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The symptom experience of newly diagnosed Chinese patients with Crohn's disease: A longitudinal qualitative study

感觉 医学 非概率抽样 检查表 疾病 定性研究 纵向研究 克罗恩病 家庭医学 心理学 内科学 社会心理学 病理 人口 社会学 认知心理学 环境卫生 社会科学
作者
L. Chen,Yunxian Zhou
出处
期刊:Journal of Advanced Nursing [Wiley]
卷期号:79 (10): 3824-3836 被引量:3
标识
DOI:10.1111/jan.15721
摘要

To longitudinally explore the symptom experience of Chinese patients with Crohn's disease within the first year following their diagnosis.A longitudinal qualitative study.Eighteen newly diagnosed Chinese patients with Crohn's disease were recruited through purposive sampling. Semi-structured interviews were conducted at four time points: soon after diagnosis, 3, 6 and 12 months post-diagnosis. Data were collected between January 2021 and February 2022. Conventional content analysis was used for data analysis of each time point. Afterwards, the data of each time point were compared longitudinally. COREQ checklist was followed.Three themes and eight sub-themes were formed through analysis: feelings towards symptoms (symptoms make me feel uneasy, symptoms make me feel inferior and symptoms make me feel helpless); acceptability of symptoms (difficult to accept, have to accept, be able to accept); functions of symptoms (assessing disease conditions and treatment effects, warning of disease management).Overall, the negative emotions related to symptoms gradually decreased over time, and the patient's acceptance of symptoms increased within the first year following diagnosis. In addition, when the disease was in remission after treatment, the warning function of symptoms gradually weakened.The process of how patients accept their symptoms found in this study provides a basis for nurses to improve patients' acceptance of symptoms and reduce their symptom-related negative emotions. This study also emphasizes the phenomenon that patients gradually ignore some symptoms with their increased acceptance level, which warrants additional health education to strengthen their awareness of self-management.No patient or public contribution was required to design or undertake this study. Patients contributed only to the data collection and member checking.
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