Literature DB >> 26856807

Evaluating outcome of prophylaxis in haemophilia: objective and self-reported instruments should be combined.

K Fischer1,2, A Nijdam1, M Holmström3,4, P Petrini3,5, R Ljung6,7, Y T van der Schouw2, E Berntorp7,8.   

Abstract

INTRODUCTION: Routine outcome assessment of prophylaxis should use validated tools, while balancing comprehensiveness and burden. Collecting overlapping information should be avoided. AIM: To assess correlations between different outcome assessment tools in haemophilia.
METHODS: From an international cross-sectional study, data on objective outcome (Haemophilia Joint Health Score (HJHS 2.1, range 0-124), radiological Pettersson score) and self-reported joint bleeding, Haemophilia Activities List (HAL, range 100-0), health-related quality of life (SF-36, including five physical and five mental domain scores, range 100-0), and Utility (SF6D and EQ-5D, range 1.0-0) were extracted. Spearman's correlations were calculated: ≥0.8 very strong, 0.60-0.79 strong, 0.40-0.59 moderate.
RESULTS: Ninety patients with severe haemophilia, on prophylaxis since median age 3.4 years, were evaluated at median 25.5 years (range 16.0-37.6). Objective outcome was favourable (median HJHS 2.1 6 points, Pettersson score 9 points). Self-reported outcome showed a median of 7 joint bleeds in 5 years, median HAL sum 96 points, high scores for physical domains of SF-36 (median 80-95) and high Utility values (median SF6D 0.87; EQ-5D 0.84). Physical examination (HJHS 2.1) showed strong correlation with radiological scores, moderate correlation with physical domains of the SF-36 and Utility, but no correlation with self-reported bleeding or limitations in activities (HAL). Bleeding was not associated with any other outcome parameter. The HAL was only correlated with the SF36 'Physical functioning' domain.
CONCLUSION: For the evaluation of patients on early prophylaxis, information on bleeding should be complemented by objective joint assessment as well as self-reported limitations in activities and quality of life.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  arthropathy; haemarthrosis; joint score; outcome; prophylaxis; quality of life

Year:  2016        PMID: 26856807     DOI: 10.1111/hae.12901

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


  6 in total

1.  Joint scores in hemophilic arthropathy in children: Developing country perspectives.

Authors:  Aritra Guha; Akash Rai; Arnab Nandy; Tanushree Mondal; Narayan Pandit; Sumantra Guha; Dipankar Gupta; Rakesh Mondal
Journal:  Eur J Rheumatol       Date:  2019-12-16

2.  MRI predicts 5-year joint bleeding and development of arthropathy on radiographs in hemophilia.

Authors:  Wouter Foppen; Irene C van der Schaaf; Frederik J A Beek; Willem P T M Mali; Kathelijn Fischer
Journal:  Blood Adv       Date:  2020-01-14

3.  Long-term impact of joint bleeds in von Willebrand disease: a nested case-control study.

Authors:  Karin P M van Galen; Piet de Kleijn; Wouter Foppen; Jeroen Eikenboom; Karina Meijer; Roger E G Schutgens; Kathelijn Fischer; Marjon H Cnossen; Joke de Meris; Karin Fijnvandraat; Johanna G van der Bom; Britta A P Laros-van Gorkom; Frank W G Leebeek; Eveline P Mauser-Bunschoten
Journal:  Haematologica       Date:  2017-06-01       Impact factor: 9.941

4.  Evidence of a disability paradox in patient-reported outcomes in haemophilia.

Authors:  Jamie O'Hara; Antony P Martin; Diane Nugent; Michelle Witkop; Tyler W Buckner; Mark W Skinner; Brian O'Mahony; Brendan Mulhern; George Morgan; Nanxin Li; Eileen K Sawyer
Journal:  Haemophilia       Date:  2021-02-17       Impact factor: 4.287

5.  Generic PROMIS item banks in adults with hemophilia for patient-reported outcome assessment: Feasibility, measurement properties, and relevance.

Authors:  Isolde A R Kuijlaars; Lorynn Teela; Lize F D van Vulpen; Merel A Timmer; Michiel Coppens; Samantha C Gouw; Marjolein Peters; Marieke J H A Kruip; Marjon H Cnossen; Jelmer J Muis; Evelien S van Hoorn; Lotte Haverman; Kathelijn Fischer
Journal:  Res Pract Thromb Haemost       Date:  2021-11-21

6.  Shortening the Haemophilia Activities List (HAL) from 42 items to 18 items.

Authors:  Isolde A R Kuijlaars; Janjaap van der Net; Tyler W Buckner; Christine L Kempton; Roger E G Schutgens; Kathelijn Fischer
Journal:  Haemophilia       Date:  2021-09-08       Impact factor: 4.263

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.