Department of Cardiothoracic Surgery, Erasmus Medical Center, Rotterdam, The Netherlands; Department of Cardiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Department of Cardiology, Erasmus Medical Center, Rotterdam, The Netherlands.
Semin Thorac Cardiovasc Surg. 2019 Autumn;31(3):496-504. doi: 10.1053/j.semtcvs.2018.10.015. Epub 2018 Nov 2.
Only few studies have reported long-term outcome of the transatrial-transpulmonary approach in the current era of management of tetralogy of Fallot (ToF). We investigated 15-year outcome of correction via a transatrial-transpulmonary approach in a large cohort of successive patients operated in the 21st century. All infant ToF patients undergoing transatrial-transpulmonary ToF correction between 2000 and 2015 were included (N = 177, 106 male, median follow-up 7.1 (interquartile range 3.0-10.9) years. Data regarding postoperative complications, reinterventions, development of atrial and ventricular arrhythmia, cardiac function, and survival were evaluated. Prior shunting was performed in 10 patients (6%). The transatrial-transpulmonary approach resulted in valve-sparing surgery in 57 patients (32%). Postoperative surgical complications included junctional ectopic tachycardia (N = 12, 7%), pericardial (N = 10, 6%) or pleural effusion (N = 7, 3%), chylothorax (N = 7, 4%), bleeding requiring reoperation (N = 4, 3%), and superficial wound infection (N = 1). Fifty-one patients underwent 68 reinterventions, mainly due to pulmonary restenosis (PS) (N = 57). ToF correction at age <2 months and double outlet or double-chambered right ventricle variants of the ToF spectrum were independent predictors for reintervention. Patients undergoing valve-sparing ToF correction had a significant longer PR-free survival than those with a transannular patch (8.5 [95% confidence interval 6.8-10.3] years vs 1.1 [95% confidence interval 0.8-1.5] years; P < 0.001). Overall mortality was 2.8%; mortality rates were higher in premature/dysmature newborns (0.7% vs 9.5%; P < 0.001). Although the 15-year outcome of the transatrial-transpulmonary approach in terms of postoperative complications and mortality rates is excellent, the high incidence of moderate and severe PR is worrisome. Valve-sparing surgery was associated with a substantially lower incidence of PR, yet was surgically not possible in the majority of patients.
仅有少数研究报道了在法洛四联症(TOF)的现代管理时代经房间隔-肺动脉途径治疗的长期结果。我们调查了 21 世纪连续接受经房间隔-肺动脉 TOF 矫正术的大量患者的 15 年结果。纳入 2000 年至 2015 年间接受经房间隔-肺动脉 TOF 矫正术的所有婴儿 TOF 患者(N=177,男 106 例,中位随访 7.1(四分位间距 3.0-10.9)年)。评估了术后并发症、再次干预、房性和室性心律失常、心功能和生存率等数据。10 例(6%)患者术前存在分流。经房间隔-肺动脉途径实现了瓣膜保留手术 57 例(32%)。术后手术并发症包括交界性异位心动过速(N=12,7%)、心包(N=10,6%)或胸腔积液(N=7,3%)、乳糜胸(N=7,4%)、需要再次手术的出血(N=4,3%)和浅表伤口感染(N=1)。51 例患者进行了 68 次再次干预,主要是由于肺动脉瓣狭窄(PS)(N=57)。TOF 矫正年龄<2 个月和 TOF 谱中的双出口或双心室右心室变异是再次干预的独立预测因素。接受瓣膜保留 TOF 矫正的患者的无 PR 生存时间显著长于接受环形补片的患者(8.5[95%置信区间 6.8-10.3]年 vs 1.1[95%置信区间 0.8-1.5]年;P<0.001)。总体死亡率为 2.8%;早产儿/不成熟儿的死亡率较高(0.7% vs 9.5%;P<0.001)。尽管经房间隔-肺动脉途径的 15 年术后并发症和死亡率结果良好,但中度和重度 PR 的高发生率令人担忧。瓣膜保留手术与 PR 发生率显著降低相关,但大多数患者无法进行手术。