Quinine, an old anti-malarial drug in a modern world: role in the treatment of malaria

被引:574
作者
Achan, Jane [1 ]
Talisuna, Ambrose O. [2 ]
Erhart, Annette [3 ]
Yeka, Adoke [4 ]
Tibenderana, James K. [5 ]
Baliraine, Frederick N. [6 ]
Rosenthal, Philip J. [6 ]
D'Alessandro, Umberto [3 ]
机构
[1] Makerere Univ, Dept Pediat & Child Hlth, Coll Hlth Sci, Kampala, Uganda
[2] Makerere Univ, Dept Epidemiol & Biostat, Sch Publ Hlth, Kampala, Uganda
[3] Inst Trop Med, Dept Parasitol, B-2000 Antwerp, Belgium
[4] Uganda Malaria Surveillance Project, Epidemiol Unit, Kampala, Uganda
[5] Malaria Consortium Africa, Communicable Dis Control Dept, Kampala, Uganda
[6] Univ Calif San Francisco, Dept Med, San Francisco, CA 94143 USA
关键词
PLASMODIUM-FALCIPARUM MALARIA; HUMAN-IMMUNODEFICIENCY-VIRUS; CHILDHOOD CEREBRAL MALARIA; IN-VITRO SUSCEPTIBILITY; INTRAVENOUS QUININE; ARTEMETHER-LUMEFANTRINE; UNCOMPLICATED MALARIA; COMBINATION THERAPY; CLINICAL-TRIAL; ORAL QUININE;
D O I
10.1186/1475-2875-10-144
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Quinine remains an important anti-malarial drug almost 400 years after its effectiveness was first documented. However, its continued use is challenged by its poor tolerability, poor compliance with complex dosing regimens, and the availability of more efficacious anti-malarial drugs. This article reviews the historical role of quinine, considers its current usage and provides insight into its appropriate future use in the treatment of malaria. In light of recent research findings intravenous artesunate should be the first-line drug for severe malaria, with quinine as an alternative. The role of rectal quinine as pre-referral treatment for severe malaria has not been fully explored, but it remains a promising intervention. In pregnancy, quinine continues to play a critical role in the management of malaria, especially in the first trimester, and it will remain a mainstay of treatment until safer alternatives become available. For uncomplicated malaria, artemisinin-based combination therapy (ACT) offers a better option than quinine though the difficulty of maintaining a steady supply of ACT in resource-limited settings renders the rapid withdrawal of quinine for uncomplicated malaria cases risky. The best approach would be to identify solutions to ACT stock-outs, maintain quinine in case of ACT stock-outs, and evaluate strategies for improving quinine treatment outcomes by combining it with antibiotics. In HIV and TB infected populations, concerns about potential interactions between quinine and antiretroviral and anti-tuberculosis drugs exist, and these will need further research and pharmacovigilance.
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