4.1 Article

Subcutaneous Interferon Beta-1a in Pediatric Multiple Sclerosis: A Retrospective Study

Journal

JOURNAL OF CHILD NEUROLOGY
Volume 28, Issue 7, Pages 849-856

Publisher

SAGE PUBLICATIONS INC
DOI: 10.1177/0883073813488828

Keywords

interferon-; multiple sclerosis; safety

Funding

  1. Merck Serono S.A., Switzerland

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To expand current knowledge, we examined the safety and tolerability of subcutaneous interferon -1a in patients with pediatric-onset multiple sclerosis. Records from 307 patients who had received at least 1 injection of subcutaneous interferon -1a for demyelinating events when aged younger than 18 years were reviewed. Overall, 168 (54.7%) patients had at least 1 prespecified medical event related to or under close monitoring with subcutaneous interferon -1a or specific to pediatric patients, 184 (59.9%) had nonserious medical events related to treatment or of unknown causality, and 12 (3.9%) had serious medical events irrespective of causality. The most common laboratory abnormalities were increased alanine (74/195; 37.9%) and aspartate aminotransferase levels (59/194; 30.4%). Annualized relapse rates were 1.79 before treatment and 0.47 during treatment. In conclusion, adult doses of subcutaneous interferon -1a (44 and 22 g, 3 times weekly) were well tolerated in pediatric patients and were associated with reduced relapse rates.

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