Sarah Marshall from Banbury on what it's like to live with the rare heart and lung disease pulmonary hypertension (PH).
Просмотров: 2275 PHA ORG UK
This short video featuring Gautam V. Ramani, M.D., Assistant Professor of Medicine at the University of Maryland School of Medicine and cardiologist at the University of Maryland Medical Center, presents an overview of pulmonary hypertension symptoms as well as the type of care patients should seek if they believe they are experiencing these symptoms. Related Links: Dr. Gautam Ramani http://findadoctor.umm.edu/Details/23506 Maryland Heart and Vascular Center http://umm.edu/programs/heart-and-vascular Pulmonary Hypertension Program http://umm.edu/programs/heart-and-vascular/services/treatments/ph Patient Success Stories http://umm.edu/programs/heart-and-vascular/about/success-stories Distributed by Tubemogul.
Просмотров: 9422 UMMCVideos
Pulmonary arterial hypertension (PAH) is a condition of high lung pressure in the blood vessels leading from the heart to the lung. It can affect anyone of any age, sex or race. However, it is more common in women aged between 30 and 50 years old. In this clip, learn about the common symptoms of PAH, its subgroups, the condition's association with connective tissue diseases (CTDs) and treatment options for PAH. This video was brought to you by the National Heart Centre Singapore (NHCS) in partnership with the Singapore General Hospital (SGH), both members of the SingHealth group.
Просмотров: 1378 SingHealth
Pulmonary hypertension Symptoms – Causes Treatment Signs and Symptoms of Pulmonary hypertension. What is pulmonary hypertension? How to identify signs symptoms of Pulmonary hypertension with pictures images photos in men women with types diagnosis prevention and treatment options. What is the life expectancy of a person with pulmonary hypertension? What is the main cause of pulmonary hypertension? Is pulmonary hypertension a terminal illness? What is the best treatment for pulmonary hypertension? Signs and symptoms of pulmonary hypertension with photos images and pictures in males females children and elderly. Check Out all our videos here https://www.youtube.com/channel/UCT4COc5wyE6rq003y9gjaIA
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Dr. Skloven explains the most common symptoms a woman with pulmonary hypertension will experience. Dr. Skloven holds board certifications in Interventional Cardiology, Nuclear Medicine, Cardiovascular Disease and Internal Medicine and practices medicine at Banner Heart Hospital in Mesa, Arizona.
Просмотров: 121 Banner Health
Eight years ago, Kate McGoey-Smith spent most of her days at home, reliant on oxygen and unable to see. “I had been diagnosed with idiopathic pulmonary arterial hypertension, a very rare disease with no cure. At the time, doctors told me I had two to five years to live.” Essentially, high blood pressure within McGoey-Smith’s lungs was putting so much pressure on the right side of heart, it was causing right-sided heart failure. As the disease progressed, she became legally blind and unable to do most of the activities she had once loved. Today, McGoey-Smith no longer relies on oxygen and her vision has returned. “It’s just really wonderful. I can more fully participate in my children’s lives… go on activities, go out and do things.” McGoey-Smith says her health began to turn around after she adopted a plant-based diet that she began to follow under the supervision of Dr. Caldwell Esselstyn, the director of the Cardiovascular Prevention and Reversal Program at the Cleveland Clinic’s Wellness Institute. “We take a certain hit, an injury, let’s say – every time certain foods pass our lips. The body is so remarkable, it repairs 90 per cent of that injury,” said Esselstyn. The remaining 10 per cent of that injury, he says, accumulates and contributes to chronic disease. Esselstyn has been studying plant-based diets for more than 30 years and has authored a number of books on the subject. He recommends patients follow a diet free of animal products and oils, focusing instead on whole grains, legumes, vegetables and fruit. “A seismic revolution in health can come about when we in the profession have the will, the grit and the determination to share with the public what is the lifestyle and most specifically, what is the nutritional literacy that will empower them to destroy chronic illness.”
