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Systematic Survey of Guidelines With Recommendations Related to Concordant Multimorbidity: Diabetes, Coronary Heart Disease and Stroke as an Example. 以糖尿病、冠心病和脑卒中为例的一致性多发病相关指南及建议的系统调查
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-01 DOI: 10.1111/jep.70385
Zijun Wang, Jie Zhang, Bingyi Wang, Huayu Zhang, Ling Wang, Zhewei Li, Di Zhu, Hongfeng He, Luyuan Sun, Xuefeng Li, Sheyu Li, Yaolong Chen, Janne Estill

Background: Although guidelines focus predominantly on individual diseases, some dedicated guidelines and recommendations exist for common combinations of comorbidities. Using diabetes, coronary heart disease (CHD) and stroke as an example, we aimed to assess the current status and quality of such guidelines.

Methods: We systematically searched literature databases, Google, guideline platforms, and websites of relevant organizations. We included guidelines published between 2020 and 2024 that addressed at least two of the following diseases: diabetes, CHD, and stroke; and included drug therapy interventions. We extracted the recommendations on drug therapy and sources of the supporting evidence, and assessed the quality of the guidelines using AGREE II and RIGHT with the help of a large language model based tool.

Results: We identified 82 guidelines: 64 focused on one disease with recommendations on comorbidities, and 18 specifically addressed a combination of diseases. China was the most frequent country of origin (n = 50, 61.0%). The methodological and reporting quality of these guidelines was moderate on average. For most guidelines (n = 54, 65.9%), the primary focus was on diabetes. We grouped the recommended drug therapies for patients with combinations of these diseases into four main categories: anti-diabetic therapy, antihypertensive therapy, lipid-lowering therapy, and anticoagulant therapy. Most recommendations were supported by RCTs, but only a third of the guidelines referred to studies done in multimorbid patients.

Conclusion: Most recommendations related to multimorbidity were found in guidelines focusing on a single target disease, and supporting evidence from multimorbid patients was rare. More primary evidence from multimorbid patients is needed.

背景:虽然指南主要侧重于单个疾病,但对于常见的合并症组合也存在一些专门的指南和建议。以糖尿病、冠心病和中风为例,我们旨在评估这些指南的现状和质量。方法:系统检索文献数据库、谷歌、指南平台及相关组织网站。我们纳入了2020年至2024年间发布的指南,涉及以下至少两种疾病:糖尿病、冠心病和中风;包括药物治疗干预。我们提取了关于药物治疗的建议和支持证据的来源,并在基于大型语言模型的工具的帮助下,使用AGREE II和RIGHT评估指南的质量。结果:我们确定了82项指南:64项侧重于一种疾病并推荐合并症,18项专门针对疾病组合。中国是最常见的原产国(n = 50, 61.0%)。这些指南的方法和报告质量平均来说是中等的。对于大多数指南(n = 54, 65.9%),主要关注的是糖尿病。我们将这些疾病合并患者的推荐药物治疗分为四大类:降糖治疗、降压治疗、降脂治疗和抗凝治疗。大多数建议都得到了随机对照试验的支持,但只有三分之一的指南参考了在多病患者中进行的研究。结论:大多数与多病相关的建议都是在针对单一目标疾病的指南中发现的,来自多病患者的支持证据很少。需要更多来自多病患者的主要证据。
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引用次数: 0
Pediatric Crush Syndrome and Injury Profiles in Earthquake Survivors: A Comprehensive Analysis From the 2023 Turkey Earthquake. 儿童挤压综合征和地震幸存者的损伤概况:来自2023年土耳其地震的综合分析。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-01 DOI: 10.1111/jep.70379
Sefika Aldas, Murat Ersoy, Mehtap Durukan Tosun, Ali Tunç, Gamze Gökulu, Esra Vatansever, Fatma Sercan Aynacı, Banu Katlan, Suna Ozdem, Berfin Ozgokce Ozmen, Sanliay Sahin

Objective: The clinical profiles of child victims admitted to hospitals following earthquakes, as well as the characteristics associated with hospital stay, are important. This study aimed to analyze the clinical outcomes of pediatric victims admitted following a sudden earthquake to enhance preparedness for accessing essential health services to reduce losses in future disasters.

