Choudhary S K, Bhan A, Sharma R, Mathur A, Airan B, Saxena A, Kothari S S, Juneja R, Venugopal P
Department of Cardiothoracic and Vascular Surgery, Cardiothoracic Center, All India Institute of Medical Sciences, New Delhi.
Ann Thorac Surg. 1999 Jul;68(1):155-9. doi: 10.1016/s0003-4975(99)00375-6.
Corrective surgery for total anomalous pulmonary venous connection in infancy still carries high morbidity and mortality rates in developing countries. The present study evaluates the factors responsible for it.
Seventy-three infants were operated on for total anomalous pulmonary venous connection from January 1987 through October 1997. Age ranged from 5 days to 12 months (mean, 3.9+/-0.24 months), with 10 (13.7%) patients younger than 1 month old. Patient weight varied from 2.0 to 5.2 kg (mean, 3.7+/-0.27 kg). Most (90.5%) patients were small for their ages (< 50th percentile). Anomalous connection was supracardiac in 42 (57.5%), cardiac in 18 (24.7%), infracardiac in 4 (5.5%), and mixed in 9 (12.3%) patients. Thirty-five patients had obstructed drainage. Preoperatively, 30 patients received antibiotic therapy for respiratory tract infection, 3 patients had balloon atrial septostomy, and 4 patients required mechanical ventilation. Fifteen patients (20.5%) were operated on as an emergency procedure. For supracardiac and infracardiac connections, a posterior approach was used for anastomosis. In cardiac type, coronary sinus was unroofed and the resultant defect along with atrial septal defect was closed with a single patch.
The operative mortality rate was 23.3% (17 of 73). Pulmonary hypertensive crisis was the cause of death in 10 patients. Emergency operation and weight less than the 25th percentile were the important risk factors for operative mortality. Young age (< 1 month) and type of drainage did not affect the mortality. Follow-up ranged from 1 to 108 months (mean, 56.4+/-26.0 months). There were two late deaths. The actuarial survival (Kaplan Meier) at 9 years was 72.87%+/-5.39%.
Failure of early recognition, and thus delayed referral, accounted for onset of cardiac cachexia, respiratory tract infection, and severe pulmonary hypertension, which had a major effect on unfavorable outcome.
在发展中国家,婴儿完全性肺静脉异位连接的矫正手术仍具有较高的发病率和死亡率。本研究评估了导致这种情况的因素。
1987年1月至1997年10月期间,对73例婴儿进行了完全性肺静脉异位连接手术。年龄范围为5天至12个月(平均3.9±0.24个月),其中10例(13.7%)患者年龄小于1个月。患者体重从2.0千克至5.2千克不等(平均3.7±0.27千克)。大多数(90.5%)患者低于其年龄的正常水平(<第50百分位数)。42例(57.5%)患者的异常连接为心上型,18例(24.7%)为心内型,4例(5.5%)为心下型,9例(12.3%)为混合型。35例患者存在引流梗阻。术前,30例患者因呼吸道感染接受了抗生素治疗,3例患者进行了球囊房间隔造口术,4例患者需要机械通气。15例患者(20.5%)作为急诊手术。对于心上型和心下型连接,采用后路进行吻合。在心内型中,切开冠状窦顶,用一块补片封闭由此产生的缺损和房间隔缺损。
手术死亡率为23.3%(73例中有17例)。10例患者死于肺动脉高压危象。急诊手术和体重低于第25百分位数是手术死亡的重要危险因素。年龄小(<1个月)和引流类型不影响死亡率。随访时间为1至108个月(平均56.4±26.0个月)。有2例晚期死亡。9年时的精算生存率(Kaplan Meier法)为72.87%±5.39%。
早期识别失败,进而导致转诊延迟,引发了心源性恶病质、呼吸道感染和严重肺动脉高压,对不良结局产生了重大影响。