Pulmonary Arterial Hypertension (PAH) is a rare yet severe condition that affects the pulmonary arteries responsible for carrying blood from the heart to the lungs. In PAH, these arteries become narrowed, causing difficulties in blood flow and raising blood pressure, which puts strain on the heart.
PAH is a progressive disease, worsening over time and potentially leading to heart failure and even death if left untreated. Early diagnosis and management of PAH are crucial to prevent complications and enhance the quality of life.
Causes of PAH remain largely unknown in most cases, but certain factors can elevate the risk of developing the condition, such as a family history of PAH, congenital heart disease, HIV infection, liver disease, sleep apnea, and the use of specific medications like fen-phen.
Several risk factors can increase the likelihood of developing PAH, including age (more common in adults over 60), gender (more prevalent in women), obesity, smoking (damaging the lungs), and living at high altitudes.
It’s essential to remember that having one or more risk factors doesn’t guarantee developing PAH. However, understanding these risk factors is crucial to taking preventive measures.
PAH symptoms can develop slowly over time and might include subtle signs such as shortness of breath, especially during exercise, fatigue, chest pain or pressure, racing heartbeat, dizziness, or fainting. If any of these symptoms are present, seeking medical attention is vital, as they could be attributed to other medical conditions.
While there is currently no cure for PAH, there are available treatment options to manage symptoms and slow the disease’s progression. These treatments may include medications to dilate the pulmonary arteries and reduce the heart’s workload, oxygen therapy to enhance blood oxygen levels, and in severe cases, a lung transplant to improve quality of life and extend survival.
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You can buy it using the link below: Bosentas 125mg Tablet exporter in india.
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