Просмотров: 5711 Fork Smart
Thank you so much for tuning in! I was diagnosed with severe Pulmonary Hypertension three years ago, after having been misdiagnosed for five years. When I was finally diagnosed, I was in heart failure (the right side of my heart was three times its normal size), I was told that I may not have much time left to live, that I may never leave the hospital again and that if I did, chances were that I would have to be on oxygen for the rest of my life! (Not the best news!) I had just booked a tour, was about to release my album, and was ready to perform my music around the world when all hell broke loose. Here I am, three years later feeling a zillion (yes, an actual zillion) times better. My pulmonary pressures have gone from 180 to 32. I am so incredibly grateful to be alive! It is my hope that some of the things I've done may be of value to YOU. For the past three years, I have utilized five key elements that I believe have played a huge role in my improvement. They are: Nutritional Lifestyle, Exercise, Mindset, Creative expression and Quality time with Family and friends. I believe that these key elements have not only allowed for the medication to work when I was told that it most likely wouldn’t (because my Pulmonary Hypertension was so severe) but that they have also allowed me to drastically reduce my meds. I am currently on very low doses of medication and I really don't experience any side effects. I get so many emails from people asking about nutrition, exercise, how to stay positive when things get difficult...basically wanting to find out what I’m doing. So I decided to create www.LifeByChloe.com. As I always say, I have no idea what could happen to me tomorrow, but I do know that today, I’m a million times better than I was. We'll be creating recipe videos, explaining why I eat the foods I eat and how they affect my body, how I order when I go to restaurants, where to eat, ways to exercise with PH, how to travel when you have PH, ways to keep your mind in the right place no matter how difficult things get, and much more. I’m not a nutritionist, so all I can do is bring you into my world and share with you what’s helped me in the hopes that it can help you, too. Don't forget to check out http://www.LifeByChloe.com and sign up with your email address to receive news, updates, recipes, exclusive content and much more! Hope to see you there :-) Hugs, Chloe FIND ME HERE: For free music, updates and more join my mailing list here: http://www.chloetemtchine.com http://www.LifeByChloe.com http://www.itunes.com/chloetemtchine (link to buy my music) http://www.youtube.com/chloesphriend (Vlog Channel) http://www.youtube.com/chloetemtchine (Music channel) http://www.facebook.com/chloetemtchine http://www.twitter.com/chloetemtchine http://www.instagram.com/chloetemtchine
Просмотров: 11131 ChloesPHriend
Dr. Raj Dasgupta discusses a case of a 29 year old healthy H1P0 woman (32 weeks of gestation) who presents to the emergency room complaining of shortness of breath from his new book Obstetrics & Gynecology Morning Report: Beyond the Pearls. Learn more here: https://www.us.elsevierhealth.com/obstetrics-gynecology-morning-report-9780323496131.html Visit our bookstore to shop for this title: US & Latin America: http://bit.ly/16mVKhy Canada: http://bit.ly/14lYZIe UK: http://bit.ly/rqJe75 Africa & Middle East: http://bit.ly/19Ag9D5 Asia: http://bit.ly/h3zIsl
Просмотров: 162 Elsevier Medical Books
Viagra and Cialis are two erectile dysfunction drugs proven to work. Now, researchers have reformulated those medications to treat another disease - pulmonary hypertension. The interesting twist here is that most patients with pulmonary hypertension are women.
Просмотров: 7035 Mayo Clinic
Pulmonary Arterial Hypertension - Aryeh Fischer, M.D. Pulmonary arterial hypertension can be a serious complication of scleroderma. New therapies offer hope to those who have been diagnosed with PAH. In this session, participants will gain a clear understanding of the biological process of PAH symptoms, how PAH is diagnosed and monitored, treatment options, and the latest research. Video Production: Magnus Media Group http://www.magnusmediausa.com (469) 252-9938
Просмотров: 6893 Scleroderma Foundation
In the pulmonary hypertension there are several factors. In the pulmonary hypertension there are some classification as for the WHO. They will also classify into clinical staging like 1, 2, 3, 4. If the person comes under clinical stage then the quality of life will be very poor. The person will be having 6 minute walk test. If the person is not able to walk for 150 meter, if the left atrial pressure is more than 14 mmHg they come under high risk category and their quality of life will be poor. Their life expectancy is around 5 to 6 years. For treatment there are endothelial receptor antagonist and methyl plasma digestrone inhibitor is there. If the patient has pulmonary hypertension secondary to the underlying lung disease. If the person is having ILD with decreased oxygen with pulmonary hypertension you have to treat with oxygen.
Просмотров: 1896 Doctors' Circle - World's Largest Health Platform
Joy Lauver has a life-threatening lung condition called pulmonary hypertension, which made her pregnancy extremely tricky for doctors; KDKA's Dr. Maria Simbra reports. FULL STORY: http://cbsloc.al/2ngUmZS
Просмотров: 701 CBS Pittsburgh
Roxana Sulica, MD, Associate Professor, Department of Medicine and Director, Pulmonary Hypertension at NYU Langone in New York City discusses the signs and symptoms of pulmonary arterial hypertension (PAH), a progressive condition that affects the heart and lungs. PAH is characterized by abnormally high blood pressure (hypertension) in the pulmonary artery, the blood vessel that carries blood from the heart to the lungs. The most common signs and symptoms are shortness of breath (dyspnea) during exertion and fainting spells. As the condition worsens, people can experience dizziness, swelling (edema) of the ankles or legs, chest pain, and a racing pulse. Most cases of PAH occur in individuals with no family history of the disorder. Although some cases are due to mutations in the BMPR2 gene and inherited in an autosomal dominant pattern, a gene mutation has not yet been identified in most individuals. When PAH is inherited from an affected relative it is called "familial" PAH. Cases with no identifiable cause may be referred to as "idiopathic" PAH. PAH can also occur secondary to an underlying disorder such as connective tissue diseases, HIV infection, chronic hemolytic anemia, and congenital heart disease, to name a few. PAH can also be induced by certain drugs and toxins, for example fenfluramine and dexfenfluramine (appetite suppressants now banned by the FDA), toxic rapeseed oil, and amphetamines.
Просмотров: 83 CheckRare
Pulmonary Hypertension is a chronic and currently incurable disease that causes the walls of the arteries of the lungs to tighten and stiffen. In someone with PAH, the right side of the heart has to work harder to push blood through narrowed arteries in the lungs. Eventually, the extra stress causes the heart to enlarge and become less flexible, compromising the heart's ability to push blood out of the heart, through the lungs, and into the rest of the body.
