Journal Article10.1111/ECHO.13699
Differences in right ventricular morphology, not function, indicate the nature of increased afterload in pulmonary hypertensive subjects with normal left ventricular function.
Farhan Raza,Catherine Dillane,Arslan Mirza,Yevgeniy Brailovsky,Sheila Weaver,Martin G. Keane,Paul R. Forfia +6 more
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TL;DR: The aim of study was to assess whether a specific morphology of the right ventricle by 2D echo predicts the hemodynamic nature of pulmonary hypertension.
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Abstract: Background The aim of study was to assess whether a specific morphology of the right ventricle (RV) by 2D echo predicts the hemodynamic nature of pulmonary hypertension (PH) Methods We reviewed clinical, 2D echo, and hemodynamic data of 100 patients with PH: divided into three groups: PH from pulmonary vascular disease (PHPVD ; n = 34) with pulmonary vascular resistance (PVR) > 3 mm Hg/L/min (Wood unit [WU]) and pulmonary artery wedge pressure (PAWP) ≤ 15 mm Hg, pulmonary venous hypertension (PVH; n = 33) with PVR 15 mm Hg and PHMIXED (n = 33) with PVR > 3 WU and PAWP > 15 mm Hg We analyzed several two-dimensional parameters of right heart morphology and function, including the degree of tapering of the RV diameter from base (just above tricuspid annulus) to apex (level of moderator band) in the apical four-chamber view P = Results Baseline characteristics were similar in all three groups: age 62 ± 144 years, 69% females, 57% Caucasians Hemodynamics and 2D echo data of PHPVD vs PVH vs PHMIXED were as follows: PVR 13 ± 6 vs 2 ± 1 vs 7 ± 2 WU, mean pulmonary artery pressure 53 ± 14 vs 34 ± 8 vs 49 ± 8 mm Hg and cardiac index 20 ± 05 vs 28 ± 07 vs 22 ± 07 L/m2 , RV base/apex ratio during systole (sRVb/a ) 13 ± 02 vs 26 ± 05 vs 15 ± 03 Thus, sRVb/a was twofold higher in the PVH vs PHPVD cohort On ROC analysis, the AUC for sRVb/a for predicting PVR > 3 WU was 0873, with optimal cutoff of 15 Conclusion Systolic RV base/apex ratio is a simple 2D index of RV shape that powerfully predicts a PVR > 3 WU and provides powerful discriminating ability between PVH and PHPVD
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Citations
Case series of seven women with uterine fibroids associated with venous thromboembolism and chronic thromboembolic disease.
Anne-Sophie Lacharite-Roberge,Farhan Raza,Riyaz Bashir,Chandra Dass,G. William Moser,William R. Auger,Yoshiya Toyoda,Paul R. Forfia,Anjali Vaidya +8 more
TL;DR: All seven women with uterine fibroids and CTEPH underwent pulmonary thromboendarterectomy (PTE) followed by marked improvement in functional, clinical, and hemodynamic status.
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Virtual echocardiography screening tool to differentiate hemodynamic profiles in pulmonary hypertension
Anjali Vaidya,Jessica R. Golbus,Natasha A. Vedage,Jeremy A. Mazurek,Farhan Raza,Paul R. Forfia +5 more
TL;DR: It is demonstrated that this novel VEST using three routine parameters that can be easily extracted from standard echocardiographic reports can successfully capture PH patients with a high likelihood of PHPVD.
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A guide to echocardiographic assessment in children and adolescents with pulmonary hypertension
TL;DR: A practical approach and a concise and clinically applicable echocardiographic guidance and present basic variables, which should be obtained at any assessment of pulmonary hypertension, are provided.
Multimodality Deep Phenotyping Methods to Assess Mechanisms of Poor Right Ventricular–Pulmonary Artery Coupling
Farhan Raza,Callyn Kozitza,Chris Lechuga,Daniel P. Seiter,Philip A. Corrado,Mohammed Merchant,Naga L. Dharmavaram,Claudia E. Korcarz,Marlowe W. Eldridge,C. Francois,Oliver Wieben,Naomi C. Chesler +11 more
TL;DR:
Diagnosis and Management of Pulmonary Hypertension and Right Ventricular Failure in the Cardiovascular Intensive Care Unit
01 Sep 2023
TL;DR: Pulmonary hypertension encompasses a broad range of conditions, including pulmonary artery hypertension, left-sided heart disease, and pulmonary and thromboembolic disorders, which require distinct management strategies.
