Pulmonary artery hypertension (PAH) is a complex and potentially life-threatening condition characterized by elevated blood pressure in the pulmonary arteries, the blood vessels that carry deoxygenated blood from the right side of the heart to the lungs. This condition leads to an increased workload on the right side of the heart, which can eventually result in heart failure. In this article, we will discuss the causes, symptoms, diagnosis, and medical treatment options and natural treatment strategies for pulmonary artery hypertension, shedding light on this debilitating condition.
Causes and Risk Factors
Mainstream medicine classifies PAH into two major categories: idiopathic (unknown cause) and associated (linked to an underlying condition). Idiopathic PAH occurs without any identifiable cause and is relatively rare. Associated PAH, on the other hand, is more prevalent and can be associated with various underlying conditions, including left sided congestive heart failure, valvular heart disease, pulmonary fibrosis, connective tissue diseases (like lupus, rheumatoid arthritis etc), congenital heart disease, liver disease, and chronic pulmonary diseases like chronic obstructive pulmonary disease (COPD).
At Natural Heart Doctor, we think disease is most often caused by violations of Eat Well, Live Well, Think Well. When I hear PAH, I think mold exposure in a water-damaged home. The mold mycotoxins get into the lungs and lead to PAH. This has been noted in the rodent model, according to this study. We suggest you test for mold mycotoxins in your urine with this test and also test your home for mold with this test from Envirobiomics.
Symptoms and Clinical Presentation
Shortness of breath is the most common symptom of PAH, usually with activity. Later in the disease process, swelling in the legs or abdomen may appear. A dry cough is another rare complaint. These symptoms are often a result of reduced blood flow and oxygenation to vital organs.
Diagnostic Procedures
The key tool in diagnosing PAH is an echocardiogram, which uses sound waves to create images of the heart and its blood vessels. It can assess the structure and function of the heart and identify any abnormalities in the pulmonary arteries. In the blood, an NT-proBNP is often elevated. Other diagnostic tests may include pulmonary function tests, blood tests, chest X-rays, CT scans, and cardiac catheterization. In my opinion, CT scans should be avoided due to the radiation exposure. MRI may be necessary to assess for congenital heart disease.
Mainstream Treatment Options
The treatment of PAH aims to improve symptoms, slow disease progression, and enhance the patient’s quality of life.
Treatment options may include:
1) Medications: Several medications are available to manage PAH. They work by dilating blood vessels and lowering inflammation. Examples include calcium channel blockers, endothelin receptor antagonists, prostacyclins, and phosphodiesterase-5 inhibitors.
2) Oxygen Therapy: Supplemental oxygen may be prescribed to improve oxygenation and alleviate symptoms of PAH.
3) Lifestyle Changes: Adopting a healthy lifestyle can play a significant role in managing PAH. This includes regular exercise as recommended by the healthcare provider, a balanced diet, smoking cessation, and managing other underlying conditions, such as obesity or sleep apnea.
4) Surgical and Interventional Procedures: In severe cases of PAH, surgical interventions may be considered. Lung transplantation and atrial septostomy (creating a hole in the wall separating the heart’s upper chambers) are examples of procedures used in specific cases.
Natural Treatment Strategies
Here are some of my favorite natural treatment solutions for pulmonary artery hypertension:
- Eat plenty of wild seafood and organs
- Get sunshine to your body, specifically your chest (lungs!)
- Get out of the chemicals
- Get out of the mold (see above)
- Biohacking strategies like sauna, red light therapy, IV nutrition, methylene blue etc.
- Natural nitric oxide boosters like Heart Beet and Vessel Support.
- Detox Programs like CellCore Foundation protocol
Prognosis and Outlook
PAH is a progressive condition, and its prognosis can vary depending on the underlying cause, the stage at which it is diagnosed, and the individual’s response to treatment. Early detection and appropriate management can significantly improve the outlook for individuals with PAH, helping to control symptoms, slow disease progression, and enhance their quality of life. However, PAH remains a serious condition, and in some cases, it can lead to complications like heart failure and respiratory infections, which can increase the risk of mortality.
Conclusion
Pulmonary artery hypertension can be a devastating condition that mainstream medicine does not have much success with. At Natural Heart Doctor, we offer natural treatment strategies to pulmonary artery hypertension, achieving much success with our patients. We can work with your local doctor.
