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Optimizing of a question prompt list to improve communication about the heart failure trajectory in patients, families, and health care professionals

机译:优化问题提示列表,以改善患者,家庭和医疗保健专业人员心力衰竭轨迹的沟通

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The aim of this study was to optimize a Question Prompt List which is designed to improve communication about the heart failure trajectory among patients, family members, and health care professionals. Data were collected in a two-round Delphi survey and a cross-sectional survey, including patients with heart failure, their family members, and health care professionals working in heart failure care in Sweden and the Netherlands. Acceptability for and demand of the Question Prompt List were assessed. A total of 96 patients, 63 family members and 26 health care professionals participated in the study. Regarding acceptability, most of the original questions were found to be relevant by the participants for inclusion in the Question Prompt List but some cultural differences exist, which resulted in two versions of the list: a Swedish version including 33 questions and a Dutch version including 38 questions. Concerning demand, participants reported that they were interested in discussing the questions in the revised Question Prompt List with a physician or a nurse. Few patients and family members reported that they were worried by the questions in the Question Prompt List and hence did not want to discuss the questions. This Question Prompt List has successfully been adapted into a Swedish version and a Dutch version and includes questions about the HF trajectory which patients, their families, and health care professionals perceived to be relevant for discussion in clinical practice. Overall, patients and family members were not worried about the content in the Question Prompt List and if used in accordance with patients’ and family members’ preferences, the Question Prompt List can help to improve communication about the heart failure trajectory.
机译:本研究的目的是优化一个问题提示清单,该列表旨在改善患者,家庭成员和医疗保健专业人员之间的心力衰竭轨迹的沟通。数据被收集在两轮德尔福调查和横断面调查中,包括心力衰竭,家人和医疗保健专业人员在瑞典和荷兰工作的心力衰竭。评估问题提示列表的可接受性和需求。共有96名患者,63名家庭成员和26名医疗专业人士参加了该研究。关于可接受性,发现大多数原始问题都是由参与者纳入问题促销列表的相关性,但存在一些文化差异,这导致了两个版本的列表:瑞典版本,包括33个问题和包括38的荷兰版本问题。关于需求,参与者报告说,他们有兴趣与医生或护士讨论修订问题提示列表中的问题。少数患者和家庭成员报告说,他们担心问题提示列表中的问题,因此不想讨论问题。此问题提示列表已成功地调整为瑞典版本和荷兰语版本,并包括关于患有患者,家庭和医疗保健专业人员在临床实践中讨论相关的HF轨迹的问题。总体而言,患者和家庭成员并不担心问题提示列表中的内容,如果根据患者和家庭成员的偏好使用,问题提示列表可以帮助改善关于心力衰竭轨迹的沟通。

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