Methods: Among 2158 patients referred to the pediatric emergency department (PED), 356 children followed at our tertiary inpatient clinic were included. Demographics, surgical interventions, and the presence of life-threatening conditions like crush syndrome and fasciotomy/amputation were investigated. Crush syndrome was defined as clinical and laboratory evidence of muscle injury accompanied by systemic complications odds ratios (OR) with 95% confidence intervals (CI) were calculated.

Results: Among the patients, 56.5% were male. The median length of hospital stay was 4 days (range: 1-120). The most common injury mechanism was entrapment under rubble, and the lower extremities were the most frequently affected injury site. Compartment syndrome developed in 31.7% of patients, and 2.8% underwent amputation. Crush syndrome was identified in 75.3% of hospitalized patients and was significantly more common among children admitted on the second day or later after the earthquake. Elevated creatine phosphokinase (CPK) levels significantly increased the likelihood of developing crush syndrome (OR: 61.7, 95% CI) and the need for fasciotomy (OR: 16.9, 95% CI). Fasciotomy was required in 28.9% of patients. Dehydration was associated with an increased risk of fasciotomy (OR: 7.2) and amputation (OR: 5.4). Elevated levels of myoglobin, uric acid, blood urea nitrogen/creatinine, and aspartate aminotransferase (AST) and alanine aminotransferase (ALT) were significantly associated with crush syndrome and fasciotomy (p < 0.001).

Conclusion: The high burden of crush-related complications in pediatric earthquake victims underscores the need for pediatric-specific trauma protocols in disaster settings. Early identification of risk factors and rapid intervention may reduce severe outcomes such as fasciotomy, renal failure, and amputation.

目的:地震后入院的儿童受害者的临床概况以及与住院有关的特征是重要的。本研究旨在分析突发性地震后入院的儿童受害者的临床结果,以加强获得基本卫生服务的准备,减少未来灾害的损失。方法:在2158例儿科急诊科(PED)的患者中,包括356名在我们三级住院诊所随访的儿童。调查了人口统计学、手术干预和存在危及生命的疾病,如挤压综合征和筋膜切开术/截肢。挤压综合征定义为伴有全身并发症的肌肉损伤的临床和实验室证据,计算95%可信区间(CI)的优势比(OR)。结果:患者中男性占56.5%。中位住院时间为4天(范围:1-120天)。最常见的损伤机制是被困在瓦砾下,下肢是最常见的损伤部位。31.7%的患者出现筋膜间室综合征,2.8%的患者截肢。在75.3%的住院患者中发现了挤压综合征,在地震后第二天或更晚入院的儿童中更为常见。肌酸磷酸激酶(CPK)水平升高显著增加发生挤压综合征的可能性(OR: 61.7, 95% CI)和筋膜切开术的必要性(OR: 16.9, 95% CI)。28.9%的患者需要行筋膜切开术。脱水与筋膜切开术(OR: 7.2)和截肢(OR: 5.4)的风险增加有关。肌红蛋白、尿酸、血尿素氮/肌酐、天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平升高与挤压综合征和筋膜切开术显著相关(p结论:儿童地震受害者挤压相关并发症的高负担强调了灾害环境中儿科创伤方案的必要性。早期识别危险因素和快速干预可以减少严重的后果,如筋膜切开术、肾功能衰竭和截肢。
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引用次数: 0
Advancing Methods to Study Clinical Variation in Healthcare. 医疗保健临床变异研究的新方法
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-01 DOI: 10.1111/jep.70383
Jason E Black, Derek S Chew, Tyler S Williamson, Braden Manns, Amity Quinn

