Department of Medical Sciences, Neurosurgery, Uppsala University, Uppsala, Sweden.
Uppsala University Hospital, Entrance 85, NIVA, 751 85, Uppsala, Sweden.
Acta Neurochir (Wien). 2024 Aug 9;166(1):330. doi: 10.1007/s00701-024-06217-5.
Decompressive craniectomy is occasionally performed as a life-saving neurosurgical intervention in patients with acute severe brain injury to reduce refractory intracranial hypertension. Subsequently, cranioplasty (CP) is performed to repair the skull defect. In the meantime, patients are living without cranial bone protection, and little is known about their daily life. This study accordingly explored daily life among patients living without cranial bone protection after decompressive craniectomy while awaiting CP.
A multiple-case study examined six purposively sampled patients, patients' family members, and healthcare staff. The participants were interviewed and the data were analyzed using qualitative content analysis.
The cross-case analysis identified five categories: "Adapting to new ways of living," "Constant awareness of the absence of cranial bone protection," "Managing daily life requires available staff with adequate qualifications," "Impact of daily life depends on the degree of recovery," and "Daily life stuck in limbo while awaiting cranioplasty." The patients living without cranial bone protection coped with daily life by developing new habits and routines, but the absence of cranial bone protection also entailed inconveniences and limitations, particularly among the patients with greater independence in their everyday living. Time spent awaiting CP was experienced as being in limbo, and uncertainty regarding planning was perceived as frustrating.
The results indicate a vulnerable group of patients with brain damage and communication impairments struggling to find new routines during a waiting period experienced as being in limbo. Making this period safe and reducing some problems in daily life for those living without cranial bone protection calls for a person-centered approach to care involving providing contact information for the correct healthcare institution and individually planned scheduling for CP.
去骨瓣减压术偶尔作为一种挽救生命的神经外科干预措施,用于治疗急性严重颅脑损伤患者,以降低难治性颅内高压。随后,进行颅骨修复术(CP)以修复颅骨缺损。在此期间,患者没有颅骨保护,他们的日常生活鲜为人知。因此,本研究探讨了去骨瓣减压术后等待 CP 期间无颅骨保护患者的日常生活。
采用多案例研究,对 6 名有目的抽样的患者、患者家属和医护人员进行了访谈。使用定性内容分析对数据进行了分析。
跨案例分析确定了五个类别:“适应新的生活方式”、“时刻意识到没有颅骨保护”、“日常生活需要有足够资格的可用工作人员”、“日常生活的影响取决于恢复程度”和“等待颅骨修复时的日常生活陷入僵局”。无颅骨保护的患者通过养成新的习惯和常规来应对日常生活,但颅骨保护的缺失也带来了不便和限制,特别是对于日常生活中独立性更强的患者。等待 CP 的时间被认为是处于僵局之中,对计划的不确定性被认为是令人沮丧的。
研究结果表明,这是一组脆弱的脑损伤和沟通障碍患者群体,他们在等待期间努力寻找新的日常生活规律,这段等待期被认为是处于僵局之中。为了使这段时间安全,并减少无颅骨保护患者日常生活中的一些问题,需要采取以患者为中心的护理方法,包括提供正确医疗机构的联系方式和为 CP 单独计划安排。