荷兰全科医生对后柯萨奇综合征患者的护理需求:对患者和全科医生的访谈研究。

IF 2 Q2 MEDICINE, GENERAL & INTERNAL
Corinne Rijpkema, Bart J Knottnerus, Rinske van den Hoek, Lisa Bosman, Liset van Dijk, Robert A Verheij, Isabelle Bos
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引用次数: 0

摘要

背景:后柯瓦兹综合征(PCS)对个人的日常生活有很大影响。由于 PCS 患者的症状多种多样,而且该疾病仍是一种相对较新的疾病,因此全科医生(GPs)很难识别、诊断和治疗 PCS 患者,从而导致难以评估和满足医疗保健需求。荷兰患者和全科医生在 PCS 方面的经历在很大程度上是未知的,因此,我们希望深入了解 PCS 患者生活的各个方面以及相关的医疗需求:2022 年 1 月至 7 月期间,我们对 13 名自述 PCS 患者(性别、年龄、教育程度和健康知识水平各不相同)和 6 名全科医生(性别、年龄和执业类型各不相同)进行了半结构式访谈。患者和全科医生很可能没有关联(不在同一诊所)。我们采用主题分析法对数据进行了分析:访谈中发现,两类 PCS 患者的经历似乎有所不同:(1) 原有健康状况良好(PEHS)的患者受到 PCS 的严重影响,难以康复;(2) PEHS 较差的患者在感染 COVID-19 后健康状况更加糟糕。与 PCS 患者和全科医生的访谈显示了两大主题,其中患者的类型有所不同:(1)PCS 患者的生活方面;PEHS 较好的患者主要在过度兴奋时出现症状,而 PEHS 较差的患者一般会持续感到疲惫不堪。(2) 医疗保健经验;全科医生强调,PEHS 良好的患者似乎可以通过仔细规划日常活动来分配精力,而 PEHS 较差的患者则需要在激活方面得到支持。患者和全科医生都强调了认真对待患者并承认其症状的重要性。最后,受访患者表示,一些全科医生对 PCS 的存在表示怀疑,导致对 PCS 的认识不足:结论:认识到两种 PCS 患者在需求和经历上的差异有助于提供更适当的护理。全科医生承认 PCS 是一种真实存在的综合征,这对患者来说非常重要,并在应对 PCS 或从 PCS 中康复的过程中发挥着重要作用。以人为本的多学科方法非常重要,可由全科医生负责协调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Care needs of patients with the post-COVID syndrome in Dutch general practice: an interview study among patients and general practitioners.

Background: The post-COVID syndrome (PCS) has a large impact on an individual's daily life. The wide variety of symptoms in PCS patients and the fact that it is still relatively new makes it difficult for general practitioners (GPs) to recognize, diagnose and treat patients with PCS, leading to difficulties in assessing and fulfilling healthcare needs. It is largely unknown what the experiences of Dutch patients and GPs are with PCS and, therefore, we gained insight into the different aspects of living with PCS and the associated healthcare needs.

Methods: Semi-structured interviews were performed with 13 self-reported PCS patients (varying in sex, age, education, and health literacy) and 6 GPs (varying in gender, age, and type of practice) between January-July 2022. Patients and GPs were most likely unrelated (not in the same practices). The data have been analysed using the Thematic Analysis method.

Results: Experiences appeared to vary between two types of PCS patients that emerged during the interviews: (1) individuals with good pre-existing health status (PEHS) who are severely affected by PCS and have difficulty recovering and (2) individuals with poorer PEHS whose health became even poorer after COVID-19 infection. The interviews with PCS patients and GPs revealed two main themes, in which the types of patients differed: (1) aspects of living with PCS; individuals with good PEHS mainly experience symptoms when overstimulated, while individuals with poorer PEHS generally feel exhausted continuously. (2) Healthcare experiences; GPs emphasized that individuals with good PEHS seem to benefit from support in distributing their energy by careful planning of daily activities, whereas individuals with poorer PEHS require support in activation. Patients and GPs emphasised the importance of taking patients seriously and acknowledging their symptoms. Finally, the patients interviewed indicated that some GPs doubted the existence of PCS, resulting in insufficient recognition.

Conclusion: Awareness of the differences in needs and experiences of the two types of PCS patients could contribute to more appropriate care. Acknowledgement of PCS by GPs as a real syndrome is important for patients and plays an important role in coping with or recovering from PCS. A multidisciplinary person-centred approach is important and can be coordinated by a GP.

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