Population pharmacokinetics of carvedilol in patients with congestive heart failure. Issue 8 (31st May 2013)

• Record Type: Journal Article
• Authors: Nikolic, Valentina N.; Jankovic, Slobodan M.; Velickovic‐Radovanović, Radmila; Apostolović, Svetlana; Stanojevic, Dragana; Zivanovic, Slavoljub; Stefanovic, Nikola; Pesic, Srdjan; Jevtovic‐Stoimenov, Tatjana; Djuric, Janko; Markovic, Veroljub; Milovanovic, Jasmina R.
• Is Part Of: Journal of pharmaceutical sciences. Volume 102:Issue 8(2013:Aug.)
• Page Start: 2851
• Page End: 2858
• Publication Date: 2013-05-31
• Subjects: population pharmacokinetics -- HPLC -- clearance -- cytohrome P450 -- genetic polymorphism -- polymerase chain reaction; Pharmacy -- Periodicals; 615.1
• DOI: 10.1002/jps.23626
• Languages: English
• ISSNs: 0022-3549

Abstract

Abstract: The aim of this study was to derive population pharmacokinetic (PK) model for clearance (CL) of carvedilol in adult patients with chronic heart failure (CHF). Medication and demographic data were obtained from 52 Caucasian patients with CHF taking carvedilol. Population PK analysis was performed by nonlinear mixed‐effects modeling (NONMEM) to estimate and identify different factors that could affect carvedilol CL. A total of 55 plasma concentrations were collected from 52 patients with mean age of 63.02 ± 11.95 years and total body weight (TBW) of 77.96 ± 13.46 kg. Total daily doses of carvedilol in the target population had wide range of variability (6.25–50 mg), followed by high variability of drug plasma concentrations (1–59.07 ng/mL). The typical mean value for carvedilol CL, estimated by the base model, in the target population was 43.8 L/h. The TBW, concomitant therapy with digoxin, and tobacco using were determinants of a derived population model. The final regression model for the CL of carvedilol is: Our results suggest that the TBW, concomitant therapy with digoxin, and tobacco using are the main subjects of carvedilol PK variability. © 2013 Wiley Periodicals, Inc. and the American Pharmacists Association J Pharm Sci 102:2851–2858, 2013