Saturday, January 4, 2020

Top 10 Medical Innovations for 2020

Cleveland Clinic Unveils Top 10 Medical Innovations for 2020

A panel of top doctors and researchers presents the medical advancements with the power to transform healthcare in the next year

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A dual-acting osteoporosis drug. Minimally invasive mitral valve surgery. New treatment for peanut allergies. These are some of the innovations that will enhance healing and change healthcare in the coming year, according to a distinguished panel of doctors and researchers.
Cleveland Clinic today announced the Top 10 Medical Innovations for 2020 at a multimedia presentation that capped off the 2019 Medical Innovation Summit. Now in its 17th year, the annual Medical Innovation Summit is organized by Cleveland Clinic Innovations, the development and commercialization arm of Cleveland Clinic.
The list of up-and-coming technologies was selected by a panel of Cleveland Clinic physicians and scientists, led by Michael Roizen, M.D., Emeritus Chief Wellness Officer at Cleveland Clinic.
“Healthcare is ever changing and we anticipate that these innovations will significantly transform the medical field and improve care for patients at Cleveland Clinic and throughout the world,” said Dr. Roizen.
Here, in order of anticipated importance, are the Top 10 Medical Innovations for 2020:
1. Dual-Acting Osteoporosis Drug
Osteoporosis is a condition in which bones become weak and brittle, effectively increasing their risk of breaking. With osteoporosis, the loss of bone occurs silently and progressively – often without symptoms until the first fracture. Providing more bone-strengthening power, the recent FDA approval of a new dual-acting drug (romosozumab) is giving patients with osteoporosis more control in preventing additional fractures.
2. Expanded Use of Minimally Invasive Mitral Valve Surgery
The mitral valve allows blood flow from the heart’s left atrium to the left ventricle. But in about 1 in 10 individuals over the age of 75, the mitral valve is defective causing the action of regurgitation. Expanding the approval of a minimally invasive valve repair device to a population of patients who have failed to get symptom relief from other therapies provides an important new treatment option.
3. Inaugural Treatment for Transthyretin Amyloid Cardiomyopathy
A disheartening cardiovascular disorder, ATTR-CM is a progressive, underdiagnosed, potentially fatal disease in which amyloid protein fibrils deposit in, and stiffen, the walls of the heart’s left ventricle. But a new agent to prevent misfolding of the deposited protein is showing a significantly reduced risk of death. Following Fast-Track and Breakthrough designations in 2017 and 2018, 2019 marked the FDA approval of tafamidis, the first-ever medication for treatment of this increasingly recognized condition.
4. Therapy for Peanut Allergies
It’s a terrifying reality for 2.5 percent of parents – the possibility that at any moment, their child might be unable to breathe due to an allergic reaction. Though emergency epinephrine has reduced the severity and risk of accidental exposure, these innovations are not enough to quell the ever-present anxiety. But development of a new oral immunotherapy medication to gradually build tolerance to peanut exposure holds the opportunity to lend protection against attack.
5. Closed-Loop Spinal Cord Stimulation
Chronic pain is a terribly frustrating condition, and a large reason for prescription of opioid medication. Spinal cord stimulation is a popular treatment for chronic pain through which an implantable device provides electrical stimulus to the spinal cord. But unsatisfactory outcomes due to subtherapeutic or overstimulation events are common. Closed-loop stimulation is allowing for better communication between the device and the spinal cord providing more optimal stimulation and relief of pain.
6. Biologics in Orthopaedic Repair
After orthopaedic surgery, the body can take anywhere from months to years to recover. But biologics – cells, blood components, growth factors, and other natural substances – have the power to replace or harness the body’s own power and promote healing. These elements are finding their way into orthopaedic care, allowing for the possibility of expedited improved outcomes.
7. Antibiotic Envelope for Cardiac Implantable Device Infection Prevention
Worldwide, roughly 1.5 million patients receive an implantable cardiac electronic device every year. In these patients, infection remains a major, potentially life-threatening complication. Antibiotic-embedded envelopes are now made to encase these cardiac devices, effectively preventing infection.

