Literature DB >> 28419637

Self-reported prevalence, description and management of pain in adults with haemophilia: methods, demographics and results from the Pain, Functional Impairment, and Quality of life (P-FiQ) study.

M Witkop1, A Neff2, T W Buckner3, M Wang3, K Batt4, C M Kessler5, D Quon6, L Boggio7, M Recht8, K Baumann9, R Z Gut10, D L Cooper10, C L Kempton11.   

Abstract

INTRODUCTION: Haemophilia is characterized by frequent haemarthrosis, leading to acute/chronic joint pain. AIM: To assess self-reported prevalence, description and management of pain in adult males with mild-to-severe haemophilia and history of joint pain/bleeding.
METHODS: Participants completed a pain survey and five patient-reported outcome instruments assessing pain, functional impairment and health-related quality of life (HRQoL).
RESULTS: Of 381 participants enrolled, median age was 34 years; 77% had haemophilia A, 71% had severe disease and 65% were overweight/obese. Many (56%) were not receiving routine infusions; 30% never received routine infusions. During the prior 6 months, 20% experienced acute pain, 34% chronic pain and 32% both acute/chronic pain. Subjects with both acute/chronic pain (vs. none, acute or chronic) were more likely to be depressed (30% vs. 0-15%), obese (35% vs. 20-29%) and have lower HRQoL (mean EQ-5D visual analog scale, 69 vs. 83-86) and function (median overall Hemophilia Activities List, 60 vs. 88-99). Most common analgesics used for acute/chronic pain during the prior 6 months were acetaminophen (62%/55%) and non-steroidal anti-inflammatory drugs (34%/49%); most common non-pharmacologic strategies were ice (65%/33%) and rest (51%/33%). Hydrocodone-acetaminophen was the most common opioid for both acute/chronic pain (30%); other long-acting opioids were infrequently used specifically for chronic but not acute pain (morphine, 7%; methadone, 6%; fentanyl patch, 2%).
CONCLUSION: Patients with chronic pain, particularly those with both acute/chronic pain, frequently experience psychological issues, functional disability and reduced HRQoL. Treatment strategies for acute pain (e.g. routine infusions to prevent bleeding) and for chronic pain (e.g. long-acting opioids) may be underused.
© 2017 The Authors. Haemophilia Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  acute pain; chronic pain; haemophilia; pain; pain management; patient-reported outcome

Mesh:

Year:  2017        PMID: 28419637     DOI: 10.1111/hae.13214

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


  28 in total

1.  Health care resource utilization and cost burden of hemophilia B in the United States.

Authors:  Tyler W Buckner; Iryna Bocharova; Kaitlin Hagan; Arielle G Bensimon; Hongbo Yang; Eric Q Wu; Eileen K Sawyer; Nanxin Li
Journal:  Blood Adv       Date:  2021-04-13

2.  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

Review 3.  Management of Hemophilia in Older Patients.

Authors:  Massimo Franchini; Pier Mannuccio Mannucci
Journal:  Drugs Aging       Date:  2017-12       Impact factor: 3.923

Review 4.  [Pain therapy for children and adolescents with hemophilia : Recommendations by an expert panel].

Authors:  W Stromer; B Messerer; R Crevenna; S H Hemberger; B Jauk; R Schwarz; W Streif; K Thom; B Wagner; K Zwiauer; R Likar
Journal:  Schmerz       Date:  2018-12       Impact factor: 1.107

5.  High prevalence of overweight/obesity in adult persons with hemophilia in Utah and a review of the literature.

Authors:  Ming Y Lim; Guo Wei; Angela P Presson; Paul Bray; George M Rodgers
Journal:  Blood Coagul Fibrinolysis       Date:  2020-12       Impact factor: 1.276

6.  Quality of life and its predictors among adult patients with haemophilic arthropathy. An observational study.

Authors:  Roberto Ucero-Lozano; José Antonio López-Pina; Alba Ortiz-Pérez; Rubén Cuesta-Barriuso
Journal:  BMC Musculoskelet Disord       Date:  2021-05-15       Impact factor: 2.362

7.  Internal consistency and item-total correlation of patient-reported outcome instruments and hemophilia joint health score v2.1 in US adult people with hemophilia: results from the Pain, Functional Impairment, and Quality of life (P-FiQ) study.

Authors:  Michael Wang; Katharine Batt; Craig Kessler; Anne Neff; Neeraj N Iyer; David L Cooper; Christine L Kempton
Journal:  Patient Prefer Adherence       Date:  2017-10-25       Impact factor: 2.711

8.  Illustration of patient-reported outcome challenges and solutions in rare diseases: a systematic review in Cushing's syndrome.

Authors:  Naomi Knoble; Gabrielle Nayroles; Cherry Cheng; Benoit Arnould
Journal:  Orphanet J Rare Dis       Date:  2018-12-19       Impact factor: 4.123

9.  Patient preferences and priorities for haemophilia gene therapy in the US: A discrete choice experiment.

Authors:  Michelle Witkop; George Morgan; Jamie O'Hara; Michael Recht; Tyler W Buckner; Diane Nugent; Randall Curtis; Brian O'Mahony; Mark W Skinner; Brendan Mulhern; Matthew Cawson; Talaha M Ali; Eileen K Sawyer; Nanxin Li
Journal:  Haemophilia       Date:  2021-07-26       Impact factor: 4.263

10.  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

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