Treat High Blood Pressure Naturally
For those of you who suffer from hypertension, you are probably interested in finding out how to treat high blood pressure naturally. Hypertension is a disease that plagues millions of people and can cause very serious health complications. Treating hypertension with prescription medications is not always the best option. In fact, there are many natural ways to control hypertension and even reverse its effects. If youve been told your hypertension is being caused by your family line of descendents, its possible that your doctor hasnt told you about all of the ways you can treat it yourself.
Hypertension has been shown to run in families. If one or more of your relatives suffer from it, chances are that you will, too. While some people get hypertension because of a rare genetic disorder, many cases of high blood pressure can be traced back to lifestyle factors that are easily corrected. To treat hypertension naturally can even result in reversing the disease completely in many cases.
Various home remedies have been proven to successfully treat high blood pressure naturally, and often much more quickly than prescription medications. While you can visit your doctor and get prescribed medications to take pressure off your heart and lungs, these often come with very serious side effects. Plus, theyre really expensive. However, there are natural remedies that you can use at home that dont cost a lot of money, but work just as well.
Natural Therapy Approach For Pulmonary Hypertension A Breathing Aid From The Sea
Since pulmonary hypertension is incurable, people who are affected suffer from a constant shortness of breath. To aid these patients, a team of researchers at the German Center for Lung Research in Giessen, Germany, have investigated the brown algae extract Fucoidan to treat pulmonary hypertension and found promising results.
When climbers reach a high peak, they struggle for air: This is because the oxygen level decreases. For patients with pulmonary hypertension, everyday life is a struggle for air even slight effort pushes them to their limits. A few stair steps or short walks can feel like high-performance sports. Pulmonary hypertension is characterized by abnormally high blood pressure in pulmonary circulation. This leads to shortness of breath and reduced physical performance, explains Dr. Ralph Schermuly, a Professor at the German Center for Lung Research at the Justus Liebig University in Giessen. As a result, says Schermuly, the heart must constantly and increasingly pump against resistance from the blood vessels constricted by the disease in order to circulate air. In the long term, the consequences are myocardial insufficiency and, ultimately, death. The organ simply no longer manages to build up enough pressure even though lung function is normal, and there is no increased blood pressure, he explains.
How To Treat Pulmonary Arterial Hypertension: Group 1
The group 1 defined by the World Health Organization includes inherited or familial PH and idiopathic PH, which means that the cause for it is unknown, as well as PH caused by determined drugs or conditions. Medication is one of the courses of treatment for group 1 pulmonary arterial hypertension. The most common drugs are meant to relax the blood vessels in the lungs and reduce excess cell growth in the blood vessels. Medication, which can be taken orally, inhaled or injected, include phosphodiesterase-5 inhibitors such as sildenafil, prostanoids, such as epoprostenol, endothelin receptor antagonists, such as bosentan and ambrisentan, and calcium channel blockers, such as diltiazem.
Physicians can prescribe one or more medications, as well as request an acute vasoreactivity test to evaluate how the pressure in the pulmonary arteries reacts to prescribed drugs. In addition, the doctor may also recommend medical and surgical procedures. During an atrial septostomy , a catheter is placed through a blood vessel of the leg into the hearts septum, which is the wall that separates the left and right atria. A tiny balloon on the tip of the tube is then inflated, creating an opening between the atria and relieving the pressure. While the atrial septostomy is a very rare procedure, lung transplants and heart-lung transplants are more common alternatives.
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Other Medical Treatments For Pulmonary Arterial Hypertension
Other medical therapies for PAH may include:
- Oxygen inhaled by patients via a nasal cannula or face mask.
- Diuretics medicine that rids the body of excess fluid that puts pressure on the heart.
- Calcium channel blockers medicine that helps to decrease blood pressure.
- Warfarin medicine that thins blood and prevents it from clotting.
Recent Evidence Indicating Beet Juice Alleviates Pah In Animal Models And Human Patients
To our keen interests, in the current issue of American Journal of Hypertension, Tawa et al. of Japan have demonstrated new evidence for therapeutic benefits of beet juice in a rat model of drug-induced PAH. They applied a low dose and high dose of nitrate to the rats with monocrotaline -induced PAH. Overall, this study conceptually confirmed a previously published work in 2012 by Baliga et al. of the United Kingdom, who first reported that chemical form of dietary nitrate reduced the right ventricular pressure and hypertrophy, and pulmonary vascular remodeling in mice exposed to 3 weeks of hypoxia. The benefits of dietary nitrate were associated with increased plasma and lung concentrations of nitrite and cGMP. A reduced beneficial effect of dietary nitrate/nitrite in the mice lacking endothelial NO synthase or treated with allopurinol suggested a role for both enzymes in catalyzing reduction of nitrite to NO. These researchers also demonstrated beneficial effects of high-dose nitrate on another etiologically distinct model of bleomycin-induced PAH. Nitrate treatment was started concomitantly with the administration of bleomycin and the pulmonary hemodynamics assessed at day 14.
While Theres No Cure For Pah There Are Effective Ways To Manage The Disease
The median survival used to be 2.5 years. Now I’d say most patients are living seven to 10 years, and some are living as long as 20 years.
