Gentles T L, Keane J F, Jonas R A, Marx G E, Mayer J E
Department of Cardiology, Children's Hospital, Boston, MA.
Circulation. 1994 Nov;90(5 Pt 2):II1-6.
Frequently the definitive operation for patients with a right ventricle (RV) that is too small to support full cardiac output is a modified Fontan operation. However, other surgical options exist that incorporate a small RV in the atriopulmonary pathway when biventricular repair is not feasible because of RV or tricuspid valve hypoplasia. The risks and benefits of these options have not been well defined.
Between 1988 and 1993, 8 patients (6 with pulmonary atresia and intact ventricular septum and 2 with tricuspid valve stenosis and RV hypoplasia) underwent a cavopulmonary connection, which allowed right atrial blood to flow either to the pulmonary artery via the RV or directly via the cavopulmonary anastomosis. Age at surgery ranged from 1.5 to 9 years. The proximal right pulmonary artery was ligated in 5 patients, and the atrial septal defect was closed during the same procedure in 7 of the 8 patients. The echocardiographic right ventricular-left ventricular volume ratio ranged from 9% to 25%, and tricuspid valve z-scores ranged from 0 to -4. There were no deaths at a median follow-up of 24 months (range, 7 to 61 months). Mild exertional limitation was evident in only one patient. Postoperative echocardiograms demonstrated pulsatile systolic flow across the RV outflow tract in 5 patients and low-velocity diastolic-systolic flow in a sixth patient with extreme tricuspid valve hypoplasia. At postoperative cardiac catheterization (6 patients) right atrial mean pressures ranged from 7 to 13 mm Hg and mixed venous saturations from 62% to 70%.
Right atrial decompression via a superior vena cava-to-pulmonary artery anastomosis allows incorporation of a small RV into the pulmonary circulation and closure of the atrial septum, with excellent results to date.
对于右心室过小无法维持全心输出量的患者,其确定性手术通常为改良Fontan手术。然而,当由于右心室或三尖瓣发育不全而无法进行双心室修复时,还存在其他手术选择,即在心房-肺循环途径中纳入小的右心室。这些选择的风险和益处尚未明确界定。
1988年至1993年间,8例患者(6例为肺动脉闭锁且室间隔完整,2例为三尖瓣狭窄合并右心室发育不全)接受了腔肺连接术,使右心房血液可通过右心室流入肺动脉或直接通过腔肺吻合口。手术年龄为1.5至9岁。5例患者结扎了右肺动脉近端,8例患者中的7例在同一手术过程中关闭了房间隔缺损。超声心动图显示右心室与左心室容积比为9%至25%,三尖瓣z值为0至-4。中位随访24个月(范围7至61个月)无死亡病例。仅1例患者有轻度运动受限。术后超声心动图显示,5例患者右心室流出道有搏动性收缩期血流,1例三尖瓣极度发育不全的患者有低速舒张期-收缩期血流。术后心脏导管检查(6例患者)显示,右心房平均压力为7至13 mmHg,混合静脉血氧饱和度为62%至70%。
通过上腔静脉-肺动脉吻合术进行右心房减压可将小的右心室纳入肺循环并关闭房间隔,迄今为止效果良好。