8. Bempedoic Acid for Cholesterol Lowering in Statin Intolerant Patients
High cholesterol is a major concern for nearly 40 percent of adults in the U.S. Left untreated, the condition could lead to serious health problems like heart attack and stroke. Though typically managed with statins, some individuals experience unacceptable muscle pain with statins. Bempedoic acid provides an alternative approach to lowering of LDL-cholesterol while avoiding these side effects.
9. PARP Inhibitors for Maintenance Therapy in Ovarian Cancer
PARP, or poly-ADP ribose polymerase, inhibitors block repair of damaged DNA in tumor cells which increases cell death, especially in tumors with deficient repair mechanisms.  One of the most recent important advances ovarian cancer treatment, PARP inhibitors have improved progression-free survival and are now being approved for first-line maintenance therapy in advanced stage disease. Several additional large-scale trials are underway with PARP inhibitors set to make great strides in improving outcomes in cancer therapy.
10. Drugs for Heart Failure with Preserved Ejection Fraction
Heart failure with preserved ejection fraction (HFpEF) – also known as diastolic heart failure – is the condition in which the ventricular heart muscles contract normally, but do not relax as they should. With preserved ejection fraction, the heart is unable to properly fill with blood – leaving less available to be pumped out to the body. Currently, recommendations for this treatment are directed at accompanying conditions and mere symptom relief. But SGLT2 inhibitors, a class of medications used in the treatment of type 2 diabetes, is now being explored in HFpEF – alluding to a potential new treatment option.
For more information on the annual Top 10 Medical Innovations including descriptions, videos, and year-by-year comparisons visit: https://innovations.clevelandclinic.org/Summit/Top-10-Medical-Innovations
About Cleveland Clinic
Cleveland Clinic is a nonprofit multispecialty academic medical center that integrates clinical and hospital care with research and education. Located in Cleveland, Ohio, it was founded in 1921 by four renowned physicians with a vision of providing outstanding patient care based upon the principles of cooperation, compassion and innovation. Cleveland Clinic has pioneered many medical breakthroughs, including coronary artery bypass surgery and the first face transplant in the United States. U.S. News & World Report consistently names Cleveland Clinic as one of the nation’s best hospitals in its annual “America’s Best Hospitals” survey. Among Cleveland Clinic’s 66,000 employees are more than 4,200 salaried physicians and researchers and 16,600 nurses, representing 140 medical specialties and subspecialties. Cleveland Clinic’s health system includes a 165-acre main campus near downtown Cleveland, 11 regional hospitals in northeast Ohio, more than 180 northern Ohio outpatient locations – including 18 full-service family health centers and three health and wellness centers – and locations in southeast Florida; Las Vegas, Nevada; Toronto, Canada; Abu Dhabi, UAE; and London, England. In 2018, there were 7.9 million total outpatient visits, 238,000 hospital admissions and observations, and 220,000 surgical cases throughout Cleveland Clinic’s health system. Patients came for treatment from every state and 185 countries. Visit us at clevelandclinic.org. Follow us at twitter.com/CCforMedia and twitter.com/ClevelandClinic. News and resources are available at newsroom.clevelandclinic.org.

