Literature DB >> 1903723

Blood loss and safety with desmopressin or placebo during aorto-iliac graft surgery.

S Lethagen1, P Rugarn, D Bergqvist.   

Abstract

In a double blind, placebo controlled study in 50 patients undergoing aorto-iliac graft surgery, we studied the effects of desmopressin given prior to surgery on blood loss and blood transfusion requirements. Desmopressin reduced the number of patients with clinically significant bleeding. Blood loss volumes and transfusion requirements were lower in the desmopressin group, but this could not be verified statistically. Even if our study population has a high incidence of generalised arteriosclerotic disease, there were no clinical manifestations of venous thromboembolism, no increase of graft occlusions and no myocardial infarction during the operative or early postoperative period. Desmopressin may be used in patients with excessive peroperative bleeding or a prolonged preoperative bleeding time. In patients where desmopressin is considered to be haemostatically efficacious, it may be used with a maintained margin of safety.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1903723     DOI: 10.1016/s0950-821x(05)80684-x

Source DB:  PubMed          Journal:  Eur J Vasc Surg        ISSN: 0950-821X


  3 in total

Review 1.  Desmopressin for minimising perioperative allogeneic blood transfusion.

Authors:  P A Carless; D A Henry; A J Moxey; D O'Connell; B McClelland; K M Henderson; K Sly; A Laupacis; D Fergusson
Journal:  Cochrane Database Syst Rev       Date:  2004

Review 2.  Pharmacological strategies to decrease transfusion requirements in patients undergoing surgery.

Authors:  Robert J Porte; Frank W G Leebeek
Journal:  Drugs       Date:  2002       Impact factor: 9.546

Review 3.  Desmopressin use for minimising perioperative blood transfusion.

Authors:  Michael J Desborough; Kathryn Oakland; Charlotte Brierley; Sean Bennett; Carolyn Doree; Marialena Trivella; Sally Hopewell; Simon J Stanworth; Lise J Estcourt
Journal:  Cochrane Database Syst Rev       Date:  2017-07-10
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.