首页> 外文期刊>BMJ Open >Establishing a population-based patient-reported outcomes study (PROMs) using national cancer registries across two jurisdictions: the Prostate Cancer Treatment, your experience (PiCTure) study
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Establishing a population-based patient-reported outcomes study (PROMs) using national cancer registries across two jurisdictions: the Prostate Cancer Treatment, your experience (PiCTure) study

机译:使用两个辖区的国家癌症登记处建立基于人群的患者报告结局研究(PROM):前列腺癌治疗,您的经验(PiCTure)研究

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Objective To establish an international patient-reported outcomes (PROMs) study among prostate cancer survivors, up to 18?years postdiagnosis, in two countries with different healthcare systems and ethical frameworks. Design A cross-sectional, postal survey of prostate cancer survivors sampled and recruited via two population-based cancer registries. Healthcare professionals (HCPs) evaluated patients for eligibility to participate. Questionnaires contained validated instruments to assess health-related quality of life and psychological well-being, including QLQ-C30, QLQ-PR25, EQ-5D-5L, 21-question Depression, Anxiety and Stress Scale (DASS-21) and the Decisional Regret Scale. Setting Republic of Ireland (RoI) and Northern Ireland (NI). Primary outcome measures Registration completeness, predictors of eligibility and response, data missingness, unweighted and weighted PROMs. Results Prostate cancer registration was 80% (95% CI 75% to 84%) and 91% (95% CI 89% to 93%) complete 2?years postdiagnosis in NI and RoI, respectively. Of 12?322 survivors sampled from registries, 53% (n=6559) were classified as eligible following HCP screening. In the multivariate analysis, significant predictors of eligibility were: being ≤59?years of age at diagnosis (p0.001), short-term survivor (5?years postdiagnosis; p0.001) and from RoI (p0.001). 3348 completed the questionnaire, yielding a 54% adjusted response rate. 13% of men or their families called the study freephone with queries for assistance with questionnaire completion or to talk about their experience. Significant predictors of response in multivariate analysis were: being ≤59?years at diagnosis (p0.001) and from RoI (p=0.016). Mean number of missing questions in validated instruments ranged from 0.12 (SD 0.71; EQ-5D-5L) to 3.72 (SD 6.30; QLQ-PR25). Weighted and unweighted mean EQ-5D-5L, QLQ-C30 and QLQ-PR25 scores were similar, as were the weighted and unweighted prevalences of depression, anxiety and distress. Conclusions It was feasible to perform PROMs studies across jurisdictions, using cancer registries as sampling frames; we amassed one of the largest, international, population-based data set of prostate cancer survivors. We highlight improvements which could inform future PROMs studies, including utilising general practitioners to assess eligibility and providing a freephone service.
机译:目的在两个具有不同医疗保健系统和道德框架的国家中,对诊断后长达18年的前列腺癌幸存者进行国际患者报告结果(PROM)研究。设计对前列腺癌幸存者进行横断面邮政调查,并通过两个基于人群的癌症登记处进行了抽样调查。医疗保健专业人员(HCP)评估了患者的参加资格。问卷包括经验证的工具,用于评估与健康相关的生活质量和心理健康,包括QLQ-C30,QLQ-PR25,EQ-5D-5L,21个问题的抑郁,焦虑和压力量表(DASS-21)和决策性问卷。后悔量表。设置爱尔兰共和国(RoI)和北爱尔兰(NI)。主要结果指标衡量注册的完整性,资格和响应的预测因素,数据缺失,未加权和加权的PROM。结果在NI和RoI诊断完成2年后,前列腺癌的注册率分别为80%(95%CI为75%至84%)和91%(95%CI为89%至93%)。从HCP筛选后,从注册表中取样的12到322名幸存者中,有53%(n = 6559)被归类为合格。在多变量分析中,是否合格的重要预测因素是:诊断时≤59岁(p <0.001),短期幸存者(诊断后<5?years; p <0.001)和RoI(p <0.001)。 3348完成了问卷,调整后的答复率为54%。 13%的男性或其家人给研究型免费电话打了电话,询问如何完成问卷调查或谈论他们的经历。多变量分析中反应的重要预测因子为:诊断时≤59岁(p <0.001)和ROI(p = 0.016)。经验证的仪器中遗漏问题的平均数量在0.12(SD 0.71; EQ-5D-5L)至3.72(SD 6.30; QLQ-PR25)之间。 EQ-5D-5L,QLQ-C30和QLQ-PR25的加权和未加权平均得分相似,抑郁,焦虑和困扰的加权和未加权患病率也相似。结论使用癌症登记处作为抽样框架,在各个辖区进行PROM研究是可行的。我们积累了最大的,国际的,基于人群的前列腺癌幸存者数据集之一。我们着重介绍可以为将来的PROM研究提供参考的改进,包括利用全科医生评估资格并提供免费电话服务。

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