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一项随机、平行研究,比较45毫克伯氨喹与75毫克布喹作为配子体杀灭剂在对血液裂殖体杀灭剂敏感的非复杂性恶性疟原虫疟疾成年患者中的安全性和疗效[国际标准随机对照试验编号:ISCRTN50134587]

A randomized, parallel study of the safety and efficacy of 45 mg primaquine versus 75 mg bulaquine as gametocytocidal agents in adults with blood schizonticide-responsive uncomplicated falciparum malaria [ISCRTN50134587].

作者信息

Gogtay N J, Kamtekar K D, Dalvi S S, Mehta S S, Chogle A R, Aigal U, Kshirsagar N A

机构信息

Department of Clinical Pharmacology, Seth G.S. Medical College and K.E.M Hospital, Parel, Mumbai 400 012, India.

出版信息

BMC Infect Dis. 2006 Feb 1;6:16. doi: 10.1186/1471-2334-6-16.

Abstract

BACKGROUND

The WHO recommends that adults with uncomplicated P. falciparum successfully treated with a blood schizonticide receive a single dose of primaquine (PQ) 45 mg as a gametocytocidal agent. An earlier pilot study suggested that 75 mg of bulaquine (BQ), of which PQ is a major metabolite, may be a useful alternate to PQ.

METHODS

In a randomized, partial blind study, 90 hospitalized adults with Plasmodium falciparum malaria that was blood schizonticide-responsive and a gametocytemia of > 55/microl within 3 days of diagnosis were randomized to receive single doses of either PQ 45 mg or BQ 75 mg on day 4. We assessed gametocytemia on days 8, 15, 22 and 29 and gametocyte viability as determined by exflagellation (2 degrees end point) on day 8.

RESULTS

On day 8, 20/31 (65%) primaquine recipients versus 19/59 (32%) bulaquine recipients showed persistence of gametocytes (P = 0.002). At day 15 and beyond, all patients were gametocyte free. On day 8, 16/31 PQ and 7/59 BQ volunteers showed gametocyte viability (p = 0.000065).

CONCLUSION

BQ is a safe, useful alternate to PQ as a Plasmodium falciparum gametocytocidal agent and may clear gametocytemia faster than PQ.

摘要

背景

世界卫生组织建议,用血液裂殖体杀灭剂成功治疗的无并发症恶性疟原虫感染成人,应接受单剂量45毫克伯氨喹(PQ)作为配子体杀灭剂。一项早期的试点研究表明,75毫克布喹(BQ,PQ是其主要代谢产物)可能是PQ的一种有效替代药物。

方法

在一项随机、部分盲法研究中,90名住院的恶性疟原虫疟疾成人患者,其感染对血液裂殖体杀灭剂有反应,且在诊断后3天内配子体血症>55/微升,在第4天被随机分配接受单剂量45毫克PQ或75毫克BQ。我们在第8、15、22和29天评估配子体血症,并在第8天通过鞭毛摆动(二级终点)测定配子体活力。

结果

在第8天,31名接受伯氨喹治疗的患者中有20名(65%)与59名接受布喹治疗的患者中有19名(32%)显示有配子体持续存在(P = 0.002)。在第15天及以后,所有患者均无配子体。在第8天,31名接受PQ治疗的志愿者中有16名和59名接受BQ治疗的志愿者中有7名显示有配子体活力(p = 0.000065)。

结论

作为恶性疟原虫配子体杀灭剂,BQ是PQ的一种安全、有效的替代药物,且清除配子体血症的速度可能比PQ更快。

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