Cheung Y F, Cheng V Y, Chau A K, Chiu C S, Yung T C, Leung M P
Division of Paediatric Cardiology, Department of Paediatrics, Grantham Hospital, The University of Hong Kong, Hong Kong, People's Republic of China.
Heart. 2002 Feb;87(2):146-52. doi: 10.1136/heart.87.2.146.
To compare the outcome of infants and children who have right atrial isomerism and normal pulmonary venous drainage with those who have anomalous drainage, and to determine factors associated with poor outcome.
Retrospective review of management and outcome of 116 infants and children determined to have right atrial isomerism between January 1980 and December 2000.
Tertiary paediatric cardiac centre.
The 116 patients presented at a median of one day (range 1 day to 3.7 years) with cyanosis in the majority (96%). No interventions were planned in 31 (27%) patients, all of whom died. The early surgical mortality for pulmonary venous repair was 25% (2 of 8), Fontan procedure 26% (5 of 19), cavopulmonary shunting 7.7% (1 of 13), and systemic pulmonary arterial shunt insertion 1.9% (1 of 53). Late mortality was related to infection (n = 10), sudden death of unknown aetiology (n = 7, 5 with history of arrhythmia), and documented arrhythmia (n = 1). Patients with obstructed anomalous pulmonary venous drainage had the worst survival (p < 0.001). The mean (SEM) survival estimates for those with normal pulmonary venous drainage at 1, 5, 10, and 15 years was 81 (5.3)%, 67 (6.6)%, 60 (7.8)%, and 43 (12)%, respectively, similar to those for patients with non-obstructed anomalous drainage (p = 0.06). Independent risk factors for mortality included pulmonary venous obstruction (relative risk 3.8, p = 0.001) and a single ventricle (relative risk 2.9, p = 0.016). An analysis of only patients with normal pulmonary venous drainage identified no risk factors for mortality.
The long term outcome of infants and children with right atrial isomerism in association with a normal pulmonary venous drainage remains unfavourable. Sepsis and sudden death that may potentially be related to cardiac arrhythmia are major causes of late mortality.
比较右心房异构且肺静脉引流正常的婴幼儿与肺静脉引流异常的婴幼儿的治疗结果,并确定与不良预后相关的因素。
回顾性分析1980年1月至2000年12月期间确诊为右心房异构的116例婴幼儿的治疗及预后情况。
三级儿科心脏中心。
116例患者就诊时的中位年龄为1天(范围1天至3.7岁),大多数患者(96%)有发绀症状。31例(27%)患者未计划进行干预,均死亡。肺静脉修复的早期手术死亡率为25%(8例中的2例),Fontan手术为26%(19例中的5例),腔肺分流术为7.7%(13例中的1例),体肺分流术为1.9%(53例中的1例)。晚期死亡率与感染有关(n = 1),不明病因的猝死(n = 7,其中5例有心律失常病史),以及记录在案的心律失常(n = 1)。肺静脉引流梗阻的患者生存率最差(p < 0.001)。肺静脉引流正常的患者在1年、5年、10年和15年的平均(标准误)生存率估计分别为81(5.3)%、67(6.6)%、60(7.8)%和43(12)%,与肺静脉引流无梗阻的患者相似(p = 0.06)。死亡的独立危险因素包括肺静脉梗阻(相对风险3.8,p = )和单心室(相对风险2.9,p = 0.016)。仅对肺静脉引流正常的患者进行分析,未发现死亡的危险因素。
右心房异构且肺静脉引流正常的婴幼儿的长期预后仍然不佳。脓毒症和可能与心律失常有关的猝死是晚期死亡的主要原因。 0.001