全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...
PLOS ONE  2013 

Benefits of Therapeutic Drug Monitoring of Vancomycin: A Systematic Review and Meta-Analysis

DOI: 10.1371/journal.pone.0077169

Full-Text   Cite this paper   Add to My Lib

Abstract:

Background and Objective The necessity of therapeutic drug monitoring (TDM) for vancomycin is controversial. The objective of the current review was to evaluate the available evidence for the necessity of TDM in patients given vancomycin to treat Gram-positive infections. Methods Medline, Embase, Web of Sciences, the Cochrane Library and two Chinese literature databases (CNKI, CBM) were searched. Randomized controlled studies and observational studies that compared the clinical outcomes of TDM groups vs. non-TDM groups were included. Two reviewers independently extracted the data. The primary outcome was clinical efficacy of therapy. Secondary outcomes included vancomycin associated nephrotoxicity, duration of vancomycin therapy, length of hospital stay, and mortality. Meta-analysis was performed using the Mantel-Haenszel fixed effect method (FEM). Odds ratios (ORs) or weighted mean differences (WMD) with 95% confidence intervals (95%CIs) were calculated for categorical and continuous outcomes, respectively. Results One randomized controlled trial (RCT) and five cohort studies were included in the meta-analysis. Compared with non-TDM groups, TDM groups had significantly higher rates of clinical efficacy (OR = 2.62, 95%CI 1.34–5.11 P = 0.005) and decreased rates of nephrotoxicity (OR = 0.25, 95%CI 0.13–0.48 P<0.0001). Subgroup analyses showed that TDM group had significantly higher rates of clinical efficacy in both cohort studies subgroup (OR = 3.04, 95%CI 1.34–6.90) and in Asian population subgroup (OR = 3.04, 95%CI 1.34–6.90). TDM group had significantly decreased rates of nephrotoxicity in all subgroup. There was no significant difference in duration of vancomycin therapy (WMD = ?0.40, 95%CI ?2.83–2.02 P = 0.74) or length of stay (WMD = ?1.01, 95%CI ?7.51-5.49 P = 0.76) between TDM and non-TDM groups. Subgroup analyses showed there were no differences in duration of vancomycin therapy. Only one study reported mortality rates. Conclusions Studies to date show that TDM significantly increases the rate of clinical efficacy and decreases the rate of nephrotoxicity in patients treated with vancomycin.

