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A multi-centre longitudinal study analysing multiple sclerosis disease-modifying therapy prescribing patterns during the COVID-19 pandemic.
Lal, Anoushka P; Foong, Yi Chao; Sanfilippo, Paul G; Spelman, Tim; Rath, Louise; Levitz, David; Fabis-Pedrini, Marzena; Foschi, Matteo; Habek, Mario; Kalincik, Tomas; Roos, Izanne; Lechner-Scott, Jeannette; John, Nevin; Soysal, Aysun; D'Amico, Emanuele; Gouider, Riadh; Mrabet, Saloua; Gross-Paju, Katrin; Cárdenas-Robledo, Simón; Moghadasi, Abdorreza Naser; Sa, Maria Jose; Gray, Orla; Oh, Jiwon; Reddel, Stephen; Ramanathan, Sudarshini; Al-Harbi, Talal; Altintas, Ayse; Hardy, Todd A; Ozakbas, Serkan; Alroughani, Raed; Kermode, Allan G; Surcinelli, Andrea; Laureys, Guy; Eichau, Sara; Prat, Alexandre; Girard, Marc; Duquette, Pierre; Hodgkinson, Suzanne; Ramo-Tello, Cristina; Maimone, Davide; McCombe, Pamela; Spitaleri, Daniele; Sanchez-Menoyo, Jose Luis; Yetkin, Mehmet Fatih; Baghbanian, Seyed Mohammad; Karabudak, Rana; Al-Asmi, Abdullah; Jakob, Gregor Brecl; Khoury, Samia J; Etemadifar, Masoud.
Afiliação
  • Lal AP; Department of Neuroscience, Central Clinical School, The Alfred, Melbourne, VIC, Australia.
  • Foong YC; Department of Neurology, The Alfred Hospital, 55 Commercial Road, Melbourne, 3004, Australia.
  • Sanfilippo PG; Department of Neuroscience, Central Clinical School, The Alfred, Melbourne, VIC, Australia.
  • Spelman T; Department of Neurology, The Alfred Hospital, 55 Commercial Road, Melbourne, 3004, Australia.
  • Rath L; Royal Hobart Hospital, Hobart, Australia.
  • Levitz D; Department of Neuroscience, Central Clinical School, The Alfred, Melbourne, VIC, Australia.
  • Fabis-Pedrini M; Department of Neuroscience, Central Clinical School, The Alfred, Melbourne, VIC, Australia.
  • Foschi M; Department of Neuroscience, Central Clinical School, The Alfred, Melbourne, VIC, Australia.
  • Habek M; Department of Neuroscience, Central Clinical School, The Alfred, Melbourne, VIC, Australia.
  • Kalincik T; Perron Institute for Neurological and Translational Science, The University of Western Australia, Perth, Australia.
  • Roos I; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, Australia.
  • Lechner-Scott J; Department of Neuroscience, MS Center, Neurology Unit, S. Maria Delle Croci Hospital, AUSL Romagna, Ravenna, Italy.
  • John N; Department of Biotechnological and Applied Clinical Sciences (DISCAB), University of L'Aquila, L'Aquila, Italy.
  • Soysal A; Department of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.
  • D'Amico E; School of Medicine, University of Zagreb, Zagreb, Croatia.
  • Gouider R; Department of Neurology, Neuroimmunology Centre, Royal Melbourne Hospital, Melbourne, Australia.
  • Mrabet S; CORe, Department of Medicine, University of Melbourne, Melbourne, Australia.
  • Gross-Paju K; Department of Neurology, Neuroimmunology Centre, Royal Melbourne Hospital, Melbourne, Australia.
  • Cárdenas-Robledo S; Hunter Medical Research Institute, University Newcastle, Newcastle, Australia.
  • Moghadasi AN; Department of Medicine, School of Clinical Sciences, Monash University, Clayton, Australia.
  • Sa MJ; Department of Neurology, Monash Health, Clayton, Australia.
  • Gray O; Bakirkoy Education and Research Hospital for Psychiatric and Neurological Diseases, Istanbul, Turkey.
  • Oh J; Medical and Surgical Sciences, Universita Di Foggia, Foggia, Italy.
