|
|
||||||||
Guest Access | Sign In via User Name/Password |
|||||||||
* From the Division of Pulmonary and Critical Care Medicine, Duke University Medical Center, Durham, NC; Division of Cardiology, University of Chicago, Chicago, IL; Division of Cardiovascular Disease, University of Michigan; Department of Pediatrics, Columbia University College of Physicians & Surgeons, New York, NY; Division of Cardiology, University of Alabama, Birmingham, AL.
Correspondence to: Victor F. Tapson, MD, FCCP, Division of Pulmonary and Critical Care Medicine, Room 351 Bell Building, Duke University Medical Center, Durham, NC, 27710; e-mail: tapso001{at}mc.duke.edu
Abstract
Background: Pulmonary arterial hypertension (PAH) is a life-threatening disease for which both continuous IV epoprostenol and continuous subcutaneous treprostinil have proven effective. With continuous IV treprostinil having potential advantages over both of the above therapies, we investigated the safety and efficacy of this regimen in patients with PAH.
Methods: We conducted a 12-week, prospective, open-label, uncontrolled, multicenter study of continuous IV treprostinil in 16 patients with PAH that was idiopathic (n = 8), related to connective tissue disease (n = 6), or related to congenital heart disease (n = 2). The primary end point was change from baseline to week 12 in exercise capacity assessed by the 6-min walk (6MW) test.
Results: Continuous IV treprostinil increased 6MW distance (mean ± SE) by 82 m from baseline (319 ± 22 m) to week 12 (400 ± 26 m) [n = 14; p = 0.001]. There were also significant improvements in the secondary end points of Naughton-Balke treadmill time (p = 0.007), Borg dyspnea score (p = 0.008), and hemodynamics (mean pulmonary artery pressure, p = 0.03; cardiac index, p = 0.002; pulmonary vascular resistance, p = 0.001) at week 12 compared with baseline. Side effects were mild and consistent with those reported with prostacyclin treatment. One death, unrelated to study drug, occurred during the 12-week study in a patient who received 3 days of treprostinil and died 2 weeks later.
Conclusions: Long-term IV infusion of treprostinil is safe and appears to be effective for the treatment of patients with PAH.
Key Words: idiopathic pulmonary arterial hypertension prostacyclin analog pulmonary arterial hypertension related to congenital heart disease pulmonary arterial hypertension related to connective tissue disease treprostinil
This article has been cited by other articles:
![]() |
A. C. Widlitz, S. McDevitt, G. R. Ward, and A. Krichman Practical Aspects of Continuous Intravenous Treprostinil Therapy Crit. Care Nurse, April 1, 2007; 27(2): 41 - 50. [Full Text] [PDF] |
||||
![]() |
M. Gomberg-Maitland Learning to pair therapies and the expanding matrix for pulmonary arterial hypertension: is more better? Eur. Respir. J., October 1, 2006; 28(4): 683 - 686. [Full Text] [PDF] |
||||
![]() |
K. C. Patterson, A. Weissmann, T. Ahmadi, and H. W. Farber Imatinib Mesylate in the Treatment of Refractory Idiopathic Pulmonary Arterial Hypertension Ann Intern Med, July 18, 2006; 145(2): 152 - 153. [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |