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Perioperative management of a heterozygous carrier of Glanzmann's thrombasthenia submitted to coronary artery bypass grafting with cardiopulmonary bypass.

Abstract
Glanzmann's thrombasthenia is a congenital hemorrhagic disorder transmitted as an autosomal recessive trait and characterized by altered production and/or assembly of the platelet membrane glycoprotein IIb/IIIa receptor. We describe the perioperative management of a heterozygous carrier of Glanzmann's thrombasthenia submitted to cardiac surgery with cardiopulmonary bypass and the case was complicated by early excessive postoperative bleeding.
AuthorsValter Casati, Armando D'Angelo, Luciano Barbato, Edoardo Rossi, Maria Antonietta Grasso, Salvatore Spagnolo, Ezio Panzeri
JournalAnesthesia and analgesia (Anesth Analg) Vol. 103 Issue 2 Pg. 309-11, table of contents (Aug 2006) ISSN: 1526-7598 [Electronic] United States
PMID16861409 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Tranexamic Acid
Topics
  • Aged
  • Cardiopulmonary Bypass
  • Coronary Artery Bypass
  • Heterozygote
  • Humans
  • Male
  • Postoperative Hemorrhage (etiology)
  • Thrombasthenia (complications)
  • Tranexamic Acid (therapeutic use)

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