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评价 SINERGIAPS,一项基于患者感知和体验的改善西班牙初级保健中心患者安全的干预措施:一项混合类型 I 随机临床试验方案。

Evaluation of SINERGIAPS, an intervention to improve patient safety in primary healthcare centers in Spain based on patients' perceptions and experiences: a protocol for a hybrid type I randomized clinical trial.

机构信息

Health Research Institute of the Balearic Islands (IdISBa), Hospital Universitari Son Espases, Palma, Spain.

Network for Research on Chronicity, Primary Care, and Health Promotion (RICAPPS), Spain.

出版信息

Front Public Health. 2024 Mar 26;12:1324940. doi: 10.3389/fpubh.2024.1324940. eCollection 2024.

Abstract

BACKGROUND

Adverse events in the primary care setting result in a direct cost equivalent to at least 2.5% of total healthcare spending. Across OECD countries, they lead to more than seven million avoidable hospital admissions annually. In this manuscript, we describe the protocol of a trial aimed at evaluating the effectiveness of SinergiAPS (a patient-centered audit and feedback intervention) in reducing avoidable hospital admission and explore the factors that may affect its implementation.

METHODS

We will conduct a 24-month, parallel, open-label, multicenter, pragmatic, hybrid type 1 randomized clinical trial. 118 primary healthcare centers with wide geographical distribution in Spain will be randomly assigned (ratio 1:1) to two groups. The intervention group will receive two audits (baseline and intermediate at 12 months) based on information collected through the administration of the PREOS-PC questionnaire (a measure of patient-reported patient safety) to a convenience sample of 100 patients per center. The intervention group will receive reports on the results of both audits, along with educational resources aimed at facilitating the design and implementation of safety improvement plans. The control group will receive care as usual. The primary outcome will be the rate of avoidable hospitalizations (administrative data). Secondary outcomes: patient-reported patient safety experiences and outcomes (PREOS-PC questionnaire); patient safety culture as perceived by professionals (MOSPSC questionnaire); adverse events reported by healthcare professionals ( questionnaire); the number of safety improvement actions which the re has implemented ( questionnaire). Outcome data will be collected at baseline and 24 months follow-up. For the evaluation of the implementation of the SinergiAPS intervention, we will draw on the Consolidated Framework for Implementation Research (CFIR). We will collect and analyze qualitative and quantitative data (30 individual interviews, implementation logbooks; questionnaires for professionals from intervention centers, and level of use of the SinergiAPS web tool).

DISCUSSION

This study will expand the scarce body of evidence existing regarding the effects and implementation of interventions aimed at promoting patient and family engagement in primary healthcare, specifically for enhancing patient safety. The study has the potential to produce an impact on clinical practice, healthcare systems, and population health.: https://clinicaltrials.gov/study/NCT05958108?term=sinergiAPS&rank=1 (NCT05958108).

摘要

背景

初级保健环境中的不良事件导致的直接成本相当于总医疗支出的至少 2.5%。在经合组织国家,这些不良事件导致每年有超过 700 万人可避免的住院。在本文中,我们描述了一项旨在评估 SinergiAPS(以患者为中心的审核和反馈干预措施)在减少可避免的住院治疗方面的有效性的试验方案,并探讨了可能影响其实施的因素。

方法

我们将进行一项为期 24 个月的、平行的、开放标签的、多中心的、实用的、混合 1 型随机临床试验。西班牙具有广泛地理分布的 118 个初级保健中心将被随机分配(比例为 1:1)到两组。干预组将根据通过管理 PREOS-PC 问卷(衡量患者报告的患者安全的措施)收集的信息,对每个中心的 100 名患者进行两次审核(基线和 12 个月时的中期审核)。干预组将收到两次审核结果的报告,以及旨在促进安全改进计划设计和实施的教育资源。对照组将接受常规护理。主要结局是可避免住院率(行政数据)。次要结局:患者报告的患者安全体验和结局(PREOS-PC 问卷);专业人员感知的患者安全文化(MOSPSC 问卷);医疗保健专业人员报告的不良事件(问卷);已实施的安全改进措施数量(问卷)。将在基线和 24 个月随访时收集结局数据。为了评估 SinergiAPS 干预措施的实施情况,我们将借鉴实施研究综合框架(CFIR)。我们将收集和分析定性和定量数据(30 次个体访谈、实施日志;干预中心专业人员的问卷,以及 SinergiAPS 网络工具的使用水平)。

讨论

这项研究将扩大现有的关于以促进患者和家属参与初级保健为重点的干预措施的效果和实施的证据基础,特别是为了增强患者安全。该研究有可能对临床实践、医疗保健系统和人口健康产生影响:https://clinicaltrials.gov/study/NCT05958108?term=sinergiAPS&rank=1(NCT05958108)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2395/11003190/24af27d32848/fpubh-12-1324940-g001.jpg

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