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婴儿期后患有充血性心力衰竭的重度瓣膜性肺动脉狭窄的肺动脉球囊瓣膜切开术

Pulmonary balloon valvotomy for severe valvular pulmonic stenosis with congestive heart failure beyond infancy.

作者信息

Shrivastava S, Kumar R K, Dev V, Kothari S S, Saxena A

机构信息

Department of Cardiology, All India Institute of Medical Sciences, New Delhi.

出版信息

Cathet Cardiovasc Diagn. 1993 Feb;28(2):137-41. doi: 10.1002/ccd.1810280209.

DOI:10.1002/ccd.1810280209
PMID:8448797
Abstract

Isolated valvular pulmonic stenosis (PS) in association with tricuspid regurgitation and congestive heart failure (CHF) is rarely encountered after infancy, and there is very little information available regarding the application of pulmonary balloon valvotomy (PBV) for this subset of patients. Since 1985, 10 patients (5 males, 5 females; mean age: 12.4 +/- 7.5 years, range 4-25 years) underwent PBV for severe valvular PS with CHF in our institution. All patients had associated tricuspid regurgitation and cardiomegaly. Before PBV, the mean peak systolic gradient across the right ventricular outflow was 131 +/- 36 mmHg and the mean right atrial pressure was 14.4 +/- 5.4 mmHg. Specific modifications in the PBV technique included the sequential use of progressively larger balloon catheters and the use of an extra stiff guidewire to support the dilatation assembly. One patient underwent PBV via the right internal jugular vein. Problems encountered during PBV included hypotension and bradycardia (2 patients) and respiratory arrest, which was transient in one patient, and prolonged and eventually fatal in one patient. A successful outcome was achieved in 8 patients (4 of these required 2 PBV attempts) with a final residual gradient of 40 mmHg or less, mean 28 +/- 7; range: 21-38 mmHg) and complete resolution of CHF. One patient has had no significant change in gradients and awaits repeat dilatation. Patients with isolated severe valvular PS with TR and CHF represent a relatively high risk group for PBV. A successful outcome is, however, feasible if a carefully planned and cautious approach is used.

摘要

婴儿期后很少见到孤立性瓣膜肺动脉狭窄(PS)合并三尖瓣反流和充血性心力衰竭(CHF)的情况,关于肺动脉球囊瓣膜成形术(PBV)应用于这类患者的资料非常少。自1985年以来,我院有10例患者(5男,5女;平均年龄:12.4±7.5岁,范围4 - 25岁)因严重瓣膜性PS合并CHF接受了PBV。所有患者均伴有三尖瓣反流和心脏扩大。PBV术前,右心室流出道的平均收缩期峰值压差为131±36 mmHg,平均右心房压力为14.4±5.4 mmHg。PBV技术的特殊改进包括依次使用逐渐增大的球囊导管以及使用超硬导丝来支撑扩张装置。1例患者经右颈内静脉进行PBV。PBV过程中遇到的问题包括低血压和心动过缓(2例患者)以及呼吸骤停,其中1例患者的呼吸骤停是短暂的,另1例患者的呼吸骤停持续时间延长并最终导致死亡。8例患者(其中4例需要进行2次PBV尝试)取得了成功的结果,最终残余压差≤40 mmHg(平均28±7;范围:21 - 38 mmHg),CHF完全缓解。1例患者的压差无明显变化,等待再次扩张。孤立性严重瓣膜性PS合并TR和CHF的患者是PBV的相对高危组。然而,如果采用精心规划和谨慎的方法,成功的结果是可行的。

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Non surgical treatment in congenital heart disease.先天性心脏病的非手术治疗
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