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Rebound activity after fingolimod cessation: A case - control study.
Barboza, Andres; Gaitán, María Inés; Alonso, Ricardo; Ysrraelit, María Célica; Luetic, Geraldine; Liwacki, Susana; Patrucco, Liliana; Halfon, Mario Javier; Burgos, Marcos; Mainella, Carolina; Pierdabuena, Raul; Recchia, Luciano; Steinberg, Judith; Tkachuk, Veronica Analia; Zanga, Gisela; Carra, Adriana; Chertcoff, Aníbal; Fernandez Liguori, Nora; Lazaro, Luciana; Menichini, Maria Laura; Miguez, Jimena; Orzuza, Gabriela; Palavecino, Alfredo; Pappolla, Agustin; Pigretti, Santiago; Pita, Cacilia; Ruiz, Emiliano; Silva, Berenice; Zentil, Guillermo.
Afiliação
  • Barboza A; Department of Neurology, Hospital Central de Mendoza, Mendoza, Argentina. Electronic address: barboza.agbarboza@gmail.com.
  • Gaitán MI; Department of Neurology, FLENI, Buenos Aires, Argentina.
  • Alonso R; Centro Universitario de Esclerosis Multiple, Hospital Ramos Mejia, Buenos Aires, Argentina; Department of Neurology, Sanatorio Güemes, Buenos Aires, Argentina.
  • Ysrraelit MC; Department of Neurology, FLENI, Buenos Aires, Argentina.
  • Luetic G; Instituto de Neurociencias de Rosario, Santa Fe, Argentina.
  • Liwacki S; Department of Neurology, Hospital Cordoba, Cordoba, Argentina; Department of Neurology, Clinica Reina Fabiola. Cordoba, Argentina.
  • Patrucco L; Department of Neurology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
  • Halfon MJ; Department of Neurology, Hospital Britanico de Buenos Aires, Buenos Aires, Argentina.
  • Burgos M; Department of Neurology, Hospital San Bernardo, Salta, Argentina.
  • Mainella C; Department of Neurology, Hospital Español de Rosario, Santa Fe, Argentina.
  • Pierdabuena R; Department of Neurology, Clinica Reina Fabiola. Cordoba, Argentina.
  • Recchia L; Department of Neurology, Hospital Central de Mendoza, Mendoza, Argentina.
  • Steinberg J; Department of Neurology, Hospital Britanico de Buenos Aires, Buenos Aires, Argentina.
  • Tkachuk VA; Department of Neurology, Hospital de Clinicas Jose de San Martin, Buenos Aires, Argentina.
  • Zanga G; Department of Neurology, ENERI, Buenos Aires, Argentina.
  • Carra A; Department of Neurology, Hospital Britanico de Buenos Aires, Buenos Aires, Argentina.
  • Chertcoff A; Department of Neurology, Hospital Britanico de Buenos Aires, Buenos Aires, Argentina.
  • Fernandez Liguori N; Department of Neurology, Sanatorio Güemes, Buenos Aires, Argentina.
  • Lazaro L; Department of Neurology, Sanatorio Güemes, Buenos Aires, Argentina.
  • Menichini ML; Instituto de Neurociencias de Rosario, Santa Fe, Argentina.
  • Miguez J; Department of Neurology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
  • Orzuza G; Department of Neurology, Hospital San Bernardo, Salta, Argentina.
  • Palavecino A; Department of Neurology, Hospital San Bernardo, Salta, Argentina.
  • Pappolla A; Department of Neurology, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
  • Pigretti S; Department of Neurology, Hospital Central de Mendoza, Mendoza, Argentina.
  • Pita C; Centro Universitario de Esclerosis Multiple, Hospital Ramos Mejia, Buenos Aires, Argentina.
  • Ruiz E; Department of Neurology, Clinica Reina Fabiola. Cordoba, Argentina.
  • Silva B; Centro Universitario de Esclerosis Multiple, Hospital Ramos Mejia, Buenos Aires, Argentina.
  • Zentil G; Department of Neurology, Hospital Central de Mendoza, Mendoza, Argentina.
Mult Scler Relat Disord ; 57: 103329, 2022 Jan.
Article em En | MEDLINE | ID: mdl-35158443
BACKGROUND: There has been an increase in the number of reports of multiple sclerosis (MS) rebound activity (RA), which is usually defined as a severe disease reactivation after natalizumab or fingolimod withdrawal that exceeds pre-treatment baseline inflammatory activity. The frequency and risk factors that could predict RA remain unknown. Fingolimod is currently the most frequently prescribed disease modifying therapy for MS in Argentina, so that there is a need to determine possible predictors of RA. OBJECTIVES: To identify risk factors for developing RA after fingolimod cessation; to describe RA characteristics, management and evolution. METHODS: The study was a multicenter, retrospective, case-control study of patients with MS who had discontinued fingolimod and were followed up to nine months after discontinuation. Demographic, clinical and paraclinical data was extracted, including age, gender, MS phenotype, reason for discontinuation, number of relapses during the year prior to suspension, time treated with fingolimod, EDSS before, during and after rebound, MRI findings. RESULTS: 26 cases of RA were matched 1:1 with patients without RA. The median time elapsed to RA was 50 days. 68% showed worsening of the EDSS in the evaluation at 3 months of RA. When compared with the control group, no difference was found in terms of age, gender, phenotype, EDSS at the moment of suspension, reason for discontinuation, number of relapses in the previous year, and time on therapy. CONCLUSION: In this case-controlled study, no risk factors could be identified to predict RA after fingolimod cessation. Further controlled, prospective, better powered studies are needed to confirm these findings.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Recidivante-Remitente / Esclerose Múltipla Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Esclerose Múltipla Recidivante-Remitente / Esclerose Múltipla Tipo de estudo: Observational_studies / Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article