A Multi-Centre Longitudinal Study Analysing Multiple Sclerosis Disease-Modifying Therapy Prescribing Patterns During the Covid-19 Pandemic
| dc.contributor.author | Lal, Anoushka P. | |
| dc.contributor.author | Foong, Yi Chao | |
| dc.contributor.author | Sanfilippo, Paul G. | |
| dc.contributor.author | Spelman, Tim | |
| dc.contributor.author | Rath, Louise | |
| dc.contributor.author | Levitz, David | |
| dc.contributor.author | Fabis-Pedrini, Marzena | |
| dc.date.accessioned | 2024-07-21T18:43:39Z | |
| dc.date.available | 2024-07-21T18:43:39Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | BackgroundThe COVID-19 pandemic raised concern amongst clinicians that disease-modifying therapies (DMT), particularly anti-CD20 monoclonal antibodies (mAb) and fingolimod, could worsen COVID-19 in people with multiple sclerosis (pwMS). This study aimed to examine DMT prescribing trends pre- and post-pandemic onset.MethodsA multi-centre longitudinal study with 8,771 participants from MSBase was conducted. Two time periods were defined: pre-pandemic (March 11 2018-March 10 2020) and post-pandemic onset (March 11 2020-11 March 2022). The association between time and prescribing trends was analysed using multivariable mixed-effects logistic regression. DMT initiation refers to first initiation of any DMT, whilst DMT switches indicate changing regimen within 6 months of last use.ResultsPost-pandemic onset, there was a significant increase in DMT initiation/switching to natalizumab and cladribine [(Natalizumab-initiation: OR 1.72, 95% CI 1.39-2.13; switching: OR 1.66, 95% CI 1.40-1.98), (Cladribine-initiation: OR 1.43, 95% CI 1.09-1.87; switching: OR 1.67, 95% CI 1.41-1.98)]. Anti-CD20mAb initiation/switching decreased in the year of the pandemic, but recovered in the second year, such that overall odds increased slightly post-pandemic (initiation: OR 1.26, 95% CI 1.06-1.49; Switching: OR 1.15, 95% CI 1.02-1.29. Initiation/switching of fingolimod, interferon-beta, and alemtuzumab significantly decreased [(Fingolimod-initiation: OR 0.55, 95% CI 0.41-0.73; switching: OR 0.49, 95% CI 0.41-0.58), (Interferon-gamma-initiation: OR 0.48, 95% CI 0.41-0.57; switching: OR 0.78, 95% CI 0.62-0.99), (Alemtuzumab-initiation: OR 0.27, 95% CI 0.15-0.48; switching: OR 0.27, 95% CI 0.17-0.44)].ConclusionsPost-pandemic onset, clinicians preferentially prescribed natalizumab and cladribine over anti-CD20 mAbs and fingolimod, likely to preserve efficacy but reduce perceived immunosuppressive risks. This could have implications for disease progression in pwMS. Our findings highlight the significance of equitable DMT access globally, and the importance of evidence-based decision-making in global health challenges. | en_US |
| dc.description.sponsorship | CAUL | en_US |
| dc.description.sponsorship | Open Access funding enabled and organized by CAUL and its Member Institutions. | en_US |
| dc.identifier.doi | 10.1007/s00415-024-12518-7 | |
| dc.identifier.issn | 0340-5354 | |
| dc.identifier.issn | 1432-1459 | |
| dc.identifier.scopus | 2-s2.0-85197450686 | |
| dc.identifier.uri | https://doi.org/10.1007/s00415-024-12518-7 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14365/5408 | |
| dc.language.iso | en | en_US |
| dc.publisher | Springer heidelberg | en_US |
| dc.relation.ispartof | Journal of Neurology | en_US |
| dc.rights | info:eu-repo/semantics/openAccess | en_US |
| dc.subject | Multiple sclerosis | en_US |
| dc.subject | COVID-19 | en_US |
| dc.subject | Disease-modifying therapy | en_US |
| dc.subject | Anti-CD20 monoclonal antibodies | en_US |
| dc.subject | Cladribine | en_US |
| dc.subject | Natalizumab | en_US |
| dc.title | A Multi-Centre Longitudinal Study Analysing Multiple Sclerosis Disease-Modifying Therapy Prescribing Patterns During the Covid-19 Pandemic | en_US |
| dc.type | Article | en_US |
| dspace.entity.type | Publication | |
| gdc.author.id | Roos, Izanne/0000-0003-0371-3666 | |
| gdc.author.id | Cardenas-Robledo, Simon/0000-0002-7612-3985 | |
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| gdc.description.department | İzmir Ekonomi Üniversitesi | en_US |
