Literature DB >> 26179213

Distress in patients with bleeding disorders: a single institutional cross-sectional study.

V Barry1,2, M E Lynch3, D Q Tran4, A Antun4, H G Cohen5, A DeBalsi1,2, D Hicks1,2, S Mattis1,2, M J A Ribeiro4, S F Stein4, C L Truss1,2, K Tyson2, C L Kempton1,2,4.   

Abstract

INTRODUCTION: Distress may affect a patient's ability to cope with and manage disease. AIM: To report distress prevalence in adult patients with bleeding disorders and determine whether specific clinical and health characteristics, including disease severity and employment status, are associated with distress.
METHODS: Patients who visited a Haemophilia Treatment Centre (HTC) between January 1st, 2012 through February 28th, 2014 and who completed a distress screen, pain screen and questionnaire were evaluated cross sectionally. Distress was measured by the National Comprehensive Cancer Network Distress Management Tool, which allowed patients to rate recent distress on a 0-10 point scale. A rating of five or more was categorized as high distress. Pain was measured by the Brief Pain Inventory Short Form, which asked patients to rate pain types on 0-10 point scales. Patients reported employment and other demographic and behavioural information on the questionnaire. Primary diagnosis, age, HIV and HCV status were abstracted from medical records. Adjusted logistic regression was used to identify distress associations.
RESULTS: High distress prevalence among 152 patients with bleeding disorders was 31.6%. Unemployment, disability, greater depressive symptoms and higher pain were associated with high distress in multivariable models. Bleeding disorder diagnosis, race/ethnicity, HIV/HCV status and on-demand treatment regimen were not associated with high distress.
CONCLUSION: Distress among patients with congenital bleeding disorders followed at a comprehensive HTC was high and similar to that reported among patients with cancer. Future research should determine whether distress impacts clinical outcomes in patients with bleeding disorders as demonstrated in other chronic disorders.
© 2015 John Wiley & Sons Ltd.

Entities:  

Keywords:  United States; depression; distress; haemophilia; pain; quality of life

Mesh:

Year:  2015        PMID: 26179213     DOI: 10.1111/hae.12748

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


  4 in total

1.  Evidence for Stress-induced Bleeding in a Patient with von Willebrand Factor Deficiency.

Authors:  Karthick Subramanian; Madhavapuri Pravallika; Vikas Menon
Journal:  Indian J Psychol Med       Date:  2018 May-Jun

2.  Fitness enhances psychosocial well-being and self-confidence in young men with hemophilia: Results from Project GYM.

Authors:  Kate Khair; Mike Holland; Sandra Dodgson; Paul McLaughlin; Simon Fletcher; Deborah Christie
Journal:  Res Pract Thromb Haemost       Date:  2021-11-26

3.  Known-group validity of patient-reported outcome instruments and hemophilia joint health score v2.1 in US adults with hemophilia: results from the Pain, Functional Impairment, and Quality of life (P-FiQ) study.

Authors:  Tyler W Buckner; Michael Wang; David L Cooper; Neeraj N Iyer; Christine L Kempton
Journal:  Patient Prefer Adherence       Date:  2017-10-11       Impact factor: 2.711

4.  A new measure to assess pain in people with haemophilia: The Multidimensional Haemophilia Pain Questionnaire (MHPQ).

Authors:  Ana Cristina Paredes; Patrício Costa; Armando Almeida; Patrícia R Pinto
Journal:  PLoS One       Date:  2018-11-28       Impact factor: 3.240

  4 in total

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