Abstract
Our aims were to elucidate the factors that affected vancomycin (VCM) serum trough levels and to find the optimal initial dose based on creatinine clearance (CrCl) and body weight (BW) to minimize inadequate trough levels in a retrospective observational study among Japanese adults. One hundred and six inpatients, in whom VCM trough levels were measured after completing the third dosing, were consecutively recruited into our study in a tertiary hospital. We considered the frequency of <30% as low. In the generalized linear model, initial VCM total daily dose, CrCl, and BW were independent risk factors of VCM trough levels. In patients with CrCl ≥30 and <50 mL/min, 1 g/day yielded low frequencies of a trough level of ≥20 mcg/mL, regardless of BW. In patients with CrCl ≥50 mL/min, 2 g/day yielded low frequencies of a trough level of <10 mcg/mL in patients weighing <55 kg, but not in patients weighing ≥55 kg. Optimal VCM initial total daily dose may be 1 g/day in patients with CrCl ≥30 and <50 mL/min regardless of BW and 2 g/day in patients weighing <55 kg with CrCl ≥50 mL/min among Japanese adults.
Similar content being viewed by others
References
Geraci JE (1977) Vancomycin. Mayo Clin Proc 52:631–634
Cook FV, Farrar WE Jr (1978) Vancomycin revisited. Ann Intern Med 88:813–818
Bailie GR, Neal D (1988) Vancomycin ototoxicity and nephrotoxicity. A review. Med Toxicol Adverse Drug Exp 3:376–386
Geraci JE, Heilman FR, Nichols DR, Wellman EW, Ross GT (1956) Some laboratory and clinical experiences with a new antibiotic, vancomycin. In: Welch H, Marti-Ibanez F (eds) Antibiotics annual 1956–1957. Medical Encyclopedia Inc., New York, pp 90–106
Cockcroft DW, Gault MH (1976) Prediction of creatinine clearance from serum creatinine. Nephron 16:31–41
Llopis-Salvia P, Jiménez-Torres NV (2006) Population pharmacokinetic parameters of vancomycin in critically ill patients. J Clin Pharm Ther 31:447–454
Moellering RC Jr, Krogstad DJ, Greenblatt DJ (1981) Vancomycin therapy in patients with impaired renal function: a nomogram for dosage. Ann Intern Med 94:343–346
Matzke GR, McGory RW, Halstenson CE, Keane WF (1984) Pharmacokinetics of vancomycin in patients with various degrees of renal function. Antimicrob Agents Chemother 25:433–437
Maeda Y, Omoda K, Fukuhara S, Ohta M, Ishii Y, Murakami T (2006) Evaluation of clinical efficacy of Maeda’s nomogram for vancomycin dosage adjustment in adult Japanese MRSA pneumonia patients. Drug Metab Pharmacokinet 21:54–60
Lake KD, Peterson CD (1985) A simplified dosing method for initiating vancomycin therapy. Pharmacotherapy 5:340–344
Pryka RD, Rodvold KA, Erdman SM (1991) An updated comparison of drug dosing methods. Part IV: vancomycin. Clin Pharmacokinet 20:463–476
Cohen E, Dadashev A, Drucker M, Samra Z, Rubinstein E, Garty M (2002) Once-daily versus twice-daily intravenous administration of vancomycin for infections in hospitalized patients. J Antimicrob Chemother 49:155–160
Rybak M, Lomaestro B, Rotschafer JC, Moellering R Jr, Craig W, Billeter M, Dalovisio JR, Levine DP (2009) Therapeutic monitoring of vancomycin in adult patients: a consensus review of the American Society of Health-System Pharmacists, the Infectious Diseases Society of America, and the Society of Infectious Diseases Pharmacists. Am J Health Syst Pharm 66:82–98. doi:10.2146/ajhp080434
Tsuji BT, Rybak MJ, Lau KL, Sakoulas G (2007) Evaluation of accessory gene regulator (agr) group and function in the proclivity towards vancomycin intermediate resistance in Staphylococcus aureus. Antimicrob Agents Chemother 51:1089–1091
Sakoulas G, Eliopoulos GM, Moellering RC Jr, Novick RP, Venkataraman L, Wennersten C, DeGirolami PC, Schwaber MJ, Gold HS (2003) Staphylococcus aureus accessory gene regulator (agr) group II: is there a relationship to the development of intermediate-level glycopeptide resistance? J Infect Dis 187:929–938
Murphy JE, Gillespie DE, Bateman CV (2006) Predictability of vancomycin trough concentrations using seven approaches for estimating pharmacokinetic parameters. Am J Health Syst Pharm 63:2365–2370
Tajiri C, Yuasa S, Kabeya M, Aoki Y, Kawai M, Kusafuka H (2009) Comparison of predictive formulas of renal function for initial dose regimen of vancomycin hydrochloride: Cockcroft & Gault, Horio and Japanese Estimated GFR Formulas. Jpn J Ther Drug Monit 26:103–110 (in Japanese, abstract in English)
Acknowledgments
The authors are grateful for the assistance of Toshiyuki Ojima, Takahiro Mochizuki, Norio Ohmagari, Taro Takeshima, Hitoshi Ando, Koichi Sakamoto, Harumi Yano, Masaki Toshima, Toyomi Kamesaki, and the Clinical Research Support Team (CRST) of Jichi Medical University. Some information about vancomycin was provided by Shionogi Co., Ltd., Osaka, Japan. The authors have declared no conflicts of interest.
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Maki, N., Ohkuchi, A., Tashiro, Y. et al. Initial dose of vancomycin based on body weight and creatinine clearance to minimize inadequate trough levels in Japanese adults. Eur J Clin Microbiol Infect Dis 31, 2537–2543 (2012). https://doi.org/10.1007/s10096-012-1593-y
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10096-012-1593-y