Houston VA HSR&D Center of Excellence, Michael E, DeBakey Veterans Affairs Medical Center, Houston, TX, USA.
BMC Health Serv Res. 2012 Aug 28;12:288. doi: 10.1186/1472-6963-12-288.
The comparative effectiveness (CE) of endoscopic screening (versus no screening) for Barrett's esophagus (BE) in patients with GERD symptoms, or among different endoscopic surveillance strategies in patients with BE, for the early detection of esophageal adenocarcinoma (EA) is unknown. Furthermore, it is unclear if patients or providers have or will adopt any of these strategies (screening only, screening and surveillance, vs. none), irrespective of their effectiveness. Endoscopic screening and surveillance is expensive and can be risky. Therefore, it is imperative to establish the CE and acceptability about the risks and outcomes related to these practices to better inform expert recommendations and provider-patient decisions.
METHODS/RESULTS: We propose a mixed methods study which will involve: (1) an analysis of secondary databases (VA and VA-Medicare linked datasets for 2004-09) to examine CE of endoscopic screening and surveillance in an observational study cohort (an estimated 680,000 patients with GERD; 25,000-30,000 with BE; and 3,000 with EA); (2) a structured electronic medical record (EMR) review on a national sample of patients using VA EMRs to verify all EA cases, identify cancer stage, cancer-targeted therapy, and validate the screening and surveillance endoscopy; and (3) qualitative in depth interviews with patients and providers to elicit preferences, norms, and behaviors to explain clinical contexts of these findings and address gaps arising from the CE study.
This study will compare clinical strategies for detecting and monitoring BE, a pre-cancerous lesion. Additionally, by eliciting acceptability of these strategies for patients and providers, we will be able to propose effective and feasible strategies that are likely to be implemented in routine use. Findings will inform recommendations for clinical practice guidelines. Our innovative approach is consistent with the methodological standards of patient-centered outcomes research, and our findings will offer a significant contribution to the literature on cancer surveillance.
胃食管反流病(GERD)患者行内镜筛查(与不筛查相比)或 Barrett 食管(BE)患者行不同内镜监测策略对食管腺癌(EA)的早期检测的比较效果(CE)尚不清楚。此外,尚不清楚患者或提供者是否已经或将要采用这些策略(仅筛查、筛查和监测,与不筛查相比),而不论其有效性如何。内镜筛查和监测费用高昂且存在风险。因此,必须确定这些实践相关的 CE 和可接受性,以及风险和结果,以便更好地为专家建议和医患决策提供信息。
方法/结果:我们提出了一项混合方法研究,将包括:(1)对 VA 和 VA-Medicare 链接数据集(2004-09 年)中的二级数据库进行分析,以在观察性研究队列中检查内镜筛查和监测的 CE(估计有 680,000 例 GERD 患者;25,000-30,000 例 BE 患者;3,000 例 EA 患者);(2)对使用 VA 电子病历(EMR)的全国患者样本进行结构化 EMR 审查,以验证所有 EA 病例,确定癌症分期、癌症靶向治疗,并验证筛查和监测内镜;(3)对患者和提供者进行深入的定性访谈,以了解偏好、规范和行为,解释这些发现的临床背景,并解决 CE 研究中出现的差距。
这项研究将比较检测和监测 BE(癌前病变)的临床策略。此外,通过了解患者和提供者对这些策略的可接受性,我们将能够提出可能在常规使用中实施的有效且可行的策略。研究结果将为临床实践指南提供建议。我们的创新方法符合以患者为中心的结局研究的方法学标准,我们的研究结果将为癌症监测文献做出重大贡献。