Просмотров: 2088 Janice Janus
Hope you enjoy my new video "Your Questions Answered - What Medication Do I Take? Pulmonary Hypertension." I'm currently taking the following medication: Tyvaso Adcirca Cell Cept Oxygen Therapy For free music, updates and more join my mailing list here: http://www.chloetemtchine.com To find out about the 5 key elements that drastically improved my health, click here: http://www.LifeByChloe.com In this video: salter labs adult micro cannulas for flows of up to 3 They left me on the plane! Join us on our Florida journey! :-) FIND ME HERE: For free music, updates and more join my mailing list here: http://www.chloetemtchine.com http://www.LifeByChloe.com http://www.itunes.com/chloetemtchine (link to buy my music) http://www.youtube.com/chloesphriend (Vlog Channel) http://www.youtube.com/chloetemtchine (Music channel) http://www.facebook.com/chloetemtchine http://www.twitter.com/chloetemtchine http://www.instagram.com/chloetemtchine Thank you so much for tuning in! I was diagnosed with severe Pulmonary Hypertension three years ago, after having been misdiagnosed for five years. When I was finally diagnosed, I was in heart failure (the right side of my heart was three times its normal size), I was told that I may not have much time left to live, that I may never leave the hospital again and that if I did, chances were that I would have to be on oxygen for the rest of my life! (Not the best news!) I had just booked a tour, was about to release my album, and was ready to perform my music around the world when all hell broke loose. Here I am, three years later feeling a zillion (yes, an actual zillion) times better. My pulmonary pressures have gone from 180 to 32. I am so incredibly grateful to be alive! It is my hope that some of the things I've done may be of value to YOU. For the past three years, I have utilized five key elements that I believe have played a huge role in my improvement. They are: Nutritional Lifestyle, Exercise, Mindset, Creative expression and Quality time with Family and friends. I believe that these key elements have not only allowed for the medication to work when I was told that it most likely wouldn’t (because my Pulmonary Hypertension was so severe) but that they have also allowed me to drastically reduce my meds. I am currently on very low doses of medication and I really don't experience any side effects. I get so many emails from people asking about nutrition, exercise, how to stay positive when things get difficult...basically wanting to find out what I’m doing. So I decided to create www.LifeByChloe.com. As I always say, I have no idea what could happen to me tomorrow, but I do know that today, I’m a million times better than I was. We'll be creating recipe videos, explaining why I eat the foods I eat and how they affect my body, how I order when I go to restaurants, where to eat, ways to exercise with PH, how to travel when you have PH, ways to keep your mind in the right place no matter how difficult things get, and much more. I’m not a nutritionist, so all I can do is bring you into my world and share with you what’s helped me in the hopes that it can help you, too. Don't forget to check out http://www.LifeByChloe.com and sign up with your email address to receive news, updates, recipes, exclusive content and much more! Hope to see you there :-) Hugs, Chloe
Просмотров: 3085 ChloesPHriend
Diagnosing Pulmonary Arterial Hypertension (PAH). Outline. Pneumonic blood vessel hypertension (PAH) is an uncommon however genuine kind of hypertension. It emulates a few other heart and lung conditions. PAH causes a considerable lot of an indistinguishable indications from coronary illness and asthma. Recognizing those conditions and PAH can be troublesome, however a few tests and instruments can enable your specialist to make a determination. What is PAH?. PAH is hypertension that influences the conduits of your lungs and the correct side of your heart. Your pneumonic supply routes and vessels convey blood from your heart to your lungs, where your blood drops off oxygen-drained cells and gets oxygen-rich cells. On the off chance that your aspiratory courses are limited or blocked, it can cause the pulse within them to rise. After some time, the expanded weight debilitates the correct side of your heart and your aspiratory courses. This can eventually prompt heart disappointment and even passing. Why PAH is difficult to analyze. PAH is hard to spot and analyze, notwithstanding when your specialist is searching for it amid a physical exam. The manifestations of PAH imitate those of other comparative conditions. Indeed, even as PAH advances, your specialist may experience difficulty recognizing it from other heart and lung conditions. Your specialist will evaluate your therapeutic history and utilize at least one tests to figure out what's causing your manifestations. Evaluating your medicinal history. To help analyze PAH, your specialist ought to evaluate your own hazard factors for the condition. For instance, they should search for any conditions that may add to PAH or exacerbate the illness. You have an expanded danger of PAH on the off chance that you have: *heart malady. *congenital heart deserts. *scleroderma. *HIV. *a family history of PAH. Your specialist may perform hereditary screening to check whether you have qualities connected to PAH. Tests used to analyze PAH. Your specialist may utilize the accompanying techniques to analyze PAH: Blood test. A blood test can enable your specialist to realize what's in your blood. They might have the capacity to recognize substances identified with PAH. It can likewise enable them to discount different conditions. Chest X-beam. On the off chance that you have progressed PAH, a chest X-beam may demonstrate the expanded piece of your heart. In any case, this imaging test doesn't generally give enough data to analyze PAH. CT filter. A CT filter makes layer-by-layer photos of your organs. This enables your specialist to check for supply route narrowing, blockages, or harm. X-ray examine. A MRI examine enables your specialist to make a photo of your body's veins. Like a CT examine, a MRI enables them to investigate the majority of the organs included. Electrocardiogram. This test measures the electrical elements of your heart, which are in charge of influencing it to pulsate routinely, in mood, and without mistake. A slight change in those electrical driving forces can have genuine results for your heart and body. Echocardiogram An echocardiogram utilizes sound waves to make a photo of your heart. With this test, your specialist can check whether any piece of your heart has become broadened or isn't thumping appropriately. Your specialist can utilize two sorts of echocardiograms. In a Doppler echocardiogram, your specialist puts a getting gadget on your chest. In a transesophageal echocardiogram, your specialist puts an imaging gadget into your throat. Your specialist can utilize an echocardiogram to analyze a few heart conditions, including PAH. By and large, they can recognize PAH with an echocardiogram. Regardless of whether they can't affirm a PAH finding, they can utilize this test to help preclude All Photos Licensed Under CC Source : www.pexels.com www.pixabay.com www.commons.wikimedia.org
Просмотров: 1571 Natural Tips
Dr. Skloven shares everything a woman may need to know about pulmonary hypertension.
