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Healthcare professionals as promoters and barriers of innovative complex outpatient interventions: A case study of an intervention to increase participation of people living with MS. 医疗保健专业人员作为创新复杂门诊干预措施的推动者和障碍:一项干预措施的案例研究,以增加MS患者的参与。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-03 DOI: 10.1016/j.zefq.2025.11.001
Susan Raths, Steffen Flessa

Objective: The German Innovation Funds project MSnetWork introduced a complex outpatient intervention to improve treatment of patients with MS. This study analyses the perception of healthcare professionals working in neurological practices to determine their ability and willingness to implement these interventions during the MSnetWork period and beyond the end of the project. The study assumes that the motivation of these professionals to implement the intervention is crucial for its success.

Methods: For this qualitative study, semi-structured interviews assessed the perception of neurological practice personnel (neurologists, assistants) of all MSnetWork practices (full sample) to determine their motivation to implement the interventions. Furthermore, challenges and opportunities of the implementation were retrieved to find out the reasons for promoting or hindering the new intervention. The interviews were transcribed and analysed using qualitative content analysis.

Results: The interviews with 26 participants from 19 neurology practices (52.8 % participation, 12 interviews with physicians and 14 interviews with assistants) were conducted from October to December 2023 and lasted about 60 minutes.. From the professionals' perspective, key motivations included improving patient care, exploring innovative approaches, and fostering collaboration. Challenges included resource limitations, unclear intervention processes, and patient engagement. The healthcare professionals also indicated that making the MSnetWork interventions an essential element of routine treatment of MS patients would require more flexibility, fair reimbursement, and specialized training.

Discussion: MSnetWork seems to have implementation potential, i.e., healthcare professionals perceive that the new services fill gaps in care that are usually not appropriately addressed due to a lack of adequate funding. However, the main barrier to implement the new scheme is its integration into routine care, given the tense situation in specialist care and the simultaneous shortage of staff.

Conclusion: The ultimate goal of innovative care projects is the transition of the pilot into routine care. The results of this interview study indicate that healthcare professionals have to be involved right from the start in both design and implementation of innovative care projects. Innovative routine care is not only a medical or technological challenge, but above all a social process that requires the joint efforts of all stakeholders. The findings indicate that the project should be transferred into routine care.

目的:德国创新基金项目MSnetWork引入了一种复杂的门诊干预措施,以改善多发性硬化患者的治疗。本研究分析了从事神经学实践的医疗保健专业人员的看法,以确定他们在MSnetWork期间和项目结束后实施这些干预措施的能力和意愿。研究假设这些专业人员实施干预的动机对其成功至关重要。方法:在这一定性研究中,半结构化访谈评估了所有MSnetWork实践(全样本)的神经实践人员(神经科医生、助理)的感知,以确定他们实施干预的动机。在此基础上,对实施过程中的挑战和机遇进行梳理,找出促进或阻碍新干预的原因。访谈记录和分析采用定性内容分析。结果:我们于2023年10月至12月对19家神经内科诊所的26名参与者进行了访谈(52.8% %,其中医生访谈12人,助理访谈14人),访谈时间约60 分钟。从专业人士的角度来看,主要动机包括改善患者护理、探索创新方法和促进合作。挑战包括资源限制、干预过程不明确和患者参与。医疗保健专业人员还指出,使MSnetWork干预成为多发性硬化症患者常规治疗的基本要素将需要更大的灵活性、公平的报销和专门的培训。讨论:MSnetWork似乎具有实施潜力,即,医疗保健专业人员认为,新的服务填补了由于缺乏足够资金而通常无法适当解决的护理空白。然而,考虑到专科护理的紧张局势和同时人员短缺,实施新计划的主要障碍是将其纳入常规护理。结论:创新护理项目的最终目标是由试点向常规护理过渡。本访谈研究的结果表明,医疗保健专业人员必须从一开始就参与创新护理项目的设计和实施。创新的常规护理不仅是一项医疗或技术挑战,而且首先是一个需要所有利益攸关方共同努力的社会进程。结果表明,该项目应转入常规护理。
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引用次数: 0
[How digital is my practice? General practitioners' attitudes towards maturity measurements - An online survey]. 我的实践有多数字化?全科医生对成熟度测量的态度-一项在线调查]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-03 DOI: 10.1016/j.zefq.2025.11.003
Timo Neunaber, Achim Mortsiefer, Sven Meister

Background: Maturity measurements are becoming increasingly important in order to record the level of digitalization of healthcare institutions. To this point, the digital maturity of GP practices has hardly been measured. This study examines GPs' interest in maturity measurements and their perceptions of factors influencing the level of digitalization.

