Literature DB >> 35347553

Health state utilities for beta-thalassemia: a time trade-off study.

Antony P Martin1, Enrico Ferri Grazzi2, Claudia Mighiu3, Manoj Chevli4, Farrukh Shah5, Louise Maher4, Anum Shaikh1, Aliah Sagar1, Hayley Hubberstey1, Bethany Franks3, Juan M Ramos-Goñi6, Mark Oppe6, Derek Tang7.   

Abstract

BACKGROUND: Beta-thalassemia (BT) is an inherited blood disorder characterized by reduced levels of functional hemoglobin resulting in phenotypes ranging from clinically asymptomatic to severely anemic. Patients with BT may require lifelong regular blood transfusions supported by appropriate iron chelation therapy (ICT). This study aimed to determine how the UK general population values BT health states associated with differing transfusion burden and ICT.
METHODS: Composite time trade-off (cTTO) methodology was employed to elicit health state utilities in BT. Relevant BT literature related to symptom and quality-of-life impact, including physical, functional, and emotional well-being, and safety profiles of BT treatments were considered when drafting health state descriptions. Eleven health state descriptions were developed and validated by hematologists and patient advocates for clinical accuracy and completeness. 200 individuals from the UK general population participated in the cTTO interviews.
RESULTS: The mean age of participants was 41.50 years (SD 16.01, range 18-81); 88 (46.8%) were female. Utility values ranged from 0.78 (SD 0.34) for non-transfusion dependent BT with oral ICT to 0.37 (SD 0.50) for high transfusion burden with subcutaneous ICT in transfusion-dependent BT.
CONCLUSIONS: This study provides health utilities for a range of BT health states from the UK general population perspective. Importantly, lower transfusion burden and lower burden of anemia were associated with higher utilities. To a lesser extent, differential modes of ICT were found to impact utility valuations in patients with BT. The utilities obtained in this study can be employed as inputs in cost-effectiveness analyses of BT therapies.
© 2022. The Author(s).

Entities:  

Keywords:  Anemia; Beta-thalassemia; Hemoglobin; Time trade-off; Transfusion burden

Year:  2022        PMID: 35347553     DOI: 10.1007/s10198-022-01449-7

Source DB:  PubMed          Journal:  Eur J Health Econ        ISSN: 1618-7598


  39 in total

1.  Relationship between health utility and psychometric health status measures.

Authors:  D A Revicki
Journal:  Med Care       Date:  1992-05       Impact factor: 2.983

Review 2.  2017 Clinical trials update in new treatments of β-thalassemia.

Authors:  Alexandros Makis; Eleftheria Hatzimichael; Ioannis Papassotiriou; Ersi Voskaridou
Journal:  Am J Hematol       Date:  2016-11       Impact factor: 10.047

Review 3.  The inherited diseases of hemoglobin are an emerging global health burden.

Authors:  David J Weatherall
Journal:  Blood       Date:  2010-03-16       Impact factor: 22.113

4.  Assessment of optimal size and composition of the U.S. National Registry of hematopoietic stem cell donors.

Authors:  Craig Kollman; Esteban Abella; Robert L Baitty; Patrick G Beatty; Ranajit Chakraborty; Cindy L Christiansen; Robert J Hartzman; Carolyn Katovich Hurley; Edgar Milford; John A Nyman; Thomas J Smith; Galen E Switzer; Randal K Wada; Michelle Setterholm
Journal:  Transplantation       Date:  2004-07-15       Impact factor: 4.939

Review 5.  Beta-thalassemia.

Authors:  Renzo Galanello; Raffaella Origa
Journal:  Orphanet J Rare Dis       Date:  2010-05-21       Impact factor: 4.123

Review 6.  Advances in the allogeneic transplantation for thalassemia.

Authors:  Guido Lucarelli; Javid Gaziev
Journal:  Blood Rev       Date:  2007-11-26       Impact factor: 8.250

Review 7.  Guidelines for diagnosis and management of Beta-thalassemia intermedia.

Authors:  Mehran Karimi; Nader Cohan; Vincenzo De Sanctis; Naji S Mallat; Ali Taher
Journal:  Pediatr Hematol Oncol       Date:  2014-10       Impact factor: 1.969

8.  Myocardial infarction in a patient with beta-thalassemia major: first report.

Authors:  Zvi G Fridlender; Deborah Rund
Journal:  Am J Hematol       Date:  2004-01       Impact factor: 10.047

Review 9.  What Unrelated Hematopoietic Stem Cell Transplantation in Thalassemia Taught us about Transplant Immunogenetics.

Authors:  Giorgio La Nasa; Adriana Vacca; Roberto Littera; Eugenia Piras; Sandro Orru; Marianna Greco; Carlo Carcassi; Giovanni Caocci
Journal:  Mediterr J Hematol Infect Dis       Date:  2016-10-20       Impact factor: 2.576

10.  Health state utilities associated with treatment for transfusion-dependent β-thalassemia.

Authors:  Louis S Matza; L Clark Paramore; Katie D Stewart; Hayley Karn; Minesh Jobanputra; Andrew C Dietz
Journal:  Eur J Health Econ       Date:  2019-12-11
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