Pulmonary Hypertension in Heart Failure. Epidemiology, Right Ventricular Function, and Survival
Patients with pulmonary hypertension due to left heart disease (PH-LHD) and a diastolic pulmonary vascular pressure gradient ≥ 7 mm Hg, representing PH out of proportion to pulmonary arterial wedge pressure, have pulmonary vascular disease and increased mortality. Little information exists on this c...
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Published in | American journal of respiratory and critical care medicine Vol. 192; no. 10; pp. 1234 - 1246 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Thoracic Society
15.11.2015
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Subjects | |
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Abstract | Patients with pulmonary hypertension due to left heart disease (PH-LHD) and a diastolic pulmonary vascular pressure gradient ≥ 7 mm Hg, representing PH out of proportion to pulmonary arterial wedge pressure, have pulmonary vascular disease and increased mortality. Little information exists on this condition, recently labeled as "combined pre- and post-capillary PH" (Cpc-PH).
To investigate epidemiology, risk factors, right ventricular function, and outcomes in patients with chronic heart failure and Cpc-PH.
The study population was identified from a retrospective chart review of a clinical database of 3,107 stable patients who underwent first diagnostic right heart catheterization and from a prospective cohort of 800 consecutive patients at a national university-affiliated tertiary center.
The retrospective cohort had 664 patients with systolic heart failure (SHF) and 399 patients with diastolic heart failure (DHF), 12% of whom were classified as Cpc-PH. The prospective cohort had 172 patients with SHF (14% Cpc-PH) and 219 patients with DHF (12% Cpc-PH). Chronic obstructive pulmonary disease (P = 0.034) and the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure ratio (P = 0.015) predicted Cpc-PH in SHF. Younger age (P = 0.004), valvular heart disease (P = 0.046), and the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure ratio predicted Cpc-PH in DHF (P = 0.016). Right ventricular-pulmonary vascular coupling was worse in Cpc-PH patients (end-systolic elastance to effective arterial elastance [Ees/Ea]: SHF: 1.05 ± 0.25; P = 0.002; DHF: 1.17 ± 0.27; P = 0.027) than in those with isolated post-capillary PH (Ees/Ea: SHF: 1.52 ± 0.51; DHF: 1.45 ± 0.29).
Cpc-PH is rare in chronic heart failure. Right ventricular-pulmonary vascular coupling is poor in Cpc-PH and could be one explanation for dismal outcomes. |
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AbstractList | RATIONALEPatients with pulmonary hypertension due to left heart disease (PH-LHD) and a diastolic pulmonary vascular pressure gradient ≥ 7 mm Hg, representing PH out of proportion to pulmonary arterial wedge pressure, have pulmonary vascular disease and increased mortality. Little information exists on this condition, recently labeled as "combined pre- and post-capillary PH" (Cpc-PH).OBJECTIVESTo investigate epidemiology, risk factors, right ventricular function, and outcomes in patients with chronic heart failure and Cpc-PH.METHODSThe study population was identified from a retrospective chart review of a clinical database of 3,107 stable patients who underwent first diagnostic right heart catheterization and from a prospective cohort of 800 consecutive patients at a national university-affiliated tertiary center.MEASUREMENTS AND MAIN RESULTSThe retrospective cohort had 664 patients with systolic heart failure (SHF) and 399 patients with diastolic heart failure (DHF), 12% of whom were classified as Cpc-PH. The prospective cohort had 172 patients with SHF (14% Cpc-PH) and 219 patients with DHF (12% Cpc-PH). Chronic obstructive pulmonary disease (P = 0.034) and the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure ratio (P = 0.015) predicted Cpc-PH in SHF. Younger age (P = 0.004), valvular heart disease (P = 0.046), and the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure ratio predicted Cpc-PH in DHF (P = 0.016). Right ventricular-pulmonary vascular coupling was worse in Cpc-PH patients (end-systolic elastance to effective arterial elastance [Ees/Ea]: SHF: 1.05 ± 0.25; P = 0.002; DHF: 1.17 ± 0.27; P = 0.027) than in those with isolated post-capillary PH (Ees/Ea: SHF: 1.52 ± 0.51; DHF: 1.45 ± 0.29).CONCLUSIONSCpc-PH is rare in chronic heart failure. Right ventricular-pulmonary vascular coupling is poor in Cpc-PH and could be one explanation for dismal outcomes. Patients with pulmonary hypertension due to left heart disease (PH-LHD) and a diastolic pulmonary vascular pressure gradient ≥ 7 mm Hg, representing PH out of proportion to pulmonary arterial wedge pressure, have pulmonary vascular disease and increased mortality. Little information exists on this condition, recently labeled as "combined pre- and post-capillary PH" (Cpc-PH). To investigate epidemiology, risk factors, right ventricular function, and outcomes in patients with chronic heart failure and Cpc-PH. The study population was identified from a retrospective chart review of a clinical database of 3,107 stable patients who underwent