NHMRC Clinical Trials Centre, The University of Sydney, Sydney, New South Wales, Australia.
Melanoma Institute Australia, North Sydney, New South Wales, Australia.
BMJ Open. 2021 Feb 11;11(2):e040751. doi: 10.1136/bmjopen-2020-040751.
To identify patient-reported outcome measures (PROMs) and patient-reported experience measures (PREMs) in clinical quality registries, for people with cutaneous melanoma, to inform a new Australian Melanoma Clinical Outcomes Registry; and describe opportunities and challenges of routine PROM/PREM collection, especially in primary care.
Systematic review.
Which PROMs and PREMs are used in clinical quality registries for people with cutaneous melanoma, how they are collected, frequency of collection, participant recruitment methods and funding models for each registry.
1134 studies were identified from MEDLINE, PreMEDLINE, Embase, PsychInfo, Cochrane Database of Abstracts of Reviews of Effects databases and TUFTS Cost-Effectiveness Analysis Registry, alongside grey literature, from database inception to 5th February 2020. Following screening, 14 studies were included, identifying four relevant registries: Dutch Melanoma Registry, Adelphi Real-World Disease-Specific Programme (Melanoma), Patient-Reported Outcomes Following Initial treatment and Long-term Evaluation of Survivorship Registry, and Cancer Experience Registry. These used seven PROMs: EuroQol-5 Dimensions, Functional Assessment of Cancer-General (FACT-G) and FACT-Melanoma (FACT-M), European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Cancer 30 (EORTC QLQ-C30), Fatigue Assessment Scale Hospital Anxiety and Depression Scale, Patient-Reported Outcome Measures Information System-29 and one PREM; EORTC QLQ-Information Module 26. PROMs/PREMs in registries were reported to improve transparency of care; facilitate clinical auditing for quality assessment; enable cost-effectiveness analyses and create large-scale research platforms. Challenges included resource burden for data entry and potential collection bias toward younger, more affluent respondents. Feedback from patients with melanoma highlighted the relevance of PROMs/PREMs in assessing patient outcomes and patient experiences.
Clinical registries indicate PROMs/PREMs for melanoma care can be incorporated and address important gaps, however cost and collection bias may limit generalisability.
CRD42018086737.
确定临床质量登记处中用于皮肤黑素瘤患者的患者报告结局测量(PROM)和患者报告体验测量(PREM),为新的澳大利亚黑素瘤临床结局登记处提供信息;并描述常规 PROM/PREM 收集的机会和挑战,特别是在初级保健中。
系统评价。
用于皮肤黑素瘤患者的临床质量登记处使用哪些 PROM 和 PREM,它们是如何收集的,收集的频率,每个登记处的参与者招募方法和资金模式。
从 MEDLINE、PreMEDLINE、Embase、PsychInfo、Cochrane 数据库的评价摘要数据库和 TUFTS 成本效益分析登记处以及灰色文献中,从数据库开始到 2020 年 2 月 5 日,共确定了 1134 项研究。经过筛选,纳入了 14 项研究,确定了四个相关的登记处:荷兰黑素瘤登记处、 Adelphi 真实世界疾病特异性计划(黑素瘤)、初始治疗后患者报告结局和生存随访登记处以及癌症体验登记处。这些登记处使用了七种 PROM:欧洲五维健康量表、癌症通用功能评估量表(FACT-G)和 FACT-黑素瘤(FACT-M)、欧洲癌症研究与治疗组织生活质量问卷-癌症 30 项(EORTC QLQ-C30)、疲劳评估量表、医院焦虑和抑郁量表、患者报告结局测量信息系统-29 和一个 PREM;EORTC QLQ-信息模块 26。登记处中的 PROMs/PREMs 据报道可以提高护理的透明度;促进临床审核以进行质量评估;使成本效益分析成为可能,并创建大规模的研究平台。挑战包括数据录入的资源负担和潜在的收集偏倚,偏向于年轻、富裕的受访者。黑素瘤患者的反馈强调了 PROMs/PREMs 在评估患者结局和患者体验方面的相关性。
临床登记处表明,黑素瘤护理可以纳入 PROMs/PREMs,并解决重要的差距,但成本和收集偏倚可能限制其普遍性。
PROSPERO 注册号:CRD42018086737。