Department of Pediatric Cardiology/Congenital Cardiology, Heidelberg University Medical Center, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.
Cardiovascular Surgery Department, Heidelberg University Medical Center, Heidelberg, Germany.
J Cardiothorac Surg. 2023 Feb 7;18(1):65. doi: 10.1186/s13019-023-02162-z.
Hybrid procedure with ductal stenting and bilateral pulmonary banding offers a temporary approach in high-risk neonates with complex congenital heart defects aiming biventricular repair. This procedure may also have negative impact concerning post-banding pulmonary stenosis resulting in right ventricular pressure load.
Between 2010 and 2021 we identified 5 patients with interrupted aortic arch and complex congenital heart defect who underwent hybrid procedure and staged biventricular repair ("hybrid-group"). Other 7 cases with interrupted aortic arch were corrected in the neonatal phase without hybrid procedure ("nonhybrid-group"). Detailed intra- and extracardiac features and surgical procedures were documented as well as pulmonary interventions during follow up. Pulmonary vessel size was assessed by diameter of left and right pulmonary artery in absolute and indexed values. RV pressure was evaluated invasively via catheterization.
Survival in cases with hybrid procedure and staged biventricular repair was 91% for a follow-up time of 40.7 months (95% CI 26-55 months) and 100% in the non-hybrid-group. Postoperative results concerning left ventricular function showed normal LV dimensions and systolic function without relevant stenosis on distal aortic arch. Hybrid procedure was associated with impaired local pulmonary arterial diameter after debanding resulting in increased right ventricular pressure and need for interventions (number intervention per patient: hybrid group 1.7 ± 0.95, non-hybrid group 0.17 ± 0.41; P 0.003).
Hybrid procedure in high-risk cases with interrupted aortic arch and staged biventricular repair shows good postoperative results with low perioperative mortality and normal left ventricular function. Due to potential risk of relevant pulmonary stenosis and right ventricular pressure load, follow up examinations must not only focus on left but also on the right heart.
对于患有复杂先天性心脏缺陷且风险较高的新生儿,采用带支架的导管和双侧肺带扎术的杂交手术提供了一种临时的双心室修复方法。但是,该手术可能会对带扎术后的肺动脉瓣狭窄产生负面影响,导致右心室压力负荷增加。
我们在 2010 年至 2021 年间共识别出 5 例患有主动脉弓中断和复杂先天性心脏缺陷的患者,他们接受了杂交手术和分期双心室修复(“杂交组”)。另有 7 例主动脉弓中断患者在新生儿期接受了无杂交手术的矫正(“非杂交组”)。我们详细记录了患者的心脏内外特征和手术过程以及随访期间的肺介入治疗。通过左、右肺动脉的直径及其绝对值和指数值来评估肺血管大小。通过心导管术评估右心室压力。
接受杂交手术和分期双心室修复的患者,其生存率为 91%,随访时间为 40.7 个月(95%可信区间 26-55 个月);非杂交组的生存率为 100%。术后左心室功能结果显示,远端主动脉弓无明显狭窄,左心室尺寸和收缩功能正常。带扎去除后,局部肺动脉直径减小,导致右心室压力增加和需要介入治疗(每位患者的介入次数:杂交组 1.7±0.95,非杂交组 0.17±0.41;P=0.003)。
对于患有主动脉弓中断和分期双心室修复高危病例,杂交手术具有良好的术后效果,围手术期死亡率低,左心室功能正常。由于存在相关肺动脉瓣狭窄和右心室压力负荷的潜在风险,随访检查不仅要关注左心,还要关注右心。