Faculty of Nursing, Graduate School of Nursing, Kansai Medical University, 2-2-2 Shinmachi, Hirakata, Osaka, 573-1004, Japan.
Department of Nursing, Faculty of Nursing, Shitennoji University, 3-2-1 Gakuenmae, Habikino, Osaka, 583-8501, Japan.
Orphanet J Rare Dis. 2024 Oct 28;19(1):401. doi: 10.1186/s13023-024-03424-2.
Adrenoleukodystrophy (ALD) is an X-linked peroxisomal disorder. Its cerebral form presents as a learning and behavioral disorder that, if untreated, leads to rapid neurological regression, disability, and death within 10 years of diagnosis. Therefore, the disease significantly impacts patients' quality of life, making quality of life assessment crucial for effective medical treatment and care. However, no disease-specific quality of life scale exists for ALD. Therefore, we conducted qualitative research to determine the experiences of patients and their families as a preliminary step toward developing one.
Four mothers of patients with cerebral ALD were interviewed. Based on classification using the qualitative content analysis method, the verbatim transcripts were grouped into four themes: support needs for patients, support needs for families, the impact of treatment, and challenges within support systems.
Support for patients and family members is required after ALD is diagnosed. In addition to addressing symptoms, daily life support and caregiving burden should be considered. Furthermore, several challenges and opportunities exist for improving treatment and support systems. Therefore, combining appropriate supporters and support systems according to the progressive and hereditary characteristics of ALD is crucial.
肾上腺脑白质营养不良(ALD)是一种 X 连锁过氧化物酶体疾病。其脑型表现为学习和行为障碍,如果未经治疗,会在诊断后 10 年内迅速导致神经退行性变、残疾和死亡。因此,这种疾病极大地影响了患者的生活质量,使生活质量评估成为有效医疗和护理的关键。然而,ALD 尚无特异性的生活质量量表。因此,我们进行了定性研究,以确定患者及其家属的体验,作为开发生活质量量表的初步步骤。
对 4 位脑型 ALD 患者的母亲进行了访谈。根据定性内容分析方法的分类,逐字记录被分为 4 个主题:患者的支持需求、家庭的支持需求、治疗的影响以及支持系统中的挑战。
ALD 确诊后,患者和家庭成员需要得到支持。除了治疗症状外,还应考虑日常生活支持和照护负担。此外,在改善治疗和支持系统方面存在一些挑战和机遇。因此,根据 ALD 的进行性和遗传性特点,结合适当的支持者和支持系统至关重要。