borderline pulmonary hypertension

Pulmonary hypertension is a cardiovascular condition characterized by an abnormally elevated pressure in the pulmonary arteries, potentially leading to impaired heart and lung function. Borderline pulmonary hypertension, also referred to as marginal pulmonary hypertension, is a state where the pulmonary artery pressure is slightly elevated above the normal range but does not yet meet the criteria for a full diagnosis of pulmonary hypertension. This condition warrants close monitoring as it may progress to more severe pulmonary hypertension if left uncontrolled.

Symptoms of borderline pulmonary hypertension can be subtle or mild, including shortness of breath, fatigue, chest pain, and fainting. These symptoms can impact a patient's daily life and ability to perform activities. The treatment objective for borderline pulmonary hypertension is to mitigate disease progression, alleviate symptoms, and prevent escalation to a more severe form of pulmonary hypertension. Therapeutic approaches may encompass pharmacological interventions, lifestyle modifications (such as smoking cessation, weight management, and increased physical activity), and regular health monitoring.

If you receive a diagnosis of borderline pulmonary hypertension, it is crucial to adhere to your physician's recommendations, engage in regular check-ups, and implement necessary preventive measures to manage the condition. Please remember not to self-administer medications and to use any medication only under a doctor's supervision. Should your symptoms worsen or new symptoms emerge, seek immediate medical care.