first diagnostic right heart catheterization and from a prospective cohort of 800 consecutive patients at a national university-affiliated tertiary center. The retrospective cohort had 664 patients with systolic heart failure (SHF) and 399 patients with diastolic heart failure (DHF), 12% of whom were classified as Cpc-PH. The prospective cohort had 172 patients with SHF (14% Cpc-PH) and 219 patients with DHF (12% Cpc-PH). Chronic obstructive pulmonary disease (P = 0.034) and the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure ratio (P = 0.015) predicted Cpc-PH in SHF. Younger age (P = 0.004), valvular heart disease (P = 0.046), and the tricuspid annular plane systolic excursion to systolic pulmonary artery pressure ratio predicted Cpc-PH in DHF (P = 0.016). Right ventricular-pulmonary vascular coupling was worse in Cpc-PH patients (end-systolic elastance to effective arterial elastance [Ees/Ea]: SHF: 1.05 ± 0.25; P = 0.002; DHF: 1.17 ± 0.27; P = 0.027) than in those with isolated post-capillary PH (Ees/Ea: SHF: 1.52 ± 0.51; DHF: 1.45 ± 0.29). Cpc-PH is rare in chronic heart failure. Right ventricular-pulmonary vascular coupling is poor in Cpc-PH and could be one explanation for dismal outcomes. |
Author | Gerges, Christian Jakowitsch, Johannes Lang, Irene M. Binder, Thomas Trip, Pia Lang, Marie B. Pistritto, Anna-Maria Gerges, Mario |
Author_xml | – sequence: 1 givenname: Mario orcidid: 0000-0003-3295-4565 surname: Gerges fullname: Gerges, Mario organization: Division of Cardiology, Department of Internal Medicine II, Vienna General Hospital, Medical University of Vienna, Vienna, Austria – sequence: 2 givenname: Christian surname: Gerges fullname: Gerges, Christian organization: Division of Cardiology, Department of Internal Medicine II, Vienna General Hospital, Medical University of Vienna, Vienna, Austria – sequence: 3 givenname: Anna-Maria surname: Pistritto fullname: Pistritto, Anna-Maria organization: Division of Cardiology, Department of Internal Medicine, Ferrarotto Hospital, University of Catania, Catania, Italy; and – sequence: 4 givenname: Marie B. surname: Lang fullname: Lang, Marie B. organization: Division of Cardiology, Department of Internal Medicine II, Vienna General Hospital, Medical University of Vienna, Vienna, Austria – sequence: 5 givenname: Pia surname: Trip fullname: Trip, Pia organization: Department of Pulmonary Medicine, Institute for Cardiovascular Research, VU University Medical Center, Amsterdam, the Netherlands – sequence: 6 givenname: Johannes surname: Jakowitsch fullname: Jakowitsch, Johannes organization: Division of Cardiology, Department of Internal Medicine II, Vienna General Hospital, Medical University of Vienna, Vienna, Austria – sequence: 7 givenname: Thomas surname: Binder fullname: Binder, Thomas organization: Division of Cardiology, Department of Internal Medicine II, Vienna General Hospital, Medical University of Vienna, Vienna, Austria – sequence: 8 givenname: Irene M. surname: Lang fullname: Lang, Irene M. organization: Division of Cardiology, Department of Internal Medicine II, Vienna General Hospital, Medical University of Vienna, Vienna, Austria |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/26181215$$D View this record in MEDLINE/PubMed |
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Keywords | pulmonary heart disease heart failure pulmonary hypertension hemodynamics |
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References | bib36 bib15 bib37 bib12 bib34 bib13 bib35 bib10 bib32 bib11 bib33 bib30 bib31 bib29 bib27 bib28 Gerges M (bib14) 2014; 35 bib40 bib25 bib26 bib23 bib24 bib21 bib22 bib20 bib9 bib7 bib8 bib5 bib18 bib6 Gerges M (bib16) 2015; 191 bib19 bib3 bib38 bib4 bib17 bib39 bib1 bib2 26568239 - Am J Respir Crit Care Med. 2015 Nov 15;192(10):1152-4 |
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Snippet | Patients with pulmonary hypertension due to left heart disease (PH-LHD) and a diastolic pulmonary vascular pressure gradient ≥ 7 mm Hg, representing PH out of... RATIONALEPatients with pulmonary hypertension due to left heart disease (PH-LHD) and a diastolic pulmonary vascular pressure gradient ≥ 7 mm Hg, representing... |
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SubjectTerms | Aged Analysis of Variance Austria - epidemiology Comorbidity Death Certificates Female Heart Failure - epidemiology Heart Failure - physiopathology Hemodynamics - physiology Humans Hypertension, Pulmonary - epidemiology Hypertension, Pulmonary - etiology Hypertension, Pulmonary - physiopathology Logistic Models Male Middle Aged Prevalence Prognosis Prospective Studies Pulmonary Heart Disease - epidemiology Pulmonary Heart Disease - physiopathology Retrospective Studies Risk Assessment Sex Distribution Survival Analysis Ventricular Dysfunction, Left - complications Ventricular Dysfunction, Left - diagnosis Ventricular Dysfunction, Left - epidemiology Ventricular Dysfunction, Right - complications Ventricular Dysfunction, Right - epidemiology Ventricular Dysfunction, Right - physiopathology |
Title | Pulmonary Hypertension in Heart Failure. Epidemiology, Right Ventricular Function, and Survival |
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