Literature DB >> 21656339

Knowledge, beliefs, and concerns about opioids, palliative care, and homecare of advanced cancer patients: a nationwide survey in Japan.

Miki Akiyama1, Toru Takebayashi, Tatsuya Morita, Mitsunori Miyashita, Kei Hirai, Motohiro Matoba, Nobuya Akizuki, Yutaka Shirahige, Akemi Yamagishi, Kenji Eguchi.   

Abstract

PURPOSE: Patients' knowledge, beliefs, or concerns about opioids, palliative care, and homecare can be potential barriers to providing quality palliative care. The primary aim of this study was to clarify knowledge about opioids, beliefs about palliative care, and concerns about homecare in advanced cancer patients.
METHODS: An anonymous questionnaire was sent to 1,619 outpatients with advanced cancer at 25 hospitals in four different regions of Japan. The respondents were asked to report their knowledge about opioids, beliefs about palliative care, and concerns about homecare, in addition to the levels of their sense of security regarding receiving cancer care in the region.
RESULTS: A total of 925 responses were received. In total, 28% believed that opioids are addictive and/or shorten life; 52% believed that palliative care is only for terminally ill patients; 75% agreed that being taken care of at home puts a heavy burden on the family; and 61% agreed that home-visit services cannot respond to sudden changes in a patient's condition. Levels of patients' sense of security were significantly higher in those who agreed that "opioids can relieve most pain caused by cancer" "palliative care relieves pain and distress", "palliative care is provided along with chemotherapy and/or radiation therapy", and "pain can be alleviated as effectively through home-visit services as it can at the hospital", and those who disagreed with the statements that "home-visit services cannot respond to sudden changes in a patient's condition" and "being taken care of at home puts a burden on the family".
CONCLUSIONS: Advanced cancer patients frequently had incorrect knowledge about opioids, a belief that palliative care is only for terminally ill patients, and concerns about homecare, especially the family burden and responses to sudden changes. Providing appropriate information about the safety of opioids, the availability of palliative care during the entire course of the disease, and realistic information about homecare is of marked importance to promote patients' sense of security.

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Year:  2011        PMID: 21656339     DOI: 10.1007/s00520-011-1161-5

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  31 in total

1.  Knowledge and beliefs about end-of-life care and the effects of specialized palliative care: a population-based survey in Japan.

Authors:  Tatsuya Morita; Mitsunori Miyashita; Makiko Shibagaki; Kei Hirai; Tomoko Ashiya; Tatsuhiko Ishihara; Tatsuhiro Matsubara; Izuru Miyoshi; Toshimichi Nakaho; Nobuaki Nakashima; Hideki Onishi; Taketoshi Ozawa; Kazuyuki Suenaga; Tsukasa Tajima; Tatsuo Akechi; Yosuke Uchitomi
Journal:  J Pain Symptom Manage       Date:  2006-04       Impact factor: 3.612

2.  A scale for measuring feelings of support and security regarding cancer care in a region of Japan: a potential new endpoint of cancer care.

Authors:  Ayumi Igarashi; Mitsunori Miyashita; Tatsuya Morita; Nobuya Akizuki; Miki Akiyama; Yutaka Shirahige; Kenji Eguchi
Journal:  J Pain Symptom Manage       Date:  2011-09-25       Impact factor: 3.612

3.  Palliative care in Japan: shifting from the stage of disease to the intensity of suffering.

Authors:  Tatsuya Morita; Mitsunori Miyashita; Satoru Tsuneto; Yasuo Shima
Journal:  J Pain Symptom Manage       Date:  2008-11-01       Impact factor: 3.612

Review 4.  Palliative care in Japan: current status and a nationwide challenge to improve palliative care by the Cancer Control Act and the Outreach Palliative Care Trial of Integrated Regional Model (OPTIM) study.