Clinical variation (a.k.a. medical practice variation) describes how patient care and outcomes differ across patients, providers, hospitals, geographic regions or other dimensions. By understanding clinical variation in patient care or outcomes that cannot be explained by patient differences, researchers and health systems can (1) highlight overuse, underuse, inefficiencies or inequities impacting patient care, (2) identify the level (e.g., patient, provider, hospital) contributing the most variation and (3) interrogate the reasons that explain the observed variation. Numerous methods exist to understand clinical variation; however, these are not well identified or characterized in the existing body of health services research literature. We aim to provide non-technical methodological guidance to researchers interested in describing and quantifying clinical variation by characterizing and comparing methods suited to this task. We present several plots to display clinical variation, including point and jitter plots, scatterplots, caterpillar plots, box plots and funnel plots. While most plots simply visualize the variation, funnel plots can characterize whether the variation is larger than expected after adjusting for relevant clinical factors that might reasonably explain clinical variation, such as case-mix. We present several basic statistical approaches to measure clinical variation, including variance, standard deviation, coefficient of variation, systematic coefficient of variation and interquartile range. Further, we describe multilevel models that measure clinical variation beyond its magnitude, including the level(s) at which variation occurs and the level-specific factors that explain the variation. We describe several statistics that quantify the clinical variation that exists in a multilevel model, such as the intraclass correlation coefficient and median odds, risk, rate and hazard ratios. We discuss key considerations when describing and quantifying clinical variation, including the appropriate measurement of patient care and outcomes, the factors explaining variation and whether it is warranted and what interventions might help reduce the variation. The objective of this review is to provide an overview of techniques to consider when describing clinical variation, serving as a resource for those examining clinical variation.

临床差异(又名医疗实践差异)描述了患者、提供者、医院、地理区域或其他维度的患者护理和结果差异。通过了解患者护理的临床变化或无法用患者差异来解释的结果,研究人员和卫生系统可以(1)突出影响患者护理的过度使用、使用不足、效率低下或不公平现象,(2)确定造成最大变化的水平(例如,患者、提供者、医院),以及(3)询问解释观察到的变化的原因。有许多方法可以理解临床变异;然而,在现有的卫生服务研究文献中,这些问题没有得到很好的确定或描述。我们的目标是通过描述和比较适合这项任务的方法,为有兴趣描述和量化临床变异的研究人员提供非技术方法指导。我们提出了几种显示临床变异的图,包括点和抖动图、散点图、毛虫图、箱形图和漏斗图。虽然大多数图只是简单地可视化变化,但漏斗图可以描述在调整了可能合理解释临床变化的相关临床因素(如病例混合)后,变化是否大于预期。我们提出了几种测量临床变异的基本统计方法,包括方差、标准差、变异系数、系统变异系数和四分位间距。此外,我们还描述了测量临床变异的多层次模型,包括变异发生的水平和解释变异的水平特异性因素。我们描述了一些量化存在于多水平模型中的临床变异的统计数据,如类内相关系数和中位几率、风险、发病率和风险比。我们讨论了描述和量化临床变异时的关键考虑因素,包括对患者护理和结果的适当测量,解释变异的因素以及是否有必要以及哪些干预措施可能有助于减少变异。这篇综述的目的是提供描述临床变异时要考虑的技术概述,为那些检查临床变异的人提供资源。
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引用次数: 0
Principles and Strategies for Interest-Holder Engagement in Health Guideline Development. 利益相关者参与健康指南制定的原则和策略。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-01 DOI: 10.1111/jep.70375
Olivia Magwood, Caitlin Shyng, Lyubov Lytvtyn, Joanne Khabsa, Alex Young-Soo Lee, Jennifer Petkovic, Vivian Welch, Kevin Pottie, Peter Tugwell

Rationale: Guidelines are statements or recommendations that help interest-holders make decisions about clinical care or health policy. Engaging a wide range of interest-holders, such as patients, providers, policymakers and members of the public in the guideline development process can help ensure that guidelines are fit-for-purpose. The MuSE Consortium is developing guidance for the engagement of interest-holders throughout the guideline development process in the form of an extension of the Guidelines International Network (GIN)-McMaster Guideline Development Checklist (GDC).

Aims and objectives: The objective of this study is to identify principles and strategies to promote interest-holder engagement across the guideline development enterprise.

Methods: We conducted interviews with 43 individuals from 10 different interest-holder groups and 15 different countries. We used a framework analysis to thematically analyze findings and identify principles and strategies relevant for engaged guideline development.

