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Tag: heart attack

  • Polly the dog to be crowned a “CPR Hero” for helping save her owner’s life during a cardiac arrest

    A golden retriever is being lauded as “the first responder” who helped saved her owner’s life when he suffered a cardiac arrest in the middle of the night.

    Hannah Cooke, from County Fermanagh in Northern Ireland, was woken up one night last year by a bark from Polly, she and her husband’s four-year-old dog, who the couple said normally sleeps quietly through the night.

    When she turned to her husband sleeping next to her, Hannah found him breathing irregularly, and then he stopped breathing entirely, according to the British Heart Foundation, which told the couple’s story ahead of a ceremony on Tuesday that will see both Hannah and Polly crowned “CPR Heroes” for their actions.

    Golden retriever Polly from Fermanagh helped save her owner Adam’s life when he had a cardiac arrest asleep in bed in 2024.

    British Heart Foundation


    “When I heard the noise Adam was making I sat bolt upright in bed, as I previously worked as a carer and it hit me that it was the same noise I’ve heard when people are taking their final breaths,” said Hannah, 33.

    She immediately sprang into action, calling an ambulance and performing CPR on her husband until paramedics arrived to whisk him to the hospital. On the way, they shocked Adam seven times with a defibrillator before his heart rate normalized.

    Adam woke up at the hospital six days later and learned that he had been diagnosed with a heart disease called dilated cardiomyopathy, which prevents the heart from pumping blood around the body effectively.

    After weeks of recovery and a procedure to have a Implantable Cardioverter Defibrillator put in his chest, Adam was finally allowed to go home — where he was reunited with Polly.

    polly-cooke.jpg

    Polly’s barking woke Adam’s wife Hannah who performed life-saving CPR and contacted the emergency services

    British Heart Foundation


    “When I got out of hospital, I’ll never forget seeing Polly again and knowing how she had intervened that night. I just cuddled her and cried for 20 minutes,” Adam said.

    The couple credit Polly with having saved Adam’s life by being “in tune” with him, and they believe she even knew what was happening.

    “Polly alerted me, possibly within seconds of Adam’s cardiac arrest, she was the first responder,” Hannah told the BHF, a charity that raises awareness of cardiovascular disease and money to fund research into treatments and cures. “Because of her, I was able to start CPR almost immediately.”

    Hannah and Polly were set to receive their honors as “CPR Heroes” at the BHF’s Heart Hero Awards ceremony in London on Tuesday evening.

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  • Can you have a heart attack without chest pains? – WTOP News

    When heart attacks happen, typically you’ll feel it in your chest first. But about 30% of people have to watch for other symptoms beyond chest pain.

    Hundreds of thousands of Americans suffer a heart attack every year, and heart disease remains the biggest cause of death here in the U.S. And when those heart attacks happen, typically you’ll feel it in your chest first.

    “Most of the time, that pain is a really bad aching, pressure feeling, although some people perceive it as a sharp pain,” said Dr. William Brady, a professor of emergency medicine at the University of Virginia. “About 70% of people that have a heart attack are going to have chest pain as the primary symptom.”

    But that means about 30%, which isn’t an insignificant number of people, have to watch for other symptoms beyond chest pain.

    “There’s a couple of other groups of the population that just don’t always have the same symptoms as most people do early on,” Brady said.

    That includes women, older Americans (especially those over 80) and someone who might be diabetic. So you need to be on the lookout for other signs too.

    “This can be like sudden, extreme weakness, terrible, extreme fatigue that happens all of a sudden, usually associated with nausea, maybe vomiting,” Brady said. “The sweating, maybe shortness of breath, sometimes the chest pain can begin to appear after the weakness and the fatigue has actually hit the patient and is making them feel bad.”

    In some cases, the pain might show up not in the chest, but the arms, your neck, or even your jaw. Brady said that’s usually called referred pain or radiating pain.

    “Most of the time, people have pain in their middle or left chest,” he noted; however, “You can have radiation of the pain to the left shoulder, the left elbow, sometimes the right shoulder, up into the jaw, the front part of your neck.

    “You may not have any chest pain,” Brady added. “I’ve seen patients that have come in and have had really bad elbow and shoulder pain on the left side without any chest pain, but they also had some nausea. They also were sweating profusely, and so that should trigger the possibility of a heart attack in the patient.”

    It’s another way that the pain people feel can be very individualized. And having a heart attack doesn’t necessarily mean you’re in cardiac arrest and will collapse right away. But left untreated, it can get to that point.

    “A heart attack is, in most cases, a blockage of one of the heart arteries that reduces or blocks blood flow to the actual muscle of the heart, and the heart muscle begins to die because of inadequate blood flow,” he said.

    You may decide you need to lie down, but you’re not going to collapse, at least initially. Still, if you feel those symptoms, you need to call for help.

    “Paramedics can treat you en route to the hospital and stabilize any complications of a heart attack,” said Brady. “Once you arrive in the emergency department, you’ll be able to be treated for the heart attack itself.”

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    © 2025 WTOP. All Rights Reserved. This website is not intended for users located within the European Economic Area.

    John Domen

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  • Woodbury teen’s Girl Scout project spurred by father’s heart attack

    Fourteen-year-old Patty Barton, or Patty Sue to her dad, has had the ‘typical’ teenage relationship with her parents, she said. There are ups and downs, but she always expected her parents would be there.

    That is until November 2024, when her dad suffered a heart attack. A shock to her family of six. Her father, Zach Barton, stayed in the hospital for 11 days and underwent triple bypass surgery.

    “After Dad’s heart attack, he and I got a lot closer,” Patty said. “I realized I wasn’t going to take things for granted anymore.”

    Patty has been in Girl Scouts since kindergarten and is preparing to receive her Silver Award, one of the highest achievements in Girl Scouting involving a community issue that requires at least 50 hours of volunteer service.

    Patty’s project is one she advocated for following her father’s heart attack. When he was in the hospital, she overheard doctors tell him he needed to pick up a low-impact sport, and biking fit the criteria. Her project, a Dero Fixit Bike Repair Station installed in Powers Lake Park near their Woodbury home, is a spot where bikers can stop and fill their tires, fix a flat or adjust about anything on a bike.

    “I wanted to do this and dedicate it to my dad because he scared me there for a while, that he wasn’t going to be able to keep his promise to me and walk me down the aisle,” Patty said, tearing up, as her father went to hold her hand.

    An unexpected hospital stay

    In early November, while doing yard work, Zach Barton felt a sudden pain in his chest. A few days after visiting the emergency room, he experienced a mild heart attack.

    The heart attack came as a surprise, he said. He’d always been healthy, eaten better than the average person, exercised regularly, never smoked and wasn’t diabetic, so it wasn’t caused by any of the things people tend to associate with heart attacks, he said.

    What he does have is familial hypercholesterolemia, a genetic disorder that causes high cholesterol in the body, which is what ultimately led to the heart attack.

    For 11 days, Barton stayed in the hospital, missing Thanksgiving with his family, he said.

    “Healing was a slow process for eight weeks,” he said. “I couldn’t lift above 10 pounds. I had to sleep kind of upright and anytime that I coughed, it hurt ever so bad.”