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Sunday, December 29, 2019

Now, one can detect cancer in just 10 seconds


Now, one can detect cancer in just 10 seconds

ANI
Published Sep 7, 2017, 8:01 am IST
Updated Sep 7, 2017, 8:01 am IST
Researchers from University of Texas, Austin invent powerful tool that rapidly and accurately identifies cancerous tissue during surgery.
The current method for diagnosing cancers, called Frozen Section Analysis, is slow and sometimes inaccurate. (Photo: Pixabay)
 The current method for diagnosing cancers, called Frozen Section Analysis, is slow and sometimes inaccurate. (Photo: Pixabay)
Washington DC: A new device can detect whether or not a tumour is cancerous in just 10 seconds.
The researchers from University of Texas, Austin invented a powerful tool that rapidly and accurately identifies cancerous tissue during surgery, delivering results in about 10 seconds-- more than 150 times as fast as existing technology.
The MasSpec Pen is an innovative handheld instrument that gives surgeons precise diagnostic information about what tissue to cut or preserve, helping improve treatment and reduce the chances of cancer recurrence.
"If you talk to cancer patients after surgery, one of the first things many will say is 'I hope the surgeon got all the cancer out,' " said team leader Livia Schiavinato Eberlin. "It's just heartbreaking when that's not the case. But our technology could vastly improve the odds that surgeons really do remove every last trace of cancer during surgery."
The current state-of-the-art method for diagnosing cancers and determining the boundary between cancer and normal tissue during surgery, called Frozen Section Analysis, is slow and sometimes inaccurate. Each sample can take 30 minutes or more to prepare and interpret by a pathologist, which increases the risk to the patient of infection and negative effects of anesthesia. And for some types of cancers, frozen section interpretation can be difficult, yielding unreliable results in as many as 10 to 20 percent of cases.
However, in tests on tissues removed from 253 human cancer patients, the MasSpec Pen took about 10 seconds to provide a diagnosis and was more than 96 percent accurate. The technology was also able to detect cancer in marginal regions between normal and cancer tissues that presented mixed cellular composition. The team expects to start testing this new technology during oncologic surgeries in 2018.
"Any time we can offer the patient a more precise surgery, a quicker surgery or a safer surgery, that's something we want to do," says James Suliburk. "This technology does all three. It allows us to be much more precise in what tissue we remove and what we leave behind."
Although maximizing cancer removal is critical to improve patient survival, removing too much healthy tissue can also have profound negative consequences for patients: For example, breast cancer patients could experience higher risk of painful side effects and nerve damage, in addition to aesthetic impacts. Thyroid cancer patients could lose speech ability or the ability to regulate the body's calcium levels in ways that are important for muscle and nerve function.
In tests performed on human samples, the device was more than 96 percent accurate for cancer diagnosis. The team has also demonstrated that it accurately diagnoses cancer in live, tumor-bearing mice during surgery without causing any observable tissue harm or stress to the animals.
Physicians can operate the disposable handheld device easily. It requires simply holding the pen against the patient's tissue, triggering the automated analysis using a foot pedal, and waiting a few seconds for a result. Meanwhile, the pen releases a drop of water onto the tissue, and small molecules migrate into the water. Then the device drives the water sample into an instrument called a mass spectrometer, which detects thousands of molecules as a molecular fingerprint.
The process is also low-impact for patients.
"When designing the MasSpec Pen, we made sure the tissue remains intact by coming into contact only with water and the plastic tip of the MasSpec Pen during the procedure," noted Zhang. "The result is a biocompatible and automated medical device that we are so excited to translate to the clinic very soon."
The research appears in the journal Science Translational Medicine.

Sunday, December 22, 2019

How I fought and recovered from a 'hidden disease' that could make me disabled for life



How I fought and recovered from a 'hidden disease' that could make me disabled for life

