Could Watching the Super Bowl Cause a Heart Attack? What local docs say about the study that says watching the big game could land you in the ER!
PHOENIX (February 3, 2010) – New medical information suggests that people getting ready for their annual Super Bowl parties may need to have the phone on speed dial to 9-1-1 due to what they say is an increase of heart attacks during the game. But before passing on watching TV this weekend, Valley residents might want to hear what one doctor at Banner Good Samaritan Medical Centers, says about the study linking football watching to heart attacks.
“The stress of watching football -just like the stress of having sex- can cause a heart attack,” says Dr. Nathan Laufer, Cardiologist at Banner Good Samaritan Medical Center. “Good stress and bad stress can lead to bad outcomes.”
The study on Super Bowl Sunday leading to an increase in heart attacks appears in the New England Journal of Medicine.
Dr. Laufer, Cardiologist at Banner Good Samaritan Medical Center and founder of the Heart and Vascular Center of Arizona, is available to talk with media regarding what stress relating to watching sports can do to your heart.
To interview Dr. Laufer please contact the Public Relations Department at Banner Good Samaritan Medical Center at 602-839-4193.
Dr. Sadhu Performs First 3-D Mapping using the St. Jude EnSite Velocity at Banner Good Samaritan Medical Center
On Friday, January 29, 2010, Dr. Ashish Sadhu, HVCA Electrophysiologist, had the opportunity to perform the first 3-D Mapping Ablation Procedure at Banner Good Samaritan Medical Center, utilizing the new St. Jude Medical EnSite Velocity 3-D Mapping System. This equipment is the latest technological advancement that the Banner Health System has added to their Electrophysiology Laboratory.
3-D Mapping provides the physician with real-time 3D graphic images of the patient heart and it's electrical activity. The new system helps minimize patient radiation exposure during the Ablation Procedure and assists in localization of the abnormal electrical circuit involved in common cardiac arrhythmias.
Heart & Vascular Center of Arizona Receives Medical Group Management Award
PRESS RELEASE
FOR IMMEDIATE RELEASE
Heart & Vascular Center of Arizona achieves MGMA 'better preformer' status
Phoenix, Arizona, January 4, 2010 - The Medical Group Management Association (MGMA) Performance and Practices of Sucessful Medical Groups: 2009 Report Based on 2008 Data indentified Heart & Vascular Center of Arizona as a "better performer" because of superior operational performance compared with similar medical practices nationwide.
Heart & Vascular Center of Arizona founded in 2001, strives to provide the highest level of cardiology care focusing on compassionate and cutting-edge preventative, diagnostic and therapeutic services to our patients. "The primary HVCA mission is maintaining high standards in providing patient care while examining and implementing ways to increase practice efficiency and productivity," states Barbara Watkins, Administrator. "We are very pleased to be recognized by MGMA. One important achievement was our Electronic Medical Records (EMR) implementation. EMR assisted us in improving medical record documentation while cost effectively communicating with primary care, referring physicians, outside laboratories and soon with our patients through our online patient portal."
The MGMA report, a benchmarking standard among medical groups for over a decade, was produced using data from respondents to the MGMA Cost Survey: 2009 Reports Based on 2008 Data as well as data from a questionaire that assesed management behaviors, practices, capacity and sucess in one or more areas of medical practice operations.
Today, MGMA's 22,500 members lead 13,700 organizations nationwide in which 275,000 physicians provide more than 40 percent of the health services delivered in the United States.
PHOENIX, Ariz. – November 17, 2009 -- The Heart & Vascular Center of Arizona today announced the availability of Corus™ CAD, the first and only gene expression test to quantify the likelihood of obstructive[i] coronary artery disease (CAD) in patients with stable chest pain. Corus CAD is a new genomic test launched in select U.S. markets, and the Heart & Vascular Center of Arizona is among the first institutions in the country to offer this first-of-its-kind gene expression test to patients with possible cardiovascular disease.
"This is a very exciting breakthrough for helping a physician evaluate the risk of obstructive coronary artery disease in our patients who have chest pain," said Dr. Alan Grossman, Medical Director of the Nuclear Cardiology and Echocardiography Laboratories at Heart and Vascular Center of Arizona. "It is a convenient, non-invasive blood test that provides fast and accurate results, which are based on information obtained literally from the cellular level within the coronary arteries. We're eager to share insights with our patients from this new cardiology tool that objectively quantifies their likelihood of severe coronary obstruction and helps us better individualize patient care."
Corus CAD is a clinically validated test that provides unique biological insight into coronary artery disease at the molecular and cellular levels for a patient. The test is performed via a simple blood draw procedure, without patient exposure to radiation, imaging agents and/or ionizing imaging contrast solutions. By combining this information with standard clinical assessments, physicians can obtain a more complete picture of their patient’s disease, and can better individualize care.
“As an oncology nurse, I’ve seen the power of preventative medicine work first-hand in my patients,” said Mandy Welsheimer, a patient of Dr. Grossman who received the Corus CAD test. "I come from a family with a history of heart disease and also have intermittent chest pain, so I visit Dr. Grossman yearly to assess my heart’s health. When he offered me the opportunity to take the new Corus CAD test that would detect my risk for coronary artery disease, I jumped at the opportunity to take advantage of the latest technology. When Dr. Grossman walked me through the test’s objective results, I immediately felt at ease to know for certain that I am unlikely to have obstructive CAD at this point."
CardioDx, a cardiovascular genomic diagnostics company that developed and launched Corus CAD, has initially launched the test in nine states, including: Kentucky, Maryland, Illinois, Washington, Wisconsin, Minnesota, North Carolina, Texas and Arizona. Patient access is expected to increase throughout the country in 2010 as Corus CAD’s availability expands to additional regions.
About Obstructive Coronary Artery Disease (CAD)
Cardiovascular disease affects tens of millions of Americans each year and is the leading cause of death in the United States. Coronary artery disease (CAD) is a narrowing or blockage of the coronary arteries (the major blood vessels that supply the heart with blood, oxygen and nutrients) that reduces blood flow to the heart muscle. As a result of the blockage, the heart does not get enough oxygenated blood, which can often cause chest pain (angina), shortness of breath and other symptoms. A severe blockage can cause a heart attack (myocardial infarction) or even death; one of every five deaths among Americans is caused by CAD. In 2008, CAD had an estimated direct and indirect cost of over $165 billion.
About Corus CAD Corus CAD is a clinically validated genomic test that integrates the expression levels of 23 genes and other patient characteristics to assess obstructive CAD. The test is intended to be used in an outpatient setting with clinically stable, non-diabetic patients who present with chest pain or who have a high risk of coronary artery disease, but without previously diagnosed myocardial infarction (heart attack) or prior revascularization procedure. Corus CAD is convenient and safe, and only requires a standard blood draw procedure. The test yields an objective result delivered to the physician in the form of a numeric score that quantifies the likelihood that a patient with stable chest pain has obstructive CAD.
About CardioDx
CardioDx is a cardiovascular genomic diagnostics company providing physicians with clinically validated tests to enable more informed and individualized patient care decisions. We are strategically focused on developing products for three forms of cardiovascular disease: coronary artery disease (CAD), cardiac arrhythmias and heart failure. The company’s first product, Corus™ CAD, is the first and only gene expression test to quantify the likelihood of obstructive coronary artery disease in a stable chest pain patient. Developed and validated in a multicenter U.S. clinical trial, Corus CAD integrates the activity of a panel of genes with other patient characteristics to assess obstructive coronary artery disease. Corus CAD is now available in nine states - Kentucky, Maryland, Illinois, Washington, Wisconsin, Minnesota, North Carolina, Texas and Arizona - via the CardioDx CLIA-certified Commercial Laboratory with broader availability expected in 2010. CardioDx was founded in 2004 and is located in Palo Alto, California. The company’s investors include leaders in life science investing: Kleiner, Perkins, Caufield & Byers, Mohr Davidow Ventures, TPG Biotech, Intel Capital and Pappas Ventures. For more information, please visit www.cardiodx.com.
About Heart & Vascular Center of Arizona
The Heart & Vascular Center of Arizona (HVCA) specializes in non-invasive, invasive and interventional cardiology as well as peripheral vascular disease and intervention. The HVCA is committed to offering their patients the highest quality, cost-effective and readily accessible cardiovascular services. With over 25 years of experience, the cardiologists at HVCA are leaders in cardiovascular diagnosis, treatment, prevention and education. Based on current evidence-based medical knowledge, the HVCA seeks to lead in the introduction of new cardiovascular tools and are committed to physician leadership and excellent patient care.
[i]Obstructive CAD is defined as at least one atherosclerotic plaque causing ≥50% luminal diameter stenosis in a major coronary artery (≥1.5mm lumen diameter) as determined by invasive quantitative coronary angiography (QCA).
