Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2005-1-11
pubmed:abstractText
Immune thrombocytopenic purpura (ITP) is an acquired autoimmune disease characterized by platelet destruction. Glucocorticoids are the first-choice treatment, resulting in a complete (CR) or partial (PR) response in 70-80% of cases. In most cases, however, response is transient or glucocorticoid-dependent. For these and for selected patients with acute refractory ITP, splenectomy may produce a good response (CR+PR) in about 60-80% of cases. We report here the long-term outcome of a large cohort of ITP splenectomized patients.
pubmed:commentsCorrections
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1592-8721
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
90
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
72-7
pubmed:meshHeading
pubmed-meshheading:15642672-Adolescent, pubmed-meshheading:15642672-Adult, pubmed-meshheading:15642672-Aged, pubmed-meshheading:15642672-Aged, 80 and over, pubmed-meshheading:15642672-Analysis of Variance, pubmed-meshheading:15642672-Child, pubmed-meshheading:15642672-Child, Preschool, pubmed-meshheading:15642672-Disease-Free Survival, pubmed-meshheading:15642672-Female, pubmed-meshheading:15642672-Humans, pubmed-meshheading:15642672-Infant, pubmed-meshheading:15642672-Male, pubmed-meshheading:15642672-Middle Aged, pubmed-meshheading:15642672-Platelet Count, pubmed-meshheading:15642672-Postoperative Complications, pubmed-meshheading:15642672-Prognosis, pubmed-meshheading:15642672-Purpura, Thrombocytopenic, Idiopathic, pubmed-meshheading:15642672-Remission Induction, pubmed-meshheading:15642672-Retrospective Studies, pubmed-meshheading:15642672-Splenectomy, pubmed-meshheading:15642672-Treatment Outcome
pubmed:year
2005
pubmed:articleTitle
Efficacy and safety of splenectomy in immune thrombocytopenic purpura: long-term results of 402 cases.
pubmed:affiliation
Hematology and Oncology Institute L. and A. Seràgnoli, University of Bologna. nvianel@med.unibo.it
pubmed:publicationType
Journal Article, Multicenter Study