Journal
MOLECULAR GENETICS AND METABOLISM
Volume 97, Issue 3, Pages 234-236Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ymgme.2009.04.007
Keywords
Mucopolysaccharidoses; Enzyme replacement therapy; Home infusion; Hunter syndrome
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The transition to home infusion therapy is described in 11 patients with mucopolysaccharide (MPS) disorders initially treated with enzyme replacement therapy (ERT) in an out-patient infusion center. Home therapy was well tolerated with no infusion-related reactions (IRR) occurring in 671 patient-weeks of treatment. In addition, compliance with the weekly treatment regimen was improved in patients on home therapy. (C) 2009 Elsevier Inc. All rights reserved.
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