Jaita Sawettachai, Madsalae Krit, Charoensakulchai Sakarn, Hanboonkunapakarn Borimas, Chotivanit Kesinee, McCarthy Anne E, Matsee Wasin
Thai Travel Clinic, Hospital for Tropical Diseases, Faculty of Tropical Medicine, Mahidol University, Bangkok 10400, Thailand.
Chulabhorn Hospital, Chulabhorn Royal Academy, Bangkok 10210, Thailand.
Trop Med Infect Dis. 2023 Jan 7;8(1):49. doi: 10.3390/tropicalmed8010049.
Artesunate is the drug of choice for treating patients with severe malaria. Post-artesunate delayed hemolysis (PADH) is an uncommon adverse event from malaria treatment. Most patients with PADH are non-immune travelers. The pathophysiology of PADH is not fully understood, but the most likely mechanism is "pitting", in which red blood cells carrying dead parasites killed by artesunate's action are directed to the spleen for clearing the dead parasites. After the cleansing process, these red blood cells re-enter the circulation but with a smaller size and impaired integrity, resulting in a shortened lifespan of 7-21 days. Therefore, most patients with PADH usually present with clinical features of hemolytic anemia 7 days or later after the initiation of artesunate. To date, the benefits of artesunate treatment outweigh its adverse events, and no fatal cases have resulted from PADH. However, the hematological follow-up of patients with malaria treated with artesunate is recommended for clinicians to detect any delayed hemolytic event early and prevent potentially serious consequences.
青蒿琥酯是治疗重症疟疾患者的首选药物。青蒿琥酯治疗后延迟性溶血(PADH)是疟疾治疗中一种罕见的不良事件。大多数PADH患者是非免疫旅行者。PADH的病理生理学尚未完全了解,但最可能的机制是“凹陷”,即携带被青蒿琥酯作用杀死的死亡寄生虫的红细胞被导向脾脏以清除死亡寄生虫。在清除过程之后,这些红细胞重新进入循环,但尺寸变小且完整性受损,导致寿命缩短至7 - 21天。因此,大多数PADH患者通常在青蒿琥酯治疗开始后7天或更晚出现溶血性贫血的临床特征。迄今为止,青蒿琥酯治疗的益处超过其不良事件,且尚无PADH导致的死亡病例。然而,建议临床医生对接受青蒿琥酯治疗的疟疾患者进行血液学随访,以便早期发现任何延迟性溶血事件并预防潜在的严重后果。