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PMID: 8532025 Published · ppublish English Clinical Trial Comparative Study Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A comparison of continuous intravenous epoprostenol (prostacyclin) with conventional therapy for primary pulmonary hypertension.

The New England journal of medicine ·Vol. 334 ·No. 5 ·1996-02-01 ·Pages 296-301

Barst RJ, Rubin LJ, Long WA, McGoon MD, Rich S, Badesch DB, Groves BM, Tapson VF, Bourge RC, Brundage BH, Koerner SK, Langleben D, Keller CA, Murali S, Uretsky BF, Clayton LM, Jöbsis MM, Blackburn SD, Shortino D, Crow JW, Primary Pulmonary Hypertension Study Group

Abstract

Primary pulmonary hypertension is a progressive disease for which no treatment has been shown in a prospective, randomized trial to improve survival. We conducted a 12-week prospective, randomized, multicenter open trial comparing the effects of the continuous intravenous infusion of epoprostenol (formerly called prostacyclin) plus conventional therapy with those of conventional therapy alone in 81 patients with severe primary pulmonary hypertension (New York Heart Association functional class III or IV). Exercise capacity was improved in the 41 patients treated with epoprostenol (median distance walked in six minutes, 362 m at 12 weeks vs. 315 m at base line), but it decreased in the 40 patients treated with conventional therapy alone (204 m at 12 weeks vs. 270 m at base line; P < 0.002 for the comparison of the treatment groups). Indexes of the quality of life were improved only in the epoprostenol group (P < 0.01). Hemodynamics improved at 12 weeks in the epoprostenol-treated patients. The changes in mean pulmonary-artery pressure for the epoprostenol and control groups were -8 percent and +3 percent, respectively (difference in mean change, -6.7 mm Hg; 95 percent confidence interval, -10.7 to -2.6 mm Hg; P < 0.002), and the mean changes in pulmonary vascular resistance for the epoprostenol and control groups were -21 percent and +9 percent, respectively (difference in mean change, -4.9 mm Hg/liter/min; 95 percent confidence interval, -7.6 to -2.3 mm Hg/liter/min; P < 0.001). Eight patients died during the study, all of whom had been randomly assigned to conventional therapy (P = 0.003). Serious complications included four episodes of catheter-related sepsis and one thrombotic event. As compared with conventional therapy, the continuous intravenous infusion of epoprostenol produced symptomatic and hemodynamic improvement, as well as improved survival in patients with severe primary pulmonary hypertension.

MeSH Terms
Adult Anticoagulants/therapeutic use Drug Administration Schedule Epoprostenol/administration & dosage,adverse effects Exercise Tolerance/drug effects Female Hemodynamics/drug effects Humans Hypertension, Pulmonary/drug therapy,mortality,therapy Infusions, Intravenous Male Platelet Aggregation Inhibitors/administration & dosage,adverse effects Prospective Studies Survival Analysis Treatment Outcome Vasodilator Agents/therapeutic use
Chemicals
Anticoagulants Platelet Aggregation Inhibitors Vasodilator Agents Epoprostenol
Authors & Affiliations
21 authors, click to expand affiliations / ORCID
Barst R J
Department of Pediatrics, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Rubin L J
Long W A
McGoon M D
Rich S
Badesch D B
Groves B M
Tapson V F
Bourge R C
Brundage B H
Koerner S K
Langleben D
Keller C A
Murali S
Uretsky B F
Clayton L M
Jöbsis M M
Blackburn S D
Shortino D
Crow J W
Primary Pulmonary Hypertension Study Group
Investigators
33 investigators, click to expand
Horn E
Kirkpatrick J
Wynne K
Knight W
Georgiou D
Beckman J
Clarke W R
Ralph D
Schrader P
Caldwell E J
Williams W
Vogel B
Ettinger N A
Canfield D
Hill N S
Carlisle C
Hinderliter A
Willis P W
Frost A E
Chafizedah K
Ross D
Claire D
Shalit E
Edwards B
Severson C
Kosberg K
Tokaraczyk T
Kaufman L
Hartle H
Summer W R
deBoisblanc B
Everett B
Krichman A
Article Info
Journal
The New England journal of medicine
Abbr.
N Engl J Med
ISSN
0028-4793
Published
1996-02-01
Pages
296-301
Language
English
Region
United States
NLM ID
0255562
Subset
IM
Corrections
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