References

[1]  Cataldo MA, Tacconelli E, Grilli E, Pea F, Petrosillo N (2012) Continuous versus intermittent infusion of vancomycin for the treatment of Gram-positive infections: systematic review and meta-analysis. J Antimicrob Chemother 67: 17–24.
[2]  Moellering RC Jr (2006) Vancomycin: a 50-year reassessment. Clin Infect Dis 42 Suppl 1: S3–4.
[3]  Levine DP (2006) Vancomycin: a history. Clin Infect Dis 42 Suppl 1: S5–12.
[4]  Rybak MJ (2006) The pharmacokinetic and pharmacodynamic properties of vancomycin. Clin Infect Dis 42 Suppl 1: S35–39.
[5]  Darko W, Medicis JJ, Smith A, Guharoy R, Lehmann DE (2003) Mississippi mud no more: cost-effectiveness of pharmacokinetic dosage adjustment of vancomycin to prevent nephrotoxicity. Pharmacotherapy 23: 643–650.
[6]  Cantu TG, Yamanaka-Yuen NA, Lietman PS (1994) Serum vancomycin concentrations: Reappraisal of their clinical value. Clin Infect Dis 18: 533–543.
[7]  Karachalios GN, Tziviskou EM (1998) Vancomycin: Is it necessary the therapeutic drug monitoring? Epitheorese Klinikes Farmakologias kai Farmakokinetikes 16: 110–119.
[8]  Pryka RD (1994) Vancomycin serum concentration monitoring: a continued debate. Ann Pharmacother 28: 1397–1399.
[9]  Moellering RC Jr (1994) Monitoring serum vancomycin levels: climbing the mountain because it is there? Clin Infect Dis 18: 544–546.
[10]  Rybak M, Lomaestro B, Rotschafer JC, Moellering R Jr, Craig W, et al. (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.
[11]  Matsumoto K, Takesue Y, Ohmagari N, Mochizuki T, Mikamo H, et al. (2013) Practice guidelines for therapeutic drug monitoring of vancomycin: a consensus review of the Japanese Society of Chemotherapy and the Japanese Society of Therapeutic Drug Monitoring. J Infect Chemother
[12]  Howden BP, Ward PB, Charles PG, Korman TM, Fuller A, et al. (2004) Treatment outcomes for serious infections caused by methicillin-resistant Staphylococcus aureus with reduced vancomycin susceptibility. Clin Infect Dis 38: 521–528.
[13]  Lodise TP, Graves J, Evans A, Graffunder E, Helmecke M, et al. (2008) Relationship between vancomycin MIC and failure among patients with methicillin-resistant Staphylococcus aureus bacteremia treated with vancomycin. Antimicrob Agents Chemother 52: 3315–3320.
[14]  Sakoulas G, Moise-Broder PA, Schentag J, Forrest A, Moellering RC Jr, et al. (2004) Relationship of MIC and bactericidal activity to efficacy of vancomycin for treatment of methicillin-resistant Staphylococcus aureus bacteremia. J Clin Microbiol 42: 2398–2402.
[15]  Hidayat LK, Hsu DI, Quist R, Shriner KA, Wong-Beringer A (2006) High-dose vancomycin therapy for methicillin-resistant Staphylococcus aureus infections: efficacy and toxicity. Arch Intern Med 166: 2138–2144.
[16]  De Cock P, Haegeman E, Goerlandt N, Vanhaesebrouck P, Stove V, et al. (2010) Focused Conference Group: P13 - Maximising benefits and minimizing harms from drugs vancomycin dosing and monitoring in children: Compliance with guidelines in a belgian teaching hospital. Basic Clin Pharmacol 107: 250–251.
[17]  Li J, Udy AA, Kirkpatrick CM, Lipman J, Roberts JA (2012) Improving vancomycin prescription in critical illness through a drug use evaluation process: a weight-based dosing intervention study. Int J Antimicrob Ag 39: 69–72.
[18]  Khotaei GT, Jam S, SeyedAlinaghi S, Motamed F, Nejat F, et al. (2010) Monitoring of serum vancomycin concentrations in pediatric patients with normal renal function. Acta Medica Iranica 48: 91–94.
[19]  Mariani-Kurkdjian P, Nebbad H, Aujard Y, Bingen E (2008) [Monitoring serum vancomycin concentrations in the treatment of Staphylococcus infections in children]. Arch Pediatr 15: 1625–1629.
[20]  Commandeur D, Giacardi C, Danguy Des Deserts M, Huynh S, Buguet-Brown ML, et al. (2011) [Monitoring vancomycin in an intensive care unit: A retrospective survey on 66 patients]. Med Mal Infect 41: 410–414.
[21]  Reis AGAC, Grisi SJFE (1996) Monitorization of blood levels of vancomycin in children with multi-resistant bacterial infections. Jornal de Pediatria 72: 225–229.
