Literature DB >> 15892434

Quality of life related to type 1 Gaucher disease: Spanish experience.

Pilar Giraldo1, Victor Solano, Juan-Ignacio Pérez-Calvo, Manuel Giralt, Daniel Rubio-Félix.   

Abstract

UNLABELLED: The impact of type 1 Gaucher disease and its therapy on health-related quality of life (QOL) was investigated and the results were compared with a Spanish adult normative group. PATIENTS AND METHODS: Between January 1998 and December 2002, a prospective clinical QOL trial was conducted by application of a Spanish version of the Health Survey SF-36 questionnaire. Patients receiving ERT (69 cases) filled in the questionnaire two times, prior to starting ERT and after two years under ERT. The patients were stratified by gender and age group. Clinical and X-ray data to assess bone disease were obtained from the Spanish Gaucher Register. Demographic, clinical, genotype and analytical data and the response to therapy were evaluated. Four grades of severity were established according to bone disease (no symptoms = 0, moderate bone pain = 1, severe bone crisis = 2, fracture/necrosis = 3). Correlation analysis was made between QOL score and grade of bone disease.
RESULTS: Mean age+/-SD 33.6+/-11.7 (range 18-66), M/F,ratio 33/36; bone disease: 0 in 27 patients (47.3%), 1 in 11 (19.3%), 2 in 5 (8.8%) and 3 in 14 (24.5%). Physical activity: 11 patients (19.3%) showed severe restriction and 41 patients (71.9%) were only limited for strenuous activities. The mean score for QOL questionnaire was 11.9+/-10.4 (range 2-46). Correlation between score and bone disease was significant only for 1 and 3 grades (p = 0.02). Improvement in self perception of global health was observed ranging from 34.3% before ERT to 91.4% after ERT (p = 0.001). Nevertheless physical activity remained unsatisfactory in 24.5% of patients due mainly to bone sequelae. COMMENTS: Physical activities and bone disease grade 1 and 3 are negatively related to QOL. Nevertheless no correlation was found with bone pain crisis, possibly due to the transitory character of this event. In spite of the improvement induced by ERT, a quarter of patients remained with physical limitations related to bone disease as well as in need of orthopaedic correction of bone sequelae. In order to improve the QOL an accurate evaluation of bone disease to define therapeutic approaches must be considered.

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Year:  2005        PMID: 15892434     DOI: 10.1007/s11136-004-0794-y

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


  7 in total

1.  Quality of life assessment in adults with type 1 Gaucher disease.

Authors:  B J Masek; K B Sims; C M Bove; M S Korson; P Short; D K Norman
Journal:  Qual Life Res       Date:  1999-05       Impact factor: 4.147

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

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

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

4.  The effect of assessment method and respondent population on utilities elicited for Gaucher disease.

Authors:  A E Clarke; M K Goldstein; D Michelson; A M Garber; L A Lenert
Journal:  Qual Life Res       Date:  1997-03       Impact factor: 4.147

5.  [The Spanish version of the SF-36 Health Survey (the SF-36 health questionnaire): an instrument for measuring clinical results].

Authors:  J Alonso; L Prieto; J M Antó
Journal:  Med Clin (Barc)       Date:  1995-05-27       Impact factor: 1.725

6.  [Quality of life in patients with eating disorders].

Authors:  N González; A Padierna; J M Quintana; I Aróstegui; M J Horcajo
Journal:  Gac Sanit       Date:  2001 Jan-Feb       Impact factor: 2.139

Review 7.  Gaucher disease. Current issues in diagnosis and treatment. NIH Technology Assessment Panel on Gaucher Disease.

Authors: 
Journal:  JAMA       Date:  1996-02-21       Impact factor: 56.272

  7 in total
  18 in total

1.  Quality of life of brazilian patients with Gaucher disease and fabry disease.

Authors:  Fabiane Lopes Oliveira; Taciane Alegra; Alicia Dornelles; Bárbara Corrêa Krug; Cristina B O Netto; Neusa Sica da Rocha; Paulo D Picon; Ida Vanessa D Schwartz
Journal:  JIMD Rep       Date:  2012-04-18

2.  Successful screening for Gaucher disease in a high-prevalence population in tabuleiro do Norte (northeastern Brazil): a cross-sectional study.

Authors:  Rigoberto Gadelha Chaves; Janice Carneiro Coelho; Kristiane Michelin-Tirelli; Tibelle Freitas Maurício; Edineide de Freitas Maia Chaves; Paulo César de Almeida; Carlos Rômulo Filgueira Maurício; Geraldo Barroso Cavalcanti
Journal:  JIMD Rep       Date:  2011-06-22

Review 3.  An overview on bone manifestations in Gaucher disease.

Authors:  Peter Mikosch; Derralynn Hughes
Journal:  Wien Med Wochenschr       Date:  2010-12

4.  Life expectancy in Gaucher disease type 1.

Authors:  Neal J Weinreb; Patrick Deegan; Katherine A Kacena; Pramod Mistry; Gregory M Pastores; Priscilla Velentgas; Stephan vom Dahl
Journal:  Am J Hematol       Date:  2008-12       Impact factor: 10.047

Review 5.  Gaucher disease - more than just a rare lipid storage disease.

Authors:  Jaehyeok Roh; Subbaya Subramanian; Neal J Weinreb; Reena V Kartha
Journal:  J Mol Med (Berl)       Date:  2022-01-23       Impact factor: 4.599

Review 6.  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

7.  Poor results of drilling in early stages of juxta-articular osteonecrosis in 12 joints affected by Gaucher disease.

Authors:  Ehud Lebel; Mici Phillips; Deborah Elstein; Ari Zimran; Menachem Itzchaki
Journal:  Acta Orthop       Date:  2009-04       Impact factor: 3.717

8.  Recommendations for the management of the haematological and onco-haematological aspects of Gaucher disease.

Authors:  Derralynn Hughes; Maria Domenica Cappellini; Marc Berger; Jan Van Droogenbroeck; Maaike de Fost; Dragana Janic; Theodore Marinakis; Hanna Rosenbaum; Jesús Villarubia; Elena Zhukovskaya; Carla Hollak
Journal:  Br J Haematol       Date:  2007-07-26       Impact factor: 6.998

9.  Improvement of bone disease by imiglucerase (Cerezyme) therapy in patients with skeletal manifestations of type 1 Gaucher disease: results of a 48-month longitudinal cohort study.

Authors:  K B Sims; G M Pastores; N J Weinreb; J Barranger; B E Rosenbloom; S Packman; P Kaplan; H Mankin; R Xavier; J Angell; M A Fitzpatrick; D Rosenthal
Journal:  Clin Genet       Date:  2008-02-27       Impact factor: 4.438

10.  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

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