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与诺伍德一期姑息手术相比,接受混合一期姑息手术治疗左心发育不全综合征患者的早期神经发育结局。

Early Neurodevelopmental Outcomes in Patients Who Undergo Hybrid Stage I Palliation Compared to Norwood Stage I Palliation for Hypoplastic Left Heart Syndrome.

作者信息

Thomas Courtney, Uzark Karen, Yu Sunkyung, Zampi Jeffrey D, Trucco Sara M, Sood Erica, Goldberg Caren

机构信息

Division of Pediatric Cardiology, Children's Mercy Hospital, Kansas City, MO, 64108, USA.

Division of Pediatric Cardiology, C.S. Mott Children's Hospital, Ann Arbor, MI, 48109, USA.

出版信息

Pediatr Cardiol. 2025 Jun 6. doi: 10.1007/s00246-025-03911-8.

Abstract

Children with congenital heart disease are at increased risk of neurodevelopmental impairment and those with hypoplastic left heart syndrome (HLHS) are among the highest risk group. The first stage of palliation for HLHS, typically performed in the newborn period, is either a Norwood stage I procedure (NS1P) or hybrid stage 1 procedure (HS1P). Our study sought to evaluate the neurodevelopmental outcomes of patients who undergo HS1P compared to NS1P using multicenter registry data. The National Pediatric Cardiology Quality Improvement Collaborative (NPC-QIC) registry was used to identify infants who had either NS1P or HS1P and completed the Ages and Stages Questionnaires-3 (ASQ-3) at age 6 months. Patient and clinical characteristics and ASQ-3 results were compared between HS1P and NS1P groups. A 6-month ASQ-3 was completed in 459 patients, 42 patients following HS1P and 417 following NS1P. Patients who underwent HS1P were more likely to have a birth weight less than 2.5 kg (14.6% vs. 4.2%, p = 0.01) and have a genetic or chromosomal anomaly (19% vs. 8.2%, p = 0.04). Gross motor skills were the most impaired of the measured domains for the entire cohort. There were no significant differences in impairment in any ASQ-3 domain between the groups, even when the analysis was adjusted for pre-operative mechanical ventilation, non-cardiac anomaly, and center. Despite patients who undergo HS1P representing a heterogenous group with other medical comorbidities, their early neurodevelopmental outcomes were comparable to patients who underwent NS1P.

摘要

患有先天性心脏病的儿童神经发育受损风险增加,而患有左心发育不全综合征(HLHS)的儿童属于风险最高的群体。HLHS的第一阶段姑息治疗通常在新生儿期进行,即诺伍德I期手术(NS1P)或混合I期手术(HS1P)。我们的研究旨在使用多中心登记数据评估接受HS1P与NS1P治疗的患者的神经发育结局。国家儿科心脏病学质量改进协作组(NPC-QIC)登记处用于识别接受NS1P或HS1P治疗并在6个月大时完成《年龄与发育阶段问卷-3》(ASQ-3)的婴儿。比较了HS1P组和NS1P组的患者及临床特征和ASQ-3结果。459例患者完成了6个月的ASQ-3评估,其中42例接受HS1P治疗,417例接受NS1P治疗。接受HS1P治疗的患者出生体重低于2.5kg的可能性更高(14.6%对4.2%,p=0.01),且有遗传或染色体异常的可能性更高(19%对8.2%,p=0.04)。在整个队列中,大运动技能是所测量领域中受损最严重的。两组在任何ASQ-3领域的受损情况均无显著差异,即使在对术前机械通气、非心脏异常和中心进行分析调整后也是如此。尽管接受HS1P治疗的患者群体存在异质性且伴有其他合并症,但其早期神经发育结局与接受NS1P治疗的患者相当。

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