Principles of pharmacological correction of pulmonary arterial hypertension

Authors

  • Liliya V. Korokina Belgorod State National Research University
  • Nina I. Zhernakova Belgorod State National Research University
  • Mikhail V. Korokin Belgorod State National Research University ORCID logo https://orcid.org/0000-0001-5402-0697
  • Olga N. Pokopejko Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University

DOI:

https://doi.org/10.3897/rrpharmacology.4.27732

Abstract

Definition and classification: Pulmonary hypertension (PH) is a group of life-threatening progressive diseases of various genesis, characterized by a progressive increase in arterial pressure (AP) in the pulmonary artery (PA), the remodeling of pulmonary vessels, which leads to an increase in pulmonary vascular resistance and pulmonary arterial pressure and more often leads to right ventricular heart failure and premature death. Pulmonary hypertension is clinically divided into five groups: patients in the first group have idiopathic pulmonary arterial hypertension (IPAH), whereas in patients of other groups secondary PH associated with cardiopulmonary or other systemic diseases is observed. The development of secondary LH is caused by congenital heart defects, collagenoses, presence of thrombus in the pulmonary artery, prolonged high pressure in the left atrium, hypoxemia, chronic obstructive pulmonary diseases (COPDs). In case of secondary PH, thrombosis and other changes in the pulmonary veins occur.

Ways of pharmacological correction of pulmonary hypertension: Over the last decade pharmacotherapy of PH has been developing rapidly, and the introduction of modern methods of treatment, especially for primary PAH, has led to positive results. However, despite the progress in treatment, the functional limitations and survival of patients remain unsatisfactory. Currently, there are two levels of treatment for pulmonary hypertension: primary and specific pathogenetic therapies. Primary therapy is aimed at the main cause of PH. It also includes supportive therapy. Pathogenetic therapy includes prostanoids, endothelin receptor antagonists, and phosphodiesterase-5 inhibitors. Tactics of therapy can be established on the basis of either clinical classification, or functional class. Prostanoids are a promising group of drugs for the treatment of pulmonary arterial hypertension (PAH), since they possess not only vasodilating, but also antiplatelet and antiproliferative actions. Therefore, it seems logical to use prostacyclin and its analogs to treat patients with various forms of PAH.

Keywords:

classification, pulmonary hypertension, pathogenetic therapy, primary therapy, prostanoids, pharmacological correction

Author Contribution

Liliya V. Korokina, Belgorod State National Research University

PhD, Associate Professor of the Department of Pharmacology and Clinical Pharmacology.

Nina I. Zhernakova, Belgorod State National Research University

Doctor of Medicine, Professor, Deputy Director of the Medical Institute for Research.

Mikhail V. Korokin, Belgorod State National Research University

Doctor of Medicine, Professor of the Department of Pharmacology and Clinical Pharmacology.

Olga N. Pokopejko, Federal State Autonomous Educational Institution of Higher Education I.M. Sechenov First Moscow State Medical University

Student of the medical faculty.

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Published

20-06-2018

How to Cite

Korokina LV, Zhernakova NI, Korokin MV, Pokopejko ON (2018) Principles of pharmacological correction of pulmonary arterial hypertension. Research Results in Pharmacology 4(2): 59–76. https://doi.org/10.3897/rrpharmacology.4.27732

Issue

Section

Review article

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