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The impact of the COVID-19 pandemic on satisfaction with healthcare services in Türkiye COVID-19 大流行对土耳其医疗服务满意度的影响
IF 3.4 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-07-10 DOI: 10.1016/j.hlpt.2024.100888
Zeynep B. Uğur , Aysenur Durak

Objectives

This study aims at evaluating whether the healthcare system in Turkey performed well or not from the perspective of patients during the COVID-19 pandemic.

Methods

For this purpose, we compare the satisfaction with healthcare services pre-pandemic and during the pandemic. We utilize the Life Satisfaction Survey conducted by Turkish Statistical Institute (TurkStat) between 2013 and 2021 and employ probit regression method.

Results

The research results do not show any change in satisfaction with healthcare services in the pandemic years of 2020 and 2021. In addition, the satisfaction with healthcare services of people with health conditions, those without health insurance, and those whose premiums are covered by the state (green card holders) did not decrease during the pandemic period. The analysis results reveal that the satisfaction of people over 65 years old and those having health conditions with healthcare services increased during the pandemic period.

Conclusion

When the findings are evaluated as a whole, we can conclude that Turkey performed well from the users’ perspective during the pandemic.

Public interest summary

This study analyzes the impact of the pandemic on satisfaction with healthcare services in Turkey. To do this, we utilize Life Satisfaction Survey between 2013 and 2021. The regression results indicate that satisfaction with healthcare services has not changed during the pandemic. Moreover, we report an increase in satisfaction scores for elderly and those with health conditions in the pandemic years. We also find satisfaction of people without health insurance, and those whose premiums are covered by the state (green card holders) does not change. Our analysis points Turkey did well in managing pandemic period in terms of healthcare services satisfaction.

本研究旨在从患者的角度评估 COVID-19 大流行期间土耳其医疗保健系统的表现是否良好。方法为此,我们比较了大流行前和大流行期间对医疗保健服务的满意度。我们利用土耳其统计研究所(TurkStat)在 2013 年至 2021 年期间进行的生活满意度调查,并采用 probit 回归方法。此外,在大流行期间,有健康状况的人、没有医疗保险的人、保费由国家承担的人(绿卡持有者)对医疗服务的满意度也没有下降。分析结果显示,在大流行期间,65 岁以上人群和有健康问题的人群对医疗服务的满意度有所上升。公共利益摘要本研究分析了大流行对土耳其医疗服务满意度的影响。为此,我们利用了 2013 年至 2021 年间的生活满意度调查。回归结果表明,医疗服务满意度在大流行期间没有发生变化。此外,我们还发现,在大流行期间,老年人和有健康问题的人的满意度得分有所提高。我们还发现,没有医疗保险的人和保费由国家承担的人(绿卡持有者)的满意度没有变化。我们的分析表明,在大流行病管理期间,土耳其的医疗服务满意度表现良好。
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引用次数: 0
Estimating a cost-effectiveness threshold for healthcare decision-making in the Greek NHS 估算希腊国家医疗服务体系医疗决策的成本效益阈值
IF 3.4 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-12 DOI: 10.1016/j.hlpt.2024.100882

Background

The introduction of new health technologies improves quality of life and longevity, but also imposes additional strains in the scarce resources of the health system. Consequently, decisions on the adoption of new technologies are typically based, among other criteria, on the difference between costs and outcomes among competing alternatives. This paper aims to estimate a cost-effectiveness threshold that can be used as an input in the decision-making process for the funding (or reimbursement) of health technologies in Greece.

Methods

For a 30-year period, we calculate the Quality-Adjusted Life Expectancy (QALE) of the Greek population and regress it against per capita public health expenditure, using an instrumental variable approach and controlling for a set of covariates. The estimated coefficients of expenditure on QALE are used to inform a cost-effectiveness threshold, estimatead as the cost per QALY gained through a permanent increase in per capita spending.

Results

Based on the estimated coefficient of health expenditure, we estimate a base case cost-effectiveness threshold of €27,117 per QALY gained for the Greek healthcare system, from a third-party payer perspective.

Conclusions

In the Greek healthcare system, which is currently in the stage of establishing a comprehensive health technology assessment process, decision rules which are not based on heuristics or “rules of thumb”, are essential.

