Department of Health Sciences, Epidemiology & Cancer Statistics Group, University of York, York, United Kingdom.
Queens Centre for Oncology and Haematology, Castle Hill Hospital, Cottingham, United Kingdom.
PLoS One. 2024 Aug 20;19(8):e0293772. doi: 10.1371/journal.pone.0293772. eCollection 2024.
Haematological malignancies (blood cancers) often follow chronic trajectories that can span many months or years. Management of these diseases typically involves periods of 'Watch & Wait', whereby patients are monitored by the hospital and only treated at progression, if or when this occurs, which might be never or on multiple occasions. Such remitting-relapsing pathways are unpredictable and can cause anxiety and distress. This study aimed to generate evidence about information preferences, with a view to underpinning future patient-facing resources; potentially mitigating psycho-social difficulties and promoting effective shared decision-making.
A qualitative study was conducted, set within a UK population-based cohort of patients with haematological malignancies. Sampling was purposive, based on age (initially around the median age of diagnosis) and disease subtype (chronic lymphocytic leukaemia, follicular lymphoma, marginal zone lymphoma and myeloma); and in-depth interviews took place with 35 patients (10 with relatives). Analysis drew on qualitative description and thematic content analysis and included critical reading and annotation of transcripts, identification of common and rare phenomena, generation of codes and coding of material, and theme development.
Patients discussed their preferences and experiences at length and rich data were generated from diagnosis onwards, across diagnostic subtypes. The overarching theme identified was 'Variations in preferences' with needs seen to differ from person to person; as well as changing over time for individuals. Five sub-themes were identified: 1) To know or not to know? 2) Needs are dynamic; 3) The polarising issue of prognosis; 4) Preferred sources; and 5) Differences in content, depth and presentation.
Varied, dynamic information preferences indicate that resources should be developed in a way that provides maximum choice, enabling patients to select relevant material at different time-points on their trajectory. The development of blood cancer subtype-specific "real-world clinical scenarios" could improve patient experiences and inform shared decision-making.
血液系统恶性肿瘤(血液癌症)通常呈现慢性发展轨迹,可能持续数月甚至数年。这些疾病的治疗通常涉及“观察与等待”阶段,在此期间,患者由医院监测,仅在疾病进展时进行治疗,如果出现进展,可能从未治疗过,也可能多次治疗。这种缓解-复发的模式是不可预测的,可能会导致焦虑和痛苦。本研究旨在生成有关信息偏好的证据,以期为未来面向患者的资源提供依据;潜在地减轻心理社会困难并促进有效的共同决策。
本研究是一项在英国基于人群的血液恶性肿瘤患者队列中开展的定性研究。采样基于年龄(最初为诊断时的中位数年龄)和疾病亚型(慢性淋巴细胞白血病、滤泡性淋巴瘤、边缘区淋巴瘤和骨髓瘤)进行有目的选择,并对 35 名患者(包括 10 名患者亲属)进行了深入访谈。分析采用定性描述和主题内容分析,包括对转录本进行批判性阅读和注释、识别常见和罕见现象、生成代码和对材料进行编码以及主题开发。
患者详细讨论了他们的偏好和经验,从诊断开始,在整个诊断亚型中都产生了丰富的数据。确定的首要主题是“偏好的变化”,即需求因人而异;并且随着时间的推移,个人的需求也会发生变化。确定了五个子主题:1)知道还是不知道?2)需求是动态的;3)预后的两极分化问题;4)首选来源;以及 5)内容、深度和呈现方式的差异。
多样化、动态的信息偏好表明,资源的开发方式应提供最大的选择,使患者能够在其病程的不同时间点选择相关材料。开发血液恶性肿瘤亚型特异性的“真实临床场景”可以改善患者的体验并为共同决策提供信息。