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Evaluating the effectiveness of AI-enhanced "One Body, Two Wings" pharmacovigilance models in China: a nationwide survey on medication safety and risk management. 评估人工智能增强的“一体两翼”药物警戒模式在中国的有效性:一项关于药物安全和风险管理的全国性调查。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-08 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1655726
Jian Yang, Yi Sun, Fan Li, Quanzhi Wei, Jincui Wei, Yingxiong Zhang

Background: This study evaluates the effectiveness of AI-enhanced "One Body Two Wings" pharmacovigilance models in China, focusing on improving medication safety and risk management. As the pharmaceutical landscape grows more complex, integrating AI into pharmacovigilance offers the potential to enhance adverse drug reaction (ADR) detection and monitoring.

Methods: A nationwide cross-sectional survey was conducted from June 25 to August 10, 2024, involving 1,000 participants from pharmacovigilance centers, hospitals, corporations, and the general public. Participants were recruited through stratified convenience sampling to ensure a broad geographical and professional representation. Data were collected through a validated questionnaire and analyzed using ANOVA, regression analysis, decision tree models, and random forest algorithms. To ensure the validity of the predictive models, resampling (SMOTE) and class weighting techniques were employed to address significant class imbalance in the outcome variable.

Results: The survey revealed that 43% of participants were hospital staff and 46% had more than 10 years of experience, with these expert groups expressing strong support for AI's role. Path analysis indicated that AI's effectiveness in processing ADR reports was strongly related to enhanced monitoring capabilities (standardized path coefficient: 0.85). Furthermore, logistic regression identified the perceived effectiveness of information systems as a significant predictor of positive attitudes toward the model (odds ratio: 1.703). Crucially, a random forest model, adjusted for class imbalance, confirmed that information systems effectiveness was the most significant predictor of the model's success (mean importance: 0.53 ± 0.05), achieving robust performance with a weighted F1-score of 0.94 and an AUC-ROC of 0.89.

Conclusion: The findings confirm AI's potential to enhance pharmacovigilance, especially in ADR monitoring. However, the study concludes that successful AI integration is predicated on a robust information systems infrastructure, which the data identified as the most critical foundational element. Therefore, optimizing pharmacovigilance in China requires prioritized investment in both this foundational IT and supportive organizational frameworks.

背景:本研究评估了人工智能增强的“一体两翼”药物警戒模型在中国的有效性,重点是改善用药安全和风险管理。随着制药领域变得越来越复杂,将人工智能整合到药物警戒中,有可能加强药物不良反应(ADR)的检测和监测。方法:于2024年6月25日至8月10日在全国范围内进行横断面调查,涉及来自药物警戒中心、医院、企业和公众的1000名参与者。参与者通过分层方便抽样招募,以确保广泛的地理和专业代表性。通过有效的问卷收集数据,并使用方差分析、回归分析、决策树模型和随机森林算法进行分析。为了确保预测模型的有效性,采用重采样(SMOTE)和类别加权技术来解决结果变量中显著的类别不平衡。结果:调查显示,43%的参与者是医院工作人员,46%的人有10年以上的工作经验,这些专家组对人工智能的作用表示强烈支持。通径分析表明,人工智能处理ADR报告的有效性与监测能力的增强密切相关(标准化通径系数:0.85)。此外,逻辑回归确定信息系统的感知有效性是对模型的积极态度的重要预测因子(优势比:1.703)。至关重要的是,一个随机森林模型,调整了班级不平衡,证实了信息系统有效性是模型成功的最显著预测因子(平均重要性:0.53±0.05),获得了加权f1得分0.94和AUC-ROC 0.89的稳健表现。结论:研究结果证实了人工智能在提高药物警戒方面的潜力,特别是在不良反应监测方面。然而,该研究得出的结论是,成功的人工智能集成是基于强大的信息系统基础设施的,数据认为这是最关键的基础要素。因此,优化中国的药物警戒需要优先投资于这一基础信息技术和支持性组织框架。
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引用次数: 0
Use of organizational change strategies and personalized agency feedback improves addressing tobacco in behavioral health outpatient treatment settings. 使用组织变革战略和个性化机构反馈可以改善行为健康门诊治疗设置中的烟草问题。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-07 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1587795
Douglas Ziedonis, Robert A Schnoll, Orrin Myers, Thomas Anthony Chavez, Amy Bachyrycz, Cesar J Ojeda, Frank T Leone, Mackenzie Hosie Quinn, Prajakta Adsul

Introduction: Implementing evidence-based interventions for tobacco use disorder (TUD) in community mental health agencies is critical, given the low adoption rates of these interventions and the high rates of TUD among patients, contributing to the high morbidity and shortened lifespan of this population. Implementation efforts require enhancing organizational preparedness to integrate these evidence-based interventions.

