Literature DB >> 9737142

The impact of Gaucher disease and its treatment on quality of life.

R P Hayes1, K A Grinzaid, E B Duffey, L J Elsas.   

Abstract

To obtain information about how Gaucher disease and its treatment, specifically enzyme replacement therapy, affect patients' health-related quality of life (HRQoL), we interviewed 16 patients with type I Gaucher disease (range 8-67 years). All but three patients had been receiving enzyme replacement therapy for at least 6 months. The quality of life factors examined for these patients included physical health, social life, emotional health, financial burden, future plans and satisfaction with health care. The results indicated that bone pain and chronic fatigue interfered with school, job and social activities and were the most debilitating symptoms of Gaucher disease. Most patients experienced a significant increase in energy level from therapy and reported significant improvements in quality of life. Most patients did not perceive an effect of Gaucher disease on their overall emotional health, but some patients expressed anxieties about the discomfort, inconvenience and high costs of therapy. We conclude that a measure of HRQoL for Gaucher patients should include a generic core of items supplemented by disease-specific items designed to assess the changes in symptoms and in the occupational, recreational, social and emotional aspects of patients' lives that occur as a result of disease progression and/or management.

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Year:  1998        PMID: 9737142     DOI: 10.1023/a:1008878425167

Source DB:  PubMed          Journal:  Qual Life Res        ISSN: 0962-9343            Impact factor:   4.147


  19 in total

Review 1.  Generic and disease-specific measures in assessing health status and quality of life.

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Journal:  Med Care       Date:  1989-03       Impact factor: 2.983

2.  Dose-dependent responses to macrophage-targeted glucocerebrosidase in a child with Gaucher disease.

Authors:  N W Barton; R O Brady; J M Dambrosia; S H Doppelt; S C Hill; C A Holder; H J Mankin; G J Murray; G C Zirzow; R I Parker
Journal:  J Pediatr       Date:  1992-02       Impact factor: 4.406

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Journal:  Med Care       Date:  1992-06       Impact factor: 2.983

Review 4.  Interpretation of quality of life changes.

Authors:  E Lydick; R S Epstein
Journal:  Qual Life Res       Date:  1993-06       Impact factor: 4.147

5.  Gaucher's disease: a pilot study of the symptomatic responses to enzyme replacement therapy.

Authors:  C L Verderese; O C Graham; C A Holder-McShane; N E Harnett; N W Barton
Journal:  J Neurosci Nurs       Date:  1993-10       Impact factor: 1.230

6.  Replacement therapy for inherited enzyme deficiency--macrophage-targeted glucocerebrosidase for Gaucher's disease.

Authors:  N W Barton; R O Brady; J M Dambrosia; A M Di Bisceglie; S H Doppelt; S C Hill; H J Mankin; G J Murray; R I Parker; C E Argoff
Journal:  N Engl J Med       Date:  1991-05-23       Impact factor: 91.245

7.  A health-related quality of life measure for multiple sclerosis.

Authors:  B G Vickrey; R D Hays; R Harooni; L W Myers; G W Ellison
Journal:  Qual Life Res       Date:  1995-06       Impact factor: 4.147

8.  Gaucher disease: gene frequencies in the Ashkenazi Jewish population.

Authors:  E Beutler; N J Nguyen; M W Henneberger; J M Smolec; R A McPherson; C West; T Gelbart
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

Review 9.  Measuring health-related quality of life.

Authors:  G H Guyatt; D H Feeny; D L Patrick
Journal:  Ann Intern Med       Date:  1993-04-15       Impact factor: 25.391

10.  Phenotype/genotype correlations in Gaucher disease type I: clinical and therapeutic implications.

Authors:  A Sibille; C M Eng; S J Kim; G Pastores; G A Grabowski
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

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  11 in total

1.  Psychological complications of patients with Gaucher disease.

Authors:  W Packman; T Wilson Crosbie; A Riesner; C Fairley; S Packman
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

Review 2.  Paediatric non-neuronopathic Gaucher disease: recommendations for treatment and monitoring.

Authors:  Antonio Baldellou; Generoso Andria; Pauline E Campbell; Joel Charrow; Ian J Cohen; Gregory A Grabowski; Chris M Harris; Paige Kaplan; Kieran McHugh; Eugen Mengel; Ashok Vellodi
Journal:  Eur J Pediatr       Date:  2003-12-16       Impact factor: 3.183

3.  Quality of life of patients with Fabry disease.

Authors:  K F Gold; G M Pastores; M F Botteman; J M Yeh; S Sweeney; W Aliski; C L Pashos
Journal:  Qual Life Res       Date:  2002-06       Impact factor: 4.147

4.  Development and validation of Gaucher disease type 1 (GD1)-specific patient-reported outcome measures (PROMs) for clinical monitoring and for clinical trials.

Authors:  Deborah Elstein; Nadia Belmatoug; Patrick Deegan; Özlem Göker-Alpan; Derralynn A Hughes; Ida Vanessa D Schwartz; Neal Weinreb; Nicola Bonner; Charlotte Panter; Donna Fountain; Andrew Lenny; Louise Longworth; Rachael Miller; Koonal Shah; Jörn Schenk; Rohini Sen; Ari Zimran
Journal:  Orphanet J Rare Dis       Date:  2022-01-06       Impact factor: 4.123

Review 5.  Imiglucerase in the treatment of Gaucher disease: a history and perspective.

Authors:  Patrick B Deegan; Timothy M Cox
Journal:  Drug Des Devel Ther       Date:  2012-04-18       Impact factor: 4.162

6.  Modelling Gaucher disease progression: long-term enzyme replacement therapy reduces the incidence of splenectomy and bone complications.

Authors:  Laura van Dussen; Marieke Biegstraaten; Marcel Gw Dijkgraaf; Carla Em Hollak
Journal:  Orphanet J Rare Dis       Date:  2014-07-24       Impact factor: 4.123

Review 7.  Rethinking fatigue in Gaucher disease.

Authors:  Y Chen Zion; E Pappadopulos; M Wajnrajch; H Rosenbaum
Journal:  Orphanet J Rare Dis       Date:  2016-04-29       Impact factor: 4.123

8.  Muscle-tendon weakness contributes to chronic fatigue syndrome in Gaucher's disease.

Authors:  Mercedes Roca-Espiau; Marcio Andrade-Campos; Jorge J Cebolla; Laura López de Frutos; Blanca Medrano-Engay; Maria-Pilar López-Royo; Pilar Giraldo
Journal:  J Orthop Surg Res       Date:  2019-11-21       Impact factor: 2.359

9.  Identification of risk features for complication in Gaucher's disease patients: a machine learning analysis of the Spanish registry of Gaucher disease.

Authors:  Marcio M Andrade-Campos; Laura López de Frutos; Jorge J Cebolla; Irene Serrano-Gonzalo; Blanca Medrano-Engay; Mercedes Roca-Espiau; Beatriz Gomez-Barrera; Jorge Pérez-Heredia; David Iniguez; Pilar Giraldo
Journal:  Orphanet J Rare Dis       Date:  2020-09-22       Impact factor: 4.123

10.  Health-related quality of life in children and adolescents living with Gaucher disease and their parents.

Authors:  Eduardo Remor; Antonio Baldellou
Journal:  Health Psychol Behav Med       Date:  2018-04-12
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