rome and Purpura--Thrombocytopenic--Idiopathic

rome has been researched along with Purpura--Thrombocytopenic--Idiopathic* in 3 studies

Reviews

1 review(s) available for rome and Purpura--Thrombocytopenic--Idiopathic

ArticleYear
Idiopathic thrombocytopenic purpura (ITP) in children.
    Pediatric blood & cancer, 2006, Oct-15, Volume: 47, Issue:5 Suppl

    Idiopathic thrombocytopenic purpura in children remits spontaneously in the majority of cases but most children require treatment. Between 1995 and 2005, 265 children (0-15 years old) have been consecutively observed and treated: 28 children with high doses of methylprednisolone (HDMP) (15 mg/kgx4 days), 63 with HDMP (7.5 mg/kgx4 days), 37 with HD dexamethasone (DXM) pulses, 29 with low doses of MP, and 51 with different doses of intravenous immunoglobulins (IVIG) (0.4 or 0.8 g/kg). Fifty-seven children have not been treated because of a platelet count>or=10x10(9)/L and no significant bleeding. Two hundred forty-four (92.1%) children reached a persistent CR, 237 (89.4%) after a first-line treatment or the wait and see strategy. No statistically significant differences in CR related to different treatments have been observed. IVIG and HDMP (7.5 mg/kg for 4 days) are the best treatments to reach quickly safe platelet levels>or=30x10(9)/L (3-6 days) and CR (7-11 days). Among non-responding (NR) patients, seven have been splenectomized and three reached stable CR. These results emphasize differences with adult ITP.

    Topics: Adolescent; Child; Child, Preschool; Humans; Infant; Infant, Newborn; Platelet Count; Purpura, Thrombocytopenic, Idiopathic; Retrospective Studies; Risk Factors; Rome; Treatment Outcome

2006

Other Studies

2 other study(ies) available for rome and Purpura--Thrombocytopenic--Idiopathic

ArticleYear
Activity and safety profile of low-dose rituximab for the treatment of autoimmune cytopenias in adults.
    Haematologica, 2007, Volume: 92, Issue:12

    We conducted a retrospective analysis of 11 consecutive patients with various autoimmune cytopenias who failed to respond to conventional treatments and received a fixed-dose regimen of rituximab (100 mg weekly for 4 consecutive weeks). Sustained complete responses were achieved in 4 out of 7 patients with idiopathic thrombocytopenic purpura and in 1 patient with autoimmune pancytopenia. A partial response was observed in 1 patient with autoimmune hemolytic anemia. The immunotherapy had no effect in 1 patient with pure red cell aplasia or in 1 patient with autoimmune neutropenia. No infusion-related or delayed toxicities attributable to rituximab were experienced by any of the patients.

    Topics: Adult; Aged, 80 and over; Anemia, Hemolytic, Autoimmune; Antibodies, Monoclonal; Antibodies, Monoclonal, Murine-Derived; Female; Humans; Immunologic Factors; London; Male; Middle Aged; Neutropenia; Pancytopenia; Purpura, Thrombocytopenic, Idiopathic; Red-Cell Aplasia, Pure; Remission Induction; Retrospective Studies; Rituximab; Rome

2007
ITP: an overview of the conference and future directions with an abbreviated ITP history.
    Journal of pediatric hematology/oncology, 2003, Volume: 25 Suppl 1

    Topics: Greece, Ancient; History, Ancient; Humans; Purpura, Thrombocytopenic, Idiopathic; Research; Research Design; Rome; T-Lymphocytes

2003