Purpose: When the Addressing Tobacco Through Organizational Change (ATTOC) model was evaluated in a cluster-randomized trial (with 13 clinics, 610 clients, and 222 staff) and compared with an education-only intervention, ATTOC proved to be better at having more TUD treatment, policies, and staff skills. This paper presents a secondary analysis focusing only on the ATTOC sites, examining whether clinic-level preparedness is associated with increased implementation activities and estimating the combined direct and indirect impact on patient referrals to evidence-based TUD interventions.

Methods: Seven sites applied the ATTOC model over 9 months, with the ATTOC Environmental Scan (ES) conducted at baseline and 3, 6, and 9 months to assess the following: (1) the environment inside and outside the building, (2) staff training and personal tobacco use, (3) clinical TUD services and documentation, and (4) tobacco policies. Summary statistics are provided, and generalized linear mixed model analyses for repeated measures were used to assess time trends and relationships among composite preparedness, activities, and number of referrals.

Results: Over the 9-month period, significant improvements were observed in ES composite preparedness (p < 0.001) and individual ES areas (p < 0.001 for each). Eight out of 11 ATTOC Dashboard items showed significant changes, including increased number of patients treated (p = 0.002); tobacco discussions (p = 0.022); provision of educational brochures (p = 0.034); referrals to a Nicotine Anonymous group (p < 0.001), an in-house wellness or tobacco group (p < 0.001), and state quitline (p = 0.012); and documentation in treatment plans (p = 0.008). Both composite preparedness (p = 0.006) and composite activities (p < 0.001) were significantly associated with the number of composite referrals.

Conclusion: Significant TUD intervention uptake was found over time through the ATTOC model organizational change intervention and tracking tools.