背景新医疗技术的引入提高了生活质量和寿命,但也给医疗系统稀缺的资源带来了额外的压力。因此,在决定是否采用新技术时,除其他标准外,通常还需考虑竞争替代方案的成本与效果之间的差异。本文旨在估算一个成本效益阈值,该阈值可作为希腊医疗技术资助(或报销)决策过程中的一项投入。方法在 30 年的时间里,我们计算了希腊人口的质量调整后预期寿命(QALE),并利用工具变量法将其与人均公共医疗支出进行回归,同时控制一组协变量。结果基于医疗支出的估计系数,我们从第三方支付者的角度估计出希腊医疗保健系统的基础成本效益阈值为每 QALY 27,117 欧元。结论希腊医疗保健系统目前正处于建立全面医疗技术评估流程的阶段,因此必须制定不以启发式或 "经验法则 "为基础的决策规则。
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引用次数: 0
Evaluating dyNamic myocardial blood flow qUantitation as a Cost-effective care modeL for diabEtic patients with coronary artery diSease (NUCLEuS): A randomized controlled trial – Rationale and Design 评估动态心肌血流激发作为冠心病患者具有成本效益的护理模式(NUCLEuS):随机对照试验 - 原理与设计
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-12 DOI: 10.1016/j.hlpt.2024.100881
Jie Jun Wong , Louis LY Teo , Fei Gao , Liang Zhong , Weimin Huang , Nicholas Graves , Ru-San Tan , Terrance SJ Chua , Felix JY Keng , Angela S. Koh

Background

Recent advancements in quantifying myocardial blood flow (MBF) and coronary flow reserve using dynamic SPECT MPI have demonstrated comparable hemodynamic correlations with invasive angiography and PET. Implementation into routine practice, however, imposes attendant demands on resources. Diabetes mellitus is a rising pandemic associated with accelerated atherosclerosis, yet there is potential for under-detection of significant ischemia.

Objectives

We postulate that quantifying myocardial blood flow (MBF) by dynamic SPECT reduces post-test resource utilization and improve economic efficiency over conventional SPECT.

Methods

NUCLEuS is an ongoing prospective open-label randomized clinical trial that will enroll 300 diabetic patients without known coronary artery disease (CAD) referred clinically for SPECT MPI from March 2022 to March 2025. The aim is to determine the incremental prognostic value and post-test resource utilization of dynamic MBF over conventional SPECT in diabetic patients with suspected CAD. The primary endpoint is diagnostic failure, defined as unnecessary coronary angiography (absence of ≥50% stenosis in ≥1 coronary artery) or additional anatomical testing (e.g., coronary computed tomography angiography) within 90 days. Secondary endpoints are referrals for angiography or revascularization, escalation of anti-anginal medications, and quality-of-life scores at 12 months. Long-term endpoints are major adverse cardiovascular events (cardiac mortality, myocardial infarction, unstable angina, revascularization) within 36 months. The incremental cost-effectiveness ratio will be estimated based on cost and clinical effectiveness.

Conclusions

NUCLEuS will be an imaging-directed clinical trial that will compare differences in outcomes and resource utilization of dynamic MBF over conventional SPECT MPI in the routine clinical management of CAD in diabetes mellitus.

背景使用动态 SPECT MPI 定量心肌血流(MBF)和冠状动脉血流储备的最新进展表明,其血流动力学相关性与有创血管造影和 PET 相当。然而,将其应用于常规临床实践对资源提出了相应的要求。方法NUCLEuS是一项正在进行的前瞻性开放标签随机临床试验,将在2022年3月至2025年3月期间招募300名临床转诊的无已知冠状动脉疾病(CAD)的糖尿病患者进行SPECT MPI检查。目的是确定动态 MBF 与传统 SPECT 相比,对疑似 CAD 的糖尿病患者的预后价值增量和检测后资源利用率。主要终点是诊断失败,定义为 90 天内不必要的冠状动脉造影(≥1 支冠状动脉没有≥50% 的狭窄)或额外的解剖检查(如冠状动脉计算机断层扫描血管造影)。次要终点是转诊进行血管造影术或血管重建术、抗心绞痛药物升级以及 12 个月的生活质量评分。长期终点为 36 个月内的主要不良心血管事件(心脏病死亡率、心肌梗死、不稳定型心绞痛、血管再通)。结论NUCLEuS 将是一项以成像为导向的临床试验,它将比较动态 MBF 与传统 SPECT MPI 在糖尿病患者 CAD 常规临床管理中的结果和资源利用率的差异。
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引用次数: 0
Digital lifestyle interventions for cardiovascular risk reduction: A systematic review and network meta-analysis 降低心血管风险的数字化生活方式干预:系统综述和网络荟萃分析
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-06 DOI: 10.1016/j.hlpt.2024.100879
Teketo Kassaw Tegegne , Desalegn Markos Shifti , Jonathan Charles Rawstorn , Paul Jansons , Yuxin Zhang , Reza Daryabeygikhotbehsara , Sheikh Mohammed Shariful Islam , Ralph Maddison

Objectives

To compare the relative effectiveness of different digital lifestyle interventions in improving cardiovascular risk factors.