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TL;DR: In this paper, a clinical classification of pulmonary hypertension (PH) was established, categorizing PH into groups which share similar pathological and hemodynamic characteristics and therapeutic approaches, and the main change was to withdraw persistent pulmonary hypertension of the newborn (PPHN) from Group 1 because this entity carries more differences than similarities with other PAH subgroups.
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Guidelines for the diagnosis and treatment of pulmonary hypertension: the Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS), endorsed by the International Society of Heart and Lung Transplantation (ISHLT)
Nazzareno Galiè,Marius M. Hoeper,Marc Humbert,Adam Torbicki,Jean-Luc Vachiery,J.A. Barberà,Maurice Beghetti,Paul A. Corris,Sean Gaine,J S R Gibbs,Miguel Ángel Gómez-Sánchez,Guillaume Jondeau,Walter Klepetko,Christian Opitz,Andrew J. Peacock,LJ Rubin,Michael J. Zellweger,Gérald Simonneau +17 more
TL;DR: In this paper, a review of the published evidence for management and/or prevention of a given condition is carried out by experts in the field and a critical evaluation of diagnostic and therapeutic procedures is performed including assessment of the risk/benefit ratio.
Survival in Patients with Primary Pulmonary Hypertension: Results from a National Prospective Registry
Gilbert E. D'Alonzo,Robyn J. Barst,Stephen M. Ayres,Edward H. Bergofsky,Bruce H. Brundage,Katherine M. Detre,Alfred P. Fishman,Roberta M. Goldring,Berton M. Groves,Janet T. Kernis,Paul S. Levy,Giuseppe G. Pietra,Lynne Reid,John T. Reeves,Stuart Rich,Carol E. Vreim,George W. Williams,Margaret Wu +17 more
TL;DR: Mortality was most closely associated with right ventricular hemodynamic function and can be characterized by means of an equation using three variables: mean pulmonary artery pressure, mean right atrial pressure, and cardiac index.
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2015 ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension: The Joint Task Force for the Diagnosis and Treatment of Pulmonary Hypertension of the European Society of Cardiology (ESC) and the European Respiratory Society (ERS): Endorsed by: Association for European Paediatric and Congenital Cardiology (AEPC), International Society for Heart and Lung Transplantation (ISHLT).
Nazzareno Galiè,Marc Humbert,Jean-Luc Vachiery,Simon Gibbs,Irene Lang,Adam Torbicki,Gérald Simonneau,Andrew Peacock,Anton Vonk Noordegraaf,Maurice Beghetti,Ardeschir Ghofrani,Miguel Angel Gomez Sanchez,Georg Hansmann,Walter Klepetko,Patrizio Lancellotti,Marco Matucci,Theresa McDonagh,Luc Pierard,Pedro T. Trindade,Maurizio Zompatori,Marius M. Hoeper +20 more
TL;DR: In this article, guidelines summarize and evaluate all available evidence on a particular issue, with the aim of assisting health professionals in selecting the best management strategies for an individual patient with a given condition, taking into account the impact on outcome, as well as the risk-benefit ratio of particular diagnostic or therapeutic means.
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Pulmonary arterial hypertension in France: results from a national registry.
Marc Humbert,Olivier Sitbon,Ari Chaouat,Michèle Bertocchi,Gilbert Habib,Virginie Gressin,Azzedine Yaici,Emmanuel Weitzenblum,Jean-François Cordier,François Chabot,Claire Dromer,Christophe Pison,Martine Reynaud-Gaubert,Alain Haloun,Marcel Laurent,Eric Hachulla,Gérald Simonneau +16 more
TL;DR: It is shown that PAH is detected late in the course of the disease, with a majority of patients displaying severe functional and hemodynamic compromise, and this contemporary registry highlights current practice.
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