在社区精神卫生机构实施基于证据的烟草使用障碍(TUD)干预措施至关重要,因为这些干预措施的采用率低,而患者中TUD的发生率高,导致这一人群的高发病率和寿命缩短。实施工作需要加强组织准备,以整合这些以证据为基础的干预措施。目的:通过组织变革解决烟草问题(ATTOC)模型在一项集群随机试验(13家诊所,610名客户和222名工作人员)中进行评估,并与仅进行教育干预相比,ATTOC在更多的TUD治疗、政策和工作人员技能方面表现更好。本文提出了一项仅关注ATTOC站点的二次分析,检查临床水平的准备是否与增加的实施活动有关,并估计对患者转诊到循证TUD干预措施的直接和间接综合影响。方法:七个站点在9个月内应用了ATTOC模型,并在基线和第3、6和9个月进行了ATTOC环境扫描(ES),以评估以下内容:(1)建筑物内外环境,(2)员工培训和个人吸烟情况,(3)临床TUD服务和文件,以及(4)烟草政策。提供了汇总统计数据,并使用重复测量的广义线性混合模型分析来评估复合准备,活动和转诊数量之间的时间趋势和关系。结果:在9个月的时间里,观察到ES复合准备的显著改善(p p p = 0.002);烟草讨论(p = 0.022);提供教育小册子(p = 0.034);转介到尼古丁匿名小组(p p p = 0.012);治疗方案的记录(p = 0.008)。结论:通过ATTOC模型、组织变革干预和跟踪工具,随着时间的推移,发现显著的TUD干预吸收。
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引用次数: 0
Working in partnership with people from under-represented groups to develop person-centred social and health care practices: methodological insights from the CICADA study. 与代表性不足的群体合作,发展以人为本的社会和保健做法:来自CICADA研究的方法见解。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-07 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1563354
Carol Rivas, Amanda P Moore, Kusha Anand, Feryal Awan, Samina Begum, Neelam Heera, Sarabajaya Kumar, Sudhir Shah, Yesmin Shahid, Alison Thomson
<p><strong>Introduction: </strong>The COVID-19 pandemic both exposed and exacerbated the multiple pre-existing societal inequities for disabled people and those from minoritised ethnic groups in the UK, especially those who were on temporary visas, or were asylum seekers or undocumented migrants. Inequities in their health and social care were marked and poorly managed. Therefore, within the mixed-methods CICADA study, we explored their person-centred health and social care, with the primary aim of making recommendations for its improvement, focusing on the intersection of ethnicity, disability, and citizenship status. We used embodiment models of disability with an assets/strengths-based approach to develop useful person-centred solutions to issues. Person-centred care prioritises individuals' diverse contexts and their inclusion in care decisions, thus its improvement is particularly suited to participatory research methods which formed a substantial component of the CICADA study; this alignment is the paper's focus as a methodological discussion.</p><p><strong>Methods: </strong>Within the qualitative strand of the study, the topic of this paper, one aim was to explore the effectiveness of different types of collaborative approaches in successfully including recent migrants. Co-researchers from minoritised communities worked autonomously alongside the central team to conduct semi-structured interviews across England. Two community groups, working independently in parallel, interviewed further participants, produced autonomous reports, and helped practically. The study's public advisory group (PAG) joined the co-researcher team to facilitate knowledge exchange workshops (to develop mutual understanding) and mixed patient-professional co-design sessions (for patient-centred outputs and interventions).</p><p><strong>Results: </strong>The mix of different participatory methods proved an effective research approach and enabled the involvement of undocumented migrants and those of precarious migration status who would be excluded by other approaches. We were able to show, for example, how recent and undocumented migrants navigated UK healthcare systems with difficulty, meeting systemic cultural, bureaucratic and socioeconomic barriers that led to patient-provider misalignment rather than person-centred care. Co-design workshops produced collaboratively designed solutions, including improved communication strategies.</p><p><strong>Discussion: </strong>The CICADA study underscored the importance of participatory methods in developing more person-centred care, by addressing structural inequities in research involvement that mirror those within health and social care services. It also showed the significance of choosing different participatory approaches depending on the specific needs, and some issues with their use in practice. Institutional constraints, such as funding and bureaucratic barriers, and time limitations, posed challenges to fully realisin
2019冠状病毒病大流行暴露并加剧了英国残疾人和少数族裔群体,特别是那些持有临时签证、寻求庇护者或无证移民的社会不平等现象。他们的健康和社会护理方面存在明显的不平等现象,而且管理不善。因此,在混合方法CICADA研究中,我们探讨了他们以人为本的健康和社会护理,主要目的是提出改进建议,重点关注种族、残疾和公民身份的交集。我们使用残疾的体现模型和基于资产/优势的方法来开发有用的以人为本的问题解决方案。以人为本的护理优先考虑个人的不同背景及其在护理决策中的纳入,因此其改进特别适合于构成CICADA研究实质性组成部分的参与性研究方法;这种一致性是本文作为方法论讨论的重点。方法:在研究的定性链中,本文的主题之一是探索不同类型的合作方法在成功纳入新移民方面的有效性。来自少数民族社区的共同研究人员与中央团队一起自主工作,在英格兰各地进行半结构化访谈。两个社区团体并行地独立工作,采访了更多的参与者,编写了自主报告,并提供了实际帮助。该研究的公共咨询小组(PAG)加入了联合研究小组,以促进知识交流研讨会(以发展相互理解)和混合患者-专业人员共同设计会议(以患者为中心的产出和干预措施)。结果:不同参与方法的混合证明是一种有效的研究方法,并使无证移民和不稳定移民身份的人能够参与进来,而其他方法将把他们排除在外。例如,我们能够展示最近和无证移民如何难以驾驭英国医疗保健系统,遇到系统性文化,官僚主义和社会经济障碍,导致患者-提供者错位,而不是以人为本的护理。共同设计研讨会产生了协作设计的解决方案,包括改进的沟通策略。讨论:CICADA的研究强调了参与式方法在发展更加以人为本的护理方面的重要性,方法是解决研究参与方面的结构性不平等,这种不平等反映了保健和社会护理服务中的不平等。它还显示了根据具体需要选择不同参与性方法的重要性,以及在实践中使用这些方法的一些问题。资金和官僚障碍等体制限制以及时间限制对充分实现公平参与构成挑战。该研究有助于讨论参与式方法的严谨性和可扩展性,以及对更具包容性、与文化相适应和以人为本的护理系统的影响,以及对个体患者与医生互动的影响。结论:通过将参与式方法与基于交叉资产的方法相结合,CICADA研究推进了以人为本的护理研究,并倡导进行系统性变革,以加强对少数群体的研究和护理。
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引用次数: 0
The real experience of nurse role reconstruction under the implementation of the no-attendant care policy in Shanghai hospitals: a qualitative study. 上海医院实施无陪护政策下护士角色重构的真实经验:一项质的研究。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-03 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1663682
Yuhan Cheng, Sibei Wan, Yifan Jiang, Yi Sheng, Qian Wu, Yan Shi, Li Wang

Objective: To explore nurse role reconstruction under the implementation of no-attendant care services in Shanghai hospitals, and to identify challenges and strategies for optimization.

Methods: A phenomenological qualitative design was adopted. From June 1 to July 1, 2025, semi-structured face-to-face interviews were conducted with 14 registered nurses from no-attendant care wards in three tertiary hospitals in Shanghai. Data were transcribed verbatim and analyzed using Colaizzi's seven-step method. Two researchers independently coded, discrepancies were resolved through discussion and methodological arbitration, and results were validated through member checking to ensure rigor.

Results: Four main themes and eleven subthemes were extracted: (1) Expanded Responsibilities and Intensified Workload: Significant Increase in Work Intensity; New Challenges in Professional Competence; Multidimensional Accumulation of Occupational Stress. (2) Positive Impacts on Patients and Families: Effective Relief of Family Care Burden; Enhanced Perceived Value of High-Quality Nursing. (3) Challenges in the Implementation Process: Blind Spots in Patient Safety Management; Need to Improve Nurse-Patient Communication Efficiency; Inadequate Mechanisms for Accountability. (4) Optimization Strategies: Establish a Legal Safeguard System; Improve Insurance Payment Coordination Mechanism; Strengthen Training Mechanisms for Nursing Assistants. A few minority or dissenting perspectives were incorporated as contextual modifiers.

