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Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen最新文献

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Ambulante Diagnosen in der Grundversorgung: mehr Transparenz im Bereich der ambulanten Diagnosen 【初级保健门诊诊断:增加门诊诊断领域的透明度】。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2026-01-08 DOI: 10.1016/j.zefq.2025.11.010
Aurélien Sallin , Joseph Rohrer , Marco Ruhstaller , Caroline Bähler , Eva Blozik

Introduction

In Switzerland, there is no obligation to record outpatient diagnoses. PraxisGruppe Schweiz (PraxiS), a network of about 30 GP and specialist practices in predominantly rural German-speaking regions in Switzerland, assign diagnosis codes per patient and consultation using the ICD-10 classification system. We compare these diagnoses with approximate ones, the so-called Pharmaceutical Cost Groups (PCGs), based on claims data from SWICA health insurance. We suspected that the distributions of diagnoses differed significantly between the two samples.

Methods

The PraxiS database was used to identify patients with at least one consultation between 2020 and 2022 who were insured with SWICA. Claims data identified patients who had at least one consultation with a PraxiS network clinician in the same period.
Diagnoses (ICD-10) were analyzed, and the ten most frequent diagnoses per age group were reported. The number of consultations per patient and age group were calculated. PCG information was derived from claims data following the official Swiss risk equalization definition, based on defined daily doses in the last observation year. Differences in diagnosis distributions between the two samples were tested using a Pearson χ2 test.

Results

High cholesterol, hypertension, diabetes, and depression are amongst the most frequently recorded diagnoses in both data sources. Furthermore, acute events (e.g., infections of the upper respiratory tract) and non-specific symptoms or problems that cannot be clearly assigned to a certain diagnosis occur frequently in primary care, while thyroid diseases, asthma/COPD and glaucoma are more commonly recorded in the claims data, since they are associated with regular medication intake. For 6 of the 32 PCG diagnoses, we rejected the null hypothesis of identical distributions, i.e., the diagnosis prevalences differ significantly between the two samples.

Discussion and conclusion

While the GPs’ diagnoses reflect the most frequent reasons for consultations, claims data also include prescriptions from outside primary care. Both data sources must be used in a complementary manner. Claims data should be used to analyze morbidity and medication use in a population. To gain a deeper understanding of the care situation, the data generated by GPs should be used. Particularly in times of GP shortages, when it is necessary to think about alternative or advanced forms of primary care, a detailed analysis of the care needs and care situations of the affected patient groups is necessary. Efforts in this direction should be supported.
简介:在瑞士,没有义务记录门诊诊断。PraxisGruppe Schweiz (PraxiS)是一个由大约30个全科医生和专家诊所组成的网络,主要分布在瑞士的农村德语地区,该网络使用ICD-10分类系统为每位患者分配诊断代码和咨询。我们将这些诊断与近似的诊断进行比较,即所谓的药物成本组(pcg),基于SWICA健康保险的索赔数据。我们怀疑两个样本之间的诊断分布有显著差异。方法:使用PraxiS数据库识别在2020年至2022年期间至少咨询过一次SWICA保险的患者。索赔数据确定了在同一时期至少与PraxiS网络临床医生进行过一次咨询的患者。分析诊断(ICD-10),并报告每个年龄组最常见的10种诊断。计算每个患者和年龄组的咨询次数。PCG信息来自根据瑞士官方风险均衡定义的索赔数据,基于上一个观察年的规定日剂量。两样本间诊断分布差异采用Pearson χ2检验。结果:高胆固醇、高血压、糖尿病和抑郁症是两个数据来源中最常见的诊断记录。此外,急性事件(例如,上呼吸道感染)和非特异性症状或问题在初级保健中经常发生,无法明确地归属于某种诊断,而甲状腺疾病、哮喘/慢性阻塞性肺病和青光眼更常记录在索赔数据中,因为它们与定期服药有关。对于32例PCG诊断中的6例,我们拒绝了相同分布的零假设,即两个样本之间的诊断患病率存在显着差异。讨论和结论:虽然全科医生的诊断反映了最常见的咨询原因,但索赔数据也包括来自初级保健以外的处方。这两个数据源必须以互补的方式使用。索赔数据应用于分析人群中的发病率和药物使用情况。为了更深入地了解护理情况,应使用全科医生生成的数据。特别是在全科医生短缺的时候,当有必要考虑替代或高级形式的初级保健时,对受影响患者群体的护理需求和护理情况的详细分析是必要的。应该支持这方面的努力。
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引用次数: 0
Qualitätsindikatoren aus der S3-Leitlinie Palliativmedizin für Patient*innen mit einer nicht-heilbaren Krebserkrankung: Identifikation von Dokumentationsprozessen, Datenquellen und Herausforderungen auf Palliativstationen [S3指南对不治之症患者姑息治疗的质量指标:确定姑息治疗单位的文件编制过程、数据来源和挑战]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2026-01-12 DOI: 10.1016/j.zefq.2025.10.009
Alexandra Glizner , Franziska Schade , Hannah Verena Frerichs, Stephanie Stiel, Katharina van Baal

