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首页> 外文期刊>Tropical Medicine and International Health: TM and IH >Chloroquine prophylaxis against vivax malaria in pregnancy: a randomized, double-blind, placebo-controlled trial.
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Chloroquine prophylaxis against vivax malaria in pregnancy: a randomized, double-blind, placebo-controlled trial.

机译:孕期氯喹预防间日疟原虫:一项随机,双盲,安慰剂对照试验。

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Objective To assess the safety of chloroquine (CQ) as prophylaxis against Plasmodium vivax infection during pregnancy. Method One thousand pregnant Karen women were enrolled in a randomized, double-blind, placebo-controlled trial of chemoprophylaxis with chloroquine (500 mg phosphate (or 300 mg base) weekly). Women received a median (range) chloroquine phosphate total dose of 9500 (1500-17 500) mg. The mothers were actively followed from inclusion to delivery and their infants until 12 months of age. Results Chloroquine prophylaxis completely prevented P. vivax episodes; 10.1% (95%CI: 7.3-14.5) of women in the placebo group experienced at least one episode of vivax malaria but no episode occurred in women in the CQ group. By contrast, the numbers of P. falciparum episodes were similar in each group: 7.4% (95%CI: 3.7-11.1) and 5.6% (95%CI: 3.3-7.9) in the placebo and CQ groups respectively (P = 0.56). Chloroquine prophylaxis was well tolerated and there was no difference in the proportions of reported side effects between CQ treated and placebo groups except for the duration of palpitations and sleeping disorders which were more frequent in those who had received CQ. Chloroquine prophylaxis had no impact on maternal anaemia, birth weight, gestational age, development of newborns or on growth, neurological development or visual acuity in infants at 1 year of age. Conclusion Chloroquine is safe and effective as prophylaxis against P. vivax during pregnancy in this population.
机译:目的评估氯喹(CQ)预防妊娠期间日疟原虫感染的安全性。方法将一千名Karen孕妇纳入一项随机,双盲,安慰剂对照的化学预防方案,以氯喹(每周500 mg磷酸盐(或300 mg碱))进行化学预防。妇女接受的中位(范围)磷酸氯喹的总剂量为9500(1500-17 500)毫克。从入选到分娩及其婴儿一直到12个月大为止,母亲一直受到积极跟踪。结果氯喹预防完全预防了间日疟原虫的发作。安慰剂组的女性中有10.1%(95%CI:7.3-14.5)经历过至少一次间日间疟疾发作,但CQ组的女性中没有发作。相比之下,每组恶性疟原虫发作的次数相似:安慰剂组和CQ组分别为7.4%(95%CI:3.7-11.1)和5.6%(95%CI:3.3-7.9)(P = 0.56 )。氯喹的预防耐受性良好,CQ治疗组与安慰剂组之间报告的副作用比例没有差异,除了心C持续时间和睡眠障碍在接受CQ的患者中更常见。预防氯喹对产妇贫血,出生体重,胎龄,新生儿发育或1岁婴儿的生长,神经发育或视敏度没有影响。结论氯喹是预防该人群妊娠间日疟原虫安全有效的方法。

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