Alessandro Maresta. M.D., Vice President and Head of Global Medical Affairs, Actelion PharmaceuticalsShare
On a physiological level, there are several different biological mechanismsknown as pathwaysrelated to how blood vessels work that are believed to play a role in PAH.
“The guidelines strongly recommend that when a patient is diagnosed with PAH, they start a combination of drugs to target two different pathways,” Maresta says. “You might get one drug first, and then start on the second one within six months.” Maresta adds that current studies are now suggesting that targeting three pathways at once has the potential to lead to better outcomes.
While there’s currently no cure for PAH, the typical prognosis is much better today than it was 25 years ago. “The median survival used to be 2.5 years,” Maresta says. “Now I’d say most patients are living seven to 10 years, and some are living as long as 20 years.”
The main focus today, adds Maresta, is to find a new pathway and an effective drug to target itfor which research is currently underway. “We’re dedicated to making it happen,” Maresta says.
Ayurvedic Aspect For Hypertension
According to Ayurveda, the balance between three doshas of the body are responsible for a healthy body. When there is an imbalance between these three doshas, the disease occurs. High blood pressure comes under two doshas that are Vata and Pitta doshas, mainly seen due to instability of Rakta Dhatu .
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Expanding Pulmonary Hypertension Clinical Trials
In addition to currently available therapies, the Pulmonary Hypertension Program is working to vastly expand therapeutic options by providing patients with access to new classes of medications currently undergoing clinical trial. We are participating in many multi-center treatment trials that investigate medications with varied mechanisms of action, new delivery systems for parenteral therapies, and treatment of various forms of pulmonary hypertension previously considered untreatable, says Dr. Sulica.
The team is already recruiting PH patients for trials of orphan drug bardoxolone methyl, an oral once-daily antioxidant inflammation modulator, including a study focused specifically on the efficacy and safety of the drug in patients with connective tissue diseaseassociated pulmonary arterial hypertension.
In another ongoing multi-center trial, Dr. Sulica and fellow investigators are testing the use of pulsed inhaled nitric oxide in pulmonary hypertension patients with chronic obstructive pulmonary disease , a form of the disease for which current treatments are ineffective. A molecule naturally produced in endothelial cells that promotes vasodilation, the nitric oxide in this system is delivered as a gas via a portable device that adjusts dosage in response to the patients breathing patterns. It has been shown in earlier studies to improve blood flow and increase patients exercise capacityand has the potential to be the first drug approved for PH-COPD.
What Is Pulmonary Hypertension
Pulmonary Hypertension — basically high blood pressure in the lungs, or rather the vascular system servicing the lungs — is a serious medical condition that be overall degenerative to your health and lead eventually to death. As blood vessels running between the lungs and heart become blocked or damaged, lung function is impaired and oxygenation of the heart and blood is reduced. This results in increased damage to the heart and lungs, causing fatigue and general ill health.
Symptoms of Pulmonary Hypertension include fatigue and dizziness, chest pain or pressure, heart palpitations, edema, and an inability to catch your breath that worsens over time.
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Additional Pharmacotherapy: Cardiac Glycosides Diuretics Antiarrhythmic Therapy Inotropic Agents And Nitrates
Although controversy persists regarding the value of digitalis in primary pulmonary hypertension , the present authors believe that children with right-sided heart failure may benefit from digitalis, in addition to diuretic therapy. Diuretic therapy must be initiated cautiously, since these patients appear to be extremely dependent on preload to maintain optimal cardiac output. Despite this, relatively high doses of diuretic therapy are commonly needed.
Although malignant arrhythmias are rare in pulmonary hypertension, they require treatment if documented. Atrial flutter or fibrillation often precipitates an abrupt decrease in cardiac output and clinical deterioration once atrial systole is lost. As opposed to healthy children, in whom atrial systole is responsible for 25% of the cardiac output, atrial systole in children with primary pulmonary hypertension often contributes as much as 70% of the cardiac output. Therefore, aggressive treatment of atrial flutter of fibrillation is advised. The treatment of children with clinically significant supraventricular tachycardias as well as frequent episodes of nonsustained ventricular tachycardia and complex ventricular arrhythmias is recommended, but it should probably be avoided for the treatment of lesser grades of arrhythmia.
What Are The Causes Of Pulmonary Hypertension
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The Lungs An Efficient Manager Of Gas
About 300 million alveoli, which provide a surface area of 100 to 140 square meters, channel oxygen into our body. This is about half a liter per minute of these vital gas molecules. The lungs are not consistently evenly ventilated: Small mucus plugs, for example, occupy areas into which hardly any oxygen can enter while breathing. If the blood were to flow through this part, the red blood cells would not be able to absorb any O2 molecules this would result in a lack of oxygen. This is why the lungs have developed into an intelligent mechanism. They allow the blood to flow only where the pulmonary alveoli can also fill up with air, i.e. where O2 is available. The respiratory organ can measure this mechanism efficiently, down to the second.
