Department of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Division of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu, 433-8558, Japan.
Jpn J Clin Oncol. 2024 Nov 2;54(11):1171-1179. doi: 10.1093/jjco/hyae092.
The diversification of information sources and changes in social structures necessitates updates on the state of public awareness of palliative care. Therefore, we clarified the status and determinants of awareness, information sources, and beliefs, regarding palliative care in Japan.
This nationwide cross-sectional survey included 10 000 participants aged ≥20 years enrolled through random sampling using a two-stage stratification in 2023. We used a mailed self-administered questionnaire (INFORM Study 2023). The questionnaire items were selected (partially modified) from the Health Information National Trends Survey (USA) to ensure comparability, included palliative care awareness, information sources, and beliefs. Weighted logistic regression was conducted to explore the determinants of awareness.
Of the 3452 participants that responded (response rate: 35.3%), 65.2% had palliative care awareness. The weighted logistic regression analysis revealed that respondents less likely to have any palliative care awareness were younger, were male, had limited education history, had lower household income, and were non-Internet users. Of these, sex had the clear association (adjusted odds ratio for female vs. male: 3.20 [95% CI: 2.66-3.85]). Across all age groups, healthcare professionals (58.5%) and the Internet (30.5%) were the most trusted source of information. Younger participants frequently received information online. Most participants believed that palliative care was beneficial, although 82.0% associated it with death.
The Japanese population had a relatively high palliative care awareness, with the majority trusting information from healthcare professionals rather than the Internet. Further efforts are warranted to address barriers to receiving trustworthy palliative care information.
信息来源的多样化和社会结构的变化要求更新公众对姑息治疗的认知状况。因此,我们明确了日本公众对姑息治疗的认知、信息来源和信念的现状和决定因素。
本项全国性横断面调查于 2023 年采用两阶段分层随机抽样方法纳入了 10000 名年龄≥20 岁的参与者。我们使用邮寄自填式问卷(INFORM 研究 2023 年)。问卷项目选自健康信息国家趋势调查(美国),(部分修改)以确保可比性,包括姑息治疗认知、信息来源和信念。采用加权逻辑回归分析探索认知的决定因素。
在 3452 名回应者中(回应率:35.3%),65.2%的人有姑息治疗认知。加权逻辑回归分析显示,不太可能具有任何姑息治疗认知的受访者更年轻、为男性、受教育程度有限、家庭收入较低且非互联网用户。其中,性别具有明确的关联(女性与男性相比的调整优势比:3.20[95%CI:2.66-3.85])。在所有年龄组中,医疗保健专业人员(58.5%)和互联网(30.5%)是最受信任的信息来源。年轻的参与者经常在线获取信息。大多数参与者认为姑息治疗是有益的,尽管 82.0%的人将其与死亡联系在一起。
日本民众对姑息治疗的认知度相对较高,大多数人信任来自医疗保健专业人员的信息,而不是互联网。需要进一步努力解决获得可信姑息治疗信息的障碍。