Care trajectories and adherence to respiratory management recommendations in persons living with amyotrophic lateral sclerosis: a ten-year cohort study in a French tertiary university centre.

Pierre Tankéré, Estelle Cascarano, Christel Saint Raymond, Martial Mallaret, Cristina Toribio Ruiz, Eléonore Herquelot, Helene Denis, Mallory Cals Maurette, Renaud Tamisier, Jean Louis Pépin
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Abstract

Objective: 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. Methods: 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. Results: 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. Conclusions: 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.

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肌萎缩性侧索硬化症患者的护理轨迹和对呼吸管理建议的依从性:一项在法国高等教育大学中心进行的十年队列研究
目的:本研究确定肌萎缩性侧索硬化症(ALS)患者开始无创通气(NIV)前后的现实生活护理轨迹。护理人员对呼吸管理建议的依从性和ALS患者的相关生存率也进行了评估。方法:数据来自三级中心前瞻性ALS数据库,包括10年ALS患者的随访数据。结果通过K聚类(TAK)表示进行数值和图形时间序列分析。Kaplan Meier和Cox模型用于确定生存率和相关预后因素。结果:纳入109例ALS患者;随访中位[四分位间距]为25.0个月[15.3-43.3]。在研究期间,患者的中位临床就诊次数为4.0次[2.0-6.0];死亡发生率为54.1%。临床就诊间隔时间中位数为3.9[2.8-6.5]个月,动脉血气间隔时间为4.3个月[3.0-6.6],肺活量测定间隔时间为5.8个月[4.1-8.2],夜间血氧测定间隔时间为4.4个月[3.0-7.8]。照护轨迹可视化TAK显示在生存、开始使用NIV的时间和开始使用NIV到死亡的时间上有明显的异质性。死亡率与NIV启动和动脉二氧化碳压升高有关。结论:ALS指南的现行框架应适应ALS疾病分期和个体患者特征。了解肌萎缩性侧索硬化症患者的亚群如何随着时间的推移使用医疗保健服务,有助于突出脆弱领域和护理资源分配和最佳实践实施的优先事项。
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Estimating the minimum important difference in the ALSFRS-R-instrument in people living with MND. Quantitative susceptibility mapping in amyotrophic lateral sclerosis: automatic quantification of the magnetic susceptibility in the subcortical nuclei. Treatment continuity of amyotrophic lateral sclerosis with available riluzole formulations: state of the art and current challenges in a 'real-world' setting. Occupational lead exposure and amyotrophic lateral sclerosis survival in the Danish National Patient Registry. Jean Marie Baptiste Vianney de Jong (1937-2024).
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