Method: General practitioners in Germany were surveyed using web-based questionnaires on demographic information, their interest in maturity assessments, and factors influencing the level of digitalization. Multiple regression analysis was used to investigate the influence of demographic characteristics on interest in maturity level measurements. Using a mean value comparison, a ranking of the most important factors influencing the level of digitalization from the GPs' perspective was established.

Results: 201 data sets were included in the analysis. The average interest of GPs in maturity measurements was 3.61 out of 5. The levels of digitalization of the practice and digital health literacy of patients were positively associated with interest in maturity measurements. The highest perceived influences on the level of digitalization were related to the technical infrastructure of medical practices.

Conclusion: In order to establish maturity level measurements in primary care, the interest of potential users such as GPs should be strengthened at an early stage by including their perspectives. The added value of the surveys in the development of maturity models should be worked out and clearly communicated to GPs.

背景:为了记录医疗机构的数字化水平,成熟度测量变得越来越重要。到目前为止,全科医生实践的数字化成熟度几乎没有得到衡量。本研究考察了全科医生对成熟度测量的兴趣以及他们对影响数字化水平的因素的看法。方法:采用基于网络的调查问卷对德国全科医生进行人口统计信息、对成熟度评估的兴趣以及影响数字化水平的因素等方面的调查。多元回归分析用于调查人口统计学特征对成熟度水平测量兴趣的影响。采用均值比较法,从全科医生的角度对影响数字化水平的最重要因素进行排序。结果:201个数据集被纳入分析。普通合伙人对期限测量的平均兴趣为3.61(满分5分)。实践的数字化水平和患者的数字健康素养与成熟度测量的兴趣呈正相关。对数字化水平影响最大的是医疗实践的技术基础设施。结论:为了在初级保健中建立成熟度水平测量,应在早期阶段加强潜在用户(如全科医生)的兴趣,包括他们的观点。应厘清调查在发展成熟度模型方面的附加价值,并清楚地传达给全科医生。
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引用次数: 0
Umsetzung des Widerrufrechtes bei der Verarbeitung von Gesundheitsdaten in Forschungsprojekten [落实撤回对研究项目中健康数据处理的同意的权利]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/j.zefq.2025.09.003
Christoph Gerst , Florian Gottschalk , Eva Hummers , Falk Schlegelmilch

Background

Processing data in health services research requires informed patient consent. When this consent is withdrawn, researchers face the challenge of correctly implementing legal requirements regarding data protection. This article aims to identify and analyze the tasks research institutions must undertake when processing a withdrawal of consent for data processing.

Methods

Using a withdrawal case from the RADARplus research project, we conducted a legal analysis of requirements under the General Data Protection Regulation (GDPR) and other relevant legal frameworks. Based on this analysis, we discuss implementation approaches.

Results

The analysis reveals the complexity of implementing a withdrawal of consent procedure: Data may exist in various systems (research databases, backup systems, paper records) and must be identified accordingly. Different retention requirements apply depending on the type of data and legal basis. We outline responsibilities and practical approaches to restricting data processing, such as technical access limitations and blocking notices.

Discussion

The practical implementation of the right to withdraw consent presents complex challenges for research institutions. Open questions remain, particularly regarding pseudonymized data, long-term data storage, and collaboration with multiple research partners. While the suggested guidance provides a structured approach for legally compliant processing of withdrawals, it does not eliminate the need for data protection assessment and proper documentation.
背景:在卫生服务研究中处理数据需要患者知情同意。当这种同意被撤回时,研究人员面临着正确实施有关数据保护的法律要求的挑战。本文旨在识别和分析研究机构在处理撤销数据处理同意时必须承担的任务。方法:利用RADARplus研究项目的撤回案例,我们对《通用数据保护条例》(GDPR)和其他相关法律框架下的要求进行了法律分析。在此基础上,讨论了实现方法。结果:分析揭示了实施撤回同意程序的复杂性:数据可能存在于各种系统(研究数据库、备份系统、纸质记录)中,必须相应地识别。根据数据类型和法律依据,适用不同的保留要求。我们概述了限制数据处理的责任和实际方法,例如技术访问限制和阻止通知。讨论:撤回同意权的实际实施对研究机构提出了复杂的挑战。悬而未决的问题仍然存在,特别是关于假名数据、长期数据存储以及与多个研究伙伴的合作。虽然建议的指导方针为符合法律要求的提款处理提供了结构化的方法,但它并没有消除对数据保护评估和适当文件的需求。
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引用次数: 0
Unzufriedenheit mit dem DMP KHK: explorativer Survey mit Hausärzt*innen zu den DMP Diabetes mellitus Typ 2 und Koronare Herzkrankheit [对冠心病DMP的不满:全科医生对2型糖尿病和冠心病疾病管理方案(DMP)的探索性调查]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/j.zefq.2025.05.008
Larisa Pilic , Lisa Kupsch , Marcus Redaèlli , Kira Molkentin , Beate Sigrid Müller , Stephanie Stock , Stefan Wilm

