Emerging therapies and new directions in the treatment of pulmonary arterial hypertension
Jazyk angličtina Země Polsko Médium print-electronic
Typ dokumentu časopisecké články, přehledy
PubMed
39743894
DOI
10.33963/v.phj.104053
PII: VM/OJS/J/104053
Knihovny.cz E-zdroje
- Klíčová slova
- activin signaling inhibitors, novel therapies, risk assessment, sotatercept, treatment strategy,
- MeSH
- antihypertenziva terapeutické užití MeSH
- inhibitory fosfodiesterasy 5 terapeutické užití MeSH
- lidé MeSH
- plicní arteriální hypertenze * farmakoterapie MeSH
- plicní hypertenze farmakoterapie terapie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- antihypertenziva MeSH
- inhibitory fosfodiesterasy 5 MeSH
Pulmonary arterial hypertension (PAH) is a severe and progressive disease with limited survival prospects under currently available therapies. Since the 2022 edition of the European Society of Cardiology and European Respiratory Society guidelines on pulmonary hypertension, substantial clinical evidence has emerged, supporting a new treatment algorithm for PAH as presented at the 7th World Symposium on Pulmonary Hypertension 2024 and the following proceeding papers. Key updates include the introduction of sotatercept as a second-line therapy leading to a revised definition of maximal medical therapy now encompassing agents from four therapeutic groups (phosphodiesterase-5 inhibitors/soluble guanylate cyclase stimulators, endothelin receptor antagonists, prostacyclin pathway agents, and sotatercept), instead of three (phosphodiesterase-5 inhibitors/soluble guanylate cyclase stimulators, endothelin receptor antagonists, prostacyclin pathway agents). Other novelties include the elimination of a distinct pathway for patients with cardiopulmonary comorbidities in favor of an individualized approach, a reduction in the initial patient assessment risk categories from three to two, and a follow-up interval shortened from 3-6 months to 3-4 months post-treatment initiation. This review presents these advancements and emphasizes the need for their widespread implementation in clinical practice. At the end, we present new opportunities and challenges in the treatment of pulmonary arterial hypertension in eight Central and Eastern European countries.
'Carol Davila' University of Medicine and Pharmacy Bucharest Romania
Clinical Department of Cardiology and Angiology General University Hospital Prague Czech Republic
Department for Respiratory Diseases Jordanovac University Hospital Centre Zagreb Zagreb Croatia
Department of Cardiology Medical Academy Lithuanian University of Health Sciences Kaunas Lithuania
Department of Pulmonary Diseases and Allergy Ljubljana University Medical Center Ljubljana Slovenia
Institute of Cardiology Lithuania University of Health Sciences Kaunas Lithuania
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