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How To Live With Pulmonary Hypertension

Pah Is Difficult To Diagnose

How long can a Person live with Pulmonary Hypertension

Given how rare PAH is, when a patient complains about such symptoms as exhaustion and labored breathing, it’s not unusual for a doctor to first order testing for conditions like asthma and congestive heart failure.

While that makes sense on some levelthose issues are much more common than PAH, explains Galiéit also means that getting diagnosed with PAH may sometimes take a while.

“You might see a general practitioner, then a specialist for asthma, then another specialist and so on before finally seeing a pulmonologist or cardiologist who diagnoses the PAH,” Maresta explains. “It usually takes one year from the presentation of symptoms to get a correct and final diagnosis of PAH.”

Plus, notes Galié, “your doctor will also need to rule out all other forms of pulmonary hypertension before giving a diagnosis of PAH.”

But the good news is that the timeline to PAH diagnosis is starting to speed up a little. “Things are slowly changing, as more doctors now know what PAH is and how to identify it,” Maresta explains.

Once your physician suspects PAH, your doctor will order a series of tests that may include a chest X-ray, pulmonary function test and exercise tolerance test. If all signs still point to PAH following the results of these tests, you’ll probably require a right-heart catheterization, which measures the pressure inside the pulmonary arteries.

Eat A Diet High In Fiber

Adhering to a nutritional diet, high in fiber and low in fat and sugar, is a good recommendation for anyone wanting to lead a healthy life. For those with a pulmonary disorder, this type of diet is critical. Eating fruits, vegetables, and whole grains can help the body flush out excess fluid and salt, as well as keep arteries clear of fat sediments. Lean meats and fish are also essential to maintaining a heart-happy nutritional program.

Classification Of Primary And Secondary Pulmonary Hypertension

The conventional classification, primary and secondary pulmonary hypertension, which also is called pulmonary arterial hypertension, has been reclassified and is now based on the main underlying cause, characteristics, and treatments of pulmonary hypertension. These terms were updated in 2013. This system classifies the condition based on five classes.

Class 1 includes:

Pulmonary arterial hypertension including idiopathic previously referred to as primary pulmonary arterial hypertension), inherited pulmonary arterial hypertension, drug-induced pulmonary arterial hypertension

Pulmonary arterial hypertension associated with the following:

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Going Home With Oxygen

In the hospital, you received oxygen treatment. You may need to use oxygen at home. Do not change how much oxygen is flowing without asking your doctor.

Have a backup supply of oxygen at home or with you when you go out. Keep the phone number of your oxygen supplier with you at all times. Learn how to use oxygen safely at home.

If you check your oxygen with an oximeter at home and your number often drops below 90%, call your doctor.

Make sure you have enough supply of your medicines. Abruptly stopping them can lead to serious illness.

Stay Away From Infections

Pulmonary Hypertension  An Overview

You should:

  • Get a flu shot every year. Ask your doctor if you should get a pneumonia vaccine.
  • Wash your hands often. Always wash them after you go to the bathroom and when you are around people who are sick.
  • Stay away from crowds.
  • Ask visitors with colds to wear masks, or to visit you after their colds are gone.

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Living With Pulmonary Hypertension: Everything You Need To Know

Feb 28, 2018 6:51:41 AM / byDuke Reeves

Pulmonary hypertension is a serious, chronic disease that affects the heart and the blood vessels in the lungs. Although it is somewhat rare, the disease can result from a large number of health conditions, genetics, or even occur spontaneously.

Unfortunately, most cases of pulmonary hypertension are chronic and incurable. But especially with early diagnosis and proper medical treatment, people with the disease are able to manage the symptoms of pulmonary hypertension and maintain a good quality of life.

In the early stages of the disease, people who have pulmonary hypertension tend to experience fatigue and shortness of breath during physical activity. But symptoms worsen and multiply as the disease progresses.

