Therapeutic Use of an Inhaled Drug Delivery in Pulmonary Hypertension: A Review

Pulmonary arterial hypertension (PAH) is a serious condition in which there is increased blood pressure in arteries of the lungs (pulmonary arteries). The therapies or drugs for PAH have expanded with the revelation of three key pathological processes - encompassing prostacyclin, nitric oxide (NO), and endothelin pathways. An outlook for patients suffering from PAH is still mediocre amidst recent advancements. The evolution of pre-clinical and clinical research on PAH has facilitated the identification of several new targeted therapies for the disease. In this article, we examine recent data on new pulmonary hypertension physiological pathways, primarily concentrating on administering drugs through the inhalation route and their effects. Although they have been given clinical use approval, medications based on these routes are presently being studied in clinical or pre-clinical settings. To confirm these innovative medicines' therapeutic efficacy and safety, extensive clinical trials are needed.

Automated summary

New insights into the treatment options and drugs for pulmonary arterial hypertension (PAH) have been discovered, but the prognosis for the disease remains mediocre. Recent research has identified several new targeted therapies, primarily focused on administering drugs through the inhalation route. Although these drugs have received clinical approval, extensive clinical trials are still needed to confirm their therapeutic efficacy and safety.