Dr. Laufer to be Profiled in Marquis Who's Who Publication
NEWS RELEASE
Media Contact: Barbara Watkins
Phone: 602-322-5057
Nathan Laufer, MD To Be Profiled in a Marquis Who’s Who® Publication
Phoenix, Arizona – November 17, 2009 – Nathan Laufer, MD, of Phoenix, Arizona has been selected to be included in a biographical directory published by Marquis Who’s Who®, the leading biographical reference publisher of the highest achievers and contributors from across the country and around the world. Dr. Laufer will be profiled in the 2010 edition of Who’s Who in Medicine, which will be available in December.
Since 1899, when A.N. Marquis printed the First Edition of Who’s Who in America®, Marquis Who’s Who has chronicled the lives of the most accomplished individuals and innovators from every significant field of endeavor – including politics, business, medicine, law, education, art, religion and entertainment. Today, Who’s Who in America® remains an essential biographical source for thousands of researchers, journalists, librarians and executive search firms around the world.
Marquis now publishes many Who’s Who titles, including Who’s Who in America®, Who’s Who in the World®, Who Was Who in America®, Who’s Who in Finance and BusinessTM, Who’s Who in American Law®, Who’s Who in Medicine and Healthcare®, Who’s Who in Science and Engineering®, and Who’s Who of American Women®. To nominate colleagues for a Marquis publication, you may visit the official Marquis Who’s Who Web site at www.marquiswhoswho.com.
Heart & Vascular Center of Arizona Launches New Web Site
The Heart & Vascular Center of Arizona launched a new patient web site to better service patients. The new site has a new look and will be the link to a new patient portal that will be launched in the next month. The new patient portal will make it easier for patients to access key information on their overall health. Watch the site for new information on when the patient portal will be accessible.
For more information contact the Heart & Vascular Center of Arizona at (602) 307-0070.
In the next month, the Heart & Vascular Center of Arizona will be launching a new patient portal which will be accessible from their new web site. Patients will click on the "Patient Portal" button on the right hand side of their screen to login to the portal. A user name and password will be used to access their own patient information, get forms, schedule appointments and many other items to make it more convenient for patients to get information at any time of day.
New patients will be able to register ahead of their new appointment time, filling out all of the necessary paperwork normally handled in the office.
For more information, contact the Heart & Vascular Center of Arizona at (602) 307-0070.
American Heart Association Announces Dr. Sorof New Board President
American Heart Association Announces New Board Members; Selection Reflects Local Professional Diversity
PHOENIX, March 2009 - The appointment of two new members to the American Heart Association’s Board of Directors was announced by Valerie Jones, executive director of the American Heart Association in Phoenix.
Suzanne A. Sorof, M.D. will serve as President of the 2009 board of directors. Dr. Sorof is Board Certified in Internal Medicine, Cardiology and Interventional Cardiology, and practices at Heart and Vascular Center of Arizona. Her Interests include Coronary Artery disease, Peripheral Artery Disease, Consultative Cardiology, and Women’s Preventive and Cardiology. Originally from New York, She graduated from medical School at Baylor College of Medicine and completed her internal medicine residency there.
Peter Harper will begin his reign as Chairman of the Board. Harper serves a Chief Financial Officer of Scottsdale Insurance. Pete Harper joined SIC in 2005. He is responsible for all financial operations at Scottsdale, including business planning and financial reporting. He brings more than 20 years of finance leadership experience to the role, including senior leadership positions with some of the largest corporations in the country. A San Francisco Bay area native, Pete earned his B.S. in Business Administration, Finance from San Jose State University in San Jose, California.
About the American Heart Association
Founded in 1924, the American Heart Association today is the nation’s oldest and largest voluntary health organization dedicated to reducing disability and death from diseases of the heart and stroke. These diseases, America’s No. 1 and No. 3 killers, and all other cardiovascular diseases claim over 870,000 lives a year. In fiscal year 2005–06 the association invested over $543 million in research, professional and public education, advocacy and community service programs to help all Americans live longer, healthier lives. To learn more, call 1-800-AHA-USA1 or visit americanheart.org.
MEDIA CONTACT:
Nancy Keane, communications director – 602-414-5341
Physicians at the Heart & Vascular Center of Arizona have been selected along with a handful of interventional cardiac specialists from around the country to participate in a prestigious trial called PROTECT 2. Dr. Ashish Pershad, Interventional Cardiologist, performed the first procedure in Maricopa County on a 79 year old patient that was felt to be too high risk for coronary bypass surgery at Banner Good Samaritan Medical Center last week.
The PROTECT 2 trial compares the new left ventricular assist device, Impella, with the current standard of care. Through a minor groin incision the Impella Device is placed. This device artificially supports circulation much like being on a bypass machine. In this way, the cardiac interventionalist can perform the high risk angioplasty that opens up the narrowed coronary arteries.
“This left ventricular assist device satisfies an unmet need in the field of cardiovascular medicine and is a significant advance,” states cardiologist Dr. Ashish Pershad. He continues, “This device allows cardiologists to safely treat those patients who are too high risk for angioplasty and do poorly with traditional coronary artery bypass surgery.”
AHA Announces Dr. Nathan Laufer New Board President
American Heart Association Announces New President
PHOENIX, Feb 12 - The American Heart Association announces the appointment of Dr. Nathan Laufer as President of the 2006 board of directors. Dr. Laufer is board certified in internal medicine, cardiology, and interventional cardiology, and has been in practice since 1984. He received his undergraduate degree and M.D. from McGill University in Montreal, Canada. He completed his internal medicine residency at the University of Toronto and a cardiology fellowship at the University of Michigan, whose faculty he then joined. Dr. Laufer is a clinical assistant professor of medicine at the University of Arizona, a member of the teaching faculty at Good Samaritan Regional Medical Center, and is president and founder of the Cardiovascular Society of Arizona. He is also past director of the Coronary Care Unit and present Director of Interventional Cardiology Fellowship at Banner Good Samaritan Hospital. He also serves as Medical Director of the Heart and Vascular Center of Arizona and Chief of Cardiology at Banner Estrella Medical Center. He regularly holds workshops for cardiologists throughout the country and is an industry advisor on interventional products. He also holds many awards for excellence in his field. Dr. Laufer was born in Montreal, Canada.
HVCA Nuclear Cardiology Lab Obtains National Accreditation
DATE: June 15, 2005
TO: Phoenix Business Journal
CONTACT: Barbara Watkins
602-322-5057
bfahl@heartcenteraz.com
Topic: Heart & Vascular Center of Arizona Nuclear Cardiology Laboratory obtains national accreditation
Heart & Vascular Center of Arizona located in Phoenix, Arizona, was granted accreditation by ICANL-Intersocietal Commission for the Accreditation of Nuclear Medicine Laboratories. ICANL provides a peer review mechanism to encourage and recognize the provision of quality nuclear cardiology and nuclear medicine diagnostic evaluations. A non-profit organization, the ICANL is dedicated to ensuring high quality patient care and to promoting health care. Dr. Alan Grossman, Director of Nuclear Cardiology at Heart & Vascular Center of Arizona states, “The accreditation process is voluntary and evaluates every aspect of the laboratory’s daily operations. Actual case studies are submitted for review. These case studies are crucial in determining compliance with ICANL Standards.”
This accreditation status signifies that the facility has been reviewed by an independent agency that recognizes the laboratory’s commitment to quality testing for the diagnosis of heart disease. According to Dr. Nathan Laufer, Medical Director of Heart & Vascular Center of Arizona, “the heart is evaluated at rest and during exercise using a small amount of radioisotope during the noninvasive procedure. A complex imaging technique, nuclear cardiology testing relies on the experience and training of both the physician and the technologist.” Their interpretive and technical abilities determine the diagnostic accuracy of the examination. The physicians are able to detect the presence of cardiovascular disease and may also discover important information regarding the occurrence of future heart attacks.
Cardiovascular disease is the leading cause of death in the United States, causing society over 83.7 billion dollars each year in health services, medications and lost work time due to disability. Early detection not only saves lives but decreases lost productivity.
Heart & Vascular Center of Arizona currently has two locations; the main facility at 1331 N. 7th Street, Suite 375, Phoenix, and a west valley location at 9305 W. Thomas Road, Suite 270, Phoenix. Both clinics provide nuclear cardiology testing and are accredited for a period of three years.