I could have made my peace with dying while my mind and body withered away, but to have no relief from the suffering was unbearable to think about.
I graduated from Delhi University in May 2014. I was determined to become a lecturer, and had even applied to a couple of universities across the country. Unfortunately, I didn't apply to enough, and couldn't get through any college, so I had to wait the year out.
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That was when I was diagnosed with Multiple sclerosis (MS). MS Kanika Juneja (right) It started towards the end of September. My body had been getting tired faster and I was experiencing spells of dizziness. I'd told my parents, who, in their wisdom, thought it was my diet and advised me to eat better and exercise more. Still, the feeling of dizziness persisted, and I finally visited a doctor, only to be told the same things that my parents suggested, “You'll be fine, just eat better.” A few days later, on October 2, 2014, I was sleeping over at my best friend, Richa's home. We'd been out with friends, and by the time we got to her house, I was feeling extremely nauseous and dizzy. I finally slept, only to realise that upon waking up I kept getting bites on the inside of my cheeks (my teeth were involuntarily biting the inside of my cheeks). The symptoms, even then, were so little, that my parents and I didn't think of them as serious, at all. Three days later, I felt this odd feeling in my leg that wouldn't go away. I couldn't describe it even to doctors and attendants, who we'd visited, after I insisted that I was in discomfort. This time, my doctor, seemed a bit perplexed, and worried, by my symptoms of cheek bites, numbness, and this uncomfortable and odd sensation in my legs.
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The doctor advised us to visit AIIMS, Delhi, as soon as possible. I was to see a neuro-specialist. The same night, when my mother handed me a glass of warm milk. She warned me how that the glass was hot. I couldn't understand, as the glass I was holding, didn't feel warm, at all. I transferred the glass to my left hand, only to drop it because of how hot it was. By then, I had no clue about what was happening to me, but I was fairly sure it was nothing grave. The next day, when the neurologist was administering a reflex test, during which, I had to touch my finger with his finger, I could do it with my left hand, but no matter how steadily I tried, I couldn't do it with my right. The neurologist suggested my father to get an 'urgent' contrast MRI of my brain. Even on the prescription, he wrote– 'urgent'.
Things were a blur those days, because every test and every referral was 'urgent'.
I, who had never had the opportunity to observe the medical world up close, was very fascinated by all the machines and instruments. Besides, in my mind, I was sure it was nothing major.
Serious illnesses are for other people. That's what everybody thinks.
I remember the doctor's face while he looked at my MRI scans, he looked very grave and immediately asked me to pack some clothes because I had to be admitted. By this time, it was July, 2015. Kanika and her mother Kanika and her mother The morning after I was admitted to AIIMS, a full panel of doctors came to ascertain my condition. They were worried about what my MRI showed, and wanted to conduct further tests. In the middle of their discussion, I had to go use the toilet, so I excused myself.
The moment I got off the bed, I staggered and fell. I tried standing up, only to fall back down, again. That was the first time, I was scared. A realisation that something was wrong had just hit me.
The doctors chose to start me on a treatment of steroids. My perception of steroids, at the time, had been limited to knowing it was used by bodybuilders and sports people to bulk up. I was even starting to get wary of staying in the hospital bed. The novelty was wearing off. We would ask the doctors what was happening, but they only said they were still diagnosing. I was undergoing blood tests, scans, etc, but I still didn't know what was making me ill.
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One day, the doctor came and asked me how the 'pins and needles' sensation in my legs was, I finally had the phrase to describe the uncomfortable feeling. You see, I had gradually started feeling it all across my body, and hadn't been able to describe the feeling until he mentioned 'pins and needles'. It was a relief, at least they knew what they were doing. Soon, the steroids took effect, and I could walk again. The doctor's explained I had what was known as a 'clinically isolated syndrome' typically consistent with an attack of Multiple Sclerosis, but they couldn't confirm until another attack hit. whatsapp-image-2017-07-09-at-11-38-30-pm Multiple sclerosis is an autoimmune disease for which there is no known cure. It involves the immune system misfiring and attacking the neurons in the brain, which causes the organs not to receive the signals sent by the brain.
It could mean that any organ in my body, at any time, could stop functioning the way it was supposed to.
The doctor further explained that it could happen to anyone, however it was most common in temperate climates, and that women were more likely to get it. They sent me home with a warning to be on the look-out for another attack which could affect any part of my body. I was still optimistic, hoping that it was just the one attack, and that I couldn't possibly have anything more. Unfortunately, the next attack came only a month later, this time, I couldn't move my eye. I could see out of it, but if I tried to blink or close it, it wouldn't respond. The third attack came close behind the second, I couldn't move my right hand. I would suddenly drop anything I was holding, and off to the hospital we went again, for the usual contrast MRI of my brain and spine. whatsapp-image-2017-07-09-at-11-41-52-pm This time, when the doctor entered my room, he looked visibly concerned.
“Kanika, I am sorry. Your disease is very aggressive in nature. Normally, people don't get attacks as frequent as you've had. I am afraid this can leave you with any disability very soon and we will have to start you on injections right away.”
I asked him, thoroughly nonplussed, “Will the injections cure me?” “No, they will only postpone the attacks for six months or so, provided you take them every week.” “Then, what's the point of taking the injections?” I asked, even more confused. “The more frequently you get attacks, the faster you become disabled. These injections will defer your disability. Cause it to progress at a slower rate.” Then, I asked him the question we all were wondering after proclamation of such a serious prognosis, “Is the disease terminal?”
