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分析结直肠疾病患者及其照顾者的心理社会功能:比较诊断、性别和发育功能。

Analysis of patients' and caregivers' psychosocial functioning in colorectal conditions: comparison of diagnosis, gender, and developmental functioning.

机构信息

Department of Psychiatry, Child and Adolescent Mental Health Division, University of Colorado Anschutz Medical Campus, 13123 E. 16th Ave, Aurora, CO, 80045, USA.

Pediatric Mental Health Institute, Children's Hospital Colorado, Aurora, CO, USA.

出版信息

Pediatr Surg Int. 2021 Apr;37(4):437-444. doi: 10.1007/s00383-020-04836-4. Epub 2021 Jan 9.

DOI:10.1007/s00383-020-04836-4
PMID:33423102
Abstract

PURPOSE

To evaluate the psychosocial functioning of caregivers and patients with anorectal malformation (ARM), Hirschsprung disease (HD), spinal conditions, and idiopathic constipation (IC) during the beginning of participation in bowel management program (BMP).

METHODS

In this retrospective study, Parent Stress Scale (PSS, parent-report) and Strengths and Difficulties Questionnaire (SDQ, parent-proxy; SDQ-S, self-report for 11 years and older) were used to evaluate parental stress levels and behavioral functioning, respectively. Descriptive and comparative statistical approaches were applied to summarize the data and to determine differences in scores between diagnoses, gender, and developmental functioning.

RESULTS

Two hundred patients and caregivers participated in BMP during the study period. PSS scores were significantly higher for caregivers of patients with IC than ARM. Statistical differences in SDQ were found for patients with IC versus those with ARM, male versus female patients, and patients with developmental delays versus those without delays. No significant differences were found in SDQ-S scores between these groups.

CONCLUSION

Key findings suggest that level of parental stress and behavioral concerns were significantly influenced by diagnoses, and partly by gender and presence of developmental delay. Thus, psychosocial support may need to be tailored based on these findings to provide optimum quality of care for patients and families.

摘要

目的

评估肛门直肠畸形(ARM)、先天性巨结肠(HD)、脊柱疾病和特发性便秘(IC)患儿及其照顾者在开始参与肠道管理计划(BMP)时的心理社会功能。

方法

在这项回顾性研究中,使用父母压力量表(PSS,父母报告)和长处和困难问卷(SDQ,父母代理;SDQ-S,11 岁及以上的自我报告)分别评估父母的压力水平和行为功能。采用描述性和比较性统计方法来总结数据,并确定诊断、性别和发育功能之间的评分差异。

结果

在研究期间,有 200 名患儿及其照顾者参与了 BMP。与 ARM 患儿的照顾者相比,IC 患儿的照顾者的 PSS 评分明显更高。在 SDQ 方面,IC 患儿与 ARM 患儿、男性患儿与女性患儿以及发育迟缓患儿与无发育迟缓患儿之间存在统计学差异。而在 SDQ-S 评分方面,这些组之间没有发现显著差异。

结论

主要发现表明,父母的压力水平和行为问题显著受到诊断的影响,部分受到性别和发育迟缓的影响。因此,可能需要根据这些发现提供有针对性的社会心理支持,为患儿及其家庭提供最佳的护理质量。

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