Dr. Ashish Pershad Performs First Non-Surgical Aortic Aneurysm Repair
FOR IMMEDIATE RELEASE
CONTACT:
Barbara Fahl-Watkins
Heart & Vascular Center of Arizona
Phone: 602-307-0070
Local Cardiologist Performs First Non-Surgical Aortic Aneurysm Repair
Phoenix, AZ(February 2005) - The Heart & Vascular Center of Arizona is pleased to announce that a minimally invasive technique for treating abdominal aortic aneurysms has been taken to the next level. Grafts for treating aneurysms are now being placed in the aorta without need for not only open surgery but without the need for “surgical cut-down” or surgical exposure of the femoral arteries. This procedure will allow thousands of patients to benefit from a minimally invasive procedure that may revolutionize treatment for abdominal aortic aneurysms.
Dr. Ashish Pershad, an interventional cardiologist of Heart & Vascular Center of Arizona has been performing the aneurysm repair procedure in Phoenix for the past three years. “This procedure is an alternative to open surgery that involves a catheter placed in the groin. Traditional surgery requires a large surgical incision in the abdomen, general anesthesia and may not be the procedure of choice for patients with other medical illnesses. Complete percutaneous aneurysm exclusion is a major step forward in the treatment of this disease. We look forward to offering this new technique to our patients and eventually doing this procedure under local anesthesia” said Ashish Pershad MD.
CONTACT:
Barbara Fahl-Watkins
Heart & Vascular Center of Arizona
1331 N. 7th Street, Ste. 375
Phoenix, AZ 85006
Phone: 602-307-0070
Email: bfahl@heartcenteraz.com
Web site: http://www.heartcenteraz.com
Local Cardiologist Lauds FDA Approved Procedure
Phoenix, AZ (August 31, 2004) - The Heart & Vascular Center of Arizona is pleased to announce the U.S. Food and Drug Administration (FDA) approval of a new technique for treating life-threatening blockages of the carotid arteries, which are the major blood vessels in the neck that supply blood to the brain. Blockages in the carotid artery are one of the leading causes of stroke. This procedure will allow thousands of patients to benefit from a minimally invasive procedure that may revolutionize treatment for stroke prevention.
The procedure is a combination of two standard cardiovascular procedures for opening blocked or partially blocked arteries - angioplasty and stenting. Added to the procedure is an innovative filter catheter which prevents blood clots from floating to the brain.
Dr. Nathan Laufer, Medical Director of Heart & Vascular Center of Arizona has been performing the carotid stent procedure in Phoenix for the past four years under an FDA approved protocol and also for compassionate use. “This procedure is an alternative to surgery that involves a small catheter placed in the groin. Traditional carotid surgery requires a large surgical incision in the neck, general anesthesia and may not be the procedure of choice for patients with other serious illnesses. Carotid stenting is a major step forward in the prevention of stroke using minimally invasive techniques. We look forward to offering this technique to our patients,” said Dr. Nathan Laufer who is also Director of the 4th Year Interventional Cardiology Training Program, Banner Good Samaritan Regional Medical Center and the Chief of Cardiovascular Services at the new Banner Estrella Medical Center. Dr. Laufer will be assisting in the development of physician training courses for this new technique.
For information: http://www.heartcenteraz.com
Contact: bfahl@heartcenteraz.com
Phone: 602-307-0070
# # #
HVCA Receives Reaccreditation of Nuclear Medicine Laboratories by ICANL
Dr. Alan Grossman, Medical Director of Nuclear Medicine at Heart & Vascular Center of Arizona, received the news today that Heart & Vascular Center of Arizona has been awarded reaccreditation from the Intersocietal Commission for the Accreditation of Nuclear Medicine Laboratories (ICANL). This accreditation shows our committment to high quality patient care by voluntarily demonstrating compliance to the requirements outlined in the ICANL Standards.
The ICANL Standards are extensive and define the minimal requirements for nuclear cardiology laboratories to provide high quality care. Through the accreditation process, we assess every aspect of our daily operation and its impact on the quality of health care provided to patients. Because accreditation is renewed every three years, a long-term commitment to quality and self-assessment is developed and maintained.
Heart & Vascular Center of Arizona is pleased to announce the opening of our Patient Portal - Secure Online Patient Services. We are excited to be one of the few offices in the state of Arizona utilizing secure messaging technology with our patients.
Secure eMail communication is convenient and efficient. It works for many of the non-urgent questions, requests or messages patients may have for our doctors and staff. Copies of the messages can be placed in the patient's medical record. Patients do need to keep in mind that although Secure eMail can be a very effective tool, it is not a substitue for an examination by their doctor.
Three Heart & Vascular Center Physicians are Named to Top Docs List for 2010!
Dr. Nathan Laufer, Dr. Ashish Pershad and Dr. Ashish Sadhu were listed on this year's Top Docs Phoenix List. Look for them in the April 2010 Phoenix Magazine! Dr. Laufer, Medical Director of Heart & Vascular Center of Arizona, is a nine year Top Docs Award Winner for Cardiology.
Dr. Pershad is featured this year in Phoenix Magazine's "Fantastic Five." The article features five of the Valley's most innovative physicians. An HVCA Interventional Cardiologist, Ashish Pershad, MD is one of a dozen doctors in the country performing the retrograde approach to coronary recanilization.
Dr. Ashish Sadhu, an Electrophysiologist at HVCA, was recognized this year for the first time. Electrophysiologists are cardiologists who have additional education and training in the diagnosis and treatment of abnormal heart rhythms.
February is Heart Month! Join Heart & Vascular Center at the Heart Walk on February 27th!
Join Heart & Vascular Center of Arizona's physicians and staff at the 2010 Phoenix "Start!" Heart Walk. Opening Ceremonies begins at 8:30am on Saturday, February 27th, Tempe Town Lake.
Maricopa County Medical Society Announces 2010 Officers - Nathan Laufer MD President-Elect
Maricopa County Medical Society announced the 2010 slate of officers this month. Dr. Nathan Laufer was named President-Elect. Dr. Laufer has been a member of the medical society since 1985. The Maricopa Medical Society continues to promote excellence in the quality of care and to represent its members by acting as a strong, collective physician voice.
URGENT CALL TO ACTION!! Access to Cardiology Care at Risk!!
Campaign for Patient Access
Cardiovascular Patients. Cardiovascular Practices. At Risk.
The Centers for Medicare & Medicaid Services (CMS) 2010 Physician Fee Schedule Rule issued in late October will have a devastating impact on cardiovascular practices.
For millions of heart patients in America the results could be severe — less access, higher fees, longer waits, impersonal care. This is why heart patients and cardiovascular professionals are coming together NOW to fight the CMS cuts. Learn more »
Cardiology is fighting for our very survival – and for our patients. CMS issued the final 2010 Physician Fee Schedule rule in late October, and the consequences are severe. This is bad public policy - and it cannot stand. We need every cardiovascular professional in the U.S. to get involved TODAY.
Thanks to this rule, outpatient cardiology is on the critical list, and that means patients won’t get the cardiovascular care they need to survive. The odds against completely stopping the cuts are high, but your College needs you in the effort to fight the cuts.
Get Involved in the Fight for Survival. Oppose the Rule.
Heart & Vascular Center Physicians Embrace E-Prescribing
Heart & Vascular Center of Arizona is proud to be using the latest technology in communicating patient presciptions to over 200 pharmacies in Arizona! E-Prescribing is safer, more convenient for our patients and more efficient for the pharmacy. Within seconds the pharmacist receives an electronic transmission of your prescription and it is ready for processing. No phone calls, no faxing and no paper!
The first step in refilling a medication is the patient alerting the pharmacy of the need for a refill. The pharmacy sends our office an electronic request for the refill. Our office can respond faster and more efficiently. No calling our office....Call your pharmacy instead!
Abiomed will be honoring a site within the PROTECT II Clinical Trial community each month that has displayed outstanding excellence and enthusiasm. This month we would like to highlight Banner Good Sam in Phoenix, Arizona. They were late to enter the trial but they successfully recruited six patients within five months of their activation date. They have displayed great enthusiasm in helping PROTECT II become a successful trial. “I think the Impella device is a true game changer in the field of interventional cardiology. The ease of use is truly a huge advantage for these high risk PCI procedures. I am anxiously awaiting the completion of PROTECT 2 so that we can identify “the patient” who would benefit most from this device and confirm our proof of concept about superiority over the balloon pump,” said Dr. Ashish Pershad, PI at Banner Good Sam.
For such a successful trial, Gabriella Diaz, RN recommends, “Collaborative education is one of the largest assets for success in not just enrolling subjects in the study, also obtaining the large data set required. The cooperation of multiple specialties to include, Cardiac Catheterization Lab, Pre-Op, holding area and bedside staff has been the key to achieving research goals. We are not islands unto ourselves. Respecting all the professionals involved through education and cooperation is a catalyst to obtaining clean, quality data that will support subject safety and industry quality.”