Background

Routine documentation in inpatient palliative care units takes up a significant amount of caregivers’ workload, but at the same time offers many opportunities for data use, e.g. for quality assurance. The S3 guideline on palliative medicine formulates eleven quality indicators (QIs). It is currently unknown how or to what extent QIs are documented on palliative care units.

Method

Semi-structured planning interviews were conducted at seven palliative care units in the catchment area of the Comprehensive Cancer Center of Lower Saxony to determine the extent to which routine documentation contains data sources for measuring ten of the eleven QIs. The documentation systems, data sources and assessments used were recorded and compared with regard to the individual QIs of the S3 guideline on palliative medicine, at the same time identifying challenges in documentation.

Results

There is no explicit documentation of all QIs across palliative care units, and the fulfilment of QIs can only be determined secondarily from routine documentation. For all seven palliative care units, the data sources are the baseline palliative care assessment, assessments such as MIDOS, IPOS or individual instruments, the progress documentation in text form and the letter from the attending physician. Challenges regarding documentation include duplicate documentation of content, technical difficulties, and inconsistent documentation procedures of different caregivers.

Discussion

Routine documentation in palliative care units is heterogeneous. To determine compliance with the ten QIs, different data sources must be used for each palliative care unit, which makes comparisons between palliative care units difficult. The challenges mentioned above influence the use of data for scientific purposes. In research projects, sufficient time should be allowed for the use of pseudonymised secondary data, in particular to enable data protection coordination.

Conclusion

Documentation in palliative care units provides important data sources for measuring QIs, and at the same time, scientific analysis is subject to many limitations. Further research is needed to identify which aspects can motivate the implementation and systematic documentation of QIs.
背景:住院姑息治疗单位的常规文件占用了大量护理人员的工作量,但同时也为数据使用提供了许多机会,例如质量保证。S3姑息医学指南制定了11个质量指标。目前尚不清楚如何或在多大程度上在姑息治疗单位记录QIs。方法:在下萨克森州综合癌症中心集水区的七个姑息治疗单位进行半结构化计划访谈,以确定常规文件包含测量11个QIs中的10个的数据源的程度。记录使用的文件系统、数据来源和评估,并与S3姑息医学指南的单个QIs进行比较,同时确定文件方面的挑战。结果:姑息治疗单位没有明确的质量指标文件,质量指标的实现只能从常规文件中确定。对于所有七个姑息治疗单位,数据来源是基线姑息治疗评估、MIDOS、IPOS或个人仪器等评估、文本形式的进展文件和主治医生的信函。文档方面的挑战包括内容的重复文档、技术困难以及不同护理人员的不一致文档程序。讨论:姑息治疗单位的常规文件是异质的。为了确定对十个质量指标的依从性,每个姑息治疗单位必须使用不同的数据源,这使得姑息治疗单位之间的比较变得困难。上述挑战影响到为科学目的使用数据。在研究项目中,应该有足够的时间来使用假名化的次要数据,特别是为了实现数据保护协调。结论:姑息治疗单位文献资料为量化QIs提供了重要的数据来源,但科学分析存在诸多局限性。需要进一步的研究来确定哪些方面可以激励QIs的实施和系统的文档。
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引用次数: 0
Dank an die Gutachter*innen des Jahres 2025 感谢2025年的评估师
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2026-02-09 DOI: 10.1016/j.zefq.2026.01.003
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引用次数: 0
Delegation ärztlicher Aufgaben an nichtärztliche Mitarbeitende: qualitative Analyse von Erfahrungen im Rahmen der DELIVER-CARE Studie [将临床任务委托给医疗实践助理:对DELIVER CARE研究经验的定性分析]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2025-11-19 DOI: 10.1016/j.zefq.2025.10.006
Kathrin Damm , Juliana Hoeper , Maike Kriependorf , Lukas Noll , Torsten Witte , Kirsten Hoeper

