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.

IF 3.1 Q2 PHARMACOLOGY & PHARMACY
Clinical Pharmacology : Advances and Applications Pub Date : 2017-05-09 eCollection Date: 2017-01-01 DOI:10.2147/CPAA.S131351
Osede I Iribhogbe, Igue Emmanuel, Marylove Odianosen
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引用次数: 9

Abstract

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.

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固定剂量青蒿琥酯/阿莫地喹与蒿甲醚/氨苯曲明联合治疗妊娠期无并发症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。
进行了一项比较临床研究,以评估两种常用的固定剂量以青蒿素为基础的复方治疗妊娠中期和晚期无并发症恶性疟原虫疟疾的安全性和耐受性。为了实现这一目标,研究人员共招募了155名参与者。其中80名来自接受常规产前护理的孕妇,而40名未怀孕的参与者来自社区中明显健康的女性。80名未合并恶性疟原虫的孕妇随机分为青蒿琥酯/阿莫地喹(AA)治疗组和蒿甲醚/氨苯曲明(AL)治疗组,40名非孕妇和35名非疟疾孕妇作为对照。干预组给予标准固定剂量AA (100/270 mg)每日或AL (20/120 mg)每日2次,连用3天。在第4天采集血样,并密切随访患者以确定药物的安全性。该研究显示了显著的(p
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来源期刊
CiteScore
4.60
自引率
0.00%
发文量
14
审稿时长
16 weeks
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