Methods

A comprehensive systematic review and network meta-analysis (NMA) of randomized controlled trials (RCTs) was conducted. Seven electronic databases were searched from 1990 to April 4, 2024. The certainty of evidence was evaluated using the Grading of Recommendations, Assessment, Development, and Evaluations (GRADE) approach. A Bayesian random-effects network meta-analysis (NMA) was performed. Continuous outcomes are reported as mean differences (MD) with their 95 % credible intervals (CrI).

Results

The combinations of physical activity + diet + smoking cessation (PA+D+Sm), and physical activity + diet (PA+D) components were the most effective interventions, leading to substantial improvements in multiple cardiovascular risk factors compared to usual care or some other digital lifestyle interventions with low to high certainty. Dietary interventions significantly reduced body weight and glycosylated hemoglobin (HbA1c) compared to usual care. Although the effect sizes did not meet established clinical significance thresholds for most cardiovascular risk factors, they still hold clinical relevance, highlighting the potential for significant health improvements.

Conclusions

Multifactorial digital lifestyle interventions, particularly those combining PA+D+Sm and PA+D components, appear the most promising for reducing cardiovascular risk factors.

方法 对随机对照试验(RCT)进行了全面的系统综述和网络荟萃分析(NMA)。检索了 1990 年至 2024 年 4 月 4 日期间的七个电子数据库。采用建议、评估、发展和评价分级法(GRADE)对证据的确定性进行了评估。进行了贝叶斯随机效应网络荟萃分析(NMA)。结果体育锻炼+饮食+戒烟(PA+D+Sm)和体育锻炼+饮食(PA+D)的组合是最有效的干预措施,与常规护理或其他一些低到高确定性的数字生活方式干预措施相比,能显著改善多种心血管风险因素。与常规护理相比,饮食干预能明显降低体重和糖化血红蛋白(HbA1c)。结论多因素数字化生活方式干预,尤其是那些结合了 PA+D+Sm 和 PA+D 成分的干预,似乎最有希望降低心血管风险因素。
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引用次数: 0
“Following the data”: Perceptions of and willingness to use clinical decision support tools to inform HIV care among Haitian clinicians "跟踪数据":海地临床医生对使用临床决策支持工具为艾滋病毒护理提供信息的看法和意愿
IF 3.4 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-05 DOI: 10.1016/j.hlpt.2024.100880
Andrew M. Secor , John Justafort , Chenet Torrilus , Jean Guy Honoré , Sharon Kiche , Tracy K. Sandifer , Kristin Beima-Sofie , Anjuli D. Wagner , Jillian Pintye , Nancy Puttkammer

Background

Clinical decision support (CDS) tools can support HIV care, including through case tracking, treatment and medication monitoring, and promoting provider compliance with care guidelines. There has been limited research into the technical, organizational, and behavioral factors that impact perceptions of and willingness to use CDS tools at scale in resource-limited settings, including in Haiti.

Methods

Our sample included fifteen purposively chosen Haitian HIV program experts, including active clinicians and HIV program managers. Participants completed structured quantitative surveys and one-on-one qualitative semi-structured interviews.

Results

Study participants had high levels of familiarity and experience with CDS tools. The primary motivator for CDS tool use was a perceived benefit to quality of care, including improved provider time use, efficiency, and decision-making ability, and patient outcomes. Participants highlighted decision-making autonomy and how CDS tools could support provider decision making but should not supplant provider knowledge and experience. Participants highlighted the need for sufficient provider training/sensitization, inclusion of providers in the system design process, and prioritization of tool user-friendliness as key mechanisms to drive tool use and impact. Some participants noted that systemic issues, such as limited laboratory capacity, may reduce the usefulness of CDS alerts, particularly concerning differentiated care and priority viral load testing.

Conclusion

Respondents had largely positive perceptions of EMRs and CDS tools, particularly due to perceived improvements in quality of care. To improve tool use, stakeholders should prioritize tool user-friendliness and provider training. Addressing systemic health system issues is necessary to unlock the full potential of these tools.