    Related Articles

    Patty, who believes herself to be a ‘model Girl Scout,’ someone who is a go-getter, innovator, risk-taker and leader, had her heart set on her Silver Award project for months before the heart attack. Her first few ideas: outdoor classrooms for local schools. However, three separate times, her projects fell through.

    When her dad was in the hospital, her priorities changed.

    “I had given up hope on my silver,” Patty said. “I was like, ‘I’ve already gotten three rejections, Dad’s in the hospital, this is the last thing I need to be worried about right now.’”

    Until she overheard that conversation between her parents and her father’s cardiologist, who recommended a low-impact sport.

    “Biking is a form of low-impact exercise,” Patty said.

    The Fixit Bike Repair Station

    When Patty was younger, she and her family would bike together regularly, and during the early years of the COVID pandemic, they even committed to biking 100 miles together one season, resulting in the grand prize of a family visit to Chuck E Cheese.

    Reminiscing on the memories she had of biking with her dad, the idea for the Fixit station came to Patty, as she’d seen one at a national park many years ago. She presented the idea to her troop leader (her mom, Joanna) and explained why exactly her idea was important.

    “This bike Fixit station is there to help the community and to make sure that other girls can continue biking with their dads,” Patty said.

    The repair station includes ‘all the tools necessary to perform basic bike repairs and maintenance,’ according to Dero. Tools attached to the station can change a flat tire, adjust brakes and derailleurs, fill tires with air, assist in changing seat levels and more. The station also includes a QR code that can be scanned to explain use and provides a map of all other Fixit stations in the state.

    While there is one other FixIt station in Woodbury, Patty said, it’s all the way in Carver Lake Park, on the opposite side of town.

    “I am hoping that there will be more of these in Woodbury because Woodbury is extending their trails,” Patty said. “I am hoping that there will be more of these because I’ve been in a sticky situation where I don’t have a bike pump on me or I’ve thrown a chain while mountain biking.”

    A stronger father-daughter bond

    After being released from the hospital on Dec. 1, 2024, Zach Barton said all four of his children were by his side, every step of the way.

    “Any time that I would call, or if they were within 10 feet of me, and they saw that I was in pain, they’d come and squeeze my arm and latch onto my arm until I finished coughing, bring me my heart pillow, bring me water, bring me whatever it was, and say, ‘Dad, are you okay? Is there anything else that you need?’”

    Patty, whose birthday is Dec. 19, said she was happy that her dad was able to be there to see her turn one year older, and that the two could continue their tradition of hanging Christmas lights together. Except this time, when her dad tried to leave the house, she would yell at him to go back inside and rest. It was out of love, she said, as his close friends were there to help hang the lights while he watched in support.

    Now the family takes turns going on daily bike rides with their dad, something Patty said she’ll never again overlook.

    “I’m trying to prioritize health, I’m trying to prioritize diet, so it gives me the best chance for longevity,” Zach Barton said. “All four of these amazing kids and my wonderful wife are there helping me.”

    Related Articles

    In the spring, Patty will receive her Silver Girl Scout Award for her Fixit bike station project, which she paid for using money she’d saved from selling Girl Scout cookies. The station itself cost $2,200, a couple of years’ worth of cookie sales. The city paid for the concrete pad and installation, her father said.

    “I think she did an amazing job. I think it was worth Gold,” 10-year-old brother and Boy Scout Danny Barton said. “If I were a Girl Scout, I don’t think I could do a better solo project.”

    Recently, Patty was sent a Facebook post from a Woodbury resident who’d snapped a picture of the station and captioned it, ‘Thank you to whoever did this. I got a flat and I really appreciate it.’ The post brought a smile to her face; it wasn’t just helpful for her family, but for her broader community too.

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  • 18-year-old survives heart attack, hopes to inspire change

    18-year-old survives heart attack, hopes to inspire change

    Heart disease is the leading cause of death for women in the U.S., and it’s something that can affect people of all ages.A drive to work on July 4 changed 18-year-old Ella Beveridge’s life.”I was at a stoplight right by a gas station, and after I had called my mom, I thought I should pull over because it hurt so bad,” Beveridge said.Her trip to the hospital turned into a 12-day stay because that pain was a heart attack.“I didn’t think that’s what it was. I thought it was something else. Just because I’m so young,” Beveridge said.Beveridge is still recovering as doctors search for answers on why and how she developed a blood clot.“It was really surprising. I was a very healthy kid. I’ve never had any health problems,” Beveridge said.Since July 4, everyday life for the 18-year-old looks different. She now wears a defibrillator.​“If it’s too bad of an irregularity, this will start beeping and say it wants to shock me, and I’ll have to hit these two buttons on either side of it,” she said.Beveridge continues her journey to wellness; she’s also on a new mission: advocacy.“I want people my age to listen to their bodies more just so that, like, if they think something is wrong, they need to go talk to someone,” Beveridge said.She hopes sharing her story can lead to more research. The statistics could finally change where, one day, heart disease won’t be the number one cause of death for women.Ella and her mom will be sharing their story at a fundraiser for the American Heart Association.Tickets are still available online.

    Heart disease is the leading cause of death for women in the U.S., and it’s something that can affect people of all ages.

    A drive to work on July 4 changed 18-year-old Ella Beveridge’s life.

    “I was at a stoplight right by a gas station, and after I had called my mom, I thought I should pull over because it hurt so bad,” Beveridge said.

    Her trip to the hospital turned into a 12-day stay because that pain was a heart attack.

    “I didn’t think that’s what it was. I thought it was something else. Just because I’m so young,” Beveridge said.

    Beveridge is still recovering as doctors search for answers on why and how she developed a blood clot.

    “It was really surprising. I was a very healthy kid. I’ve never had any health problems,” Beveridge said.

    Since July 4, everyday life for the 18-year-old looks different. She now wears a defibrillator.​

    “If it’s too bad of an irregularity, this will start beeping and say it wants to shock me, and I’ll have to hit these two buttons on either side of it,” she said.

    Beveridge continues her journey to wellness; she’s also on a new mission: advocacy.

    “I want people my age to listen to their bodies more just so that, like, if they think something is wrong, they need to go talk to someone,” Beveridge said.

    She hopes sharing her story can lead to more research. The statistics could finally change where, one day, heart disease won’t be the number one cause of death for women.

    Ella and her mom will be sharing their story at a fundraiser for the American Heart Association.

    Tickets are still available online.

