A randomized trial to monitor the efficacy and effectiveness by QT-NASBA of artemether-lumefantrine versus dihydroartemisinin-piperaquine for treatment and transmission control of uncomplicated Plasmodium falciparum malaria in western Kenya.
A randomized trial to monitor the efficacy and effectiveness by QT-NASBA of artemether-lumefantrine versus dihydroartemisinin-piperaquine for treatment and transmission control of uncomplicated Plasmodium falciparum malaria in western Kenya.
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DOI:
10.1186/1475-2875-7-237
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发表时间:
2008-11-18
期刊:
影响因子:
3
通讯作者:
Kager, Piet A.
中科院分区:
文献类型:
--
作者:
Mens, Petra F.;Sawa, Patrick;van Amsterdam, Sandra M.;Versteeg, Inge;Omar, Sabah A.;Schallig, Henk D. F. H.;Kager, Piet A.
Many countries have implemented artemisinin-based combination therapy (ACT) for the first-line treatment of malaria. Although many studies have been performed on efficacy and tolerability of the combination arthemeter-lumefantrine (AL) or dihydroartemisinin-piperaquine (DP), less is known of the effect of these drugs on gametocyte development, which is an important issue in malaria control. In this two-arm randomized controlled trial, 146 children were treated with either AL or DP. Both groups received directly observed therapy and were followed for 28 days after treatment. Blood samples were analysed with microscopy and NASBA. In comparison with microscopy NASBA detected much more gametocyte positive individuals. Moreover, NASBA showed a significant difference in gametocyte clearance in favour of AL compared to DP. The decline of parasitaemia was slower and persistence or development of gametocytes was significantly higher and longer at day 3, 7 and 14 in the DP group but after 28 days no difference could be observed between both treatment arms. Although practical considerations could favour the use of one drug over another, the effect on gametocytogenesis should also be taken into account and studied further using molecular tools like NASBA. This also applies when a new drug is introduced. Current controlled trials ISRCTN36463274
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影响因子:
2.9
作者:
Sokhna, CS;Trape, JF;Robert, V
通讯作者:
Robert, V
DOI:
10.1371/journal.pctr.0020020
发表时间:
2007-05-18
期刊:
PLoS clinical trials
影响因子:
--
作者:
Kamya, Moses R;Yeka, Adoke;Dorsey, Grant
通讯作者:
Dorsey, Grant
影响因子:
6.4
作者:
Ashley, EA;Krudsood, S;White, NJ
通讯作者:
White, NJ
影响因子:
11.8
作者:
Ashley, EA;McGready, R;Nosten, F
通讯作者:
Nosten, F
影响因子:
15.8
作者:
Sutherland, CJ;Ord, R;Targett, GAT
通讯作者:
Targett, GAT