背景临床决策支持(CDS)工具可以通过病例追踪、治疗和药物监测以及促进医疗服务提供者遵守医疗指南等方式支持艾滋病护理。在资源有限的环境中,包括在海地,对影响大规模使用 CDS 工具的看法和意愿的技术、组织和行为因素的研究还很有限。方法 我们的样本包括 15 名特意挑选的海地 HIV 项目专家,其中包括活跃的临床医生和 HIV 项目经理。参与者完成了结构化定量调查和一对一半结构化定性访谈。使用 CDS 工具的主要动机是认为它有利于提高医疗质量,包括改善医疗服务提供者的时间利用、效率和决策能力,以及改善患者的治疗效果。与会者强调了决策自主权以及 CDS 工具如何支持医疗服务提供者的决策,但不应取代医疗服务提供者的知识和经验。与会者强调,作为推动工具使用和影响的关键机制,需要对医疗服务提供者进行充分的培训/宣传,将医疗服务提供者纳入系统设计过程,并优先考虑工具的用户友好性。一些参与者指出,实验室能力有限等系统性问题可能会降低 CDS 警报的效用,特别是在有区别的护理和优先病毒载量检测方面。为提高工具的使用率,相关方应优先考虑工具的易用性和对提供者的培训。要充分释放这些工具的潜力,就必须解决系统性的医疗系统问题。
{"title":"“Following the data”: Perceptions of and willingness to use clinical decision support tools to inform HIV care among Haitian clinicians","authors":"Andrew M. Secor ,&nbsp;John Justafort ,&nbsp;Chenet Torrilus ,&nbsp;Jean Guy Honoré ,&nbsp;Sharon Kiche ,&nbsp;Tracy K. Sandifer ,&nbsp;Kristin Beima-Sofie ,&nbsp;Anjuli D. Wagner ,&nbsp;Jillian Pintye ,&nbsp;Nancy Puttkammer","doi":"10.1016/j.hlpt.2024.100880","DOIUrl":"10.1016/j.hlpt.2024.100880","url":null,"abstract":"<div><h3>Background</h3><p>Clinical decision support (CDS) tools can support HIV care, including through case tracking, treatment and medication monitoring, and promoting provider compliance with care guidelines. There has been limited research into the technical, organizational, and behavioral factors that impact perceptions of and willingness to use CDS tools at scale in resource-limited settings, including in Haiti.</p></div><div><h3>Methods</h3><p>Our sample included fifteen purposively chosen Haitian HIV program experts, including active clinicians and HIV program managers. Participants completed structured quantitative surveys and one-on-one qualitative semi-structured interviews.</p></div><div><h3>Results</h3><p>Study participants had high levels of familiarity and experience with CDS tools. The primary motivator for CDS tool use was a perceived benefit to quality of care, including improved provider time use, efficiency, and decision-making ability, and patient outcomes. Participants highlighted decision-making autonomy and how CDS tools could support provider decision making but should not supplant provider knowledge and experience. Participants highlighted the need for sufficient provider training/sensitization, inclusion of providers in the system design process, and prioritization of tool user-friendliness as key mechanisms to drive tool use and impact. Some participants noted that systemic issues, such as limited laboratory capacity, may reduce the usefulness of CDS alerts, particularly concerning differentiated care and priority viral load testing.</p></div><div><h3>Conclusion</h3><p>Respondents had largely positive perceptions of EMRs and CDS tools, particularly due to perceived improvements in quality of care. To improve tool use, stakeholders should prioritize tool user-friendliness and provider training. Addressing systemic health system issues is necessary to unlock the full potential of these tools.</p></div>","PeriodicalId":48672,"journal":{"name":"Health Policy and Technology","volume":"13 3","pages":"Article 100880"},"PeriodicalIF":3.4,"publicationDate":"2024-06-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141398396","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
How do self-motivation and social motivation contribute to consumers’ acceptance of m-health services? 自我激励和社会激励如何促进消费者接受移动医疗服务?
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-05 DOI: 10.1016/j.hlpt.2024.100878
Da Tao , Kaifeng Liu

Objectives

The study aimed to propose a unified model integrating the technology acceptance model (TAM), social-determination theory (SDT), and social motivation to examine the roles of self-motivation (i.e., autonomy, relatedness, and competency) and social motivation (i.e., social influence and social recognition) in consumer acceptance of m-health services. In addition, the study aimed to explore whether relationships among the antecedent factors and consumer acceptance of m-health services would be moderated by consumers’ demographic characteristics.

Methods

Partial least squares structural equation modelling (PLS-SEM) approach was used to test the proposed model with data from 614 Chinese m-health users. Multi-group analyses were performed to examine whether the results were different or equivalent across demographic backgrounds.

Results

Usage behavior was significantly influenced by behavioral intention. While self-motivations mostly exerted impacts on behavioral intention through the mediating roles of perceived usefulness and perceived ease of use, social motivations affected behavioral intention both directly and indirectly through the mediating roles of perceived usefulness. In addition, most of the hypothesized relations remained unchanged across gender, age, and usage experience.

Conclusions

This study reveals the important roles of varied self- and social motivations in developing consumer acceptance of m-health services. To facilitate consumers’ acceptance, m-health services should be designed to meet consumers’ internal requirements on autonomy and relatedness and earn recognition from social perspectives. The findings provide insights into the design and implementation of m-health services in support of consumer acceptance across different demographic backgrounds.

