Bhaskar Jayapadman, Galati John C, Brooks Paul, Oppido Guido, Konstantinov Igor E, Brizard Christian P, d'Udekem Yves
Department of Cardiac Surgery, Royal Children's Hospital, Melbourne, Australia.
The Clinical Epidemiology and Biostatistics Unit, Murdoch Children's Research Institute, Melbourne, Australia; Department of Mathematics and Statistics, La Trobe University, Melbourne, Australia.
J Thorac Cardiovasc Surg. 2015 Jun;149(6):1509-13. doi: 10.1016/j.jtcvs.2015.01.038. Epub 2015 Jan 24.
To identify determinants of adverse outcomes in patients with atrial isomerism.
Determinants of survival were analyzed for the group as a whole as well as separately for left and right atrial isomerism.
There were 78 cases with right and 104 with left atrial isomerism. Nineteen patients were not offered surgery; 49 (47%) of those with left atrial isomerism and 60 (77%) with right atrial isomerism were directed to single ventricle palliation. A total of 67 patients died. Survival to 25 years was 62% (95% confidence interval [CI], 53%-69%). Independent predictors of mortality were obstructed total anomalous pulmonary venous drainage (P < .001; hazard ratio [HR], 5.2; 95% CI, 2.7-9.7) and asplenia (P = .008; HR, 2; 95% CI, 1.2-3.3). There was no evidence that patients born in the recent era had improved survival (P = .47; HR, 1.1; 95% CI, 0.8-1.5). Survival was better for patients with left than right atrial isomerism: 18 years survival 74% (95% CI, 63%-82%) versus 50% (95% CI, 38%-60%). Independent predictors of mortality for patients with left atrial isomerism were dextrocardia (P = .009; HR, 3.0; 95% CI, 1.3-6.7) and pulmonary stenosis (P = .042; HR, 0.3; 95% CI, 0.1-0.9) and patients with right atrial isomerism, biventricular repair (P < .001; HR, 6.0; 95% CI, 2.8-13), and obstructed total anomalous pulmonary venous drainage (P < .001; HR, 4.2; 95% CI, 2.0-8.6).
A significant proportion of patients with isomerism still die before reaching adulthood. Only a fraction of those with obstructed pulmonary veins survive. Having biventricular repair does not confer a survival advantage to those born with right atrial isomerism.
确定心房异构患者不良结局的决定因素。
对整个队列以及分别对左、右心房异构患者的生存决定因素进行分析。
有78例右心房异构患者和104例左心房异构患者。19例患者未接受手术;左心房异构患者中有49例(47%)、右心房异构患者中有60例(77%)接受了单心室姑息治疗。共有67例患者死亡。25年生存率为62%(95%置信区间[CI],53%-69%)。死亡的独立预测因素为完全性肺静脉异位引流梗阻(P <.001;风险比[HR],5.2;95% CI,2.7-9.7)和无脾(P =.008;HR,2;95% CI,1.2-3.3)。没有证据表明近期出生的患者生存率有所提高(P =.47;HR,1.1;95% CI,0.8-1.5)。左心房异构患者的生存率高于右心房异构患者:18年生存率分别为74%(95% CI,63%-82%)和50%(95% CI,38%-60%)。左心房异构患者死亡的独立预测因素为右位心(P =.009;HR,3.0;95% CI,1.3-6.7)和肺动脉狭窄(P =.042;HR,0.3;95% CI,0.1-0.9),右心房异构患者死亡的独立预测因素为双心室修复(P <.ooo1;HR,6.0;95% CI,2.8-13)和完全性肺静脉异位引流梗阻(P <.001;HR,4.2;95% CI,2.0-8.6)。
相当一部分异构患者在成年前仍会死亡。只有一小部分肺静脉梗阻患者能存活。双心室修复并不能给右心房异构患者带来生存优势。