http://www.neurology.org/content/84/14_Supplement/P4.301.short
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Neurology April 6, 2015 vol. 84 no. 14 Supplement P4.301
- Abstract
Abstract
Background: Temporary discontinuation of warfarin for endovascular procedures is necessary to avoid risk of bleeding complications. The
risks and benefits associated with such discontinuation are not well described.
Methods: We reviewed the medical
records of patients who underwent discontinuation of warfarin prior to
endovascular procedures. The
primary end point was ischemic stroke during
warfarin discontinuation, occurrence of death, cerebral infarction, and
unplanned
or urgent endovascular or surgical intervention.
The primary safety end point was bleeding, for which complications were
classified
according to the Thrombolysis in Myocardial
Infarction scheme as major (hemoglobin decrease of more than 5 g/dl),
minor (hemoglobin
decrease of 3-5 g/dl), or insignificant.
Results: Seventy three patients
(mean age, 68.4 ± 70.4 yr; 43 men) underwent discontinuation of warfarin
prior to endovascular procedure.
Low molecular weight heparin was instituted after
discontinuation of warfarin in 27 of 73 patients. Mean (±SD)
international
normalized ratio was 1.1 ± 0.2 prior to procedure.
Warfarin was restarted within 1 day (n=9), 2-4 days (n=17) or greater
than
4 days (n=1) after procedure. Among the 27 patients
who underwent discontinuation, no intracerebral hemorrhages and 2 and
5 ischemic strokes occurred during the period of
warfarin discontinuation in bridging and without bridging therapy or
during
1-month follow-up period, respectively. Stroke
events occurred within 1 day (n=0), 2-4 days (n=0) or greater than 4
days (n=2)
after procedure. There was one episode of major
bleeding from the femoral insertion site. The risk of ischemic stroke
was
similar in patients who did or did not receive
interim low molecular weight heparin (2 of 27 versus 5 of 46, p=0.7).
The duration
of warfarin discontinuation was correlated with
risk of ischemic stroke.
Conclusions: The risk of ischemic stroke during discontinuation of warfarin is higher than expected and requires a careful evaluation
of risk and benefits.
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