Cotrimoxazole Prophylaxis Versus Mefloquine Intermittent Preventive Treatment to Prevent Malaria in HIV-Infected Pregnant Women: Two Randomized Controlled Trials

被引:29
|
作者
Denoeud-Ndam, Lise [1 ,2 ]
Zannou, Djimon-Marcel [3 ,4 ]
Fourcade, Camille [1 ,2 ]
Taron-Brocard, Clement [1 ,2 ]
Porcher, Raphael [5 ]
Atadokpede, Felix [6 ]
Komongui, Didier G. [7 ]
Dossou-Gbete, Lucien [8 ]
Afangnihoun, Aldric [9 ]
Ndam, Nicaise T. [1 ,2 ]
Girard, Pierre-Marie [10 ,11 ]
Cot, Michel [1 ,2 ]
机构
[1] Inst Rech Dev, UMR 216, Paris, France
[2] Univ Paris 05, Fac Pharm, Paris, France
[3] Ctr Natl Hosp Univ Hubert Koutoukou Maga, Ctr Traitement Ambulatoire, Cotonou, Benin
[4] Univ Abomey Calavi, Fac Sci Sante, Abomey Calavi, Benin
[5] Hop St Louis, INSERM, U717, Paris, France
[6] Hop Instruct Armees, Serv Med Interne, Cotonou, Benin
[7] Hop Mere & Enfant Lagune, Gynecol Serv, Cotonou, Benin
[8] Clin Louis Pasteur, Porto Novo, Benin
[9] Hop Zone Suru Lere, Ctr Traitement Ambulatoire, Cotonou, Benin
[10] Hop St Antoine, APHP, Serv Malad Infect & Trop, F-75571 Paris, France
[11] Univ Paris 06, INSERM, U707, Paris, France
关键词
malaria during pregnancy; mefloquine; cotrimoxazole; HIV; randomized controlled trial; TO-CHILD TRANSMISSION; SULFADOXINE-PYRIMETHAMINE; PLACENTAL MALARIA; ANTIRETROVIRAL THERAPY; MOLECULAR MARKERS; IMPACT; PREVALENCE; PARASITEMIA; RESISTANCE; INCREASES;
D O I
10.1097/QAI.0000000000000058
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:198 / 206
页数:9
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