Просмотров: 698 EmpowHER
Aspiratory Arterial Hypertension. What is essential aspiratory hypertension?. Essential aspiratory hypertension is currently known as pneumonic blood vessel hypertension (PAH). The name was changed in 1998 on the grounds that it was resolved to be more spellbinding of the condition. PAH is a turmoil described by an anomalous increment in aspiratory course weight, typical pneumonic narrow wedge weight, and expanded aspiratory vascular protection. A progressive increment of pneumonic supply route weight can prompt possible right-heart disappointment and passing. Increments in aspiratory blood vessel weight are the most imperative pointers of PAH. Imaging tests are utilized to glimpse inside the body for a determination. Developed supply routes or harm to the heart are certain indications of PAH. Medicines are utilized to moderate heart harm and manage side effects. Indeed, even with treatment, around 33% of individuals with PAH will pass on inside three years of conclusion. On account of new medications, this number is a change from the 50 percent who used to pass on inside 3 years. The therapeutic group would like to discover a cure to stop the harm of PAH. Reasons for pneumonic blood vessel hypertension The reason for PAH can be either idiopathic (IPAH) or familial (FPAH). Idiopathic infections emerge suddenly, and their causes are obscure. Familial sicknesses are hereditarily gone down through families. Natural variables and pharmaceuticals are accepted to be conceivable reasons for IPAH. Conceivable reasons for IPAH: hunger suppressants (aminorex, fenfluramine, dexfenfluramine, and so on.). hormone treatment (which may clarify why a greater number of ladies than men have the sickness). Most instances of FPAH emerge from a change in the BMPR2 quality. Extreme cases are for the most part connected to the nearness of the transformation. Despite the fact that the change might be available during childbirth, the illness may take months or years to show up. Indications of pneumonic blood vessel hypertension The trademark indication of PAH is an expansion in pneumonic vascular protection. This causes an expansion in weight on the correct ventricle of the heart. That issue prompts inconvenience in filling the left piece of the heart. In the end, the heart bombs therefore. Normal manifestations of PAH are: troublesome or worked breathing on effort. weariness, caused by the heart pumping increasingly hard. about blacking out. swooning. Medicines for PAH are intended to diminish side effects and drag out life. Specialists frequently start medications late in the sickness, since it's difficult to distinguish. All Photos Licensed Under CC Source : www.pexels.com www.pixabay.com www.commons.wikimedia.org
Просмотров: 1966 Beauty & Health Tips
Pulmonary hypertension is a rare type of high blood pressure that affects fewer than 200,000 US patients per year. Many people who suffer from the disease are undiagnosed because the symptoms are similar to more common diseases, such as the flu. On this month's episode of Picture of Health, host Stephen Barnes chats with Angela Mann, an advanced nurse practitioner from Lakeland Regional Health, and Joy Morgan, the leader of the Central Florida Pulmonary Hypertension Support Group, to learn more about the disease and how it affects daily life. Also on this episode, Whitney Fung from the University of Florida IFAS Extension shares another nutrition tip. To see more videos like this, go to the PGTV webpage at http://www.Polk-County.net/PGTV.
