Variant clinical courses in children with immune thrombocytopenic purpura: Sixteen year experience of a single medical center

Bibliographic Details
Title: Variant clinical courses in children with immune thrombocytopenic purpura: Sixteen year experience of a single medical center
Authors: Işın Yaprak, Berna Atabay, İkbal Durak, Meral Türker, Haldun Öniz, Esra Arun Özer
Source: Turkish Journal of Hematology, Vol 27, Iss 3, Pp 147-155 (2010)
Publisher Information: Galenos Publishing House, 2010.
Publication Year: 2010
Collection: LCC:Diseases of the blood and blood-forming organs
Subject Terms: immune thrombocytopenic purpura, children, clinical course, chronic, recurrent, outcome, Diseases of the blood and blood-forming organs, RC633-647.5
More Details: OBJECTIVE: Immune thrombocytopenic purpura (ITP) is the most common cause of acquired thrombocytopenia in children. The objective of this study was to evaluate the presenting features, variation in the clinical courses, initial response rate to therapy, and long-term outcome in patients with ITP. METHODS: Three hundred and fifty out of 491 newly diagnosed patients with ITP between the initial diagnosis ages of 6 months to 16 years were included in this retrospective, descriptive study. Patients with acute vs chronic ITP, acute vs recurrent ITP and chronic vs recurrent ITP were compared in terms of age at diagnosis, gender, initial platelet count, response rate to initial therapy, long-term outcome, and total duration of follow-up. RESULTS: The clinical courses of the patients were determined as acute, chronic and recurrent in 63.8%, 29.1%, and 7.1%, respectively. Platelet count >20x109/L and initial diagnosis age >10 years were found to increase the probability of chronic outcome by at least two-fold. CONCLUSION: It is concluded that ITP in childhood is a common disease with low morbidity and mortality. In addition to the acute and chronic form, a rare recurrent form, which accounts for about 4-7% of all ITP patients, should be considered.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1308-5263
Relation: https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-44227; https://doaj.org/toc/1308-5263
DOI: 10.5152/tjh.2010.21
Access URL: https://doaj.org/article/f5007f5000cd495bbf565c5be92085fe
Accession Number: edsdoj.f5007f5000cd495bbf565c5be92085fe
Database: Directory of Open Access Journals
More Details
ISSN:13085263
DOI:10.5152/tjh.2010.21
Published in:Turkish Journal of Hematology
Language:English