Results: Guideline development initiatives may better engage interest-holders by shifting from vertical to horizontal power structures, emphasizing collaboration and shared decision-making. We identified a need for epistemic justice, promoting fairness and equality in knowledge production and validation, particularly for patients and members of the public. Representation is a crucial key issue, necessitating diverse perspectives in guideline development groups. Strategies include involving interest-holders early and meaningfully in the guideline development process through governance, setting clear expectations and timelines, and providing fair compensation. Dissemination activities should extend beyond academic publications, empowering all interest-holders to contribute to activities such as presentations, educational sessions, or social media campaigns. While engagement is desirable, limitations may arise in emergency contexts or resource-constrained settings.

Conclusions: Guideline developers may need to make pragmatic decisions as to who they engage in guideline development and how. Capacity strengthening in low- and middle-income countries may help address current disparities in engagement in guideline development. Future research should explore issues around representativeness of interest-holders.

基本原理:指南是帮助利益相关者做出临床护理或卫生政策决策的声明或建议。让广泛的利益相关者,如患者、提供者、政策制定者和公众参与指南制定过程,有助于确保指南符合目的。缪斯联盟正在以指南国际网络(GIN)-麦克马斯特指南制定清单(GDC)的扩展形式,为利益攸关方在指南制定过程中的参与制定指南。目的和目标:本研究的目的是确定原则和策略,以促进整个指南制定企业的利益相关者参与。方法:我们对来自10个不同利益集团和15个不同国家的43名个人进行了访谈。我们使用一个框架分析来对发现进行主题分析,并确定与参与指南制定相关的原则和策略。结果:通过从纵向权力结构转向横向权力结构,强调协作和共享决策,指南制定计划可能更好地吸引利益相关者。我们确定需要认识正义,促进知识生产和验证的公平和平等,特别是对患者和公众。代表性是一个至关重要的关键问题,在指南制定小组中需要不同的观点。策略包括通过治理、设定明确的期望和时间表以及提供公平的补偿,使利益相关者尽早并有意地参与指南制定过程。传播活动应扩展到学术出版物之外,使所有利益相关者都能参与诸如演讲、教育会议或社交媒体活动等活动。虽然参与是可取的,但在紧急情况下或资源有限的情况下可能会产生限制。结论:指南制定者可能需要就谁参与指南制定以及如何参与指南制定做出务实的决定。加强低收入和中等收入国家的能力可能有助于解决目前在参与指南制定方面的差距。未来的研究应围绕利益相关者的代表性问题进行探讨。
{"title":"Principles and Strategies for Interest-Holder Engagement in Health Guideline Development.","authors":"Olivia Magwood, Caitlin Shyng, Lyubov Lytvtyn, Joanne Khabsa, Alex Young-Soo Lee, Jennifer Petkovic, Vivian Welch, Kevin Pottie, Peter Tugwell","doi":"10.1111/jep.70375","DOIUrl":"10.1111/jep.70375","url":null,"abstract":"<p><strong>Rationale: </strong>Guidelines are statements or recommendations that help interest-holders make decisions about clinical care or health policy. Engaging a wide range of interest-holders, such as patients, providers, policymakers and members of the public in the guideline development process can help ensure that guidelines are fit-for-purpose. The MuSE Consortium is developing guidance for the engagement of interest-holders throughout the guideline development process in the form of an extension of the Guidelines International Network (GIN)-McMaster Guideline Development Checklist (GDC).</p><p><strong>Aims and objectives: </strong>The objective of this study is to identify principles and strategies to promote interest-holder engagement across the guideline development enterprise.</p><p><strong>Methods: </strong>We conducted interviews with 43 individuals from 10 different interest-holder groups and 15 different countries. We used a framework analysis to thematically analyze findings and identify principles and strategies relevant for engaged guideline development.</p><p><strong>Results: </strong>Guideline development initiatives may better engage interest-holders by shifting from vertical to horizontal power structures, emphasizing collaboration and shared decision-making. We identified a need for epistemic justice, promoting fairness and equality in knowledge production and validation, particularly for patients and members of the public. Representation is a crucial key issue, necessitating diverse perspectives in guideline development groups. Strategies include involving interest-holders early and meaningfully in the guideline development process through governance, setting clear expectations and timelines, and providing fair compensation. Dissemination activities should extend beyond academic publications, empowering all interest-holders to contribute to activities such as presentations, educational sessions, or social media campaigns. While engagement is desirable, limitations may arise in emergency contexts or resource-constrained settings.</p><p><strong>Conclusions: </strong>Guideline developers may need to make pragmatic decisions as to who they engage in guideline development and how. Capacity strengthening in low- and middle-income countries may help address current disparities in engagement in guideline development. Future research should explore issues around representativeness of interest-holders.</p>","PeriodicalId":15997,"journal":{"name":"Journal of evaluation in clinical practice","volume":"32 1","pages":"e70375"},"PeriodicalIF":2.1,"publicationDate":"2026-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12917349/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146220037","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Altruism and Missed Nursing Care Among Intensive Care Nurses: A Descriptive Correlational Study. 重症监护护士的利他主义与护理缺失:一项描述性相关研究。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-02-01 DOI: 10.1111/jep.70381
Sümeyye Akçoban, Betül Tosun

