Reddy V M, McElhinney D B, Sagrado T, Parry A J, Teitel D F, Hanley F L
Division of Cardiothoracic Surgery, University of California-San Francisco, USA.
J Thorac Cardiovasc Surg. 1999 Feb;117(2):324-31. doi: 10.1016/S0022-5223(99)70430-7.
Published data suggest that low birth weight is a risk factor for poor outcome in corrective surgery for many cardiac defects. Congenital heart defects in low birth weight infants are typically managed with supportive therapy or palliative operations, with definitive repair delayed. The morbidity associated with such approaches is high.
Since 1990 complete repair of congenital heart defects (other than patent ductus arteriosus) has been performed in 102 infants no larger than 2500 g (median 2100 g, range 700-2500 g), including 16 no larger than 1500 g. Defects included ventricular septal defect (n = 22), tetralogy of Fallot complexes (n = 20), transposition complexes (n = 13), aortic coarctation (n = 12), interrupted arch (n = 10), truncus arteriosus (n = 8), atrioventricular septal defect (n = 6), total anomalous pulmonary venous return (n = 5), and other (n = 6).
Preoperative morbidity was more common among patients referred late for surgical correction. There were 10 early deaths (10%) attributable to cardiac failure (n = 4), arrhythmia (n = 1), multiorgan failure (n = 1), sepsis (n = 1), idiopathic coronary artery intimal necrosis (n = 1), foot gangrene (n = 1), and pulmonary hemorrhage (n = 1). No patient had postbypass intracerebral hemorrhage. At follow-up (median 36 months) there were 8 late deaths, and 8 patients underwent 10 reinterventions. There was no evidence of neurologic sequelae attributable to the operation.
In general, delaying repair of congenital heart defects in low birth weight infants does not confer a benefit and is associated with higher preoperative morbidity. Complete repair of both simple and complex lesions can be achieved in such cases with good results. Growth after repair approximates the normal curve for low birth weight infants without heart disease. It is recommended that such infants, especially when they have symptoms, undergo early surgical repair rather than prolonged medical management or other forms of palliation.
已发表的数据表明,低出生体重是许多心脏缺陷矫正手术预后不良的一个危险因素。低出生体重婴儿的先天性心脏缺陷通常采用支持性治疗或姑息性手术进行处理,确定性修复则推迟进行。此类方法相关的发病率很高。
自1990年以来,对102例体重不超过2500克(中位数2100克,范围700 - 2500克)的婴儿进行了先天性心脏缺陷(动脉导管未闭除外)的完全修复,其中包括16例体重不超过1500克的婴儿。缺陷包括室间隔缺损(n = 22)、法洛四联症复合体(n = 20)、大动脉转位复合体(n = 13)、主动脉缩窄(n = 12)、主动脉弓中断(n = 10)、动脉干(n = 8)、房室间隔缺损(n = 6)、完全性肺静脉异位引流(n = 5)以及其他(n = 6)。
术前发病率在手术矫正转诊较晚的患者中更为常见。有10例早期死亡(10%),原因包括心力衰竭(n = 4)、心律失常(n = 1)、多器官衰竭(n = 1)、败血症(n = 1)、特发性冠状动脉内膜坏死(n = 1)、足部坏疽(n = 1)以及肺出血(n = 1)。没有患者发生体外循环后脑出血。在随访(中位数36个月)时有8例晚期死亡,8例患者接受了10次再次干预。没有证据表明手术导致神经后遗症。
一般而言,推迟低出生体重婴儿先天性心脏缺陷的修复并无益处,且与较高的术前发病率相关。在这种情况下,简单和复杂病变均可实现完全修复,效果良好。修复后的生长接近无心脏病的低出生体重婴儿的正常曲线。建议此类婴儿,尤其是出现症状时,应尽早接受手术修复,而非长期药物治疗或其他形式的姑息治疗。