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  • 18-year-old survives heart attack, hopes to inspire change

    18-year-old survives heart attack, hopes to inspire change

    Heart disease is the leading cause of death for women in the U.S., and it’s something that can affect people of all ages.A drive to work on July 4 changed 18-year-old Ella Beveridge’s life.”I was at a stoplight right by a gas station, and after I had called my mom, I thought I should pull over because it hurt so bad,” Beveridge said.Her trip to the hospital turned into a 12-day stay because that pain was a heart attack.“I didn’t think that’s what it was. I thought it was something else. Just because I’m so young,” Beveridge said.Beveridge is still recovering as doctors search for answers on why and how she developed a blood clot.“It was really surprising. I was a very healthy kid. I’ve never had any health problems,” Beveridge said.Since July 4, everyday life for the 18-year-old looks different. She now wears a defibrillator.​“If it’s too bad of an irregularity, this will start beeping and say it wants to shock me, and I’ll have to hit these two buttons on either side of it,” she said.Beveridge continues her journey to wellness; she’s also on a new mission: advocacy.“I want people my age to listen to their bodies more just so that, like, if they think something is wrong, they need to go talk to someone,” Beveridge said.She hopes sharing her story can lead to more research. The statistics could finally change where, one day, heart disease won’t be the number one cause of death for women.Ella and her mom will be sharing their story at a fundraiser for the American Heart Association.Tickets are still available online.

    Heart disease is the leading cause of death for women in the U.S., and it’s something that can affect people of all ages.

    A drive to work on July 4 changed 18-year-old Ella Beveridge’s life.

    “I was at a stoplight right by a gas station, and after I had called my mom, I thought I should pull over because it hurt so bad,” Beveridge said.

    Her trip to the hospital turned into a 12-day stay because that pain was a heart attack.

    “I didn’t think that’s what it was. I thought it was something else. Just because I’m so young,” Beveridge said.

    Beveridge is still recovering as doctors search for answers on why and how she developed a blood clot.

    “It was really surprising. I was a very healthy kid. I’ve never had any health problems,” Beveridge said.

    Since July 4, everyday life for the 18-year-old looks different. She now wears a defibrillator.​

    “If it’s too bad of an irregularity, this will start beeping and say it wants to shock me, and I’ll have to hit these two buttons on either side of it,” she said.

    Beveridge continues her journey to wellness; she’s also on a new mission: advocacy.

    “I want people my age to listen to their bodies more just so that, like, if they think something is wrong, they need to go talk to someone,” Beveridge said.

    She hopes sharing her story can lead to more research. The statistics could finally change where, one day, heart disease won’t be the number one cause of death for women.

    Ella and her mom will be sharing their story at a fundraiser for the American Heart Association.

    Tickets are still available online.

    Source link

  • Xylitol sugar substitute linked to increased risk of heart attack and stroke, study finds

    Xylitol sugar substitute linked to increased risk of heart attack and stroke, study finds

    Xylitol is the latest sugar substitute to be linked to potential negative health impacts.

    In a study from the Cleveland Clinic, published Thursday in the European Heart Journal, researchers found higher amounts of xylitol are associated with an increased risk of heart attack and stroke. 

    Xylitol, a sugar alcohol found naturally in some plants, is not the most common sweetening agent in sugar-free food products in the U.S. but is often found in sugarless gum and some toothpastes.

    The study, which included more than 3,000 participants in the U.S. and UK, was observational, meaning it does not prove causation. Still, it prompts pause when it comes to the use of artificial sweeteners, especially as they continue to gain popularity as healthy alternatives.  

    “This study again shows the immediate need for investigating sugar alcohols and artificial sweeteners, especially as they continue to be recommended in combatting conditions like obesity or diabetes,” said research lead Dr. Stanley Hazen in a news release. “It does not mean throw out your toothpaste if it has xylitol in it, but we should be aware that consumption of a product containing high levels could increase the risk of blood clot related events.” 

    The authors note further studies are warranted to better understand the potential health risks. 

    Last year, the same research team found erythritol, a zero-calorie sugar substitute used to sweeten low-cal, low-carb and “keto” products, to have similar effects on the heart.

    While this study also didn’t definitively show causation, then-CBS News medical contributor Dr. David Agus said there was “certainly enough data to make you very worried.”

    In response to the erythritol study, Robert Rankin, executive director of the Calorie Control Council, an international association representing the low- and reduced-calorie food and beverage industry, told CBS News the results are “contrary to decades of scientific research showing low- and no-calorie sweeteners like erythritol are safe, as evidenced by global regulatory permissions for their use in foods and beverages, and should not be extrapolated to the general population, as the participants in the intervention were already at increased risk for cardiovascular events.” 

    CBS News has reached out to the Calorie Control Council for comment on the latest research involving xylitol. 

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  • The Truth About Heart Stents | NutritionFacts.org

    The Truth About Heart Stents | NutritionFacts.org

    Coronary artery disease, the number one killer of men and women, involves blockages in the blood vessels that supply the heart muscle. As discussed in my video Do Angioplasty Heart Stent Procedures Work?, low blood flow can lead to a type of chest pain called angina or, if severe enough, a heart attack. Plant-based diets and lifestyle programs have been shown to help reverse these blockages by treating the cause of why our arteries are clogging up in the first place. But, for those unable or unwilling to change their diets, there are drugs that may help, as well as more invasive surgical treatments.

    What Is a Heart Stent?

    You may have heard of open-heart surgery, performed to try to bypass the blockage, or percutaneous coronary intervention. As discussed in my video Why Angioplasty Heart Stents Don’t Work Better, historically, the more common procedure was angioplasty, wherein a tiny balloon is inserted into a narrowed coronary artery feeding your heart to force it to open wider to improve blood flow. Then, stents came into vogue. Instead of just ballooning up the artery, how about permanently inserting a metal mesh tube to prop open the artery? Stents are typically inserted in the groin and threaded all the way up into the heart, and, while stents used to be mostly bare metal, there are now fancy new drug-eluting stents that not only force open arteries, but they also slowly release pharmaceuticals.

    How Serious Is Having a Stent Put In?

    The surgical procedure carries risks—including death. In an emergency setting, while you’re actively having a heart attack, angioplasty can be lifesaving, but hundreds of thousands of these procedures are for stable coronary artery disease, for which there appears to be little or no benefits. As discussed in my video The Risks of Heart Stents, doctors appear to be killing or stroking out thousands of people a year for nothing, and that isn’t even counting the tens of thousands of silent mini-strokes caused by these procedures that may contribute to cognitive decline. Indeed, 11 to 17 percent of people who go through angioplasty or stenting come away with new brain lesions—up to one in six patients.

    Do Stents Work?

    Angioplasty and stents for non-emergency coronary artery disease are among the most common invasive procedures performed in the United States. Millions of people have gotten stents for stable coronary artery disease, yet it now appears that for such patients, angioplasty and stent placement do not actually prevent heart attacks, do not offer long-term angina pain relief, and do not improve survival. Why? Because the most dangerous plaques—the ones most vulnerable to rupture leading to a heart attack—are not the ones doctors put stents into. They often aren’t the ones that are even seen on angiogram to be obstructing blood flow.

    Indeed, in 2007, we learned from the COURAGE trial that angioplasty and stents don’t reduce the risk of death or heart attack, but patients didn’t seem to get the memo. As discussed in my video Why Are Stents Still Used If They Don’t Work?, only 1 percent realize there was no mortality or heart attack benefit, perhaps because most cardiologists failed to happen to mention that fact. One can imagine that if patients actually understood all they were getting was symptomatic relief, they’d be less likely to go under the knife. Ten years later, the ORBITA trial was published, showing even the promise of symptom relief was an illusion.

    Are Stents Really Necessary?

