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Tag: transplant

  • New Mexico boy receives life-changing heart transplant

    Hunter Rael, an 8-year-old boy from New Mexico, has received a new heart after experiencing Kawasaki disease, a rare illness that causes inflammation of the blood vessels and serious heart issues.Hunter’s family received a life-changing phone call on Tuesday, informing them that a new heart was available for him. “We were in shock. We were a mix of emotions. We were crying,” Anna Moya, his mother, said.The news comes right around Hunter’s three-year anniversary of his Kawasaki disease diagnosis. On Nov. 1, 2022, Hunter was diagnosed with the rare illness. It primarily affects young children and causes inflammation of blood vessels throughout the body, but in Hunter’s case, it caused serious heart issues.According to the Mayo Clinic, Kawasaki disease most often affects the heart arteries in children. Kids with the illness sometimes have a high fever, swollen hands and feet with skin peeling, red eyes, and tongue. The Mayo Clinic reports that with early treatment, most children get better and have no long-lasting symptoms. On Tuesday, Hunter just got back to New Mexico after traveling to Colorado for a checkup at Children’s Hospital Colorado. Around 11 that morning, he received a phone call he’s been waiting for. “You need to come back. We found Hunter a heart, and it’s go time,” said Moya. He and his mom immediately got on a plane and headed to Colorado.At 5 a.m. Wednesday, Hunter underwent surgery. Cell phone video shared by his family shows the 8-year-old being wheeled back to surgery as he listens to his favorite artist, Jelly Roll. Hunter said Jelly Roll’s music helps keep him calm and gets him through tough times.In October, Hunter got a surprise package from Jelly Roll’s team. It included some gifts and a signed album. According to Hunter, meeting the artist would be a dream come true.Doctors found a bleed flooding the transplant, but were able to fix it. Hunter’s family says right now, Hunter is in stable condition after having a rough night.As of Thursday, Hunter was on an ECMO machine to allow his heart and lungs to rest and heal. His family told sister station KOAT that things are looking good, but it’s going to take some time to see how his body adjusts to the new heart.”They’re slowly starting to kind of wake him up off the sedation. He’ll probably be on that for a few more days. Then we’ll probably have more like of an understanding, make sure everything’s going good, no brain damage, because he’s had a hard hit,” said Moya. “It’s really affecting his body. He’s kind of swollen right now, and they’re trying just to get everything under control.”Hunter and his family want to thank everyone who’s reached out and has been following his journey. “We appreciate all the prayers. Just keep rooting for him. Just keep praying,” said Moya. ‘”As soon as I’m able to show you guys his beautiful face and he’s awake, I will, I will do that … we’ll get him singing Jelly Roll again and we’re going to get there. It’s just going to take time.”

    Hunter Rael, an 8-year-old boy from New Mexico, has received a new heart after experiencing Kawasaki disease, a rare illness that causes inflammation of the blood vessels and serious heart issues.

    Hunter’s family received a life-changing phone call on Tuesday, informing them that a new heart was available for him.

    “We were in shock. We were a mix of emotions. We were crying,” Anna Moya, his mother, said.

    The news comes right around Hunter’s three-year anniversary of his Kawasaki disease diagnosis. On Nov. 1, 2022, Hunter was diagnosed with the rare illness. It primarily affects young children and causes inflammation of blood vessels throughout the body, but in Hunter’s case, it caused serious heart issues.

    According to the Mayo Clinic, Kawasaki disease most often affects the heart arteries in children. Kids with the illness sometimes have a high fever, swollen hands and feet with skin peeling, red eyes, and tongue. The Mayo Clinic reports that with early treatment, most children get better and have no long-lasting symptoms.

    On Tuesday, Hunter just got back to New Mexico after traveling to Colorado for a checkup at Children’s Hospital Colorado. Around 11 that morning, he received a phone call he’s been waiting for.

    “You need to come back. We found Hunter a heart, and it’s go time,” said Moya.

    He and his mom immediately got on a plane and headed to Colorado.

    At 5 a.m. Wednesday, Hunter underwent surgery. Cell phone video shared by his family shows the 8-year-old being wheeled back to surgery as he listens to his favorite artist, Jelly Roll. Hunter said Jelly Roll’s music helps keep him calm and gets him through tough times.

    In October, Hunter got a surprise package from Jelly Roll’s team. It included some gifts and a signed album. According to Hunter, meeting the artist would be a dream come true.