Conclusion: No-attendant care improves patient experience and alleviates family caregiving burden, but simultaneously places heavier physical, risk, and relational demands on nurses, highlighting the complexity of role reconstruction. This study demonstrates the essential features of nurses' lived experiences under this model and emphasizes the need for systemic support, such as legal frameworks, insurance coverage, and workforce training, to optimize care delivery and sustain professional resilience.

目的:探讨上海医院实施无陪护服务下的护士角色重构,并找出优化挑战和策略。方法:采用现象学定性设计。于2025年6月1日至7月1日,对上海三所三级医院无护理病房的14名注册护士进行半结构化面对面访谈。数据逐字记录,并使用Colaizzi的七步法进行分析。两位研究人员独立编码,通过讨论和方法仲裁解决差异,并通过成员检查验证结果以确保严谨性。结果:提取出4个主旋律和11个副旋律:(1)职责扩大、工作量加大:工作强度显著增加;专业能力面临的新挑战职业压力的多维累积。(2)对患者和家庭的积极影响:有效减轻家庭护理负担;提高高质量护理的感知价值。(3)实施过程中的挑战:患者安全管理的盲点;提高护患沟通效率的必要性问责机制不足。(4)优化策略:建立法律保障体系;完善保险支付协调机制;强化护理员培训机制。少数少数或反对的观点被纳入上下文修饰语。结论:无护理改善了患者体验,减轻了家庭护理负担,但同时加重了护士的身体、风险和关系需求,凸显了角色重构的复杂性。本研究展示了该模式下护士生活经历的基本特征,并强调需要系统支持,如法律框架、保险覆盖和劳动力培训,以优化护理服务和维持专业弹性。
{"title":"The real experience of nurse role reconstruction under the implementation of the no-attendant care policy in Shanghai hospitals: a qualitative study.","authors":"Yuhan Cheng, Sibei Wan, Yifan Jiang, Yi Sheng, Qian Wu, Yan Shi, Li Wang","doi":"10.3389/frhs.2025.1663682","DOIUrl":"10.3389/frhs.2025.1663682","url":null,"abstract":"<p><strong>Objective: </strong>To explore nurse role reconstruction under the implementation of no-attendant care services in Shanghai hospitals, and to identify challenges and strategies for optimization.</p><p><strong>Methods: </strong>A phenomenological qualitative design was adopted. From June 1 to July 1, 2025, semi-structured face-to-face interviews were conducted with 14 registered nurses from no-attendant care wards in three tertiary hospitals in Shanghai. Data were transcribed verbatim and analyzed using Colaizzi's seven-step method. Two researchers independently coded, discrepancies were resolved through discussion and methodological arbitration, and results were validated through member checking to ensure rigor.</p><p><strong>Results: </strong>Four main themes and eleven subthemes were extracted: (1) Expanded Responsibilities and Intensified Workload: Significant Increase in Work Intensity; New Challenges in Professional Competence; Multidimensional Accumulation of Occupational Stress. (2) Positive Impacts on Patients and Families: Effective Relief of Family Care Burden; Enhanced Perceived Value of High-Quality Nursing. (3) Challenges in the Implementation Process: Blind Spots in Patient Safety Management; Need to Improve Nurse-Patient Communication Efficiency; Inadequate Mechanisms for Accountability. (4) Optimization Strategies: Establish a Legal Safeguard System; Improve Insurance Payment Coordination Mechanism; Strengthen Training Mechanisms for Nursing Assistants. A few minority or dissenting perspectives were incorporated as contextual modifiers.</p><p><strong>Conclusion: </strong>No-attendant care improves patient experience and alleviates family caregiving burden, but simultaneously places heavier physical, risk, and relational demands on nurses, highlighting the complexity of role reconstruction. This study demonstrates the essential features of nurses' lived experiences under this model and emphasizes the need for systemic support, such as legal frameworks, insurance coverage, and workforce training, to optimize care delivery and sustain professional resilience.</p>","PeriodicalId":73088,"journal":{"name":"Frontiers in health services","volume":"5 ","pages":"1663682"},"PeriodicalIF":2.7,"publicationDate":"2025-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12531242/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145330978","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Impact analysis of DRG payment reform on hospitalization expenses and length of stay for lung cancer inpatients (2019-2023). DRG支付改革对2019-2023年肺癌住院患者住院费用和住院时间的影响分析
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-03 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1661995
Mingbo Chen, Dongfeng Pan, Ting Pan, Zhuo Liu, Yuhui Geng, Xiaojuan Ma, Peifeng Liang

Objective: Globally adopted as a contemporary hospital management methodology, DRG payment systems aim to improve cost-efficiency, advance clinical service quality, and maintain treatment safety. Through empirical analysis of lung cancer inpatient data, this study quantifies the policy's effects on medical expenditure patterns and efficiency metrics, offering evidence-based insights for optimizing healthcare resource management.

