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Comparative analysis of the safety and tolerability of fixed-dose artesunate/amodiaquine versus artemether/lumefantrine combinations for uncomplicated falciparum malaria in pregnancy: a randomized open label study

机译:固定剂量青蒿琥酯/阿莫地喹与蒿甲醚/氟美汀联合治疗未发生复杂性恶性疟疾的安全性和耐受性比较分析:一项随机开放标签研究

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摘要

A comparative clinical study was conducted to evaluate the safety and tolerability of two commonly used fixed dose artemisinin-based combinations for the treatment of uncomplicated Plasmodium falciparum malaria in the second and third trimester of pregnancy. To achieve this, a total of 155 participants were recruited for the study. Eighty of these were drawn from pregnant women who came for routine antenatal care while 40 nonpregnant participants were recruited from apparently healthy females in the community. Eighty pregnant participants with uncomplicated P. falciparum malaria were randomized into artesunate/amodiaquine (AA) and artemether/lumefantrine (AL) treatment arms while 40 nonpregnant and 35 nonmalarious pregnant women were used as control. The interventional groups received standard fixed dose combinations of AA (100/270 mg) daily or AL (20/120 mg) twice daily for 3 days. Blood samples were collected on day 4 and patients were followed-up closely to ascertain the safety of the drugs. The study showed a significant (p<0.0001) elevation of alkaline phosphatase in the AA and AL group compared to the nonpregnant control and a significant (p<0.05) elevation of alanine transaminase and aspartate transaminase level in the AL combination group when compared with the AA group. The elevated hepatic enzymes were within the normal range for pregnancy and were not clinically significant. Adverse event rate was higher in the AA group (n=28 [70%]) when compared to the AL group (n=4 [10%]) although the drugs were well-tolerated in both treatment arms. In conclusion, the use of these combinations is safe in the second and third trimester of pregnancy. However, we recommend active pharmacovigilance and spontaneous drug reporting of the agents in order to continuously monitor safety in the vastly heterogeneous population.
机译:进行了一项比较性临床研究,以评估两种常用的基于青蒿素的固定剂量固定剂量联合用药在妊娠中期和中期妊娠中治疗单纯性恶性疟原虫的安全性和耐受性。为了实现这一目标,总共招募了155名参与者进行这项研究。其中有80名是从孕妇那里接受常规产前检查的,而40名未怀孕的参与者是从该社区中看似健康的女性中招募的。 80名患有单纯性恶性疟原虫疟疾的怀孕参与者被随机分为青蒿琥酯/阿莫地喹(AA)和青蒿醚/荧光粉(AL)治疗组,而40例未妊娠和35例无疟疾孕妇被用作对照。干预组接受标准的固定剂量组合,每日两次AA(100/270 mg)或每天两次AL(20/120 mg),共3天。在第4天收集血样,并密切随访患者以确定药物的安全性。研究显示,与未妊娠对照组相比,AA和AL组的碱性磷酸酶升高(p <0.0001),而与AL组相比,AL组合组的丙氨酸转氨酶和天冬氨酸转氨酶水平显着(p <0.05)升高。 AA小组。肝酶升高在怀孕的正常范围内,在临床上不显着。与AL组相比,AA组的不良事件发生率更高(n = 28 [70%])(n = 4 [10%]),尽管两个治疗组的药物耐受性都很好。总之,在妊娠中期和中期使用这些组合是安全的。但是,我们建议对药物进行积极的药物警戒和自发性药物报告,以便持续监控广泛异质人群的安全性。

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