Tláskal T, Hucín B, Hruda J, Marek J, Chaloupecký V, Kostelka M, Janousek J, Skovránek J
Kardiocentrum, University Hospital Motol, Prague, Czech Republic. tomas tlaskal@1f motol.cuni.cz
Eur J Cardiothorac Surg. 1998 Sep;14(3):235-42. doi: 10.1016/s1010-7940(98)00184-5.
Early results of primary and two-stage repair of interrupted aortic arch have improved. Experience with different surgical approaches should be analysed and compared.
Forty neonates and infants with interrupted aortic arch underwent primary repair (19 patients) or palliative operation (21 patients). Twenty (50%) patients were followed-up for 5.1+/-4.3 years. All patients were regularly examined with the aim of determining clinical development, presence of residual lesions or complications and need for re-intervention. Aortic arch and the left ventricular outflow tract growth were assessed by echocardiographic examination. Data from hospital and outpatient department records were analysed.
The early mortality was 61.9% after palliative operations and 36.8% after the primary repair. Presence of complications (P < 0.001), earlier year of surgery (P < 0.01), bad clinical condition and acidosis (P < 0.05) represented statistically significant risk factors for death in the whole series. In seven (87.5%) out of eight early survivors, after the initial palliative operation, closure of ventricular septal defect and debanding were done, and in three (37.5%) patients, re-operation for aortic arch obstruction was also required. Out of 12 patients, after the primary repair, one required early re-operation for persistent left ventricular outflow tract obstruction and two needed late re-intervention for left bronchus obstruction. In three (25%) patients, after the primary repair, left ventricular outflow tract obstruction with a maximal systolic pressure gradient higher than 30 mmHg developed. At present, all 20 early survivors are alive. Five patients, after palliative operation, are in NYHA class 1, but in three patients, who are in class III or IV, the outcome is influenced by severe complications. All patients after the primary repair are in class I or II.
Our experience confirmed better results after the primary repair of interrupted aortic arch, which was associated with lower mortality, prevalence of severe complications and need for re-intervention. Higher prevalence of subaortic stenosis after primary repair could be explained by patient selection early in our experience. We recommend the primary repair of interrupted aortic arch and associated heart lesions in neonates, however, in unfavourable conditions an individualised surgical approach with initial palliative surgery should be considered.
主动脉弓中断一期修复和两期修复的早期结果已有所改善。应对不同手术方法的经验进行分析和比较。
40例主动脉弓中断的新生儿和婴儿接受了一期修复(19例)或姑息性手术(21例)。20例(50%)患者接受了5.1±4.3年的随访。对所有患者进行定期检查,目的是确定临床发育情况、是否存在残余病变或并发症以及再次干预的必要性。通过超声心动图检查评估主动脉弓和左心室流出道的生长情况。对医院和门诊记录的数据进行分析。
姑息性手术后早期死亡率为61.9%,一期修复后为36.8%。并发症的存在(P<0.001)、手术年份较早(P<0.01)、临床状况不佳和酸中毒(P<0.05)是整个系列中具有统计学意义的死亡危险因素。在8例早期幸存者中的7例(87.5%),在最初的姑息性手术后,进行了室间隔缺损修补和解除束带术,3例(37.5%)患者还需要再次手术治疗主动脉弓梗阻。在12例一期修复后的患者中,1例因持续性左心室流出道梗阻需要早期再次手术,2例因左支气管梗阻需要后期再次干预。在3例(25%)一期修复后的患者中,出现了最大收缩压梯度高于30 mmHg的左心室流出道梗阻。目前,所有20例早期幸存者均存活。5例接受姑息性手术的患者心功能分级为Ⅰ级,但3例心功能分级为Ⅲ级或Ⅳ级的患者,其预后受严重并发症影响。所有一期修复后的患者心功能分级为Ⅰ级或Ⅱ级。
我们的经验证实,主动脉弓中断一期修复后的结果更好,这与较低的死亡率、严重并发症的发生率和再次干预的必要性相关。一期修复后主动脉瓣下狭窄发生率较高可通过我们早期经验中的患者选择来解释。我们建议对新生儿主动脉弓中断及相关心脏病变进行一期修复,然而,在不利情况下,应考虑采用个体化手术方法,首先进行姑息性手术。