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脊髓损伤超过20年患者的心理困扰及医疗保健服务体验

Psychological distress and user experiences with health care provision in persons living with spinal cord injury for more than 20 years.

作者信息

Jakimovska V M, Kostovski E, Biering-Sørensen F, Lidal I B

机构信息

Sunnaas Rehabilitation Hospital, Science Department, Nesoddtangen, Norway.

Faculty of Medicine, Department of Physical Medicine and Rehabilitation, University of Oslo, Oslo, Norway.

出版信息

Spinal Cord. 2017 Sep;55(9):864-869. doi: 10.1038/sc.2017.29. Epub 2017 Mar 21.

DOI:10.1038/sc.2017.29
PMID:28322242
Abstract

STUDY DESIGN

Descriptive cross-sectional and retrospective study.

OBJECTIVES

To gain more insight into the long-term health status in persons with traumatic spinal cord injury (SCI), especially perceived psychological distress as well as self-reports of utilization of healthcare services.

SETTING

Sunnaas Rehabilitation Hospital, Norway.

METHODS

In total, 147 persons with SCI were examined for more than 20 years and interviewed (in 2004/2005) using a self-administrated questionnaire and General Health Questionnaire (GHQ-20). Descriptive statistics and a logistic regression analysis were conducted to identify variables associated with psychological distress.

RESULTS

Most participants had received SCI follow-up health services at least once after initial rehabilitation; 34% were satisfied, 51% neutral and 18% unsatisfied with the health services provided. Concerning psychological distress, 34 persons were cases according to the GHQ-20. The cases did not differ from non-cases concerning demography, time since injury, injury aetiology, injury severity, marital status or employment status. The regression analysis revealed that cases were associated (P<0.05) with more use of SCI-specific follow-ups.

CONCLUSION

In a 20+ years' post-injury SCI population, psychological distress is common and associated with the use of follow-up services. The varying satisfaction of people with SCI about healthcare services is notable, as is the finding that 20% of people with paraplegia did not use specific SCI follow-up services. The experiences of people with SCI with healthcare services need further investigation, and there is also a need for studies that examine the effects of interventions aimed at improving services and patient satisfaction.

摘要

研究设计

描述性横断面研究和回顾性研究。

目的

更深入了解创伤性脊髓损伤(SCI)患者的长期健康状况,尤其是感知到的心理困扰以及医疗服务利用情况的自我报告。

地点

挪威松讷斯康复医院。

方法

共有147名脊髓损伤患者接受了20多年的检查,并于2004/2005年使用自填式问卷和一般健康问卷(GHQ - 20)进行了访谈。进行描述性统计和逻辑回归分析以确定与心理困扰相关的变量。

结果

大多数参与者在初次康复后至少接受过一次脊髓损伤随访健康服务;34%对所提供的健康服务感到满意,51%持中立态度,18%不满意。关于心理困扰,根据GHQ - 20,有34人属于病例。病例在人口统计学、受伤时间、损伤病因、损伤严重程度、婚姻状况或就业状况方面与非病例没有差异。回归分析显示,病例与更多使用脊髓损伤特异性随访相关(P<0.05)。

结论

在受伤20多年后的脊髓损伤人群中,心理困扰很常见,且与随访服务的使用有关。脊髓损伤患者对医疗服务的满意度各不相同,这一点值得注意,同样值得注意的是,20%的截瘫患者未使用特定的脊髓损伤随访服务。脊髓损伤患者的医疗服务体验需要进一步研究,也需要研究来检验旨在改善服务和患者满意度的干预措施的效果。

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