    Doctors found a bleed flooding the transplant, but were able to fix it. Hunter’s family says right now, Hunter is in stable condition after having a rough night.

    As of Thursday, Hunter was on an ECMO machine to allow his heart and lungs to rest and heal. His family told sister station KOAT that things are looking good, but it’s going to take some time to see how his body adjusts to the new heart.

    “They’re slowly starting to kind of wake him up off the sedation. He’ll probably be on that for a few more days. Then we’ll probably have more like of an understanding, make sure everything’s going good, no brain damage, because he’s had a hard hit,” said Moya. “It’s really affecting his body. He’s kind of swollen right now, and they’re trying just to get everything under control.”

    Hunter and his family want to thank everyone who’s reached out and has been following his journey.

    “We appreciate all the prayers. Just keep rooting for him. Just keep praying,” said Moya. ‘”As soon as I’m able to show you guys his beautiful face and he’s awake, I will, I will do that … we’ll get him singing Jelly Roll again and we’re going to get there. It’s just going to take time.”

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  • 10/31: CBS Morning News



    10/31: CBS Morning News – CBS News










































    Watch CBS News



    Pres. Trump calls on Senate Republicans to get rid of the filibuster to reopen the government; a heart transplant recipient is raising awareness for nonprofit Harboring Hearts during the NYC marathon.

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  • Her little sister needed a kidney. The donation let them both live their dreams

    Her little sister needed a kidney. The donation let them both live their dreams

    As children, sisters Amaris and Dominique Elston were inseparable. Their parents remember the two of them sharing everything and always having each others’ backs, no matter the situation. 

    That bond didn’t change as they grew older, and when an 18-year-old Dominique was diagnosed with focal segmental
    glomerulosclerosis, a chronic kidney disease that soon led to kidney failure, Amaris was again ready to help her sister.

    “I told Amaris ‘Dominique is in kidney failure. Her kidney function was at 19%, and she’s going to need a kidney transplant eventually,'” Denise Elston, their mother, said. “Thirty seconds later, Amaris said, ‘Can I give her one?'” 

    Amaris (back) and Dominique (front) Elston as children. 

    The Elston family


    Amaris, then interviewing for medical schools, knew her family had a history of kidney disease, so she wasn’t sure she’d be able to donate. Dominique didn’t want her sister to put her life on hold but as her condition deteriorated and her kidney function dropped to just 5%, despite dialysis treatments, Amaris knew she had to do something. Without telling Dominique, she got tested and learned she was a match. 

    “She’s my little sister,” Amaris said. “As a big sister, it’s natural to want to jump in and save her from everything that life has to offer, even failing kidneys. I knew this was the best option that she had at getting back on track with life and doing all the things she wanted to do. It was never really a question.” 

    Avoiding years on a waiting list 

    About 140,000 people are on the waiting list for a kidney transplant in the United States, according to Dr. Kelly Birdwell, medical director of kidney transplantation at Vanderbilt University Medical Center, who was not involved in the Elston sisters’ care.

    The average American waits about five years for a kidney donation through the waiting list. Black Americans are also disproportionately represented on the waiting list, Birdwell said. Black people are more likely to have Type B blood, which has fewer compatible donors, she said, and there is also “an excess risk of kidney disease in the African American population.” 

    In 2019, more than 14,000 Black kidney transplant candidates were moved up on the national waitlist after it was found a widely-used test was overestimating how well Black people’s kidneys were functioning, making them seem healthier than they were and extending the amount of time they waited. 


    Thousands of Black kidney transplant candidates moved up on waitlist after testing bias found

    03:20

    Amaris said all of those factors were on her mind when she decided she wanted to donate to her sister. In 2023, 21,765 kidney transplants were completed, with 6,294 of those organs coming from living donors. About 60% of living donors are related to the recipient, Birdwell said. 

    To donate a kidney, interested family members do a round of initial testing that confirms the donor is compatible with the recipient. That’s followed by a longer evaluation, Birdwell explained, to make sure the donation won’t put the potential donor at risk. The evaluation includes bloodwork and imaging to confirm the potential donor is in good health. Once those stages are successfully completed, it’s just a matter of scheduling the surgery. 

