Tankéré Pierre, Cascarano Estelle, Saint Raymond Christel, Mallaret Martial, Toribio Ruiz Cristina, Herquelot Eléonore, Denis Helene, Cals Maurette Mallory, Tamisier Renaud, Pépin Jean Louis
University Grenoble Alpes, Grenoble, France.
Center for Sleep Medicine, Croix-Rousse Hospital, Hospices Civils de Lyon, Lyon, France.
Amyotroph Lateral Scler Frontotemporal Degener. 2025 May;26(3-4):259-267. doi: 10.1080/21678421.2024.2447911. Epub 2025 Jan 3.
: This study determined real-life care trajectories before and after initiation of noninvasive ventilation (NIV) in patients with amyotrophic lateral sclerosis (ALS). Caregiver adherence to respiratory management recommendations and the associated survival rate of people with ALS were also assessed. : Data were obtained from a tertiary center prospective ALS database that included 10 years of follow-up data for people with ALS. Results are presented numerically and with graphical time sequence analysis through K clustering (TAK) representation. Kaplan Meier and Cox models were used to determine survival and associated prognostic factors. 109 patients with ALS patients were included; median [interquartile range] follow-up was 25.0 months [15.3-43.3]. During study timeframe patients had a median of 4.0 [2.0-6.0] clinical visits; death occurred in 54.1%. Median time between clinical visits was 3.9 [2.8-6.5] months, between arterial blood gases was 4.3 months [3.0-6.6], between spirometry testing was 5.8 months [4.1-8.2], and between nocturnal oximetry was 4.4 months [3.0-7.8]. Visualization of care trajectories TAK show marked heterogeneity in survival, time to NIV initiation, and time from NIV initiation to death. Mortality was correlated with NIV initiation and arterial carbon dioxide pressure increase. : The current framework in ALS guidelines should be adapted to the ALS disease stage and individual patient characteristics. Understanding how subgroups of patients with ALS use healthcare services over time could help to highlight fragility areas and priorities in the allocation of care resources and implementation of best practices.
本研究确定了肌萎缩侧索硬化症(ALS)患者在开始无创通气(NIV)之前和之后的实际护理轨迹。还评估了护理人员对呼吸管理建议的依从性以及ALS患者的相关生存率。:数据来自一个三级中心前瞻性ALS数据库,该数据库包含了ALS患者10年的随访数据。结果以数字形式呈现,并通过K聚类(TAK)表示进行图形时间序列分析。使用Kaplan Meier和Cox模型来确定生存率和相关的预后因素。纳入了109例ALS患者;中位[四分位间距]随访时间为25.0个月[15.3 - 43.3]。在研究期间,患者的临床就诊中位数为4.0[2.0 - 6.0]次;54.1%的患者死亡。临床就诊之间的中位时间为3.9[2.8 - 6.5]个月,动脉血气检查之间为4.3个月[3.0 - 6.6],肺活量测定检查之间为5.8个月[4.1 - 8.2],夜间血氧饱和度测定之间为4.4个月[3.0 - 7.8]。护理轨迹TAK的可视化显示,在生存率、开始NIV的时间以及从开始NIV到死亡的时间方面存在明显的异质性。死亡率与开始NIV和动脉二氧化碳压力升高相关。:ALS指南中的当前框架应根据ALS疾病阶段和个体患者特征进行调整。了解ALS患者亚组如何随时间使用医疗保健服务,有助于突出护理资源分配和最佳实践实施中的脆弱领域和重点。