A systematic review of the safety and efficacy of artemether-lumefantrine against uncomplicated Plasmodium falciparum malaria during pregnancy

被引:40
作者
Manyando, Christine [1 ]
Kayentao, Kassoum [2 ]
D'Alessandro, Umberto [3 ,4 ]
Okafor, Henrietta U. [5 ]
Juma, Elizabeth [6 ]
Hamed, Kamal [7 ]
机构
[1] Trop Dis Res Ctr, Ndola, Zambia
[2] Malaria Res & Training Ctr, Bamako, Mali
[3] Inst Trop Med, B-2000 Antwerp, Belgium
[4] MRC Unit, Fajara, Gambia
[5] Univ Nigeria, Dept Paediat, Coll Med, Enugu, Nigeria
[6] Kenya Govt Med Res Ctr, Kisumu, Kenya
[7] Novartis Pharmaceut, E Hanover, NJ USA
来源
MALARIA JOURNAL | 2012年 / 11卷
关键词
Artemether-lumefantrine; Artemisinin-based combination therapy (ACT); Pregnancy; Malaria; Plasmodium falciparum; POPULATION PHARMACOKINETICS; DEVELOPMENTAL TOXICITY; RETICULOCYTE COUNT; INTERACTION TRIAL; WOMEN; ARTESUNATE; ARTEMISININS; ANTIMALARIALS; UGANDA; ARTEMETHER/LUMEFANTRINE;
D O I
10.1186/1475-2875-11-141
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Malaria during pregnancy, particularly Plasmodium falciparum malaria, has been linked to increased morbidity and mortality, which must be reduced by both preventive measures and effective case management. The World Health Organization (WHO) recommends artemisinin-based combination therapy (ACT) to treat uncomplicated falciparum malaria during the second and third trimesters of pregnancy, and quinine plus clindamycin during the first trimester. However, the national policies of many African countries currently recommend quinine throughout pregnancy. Therefore, the aim of this article is to provide a summary of the available data on the safety and efficacy of artemether-lumefantrine (AL) in pregnancy. An English-language search identified 16 publications from 1989 to October 2011 with reports of artemether or AL exposure in pregnancy, including randomized clinical trials, observational studies and systematic reviews. Overall, there were 1,103 reports of AL use in pregnant women: 890 second/third trimester exposures; 212 first trimester exposures; and one case where the trimester of exposure was not reported. In the second and third trimesters, AL was not associated with increased adverse pregnancy outcomes as compared with quinine or sulphadoxine-pyrimethamine, showed improved tolerability relative to quinine, and its efficacy was non-inferior to quinine. There is evidence to suggest that the pharmacokinetics of antimalarial drugs may change in pregnancy, although the impact on efficacy and safety needs to be studied further, especially since the majority of studies report high cure rates and adequate tolerability. As there are fewer reports of AL safety in the first trimester, additional data are required to assess the potential to use AL in the first trimester. Though the available safety and efficacy data support the use of AL in the second and third trimesters, there is still a need for further information. These findings reinforce the WHO recommendation to treat uncomplicated falciparum malaria with quinine plus clindamycin in early pregnancy and ACT in later pregnancy.
引用
收藏
页数:13
相关论文
共 60 条
[11]   Implementation of the Zambia Electronic Perinatal Record System for comprehensive prenatal and delivery care [J].
Chi, Benjamin H. ;
Vwalika, Bellington ;
Killam, William P. ;
Wamalume, Chibesa ;
Giganti, Mark J. ;
Mbewe, Reuben ;
Stringer, Elizabeth M. ;
Chintu, Namwinga T. ;
Putta, Nande B. ;
Liu, Katherine C. ;
Chibwesha, Carla J. ;
Rouse, Dwight J. ;
Stringer, Jeffrey S. A. .
INTERNATIONAL JOURNAL OF GYNECOLOGY & OBSTETRICS, 2011, 113 (02) :131-136
[12]   Developmental toxicity of artesunate in the rat: Comparison to other artemisinins, comparison of embryotoxicity and kinetics by oral and intravenous routes, and relationship to maternal reticulocyte count [J].
Clark, Robert L. ;
Lerman, Steven A. ;
Cox, Estella M. ;
Gristwood, William E. ;
White, Tacey E. K. .
BIRTH DEFECTS RESEARCH PART B-DEVELOPMENTAL AND REPRODUCTIVE TOXICOLOGY, 2008, 83 (04) :397-406
[13]   Effects of artemisinins on reticulocyte count and relationship to possible embryotoxicity in confirmed and unconfirmed malarial patients [J].
Clark, Robert L. .
BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY, 2012, 94 (02) :61-75
[14]   Pregnancy Exposure Registries for Assessing Antimalarial Drug Safety in Pregnancy in Malaria-Endemic Countries [J].
Dellicour, Stephanie ;
ter Kuile, Feiko O. ;
Stergachis, Andy .
PLOS MEDICINE, 2008, 5 (09) :1310-1314
[15]   The safety of artemisinins during pregnancy: a pressing question [J].
Dellicour, Stephanie ;
Hall, Susan ;
Chandramohan, Daniel ;
Greenwood, Brian .
MALARIA JOURNAL, 2007, 6 (1)
[16]   Quantifying the Number of Pregnancies at Risk of Malaria in 2007: A Demographic Study [J].
Dellicour, Stephanie ;
Tatem, Andrew J. ;
Guerra, Carlos A. ;
Snow, Robert W. ;
ter Kuile, Feiko O. .
PLOS MEDICINE, 2010, 7 (01)
[17]   Epidemiology and burden of malaria in pregnancy [J].
Desai, Meghna ;
ter Kuile, Feiko O. ;
Nosten, Francois ;
McGready, Rose ;
Asamoa, Kwame ;
Brabin, Bernard ;
Newman, Robert D. .
LANCET INFECTIOUS DISEASES, 2007, 7 (02) :93-104
[18]   Understanding the pharmacokinetics of Coartem® [J].
Djimde, Abdoulaye ;
Lefevre, Gilbert .
MALARIA JOURNAL, 2009, 8
[19]   Pharmacokinetics and pharmacodynamics of lumefantrine (benflumetol) in acute falciparum malaria [J].
Ezzet, F ;
van Vugt, M ;
Nosten, F ;
Looareesuwan, S ;
White, NJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (03) :697-704
[20]   Lopinavir/Ritonavir Affects Pharmacokinetic Exposure of Artemether/Lumefantrine in HIV-Uninfected Healthy Volunteers [J].
German, Polina ;
Parikh, Sunil ;
Lawrence, Jody ;
Dorsey, Grant ;
Rosenthal, Philip J. ;
Havlir, Diane ;
Charlebois, Edwin ;
Hanpithakpong, Warunee ;
Lindegardh, Niklas ;
Aweeka, Francesca T. .
JAIDS-JOURNAL OF ACQUIRED IMMUNE DEFICIENCY SYNDROMES, 2009, 51 (04) :424-429