Background

The primary objective of the DELIVER-CARE study was to evaluate a generic model for the delegation of clinical tasks to medical practice assistants (MPAs) in the outpatient treatment of chronic inflammatory diseases in the form of an MPA consultation. In addition to proving that the model is not inferior to standard care, permanent implementation also requires a positive evaluation by those involved and knowledge of the barriers and success factors. Therefore, the aim of this study was to investigate the perspectives of those involved from the specialist fields of rheumatology, gastroenterology, and dermatology on the delegation of medical activities to MPAs and to identify both success factors and barriers to transferring the model to standard care. The focus here will be on the experience of setting up and running an MPA consultation.

Material and methods

Qualitative, semi-structured guided interviews were conducted with doctors, medical assistants and patients in the fields of rheumatology, gastroenterology, and dermatology (convenience sample). Qualitative content analysis of interview transcripts was used.

Results

In 2022, 61 interviews were conducted with physicians (n = 21), medical assistants (n = 18), and patients (n = 22). In addition to the general willingness expressed by the majority of participants to continue using the delegation or MPA consultation model, aspects from the following areas were identified: (1) goals and motives for participating, (2) the participants’ experiences with the intervention as well as current barriers to and challenges of long-term implementation. In summary, the interviewees were mostly pleased with the model and saw advantages, such as easing the workload of doctors, appreciating the work of medical assistants, and improving patient care). However, lack of a funding concept and general staffing conditions (fluctuation, lack of specialist staff) have made it difficult to implement the model.

Discussion

Considering the shortage of medical resources, MPA visits can be a key element in the transformation of outpatient care. However, further research and discussion is needed to specify the delegation model before it can be permanently integrated into standard care (i. e., regarding the mandatory face-to-face encounter between doctors and patients, remuneration for services, and the competency framework for medical assistants).
背景:DELIVER-CARE研究的主要目的是评估在门诊治疗慢性炎症性疾病时,以MPA会诊的形式将临床任务委托给医疗实践助理(MPA)的通用模型。除了证明该模式不逊色于标准护理之外,永久实施还需要参与者的积极评价,以及对障碍和成功因素的了解。因此,本研究的目的是调查风湿病学、胃肠病学和皮肤病学等专业领域的相关人员对将医疗活动委托给mpa的看法,并确定将该模式转移到标准护理的成功因素和障碍。这里的重点将是建立和运行MPA咨询的经验。材料和方法:对风湿病学、胃肠病学和皮肤病学领域的医生、医疗助理和患者(方便样本)进行定性、半结构化的引导访谈。对访谈笔录进行定性内容分析。结果:2022年共对医生(n = 21)、医疗助理(n = 18)和患者(n = 22)进行了61次访谈。除了大多数参与者普遍表示愿意继续使用委托或MPA咨询模式外,还确定了以下方面:(1)参与的目标和动机;(2)参与者的干预经验以及目前长期实施的障碍和挑战。综上所述,受访者大多对这种模式感到满意,并看到了优点(如减轻了医生的工作量,赞赏了医疗助理的工作,改善了病人的护理)。然而,由于缺乏筹资概念和一般的人员配置条件(波动、缺乏专业工作人员),使该模式难以实施。讨论:考虑到医疗资源的短缺,MPA访问可以成为门诊护理转型的关键因素。然而,在将授权模式永久纳入标准护理(即关于医生和病人之间的强制性面对面接触、服务报酬和医疗助理的能力框架)之前,需要进一步研究和讨论以具体说明授权模式。
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引用次数: 0
Mehr Patientensicherheit durch mehr-patientensicherheit.de – Wie ein neues Portal die Patientenperspektive stärkt 通过meh -patientensicherheit.de提高患者安全?新平台如何加强患者视角]。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2025-12-16 DOI: 10.1016/j.zefq.2025.11.002
Clara Monaca , Saskia Huckels-Baumgart , Marcus Rall