Background

Disease management programs (DMPs) were implemented in 2002 to improve the care for a growing number of chronically ill people in Germany. However, the current state of research on the effectiveness and acceptance of DMPs does not allow valid comparisons between them. The aim of the survey was to compare general practitioners’ (GPs’) experiences with DMPs for type 2 diabetes mellitus (T2DM) and coronary heart disease (CHD). The survey complements the results of a qualitative study conducted in 2020.

Methods

Cross-sectional exploratory study using an online survey among GPs in the area of the North Rhine Association of Statutory Health Insurance Physicians in 2023. In addition to general questions on DMPs, the DMPs for T2DM and CHD were compared in regard to three main topics: (1) perceived effectiveness of DMPs, (2) satisfaction with DMPs, and (3) perceived self-management of patients in the DMPs. A total of 42 items were used.

Results

The survey was completed by 186 GPs, resulting in a response rate of 10.4%. 96% were practice owners, all of whom had experience in implementing these DMPs. Significant differences were observed in the perceived effectiveness of the two DMPs, e.g. in reducing complications and hospitalizations, with consistently lower ratings for the DMP for CHD. This was also evident in the thematic blocks on satisfaction with DMPs, with regard to enrolment patterns and documentation, as well as patients’ self-management in terms of health behaviour and personal responsibility.

Conclusion

Future studies should examine DMPs in GP care separately, given the significant differences in how they are evaluated by GPs. In addition, DMPs should be analysed in more detail regarding effectiveness, feasibility, and acceptance, especially the DMP for CHD.
背景:疾病管理计划(dmp)于2002年实施,以改善对德国越来越多的慢性病患者的护理。然而,目前关于dmp的有效性和接受度的研究状况不允许对它们进行有效的比较。该调查的目的是比较全科医生(gp)和dmp治疗2型糖尿病(T2DM)和冠心病(CHD)的经验。该调查补充了2020年进行的一项定性研究的结果。方法:采用横断面探索性研究方法,于2023年对北莱茵地区法定健康保险医师协会全科医生进行在线调查。除了关于dmp的一般问题外,T2DM和CHD的dmp在三个主要主题上进行了比较:(1)dmp的感知有效性,(2)对dmp的满意度,(3)dmp患者的感知自我管理。总共使用了42个项目。结果:共有186名全科医生完成调查,回复率为10.4%。96%是实践业主,他们都有实施这些dmp的经验。在两种DMP的感知有效性方面观察到显著差异,例如在减少并发症和住院方面,DMP治疗冠心病的评分一直较低。这一点也体现在对医疗保健方案的满意度、登记模式和文件以及患者在健康行为和个人责任方面的自我管理方面的专题块中。结论:考虑到全科医生评估dmp的方式存在显著差异,未来的研究应单独检查全科医生护理中的dmp。此外,应更详细地分析DMP的有效性、可行性和可接受性,特别是用于冠心病的DMP。
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引用次数: 0
Developing a roadmap for consultations on patient-reported outcomes: Insights from the PROCES study 制定关于患者报告结果的磋商路线图:来自processes研究的见解。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/j.zefq.2025.09.006
Alizé Rogge , Felix Fischer , Sophie Dombrowski , Matthias Rose , Gregor Liegl

Introduction

Patient-reported outcomes (PROs) are increasingly recognized for their potential to enhance patient-centered and value-based healthcare. However, their implementation remains inconsistent, often hindered by fragmented approaches and a lack of sufficient expertise, leaving stakeholders without adequate practical support. To bridge this gap, a structured framework for PRO consulting services is crucial, yet currently absent in Germany. The PROCES study aimed to develop a roadmap as a first step to enable standardized, context-adaptive, and resource-efficient PRO implementation in both research and clinical care.

