New device to remove stroke-causing blood clots proves better than standard tool
The Solitaire™ FR Revascularization Device is a new device that restores blood flow and
retrieves clots from blocked blood vessels in patients experiencing acute ischemic stroke.
August 26, 2012
By Amy Albin
Stroke is the fourth leading cause of death and a common cause of long-term disability in the United States,
but doctors have very few proven treatment methods. Now a new device that mechanically removes stroke-causing
clots from the brain is being hailed as a game-changer.
Lately, with all of
the pradaxa lawsuits surfacing,
many anticoagulants commonly used to prevent stroke and heart attack due to blood clotting are coming under intense scrutiny.
A quick visit to DrugNews.net and one can read all about the latest health risks and
lawsuits emerging in the medical world. With patient safety on the line, the debut of the SOLITAIRE Flow Restoration Device
is making positive waves across the medical community.
In a recent clinical trial, the SOLITAIRE Flow Restoration Device dramatically outperformed the standard mechanical treatment.
Findings from the trial, called SOLITAIRE With the Intention for Thrombectomy (SWIFT), are published online today in the journal
and will also appear in a later print edition of the journal.
SOLITAIRE, which was approved by the U.S. Food and Drug Administration in March, is among an entirely new generation of
devices designed to remove blood clots from blocked brain arteries in patients experiencing an ischemic stroke.
It has a self-expanding, stent-like design, and once inserted into a blocked artery using a thin catheter tube,
it compresses and traps the clot. The clot is then removed by withdrawing the device, reopening the blocked blood vessel.
"This new device is significantly changing the way we can treat ischemic stroke," said the study's lead author,
Dr. Jeffrey L. Saver, director of the
UCLA Stroke Center
and a professor of neurology at the
David Geffen School of Medicine at UCLA.
"We are going from our first generation of clot-removing procedures, which were only moderately good in reopening target arteries,
to now having a highly effective tool."
Results of the study showed that the device opened blocked vessels without causing symptomatic bleeding in or around the brain
in 61 percent of patients. The standard FDA–approved mechanical device — a corkscrew-type clot remover called the MERCI
Retriever — was effective in 24 percent of cases.
The use of SOLITAIRE also led to better survival three months after a stroke. There was a 17.2 percent mortality rate with the
new device, compared with a 38.2 percent rate with the older one.
About 87 percent of all strokes are caused by blood clots blocking a blood vessel supplying the brain. The stroke treatment
that has received the most study is an FDA–approved clot-busting drug known as tissue plasminogen activator, but this drug
must be given within four-and-a-half hours of the onset of stroke symptoms, and even more quickly in older patients.
When clot-busting drugs cannot be used or are ineffective, the clot can sometimes be mechanically removed during, or beyond,
the four-and-a-half–hour window. The current study, however, did not compare mechanical clot removal to drug treatment.
For the trial, researchers randomly assigned 113 stroke patients at 18 hospitals to receive either SOLITAIRE or MERCI therapy
within eight hours of stroke onset, between January 2010 and February 2011. The patients' average age was 67, and 68 percent
were male. The time from the beginning of stroke symptoms to the start of the clot-retriever treatment averaged 5.1 hours.
Forty percent of the patients had not improved with standard clot-busting medication prior to the study, while the remainder
had not received it.
At the suggestion of a safety monitoring committee, the trial was ended nearly a year earlier than planned due to significantly
better outcomes with the experimental device.
Other statistically significant findings included:
•2 percent of SOLITAIRE-treated patients had symptoms of bleeding in the brain, compared with 11 percent of MERCI patients.
•At the 90-day follow-up, overall adverse event rates, including bleeding in the brain, were similar for the two devices.
•58 percent of SOLITAIRE-treated patients had good mental/motor functioning at 90 days, compared with 33 percent of MERCI patients.
•The SOLITARE device also opened more vessels when used as the first treatment approach, necessitating fewer subsequent attempts
with other devices or drugs.
"Nearly a decade ago, our UCLA Stroke Center team invented the first stroke retrieval device — the MERCI Retriever — and now
we are pleased to have helped develop and successfully test a superior, next-generation clot removing device," said Dr. Reza Jahan,
associate professor of radiology at UCLA and the study's principal neurointerventional investigator, who also led the pre-clinical
studies. "It is exciting to have a highly effective new tool that can improve the outcomes for more stroke patients."
Additional co-authors included Dr. Elad Levy, Dr. Tudor G. Jovin, Dr. Blaise Baxter, Dr. Raul Nogueira, Dr. Wayne Clark,
Dr. Ronald Budzik, Dr. Osama O. Zaidat and the SWIFT trial investigators.
Covidien, the manufacturer of the SOLITAIRE device, funded the study. The SOLITAIRE device is cleared by the FDA for use
in the United States and is also approved for use in Europe.
Saver and Jahan received compensation from Covidien as scientific consultants for the design and conduct of the trial.
The UCLA Stroke Center,
recognized as one of the world's leading centers for the management of cerebral vascular disease,
treats simple and complex vascular disorders by incorporating recent developments in emergency medicine, stroke neurology,
microneurosurgery, interventional neuroradiology, stereotactic radiology, neurointensive care, neuroanesthesiology and
rehabilitation neurology. The program is unique in its ability to integrate clinical and research activities across multiple
disciplines and departments. Founded in 1994, the UCLA Stroke Center is designated as a certified Primary Stroke Center by
the national Joint Commission on Accreditation of Healthcare Organizations.