First Patient from ETMC Enrolled in New St. Jude Medical Trial
ETMC will contribute to study of device that could help detect coronary
events
The East Texas Medical Center Cardiovascular
Institute has enrolled its first patient in a new trial sponsored by St. Jude
Medical that will contribute to the study of a device that could help detect
acute coronary syndrome events, such as a heart attack.
"We are proud to participate in this trial in
conjunction with Cardiovascular Associates of East Texas," commented John
Stewart, vice president of ETMC. "We recognize the potential this new feature
has to help save lives and enhance the care we can provide to patients. We look
forward to contributing to the study."
ETMC is one of 200 nationwide centers participating
in the ST Monitoring to Detect ACS (Acute
Coronary Syndrome) Events in ICD Patients study, known as the Analyze ST trial.
The trial will study the safety and effectiveness of a new feature in the
device maker's Fortify® ST implantable cardioverter defibrillator (ICD) system.
Dr. Noah Israel with CAET performed the procedure at ETMC.
More than half of patients experiencing a heart
attack die before reaching a hospital. Even patients with stable coronary
artery disease (CAD) are at high risk of having a life-threatening or
potentially fatal coronary event. Additionally, 15 to 20 percent of patients
who have had an ischemic event have recurrent events. As a result, CAD needs to
be managed on an ongoing basis to avoid a more unstable or life threatening
acute coronary event.
Approximately two thirds of ICD patients have
cardiac ischemia (narrowing or blockage responsible for significantly obstructing
the flow of blood to a patient's heart muscle), with many more having risk
factors for developing cardiovascular disease.
The ST monitoring feature in the Fortify ST ICD is
designed to detect a coronary event, such as a heart attack, by monitoring
changes in a specific section of the patient's heartbeat – the ST segment.
Changes in the ST segment have long been studied via surface
electrocardiograms. This unique feature adds a new diagnostic capability to the
ICD system so that physicians can automatically monitor the ST segment from
inside the body and on a continual basis.
The Analyze ST study will determine if this
diagnostic capability can provide detection of acute coronary syndrome events,
and may provide important insights leading up to an event. The study will also
provide key insights on the value of such a diagnostic feature in possibly
reducing the event-to-treatment time and positively impacting patient outcomes.
As part of this new feature, a transmitter will
provide updates to physicians who will then be able to remotely monitor their
patients' ST segment changes. The device can also alert the patient to a change
in the ST segment, prompting them to seek medical attention.
Earlier this year, St. Jude Medical received
investigational device exemption (IDE) approval from the U.S. Food and Drug
Administration (FDA) to start its Analyze
ST trial. The technology has been an available
feature in St. Jude Medical ICDs in Europe since 2008, but this is the first
trial to study the device's use in the U.S. In all, more than 5,000
patients will participate in the study to evaluate the effectiveness and safety
of the new ST monitoring feature.
For more information on the Analyze ST trial, visit www.sjm.com
and www.etmc.org