Methods: Using ITS analysis, we developed a segmented regression model to evaluate the longitudinal effects of DRG-based payment reform on healthcare expenditure and LOS for lung cancer patients at a regional tertiary hospital in Northwest China.

Results: The analytical cohort comprised 1,076 consecutively admitted lung cancer patients. ITS analysis revealed: (1) No significant immediate changes in total hospitalization costs (β 2 = -1,365.532, P = 0.684), treatment expenses [(β 2 = +147.512, P = 0.524)], or LOS [(β 2 = -0.104 days, P = 0.944)], with stable longitudinal trends post-implementation; (2) Material expenses showed no reduction [(β 2 = -1,433.072, P = 0.426)]; (3) Diagnosis expenses exhibited a significant immediate increase [(β 2 = +1,953.740, P < 0.001)] and progressive monthly escalation [(β 3 = +72.184, P = 0.035)], while drug costs showed a pronounced policy-induced surge [(β 2 = +4,963.668, P < 0.001)] with accelerated growth [(β 3 =+147.378 per month, P = 0.001)].

Conclusion: While DRG reform serves as an essential resource allocation mechanism, our findings reveal paradoxical outcomes. The implementation showed limited efficacy in reducing aggregate costs and LOS while provoking structural cost shifts marked by escalated diagnostic and pharmaceutical expenditures. These unintended economic consequences may distort clinical practices, potentially compromising both pharmacoeconomic efficiency and service quality.

目的:作为一种现代医院管理方法,DRG支付系统在全球范围内被采用,旨在提高成本效益,提高临床服务质量,维护治疗安全。本研究通过对肺癌住院患者数据的实证分析,量化政策对医疗支出模式和效率指标的影响,为优化医疗资源管理提供循证见解。方法:采用ITS分析方法,建立分段回归模型,对西北地区某区域性三级医院基于drg的支付改革对肺癌患者医疗费用和住院时间的纵向影响进行评价。结果:分析队列包括1076例连续入院的肺癌患者。ITS分析显示:(1)总住院费用(β 2 = -1,365.532, P = 0.684)、治疗费用[(β 2 = +147.512, P = 0.524)]、住院时间(LOS) [(β 2 = -0.104天,P = 0.944)]即刻无显著变化,实施后纵向趋势稳定;(2)材料费用没有减少[(β 2 = - 1433.072, P = 0.426)];(3)诊断费用立即显著增加[(β 2 =+ 1,953.740, P β 3 =+ 72.184, P = 0.035)],而药品费用则因政策而显著增加[(β 2 =+ 4,963.668, P β 3 =+147.378, P = 0.001)]。结论:虽然DRG改革是一种重要的资源配置机制,但我们的研究结果揭示了矛盾的结果。实施表明,在降低总成本和LOS方面效果有限,同时引发了以诊断和药品支出升级为标志的结构性成本转移。这些意想不到的经济后果可能扭曲临床实践,潜在地损害药物经济效率和服务质量。
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引用次数: 0
Standardizing patient-reported outcomes across diseases: development of a novel generic patient-reported outcome set. 标准化患者报告的结果跨越疾病:一个新的通用患者报告的结果集的发展。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-02 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1497055
Preston Long, Alize Rogge, Ann-Kristin Porth, Evelyn Gross, Liselotte Fierens, Belle H de Rooij, Nadia Kamminga, Tanja Stamm

Objectives: Patient-reported outcomes (PROs) are an essential component in the implementation of value-based health care. Up to now, no consensus exists on the appropriateness of PROs used across diseases, e.g., to allow for comparability or to assess disease impact. The aim of this study was to develop an international, multi-stakeholder consensus on a generic PRO set applicable for different stakeholders and diseases within of the Health Outcomes Observatory (H2O) project funded by the EU Innovative Medicines Initiative.

Methods: To begin, a literature review was conducted to identify the most frequently utilized generic PROs followed by a three-round Delphi consensus procedure. The resulting outcome set was then cross-referenced with disease-specific outcome sets for lung and metastatic breast cancer, diabetes, and inflammatory bowel diseases to identify overlaps and gaps. Lastly, the identified generic outcome domains were mapped to the Max Neef's human needs model to explore the degree to which the generic domains address a general concept of wellbeing.

Results: The literature search resulted in 2357 articles from which 190 PROMs and their measured domains were extracted. The Delphi consensus procedure reduced these to 10 core domains (mental, physical and social wellbeing, overall health status, fatigue, pain, sleep quality, sexuality, self-efficacy, treatment satisfaction). In comparison to the human needs model, needs such as identity and leisure were disregarded.

Conclusions: The H2O generic outcome set presents a disease-generic, domain-centered PRO framework building the groundwork for health data spaces and supporting consistency in treatment outcomes across different sites, settings, and patient populations.

