Kanter K R, Vincent R N, Raviele A A
Division of Cardio-Thoracic Surgery, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Ann Thorac Surg. 1999 Sep;68(3):969-74; discussion 974-5. doi: 10.1016/s0003-4975(99)00782-1.
Children with chronic cyanotic heart disease often develop systemic-to-pulmonary collateral arteries that can be deleterious at the time of a Fontan procedure due to excessive pulmonary blood flow. We therefore occlude all significant collaterals during cardiac catheterization.
From June 1993 to May 1998, 93 children aged 1.5 to 15.8 years (median 2.5 years) underwent a fenestrated lateral tunnel Fontan procedure. Eighty-nine (96%) had a previous bidirectional Glenn anastomosis, including 31 (33%) with a Norwood procedure.
Preoperatively, 33 children (35%) required occlusion of 1 to 11 (mean 3.6) collateral vessels. Two of the three perioperative deaths (operative survival 97%) were due to excessive pulmonary blood flow from unrecognized collaterals in one and uncontrollable collaterals in the other. Postoperatively, 19 children (20%) required coil occlusion of 1 to 21 (mean 5.6) collaterals for elevated pulmonary artery pressures, heart failure, or prolonged chest tube drainage. Duration of inotropic support, postoperative ventilation, intensive care unit stay, and postoperative hospitalization were all significantly longer in the patients who had postoperative occlusion of collaterals. On follow-up of 2 to 67 months (mean 35 months), there have been four late deaths (two infections, two heart failures); 6 patients underwent successful cardiac transplantation for refractory heart failure. All 8 patients with ventricular failure required occlusion of significant collaterals postoperatively.
Hemodynamically significant collaterals are not uncommon in Fontan candidates, and aggressive control can result in good operative and medium-term survival. After the Fontan, significant collaterals may be a marker for eventual cardiac failure because 8 of 18 patients requiring postoperative coils went on to transplantation or died of heart failure.
患有慢性紫绀型心脏病的儿童常出现体肺侧支动脉,在实施Fontan手术时,由于肺血流量过多,这些侧支动脉可能有害。因此,我们在心脏导管插入术期间封堵所有重要的侧支动脉。
1993年6月至1998年5月,93名年龄在1.5至15.8岁(中位数2.5岁)的儿童接受了开窗侧隧道Fontan手术。89名(96%)患儿此前接受过双向格林吻合术,其中31名(33%)还接受过诺伍德手术。
术前,33名儿童(35%)需要封堵1至11支(平均3.6支)侧支血管。围手术期死亡的3名患儿中有2名(手术存活率97%),1名死于未识别出的侧支动脉导致的肺血流量过多,另1名死于难以控制的侧支动脉。术后,19名儿童(20%)因肺动脉压力升高、心力衰竭或胸腔引流管引流时间延长,需要用弹簧圈封堵1至21支(平均5.6支)侧支血管。接受术后侧支血管封堵的患者,其使用正性肌力药物支持的时间、术后通气时间、重症监护病房停留时间和术后住院时间均显著延长。在2至67个月(平均35个月)的随访中,有4例晚期死亡(2例感染,2例心力衰竭);6例患者因难治性心力衰竭接受了成功的心脏移植。所有8例心力衰竭患者术后均需要封堵重要的侧支动脉。
在Fontan手术候选患儿中,具有血流动力学意义的侧支动脉并不少见,积极控制可带来良好的手术效果和中期生存率。Fontan手术后,重要的侧支动脉可能是最终发生心力衰竭的一个标志,因为18例术后需要使用弹簧圈的患者中有8例最终接受了心脏移植或死于心力衰竭。