Contemporary Approach to Managing Young Symptomatic Infants With Tetralogy of Fallot in the United Kingdom.

Ines Hribernik, Stacey Boardman, David Crossland, Antony Hermuzi, Hannah Bellsham-Revell, Patrick Elnazir, Andrew Ho, Norah Yap, Demetris Taliotis, Jack Gibb, James R Bentham
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Abstract

ObjectivesWe set out to determine the characteristics and outcomes of symptomatic infants with tetralogy of Fallot who due to insufficient pulmonary blood flow required transcatheter or surgical intervention in early infancy.MethodsFive centers in the United Kingdom contributed data for infants born with tetralogy of Fallot who underwent an initial procedure between January 2015 and January 2022. The studied group were infants requiring palliative or reparative procedure at less than three months of age. The primary outcome was survival to one year; secondary outcomes were periprocedural complications, cumulative mechanical ventilation time, length of hospital stay, and need for reintervention.ResultsA total of 535 infants with tetralogy of Fallot were identified during the study period. 96 infants underwent initial palliation (58 right ventricular outflow tract stent, 7 ductal stent, 17 balloon pulmonary valvuloplasty, 9 modified Blalock-Taussig-Thomas shunt, and 5 right ventricular outflow tract patch augmentation). 37 infants underwent primary repair at less than three months of age, 402 infants had primary repair at 3 to 12 months of age. Median age and weight were 26 days and 3.1 kg for initial palliation; 68 days and 4.7 kg for primary repair under three months (P < .001). One year survival post-procedure was 95.7% for initial palliation, and 97.3% for primary repair under three months (P = .55, hazard ratio [HR] 1.97, 95% confidence interval [CI] 0.33-11.67). Five-year freedom from reintervention on the right ventricle-to-pulmonary artery segment was 76% after staged repair and 88% after primary repair under three months (P = .23, HR 1.90, 95% CI 0.75-4.80).ConclusionsInitial palliation with staged repair remains the predominantly employed approach for the highest risk young infants with tetralogy of Fallot in the United Kingdom. Survival outcomes are excellent; concerns remain regarding increased cumulative costs and associated reintervention rates. Primary repair under three months of age has also proven to be feasible with excellent results, although with individual candidate selection bias.

当代方法处理年幼婴儿法洛四联症在英国。
目的:研究有症状的法洛四联症患儿在婴儿期早期因肺血流不足需要经导管或手术治疗的特点和结局。方法英国的五个中心提供了2015年1月至2022年1月期间接受初始手术的法洛四联症婴儿的数据。研究组是需要姑息治疗或修复手术的婴儿,年龄小于3个月。主要结局是存活至1年;次要结局是围手术期并发症、累计机械通气时间、住院时间和再次干预的需要。结果本研究期间共检出法洛四联症患儿535例。96名婴儿接受了最初的姑息治疗(58例右心室流出道支架,7例导管支架,17例球囊肺动脉瓣成形术,9例改良Blalock-Taussig-Thomas分流术,5例右心室流出道贴片增强术)。37名婴儿在不到3个月大时进行了初级修复,402名婴儿在3至12个月大时进行了初级修复。初始缓解时的中位年龄和体重为26天,3.1 kg;68天,3个月内一次修复4.7公斤(P =。55,风险比[HR] 1.97, 95%可信区间[CI] 0.33 ~ 11.67)。在3个月内,分期修复后的5年再干预自由率为76%,初次修复后为88% (P =。23, hr 1.90, 95% ci 0.75-4.80)。结论:在英国,对于高风险的法洛四联症婴儿,初始姑息和分期修复仍然是主要的治疗方法。生存结果非常好;人们仍然担心累积成本的增加和相关的再干预率。3个月以下的初级修复也被证明是可行的,效果很好,尽管存在个体候选人选择偏差。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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