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恶性疟原虫根治期间伯氨喹致严重溶血:两项系统评价和个体患者数据描述性分析。

Severe Hemolysis during Primaquine Radical Cure of Plasmodium vivax Malaria: Two Systematic Reviews and Individual Patient Data Descriptive Analyses.

机构信息

Jimma University Clinical Trial Unit, Department of Internal Medicine, Jimma University, Jimma, Ethiopia.

WorldWide Antimalarial Resistance Network, Oxford, United Kingdom.

出版信息

Am J Trop Med Hyg. 2023 Aug 21;109(4):761-769. doi: 10.4269/ajtmh.23-0280. Print 2023 Oct 4.

Abstract

Primaquine (PQ) kills Plasmodium vivax hypnozoites but can cause severe hemolysis in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency. We conducted two systematic reviews. The first used data from clinical trials to determine the variety of definitions and frequency of hematological serious adverse events (SAEs) related to PQ treatment of vivax malaria. The second used data from prospective studies and case reports to describe the clinical presentation, management, and outcome of severe PQ-associated hemolysis necessitating hospitalization. In the first review, SAEs were reported in 70 of 249 clinical trials. There were 34 hematological SAEs among 9,824 patients with P. vivax malaria treated with PQ, nine of which necessitated hospitalization or blood transfusion. Criteria used to define SAEs were diverse. In the second review, 21 of 8,487 articles screened reported 163 patients hospitalized after PQ radical cure; 79.9% of whom (123 of 154) were prescribed PQ at ≥ 0.5 mg/kg/day. Overall, 101 patients were categorized as having probable or possible severe PQ-associated hemolysis, 96.8% of whom were G6PD deficient (< 30% activity). The first symptoms of hemolysis were reported primarily on day 2 or 3 (45.5%), and all patients were hospitalized within 7 days of PQ commencement. A total of 57.9% of patients (77 of 133) had blood transfusion. Seven patients (6.9%) with probable or possible hemolysis died. Even when G6PD testing is available, enhanced monitoring for hemolysis is warranted after PQ treatment. Clinical review within the first 5 days of treatment may facilitate early detection and management of hemolysis. More robust definitions of severe PQ-associated hemolysis are required.

摘要

伯氨喹(PQ)可杀灭间日疟原虫休眠子,但可导致葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症患者严重溶血。我们进行了两项系统评价。第一项使用临床试验数据,确定与间日疟原虫疟疾 PQ 治疗相关的各种定义和血液学严重不良事件(SAE)的频率。第二项使用前瞻性研究和病例报告的数据,描述需要住院治疗的严重 PQ 相关溶血性贫血的临床表现、管理和结局。在第一项评价中,249 项临床试验中有 70 项报告了 SAE。9824 例间日疟患者接受 PQ 治疗后发生 34 例血液学 SAE,其中 9 例需要住院或输血。用于定义 SAE 的标准各不相同。在第二项评价中,经筛选的 8487 篇文章中有 21 篇报道了 163 例接受 PQ 根治治疗后住院的患者;其中 154 例中有 123 例(79.9%)处方 PQ 剂量≥0.5mg/kg/天。总体而言,101 例患者被归类为可能或可能严重的 PQ 相关溶血性贫血,其中 96.8%(101/104)为 G6PD 缺乏症(活性<30%)。溶血性贫血的首发症状主要发生在第 2 或 3 天(45.5%),所有患者在 PQ 开始后 7 天内住院。共有 57.9%(77/133)的患者需要输血。7 例(6.9%)疑似或可能溶血的患者死亡。即使有 G6PD 检测,PQ 治疗后也需要加强溶血监测。治疗后前 5 天内的临床评估可能有助于早期发现和管理溶血。需要更严格的严重 PQ 相关溶血性贫血定义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e253/10551063/ac61abb0ae7b/ajtmh.23-0280f1.jpg

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