Nitric Oxide Dysregulation Contributes To Pathogenesis Of Pah
Similar to its well-appreciated role in systemic hypertension, a decreased tissue level and/or bioavailability of nitric oxide , one of the most crucial vasodilatory molecules and cell signaling transmitters, has also been considered as an important pathologic mechanism of PAH. In 2005, Girgis et al. measured endogenous NO metabolites in 24-hour urine and NO levels in exhaled breath air collected from 10 patients with untreated PAH and 12 control subjects. They found that both exhaled NO and urinary NO metabolites were significantly reduced in patients with PAH compared with control subjects. Interestingly, treatment with bosentan reversed these NO abnormalities.
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Oxygen Therapy For Pulmonary Hypertension
People with group 3 pulmonary hypertension caused by conditions such as chronic obstructive pulmonary disease , interstitial lung disease, and sleep apnea may develop hypoxia, or low levels of oxygen in the blood. If you are diagnosed with hypoxia, you may benefit from supplemental oxygen through oxygen therapy. Oxygen therapyis only available by prescription.
Some people with hypoxia only require oxygen therapy when they are walking, eating, sleeping, or during airline flights. Others may have resting hypoxia and need supplemental oxygen even when they are sitting still. When someone needs oxygen therapy 24 hours a day, this is known as long-term oxygen therapy . Those who require LTOT must use it at least 15 hours a day to experience benefits. However, for maximum benefits, those who need LTOT should use oxygen therapy 24 hours a day.
There are three main types of oxygen delivery devices: oxygen-gas cylinders, oxygen concentrators, and liquid-oxygen devices. Read more about oxygen therapy.
Questions To Ask Your Doctor
- How do you know whats causing my pulmonary hypertension?
- Is the underlying condition treatable?
- What kind of tests will I need? Are they covered by insurance?
- Is it safe for me to exercise? What kinds of exercise can I do?
- I have other health problems. Will treatment of pulmonary hypertension affect the treatment of my other health problems?
- Will I need surgery? What does surgery entail?
- Do I need oxygen for my pulmonary hypertension?
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Estrogen Treatment May Help Reverse Severe Pulmonary Hypertension
- University of California – Los Angeles Health Sciences
- Researchers have found that the hormone estrogen may help reverse advanced pulmonary hypertension, a rare and serious condition that affects 2 to 3 million individuals in the US, mostly women, and can lead to heart failure. The preclinical study shows that in rats, estrogen treatment can reverse the progression of pulmonary hypertension to heart failure and can restore lung and ventricle structure and function.
UCLA researchers have found that the hormone estrogen may help reverse advanced pulmonary hypertension, a rare and serious condition that affects 2 to 3 million individuals in the U.S., mostly women, and can lead to heart failure.
The condition causes a progressive increase in blood pressure in the main pulmonary artery, which originates in the heart’s right ventricle and delivers blood to the lungs. The rise in pressure impairs heart function by enlarging the right ventricle, potentially leading to heart failure.
Published in the Sept. 15 issue of the American Journal of Respiratory and Critical Care Medicine, the preclinical study shows that in rats, estrogen treatment can reverse the progression of pulmonary hypertension to heart failure and can restore lung and ventricle structure and function.
All rats with severe pulmonary hypertension that were treated with estrogen survived by the study’s end. Only 25 percent of the untreated rats survived.
Testing And Diagnosis Of Pulmonary Hypertension
Our involvement starts at the first phone call or Hospital visit, when we evaluate the history and symptoms to determine how urgently your child needs to be seen or treated. During your child’s evaluation for PH:
Because PH is a rare and complex disease and is difficult to diagnose, your child’s treatment team should have special expertise in the disease. At Children’s Hospital of Philadelphia, we provide in-hospital treatment to more than 20 children with PH every day, so PH is understood by every member of your CHOP team, from the emergency room to the intensive care.
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What Is The Panchakarma Treatment For Pulmonary Arterial Hypertension
If the condition of the patient is stable than panchakarma treatment is advised otherwise ayurvedic medicines are sufficient. The panchkarma therapies that are recommended to these patients are:
- Abhayanga: In this massage with herbal oils are recommended to the patients.
- Patra potli pind sweda: In this procedure, a potli is prepared with medicated leaves after that it is put in medicated oil. The massage of whole body is done with this potli over the chest region.
- Urobasti: In this a ring like structure of flour is made on the chest region. After that lukewarm oil is put in this ring let it for few minutes after that with sponge it is soaked. This is repeated three to four times.
Stay Away From Stimulants
Avoiding caffeine and other stimulants, such as alcohol, is necessary for regulating your blood pressure. Try tea and coffee substitutes like chicory if you like a hot beverage in the morning. Carbonated juices and mock-tails can replace a drink at the end of the day.
Bonus tip: Cutting back on stimulants can also help you sleep better.
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Cut Back On Salt And Sodium
One of the most common bits of advice youll hear from doctors is to lower your salt intake. Salt hides in many packaged, pickled, and canned foods, so choosing fresh ingredients can help limit the amount of sodium you consume. Try tasting your food before adding salt. Many people add salt out of habit, and a little goes a long way.
Bonus tip: If youre worried about losing flavor, try experimenting with spices like cumin, and herbs like garlic.