摘要
目的:分析室间隔缺损合并重度肺动脉高压(pulmonary hypertension,PH)患者的诊断性治疗及远期随访结果,总结先天性心脏病(先心病)合并重度肺动脉高压患者的诊断性治疗体会。方法:2005年10月至2010年12月,收治室间隔缺损合并重度肺动脉高压患者65例,分别给与选择性扩张肺动脉药物治疗,以不吸氧状态下末梢氧饱和度稳定在95%以上为主要标准,判断手术指征。结果:手术54例,均在体外循环下行室间隔缺损修补术。围手术期死亡1例,无远期死亡,11例不具备手术条件,继续药物治疗。随访12~36个月,平均肺动脉压力低于40 mmHg(1 mmHg=0.133 kPa)。未手术患者肺动脉压力明显降低,心功能明显改善。结论:通过药物对重度肺动脉高压患者进行诊断性治疗,可以对肺动脉高压性质做出准确的判断,能获得良好的疗效。
Objective:To evaluate the standard of operative indications and the perioperative manage- ment of ventricular septal defect complicated with severe pulmonary hypertension. Methods: From October 2005 to December 2010, 65 patients suffered ventricular septal defect accompanying with severe pulmonary hy- pertension were given selective dilation of the pulmonary vasodilator drugs. Standard of operative indications was on the base of change of SpO2, echocardiogram and X-ray. Results : After the pre-operation preparative, 54 ca- ses operation was performed, 1 patient died in hospital. The follow-up showed that the pulmonary pressure was significantly decreased. Conclusion: Satisfactory result can be achieved in treatment of ventricular septal defect complicated with severe pulmonary hypertension by comprehensive preoperative management and preoperative a- nalysis of surgical indications.
出处
《心肺血管病杂志》
CAS
2012年第4期402-404,共3页
Journal of Cardiovascular and Pulmonary Diseases
关键词
先天性心脏病
室间隔缺损
肺动脉高压
Ventricular septal defect
Pulmonary arterial hypertension
Congenital heart disease