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疟疾后贫血在马拉维伴有疟疾性脑病的儿童中罕见。

Post-Malaria Anemia Is Rare in Malawian Children with Cerebral Malaria.

机构信息

1Department of Pediatrics, Children's National Medical Center, Washington, District of Columbia.

2Blantyre Malaria Project, University of Malawi College of Medicine, Blantyre, Malawi.

出版信息

Am J Trop Med Hyg. 2021 Apr 26;104(6):2146-2151. doi: 10.4269/ajtmh.20-1668.

DOI:10.4269/ajtmh.20-1668
PMID:33901002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8176486/
Abstract

Artesunate therapy for severe malaria syndromes has been associated with post-treatment hemolysis and anemia. We defined post-malaria anemia as any decrease in hematocrit between the index hospitalization for severe malaria and 1 month after. We determined the incidence and severity of post-malaria anemia in Malawian children surviving cerebral malaria (CM) by analyzing hospital and follow-up data from a long-standing study of CM pathogenesis. Children enrolled before 2014 and treated with quinine (N = 258) were compared with those admitted in 2014 and after, and treated with artesunate (N = 235). The last hematocrit value obtained during hospitalization was compared with the 1-month post-hospitalization hematocrit value. The overall rate of a post-hospitalization decrease in hematocrit in children surviving CM was 5.3% (11 of 235 or 4.7% for quinine, 15 of 258 or 5.8% for artesunate; odds ratio, 3.23 [0.88, 18.38]); no patients with a decrease in hematocrit were symptomatic, and none required transfusion after hospitalization. Of the 26 children who had a decrease in hematocrit 1 month after hospitalization, 23.1% had evidence of a new malaria infection. When children treated with quinine and artesunate were combined, a higher hematocrit level on admission, lower quantitative histidine-rich protein level, and splenomegaly were associated independently with post-malaria anemia. In African survivors of CM, post-malaria anemia is rare, mild, and unassociated with the anti-malarial treatment received.

摘要

青蒿琥酯治疗严重疟疾综合征与治疗后溶血和贫血有关。我们将疟疾后贫血定义为严重疟疾住院期间和 1 个月后之间的血细胞比容下降。我们通过分析一项长期疟疾发病机制研究的住院和随访数据,确定了在马拉维幸存的脑疟疾(CM)儿童中疟疾后贫血的发生率和严重程度。与 2014 年之前入院并接受奎宁治疗的儿童(N = 258)相比,比较了在 2014 年及以后入院并接受青蒿琥酯治疗的儿童(N = 235)。将住院期间最后一次获得的血细胞比容值与住院后 1 个月的血细胞比容值进行比较。CM 幸存儿童中,住院后血细胞比容下降的总体发生率为 5.3%(235 例中的 11 例,奎宁为 4.7%,258 例中的 15 例,青蒿琥酯为 5.8%;比值比,3.23[0.88, 18.38]);没有血细胞比容下降的患者有症状,且住院后无需输血。在 26 例住院后血细胞比容下降的儿童中,23.1%有新疟疾感染的证据。当将接受奎宁和青蒿琥酯治疗的儿童合并时,入院时较高的血细胞比容水平、较低的定量组氨酸丰富蛋白水平和脾肿大与疟疾后贫血独立相关。在非洲 CM 幸存者中,疟疾后贫血罕见、轻度且与接受的抗疟治疗无关。

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