    For the Elstons, that meant waiting until Amaris finished her first semester of medical school at the University of Alabama at Birmingham. In December 2018, the sisters were again side-by-side, waiting for their operations at the University of Vanderbilt’s Transplant Center. Amaris’ operation was first. Birdwell estimates that a donor surgery is about two hours, while a recipient’s surgery, scheduled for later in the day, is about three hours. 

    When Amaris and Dominique reunited after their operations, the eldest of the two could already see a change in her baby sister. 

    “I remember laying in the bed and being in a lot [of] pain, and Dominique walking down the hallways like ‘No big deal,’ and in that moment, it solidified that I knew I had made the right decision,” Amaris said. “She looked like a whole new person, in less than 24 hours. She was just bopping in my room, sitting in my chair. It was worth it.” 

    02.jpg
    Dominique (left) and Amaris (right) after transplant. 

    The Elston family


    Working together to save lives 

    Amaris gave her younger sister more than a kidney. She also gave Dominique the chance to follow her sister into the field of medicine. 

    Amaris graduated from UAB’s Heersink School of Medicine in 2022. Just two years later, Dominique graduated from the UAB School of Nursing with her bachelor’s degree in nursing. Amaris cheered her on from the audience. 

    “After going through what we went through, it was kind of like a calling for me to go into (nursing),” Dominique said. “It wasn’t really something I had to think about. I felt like it was something that was meant for me.” 

    1.png
    Dominique (left) and Amaris (right) at Dominique’s graduation ceremony from UAB. 

    The Elston family/UAB


    Now, both sisters are working in the neurology field. Amaris is a neurology resident at the Medical University of South Carolina, and Dominique is a neurology intensive care unit nurse at UAB. The two are the first members of their family to enter the medical field. Though the sisters are now separated by more than more than 400 miles, their bond is stronger than ever. 

    “It’s been fun having somebody that is with you through everything, because if you want to talk about the bad parts, the good parts, you can,” Amaris said. “It feels good to know that there’s somebody right beside you that can understand how you feel and what you’re going through. We’ve been each other’s best friends amid some of our darkest moments, so this is just another journey that we’re on together.”  

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  • World Heart Day: A Leesburg father’s urgent message on heart failure after he was diagnosed at 41 – WTOP News

    World Heart Day: A Leesburg father’s urgent message on heart failure after he was diagnosed at 41 – WTOP News

    A Loudoun County man had a mysterious illness until his doctor got a hunch and ordered a heart X-ray. The doctor gave the Leesburg father of three a surprising diagnosis.

    Son Vang with his family. He was diagnosed with congestive heart failure.
    (Courtesy Son Bang)

    Courtesy Son Bang

    At 41 years old, Son Vang didn’t fit the mold of a typical heart failure patient.
    (Courtesy Son Bang)

    Courtesy Son Bang

    Dr. Robert Kormos, a cardiothoracic surgeon and professor emeritus at the University of Pittsburgh, said many times heart failure masquerades as cold symptoms because fluid from the heart builds up in the lungs, causing an incessant cough and congestion.
    (Courtesy Robert Kormos)

    Courtesy Robert Kormos

    Editor’s note: This story has been updated to correct the spelling of Son Vang.

    Five years ago, Son Vang battled a dry cough that wouldn’t go away.

    It was a mysterious illness until his doctor got a hunch and ordered a heart X-ray. The doctor gave the Leesburg, Virginia, father of three a surprising diagnosis.

    “The cardiologist came into my hospital room and said, ‘Look, you have congestive heart failure,’” Vang told WTOP. “I was pretty scared at that time.”

    Vang didn’t fit the mold of a typical heart failure patient. At 41 years old, he was young, a nonsmoker and had no family history of the condition.

    But the discovery was a relief for him because doctors had a path to wellness. It included getting on a long heart transplant list. And last year, he got an artificial heart pump, giving him more time with his wife and three girls.

    “I’ve been feeling better than I have the last five or 10 years,” he said. “You don’t realize how sick you were with your heart not pumping enough blood to the rest of your organs. Now that my heart is pumping full speed, I can be active and play with my kids.”

    Sunday is World Heart Day, when doctors and patients around the globe bring attention to heart disease and explore ways to make the organ healthier.

    Vang said his journey is a message to others to get checked for heart failure early.

    “You can’t tell a person who’s having heart failure,” he said. “It doesn’t show. It’s not like you break your leg and you can see it. With the declining of your heart, you can’t tell.”