| gdc.description.departmenttemp | [Lal, Anoushka P.; Foong, Yi Chao; Sanfilippo, Paul G.; Spelman, Tim; Rath, Louise; Levitz, David; Butzkueven, Helmut; Van der Walt, Anneke] The Alfred, Cent Clin Sch, Dept Neurosci, Melbourne, Vic, Australia; [Lal, Anoushka P.; Foong, Yi Chao; Butzkueven, Helmut; Van der Walt, Anneke] The Alfred Hosp, Dept Neurol, 55 Commercial Rd, Melbourne, Vic 3004, Australia; [Fabis-Pedrini, Marzena; Kermode, Allan G.] Univ Western Australia, Perron Inst Neurol & Translat Sci, Perth, WA, Australia; [Fabis-Pedrini, Marzena; Kermode, Allan G.] Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia; [Foschi, Matteo; Surcinelli, Andrea] S Maria Croci Hosp, Dept Neurosci, Neurol Unit, AUSL Romagna,MS Ctr, Ravenna, Italy; [Foschi, Matteo] Univ Aquila, Dept Biotechnol & Appl Clin Sci DISCAB, Laquila, Italy; [Habek, Mario] Univ Hosp Ctr Zagreb, Dept Neurol, Zagreb, Croatia; [Habek, Mario] Univ Zagreb, Sch Med, Zagreb, Croatia; [Kalincik, Tomas; Roos, Izanne] Royal Melbourne Hosp, Neuroimmunol Ctr, Dept Neurol, Melbourne, Vic, Australia; [Kalincik, Tomas] Univ Melbourne, Dept Med, CORE, Melbourne, Australia; [Lechner-Scott, Jeannette] Univ Newcastle, Hunter Med Res Inst, Newcastle, NSW, Australia; [John, Nevin] Monash Univ, Sch Clin Sci, | en_US |
| gdc.description.departmenttemp | [Lal, Anoushka P.; Foong, Yi Chao; Sanfilippo, Paul G.; Spelman, Tim; Rath, Louise; Levitz, David; Butzkueven, Helmut; Van der Walt, Anneke] The Alfred, Cent Clin Sch, Dept Neurosci, Melbourne, Vic, Australia; [Lal, Anoushka P.; Foong, Yi Chao; Butzkueven, Helmut; Van der Walt, Anneke] The Alfred Hosp, Dept Neurol, 55 Commercial Rd, Melbourne, Vic 3004, Australia; [Fabis-Pedrini, Marzena; Kermode, Allan G.] Univ Western Australia, Perron Inst Neurol & Translat Sci, Perth, WA, Australia; [Fabis-Pedrini, Marzena; Kermode, Allan G.] Murdoch Univ, Ctr Mol Med & Innovat Therapeut, Perth, WA, Australia; [Foschi, Matteo; Surcinelli, Andrea] S Maria Croci Hosp, Dept Neurosci, Neurol Unit, AUSL Romagna,MS Ctr, Ravenna, Italy; [Foschi, Matteo] Univ Aquila, Dept Biotechnol & Appl Clin Sci DISCAB, Laquila, Italy; [Habek, Mario] Univ Hosp Ctr Zagreb, Dept Neurol, Zagreb, Croatia; [Habek, Mario] Univ Zagreb, Sch Med, Zagreb, Croatia; [Kalincik, Tomas; Roos, Izanne] Royal Melbourne Hosp, Neuroimmunol Ctr, Dept Neurol, Melbourne, Vic, Australia; [Kalincik, Tomas] Univ Melbourne, Dept Med, CORE, Melbourne, Australia; [Lechner-Scott, Jeannette] Univ Newcastle, Hunter Med Res Inst, Newcastle, NSW, Australia; [John, Nevin] Monash Univ, Sch Clin Sci, | en_US |
| gdc.description.endpage | 5824 | |
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| gdc.description.volume | 271 | |
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| gdc.identifier.pmid | 38935148 | |
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| gdc.oaire.keywords | Male | |
| gdc.oaire.keywords | Adult | |
| gdc.oaire.keywords | Multiple Sclerosis | |
| gdc.oaire.keywords | Immunologic Factors / therapeutic use | |
| gdc.oaire.keywords | 610 | |
| gdc.oaire.keywords | cladribine | |
| gdc.oaire.keywords | multiple sclerosis | |
| gdc.oaire.keywords | COVID-19 / epidemiology | |
| gdc.oaire.keywords | Multiple sclerosis | |
| gdc.oaire.keywords | natalizumab | |
| gdc.oaire.keywords | Fingolimod Hydrochloride / therapeutic use | |
| gdc.oaire.keywords | Medicine and Health Sciences | |
| gdc.oaire.keywords | Practice Patterns, Physicians' / statistics & numerical data | |
| gdc.oaire.keywords | Disease-modifying therapy | |
| gdc.oaire.keywords | Humans | |
| gdc.oaire.keywords | Immunologic Factors | |
| gdc.oaire.keywords | Longitudinal Studies | |
| gdc.oaire.keywords | Practice Patterns, Physicians' | |
| gdc.oaire.keywords | Alemtuzumab | |
| gdc.oaire.keywords | Original Communication | |
| gdc.oaire.keywords | Fingolimod Hydrochloride | |
| gdc.oaire.keywords | Anti-CD20 monoclonal antibodies | |
| gdc.oaire.keywords | Natalizumab | |
| gdc.oaire.keywords | COVID-19 | |
| gdc.oaire.keywords | Multiple Sclerosis / epidemiology | |
| gdc.oaire.keywords | Middle Aged | |
| gdc.oaire.keywords | anti-CD20 monoclonal antibodies | |
| gdc.oaire.keywords | Alemtuzumab / therapeutic use | |
| gdc.oaire.keywords | disease-modifying therapy | |
| gdc.oaire.keywords | Natalizumab / therapeutic use | |
| gdc.oaire.keywords | Anti-CD20 monoclonal antibodies; COVID-19; Cladribine; Disease-modifying therapy; Multiple sclerosis; Natalizumab | |
| gdc.oaire.keywords | Cladribine / therapeutic use | |
| gdc.oaire.keywords | Multiple Sclerosis / drug therapy | |
| gdc.oaire.keywords | Cladribine | |
| gdc.oaire.keywords | Female | |
| gdc.oaire.keywords | Immunosuppressive Agents / therapeutic use | |
| gdc.oaire.keywords | Immunosuppressive Agents | |
| gdc.oaire.keywords | Clinical Medical Sciences | |
| gdc.oaire.keywords | Biomedicine and Health Sciences | |
| gdc.oaire.keywords | neurologija | |
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