Public interest summary

M-health has long been considered as a promising tool to support individuals’ health care activities and achieve improved efficiency and quality in the delivery of health care services. However, the introduction of m-health to consumers has proven difficult, and wide acceptance has not been achieved. We conducted a field survey of 614 Chinese m-health users to identify the roles of self-motivation and social motivation in consumers’ acceptance of m-health services. We found that self-motivation can exert impacts on consumers’ acceptance through the mediating roles of perceived usefulness and perceived ease of use, while social motivation affected acceptance both directly and indirectly through the mediating roles of perceived usefulness. In addition, these effects mostly remained unchanged across consumers’ gender, age, and usage experience. Based on our findings, we propose implications to design and implement m-health services in support of consumer acceptance across different demographic backgrounds.

目的本研究旨在提出一个整合了技术接受模型(TAM)、社会决定理论(SDT)和社会动机的统一模型,以探讨自我动机(即自主性、相关性和能力)和社会动机(即社会影响和社会认可)在消费者接受移动医疗服务中的作用。此外,该研究还旨在探讨消费者的人口统计学特征是否会调节前因因素与消费者对移动医疗服务接受度之间的关系。结果使用行为受到行为意向的显著影响。自我动机主要通过感知有用性和感知易用性的中介作用对行为意向产生影响,而社会动机则通过感知有用性的中介作用直接或间接地影响行为意向。此外,大多数假设关系在不同性别、年龄和使用经验的情况下保持不变。为促进消费者的接受,移动医疗服务的设计应满足消费者对自主性和相关性的内在要求,并从社会角度赢得认可。研究结果为移动医疗服务的设计和实施提供了见解,以支持不同人口背景的消费者接受移动医疗服务。 公益摘要移动医疗一直被认为是支持个人医疗保健活动、提高医疗保健服务效率和质量的有效工具。然而,事实证明,向消费者介绍移动医疗是困难的,而且尚未获得广泛接受。我们对 614 名中国移动医疗用户进行了实地调查,以确定自我激励和社会激励在消费者接受移动医疗服务中的作用。我们发现,自我动机可以通过感知有用性和感知易用性的中介作用对消费者的接受度产生影响,而社会动机则通过感知有用性的中介作用直接或间接地影响消费者的接受度。此外,这些效应在不同性别、年龄和使用经验的消费者中大多保持不变。根据我们的研究结果,我们提出了设计和实施移动医疗服务的启示,以支持不同人口背景的消费者接受移动医疗服务。
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引用次数: 0
Public database on pharmaceutical ties in Japan: Traffic and user attitudes on industry-professional relationships 日本医药关系公共数据库:交通和用户对行业与专业关系的态度。
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-01 DOI: 10.1016/j.hlpt.2024.100847
Yosuke Suzuki , Anju Murayama , Akihiko Ozaki , Hiroaki Saito , Toyoaki Sawano , Erika Yamashita , Tetsuya Tanimoto

Background

It is imperative to understand the specific details of the usage of the databases documenting financial ties between pharmaceutical companies and the healthcare sector and the attitudes of such database in evaluating how the citizens would recognize this issue. This study aimed to elucidate usage patterns and user attitudes regarding value transfers by analyzing data from the Yen For Docs Database in Japan (YDJ).

Methods and Materials

The study spanned the entire available data period, from January 15, 2019, to May 24, 2021, using Google Analytics to extract YDJ visitor data, including details on unique users, sessions, page views, and access paths over time. All visitors were invited to participate in a questionnaire survey gauging their attitudes towards value transfers from pharmaceutical firms to healthcare professionals. The survey data were analyzed separately for distinct groups, including non-healthcare or industry respondents, healthcare professionals, and those affiliated with pharmaceutical companies.

Results

YDJ received 604,903 accesses from 354,863 unique users, viewing 5,635,087 pages. Usage spiked initially and at later points. A survey of 399 respondents revealed negative views on value transfers from pharmaceutical companies, with over half finding it unethical. More than two-thirds supported stricter regulations. Non-healthcare respondents were less favorable compared to healthcare professionals and those affiliated with pharmaceutical companies.

Conclusion

YDJ achieved substantial user engagement, and the embedded questionnaire survey revealed prevalent critical perspectives among users regarding value transfers from pharmaceutical companies to the healthcare sector. Non-healthcare or industry respondents, in particular, expressed the most negative views about such relationships.

