Beraprost therapy for pulmonary arterial hypertension
Robyn J. Barst, MD, FACC*,*,
Michael McGoon, MD ,
Vallerie McLaughlin, MD, FACC ,
Victor Tapson, MD, FCCP ,
Ronald Oudiz, MD, FACC||,
Shelley Shapiro, MD¶,
Ivan M. Robbins, MD#,
Richard Channick, MD**,
David Badesch, MD ,
Barry K. Rayburn, MD, FACC ,
Robin Flinchbaugh, BS ,
Jeff Sigman, BA ,
Carl Arneson, MStat ,
Roger Jeffs, PhD Beraprost Study Group
* Columbia University College of Physicians and Surgeons, New York, New York, USA
Mayo Clinic, Rochester, Minnesota, USA
Rush Presbyterian-St. Lukes Medical Center, Chicago, Illinois, USA
Duke University Medical Center, Durham, North Carolina, USA
|| Research and Education Institute at Harbor-UCLA Medical Center, Torrance, California, USA
¶ USC Medical Center, Los Angeles, California, USA
# Vanderbilt University Medical Center, Nashville, Tennessee, USA
** University of California-San Diego Medical Center, La Jolla, California, USA
 University of Colorado Health Sciences Center, Denver, Colorado, USA
 University of Alabama at Birmingham, Birmingham, Alabama, USA
 United Therapeutics Corporation, Research Triangle Park, North Carolina, USA

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Figure 1 Median change in 6-min walking distance from baseline to months 3, 6, 9, and 12 in the placebo and beraprost sodium (BPS) groups; p = 0.010 at 3 months; p = 0.016 at 6 months; p = 0.098 at 9 months; and p = 0.180 at 12 months (adjusted for center, etiology, and baseline peak oxygen consumption, 6-min walk, Borg dyspnea score, and vasodilator use). Worst rank for all missing data.
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Figure 2 Mean change in Borg dyspnea score from baseline to months 3, 6, 9, and 12 in the placebo and beraprost sodium (BPS) groups; p = 0.24 at 3 months; p = 0.27 at 6 months; p = 0.92 at 9 months; and p = 0.75 at 12 months (analysis of covariance adjusted for center, etiology, and baseline peak oxygen consumption, 6-min walk distance, Borg dyspnea score, and vasodilator use). Black bars = BPS; white bars = placebo. Number in the bars = exact mean rates; lines = standard error of the mean.
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