Charité-Universitätsmedizin Berlin, Institute of Medical Sociology and Rehabilitation Science, Berlin, Germany.
Emergency and Acute Medicine (CVK, CCM), Charité-Universitätsmedizin Berlin, Berlin, Germany.
PLoS One. 2022 Aug 24;17(8):e0273115. doi: 10.1371/journal.pone.0273115. eCollection 2022.
This study aims to improve emergency department (ED) care for patients suffering from atraumatic abdominal pain. An application-supported pathway for the ED will be implemented, which supports quick, evidence-based, and standardized diagnosis and treatment steps for patients with atraumatic abdominal pain at the ED. A mixed-methods multicentre cluster randomized controlled stepped wedge trial design will be applied. A total of 10 hospitals with EDs (expected n = 2.000 atraumatic abdominal pain patients) will consecutively (every 4 months) be randomized to apply the intervention. Inclusion criteria for patients are a minimum age of 18 years, suffering from atraumatic abdominal pain and being insured with a German statutory health insurance. Primary outcomes: acute pain score at time of discharge from ED, duration of treatment at the ED, patient-reported satisfaction. Secondary endpoints include patient safety and quality of care parameters, process evaluation parameters, and costs and cost-effectiveness parameters. Quantitative data will be gathered from patient-surveys, clinical records, and routine data from hospital information systems as well as from a participating German statutory health insurance. Descriptive and analytic statistical analysis will be performed to provide summaries and associations for primary patient-reported outcomes, process measures, quality measures, and costs. Qualitative data collection consists of participatory patient observations and semi-structured expert interviews, which will be inductively analysed. Findings will be disseminated in publications in peer-reviewed journals, on conferences, as well as via a project website. To ensure data protection, appropriate technical and organisational measures will be taken. Trial registration: DRKS00021052.
本研究旨在改善急诊科(ED)对非创伤性腹痛患者的治疗。将实施一种应用支持的 ED 路径,该路径支持对 ED 中非创伤性腹痛患者进行快速、基于证据和标准化的诊断和治疗步骤。将采用混合方法多中心集群随机对照分步楔形试验设计。总共将有 10 家拥有急诊科的医院(预计 n = 2000 例非创伤性腹痛患者)连续(每 4 个月)随机应用干预措施。患者纳入标准为年龄至少 18 岁、患有非创伤性腹痛且参加德国法定健康保险。主要结局指标:ED 出院时的急性疼痛评分、ED 治疗时间、患者报告的满意度。次要结局指标包括患者安全性和护理质量参数、过程评估参数以及成本和成本效益参数。定量数据将从患者调查、临床记录和医院信息系统的常规数据以及参与的德国法定健康保险中收集。将对描述性和分析性统计分析进行汇总和关联,以提供主要患者报告结局、过程指标、质量指标和成本的分析。定性数据收集包括参与式患者观察和半结构化专家访谈,将对其进行归纳分析。研究结果将通过同行评审期刊上的出版物、会议以及项目网站进行传播。为确保数据保护,将采取适当的技术和组织措施。试验注册:DRKS00021052。