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dc.contributor.authorNaranjo, M.
dc.contributor.authorRosenzweig, E.B.
dc.contributor.authorHemnes, A.R.
dc.contributor.authorJacob, M.
dc.contributor.authorDesai, A.
dc.contributor.authorHill, N.S.
dc.contributor.authorLarive, A.B.
dc.contributor.authorFinet, J.E.
dc.contributor.authorLeopold, J.
dc.contributor.authorHorn, E.
dc.contributor.authorFrantz, R.
dc.contributor.authorRischard, F.
dc.contributor.authorErzurum, S.
dc.contributor.authorBeck, G.
dc.contributor.authorMathai, S.C.
dc.contributor.authorHassoun, P.M.
dc.date.accessioned2024-08-17T19:50:09Z
dc.date.available2024-08-17T19:50:09Z
dc.date.issued2023-08-21
dc.identifier.citationNaranjo M, Rosenzweig EB, Hemnes AR, Jacob M, Desai A, Hill NS, Larive AB, Finet JE, Leopold J, Horn E, Frantz R, Rischard F, Erzurum S, Beck G, Mathai SC, Hassoun PM. Frequency of acute vasodilator response (AVR) in incident and prevalent patients with pulmonary arterial hypertension: results from the pulmonary vascular disease phenomics study. Pulm Circ. 2023; 13:e12281.
dc.identifier.issn2045-8932
dc.identifier.doi10.1002/pul2.12281
dc.identifier.urihttp://hdl.handle.net/10150/674490
dc.description.abstractThe prevalence of acute vasodilator response (AVR) to inhaled nitric oxide (iNO) during right heart catheterization (RHC) is 12% in idiopathic pulmonary arterial hypertension (IPAH). AVR, however, is reportedly lower in other disease-associated pulmonary arterial hypertension (PAH), such as connective tissue disease (CTD). The prevalence of AVR in patients on PAH therapy (prevalent cases) is unknown. We sought to determine AVR prevalence in Group 1 PH in the PVDOMICS cohort of incident and prevalent patients undergoing RHC. AVR was measured in response to 100% O2 and O2 plus iNO, with positivity defined as (1) decrease in mean pulmonary artery pressure (mPAP) by ≥10 mmHg to a value ≤40 mmHg, with no change or an increase in cardiac output (definition 1); or (2) decrease in mPAP by ≥12% and pulmonary vascular resistance by ≥30% (definition 2). AVR rates and cumulative survival were compared between incident and prevalent patients. In 338 mainly prevalent (86%) patients, positive AVR to O2-only was <2%, and 5.1% to 16.9%, based on definition 1 and 2 criteria, respectively; following O2 + iNO. IPAH AVR prevalence (4.1%–18.7%) was similar to prior reports. AVR positivity was 7.7% to 15.4% in mostly CTD-PAH prevalent cases, and 2.6% to 11.8% in other PAH groups. Survival was 89% in AVR responders versus 77% in nonresponders from PAH diagnosis, and 91% versus 86% from PVDOMICS enrollment (log-rank test p = 0.04 and p = 0.05, respectively). In conclusion, AVR in IPAH patients is similar to prior studies. AVR in non-IPAH patients was higher than previously reported. The relationship between PAH therapy, AVR response, and survival warrants further investigation. © 2023 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute.
dc.language.isoen
dc.publisherJohn Wiley and Sons Inc
dc.rights© 2023 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License.
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectpulmonary arterial hypertension
dc.subjectsurvival
dc.subjectvasoreactivity
dc.titleFrequency of acute vasodilator response (AVR) in incident and prevalent patients with pulmonary arterial hypertension: Results from the pulmonary vascular disease phenomics study
dc.typeArticle
dc.typetext
dc.contributor.departmentDepartment of Medicine, College of Medicine, The University of Arizona
dc.identifier.journalPulmonary Circulation
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitlePulmonary Circulation
refterms.dateFOA2024-08-17T19:50:09Z


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© 2023 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License.
Except where otherwise noted, this item's license is described as © 2023 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial License.