Nottingham University Hospitals NHS Trust, Nottingham, UK.
University of Lincoln, Lincoln, UK.
Support Care Cancer. 2024 Jul 2;32(7):481. doi: 10.1007/s00520-024-08675-0.
PURPOSE: This longitudinal study investigated distress rates in patients with advanced ovarian cancer during the COVID-19 pandemic and examined whether time, illness representations, and coping strategies predicted distress levels. METHODS: UK patients with stage 3 or 4 ovarian cancer were recruited between September 2020 and March 2021. Data were collected at baseline (T0), 2 months (T1), and 4 months (T2) post-enrolment. Validated questionnaires assessed distress (anxiety, depression, PTSD, fear of progression) and predictors (coping strategies and illness perceptions), analysed via multilevel modelling. RESULTS: Seventy-two participants returned a questionnaire at T0, decreasing to 49 by T2. High distress was observed, with over 50% of participants experiencing anxiety and depression consistently. Nearly 60% reported clinical levels of fear of progression at some point. PTSD rates resembled the general population. Although distress levels remained stable over time, some individual variability was observed. Time had minimal effect on distress. Coping strategies and illness perceptions remained stable. Threatening illness perceptions consistently predicted distress, while specific coping strategies such as active coping, acceptance, self-blame, and humour predicted various aspects of distress. Together, these factors explained up to half of the distress variance. CONCLUSION: The findings have implications for routine screening for distress and the inclusion of psychological treatment pathways in advanced ovarian cancer care. Addressing illness representations is crucial, with attention to informational support. Future research should explore the long-term effects of heightened distress and the effectiveness of interventions targeting illness perceptions. This study informs current clinical practice and future pandemic preparedness in cancer care.
目的:本纵向研究调查了 COVID-19 大流行期间晚期卵巢癌患者的困扰率,并探讨了时间、疾病认知和应对策略是否预测了困扰水平。
方法:2020 年 9 月至 2021 年 3 月期间,招募了英国 III 期或 IV 期卵巢癌患者。在入组后 2 个月(T1)和 4 个月(T2)时收集基线(T0)和数据。使用验证问卷评估困扰(焦虑、抑郁、创伤后应激障碍、对进展的恐惧)和预测因素(应对策略和疾病认知),通过多层次模型进行分析。
结果:72 名参与者在 T0 时返回了问卷,到 T2 时减少到 49 名。观察到高困扰率,超过 50%的参与者持续出现焦虑和抑郁。近 60%的人在某些时候报告了临床水平的对进展的恐惧。创伤后应激障碍的发生率与一般人群相似。尽管困扰水平随时间保持稳定,但观察到了一些个体差异。时间对困扰的影响很小。应对策略和疾病认知保持稳定。威胁性疾病认知始终预测困扰,而特定的应对策略,如积极应对、接受、自责和幽默,预测了困扰的各个方面。这些因素共同解释了困扰变异的一半左右。
结论:研究结果对常规筛查困扰和在晚期卵巢癌护理中纳入心理治疗途径有影响。解决疾病认知至关重要,要关注信息支持。未来的研究应探索困扰加剧的长期影响和针对疾病认知的干预措施的有效性。本研究为当前的临床实践和癌症护理未来的大流行准备提供了信息。
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