气管麻痹大动脉切除术后与健康相关的生活质量:一项横断面研究。

0 CARDIAC & CARDIOVASCULAR SYSTEMS Interdisciplinary cardiovascular and thoracic surgery Pub Date : 2024-07-03 DOI:10.1093/icvts/ivae121
Bethany L Brockbank, Greg S J Dewar, Richard J Hewitt, Colin R Butler, Jo Wray
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引用次数: 0

摘要

目的目的:测量儿童在接受主动脉瓣成形术治疗全因气管异位症后的健康相关生活质量(HRQoL):方法:年龄≥5 岁的儿童及其父母:共收到 35 位家长(65%)和 10 位儿童(38%)填写的调查问卷。主动脉成形术时的中位年龄为 9.8 个月(1 个月-12.7 岁),随访的中位年数为 2.6 年(4 个月-6.9 年)。填写问卷的儿童中位年龄为 8.4(5.7-13.4)岁。家长和儿童报告的 PedsQL 总分分别为 69.61 分(标准差:19.74)和 63.15 分(标准差:20.40)。半数家长和 80% 的儿童报告的得分表明他们的 HRQoL 状况不佳。家长报告的总分、身体得分和心理社会得分均低于健康儿童和患有急性疾病的儿童,但与患有慢性疾病和心血管疾病的儿童相当。同样,儿童自己报告的总分与患有慢性疾病的儿童相当,但主动脉瓣成形术组儿童报告的社会心理分数低于任何其他组别。儿童生活质量量化评分与不良症状的原因、年龄或主动脉瓣成形术后的时间之间没有关联。复杂先天性合并症的存在对评分有显著影响(p 结论):主动脉瓣成形术后,儿童的 HRQoL 仍有可能较差,尤其是那些患有复杂合并症的儿童。父母和患儿报告的 HRQoL 为了解手术后患儿的生活提供了重要依据。需要进一步开展纵向和定性研究,以更好地了解这一复杂群体。
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Health-related quality of life following aortopexy for tracheomalacia: a cross-sectional study.

Objectives: The objective was to measure health-related quality of life (HRQoL) of children following treatment of all-cause tracheomalacia with aortopexy.

Methods: Children ≥5 years and parents of children <18 years who had undergone aortopexy completed the Paediatric Quality of Life Inventory (PedsQL4.0). Scores were compared to published norms.

Results: Completed questionnaires were received from 35 parents (65%) and 10 children (38%). Median age at aortopexy was 9.8 months (1 month-12.7 years) and median years of follow-up was 2.6 (4 months-6.9 years). Children who completed questionnaires had a median age of 8.4 (5.7-13.4) years. Parent and child-reported total PedsQL scores were 69.61 (SD : 19.74), and 63.15 (SD : 20.40) respectively. Half of parents and 80% of children reported scores suggesting poor HRQoL outcomes. Parent-reported total, physical and psycho-social scores were lower than those of healthy children and those with acute illness but comparable to children with chronic health conditions and cardiovascular disease. Similarly, children themselves reported comparable total scores to children with chronic illness but child-reported psycho-social scores were lower in the aortopexy group than any other group. There was no association between PedsQL scores and cause of malacia, age or time since aortopexy. The presence of complex congenital comorbidities had a significant (p < 0.05) impact on HRQoL scores.

Conclusions: Following aortopexy children remain at risk of poor HRQoL, especially those with complex comorbidities. HRQoL reported by both parent and child provides important insight into the lives of children following this procedure. Further longitudinal and qualitative study are required to better understand this complex group.

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