Authors:  Akemi Yamagishi; Tatsuya Morita; Mitsunori Miyashita; Nobuya Akizuki; Yoshiyuki Kizawa; Yutaka Shirahige; Miki Akiyama; Tadashi Kudo; Takuhiro Yamaguchi; Asuka Fukushima; Kenji Eguchi
Journal:  Am J Hosp Palliat Care       Date:  2008-07-03       Impact factor: 2.500

5.  Palliative family caregivers' accounts of health care experiences: the importance of "security".

Authors:  Laura M Funk; Diane E Allan; Kelli I Stajduhar
Journal:  Palliat Support Care       Date:  2009-12

6.  Late referrals to specialized palliative care service in Japan.

Authors:  Tatsuya Morita; Tatsuo Akechi; Masayuki Ikenaga; Yoshiyuki Kizawa; Hiroyuki Kohara; Taketo Mukaiyama; Toshimichi Nakaho; Nobuaki Nakashima; Yasuo Shima; Tatsuhiro Matsubara; Yosuke Uchitomi
Journal:  J Clin Oncol       Date:  2005-02-22       Impact factor: 44.544

7.  Feeling like a burden: exploring the perspectives of patients at the end of life.

Authors:  Christine J McPherson; Keith G Wilson; Mary Ann Murray
Journal:  Soc Sci Med       Date:  2006-10-27       Impact factor: 4.634

8.  Self-perceived burden in terminally ill cancer patients: a categorization of care strategies based on bereaved family members' perspectives.

Authors:  Terukazu Akazawa; Tatsuo Akechi; Tatsuya Morita; Mitsunori Miyashita; Kazuki Sato; Satoru Tsuneto; Yasuo Shima; Toshiaki A Furukawa
Journal:  J Pain Symptom Manage       Date:  2010-06-11       Impact factor: 3.612

9.  Barriers to referral to inpatient palliative care units in Japan: a qualitative survey with content analysis.

Authors:  Mitsunori Miyashita; Kei Hirai; Tatsuya Morita; Makiko Sanjo; Yosuke Uchitomi
Journal:  Support Care Cancer       Date:  2007-02-21       Impact factor: 3.603

10.  Supportive versus palliative care: what's in a name?: a survey of medical oncologists and midlevel providers at a comprehensive cancer center.

Authors:  Nada Fadul; Ahmed Elsayem; J Lynn Palmer; Egidio Del Fabbro; Kay Swint; Zhijun Li; Valerie Poulter; Eduardo Bruera
Journal:  Cancer       Date:  2009-05-01       Impact factor: 6.860

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  5 in total

1.  Effective Canadian policy to reduce harms from prescription opioids: learning from past failures.

Authors:  Benedikt Fischer; Jürgen Rehm; Mark Tyndall
Journal:  CMAJ       Date:  2016-11-07       Impact factor: 8.262

2.  The effects of community-wide dissemination of information on perceptions of palliative care, knowledge about opioids, and sense of security among cancer patients, their families, and the general public.

Authors:  Miki Akiyama; Kei Hirai; Toru Takebayashi; Tatsuya Morita; Mitsunori Miyashita; Ayano Takeuchi; Akemi Yamagishi; Hiroya Kinoshita; Yutaka Shirahige; Kenji Eguchi
Journal:  Support Care Cancer       Date:  2015-06-16       Impact factor: 3.603

3.  Validation of the Japanese version of the barriers questionnaire II in cancer pain management: a cross-sectional study.

Authors:  Naoki Sakakibara; Hiroko Komatsu; Mikako Takahashi; Hideko Yamauchi; Teruo Yamauchi; Ardith Z Doorenbos
Journal:  BMC Palliat Care       Date:  2020-07-09       Impact factor: 3.234

4.  Psychological barriers to the use of opioid analgesics for treating pain in patients with advanced recurrent cancer (BAROC): protocol for a multicentre cohort study.

Authors:  Takehiko Tsuno; Tatsuhiro Fujimiya; Takashi Kawaguchi; Ryota Yanaizumi; Keiko Kojima; Akime Miyasato; Kanako Azuma; Tomoya Saeki; Hironori Mawatari; Takashi Igarashi; Tomofumi Miura; Hiroyuki Ogura; Junichi Kondo; Tadashi Tanoue; Hiroshi Hamada; Yu Oyama; Akira Kotani; Takuhiro Yamaguchi; Hideki Hakamata
Journal:  BMJ Open       Date:  2022-03-31       Impact factor: 2.692

5.  Palliative care utilization in oncology and hemato-oncology: a systematic review of cognitive barriers and facilitators from the perspective of healthcare professionals, adult patients, and their families.

Authors:  Marco Bennardi; Nicola Diviani; Claudia Gamondi; Georg Stüssi; Piercarlo Saletti; Ivan Cinesi; Sara Rubinelli
Journal:  BMC Palliat Care       Date:  2020-04-13       Impact factor: 3.234

  5 in total

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