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直肠癌随访:开发并测试一项新型患者主导的随访计划。研究方案。

Follow-up after rectal cancer: developing and testing a novel patient-led follow-up program. Study protocol.

作者信息

Hovdenak Jakobsen Ida, Juul Therese, Bernstein Inge, Christensen Peter, Jensen Frank Svendsen, Johansen Christoffer, Lindhardt Larsen Susie, Laurberg Søren, Madsen Mogens Rørbæk, Thorlacius-Ussing Ole, Vind Thaysen Henriette

机构信息

a Department of Surgery P , Aarhus University Hospital , Aarhus , Denmark.

b Department of Surgery , Aalborg University Hospital , Aalborg , Denmark.

出版信息

Acta Oncol. 2017 Feb;56(2):307-313. doi: 10.1080/0284186X.2016.1267400. Epub 2017 Jan 9.

Abstract

BACKGROUND

The main treatment for non-metastatic rectal cancer (RC) is surgical resection. Late adverse effects that are highly prevalent and negatively impact patients' symptom burden and quality of life are: bowel-, urological and sexual dysfunctions; psychological distress; fear of recurrence. Patients and clinicians have requested a more patient-centred follow-up, balancing the focus on detection of recurrence, and physiological and psychological late adverse effects. The current follow-up program primarily focuses on detection of recurrence, with less attention on late adverse effects. As a consequence, the randomized controlled trial Follow-up after Rectal Cancer (FURCA) has been launched, testing the effect of a new patient-led, follow-up program. The aim of this paper is to describe the methodology used in the FURCA study and to report results from the development of the patient-led, follow-up program. Adult patients, treated with curative intent for primary adenocarcinoma in the rectum are included from four Danish centers.

MATERIAL AND METHODS

Patients are randomized into an intervention group, receiving standardized education and access to self-referral to an assigned project nurse, or a control group following the current follow-up program with routine medicals. The primary outcomes are symptom burden and quality of life, measured by the Functional Assessment of Cancer Therapy - Colorectal (FACT-C) questionnaire. Other outcome and demographic data are collected as patient-reported measures and register-based data. Results from developing the intervention: The education program is based on data from two focus group interviews and the feedback from experts. An algorithm is developed in order to qualify the research nurses' responses to patients' self-referral. Discussion and perspectives: The results of the FURCA study will strengthen the evidence base for RC follow-up, and qualify the ongoing transformation in cancer follow-up programs.

摘要

背景

非转移性直肠癌(RC)的主要治疗方法是手术切除。晚期不良反应非常普遍,对患者的症状负担和生活质量产生负面影响,包括:肠道、泌尿和性功能障碍;心理困扰;对复发的恐惧。患者和临床医生要求采用更以患者为中心的随访方式,在关注复发检测以及生理和心理晚期不良反应之间取得平衡。目前的随访计划主要侧重于复发检测,而对晚期不良反应关注较少。因此,开展了直肠癌随访(FURCA)随机对照试验,以测试一项新的由患者主导的随访计划的效果。本文旨在描述FURCA研究中使用的方法,并报告由患者主导的随访计划的开发结果。来自丹麦四个中心的成年患者被纳入研究,这些患者接受了针对直肠原发性腺癌的根治性治疗。

材料与方法

患者被随机分为干预组和对照组。干预组接受标准化教育,并可自行转介给指定的项目护士;对照组遵循当前的随访计划,进行常规体检。主要结局指标为症状负担和生活质量,通过癌症治疗功能评估-结直肠癌(FACT-C)问卷进行测量。其他结局指标和人口统计学数据通过患者报告的测量方法和基于登记的数据进行收集。干预措施开发的结果:教育计划基于两次焦点小组访谈的数据和专家的反馈。开发了一种算法,以使研究护士对患者自行转介的回复标准化。讨论与展望:FURCA研究的结果将加强直肠癌随访的证据基础,并使癌症随访计划正在进行的转变更加合理。

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