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法洛四联症分期修复的中期结果

Intermediate Outcomes of Staged Tetralogy of Fallot Repair.

作者信息

Mahajan Poonam, Ebenroth Eric S, Borsheim Kirsten, Husain Sabena, Bo Na, Herrmann Jeremy L, Rodefeld Mark D, Turrentine Mark W, Brown John W, Patel Jyoti K

机构信息

Division of Cardiology, Department of Pediatrics, Riley Hospital for Children at Indiana University Health, Indianapolis, IN, USA.

Department of Pediatrics, Riley Hospital for Children at Indiana University Health, Indianapolis, IN, USA.

出版信息

World J Pediatr Congenit Heart Surg. 2019 Nov;10(6):694-701. doi: 10.1177/2150135119874035.

Abstract

BACKGROUND

The optimal surgical strategy for tetralogy of Fallot (TOF) repair in neonates and young infants requiring early surgical intervention remains controversial. Our surgical center follows the uniform strategy of a staged approach with initial systemic-to-pulmonary artery shunt the majority of time when early surgical intervention is required. We characterized a contemporary cohort of patients with TOF with pulmonary stenosis (PS) undergoing staged repair in order to determine the rate of pulmonary valve-sparing repair (PVSR), growth of the pulmonary valve annulus and pulmonary arteries, postoperative morbidity and mortality, and need for reintervention.

METHODS

We retrospectively studied patients with TOF/PS who underwent staged repair from 2000 to 2017. Surgical details, postoperative course, and reinterventions were noted. Echocardiographic measurements and Z-score values of pulmonary valve annulus, main pulmonary artery (MPA), right pulmonary artery (RPA), and left pulmonary artery (LPA) diameters were evaluated.

RESULTS

Of the 59 patients with staged TOF/PS, PVSR was performed in 25 (42%). There was a 5% incidence of postoperative arrhythmia. The Z-scores of MPA, RPA, and LPA were significantly higher before complete repair when compared to before palliative shunt. The 5 and 10-year survival rates were both 93%, and the probability of freedom from reoperation at 5 and 10 years was 87% and 82%, respectively.

CONCLUSIONS

Staged repair of TOF in young symptomatic infants results in 42% receiving PVSR, pulmonary artery growth, low incidence of postoperative arrhythmia, and relatively low rate of reoperations.

摘要

背景

对于需要早期手术干预的新生儿和小婴儿法洛四联症(TOF)修复的最佳手术策略仍存在争议。我们的手术中心遵循统一的分期方法策略,在大多数需要早期手术干预的情况下,首先进行体肺分流术。我们对一组当代患有肺动脉狭窄(PS)的TOF患者进行分期修复的情况进行了特征分析,以确定保留肺动脉瓣修复(PVSR)的比例、肺动脉瓣环和肺动脉的生长情况、术后发病率和死亡率以及再次干预的必要性。

方法

我们回顾性研究了2000年至2017年期间接受分期修复的TOF/PS患者。记录手术细节、术后病程和再次干预情况。评估肺动脉瓣环、主肺动脉(MPA)、右肺动脉(RPA)和左肺动脉(LPA)直径的超声心动图测量值和Z评分值。

结果

在59例分期TOF/PS患者中,25例(42%)进行了PVSR。术后心律失常的发生率为5%。与姑息性分流术前相比,完全修复前MPA、RPA和LPA的Z评分显著更高。5年和10年生存率均为93%,5年和10年免于再次手术的概率分别为87%和82%。

结论

对有症状的小婴儿进行TOF分期修复,42%的患者接受了PVSR,肺动脉生长,术后心律失常发生率低,再次手术率相对较低。

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