Identification of the most important factors related to people with cancer starting a palliative care conversation: A survey study

对话 缓和医疗 心理干预 逻辑回归 非概率抽样 心理学 家庭医学 医学 优势比 横断面研究 可能性 护理部 内科学 人口 环境卫生 沟通 病理
作者
Anne-Lore Scherrens,Kim Beernaert,Luc Deliens,Lore Lapeire,Martine De Laat,Christine Biebuyck,Karen Geboes,Charles Van Praet,Ine Moors,Benedicte Deforche,Joachim Cohen
出处
期刊:Psycho-oncology [Wiley]
卷期号:31 (11): 1843-1851
标识
DOI:10.1002/pon.6039
摘要

A late conversation about palliative care needs can lead to suboptimal care in the final months/weeks of life. Insight into factors related to patients' communication about palliative care is needed. This study aims to identify the factors associated with starting/intending to start a conversation about palliative care with the physician.We performed a cross-sectional interviewer-administered survey among people with incurable cancer. Purposive sampling was used, taking into account theoretically relevant heterogeneity. The questionnaire was developed based on the theory of planned behavior. Uni- and multivariable logistic regression analyses were performed.Out of 80 participants, ten (13%) started the palliative care conversation and 18 (23%) intended to do so. People holding a positive attitude towards starting/intending to start the conversation (odds ratio [OR] 4.74; 95% CI 2.35-9.54), perceiving more benefits of it (OR 2.60; 95% CI 1.37-4.96) and perceiving a positive attitude towards the behavior in family/friends (OR 2.07; 95% CI 1.26-3.41) and the physician (OR 2.19; 95% CI 1.39-3.45) were more likely to start/intend to start a palliative care conversation; people perceiving more disadvantages (OR 0.53; 95% CI 0.32-0.87) and barriers (OR 0.31; 95% CI 0.15-0.63) were less likely to do so. These factors explained 64% of the variance.Our findings show that psychological and perceived socio-environmental factors, particularly patients' attitudes, are associated with starting a conversation about palliative care. Theory-based interventions targeting these strong associations might have a high potential to empower people with cancer to take the initiative in communication about palliative care and to improve timely initiation of palliative care.
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