Просмотров: 786 Polk Government
The Pulmonary Hypertension Pathology video reviews the classification and histopathologic features of pulmonary hypertensive vasculopathy. Visit http://www.ccfcme.org/PHvideo to claim CME credit or learn more about the Pulmonary Hypertension Webcast Series. The PH pathology video features expert faculty member, Dr. Carol Farver, of Cleveland Clinic. The video was produced by Cleveland Clinic Foundation Center for Continuing Education and Cleveland Clinic Respiratory Institute. Interested in related CME education? Visit http://www.clevelandclinicmeded.com/specialties/Pulmonology.aspx?id=145&name=Pulmonology
Просмотров: 1121 ClevelandClinicCME
In March of 2012, Sheryl Albin was given the grim prognosis of having only three to five years left to live. The active mother was diagnosed with pulmonary arterial hypertension, a disease that causes the arteries in the lungs to become narrow or blocked, raising blood pressure in the lungs and causing the heart to work in overdrive to keep up. Subscribe to WDSU on YouTube now for more: http://bit.ly/1n00vnY Get more New Orleans news: http://wdsu.com Like us: http://facebook.com/wdsutv Follow us: http://twitter.com/wdsu Google+: https://plus.google.com/+wdsu
Просмотров: 75 WDSU News
November is Pulmonary Hypertension Awareness Month. Pulmonary hypertension is a disease that, because of its name, sometimes is confused with high blood pressure. But, pulmonary hypertension is different. Mayo Clinic pulmonologist Dr. Charles Burger says pulmonary hypertension means the pressures inside the lung are elevated, forcing the right side of the heart to work harder to increase blood flow. Eventually, the heart enlarges and fails. About 20,000 people in the U.S. are being treated for this disease. There is treatment, but no cure. In this Mayo Clinic Minute, reporter Vivien Williams talks to Dr. Burger about pulmonary hypertension. More health and medical news on the Mayo Clinic News Network http://newsnetwork.mayoclinic.org/
Просмотров: 1577 Mayo Clinic
Pneumonic Arterial Hypertension (PAH) Risk Factors. Understanding pneumonic blood vessel hypertension (PAH). Pneumonic blood vessel hypertension (PAH) happens when the corridors in the lungs have lifted pulse, and the correct side of the heart needs to work harder to draw blood to the lungs. After some time, as the heart must keep on working harder, the muscle debilitates and heart disappointment happens. In spite of the fact that PAH isn't reparable, it's treatable with drugs and way of life changes. Sorts of PAH. There are two wide kinds of pneumonic blood vessel hypertension: *idiopathic PAH. *secondary PAH. The two sorts are extremely uncommon. With idiopathic PAH, there's no known reason for the condition. It appears to have created without anyone else, however infrequently there's a hereditarily acquired part. In optional PAH, the condition has created because of some other hidden condition. Manifestations of PAH. Huge numbers of the signs and indications of PAH are like those of other heart and lung conditions. These indications may include: *shortness of breath. *dizziness or blacking out. *racing heartbeat or heart palpitations. *fatigue. *weakness. *chest torment. *cough. *abdominal swelling, or swelling of the arms, legs, or lower legs. *blue or pasty skin, particularly at the fingertips. Normal hazard factors. Anybody can create PAH. There are various hazard factors that can make somebody more vulnerable to this and other heart and lung conditions, for example, *age. *gender. *family history. *other wellbeing conditions. *drug utilize. *high height. *Age and sex: In spite of the fact that PAH can strike at any age, it's only found in grown-ups. The most widely recognized window is in the vicinity of 20 and 60 years old. With respect to sexual orientation, idiopathic PAH is twice as regular in ladies as in men, as indicated by the Pulmonary Hypertension Association. More youthful ladies of childbearing age are particularly liable to build up the condition. Family history. Idiopathic PAH creates with no noticeable reason. Now and again, family history appears to assume a part, which would show a hereditary connection. Truth be told, a hereditary marker has been found for PAH. Nonetheless, not every person with idiopathic PAH has this marker, or any family history of the condition. Realize why it's critical to comprehend your family wellbeing history. Other wellbeing conditions. Other wellbeing conditions that are hazard factors for PAH include: *obesity and rest apnea, which deny the group of oxygen, constraining the heart to work harder to draw blood to the lungs for oxygenation. *HIV contamination. *heart and lung conditions, including perpetual obstructive aspiratory illness (COPD) and maladies of the left half of the heart. *history of blood clumps in the aspiratory veins. *liver sickness. *lupus and different sicknesses of the connective tissues. *pregnancy, which appears to somewhat raise the danger of PAH. Ladies officially living with PAH who wind up pregnant have a high danger of death because of heart disappointment. Ladies with PAH ought to talk about the dangers completely with their specialist if thinking about getting to be pregnant. Medication utilize. Recreational medications, for example, methamphetamines and cocaine, and in addition eating routine medications, for example, Fen-Phen, have been appeared to cause PAH. Once in a while the condition doesn't create until the point that numerous years after medication utilize has finished. High height. The individuals who inhabit high elevation for stretched out periods will probably create PAH. Research has demonstrated that this condition can be turned around if the individual moves back close ocean level. The individuals who as of now have PAH and go to high elevations may find that their side effects exacerbate amid their excursion. Overseeing PAH. A significant number of these hazard factors are hard to control, if certainly feasible. What you can control is the manner by which you respond to indications of PAH or other heart and lung conditions. All Photos Licensed Under CC Source : www.pexels.com www.pixabay.com www.commons.wikimedia.org
Просмотров: 1132 Red Health Care
