摘要
目的:探讨并发重度肺动脉高压的先天性心脏病患者的外科手术方式。方法:采用房水平单向活瓣补片对48例本病患者进行手术治疗。其中,室间隔缺损30例,房间隔缺损3例,室间隔缺损并发房间隔缺损8例,室间隔缺损伴动脉导管未闭7例。结果:术后1例(2%)死于低心排综合征。术后早期均有明显低氧血症。术后1周仍出现跨单向活瓣补片分流40例,术后3个月活瓣仍开放10例,术后26个月提示活瓣均关闭,分流消失,经皮血氧均为95%以上,肺动脉压均明显下降。结论:房水平单向活瓣式补片治疗先天性心脏病并发肺动脉高压,使患者度过术后危险期,提高手术成功率。
AIM: To study the surgical treatment of patients with congenital heart disease (CHD) with severe pulmonary hypertension (PH). METHODS: One-way valved patch was used during surgical treatment for 48 patients with CHD with PH. Patients included represented 30 cases of ventricular septal defect (VSD) , three cases of atrial septal defect (ASD), eight cases of ~SD with ASD, and seven cases of VSD with patent ductus arteriosus (PDA). RESULTS : One patient died postoperatively due to low cardiac output syndrome. All patients suffered from hypoxia postoperatively. After the first postoperative week, transpatch shunt was observed in 40 patients and after 3 postoperative months, open valves were seen in ten cases. Twenty-six months postoperatively, valves closed and shunting disappeared. Transeutaneous oxygen was 〉 95 % and pulmonary artery pressure decreased significantly. CONCLUSION: Application of one-way valved patch in surgical treatment of congenital heart disease with pulmonary hypertension enhances the rate of successful surgeries and more rapid recovery.
出处
《心脏杂志》
CAS
2012年第5期636-638,共3页
Chinese Heart Journal
关键词
心脏病
先天性
肺动脉高压
手术治疗
congenital heart disease
secondary pulmonary hypertension
surgery