Life expectancy and treatment options depend mostly on how early the disease was caught and what cause, if any, doctors can find for the disease. In this guide, we will help you better understand pulmonary hypertension, what causes it, and what kind of treatments options are out there to help patients manage the disease.

Phas Resources To Improve Living With Pulmonary Hypertension

The association believes that PH patients can benefit from the experience of thousands of other patients who have learned to effectively manage the disease. Therefore, PHA offers a section with tips, tools and resources to help living with pulmonary hypertension.

  • Empowered Patient Online Toolkit includes downloadable PH-specific templates and checklists to create a personalized medical binder.
  • Day-to-Day Living can help simplify the daily routine with tips from long-term survivors.
  • Coping with PH helps patients identify strategies for coping with the emotional and social aspects of PH.
  • Health and Medication Management is a guide to manage the medications and coordinate the overall healthcare.
  • Emergency Situations helps patients prepare for emergencies before they happen.
  • Caregiver Shout-Outs are meant to honor family members and friends in the PH community who provide patients with daily encouragement and support.
  • Working with PH is a guide to make and keep a place for patients within the workforce by listening to their body and knowing their rights.
  • Diet and Nutrition offers recommendations on keeping the diet on track with advice from PH experts.
  • Exercise and PH is a guide on getting active without overexerting your body.
  • Traveling with PH includes recommendations to plan ahead for safe and comfortable travel with PH by car, plane or train.
  • Climate and PH is a guide for patients to prepare weather and altitude alterations.

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Which Diseases Are Common In People With The Condition

There are no clear statistical data on the prevalence of pulmonary hypertension. Since pulmonary hypertension is seen in multiple different conditions, it is perhaps better to look at the prevalence in each condition. It is fairly common in patients with heart failure, COPD, and sleep apnea. It occurs in 7% to 12% of patients with collagen vascular disease, and in less than 5% of HIV patients.

  • People may also complain of chest pain and angina.
  • Depending on the underlying associated disease, pulmonary artery hypertension can have other manifestations. For example, characteristic skin changes seen in scleroderma, or the signs of liver disease seen in portopulmonary hypertension.
  • Signs of pulmonary hypertension may include:

  • Rapid breathing, hypoxia , and swelling in the legs.
  • In severe pulmonary hypertension, the health care professional may hear louder than normal components of heart sounds when he or she listens to the heart with a stethoscope .
  • The doctor may also feel elevation of the chest wall when the heart pumps and this may indicate enlargement of the right side of the heart suggestive of pulmonary hypertension .
  • Pah Is Complicated1tracking Your Pah Data Doesnt Have To Be

    Can I live with Pulmonary Hypertension

    It can often be difficult to remember everything that happened between doctor visits, particularly symptoms youâve experienced and how youâve been feeling on a day-to-day basis. Using the tools within Care4Today® Connect to track these experiences can help empower you to take an active role in your health â and by sharing your PAH data with your doctor you can help ensure you receive data-driven care. Care4Today® Connect can help you:

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    Yales Pulmonary Vascular Disease Program: One Of Just A Few Nationally

    McGrath was referred to the Yale Medicine PVD Program because it is one of the few centers in the nation accredited by the Pulmonary Hypertension Association, and the only such program in the state. The PVD Program allows pulmonary specialists to collaborate with physicians in cardiology, rheumatology, hepatology, cardiothoracic surgery, diagnostic radiology, and pathology, making it a single destination to manage complex cases. Depending on how serious the condition is, treatment options include medications taken orally and those delivered intravenously through a continuous pump.

    At the time, however, McGrath, a married mother of three and grandmother of five, had no idea how complicated her disease was or how much her life would change because of it.

    There are four functional classes of PH disease with class 4 being the most severe, Dr. Singh explains. When he first met McGrath, she was already at class 4. Because of that severity, Dr. Singh put her on two oral medications and a continuous IV medication delivered through an external pump. Today, McGrath wears the pump, which is about the length of her smartphone, at all times on the side of her body. The pump has a 4-foot IV line that attaches to a catheter in her chest and delivers medication to a vein near her heart. McGrath receives the medications by mail and puts them in her pump.