Dr. Roger Seheult explains the key aspects of pulmonary hypertension: 0:14 - Definition of pulmonary hypertension 0:20 - Mean pulmonary artery pressure 1:00 - Using systolic to estimate pulmonary hypertension with echocardiogram 1:18 - 5 different WHO pulmonary hypertension groups 1:30 - Pulmonary arteriolar hypertension (PAH), Idiopathic pulmonary hypertension, collagen vascular diseases, portal HTN 3:35 - BMPR2 4:00 - Left heart failure 4:10 - Lung disease, COPD, OSA, idiopathic pulmonary fibrosis 4:35 - Pulmonary embolism, chronic VTE 4:50 - Hematologic disorders, sarcoidosis, glycogen storage diseases, renal failure 5:40 - Amphetamines 5:50 - Diagnosis of pulmonary hypertension and physical exam findings 6:07 - Heart sounds, loud P2, tricuspid regurgitation, RV heave 6:35 - JVP, c,v waves liver pulsatile, edematous legs 6:58 - Chest Xray findings with pulmonary hypertension 7:36 - ECG/EKG findings with pulmonary hypertension, RVH, RBBB 8:17 - Echocardiogram findings with pulmonary hypertension 9:03 - Tricuspid regurgitation, regurgitant jet, Modified Bernoulli Equation 10:40 - Advantages of echocardiogram: PASP, 11:10 - Echo bubble study 11:25 - Right heart catheter, wedge pressure, Left atrial pressure (LAP), mean artery pressure (MAP) Speaker: Roger Seheult, MD Clinical and Exam Preparation Instructor Board Certified in Internal Medicine, Pulmonary Disease, Critical Care, and Sleep Medicine. MedCram: Medical topics explained clearly including: Asthma, COPD, Acute Renal Failure, Mechanical Ventilation, Oxygen Hemoglobin Dissociation Curve, Hypertension, Shock, Diabetic Ketoacidosis (DKA), Medical Acid Base, VQ Mismatch, Hyponatremia, Liver Function Tests, Pulmonary Function Tests (PFTs), Adrenal Gland, Pneumonia Treatment, any many others. New topics are often added weekly- please subscribe to help support MedCram and become notified when new videos have been uploaded. Subscribe: https://www.youtube.com/subscription_... Recommended Audience: Health care professionals and medical students: including physicians, nurse practitioners, physician assistants, nurses, respiratory therapists, EMT and paramedics, and many others. Review for USMLE, MCAT, PANCE, NCLEX, NAPLEX, NDBE, RN, RT, MD, DO, PA, NP school and board examinations. More from MedCram: Complete Video library: https://www.youtube.com/c/medcram Facebook: https://www.facebook.com/MedCram Google+: https://plus.google.com/u/1/+Medcram Twitter: https://twitter.com/MedCramVideos Produced by Kyle Allred PA-C Please note: MedCram medical videos, medical lectures, medical illustrations, and medical animations are for medical educational and exam preparation purposes, and not intended to replace recommendations by your health care provider.
Просмотров: 118392 MedCram - Medical Lectures Explained CLEARLY
Dr Greg Kier provides a snapshot of Pulmonary Arterial Hypertension, what it is and highlights the symptoms, diagnosis and treatment.
Просмотров: 243 Lung Foundation Australia
Roxana Sulica, MD, Associate Professor, Department of Medicine and Director, Pulmonary Hypertension at NYU Langone in New York City discusses some of the emerging tretment options for pulmonary arterial hypertension (PAH). One of these emerging therapies is the INOpulse system developed by Bellerophon Therapeutics. Bellerophon is testing its investigative INOpulse system for several forms of pulmonary hypertension (PH). PAH a progressive condition that affects the heart and lungs. PAH is characterized by abnormally high blood pressure (hypertension) in the pulmonary artery, the blood vessel that carries blood from the heart to the lungs. The most common signs and symptoms are shortness of breath (dyspnea) during exertion and fainting spells. As the condition worsens, people can experience dizziness, swelling (edema) of the ankles or legs, chest pain, and a racing pulse. Most cases of PAH occur in individuals with no family history of the disorder. Although some cases are due to mutations in the BMPR2 gene and inherited in an autosomal dominant pattern, a gene mutation has not yet been identified in most individuals. When PAH is inherited from an affected relative it is called "familial" PAH. Cases with no identifiable cause may be referred to as "idiopathic" PAH. PAH can also occur secondary to an underlying disorder such as connective tissue diseases, HIV infection, chronic hemolytic anemia, and congenital heart disease, to name a few. PAH can also be induced by certain drugs and toxins, for example fenfluramine and dexfenfluramine (appetite suppressants now banned by the FDA), toxic rapeseed oil, and amphetamines.
Просмотров: 345 CheckRare
The 27-year-old music teacher from Chelmsford, Essex, was diagnosed with an incurable heart condition called pulmonary arterial hypertension (PAH) in her teens.The debilitating disease which affects blood vessels in the lungs, leads to heart failure, meaning that Tess will eventually need a heart transplant.“I was well enough to walk down the aisle and was symptom-free all day,” she says.“It was a very emotional day not only because of my health but because my dad Chris, who passed away in 2014, wasn’t there to share the day.“But we released a dove in his memory and I loved having my mum Val walk me up the aisle.” and for many sufferers the cause is a mystery. Related articles Heart disease treatment: Beta blockers could cure DEADLY lung condion High blood pressure affecting lungs could be treated with THIS Women are more than twice as likely to be affected as men and it often occurs in young people.It is a chronic disease that leaves sufferers feeling breathless, exhausted and in severe pain.After diagnosis only 50 per cent of those affected will survive for another five years. The only cure is a heart and lung transplant, which has associated risks and complications.Although PAH can be inherited, in Tess’s case it was caused by a hole in her heart which was discovered when she was 17 and studying for her A-levels at college.“I was angry when I found out my condition was incurable,” she recalls.“I thought, ‘Why me?’ and I was sad. I was a trumpet player and that was my life, although I also played piano and cello.“But I loved the trumpet. I was told I would never be able to play it again as it was putting too much pressure on my heart. That was the worst news for me.” Current treatments for PAH including macitentan and sildenafil can only target symptoms and can have unpleasant side effects such as nausea, limb pain, vomiting and diarrhoea.Tess, who takes both medications, says: “I get headaches, migraines and nausea but it’s got me through the last 10 years so I know that holding out through the side effects will be better for me in the long run.”Despite her condition, which often involves long stays in hospital, Tess managed to get a place at Southampton University to study music and obtain her degree.She travelled around Europe with an orchestra until she was 21 and worked in the Middle East before returning to the UK to become a music teacher.“I have always been a positive person,” she says. “But I never know what the next day will bring. I have to wake up and see how I feel.“If I go out and start to feel sick I have to go home. I also find that if I go out and let my hair down I have to take the next day off as I will spend the day in bed. I went on holiday with friends last year and spent the next week in hospital.“I will have a wonderful time but I will pay for it. But that is my decision. If I didn’t I would feel left out. I live life to the full as I don’t know what is around the corner.”But now thanks to new research, Tess has
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Please visit: http://www.diseasesandtreatment.com for more information about diseases and treatment option.
