Abstract

ABSTRACTObjectives: To describe routine treatment and clinical characteristics of patients with chronic ITP (cITP).Methods: We used data from Danish nationwide registers and medical records to examine routine clinical care, including splenectomy and medical treatment, of Danish patients with chronic immune thrombocytopenia (cITP, defined as two or more ITP diagnoses at least 6 months apart), i.e. treatment initiation before cITP diagnosis and treatment initiation within one year post-diagnosis for treatment-naïve patients.Results: Nearly half of all 964 cITP patients diagnosed during 2009–2015 initiated treatment between initial ITP diagnosis and chronic onset; 43% received glucocorticoids, 12% received IVIG and 18% received rituximab. Within one year post-diagnosis, 9.2% of previously untreated patients commenced therapy, most often corticosteroids and rituximab.Discussion: Our results are in line with findings of recent studies from other countries.Conclusion: We found that corticosteroids, IVIG, and rituximab are common first- choice of ITP drugs. Bleeding events occurred in nearly one third of treated patients in the year before cITP diagnosis and in 5% of the treatment-naïve patients. A substantial number of patients do not need treatment during the first 6–12 months. However, some of these patients will subsequently need treatment as the disease may worsen, indicating the need for continuous follow-up of these patients.

Highlights

  • Immune thrombocytopenic purpura (ITP) is an autoimmune disease characterized by platelet destruction and decreased production [1]

  • Half (n = 469, 49%) of patients were treated between their initial ITP diagnosis date and their subsequent chronic ITP (cITP) diagnosis date

  • 43% had a record of treatment with corticosteroids, 18% with rituximab, 12% with intravenous immunoglobulin (IVIG), 3.7% with splenectomy, 3.1% with Thrombopoietin receptor agonists (TPO-RA), and 12% with supportive treatment (Table 2)

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Summary

Introduction

Immune thrombocytopenic purpura (ITP) is an autoimmune disease characterized by platelet destruction and decreased production [1]. Patients with low platelet counts may present with a spectrum of symptoms, ranging from being asymptomatic to severe bleeding diathesis [2]. Severe bleeding events occur in about 10% of adult ITP patients [3]. Corticosteroids alone or in combination with intravenous immunoglobulin (IVIG) are considered as the first-line therapies in ITP, whereas splenectomy, immunosuppressive treatment and Thrombopoietin receptor agonists (TPO-RA) are used in patients failing steroids [4]. Treatment is recommended for patients with bleeding symptoms or at high risk of bleeding. Initiation of treatment is recommended if platelet counts fall below 30 × 109/L [4,5]

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