    The implications are profound and far-reaching. First and foremost, the results showed unequivocally that there are no benefits to non-emergency angioplasty and stents for stable heart disease. Basically, patients would be risking harm for no benefit whatsoever, so it’s hard to imagine a scenario where a fully-informed patient would choose an invasive procedure for nothing.

    Yet angioplasty and stent placement continue to be frequently performed for patients with non-emergency coronary artery disease, despite clear evidence that it provides minimal benefit, as discussed in my video Angioplasty Heart Stent Risks vs. Benefits. For example, it does not prevent heart attacks or death, yet as many as nine out of ten patients mistakenly believed that the procedure would reduce their chances of having a heart attack.

    What Are the Side Effects of Heart Stents?

    Stent placement and the blood-thinner drugs you have to go on after the surgery can cause complications, including heart failure, stroke, and death. The risks are relatively low; there’s less than a 1 percent chance it will kill you or stroke you out. The 15 percent risk of heart attack is only if your stent clogs at a later date, which only happens about 1 percent of the time in the near-term. There is a 13 percent risk of kidney injury, due to the dyes that must be injected, but that typically heals on its own. The most serious complications—including death—only happen in about 1 in 150 cases. However, you have to multiply that by the fact that hundreds of thousands of these procedures are performed every year.

    And, again, although stents appeared to offer immediate relief of angina chest pain in stable patients with coronary artery disease, they do not offer long-term angina pain relief and they didn’t actually translate into lower risk of heart attack or death. More on this in my video Do Heart Stent Procedures Work for Angina Chest Pain?.

    Diet After Heart Attack and Stents

    Should we be surprised that angioplasty and stents fail to improve prognosis? After all, neither does anything to modify the underlying disease process itself. In other words, they don’t treat the cause. As discussed in my video Heart Stents and Upcoding: How Cardiologists Game the System, even if stents helped with symptoms beyond the placebo effect, they would still just be treating the symptoms, not the disease, so it’s no wonder the disease continues to progress until the patient is disabled into death.

    Thankfully, we are on the cusp of a seismic revolution in health: not another pill, procedure, or operation, but, instead, treating the underlying cause of heart disease with whole food, plant-based nutrition, the mightiest tool medicine has ever had in its toolbox.

    Heart-Healthy Eating

    The most likely reason the majority of our loved ones will die is heart disease. Atherosclerosis, or hardening of the arteries, begins in childhood, as discussed in my video How Not to Die from Heart Disease. The arteries of nearly all kids raised on the standard American diet already have fatty streaks marking the first stage of the disease—by the time they are ten years old. After that, the plaques start forming in our 20s, get worse in our 30s, and can then start killing us off. In our heart, it’s called a heart attack; in our brain, it can manifest as a stroke. So, for anyone reading this who is older than ten, the choice isn’t whether or not to eat healthfully to prevent heart disease—it’s whether or not you want to reverse the heart disease you likely already have.

    Is that even possible? When researchers took people with heart disease and put them on the kind of plant-based diet followed by populations who did not get epidemic heart disease, their hope was that it might slow down the disease process or maybe even stop it. Instead, something miraculous happened. The disease actually started to reverse. It started to get better. As soon as patients stopped eating artery-clogging diets, their bodies were able to start dissolving away some of the plaque, opening up arteries without drugs and without surgery, suggesting their bodies wanted to heal all along, but just were never given the chance. That improvement in blood flow to the heart muscle itself was after just three weeks of eating healthfully.

    Plant-based diets aren’t just safer and cheaper. They can work better because they let us treat the actual cause of the disease.

    Michael Greger M.D. FACLM

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  • Priscilla Presley Defends Elvis For Dating Her When She Was 14 And He Was 24

    Priscilla Presley Defends Elvis For Dating Her When She Was 14 And He Was 24

    Opinion

    Sources: YouTube Screenshots, Piers Morgan Uncensored, Pop Culture Club

    Priscilla Presley is speaking out to defend the late legendary singer Elvis Presley for initiating their relationship when he was 24 and she was only 14.

    Priscilla Defends Elvis

    Fox News reported that Priscilla was only 14 years-old when she met Elvis at a party in Germany, where the 24 year-old was stationed while serving in the U.S. military. Backlash has grown in recent years over both their 10 year age gap and Priscilla being a minor when they met, but she was quick to defend Elvis in a new interview.

    “My relationship with Elvis, you know, people go, ‘Oh my god, how could this happen?’ It was not a sexual relationship, being 14 years old,” Priscilla, now 78, told Fox 32 Chicago. “What I think really attracted him to me was the fact that, and I’ve gone over this many times, ‘Why me? Why me?’ was because I was like the listener. He poured his heart out to me in Germany. He was very, very lonely.”

    Priscilla went on to explain that Elvis had recently lost his mother when they met, something that she described as being  “a big issue for him.”

    “He just trusted me with a lot of things that he shared,” she explained.

    Priscilla further opened up about her and Elvis’ age gap earlier this year.

    “It was very difficult for my parents to understand that Elvis would be so interested in me and I really do think because I was more of a listener,” Priscilla said back in September, according to Entertainment Weekly. “Elvis would pour his heart out to me, his fears, his hopes, the loss of his mother which he never ever got over, and I was the person who really really sat there to listen and to comfort him.”

    “I was a little bit older in life than in numbers and that was the attraction,” she continued. “And you know, people think, Oh, it was sex… Not at all. I never had sex with him. He was very kind, very soft, very loving. But he also respected the fact that I was only 14 years old. We were more in mind and thought. And that was our relationship.”

    Related: Priscilla Presley Confesses Real Reason She Never Married Again After Elvis – ‘No One Could Ever Match Him

    Priscilla Remembers Christmases With Elvis

    Some of Priscilla’s fondest memories of Elvis are spending Christmases with him at his Graceland estate in Memphis, Tennessee.

    “Yes, that was his special time,” she said of these holidays. “He loved all the decorations. I would do the tree, I would put all the lightbulbs on the tree and the lights, and he would take the tinfoil and stand in the back where the dining room table is and curl it all up, squish it together and throw it. And I go, ‘No, that’s not how you put tinsel on and so I would take it and put a little bit and he would just take it and throw the tinsel on.”

    Priscilla and Elvis were married from 1967 until they divorced in 1973, and he tragically died four years later from a heart attack at the age of 42. Despite their split, Priscilla still views Elvis as the love of her life, and she has never remarried in the decades since his passing.

    “To be honest with you, I never wanted to marry after him. I never had any desire,” Priscilla told People Magazine last month. “No one could ever match him.”

    Related: Priscilla Presley Reveals She’ll Be Buried Next To Ex-Husband Elvis After Her Death

    Priscilla To Be Buried Near Elvis

    Page Six reported that this came days after a judge signed off on official documents stating that after her death, Priscilla will be buried near Elvis and their daughter Lisa Marie in Graceland’s Meditation Garden in Memphis, Tennessee.

    “That’s what I want and wanted,” Priscilla told the British media personality Piers Morgan afterwards of these burial plans.

    “So you will be buried there?” Piers asked, to which Priscilla replied with an emphatic, “Yes.”

