Immune thrombocytopenia: no longer 'idiopathic'

Cleve Clin J Med. 2011 Jun;78(6):358-73. doi: 10.3949/ccjm.78gr.10005.

Abstract

Immune thrombocytopenia (ITP) is a common hematologic disorder. Its pathogenesis involves both accelerated platelet destruction and impaired platelet production. First-line agents are usually effective initially but do not provide long-term responses. Splenectomy remains an effective long-term therapy, as does rituximab (Rituxan) in a subset of patients. Thrombopoietic agents offer a new alternative, although their place in the overall management of ITP remains uncertain.

Publication types

  • Review

MeSH terms

  • Adrenal Cortex Hormones / therapeutic use
  • Anti-Inflammatory Agents / therapeutic use
  • Antibodies, Monoclonal, Murine-Derived / therapeutic use
  • Humans
  • Immunologic Factors / therapeutic use
  • Purpura, Thrombocytopenic, Idiopathic / diagnosis
  • Purpura, Thrombocytopenic, Idiopathic / etiology
  • Purpura, Thrombocytopenic, Idiopathic / therapy*
  • Receptors, Thrombopoietin / agonists
  • Rituximab
  • Splenectomy

Substances

  • Adrenal Cortex Hormones
  • Anti-Inflammatory Agents
  • Antibodies, Monoclonal, Murine-Derived
  • Immunologic Factors
  • Receptors, Thrombopoietin
  • Rituximab