儿童心肺移植患者健康相关生活质量的未知领域:范围综述

Fabienne Dobbels MSc, PhD , Nathalie Duerinckx APN, PhD
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摘要

虽然儿童心脏移植(HTx)后生存率良好,儿童肺移植(LTx)后生存率稳步提高,但尚不清楚这是否也转化为令人满意的健康相关生活质量(HRQOL)。方法本综述总结了截至2025年1月23日在PubMed上发表的HTx或LTx后儿科患者总体HRQOL的研究结果。HTx和LTx的研究设计、人群特征、测量方法、HRQOL定义和结果分别制成表格并进行叙述。结果共有27篇论文24篇原创研究(定性研究3篇,定量研究21篇)报道了小儿HTx患者的HRQOL。大多数定量研究表明,他们的HRQOL总体上是良好的,无论是在童年时期还是成年时期,都与健康同龄人或患有其他慢性病的儿童相当。然而,这3项定性研究描绘了更多不同的经历,tx后的轨迹以起起落落为标志。仅有4篇论文关注儿科LTx患者的HRQOL。两项前瞻性研究显示,术后早期HRQOL较好,而两项定性研究也报告了更多的混合体验。然而,研究通常规模较小,没有定义HRQOL,使用多种测量方法,并显示出大量的排除率和拒绝率。结论:虽然大多数研究对儿科患者的HRQOL持乐观态度,但由于目前证据基础中存在方法学异质性和选择偏倚,这些研究结果应谨慎解读。本文综述了今后研究方法改进的几个方向,旨在加深我们对ALL儿童心胸移植患者HRQOL的认识。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Uncharted territories on pediatric heart and lung transplant patients’ health-related quality of life: A scoping review

Background

Although survival is good after pediatric heart transplantation (HTx) and steadily improving after pediatric lung transplantation (LTx), it remains unclear whether this also translates into a satisfactory health-related quality of life (HRQOL).

Methods

This scoping review summarizes the findings on pediatric patients’ overall HRQOL after HTx or LTx published in PubMed up to January 23, 2025. Data on study design, population characteristics, measurement methods, HRQOL definitions, and results are tabulated and described narratively for HTx and LTx separately.

Results

Twenty-seven papers covering 24 original studies (3 qualitative and 21 quantitative) report on pediatric HTx’ patients HRQOL. Most quantitative studies indicate that their HRQOL is generally good, both during childhood and into adulthood, and is comparable to that of healthy peers or children with other chronic conditions. However, the 3 qualitative studies portray more varied experiences, with the post-Tx trajectory being marked by ups and downs. Only 4 papers focus on pediatric LTx patients’ HRQOL. The 2 prospective studies show a favorable HRQOL early post-Tx, while the 2 qualitative studies also report more mixed experiences. Nevertheless, studies are generally small, do not define HRQOL, use diverse measures, and exhibit substantial exclusion and refusal rates.

Conclusions

While most studies present an optimistic view of pediatric patients’ HRQOL, these findings should be interpreted with caution due to the methodological heterogeneity and selection bias present within the current evidence base. This review offers several directions for methodological improvement in future research, aiming to deepen our understanding of HRQOL in ALL pediatric cardiothoracic transplant patients.
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