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Awareness, information sources, and beliefs regarding palliative care in the general population in Japan: a nationwide cross-sectional survey (INFORM study 2023).
Uneno, Yu; Mori, Masanori; Saito, Junko; Otsuki, Aki; Kuchiba, Aya; Sakurai, Naomi; Nakaya, Naoki; Fujimori, Maiko; Shimazu, Taichi.
Afiliación
  • Uneno Y; Department of Therapeutic Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
  • Mori M; Division of Palliative and Supportive Care, Seirei Mikatahara General Hospital, Hamamatsu, 433-8558, Japan.
  • Saito J; Division of Behavioral Sciences, National Cancer Center Institute for Cancer Control, National Cancer Center, Tokyo, Japan.
  • Otsuki A; Division of Behavioral Sciences, National Cancer Center Institute for Cancer Control, National Cancer Center, Tokyo, Japan.
  • Kuchiba A; Graduate School of Health Innovation, Kanagawa University of Human Services, Kanagawa, Japan.
  • Sakurai N; Division of Biostatistical Research, Institution for Cancer Control/Biostatistics Division, Center for Research Administration and Support, National Cancer Center Hospital, Tokyo, Japan.
  • Nakaya N; Cancer Solutions, Inc, Tokyo, Japan.
  • Fujimori M; Tohoku Medical Megabank Organization, Tohoku University, Sendai, Japan.
  • Shimazu T; Division of Survivorship Research, National Cancer Center Institute for Cancer Control, National Cancer Center, Tokyo, 104-0045, Japan.
Jpn J Clin Oncol ; 2024 Jul 20.
Article en En | MEDLINE | ID: mdl-39033085
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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Jpn J Clin Oncol Año: 2024 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Jpn J Clin Oncol Año: 2024 Tipo del documento: Article País de afiliación: Japón
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