  • Reddel S; Department of Neurology, LR 18SP03, Clinical Investigation Centre Neurosciences and Mental Health, Razi University Hospital, Tunis, Tunisia.
  • Ramanathan S; Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis, Tunisia.
  • Al-Harbi T; Department of Neurology, LR 18SP03, Clinical Investigation Centre Neurosciences and Mental Health, Razi University Hospital, Tunis, Tunisia.
  • Altintas A; Faculty of Medicine of Tunis, University of Tunis El Manar, Tunis, Tunisia.
  • Hardy TA; Multiple Sclerosis Centre, West-Tallinn Central Hospital, Tallinn, Estonia.
  • Ozakbas S; Department of Neurology, Centro de Esclerosis Múltiple (CEMHUN), Hospital Universitario Nacional de Colombia Bogota, Bogota, Colombia.
  • Alroughani R; Departamento de Medicina InternaFacultad de Medicina, Universidad Nacional de Colombia, Bogota, Colombia.
  • Kermode AG; Multiple Research Centre, Neuroscience Institute, Tehran University of Medical Science, Tehran, Iran.
  • Surcinelli A; Department of Neurology, Centro Hospitalar Universitario de Sao Joao, Porto, Portugal.
  • Laureys G; South Eastern HSC Trust, Belfast, UK.
  • Eichau S; St. Michael's Hospital, Toronto, Canada.
  • Prat A; Department of Neurology, Concord Repatriation General Hospital, Sydney, Australia.
  • Girard M; Translational Neuroimmunology Group, Kids Neuroscience Centre and Brain and Mind Centre, Concord Hospital, Sydney, Australia.
  • Duquette P; Neurology Department, King Fahad Specialist Hospital-Dammam, Dammam, Saudi Arabia.
  • Hodgkinson S; Department of Neurology, School of Medicine and Koc University Research Center for Translational Medicine (KUTTAM), Istanbul, Turkey.
  • Ramo-Tello C; Department of Neurology, Concord Repatriation General Hospital, Sydney, Australia.
  • Maimone D; Izmir University of Economics, Medical Point Hospital, Izmir, Turkey.
  • McCombe P; Multiple Sclerosis Research Association, Izmir, Turkey.
  • Spitaleri D; Division of Neurology, Department of Medicine, Amiri Hospital, Sharq, Kuwait.
  • Sanchez-Menoyo JL; Perron Institute for Neurological and Translational Science, The University of Western Australia, Perth, Australia.
  • Yetkin MF; Centre for Molecular Medicine and Innovative Therapeutics, Murdoch University, Perth, Australia.
  • Baghbanian SM; Department of Neuroscience, MS Center, Neurology Unit, S. Maria Delle Croci Hospital, AUSL Romagna, Ravenna, Italy.
  • Karabudak R; Department of Neurology, University Hospital Ghent, Ghent, Belgium.
  • Al-Asmi A; Department of Neurology, Hospital Universitario Virgen Macarena, Seville, Spain.
  • Jakob GB; CHUM and Universite de Montreal, Montreal, Canada.
  • Khoury SJ; CHUM and Universite de Montreal, Montreal, Canada.
  • Etemadifar M; CHUM and Universite de Montreal, Montreal, Canada.
J Neurol ; 271(9): 5813-5824, 2024 Sep.
Article em En | MEDLINE | ID: mdl-38935148
ABSTRACT

BACKGROUND:

The 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.

METHODS:

A 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.

RESULTS:

Post-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)].

CONCLUSIONS:

Post-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.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cloridrato de Fingolimode / Natalizumab / COVID-19 / Imunossupressores / Esclerose Múltipla Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cloridrato de Fingolimode / Natalizumab / COVID-19 / Imunossupressores / Esclerose Múltipla Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2024 Tipo de documento: Article