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[痴呆症患者居家和社区服务非医疗部门与医疗部门之间的接口处的医生]

[Physicians at the Interface to the Non-Medical Sector of Home- and Community-Based Services for People with Dementia].

作者信息

Cording Linda, Beyer Annette, Boettcher Aisha Meriel, Schattschneider Ralf, Busch Susanne

机构信息

Competence Center Gesundheit, Hochschule für Angewandte Wissenschaften Hamburg, Hamburg.

出版信息

Gesundheitswesen. 2019 Apr;81(4):319-324. doi: 10.1055/s-0042-124662. Epub 2017 Jun 30.

Abstract

OBJECTIVE

The study examined the function of physicians between the medical and nonmedical sector of home- and community-based services in the ambulatory care of people with dementia and their relatives. Therefore, the study took a differentiated look at the status quo of physicians' activities regarding non-medical home- and community-based services as well as approaches for optimizing the current situation from the physicians' perspective.

METHODS

An explorative cross-sectional study was conducted using a standardized postal survey (based on a qualitative preliminary study with 6 physicians). Data from 177 GPs and specialists in Hamburg could be collected and analyzed with descriptive statistics.

RESULTS

The majority of physicians (88.1%) inform their patients with dementia and their carers about home- and community-based services. 'Home care' presents the most often and 'services for carers' the least considered aspect. Approaches that address the optimization of information material are assessed as most supportive.

CONCLUSION

The results can be used as a basis for further development of the care landscape in Hamburg. What has to be discussed is the monoperspective data collection only from physician's point of view. The utilization of the results requires an inclusion of the perspective of affected persons themselves as well as other actors in the non-medical care landscape.

摘要

目的

本研究探讨了在为痴呆症患者及其亲属提供门诊护理时,家庭和社区服务的医疗与非医疗部门中医师的职能。因此,该研究从不同角度审视了中医师在非医疗家庭和社区服务方面的活动现状,以及从中医师角度优化当前状况的方法。

方法

采用标准化邮政调查进行探索性横断面研究(基于对6名医师的定性初步研究)。对汉堡的177名全科医生和专科医生的数据进行收集,并运用描述性统计方法进行分析。

结果

大多数医师(88.1%)会告知痴呆症患者及其护理人员有关家庭和社区服务的信息。“居家护理”是最常被提及的方面,而“护理人员服务”则是最少被考虑的方面。被认为最具支持性的方法是优化信息材料。

结论

研究结果可作为汉堡护理格局进一步发展的基础。需要讨论的是仅从医师角度进行的单视角数据收集。要利用这些结果,还需要纳入受影响者自身以及非医疗护理领域其他参与者的视角。

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