Jin Di, Shen Le, Huang Yuguang
Department of Anesthesiology, Peking Union Medical College Hospital, Beijing, China.
State Key Laboratory of Complex Severe and Rare Diseases (Peking Union Medical College Hospital), Beijing, China.
Front Physiol. 2022 Jun 30;13:926398. doi: 10.3389/fphys.2022.926398. eCollection 2022.
Hereditary spherocytosis is a common red blood cell disease caused by an inherited red blood cell membrane defect, leading to a spherical shape and propensity for hemolysis. There is a lack of reports on intraoperative autologous blood transfusion for hereditary spherocytosis patients. We hereby report our recent experience with using the Cell Saver system for intraoperative red blood cell salvage on a hereditary spherocytosis patient. There was a drastic increase in salvaged blood free-hemoglobin compared with the preoperative sample (82.6 mg/dl vs. 6.2 mg/dl) which indicated severe hemolysis. Although our patient recovered smoothly with a normal liver and renal function test and reported no adverse reaction during follow-up, it is noteworthy that severe hemolysis could happen during the cell salvage process for patients with hemolytic anemia, as there are similar reports on sickle cell anemia, beta-thalassemia intermedia, and paroxysmal nocturnal hemoglobinuria. Therefore, more clinical attention and thorough research should be drawn into this perspective, namely, hemolysis during the red blood cell salvage process for patients with hemolytic anemia.
遗传性球形红细胞增多症是一种常见的红细胞疾病,由遗传性红细胞膜缺陷引起,导致红细胞呈球形并易于溶血。关于遗传性球形红细胞增多症患者术中自体输血的报道较少。我们在此报告我们最近使用细胞回收系统对一名遗传性球形红细胞增多症患者进行术中红细胞回收的经验。与术前样本相比,回收血液中的游离血红蛋白急剧增加(82.6毫克/分升对6.2毫克/分升),这表明存在严重溶血。尽管我们的患者恢复顺利,肝肾功能测试正常,且随访期间未报告不良反应,但值得注意的是,对于溶血性贫血患者,在细胞回收过程中可能会发生严重溶血,镰状细胞贫血、中间型β地中海贫血和阵发性夜间血红蛋白尿也有类似报道。因此,应从这一角度,即溶血性贫血患者红细胞回收过程中的溶血,引起更多的临床关注和深入研究。