Patient's Action Network for Health System Reform Updates
Congress is closer than ever to passing a health system reform bill, and we can't lose this opportunity for real health reform. However, members of the AMA's Patients' Action Network and doctors from around the country--in states like Florida, Nebraska, Colorado, Texas and Missouri--are all concerned about how this legislation will affect your access to your doctor.
In the U.S. Senate, the health reform bill that's been proposed would use Medicare as a foundation--and that foundation is crumbling because of an archaic payment system already in place. This system is scheduled to cut Medicare physician payments by more than 20 percent Jan. 1, 2010, with repeated annual cuts coming after that.
These annual cuts are a huge problem for patients--and for many families--because they will prevent doctors from taking on new Medicare patients, discourage many from investing in new health technology and make some think about closing their medical practices altogether.
Right now, the Senate is promoting another one-year Band-Aid for this problem, which means that we’ll be dealing with an even bigger problem next year.
Please don't put this off. Your senators need to hear from you now, to protect your family's access to health care today and in the future. Tell your senators that the short-term, Band-Aid approaches used in the past will no longer do. Real health system reform must include Medicare reform.
American Heart Association, Arizona Cardinals Preparatory Academy, and Phoenix Fire Team Up to Share the Gift of CPR with Students!
First-of-its-kind program for Maricopa County students to kickoff on September 22, 2009
Phoenix, AZ--- The American Heart Association has teamed up with Cardinals Charities, the Arizona Cardinals Preparatory Academy and the City of Phoenix Fire Department, to kickoff a special CPR instructional program for 7th and 8th grade students. Through the use of the CPR Anytime kit, students will each be given their own mini blow-up mannequin and instructional DVD and workbook. Phoenix Fire personnel will facilitate the training.
The program, called Heartbeat of Arizona, will teach students across Maricopa County the skills needed to perform cardiopulmonary resuscitation in only 22 minutes.
On Tuesday, September 22, 2009 from 1 p.m. – 2p.m., students at the Arizona Cardinals Preparatory Academy will be the first in Maricopa County to be trained with the CPR Anytime program. The campus is located at the Royal Palms Middle School on the corner of Butler Ave. and 19th Ave. in the Washington Elementary School District. The training will take place at the campus Community Center. Cardinals Quarterback Kurt Warner, along with his wife Brenda, and other Arizona Cardinals players will be on hand to help train the students.
“Teaching the lifesaving skill of CPR reinforces the mission of the academy and the school district and that is to cultivate student achievement, prepare all students to become responsible and successful contributors to our diverse society. We’re honored that Cardinals Charities and the American Heart Association chose our academy to kickoff this great educational opportunity," says Principal Jackie Jackson, Ed D.
"The Phoenix Fire Department is excited about partnering with the American Heart Association and the Arizona Cardinals Preparatory Academy to bring CPR knowledge to Maricopa County students," said Chief Bob Khan. "Not only are we empowering children in the fight against sudden cardiac arrest, we are bringing that knowledge into the home, where the majority of these kinds of emergencies occur."
“The American Heart Association has found that only 6.4% of sudden cardiac arrest victims survive because the vast majority of those witnessing the incident are people who do not know how to perform CPR,” says Suzanne Sorof, MD, and board president of the Phoenix American Heart Association. Cities such as Seattle that have implemented heart safe programs boast survival rates around 40 percent, according to the American Heart Association. When sudden cardiac arrest occurs, the victim collapses, becomes unresponsive to gentle shaking, stops normal breathing and after two rescue breaths, still isn't breathing normally, coughing or moving. CPR helps maintain vital blood flow to the heart and brain and increases the amount of time that an electric shock from a defibrillator can be effective, according to the American Heart Association.
Recent studies have shown that students as young as 9 years are able to successfully and effectively learn basic life support skills including AED [automated external defibrillator] deployment, correct recovery position and emergency calling. A critical component of the program is that after kids learn CPR in the classroom, they then take the CPR Anytime kit home to share it with family and friends.
Heartbeat of Arizona is made possible by generous funding from Phoenix area businesses including the Cardinals Charities, Blue Cross Blue Shield of Arizona and Aetna. More than $1 million dollars is needed to sustain the program over the next three years.
About The Cardinals Academy:
The Cardinals Academy offers accelerated instruction to help students focus on their education and service learning to help students achieve success. The academy promotes a small school environment of not more than 120 students, quality teachers, and community resources delivered in an accessible way to reduce or eliminate nonscholastic barriers to staying in school.
About the American Heart Association:
Founded in 1924, the American Heart Association today is the nation’s oldest and largest voluntary health organization dedicated to reducing disability and death from diseases of the heart and stroke. These diseases, America’s No. 1 and No. 3 killers, and all other cardiovascular diseases claim over 870,000 lives a year. In fiscal year 2005–06 the association invested over $543 million in research, professional and public education, advocacy and community service programs to help all Americans live longer, healthier lives. To learn more, call 1-800-AHA-USA1 or visit americanheart.org.
Additional Facts on Sudden Cardiac Arrest and CPR:
- About 80 percent of all out-of-hospital cardiac arrests occur in private residential settings, so being trained to perform cardiopulmonary resuscitation (CPR) can mean the difference between life and death for a loved one.
- Effective bystander CPR, provided immediately after cardiac arrest, can double a victim’s chance of survival.
- CPR helps maintain vital blood flow to the heart and brain and increases the amount of time that an electric shock from a defibrillator can be effective.
- Approximately 93 percent of sudden cardiac arrest victims die before reaching the hospital.
- Death from sudden cardiac arrest is not inevitable. If more people knew CPR, more lives could be saved.
- Brain death starts to occur four to six minutes after someone experiences cardiac arrest if no CPR and defibrillation occurs during that time.
- If bystander CPR is not provided, a sudden cardiac arrest victim’s chances of survival fall 7 percent to 10 percent for every minute of delay until defibrillation. Few attempts at resuscitation are successful if CPR and defibrillation are not provided within minutes of collapse.
- Coronary heart disease accounts for about 446,000 of the over 864,000 adults who die each year as a result of cardiovascular disease.
- There are 294,851 emergency medical services-treated out-of-hospital cardiac arrests annually in the United States.
- There are about 138,000 coronary heart disease deaths within one hour of symptom onset each year in the United States.
- Sudden cardiac arrest is most often caused by an abnormal heart rhythm called ventricular fibrillation (VF). Cardiac arrest can also occur after the onset of a heart attack or as a result of electrocution or near-drowning.
- When sudden cardiac arrest occurs, the victim collapses, becomes unresponsive to gentle shaking, stops normal breathing and after two rescue breaths, still isn’t breathing normally, coughing or moving.
Date and Time: Tuesday, September 22, 2009 from 1 p.m. – 2p.m
ABSTRACT: Objective. The treatment of long superficial femoral artery (SFA) chronic total occlusions (CTOs) remains controversial. There are several percutaneous treatment options available for the recanalization of these lesions. Percutaneous transluminal angioplasty (PTA) alone, nitinol stents, and expanded PTFE-lined nitinol stents are all viable treatment alternatives to femoral-popliteal bypass surgery. There are, however, limited data on outcomes of patients with SFA CTOs undergoing endovascular treatment. This study was performed to evaluate the safety, efficacy and 1-year patency rates of the Viabahn (WL Gore and Associates, Flagstaff, Arizona) e-polytetrafluoroethylene (e-PTFE) stent grafts at a major medical center in Phoenix, Arizona. Methods. Thirty patients (32 limbs) were prospectively treated for activity-limiting claudication after failing medical therapy. These patients received traditional angioplasty and stenting techniques using the Viabahn e-PTFE stent graft. Follow-up ankle-brachial index (ABI) examinations and duplex surveillance were completed at 6 and 12 months in all patients. Results. The mean age of the patients was 58.4 years. There were 12 women (40%) and 18 men (60%). Five of the patients (16.67%) were diabetics. The procedural success rate was 100%, with no in-hospital morbidity or mortality. The mean preprocedural ABI was 0.54 and the mean SFA occlusion length was 15.4 cm. The mean stented length was 24.6 cm. The median stent diameter was 6 mm. One patient (3.3%) did have subacute stent thrombosis at 4 months. On follow-up testing, the mean post-procedure ABI at 1 year was 0.76 with a primary patency rate of 80% and a primary assisted patency rate of 86%. Silent asymptomatic occlusions were noted in 10% (3/30) of the patients. Restenosis was a prespecified endpoint and was defined as being significant if the proximal peak velocity ratio (PVR) exceeded 2.4 on duplex interrogation. This endpoint was detected in 6.6% of the patient population (2/30) (proximal peak velocity ratio is the ratio of the maximum intrastenotic PSV and the maximum prestenotic PSV). Conclusions. Percutaneous e-PTFE stent-grafting with the Viabahn stent graft is a viable treatment option for TASC D occlusions in the SFA in claudicants and patients with critical limb ischemia. Primary and primary assisted patency rates at 1 year are comparable to historical surgical outcomes using PTFE grafts as bypass conduits. Long-term data (> 5 years) in a larger patient cohort are necessary before definite conclusions can be drawn.