Aim: This study aims to assess the relationship between altruism and the level of missed nursing care among nurses working in Intensive Care Units (ICU).

Design: The study was descriptive and correlational.

Methods: This study was conducted between 15 January and 15 June 2025 with 210 ICU nurses working in two public hospitals. Data were collected using the "Nurse Demographic Information Form", the "Altruism Scale" and the "Missed Nursing Care Survey (MISSCARE)". Data analysis included descriptive statistics, Independent Student's t test, One-Way ANOVA, and Pearson correlation analysis.

Results: The nurses' mean age was 29.30 ± 5.23 years, with 72.4% being female and 80.0% holding a bachelor's degree. It was found that 78.6% of the participants experienced delays in providing patient care due to material shortages and high workload, while 97.1% reported delivering care with an altruistic approach. A significant, moderate, and negative correlation was identified between the altruism scale and the amount of missed nursing care (MISSCARE A) (r = -0.389, p < 0.001).

Patient or public contribution: A higher level of altruism among ICU nurses appears to contribute to a lower incidence of missed nursing care. The correlation between missed nursing care and altruism underscores the importance of altruistic attitudes in patient care. However, the high significance of the reasons for missed nursing care highlights issues related to working conditions in ICU settings. To enable altruistic nurses to provide high-quality care without disruptions, healthcare policies should prioritize improving working conditions, adjusting staffing levels, and addressing medical supply shortages.

目的:本研究旨在探讨重症监护病房护士利他行为与护理缺失的关系。设计:本研究为描述性和相关性研究。方法:于2025年1月15日至6月15日对两所公立医院的210名ICU护士进行研究。数据收集采用“护士人口统计信息表”、“利他主义量表”和“护理缺失调查(MISSCARE)”。数据分析包括描述性统计、独立学生t检验、单因素方差分析和Pearson相关分析。结果:护理人员平均年龄29.30±5.23岁,女性占72.4%,本科学历占80.0%。研究发现,78.6%的参与者由于材料短缺和高工作量而延迟提供患者护理,而97.1%的参与者报告以利他的方式提供护理。利他主义量表与护理遗漏量之间存在显著、中度和负相关(r = -0.389, p)。患者或公众贡献:ICU护士的利他主义水平越高,护理遗漏率越低。错过护理和利他主义之间的相关性强调了利他态度在病人护理中的重要性。然而,错过护理的原因的高度重要性突出了与ICU设置的工作条件有关的问题。为了使无私的护士能够不受干扰地提供高质量的护理,医疗保健政策应优先考虑改善工作条件、调整人员配备水平和解决医疗供应短缺问题。
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引用次数: 0
Beyond Accuracy: How Patient Families in South Korea Evaluate Medical Information and Build Institutional Trust 超越准确性:韩国患者家属如何评估医疗信息并建立机构信任。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-22 DOI: 10.1111/jep.70368
SangYoon Lim

Background

In the evolving patient-centred healthcare market, family members often act as ‘surrogate information seekers’, playing a pivotal role in medical decision-making and hospital selection. However, unlike healthcare professionals, these lay consumers face significant challenges in evaluating the quality of online medical information. This study applies the Technology Acceptance Model (TAM) to examine how patient families perceive medical information quality and how these perceptions influence their satisfaction and intention to revisit medical institutions.

