Quality of life outcomes in children after surgery for Hirschsprung disease and anorectal malformations: a systematic review and meta-analysis.

IF 0.8 4区 医学 Q4 PEDIATRICS World Journal of Pediatric Surgery Pub Date : 2022-11-10 eCollection Date: 2022-01-01 DOI:10.1136/wjps-2022-000447
Irina Oltean, Lamia Hayawi, Victoria Larocca, Vid Bijelić, Emily Beveridge, Manvinder Kaur, Viviane Grandpierre, Jane Kanyinda, Ahmed Nasr
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Abstract

Background: No systematic review and meta-analysis to date has examined multiple child and parent-reported social and physical quality of life (QoL) in pediatric populations affected by Hirschsprung's disease (HD) and anorectal malformations (ARM). The objective of this systematic review is to quantitatively summarize the parent-reported and child-reported psychosocial and physical functioning scores of such children.

Methods: Records were sourced from the CENTRAL, EMBASE, and MEDLINE databases. Studies that reported child and parent reported QoL in children with HD and ARM, regardless of surgery intervention, versus children without HD and ARM, were included. The primary outcome was the psychosocial functioning scores, and the secondary outcomes were the presence of postoperative constipation, postoperative obstruction symptoms, fecal incontinence, and enterocolitis. A random effects meta-analysis was used.

Results: Twenty-three studies were included in the systematic review, with 11 studies included in the meta-analysis. Totally, 1678 total pediatric patients with HD and ARM underwent surgery vs 392 healthy controls. Pooled parent-reported standardized mean (SM) scores showed better social functioning after surgery (SM 91.79, 95% CI (80.3 to 103.3), I2=0). The pooled standardized mean difference (SMD) showed evidence for parent-reported incontinence but not for constipation in children with HD and ARM after surgery that had a lower mean QoL score compared with the normal population (SMD -1.24 (-1.79 to -0.69), I2=76% and SMD -0.45, 95% CI (-1.12 to 0.21), I2=75%). The pooled prevalence of child-reported constipation was 22% (95% CI (16% to 28%), I2=0%). The pooled prevalence of parent-reported postoperative obstruction symptoms was 61% (95% CI (41% to 81%), I2=41%).

Conclusion: The results demonstrate better social functioning after surgery, lower QoL scores for incontinence versus controls, and remaining constipation and postoperative obstruction symptoms after surgery in children with HD and ARM.

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赫氏胃肠病和肛门直肠畸形手术后儿童的生活质量:系统回顾和荟萃分析。
背景:迄今为止,还没有系统性综述和荟萃分析研究过受赫氏包虫病(HD)和肛门直肠畸形(ARM)影响的儿童群体中儿童和家长报告的社会和身体生活质量(QoL)。本系统性综述旨在定量总结此类儿童的家长报告和儿童报告的社会心理和身体功能评分:方法:记录来自 CENTRAL、EMBASE 和 MEDLINE 数据库。方法:从 CENTRAL、EMBASE 和 MEDLINE 数据库中获取记录,纳入了报告 HD 和 ARM 患儿(无论手术干预与否)与非 HD 和 ARM 患儿的儿童和家长 QoL 的研究。主要研究结果为社会心理功能评分,次要研究结果为术后便秘、术后梗阻症状、大便失禁和肠结肠炎。研究采用随机效应荟萃分析法:系统综述纳入了 23 项研究,荟萃分析纳入了 11 项研究。共有1678名患有HD和ARM的儿童患者接受了手术治疗,健康对照组为392人。汇总的家长报告标准化平均分(SM)显示,手术后的社会功能更好(SM 91.79,95% CI (80.3 to 103.3),I2=0)。汇总标准化均值差异(SMD)显示,与正常人群相比,HD患儿和ARM患儿术后的平均QoL评分较低,有证据显示家长报告的尿失禁情况较好(SMD-1.24(-1.79至-0.69),I2=76%;SMD-0.45,95% CI(-1.12至0.21),I2=75%),但便秘情况较差。儿童报告的便秘汇总患病率为 22%(95% CI (16% to 28%),I2=0%)。家长报告的术后梗阻症状的汇总发生率为61%(95% CI(41%至81%),I2=41%):结果表明,与对照组相比,HD和ARM患儿术后的社会功能更好,尿失禁的QoL评分更低,术后仍有便秘和术后梗阻症状。
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来源期刊
CiteScore
1.40
自引率
12.50%
发文量
38
审稿时长
13 weeks
期刊最新文献
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