Atherosclerotic peripheral vascular disease (PVD) is often an underdiagnosed, undertreated and debilitating disease.1 The 2007 Trans-Atlantic Inter-Society Consensus (TASC) for the Management of Peripheral Arterial Disease document estimates that there are currently 27 million people in Europe and North America who are afflicted with this disease. There are also an estimated 413,000 hospital discharges per year due to chronic PVD.2 The prevalence of PVD increases progressively with age, beginning after the age of 40, a relationship demonstrated by the National Health and Nutrition Examination Survey. The authors found that PVD was present in 0.9% of those between the ages of 40–49 years, 2.5% of those 50–59 years old, 4.7% in the 60–69 year-old group and 14.5% in those ≥ 70 years.3 PVD will thus continue to grow in clinical significance as the world’s population ages.
The use of percutaneous transluminal angioplasty (PTA) to revascularize the superficial femoral artery (SFA) can result in initial technical success rates > 95%, with a low risk of complications.4 However, late clinical failure remains an important concern. Restenosis occurs in 40–60% of treated segments after 1 year. The use of angioplasty to treat extensive disease of the SFA has particularly poor results: at 1 year, the rates of restenosis exceed 70% for lesions longer than 10 cm.5
Stents avoid the problems of early recoil and flow-limiting dissection after balloon angioplasty and can thus be used for the treatment of long and complex lesions. Initial studies of stenting of the SFA reported promising results, with patency rates > 85% at 18 months.6 However, subsequent studies found that exaggerated neointimal hyperplasia frequently leads to in-stent restenosis, and randomized, controlled trials failed to demonstrate any benefit of a stainless-steel stent over angioplasty alone.7
Investigation into evaluating efficacy of percutaneous stenting versus angioplasty alone has yielded conflicting results. The VIENNA trial demonstrated a 37% restenosis rate at 12 months in those with SFA stenting versus a 64% restenosis rate for those with angioplasty alone.8 This was further supported by the RESILIENT trial, which demonstrated superiority with target vessel revascularization (TVR) at 12 months in those with SFA stenting over angioplasty alone.9 It is important to note that the RESILIENT results were primarily from TASC A and B lesions, with significantly higher crossover than previous studies. In contrast, the FAST trial demonstrated no difference in binary restenosis at 12 months between PTA and stenting compared to PTA alone.10 This finding was confirmed by a recent meta-analysis, which concluded that while initial procedural success is higher with routine stenting, there was no detectable difference in restenosis or TVR in long-term follow up.11 Stenting of the SFA for TASC A and B lesions is currently recommended only as a bailout procedure after technical failure of angioplasty.12
The last decade has ushered in many new endovascular treatment modalities for PVD including endovascular cryoplasty, cutting-balloon angioplasty, subintimal angioplasty, excisional atherectomy, excimer laser-assisted angioplasty, drug-eluting stents, biodegradable stents and e-PTFE covered self-expanding stents.13,14 The TASC II guidelines recommend endovascular treatment for TASC A and B lesions. Surgical revascularization has been the recommendation for TASC D lesions (lesion classifications are provided in Table 1). The guidelines are ambiguous as to how TASC C lesions are approached. There remains equipoise, with some recommending a trial of endovascular therapy first, while others suggest open surgical techniques as the frontline therapy. Though the guidelines recommend open surgery for the more severe cases (TASC C and D), many of these patients may benefit from less invasive endovascular treatments because they are not candidates for surgery due to a prohibitively high perioperative cardiovascular risk or other medical comorbidities. Many of these patients are denied any treatment, and thus frequently end up with the catastrophic consequence of limb loss.
Chronic total occlusions (CTOs) of the SFA are a particularly challenging lesion subset. Recanalization rates in CTOs are reported as > 85%. Pooled results also show 1- and 3-year patency rates for CTOs of 65% and 48% for PTA alone, and 73% and 64% for PTA/stent.15 There are no long-term data for PTA/stent, but the 5-year patency rates of PTA alone for stenosis and occlusion are 55% and 42%, respectively. Because of these success rates, many feel that patients with more extensive disease should be considered for percutaneous treatment and then referred for surgery if this approach fails. Bypass surgery with venous grafts must still be considered the most durable and extensively studied revascularization technique for patients with chronic limb ischemia and extensive disease of the SFA. The Bypass Surgery versus Angioplasty in Severe Ischemia of the Leg trial found that the rates of amputation-free survival after surgery and balloon angioplasty were similar for at least the first 2 years.18
Nitinol stents may be an effective alternative to surgical revascularization for longer lesions in patients who are poor candidates for surgery, such as those with severe coexisting cardiovascular conditions. Furthermore, stenting may be an option for patients without available saphenous vein grafts, since the 12-month patency data for stents are similar to those for prosthetic bypass grafts, and stenting has a considerably lower rate of complications. However, the endovascular approach seems justified as long as the rates of complications are low and the surgical target zone for the distal anastomosis of a potential secondary bypass operation remains unaffected by the interventional procedure.
This study, conducted at a major teaching hospital, evaluated the safety, efficacy and 1-year patency rates of the Viabahn expanded-PTFE (e-PTFE) stent grafts (WL Gore and Associates, Flagstaff, Arizona) in patients with SFA disease and Functional Class II and III claudication.
Methods
Thirty patients (32 limbs) were prospectively treated for activity and lifestyle-limiting claudication. All patients included in this study were symptomatic and refractory to maximal outpatient medical management including smoking cessation, use of cilostazol and exercise therapy. Asymptomatic patients, despite known severe SFA stenoses or occlusions, were not included in this investigation. Twenty-eight patients (93.33%) were Functional Class III–IV claudicants, while 2 patients (6.67%) presented with critical limb ischemia. None of the patients had tissue loss.
Traditional angioplasty and stenting techniques were employed in all patients. During the procedure, these patients received the Viabahn e-PTFE stent graft. Access for the intervention was obtained from the contralateral route in 22 patients (73.3%), via the antegrade ipsilateral route in 4 patients (13.3%), and via the ipsilateral popliteal approach in 6 patients (20%). No stent grafts < 5 mm in diameter were implanted, as these have known higher graft occlusion and lower graft patency rates. Stent grafts were not implanted in heavily calcified arteries that were resistant to balloon angioplasty due to known lower graft patency rates in this population. All patients were subsequently discharged on lifelong aspirin and clopidogrel. Follow-up clinical visits with ABI examinations and duplex surveillance were completed at 6 and 12 months for all patients.
Results
The mean age of the patients was 58.4 years. In all, there were 12 women (40%) and 18 men (60%). Five of the patients (16.67%) were diabetic. The technical success rate was 100%, with no in-hospital morbidity or mortality. There were no incidents of myocardial infarction, pseudoaneurysm, groin infection or death. One patient (3.3%) did have stent thrombosis at 4 months. The patient presented with acute limb ischemia and was treated with an open surgical approach using an autologous vein for a femoral-popliteal bypass procedure. The angiogram was consistent with a thrombotic occlusion of the stent graft, and no attempt was made to perform thrombectomy as an alternative treatment strategy. The mean preprocedure ABI was 0.54, and the mean SFA length of occlusion was 15.4 cm. The mean stented length was 24.6 cm. The median stent diameter was 6 mm. On follow-up testing, the mean post-procedure ABI at 1 year was 0.76 (Figure 1), with a primary patency rate of 80% at 1 year. Silent asymptomatic occlusions were noted in 10% (3/30) of the patients. Restenosis was detected on duplex surveillance in 6.6% (2/30) of the patients, with subsequent TVR via PTA. The 1-year primary assisted patency rate was 86%.
Discussion
The advent of endovascular treatment modalities has heralded a new era in caring for those with PVD. However, early adoption was limited to those with milder forms of disease (short focal stenosis or occlusions). In addition, the poor results seen in the early days of PTA/stenting had resulted in less acceptance of this strategy as a primary form of treatment for the more severe cases. As stents were initially used provisionally for unfavorable PTA results, earlier studies may have had a bias against stenting.17 However, with the advancement in technology and the introduction of nitinol stents, as well as e-PTFE-lined stents, PTA/stenting can finally be applied as a primary treatment in a large number of patients.
