Hearn Jasmine Heath, Selvarajah Sen, Kennedy Paul, Taylor Julian
1The University of Buckingham Medical School, Hunter Street, Buckingham, UK.
2Stoke Mandeville Spinal Research, The National Spinal Injuries Centre, Buckinghamshire Healthcare NHS Trust, Aylesbury, UK.
Spinal Cord Ser Cases. 2018 Feb 12;4:12. doi: 10.1038/s41394-018-0042-2. eCollection 2018.
Qualitative, phenomenological design.
Neurogenic bladder dysfunction and urinary tract infection (UTI) are common secondary consequences to neurological damage to the spinal cord. This study sought to establish the impact of chronic, recurrent UTIs on people with spinal cord injury (SCI).
Community sample, United Kingdom.
Twelve participants with SCI, aged between 28 and 68 years, who had experienced at least three recurrent UTI events within the previous 12 months were recruited. Detailed qualitative information was obtained from semi-structured interviews, which lasted between 30 and 60 min. Interpretative Phenomenological Analysis was performed to explore the lived experience of UTIs.
Interview findings identified a range of factors related to the experience of recurrent UTIs in people with SCI. These were classified into the following themes: (1) Symptom Management Precedence, (2) Stigma-Motivated Risk Management and (3) Exhaustive Exploration of Treatment Options. Participants discussed management of acute exacerbations. Distress arose from perceptions of UTIs as potentially stigmatizing and fear of relying on antibiotics. Arising from this fear, many participants sought alternative prevention and management strategies.
These results suggest that chronic recurrent UTIs act as major barriers to social participation, with adverse effects on quality of life of people with a neurogenic bladder after SCI. People with SCI would benefit from additional assessment of the impact of recurrent UTIs, so that healthcare professionals can address specific concerns, such as the psychosocial impact of urinary incontinence and stigmatizing views. Additional support to enhance self-management and facilitate social participation should be provided.
定性、现象学设计。
神经源性膀胱功能障碍和尿路感染(UTI)是脊髓神经损伤常见的继发后果。本研究旨在确定慢性复发性尿路感染对脊髓损伤(SCI)患者的影响。
英国社区样本。
招募了12名年龄在28至68岁之间、在过去12个月内经历过至少三次复发性尿路感染事件的脊髓损伤患者。通过持续30至60分钟的半结构化访谈获取详细的定性信息。采用解释现象学分析来探究尿路感染的生活经历。
访谈结果确定了一系列与脊髓损伤患者复发性尿路感染经历相关的因素。这些因素分为以下几个主题:(1)症状管理优先级,(2)因耻辱感而进行风险管理,(3)对治疗方案的详尽探索。参与者讨论了急性加重期的管理。因认为尿路感染可能带来耻辱感以及害怕依赖抗生素而产生困扰。出于这种恐惧,许多参与者寻求替代的预防和管理策略。
这些结果表明,慢性复发性尿路感染是社会参与的主要障碍,对脊髓损伤后神经源性膀胱患者的生活质量产生不利影响。脊髓损伤患者将受益于对复发性尿路感染影响的额外评估,以便医疗保健专业人员能够解决特定问题,如尿失禁的心理社会影响和耻辱性观念。应提供额外支持以加强自我管理并促进社会参与。