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Safety, tolerability and pharmacokinetics of an intravenous bolus of sildenafil in patients with pulmonary arterial hypertension

Authors :
Xiang Gao
Robert Naeije
Hunter Gillies
Sandrine Huez
Naoto Hayashi
Jean-Luc Vachiery
Gary Layton
Source :
British Journal of Clinical Pharmacology. 71:289-292
Publication Year :
2011
Publisher :
Wiley, 2011.

Abstract

WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT Pulmonary arterial hypertension (PAH) is a rare syndrome of dyspnoea and fatigue due to an increase in pulmonary vascular resistance. Although the disease remains incurable, targeted therapies have been shown to be beneficial to patients. Oral sildenafil (20 mg three times daily) is a phosphodiesterase type 5 inhibitor with proven efficacy on exercise capacity, symptoms and pulmonary haemodynamics in patients with PAH. WHAT THIS STUDY ADDS It is advisable that chronic therapies for PAH, including oral sildenafil, not be interrupted. However, patients may not be able to take their medication because of an intervening illness or a requirement to undergo general anaesthesia, preventing oral drug administration. This study demonstrates that an intravenous bolus of 10 mg sildenafil in stable patients with PAH is safe, well tolerated and maintains plasma levels to preserve drug exposure. AIMS To assess pharmacokinetics and pharmacodynamics of a 10 mg intravenous sildenafil bolus in pulmonary arterial hypertension (PAH) patients stabilized on 20 mg sildenafil orally three times daily. METHODS Pharmacokinetic parameters were calculated using noncompartmental analysis. RESULTS After an acute increase, plasma concentrations stabilized within the range reported previously for a 20 mg oral tablet. At 0.5 h, mean ± SD changes from baseline were βˆ’8.4 ± 11.7 mmHg (systolic pressure), βˆ’2.6 ± 7.3 mmHg (diastolic pressure) and βˆ’3.5 ± 10.4 beats minβˆ’1 (heart rate). There was no symptomatic hypotension. CONCLUSIONS Although further research is warranted, a 10 mg sildenafil intravenous bolus appears to provide similar exposure, tolerability and safety to the 20 mg tablet.

Details

ISSN :
03065251
Volume :
71
Database :
OpenAIRE
Journal :
British Journal of Clinical Pharmacology
Accession number :
edsair.doi...........2819bc5602d8f89594163857f53f0b79