Follow-up tricuspid annular plane systolic excursion predicts survival in pulmonary arterial hypertension
- PMID: 28597759
- PMCID: PMC5467921
- DOI: 10.1177/2045893217694175
Follow-up tricuspid annular plane systolic excursion predicts survival in pulmonary arterial hypertension
Abstract
Few studies have examined the utility of serial echocardiography in the evaluation, management, and prognosis of patients with pulmonary arterial hypertension (PAH). Therefore, we sought to evaluate the prognostic significance of follow-up tricuspid annular plane systolic excursion (TAPSE) in PAH. We prospectively studied 70 consecutive patients with PAH who underwent baseline right heart catheterization (RHC) and transthoracic echocardiogram, who survived to follow-up echocardiogram after initiation of PAH therapy. Baseline TAPSE was 1.6 ± 0.5 cm which increased to 2.0 ± 0.4 cm on follow-up ( P < 0.0001). The cohort was dichotomized by TAPSE at one-year follow-up: Group 1 (n = 37): follow-up TAPSE ≥ 2 cm; Group 2 (n = 33): follow-up TAPSE < 2 cm. Group 1 participants were significantly more likely to reach WHO functional class I-II status and achieve a higher six-minute walk distance on follow-up. Of the 68 patients who survived more than one year, 18 died (26.5%) over a median follow-up of 941 days (range, 3-2311 days), with significantly higher mortality in Group 2 versus Group 1 (41.9% vs. 13.5%; P = 0.003). While baseline TAPSE stratified at 2 cm did not predict survival in this cohort, TAPSE ≥ 2 cm at follow-up strongly predicted survival in bivariable models (hazard ratio, 0.21; 95% confidence interval, 0.08-0.60). In conclusion, follow-up TAPSE ≥ 2 cm is a prognostic marker and potential treatment target in a PAH population.
Keywords: follow-up; pulmonary arterial hypertension (PAH); right ventricular function; survival; tricuspid annular plane systolic excursion (TAPSE).
Figures
References
-
- Vonk-Noordegraaf A, Haddad F, Chin KM, et al. Right heart adaptation to pulmonary arterial hypertension: Physiology and pathobiology. J Am Coll Cardiol 2013; 62(Suppl. 25): D22–33. - PubMed
-
- Mazurek JA, Forfia PR. Enhancing the accuracy of echocardiography in the diagnosis of pulmonary arterial hypertension: Looking at the heart to learn about the lungs. Curr Opin Pulm Med 2013; 19: 437–445. - PubMed
-
- Girgis RE. Predicting long-term survival in pulmonary arterial hypertension: More than just pulmonary vascular resistance. J Am Coll Cardiol 2011; 58: 2520–2521. - PubMed
-
- D'Alonzo GE, Barst RJ, Ayres SM, et al. Survival in patients with primary pulmonary hypertension. Results from a national prospective registry. Ann Intern Med 1991; 115: 343–349. - PubMed
-
- Thenappan T, Shah SJ, Rich S, et al. A USA-based registry for pulmonary arterial hypertension: 1982–2006. Eur Respir J 2007; 30: 1103–1110. - PubMed
LinkOut - more resources
Full Text Sources
Other Literature Sources
