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Published on 10 February 2012

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Rivaroxaban ‘safer’ than warfarin for stroke prevention

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Rivaroxaban may be better than warfarin at preventing clot-related strokes in patients with atrial fibrillation while minimising the risk of causing a bleeding stroke, according to research presented at the American Stroke Association’s International Stroke Conference 2012.

The finding stems from a sub-analysis of data in a large, randomised clinical trial called ROCKET AF, conducted in 45 countries at 1,178 sites.

Among patients with the most common type of atrial fibrillation, without any history of heart valve damage, those who received rivaroxaban were 34% less likely to experience an intracranial haemorrhage, compared with those on warfarin, the study found.

“We have to be very careful about giving anticoagulants to patients at risk of bleeding into the brain, and therefore need to be able to identify who these patients are,” said lead author Graeme Hankey, Neurologist at the Royal Perth Hospital and University of Western Australia.

“Anticoagulant drugs can prevent ischemic strokes, but paradoxically, they can cause intracranial bleeding, including haemorrhagic strokes.”

The new study also identified five risk factors, independent of the treatment used, that increased the likelihood that AF patients would suffer intracranial bleeding:

  • Blacks had a 4.2-fold increased risk compared to whites; Asians’ increased risk was two-fold. Other races did not have a meaningful higher risk.
  • In older people, risk increased by one third for every 10 years of age.
  • A prior stroke or transient ischemic attack (TIA) boosted the risk 51%.
  • Decreased levels of serum albumin, a protein that helps keep fluid from leaking out of blood vessels, increased the risk 42% for every decrease in albumin by 0.5 g/l.
  • A low platelet count also increased the risk of intracranial bleeding.

 

ROCKET AF’s primary finding, reported last year at the American Heart Association’s Scientific Sessions 2010, showed rivaroxaban equal to warfarin in preventing stroke or systemic blood clots in the AF patients.

However, rivaroxaban patients had less intracranial bleeding and fatal bleeding. The new research aimed to determine the rate and locations of intracranial bleeding that occurred in ROCKET AF.

None of the study participants had experienced intracranial bleeding at enrollment, but 53% had suffered a prior ischemic stroke.

After a median follow-up of about two years, researchers found 136 of the 14,264 participants had experienced an intracranial bleed – a low rate overall of about 0.5% per year according to Hankey.

Use of aspirin or a thienopyridine drug was associated with an increased risk of intracranial bleeding during the trial. However, taking rivaroxaban during the trial was associated with a lower risk of intracranial hemorrhage than taking warfarin.

The findings apply only to nonvalvular AF patients at moderate or high risk of stroke, such as those enrolled in the ROCKET AF trial, Hankey said. The validity of these findings in other populations of patients with AF awaits further study.

International Stroke Conference



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