Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription

Introduction: None of the approved immunomodulatory drugs in adults Multiple Sclerosis (MS) patients have been officially approved for the pediatric patients and are currently used off-label in this population. Objectives: In this study, we evaluated the effectiveness and tolerability of intramuscul...

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Main Authors: Amir Hadi Maghzi, Zahra Fatehi, Vahid Shaygannejad, Fereshteh Ashtari, Fatemeh Derakhshan, Masood Etemadifar, Keivan Basiri, Farzad Fatehi
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2012-02-01
Series:Acta Medica Iranica
Subjects:
Online Access:http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/20205.pdf&manuscript_id=20205
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spelling doaj-5819526eedf24916b9c2aad0ccd756922020-11-25T04:00:33ZengTehran University of Medical SciencesActa Medica Iranica0044-60250173-59692012-02-0150297100Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term PrescriptionAmir Hadi MaghziZahra FatehiVahid ShaygannejadFereshteh AshtariFatemeh DerakhshanMasood EtemadifarKeivan BasiriFarzad FatehiIntroduction: None of the approved immunomodulatory drugs in adults Multiple Sclerosis (MS) patients have been officially approved for the pediatric patients and are currently used off-label in this population. Objectives: In this study, we evaluated the effectiveness and tolerability of intramuscular interferon beta1-a (Avonex®) and subcutaneously injected interferon beta1-b (Betaferon®) in children with definite relapsing-remitting MS (RRMS). Thirteen patients aged younger than 16, who were recently diagnosed with definite RRMS according to the McDonalds criteria, were enrolled in this study. Six patients were treated with Avonex® 30 μg, intramuscularly every week, and seven patients were treated with Betaferon® 250 μg, subcutaneously every other day. All patients were treated with adult doses; initially interferon-beta was prescribed with half dose, and it was increased to full adult dose steadily. Results: Eleven girls and two boys, mean (SD) age of 14.7 (1.9) years, were studied. Following nine months of using interferon-beta, nine patients (69.2%) had no relapses and the remaining four, experienced only one relapse. The mean EDSS score was decreased significantly after the study period. Conclusion: The present study provides reasonable data for the use of interferon-beta in Pediatric MS due to lack of short-term complications and safety. Studies with larger sample size and longer follow up duration are required to shed light on the long term impact of the interferon-beta therapy in children.http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/20205.pdf&manuscript_id=20205Multiple SclerosisPediatricsChildhoodInterferons
collection DOAJ
language English
format Article
sources DOAJ
author Amir Hadi Maghzi
Zahra Fatehi
Vahid Shaygannejad
Fereshteh Ashtari
Fatemeh Derakhshan
Masood Etemadifar
Keivan Basiri
Farzad Fatehi
spellingShingle Amir Hadi Maghzi
Zahra Fatehi
Vahid Shaygannejad
Fereshteh Ashtari
Fatemeh Derakhshan
Masood Etemadifar
Keivan Basiri
Farzad Fatehi
Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription
Acta Medica Iranica
Multiple Sclerosis
Pediatrics
Childhood
Interferons
author_facet Amir Hadi Maghzi
Zahra Fatehi
Vahid Shaygannejad
Fereshteh Ashtari
Fatemeh Derakhshan
Masood Etemadifar
Keivan Basiri
Farzad Fatehi
author_sort Amir Hadi Maghzi
title Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription
title_short Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription
title_full Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription
title_fullStr Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription
title_full_unstemmed Interferon-Beta in Pediatric Multiple Sclerosis Patients: Safety in Short-Term Prescription
title_sort interferon-beta in pediatric multiple sclerosis patients: safety in short-term prescription
publisher Tehran University of Medical Sciences
series Acta Medica Iranica
issn 0044-6025
0173-5969
publishDate 2012-02-01
description Introduction: None of the approved immunomodulatory drugs in adults Multiple Sclerosis (MS) patients have been officially approved for the pediatric patients and are currently used off-label in this population. Objectives: In this study, we evaluated the effectiveness and tolerability of intramuscular interferon beta1-a (Avonex®) and subcutaneously injected interferon beta1-b (Betaferon®) in children with definite relapsing-remitting MS (RRMS). Thirteen patients aged younger than 16, who were recently diagnosed with definite RRMS according to the McDonalds criteria, were enrolled in this study. Six patients were treated with Avonex® 30 μg, intramuscularly every week, and seven patients were treated with Betaferon® 250 μg, subcutaneously every other day. All patients were treated with adult doses; initially interferon-beta was prescribed with half dose, and it was increased to full adult dose steadily. Results: Eleven girls and two boys, mean (SD) age of 14.7 (1.9) years, were studied. Following nine months of using interferon-beta, nine patients (69.2%) had no relapses and the remaining four, experienced only one relapse. The mean EDSS score was decreased significantly after the study period. Conclusion: The present study provides reasonable data for the use of interferon-beta in Pediatric MS due to lack of short-term complications and safety. Studies with larger sample size and longer follow up duration are required to shed light on the long term impact of the interferon-beta therapy in children.
topic Multiple Sclerosis
Pediatrics
Childhood
Interferons
url http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/20205.pdf&manuscript_id=20205
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