1.Suggestions and recommendations from health care professionals involved in regional palliative care program
Tatsuya Morita ; Chizuru Imura ; Yoshiko Nozue ; Satoshi Suzuki ; Mie Shibuya ; Hiroya Kinoshita ; Kumiko Harada ; Yutaka Shirahige ; Mika Hirayama ; Kenji Eguchi
Palliative Care Research 2012;7(1):163-171
The aim of this study is to collect the suggestions and recommendations of health care professionals involved in the regional palliative care program (OPTIM-study). A total of 101 multidisciplinary health care professionals who participated in the intervention program were interviewed, and 107 meaningful units were obtained from 89 valid interviews. The responses were categorized into “suggestions regardless of profession” (n=59), including “Participate in a multi-disciplinary conference to expand the network of people”, “Try to understand the situation of others”, “Seek support from others when you cannot solve the problem by yourself”, “Pursue all possibilities before giving up”, and “Do not try too hard”. As suggestions to those engaged in each profession, “Suggestions to community pharmacies” and “Suggestions to care managers” are frequently described. An examination of suggestions by the participants in the regional palliative care program could provide some insights to improve community palliative care.
2.What is the greatest impact of the regional palliative care program?: the OPTIM-study
Tatsuya Morita ; Chizuru Imura ; Yoshiko Nozue ; Satoshi Suzuki ; Mie Shibuya ; Hiroya Kinoshita ; Kumiko Harada ; Yutaka Shirahige ; Mika Hirayama ; Kenji Eguchi
Palliative Care Research 2012;7(2):209-217
The purpose of this study was to identify the greatest impact of the regional palliative care program on community health care professionals. Interviews were conducted involving 101 people who became involved in the intervention program implemented in 4 areas across Japan, and 96 valid responses were collected. The following were cited as the greatest impact: [I developed a network of people, and realized the importance of collaboration] (n=61; “I was able to develop an interpersonal relationship” and “Now I understand the significance of collaboration”), [My knowledge and skills regarding palliative care were improved] (n=18; “Knowledge and support helped me respond to patients with confidence” and “I have come to think that there is more to palliative care than terminal care”), [I rediscovered my role through a wide variety of experiences] (n=10), [Both collaboration and palliative knowledge/skills meant a lot to me] (n=4), [What I experienced in this program will help me play my role] (n=2), and [Patients and their families became satisfied] (n=1). The community palliative care program was most effective in facilitating collaboration, and helped participants develop knowledge and skills concerning palliative care.
3.The effect of an intervention of a regional palliative care intervention program on home hospice utilization and hospital staff’s perceptions about home care: an observation from the OPTIM-study
Yutaka Shirahige ; Takatoshi Noda ; Minoru Hojo ; Shinichi Goto ; Shiro Tomiyasu ; Masahiro Deguchi ; Sadayuki Okudaira ; Masakazu Yasunaka ; Mika Hirayama ; Ritsuko Yoshihara ; Taeko Funamoto ; Ayumi Igarashi ; Mitsunori Miyashita ; Tatsuya Morita
Palliative Care Research 2012;7(2):389-394
This study aimed to clarify whether a regional palliative care intervention program, the OPTIM project, increased home hospice utilization, and explore the potential association between the home hospice utilization and the hospital staff's perceptions on home care. A questionnaire survey was conducted involving 154 physicians and 469 nurses. The rate of patients who made the transition to home-based care increased 967% in A Hospital, 295% in B Hospital, and 221% in C Hospital in 2010 compared to 2007, which was assumed to be 100. Staff of a hospital where many patients made the transition to home-based care were more likely to agree with the following statements concerning home care perspectives: “I started to consider that even cancer patients can be treated at home until the last moment of their life”, “I usually ask patients whether they wish to receive home-based care”, “We decided on coping strategies for sudden changes in the course of disease and a place to contact in advance”, and “I started to simplify treatment procedures, such as prescriptions during hospitalization for patients and their families to prepare for home-based care“.