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Dr. Skloven shares everything a woman may need to know about pulmonary hypertension. Dr. Skloven attended medical school at the University of Maryland School of Medicine, graduating Cum Laude, and now treats patients at Banner Heart Hospital in Mesa, Arizona.
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Unlike other conditions, pulmonary hypertension has symptoms that can be hard to identify in order to give the patients the right diagnosis. Misdiagnosis can not only worsen the symptoms, but also make treatment that much harder in the long run.
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Roxana Sulica, MD, Associate Professor, Department of Medicine and Director, Pulmonary Hypertension at NYU Langone in New York City discusses the current tretment options of pulmonary arterial hypertension (PAH), a progressive condition that affects the heart and lungs. PAH is characterized by abnormally high blood pressure (hypertension) in the pulmonary artery, the blood vessel that carries blood from the heart to the lungs. The most common signs and symptoms are shortness of breath (dyspnea) during exertion and fainting spells. As the condition worsens, people can experience dizziness, swelling (edema) of the ankles or legs, chest pain, and a racing pulse. Most cases of PAH occur in individuals with no family history of the disorder. Although some cases are due to mutations in the BMPR2 gene and inherited in an autosomal dominant pattern, a gene mutation has not yet been identified in most individuals. When PAH is inherited from an affected relative it is called "familial" PAH. Cases with no identifiable cause may be referred to as "idiopathic" PAH. PAH can also occur secondary to an underlying disorder such as connective tissue diseases, HIV infection, chronic hemolytic anemia, and congenital heart disease, to name a few. PAH can also be induced by certain drugs and toxins, for example fenfluramine and dexfenfluramine (appetite suppressants now banned by the FDA), toxic rapeseed oil, and amphetamines.
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Though the commonly accepted ratio is 3:1 women, longtime clinicians suggest PAH ratio is more likely closer to 4:1.
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Local man is alive because of new surgery
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The Toronto Western Hospital Pulmonary Rehabilitation Home Exercise DVD was created to help people with chronic lung disease learn to: - Be more active - Stay active - Keep their independence - Improve their quality of life Symptoms of fatigue and shortness of breath can make people with chronic lung disease feel disabled. The TWH Pulmonary Rehabilitation Home Exercise DVD teaches you how to use breathing techniques while working on gradually building momentum. The exercise DVD combines gentle movements, stretches, strength training, balance and flexibility movements that you can follow at your own pace. The information within this video is not intended to replace any advice provided to you by your health care team. For your safety, we ask that you do not act on the information within these videos without first discussing your treatment or healthy living plan with your qualified health care providers. For more information about UHN Patient & Family Education, visit http://www.uhnpatienteducation.ca.
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Shortness of breath? Learn more and get a better lung disease treatment plan with top experts. Visit our Online Expert Centers at https://diagnosticdetectives.com/expert-centers/ Exclusive interview / Dr. Anton Titov MD and Professor Dr. Aaron Waxman MD, leading pulmonary arterial hypertension, right heart failure and lung disease expert. Find out exact cause if you have shortness of breath - get a precise diagnosis and best treatment for shortness of breath root cause. - Your research focuses on how blood vessels and lungs change in disease. You show that inflammation in lungs leads to change in vascular architecture, the lung undergoes, the blood vessels undergo remodeling process. You also have a mouse model that mimics closely the pulmonary arterial hypertension. So how does your research help people with lung disease? What are the current directions of your research in pulmonary arterial hypertension and other lung vascular diseases? I think the things that we've learned from some of the work we've done here, is really the role of inflammation in driving vascular remodeling. We've looked at several aspects of inflammation and we've used a number of models. You mentioned the mouse model that was an IL-6 over-producer that remodeled their lung blood vessels much like human disease. Although it's still not a clean model of human disease. Also in collaboration with Dr. Jane Leopold in cardiology, we've developed a large animal model using a pig model, where we can tie off the inferior pulmonary vein and that drives a timed remodeling of the pulmonary vascular bed and the right heart. So we've been able to use that as a model of progressive pulmonary vascular remodeling and kind of an accurate timing of right heart dysfunction and eventually right heart failure. And we've been able to look at different things like administering stem cells using an intracoronary approach and showing viability of those stem cells. That model may also allow us to ask the question about devices. And could we put in a ventricular assist device in the setting of right heart failure that might actually help remodel the vascular bed and obviously support the right ventricle? But questions about pulsatile blood flow versus non-pulsatile flow... There may be benefit to non-pulsatile blood flow in the pulmonary vascular bed. But I think getting back to your question about how it is affected how we treat patients, we right now start to do clinical trials in anti-inflammatory treatments, including anti IL-6 or medicines that affect targets to the IL-6 receptors and downstream effectors of those receptors as well as stem-cell approaches, and even device approaches. - It's certainly very interesting because it has direct clinical implications and can help understand the pathophysiology of the lung disease better for patients with lung diseases.
