The Current Status of Palliative Care for Non-cancer Patients in Japan: Field Survey on the Representatives of the Japanese Society for Palliative Medicine

Iwao Osaka; Akihiro Sakashita; Yoshiyuki Kizawa; Toyoshi Hosokawa

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The Current Status of Palliative Care for Non-cancer Patients in Japan: Field Survey on the Representatives of the Japanese Society for Palliative Medicine

VernacularTitle:The Current Status of Palliative Care for Non-cancer Patients in Japan: Field Survey on the Representatives of the Japanese Society for Palliative Medicine
Author: Iwao OSAKA ¹ ; Akihiro SAKASHITA ² ; Yoshiyuki KIZAWA ² ; Toyoshi HOSOKAWA ³
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1. Division of Palliative Medicine, Shizuoka Cancer Center Hospital
2. Department of Palliative Medicine, Kobe University Graduate School of Medicine
3. Department of Pain Management and Palliative Care Medicine, Kyoto Prefectural University of Medicine
Keywords: non-cancer; palliative care; internet survey
From:Palliative Care Research 2018;13(1):31-37
CountryJapan
Language:Japanese
Abstract: Purpose: The field survey was conducted to evince the current status of palliative care for non-cancer patients. Methods: The on-line questionnaire survey was conducted covering 196 representatives of the Japanese Society for Palliative Medicine. Multiple-choice questions were asked about their medical experiences with non-cancerous diseases, their attitudes towards palliative care, their feelings of bewilderment upon providing palliative care, and what they thought would be required for future education in this field. Results: One-hundred and eleven (111) representatives (57%) responded the survey. Ninety-nine (99)% of the respondents experienced providing non-cancer patients with palliative care, but 63% of them experienced less than 50 patients in the terminal phases even in cumulative total. Eighty (80)% of them said they were feeling insecure about providing non-cancer patients with palliative care, and 83% of them were feeling difficulty when they had to do so. The reasons listed included that prognostic prediction for such cases wouldn’t be easy and that it wouldn’t be covered by public health insurances. What they felt necessary about future education included communication and multi-disciplinary team medicine, in this order. Conclusions: The representatives of the Japanese Society for Palliative Medicine are well-aware of the demands for palliative care for non-cancer patients, but not many of them have experienced such cases and more than 80% of them are feeling insecure and difficulty about providing it.