Methods

A cross-sectional survey was conducted with 318 patient families who had utilised healthcare services in the southern region of Gyeonggi Province, South Korea. The collected data were analysed using Structural Equation Modelling (SEM) to test the hypothesised relationships between information quality dimensions (accuracy, reliability, timeliness, accessibility), perceived usefulness, perceived ease of use, and behavioural intentions.

Results

The findings indicate that reliability, timeliness, and accessibility significantly enhance both perceived usefulness and perceived ease of use. Notably, the accuracy of information did not exert a significant influence on users' perceptions, suggesting that lay families may rely more on heuristic cues like accessibility and timeliness than on technical precision. Furthermore, satisfaction with medical information was found to significantly increase hospital satisfaction, which in turn served as a strong predictor of the intention to revisit.

Conclusion

These results suggest that for healthcare providers, merely claiming information accuracy is insufficient to engage patient families. Instead, institutions should prioritise communication strategies that ensure information is easily accessible and transparently reliable. By lowering barriers to information and enhancing usability, providers can reduce family anxiety, improve satisfaction, and ultimately build long-term institutional trust.

背景:在不断发展的以患者为中心的医疗保健市场中,家庭成员经常充当“替代信息寻求者”,在医疗决策和医院选择中发挥关键作用。然而,与医疗保健专业人员不同,这些外行消费者在评估在线医疗信息的质量方面面临着重大挑战。本研究运用技术接受模型(TAM)来检视病患家属对医疗资讯品质的认知,以及这些认知如何影响他们对医疗机构的满意度和再访意愿。方法:对韩国京畿道南部地区318个利用医疗保健服务的患者家庭进行横断面调查。使用结构方程模型(SEM)对收集到的数据进行分析,以检验信息质量维度(准确性、可靠性、及时性、可访问性)、感知有用性、感知易用性和行为意图之间的假设关系。结果:信度、时效性和可及性显著提高了感知有用性和感知易用性。值得注意的是,信息的准确性并没有对用户的感知产生显著影响,这表明外行家庭可能更多地依赖于启发式线索,如可访问性和及时性,而不是技术精度。此外,对医疗信息的满意度显著增加了医院满意度,这反过来又成为再次访问意愿的强烈预测因子。结论:这些结果表明,对于医疗保健提供者,仅仅声称信息的准确性是不够的,以吸引患者家属。相反,机构应该优先考虑确保信息容易获取和透明可靠的传播策略。通过降低信息障碍和提高可用性,提供者可以减少家庭焦虑,提高满意度,最终建立长期的机构信任。
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引用次数: 0
Redefining Evidence-Based Practice Through Patient Values: A Theoretical Innovation for Person-Centered, Value-Based Care 通过患者价值重新定义循证实践:以人为本、价值为基础的护理的理论创新。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-22 DOI: 10.1111/jep.70344
Sandra D. Shapiro, Ilana Logvinov, Rachel McMahan Thomas

Rationale

Before evidence-based practice (EBP) was formally adopted, healthcare decisions relied on critical thinking and clinical judgment informed by disciplinary knowledge, theory, and research, but lacked full integration of patient values with clinical expertise. Sackett et al. redefined EBP as the integration of the best available evidence, clinical expertise, and patient values. This framework has been embraced by nursing and other healthcare disciplines, embedding EBP into education, clinical protocols, and quality improvement efforts. Despite widespread adoption, traditional conceptualizations prioritize empirical evidence above patient values, potentially undermining individualized care.

Aims and Objectives

This paper proposes a reconceptualization that places patient and client values—their why—at the center of EBP, inspired by Simon Sinek's Golden Circle model which emphasizes starting with purpose to influence behavior effectively. Prioritizing the patient's values before incorporating empirical evidence into a care plan ensures that care aligns with their personal goals and definitions of health, fostering therapeutic relationships and supporting meaningful behavior change.

