| Literature DB >> 27129318 |
Işıl Bavunoğlu1, Ahmet Emre Eşkazan2, Muhlis Cem Ar3, Mahir Cengiz1, Serap Yavuzer1, Ayşe Salihoğlu2, Şeniz Öngören2, Aydın Tunçkale1, Teoman Soysal2.
Abstract
Immune thrombocytopenia (ITP) is the most frequent cause of acquired thrombocytopenia. In adult ITP patients, corticosteroids and intravenous immunoglobulin (IVIg) are used as first-line treatment. The aim of the present study was to investigate retrospectively the demographic and etiologic characteristics of patients with ITP admitted to the emergency room at our hospital. Seventy-five adult patients with ITP were included, and demographic data, bleeding characteristics, etiologic features and responses to treatments were evaluated retrospectively. Fifty-six patients (75 %) were female, and the median age was 43 years. Eighteen patients had a history of ITP, whereas in 57, thrombocytopenia was identified for the first time. During admission, the median platelet count was 5 × 10(9)/L. Cutaneous and/or mucosal bleeding was the most common clinical feature. High-dose dexamethasone was administered in 60 episodes, whereas IVIg and conventional-dose methylprednisolone were used in nine and six episodes, respectively. The overall response rate of the entire cohort following first-line treatments was 67 %, and complete remission was achieved in 31 patients, 19 patients achieved partial remission, and 25 patients were non-responders. In cases with life-threatening bleeding, concomitant infection, post-traumatic bleeding and need for emergency surgery, IVIg can be used as the first line of treatment option in addition to platelet transfusions.Entities:
Keywords: Conventional-dose methylprednisolone; Emergency room; High-dose dexamethasone; Immune thrombocytopenia; Intravenous immunoglobulin
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Year: 2016 PMID: 27129318 DOI: 10.1007/s12185-016-2003-5
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.490