    Nearly seven million people in the U.S. are diagnosed with heart failure each year, according to the Centers for Disease Control. Many live undiagnosed for years, battling puzzling symptoms, which include:

    • Shortness of breath
    • Extreme fatigue
    • A constant, dry cough
    • Swelling in the legs, ankles and feet

    Dr. Robert Kormos, a cardiothoracic surgeon and professor emeritus at the University of Pittsburgh, said many times heart failure masquerades as cold symptoms because fluid from the heart builds up in the lungs, causing an incessant cough and congestion.

    Kormos said patients and doctors could get to the root of the illness faster with tests designed to spot heart failure.

    “Heart failure is lethal. It kills more people than the cancer we treat,” Kormos told WTOP. “The important thing is if you have symptoms, you need another level of investigation. You need to go deeper.”

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    © 2024 WTOP. All Rights Reserved. This website is not intended for users located within the European Economic Area.

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  • Race removed as factor in kidney function test, allowing Minneapolis woman to receive transplant sooner

    Race removed as factor in kidney function test, allowing Minneapolis woman to receive transplant sooner

    MINNEAPOLIS — A major change in the medical world is helping make kidney transplants more racially equitable.

    Race is no longer being considered an important test to estimate kidney function.

    Bernadeia Johnson, a Black woman from Minneapolis, had kidney transplant surgery last month.

    “I’m doing so well,” she said.

    Living with stage five chronic kidney disease, Johnson had five donors fall through until the sixth turned out to be the charm.

    “I had to show some level of strength, but I have to tell you, nobody should have to show this much strength,” she said. “It was very hard.”

    There are several factors that go into someone’s placement on the transplant waiting list, including, of course, if there’s a match out there, but one of the factors is how long the wait has been.

    Johnson got a big boost there.

    10p-pkg-kidney-test-wcco5hka-00-01-3719.jpg

    Bernadeia Johnson


    “I was on the list for two years, but after they did the recalculation, I was on the list for five years and eight months,” she said.

    That adjustment was the result of race being removed as a component in a test that estimates kidney function.

    “I could still be waiting,” Johnson said.

    Dr. Kirsten Johansen, Hennepin Healthcare’s chief of nephrology, says the test had been systematically causing Black people’s results to come back as higher, which, in some cases, may have affected their eligibility for a transplant.

    “They required all transplant centers to go back and reevaluate…and then go through the charts of all Black patients to see whether they could document that they would have, under the newer equation, had a lower estimated kidney function sooner, and then to adjust their time back,” Johansen said.

    Johansen says there’s still plenty of work to do to address racial disparities in health outcomes.

    “Among people with kidney failure, requiring dialysis or transplant, it’s almost four times higher for Black people than for white people,” she said. “It’s also higher among Hispanics.”

    In Johnson’s case, the culprits were diabetes and hypertension — two risk factors that occur at higher rates in Black people.

    “There’s no silver bullet to any of this,” she said. “Just trying to take control of my own health and becoming my best advocate.”

    David Schuman

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  • Doctors perform first-ever combined heart pump and pig kidney transplant

    Doctors perform first-ever combined heart pump and pig kidney transplant

    For the first time, surgeons at NYU Langone Health performed a combined mechanical heart pump and gene-edited pig kidney transplant, helping a 54-year-old woman with heart and kidney failure.

    Before the two procedures, which took place earlier this month, New Jersey native Lisa Pisano faced heart failure and end-stage kidney disease that required routine dialysis, and she was not a candidate for a human transplant.

    “I was pretty much done,” Pisano told CBS News chief medical correspondent Dr. Jon LaPook, who is also a professor at NYU Langone. “I couldn’t go up the stairs. I couldn’t drive. I couldn’t play with my grandkids. So when this opportunity came to me I was taking it.”

    Now, she says, she’s feeling “great today compared to other days.” 

    Dr. Robert Montgomery, NYU Langone Transplant Institute director, said she is currently “doing very well” in recovery. 

    Pisano received only the second known transplant of a gene-edited pig kidney into a living person, and the first to include the pig’s thymus gland to aid against rejection, the hospital said. The transplant surgery took place on April 12, eight days after the heart pump, called a left ventricular assist device, or LVAD, was implanted on April 4.

    Last month, surgeons at Massachusetts General Hospital in Boston transplanted a pig kidney into 62-year-old Rick Slayman, marking the first successful procedure of its kind in a living human patient in the world. 

