Kaulitz R, Ziemer G, Luhmer I, Kallfelz H C
Division of Pediatric Cardiology, Children's Hospital, Hannover, Germany.
J Thorac Cardiovasc Surg. 1996 Sep;112(3):658-64. doi: 10.1016/S0022-5223(96)70049-1.
The modified Fontan operation has been proposed as definitive palliation for an increasing variety of hearts with complex univentricular anatomy. To eliminate the influence of different surgical strategies, only patients undergoing total cavopulmonary anastomosis were included in this retrospective study.
Seventy-two patients had been operated on at ages ranging from 7 to 219 months, with 29 patients younger than 4 years. Twenty-three patients had mean pulmonary artery pressures higher than 15 mm Hg, elevated pulmonary arteriolar resistances (> 3 U.m2), or elevated end-diastolic ventricular pressure (> 12 mm Hg). Associated systemic or pulmonary venous anomalies were present in 22 patients (30%), and atrioventricular valve incompetence was present in 21 patients (29%).
The overall mortality rate was 9.7% (7/72). Variables with significant effects on postoperative mortality were associated systemic or pulmonary venous anomalies, atrioventricular valve incompetence, mean pulmonary artery pressure greater than 15 mm Hg, and prolonged cardiopulmonary bypass time. Postoperative morbidity resulted mainly from atrial arrhythmia (20%). Clinical signs of protein-losing enteropathy or atrial thrombi were rare (3% and 6%, respectively). Postoperative hemodynamic data from 48 surviving patients (74%) revealed a mean transpulmonary gradient of 6.3 mm Hg, systemic venous pressure greater than 12 mm Hg in only 10 patients, and cardiac index less than 3 L.min-1.m-2 in 18 patients.
In a high proportion of hearts with complex univentricular anatomy, associated anomalies, and borderline hemodynamics, the Fontan operation can be performed as a total cavopulmonary anastomosis with acceptable intermediate postoperative morbidity and hemodynamic results.
改良Fontan手术已被提议作为越来越多具有复杂单心室解剖结构心脏的最终姑息治疗方法。为消除不同手术策略的影响,本回顾性研究仅纳入接受全腔静脉肺动脉吻合术的患者。
72例患者接受手术时年龄在7至219个月之间,其中29例年龄小于4岁。23例患者平均肺动脉压高于15 mmHg,肺小动脉阻力升高(>3 U.m²),或舒张末期心室压力升高(>12 mmHg)。22例患者(30%)存在相关的体循环或肺静脉异常,21例患者(29%)存在房室瓣关闭不全。
总死亡率为9.7%(7/72)。对术后死亡率有显著影响的变量包括相关的体循环或肺静脉异常、房室瓣关闭不全、平均肺动脉压大于15 mmHg以及体外循环时间延长。术后并发症主要源于房性心律失常(20%)。蛋白丢失性肠病或心房血栓的临床体征罕见(分别为3%和6%)。48例存活患者(74%)的术后血流动力学数据显示,平均跨肺压差为6.3 mmHg,仅10例患者体循环静脉压大于12 mmHg,18例患者心脏指数小于3 L.min⁻¹.m⁻²。
在很大比例的具有复杂单心室解剖结构、相关异常和临界血流动力学的心脏中,Fontan手术可作为全腔静脉肺动脉吻合术进行,术后中期并发症和血流动力学结果可接受。