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儿童先天性心脏病的机械瓣膜置换术。

Mechanical valve replacement in congenital heart disease in children.

作者信息

Lubiszewska B, Rozanski J, Szufladowicz M, Szaroszyk W, Hoffman P, Ksiezycka E, Rydlewska-Sadowska W, Ruzyllo W

机构信息

Dept. of General Cardiology, National Institute of Cardiology, Warsaw, Poland.

出版信息

J Heart Valve Dis. 1999 Jan;8(1):74-9.

Abstract

BACKGROUND AND AIM OF THE STUDY

The study aim was to analyze predictive factors of long-term results after mechanical heart valve replacement in children.

METHODS

Forty-four patients (19 males, 25 females; mean age 8.9+/-3.9 years, median 7.0 years, range: 1.3 to 15 years) underwent heart valve replacement with mechanical prostheses. Of these patients, 25 had left atrioventricular valve replacement (LavVR) (18 mitral, six tricuspid in corrected transposition of the great arteries (TGA), one common in a univentricular heart), 13 had aortic valve replacement (AVR) and six had tricuspid valve replacement (TVR). The etiology of the valvular disease was congenital in all patients, and complicated by infective endocarditis in seven (16%). Fifteen patients had undergone previous procedures and 16 required simultaneous repair of associated lesions. The mean size of the implanted prosthesis was 26 mm (range: 19-29 mm) for LavVR, 29.7 mm (range: 23-33 mm) for TVR, and 21.9 mm (range: 19-25 mm) for AVR. Postoperatively, all patients received oral anticoagulation. The mean follow up was 6.8+/-3.5 years (total 290 patient-years).

RESULTS

There was no early mortality, but three patients (7%) died later; all late deaths occurred in patients with LavVR. There were two sudden deaths, both in patients with complex congenital heart disease and heart failure (before the ACE inhibitor era), and one valve-related death from thrombotic occlusion of a mitral prosthesis. Five patients were reoperated on; three for patient-prosthesis mismatch, one for periprosthetic leak, and one for aortic dissection due to Marfan's syndrome. Thrombotic obstruction occurred in three patients; two in the tricuspid position were treated successfully with thrombolysis, but one in the left atrioventricular position proved fatal. After seven years, the survival rate was 93.4%.

CONCLUSIONS

Mechanical heart valve replacement in children aged over one year with congenital heart disease can be performed with satisfactory early and late results. Mechanical valves of >23 mm diameter in the atrioventricular position in the systemic ventricle, and >21 mm in the aortic orifice, can offer excellent long-lasting hemodynamic performance. However, mechanical valves in the tricuspid position are prone to develop thrombotic occlusion.

摘要

研究背景与目的

本研究旨在分析儿童机械心脏瓣膜置换术后长期疗效的预测因素。

方法

44例患者(男19例,女25例;平均年龄8.9±3.9岁,中位数7.0岁,范围:1.3至15岁)接受了机械瓣膜置换术。其中,25例行左房室瓣置换术(LavVR)(18例二尖瓣置换,6例三尖瓣置换,其中矫正型大动脉转位(TGA)患者6例,单心室心脏患者1例),13例行主动脉瓣置换术(AVR),6例行三尖瓣置换术(TVR)。所有患者瓣膜疾病的病因均为先天性,7例(16%)合并感染性心内膜炎。15例患者曾接受过先前手术,16例需要同时修复相关病变。LavVR植入人工瓣膜的平均尺寸为26mm(范围:19 - 29mm),TVR为29.7mm(范围:23 - 33mm),AVR为21.9mm(范围:19 - 25mm)。术后,所有患者均接受口服抗凝治疗。平均随访时间为6.8±3.5年(总计290患者 - 年)。

结果

无早期死亡病例,但有3例患者(7%)后期死亡;所有晚期死亡均发生在LavVR患者中。有2例猝死,均发生在患有复杂先天性心脏病和心力衰竭的患者中(在ACE抑制剂时代之前),1例因二尖瓣人工瓣膜血栓闭塞导致瓣膜相关死亡。5例患者接受了再次手术;3例因患者 - 人工瓣膜不匹配,1例因人工瓣膜周漏,1例因马凡综合征导致主动脉夹层。3例患者发生血栓阻塞;2例三尖瓣位置的血栓阻塞经溶栓治疗成功,但1例左房室位置的血栓阻塞导致死亡。7年后,生存率为93.4%。

结论

1岁以上先天性心脏病儿童进行机械心脏瓣膜置换术,早期和晚期结果均令人满意。在体心室的房室位置,直径>23mm的机械瓣膜,以及在主动脉瓣口直径>21mm的机械瓣膜,可提供出色的长期血流动力学性能。然而,三尖瓣位置的机械瓣膜容易发生血栓阻塞。

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