Department of Psychiatry, McGill University, Montreal, Canada.
Department of Psychology, Crandall University, Moncton, Canada.
BMC Health Serv Res. 2022 May 23;22(1):693. doi: 10.1186/s12913-022-07946-y.
Research on patients' perceptions of cancer care often documents sub-optimal experiences. Cancer care quality issues include restricted service access, lack of care coordination, gaps in follow-up and "generic" rather than person-centered care. Recent reports underscore that proactively and periodically seeking user feedback is crucial for timely care quality improvement. The present study aimed to analyze and thematically organize a large amount of feedback from patients who had been treated for cancer within the last 6 months.
Randomly selected participants (N = 3,278) from 3 University-affiliated cancer centres in Montreal, Quebec, Canada completed the Ambulatory Oncology Patient Satisfaction Survey (AOPSS) and an open-ended question on their perceptions of the care they received. 692 participants responded to the latter. Guided by the Cancer Experience Measurement Framework (CEMF), their feedback was analyzed using a qualitative thematic approach.
Cancer care perceptions included sub-themes of care access and coordination, continuity/transition, and perceived appropriateness/personalisation of care. The most salient theme was captured by care access and coordination with 284 comments (44%) directly addressing these issues. The ways in which health care services were structured including setting, schedule, and location were often raised as cause for concerns. Issues surrounding cancer information/education, emotional support, and physical comfort were frequently reported as unmet needs. In addition, limited access to cancer services led patients to seek alternatives such as going to emergency departments and/or private care.
These findings are timely as they show that most patients are well aware of quality issues in cancer care and are willing to report candidly on these. Patient feedback also underscore the importance for cancer care institutions to periodically gather patient-reported data so that systems can re-calibrate their service offerings according to these data. Ultimately, patient reports will translate into enhanced quality, personalization, and safer cancer care provision.
对患者对癌症护理的认知的研究常常记录到不尽如人意的体验。癌症护理质量问题包括服务机会受限、护理协调不足、随访空白以及缺乏以患者为中心的常规护理。最近的报告强调,主动且定期征求用户反馈对于及时改善护理质量至关重要。本研究旨在分析和组织来自最近 6 个月内接受癌症治疗的患者的大量反馈。
从加拿大魁北克省蒙特利尔的 3 家大学附属癌症中心随机抽取参与者(N=3278),完成门诊肿瘤患者满意度调查(AOPSS)和对他们所接受的护理的看法的开放性问题。有 692 名参与者对后者做出了回应。在癌症体验测量框架(CEMF)的指导下,采用定性主题分析方法对他们的反馈进行了分析。
癌症护理认知包括护理机会和协调、连续性/过渡以及护理的适当性/个性化等亚主题。最突出的主题是护理机会和协调,有 284 条评论(44%)直接针对这些问题。经常提出医疗服务的结构方式,包括设置、日程安排和地点,这引起了人们的关注。癌症信息/教育、情感支持和身体舒适等方面的问题经常被报道为未满足的需求。此外,癌症服务机会有限,导致患者寻求替代方案,如去急诊室和/或私人护理。
这些发现是及时的,因为它们表明大多数患者非常了解癌症护理中的质量问题,并愿意坦诚地报告这些问题。患者反馈还强调了癌症护理机构定期收集患者报告数据的重要性,以便系统能够根据这些数据重新调整其服务提供。最终,患者报告将转化为增强质量、个性化和更安全的癌症护理提供。