首页> 外文期刊>BMC Medical Informatics and Decision Making >Feasibility test of a UK-scalable electronic system for regular collection of patient-reported outcome measures and linkage with clinical cancer registry data: The electronic Patient-reported Outcomes from Cancer Survivors (ePOCS) system
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Feasibility test of a UK-scalable electronic system for regular collection of patient-reported outcome measures and linkage with clinical cancer registry data: The electronic Patient-reported Outcomes from Cancer Survivors (ePOCS) system

机译:英国可扩展的电子系统的可行性测试,用于定期收集患者报告的结局指标并与临床癌症登记数据关联:电子报告的癌症幸存者结果(ePOCS)系统

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Background Cancer survivors can face significant physical and psychosocial challenges; there is a need to identify and predict which survivors experience what sorts of difficulties. As highlighted in the UK National Cancer Survivorship Initiative, routine post-diagnostic collection of patient reported outcome measures (PROMs) is required; to be most informative, PROMs must be linked and analysed with patients' diagnostic and treatment information. We have designed and built a potentially cost-efficient UK-scalable electronic system for collecting PROMs via the internet, at regular post-diagnostic time-points, for linking these data with patients' clinical data in cancer registries, and for electronically managing the associated patient monitoring and communications; the electronic Patient-reported Outcomes from Cancer Survivors (ePOCS) system. This study aims to test the feasibility of the ePOCS system, by running it for 2 years in two Yorkshire NHS Trusts, and using the Northern and Yorkshire Cancer Registry and Information Service. Methods/Design Non-metastatic breast, colorectal and prostate cancer patients (largest survivor groups), within 6 months post-diagnosis, will be recruited from hospitals in the Yorkshire Cancer Network. Participants will be asked to complete PROMS, assessing a range of health-related quality-of-life outcomes, at three time-points up to 15 months post-diagnosis, and subsequently to provide opinion on the ePOCS system via a feedback questionnaire. Feasibility will be examined primarily in terms of patient recruitment and retention rates, the representativeness of participating patients, the quantity and quality of collected PROMs data, patients' feedback, the success and reliability of the underpinning informatics, and the system running costs. If sufficient data are generated during system testing, these will be analysed to assess the health-related quality-of-life outcomes reported by patients, and to explore if and how they relate to disease, treatment and/or individual differences characteristics. Discussion There is currently no system in the UK for collecting PROMs online and linking these with patients' clinical data in cancer registries. If feasible, ePOCS has potential to provide an affordable UK-scalable technical platform to facilitate and support longitudinal cohort research, and improve understanding of cancer survivors' experiences. Comprehensive understanding of survivorship difficulties is vital to inform the development and provision of supportive services and interventions.
机译:背景癌症幸存者可能面临重大的生理和心理挑战。有必要确定和预测哪些幸存者会遇到什么样的困难。正如英国国家癌症生存计划所强调的那样,需要对患者报告的结局指标进行常规的诊断后收集;为了提供更多信息,PROM必须与患者的诊断和治疗信息联系起来并进行分析。我们设计并构建了具有潜在成本效益的英国可扩展电子系统,用于在常规诊断后时间点通过互联网收集PROM,将这些数据与癌症登记处的患者临床数据链接,并以电子方式管理相关的病人监测和沟通;癌症幸存者(ePOCS)系统的电子患者报告结果。这项研究旨在通过在两个约克郡NHS信托基金中运行ePOCS系统2年,并使用Northern and Yorkshire Cancer Registry and Information Service来测试ePOCS系统的可行性。方法/设计在诊断后的6个月内,将从纽约约克郡癌症网络的医院招募非转移性乳腺癌,结直肠癌和前列腺癌患者(最大的幸存者组)。将要求参与者在诊断后15个月内的三个时间点完成PROMS,评估一系列与健康相关的生活质量结果,然后通过反馈调查表对ePOCS系统提出意见。将主要从患者招募和保留率,参与患者的代表性,所收集的PROMs数据的数量和质量,患者的反馈,基础信息学的成功和可靠性以及系统运行成本等方面来检查可行性。如果在系统测试期间生成了足够的数据,将对这些数据进行分析,以评估患者报告的与健康相关的生活质量结果,并探讨它们是否以及如何与疾病,治疗和/或个体差异特征相关。讨论目前,英国尚无在线收集PROM并将其与癌症登记中患者临床数据联系起来的系统。如果可行,ePOCS有潜力提供可负担的英国可扩展技术平台,以促进和支持纵向队列研究,并增进对癌症幸存者经验的理解。全面了解生存困难对于为支持服务和干预措施的开发和提供至关重要。

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