Literature DB >> 8353277

Home treatment with intravenous enzyme replacement therapy for Gaucher disease: an international collaborative study of 33 patients.

A Zimran1, C E Hollak, A Abrahamov, M H van Oers, M Kelly, E Beutler.   

Abstract

Intravenous enzyme replacement therapy (Alglucerase; Ceredase; Genzyme Corp, Boston, MA) is an effective and safe treatment for patients with type 1 Gaucher disease. In an attempt to reduce its high cost, a "low-dose high-frequency" protocol (30 U/kg/mo, 3 times a week) was introduced and found to be as effective as the original high-dose protocol (60 U/kg every 2 weeks). Because receiving frequent infusions creates a burden for many patients, we have implemented a program of home treatment for our patients. We now report the safety and feasibility of low-dose/high-frequency home intravenous enzyme-replacement therapy in 33 patients with Gaucher disease. The chronic nature of the treatment, its safety, lack of adverse effects, the stable condition of most patients, and the need to reduce the high cost make enzyme replacement for Gaucher disease a good candidate for intravenous home therapy.

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Year:  1993        PMID: 8353277

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  10 in total

1.  Alglucerase for Gaucher's disease: dose, costs and benefits.

Authors:  E Beutler; A M Garber
Journal:  Pharmacoeconomics       Date:  1994-06       Impact factor: 4.981

Review 2.  Treatment of lysosomal storage disorders : progress with enzyme replacement therapy.

Authors:  Marianne Rohrbach; Joe T R Clarke
Journal:  Drugs       Date:  2007       Impact factor: 9.546

3.  The health-related quality of life of adults with Gaucher's disease receiving enzyme replacement therapy: results from a retrospective study.

Authors:  A M Damiano; G M Pastores; J E Ware
Journal:  Qual Life Res       Date:  1998-07       Impact factor: 4.147

Review 4.  Alglucerase (Ceredase).

Authors:  E H Wiltink; C E Hollak
Journal:  Pharm World Sci       Date:  1996-01

5.  A case with Gaucher disease unable to reach enzyme replacement therapy because of COVID-19 quarantine: The first case from Turkey.

Authors:  Merve Koç Yekedüz; Engin Köse; Fatma Tuba Eminoğlu
Journal:  Turk Arch Pediatr       Date:  2021-05-01

Review 6.  Alglucerase. A pharmacoeconomic appraisal of its use in the treatment of Gaucher's disease.

Authors:  R Whittington; K L Goa
Journal:  Pharmacoeconomics       Date:  1995-01       Impact factor: 4.981

7.  Considerations for Home-Based Treatment of Fabry Disease in Poland during the COVID-19 Pandemic and Beyond.

Authors:  Michał Nowicki; Stanisława Bazan-Socha; Mariusz Kłopotowski; Beata Błażejewska-Hyżorek; Mariusz Kusztal; Krzysztof Pawlaczyk; Jarosław Sławek; Andrzej Oko; Zofia Oko-Sarnowska
Journal:  Int J Environ Res Public Health       Date:  2021-08-04       Impact factor: 3.390

8.  Treatment adherence and patients' acceptance of home infusions with adenosine 5'-triphosphate (ATP) in palliative home care.

Authors:  Sandra Beijer; Nicole E G Wijckmans; Erik van Rossum; Cor Spreeuwenberg; Ron A G Winkens; Lisette Ars; Pieter C Dagnelie
Journal:  Support Care Cancer       Date:  2008-09-23       Impact factor: 3.603

Review 9.  Imiglucerase in the management of Gaucher disease type 1: an evidence-based review of its place in therapy.

Authors:  Christine Serratrice; Sebastian Carballo; Jacques Serratrice; Jérome Stirnemann
Journal:  Core Evid       Date:  2016-10-14

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

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

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