    Rejection issues with animal-to-human transplants, or xenotransplantation, have led to failures, largely due to people’s immune systems attacking the foreign tissue. Now, scientists are using genetic modification to better match those organs to humans.

    “The human immune system rejects organs from animals, but Dr. Montgomery and his team used a pig kidney with one gene altered to make it more compatible,” LaPook explains.

    Montgomery says this is about more than just the organ itself.

    “This isn’t just about keeping somebody alive, it’s restoring them to their their lives,” he says. 

    For Pisano, it means dreams of playing with her two young grandchildren for the first time in years, she says.

    LaPook adds this procedure was done under the FDA’s “compassionate use” protocol. “So it’s not approved yet — but what an amazing technological tour de force,” he said. 

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  • Capital Region chef receives kidney transplant

    Capital Region chef receives kidney transplant

    ALBANY, N.Y. (NEWS10) — The family of a beloved Capital Region chef and philanthropist shared an update on his health. Yono Purnomo received a kidney from a living donor on Tuesday.

    Purnomo had been on a months-long search for a kidney after being diagnosed with end stage renal failure in 2023. NEWS10’s Trishna Begam interviewed the restauranteur about his health and how dialysis multiple times a day changed his life.

    His surgery took place Tuesday morning at New York City’s Presbyterian Hospital. He and his donor are both recovering. Purnomo’s family said both are doing well, and they thank everyone for their continued support and prayers.

    Courtney Ward

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  • US surgeons transplant genetically modified pig kidney into patient

    US surgeons transplant genetically modified pig kidney into patient

    NEW YORK — Doctors in Boston announced Thursday they have transplanted a pig kidney into a 62-year-old patient.

    Massachusetts General Hospital said it’s the first time a genetically modified pig kidney has been transplanted into a living person. Previously, pig kidneys have been temporarily transplanted into brain-dead donors. Also, two men received heart transplants from pigs, although both died within months.

    The experimental transplant was done at the Boston hospital on Saturday. The patient, Richard “Rick” Slayman of Weymouth, Massachusetts, is recovering well and is expected to be discharged soon, doctors said Thursday.

    Slayman had a kidney transplant at the hospital in 2018, but had to go back on dialysis last year when it showed signs of failure. When dialysis complications arose, his doctors suggested a pig kidney transplant, he said in a statement released by the hospital.

    “I saw it not only as a way to help me, but a way to provide hope for the thousands of people who need a transplant to survive,” said Slayman.

    The announcement marks the latest development in xenotransplantation, the term for efforts to try to heal human patients with cells, tissues, or organs from animals. For decades, it didn’t work – the human immune system immediately destroyed foreign animal tissue. More recent attempts have involved pigs that have been modified so their organs are more humanlike – increasing hope that they might one day help fill a shortage of donated organs.

    More than 100,000 people are on the national waiting list for a transplant, most of them kidney patients, and thousands die every year before their turn comes.

    ___

    The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group. The AP is solely responsible for all content.

    Copyright © 2024 by The Associated Press. All Rights Reserved.

    AP

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  • Transplant Season 4 Episode 4 Release Date & Time on Peacock

    Transplant Season 4 Episode 4 Release Date & Time on Peacock

    The Transplant Season 4 Episode 4 release date and time have been revealed. The episode will air on CTV and then will be available for streaming on Peacock. It is titled as ‘Decisions’. This series centers on charismatic Dr. Bashir Hamed, who flees from his war-torn country to build a better life in Canada. However, it is not going to be easy as Dr. Hamed rebuilds himself completely in a new environment.

    Here’s when the episode is coming out.

    When is the Transplant Season 4 Episode 4 release date and time?

    The Transplant season 4 episode 4 Peacock release date is October 28, 2023. Episode 4 will air on CTV on October 27, 2023, and it will be then available for streaming on Peacock on the following day.

    The Transplant season 4 episode 4 release time is:

    • 6:00 P.M. Pacific Time Zone (PT)
    • 9:00 P.M. Eastern Time Zone (ET)
    • 2:00 A.M. British Summer Time (BST)
    • 3:00 A.M. Central European Summer Time (CEST)

    Where to watch Transplant Season 4 Episode 4

    Viewers can watch the upcoming episode on Peacock.