    What Are The Causes Of Pulmonary Hypertension

  • Primary pulmonary hypertension often has no determined cause. People who develop PPH may be genetically predisposed to the condition, or sensitive to substances that cause the blood vessels to constrict, including stimulants. PPH may also be triggered by other illnesses, including autoimmune diseases such as lupus, as well as AIDS, scleroderma and sickle-cell anemia.
  • Secondary pulmonary hypertension is linked to other heart and lung related medical problems, including:
  • Pathology of the lungs, such as blood clots, pulmonary fibrosis, and chronic obstructive pulmonary diseases such as emphysema
  • Heart disease, including congenital heart conditions and left-sided heart failure
  • Connective tissue disorders, such as scleroderma
  • Sleep apnea
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    Strengths And Limitations Of This Study

    • This is the first ethnographic study to investigate the experiences of patients living with pulmonary hypertension and uncovers a number of findings that would not typically be revealed by other qualitative approaches.
    • The study included an international sample of patients with an array of demographic features in order to provide a wide range of perspectives on living with the disease and to identify trends.
    • A larger study including more patients across additional countries is warranted to allow subanalyses to be undertaken according to demographic variables, country and disease type.

    Store Things At Eye Level

    59 best images about Community Support: Pulmonary Hypertension on ...

    Stack your favorite T-shirts in the top drawer. Keep your go-to kitchen items on the countertop. Put laundry soap next to or just above the machine. Move your bathroom products from under the sink up to the medicine cabinet. You want your chest to stay upright during the day. Bending over too often could trigger PAH symptoms or make them worse.

    6

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    Pah Affects Women More Than Men

    The idiopathic and heritable forms of PAH are at least twice as common in women compared to men, according to the Pulmonary Hypertension Association. In fact, PAH is most often diagnosed in women between the ages of 30 and 60.

    It’s not currently known why females are more susceptible, but some theories under investigation have to do with the role of estrogen, changes that occur during pregnancy and links to autoimmune issues, which also tend to be more prevalent in women.

    Ive Been Diagnosed With Mild Pulmonary Hypertension How Is This Treated

    HelloI had an echo done due to chest x-ray at ER because of possible enlarged heart. Due to severe anemia 4.5, I had transfusions of blood and I am on iron therapy for 3 months now. The symptoms that sent me to ER were racing heartI could not walk without having to stop and let my heart calm downI had pitting edema in front of lower legs, but that has been present since my 20sbut I started swelling in feet and ankles. Since treatment, I can walk miles with no fast heart rate, no more swelling even in lower legs..my echo showed moderate mitral regurgitation, mild tricuspid regurgitation, left atrial mildly enlarged, with an RSVP of 37mild pulmonary hypertension. All valves are normal in sizeno stenosis, and no pericardial effusion, no pleural effusionEF of 55%-60%. Everything else normal. My cardiologist is having me back in 3 months. He did not give me any blood pressure medicine nothingjust monitoring. Is this normal or even safe with mild pulmonary hypertension? Is it possible I dont have it? And can it be reversed or treated if it is secondary to mitral valve regurg? Been worried sick!

    Submitted by Teresa from Middletown, Ohio on 11/08/2014

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    Group : Pulmonary Arterial Hypertension

    Group 1 PH, also known as pulmonary arterial hypertension, can be caused by many factors. In some cases, there is no known cause of the disease . In other cases, it can be caused by genetics , drugs and toxins , or other underlying diseases such as:

    • Autoimmune conditions, such as scleroderma
    • Liver disease
    • Congenital heart disease
    • HIV infection

    Underlying conditions that cause PH can also affect disease outcomes. For example, individuals with both PH and scleroderma have a 40 percent chance of living two years after diagnosis.

