Contact