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本文引用的文献

1
Artemisinin resistance in Plasmodium falciparum malaria.恶性疟原虫疟疾中的青蒿素耐药性。
N Engl J Med. 2009 Jul 30;361(5):455-67. doi: 10.1056/NEJMoa0808859.
2
Changes in the treatment responses to artesunate-mefloquine on the northwestern border of Thailand during 13 years of continuous deployment.在持续使用13年期间,泰国西北边境地区对青蒿琥酯-甲氟喹治疗反应的变化。
PLoS One. 2009;4(2):e4551. doi: 10.1371/journal.pone.0004551. Epub 2009 Feb 23.
3
Evidence of artemisinin-resistant malaria in western Cambodia.柬埔寨西部出现青蒿素耐药性疟疾的证据。
N Engl J Med. 2008 Dec 11;359(24):2619-20. doi: 10.1056/NEJMc0805011. Epub 2008 Dec 8.
4
The relationship between the haemoglobin concentration and the haematocrit in Plasmodium falciparum malaria.恶性疟原虫疟疾中血红蛋白浓度与血细胞比容之间的关系。
Malar J. 2008 Aug 2;7:149. doi: 10.1186/1475-2875-7-149.
5
Declining artesunate-mefloquine efficacy against falciparum malaria on the Cambodia-Thailand border.在柬埔寨-泰国边境,青蒿琥酯-甲氟喹对抗恶性疟的疗效正在下降。
Emerg Infect Dis. 2008 May;14(5):716-9. doi: 10.3201/eid1405.071601.
6
Qinghaosu (artemisinin): the price of success.青蒿素:成功的代价
Science. 2008 Apr 18;320(5874):330-4. doi: 10.1126/science.1155165.
7
World Antimalarial Resistance Network I: clinical efficacy of antimalarial drugs.世界抗疟药物耐药性网络I:抗疟药物的临床疗效。
Malar J. 2007 Sep 6;6:119. doi: 10.1186/1475-2875-6-119.
8
Pfmdr1 and in vivo resistance to artesunate-mefloquine in falciparum malaria on the Cambodian-Thai border.Pfmdr1与柬埔寨-泰国边境恶性疟原虫对青蒿琥酯-甲氟喹的体内抗性
Am J Trop Med Hyg. 2007 Apr;76(4):641-7.
9
Efficacy of artemether-lumefantrine for the treatment of uncomplicated falciparum malaria in northwest Cambodia.蒿甲醚-本芴醇治疗柬埔寨西北部非复杂性恶性疟的疗效
Trop Med Int Health. 2006 Dec;11(12):1800-7. doi: 10.1111/j.1365-3156.2006.01739.x.
10
Surveillance of the efficacy of artesunate and mefloquine combination for the treatment of uncomplicated falciparum malaria in Cambodia.柬埔寨青蒿琥酯与甲氟喹联合治疗非复杂性恶性疟疗效监测
Trop Med Int Health. 2006 Sep;11(9):1360-6. doi: 10.1111/j.1365-3156.2006.01690.x.

体内寄生虫学青蒿素敏感性测量。

In vivo parasitological measures of artemisinin susceptibility.

机构信息

Mahidol-Oxford Tropical Medicine Research Unit, Mahidol University, Bangkok, Thailand.

出版信息

J Infect Dis. 2010 Feb 15;201(4):570-9. doi: 10.1086/650301.

DOI:10.1086/650301
PMID:20085495
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4291277/
Abstract

Parasite clearance data from 18,699 patients with falciparum malaria treated with an artemisinin derivative in areas of low (n=14,539), moderate (n=2077), and high (n=2083) levels of malaria transmission across the world were analyzed to determine the factors that affect clearance rates and identify a simple in vivo screening measure for artemisinin resistance. The main factor affecting parasite clearance time was parasite density on admission. Clearance rates were faster in high-transmission settings and with more effective partner drugs in artemisinin-based combination treatments (ACTs). The result of the malaria blood smear on day 3 (72 h) was a good predictor of subsequent treatment failure and provides a simple screening measure for artemisinin resistance. Artemisinin resistance is highly unlikely if the proportion of patients with parasite densities of <100,000 parasites/microL given the currently recommended 3-day ACT who have a positive smear result on day 3 is <3%; that is, for n patients the observed number with a positive smear result on day 3 does not exceed (n + 60)/24.

摘要

从全世界疟疾传播水平低(n=14539)、中(n=2077)和高(n=2083)地区采用青蒿素衍生物治疗的 18699 例恶性疟患者的寄生虫清除数据进行分析,以确定影响清除率的因素,并鉴定一种简单的青蒿素耐药性体内筛选方法。影响寄生虫清除时间的主要因素是入院时寄生虫密度。在高传播地区以及在基于青蒿素的联合治疗(ACT)中采用更有效的联合药物时,清除率更快。第 3 天(72 小时)疟疾病血涂片的结果是随后治疗失败的良好预测指标,并提供了一种简单的抗疟药耐药性筛选方法。如果在目前推荐的 3 天 ACT 治疗中,寄生虫密度<100,000 个/微升的患者中,第 3 天阳性血涂片结果的比例<3%(即 n 个患者中,第 3 天阳性血涂片结果的观察数不超过(n+60)/24),那么出现青蒿素耐药的可能性极小。