News

Stroke Study Expands Window
of Clot Removal Treatment
for Some Patients

A procedure to remove clots from blocked brain vessels—known as thrombectomy—may be beneficial for some stroke patients even if they come in to the emergency room beyond the six-hour treatment window that current guidelines endorse, according to a groundbreaking study conducted by an international team of physicians and researchers led by the University of Pittsburgh Medical Center (UPMC) and Emory University.

The results, which were first announced in May at the European Stroke Organization Conference, were published Saturday, November 11, in the New England Journal of Medicine.

"When the irreversibly damaged brain area affected by the stroke is small, we see that clot removal can make a significant positive difference, even if performed outside the six hour window," says Tudor Jovin, MD, director of the UPMC Stroke Institute, director of the UPMC Center for Endovascular Therapy, and a professor of neurology and neurosurgery at the University of Pittsburgh who coled the trial. "However, this does not diminish urgency with which patients must be rushed to the [emergency room] in the event of a stroke. The mantra 'time is brain' still holds true."

In the study, researchers randomly assigned stroke victims who arrived at the hospital outside the six-hour time window to either thrombectomy or to standard medical therapy. To select patients for the trial, the researchers used a new paradigm, which used brain imaging and clinical criteria as opposed to just time alone.

"Looking at the physiological state of the brain and evaluating the extent of damage and other clinical factors may be a better way to decide if thrombectomy will benefit patients as opposed to adhering to a rigid time window," says coprincipal investigator Raul Nogueira, MD, a professor of neurology, neurosurgery, and radiology at Emory University School of Medicine and director of neuroendovascular service at Marcus Stroke & Neuroscience Center, Grady Memorial Hospital.

Brain imaging and clinical information (neurological deficit) was used to identify and enroll patients who had a small area of irreversibly damaged brain and a significantly larger brain tissue area that was imminently threatened by loss of blood supply, but still alive—a criterion known as clinical infarct mismatch.

The results showed that almost one-half of the patients (48.6%) receiving endovascular therapy had a good outcome—defined as the patient being independent in activities of daily living—at 90 days after treatment and showed clinical benefit, while only 13.1% showed benefit in the group that received clot-busting drugs alone. There was no difference in mortality between the two groups.

The researchers planned to enroll a maximum of 500 patients over the course of the study period. However, a preplanned intermediate review of the treatment effectiveness when 200 patients were enrolled led the independent Data Safety Monitoring Board overseeing the study to recommend early termination of the trial based on predefined criteria demonstrating that clot removal provided significant clinical benefit in the selected patients.

The multicenter international study known as the DAWN trial included trial locations in the United States, Spain, France, Australia, and Canada. The trial was sponsored by Stryker Corporation, which manufactures the clot removal devices used in the study.