了解你的病人:病人对促进以人为本的护理问卷回答的内容分析。

Q2 Medicine
Juno Hk Bergers, Hester Wessels-Wynia, Tatjana Seute, Astrid Janssens, Johannes Jm van Delden
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引用次数: 0

摘要

背景:以人为本的护理(PCC)鼓励患者积极参与医疗保健,从而促进适合患者生活的护理。因此,医疗保健专业人员(HCPs)需要了解病人。作为改善 PCC 的广泛政策的一部分,此前已开发了由 5 个问题组成的数字问卷("我们想了解您"),以帮助医护人员在患者和员工的参与下了解患者:本研究旨在深入了解问卷的内容和目的,以了解其潜力和可用性:我们使用 NVivo Pro(QSR International)对患者的回答进行了定性、回顾性内容分析。该问卷在荷兰一家学术医院的神经肿瘤科门诊使用:在 374 名受邀患者中,78 人(20.9%)完成了问卷调查。我们从 78 名患者中抽取了 42 人(54%)作为样本。患者在每个问题上的用词中位数为 16(IQR 7-27)个单词,大多数答案都很容易理解。当被问及重要活动时,最常提及的是社交活动、体育运动或维持正常生活。患者还写到了对疾病的恐惧、疾病可能对生活造成的影响或对未来的恐惧。患者希望保健医生了解他们的护理和沟通偏好,或分享个人信息。他们对有效治疗、沟通和护理过程提出了期望:该问卷似乎是可用的,因为患者提供了可解释的答案,只需花很少的时间阅读,而保健医生可以利用这些答案进行个性化护理。我们的研究表明,该问卷具有帮助提供 PCC 的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Getting to Know Your Patient: Content Analysis of Patients' Answers to a Questionnaire for Promoting Person-Centered Care.

Background: Person-centered care (PCC) encourages patients to actively participate in health care, thus facilitating care that fits the life of the patient. Therefore, health care professionals (HCPs) need to know the patient. As part of a broad policy for improving PCC, a digital questionnaire ("We would like to know you") consisting of 5 questions has previously been developed to help HCPs to get to know the patient with the help of patient and staff involvement.

Objective: The purpose of this study was to provide insight into the content and aims of the questionnaire to understand its potential and usability.

Methods: We conducted a qualitative, retrospective content analysis of patients' answers using NVivo Pro (QSR International). The questionnaire was used in the outpatient neuro-oncology department of a Dutch academic hospital.

Results: Of 374 invited patients, 78 (20.9%) completed the questionnaire. We selected a sample of 42 (54%) of the 78 patients. Patients used a median of 16 (IQR 7-27) words per question, and most answers were easily interpretable. When asked about important activities, social activities, sports, or maintaining a normal life were most frequently mentioned. Patients wrote about fear of the disease, its possible influence on life, or fear of the future in general. Patients wanted HCPs to know about their care and communication preferences or shared personal information. They formulated expectations about effective treatment, communication, and the care process.

Conclusions: The questionnaire seems usable because patients provide interpretable answers that take little time to read, which HCPs can use to personalize care. Our study shows the potential of the questionnaire to help deliver PCC.

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来源期刊
Journal of Participatory Medicine
Journal of Participatory Medicine Medicine-Medicine (miscellaneous)
CiteScore
3.20
自引率
0.00%
发文量
8
审稿时长
12 weeks
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