help button home button
AJRCCM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH

Published ahead of print on August 3, 2006, doi:10.1164/rccm.200604-547OC

Am. J. Respir. Crit. Care Med., Volume 174, Number 9, November 2006, 1034-1041

A more recent version of this article appeared on November 1, 2006
This Article
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
200604-547OCv1
174/9/1034    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Forfia, P. R
Right arrow Articles by Hassoun, P. M
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Forfia, P. R
Right arrow Articles by Hassoun, P. M

Submitted on April 20, 2006
Accepted on August 3, 2006

Tricuspid Annular Displacement Predicts Survival in Pulmonary Hypertension

Paul R Forfia1, Micah R Fisher2, Stephen C Mathai2, Traci Housten-Harris2, Anna R Hemnes2, Barry A Borlaug1, Elzbieta Chamera1, Mary C Corretti1, Hunter C Champion1, Theodore P Abraham1, Reda E Girgis2, and Paul M Hassoun2*

1 Department of Medicine, Division of Cardiology, Johns Hopkins University, Baltimore, Maryland, USA, 2 Department of Medicine, Division of Pulmonary and Critical Care Medicine, Johns Hopkins University, Baltimore, Maryland, USA

* To whom correspondence should be addressed. E-mail: phassoun{at}jhmi.edu.

Rationale: Right ventricular (RV) function is an important determinant of prognosis in pulmonary hypertension. However, noninvasive assessment of the RV is often limited by complex geometry and poor endocardial definition. Objectives: To test whether the degree of tricuspid annular displacement (tricuspid annular plane systolic excursion; TAPSE) is a useful echo-derived measure of RV function with prognostic significance in pulmonary hypertension (PH). Methods: We prospectively studied 63 consecutive patients with PH who were referred for a clinically indicated right heart catheterization. Patients underwent right heart catheterization immediately followed by transthoracic echocardiogram and TAPSE measurement. Results: In the overall cohort, a TAPSE < 1.8 cm was associated with greater RV systolic dysfunction (cardiac index-1.9 vs. 2.7 l/min/m2; RV % area change-24 vs. 33%), right heart remodeling (right atrial area index-17.0 vs. 12.1 cm2/m), and RV-LV disproportion (RV/LV diastolic area-1.7 vs. 1.2; all P<0.001) vs. a TAPSE ≥ 1.8 cm. In patients with pulmonary arterial hypertension (PAH, n=47), survival estimates at one/two years were 94%/88% in those with a TAPSE ≥ 1.8 cm vs. 60%/50% in subjects with a TAPSE < 1.8 cm. The unadjusted risk of death (HR) in patients with a TAPSE < 1.8 vs. ≥ 1.8 cm was 5.7 (95% CI 1.3-24.9, P=0.02) for the PAH cohort. For every one millimeter decrease in TAPSE, the unadjusted risk of death increased by 17% (HR 1.17, 95% CI 1.05-1.30, P=0.006), which persisted after adjusting for other echocardiographic and hemodynamic variables and baseline treatment status. Conclusions: TAPSE powerfully reflects RV function and prognosis in PAH.


Key words: TAPSE. Tricuspid annular displacement, right ventricular function, pulmonary arterial hypertension, prognosis




This article has been cited by other articles:


Home page
Eur Respir JHome page
A. Chaouat, R. Naeije, and E. Weitzenblum
Pulmonary hypertension in COPD
Eur. Respir. J., November 1, 2008; 32(5): 1371 - 1385.
[Abstract] [Full Text] [PDF]


Home page
Circ Heart FailHome page
R. J. Tedford, A. R. Hemnes, S. D. Russell, I. S. Wittstein, M. Mahmud, A. L. Zaiman, S. C. Mathai, D. R. Thiemann, P. M. Hassoun, R. E. Girgis, et al.
PDE5A Inhibitor Treatment of Persistent Pulmonary Hypertension After Mechanical Circulatory Support
Circ Heart Fail, November 1, 2008; 1(4): 213 - 219.
[Abstract] [Full Text] [PDF]


Home page
Proc Am Thorac SocHome page
C. E. Ventetuolo, R. L. Benza, A. J. Peacock, R. T. Zamanian, D. B. Badesch, and S. M. Kawut
Surrogate and Combined End Points in Pulmonary Arterial Hypertension
Proceedings of the ATS, July 15, 2008; 5(5): 617 - 622.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Respir. Crit. Care Med.Home page
P. R. Forfia, S. C. Mathai, M. R. Fisher, T. Housten-Harris, A. R. Hemnes, H. C. Champion, R. E. Girgis, and P. M. Hassoun
Hyponatremia Predicts Right Heart Failure and Poor Survival in Pulmonary Arterial Hypertension
Am. J. Respir. Crit. Care Med., June 15, 2008; 177(12): 1364 - 1369.
[Abstract] [Full Text] [PDF]


Home page
J Am Coll CardiolHome page
K. M. Chin and L. J. Rubin
Pulmonary arterial hypertension.
J. Am. Coll. Cardiol., April 22, 2008; 51(16): 1527 - 1538.
[Abstract] [Full Text] [PDF]


Home page
CirculationHome page
T. P. Abraham, V. L. Dimaano, and H.-Y. Liang
Role of Tissue Doppler and Strain Echocardiography in Current Clinical Practice
Circulation, November 27, 2007; 116(22): 2597 - 2609.
[Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
Proc. Am. Thorac. Soc. Am. J. Respir. Cell Mol. Biol.
Copyright © 2006 American Thoracic Society
  ATS Sleep Tracings Quiz