目标:患者报告的结果(PROs)是实施基于价值的医疗保健的重要组成部分。到目前为止,对于跨疾病使用pro的适当性,例如允许可比性或评估疾病影响,尚未达成共识。本研究的目的是在欧盟创新药物倡议资助的健康结果观察站(H2O)项目中,就适用于不同利益相关者和疾病的通用PRO集达成国际、多利益相关者共识。方法:首先,进行文献综述,确定最常用的通用PROs,然后进行三轮德尔菲共识程序。然后将结果集与肺癌和转移性乳腺癌、糖尿病和炎症性肠病的疾病特异性结果集进行交叉对照,以确定重叠和空白。最后,将确定的通用结果域映射到Max Neef的人类需求模型中,以探索通用域在多大程度上解决了幸福的一般概念。结果:共检索到2357篇文献,提取出190个PROMs及其测量域。德尔菲共识程序将这些减少到10个核心领域(心理,身体和社会福祉,整体健康状况,疲劳,疼痛,睡眠质量,性,自我效能感,治疗满意度)。与人类需求模型相比,身份和休闲等需求被忽视了。结论:H2O通用结果集提供了一个疾病通用的、以领域为中心的PRO框架,为健康数据空间奠定了基础,并支持不同地点、环境和患者群体的治疗结果一致性。
{"title":"Standardizing patient-reported outcomes across diseases: development of a novel generic patient-reported outcome set.","authors":"Preston Long, Alize Rogge, Ann-Kristin Porth, Evelyn Gross, Liselotte Fierens, Belle H de Rooij, Nadia Kamminga, Tanja Stamm","doi":"10.3389/frhs.2025.1497055","DOIUrl":"10.3389/frhs.2025.1497055","url":null,"abstract":"<p><strong>Objectives: </strong>Patient-reported outcomes (PROs) are an essential component in the implementation of value-based health care. Up to now, no consensus exists on the appropriateness of PROs used across diseases, e.g., to allow for comparability or to assess disease impact. The aim of this study was to develop an international, multi-stakeholder consensus on a generic PRO set applicable for different stakeholders and diseases within of the Health Outcomes Observatory (H2O) project funded by the EU Innovative Medicines Initiative.</p><p><strong>Methods: </strong>To begin, a literature review was conducted to identify the most frequently utilized generic PROs followed by a three-round Delphi consensus procedure. The resulting outcome set was then cross-referenced with disease-specific outcome sets for lung and metastatic breast cancer, diabetes, and inflammatory bowel diseases to identify overlaps and gaps. Lastly, the identified generic outcome domains were mapped to the Max Neef's human needs model to explore the degree to which the generic domains address a general concept of wellbeing.</p><p><strong>Results: </strong>The literature search resulted in 2357 articles from which 190 PROMs and their measured domains were extracted. The Delphi consensus procedure reduced these to 10 core domains (mental, physical and social wellbeing, overall health status, fatigue, pain, sleep quality, sexuality, self-efficacy, treatment satisfaction). In comparison to the human needs model, needs such as identity and leisure were disregarded.</p><p><strong>Conclusions: </strong>The H2O generic outcome set presents a disease-generic, domain-centered PRO framework building the groundwork for health data spaces and supporting consistency in treatment outcomes across different sites, settings, and patient populations.</p>","PeriodicalId":73088,"journal":{"name":"Frontiers in health services","volume":"5 ","pages":"1497055"},"PeriodicalIF":2.7,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12528166/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145330963","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Social enterprise as a strategy to advance patient-oriented health services innovation: learning from the Alberta Family Integrated Care model. 社会企业是推动以病人为导向的保健服务创新的战略:借鉴艾伯塔省家庭综合护理模式。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-02 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1638587
Anmol Shahid, Kristen Graham, Karen Benzies

This community case study outlines the conceptualization, development, implementation, and commercialization of the Alberta Family Integrated Care (Alberta FICare) model, offering insights into a unique way of sustaining patient-oriented innovations through social enterprise. Our team developed the Alberta FICare model to include families as partners in care in neonatal intensive care units (NICUs). Research phases of our model showed improved outcomes for neonates (shorter hospital stays), their families (greater caregiving self-efficacy, reduced psychosocial distress), and the health system (cost avoidance). Despite co-development of the model with families, providers, and leaders, rigorous testing (cluster randomized controlled trial), and province-wide scale-up (now standard of care in all 14 Alberta NICUs) efforts to sustain the model stalled due to shifting health system priorities. To address this challenge, we incorporated a social enterprise (Liminality Innovations Inc.) to sustain the model of care and support broader dissemination of family integrated care practices in NICUs beyond Alberta. While this strategy fostered sustainment and growth of our model, it also raised challenges. Some of these challenges included tackling perceptions within the research and practice communities that commercialization undermines research integrity. We share our experiences to highlight the potential of ethical, mission-driven commercialization through social enterprise to support innovation in learning health systems through ongoing interest holder engagement, responsible stewardship, and improving learning health system outcomes as the central goal.

