首页> 外文期刊>Emerging Infectious Diseases >Severe Delayed Hemolysis Associated with Regulated Parenteral Antimalarial Drug (http://wwwnc.cdc.gov/eid/article/21/1/14-0147)
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Severe Delayed Hemolysis Associated with Regulated Parenteral Antimalarial Drug (http://wwwnc.cdc.gov/eid/article/21/1/14-0147)

机译:与经肠胃外抗疟药物管理相关的严重延迟溶血(ht​​tp://wwwnc.cdc.gov/eid/article/21/1/14-0147)

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To the Editor: Intravenous artesunate is recommended by the World Health Organization as first-line treatment for severe malaria. While artemisinin-based therapies are well tolerated, recent studies have reported cases of severe delayed hemolysis after artesunate treatment for malaria ( 1 – 5 ). To date, all reported cases have been associated with the use of artesunate not produced under Good Manufacturing Practice (GMP) standards. The United States and Canada are the only countries that use GMP artesunate, and a recent review concluded that delayed hemolysis may be related to differences in GMP versus non-GMP artemisinins ( 5 ). We report a case of severe delayed hemolysis after administration of GMP artesunate to treat a patient with severe malaria.
机译:致编辑:世界卫生组织推荐静脉青蒿琥酯作为严重疟疾的一线治疗。尽管基于青蒿素的疗法耐受性良好,但最近的研究报道了青蒿琥酯治疗疟疾后严重延迟溶血的病例(1-5)。迄今为止,所有报告的病例都与使用非按照良好生产规范(GMP)标准生产的青蒿琥酯有关。美国和加拿大是唯一使用GMP青蒿琥酯的国家,最近的一项审查得出结论,溶血延迟可能与GMP与非GMP青蒿素的差异有关(5)。我们报告了在给予GMP青蒿琥酯治疗严重疟疾后严重延迟溶血的情况。

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