TY - JOUR
T1 - Sublingual administration of furosemide
T2 - New application of an old drug
AU - Haegeli, Laurent
AU - Brunner-La Rocca, Hans Peter
AU - Wenk, Markus
AU - Pfisterer, Matthias
AU - Drewe, Jürgen
AU - Krähenbühl, Stephan
PY - 2007/12
Y1 - 2007/12
N2 - Background: In patients with decompensated heart failure, absorption of orally administered furosemide may be delayed, possibly leading to impaired pharmacodynamic effects. Sublingual administration may represent an alternative in such situations. Methods: In a crossover study including 11 healthy men, 20 mg furosemide was administered intravenously, orally and sublingually on three different days. Pharmacokinetics and pharmacodynamics were assessed from repeated blood and urine samples. Results: Compared with oral administration, sublingual administration was associated with 43% higher Cmax [difference 215 ng ml-1, 95% confidence interval (CI) 37, 392], a higher urinary recovery (8.9 vs. 7.3 mg, difference 1.6 mg, 95% CI 0.3, 2.9), an 28% higher AUC (difference 328 ng h-1 ml-1, 95% CI 24, 632) and a higher bioavailability of furosemide (59 vs. 47%, difference 12.0%, 95% CI -1.2, 25.2). Sodium excretion was higher after sublingual compared with oral administration (peak excretion rate 1.8 vs. 1.4 mmol min-1, P < 0.05), whereas urine volume did not differ significantly between the two application modes. In comparison, intravenous administration showed the expected more rapid and intense response. Conclusion: Sublingually administered furosemide tablets differ in certain kinetic and dynamic properties from identical tablets given orally. Sublingual administration of furosemide may offer therapeutic advantages in certain groups of patients.
AB - Background: In patients with decompensated heart failure, absorption of orally administered furosemide may be delayed, possibly leading to impaired pharmacodynamic effects. Sublingual administration may represent an alternative in such situations. Methods: In a crossover study including 11 healthy men, 20 mg furosemide was administered intravenously, orally and sublingually on three different days. Pharmacokinetics and pharmacodynamics were assessed from repeated blood and urine samples. Results: Compared with oral administration, sublingual administration was associated with 43% higher Cmax [difference 215 ng ml-1, 95% confidence interval (CI) 37, 392], a higher urinary recovery (8.9 vs. 7.3 mg, difference 1.6 mg, 95% CI 0.3, 2.9), an 28% higher AUC (difference 328 ng h-1 ml-1, 95% CI 24, 632) and a higher bioavailability of furosemide (59 vs. 47%, difference 12.0%, 95% CI -1.2, 25.2). Sodium excretion was higher after sublingual compared with oral administration (peak excretion rate 1.8 vs. 1.4 mmol min-1, P < 0.05), whereas urine volume did not differ significantly between the two application modes. In comparison, intravenous administration showed the expected more rapid and intense response. Conclusion: Sublingually administered furosemide tablets differ in certain kinetic and dynamic properties from identical tablets given orally. Sublingual administration of furosemide may offer therapeutic advantages in certain groups of patients.
KW - Absorption
KW - Furosemide
KW - Pharmacodynamics
KW - Pharmacokinetics
KW - Sublingual administration
UR - https://www.scopus.com/pages/publications/36849046822
U2 - 10.1111/j.1365-2125.2007.03035.x
DO - 10.1111/j.1365-2125.2007.03035.x
M3 - Article
C2 - 17875188
AN - SCOPUS:36849046822
SN - 0306-5251
VL - 64
SP - 804
EP - 809
JO - British Journal of Clinical Pharmacology
JF - British Journal of Clinical Pharmacology
IS - 6
ER -