    Do you think Elvis deserves backlash for beginning a relationship with Priscilla when she was only 14, or should people let this one go? Let us know in the comments section.

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    James Conrad

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  • Young nurse practicing cardiac arrest treatment goes into cardiac arrest

    Young nurse practicing cardiac arrest treatment goes into cardiac arrest

    Concord, N.H. — Andy Hoang eagerly began her first nursing job this year in New Hampshire, with a desire to specialize in cardiac care.

    She was excited about attending a November practice session on how to respond to someone in cardiac arrest. But as things were getting under way at Dartmouth-Hitchcock Medical Center, Hoang, 23, started to feel dizzy and nauseous. She felt she needed to sit down.

    “That’s the last thing I remember,” she told The Associated Press in an interview. “I woke up to a room full of doctors and nurses.”

    Nurse Cardiac Arrest New Hampshire
    Andy Hoang, 23, a recent nursing graduate, center, poses on Dec. 5, 2023, in Lebanon, N.H. with co-workers Lisa Davenport, left, and Justina Terino at the spot where she was stricken the month before during a cardiac training session at the Dartmouth-Hitchcock Medical Center.

    Charles Krupa / AP


    It turned out that she, herself, had gone into cardiac arrest and needed help immediately. Her colleagues sprang into action – instead of practicing chest compressions on a mannequin in a simulated environment, they went to work on her.

    “One checked her carotid, one her femoral (arteries), and she did not have a pulse,” instructor Lisa Davenport said.

    The nurses started CPR and a “code blue,” or medical emergency, team was called.

    A first  

    “What was really stressful about the situation was that we never had a real code blue in the center,” Davenport said. “We train for them all the time.”

    Davenport shouted for help. Luckily, the Lebanon hospital’s critical care team was nearby, attending a separate session. More nurses came in, hooked Hoang up to defibrillator for monitoring, inserted an IV line and placed her on oxygen. A doctor and nurse from another department rushed in with crash carts.

    Hoang was waking up by the time an emergency team arrived. Davenport estimated 15 minutes passed from the time Hoang slumped over to when they got her on a stretcher and sent her to the emergency department. But it felt longer.

    “It worked out, but it was pretty frightening for all of us,” she said. “You just don’t expect that to happen with someone as young as Andy.”

    Charmaine Martin, one of the nurses at the scene, agreed it was a scary moment, but also one “where I saw and felt supported and we all worked as a team,” she said in a statement.

    Hoang, who recently returned to work, couldn’t believe what had happened either.

    “I would say I’m your pretty average healthy 23-year-old,” she said. She goes to the gym four times a week, runs, and eats well. “I’m on my feet 12, 13 hours a day at work, so I want to make sure that I’m in shape for that.”

    Cardiac arrest vs. heart attacks  

    Cardiac arrest – the sudden loss of heart function – causes more than 436,000 deaths in the United States each year, according to the American Heart Association. It is different from a heart attack, which happens when blood flow to the heart is blocked.

    A person can suffer cardiac arrest after having a heart attack, but the association says other conditions can also disrupt the heart’s rhythm and lead to cardiac arrest, including having a thickened heart muscle or cardiomyopathy, heart failure, arrhythmias and more.

    According to information compiled by the National Heart, Lung and Blood Institute, a person’s risk of cardiac arrest increases with age. It is rare in someone younger than 30. Genetic arrhythmias, problems with the structure of the heart or coronary arteries, heart inflammation and substance abuse are the main risk factors in younger people. Most cardiac arrests also occur in men and women’s risk increases after menopause.

    Unlikely victim  

    Hoang said before the day she suffered cardiac arrest, she had passed out twice before. The first time, she hadn’t eaten and her blood sugar was low. The second time was preceded by a sharp pain in her abdomen.

    “So, nothing like this, nothing to this extent,” she said.

    Hoang, who grew up in Vietnam and came to the United States in 2016 as a student, said her family has no history of heart problems. She had been living with a family in Montana before she got her nursing degree in Michigan, then headed to New Hampshire.

    While recovering, Hoang wore a patch that recorded the electrical activity of her heart. Doctors hope to learn more from the data.

    The experience has strengthened her relationship with the other nurses – Hoang now regards them as best friends. “We basically went through this whole life-or-death experience,” she said.

    “I am so grateful for Andy and her courage. She is an excellent nurse and someone I call friend,” Martin said.

    Hoang said she feels like she’s part of a family at work, not just an employee. Her family told the AP they are extremely grateful that she was surrounded by medical personnel when she went into cardiac arrest.

    It was care given by nurses to her grandfather, who died a couple of years ago, that made Hoang want to switch her career focus from graphic design to nursing. But she never expected she would become a patient.

    “It really changed my perspective on how I view life, like ‘Hug your family a little longer,’” she said. “Tell them that you love them, because it might be the last time you get to say it to them. And just cherish life for what you’ve been given. It’s precious, and I didn’t realize how precious it was until I nearly lost it.”

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  • The CRISPR Era Is Here

    The CRISPR Era Is Here

    When Victoria Gray was still a baby, she started howling so inconsolably during a bath that she was rushed to the emergency room. The diagnosis was sickle-cell disease, a genetic condition that causes bouts of excruciating pain—“worse than a broken leg, worse than childbirth,” one doctor told me. Like lightning crackling in her body is how Gray, now 38, has described the pain. For most of her life, she lived in fear that it could strike at any moment, forcing her to drop everything to rush, once again, to the hospital.

    After a particularly long and debilitating hospitalization in college, Gray was so weak that she had to relearn how to stand, how to use a spoon. She dropped out of school. She gave up on her dream of becoming a nurse.

    Four years ago, she joined a groundbreaking clinical trial that would change her life. She became the first sickle-cell patient to be treated with the gene-editing technology CRISPR—and one of the first humans to be treated with CRISPR, period. CRISPR at that point had been hugely hyped, but had largely been used only to tinker with cells in a lab. When Gray got her experimental infusion, scientists did not know whether it would cure her disease or go terribly awry inside her. The therapy worked—better than anyone dared to hope. With her gene-edited cells, Gray now lives virtually symptom-free. Twenty-nine of 30 eligible patients in the trial went from multiple pain crises every year to zero in 12 months following treatment.

    The results are so astounding that this therapy, from Vertex Pharmaceuticals and CRISPR Therapeutics, became the first CRISPR medicine ever approved, with U.K. regulators giving the green light earlier this month; the FDA appears prepared to follow suit in the next two weeks. No one yet knows the long-term effects of the therapy, but today Gray is healthy enough to work full-time and take care of her four children. “Now I’ll be there to help my daughters pick out their wedding dresses. And we’ll be able to take family vacations,” she told NPR a year after her treatment. “And they’ll have their mom every step of the way.”

    The approval is a landmark for CRISPR gene editing, which was just an idea in an academic paper a little more than a decade ago—albeit one already expected to cure incurable diseases and change the world. But how, specifically? Not long after publishing her seminal research, Jennifer Doudna, who won the Nobel Prize in Chemistry with Emmanuelle Charpentier for their pioneering CRISPR work, met with a doctor on a trip to Boston. CRISPR could cure sickle-cell disease, he told her. On his computer, he scrolled through DNA sequences of cells from a sickle-cell patient that his lab had already edited with CRISPR. “That, for me, personally, was one of those watershed moments,” Doudna told me. “Okay, this is going to happen.” And now, it has happened. Gray and patients like her are living proof of gene-editing power. Sickle-cell disease is the first disease—and unlikely the last—to be transformed by CRISPR.