Methods

A conceptual analysis was conducted using Simon Sinek's Golden Circle model as a guiding framework. This model emphasizes starting with purpose to influence behavior effectively. The analysis explores how integrating patient values first, followed by empirical evidence and clinical expertise, can operationalize person-centered EBP.

Results

The reconceptualized framework positions patient values as the foundation of care planning. By aligning interventions with patients' personal goals and values first, clinicians can strengthen therapeutic relationships and support individualized care.

Conclusion

Effective nursing clinicians and leaders must embrace this patient-first approach to truly operationalize person-centered, evidence-based care that respects the diverse needs and motivations of patients.

理由:在正式采用循证实践(EBP)之前,医疗保健决策依赖于由学科知识、理论和研究提供的批判性思维和临床判断,但缺乏患者价值观与临床专业知识的充分整合。Sackett等人将EBP重新定义为可获得的最佳证据、临床专业知识和患者价值的整合。该框架已被护理和其他医疗保健学科所采用,将EBP嵌入到教育、临床协议和质量改进工作中。尽管被广泛采用,传统的概念优先考虑经验证据高于病人的价值,潜在地破坏个性化护理。目的和目标:本文提出了一个重新概念,将病人和客户的价值——他们为什么——放在EBP的中心,灵感来自西蒙·斯涅克的黄金圈模型,该模型强调从目的开始,有效地影响行为。在将经验证据纳入护理计划之前,优先考虑患者的价值观,确保护理符合他们的个人目标和健康定义,促进治疗关系并支持有意义的行为改变。方法:以Simon Sinek的黄金圈模型为指导框架进行概念分析。这种模式强调从目标开始,有效地影响行为。分析探讨了如何首先整合患者价值,其次是经验证据和临床专业知识,从而实现以人为本的EBP。结果:重新定义的框架将患者价值定位为护理计划的基础。通过首先将干预措施与患者的个人目标和价值观结合起来,临床医生可以加强治疗关系并支持个性化护理。结论:有效的护理临床医生和领导者必须接受这种以病人为先的方法,真正实施以人为本的循证护理,尊重病人的不同需求和动机。
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引用次数: 0
Selecting the Right Journal for Publication: Points to Ponder for Medical Students and Faculty 选择合适的期刊:医学生和教师的思考。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-22 DOI: 10.1111/jep.70367
Preeti Sharma, Vijay Wadhwan
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引用次数: 0
Rethinking Evidence in Contemporary Evidence-Based Medicine: A Critical Examination Into Emerging Forms of Clinical Practice 重新思考当代循证医学中的证据:对新兴临床实践形式的批判性考察。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-22 DOI: 10.1111/jep.70369
Wenxiu Qi

Background

With the increasing integration of digital technologies, precision medicine, and artificial intelligence into contemporary evidence-based medicine (EBM), a range of novel methodological approaches, such as real-world data, synthetic control arms, N-of-1 trials, and large-scale predictive models, have been introduced into clinical decision-making as complementary forms of practice beyond traditional randomized controlled trials. Although these approaches have gained traction in both technical implementation and institutional adoption, their epistemic status as “evidence” and their appropriate positioning within the existing EBM hierarchy remain insufficiently examined.

Objective

This study adopts a perspective from philosophy of science and epistemology to analyze the inferential structures and causal assumptions underpinning these emerging evidence forms, and to assess their applicability in guiding clinical action, supporting explanation, and bearing normative responsibility.

Results

We argue that in the post-EBM era, the concept of evidence must evolve beyond a monolithic methodological paradigm toward a more pluralistic and practice-oriented framework, which is capable of addressing the growing complexity, uncertainty, and individual variability in modern medical decision-making.

