Oncology, Rambam Health Care Campus, Haifa, Israel; Gastrointestinal Tract Cancer Group, EORTC, Brussels, Belgium.
Oncology, Rambam Health Care Campus, Haifa, Israel.
ESMO Open. 2020 May;5(3):e000651. doi: 10.1136/esmoopen-2019-000651.
Digital social networks have become a key player in the ecosystem of young patients with cancer, with regard to their unique perspectives and unmet needs. This study aims to investigate the web-based social community tools and to characterise the user profile, unmet needs and goals of young patients with cancer.
A web-based survey was distributed via large-scale social network designated for young patients with cancer (age 18-45 years) Stop Cancer. The survey collected demographic data and oncological status. Primary outcome was potential goals of accessing the network; secondary outcomes were emotional impact, effect of disease status, education, marital status and employment, on user satisfaction rate.
The survey was available for 5 days (10/2018) and was filled by 523 participants. Breast cancer, haematological malignancies and colorectal cancer were the most common diagnoses. The majority had non-metastatic disease at diagnosis, 79% had no evidence of disease at time of the survey. Forty-five per cent considered the network as a reliable source for medical information. Academic education was associated with higher satisfaction from the platform. There were no differences between cancer survivors and patients with active disease in patterns of platform usage. The social network had an allocated section for 'patient mentoring' of newly diagnosed members by survivors.
Our study portrayed the user prototype of a social digital network among young adult patients with cancer, indicating challenging trends. Whereas social media may prove a powerful tool for patients and physicians alike, it may also serve as a research tool to appraise wide practices within a heterogeneous population. Nevertheless, it acts as a double-edged sword in the setting of uncontrolled medical information. It is our role as healthcare providers to join this race and play an active role in shaping its medical perspectives.
数字社交网络已成为癌症青年患者生态系统中的重要参与者,其独特的视角和未满足的需求不容忽视。本研究旨在调查网络社交社区工具,并描述癌症青年患者的用户特征、未满足需求和目标。
通过面向年轻癌症患者(18-45 岁)的大型社交网络 Stop Cancer 分发了一项基于网络的调查。该调查收集了人口统计学数据和肿瘤学状况。主要结果是访问网络的潜在目标;次要结果是疾病状况、教育、婚姻状况和就业对用户满意度的影响。
该调查开放了 5 天(2018 年 10 月),共有 523 名参与者填写了问卷。乳腺癌、血液恶性肿瘤和结直肠癌是最常见的诊断。大多数患者在诊断时为非转移性疾病,79%的患者在调查时无疾病证据。45%的参与者认为该网络是获取医疗信息的可靠来源。学术教育与对平台更高的满意度相关。癌症幸存者和活动期患者在平台使用模式上没有差异。该社交网络为新诊断成员分配了由幸存者担任的“患者指导”版块。
本研究描绘了癌症青年患者社交数字网络的用户原型,显示出具有挑战性的趋势。尽管社交媒体可能是患者和医生的有力工具,但它也可以作为一种研究工具,评估在异质人群中广泛的实践。然而,在不受控制的医疗信息背景下,它也有两面性。我们作为医疗保健提供者的角色是加入这场竞赛,并在塑造其医学观点方面发挥积极作用。