Zhonghua Xue Ye Xue Za Zhi. 2024 Feb 14;45(2):109-114. doi: 10.3760/cma.j.cn121090-20230927-00145.
Paroxysmal nocturnal hemoglobinuria (PNH) is a rare clonal disease with abnormal hematopoietic stem cells that causes intravascular hemolytic anemia, thrombosis, and peripheral blood cytopenia. It has a chronic progressive course and can be fatal in severe cases if not treated aggressively. Complement inhibitors are the first-line recommended treatment for hemolysis-related symptoms of PNH. With the rapid development of new complement inhibitors, it is critical to quickly screen and confirm the diagnosis, identify patients with complement inhibitor indications, and monitor breakthrough hemolysis and extravascular hemolysis during complement inhibitor therapy. Drawing on the most recent guidelines, works of literature, and meta-reviews from around the world, as well as combining with experience from the experts, this consensus focused on PNH screening principles, the significance of PNH cloning detection, and post-treatment monitoring of terminal complement inhibitors, which may contribute to a better understanding of diagnosis and treatment monitoring in the era of complement inhibitors.
阵发性睡眠性血红蛋白尿(PNH)是一种罕见的克隆性疾病,造血干细胞异常,可导致血管内溶血、血栓形成和外周血细胞减少。它病程呈慢性进行性,如果不积极治疗,严重时可致命。补体抑制剂是PNH溶血相关症状的一线推荐治疗药物。随着新型补体抑制剂的快速发展,快速筛查和确诊、识别有补体抑制剂适应证的患者以及监测补体抑制剂治疗期间的突破性溶血和血管外溶血至关重要。借鉴全球最新指南、文献和荟萃综述,并结合专家经验,本共识聚焦于PNH筛查原则、PNH克隆检测的意义以及终末补体抑制剂治疗后的监测,这可能有助于更好地理解补体抑制剂时代的诊断和治疗监测。