Literature DB >> 28429867

Health-related quality of life questionnaires in individuals with haemophilia: a systematic review of their measurement properties.

P F Limperg1, C B Terwee2, N L Young3, V E Price4, S C Gouw5, M Peters5, M A Grootenhuis1, V Blanchette6, L Haverman1.   

Abstract

BACKGROUND: The evaluation of health related quality of life (HRQOL) is essential for a full assessment of the influence of an illness on patients' lives. The aim of this paper is to critically appraise and compare the measurement properties of HRQOL questionnaires studied in haemophilia.
METHODS: Bibliographic databases (Embase, Medline, Cinahl and PsycInfo) were searched for articles evaluating measurement properties of HRQOL questionnaires in haemophilia. Articles were excluded that did not report HRQOL measurement properties, or when <50% of the study population had haemophilia. The methodological quality of the selected studies was evaluated using the COSMIN checklist. The measurement properties of the HRQL questionnaires were rated as 'positive', 'indeterminate' or 'negative', accompanied by levels of evidence.
RESULTS: The search resulted in 1597 unique hits, of which 22 studies were included. These articles evaluated three questionnaires for children (CHO-KLAT, Haemo-QoL and one unnamed measure) and five for adults (Hemofilia-QoL, Haemophilia Well-Being Index, HAEMO-QoL-A, Haem-A-QoL, and SF-36). The CHO-KLAT was the paediatric measure that showed the strongest measurement properties in high-quality studies. The Haemophilia Well-Being Index and HAEMO-QoL-A performed best among the adult measures. None of the studies reported measurement error and responsiveness.
CONCLUSION: Our findings suggest that there is no need for new disease-specific HRQOL questionnaires for haemophilia, but rather that additional research is necessary to document the measurement properties of the currently available questionnaires, specifically focusing on the structural validity, measurement error and responsiveness of these questionnaires.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  adults; children; haemophilia; health-related quality of life; measurement properties; questionnaires; systematic review

Mesh:

Year:  2017        PMID: 28429867     DOI: 10.1111/hae.13197

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


  14 in total

1.  Psychometric Validation of the Haemo-QOL-A in Participants with Hemophilia A Treated with Gene Therapy.

Authors:  Jennifer Quinn; Kathleen A Delaney; Wing Yen Wong; Wolfgang Miesbach; Monika Bullinger
Journal:  Patient Relat Outcome Meas       Date:  2022-07-18

2.  Persistence of haemostatic response following gene therapy with valoctocogene roxaparvovec in severe haemophilia A.

Authors:  K John Pasi; Michael Laffan; Savita Rangarajan; Tara M Robinson; Nina Mitchell; Will Lester; Emily Symington; Bella Madan; Xinqun Yang; Benjamin Kim; Glenn F Pierce; Wing Yen Wong
Journal:  Haemophilia       Date:  2021-08-11       Impact factor: 4.263

Review 3.  Haemophilia.

Authors:  Erik Berntorp; Kathelijn Fischer; Daniel P Hart; Maria Elisa Mancuso; David Stephensen; Amy D Shapiro; Victor Blanchette
Journal:  Nat Rev Dis Primers       Date:  2021-06-24       Impact factor: 52.329

4.  Patient-relevant health outcomes for hemophilia care: Development of an international standard outcomes set.

Authors:  Erna C van Balen; Brian O'Mahony; Marjon H Cnossen; Gerard Dolan; Victor S Blanchette; Kathelijn Fischer; Deborah Gue; Jamie O'Hara; Alfonso Iorio; Shannon Jackson; Barbara A Konkle; Diane J Nugent; Donna Coffin; Mark W Skinner; Cees Smit; Alok Srivastava; Fred van Eenennaam; Johanna G van der Bom; Samantha C Gouw
Journal:  Res Pract Thromb Haemost       Date:  2021-03-06

5.  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

6.  Recommended primary outcomes for clinical trials evaluating hemostatic blood products and agents in patients with bleeding: Proceedings of a National Heart Lung and Blood Institute and US Department of Defense Consensus Conference.

Authors:  Philip C Spinella; Nahed El Kassar; Andrew P Cap; Andrei L Kindzelski; Christopher S Almond; Alan Barkun; Terry B Gernsheimer; Joshua N Goldstein; John B Holcomb; Alfonso Iorio; Dennis M Jensen; Nigel S Key; Jerrold H Levy; Stephan A Mayer; Ernest E Moore; Simon J Stanworth; Roger J Lewis; Marie E Steiner
Journal:  J Trauma Acute Care Surg       Date:  2021-08-01       Impact factor: 3.697

7.  Impact of prophylaxis on health-related quality of life of boys with hemophilia: An analysis of pooled data from 9 countries.

Authors:  Koyo Usuba; Victoria E Price; Victor Blanchette; Audrey Abad; Carmen Altisent; Loretta Buchner-Daley; Jorge D A Carneiro; Brian M Feldman; Kathelijn Fischer; John Grainger; Susanne Holzhauer; Koon-Hung Luke; Sandrine Meunier; Margareth Ozelo; Ling Tang; Sandra V Antunes; Paula Villaça; Cindy Wakefield; Gilian Wharfe; Runhui Wu; Nancy L Young
Journal:  Res Pract Thromb Haemost       Date:  2019-04-23

8.  Evaluation of quality of life in hemophilia patients using the WHOQOL-bref and Haemo-A-Qol questionnaires.

Authors:  Gustavo Cambraia Trindade; Luíza Gabrielle de Lacerda Viggiano; Enderson Resende Brant; Carlos Alexandre de Oliveira Lopes; Mateus Lopes de Faria; Pedro Henrique Nery de Sá Ribeiro; Ana Flávia do Carmo Silva; Diana Maria de Resende Souza; Aline de Freitas Lopes; João Marcos Arantes Soares; Melina de Barros Pinheiro
Journal:  Hematol Transfus Cell Ther       Date:  2019-07-04

9.  Health-related quality of life, developmental milestones, and self-esteem in young adults with bleeding disorders.

Authors:  P F Limperg; L Haverman; H Maurice-Stam; M Coppens; C Valk; M J H A Kruip; J Eikenboom; M Peters; M A Grootenhuis
Journal:  Qual Life Res       Date:  2017-09-12       Impact factor: 4.147

10.  Clinical outcomes in hemophilia: Towards development of a core set of standardized outcome measures for research.

Authors:  Saunya Dover; Victor S Blanchette; Alok Srivastava; Kathelijn Fischer; Audrey Abad; Brian M Feldman
Journal:  Res Pract Thromb Haemost       Date:  2020-04-09
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