Literature DB >> 35849155

Thrombopoietin receptor agonist discontinuation rates and reasons among patients with immune thrombocytopenia: a study of administrative claims linked with medical chart review.

Adam Cuker1, Lincy Lal2, Anuja Roy3, Caitlin Elliott2, Maureen Carlyle2, Carolyn Martin4, Jens Haenig5, Ricardo Viana5.   

Abstract

Administrative claims provide a rich data source for retrospective studies of real-world clinical practice, yet some important data may be inconsistent or unavailable. This study explored factors influencing discontinuation of thrombopoietin receptor agonists (TPO-RAs) among patients with immune thrombocytopenia (ITP), by adding medical chart abstraction for additional details. Adult (≥ 18 years) patients with continuous commercial or Medicare Advantage with Part D health insurance coverage were included. Inclusion criteria were ≥ 1 claim for eltrombopag or romiplostim and ≥ 2 diagnoses of ITP between December 31, 2017, and January 1, 2020. Providers were asked to provide access to medical charts for abstraction. The analyses included only patients who discontinued TPO-RA and described patient characteristics, treatment patterns, platelet values, and reasons for discontinuation. Among 207 ITP patients treated with a TPO-RA, 137 (66%) discontinued treatment during the observation period. The mean TPO-RA treatment duration was 185 days. Mean platelet count at the time of discontinuation was 197 × 109/L. The most common reason for discontinuation was improvement of the patient's condition (42%). Other reasons included worsening of ITP/lack of response (12%), adverse events (12%), and cost-related or social reasons (23%). No reason was reported for 10%. Notably 26% of patients who discontinued remained off all ITP therapy for the remainder of the study, with a mean treatment-free period of 262 days. These results emphasize that some patients with ITP are able to discontinue TPO-RA therapy and achieve durable treatment-free periods.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Administrative claims; Discontinuation; Eltrombopag; Immune thrombocytopenia; Medical chart review; Observational; Platelet response; Retrospective study; Romiplostim

Mesh:

Substances:

Year:  2022        PMID: 35849155     DOI: 10.1007/s00277-022-04888-7

Source DB:  PubMed          Journal:  Ann Hematol        ISSN: 0939-5555            Impact factor:   4.030


  25 in total

Review 1.  The ITP syndrome: pathogenic and clinical diversity.

Authors:  Douglas B Cines; James B Bussel; Howard A Liebman; Eline T Luning Prak
Journal:  Blood       Date:  2009-04-24       Impact factor: 22.113

2.  Standardization of terminology, definitions and outcome criteria in immune thrombocytopenic purpura of adults and children: report from an international working group.

Authors:  Francesco Rodeghiero; Roberto Stasi; Terry Gernsheimer; Marc Michel; Drew Provan; Donald M Arnold; James B Bussel; Douglas B Cines; Beng H Chong; Nichola Cooper; Bertrand Godeau; Klaus Lechner; Maria Gabriella Mazzucconi; Robert McMillan; Miguel A Sanz; Paul Imbach; Victor Blanchette; Thomas Kühne; Marco Ruggeri; James N George
Journal:  Blood       Date:  2008-11-12       Impact factor: 22.113

3.  Updated international consensus report on the investigation and management of primary immune thrombocytopenia.

Authors:  Drew Provan; Donald M Arnold; James B Bussel; Beng H Chong; Nichola Cooper; Terry Gernsheimer; Waleed Ghanima; Bertrand Godeau; Tomás José González-López; John Grainger; Ming Hou; Caroline Kruse; Vickie McDonald; Marc Michel; Adrian C Newland; Sue Pavord; Francesco Rodeghiero; Marie Scully; Yoshiaki Tomiyama; Raymond S Wong; Francesco Zaja; David J Kuter
Journal:  Blood Adv       Date:  2019-11-26

4.  The bleeding risk and natural history of idiopathic thrombocytopenic purpura in patients with persistent low platelet counts.

Authors:  Y C Cohen; B Djulbegovic; O Shamai-Lubovitz; B Mozes
Journal:  Arch Intern Med       Date:  2000-06-12

5.  Fatigue in adult patients with primary immune thrombocytopenia.

Authors:  Julia L Newton; Jessica A Reese; Shirley I Watson; Sara K Vesely; Paula H B Bolton-Maggs; James N George; Deirdra R Terrell
Journal:  Eur J Haematol       Date:  2011-03-23       Impact factor: 2.997

Review 6.  The incidence of immune thrombocytopenic purpura in children and adults: A critical review of published reports.

Authors:  Deirdra R Terrell; Laura A Beebe; Sara K Vesely; Barbara R Neas; Jodi B Segal; James N George
Journal:  Am J Hematol       Date:  2010-03       Impact factor: 10.047

Review 7.  Chronic immune thrombocytopenia in adults: epidemiology and clinical presentation.

Authors:  Patrick F Fogarty
Journal:  Hematol Oncol Clin North Am       Date:  2009-12       Impact factor: 3.722

Review 8.  The geoepidemiology of immune thrombocytopenic purpura.

Authors:  Sean Deane; Suzanne S Teuber; M Eric Gershwin
Journal:  Autoimmun Rev       Date:  2009-11-27       Impact factor: 9.754

9.  Self-reported health-related quality of life in adults with chronic immune thrombocytopenic purpura.

Authors:  Robert McMillan; James B Bussel; James N George; Deepa Lalla; Janet L Nichol
Journal:  Am J Hematol       Date:  2008-02       Impact factor: 10.047

10.  American Society of Hematology 2019 guidelines for immune thrombocytopenia.

Authors:  Cindy Neunert; Deirdra R Terrell; Donald M Arnold; George Buchanan; Douglas B Cines; Nichola Cooper; Adam Cuker; Jenny M Despotovic; James N George; Rachael F Grace; Thomas Kühne; David J Kuter; Wendy Lim; Keith R McCrae; Barbara Pruitt; Hayley Shimanek; Sara K Vesely
Journal:  Blood Adv       Date:  2019-12-10
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