Methods

PROCES employed a mixed-methods approach, including (1) semi-structured qualitative interviews with 28 stakeholders at one university hospital, (2) an anonymous survey of 17 PRO experts across seven European countries, and (3) a two-day on-site workshop with PRO experts to refine findings. Data were analyzed using qualitative content analysis and descriptive statistics.

Results

The study identified three main challenges: diverse stakeholder needs, increasing demand for consultations, and limited funding. A roadmap was proposed, including a decision-support flowchart for routine care and a filter scheme to manage incoming PRO requests to optimize resource allocation. Additionally, 75 % of surveyed experts supported the establishment of an international PRO network to standardize consultancy practices.

Discussion

The PROCES findings represent a significant step toward standardized PRO consultancy services in Germany, emphasizing a construct-centered, instrument-independent approach. Future research should evaluate its adaptability and explore its potential as a blueprint for fostering a national PRO approach in Germany.

Conclusion

This roadmap addresses key barriers to PRO implementation, including unstructured consultations and fragmented efforts, while promoting sustainable and efficient implementation.
简介:患者报告的结果(pro)因其增强以患者为中心和基于价值的医疗保健的潜力而日益得到认可。然而,它们的实施仍然不一致,往往受到支离破碎的方法和缺乏足够专业知识的阻碍,使利益攸关方得不到足够的实际支持。为了弥补这一差距,一个结构化的PRO咨询服务框架是至关重要的,但目前在德国还没有。process研究旨在制定一个路线图,作为在研究和临床护理中实现标准化、环境适应性和资源高效的PRO实施的第一步。方法:PROCES采用混合方法,包括(1)对一家大学医院的28名利益相关者进行半结构化定性访谈,(2)对7个欧洲国家的17名PRO专家进行匿名调查,以及(3)与PRO专家进行为期两天的现场研讨会,以完善研究结果。数据分析采用定性内容分析和描述性统计。结果:研究确定了三个主要挑战:不同的利益相关者需求、不断增加的咨询需求和有限的资金。提出了一种路线图,包括日常护理的决策支持流程图和管理传入PRO请求的过滤方案,以优化资源分配。此外,75% %的受访专家支持建立一个国际PRO网络来规范咨询业务。讨论:process的研究结果代表了德国向标准化PRO咨询服务迈出的重要一步,强调了以构建为中心、仪器独立的方法。未来的研究应评估其适应性,并探索其作为促进德国国家PRO方法的蓝图的潜力。结论:该路线图解决了实施PRO的主要障碍,包括非结构化磋商和分散的努力,同时促进了可持续和高效的实施。
{"title":"Developing a roadmap for consultations on patient-reported outcomes: Insights from the PROCES study","authors":"Alizé Rogge ,&nbsp;Felix Fischer ,&nbsp;Sophie Dombrowski ,&nbsp;Matthias Rose ,&nbsp;Gregor Liegl","doi":"10.1016/j.zefq.2025.09.006","DOIUrl":"10.1016/j.zefq.2025.09.006","url":null,"abstract":"<div><h3>Introduction</h3><div>Patient-reported outcomes (PROs) are increasingly recognized for their potential to enhance patient-centered and value-based healthcare. However, their implementation remains inconsistent, often hindered by fragmented approaches and a lack of sufficient expertise, leaving stakeholders without adequate practical support. To bridge this gap, a structured framework for PRO consulting services is crucial, yet currently absent in Germany. The PROCES study aimed to develop a roadmap as a first step to enable standardized, context-adaptive, and resource-efficient PRO implementation in both research and clinical care.</div></div><div><h3>Methods</h3><div>PROCES employed a mixed-methods approach, including (1) semi-structured qualitative interviews with 28 stakeholders at one university hospital, (2) an anonymous survey of 17 PRO experts across seven European countries, and (3) a two-day on-site workshop with PRO experts to refine findings. Data were analyzed using qualitative content analysis and descriptive statistics.</div></div><div><h3>Results</h3><div>The study identified three main challenges: diverse stakeholder needs, increasing demand for consultations, and limited funding. A roadmap was proposed, including a decision-support flowchart for routine care and a filter scheme to manage incoming PRO requests to optimize resource allocation. Additionally, 75 % of surveyed experts supported the establishment of an international PRO network to standardize consultancy practices.</div></div><div><h3>Discussion</h3><div>The PROCES findings represent a significant step toward standardized PRO consultancy services in Germany, emphasizing a construct-centered, instrument-independent approach. Future research should evaluate its adaptability and explore its potential as a blueprint for fostering a national PRO approach in Germany.</div></div><div><h3>Conclusion</h3><div>This roadmap addresses key barriers to PRO implementation, including unstructured consultations and fragmented efforts, while promoting sustainable and efficient implementation.</div></div>","PeriodicalId":46628,"journal":{"name":"Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen","volume":"198 ","pages":"Pages 54-61"},"PeriodicalIF":1.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145423163","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Herausgeberkollegium / Editorial Board Herausgeberkollegium编委会
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/S1865-9217(25)00220-X
{"title":"Herausgeberkollegium / Editorial Board","authors":"","doi":"10.1016/S1865-9217(25)00220-X","DOIUrl":"10.1016/S1865-9217(25)00220-X","url":null,"abstract":"","PeriodicalId":46628,"journal":{"name":"Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen","volume":"198 ","pages":"Page ii"},"PeriodicalIF":1.7,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145625168","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial: Gesundheitsökonomische Evaluation komplexer Interventionen – Zeit den Horizont zu erweitern 编辑:复杂干预措施的卫生经济评估:是时候扩大视野了。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/j.zefq.2025.09.001
Juliane Köberlein-Neu , Andrea Icks
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引用次数: 0
Kosten informeller Pflege bei Menschen mit kognitiven Beeinträchtigungen: eine Kostenstudie aus dem Digitalen Demenzregister Bayern (digiDEM Bayern) [对认知障碍患者的非正式护理成本:基于巴伐利亚数字痴呆症登记处(digiDEM Bayern)的成本研究]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/j.zefq.2025.10.001
Florian Weidinger , Jana Räbel , Elmar Gräßel , Thomas Ganslandt , Peter Kolominsky-Rabas , Martin Emmert

