Literature DB >> 16100158

Bosentan improves exercise tolerance and Tei index in patients with pulmonary hypertension and prostanoid therapy.

Hans-Jürgen Seyfarth1, Hans Pankau, Stefan Hammerschmidt, Joachim Schauer, Hubert Wirtz, Jörg Winkler.   

Abstract

STUDY
OBJECTIVE: Pulmonary arterial hypertension (PAH) is a progressive disease with a bad prognosis. Prostanoids are well established in the medical treatment of this disease. Treatment of patients with progressive disease despite prostanoids remains a therapeutic challenge. In this study, we examined the effect of adding bosentan, an endothelin antagonist, to existing prostanoid therapy on exercise capacity (6-min walking distance [6MWD]) and right ventricular (RV) function (Tei index) in patients with progressive pulmonary hypertension.
DESIGN: Prospective, nonrandomized, open-label study.
SETTING: University hospital. PATIENTS: Sixteen patients with pulmonary hypertension (PAH, n = 10; pulmonary hypertension due to other cause, n = 6) with progressive disease receiving either beraprost (n = 3), inhaled iloprost (n = 10), or iloprost IV (n = 3).
INTERVENTIONS: Combination therapy with bosentan (final dosage, 125 mg bid) was initiated following an interval of 3-months minimum of unchanged prostanoid therapy. MEASUREMENTS AND
RESULTS: Tei index, 6MWD, and New York Heart Association (NYHA) functional class were assessed prior to the initiation of combination therapy (baseline), at 6 months after initiation of combination therapy, and every 3 months thereafter. Two patients were followed up for 6 months only; all remaining patients reached a mean follow-up period (+/- SD) of 13.5 +/- 5.0 months (range, 9 to 22 months). 6MWD increased by 42.5 +/- 66 m at 6 months and 44.6 +/- 66 m at the last follow-up (both time points vs baseline, p < 0.001), and Tei index improved by -0.13 +/- 0.08 at 6 months and - 0.13 +/- 0.11 at the last follow-up (both time points vs baseline, p < 0.001). All patients reported subjective improvements. Nine of 16 patients exhibited improvement in NYHA functional class at 6 months. No side effects occurred that required dose adjustment or discontinuation of the study medication.
CONCLUSION: Bosentan administered to patients with progressive pulmonary hypertension receiving prostanoids resulted in an increased exercise capacity and an improved RV function. Bosentan therefore appears to be well suited for combination therapy with prostanoids in selected patients pending results of ongoing randomized trials.

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Year:  2005        PMID: 16100158     DOI: 10.1378/chest.128.2.709

Source DB:  PubMed          Journal:  Chest        ISSN: 0012-3692            Impact factor:   9.410


  9 in total

1.  Use of the myocardial performance index to assess right ventricular function in infants with pulmonary hypertension.

Authors:  Neil Patel; John F Mills; Michael M H Cheung
Journal:  Pediatr Cardiol       Date:  2008-08-15       Impact factor: 1.655

2.  Effect of imatinib as add-on therapy on echocardiographic measures of right ventricular function in patients with significant pulmonary arterial hypertension.

Authors:  Amil M Shah; Patricia Campbell; Gabriela Querejeta Rocha; Andrew Peacock; Robyn J Barst; Debbie Quinn; Scott D Solomon
Journal:  Eur Heart J       Date:  2014-02-23       Impact factor: 29.983

3.  Long-term oral bosentan treatment in patients with pulmonary arterial hypertension related to congenital heart disease: a 2-year study.

Authors:  S C Apostolopoulou; A Manginas; D V Cokkinos; S Rammos
Journal:  Heart       Date:  2006-09-15       Impact factor: 5.994

4.  Identification of Transporters Involved in Beraprost Sodium Transport In Vitro.

Authors:  Keiyu Oshida; Masahiro Shimamura; Kazuhiro Seya; Akihiro Ando; Yohei Miyamoto
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2017-02       Impact factor: 2.441

5.  Standard PAH therapy improves long term survival in CTEPH patients.

Authors:  Hans-Juergen Seyfarth; Michael Halank; Heinrike Wilkens; Hans-Joachim Schäfers; Ralf Ewert; Martin Riedel; Ernst Schuster; Hans Pankau; Stefan Hammerschmidt; Hubert Wirtz
Journal:  Clin Res Cardiol       Date:  2010-04-25       Impact factor: 5.460

6.  Right ventricular to left ventricular diameter ratio at end-systole in evaluating outcomes in children with pulmonary hypertension.

Authors:  Pei-Ni Jone; Julie Hinzman; Brandie D Wagner; David Dunbar Ivy; Adel Younoszai
Journal:  J Am Soc Echocardiogr       Date:  2013-12-08       Impact factor: 5.251

7.  Survival with sildenafil and inhaled iloprost in a cohort with pulmonary hypertension: an observational study.

Authors:  Henning Gall; Natascha Sommer; Katrin Milger; Manuel J Richter; Robert Voswinckel; Dirk Bandorski; Werner Seeger; Friedrich Grimminger; Hossein-Ardeschir Ghofrani
Journal:  BMC Pulm Med       Date:  2016-01-12       Impact factor: 3.317

Review 8.  Inhaled iloprost for the control of pulmonary hypertension.

Authors:  Sabine Krug; Armin Sablotzki; Stefan Hammerschmidt; Hubert Wirtz; Hans-Juergen Seyfarth
Journal:  Vasc Health Risk Manag       Date:  2009

9.  A meta-analysis of the safety and efficacy of bosentan therapy combined with prostacyclin analogues or phosphodiesterase type-5 inhibitors for pulmonary arterial hypertension.

Authors:  Zhan-Cui Dang; Bo Tang; Bin Li; Shou Liu; Ri-Li Ge; Zhan-Qiang Li; Dian-Xiang Lu
Journal:  Exp Ther Med       Date:  2019-10-29       Impact factor: 2.447

  9 in total

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