Background

The active involvement of patients is considered a key factor in improving patient safety. With the model project Mehr Patientensicherheit, Germany has, for the first time, implemented a Critical Incident Reporting System (CIRS) specifically for patients and their relatives, enabling the anonymous reporting of patient safety events. This study aimed to analyze the demographic characteristics of reporters, assess their evaluations of information status, severity, and recurrence risk of incidents, test hypotheses regarding potential influencing factors, and derive implications for the further development of the platform.

Methods

A cross-sectional observational study analyzed 1,390 reports submitted via the online platform www.mehr-patientensicherheit.de between January and October 2024. Data were collected anonymously using a structured questionnaire containing open-ended and closed-ended items. Descriptive analyses, chi-square tests, and Mann–Whitney U tests were applied.

Results

Of all reports, 73 % originated directly from patients, while 24.4 % were submitted by relatives reporting on behalf of patients. The majority of reports concerned female patients (62.2 %). Age distribution was as follows: >80 years (9.9 %), 70–79 years (12.4 %), 50–69 years (32.1 %), 30–49 years (29.1 %), 15–29 years (10.8 %), and <15 years (4.2 %). The majority of the incidents were reported from ambulatory and in-patient care settings. Overall, 71 % of reports indicated insufficient information regarding patient safety measures.

Discussion

The findings demonstrate that patients can actively contribute to patient safety. The reports submitted provide novel insights into subjectively perceived risks, thereby complementing existing reporting systems with a previously underrepresented perspective. At the same time, the results highlight structural deficiencies, particularly in communication and feedback processes following serious incidents.

