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先天性心脏病患儿行 Norwood 手术后的学龄期和青春期心力衰竭。

School age and adolescent heart failure following the Norwood procedure.

机构信息

Children's Healthcare of Atlanta and Department of Pediatrics, Division of Cardiology, Emory University, Atlanta, Georgia.

Emory University School of Medicine, Department of Pediatrics, Atlanta, Georgia.

出版信息

J Heart Lung Transplant. 2024 Mar;43(3):453-460. doi: 10.1016/j.healun.2023.10.012. Epub 2023 Oct 20.

Abstract

BACKGROUND

Heart failure results in significant morbidity and mortality for young children with hypoplastic left heart syndrome (HLHS) following the Norwood procedure. The trajectory in later childhood is not well described.

METHODS

We studied the outcome into adolescence of participants enrolled in the Single Ventricle Reconstruction trial who underwent the Fontan procedure or survived to 6 years without having undergone Fontan procedure. The primary outcome was heart failure events, defined as heart transplant listing or death attributable to heart failure. Symptomatic heart failure for participants surviving 10 or more years was also assessed utilizing the Pediatric Quality of Life Inventory (PedsQL).

RESULTS

Of the 345 participants who underwent a Fontan operation or survived to 6 years without Fontan, 25 (7.2%) had a heart failure event before the age of 12 years. Among these, 21 were listed for heart transplant, and 4 died from heart failure. Nineteen participants underwent heart transplant, all of whom survived to age 12 years. Factors associated with a heart failure event included longer Norwood hospital length of stay, aortic atresia, and no Fontan operation by age 6 years. Assessment of heart failure symptoms at 12 years of age revealed that 24 (12.2%) of 196 PedsQL respondents "often" or "almost always" had difficulty walking more than one block.

CONCLUSIONS

Heart failure events occur in over 5% of children with palliated HLHS between preschool age and adolescence. Outcomes for children listed for transplant are excellent. However, a substantial portion of palliated HLHS children have significant symptoms of heart failure at 12 years of age.

摘要

背景

左心发育不全综合征(HLHS)患儿在接受 Norwood 手术后,心力衰竭导致其发病率和死亡率显著增加。但对于他们在儿童后期的病程情况,目前尚缺乏详细的描述。

方法

我们研究了参加单心室重建试验的参与者在 Fontan 手术后的青少年结局,或在没有进行 Fontan 手术的情况下生存至 6 岁。主要结局是心力衰竭事件,定义为心脏移植名单或归因于心力衰竭的死亡。对于存活 10 年或以上的参与者,通过儿童生活质量量表(PedsQL)评估心力衰竭的症状。

结果

在 345 名接受 Fontan 手术或在 6 岁时未接受 Fontan 手术而存活的患者中,有 25 名(7.2%)在 12 岁之前发生心力衰竭事件。其中,21 人被列入心脏移植名单,4 人死于心力衰竭。19 名患者接受了心脏移植,他们都存活至 12 岁。与心力衰竭事件相关的因素包括 Norwood 住院时间较长、主动脉瓣闭锁和 6 岁时未进行 Fontan 手术。在 12 岁时评估心力衰竭症状时,发现 196 名 PedsQL 应答者中的 24 名(12.2%)“经常”或“几乎总是”在行走一个街区以上时感到困难。

结论

在学龄前到青春期之间,接受 HLHS 姑息治疗的儿童中,有超过 5%的儿童发生心力衰竭事件。接受移植名单的儿童的结局非常好。然而,相当一部分姑息治疗的 HLHS 儿童在 12 岁时存在严重的心力衰竭症状。

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