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Abstract
- The standard anticoagulant for preventing
thromboembolic events after
hip or knee replacement surgery is a
subcutaneous low-molecular-weight
heparin such as enoxaparin.
- Dabigatran, a specific thrombin
inhibitor, was recently licensed for oral
prophylaxis in this setting, as dabigatran
etexilate (mesilate), a prodrug.
- The clinical evaluation of dabigatran
in this indication is based on two comparative
double-blind trials with similar
protocols, comparing dabigatran
150 mg or 220 mg/day versus enoxaparin
in 3494 patients undergoing hip
replacement surgery and 2101 patients
undergoing knee replacement surgery.
- The results were virtually identical:
compared with enoxaparin, dabigatran
did not reduce overall mortality
(almost zero in the different groups),
the frequency of symptomatic pulmonary
embolism (almost zero in the
different groups), or the frequency of
symptomatic deep venous thrombosis
(0.1% to 1.2%).
- There was no difference between
the groups with respect to the frequency
of severe bleeding (about
1.5%), hepatic disorders (about 4%), or
acute coronary events (a few cases).
But dabigatran was associated with
surgical wound seepage in 7% of
patients, versus 4.7% with enoxaparin.
- The anticoagulant effect of dabigatran,
and therefore the frequency of
haemorrhage, increases with age and
in cases of renal failure. However, clinical
trials included relatively few elderly
patients and/or patients with renal failure,
who nonetheless represent a large
proportion of the candidates for hip or
knee replacement.
- Dabigatran becomes more potent
when combined with P-glycoprotein
inhibitors or with drugs that impair
renal function. Combination with other
antithrombotic drugs should be avoided.
- Dabigatran is administered orally,
while enoxaparin requires daily subcutaneous
injections. Dabigatran therapy
does not necessitate laboratory
monitoring, while the platelet count
must be monitored with enoxaparin.
There is no known antidote for dabigatran
overdose.