    Personality And Daily Routine

    Living with Pulmonary Arterial Hypertension (PAH): Meet Kathryn

    The symptoms of PH limited a patient’s lifestyle, and their personality often changed accordingly, as illustrated by the following comment from a patient: If my illness was a person it would probably feel quite depressed and angry at times, because it could not do what it wants to do when it wants to do it. Many patients also reported deliberately adapting their personality to match the limitations placed on them by their disease, using phrases such as I don’t like sports, going out isn’t for me and I like staying in.

    In terms of disease-coping strategies, patients fell into two categories . Solution seekers developed tactics to cope with PH on a daily basis, were less dependent on caregivers and were generally optimistic and motivated. This resulted in these patients maintaining a social life and being able to work part time. Conversely, disease-dominated patients had a more passive attitude towards PH, a greater dependency on caregivers, a reliance on medication and were generally more pessimistic and more likely to experience depression. For example, one disease-dominated patient stated, the disease limits me. Regardless of the coping strategy adopted, patients stated that extensive planning and adherence to daily routines were essential in everyday life and made statements such as Walking is difficult so when I have to meet someone I have to leave the house early and My feet are stuck in mud but with patience I can get them out.

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    What Does Treatment Look Like

    These medications are called vasodialators. They basically open the vessels to help the flow of the blood in your body. Thats where a lot of the side effects come in. Theres a lot of pain, like flushing pressure headaches and pain in my legs and feet. It affects other organs as well, like the bowels and stomach .

    Causes Of Miscellaneous Pulmonary Hypertension

    • Blood Diseases: Certain blood diseases, such as bone marrow disease, are associated with pulmonary hypertension. Doctors postulate that, because these blood diseases cause the body to produce excess red blood cells, they can contribute to pulmonary hypertension.
    • Systemic Disorders: Some systemic disorders cause a condition called vasculitis, a kind of inflammation that affects blood vessels throughout the body. Over time this can narrow blood vessels and restrict blood flow to vital organs and tissues, including the lungs, which can result in pulmonary hypertension.
    • Tumors: Certain conditions cause tumors to develop in the lungs or chest. These tumors can press against the pulmonary arteries, restricting blood flow and causing pulmonary hypertension.
    • Metabolic Disorders: Some metabolic disorders, including thyroid disorders, Gaucher disease, and glycogen storage disease, can result in pulmonary hypertension.

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    How Pulmonary Hypertension Affects Your Body

    To understand how pulmonary hypertension affects your body, you first have to understand the basics of how blood circulates through the heart and lungs. The following diagram of the heart and pulmonary arteries should help you follow along.The heart is divided into two main sides: right and left. The heart is further divided from top to bottom, to make four heart chambers total.

    The top two heart chambers are called ventricles, and they receive blood from other parts of the body. The bottom chambers are called ventricles, and they pump blood out to the rest of the body.

    Pulmonary hypertension mainly effects the right ventricle of the heart, which is responsible for pumping blood out of the heart and into the lungs. When the blood vessels in the lungs become stiff, narrow, or blocked, it creates back-pressure when the right ventricle tries to pump blood into the pulmonary arteries.

    As a result, the blood pressure in the lungs goes up and the heart’s right ventricle has to work harder and harder to push blood through the constricted arteries. Eventually, the resistance causes the right ventricle to enlarge and become weaker.

    Over time, pulmonary hypertension causes the heart to continue to enlarge and get weaker and weaker, until it eventually is unable to pump blood into the lungs at all. The resulting heart failure is a major cause of death for people who are diagnosed with pulmonary hypertension.

    Treatment Therapy And Medication Options

    How Long Does a Person Live with Pulmonary Hypertension?

    Theres no one-size-fits-all approach to treatment for PAH. Instead, your doctor will base your treatment strategy on the severity of your symptoms, results of diagnostic tests, and factors like how much you can commit to certain treatment strategies with or without help at home.

    While combinations of different drugs are usually considered the main treatment for PAH, your doctor may also recommend additional treatment options.

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