本社区案例研究概述了艾伯塔省家庭综合护理(Alberta FICare)模式的概念化、发展、实施和商业化,为通过社会企业维持以患者为导向的创新提供了独特的方式。我们的团队开发了艾伯塔省FICare模型,将家庭作为新生儿重症监护病房(NICUs)护理的合作伙伴。我们模型的研究阶段显示,新生儿(缩短住院时间)、他们的家庭(提高护理自我效能、减少心理社会困扰)和卫生系统(避免成本)的结果有所改善。尽管与家庭、提供者和领导共同开发了该模式,进行了严格的测试(集群随机对照试验),并在全省范围内扩大了规模(现在是艾伯塔省所有14个新生儿重症监护病房的护理标准),但由于卫生系统优先事项的转移,维持该模式的努力陷入了停滞。为了应对这一挑战,我们成立了一家社会企业(Liminality Innovations Inc.),以维持护理模式,并支持在阿尔伯塔省以外的新生儿重症监护病房更广泛地推广家庭综合护理实践。虽然这一战略促进了我们模式的维持和发展,但它也带来了挑战。其中一些挑战包括解决研究和实践团体内部的看法,即商业化破坏了研究的完整性。我们分享我们的经验,强调通过社会企业实现道德、使命驱动的商业化的潜力,通过利益相关者的持续参与、负责任的管理和改善学习型卫生系统成果作为中心目标,支持学习型卫生系统的创新。
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引用次数: 0
Development of methods for WHO quality standards for child and youth mental health services to improve quality of care and patient safety in the WHO European region. 制定世卫组织儿童和青年精神卫生服务质量标准的方法,以提高世卫组织欧洲区域的护理质量和患者安全。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-02 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1644419
Jennifer Hall, Katie H Atmore, Rimma Belikova, Chris Boyd-Skinner, Lisa Corrigan, Anastasia Giannaki, Ana Isabel F Guerreiro, Penny Kalpaxi, Colette Kelly, Konstantinos Kotsis, Dennis Ougrin, Catalina Popoviciu, Anne Marie Råberg Christensen, Dion Ras, Cassie Redlich, Tatiana Taylor Salisbury, Raffaella Sibilio, Ana Maria Tijerino, Ledia Lazeri, Joao Breda

Background: Child and youth mental health care is of varying quality across the WHO European Region, with many settings being low-resourced. To improve and standardize quality of care, WHO Regional Office for Europe is developing quality standards for child and youth mental health services. This research aims to develop evidence informed methods to develop these quality standards.

Methods: Desk reviews of grey literature aimed to understand what approaches have been used or recommended to develop quality standards for child and youth mental health/health for use across a range of different countries, and consultation was sought from an expert steering group. A thematic approach was used to synthesize relevant themes. The methods were developed based on the results of these steps.

Results: Desk reviews identified variation in approaches used and recommended to develop quality standards, with limited available guidance applicable across different resource settings. Nine key themes from stakeholder consultations were highlighted. Based on these results, a seven-step methodology was created to develop the quality standards for child and youth mental health which prioritizes using an evidence-based approach and inputs from a wide range of stakeholders.

Discussion: The methods taken to develop quality standards need to be rigorous to ensure that standards accurately define high-quality care for a service. There is a need to develop a unified approach to developing quality standards. It is hoped that this paper will provide inspiration for others developing quality standards for child and youth mental health services and spark research in this area.

背景:世卫组织欧洲区域的儿童和青年精神卫生保健质量参差不齐,许多环境资源不足。为了改善护理质量并使其标准化,世卫组织欧洲区域办事处正在制定儿童和青年精神卫生服务的质量标准。本研究旨在开发循证方法来制定这些质量标准。方法:对灰色文献进行案头审查,旨在了解在制定儿童和青少年心理健康/健康质量标准方面已采用或建议采用哪些方法,供不同国家使用,并寻求专家指导小组的咨询。采用主题方法综合相关主题。这些方法是根据这些步骤的结果发展起来的。结果:案头审查确定了使用方法的差异,并建议制定质量标准,有限的可用指导适用于不同的资源设置。会议强调了利益攸关方磋商的九个关键主题。根据这些结果,制定了一套七步方法,以制定儿童和青少年心理健康质量标准,其中优先采用循证方法和广泛利益攸关方的投入。讨论:制定质量标准的方法需要严格,以确保标准准确地定义服务的高质量护理。有必要制定一种统一的方法来制定质量标准。希望本文能够为制定儿童和青少年心理健康服务质量标准的其他人提供启发,并激发这一领域的研究。
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引用次数: 0
Rectal treatment in ulcerative colitis; a qualitative study exploring reasons for under utilisation. 溃疡性结肠炎的直肠治疗质性研究,探讨资源利用不足的原因。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-01 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1654520
Jean-Pierre Rothen, Florence Moerlen, Céline von Büren, Samuel Allemann, Isabelle Arnet

Introduction: Ulcerative colitis is an inflammatory bowel disease that is limited to the colon. First-line treatment consists of rectally administered suppositories, foam or enema. Adherence to rectal treatment is very low in people with ulcerative colitis. We aimed to explore modifiable factors influencing adherence to rectal treatment among patients, healthcare providers (HCP), and pharmaceutical companies, and to delineate new approaches to improve adherence to rectal medicines.

