Literature DB >> 16628169

Intravenous enzyme replacement therapy: better in home or hospital?

A Milligan1, D Hughes, S Goodwin, L Richfield, A Mehta.   

Abstract

This article evaluates satisfaction with enzyme replacement therapy (ERT) at home and at hospital in adult patients with Fabry and Gaucher diseases. A questionnaire was developed and sent to 34 patients with Fabry disease who were receiving ERT with agalsidase alfa (Replagal) and to 49 patients with type I Gaucher disease who were receiving ERT with glucocerebrosidase (Cerezyme). Of the 45 returned questionnaires, 20 were from patients with Fabry disease and 25 from patients with Gaucher disease. Hospital treatment visits were reported as stressful by 18 patients (40%), whereas only 4 (9%) patients reported that home therapy was stressful. Both groups of patients adjusted well to receiving home-based therapy. Nearly all of the patients with Fabry disease (19 patients, 95%) and Gaucher disease (21 patients, 84%) preferred home-based therapy. Treatment in the home was reported as more comfortable, less stressful, more effective and had less impact on family life. Only 4 (9%) patients chose to continue receiving infusions in hospital. The majority of patients with Fabry disease and Gaucher disease found home-based therapy to be more convenient and less stressful than hospital-based therapy.

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Year:  2006        PMID: 16628169     DOI: 10.12968/bjon.2006.15.6.20681

Source DB:  PubMed          Journal:  Br J Nurs        ISSN: 0966-0461


  17 in total

1.  Burden associated with Fabry disease and its treatment in 12-15 year olds: results from a European survey.

Authors:  Lisa Bashorum; Gerard McCaughey; Owen Evans; Ashley C Humphries; Richard Perry; Alasdair MacCulloch
Journal:  Orphanet J Rare Dis       Date:  2022-07-15       Impact factor: 4.303

2.  Home treatment with Elaprase and Naglazyme is safe in patients with mucopolysaccharidoses types II and VI, respectively.

Authors:  S Bagewadi; J Roberts; J Mercer; S Jones; J Stephenson; J E Wraith
Journal:  J Inherit Metab Dis       Date:  2008-10-19       Impact factor: 4.982

3.  Stepwise shortening of agalsidase beta infusion duration in Fabry disease: Clinical experience with infusion rate escalation protocol.

Authors:  Eleonora Riccio; Mario Zanfardino; Monica Franzese; Ivana Capuano; Pasquale Buonanno; Lucia Ferreri; Maria Amicone; Antonio Pisani
Journal:  Mol Genet Genomic Med       Date:  2021-03-23       Impact factor: 2.183

Review 4.  Update on role of agalsidase alfa in management of Fabry disease.

Authors:  Uma Ramaswami
Journal:  Drug Des Devel Ther       Date:  2011-03-14       Impact factor: 4.162

5.  The role of enzyme replacement therapy in severe Hunter syndrome-an expert panel consensus.

Authors:  Joseph Muenzer; Olaf Bodamer; Barbara Burton; Lorne Clarke; Gudrun Schulze Frenking; Roberto Giugliani; Simon Jones; Maria Verónica Muñoz Rojas; Maurizio Scarpa; Michael Beck; Paul Harmatz
Journal:  Eur J Pediatr       Date:  2011-10-29       Impact factor: 3.183

6.  Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease.

Authors:  Maurizio Scarpa; Zsuzsanna Almássy; Michael Beck; Olaf Bodamer; Iain A Bruce; Linda De Meirleir; Nathalie Guffon; Encarna Guillén-Navarro; Pauline Hensman; Simon Jones; Wolfgang Kamin; Christoph Kampmann; Christina Lampe; Christine A Lavery; Elisa Leão Teles; Bianca Link; Allan M Lund; Gunilla Malm; Susanne Pitz; Michael Rothera; Catherine Stewart; Anna Tylki-Szymańska; Ans van der Ploeg; Robert Walker; Jiri Zeman; James E Wraith
Journal:  Orphanet J Rare Dis       Date:  2011-11-07       Impact factor: 4.123

Review 7.  Quality of life in patients with Fabry disease: a systematic review of the literature.

Authors:  Maarten Arends; Carla E M Hollak; Marieke Biegstraaten
Journal:  Orphanet J Rare Dis       Date:  2015-06-16       Impact factor: 4.123

8.  Seven-year safety and efficacy with velaglucerase alfa for treatment-naïve adult patients with type 1 Gaucher disease.

Authors:  Ari Zimran; Nan Wang; Carol Ogg; Eric Crombez; Gabriel M Cohn; Deborah Elstein
Journal:  Am J Hematol       Date:  2015-05-28       Impact factor: 10.047

9.  Review of the safety and efficacy of imiglucerase treatment of Gaucher disease.

Authors:  Deborah Elstein; Ari Zimran
Journal:  Biologics       Date:  2009-09-15

Review 10.  Guidelines for diagnosis and treatment of Hunter Syndrome for clinicians in Latin America.

Authors:  Roberto Giugliani; Martha Luz Solano Villarreal; C Araceli Arellano Valdez; Antonieta Mahfoud Hawilou; Norberto Guelbert; Luz Norela Correa Garzón; Ana Maria Martins; Angelina Acosta; Juan Francisco Cabello; Aída Lemes; Mara Lucia Schmitz Ferreira Santos; Hernán Amartino
Journal:  Genet Mol Biol       Date:  2014-06       Impact factor: 1.771

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