[先天性心脏缺陷的外科治疗:当前进展及一些病例示例]

[Surgery in congenital heart defects: current developments and a few case examples].

作者信息

Carrel T

机构信息

Thorax-, Herz- und Gefässchirurgie, Inselspital Bern.

出版信息

Praxis (Bern 1994). 1997 Apr 23;86(17):704-9.

DOI:
PMID:9221478
Abstract

Congenital heart surgery includes the palliative treatment and surgical complete repair of cardiac malformations in newborns, children and adolescents. Palliative surgery allows early or long-term survival, depending on the primary malformation and the condition of the patient. Confection of a systemic-to-pulmonary shunt (the modified Blalock-Taussig shunt) allows in general recovery from severe cyanosis and leads to development of the hypoplastic pulmonary vascular tree in newborns with severe pulmonary stenosis. Longterm palliation can be applied to all patients in whom establishment of a biventricular heart can not be realized. The total cavo-pulmonary connection represents one possibility to bypass a single ventricle in these complex cases. Total repair allows the restitution of a completely normal anatomy and physiology after surgery; usually, this type of surgery is followed by a normalization of life expectancy with minimal pharmacotherapy. Preoperative diagnosis of congenital heart disease is reasonably performed by transthoracic echocardiography in the majority of cases. Cardiac catheterism is reserved for complex cases and those in which full hemodynamic evaluation is required for proper planning of surgery. Continuous improvement has been realized in the fields of cardiac anesthesiology and pediatric intensive care during the last decade; hence more and more complex cases have been accepted without any negative effect on the operative mortality. Additionally there has been a number of improvements in surgical and perfusion techniques, thus allowing open heart surgery in newborns with a minimal weight of 2000 g. Intraoperative transesophageal echocardiography is performed routinely and allows the proper control of surgical repair; furthermore this examination may be helpful during the weaning period from the extracorporeal circulation. There is a number of interesting topics that will take importance or will be developed in the near future: the role of interventional cardiology in pediatric patients gains more and more importance. There is a potential for minimally-invasive surgery and the number of potential candidates for heart transplantation may increase, due to the fate of long-term survivors after palliative surgery.

摘要

先天性心脏手术包括对新生儿、儿童和青少年心脏畸形进行姑息治疗和手术完全修复。姑息手术能使患者实现早期或长期存活,这取决于原发性畸形和患者状况。构建体肺分流术(改良布莱洛克 - 陶西格分流术)通常可使严重青紫症状得到缓解,并促使患有严重肺动脉狭窄的新生儿发育不全的肺血管树得到发展。长期姑息治疗适用于所有无法实现双心室心脏构建的患者。在这些复杂病例中,全腔静脉 - 肺动脉连接术是绕过单心室的一种可行方法。完全修复可使术后解剖结构和生理功能完全恢复正常;通常,这类手术后通过最少的药物治疗,预期寿命可恢复正常。在大多数情况下,先天性心脏病的术前诊断通过经胸超声心动图就能合理完成。心导管检查则用于复杂病例以及那些为正确规划手术需要进行全面血流动力学评估的病例。在过去十年里,心脏麻醉学和儿科重症监护领域持续取得进展;因此,越来越多复杂病例得以接受,且对手术死亡率没有任何负面影响。此外,手术和灌注技术也有多项改进,从而使体重低至2000克的新生儿也能进行心脏直视手术。术中常规进行经食管超声心动图检查,有助于对手术修复进行适当控制;此外,在脱离体外循环的撤机阶段,这项检查也可能会有帮助。有许多有趣的话题在不久的将来会变得重要或得到发展:介入心脏病学在儿科患者中的作用越来越重要。由于姑息手术后长期存活者的情况,微创手术有发展潜力,且心脏移植的潜在候选者数量可能会增加。

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