Data have been scarce from randomized clinical trials comparing surgical bypass with percutaneous intervention. This can be attributed to the fact that the two procedures have been historically reserved for different patient subsets. In 2005, Adam et al published a randomized study of 452 patients evaluating the efficacy of angioplasty and surgery in patients with severe lower-extremity ischemia. In this study, the authors found no difference in amputation-free survival at 1 year.18 In contrast to this, Wolf et al conducted a multicenter, prospective randomized trial comparing PTA to bypass surgery in 263 male patients with iliac, femoral or popliteal obstruction. However, in the 56 patients with long SFA stenoses, the 1-year primary patency rates after PTA and surgery were 43% and 82%, respectively.19 The results of this study, however, suggest otherwise, even in the toughest subset of patients, and are more in line with results obtained by Shaikh et al.20 The primary and primary-assisted patency rates obtained at 1 year, 80% and 86%, respectively, are encouraging and comparable to autologous vein bypass surgery.
Long-term patency, however, continues to be an issue of concern with endovascular treatment in the SFA. Coverage of side branches that supply collaterals has also been suggested as a potential problem in using stent grafts in the SFA. In this small study, neither of these issues seemed to be a significant problem. Dual antiplatelet therapy was rigorously enforced and may have had a favorable impact on the low incidence of stent thrombosis (1/30 patients: 3.3%) in this study. The current generation of heparin-coated Viabahn stent grafts were not used in this study. The potential for further reducing thrombotic risk with heparin coating appears promising.
The anatomy of the SFA plays a major role in long-term success, or lack thereof, using endovascular intervention. The SFA is subject to extrinsic dynamic forces (compression, torsion, elongation) that predispose stents to restenosis and fracture.21–23 The Viabahn stent graft consists of an e-PTFE liner attached to an external nitinol stent structure with significant flexibility, which enables it to be more easily placed across tortuous segments of the SFA and conform more closely to the anatomy of the artery. The procedural success rate and 1-year primary and primary assisted patency rates seen in this study indicate that percutaneous e-PTFE stent grafting with the Viabahn stent graft is a viable treatment option for TASC D occlusions in the SFA in claudicants and the occasional patient with critical limb ischemia. Long-term data (> 5 years) in a larger patient cohort are necessary before definite conclusions can be drawn.
Study limitations. This is not a randomized study comparing stents with surgery. The number of patients enrolled in this single-center registry was small, and follow up, though 100%, was reported only for 1 year. In spite of these limitations, this study is thought-provoking and adds to the body of evidence that endovascular treatment for TASC D SFA lesions may not be farfetched, and a randomized, controlled trial comparing surgery and stenting for TASC C and D lesions is warranted to better define the preferred treatment approach for this difficult lesion subset.
_________________________
From the *Cardiology Fellowship, §Interventional Cardiology Fellowship, Banner Good Samaritan Medical Center and £Heart and Vascular Center of Arizona, Phoenix, Arizona.
The authors report no conflicts of interest regarding the content herein.
Manuscript submitted December 30, 2008, provisional acceptance given February 5, 2009, final version accepted February 16, 2009.
Address for correspondence: Nahel Farraj, DO, 7004 West Keim Dr., Glendale, AZ 85303. E-mail: nahelfarraj@yahoo.com
References:
1. Dippel E, Shammas N, Takes V, et al. Twelve-month results of percutaneous endovascular reconstruction for chronically occluded superficial femoral arteries: A quality-of-life assessment. J Invasive Cardiol 2006;18:316–321.
2. Galaria I, Surowiec S, Rhodes J, et al. Implications of early failure of superficial femoral artery endoluminal interventions. Ann Vasc Surg 2005;19:787–792.
3. Selvin E, Erlinger TP. Prevalence of and risk factors for peripheral arterial disease in the United States: Results from the National Health and Nutrition Examination Survey, 1999–2000. Circulation 2004;110:738.
4. Dormandy JA, Rutherford B. Management of peripheral arterial disease. J Vasc Surg 2000;31:251–296.
5. Capek P, McLean GK, Berkowitz HD. Femoro-popliteal angioplasty: Factors influencing long term success. Circulation 1991;83:(Suppl 2):170–180.
6. Henry M, Amor M, Beyar I, et al. Clinical experience with a new mitinol self expanding stent in peripheral arterial disease. J Endovasc Surg 1996;3:369–379.
7. Becquemin JP, Favre JP, Marzella J, et al. Systematic versus selective stent placement after superficial femoral artery balloon angioplasty: A multicenter prospective randomized study. J Vasc Surg 2003;37:487–494.
8. Schillinger M, Sabeti S, Loewe C, et al. Balloon Angioplasty versus implantation of nitinol stents in the superficial femoral artery. N Engl J Med 2006;354:1879–1888.
9. Katzen BT, Laird J; RESILIENT investigators. The RESILIENT trial. 12-Month analysis. TCT 2007 (Transcatheter Cardiovascular Therapeutics). Washington, D.C., 20–25 October 2007. http://www.cardiosource.com/clinicaltrials/trial.asp?trialID51615 (5 November 2008).
10. Krankenberg H, Schlüter M, Steinkamp HJ, et al. Nitinol stent implantation versus percutaneous transluminal angioplasty in superficial femoral artery lesions up to 10 cm in length: The Femoral Artery Stenting Trial (FAST). Circulation 2007;116:285–292.
11. Kasapis C, Henke PK, Chetcuti SJ, et al. Routine stent implantation vs. percutaneous transluminal angioplasty in femoropopliteal artery disease: A meta-analysis of randomized controlled trials. Eur Heart J2009;30:44–55.
12. Hirsch AT, Haskal ZJ, Hertzer NR, et al. ACC/AHA Guidelines for the Management of Patients with Peripheral Arterial Disease (Lower Extremity, Renal, Mesenteric, and Abdominal Aortic): A Collaborative Report from the American Association for Vascular Surgery/Society for Vascular Surgery, Society for Cardiovascular Angiography and Interventions, Society of Interventional Radiology, Society for Vascular Medicine and Biology, and the American College of Cardiology/American Heart Association Task Force on Practice Guidelines (Writing Committee to Develop Guidelines for the Management of Patients With Peripheral Arterial Disease). American College of Cardiology Web Site. Available at: http://www.acc.org/clinical/guidelines/pad/ index.pdf.
13. Lyden S, Shimshak T. Contemporary endovascular treatment for disease of the superficial femoral and popliteal arteries: An integrated device-based strategy. J Endovasc Ther 2006;13(Suppl II):II41–II51.
14. Tepe G, Schmehl J, Heller S, et al. Superficial femoral artery: Current treatment options. Eur Radiol 2006;16:316–1322.
15. Norgren L, Hiatt WR, Dormandy JA, et al. Inter-society consensus for the management of peripheral arterial disease (TASC II). Eur J Vasc Endovasc Surg 2007;33:S1–S70.
16. Duda SH, Pusich B, Richter G, et al. Sirolimus eluting stents for the treatment of obstructive superficial femoral artery disease: 6-Month results. Circulation 2002;106:1505–1509.
17. Gordon I, Conroy R, Arefi M, et al. Three-year outcome of endovascular treatment of superficial femoral artery occlusion. Arch Surg 2001;136:221–228.
18. Adam DJ, Beard JD, Cleveland, T, et al. Bypass versus angioplasty in severe ischemia of the leg (BASIL): Multicenter randomized controlled trial. Lancet 2005;366:1925–1934.
19. Wolf G, Wilson S, Cross A, et al. Surgery or balloon angioplasty for peripheral vascular disease: A randomized clinical trial. Principal Investigators and their Associates of Veterans Administration Cooperative Study Number 199. J Vasc Interv Radiol 1993;4:639–648.
20. Shaikh F, Djelmami-Hani M, Solis J, et al. Percutaneous endovascular treatment of SFA disease using the Gore Viabahn® endoprosthesis. Do the procedural success and 1-year follow-up data make this the treatment of choice? Endovasc Today 2007(Suppl).
21. Laird J. Limitations of percutaneous transluminal angioplasty and stenting for the treatment of disease of the superficial femoral and popliteal arteries. J Endovasc Ther 2006;13(Supp II):II30–II40
22. Ferreira M, Lanziotti L, Monteiro M, et al. Superficial femoral artery recanalization with self-expanding nitinol stents: Long-term follow-up results. Eur J Vasc Endovasc Surg 2007;34:702–708.
23. Kessel D, Wijesinghe L, Robertson I, et al. Endovascular stent-grafts for superficial femoral artery disease: Results of 1-year follow-up. J Vasc Interv Radiol 1999;10:289–296.
Dr. Suzanne Sorof, President of AHA-Phoenix Chapter Speaks at the Go Red For Women Luncheon
American Heart Association's - Go Red For Women Luncheon
More than 600 women from across the Valley took part in the Go Red For Women Luncheon on Friday, May 1 at 11:45 a.m. The 5th annual luncheon, was held at the Sheraton Phoenix Downtown Hotel, will raise awareness around heart disease, the No.1 killer of women. The American Heart Associations Go Red For Women campaign encourages women to take charge of their heart health and make it a top priority to live a stronger and healthier life.
