Oklahoma Children's Hospital at OU Health, Oklahoma City, Oklahoma.
J Extra Corpor Technol. 2021 Jun;53(2):137-139. doi: 10.1182/ject-2000060.
Little is reported in the literature regarding hereditary spherocytosis (HS) and cardiopulmonary bypass (CPB). We present a case of a 19-month-old girl child who was referred for an atrioventricular septal defect (AVSD) and HS. The patient underwent surgical repair, and an exchange transfusion was performed at the initiation of CPB. No significant hemolysis or events attributed to HS were observed during or after CPB. The surgical repair of an AVSD in a pediatric patient with HS and total volume exchange transfusion is herein reported.
关于遗传性球形红细胞增多症(HS)和体外循环(CPB),文献报道甚少。我们报告了一例 19 个月大的女孩,因房间隔和室间隔缺损(AVSD)和 HS 而转诊。患者接受了手术修复,在 CPB 开始时进行了换血。在 CPB 过程中和之后,没有观察到明显的溶血或归因于 HS 的事件。本文报告了一例 HS 合并全血容量换血的小儿患者的 AVSD 手术修复。