一项探讨儿科风湿病治疗经验的定性研究-儿童,年轻人,父母和护理者的观点。

IF 2.8 3区 医学 Q1 PEDIATRICS
Kassie Gracella Putri, Sunil Sampath, Charlotte Lucy Richardson, Alice McCloskey, Adam Pattison Rathbone
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引用次数: 0

摘要

背景:从儿童和青少年(CYP)及其父母或照顾者(PC)的角度描述整体生活医疗经历的儿科风湿病学文献有限。这很重要,因为它可能对依从性有影响。本研究旨在探讨CYP和PC在儿科风湿病科的治疗经验。方法:参与者在三级儿科风湿病中心的静脉输液日病例单位招募。采用与CYP和PC的联合定性半结构化访谈来收集数据。使用NVivo 12.4对数据进行转录、质量检查和主题分析以确定发现。结果:32名参与者(15名年龄在6 - 16岁之间的CYP, 17名PC)参加了平均时长41分钟43秒的访谈。参与者描述了使用英夫利昔单抗,其次是托珠单抗和阿巴接受的经历。参与者经历了一个波动,在积极和消极的轨迹之间摇摆。医学治疗的经验被描述为暂时的,最终改变并导致治疗改变或停止。行为受到躯体因素(疼痛、功能)、社会因素(卫生专业人员的建议、朋友、家人和老师的鼓励、在学校、工作和财务方面使用治疗的实用性)和认知因素(害怕针头、害怕特定药物、相信必要性)的影响。结论:总的来说,研究结果表明,医疗经验反映了许多儿科风湿病的性质,在积极和消极轨迹之间摇摆。当治疗被认为是“成功的”时,身体、社会和认知体验可能是积极的。消极的身体、社会或认知经历导致诸如不坚持治疗等行为。该研究的一个局限性是访谈是与CYP和PC联合进行的,这可能会影响参与者在彼此面前愿意说的话,但这确实意味着研究结果与CYP和PC都相关,因此可能是干预措施的合适目标,以提高依从性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A qualitative study exploring experiences of treatment in paediatric rheumatology - children's, young people's, parents' and carers' perspectives.

Background: There is limited literature in paediatric rheumatology describing holistic lived experiences of medical treatment from perspectives of children and young people (CYP) and their parents or carers (PC). This is important as it could have implications for adherence. This study aimed to explore treatment experiences of CYP and PC in a paediatric rheumatology service.

Methods: Participants were recruited at a day-case unit for intravenous infusions at a tertiary paediatric rheumatology centre. Joint qualitative semi-structured interviews with CYP and PC were used to collect data. Data were transcribed, quality checked and thematically analysed using NVivo 12.4 to identify findings.

Results: Thirty-two participants (15 CYP between the ages of 6 and 16 years, 17 PC) took part in interviews lasting 41 min and 43 s, on average. Participants described experiences using infliximab, followed by tocilizumab and abatacept. Participants experienced a wave, oscillating between positive and negative trajectories. Experiences of medical treatments were described as temporary, eventually changing and leading to treatment changes or cessation. Behaviours were influenced through somatic factors (pain, function), social factors (advice from health professionals, encouragement from friends, family and teachers, practicality of using treatment in relation to school, work and finance) and cognitive factors (fear of needles, fear of specific medications, beliefs about necessity).

Conclusions: Collectively, findings demonstrate experiences of medical treatment reflect the nature of many paediatric rheumatology conditions, oscillating between periods of positive and negative trajectories. Somatic, social and cognitive experiences can be positive, when treatment is considered 'successful'. Negative somatic, social or cognitive experiences led to behaviours such as treatment non-adherence. A limitation of the study is interviews were conducted jointly with CYP and PC, which may have influenced what participants were willing to say in front of one another however this does mean findings relate to both CYP and PC and so could be suitable targets for interventions to improve adherence.

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来源期刊
Pediatric Rheumatology
Pediatric Rheumatology PEDIATRICS-RHEUMATOLOGY
CiteScore
4.10
自引率
8.00%
发文量
95
审稿时长
>12 weeks
期刊介绍: Pediatric Rheumatology is an open access, peer-reviewed, online journal encompassing all aspects of clinical and basic research related to pediatric rheumatology and allied subjects. The journal’s scope of diseases and syndromes include musculoskeletal pain syndromes, rheumatic fever and post-streptococcal syndromes, juvenile idiopathic arthritis, systemic lupus erythematosus, juvenile dermatomyositis, local and systemic scleroderma, Kawasaki disease, Henoch-Schonlein purpura and other vasculitides, sarcoidosis, inherited musculoskeletal syndromes, autoinflammatory syndromes, and others.
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