    All of sickle-cell disease’s debilitating and ultimately deadly effects originate from a single genetic typo. A small misspelling in Gray’s DNA—an A that erroneously became a T—caused the oxygen-binding hemoglobin protein in her blood to clump together. This in turn made her red blood cells rigid, sticky, and characteristically sickle shaped, prone to obstructing blood vessels. Where oxygen cannot reach, tissue begins to die. Imagine “if you put a tourniquet on and walked away, or if you were having a heart attack all the time,” says Lewis Hsu, a pediatric hematologist at the University of Illinois at Chicago. These obstructions are immensely painful, and repeated bouts cause cumulative damage to the body, which is why people with sickle cell die some 20 years younger on average.

    Not everyone with the sickle-cell mutation gets quite so sick. As far back as the 1940s, a doctor noticed that the blood of newborns with sickle-cell disease did not, surprisingly, sickle very much. Babies in the womb actually make a fetal version of the hemoglobin protein, whose higher affinity for oxygen pulls the molecule out of their mother’s blood. At birth, a gene that encodes fetal hemoglobin begins to turn off. But adults do sometimes still make varying amounts of fetal hemoglobin, and the more they make, scientists observed, the milder their sickle-cell disease, as though fetal hemoglobin had stepped in to replace the faulty adult version. Geneticists eventually figured out the exact series of switches our cells use to turn fetal hemoglobin on and off. But there, they remained stuck: They had no way to flip the switch themselves.

    Then came CRISPR. The basic technology is a pair of genetic scissors that makes fairly precise cuts to DNA. CRISPR is not currently capable of fixing the A-to-T typo responsible for sickle cell, but it can be programmed to disable the switch suppressing fetal hemoglobin, turning it back on. Snip snip snip in billions of blood cells, and the result is blood that behaves like typical blood.

    Sickle cell was a “very obvious” target for CRISPR from the start, says Haydar Frangoul, a hematologist at the Sarah Cannon Research Institute in Nashville, who treated Gray in the trial. Scientists already knew the genetic edits necessary to reverse the disease. Sickle cell also has the advantage of affecting blood cells, which can be selectively removed from the body and gene-edited in the controlled environment of a lab. Patients, meanwhile, receive chemotherapy to kill the blood-producing cells in their bone marrow before the CRISPR-edited ones are infused back into their body, where they slowly take root and replicate over many months.

    It is a long, grueling process, akin to a bone-marrow transplant with one’s own edited cells. A bone-marrow transplant from a donor is the one way doctors can currently cure sickle-cell disease, but it comes with the challenge of finding a matched donor and the risks of an immune complication called graft-versus-host disease. Using CRISPR to edit a patient’s own cells eliminates both obstacles. (A second gene-based therapy, using a more traditional engineered-virus technique to insert a modified adult hemoglobin gene into DNA semi-randomly, is also expected to receive FDA approval  for sickle-cell disease soon. It seems to be equally effective at preventing pain crises so far, but development of the CRISPR therapy took much less time.)

    In another way, though, sickle-cell disease is an unexpected front-runner in the race to commercialize CRISPR. Despite being one of the most common genetic diseases in the world, it has long been overlooked because of whom it affects: Globally, the overwhelming majority of sickle-cell patients live in sub-Saharan Africa. In the U.S., about 90 percent are of African descent, a group that faces discrimination in health care. When Gray, who is Black, needed powerful painkillers, she would be dismissed as an addict seeking drugs rather than a patient in crisis—a common story among sickle-cell patients.

    For decades, treatment for the disease lagged too. Sickle-cell disease has been known to Western medicine since 1910, but the first drug did not become available until 1998, points out Vence Bonham, a researcher at the National Human Genome Research Institute who studies health disparities. In 2017, Bonham began convening focus groups to ask sickle-cell patients about CRISPR. Many were hopeful, but some had misgivings because of the history of experimentation on Black people in the U.S. Gray, for her part, has said she never would have agreed to the experimental protocol had she been offered it at one of the hospitals that had treated her poorly. Several researchers told me they hoped the sickle-cell therapy would make a different kind of history: A community that has been marginalized in medicine is the first in line to benefit from CRISPR.


    Doctors aren’t willing to call it an outright “cure” yet. The long-term durability and safety of gene editing are still unknown, and although the therapy virtually eliminated pain crises, Hsu says that organ damage can accumulate even without acute pain. Does gene editing prevent all that organ damage too? Vertex, the company that makes the therapy, plans to monitor patients for 15 years.

    Still, the short-term impact on patients’ lives is profound. “We wouldn’t have dreamed about this even five, 10 years ago,” says Martin Steinberg, a hematologist at Boston University who also sits on the steering committee for Vertex. He thought it might ameliorate the pain crises, but to eliminate them almost entirely? It looks pretty damn close to a cure.

    In the future, however, Steinberg suspects that this currently cutting-edge therapy will seem like only a “crude attempt.” The long, painful process necessary to kill unedited blood cells makes it inaccessible for patients who cannot take months out of their life to move near the limited number of transplant centers in the U.S.—and inaccessible to patients living with sickle-cell disease in developing countries. The field is already looking at techniques that can edit cells right inside the body, a milestone recently achieved in the liver during a CRISPR trial to lower cholesterol. Scientists are also developing versions of CRISPR that are more sophisticated than a pair of genetic scissors—for example, ones that can paste sequences of DNA or edit a single letter at a time. Doctors could one day correct the underlying mutation that causes sickle-cell disease directly.

    Such breakthroughs would open CRISPR up to treating diseases that are out of reach today, either because we can’t get CRISPR into the necessary cells or because the edit is too complex. “I get emails now daily from families all over the world asking, ‘My son or my loved one has this disease. Can CRISPR fix it?’” says Frangoul, who has become known as the first doctor to infuse a sickle-cell patient in a CRISPR trial. The answer, usually, is not yet. But clinical trials are already under way to test CRISPR in treating cancer, diabetes, HIV, urinary tract infections, hereditary angioedema, and more. We have opened the book on CRISPR gene editing, Frangoul told me, but this is not the final chapter. We may still be writing the very first.

    Sarah Zhang

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  • The Future of Obesity Drugs Just Got Way More Real

    The Future of Obesity Drugs Just Got Way More Real

    A wild idea recently circulated about the future of aviation: If passengers lose weight via obesity drugs, airlines could potentially cut down on fuel costs. In September, analysts at Jefferies Bank estimated that in the “slimmer society” obesity drugs will create, United Airlines could save up to $80 million in jet fuel annually.

    In the past year, as more Americans have learned about semaglutide, which is sold for diabetes under the brand name Ozempic and for obesity under the name Wegovy, hype has become completely divorced from reality. For all the grand predictions, just a fraction of Americans who qualify for obesity drugs are on them. With a list price of roughly $1,350 a month, Wegovy is far too expensive, under-covered by insurance, and in limited supply to be a routine part of health care.

