Literature DB >> 22289484

Prognostic factors in severe pulmonary hypertension patients who need parenteral prostanoid therapy: the impact of late referral.

Roberto Badagliacca1, Beatrice Pezzuto, Roberto Poscia, Massimo Mancone, Silvia Papa, Serena Marcon, Gabriele Valli, Gennaro Sardella, Fabio Ferrante, Carlo Iacoboni, Daniela Parola, Francesco Fedele, Carmine Dario Vizza.   

Abstract

BACKGROUND: Oral drugs have made the treatment of pulmonary hypertension (PH) feasible in non-expert centers, which could delay patient access to prostanoid therapy.
METHODS: Fifty-seven consecutive patients with precapillary PH received a prostanoid in our center. Data at prostanoid initiation included modality of center referral, medical history, New York Heart Association [NYHA] class, exercise capacity, echocardiographic parameters, and hemodynamics.
RESULTS: Overall survival at 1, 2, and 3 years was 85%, 69%, 55%, respectively. Non-survivors had worse NYHA class III/IV (17/12) than survivors (27/1; p < 0.01) and exercise capacity on 6-minute-walk distance (254 ± 114 vs 354 ± 91 meters; p < 0.01). Non-survivors were more frequently referred on oral therapy (83% vs 36%; p < 0.01) and had a higher rate of urgent prostanoid treatment (69% vs 17%; p < 0.0001). Multivariate analysis (hazard ratio [95% confidence interval]) found the independent prognostic factors were urgent prostanoid therapy (2.0 [1.1-3.9]) and NYHA class (3.5 [1.5-8.2]). Survivors had a significant response to prostanoid, improving NYHA class from 2.8 ± 0.4 to 2.3 ± 0.5 (p = 0.002), 6-minute walk distance from 354 ± 91 to 426 ± 82 meters (p = 0.0001), and pulmonary hemodynamics (pulmonary artery pressure from 56 ± 13 to 44 ± 18 mm Hg [p < 0.05]; cardiac index from 2.0 ± 1.2 to 3.1 ± 1.2 liters/min/m(2) [p = 0.002], and pulmonary vascular resistance from 17 ± 10 to 8 ± 6 WU [p = 0.001]).
CONCLUSIONS: Referral of patients on oral treatment to a tertiary PH center is delayed and significantly affects prognosis. Copyright Â
© 2012 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22289484     DOI: 10.1016/j.healun.2011.12.011

Source DB:  PubMed          Journal:  J Heart Lung Transplant        ISSN: 1053-2498            Impact factor:   10.247


  6 in total

Review 1.  An update on medical therapy for pulmonary arterial hypertension.

Authors:  Yan Wu; Dermot S O'Callaghan; Marc Humbert
Journal:  Curr Hypertens Rep       Date:  2013-12       Impact factor: 5.369

Review 2.  Medical Therapies for the Treatment of Pulmonary Arterial Hypertension: How Do We Choose?

Authors:  Alison M MacKenzie; Andrew J Peacock
Journal:  Curr Hypertens Rep       Date:  2015-07       Impact factor: 5.369

3.  Ivabradine in pulmonary arterial hypertension: can we delay the need for parenteral prostanoid therapy?

Authors:  Michele Correale; Deodata Montrone; Riccardo Ieva; Matteo Di Biase; Natale Daniele Brunetti
Journal:  Clin Res Cardiol       Date:  2013-02-07       Impact factor: 5.460

4.  Short-term improvement in pulmonary hemodynamics is strongly predictive of long-term survival in patients with pulmonary arterial hypertension.

Authors:  Henning Tiede; Natascha Sommer; Katrin Milger; Robert Voswinckel; Dirk Bandorski; Ralph T Schermuly; Norbert Weissmann; Friedrich Grimminger; Werner Seeger; Hossein A Ghofrani
Journal:  Pulm Circ       Date:  2013-11-19       Impact factor: 3.017

5.  Resource utilization at the time of prostacyclin initiation in children in pulmonary arterial hypertension: a multicenter analysis.

Authors:  Stephen A Hart; Gaurav Arora; Brian Feingold
Journal:  Pulm Circ       Date:  2018-01-09       Impact factor: 3.017

Review 6.  Echocardiographic findings associated with mortality ortransplant in patients with pulmonary arterial hypertension:A systematic review and meta-analysis.

Authors:  V J M Baggen; M M P Driessen; M C Post; A P van Dijk; J W Roos-Hesselink; A E van den Bosch; J J M Takkenberg; G T Sieswerda
Journal:  Neth Heart J       Date:  2016-06       Impact factor: 2.380

  6 in total

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