    To watch episode 4, you can sign up for Peacock streaming services. Peacock subscription plans will offer users access to its entire lineup, including NBC shows, WWE Network, Sunday Night Football, and more. It offers two subscription plans to users:

    • Peacock Premium Plan – It is priced at $5.99 a month
    • Peacock Premium Plus Plan – It is priced at $11.99 a month

    This series follows Dr. Bashir Hamed, a civil Syrian refugee in Canada, as he navigates through several challenges while building his new life. Season 4 premiered on October 6, 2023, and follows a weekly release schedule.

    The official synopsis for Transplant reads:

    “Dr. Bashir Hamed, a Syrian doctor with battle-tested skills in emergency medicine, makes the difficult decision to flee his country and build a new life in Canada with his younger sister Amira. Bash works to navigate a new environment after earning a coveted residency in the Emergency Department of one of the best hospitals in Toronto, York Memorial.”



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  • Experts ID Likely Cause of Mysterious Hepatitis Outbreak in Kids

    Experts ID Likely Cause of Mysterious Hepatitis Outbreak in Kids

    April 4, 2023 – Researchers have found that co-infection by multiple common viruses may have caused a mysterious hepatitis outbreak in kids worldwide. 

    Since October 2021, these hepatitis cases in young children affected more than 1,000 kids in 35 countries. Although most children survived, of about 350 patients identified in the United States until May 2022, 22 required a liver transplant and 13 died.

    Most of these children were under 6 years old. 

    Not only are these hepatitis cases acute and severe, but what’s causing them is a mystery. They don’t fit into the common categories of liver inflammation, known as hepatitis A through E. 

    Now, researchers have zeroed in on a possible culprit. They identified a strain of virus, called adeno-associated virus type 2 (AAV2), as the central player in the outbreak. And if they are correct, AAV2 is not acting alone. 

    In fact, this virus is not strong enough to cause these severe cases without help. Instead, affected children must have at least one other “helper” virus at the same time, such as a human adenovirus (which can cause symptoms similar to the common cold or flu, according to the CDC), Epstein-Barr virus, and/or human herpesvirus 6. 

    The new study was published online March 30 in the journal Nature

    Pointing to the Pandemic

    The researchers say there is no evidence linking the illnesses to the virus that causes COVID-19, but the pandemic may still be a factor in these infections. Because many children were not exposed to the viruses linked to the hepatitis cases during lockdowns and social isolation, as they normally would be, they did not build up immunity to them.  

    “So it is possible once restrictions were lifted, they were suddenly exposed over a short period of time to multiple viruses,” said senior study author Charles Chiu, MD, PhD, a laboratory medicine and infectious disease specialist at the University of California San Francisco School of Medicine. 

    This setup and lack of a strong immune system to deal with these specific viruses “would have increased their risk of developing severe disease.”

    William Balistreri, MD, a pediatric hepatitis specialist who was not affiliated with the study, agreed this was possible. 

    This has been a popular theory, especially in view of the timing of the bulk of cases, peaking during the height of the COVID-19 pandemic and associated isolation procedures,” said Balistreri, who is also a professor of pediatrics and director emeritus of the Pediatric Liver Care Center at Cincinnati Children’s Hospital Medical Center. 

    What to Watch for in Kids

    As for his take-home message for parents and health care providers, “the keys are awareness and reassurance,” Balistreri said. 

    Vigilance also is warranted, he said, if a child has symptoms that often come right before hepatitis, including respiratory symptoms, nausea, vomiting, diarrhea, and belly pain. Also, If jaundice or yellowing of the eyes from jaundice, called scleral icterus, develops, then hepatitis should be suspected. 

    “Reassurance is based on the good news that most children with acute hepatitis get better. If a case arises, it is good practice to keep the child well-hydrated, offer a normal diet, and avoid medications that may be cleared by the liver,” Balistreri said, noting that COVID vaccination is “strongly suggested.”

    Working to Solve the Mystery

    Chiu and colleagues were not completely in the dark at first. They knew from previous research that adenoviruses might be involved. So they used genomic sequencing and other advanced technologies to look for the virus in 27 blood, stool, and other samples from 16 children with this severe hepatitis. They also wanted to know what other viruses might be present. 

    And for comparison, they searched for the same viruses in a group of 113 children without this severe hepatitis of unknown origin.

    Strengthening their findings were two other studies that were done at different institutions and published in the same journal at the same time. One was a genomic study confirming the presence of AAV2 and other suspected viruses, and the other was a genomic and laboratory study further supporting the results.

