Recent discoveries in the disease pathophysiology of pulmonary arterial hypertension have been translated into effective therapies tested in clinical trials. The studies have focused on surrogate and intermediate end points, thought to reflect quantity and quality of life, respectively The authors present the necessary requirements for establishing the reliability and validity of such end points before they may be used dependably. The authors also review the available data, strengths, and weaknesses of potential end points in pulmonary arterial hypertension.
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Baylor Coll Med, Div Pulm & Crit Care Med, Houston, TX 77030 USAUniv Bologna, Inst Cardiol, I-40138 Bologna, Italy
Safdar, Zeenat
Shapiro, Shelley
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Univ Calif Los Angeles, David Geffen Sch Med, Greater Los Angeles Vet Affairs Healthcare Syst, Los Angeles, CA 90095 USAUniv Bologna, Inst Cardiol, I-40138 Bologna, Italy
Shapiro, Shelley
White, R. James
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Univ Rochester, Div Pulm & Crit Care Med, Rochester, NY USAUniv Bologna, Inst Cardiol, I-40138 Bologna, Italy
White, R. James
Chan, Melanie
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Eli Lilly & Co, Toronto, ON, CanadaUniv Bologna, Inst Cardiol, I-40138 Bologna, Italy