Bender Jacqueline L, Scruton Sarah, Wong Geoff, Abdelmutti Nazek, Berlin Alejandro, Easley Julie, Liu Zhihui Amy, McGee Sharon, Rodin Danielle, Sussman Jonathan, Urquhart Robin
Cancer Rehabilitation and Survivorship, Department of Supportive Care, Princess Margaret Cancer Centre, Toronto, Ontario, Canada.
Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.
Cancer Med. 2024 Feb;13(4):e6948. doi: 10.1002/cam4.6948.
The purpose of this study was to investigate associations between self-reported distress (anxiety/depression) and satisfaction with and desire for virtual follow-up (VFU) care among cancer patients during and beyond the COVID-19 pandemic.
Breast and prostate cancer patients receiving VFU at an urban cancer centre in Toronto, Canada completed an online survey on their sociodemographic, clinical, and technology, characteristics and experience with and views on VFU. EQ5D-5 L was used to assess distress. Statistical models adjusted for age, gender, education, income and Internet confidence.
Of 352 participants, average age was 65 years, 48% were women,79% were within 5 years of treatment completion, 84% had college/university education and 74% were confident Internet users. Nearly, all (98%) had a virtual visit via phone and 22% had a virtual visit via video. The majority of patients (86%) were satisfied with VFU and 70% agreed that they would like VFU options after the COVID-19 pandemic. Participants who reported distress and who were not confident using the Internet for health purposes were significantly less likely to be satisfied with VFU (OR = 0.4; 95% CI: 0.2-0.8 and OR = 0.19; 95% CI: 0.09-0.38, respectively) and were less likely to desire VFU option after the COVID-19 pandemic (OR = 0.49; 95% CI: 0.30-0.82 and OR = 0.41; 95% CI: 0.23-0.70, respectively).
The majority of respondents were satisfied with VFU and would like VFU options after the COVID-19 pandemic. Future research should determine how to optimize VFU options for cancer patients who are distressed and who are less confident using virtual care technology.
本研究旨在调查在2019冠状病毒病大流行期间及之后,癌症患者自我报告的痛苦(焦虑/抑郁)与对虚拟随访(VFU)护理的满意度及需求之间的关联。
在加拿大多伦多一家城市癌症中心接受VFU的乳腺癌和前列腺癌患者完成了一项关于其社会人口统计学、临床和技术特征以及VFU体验与看法的在线调查。使用EQ5D - 5L评估痛苦程度。统计模型对年龄、性别、教育程度、收入和互联网信心进行了调整。
在352名参与者中,平均年龄为65岁,48%为女性,79%在完成治疗的5年内,84%拥有大专/本科学历,74%是自信的互联网用户。几乎所有患者(98%)通过电话进行过虚拟就诊,22%通过视频进行过虚拟就诊。大多数患者(86%)对VFU感到满意,70%的患者同意在2019冠状病毒病大流行后希望有VFU选项。报告有痛苦且对出于健康目的使用互联网缺乏信心的参与者对VFU感到满意的可能性显著降低(比值比分别为0.4;95%置信区间:0.2 - 0.8和0.19;95%置信区间:0.09 - 0.38),并且在2019冠状病毒病大流行后希望有VFU选项的可能性也降低(比值比分别为0.49;95%置信区间:0.30 - 0.82和0.41;95%置信区间:0.23 - 0.70)。
大多数受访者对VFU感到满意,并希望在新冠疫情大流行后有VFU选项。未来的研究应确定如何为感到痛苦且对使用虚拟护理技术缺乏信心的癌症患者优化VFU选项。