Awareness, information sources, and beliefs regarding palliative care in the general population in Japan: a nationwide cross-sectional survey (INFORM study 2023).

IF 1.9 4区 医学 Q3 ONCOLOGY
Yu Uneno, Masanori Mori, Junko Saito, Aki Otsuki, Aya Kuchiba, Naomi Sakurai, Naoki Nakaya, Maiko Fujimori, Taichi Shimazu
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引用次数: 0

Abstract

Background: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

日本普通民众对姑息关怀的认识、信息来源和信念:一项全国性横断面调查(INFORM 研究 2023)。
背景:随着信息来源的多样化和社会结构的变化,有必要更新公众对姑息关怀的认识状况。因此,我们阐明了日本公众对姑息关怀的认识、信息来源和信念的现状及决定因素:这项全国性横断面调查在 2023 年通过两阶段分层随机抽样的方式纳入了 10 000 名年龄≥20 岁的参与者。我们使用邮寄的自填式问卷(INFORM 研究 2023)。问卷项目选自(部分修改)美国健康信息全国趋势调查,以确保可比性,包括姑息关怀意识、信息来源和信念。研究人员采用加权逻辑回归法来探讨认知度的决定因素:在 3452 名回复者(回复率:35.3%)中,65.2% 具有姑息关怀意识。加权逻辑回归分析表明,较少具有姑息关怀意识的受访者年龄较小、为男性、受教育经历有限、家庭收入较低且不使用互联网。其中,性别具有明显的相关性(女性与男性的调整赔率比:3.20 [95% CI:2.66-3.85])。在所有年龄组中,医护人员(58.5%)和互联网(30.5%)是最值得信赖的信息来源。年轻的参与者经常从网上获取信息。大多数参与者认为姑息关怀是有益的,尽管 82.0% 的人将姑息关怀与死亡联系在一起:日本人对姑息关怀的认知度相对较高,大多数人相信医疗保健专业人员提供的信息,而不是互联网。有必要进一步努力,以解决获得值得信赖的姑息关怀信息的障碍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
8.30%
发文量
177
审稿时长
3-8 weeks
期刊介绍: Japanese Journal of Clinical Oncology is a multidisciplinary journal for clinical oncologists which strives to publish high quality manuscripts addressing medical oncology, clinical trials, radiology, surgery, basic research, and palliative care. The journal aims to contribute to the world"s scientific community with special attention to the area of clinical oncology and the Asian region. JJCO publishes various articles types including: ・Original Articles ・Case Reports ・Clinical Trial Notes ・Cancer Genetics Reports ・Epidemiology Notes ・Technical Notes ・Short Communications ・Letters to the Editors ・Solicited Reviews
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