Objective: To report the initial clinical experience with fibrinogen d
epletion using ancrod as prophylaxis and treatment for deep vein throm
bosis and pulmonary embolism (DVT/PE) in patients with multiple trauma
. Design: A series of cases, selected because of their extreme risk of
DVT/PE or because of the appearance of thromboembolic complications d
espite prophylaxis using conventional methods. Setting: University tea
ching hospital. Patients: A referred sample comprising 30 patients wit
h multiple blunt trauma. The mean injury severity score was 30. Most c
ases involved a combination of lower extremity, pelvic and chest injur
ies. Interventions: Fibrinogen was slowly depleted over 24 to 36 hours
and the concentration maintained at 0.2 to 0.5 g/L thereafter. Ancrod
was continued prophylactically (22 patients) or for established DVT/P
E (8 patients) until the patients were mobilized or until there was no
longer a contraindication to heparin, or until treatment with warfari
n became practical. Main Outcome Measure: Monitoring for DVT by duplex
ultrasonography or iodine-125-labelled-fibrinogen scanning, whichever
could be applied. Results: Twenty patients were treated with ancrod f
or prophylaxis from the outset because it offered theoretic and practi
cal benefits over other methods. No patient treated with ancrod for pr
ophylaxis suffered a clinically significant DVT/PE. Patients in whom h
eparin prophylaxis failed and who experienced thromboembolic complicat
ions were effectively managed with ancrod. There were no deaths and no
bleeding complications specifically due to the therapy. Conclusions:
Slow depletion of fibrinogen with ancrod may provide a safe and effect
ive means to prevent DVT/PE in multiple trauma patients or to treat DV
T/PE when the risk of bleeding from heparin is great. This initial exp
erience should be evaluated by a randomized controlled trial.