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首页> 外文期刊>BMC Infectious Diseases >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]
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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]

机译:随机,平行研究45毫克原序与75毫克风格的血液分解症 - 血液分解症 - 响应性松果疟疾(Iscrtn50134587)的成人血杂小杂交剂

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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/μl 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° 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.
机译:背景技术谁建议将成年人具有不复杂的P. falciparum用血液分解症成功处理,得到单剂量的原序(PQ)45mg作为配子杂交剂。较早的试点研究表明,75毫克的风质(BQ),其中PQ是主要的代谢物,可能是对PQ有用的交替。方法在随机,部分盲目研究中,90名住院成人具有血液鞘癫痫患者的疟原虫疟疾疟疾的疟疾响应性,3天内诊断3天内> 55 /μl的配子键血症被随机化,以接收单剂量的PQ 45mg或BQ 75 mg在第4天。我们在第8天通过Exflagelation(2°终点)确定的第8,15,22和29天和的配子细胞活力评估了配子键血症和配子细胞活力。结果第8天,20/31(65%)原始受体与19天/ 59(32%)万全受者显示出持久性的配子细胞(P = 0.002)。在第15天及以后,所有患者均为无菌细胞。在第8天,16/31 PQ和7/59 BQ志愿者显示有配子织物的活力(P = 0.000065)。结论BQ是PQ的安全性,有用的交替,作为恶性疟原虫配子腺苷酸代理,可能比PQ更快地清除配子键虫。

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