Literature DB >> 9556088

Idiopathic thrombocytopenic purpura: a guideline for diagnosis and management of children and adults. American Society of Hematology.

J N George1, S H Woolf, G E Raskob.   

Abstract

Idiopathic thrombocytopenic purpura (ITP, also known as immune thrombocytopenic purpura) affects both children and adults. In childhood, the peak age is 2-4 years, girls and boys are equally affected, and in most children, the disease is self-limited with spontaneous recovery occurring in several weeks to several months. In adults, ITP is most common among young women, and the disease is more insidious in its onset and chronic in its course. In both children and adults, there are important unresolved issues in diagnosis and management that have major cost implications. For this reason, the American Society of Hematology chose ITP as the disease topic for its initial practice guideline in 1993. In 1996, the practice guideline was published in Blood, the Journal of the American Society of Hematology. This review describes the principle features of ITP in children and adults, the process of development of the practice guideline for ITP, and the implications of the guideline for the diagnosis and management of patients with ITP.

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Year:  1998        PMID: 9556088     DOI: 10.3109/07853899808999383

Source DB:  PubMed          Journal:  Ann Med        ISSN: 0785-3890            Impact factor:   4.709


  5 in total

1.  CNR2 functional variant (Q63R) influences childhood immune thrombocytopenic purpura.

Authors:  Francesca Rossi; Silvia Mancusi; Giulia Bellini; Domenico Roberti; Francesca Punzo; Simona Vetrella; Sofia Maria Rosaria Matarese; Bruno Nobili; Sabatino Maione; Silverio Perrotta
Journal:  Haematologica       Date:  2011-08-09       Impact factor: 9.941

Review 2.  Treatment of immune thrombocytopenic purpura in children : current concepts.

Authors:  Aziza T Shad; Corina E Gonzalez; S G Sandler
Journal:  Paediatr Drugs       Date:  2005       Impact factor: 3.022

3.  Correction of Th1-dominant cytokine profiles by high-dose dexamethasone in patients with chronic idiopathic thrombocytopenic purpura.

Authors:  Chengshan Guo; Xiaoxia Chu; Yan Shi; Weidong He; Lizhen Li; Lin Wang; Yingxue Wang; Jun Peng; Ming Hou
Journal:  J Clin Immunol       Date:  2007-07-06       Impact factor: 8.317

4.  A case of refractory immune thrombocytopenia in pregnancy managed with elthrombopag.

Authors:  Jyothis Purushothaman; Kochuthresia J Puthumana; Aswath Kumar; Susheela J Innah; Sareena Gilvaz
Journal:  Asian J Transfus Sci       Date:  2016 Jul-Dec

5.  When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura.

Authors:  Ying-Ying Jin; Jing Wu; Tong-Xin Chen; Ji Chen
Journal:  Front Immunol       Date:  2019-07-09       Impact factor: 7.561

  5 in total

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