This years luncheon featured Dr. Suzanne Sorof, interventional cardiologist from the Heart & Vascular Center of Arizona who shared the warning signs of heart disease and heart disease prevention tips. In addition, Elaine Lundberg, MA a nationally recognized humor therapist, Dr. Iva Smolens, a local cardiothoracic surgeon and Lin Sue Cooney, anchor - 12 News, served as Emcee of this years event. This special day began at 9 am with educational sessions on healthy cooking and heart disease prevention.
"Heart disease and stroke claim more womens lives each year than the next seven causes of death combined, and nearly twice as many as all forms of cancer, including breast cancer,¨ says Valerie Jones, executive director of the American Heart Association in Phoenix. In Arizona, nearly 5,000 women die from heart disease every year.¨ Ninety percent of women feel they have power over their health but only 27 percent say their health is a top priority according to a recent American Heart Association survey.
This lack of urgency about such a serious health threat contributes to the deaths of more than 500,000 American women every year. The campaign is sponsored nationally by Macys and Merck, and locally by University of Phoenix, Banner Health, and Safeway. Our focus is to empower women to reduce their risk of heart disease,¨ says Jones. The Go Red For Women Luncheon empowers women to take action against heart disease and make heart disease prevention a part of their life, because your heart is your life.¨
By calling 1-888-MY-HEART or visiting http://www.americanheart.org/women americanheart.org, women will receive a Heart Health Tool Kit with tips and information, including:
*A comprehensive brochure with information on heart disease and stroke risk factors and warning signs
*A bookmark with information on how women can reduce their risk for heart disease and stroke
* A wallet card with questions to ask a doctor and a chart to track blood pressure, cholesterol and weight
*An American Heart Association red dress pin to wear to show support for the women and heart disease cause.
About the American Heart Association Founded in 1924, the American Heart Association today is the nation¡¦s oldest and largest voluntary health organization dedicated to reducing disability and death from diseases of the heart and stroke. These diseases, Americas No. 1 and No. 3 killers, and all other cardiovascular diseases claim over 870,000 lives a year. In fiscal year 2005-06 the association invested over $543 million in research, professional and public education, advocacy and community service programs to help all Americans live longer, healthier lives. To learn more, call 1-800-AHA-USA1 or visit americanheart.org.
Go Red For Women Campaign Encourages Healthy Hearts
Reported by: Eva Bowen
Email: ebowen@abc15.com
Last Update: 2/17 8:17 am
Women across Arizona will Go Red For Women throughout February to raise awareness of cardiovascular disease, women's number one health threat.
The American Heart Association's campaign invites women to take charge of their heart health, and make it a top priority for a stronger, longer life.
Red is the American Heart Association's color for women and heart disease.
"We need a bold color like red to draw attention to heart disease, which is women's greatest health threat," said Suzanne Sorof, MD, interventional cardiologist and president of the American Heart Association's board of directors in Phoenix.
"Red symbolizes women's power to take control of their health and passion for the women whose lives have been affected," said Sorof.
The association is encouraging everyone to wear red - such as a red dress, shirt, hat or other item - throughout February in support of all women who have been touched by heart disease or stroke.
"Our focus is to empower women to reduce their risk of heart disease." The American Heart Association's Go Red For Women movement, sponsored by Macy's and Merck, encourages women to become more aware of their risk for heart disease and stroke, as well as what they can do to reduce their risk.
For more information, please contact Nancy Keane, Director of Marketing Communications, American Heart Association/American Stroke Association at 602-414-5341 or 480-495-7131. - nancy.keane@heart.org.
Dr. Suzanne Sorof is an interventional cardiologist at Banner Estrella and Banner Good Samaritan medical centers, specializing in women's cardiology.
Question: I am a 61-year-old woman with diabetes, and I have read that I am at increased risk for a heart attack. What should I know about heart disease?
Answer: The more risk factors you have, the greater your chances are of developing coronary artery disease. Age, sex and genetics are risk factors you cannot control. However, you can influence other risk factors, including avoiding tobacco smoke, controlling cholesterol and blood pressure and increasing your level of physical activity.
Children of parents with heart disease are more likely to develop the disease. African-Americans have a higher risk of high blood pressure and heart disease than others. Also, minorities have high rates of obesity and diabetes, which also predispose them to heart disease. Women with diabetes have more than double the risk of heart attack than non-diabetic women.
Although men are more likely to suffer heart attacks, once a woman completes menopause, she is more likely to suffer a fatal heart attack. The symptoms women experience are often misdiagnosed as gastric reflux, anxiety or even the flu. They can include shortness of breath, nausea, back pain, fatigue, malaise and dizziness. Symptoms are often mild and difficult to diagnose. In many cases, this delay of treatment results in complications and increased mortality. Diabetics often do not feel chest pain, and their symptoms are overlooked as upper-respiratory infection.
In general, women wait longer than men to go to an emergency room and physicians are slower to recognize the symptoms.
Specialty: Cardiology Medical School: McGill University, Montreal, Canada Years Practicing: 24 Hometown: Montreal, Canada
What brought you to Phoenix?
“I recognized an opportunity, and I liked to teach and do research, and I didn’t want to have to worry about tenure and the university politics. I came here and was able to do everything in the realm of private practice. I was the coronary care unit director at Good Sam from 1986 until 1991. Now I am the director of Banner Health’s interventional cardiology fellowship program, which teaches young doctors how to do angioplasty and stints.”
Are people here healthier than in other places you’ve worked, such as Michigan?
“I don’t think people are healthier necessarily. I think younger people are healthier, but we have a lot of people that move here from elsewhere who have cardiac problems. The chance of having a heart attack today is going down across the country because patients in general are taking better care of themselves. But there is certainly plenty of coronary disease to keep us busy.”
Why do you think coronary disease is still so prevalent?
“I think a lot of the public is looking for a quick fix – a magic pill – and do not want to do the things that are necessary, such as diet and exercise. The public wants instant gratification. They want laser [treatment] for their carotid arteries rather than preventing these things to begin with. They view medicine as a pit stop in the race of life, whereas a little preventive maintenance goes a lot further.”
We live in a caffeinated society. How does that affect our tickers?
Too much of anything is never good. Everything in moderation should be the motto. One to two cups of coffee a day are best, no more. Caffeine is also a mild diuretic. People think that because there is water in coffee, it hydrates you. But actually, it’s just the opposite.
POSTED: 12:04 pm MST November 26, 2007
UPDATED: 12:06 pm MST November 26, 2007
PHOENIX -- Drugs, diet and exercise are the most common ways to prevent a heart attack in the long run, but what about a quick fix when the symptoms hit hard and fast?
CBS 5 News learned of a potentially life-saving technique that may help hold off a heart attack if you feel one coming on.
An e-mail says you may be able to cough your way out of a blackout, but is that really true?
"Coughing can help and can keep you awake enough that you can call 911," said Dr. Nathan Laufer.
Laufer, a renowned Valley cardiologist, said coughing deeply forces blood to the brain and can contract an erratic heart. That can keep you awake long enough to get help.
"It won't prevent a heart attack, but the problem with heart attacks is that 50 percent of patients don't make it to the hospital because they die suddenly," Laufer said.
Coughing buys time, but you must start coughing immediately and deeply. If it really is a heart attack, you have only about five to 10 seconds before you'll pass out.
"It doesn't last forever because eventually you get fatigued and tired and you will pass out. But it may give you those extra few seconds or minutes where you can actually get to a telephone," Laufer said.
Laufer said he uses the coughing technique in his office if one of his patients goes into arrhythmia.
Copyright 2007 by KPHO.com. All rights reserved.
This material may not be published, broadcast, rewritten or redistributed.
Improving one's diet and exercise vs. having a stent implanted may be equal in terms of preventing a heart attack, but the two appraches may vary greatly in their effects on your quality of life, according to a Valley cardiology expert.
"You have to ask, why are we doing these procedures?" asked Dr. Nathan Laufer, director of interventional cardiology at Banner Good Samaritan Medical Center, where about 3,500 stent interventions are performed every year.
The number of angioplasties performed in Arizona has risen over the past several years. In 2000, there were 11,854 of the procedures; in 2005, there were 17,039.
Having a stent implanted is "not necessarily to make the patient live longer, but to help them live better."
In Canada, where angioplasties are not as common as in the United States, many patients improve their diet and exercise but are still medically disabled.
Although exercise can relive pain and tightness, it doesn't mean ite will go away. An angiioplasty can improve those chances, said Laufer, who also is medical director of the Heart & Vascular Center of Arizona.
Intermediate Term (2 YEAR) Outcomes Following Unprotected Left Main Trunk Percutaneous Intervention With Drug Eluting Stents.
