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Patients' preferences for involvement in treatment decision making in Japan

机译:在日本患者对参与治疗决策的偏好

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Background A number of previous studies have suggested that the Japanese have few opportunities to participate in medical decision-making, as a result both of entrenched physician paternalism and national characteristics of dependency and passivity. The hypothesis that Japanese patients would wish to participate in treatment decision-making if adequate information were provided, and the decision to be made was clearly identified, was tested by interview survey. Methods The subjects were diabetic patients at a single outpatient clinic in Kyoto. One of three case study vignettes (pneumonia, gangrene or cancer) was randomly assigned to each subject and, employing face-to-face interviews, the subjects were asked what their wishes would be as patients, for treatment information, participation in decision-making and family involvement. Results 134 patients participated in the study, representing a response rate of 90%. The overall proportions of respondents who preferred active, collaborative, and passive roles were 12%, 71%, and 17%, respectively. Respondents to the cancer vignette were less likely to prefer an active role and were more likely to prefer family involvement in decision-making compared to non-cancer vignette respondents. If a physician's recommendation conflicted with their own wishes, 60% of the respondents for each vignette answered that they would choose to respect the physician's opinion, while few respondents would give the family's preference primary importance. Conclusions Our study suggested that a majority of Japanese patients have positive attitudes towards participation in medical decision making if they are fully informed. Physicians will give greater patient satisfaction if they respond to the desire of patients for participation in decision-making.
机译:背景技术先前的许多研究表明,由于根深蒂固的医师家长制以及依赖和消极的民族特征,日本人很少有机会参与医疗决策。通过访谈调查检验了日本患者希望提供足够信息并明确确定了要做出的决定的日本患者希望参加治疗决策的假设。方法研究对象是在京都一家门诊诊所的糖尿病患者。将三个案例研究小插曲(肺炎,坏疽或癌症)之一随机分配给每个受试者,并通过面对面访谈,询问受试者作为患者的意愿,治疗信息,参与决策和家庭参与。结果134例患者参加了该研究,反应率为90%。偏好主动,协作和被动角色的受访者的总比例分别为12%,71%和17%。与非癌症小插图的受访者相比,癌症小插图的受访者不太可能喜欢扮演积极角色,而更倾向于家庭参与决策。如果医师的建议与自己的意愿相抵触,则每个小插图的60%的受访者回答说,他们将选择尊重医师的意见,而很少有受访者将家庭的偏好放在首位。结论我们的研究表明,如果日本患者充分了解情况,他们对参与医疗决策会持积极态度。如果医师响应患者参与决策的愿望,他们将给予患者更大的满意度。

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