研究背景 了解记录制药公司与医疗保健部门之间财务关系的数据库的具体使用细节以及这些数据库在评估公民如何认识这一问题时所持的态度是非常必要的。本研究旨在通过分析日本Yen For Docs数据库(YDJ)的数据,阐明用户对价值转移的使用模式和态度。研究方法和材料本研究跨越了从2019年1月15日到2021年5月24日的整个可用数据期,使用Google Analytics提取YDJ访客数据,包括独立用户、会话、页面浏览量和访问路径的详细信息。我们邀请所有访问者参与问卷调查,以了解他们对制药公司向医疗保健专业人员转移价值的态度。调查数据按不同的群体分别进行了分析,包括非医疗保健或行业受访者、医疗保健专业人员以及制药公司的附属人员。结果YDJ 收到了来自 354,863 位独立用户的 604,903 次访问,浏览了 5,635,087 个页面。最初和后来的使用量都激增。对 399 名受访者进行的调查显示,他们对制药公司的价值转移持负面看法,一半以上的受访者认为这种行为不道德。超过三分之二的受访者支持制定更严格的法规。结论YDJ 实现了大量的用户参与,嵌入式问卷调查显示,用户普遍对制药公司向医疗保健行业的价值转移持批评观点。尤其是非医疗保健或行业受访者对这种关系表达了最消极的看法。
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引用次数: 0
Working with epistemic uncertainties: Emerging entanglements within conditional reimbursement practices 与认识上的不确定性打交道:有条件报销实践中新出现的纠葛
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-01 DOI: 10.1016/j.hlpt.2024.100850
Rik Wehrens, Bert de Graaff
<div><h3>Objectives</h3><p>HTA agencies are experimenting with conditional reimbursement approaches allowing greater flexibility to cope with epistemic uncertainties generated by new health technologies and pharmaceuticals lacking evidence. While some research into promises and effects of conditional reimbursement is conducted, little empirical research investigates how such policies play out in practice. In this paper, we analyze two cases of conditional reimbursement in the Netherlands.</p></div><div><h3>Methods</h3><p>Case studies were purposively selected. We conducted document analysis combined with semi-structured in-depth interviews (<em>n</em> = 28). We analyzed both case studies together through initial thematic analysis and additional abductive analysis. Results were verified through data triangulation. We performed a member check in which we presented our preliminary analysis during a reflection meeting with key stakeholders.</p></div><div><h3>Results</h3><p>We identified three tensions in the practices of CED-schemes: proceduralism versus improvisation, steering professionals versus providing leeway, involving patients as data subjects versus legitimate stakeholders. These tensions explicate several sources of epistemic uncertainties that extend beyond methodological and more well-known socio-political pressures such as from industry on regular reimbursement decision-making process. We note the importance of improvisation work, of normative considerations, and of epistemic hierarchies.</p></div><div><h3>Conclusions</h3><p>We postulate that the emerging uncertainties within the practice of CED-schemes are to an extent unavoidable as they emerge from the necessarily interactive and normative nature of human relations. We conceptualize this with the notion of ‘epistemic entanglements’, which highlights how normative and scientific dimensions are interwoven in reimbursement decisions. As epistemic uncertainties are difficult to reduce and tame in practice the need for a more reflexive and inclusive approach to conditional reimbursement decision-making becomes apparent.</p></div><div><h3>Public interest abstract</h3><p>New technologies and personalized medicines can have great health benefits for patients, but often not enough knowledge is available to assess whether these innovations live up to their expectations. At the same time, despite this uncertainty, governments need to make a decision about whether or not to reimburse these innovations. Many countries are experimenting with forms of conditional reimbursement: temporarily reimbursement of technologies until more evidence is collected regarding (cost-)effectiveness in practice. Although much literature addresses potential benefits and drawbacks of conditional reimbursement policies, few studies look into how such policies play out in practice. In our research we study two examples of conditional reimbursement practices. We show conditional reimbursement practices lead to three new t
目的 卫生和药品管理局正在尝试采用有条件报销的方法,以便更灵活地应对新医疗技术和缺乏证据的药品所带来的认识上的不确定性。虽然对有条件报销的承诺和效果进行了一些研究,但很少有实证研究调查此类政策在实践中是如何发挥作用的。本文分析了荷兰有条件报销的两个案例。我们进行了文件分析和半结构式深度访谈(n = 28)。我们通过初步的主题分析和额外的归纳分析对两个案例研究进行了综合分析。我们通过数据三角分析对结果进行了验证。我们进行了一次成员检查,在与主要利益相关者的反思会议上介绍了我们的初步分析。结果我们在 CED 计划的实践中发现了三种紧张关系:程序主义与随机应变、指导专业人员与提供回旋余地、患者作为数据主体参与与合法利益相关者参与。这些矛盾解释了认识论不确定性的几个来源,这些不确定性超出了方法论的范畴,也超出了众所周知的社会政治压力,例如来自行业对常规报销决策过程的压力。我们注意到即兴工作、规范性考虑和认识论等级的重要性。结论我们推测,CED 计划实践中新出现的不确定性在某种程度上是不可避免的,因为它们产生于人类关系必然的互动性和规范性。我们用 "认识上的纠葛 "这一概念来概括这一点,它强调了规范性和科学性是如何在补偿决策中交织在一起的。由于认识论上的不确定性在实践中难以减少和控制,因此显然需要一种更具反思性和包容性的方法来进行有条件的报销决策。公众利益摘要新技术和个性化药物可以为患者带来巨大的健康益处,但往往没有足够的知识来评估这些创新是否符合他们的期望。同时,尽管存在这种不确定性,政府仍需要决定是否对这些创新进行报销。许多国家正在尝试有条件报销的形式:在收集到更多有关实际(成本)效益的证据之前,暂时对技术进行报销。尽管许多文献都论述了有条件报销政策的潜在好处和弊端,但很少有研究探讨此类政策在实践中是如何发挥作用的。在我们的研究中,我们研究了两个有条件报销实践的例子。我们发现,有条件报销做法导致了三种新的紧张局势。我们的结论是,认识到证据开发和规范考虑因素相互交织的方法将使 HTA 机构受益。
