Is Cardiac Arrest Contagious?

Sudden cardiac arrest is what happens when the heart stops beating suddenly and unexpectedly. It is the leading cause of death of adults in this country. However, it is not just an adult thing. It is linked to 10% of SIDS deaths; is the leading cause of death of student athletes; and takes the lives of thousands of children every year.

Is it contagious?

Last week, two stories broke about the risk of sudden cardiac arrest in athletes. Cameron Smith, a twenty-four year old linebacker with the Minnesota Vikings, discovered a heart condition (bicuspid aortic valve) after being diagnosed with COVID-19. Biscupid aortic valve is a condition where the aortic valve has two leaflets instead of three. The aortic valve regulates blood flow from heart to the aorta. This is a structural heart condition and is usually inherited.

Then, the Big Ten reported at least ten players were diagnosed with myocarditis after testing positive for COVID-19. Myocarditis is an inflammation of the heart muscle (called myocardium) that limits the heart’s ability to pump blood. This condition is also structural, but it is acquired. It is caused by things like a virus or a drug interaction.

“We know that COVID-19 can attack the heart, said David Shipon, a cardiologist at Jefferson University Hospital and Chief Medical Officer of Simon’s Heart. “Typically, the worse the symptoms are from COVID, the greater the likelihood that the heart will become inflamed. But, all physically active individuals who are diagnosed with COVID should get their hearts screened because we are still learning about the effects of this virus.”

These stories amplify our message – testing and screening are so important. It is not enough for us to assume that Cameron’s heart was healthy for the first two decades of his life. He and all of his high school classmates should have been screened. He is an elite athlete. He won a state championship in high school, played at USC for four years, and was drafted by the NFL. Should he have to wait for a pandemic to find something so significant?

The case of the Big Ten players underscores the importance of screening for a different reason. It is not enough to report positive tests, hospitalizations and fatalities of COVID-19. We need to understand how this virus is compromising the hearts and other parts of our children. Over 300,000 children have tested positive for coronavirus, and while the mortality rate is very low today, how many of these children will suffer from heart failure or cardiac arrest in the future? We won’t know unless we screen and conduct research.

Sudden cardiac arrest is not contagious, although viruses like COVID-19 that can cause myocarditis are. Whether the conditions are inherited or acquired, we can prevent sudden cardiac arrest through screening and research. Our children don’t have to die from detectable and treatable heart conditions.

Jake Berman

“I attended a heart screening at Colonial Middle School when I was ten. I was in the marching band and liked to hike and rock climb. I was diagnosed with Wolff Parkinson White Syndrome. After my procedure, I kept doing the same things.”

Whitney Jones

Whitney’s commitment to heart health advocacy began at 10 years old when she and her mother, Rayna, were diagnosed with Long QT Syndrome during a Simon’s Heart screening at Downingtown West High School. Despite the diagnosis, Whitney pursued her passion for cheerleading and continued to thrive in the sport through her college years at St. Joseph’s University. After graduating, Whitney joined Stryker Instruments as the Senior Specialist for Off-Site Meeting and Events, where she skillfully orchestrates events that promote health and medical innovation. Further extending her impact, Whitney is an active member of the Simon’s Heart Young Professionals Committee, while her mother Rayna contributes her expertise on the Board of Directors.

Katie Asper

“I attended a heart screening at Upper Dublin High School when I was ten. I played soccer. I was diagnosed with Wolff Parkinson White Syndrome and had an ablation to fix the problem. I attend Temple University.”

Matthew Green

“I attended a heart screening in Mason, Ohio, when I was ten. I participated in baseball, basketball, and diving. I was diagnosed with an atrial septal defect. I had surgery to repair the hole and started wearing a protective shirt during activity. I am graduating from Miami University.”

Valerie Krawitz

“I attended a heart screening at Colonial Middle School when I was ten. I played baseball, soccer, and track. I was diagnosed with Long QT Syndrome and an atrial septal defect. I had heart surgery to repair the hole and I take medicine for the Long QT. I can’t play competitive sports like I once did, but found other activities. Next year, I’m attending Penn State University.”

Drew Harrington

“I attended a heart screening at Radnor High School when I was ten. I played lacrosse, tennis, and basketball. I was diagnosed with Wolff Parkinson White Syndrome. I used to feel my heart beat really fast, but just assumed it was fine. Coincidentally, on Simon’s 7th birthday, I had a procedure called an ablation. Today, my heart is fine and I attend the University of Richmond.”

Alaysia Keeley

“I attended a heart screening at Norristown High School when I was ten. I played softball and enjoyed going to the mall with my friends. I was diagnosed with Long QT Syndrome. I had to stop playing sports and drinking soda. Now, I take medication and live a normal life.”

Kyle McCabe

“I attended a heart screening at Norristown High School when I was ten. I played baseball, basketball, and football. I was diagnosed with Long QT Syndrome. I stopped playing sports to protect my heart, but I still manage to have fun.”

Melissa Fair

“I attended a heart screening at Colonial Middle School when I was ten. I loved dancing and hanging out with my friends. I was diagnosed with Partial Anomolous Pulmonary Venous Return and Atrial Septal Defect. The doctor told me that my life would have been cut short if I hadn’t found out. I’m graduating from Penn State University this year.”

Zach Steffens

“I attended a heart screening at Stillman Elementary School in Tenafly, N.J., when I was fourteen years old. I love running, Tae Kwon Do, and Armenian cultural dancing. I was diagnosed with a rare congenital defect called ALCAPA (Anomalous Left Coronary Artery from the Pulmonary Artery). I had open-heart surgery and recovered well. One month later, I suffered a cardiac arrest and an automated external defibrillator (AED) saved my life. I now have an implantable cardioverter defibrillator (ICD) and am healthier than ever. I will be attending The College of New Jersey and majoring in biomedical engineering.”

Annie FitzPatrick

“I went into sudden cardiac arrest at a local convenience store when I was 19 years old. My heart stopped and the only reason I am alive today is because an AED was readily available. I was diagnosed with Long QT Syndrome shortly after and was introduced to Darren and Phyllis with Simon’s Heart. I have been an active volunteer ever since. I went on to graduate Cum Laude from Drexel University with a double major in Business Analytics and Marketing and now work at a leading chemical company.”

Maeve Quinn

"I had a sudden cardiac arrest during softball tryouts at my high school. I was 15 years old. Thanks to the quick thinking of my coach and athletic trainer, they started doing CPR and using an AED immediately. This helped save my life. I had an implantable defibrillator surgically placed in case this happens again. I volunteer to educate people on the importance of screenings, learning CPR and the use of AEDs. Anyone can save a life like mine! I am planning on going to college for nursing."