Rao V, Kadletz M, Hornberger L K, Freedom R M, Black M D
Division of Cardiology, The Hospital for Sick Children, University of Toronto, Ontario, Canada.
Ann Thorac Surg. 2000 Jan;69(1):176-9; discussion 179-80. doi: 10.1016/s0003-4975(99)01152-2.
Surgical repair of congenital lesions associated with right ventricular outflow tract obstruction frequently requires the destruction of pulmonary valve (PV) components including the valve annulus. The resultant pulmonary insufficiency may lead to late functional deterioration of right ventricular performance. Acute right ventricular dysfunction has been associated with poor pulmonary runoff, tricuspid valve regurgitation, and pulmonary hypertension. Preservation of PV competence may prevent both early and late right ventricular failure. However, the recent trend towards earlier repair of tetralogy of Fallot (TOF) may preclude preservation of the PV in favor of a transannular patch. We reviewed our experience with surgical repair of TOF to determine if age and/or body size affected the ability to repair the PV.
We reviewed the clinical records of 50 consecutive children who underwent surgical repair of TOF by one surgeon. The latter 27 patients underwent repair with an intention to preserve their pulmonary valve. In total, 28 patients underwent repair with preservation of their pulmonary valve, and form the basis of this study. Serial echocardiographic assessments were performed early (3 to 6 months) and late (12 months) after surgery.
Pulmonary valve preservation was possible in the majority of children (89%) in whom it was intended. Pulmonary valve competence was observed in 68% of children, with only 5 (16%) children demonstrating severe insufficiency at follow-up. Residual right ventricular outflow tract obstruction was present in only 1 child who underwent repair with pulmonary valve preservation at greater than 2 years of age.
Our data suggest that earlier repair of TOF does not preclude preservation of the pulmonary valve and may indeed facilitate repair. The pulmonary valve remains competent at 12 months, with acceptable gradients, and should participate in somatic growth. Pulmonary valve preservation during repair of TOF may prevent free pulmonary insufficiency, progressive right ventricular dilation, and the need for future prosthetic pulmonary valve replacement.
与右心室流出道梗阻相关的先天性病变的手术修复常常需要破坏包括瓣环在内的肺动脉瓣(PV)组件。由此产生的肺动脉瓣关闭不全可能导致右心室功能的晚期恶化。急性右心室功能障碍与肺血流减少、三尖瓣反流和肺动脉高压有关。保留肺动脉瓣功能可能预防早期和晚期右心室衰竭。然而,近期法洛四联症(TOF)早期修复的趋势可能不利于保留肺动脉瓣,而倾向于采用跨瓣环补片。我们回顾了我们对TOF手术修复的经验,以确定年龄和/或体型是否会影响肺动脉瓣修复的能力。
我们回顾了由一位外科医生连续为50例儿童进行TOF手术修复的临床记录。后27例患者手术的目的是保留其肺动脉瓣。总共28例患者接受了保留肺动脉瓣的修复,并构成了本研究的基础。术后早期(3至6个月)和晚期(12个月)进行了系列超声心动图评估。
大多数计划保留肺动脉瓣的儿童(89%)实现了肺动脉瓣保留。68%的儿童观察到肺动脉瓣功能正常,随访时只有5例(16%)儿童表现为严重关闭不全。仅1例年龄大于2岁且接受了肺动脉瓣保留修复的儿童存在残余右心室流出道梗阻。
我们的数据表明,TOF的早期修复并不排除保留肺动脉瓣,实际上可能有助于修复。肺动脉瓣在12个月时功能仍然正常,压力阶差可接受,并且应该参与身体生长。TOF修复过程中保留肺动脉瓣可能预防自由性肺动脉瓣关闭不全、右心室进行性扩张以及未来人工肺动脉瓣置换的需要。