Literature DB >> 20304507

Quality of life and functional capacity can be improved in patients with Eisenmenger syndrome with oral sildenafil therapy.

Edgar L W Tay1, Maria Papaphylactou, Gerhard Paul Diller, Rafael Alonso-Gonzalez, Ryo Inuzuka, Georgios Giannakoulas, Carl Harries, Stephen John Wort, Lorna Swan, Konstantinos Dimopoulos, Michael A Gatzoulis.   

Abstract

BACKGROUND: Patients with Eisenmenger syndrome (ES) have a decreased exercise capacity and poor quality of life (QoL). While patients may survive to middle adulthood, the burden of disease is disabling. Sildenafil seems to improve exercise tolerance and hemodynamics, but there is no data to date on its impact on QoL.
METHODS: Eisenmenger patients in New York Heart Association (NYHA) class III were recruited in a prospective study of efficacy and safety of oral sildenafil. The QoL endpoint was assessed using a disease-specific questionnaire (CAMPHOR). Exercise capacity was assessed by means of six minute walk test (6MWT). All patients underwent comprehensive assessment at baseline and after 3months of treatment.
RESULTS: Twelve patients (mean age was 34.3±10.2, 83% female) with various cardiac anatomies were recruited. No major adverse events during the follow-up or significant drop in resting oxygen saturation were recorded. After 3months of oral sildenafil therapy, all patients improved to NYHA II with a concomitant improvement in 6MWT distance (347.3±80.7 to 392.5±82.0m, p=0.002). All components of the CAMPHOR score, relating to symptoms, activity and QoL, improved significantly resulting in substantial improvement in the total CAMPHOR score (27.6±10.5 to 15.8±10.4, p=0.002).
CONCLUSIONS: Three months of sildenafil therapy in adults with ES was well tolerated and associated with significant improvement in the QoL CAMPHOR questionnaire and in NYHA class and exercise capacity. Larger studies are warranted to assess long term efficacy of oral sildenafil and potential impact on survival.
Copyright © 2010 Elsevier Ireland Ltd. All rights reserved.

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Year:  2010        PMID: 20304507     DOI: 10.1016/j.ijcard.2010.02.020

Source DB:  PubMed          Journal:  Int J Cardiol        ISSN: 0167-5273            Impact factor:   4.164


  8 in total

1.  Life span of patients with Eisenmenger syndrome is not superior to that of patients with other causes of pulmonary hypertension.

Authors:  Béatrice Bonello; Sébastien Renard; Julien Mancini; Sandrine Hubert; Gilbert Habib; Alain Fraisse
Journal:  Cardiovasc Diagn Ther       Date:  2014-10

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.  Palliative care in pulmonary hypertension associated with congenital heart disease: systematic review and expert opinion.

Authors:  Andrew Constantine; Robin Condliffe; Paul Clift; Robert Tulloh; Konstantinos Dimopoulos
Journal:  ESC Heart Fail       Date:  2021-03-03

4.  Rapid transition from inhaled iloprost to inhaled treprostinil in patients with pulmonary arterial hypertension.

Authors:  Robert C Bourge; Victor F Tapson; Zeenat Safdar; Raymond L Benza; Richard N Channick; Erika B Rosenzweig; Shelley Shapiro; R James White; Christopher Shane McSwain; Stephen Karl Gotzkowsky; Andrew C Nelsen; Lewis J Rubin
Journal:  Cardiovasc Ther       Date:  2013-02       Impact factor: 3.023

Review 5.  The Changing Landscape of Pulmonary Arterial Hypertension in the Adult with Congenital Heart Disease.

Authors:  Alexandra C van Dissel; Barbara J M Mulder; Berto J Bouma
Journal:  J Clin Med       Date:  2017-03-30       Impact factor: 4.241

6.  Patent ductus arteriosus with persistent pulmonary artery hypertension after transcatheter closure.

Authors:  Jianqi Feng; Xiangqing Kong; Yanhui Sheng; Rong Yang
Journal:  Ther Clin Risk Manag       Date:  2016-11-03       Impact factor: 2.423

7.  Use of sildenafil citrate in a cat with Eisenmenger's syndrome and an atrial septal defect.

Authors:  Ke Shuan Chow; Niek J Beijerink; Stephen Ettinger; Reuben Fliegner; Julia A Beatty; Vanessa R Barrs
Journal:  JFMS Open Rep       Date:  2015-04-28

8.  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

  8 in total

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