背景:随着数字技术、精准医学和人工智能日益融入当代循证医学(EBM),一系列新的方法学方法,如真实世界数据、合成对照臂、N-of-1试验和大规模预测模型,已被引入临床决策,作为传统随机对照试验之外的补充实践形式。尽管这些方法在技术实施和机构采用上都获得了牵引力,但它们作为“证据”的认知地位以及它们在现有循证医学等级体系中的适当定位仍然没有得到充分的检验。目的:本研究采用科学哲学和认识论的视角,分析支撑这些新兴证据形式的推理结构和因果假设,并评估其在指导临床行动、支持解释和承担规范责任方面的适用性。结果:我们认为,在后循证医学时代,证据的概念必须超越单一的方法论范式,向更加多元化和以实践为导向的框架发展,从而能够解决现代医疗决策中日益增长的复杂性、不确定性和个体可变性。
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引用次数: 0
Variation in Variation Measurement: A Mapping Review of Methods to Study Clinical Variation 变异测量中的变异:临床变异研究方法的制图综述。
IF 2.1 4区 医学 Q3 HEALTH CARE SCIENCES & SERVICES Pub Date : 2026-01-22 DOI: 10.1111/jep.70350
Amity E. Quinn, Jason E. Black, Derek Chew, Tyler S. Williamson, Dean Yergens, Peter Faris, Flora Au, Jane M. Fletcher, Simarprit Sidhu, Rachelle Drummond, Becky Skidmore, Braden Manns

Rationale

Variation in health care delivery exists at many levels (e.g., provider, practice, system) and can often be explained by various factors at each level. Understanding clinical variation presents an opportunity to improve the value of health care by identifying low-value care (overuse), gaps in high-value care (underuse), and how they can be improved. Numerous methods exist to describe or quantify clinical variation; however, these are not well identified or applied consistently.

Aim

A mapping review was used to identify and characterize available methods to describe and quantify clinical variation.

Method

We systematically searched health care and health services-related literature for variation and related terms used in titles and abstracts. Titles and abstracts were screened for inclusion. We then identified graphical and statistical methods used, health care specialty, study setting, and health system performance area (e.g., quality, access, costs) using a keyword analysis.

Results

Of the 16,969 papers screened, we excluded 10,866 that did not measure a care process or health outcome, measure variation at the person-level or higher, or analyze routinely collected data. We included 6,103 full-text studies, which were analyzed using a keyword analysis. Most studies used basic methodological approaches (e.g., regression, crude comparisons, ranges). Fewer than 1000 studies used multilevel models, a more advanced methodologic approach that quantifies the magnitude and source of variation. Multilevel models were not commonly used to study variation in health care quality.

Conclusions

While understanding clinical variation is important for all health systems, the methods used are usually able to identify but not quantify or explain variation. This review advances our knowledge of the scope and application of these methods and can be used to improve the measurement of variation to increase the value and equity of health care.

理由:卫生保健提供的差异存在于许多层面(例如,提供者、实践、系统),并且通常可以用每个层面的各种因素来解释。了解临床差异提供了一个机会,通过确定低价值护理(过度使用)、高价值护理(使用不足)方面的差距,以及如何改进它们,来提高医疗保健的价值。有许多方法可以描述或量化临床变异;然而,这些都没有很好地识别或一致地应用。目的:一项地图回顾用于识别和表征可用的方法来描述和量化临床变异。方法:系统检索卫生保健和卫生服务相关文献,查找标题和摘要中使用的变异和相关术语。对标题和摘要进行筛选以纳入。然后,我们使用关键字分析确定所使用的图形和统计方法,医疗保健专业,研究设置和卫生系统绩效领域(例如,质量,获取,成本)。结果:在筛选的16,969篇论文中,我们排除了10,866篇没有测量护理过程或健康结果、测量个人水平或更高水平的变化或分析常规收集数据的论文。我们纳入了6103篇全文研究,使用关键字分析对其进行了分析。大多数研究使用基本的方法方法(例如,回归、粗略比较、范围)。不到1000项研究使用了多层模型,这是一种更先进的方法方法,可以量化变化的幅度和来源。多层模型不常用于研究卫生保健质量的变化。结论:虽然了解临床变异对所有卫生系统都很重要,但所使用的方法通常能够识别但不能量化或解释变异。这篇综述提高了我们对这些方法的范围和应用的认识,并可用于改进变异的测量,以增加医疗保健的价值和公平性。
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引用次数: 0
期刊
Journal of evaluation in clinical practice
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