Daisuke Toda, Ai Hirose, M. Hata, Mari Sasaki, Saki Ojyara, Yuya Takayama, Syoryoku Hino, Tatsuru Kitamura
{"title":"轻度痴呆患者临终关怀偏好及与家庭照顾者临终关怀期望差异调查","authors":"Daisuke Toda, Ai Hirose, M. Hata, Mari Sasaki, Saki Ojyara, Yuya Takayama, Syoryoku Hino, Tatsuru Kitamura","doi":"10.14442/generalist.44.45","DOIUrl":null,"url":null,"abstract":"Introduction: We investigated the end-of-life care preferences of patients with mild dementia and compared them with the hopes of caregivers regarding end-of-life care for patients. Methods: A questionnaire survey was conducted among outpatients with mild dementia or mild cognitive impairment and their family caregivers who visited the Medical Center for Dementia. Results: We analyzed 50 pairs of dementia patients and their family caregivers. Of people with dementia, 24 respondents (48.0%) preferred“antibiotics and infusions for pneumonia”at the end of life. Eleven respondents (22.0%) preferred“central parenteral nutrition”. Eight respondents (16.0%) preferred“resuscitation”. For each end-of-life care item, the concordance rate between patients and caregivers on“prefer”/“do not prefer”was 0%-76%. Patients and their families who discussed end-of-life care had a significantly higher concordance rate for“resuscitation” preference than those who did not. Conclusion: For patients and their families to be able to make decisions they do not regret, it is important to promote discussions about end-of-life medical care before the patient’s condition becomes severe.","PeriodicalId":211485,"journal":{"name":"An Official Journal of the Japan Primary Care Association","volume":"7 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Survey of the End-of-life Care Preferences of Patients with Mild Dementia and Differences from Hopes of Familial Caregivers Regarding End-of-life Care for Patients\",\"authors\":\"Daisuke Toda, Ai Hirose, M. Hata, Mari Sasaki, Saki Ojyara, Yuya Takayama, Syoryoku Hino, Tatsuru Kitamura\",\"doi\":\"10.14442/generalist.44.45\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction: We investigated the end-of-life care preferences of patients with mild dementia and compared them with the hopes of caregivers regarding end-of-life care for patients. Methods: A questionnaire survey was conducted among outpatients with mild dementia or mild cognitive impairment and their family caregivers who visited the Medical Center for Dementia. Results: We analyzed 50 pairs of dementia patients and their family caregivers. Of people with dementia, 24 respondents (48.0%) preferred“antibiotics and infusions for pneumonia”at the end of life. Eleven respondents (22.0%) preferred“central parenteral nutrition”. Eight respondents (16.0%) preferred“resuscitation”. For each end-of-life care item, the concordance rate between patients and caregivers on“prefer”/“do not prefer”was 0%-76%. Patients and their families who discussed end-of-life care had a significantly higher concordance rate for“resuscitation” preference than those who did not. Conclusion: For patients and their families to be able to make decisions they do not regret, it is important to promote discussions about end-of-life medical care before the patient’s condition becomes severe.\",\"PeriodicalId\":211485,\"journal\":{\"name\":\"An Official Journal of the Japan Primary Care Association\",\"volume\":\"7 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-06-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"An Official Journal of the Japan Primary Care Association\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14442/generalist.44.45\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"An Official Journal of the Japan Primary Care Association","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14442/generalist.44.45","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Survey of the End-of-life Care Preferences of Patients with Mild Dementia and Differences from Hopes of Familial Caregivers Regarding End-of-life Care for Patients
Introduction: We investigated the end-of-life care preferences of patients with mild dementia and compared them with the hopes of caregivers regarding end-of-life care for patients. Methods: A questionnaire survey was conducted among outpatients with mild dementia or mild cognitive impairment and their family caregivers who visited the Medical Center for Dementia. Results: We analyzed 50 pairs of dementia patients and their family caregivers. Of people with dementia, 24 respondents (48.0%) preferred“antibiotics and infusions for pneumonia”at the end of life. Eleven respondents (22.0%) preferred“central parenteral nutrition”. Eight respondents (16.0%) preferred“resuscitation”. For each end-of-life care item, the concordance rate between patients and caregivers on“prefer”/“do not prefer”was 0%-76%. Patients and their families who discussed end-of-life care had a significantly higher concordance rate for“resuscitation” preference than those who did not. Conclusion: For patients and their families to be able to make decisions they do not regret, it is important to promote discussions about end-of-life medical care before the patient’s condition becomes severe.