Literature DB >> 23553708

Impact of sildenafil on survival of patients with Eisenmenger syndrome.

Yun-Juan Sun1, Tao Yang, Wei-Jie Zeng, Qing Gu, Xin-Hai Ni, Zhi-Hui Zhao, Zhi-Hong Liu, Chang-Ming Xiong, Jian-Guo He.   

Abstract

The favorable effects of short-term use of sildenafil on patients with Eisenmenger syndrome have been reported. We further studied the impact of long-term use of sildenafil on survival of these patients. In this study, the baseline data of patients newly diagnosed as Eisenmenger syndrome in our hospital between January 2005 and December 2009 were retrospectively collected. Patients were followed-up either by telephone contacts or during visits in our out-patient clinic. A total of 121 patients (68 patients in conventional group and 53 patients in sildenafil group) were finally included and 29 patients were re-evaluated after sildenafil therapy for 3-4 months. Compared with the baseline, a 6-minute walk distance, functional classes, plasma hemoglobin level, and hemodynamics were significantly improved after sildenafil treatment. During a median follow-up period of 35.8 months, 15 patients died (11 patients in conventional group). The 1- and 3-year survival rates in sildenafil group were 97.0% and 95.2%, significantly higher than 90.6% and 82.9% in conventional group P = .025). Multivariate analysis showed that sildenafil therapy, functional class and mean pulmonary arterial pressure were independently associated with survival. Therefore, long-term sildenafil therapy improved survival in patients with Eisenmenger syndrome.
© The Author(s) 2013.

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Year:  2013        PMID: 23553708     DOI: 10.1002/jcph.78

Source DB:  PubMed          Journal:  J Clin Pharmacol        ISSN: 0091-2700            Impact factor:   3.126


  6 in total

1.  Current therapy and outcome of Eisenmenger syndrome: data of the German National Register for congenital heart defects.

Authors:  Gerhard-Paul Diller; Marc-André Körten; Ulrike M M Bauer; Oliver Miera; Oktay Tutarel; Harald Kaemmerer; Felix Berger; Helmut Baumgartner
Journal:  Eur Heart J       Date:  2016-02-02       Impact factor: 29.983

Review 2.  Adult congenital heart disease with pulmonary arterial hypertension: mechanisms and management.

Authors:  Michail Papamichalis; Andrew Xanthopoulos; Panagiotis Papamichalis; John Skoularigis; Filippos Triposkiadis
Journal:  Heart Fail Rev       Date:  2020-09       Impact factor: 4.214

3.  The role of phosphodiesterase inhibitors in the management of pulmonary vascular diseases.

Authors:  Ghazwan Butrous
Journal:  Glob Cardiol Sci Pract       Date:  2014-10-16

4.  Evaluation of Macitentan in Patients With Eisenmenger Syndrome.

Authors:  Michael A Gatzoulis; Michael Landzberg; Maurice Beghetti; Rolf M Berger; Michela Efficace; Sophie Gesang; Jian'guo He; Kelly Papadakis; Tomás Pulido; Nazzareno Galiè
Journal:  Circulation       Date:  2019-01-02       Impact factor: 29.690

5.  Clinical features and outcome of dogs and cats with bidirectional and continuous right-to-left shunting patent ductus arteriosus.

Authors:  Victoria Greet; Elizabeth F Bode; Joanna Dukes-McEwan; Pedro Oliveira; David J Connolly; Julia Sargent
Journal:  J Vet Intern Med       Date:  2021-02-26       Impact factor: 3.333

6.  Management dilemmas in pulmonary arterial hypertension associated with congenital heart disease.

Authors:  R Condliffe; P Clift; K Dimopoulos; R M R Tulloh
Journal:  Pulm Circ       Date:  2018-07-23       Impact factor: 3.017

  6 in total

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