Conclusion

The patient-centered CIRS has the potential to foster cross-sector learning and advance the development of patient safety culture. The systematic inclusion of the patient perspective and the institutionalization of the system should be actively encouraged.
背景:患者的积极参与被认为是提高患者安全的关键因素。通过“Mehr Patientensicherheit”模型项目,德国首次实施了专门针对患者及其亲属的关键事件报告系统(CIRS),使患者安全事件能够匿名报告。本研究旨在分析记者的人口统计学特征,评估他们对信息状况、严重程度和事件复发风险的评估,检验有关潜在影响因素的假设,并得出平台进一步发展的启示。方法:一项横断面观察研究分析了2024年1月至10月期间通过在线平台www.mehr-patientensicherheit.de提交的1390份报告。数据匿名收集使用结构化问卷,包括开放式和封闭式项目。采用描述性分析、卡方检验和Mann-Whitney U检验。结果:在所有报告中,73% %直接来自患者,24.4% %由亲属代表患者报告。大多数报告涉及女性患者(62.2% %)。年龄分布如下:bb0 ~ 80岁(9.9 %),70 ~ 79岁(12.4 %),50 ~ 69岁(32.1 %),30 ~ 49岁(29.1 %),15 ~ 29岁(10.8 %),讨论:研究结果表明患者可以积极为患者安全做出贡献。所提交的报告对主观感知的风险提供了新的见解,从而补充了现有的报告制度和以前代表性不足的观点。与此同时,调查结果突出了结构性缺陷,特别是在严重事件发生后的沟通和反馈过程中。结论:以患者为中心的CIRS具有促进跨部门学习和促进患者安全文化发展的潜力。应积极鼓励系统地纳入患者观点,并使该制度制度化。
{"title":"Mehr Patientensicherheit durch mehr-patientensicherheit.de – Wie ein neues Portal die Patientenperspektive stärkt","authors":"Clara Monaca ,&nbsp;Saskia Huckels-Baumgart ,&nbsp;Marcus Rall","doi":"10.1016/j.zefq.2025.11.002","DOIUrl":"10.1016/j.zefq.2025.11.002","url":null,"abstract":"<div><h3>Background</h3><div>The active involvement of patients is considered a key factor in improving patient safety. With the model project <em>Mehr Patientensicherheit</em>, Germany has, for the first time, implemented a Critical Incident Reporting System (CIRS) specifically for patients and their relatives, enabling the anonymous reporting of patient safety events. This study aimed to analyze the demographic characteristics of reporters, assess their evaluations of information status, severity, and recurrence risk of incidents, test hypotheses regarding potential influencing factors, and derive implications for the further development of the platform.</div></div><div><h3>Methods</h3><div>A cross-sectional observational study analyzed 1,390 reports submitted via the online platform <span><span>www.mehr-patientensicherheit.de</span><svg><path></path></svg></span> between January and October 2024. Data were collected anonymously using a structured questionnaire containing open-ended and closed-ended items. Descriptive analyses, chi-square tests, and Mann–Whitney U tests were applied.</div></div><div><h3>Results</h3><div>Of all reports, 73 % originated directly from patients, while 24.4 % were submitted by relatives reporting on behalf of patients. The majority of reports concerned female patients (62.2 %). Age distribution was as follows: &gt;80 years (9.9 %), 70–79 years (12.4 %), 50–69 years (32.1 %), 30–49 years (29.1 %), 15–29 years (10.8 %), and &lt;15 years (4.2 %). The majority of the incidents were reported from ambulatory and in-patient care settings. Overall, 71 % of reports indicated insufficient information regarding patient safety measures.</div></div><div><h3>Discussion</h3><div>The findings demonstrate that patients can actively contribute to patient safety. The reports submitted provide novel insights into subjectively perceived risks, thereby complementing existing reporting systems with a previously underrepresented perspective. At the same time, the results highlight structural deficiencies, particularly in communication and feedback processes following serious incidents.</div></div><div><h3>Conclusion</h3><div>The patient-centered CIRS has the potential to foster cross-sector learning and advance the development of patient safety culture. The systematic inclusion of the patient perspective and the institutionalization of the system should be actively encouraged.</div></div>","PeriodicalId":46628,"journal":{"name":"Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen","volume":"200 ","pages":"Pages 21-30"},"PeriodicalIF":1.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145776088","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
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 : 2026-02-01 Epub 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。
{"title":"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","authors":"Susan Raths,&nbsp;Steffen Flessa","doi":"10.1016/j.zefq.2025.11.001","DOIUrl":"10.1016/j.zefq.2025.11.001","url":null,"abstract":"<div><h3>Objective</h3><div>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.</div></div><div><h3>Methods</h3><div>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.</div></div><div><h3>Results</h3><div>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.</div></div><div><h3>Discussion</h3><div>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.</div></div><div><h3>Conclusion</h3><div>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.</div></div>","PeriodicalId":46628,"journal":{"name":"Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen","volume":"200 ","pages":"Pages 83-93"},"PeriodicalIF":1.7,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145678855","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
Practice test of the German S3 guideline “Thyroid Nodules in Adults in General Practice”: Evaluating feasibility, comprehensibility, and acceptance 德国S3指南“成人甲状腺结节全科治疗”的实践试验:评估可行性、可理解性和可接受性。
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2025-11-13 DOI: 10.1016/j.zefq.2025.10.007
Victoria Kyriacou , Karola Mergenthal , Corina Güthlin , Ferdinand M. Gerlach , Marjan van den Akker , Sandra Salm

