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先天性巨结肠症和肛门直肠畸形患儿术后的生活质量结局:一项系统评价和荟萃分析

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

作者信息

Oltean Irina, Hayawi Lamia, Larocca Victoria, Bijelić Vid, Beveridge Emily, Kaur Manvinder, Grandpierre Viviane, Kanyinda Jane, Nasr Ahmed

机构信息

Department of Surgery, Children's Hospital of Eastern Ontario, Ottawa, Ontario, Canada.

Clinical Research Unit, Children's Hospital of Eastern Ontario Research Institute, Ottawa, Ontario, Canada.

出版信息

World J Pediatr Surg. 2022 Nov 10;5(4):e000447. doi: 10.1136/wjps-2022-000447. eCollection 2022.

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), I=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), I=76% and SMD -0.45, 95% CI (-1.12 to 0.21), I=75%). The pooled prevalence of child-reported constipation was 22% (95% CI (16% to 28%), I=0%). The pooled prevalence of parent-reported postoperative obstruction symptoms was 61% (95% CI (41% to 81%), I=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.

摘要

背景

迄今为止,尚无系统评价和荟萃分析研究受先天性巨结肠(HD)和肛门直肠畸形(ARM)影响的儿科人群中多种儿童及家长报告的社会和身体生活质量(QoL)。本系统评价的目的是定量总结此类儿童家长报告和儿童报告的心理社会及身体功能评分。

方法

记录来源于CENTRAL、EMBASE和MEDLINE数据库。纳入报告HD和ARM患儿及家长报告的生活质量,且无论是否进行手术干预,并与无HD和ARM患儿进行对比的研究。主要结局为心理社会功能评分,次要结局为术后便秘、术后梗阻症状、大便失禁和小肠结肠炎的存在情况。采用随机效应荟萃分析。

结果

系统评价纳入23项研究,荟萃分析纳入11项研究。共有1678例HD和ARM患儿接受手术,与392例健康对照进行对比。汇总的家长报告标准化均值(SM)评分显示术后社会功能较好(SM 91.79,95%CI(80.3至103.3),I=0)。汇总的标准化均值差(SMD)显示,与正常人群相比,HD和ARM患儿术后家长报告存在大便失禁的证据,但不存在便秘证据(SMD -1.24(-1.79至-0.69),I=76%;SMD -0.45,95%CI(-1.12至0.21),I=75%)。儿童报告便秘的汇总患病率为22%(95%CI(16%至28%),I=0%)。家长报告术后梗阻症状的汇总患病率为61%(95%CI(41%至81%),I=41%)。

结论

结果表明,HD和ARM患儿术后社会功能较好,与对照组相比,失禁导致的生活质量评分较低,术后仍存在便秘和术后梗阻症状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d529/9716859/41ddc63367fa/wjps-2022-000447f01.jpg

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