    Of the 16 affected children studied by Chiu and colleagues, the average age was 3. About half were boys. These children were diagnosed with severe hepatitis starting when it was first detected on Oct. 1, 2021, until May 22, 2022. 

    Key Findings

    Of the three studies published in Nature, using different diagnostic tools, there was a consistent presence of the adeno-associated virus type 2 in all or almost all of children, while the “helper” viruses of varying types were also discovered.

    Also striking in the studies: what was not found. Of 113 children in one comparison group, among those with diagnoses other than the mystery ailments — including stomach flu, hepatitis of known origin, and those admitted to a hospital for liver failure — AAV2 was much less common. 

    There was also hardly any evidence of the “helper” viruses. 

    “I am quite confident that we have identified the key viruses” because they used  comprehensive genetic sequencing “to look for potential infections from any virus or non-viral pathogen,” Chu said.

    Moving Forward

    The next steps in the research could go beyond identifying presence of these viruses and figuring out which one – or ones – are adding the most to the acute pediatric hepatitis. 

    There was also a study in the United Kingdom that identified a specific genetic factor linked to the condition, and Chiu and colleagues might look into that further. 

    They also said they might study other things linked to the COVID pandemic, including if and how long COVID fits into this and resurgence of other viruses, such as respiratory syncytial virus (RSV) and the flu.

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  • Investigation finds failures in organ transplant system:

    More than 100,000 people in the United States are waiting for an organ transplant. But only slightly more than half of them are expected to receive an organ within five years.  

    Now, a congressional investigation is raising serious questions about whether non-profit groups meant to secure organs for transplants from deceased donors are doing enough. 

    The groups, called organ procurement organizations, or OPOs, are “failing” to secure many organs that could be recovered, according to a House subcommittee investigating the organ donation and transplant system.

    “Seventeen to 20 people a day die on the wait list because they can’t get organs, and the OPOs are just not recovering enough organs and making sure they’re getting into people who need them,” said Rep. Raja Krishnamoorthi, who chairs the House subcommittee.

    In August, the Senate Committee on Finance said a 2.5-year investigation found “from the top down, the U.S. transplant network is not working, putting Americans’ lives at risk.”   

    And in a letter sent to OPOs on Thursday, the House subcommittee raised questions about whether data provided by OPOs may be “inaccurate and incomplete.”

    “If you don’t have proper data, then you don’t know what organs exist and are usable to go into people who need them,” said Krishnamoorthi.

    Several OPOs told CBS News their data is “accurate,” and they’re committed to saving lives.  

    The United Network for Organ Sharing, UNOS, said its “systems are audited annually.” 

    “The data clearly demonstrates that year over year our transplant system continues to be more and more successful,” UNOS’ Dr. Matt Cooper told CBS News in May, when he was board president.

    But not everyone in the system agrees. 

    Matt Wadsworth, who heads Life Connection, an OPO in Ohio, said he believes many OPOs nationwide are failing. 

    He became emotional during his interview with CBS News, breaking down in tears and leaving for a moment to compose himself.

    “There’s people dying,” he said.   

    In Wadsworth’s first two years at his organization, they doubled the number of organ donors in his region, which meant many more lives saved. He told members of Congress at a House subcommittee’s hearing in 2021 that other OPOs should be doing better, too, and that OPOs are “grossly inefficient and unaccountable.” 

    They’re unaccountable, he said, because before this year, when the government changed the way OPOs are evaluated, some OPOs were able to make their numbers look better than they actually were.

    In manipulating their data, OPOs made it look like “they were going after every opportunity every time, they were converting every possible patient to be a successful organ donor.”

    “And that’s just not the truth,” he said. “And they’re the same bad players. If you look at the data, it’s the same people low performing year after year.”

    The Association of Organ Procurement Organizations said its members are doing a good job and that OPOs have increased the number of deceased organ donors by 35% in the last five years. But it agreed “improvements are necessary” to advance care for patients.

    One of those patients is LaQuayia Goldring, who has been waiting seven years for a kidney transplant to keep her alive.

    For four hours a day, five days a week, she sits hooked up to a machine for home dialysis – the only way to clean her blood while she waits.

    “I only have one shot at a transplant, and until I get that call, my life is dependent upon a machine,” she said. “A lot of dialysis patients are sitting around like me just wondering, ‘When will we get the call?'” 

    “I feel like the longer that I wait, the closer I am to death,” she said. 

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