    But that possibility is beginning to seem very real. The results of a highly anticipated study published on Saturday indicate that Wegovy can have profound effects on heart health, which potentially opens up the drug to even more patients. A few days earlier, the FDA approved Zepbound, an obesity drug that is a bit cheaper and appears more potent than Wegovy. If there was any doubt before, now it is undeniable: Obesity drugs “are here to stay,” Kyla Lara-Breitinger, a cardiologist at the Mayo Clinic, told me. “There’s only going to be more and more of them.” They are now poised to become deeply entrenched in American health care, perhaps eventually even joining the ranks of commonly used drugs such as statins and metformin.

    Considering that obesity is linked to all sorts of major heart ailments, it is no big surprise that a weekly shot for weight loss might have some cardiovascular benefits. But because this class of obesity drugs, known as GLP-1 agonists for the hunger hormone they target, is so new, doctors did not know that for sure. Starting in 2018, Novo Nordisk, the company that manufactures semaglutide, began to look for answers in a study of more than 17,600 people with obesity and cardiovascular disease. In this group, results of a trial named SELECT show that Wegovy reduced the risk of major cardiac events—stroke, heart attack, death—by 20 percent. Even compared with studies on common heart medications such as Praluent and Repatha, the Wegovy results are “impressive,” Eugene Yang, a cardiologist and professor of medicine at the University of Washington, told me.

    How exactly the drug prevents major cardiac events isn’t fully understood. Some of the effects can likely be chalked up to weight loss itself, which is associated with improvements in metrics that influence heart health, such as blood pressure, Yang said. But mechanisms independent of weight loss may also be at work. In the trial, lower rates of cardiovascular events began showing up before participants lost weight. One explanation is the drug’s impact on inflammation, which is associated with heart disease: C-reactive protein, a rough proxy for inflammation, dropped by nearly 40 percent in study participants.

    Regardless of how Wegovy works, Yang said, “it has the potential benefit of being very significant” as a new line of treatment for heart disease, the leading cause of death nationwide. Novo Nordisk has already applied for expanded FDA approval and anticipates receiving it within six months. Approval would also show that Wegovy has a medical benefit beyond weight loss, pressuring insurers to cover it. Right now, for instance, Medicare does not, in part because obesity has long been viewed as a cosmetic issue, not a medical one. Even with private coverage, the drug is still frequently out of reach. The SELECT trial makes it “unequivocally clear” that obesity is a health condition that can be treated with drugs, Ted Kyle, an obesity-policy expert, told me. Still, the study leaves room for pushback: The absolute risk reduction of cardiovascular events was 1.5 percent, which is, by some reckonings, quite small. A higher risk reduction would have “put more pressure” on insurers and manufacturers to make the drugs more affordable for Americans, Lara-Breitinger said.

    Still, the findings are robust enough that it seems likely that the heart benefits of obesity drugs will lead more Americans to take them—if not immediately, then eventually. The approval of a new drug could do the same. Tirzepatide, which Eli Lilly has sold as a diabetes drug under the name Mounjaro, will be marketed as Zepbound for obesity—and it is coming for Wegovy’s throne. In one study, people on tirzepatide lost an average of 18 percent of their body weight; for comparison, in another study patients on Wegovy lost an average of 15 percent. At a little over $1,000 a month, Zepbound is not cheap, but its list price is hundreds of dollars lower than that of Wegovy. (The manufacturers of both drugs have said that most insured patients pay far less than that.)

    Zepbound’s approval is just the beginning. Unlike semaglutide, which targets only one hormone, GLP-1, to exert its effects on appetite and fullness, tirzepatide targets two. Other drugs that target two or even three hormones are in the works, as are versions that come in a more appealing pill format rather than as an injection. Generic versions of these drugs, likely beginning with liraglutide, a predecessor to semaglutide sold as Saxenda, could become available soon, Yang said. This competition will help bring down costs, but it will go only so far. Drug pricing is “a little bit screwy,” Kyle said, complicated by the wide gap between the list price and the net price created by manufactures, insurers, and intermediaries between them.

    Each new competitor and new study is a step toward a future in which a substantial proportion of Americans with obesity are routinely prescribed these drugs. In a single week, obesity drugs leapt a new era—one in which they are about to become significantly more mainstream. No doubt that future is a bright one for millions of people who might benefit from treatment. Still, many questions about the drugs remain unanswered, such as their long-term safety and endless supply shortages.

    But the potential for obesity drugs to truly change America has never felt closer—with all of the dizzying questions this creates about what “a slimming society” might mean for exercise, the food industry, and apparently even airline jet fuel.

    Yasmin Tayag

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  • A ‘game-changing’ study backs Wegovy use to cut heart attacks and strokes: ‘This is not just about weight and appearance’

    A ‘game-changing’ study backs Wegovy use to cut heart attacks and strokes: ‘This is not just about weight and appearance’

    Novo Nordisk A/S unveiled details from a closely watched study that support use of Wegovy, its blockbuster weight-loss drug, to cut heart attacks and strokes in obesity patients with a history of cardiovascular disease.

    People taking the highest dose of Wegovy saw a drop in blood sugar levels and inflammation — two harbingers of heart disease — that help explain the 20% reduction in cardiovascular events that Novo reported in August. While none of the patients had diabetes, two-thirds started the study with blood sugar levels in the prediabetic range, which is associated with a higher risk of heart disease and death. Patients also saw significant reductions in blood pressure.

    Three-quarters of patients had suffered heart attacks before the study began and a quarter had heart failure. In this highly vulnerable population, the results help cement the argument for using Novo’s drug as a heart treatment alongside statins and blood pressure therapies. Patients on Wegovy also lost weight in the trial.

    The results, presented on Saturday at the American Heart Association’s annual conference in Philadelphia, are “game-changing,” Eugene Yang, the chair of the American College of Cardiology’s prevention section, said in an interview. The room at the city’s Convention Center erupted into several rounds of applause when the data were presented.

    Heart disease is the number one killer in the US and accounts for about a third of deaths globally. While obesity is known to raise the risk for such ailments, Novo’s trial was designed to show whether Wegovy could ward off future heart attacks and strokes in people with established cardiovascular disease.

    Novo said it will seek expanded US approval for reducing risk of major adverse cardiovascular events in adults with a body mass index, or BMI, of 27 or higher and established cardiovascular disease.

    Read More: All About the New Obesity Drugs Causing a Big Stir

    “Increasingly, physicians are understanding that this is not just about weight and appearance,” Lars Fruergaard Jorgensen, Novo’s chief executive officer, said in an interview on Friday before the details were released. “It’s about real health benefits.”

    Weight-loss drugs such as Wegovy, which increased sales more than 700% last quarter, have become a phenomenon this year. Celebrities are touting their benefits, while investors handicap how much they will disrupt a wide swath of sectors that includes apparel companies, restaurants and packaged food producers. Novo is already struggling to keep up with demand. And competition is increasing with Eli Lilly & Co. just receiving approval for its weight-loss drug, Zepbound.