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引用次数: 0
Telemedicine decision-making in primary care during the COVID-19 pandemic: Balancing patient agency and provider expertise COVID-19 大流行期间初级保健中的远程医疗决策:平衡患者代理与医疗服务提供者的专业知识
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-01 DOI: 10.1016/j.hlpt.2024.100839
Kimberly A. Muellers , Katerina Andreadis , Rahma S. Mkuu , Jenny J. Lin , Carol R. Horowitz , Rainu Kaushal , Jessica S. Ancker
<div><h3>Objectives</h3><p>The COVID-19 pandemic precipitated the expansion of telemedicine use worldwide, introducing a new dimension of healthcare decision-making – choosing a visit format – not previously experienced by most patients or providers. To date, the pandemic's impact on decisions about using telemedicine versus in-person visits in primary care has not been fully explored. The purpose of this study was to examine patient and provider accounts of decision-making about the choice between telemedicine and in-person care during the COVID-19 pandemic.</p></div><div><h3>Methods</h3><p>Primary care providers and patients were recruited from four healthcare systems across three states in the United States. Participants completed semi-structured interviews about their experiences using telemedicine for primary care during the pandemic. Data pertaining to decision-making about telemedicine were examined as a secondary analysis using interpretive description.</p></div><div><h3>Results</h3><p>Twenty-one providers and 65 patients completed interviews. Patients’ ability to choose their own visit format influenced their level of satisfaction with telemedicine care, while providers expressed concern about leaving visit format entirely up to their patients. Patients and providers generally agreed that telemedicine was well-suited for routine follow-ups, reviewing results, and medication management. However, in cases of urgent health problems, patients and providers differed in their criteria for determining what visit format is most appropriate but agreed that telemedicine could be a useful tool for “quick fixes” and for fast and effective triage.</p></div><div><h3>Conclusions</h3><p>Primary care patients and providers emphasized the importance of agency during care delivery and shared opportunities for effective triage via telemedicine. Further research should focus on developing tools to support shared healthcare decisions regarding telemedicine use under changing healthcare conditions, particularly for urgent health questions.</p></div><div><h3>Public Interest Summary</h3><p>The COVID-19 pandemic has increased telemedicine use around the world. This study looked at patient and provider decisions about using telemedicine versus in-person care during the pandemic. We asked 21 primary care providers and 65 patients from four healthcare systems across three U.S. states about their experiences using telemedicine during the pandemic. Patients were more satisfied if they were able to choose whether to have an in-person or video visit, while providers worried that allowing patients to choose the visit format could get in the way of care when patients need physical exams or laboratory testing. Patients and providers gave different reasons for choosing a visit format, but both agreed that telemedicine was useful for “quick fixes” and making decisions together in emergencies. Healthcare systems should create tools to help patients and providers decide when t
目的 COVID-19 大流行促进了远程医疗在全球范围内的推广使用,为医疗决策引入了一个新的维度--选择就诊形式--这是大多数患者或医疗服务提供者以前从未经历过的。迄今为止,人们尚未充分探讨大流行对初级保健中使用远程医疗与亲自就诊决策的影响。本研究的目的是探讨在 COVID-19 大流行期间,患者和医疗服务提供者在选择远程医疗还是面对面就诊时的决策情况。方法从美国三个州的四个医疗保健系统中招募初级医疗服务提供者和患者。参与者完成了半结构化访谈,讲述了他们在大流行期间使用远程医疗进行初级保健的经历。结果21 名医疗服务提供者和 65 名患者完成了访谈。患者能够选择自己的就诊形式影响了他们对远程医疗的满意度,而医疗服务提供者则对完全由患者决定就诊形式表示担忧。患者和医疗服务提供者普遍认为,远程医疗非常适合常规随访、检查结果和药物管理。然而,在出现紧急健康问题时,患者和医疗服务提供者在确定何种就诊形式最合适的标准上存在分歧,但他们一致认为远程医疗可以成为 "快速解决问题 "和快速有效分诊的有用工具。结论初级医疗患者和医疗服务提供者都强调了在提供医疗服务过程中代理的重要性,并分享了通过远程医疗进行有效分诊的机会。进一步的研究应侧重于开发工具,以支持在不断变化的医疗条件下就远程医疗的使用做出共同的医疗决策,尤其是针对紧急的健康问题。本研究调查了患者和医疗服务提供者在大流行期间使用远程医疗与面对面医疗的决策。我们询问了来自美国三个州四个医疗保健系统的 21 名初级保健提供者和 65 名患者在大流行期间使用远程医疗的经验。如果患者能够选择亲自就诊还是视频就诊,他们会更满意;而医疗服务提供者则担心,如果允许患者选择就诊形式,可能会在患者需要体检或化验时妨碍医疗服务。患者和医疗服务提供者对选择就诊形式给出了不同的理由,但他们都认为远程医疗对于 "快速解决问题 "和在紧急情况下共同做出决定非常有用。医疗系统应开发工具,帮助患者和医疗服务提供者决定何时使用远程医疗,尤其是在处理紧急健康问题时。
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引用次数: 0
Apps don't work for patients who don't use them: Towards frameworks for digital therapeutics adherence 对于不使用应用程序的患者来说,应用程序不起作用:建立数字治疗依从性框架
IF 6 3区 医学 Q1 HEALTH POLICY & SERVICES Pub Date : 2024-06-01 DOI: 10.1016/j.hlpt.2024.100848
David G. Schwartz , Sivan Spitzer , Michael Khalemsky , Arturo Heyner Cano-Bejar , Soumya Ray , Jeng-Yuan Chiou , Rizan Sakhnini , Raya Lanin , Menachem M. Meir , Ming-Che Tsai

