Literature DB >> 14987245

Development and testing of an instrument to assess the Quality of Life of Children with Haemophilia in Europe (Haemo-QoL).

S von Mackensen1, M Bullinger.   

Abstract

In spite of an increased interest in the assessment of quality of life (QoL) in children, so far no instrument for children with haemophilia is available. Because of the low prevalence of the condition, such an instrument should also be cross-culturally applicable. In the study presented, a (QoL) assessment instrument for children with haemophilia (the Haemo-QoL questionnaire) was developed and tested in six countries (France, Germany, Italy, the Netherlands, Spain and the United Kingdom) for psychometric properties in 339 children with haemophilia and their parents. The Haemo-QoL is a self-reported questionnaire for children in the age ranges 4-7 (I: 21 items), 8-12 (II: 64 items), 13-16 years (III: 77 items) as well as for parent rating containing 9-11 subscales (depending on age-group versions). Psychometric testing involved the examination of reliability and validity. The three age-group versions of the Haemo-QoL had acceptable internal consistency and retest reliability values, as well as possessing sufficient discriminant and convergent validity. However, in young children when compared to older children, these indicators were less satisfactory. The Haemo-QoL full version is now available for children of three age groups and their parents and is ready for use in clinical research.

Entities:  

Mesh:

Year:  2004        PMID: 14987245     DOI: 10.1111/j.1355-0691.2004.00875.x

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  22 in total

Review 1.  Estimates of utility weights in hemophilia: implications for cost-utility analysis of clotting factor prophylaxis.

Authors:  Scott D Grosse; Shraddha S Chaugule; Joel W Hay
Journal:  Expert Rev Pharmacoecon Outcomes Res       Date:  2015-01-14       Impact factor: 2.217

2.  Pilot randomized, non-inferiority, cross-over trial of once-weekly vs. three times-weekly recombinant factor VIII prophylaxis in adults with severe haemophilia A.

Authors:  M V Ragni; J G Yabes; P F Fogarty; N C Josephson; C M Kessler; A T Neff; L Raffini; K Brummel-Ziedins; C G Moore
Journal:  Haemophilia       Date:  2016-12-11       Impact factor: 4.287

3.  Patient preference for needleless factor VIII reconstitution device: the Italian experience.

Authors:  Roberto Musso; Rita Santoro; Antonio Coppola; Maura Marcucci; Gianluca Sottilotta; Roberto Targhetta; Ezio Zanon; Massimo Franchini
Journal:  Int J Gen Med       Date:  2010-07-21

4.  Measuring the impact of hemophilia on families: Development of the Hemophilia Family Impact Tool (H-FIT).

Authors:  Saunya Dover; Nancy L Young; Victor S Blanchette; Robert J Klaassen; Anthony K Chan; Cindy Wakefield; Vanessa Bouskill; Manuel Carcao; Mark Belletrutti; Aisha A K Bruce; Victoria E Price
Journal:  Res Pract Thromb Haemost       Date:  2021-05-07

5.  Content comparison of haemophilia specific patient-rated outcome measures with the international classification of functioning, disability and health (ICF, ICF-CY).

Authors:  Silvia Riva; Monika Bullinger; Edda Amann; Sylvia von Mackensen
Journal:  Health Qual Life Outcomes       Date:  2010-11-25       Impact factor: 3.186

6.  The effect of an exercise intervention on aerobic fitness, strength and quality of life in children with haemophilia (ACTRN012605000224628).

Authors:  Carolyn R Broderick; Robert D Herbert; Jane Latimer; Julie A Curtin; Hiran C Selvadurai
Journal:  BMC Blood Disord       Date:  2006-05-29

7.  The effect of yoga on the quality of life in the children and adolescents with haemophilia.

Authors:  Noushin Beheshtipoor; Shahapar Bagheri; Fatemeh Hashemi; Najaf Zare; Mehran Karimi
Journal:  Int J Community Based Nurs Midwifery       Date:  2015-04

8.  Measuring disease-specific quality of life in rare populations: a practical approach to cross-cultural translation.

Authors:  Victoria E Price; Robert J Klaassen; Paula H B Bolton-Maggs; John D Grainger; Christine Curtis; Cindy Wakefield; Gustavo Dufort; Arne Riedlinger; Christophe Soltner; Victor S Blanchette; Nancy L Young
Journal:  Health Qual Life Outcomes       Date:  2009-10-23       Impact factor: 3.186

Review 9.  Issues in pediatric haemophilia care.

Authors:  Paola Giordano; Massimo Franchini; Giuseppe Lassandro; Maria Felicia Faienza; Roberto Valente; Angelo Claudio Molinari
Journal:  Ital J Pediatr       Date:  2013-04-20       Impact factor: 2.638

10.  Psychological interventions for people with hemophilia.

Authors:  Laura Palareti; Giannino Melotti; Frederica Cassis; Sarah J Nevitt; Alfonso Iorio
Journal:  Cochrane Database Syst Rev       Date:  2020-03-18
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