Literature DB >> 14555600

Successful withdrawal of long-term epoprostenol therapy for pulmonary arterial hypertension.

Nick H Kim1, Richard N Channick, Lewis J Rubin.   

Abstract

BACKGROUND: IV epoprostenol treatment of pulmonary arterial hypertension (PAH) has been believed to require an indefinite duration of therapy
OBJECTIVE: To describe the successful discontinuation of long-term epoprostenol therapy in four patients
DESIGN: Case reports
SETTING: Outpatient clinic, tertiary-care hospital PATIENTS: Four patients with acutely nonvasoreactive, World Health Organization (WHO) functional class IV PAH received long-term epoprostenol therapy. All patients subsequently demonstrated normalization of pulmonary arterial pressures on epoprostenol treatment. These patients were selected for epoprostenol withdrawal INTERVENTION: Down-titration and discontinuation of epoprostenol
RESULTS: All four patients were safely transitioned from epoprostenol to oral therapies and have maintained WHO functional class I-II for a mean of 11 months (range, 8 to 16 months). The duration of epoprostenol therapy prior to discontinuation averaged 5.7 years (range, 2.4 to 13.5 years)
CONCLUSION: Epoprostenol may sufficiently reverse the pathogenic process in select patients with PAH to allow a transition to less complex and less invasive treatment modalities.

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Year:  2003        PMID: 14555600

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


  10 in total

1.  Weaning and discontinuation of epoprostenol in children with idiopathic pulmonary arterial hypertension receiving concomitant bosentan.

Authors:  D Dunbar Ivy; Aimee Doran; Lori Claussen; Deborah Bingaman; Anji Yetman
Journal:  Am J Cardiol       Date:  2004-04-01       Impact factor: 2.778

2.  Pulmonary arterial hypertension in a patient with β-thalassemia intermedia and reversal with infusion epoprostenol then transition to oral calcium channel blocker therapy: review of literature.

Authors:  Kamonpun Ussavarungsi; Charles D Burger
Journal:  Pulm Circ       Date:  2014-09       Impact factor: 3.017

3.  Transition from prostacyclin analogue infusion to oral therapy in patients with pulmonary arterial hypertension: a 5-year follow-up.

Authors:  Esteban Escolar; Andrés M Pineda; Barbara Correal; Tahir Ahmed
Journal:  Pulm Circ       Date:  2013-12       Impact factor: 3.017

4.  Response to bosentan in children with pulmonary hypertension.

Authors:  S Maiya; A A Hislop; Y Flynn; S G Haworth
Journal:  Heart       Date:  2005-10-10       Impact factor: 5.994

Review 5.  Transition from intravenous epoprostenol to oral or subcutaneous therapy in pulmonary arterial hypertension: a retrospective case series and systematic review.

Authors:  Kirily Park; David Ostrow; Robert D Levy; John Swiston
Journal:  Can Respir J       Date:  2011 May-Jun       Impact factor: 2.409

6.  A systematic review of transition studies of pulmonary arterial hypertension specific medications.

Authors:  Avraham Sofer; Michael J Ryan; Ryan J Tedford; Joel A Wirth; Wassim H Fares
Journal:  Pulm Circ       Date:  2017-05-12       Impact factor: 3.017

7.  Withdrawal of long-term epoprostenol therapy in pulmonary arterial hypertension (PAH).

Authors:  George Calcaianu; Mihaela Calcaianu; Matthieu Canuet; Irina Enache; Romain Kessler
Journal:  Pulm Circ       Date:  2017-03-13       Impact factor: 3.017

8.  Safety and tolerability of bosentan in the management of pulmonary arterial hypertension.

Authors:  Kari E Roberts; Ioana R Preston
Journal:  Drug Des Devel Ther       Date:  2009-09-21       Impact factor: 4.162

Review 9.  Optimizing endothelin receptor antagonist use in the management of pulmonary arterial hypertension.

Authors:  M Kathryn Steiner; Ioana R Preston
Journal:  Vasc Health Risk Manag       Date:  2008

10.  Weaning from intravenous prostanoids and normalization of hemodynamics by long-term imatinib therapy in severe idiopathic pulmonary arterial hypertension.

Authors:  Rudolf Speich; Ursula Treder; Guido Domenighetti; Lars C Huber; Silvia Ulrich
Journal:  Int J Clin Pharm       Date:  2013-11-28
  10 in total

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