Literature DB >> 11966854

Pilot testing of the 'Haemo-QoL' quality of life questionnaire for haemophiliac children in six European countries.

M Bullinger1, S von Mackensen, K Fischer, K Khair, C Petersen, U Ravens-Sieberer, A Rocino, P Sagnier, J M Tusell, M van den Berg, M Vicariot.   

Abstract

In a multinational working group, an instrument (Haemo-QoL) to assess quality of life in children/adolescents with haemophilia and their parents has been developed. In co-operation with haemophilia treatment centres in six European countries, approximately 10 children/adolescents with haemophilia per country and their parents were asked to participate in the pilot-testing. Both self-reported and parent-reported questionnaires were provided for two age-groups of children (4-16 years). Medical data was collected from physicians from patient files. Answers to open questions from participants (58 children and 57 parents) confirmed the content of 116 of the preliminary items. Cognitive debriefing revealed that the majority of the Haemo-QoL was rated favourably, but 29 questions were recommended to be omitted and several items to be reformulated. Preliminary psychometric testing of the revised 77 item questionnaire in the same sample showed acceptable reliability and validity, which will be examined in a subsequent study with a larger patient sample.

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Year:  2002        PMID: 11966854     DOI: 10.1046/j.1351-8216.2001.114.doc.x

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


  9 in total

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4.  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

5.  The European DISABKIDS project: development of seven condition-specific modules to measure health related quality of life in children and adolescents.

Authors:  Rolanda M Baars; Clare I Atherton; Hendrik M Koopman; Monika Bullinger; Mick Power
Journal:  Health Qual Life Outcomes       Date:  2005-11-13       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.  Reliability of patient-reported outcome instruments in US adults with hemophilia: the Pain, Functional Impairment and Quality of life (P-FiQ) study.

Authors:  Christine L Kempton; Michael Wang; Michael Recht; Anne Neff; Amy D Shapiro; Amit Soni; Roshni Kulkarni; Tyler W Buckner; Katharine Batt; Neeraj N Iyer; David L Cooper
Journal:  Patient Prefer Adherence       Date:  2017-09-19       Impact factor: 2.711

9.  Developing and pretesting a new patient reported outcome measure for paediatric Chronic Fatigue Syndrome/ Myalgic Encephalopathy (CFS/ME): cognitive interviews with children.

Authors:  Roxanne M Parslow; Alison Shaw; Kirstie L Haywood; Esther Crawley
Journal:  J Patient Rep Outcomes       Date:  2019-11-09
  9 in total

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