Background

Thyroid nodules are commonly discovered incidentally during routine examinations in general practice, which often leads to extensive diagnostics and overtreatment. To provide general practitioners (GPs) with evidence-based guidance on the diagnosis and management of thyroid nodules, the S3 guideline “Thyroid Nodules in Adults” by the German Society for General and Family Medicine (DEGAM) was developed in three versions: a short, a long, and a patient leaflet format. An assessment of the effectiveness of the guideline in general practice was undertaken.

Methods

We ran a practice test in 17 general practices, yielding data from 17 GPs and 94 patients. Quantitative data were collected using documentation forms and questionnaires for GPs and patients. Two semi-structured online workshops provided qualitative data. Data were analyzed using descriptive statistics and qualitative content analysis.

Results

About 50 % of GPs reported modifying their diagnostic methods, while therapy adjustments were reported in 21 % of the consultations. The patient leaflet received positive feedback from patients and GPs, but both groups requested more detailed content. The workshops revealed challenges, including limited consultation time, difficulties in explaining extended follow-up intervals to patients, and differences in approaches between primary care and specialist services.

Discussion

The guideline proved applicable in practice. The feedback served ongoing improvements, including plans for supportive tools like conversation guides, case examples, and training materials.

Conclusion

The practice test showed the level of guideline comprehensibility and acceptance in general practice, highlighting areas of improvement. These include clearer communication with patients, interprofessional alignment and modification of materials according to patient requirements.
背景:甲状腺结节通常是在常规检查中偶然发现的,这往往导致广泛的诊断和过度治疗。为了向全科医生(gp)提供甲状腺结节诊断和管理的循证指导,德国全科和家庭医学学会(DEGAM)制定了S3指南“成人甲状腺结节”,分为三个版本:短版本、长版本和患者传单格式。对该指南在一般实践中的有效性进行了评估。方法:我们在17个全科医生中进行了实践测试,获得了来自17名全科医生和94名患者的数据。通过对全科医生和患者的文件表格和问卷调查收集定量数据。两个半结构化的在线研讨会提供了定性数据。数据分析采用描述性统计和定性内容分析。结果:约50% %的全科医生报告修改了他们的诊断方法,而21% %的咨询报告了治疗调整。患者传单得到了患者和全科医生的积极反馈,但两组都要求更详细的内容。讲习班揭示了挑战,包括有限的咨询时间,向患者解释延长随访间隔的困难,以及初级保健和专科服务之间方法的差异。讨论:该指南在实践中被证明是适用的。反馈服务于持续的改进,包括支持性工具的计划,如对话指南、案例示例和培训材料。结论:实践测试显示了指南在全科实践中的可理解性和可接受性水平,突出了改进的领域。这些包括与患者更清晰的沟通,专业间的协调和根据患者的要求修改材料。
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引用次数: 0
The problem with PPI is … it keeps needing another ‘P’… PPI的问题是……它总是需要另一个“P”....
IF 1.7 Q4 HEALTH POLICY & SERVICES Pub Date : 2026-02-01 Epub Date: 2025-12-16 DOI: 10.1016/j.zefq.2025.11.006
David Jackson-Perry , David Haerry
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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 : 2026-02-01 Epub Date: 2026-03-02 DOI: 10.1016/S1865-9217(26)00028-0
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引用次数: 0
Wie digital ist meine Praxis? Einstellungen von Hausärztinnen und Hausärzten gegenüber Reifegradmessungen – eine Online-Umfrage 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 : 2026-02-01 Epub 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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Zeitschrift fur Evidenz Fortbildung und Qualitaet im Gesundheitswesen
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