AI Article Synopsis

  • The study examines the impact of thrombopoietin receptor agonists (TPO-RA) on treating immune thrombocytopenia (ITP) in adults over ten years, highlighting a shift in treatment guidelines.
  • Older patients (over 65) showed higher platelet counts and fewer bleeding issues but had more prothrombotic risks compared to younger patients.
  • The use of TPO-RAs has led to a significant decrease in the necessity for splenectomy and intravenous immunoglobulin treatments, especially in younger patients, indicating their effectiveness as a first-line treatment alternative.

Article Abstract

Background: Ten years after their availability, thrombopoietin receptor agonists (TPO-RA) have heralded a paradigm shift in the treatment of immune thrombocytopenia (ITP). This study was aimed to analyze the implementation of current recommendations in the standard practice of adult ITP patients, and how age may influence those changes.

Methods: We included 121 adult patients (> 65 years, n = 54; younger individuals, n = 67) who initiated treatment with TPO-RA between January 2012 and December 2014.

Results: Patients older than 65 years treated with TPO-RA presented at diagnosis with significantly higher platelet counts, less bleeding, and a more prothrombotic profile than younger ones. The high efficacy rates of TPO-RA, preferentially used during the last decade in non-chronic phases, precluded from further therapies in the majority of ITP patients. Their administration was associated with a sharp decline in the last decade in the use of splenectomy and intravenous immunoglobulin, especially in younger ITP individuals.

Conclusion: These results confirm (1) that there is a preferential use of TPO-RAs in elderly ITP patients with fewer bleeding complications but more unfavorable prothrombotic conditions than in younger individuals, and (2) that early use of these agents has been established as an effective therapeutic alternative to other second line therapies.

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Source
http://dx.doi.org/10.1016/j.bcmd.2020.102505DOI Listing

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