Background

Informal care costs account for the largest share of the total costs of dementia. The informal care costs of dementia have been well researched in Germany, but the group of family caregivers of people with MCI (“mild cognitive impairment”) has not been taken into account so far. The aim of this study is to evaluate the care time spent by family caregivers of people with cognitive impairment according to the severity of the disease and to estimate informal care costs.

Methods

The data is based on the multicenter, prospective registry study “Digital Dementia Regustry Bavaria – digiDEMBayern” (German title: “Digitales Demenzregister Bayern – digiDEM Bayern”). Information on informal care time was collected using the “Resource Utilization in Dementia Lite (RUD-Lite)” instrument. Informal care costs were calculated using the opportunity cost approach. Sensitivity analyses were used to determine a high and a low cost estimate and to compare them with each other. Severity-related differences were assessed using variance analyses.

Results

The survey results of 445 people with cognitive impairment and their informal caregivers were evaluated. The average care time to support activities of daily living significantly increased with greater severity (p = 0.005). The average cost of informal caregiving was between 15,057 and 30,994 EUR for people with mild cognitive impairment, between 19,785 and 38,747 EUR for people with mild dementia, and between 23,709 and 48,451 EUR for people with moderate dementia.

Discussion

Several earlier studies found an increase in the costs of informal caregiving with increasing cognitive decline in Germany. However, these studies differ in the methodologies used. There are various reasons why comparatively higher costs of informal care have been calculated in the present study.

