Literature DB >> 16778286

Efficacy of long-term subcutaneous treprostinil sodium therapy in pulmonary hypertension.

Irene Lang1, Miguel Gomez-Sanchez, Meinhard Kneussl, Robert Naeije, Pilar Escribano, Nika Skoro-Sajer, Jean-Luc Vachiery.   

Abstract

STUDY
OBJECTIVES: The aim of this long-term multicenter analysis was to investigate whether subcutaneously infused treprostinil could provide sustained improvements of exercise capacity and survival benefits in patients with pulmonary arterial hypertension (PAH) and inoperable chronic thromboembolic pulmonary hypertension (CTEPH). Subcutaneous administration of the prostacyclin analog treprostinil is an effective treatment for PAH that, unlike epoprostenol, does not require the insertion of a permanent central venous catheter.
DESIGN: Multicenter retrospective study.
SETTING: Three European university hospitals.
METHODS: Ninety-nine patients with PAH and 23 patients with CTEPH in New York Heart Association (NYHA) classes II-IV were followed up for a mean of 26.2 +/- 17.2 months (+/- SE) [range, 3 to 57 months]. Long-term efficacy was assessed by 6-min walking distance (SMWD), Borg dyspnea score, and NYHA class. Clinical events were monitored to assess survival and event-free survival.
RESULTS: At 3 years, significant improvements from baseline were observed in mean SMWD (305 +/- 11 to 445 +/- 12 m, p = 0.0001), Borg dyspnea score (5.7 +/- 0.2 to 4.5 +/- 1, p = 0.0006), and NYHA class (3.20 +/- 0.04 to 2.1 +/- 0.1, p = 0.0001). These changes were observed under a mean dose of subcutaneously infused treprostinil at 40 +/- 2.6 ng/kg/min (range, 16 to 84 ng/kg/min). Subcutaneously infused treprostinil was well tolerated, and local pain at the subcutaneous site accounted for treatment interruption in only 5% of the cases. Survival was 88.6% and 70.6% at 1 year and 3 years, respectively. At the same time points, the event-free survival rates, defined as survival without hospitalization for clinical worsening, transition to IV epoprostenol, and need for combination therapy or atrial septostomy, were 83.2% and 69%, respectively.
CONCLUSIONS: Long-term subcutaneous therapy with treprostinil appears to continuously improve exercise tolerance and symptoms in patients with PAH and inoperable CTEPH. Moreover, treatment may provide a significant survival benefit.

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Year:  2006        PMID: 16778286     DOI: 10.1378/chest.129.6.1636

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


  34 in total

1.  A clinical comparison of slow- and rapid-escalation treprostinil dosing regimens in patients with pulmonary hypertension.

Authors:  Nika Skoro-Sajer; Irene M Lang; Evis Harja; Meinhard P Kneussl; Wendy Gin Sing; Simon J R Gibbs
Journal:  Clin Pharmacokinet       Date:  2008       Impact factor: 6.447

Review 2.  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

3.  Subcutaneous treprostinil is well tolerated with infrequent site changes and analgesics.

Authors:  R James White; Yana Levin; Kathleen Wessman; Antonia Heininger; Karen Frutiger
Journal:  Pulm Circ       Date:  2013-11-18       Impact factor: 3.017

Review 4.  Pharmacologic therapy for pulmonary arterial hypertension in adults: CHEST guideline and expert panel report.

Authors:  Darren B Taichman; Joe Ornelas; Lorinda Chung; James R Klinger; Sandra Lewis; Jess Mandel; Harold I Palevsky; Stuart Rich; Namita Sood; Erika B Rosenzweig; Terence K Trow; Rex Yung; C Gregory Elliott; David B Badesch
Journal:  Chest       Date:  2014-08       Impact factor: 9.410

Review 5.  Novel putative pharmacological therapies to protect the right ventricle in pulmonary hypertension: a review of current literature.

Authors:  Gerald J Maarman; Rainer Schulz; Karen Sliwa; Ralph Theo Schermuly; Sandrine Lecour
Journal:  Br J Pharmacol       Date:  2017-02-24       Impact factor: 8.739

Review 6.  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

Review 7.  Idiopathic pulmonary arterial hypertension.

Authors:  Amy L Firth; Jess Mandel; Jason X-J Yuan
Journal:  Dis Model Mech       Date:  2010 May-Jun       Impact factor: 5.758

Review 8.  Optimal use of treprostinil in pulmonary arterial hypertension: a guide to the correct use of different formulations.

Authors:  Nika Skoro-Sajer
Journal:  Drugs       Date:  2012-12-24       Impact factor: 9.546

Review 9.  Comparative Safety and Tolerability of Prostacyclins in Pulmonary Hypertension.

Authors:  Caroline O'Connell; David Amar; Athénaïs Boucly; Laurent Savale; Xavier Jaïs; Marie-Camille Chaumais; David Montani; Marc Humbert; Gérald Simonneau; Olivier Sitbon
Journal:  Drug Saf       Date:  2016-04       Impact factor: 5.606

10.  2014 Guidelines of Taiwan Society of Cardiology (TSOC) for the Management of Pulmonary Arterial Hypertension.

Authors:  Chih-Hsin Hsu; Wan-Jing Ho; Wei-Chun Huang; Yu-Wei Chiu; Tsu-Shiu Hsu; Ping-Hung Kuo; Hsao-Hsun Hsu; Jia-Kan Chang; Chin-Chang Cheng; Chao-Lun Lai; Kae-Woei Liang; Shoa-Lin Lin; Hsao-Hsun Sung; Wei-Chuan Tsai; Ken-Pen Weng; Kai-Sheng Hsieh; Wei-Hsian Yin; Shing-Jong Lin; Kuo-Yang Wang
Journal:  Acta Cardiol Sin       Date:  2014-09       Impact factor: 2.672

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