Dunlap Julie D, Green Morton C, Shah Aali M, Kibby Brandon T, Billmire Deborah F
Department of Clinical Anaesthesia, Riley Hospital for Children, Indianapolis, IN 46202-5200, USA.
Department of Surgery, Riley Hospital for Children, Indianapolis, IN 46202-5200, USA.
Ann Card Anaesth. 2019 Apr-Jun;22(2):210-212. doi: 10.4103/aca.ACA_38_18.
A 2-month-old male infant presented for elective repair of inguinal hernias. His preoperative medical history and physical examination were unremarkable. During induction of anesthesia, the infant sustained an adverse cardiac event. The event was characterized by tachycardia, hypotension, and massive ST-segment elevation. Despite vigorous resuscitation, spontaneous hemodynamic stability could not be achieved and extracorporeal membrane oxygenation was required. A transthoracic echocardiogram revealed severe hypoplasia of the ascending aorta. As effective cardiac function did not recover and there was evidence of diffuse ischemic brain injury, life support was withdrawn. Genetic testing performed postoperatively was definitive for Williams syndrome.
一名2个月大的男婴因择期腹股沟疝修补术前来就诊。其术前病史和体格检查均无异常。在麻醉诱导期间,该婴儿发生了不良心脏事件。该事件的特征为心动过速、低血压和广泛的ST段抬高。尽管进行了积极的复苏,但仍无法实现自主血流动力学稳定,需要进行体外膜肺氧合。经胸超声心动图显示升主动脉严重发育不全。由于有效的心脏功能未恢复且有弥漫性缺血性脑损伤的证据,于是停止了生命支持。术后进行的基因检测确诊为威廉姆斯综合征。