@article{bed50ca865274c469005a3b5440793f1,
title = "Health-related quality of life and health status in adolescent and adult people with haemophilia A without factor VIII inhibitors—A non-interventional study",
abstract = "Introduction: Real-world data on health-related outcomes in persons with haemophilia A (PwHA) can provide useful information for improving patient care. The global, non-interventional study (NIS; NCT02476942) prospectively collected high-quality data in PwHA, including those without factor VIII (FVIII) inhibitors treated according to local routine clinical practice. Aim: To report health-related quality of life (HRQoL) and health status of adult/adolescent PwHA without FVIII inhibitors. Methods: Participants were PwHA without FVIII inhibitors age ≥12 years; they remained on existing episodic treatment or prophylaxis. HRQoL was assessed by Haemophilia Quality of Life Questionnaire for Adults (Haem-A-QoL) or Haemophilia-Specific Quality of Life Assessment for Children and Adolescents Short Form (Haemo-QoL-SF II). Health status was assessed through EuroQol 5-Dimensions 5-Levels (EQ-5D-5L) index utility score and visual analogue scale (EQ-VAS). Results: Ninety-four participants enrolled; median age was 34.0 years (range 12–76). Forty-five received episodic treatment and 49 received prophylaxis for a median time of 27.7 weeks and 30.4 weeks, respectively. Mean (standard deviation) baseline Haem-A-QoL total scores were 40.1 (17.0) for the episodic group and 26.6 (14.6) for the prophylaxis group, indicating impairments in HRQoL, which remained consistent over time. Mean EQ-5D-5L IUS scores were similar between treatment regimens (0.8 episodic; 0.9 prophylaxis) and consistent over time. The mean EQ-VAS scores were similar between treatment regimens, and lower on days when bleeding occurred (79.0 vs 85.0 for episodic treatment; 77.0 vs 82.0 for prophylaxis, respectively). Conclusions: Adult and adolescent PwHA without FVIII inhibitors had HRQoL impairments regardless of whether they were treated with episodic or prophylactic standard care with FVIII.",
keywords = "factor VIII, haemophilia A, health-related quality of life, inhibitors, non-interventional study, real-world data",
author = "Johannes Oldenburg and Huyen Tran and Flora Peyvandi and Ramiro N{\'u}{\~n}ez and Peter Trask and Sammy Chebon and Mahlangu, {Johnny N.} and Michaela Lehle and Victor Jim{\'e}nez-Yuste and {von Mackensen}, Sylvia",
note = "Funding Information: JO reports grants and personal fees (for travel support, participation in Advisory Boards and participation in symposia as chair or speaker) from Bayer, Biotest, CSL Behring, Novo Nordisk, Octapharma, and Shire/Takeda; as well as personal fees from Chugai Pharmaceutical Co., Grifols, Pfizer, F. Hoffmann‐La Roche Ltd, and SOBI. HT has served on Advisory Boards for F. Hoffmann‐La Roche Ltd, Takeda, Pfizer and Novartis. FP has received honoraria for participating as a speaker at educational symposia organized by Grifols, F. Hoffmann‐La Roche Ltd and Takeda; and reports participation at Advisory Boards for F. Hoffmann‐La Roche Ltd, Sanofi, SOBI and Takeda. RN has acted as a paid consultant for F. Hoffmann‐La Roche Ltd, Takeda, Novartis, Grifols, Novo Nordisk and Bayer. PT is employed by F. Hoffmann‐La Roche Ltd/Genentech, Inc. and owns stock in the companies. SC is an employee and holds shares in F. Hoffmann‐La Roche Ltd. JNM has received research grants from Bayer, Biogen, CSL Behring, Novo Nordisk and F. Hoffmann‐La Roche Ltd, has served on Advisory Boards for Baxalta, Biogen, CSL Behring, Novo Nordisk, F. Hoffmann‐La Roche Ltd, and Shire; and on speakers{\textquoteright} bureaus for Amgen, Alnylam, Bayer, Biogen, Biotest and CSL Behring. ML is an employee and holds stocks in F. Hoffmann‐La Roche Ltd. VJ‐Y has provided consultancy (including expert testimony) for F. Hoffmann‐La Roche Ltd, Novo Nordisk, Takeda, Sobi and Pfizer; and received research funding from Grifols, Novo Nordisk, Sobi, Takeda and Pfizer; as well as honoraria from F. Hoffmann‐La Roche Ltd, Novo Nordisk, Takeda, Sobi, Pfizer, Grifols, Octapharma, CSL Behring and Bayer. SvM has served as a consult or advisor for SOBI, F. Hoffmann‐La Roche Ltd/Chugai Pharmaceutical Co., Takeda and Bayer; in speakers{\textquoteright} bureaus for SOBI and CSL Behring; and received research funding from SOBI and Novo Nordisk; as well as travel, accommodations and expenses from SOBI and CSL Behring. Funding Information: The study was funded by F. Hoffmann‐La Roche Ltd. and Chugai Pharmaceutical Co., Ltd. Editorial assistance for the development of this manuscript, under the direction of the authors, was provided by Robert Harrison, PhD, and Rebecca A Bachmann, PhD, of Gardiner‐Caldwell Communications, and funded by F. Hoffmann‐La Roche Ltd. Publisher Copyright: {\textcopyright} 2021 The Authors. Haemophilia published by John Wiley & Sons Ltd. Copyright: Copyright 2021 Elsevier B.V., All rights reserved.",
year = "2021",
month = may,
doi = "10.1111/hae.14270",
language = "English",
volume = "27",
pages = "398--407",
journal = "Haemophilia",
issn = "1351-8216",
publisher = "Wiley-Blackwell",
number = "3",
}