T A Hardy, P Aouad, M H Barnett, S Blum, S Broadley, W M Carroll, D Crimmins, D Griffiths, S Hodgkinson, J Lechner-Scott, A Lee, R Malhotra, P McCombe, J Parratt, C Plummer, A Van der Walt, K Martel, R A Walker
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The primary endpoint was the average time for siponimod onboarding; secondary endpoints were adherence and sub-group analyses of variables influencing onboarding.</p><p><strong>Results: </strong>Mixed-cure modelling estimated that 58% of participants (<i>N</i> = 368, females 71%, median age of 59 years) registered in MSGo would ever initiate siponimod. The median time to initiation was 56 days (95% CI [47-59] days). Half of the participants cited 'waiting for vaccination' as the reason for initiation delay. Cox regression analyses found participants with a nominated care partner had faster onboarding (HR 2.1, 95% CI [1.5-3.0]) and were more likely to continue self-reporting daily siponimod dosing than were those without a care partner (HR 2.2, 95% CI [1.3-3.7]).</p><p><strong>Conclusions: </strong>Despite the limitations of self-reported data and the challenges of the COVID-19 pandemic, this study provides insights into siponimod onboarding in Australia and demonstrates the positive impact of care partner support.</p>","PeriodicalId":18961,"journal":{"name":"Multiple Sclerosis Journal - Experimental, Translational and Clinical","volume":"10 1","pages":"20552173231226106"},"PeriodicalIF":2.5000,"publicationDate":"2024-01-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10787529/pdf/","citationCount":"0","resultStr":"{\"title\":\"Onboarding of siponimod in secondary progressive multiple sclerosis patients in Australia: Novel, real-world evidence from the MSGo digital support programme.\",\"authors\":\"T A Hardy, P Aouad, M H Barnett, S Blum, S Broadley, W M Carroll, D Crimmins, D Griffiths, S Hodgkinson, J Lechner-Scott, A Lee, R Malhotra, P McCombe, J Parratt, C Plummer, A Van der Walt, K Martel, R A Walker\",\"doi\":\"10.1177/20552173231226106\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Siponimod is approved for use in people with secondary progressive multiple sclerosis (pwSPMS). An integrated digital platform, MSGo, was developed for pwSPMS and clinicians to help navigate the multiple steps of the pre-siponimod work-up.</p><p><strong>Objective: </strong>To explore real-world onboarding experiences of siponimod amongst pwSPMS in Australia.</p><p><strong>Methods: </strong>Retrospective, non-interventional, longitudinal, secondary analysis of data extracted from MSGo (20 April 2022). The primary endpoint was the average time for siponimod onboarding; secondary endpoints were adherence and sub-group analyses of variables influencing onboarding.</p><p><strong>Results: </strong>Mixed-cure modelling estimated that 58% of participants (<i>N</i> = 368, females 71%, median age of 59 years) registered in MSGo would ever initiate siponimod. The median time to initiation was 56 days (95% CI [47-59] days). Half of the participants cited 'waiting for vaccination' as the reason for initiation delay. Cox regression analyses found participants with a nominated care partner had faster onboarding (HR 2.1, 95% CI [1.5-3.0]) and were more likely to continue self-reporting daily siponimod dosing than were those without a care partner (HR 2.2, 95% CI [1.3-3.7]).</p><p><strong>Conclusions: </strong>Despite the limitations of self-reported data and the challenges of the COVID-19 pandemic, this study provides insights into siponimod onboarding in Australia and demonstrates the positive impact of care partner support.</p>\",\"PeriodicalId\":18961,\"journal\":{\"name\":\"Multiple Sclerosis Journal - Experimental, Translational and Clinical\",\"volume\":\"10 1\",\"pages\":\"20552173231226106\"},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-01-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10787529/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Multiple Sclerosis Journal - Experimental, Translational and Clinical\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1177/20552173231226106\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Multiple Sclerosis Journal - Experimental, Translational and Clinical","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1177/20552173231226106","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景介绍西泊尼莫德被批准用于继发性进展型多发性硬化症患者(pwSPMS)。我们为多发性硬化症患者和临床医生开发了一个综合数字平台 MSGo,以帮助他们了解西泊尼莫德治疗前的多个步骤:探索澳大利亚帕金森病患者使用西泊尼莫德的真实体验:对从 MSGo(2022 年 4 月 20 日)中提取的数据进行回顾性、非干预性、纵向、二次分析。主要终点是西泊尼莫德的平均上机时间;次要终点是依从性以及对影响上机的变量进行亚组分析:混合治愈模型估计,58%的MSGo注册参与者(N = 368,女性占71%,年龄中位数为59岁)会开始使用西泊尼莫德。开始治疗的中位时间为 56 天(95% CI [47-59] 天)。半数参与者认为 "等待疫苗接种 "是延迟开始治疗的原因。Cox回归分析发现,与没有护理伙伴的参与者相比,有指定护理伙伴的参与者入组速度更快(HR 2.1,95% CI [1.5-3.0]),更有可能继续自我报告每日服用西泊莫德(HR 2.2,95% CI [1.3-3.7]):尽管存在自我报告数据的局限性以及 COVID-19 大流行所带来的挑战,但这项研究提供了有关澳大利亚西泊尼莫德用药情况的见解,并证明了护理伙伴支持的积极影响。
Onboarding of siponimod in secondary progressive multiple sclerosis patients in Australia: Novel, real-world evidence from the MSGo digital support programme.
Background: Siponimod is approved for use in people with secondary progressive multiple sclerosis (pwSPMS). An integrated digital platform, MSGo, was developed for pwSPMS and clinicians to help navigate the multiple steps of the pre-siponimod work-up.
Objective: To explore real-world onboarding experiences of siponimod amongst pwSPMS in Australia.
Methods: Retrospective, non-interventional, longitudinal, secondary analysis of data extracted from MSGo (20 April 2022). The primary endpoint was the average time for siponimod onboarding; secondary endpoints were adherence and sub-group analyses of variables influencing onboarding.
Results: Mixed-cure modelling estimated that 58% of participants (N = 368, females 71%, median age of 59 years) registered in MSGo would ever initiate siponimod. The median time to initiation was 56 days (95% CI [47-59] days). Half of the participants cited 'waiting for vaccination' as the reason for initiation delay. Cox regression analyses found participants with a nominated care partner had faster onboarding (HR 2.1, 95% CI [1.5-3.0]) and were more likely to continue self-reporting daily siponimod dosing than were those without a care partner (HR 2.2, 95% CI [1.3-3.7]).
Conclusions: Despite the limitations of self-reported data and the challenges of the COVID-19 pandemic, this study provides insights into siponimod onboarding in Australia and demonstrates the positive impact of care partner support.