Home treatment with elaprase® and Naglazyme® is safe in patients with mucopolysaccharidoses types II and VI, respectively

S. Bagewadi, J. Roberts, J. Mercer, S. Jones, J. Stephenson, J. E. Wraith

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Enzyme replacement therapy for lysosomal storage disorders has made an important contribution to improving the quality of life of affected patients. The treatment, however, is invasive and onerous, involving weekly or biweekly intravenous infusions of product over a 3-4 h period. Such therapy can be extremely disruptive of normal family life and the provision of a safe, home treatment regimen is greatly appreciated by affected families. In this report we demonstrate the safety of home treatment with Elaprase for mucopolysaccharidosis type II (17 patients) and Naglazyme for mucopolysaccharidosis type VI (6 patients). Careful patient selection, an experienced home care company and a detailed management plan for potential anaphylaxis and infusion-associated reactions are important components in a successful home treatment programme. © Springer Science+Business Media B.V. 2008.
    Original languageEnglish
    Pages (from-to)733-737
    Number of pages4
    JournalJournal of Inherited Metabolic Disease
    Volume31
    Issue number6
    DOIs
    Publication statusPublished - 2008

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