“No, you will gradually become disabled, most likely wheelchair-bound or visually impaired, but can still go on living with it until the age of 80,” he opined.
That's when I felt the rug beneath my feet being pulled. I had been struck with a disease that had no known cause, no known cure, and it would make me miserable. I would have to live a long time being disabled. I could have made my peace with dying while my mind and body withered away, but to have no relief from the suffering, was unbearable to think about. whatsapp-image-2017-07-09-at-11-39-21-pm All around me, friends were getting jobs, going abroad and a few were even marrying, but I, who was an overachiever all throughout school, who enjoyed theatre and public speaking, was confined to a bed with the destiny of staying there. I started taking the MS injections upon going back home. The injections came with a host of side effects, extreme weakness, rashes over my body, nausea, and dizziness. The doctor advised me to always self-administer (they had a specific placing and schedule) them on Friday, so I had the entire weekend to recover from the injections.
The self-administration was also a harrowing affair because I would accidentally slip, and once even cut a significant nerve.
The overall trauma from the injections alone did nothing for my fear of them. The MS injections weren't cheap, either, as they cost my family Rs 20,000 a month. And although, they never said anything to me, I could see the worrying and discussions about money that were taking place almost daily at home. I started feeling like a burden on my family. I withdrew into a shell, knowing that while I could do nothing for myself and was suffering, I was taking my family along for the miserable ride. I, eventually, found out about the schemes for MS injections where if you needed assistance, the companies would provide one plus one month, two months plus one month, etc offers on the injections where you got one free month of injections after buying the first month or so. I had determined to receive one plus one month, but the surveyors who came to our home declared that I only qualified for the two months plus one one month, under their financial benefits scheme. I couldn't accept that. I went to my doctor and told him that I was going to stop taking the injections. If they made me disabled, so be it, but I did not have the money to pay for them anymore. He tried to persuade me, but I could no longer accept my parents being bled dry for something that was my cross to bear. whatsapp-image-2017-07-09-at-11-36-40-pm In October 2016, my luck changed, I found out about Hematopoietic stem cell transplantation (HSCT). It meant removing stem cells from the body, undergoing chemotherapy so that the immune system that had gone haywire would reset, and then reintroducing the stem cells so that the body could heal. It was a very new research based treatment that had given some very positive results in places like Russia, Chicago, Philippines, and Mexico. It was capable of stopping the progression of the disease, so in my case, where there was very little permanent disability, it was virtually a cure. I found out, that doctors didn't prescribe this treatment until the MS patient was at the last tethers of facing extreme disability or death. However, I felt it unfair.
How could they just sit there and wait for me to become disabled, and then administer the drug that could halt my disease as a last resort? I wanted to be healthy, now! That was my right.
I was determined to get the treatment. I had to at least try. Still, it was very expensive, could cost anywhere between Rs 50,00,000 – Rs 10,000,000. I spoke to my parents who said that they would try anything if it had the possibility of making my health better. I applied everywhere and was waiting, when luckily I heard that Fortis in India, had a trial that was starting HSCT for MS. I became the first person in India to undergo the procedure. whatsapp-image-2017-07-09-at-11-36-48-pm In December 2016, I had my eggs frozen, as chemotherapy radiation could cause me to go infertile. And then, after going through months of testing, in January 2017, I underwent AHSCT, which is Autologous hematopoietic stem cell transplantation, 'autologous' meaning that I used my own stem cells. I underwent the removal of stem cells, the chemotherapy, then the stem cells were reintroduced (that hurt the most), and I was kept in isolation for the duration because my immune system was practically non-existent. Thankfully, I have, so far, been free from symptoms of MS since my transplant. I have also had no need to take my medicines or injections. Things that I used to take on a daily basis. I am, also, on a mission to spread awareness about how MS is a 'hidden disease' with no physical indicators and therefore largely ignored. It occurs mostly in women, from whom weakness is expected, and therefore undiagnosed. MS is also considered a disease that affects the brain and spine, which is misunderstood as a mental illness. None of these are true, and for those who suffer from it, there is a cure. I run this website to promote awareness about both, the disease and the treatment that arrests the disease. Kanika Juneja (now) Kanika Juneja (now) I have a set of tests in December 2017, to ascertain the status of my disease. Meanwhile, I wanted to be a lecturer, but I realised I'm better at interacting with adults, so maybe I will become an adult trainer. It all depends on my results, so fingers crossed. As told to Tanvi Jain All images sourced via Kanika Juneja

Friday, December 13, 2019

confusion about early statin use as preventive

5 days ago - By Layal Liverpool A person's cholesterol levels before the age of 45 can predict their lifetime risk of developing cardiovascular disease.
by DN Vikulova - ‎2019 - ‎Cited by 3
Jul 8, 2019 - The risk burden and mortality rates were worse for women. ... further the specific cardiovascular risk profile and to enhance risk‐estimation approaches for young adults. ..... diseases predicted a higher mortality risk, whereas hyperlipidemia, .... The lack of further declines mirrors the pattern observed in the ...


These five tests better predict heart disease risk -- ScienceDaily


Mar 31, 2017 - Five simple medical tests together provide a broader and more accurate assessment of heart-disease risk than currently used methods, ...