    However, the drugs are expensive. Zepbound will cost about $1,050 for a month’s supply, which is cheaper than Wegovy’s monthly list price of roughly $1,350. The cost is a barrier to widespread access, Yang said. Based on the trial results, to prevent one heart attack or cardiovascular death, 67 people will need to be treated with Wegovy for almost three years and four months, according to a Bloomberg analysis. At list prices, this would cost $3.8 million.

    Along with reducing weight, blood sugar control and anti-inflammatory effects are likely what’s driving the benefit for heart disease shown in the study, Martin Holst Lange, Novo’s development chief, said in an interview. In the trial of more than 17,600 overweight and obese adults who were 45 and older, taking Wegovy lowered body weight by an average of 9.4% over two years, compared to a less than 1% loss in the placebo group. The treatment group also saw reduced weight circumference and blood pressure that’s often associated with shedding pounds.

    At the same time, blood sugar fell into a healthy range in two-thirds of those treated. That was enough to ward off diabetes in about 70% of patients. C-reactive protein, a liver product that’s linked to inflammation, fell about 40% among those taking Wegovy.

    Only 28% of the patients in the trial were women and just 4% were Black, meaning the results may not translate to those populations, according to the ACC’s Yang. About 17% of the patients in the trial stopped taking Wegovy due to side effects. The most common cause was gastrointestinal issues, which were responsible for most of the discontinuations.

    — With assistance from Robert Langreth

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    Madison Muller, Naomi Kresge, Bloomberg

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  • Traditional Chinese medicine proves effective in modern clinical trial

    Traditional Chinese medicine proves effective in modern clinical trial

    A traditional Chinese medicine has been shown to be effective at reducing complications following a heart attack after a large-scale, clinical trial.

    The medicine, known as tongxinluo, is made of extracts derived from seven herbs and various animals—including cockroaches, scorpions, cicadas and leeches. The compound, whose name means “to open the network of the heart,” has long been used as a traditional Chinese treatment for patients who have had heart attacks and/or strokes.

    Based on promising results in cellular and animal models, the State Food and Drug Administration of China approved its use for the treatment of stroke and angina pectoris—a heart condition characterized by reoccurring chest pain—in 1996.

    But the medicine had never been evaluated in a randomized, double-blind, placebo-controlled clinical trial—the gold standard of drug testing that is usually required to approve treatments in the United States and Europe.

    The latest study, which has been published in JAMA (formerly The Journal of the American Medical Association), represents one of the first times that a traditional Chinese medicine has been tested in a large-scale, Western-style clinical trial.

    The authors of the study, who include researchers from several Chinese universities and hospitals, in collaboration with experts from the University of Texas Southwestern Medical Center (UTSW)—found that tongxinluo reduced the risk of heart attacks (known as myocardial infarctions), deaths and other major cardiovascular complications for at least a year after a first heart attack.

    Matthew Saybolt, a cardiologist with the Hackensack Meridian Jersey Shore University Medical Center who was not involved in the latest study, told Newsweek that he found the latest research “compelling” after reviewing the paper.

    “I am not aware of any other large, well-run trials like this studying traditional Chinese medicine. This is a rarely run type of study, and I congratulate the authors for their work and publication in such a prestigious medical journal,” Saybolt said.

    The study involved 3,777 patients at 124 clinical centers in China who had suffered the most severe form of heart attack—known as ST-segment elevation myocardial infarction, or STEMI. This condition involves a blood clot that completely blocks a major vessel supplying the heart. The patients were enrolled from May 2019 to December 2020, with the last date of follow-up occurring in December 2021.

    The patients were treated within hours of symptom onset by surgical or chemical removal of the clot. While they received standard treatments over the next year—such as taking a daily aspirin or medications including beta blockers—half of the individuals were randomly selected to receive tongxinluo as well. The other half were given a placebo—designed to match the look, smell and taste of the traditional Chinese medicine—instead.

    Over the next year, the patients were followed to track the incidence of major adverse cardiac and cerebrovascular events (MACCEs), an umbrella term that covers cardiac death, repeat heart attacks (myocardial reinfarctions), stroke and emergency procedures to restore blood flow to the heart.

    The results showed that the incidence of MACCEs was around 30 percent lower in the group that took tongxinluo, compared with those participants taking the placebo at 30 days of follow-up. These benefits persisted for one year after discharge, and no major side effects were recorded, indicating that the medicine was safe to use, the authors found.

    A stock image shows a doctor prescribing medicine. A traditional Chinese medicine has been shown to be effective at reducing complications from a heart attack after a large-scale, clinical trial.
    iStock

    “Many drugs have failed to achieve effects as impressive as this traditional Chinese medicine,” Dr. Ying Xian, an author of the study who is at UTSW, said in a press release.

    Saybolt said the study was “well conducted,” with a large sample size that was “well powered” to measure the outcomes.

    “In this trial, there is clearly a benefit to patients treated with this Chinese medicine compound compared to placebo,” he said.

    He went on: “A reduction in death, reinfarction or complications after a STEMI is a very exciting finding. We have for some time been trying to bend the curve and improve mortality and complications after STEMI. Any new therapy, if safe, that can accomplish this would be very appealing to patients and physicians alike.”

    Saybolt said he also observed some weaknesses in the way the study was conducted, one of which was that the participants were entirely Chinese citizens and predominantly male.

    “Thus the findings may not be generalizable throughout the world or to women,” he said. “Furthermore, the patients were less frequently—compared to the United States, for example—treated with traditional proven medicine after their myocardial infarctions. Therefore, the effect of the Chinese medicine may have been augmented by the lack of patient exposure to proven therapies.

    “However, there was equivalent low utilization of these traditional medications in both groups,” he continued. “Furthermore, the study drug Chinese medicine compound was composed of multiple plant and insect products. Thus, we do not know which component or combination of components were the active ingredients and what is the correct dose.”

    Further research will be needed to address these matters, and the benefits shown in this study would need to be duplicated in other populations before the treatment could get approved by the U.S. Food and Drug Administration.

    Saybolt said he would be “very interested” to see another study of its kind in a broader population outside China. “We must also isolate the compound into its individual components and determine which of the components is the therapeutic ingredient.”

    Traditional Chinese medicines are seldom tested in large, randomized, placebo-controlled, blinded trials, he said.

    “The gap in research is due to a combination of bias in research towards traditional pharmaceuticals and due to funding. Large trials such as this require funding from federal agencies, grants or industry sponsorship. A generic medicine or nutritional/herbal/animal/insect compound has little financial backing in many cases,” he said.

    Eric Peterson, a senior author of the study who is at UTSW, advised and collaborated with the Chinese researchers. He told Newsweek: “Is the medicine ready for the West? No. Does it show interesting promise? Absolutely. And we should not discount it. We have shown that traditional Chinese medicines can be tested.”

    He continued: “There’s a little bit of disbelief when you just look at the ingredients that are in it. People in the West…we have our doubts. We felt similarly about some of the drugs that we had to treat malaria until we found that they were actually pretty powerful medicines. So I think there are a lot of natural cures that actually are based on some believable and truthful benefits.”