Bové Thierry, François Katrien, De Groote Katya, Suys Bert, De Wolf Daniel, Verhaaren Hendrik, Matthys Dirk, Moerman Annelies, Poelaert Jan, Vanhaesebroeck Piet, Van Nooten Guido
Department of Cardiac Surgery, University Hospital of Gent, Ghent, Belgium.
Ann Thorac Surg. 2004 Jul;78(1):181-7. doi: 10.1016/j.athoracsur.2003.12.066.
From June 1995 to January 2003, 49 consecutive neonates of less than 2,500 g underwent early surgery for congenital heart disease. A retrospective analysis was performed to evaluate the early to medium term outcome.
Major cardiac surgery for congenital heart defects included a complete correction in 31 patients (group I) and a palliative procedure in 18 patients (group II). Mean age at operation was 15.2 days (1 day-90 days) and mean weight was 2,190 g (1,300 g-2,500 g). Twenty-four children (49%) were born prematurely. All neonates were critically ill and 47% were already ventilated preoperatively. Heart defects included mainly ventricular septal defect (10), tetralogy of Fallot complexes (8), aortic coarctation (8), transposition complexes (7), single ventricle anomalies (4), pulmonary atresia with intact septum (4), interrupted aortic arch (3), totally anomalous pulmonary venous return (3), and common atrioventricular septal defect (2).
Overall surgical mortality was 18%: 4 neonates died after definitive repair and 5 after palliation; representing, respectively, 13% and 28% of each group. Postoperative morbidity occurred in half of the patients (53%). Age, weight, prematurity, type of first surgical procedure, and use of cardiopulmonary bypass did not influence the early outcome. After a mean follow-up of 2.82 years (2 months to 6 years), survival was 87% in the correction group and 54% in the palliation group. All children were in NYHA class I-II. Freedom from reintervention at 18 months was 68% after correction versus 8% after palliation.
Cardiac surgery for congenital malformations in critically ill, low weight neonates can be achieved with acceptable mortality, at the cost of an increased morbidity. Early outcome seems independent of age, weight, prematurity, use of extracorporeal perfusion, and type of first intervention. Moreover, primary correction appears to result in an early survival benefit, remaining constant over time.
1995年6月至2003年1月,49例连续出生、体重不足2500克的新生儿接受了先天性心脏病早期手术。进行回顾性分析以评估早期至中期的结果。
先天性心脏缺陷的主要心脏手术包括31例患者的完全矫正(I组)和18例患者的姑息性手术(II组)。手术平均年龄为15.2天(1天至90天),平均体重为2190克(1300克至2500克)。24名儿童(49%)为早产儿。所有新生儿病情危重,47%术前已接受通气治疗。心脏缺陷主要包括室间隔缺损(10例)、法洛四联症(8例)、主动脉缩窄(8例)、大动脉转位(7例)、单心室畸形(4例)、室间隔完整的肺动脉闭锁(4例)、主动脉弓中断(3例)、完全性肺静脉异位引流(3例)和共同房室间隔缺损(2例)。
总体手术死亡率为18%:4例新生儿在确定性修复后死亡,5例在姑息治疗后死亡;分别占每组的13%和28%。半数患者(53%)发生术后并发症。年龄、体重、早产、首次手术类型和体外循环的使用均未影响早期结果。平均随访2.82年(2个月至6年)后,矫正组生存率为87%,姑息治疗组为54%。所有儿童均为纽约心脏协会I-II级。矫正后18个月无需再次干预的比例为68%,而姑息治疗后为8%。
对于病情危重、体重低的新生儿,先天性畸形的心脏手术可以实现,死亡率可接受,但代价是发病率增加。早期结果似乎与年龄、体重、早产、体外循环的使用以及首次干预的类型无关。此外,一期矫正似乎能带来早期生存益处,并随时间保持不变。