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The authors demonstrate a successful pulmonary thromboendarterectomy, performed for a 37-year-old woman with chronic thromboembolic pulmonary hypertension. Learn more: https://www.ctsnet.org/article/pulmonary-thromboendarterectomy-chronic-thromboembolic-pulmonary-hypertension The Cardiothoracic Surgery Network (CTSNet) connects the global cardiothoracic community through communication, collaboration, education, and interaction amongst cardiothoracic surgeons and their teams across the globe. CTSNet provides a broad range of video and text-based educational content, the premier job board across all of cardiothoracic surgery, profile pages for cardiothoracic surgeons and individuals associated with the specialty, and a calendar of events related to the specialty. Find even more content on our website: https://www.ctsnet.org/ Connect with us on Facebook: https://www.facebook.com/CTSNet/ Connect with us on Twitter: https://twitter.com/ctsnetorg
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In this month's edition of Second Sunday, Channel 8 Eyewitness News profiles pulmonary hypertension services at Bryan Medical Center. Pulmonary hypertension is, essentially, high blood pressure in the lungs. It causes shortness of breath and affects the heart when blood vessels in the lungs are inflamed. It is a rare condition and typically is found in younger women. There is no cure, but with early detection and proper treatment, patients can live a normal life. Kelsie was diagnosed with pulmonary hypertension several years ago and has improved dramatically since her accurate diagnosis.
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What types of patients are the most challenging to manage? How do you treat high risk patients? An expert panel discussion on managing challenging patients with pulmonary hypertension. Moderated by Dr. Richard Channick. Discussants: Dr. Richard Krasuski, Dr. Vallerie McLaughlin, Dr. Ioana Preston, Dr. Sean Studer
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Pulmonary Hypertension is a type of high blood pressure that affects the arteries in the lungs and right side of the heart. It's a serious and progressive disease. Dr. Cecelia Smith talks about treatment options available at Reading Health System.
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Stem Cell Therapy and Treatment for Arterial Hypertension. In this video will be shown how effectivly stem cell therapy and treatment is in curing arterial hypertention. Arterial Hypertension destructive diseases, symptoms and forms with stem cell therapy and treatment abroad. http://www.placidway.com/subtreatment-detail/treatment,31,subtreatment,269.html/Stem-Cell-Treatment-for-Arterial-Hypertension-Treatment-Abroad Contact us directly: http://www.placidway.com/contact/contact-us.php Email: email@example.com Phone: +1 303 500 3821 Website: http://www.placidway.com Follow us: Youtube: http://www.youtube.com/user/placidways Pinterest: http://pinterest.com/placidway/ Google+: https://plus.google.com/u/0/+Placidway/ LinkedIn: https://www.linkedin.com/in/placidway https://www.youtube.com/watch?v=IyYMC3XhCuY Transcript: You've reached PlacidWay, the leading health tourism company! Subscribe to our YouTube channel and get instant access to all of our latest health videos. Stem Cell Treatment for Arterial Hypertension Hypertension is a potentially devastating medical condition that increases blood pressure. Known as a silent disease, hypertension generally doesn't involve symptoms that are easily recognized by most individuals until damage to blood vessels or cardiac health is realized. In most cases, hypertension, also called arterial hypertension, is treated with a variety of drugs that may involve the use of diuretics, Beta blockers, ACE inhibitors, and calcium channel blockers. Treating Hypertension with Stem Cell Embryonic stem cell treatments for hypertension have shown efficacy in reducing blood pressure, frequency of headaches, and a stabilization of blood pressure, leading to enhanced mental capacity and abilities, rejuvenation, and sexual performance and potency in men and women. Embryonic stem cells have the ability to differentiate, or become any type of cell in the human body, offering unique opportunities to replace damaged cells and tissues in the human body. A variety of facilities throughout Europe, the Netherlands, and Ukraine have offered and performed treatments, clinical trials and studies regarding the efficacy of stem cell therapies to improve heart function. Studies performed in the Netherlands have shown that allogenic stem cell therapies improved function of the right ventricular portion of the heart as well as lung capacity in small animals with pulmonary hypertension. https://www.youtube.com/watch?v=IyYMC3XhCuY Helpful tags: arterial hypertension treatment,arterial therapy with stem cells,stem cells treatment abroad arterial hypertension cost,pulmonary arterial hypertension,arterial hypertension symptoms,medical tourism stem cell treatment
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Pulmonary Hypertension is a rare, complex disease of the heart and lungs. It most commonly strikes women in childbearing years, though it can affect all ages, races and both sexes. This program will identify what pulmonary hypertension is, and how it is treated. Though there is not yet a cure for this illness, treatments have emerged over the last decade, giving patients hope for a longer, healthier life. Meet patients who are living with pulmonary hypertension and demonstrate how to improve your quality of life. We'll also outline the genesis of the Pulmonary Hypertension Association, and illustrate the power people can have to organize, draw attention to a cause and work to improve the lives of patients and families coping with serious illnesses.
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