Conclusion

It is likely that the annual costs of informal caregiving are in the range described, depending on the level of severity. The results indicate that people caring for family members with MCI bear a significant burden and that this leads to high social costs. The indirect costs of dementia increase the burden on society also from an economic perspective.
背景:非正式护理费用占痴呆症总费用的最大份额。在德国,痴呆症的非正式护理成本已经得到了很好的研究,但到目前为止,MCI(轻度认知障碍)患者的家庭照顾者群体还没有被考虑在内。本研究的目的是根据疾病的严重程度评估家庭照顾者对认知障碍患者的护理时间,并估计非正式护理费用。方法:数据基于多中心前瞻性登记研究“Digital Dementia registry Bavaria - digiDEMBayern”(德文标题:“Digitales Demenzregister Bayern - digiDEMBayern”)。使用“痴呆症生活资源利用”工具收集非正式护理时间的信息。非正式护理费用采用机会成本法计算。敏感性分析用于确定高成本和低成本估算,并相互比较。使用方差分析评估与严重程度相关的差异。结果:对445名认知障碍患者及其非正式照顾者的调查结果进行评价。支持日常生活活动的平均护理时间随着病情加重而显著增加(p = 0.005)。轻度认知障碍患者的平均非正式护理费用为15,057至30,994欧元,轻度痴呆患者的平均护理费用为19,785至38,747欧元,中度痴呆患者的平均护理费用为23,709至48,451欧元。讨论:早期的几项研究发现,在德国,随着认知能力的日益下降,非正式护理的成本也在增加。然而,这些研究在使用的方法上有所不同。在本研究中计算出相对较高的非正式护理成本有多种原因。结论:根据严重程度的不同,非正式护理的年度成本可能在描述的范围内。结果表明,照顾患有轻度认知障碍的家庭成员的人承担着很大的负担,这导致了很高的社会成本。从经济角度来看,痴呆症的间接成本也增加了社会负担。
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引用次数: 0
Inhaltsverzeichnis / Table of Contents 吸入物/目录
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/S1865-9217(25)00221-1
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引用次数: 0
Versorgungsforschung als vielfältiges Beschäftigungsfeld in Deutschland: eine Dokumentenanalyse von Stellenanzeigen [作为就业市场的医疗服务研究:招聘广告的文献分析]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2025-12-01 DOI: 10.1016/j.zefq.2025.07.002
Annika Queder , Lea Gölz , Michel Wensing , Charlotte Ullrich

Introduction

Since the mid-2010s, health services research (HSR) in Germany has been increasingly institutionalized. However, little is known about actual career paths within the field. The aim of this study was to describe the HSR job market in Germany, both in general terms and specifically for graduates of health services research master degree programs.

Methods

Over a period of three months in spring 2022, four employment websites and the websites of the German Network for HSR were searched for job advertisements containing the term “health services research”. Using document analysis, the job advertisements identified were analyzed with regard to a) employer characteristics, b) job characteristics, and c) significance of HSR.

Results

Of the 1,474 job advertisements identified, 360 were included in the analysis. These were mainly from hospitals (31.94 %, n = 115), companies (29.44 %, n = 106), and universities (23.33 %, n = 84). The majority of the positions offered required a Master’s degree or a higher qualification (57.22 %, n = 206), and for 76 positions (36.89 %) there was the additional requirement of a completed vocational training and/or main occupation in patient care. Most of the 91 job offers for graduates of a HSR master’s program were temporary (65.93 %, n = 60) and in the field of science and research (89.01 %, n = 81). About half were full-time positions (46.15 %, n = 42).

Discussion

The study shows an increasing number of job advertisements including the search term “health services research”, a broad understanding of the term and associated heterogeneous qualification requirements and job characteristics.

Conclusion

Our findings contribute to a better understanding of HSR as a professional field in Germany. The results provide guidance for students, graduates, and teachers in HSR.
导言:自2010年代中期以来,德国的卫生服务研究(HSR)日益制度化。然而,人们对该领域的实际职业道路知之甚少。本研究的目的是描述德国的高铁就业市场,包括一般术语和卫生服务研究硕士学位课程毕业生的具体情况。方法:在2022年春季的三个月时间里,对四个招聘网站和德国高铁网络网站进行搜索,搜索包含“卫生服务研究”一词的招聘广告。采用文献分析的方法,从a)雇主特征、b)工作特征和c)高铁的显著性三个方面对所识别的招聘广告进行了分析。结果:在确定的1474个招聘广告中,有360个被纳入了分析。这些是主要来自医院(31.94 %,n = 115),公司(29.44 % n = 106),和大学(23.33 % n = 84)。提供的大多数职位要求硕士学位或更高学历(57.22 %,n = 206),76个职位(36.89 %)还要求完成职业培训和/或主要职业是患者护理。高铁硕士项目毕业生获得的91份工作中,大部分是临时性的(65.93 %,n = 60)和科研领域的工作(89.01 %,n = 81)。大约一半是全职职位(46.15 %,n = 42)。讨论:研究表明,越来越多的招聘广告包括搜索词“卫生服务研究”,对术语的广泛理解以及相关的异构资格要求和工作特征。结论:我们的研究结果有助于更好地理解德国的高铁作为一个专业领域。研究结果可为高铁学生、毕业生和教师提供指导。
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引用次数: 0
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Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen
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