Type: Poster
Starts On: TBD
Presenter/Author:
Ashish Pershad, MD, Rajendran Sabapathy, MD, Adam Brodsky, Renee Espinosa, MD, Nathan Laufer, MD, Heart and Vascular Center of AZ, Phoenix, AZ
Abstract Number: 366
Background: Bypass surgery remains the revascularization strategy of choice for left main trunk coronary artery disease in an unselected group of patients. Drug eluting stents have been proposed as a viable alternative to bypass surgery for left main trunk lesions but their intermediate and long term outcomes are still under scrutiny.
Methods: A series of 50 patients with significant unprotected left main trunk stenosis (>50%) underwent revascularization with drug eluting stents (sirolimus and paclitaxel stents ) and were enrolled in a registry. Follow up angiography was clinically driven for recurrent chest pain and ischemia on MPI. Prespecified primary endpoints of this registry were major adverse cardiac event at 2 year follow up. Major adverse cardiac events were defined as death; ST elevation MI; Need for urgent CABG; Non Q MI defined as CPK -MB measurements at 3 times the upper limit of normal; persistent ischemia by nuclear imaging and target lesion revascularization. Target lesion revascularization was defined as intervention within the left main trunk or within 10mm distal to the branch vessel ostia.
Results: The mean age of patients was 68 years. 40% of the subjects were female. 32.5% of patients were diabetic and the mean EF was 45%.
Clinical follow up at 2 years was complete in all 50 patients (100%). Angiographic follow up was necessary in 20 patients (40%). The lesion treated was in the distal LMT in 24/50 (49 %) patients. Heavy fluoroscopic calcification was noted in 10/50 (20%) patients. The RCA was occluded in 3/50 (6%) patients. Peri-procedural IABP was used in 10/50 (20%) patients. Elective or bailout IIb IIIa use was in 13/50 (25%) patients. Two stents were used in 23/50 (46%) patients. Bifurcation technique used was V/T stent approach in 22/23 (95% ) and crush tehnique in 1/23 (04%) patients.
Conclusions: There were no deaths or need for urgent CABG. The incidence of Q wave MI was 1/50 (2%) and Non Q wave MI was 2/50 (4%) in follow up of 2 years. The need for TLR was noted in 4/50 (8%) patients. Thus the low cumilative major adverse cardiac event rate of 14% at 2 years warrants a randomized control trial comparing PCI with CABG.
There are approximately 2 million cases of acute coronary syndromes per year, with medical costs of $100 billion. Aggressive medical therapy with 3-hydroxyl-3-methylglutyaryl coenzyme A reductase inhibitors, beta-blockers, aspirin, platelet inhibitors, and angiotensin-converting enzyme inhibitors are part of the treatment for this ever-growing problem of coronary atherosclerosis. As technology continues to evolve, there will be new techniques to assist the interventional cardiologist in identifying a plaque and determining its primary composition.
Percutaneous Approaches to Aortic Valve Replacement
Aortic valvular disease is a common disorder often affecting elderly patients with multiple comorbidities. A percutaneous approach to aortic valve replacement would allow treatment of high-risk patients without exposing them to the risks associated with surgery and cardiopulmonary bypass. Percutaneous aortic valve replacement presents several challenges due to the valve’s proximity to the coronary ostia and mitral valve.
INDUSTRY WRAPUPS - From the October 1, 2004 print edition of Health
Heart center gets FDA nod for stroke prevention
Angela Gonzales The Business Journal
The Heart & Vascular Center of Arizona received approval to use a new technique for treating life-threatening blockages of the carotid arteries, the major blood vessels in the neck that supply blood to the brain.
The U.S. Food and Drug Administration approved the procedure, which will allow thousands of patients to benefit from a minimally invasive procedure that could revolutionize the treatment for stroke prevention.
Blockages in the carotid artery are one of the leading causes of stroke.
The technique combines two standard cardiovascular procedures for opening blocked or partially blocked arteries -- angioplasty and stenting. Added to the procedure is a filter catheter that prevents blood clots from floating to the brain.
Dr. Nathan Laufer, medical director of Heart & Vascular Center of Arizona, has been performing the carotid stent procedure in Phoenix for the past four years under an FDA-approved protocol.
During the procedure, the doctor places a small catheter in the groin, Laufer said.
"Traditional carotid surgery requires a large surgical incision in the neck, general anesthesia and may not be the procedure of choice for patients with other serious illnesses," he said. "Carotid stenting is a major step forward in the prevention of stroke using minimally invasive techniques."
Laufer, who also is the director of the fourth-year interventional cardiology training program at Banner Good Samaritan Regional Medical Center and chief of cardiovascular services at the soon-to-open Banner Estrella Medical Center, will help develop physician training courses for the new technique.
INDUSTRY WRAPUPS - From the September 26, 2003 print edition - Health Section
Local doctor investigates drug-coated coronary stent
Angela Gonzales
The Business Journal
Dr. Nathan Laufer, medical director of Heart & Vascular Center of Arizona, was the local principal investigator on Boston Scientific Corp.'s study released this week of its drug-coated coronary stent that is showing promising results.
Many times, after a stent is inserted to hold open arteries, plaque will begin to build up, causing the arteries to renarrow. For the study, the drug Paclitaxol was used to coat the stent to inhibit renarrowing of the arteries.
Boston Scientific released trial results at a national interventional cardiology meeting in Washington last week.
Physicians had expected the Boston Scientific Taxus IV trial to show a renarrowing rate of between 9 percent and 11 percent. The nine-month clinical renarrowing rate for Taxus IV patients treated with the stent was 3 percent to 4 percent, compared with 26.6 percent for a nondrug coated stent control group.
"This will further reduce the need for bypass surgery in many more patients and will reduce the cost of drug coated stents by inserting competition in the marketplace," Laufer said.
Boston Scientific officials hope to receive FDA approval for the Taxus drug eluting stent by the end of this year.
This article is reprinted with permission. Copyright 2002, East Valley & Scottsdale Tribune, a Freedom Communications, Inc. company. All rights reserved. For more information, please visit http://www.eastvalleytribune.com/.
May 5, 2003
A just-approved device expected to reduce the number of repeat procedures on hundreds of thousands of heart patients and even the need for bypass surgery in some, went through clinical trials in two Valley hospitals, including Scottsdale Healthcare Shea.
Johnson and Johnson's Cypher is the first drug-coated coronary stent available in the United States. The device dramatically reduces the need to replace the tiny metal mesh tubes used to prop open clogged coronary heart vessels.
Each year 800,000 angioplasty procedures are performed in the United States to open coronary arteries clogged with plaque, according to the FDA. In as many as 30 percent of patients, the artery becomes clogged with scar tissue within a year, requiring a second angioplasty or bypass surgery.
The Cypher — in sizes ranging from a grain of rice to a fork tine — is infused with a chemotherapy formula used to inhibit the growth of scar tissue. The metal mesh tube enters the body through a catheter inserted into an incision in the groin. The stent is then threaded into the heart vessels and introduced inside the old stent blocked with scar tissue, or into a blood vessel blocked with plaque. There, a balloon expands the scaffolding to its permanent shape. Once in place, the drug inhibits the growth of scar cells in the affected area, reducing the need for a replacement. The drug is released into the blood vessel for about one month — sufficient time to impede scarring, Rizik said.
Dr. Nathan Laufer, director of the interventional training program at Banner Good Samaritan Medical Center in Phoenix, who implanted the Cypher in 40 Arizona residents for an FDA clinical trial, said that 90 percent of people who suffer from symptomatic coronary artery disease are candidates for the Cypher.
"Lots of patients won't need a second (stent) procedure," Laufer said. And for some, the stent will eliminate the need for bypass heart surgery, he said.
The new stent will lower the need for subsequent replacements to less than 10 percent of patients, and in ideal candidates, to 2 percent, Rizik said.
Scottsdale resident Lewis Izzo, 81, was recovering Tuesday from implantation of his third stent — his first Cypher. Within 24 hours he said he was feeling more energetic.
"I felt tired all the time. I couldn't walk the length of a car," said Izzo, who at Shea hospital was Scottsdale Healthcare's first post-FDA approval Cypher patient. "This is great."
Izzo's other two stents — which he received in the past seven years — already were showing blockage.
The Cypher costs about $3,200 — three times that of a traditional stent. While it is covered by Medicare and many private insurance plans, the price is expected to drop within the next year when a second drug-coated stent is expected to pass FDA approval.
The success of drug-coated stents means the future for traditional stents is bleak, Laufer said.
"The rest of the industry may go belly-up," he said.
In 2000, 515,204 people in the United States died of coronary artery disease, making hardening of the arteries the single leading cause of death in the United States, according to the American Heart Association.
Contact Emma Johnson by email, or phone (480) 898-6373