Interdisciplinary network care collaboration in Parkinson's disease: a baseline evaluation in Germany.

Q2 Medicine
Carina Lummer, Carsten Eggers, Andreas Becker, Fenja Demandt, Tobias Warnecke
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Abstract

Background: The strengthening of interdisciplinary care collaboration in Parkinson's disease is taking on increasing importance in daily medical routine. Therefore, care providers worldwide are organizing themselves in disease-specific regional network structures. However, the existing networks are heterogeneous, and the driving key players are yet unidentified.

Objectives: To systematically identify key factors of the composition of health care professionals, who are initially interested in the development of a Parkinson network for interdisciplinary care collaboration, their motivation, and expectations, we conducted a basic evaluation in three different German regions covering a total number of 23,405 people with Parkinson's.

Methods: A specially developed semi-open questionnaire focusing on socio-demographic information, ways of contact, interdisciplinary collaboration, and connectedness was used. Statistical analyses were performed based on a predesigned codebook.

Results: The most crucial professions were outpatient therapists (physio-, occupational-, speech therapists) (36.7%), average case load of 10.1 patients/3 months and inpatient movement disorder specialists (21.1%), average case load of 197.4 patients/3 months. Before implementation of PD networks, 48.9% of outpatient therapists did not have any contact with neurologists. 58.9% of caregivers considered the current frequency of collaboration to be insufficient. The lack of political support as well as a lack of time were identified as main hurdles to increased collaboration.

Conclusion: The identified driving forces in strengthened care collaboration are assigned to different healthcare sectors. This makes networks which provide tools for specialized education and interdisciplinary, cross-sectoral communication indispensable. For an areawide rollout, a rethinking of political frameworks towards network care is strongly necessary.

帕金森病的跨学科网络护理合作:德国的基线评估。
背景:在日常医疗工作中,加强帕金森病的跨学科护理合作越来越重要。因此,世界各地的医疗服务提供者正在针对特定疾病组织区域网络结构。然而,现有的网络结构不尽相同,关键的推动因素尚未确定:为了系统地确定最初对建立帕金森病跨学科合作网络感兴趣的医护专业人员构成的关键因素、他们的动机和期望,我们在德国三个不同地区进行了一项基本评估,共涉及 23405 名帕金森病患者:方法:我们使用了一份专门开发的半开放式问卷,主要内容包括社会人口信息、接触方式、跨学科合作和联系。结果:最关键的专业是门诊:最重要的职业是门诊治疗师(物理治疗师、职业治疗师、语言治疗师)(36.7%)和住院运动障碍专家(21.1%),前者的平均病例数为 10.1 例/3 个月,后者的平均病例数为 197.4 例/3 个月。在实施帕金森病网络之前,48.9% 的门诊治疗师与神经科医生没有任何联系。58.9%的护理人员认为目前的合作频率不够。缺乏政治支持和时间不足被认为是加强合作的主要障碍:结论:加强护理合作的驱动力来自不同的医疗保健部门。因此,为专业教育和跨学科、跨部门交流提供工具的网络必不可少。要在全区范围内推广网络护理,就必须重新思考网络护理的政治框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.40
自引率
0.00%
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审稿时长
14 weeks
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