Objectives

Digital therapeutics such as mobile health applications (mHealth apps) are becoming part of patients’ treatment programs. Ensuring patients actually use (adhere to) an app as prescribed, effectively measuring and interpreting usage, and detecting clinical non-compliance are fundamental to effective treatment. Clinicians are not currently prepared to deal with issues of patients’ adherence to digital therapeutics (DTx). This study proposes and analyses potential frameworks for clinician-patient dialogue about DTx adherence.

Methods

Purposive sampling is used to select three leading adherence frameworks, one at each of the micro (patient), mesa (physician), and macro (system) levels of healthcare. The ABC taxonomy of adherence stages; Osterberg and Blaschke's medication adherence framework; and the Morisky Medication Adherence Scale-8 (MMAS8). Each framework is deconstructed and analysed from the perspective of DTx adherence.

Results

Modifications to ABC can improve suitability to conceptualize DTx adherence whilst maintaining the overall framework. Osterberg and Blaschke's framework provides many metrics adaptable to app assessment alongside some that are inapplicable. Significant modification of MMAS-8 appears necessary to build relevance to DTx adherence reporting. Specific reconceptualizations of each framework element are presented.

Conclusions

A strong basis for studying and measuring DTx adherence exists in existing treatment adherence research and practice, and can help guide policy. However, important adaptations are needed to ensure the development of methods for use in clinical environments.

目的:移动医疗应用程序(mHealth 应用程序)等数字疗法正在成为患者治疗计划的一部分。确保患者按照处方实际使用(坚持使用)应用程序、有效测量和解释使用情况以及检测临床违规行为是有效治疗的基础。目前,临床医生还没有准备好处理患者对数字疗法(DTx)的依从性问题。本研究提出并分析了临床医生与患者就数字疗法依从性进行对话的潜在框架:方法:本研究采用有目的的抽样方法,从医疗保健的微观(患者)、中观(医生)和宏观(系统)三个层面各选择一个主要的依从性框架。这三个框架分别是:坚持用药阶段的 ABC 分类法;Osterberg 和 Blaschke 的坚持用药框架;以及 Morisky Medication Adherence Scale-8 (MMAS8)。从 DTx 依从性的角度对每个框架进行了解构和分析:结果:在保持整体框架的前提下,对 ABC 进行修改可提高 DTx 依从性概念化的适用性。Osterberg和Blaschke的框架提供了许多适用于应用评估的指标,同时也提供了一些不适用的指标。对 MMAS-8 进行重大修改似乎是必要的,这样才能建立与 DTx 报告的相关性。本文介绍了对每个框架要素的具体重新认识:现有的治疗依从性研究和实践为研究和测量 DTx 依从性奠定了坚实的基础,有助于为政策提供指导。然而,还需要进行重要的调整,以确保开发出适用于临床环境的方法。
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