Thromb Haemost 1985; 53(02): 235-238
DOI: 10.1055/s-0038-1661282
Original Article
Schattauer GmbH Stuttgart

Plasma Beta-Thromboglobulin, Fibrinopeptide A and Bβ15–42 Antigen in Relation to Postoperative DVT, Malignancy and Stanozolol Treatment

Jessie T Douglas
The University Depts. of Medicine and Surgery, Glasgow Royal Infirmary, Glasgow, UK
,
S L Blamey
The University Depts. of Medicine and Surgery, Glasgow Royal Infirmary, Glasgow, UK
,
G D O Lowe
The University Depts. of Medicine and Surgery, Glasgow Royal Infirmary, Glasgow, UK
,
D C Carter
The University Depts. of Medicine and Surgery, Glasgow Royal Infirmary, Glasgow, UK
,
C D Forbes
The University Depts. of Medicine and Surgery, Glasgow Royal Infirmary, Glasgow, UK
› Author Affiliations
Further Information

Publication History

Received 20 September 1984

Accepted 17 January 1985

Publication Date:
18 July 2018 (online)

Summary

Plasma levels of betathromboglobulin (BTG), fibrinopeptide A (FPA) and Bβ15–42 fragment, indices of platelet release, thrombin generation and plasmin activity respectively, were measured in 32 high risk patients during a double blind study of a single dose of the anabolic steroid stanozolol (50 mg IM) in the prevention of DVT after major gastro-intestinal surgery. The prevalence of malignancy and the incidence of DVT (125I fibrinogen scan) were similar in the two treatment groups. On the first postoperative day, BTG, FPA and Bβ15–42 levels were increased in most patients. Plasma BTG levels were significantly increased on the first post-operative day in patients who developed a DVT (n = 14) compared to those patients who did not (n = 18). A significant increase in FPA levels was found in the DVT group, 7 days after surgery. On the morning before surgery, plasma Bβ15–42 levels were significantly increased in patients who developed a DVT. In patients undergoing surgery for early malignancy (n = 17), we observed a pre-operative increase in FPA levels when compared to patients without malignancy. At post-operative day 7, Bβ15–42 levels were significantly increased in patients who received stanozolol (n = 15), when compared to the placebo group, suggesting that intramuscular stanozolol increases fibrinolysis in vivo.

 
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