Methods: We recruited people using rectal treatment, community and clinical pharmacists, gastroenterologists, inflammatory bowel diseases (IBD) nurses, and representatives of pharmaceutical companies specialised in the production of rectal therapies. We performed semi-structured one-to-one interviews tackling the three pivotal topics knowledge and beliefs, product characteristics, and communication. We started with patient interviews whose statements served to inform the other interviews. All interviews were the subject of a keyword protocol, audio-recorded, and transcribed. Thematic analysis was used with inductive approach for the patients, and deductive approach for all other interviewees. Identified themes were compared and agreements and divergences were compiled.

Results: We interviewed eight patients (22-77 years old, 3 women) in spring 2023, and stakeholders from the hospital (3 gastroenterologists and 2 IBD nurses), ambulatory setting (4 community pharmacists) and pharmaceutical companies (2 representatives) in 2024, all in the region of Basel (Switzerland). Overall, people with ulcerative colitis often feel left alone to cope with the challenges associated with their therapies. Pretreatment concerns and difficulties experienced by these people following their first attempts at use are not adequately addressed by HCPs. Training sessions for clinicians and pharmacists, patient-oriented demonstration materials, visual aids, and tips and tricks the application of rectal treatment could help improve the use of rectal medicines by people with ulcerative colitis.

Conclusion: This study identified a detailed knowledge of the proper use of rectal treatment and frank communication between patients and HCPs as crucial for the adherence to rectally administered medicines. While these factors are broadly recognised in the literature, this study highlights their common priority among all stakeholders. In addition, solutions for future development and tailored interventions are proposed.

简介:溃疡性结肠炎是一种局限于结肠的炎症性肠病。一线治疗包括直肠注射栓剂、泡沫或灌肠。溃疡性结肠炎患者对直肠治疗的依从性非常低。我们的目的是探索影响患者、医疗保健提供者(HCP)和制药公司对直肠治疗依从性的可改变因素,并描述提高直肠药物依从性的新方法。方法:我们招募了使用直肠治疗的人,社区和临床药剂师,胃肠病学家,炎症性肠病(IBD)护士,以及专门生产直肠治疗的制药公司的代表。我们进行了半结构化的一对一访谈,讨论了三个关键主题:知识和信念、产品特性和沟通。我们从病人访谈开始,他们的陈述为其他访谈提供了信息。所有的采访都是一个关键字协议的主题,录音,并转录。对患者采用归纳法,对其他受访者采用演绎法进行主题分析。对确定的主题进行了比较,并汇编了一致意见和分歧。结果:我们于2023年春季访问了8名患者(22-77岁,3名女性),并于2024年访问了来自医院(3名胃肠病学家和2名IBD护士),门诊机构(4名社区药剂师)和制药公司(2名代表)的利益相关者,均在巴塞尔(瑞士)地区。总的来说,患有溃疡性结肠炎的人经常感到独自应对与他们的治疗相关的挑战。HCPs没有充分解决这些人在首次尝试使用后遇到的预处理问题和困难。针对临床医生和药剂师的培训课程、以患者为导向的演示材料、视觉辅助工具以及直肠治疗应用的提示和技巧可以帮助改善溃疡性结肠炎患者对直肠药物的使用。结论:本研究确定了直肠治疗正确使用的详细知识以及患者和医务人员之间的坦率沟通对于坚持直肠给药至关重要。虽然这些因素在文献中得到广泛认可,但本研究强调了所有利益相关者的共同优先事项。此外,还提出了未来发展的解决方案和量身定制的干预措施。
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引用次数: 0
Environmental sustainability, an essential outcome for implementation scientists to improve health. 环境的可持续性,是实施科学家改善健康的重要成果。
IF 2.7 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2025-10-01 eCollection Date: 2025-01-01 DOI: 10.3389/frhs.2025.1664446
Virginia Mckay, Emmanuel Tetteh, Nicholas Wong, C Bradley Kramer, Jason Burnham

While there is evidence of humans' harmful impact on the environment, translating such evidence into changes is challenging. Implementation science can facilitate a shift from a reactive to proactive approach in tackling environmental sustainability. This article aims to spur further discussion among implementation scientists to incorporate environmental sustainability within their research, while also offering concepts relevant to environmental science researchers seeking to apply implementation science principles.

虽然有证据表明人类对环境有有害影响,但将这些证据转化为变化是具有挑战性的。在处理环境可持续性问题时,实施科学可以促进从被动方法向主动方法的转变。本文旨在促进实施科学家之间的进一步讨论,将环境可持续性纳入他们的研究,同时也为寻求应用实施科学原理的环境科学研究人员提供相关概念。
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引用次数: 0
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