Beraprost therapy for pulmonary arterial hypertension

被引:495
作者
Barst, RJ
McGoon, M
McLaughlin, V
Tapson, V
Oudiz, R
Shapiro, S
Robbins, IM
Channick, R
Badesch, D
Rayburn, BK
Flinchbaugh, R
Sigman, J
Arneson, C
Jeffs, R
机构
[1] Columbia Univ, Coll Phys & Surg, New York, NY 10032 USA
[2] Mayo Clin, Rochester, MN USA
[3] Rush Presbyterian St Lukes Med Ctr, Chicago, IL 60612 USA
[4] Duke Univ, Med Ctr, Durham, NC 27706 USA
[5] Harbor UCLA Med Ctr, Res & Educ Inst, Torrance, CA 90509 USA
[6] USC Med Ctr, Los Angeles, CA USA
[7] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[8] Univ Calif San Diego, Med Ctr, La Jolla, CA 92093 USA
[9] Univ Colorado, Hlth Sci Ctr, Denver, CO 80202 USA
[10] Univ Alabama Birmingham, Birmingham, AL USA
[11] United Therapeut Corp, Res Triangle Pk, NC USA
关键词
D O I
10.1016/S0735-1097(03)00463-7
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The purpose of this study was to assess the safety and efficacy of the oral prostacyclin analogue beraprost sodium during a 12-month double-blind, randomized, placebo-controlled trial in patients with pulmonary arterial hypertension (PAH). BACKGROUND Pulmonary arterial hypertension is a progressive disease that ultimately causes right heart failure and death. Despite the risks from its delivery system, continuous intravenous epoprostenol remains the most efficacious treatment currently available. METHODS A total of 116 patients with World Health Organization (WHO) functional class II or III primary pulmonary hypertension or PAH related to either collagen vascular diseases or congenital systemic to pulmonary shunts were enrolled. Patients were randomized to receive the maximal tolerated dose of beraprost sodium (median dose 120 [,g four times a day) or placebo for 12 months. The primary end point was disease progression; i.e., death, transplantation, epoprostenol rescue, or 25% decrease in peak oxygen consumption (VO2). Secondary end points included exercise capacity assessed by 6-min walk test and peak VO2, Borg dyspnea score, hemodynamics, symptoms of PAH, and quality of life. RESULTS Patients treated with beraprost exhibited less evidence of disease progression at six months (p = 0.002), but this effect was not evident at either shorter or longer follow-up intervals. Similarly, beraprost-treated patients had improved 6-min walk distance at 3 months by 22 m from baseline and at 6 months by 31 m (p = 0.010 and 0.016, respectively) compared with placebo, but not at either 9 or 12 months. Drug-related adverse events were common and were related to the disease and/or expected prostacyclin adverse events. CONCLUSIONS These data suggest that beneficial effects may occur during early phases of treatment with beraprost in WHO functional class II or III patients but that this effect attenuates with time. (J Am Coll Cardiol 2003;41:2119-25). (C) 2003 by the American College of Cardiology Foundation.
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收藏
页码:2119 / 2125
页数:7
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