Anticoagulation in pulmonary arterial hypertension - association with mortality, healthcare utilization, and quality of life: The Pulmonary Hypertension Association Registry (PHAR).

TitleAnticoagulation in pulmonary arterial hypertension - association with mortality, healthcare utilization, and quality of life: The Pulmonary Hypertension Association Registry (PHAR).
Publication TypeJournal Article
Year of Publication2022
AuthorsGarry, JD, Kolaitis, NA, Kronmal, R, Thenappan, T, Hemnes, A, Grinnan, D, Bull, T, Chakinala, MM, Horn, E, Simon, MA, De Marco, T
Corporate/Institutional AuthorsPulmonary Hypertension Association Registry Investigators
JournalJ Heart Lung Transplant
Volume41
Issue12
Pagination1808-1818
Date Published2022 Dec
ISSN1557-3117
KeywordsFamilial Primary Pulmonary Hypertension, Humans, Hypertension, Pulmonary, Patient Acceptance of Health Care, Pulmonary Arterial Hypertension, Quality of Life, Registries
AbstractRoutine long-term anticoagulation in PAH is controversial and shown to be beneficial or neutral in idiopathic disease (IPAH) and neutral-to-harmful in connective tissue disease (CTD-PAH). Authors sought examined the association between anticoagulation and mortality, healthcare utilization, and quality of life (QoL) in PAH using PHAR data. Anticoagulation was not associated with higher mortality, but is associated with increased healthcare utilization in the PHAR. PAH-specific QoL may be worse in patients receiving anticoagulation.
DOI10.1016/j.healun.2022.08.019
Alternate JournalJ Heart Lung Transplant
PubMed ID36150996
PubMed Central IDPMC10329839
Grant ListK24 HL155891 / HL / NHLBI NIH HHS / United States