Trends in Invasive Interventions and Risk Factors for Early Critical Events in Multiple System Atrophy.

IF 2.4 3区 医学 Q3 NEUROSCIENCES
Monami Tarisawa, Masaaki Matsushima, Akihiko Kudo, Taichi Nomura, Hisashi Uwatoko, Shinichi Shirai, Ikuko Takahashi-Iwata, Ken Sakushima, Hiroaki Yaguchi, Isao Yokota, Naoki Nishimoto, Jun Sawada, Takeshi Matsuoka, Haruo Uesugi, Naoya Minami, Kazuya Sako, Asako Takei, Shin Hisahara, Yasuhiro Kanatani, Akiko Tamakoshi, Norihiro Sato, Ichiro Yabe
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Abstract

Multiple system atrophy (MSA) is a progressive, adult-onset neurodegenerative disorder involving autonomic failure, cerebellar ataxia, and parkinsonism. Patients often require invasive interventions, such as gastrostomy or tracheostomy, and sudden death is common. This study aimed to elucidate patterns of invasive treatment and identify risk factors for tracheostomy or sudden death within 5 years of onset. In total, 214 patients diagnosed with MSA between November 2014 and October 2024 across 66 institutions in Hokkaido were enrolled in the Hokkaido Rare Disease Consortium for MSA (HoRC-MSA). Patients were grouped by clinical course and interventions. We analyzed use of invasive procedures, including enteral nutrition via gastrostomy, enterostomy, esophagostomy, nasogastric tube insertion, central venous nutrition, tracheostomy, and ventilator support. Multivariable analyses were performed to compare patients with and without early critical events, defined as tracheostomy or sudden death within 5 years of disease onset. Invasive procedures were performed in 63.1% of patients. Patients receiving enteral nutrition and tracheostomy had prolonged survival. Early events correlated with older onset age (mean, 65.9 years), orthostatic hypotension, stridor, and an elevated apnea-hypopnea index (median, 32.45). Patients with preserved activities of daily living (ADL) in the Unified MSA Rating Scale part Ⅳ also had an increased risk of early critical events. Autonomic dysfunction, sleep-disordered breathing, and vocal cord impairment predict key risk factors for early mortality in patients with MSA. Monitoring is necessary, regardless of preserved ADL. The impact of invasive interventions on quality of life should be further explored.

多系统萎缩早期关键事件的侵入性干预和危险因素趋势。
多系统萎缩(MSA)是一种进行性、成人发病的神经退行性疾病,涉及自主神经衰竭、小脑性共济失调和帕金森病。患者通常需要侵入性干预,如胃造口术或气管造口术,猝死很常见。本研究旨在阐明有创治疗模式,并确定发病5年内气管切开术或猝死的危险因素。2014年11月至2024年10月,北海道66家机构共有214名被诊断为MSA的患者加入了北海道罕见病联盟(HoRC-MSA)。患者按临床病程和干预措施进行分组。我们分析了侵入性手术的使用,包括通过胃造口、肠造口、食管造口、鼻胃管插入、中心静脉营养、气管造口和呼吸机支持进行肠内营养。进行多变量分析,比较有和没有早期关键事件的患者,定义为疾病发病5年内的气管切开术或猝死。63.1%的患者接受了有创手术。接受肠内营养和气管切开术的患者生存期延长。早期事件与发病年龄较大(平均65.9岁)、体位性低血压、喘鸣和呼吸暂停低通气指数升高相关(中位数,32.45)。在统一MSA评定量表Ⅳ中保留日常生活活动(ADL)的患者早期危急事件的风险也增加。自主神经功能障碍、睡眠呼吸障碍和声带损伤预测MSA患者早期死亡的关键危险因素。无论保存的ADL如何,都必须进行监测。有创性干预对生活质量的影响有待进一步探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Cerebellum
Cerebellum 医学-神经科学
CiteScore
6.40
自引率
14.30%
发文量
150
审稿时长
4-8 weeks
期刊介绍: Official publication of the Society for Research on the Cerebellum devoted to genetics of cerebellar ataxias, role of cerebellum in motor control and cognitive function, and amid an ageing population, diseases associated with cerebellar dysfunction. The Cerebellum is a central source for the latest developments in fundamental neurosciences including molecular and cellular biology; behavioural neurosciences and neurochemistry; genetics; fundamental and clinical neurophysiology; neurology and neuropathology; cognition and neuroimaging. The Cerebellum benefits neuroscientists in molecular and cellular biology; neurophysiologists; researchers in neurotransmission; neurologists; radiologists; paediatricians; neuropsychologists; students of neurology and psychiatry and others.
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