Literature DB >> 15230953

Development of a new disease-specific quality-of-life questionnaire to adults living with haemophilia.

P Arranz1, E Remor, M Quintana, A Villar, J L Díaz, M Moreno, J Monteagudo, A Ugarriza, I Soto, R Pérez, J Chacón, M García-Luaces, A Cid, I Balda, M F López, M J Gutíerrez, E Martínez, C Marrero, M Prieto, C Sedano, R Vaca, C Altisent, F Hernández-Navarro.   

Abstract

A haemophilia-specific health-related quality-of-life questionnaire (named 'Hemofilia-QoL') was developed to assess quality-of-life in adults with haemophilia, and was psychometrically tested. Seventy-three interviews with haemophilia patients and health care professionals were used to generate the items included in the questionnaire, and expert ratings on the items formulated were used to screen them for potential omission. This was followed by psychometric testing in a sample of 35 patients. Preliminary psychometric testing of the revised questionnaire version, which contains 10 domains (physical health, physical role, joint damage, pain, treatment satisfaction, emotional role, mental health, social support), showed acceptable reliability (alpha = 0.94 for the Hemofilia-QoL total score) and validity, and this will be examined in a subsequent study with a larger patient sample.

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Mesh:

Year:  2004        PMID: 15230953     DOI: 10.1111/j.1365-2516.2004.00918.x

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


  12 in total

Review 1.  Routine provision of feedback from patient-reported outcome measurements to healthcare providers and patients in clinical practice.

Authors:  Chris Gibbons; Ian Porter; Daniela C Gonçalves-Bradley; Stanimir Stoilov; Ignacio Ricci-Cabello; Elena Tsangaris; Jaheeda Gangannagaripalli; Antoinette Davey; Elizabeth J Gibbons; Anna Kotzeva; Jonathan Evans; Philip J van der Wees; Evangelos Kontopantelis; Joanne Greenhalgh; Peter Bower; Jordi Alonso; Jose M Valderas
Journal:  Cochrane Database Syst Rev       Date:  2021-10-12

2.  Development and psychometric testing of the Hemophilia Well-being Index.

Authors:  Eduardo Remor
Journal:  Int J Behav Med       Date:  2013-12

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.  Development of a disease-specific quality of life questionnaire for adult patients with hereditary angioedema due to C1 inhibitor deficiency (HAE-QoL): Spanish multi-centre research project.

Authors:  Nieves Prior; Eduardo Remor; Carmen Gómez-Traseira; Concepción López-Serrano; Rosario Cabañas; Javier Contreras; Ángel Campos; Victoria Cardona; Stefan Cimbollek; Teresa González-Quevedo; Mar Guilarte; Dolores Hernández Fernández de Rojas; Carmen Marcos; María Rubio; Miguel Ángel Tejedor-Alonso; Teresa Caballero
Journal:  Health Qual Life Outcomes       Date:  2012-07-20       Impact factor: 3.186

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.  Combination of qualitative and quantitative methods for developing a new Health Related Quality of Life measure for patients with anogenital warts.

Authors:  Xavier Badia; Jose Antonio Colombo; Nuria Lara; M Angels Llorens; Luis Olmos; Miguel Sainz de los Terreros; Jose Antonio Varela; Juan Jose Vilata
Journal:  Health Qual Life Outcomes       Date:  2005-04-07       Impact factor: 3.186

7.  The Patient Reported Outcomes, Burdens and Experiences (PROBE) Project: development and evaluation of a questionnaire assessing patient reported outcomes in people with haemophilia.

Authors:  M W Skinner; C Chai-Adisaksopha; R Curtis; N Frick; M Nichol; D Noone; B O'Mahony; D Page; J S Stonebraker; A Iorio
Journal:  Pilot Feasibility Stud       Date:  2018-02-27

8.  Psychometric properties of the Greek Haem-A-QoL for measuring quality of life in Greek haemophilia patients.

Authors:  Agoritsa Varaklioti; Nick Kontodimopoulos; Olga Katsarou; Dimitris Niakas
Journal:  Biomed Res Int       Date:  2014-05-06       Impact factor: 3.411

Review 9.  Patient involvement in the development of patient-reported outcome measures: a scoping review.

Authors:  Bianca Wiering; Dolf de Boer; Diana Delnoij
Journal:  Health Expect       Date:  2016-02-18       Impact factor: 3.377

Review 10.  Measuring therapeutic relationship in the care of patients with haemophilia: A scoping review.

Authors:  Erin McCabe; Maxi Miciak; Liz Dennett; Patricia Manns; Christine Guptill; Jeremy Hall; Douglas P Gross
Journal:  Health Expect       Date:  2018-08-29       Impact factor: 3.377

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