[22]  Pea F, Poz D, Baraldo M, Furlanut M (2000) Optimisation of vancomycin regimen in neutropenic haematological patients with normal renal function - Multiple daily doses may be preferable. Clin Drug Invest 19: 213–218.
[23]  Miles MV, Li L, Lakkis H, Youngblood J, McGinnis P (1997) Special considerations for monitoring vancomycin concentrations in pediatric patients. Ther Drug Monit 19: 265–270.
[24]  Hochart C, Berthon C, Corm S, Gay J, Cliquennois M, et al. (2011) Vancomycin serum concentration during febrile neutropenia in patients with acute myeloid leukemia. Med Mal Infect 41: 652–656.
[25]  Marengo LL, Del Fiol Fde S, Oliveira Sde J, Nakagawa C, Croco EL, et al. (2010) Vancomycin: the need to suit serum concentrations in hemodialysis patients. Braz J Infect Dis 14: 203–208.
[26]  Eiland LS, English TM, Eiland EH (2011) Assessment of vancomycin dosing and subsequent serum concentrations in pediatric patients. Ann Pharmacother 45: 582–589.
[27]  Wells GS, Shea B, O'Connell D, Peterson J, Welch V, et al. (2005) The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. http://www.ohri.ca/programs/clinical_epi?demiology/oxford.htm (20 Apirl 2013, data last accessed).
[28]  Begg CB, Mazumdar M (1994) Operating characteristics of a rank correlation test for publication bias. Biometrics 50: 1088–1101.
[29]  Egger M, Davey Smith G, Schneider M, Minder C (1997) Bias in meta-analysis detected by a simple, graphical test. BMJ 315: 629–634.
[30]  Welty TE, Copa AK (1994) Impact of vancomycin therapeutic drug monitoring on patient care. Ann Pharmacother 28: 1335–1339.
[31]  Fernandez de Gatta MD, Calvo MV, Hernandez JM, Caballero D, San Miguel JF, et al. (1996) Cost-effectiveness analysis of serum vancomycin concentration monitoring in patients with hematologic malignancies. Clin Pharmacol Ther 60: 332–340.
[32]  Iwamoto T, Kagawa Y, Kojima M (2003) Clinical efficacy of therapeutic drug monitoring in patients receiving vancomycin. Biol Pharm Bull 26: 876–879.
[33]  Sato S, Saito Y (2007) Evaluation of the usefulness of vancomycin dosage design based on pharmacokinetics/pharmacodynamics theory. Jpn J Chemother 55: 220–224.
[34]  Mochizuki T, Sato T, Okinaka K, Kishida N, Fujita T, et al. (2010) Efficacy and safety for vancomycin in uncomplicated catheter-related bloodstream infection by coagulase negative Staphylococcus. Jpn J Chemother 58: 233–238.
[35]  Huang YZ, Mao MY, Yuan KX (2011) Clinical application of drug monitoring of vancomycin. Chin J Infec Chemother 11: 295–298.
[36]  Jeffres MN, Isakow W, Doherty JA, McKinnon PS, Ritchie DJ, et al. (2006) Predictors of mortality for methicillin-resistant Staphylococcus aureus health-care-associated pneumonia: specific evaluation of vancomycin pharmacokinetic indices. Chest 130: 947–955.
[37]  Zhang C, Zhai SD, Liu F (2009) Necessarity of therapeutic drug monitoring of vancomycin in clinical use: a systematicreview. Chin J Clin Pharmacol 25: 329–333.
[38]  Long C, Che Amin N, Manan M (2011) Population pharmacokinetics of vancomycin in hospitalized adult patients at a Malaysian tertiary care hospital. Eur J Pharm Sci 44: 195–196.
[39]  van de Vijsel LM, Walker SA, Walker SE, Yamashita S, Simor A, et al. (2010) Initial vancomycin dosing recommendations for critically ill patients undergoing continuous venovenous hemodialysis. Can J Hosp Pharm 63: 196–206.
[40]  Vazquez M, Fagiolino P, Boronat A, Buroni M, Maldonado C (2008) Therapeutic drug monitoring of vancomycin in severe sepsis and septic shock. Int J Clin Pharmacol Ther 46: 140–145.
[41]  Lau AH, John E (1988) Elimination of vancomycin by continuous arteriovenous hemofiltration. Child Nephrol Urol 9: 232–235.
[42]  Pea F, Porreca L, Baraldo M, Furlanut M (2000) High vancomycin dosage regimens required by intensive care unit patients cotreated with drugs to improve haemodynamics following cardiac surgical procedures. J Antimicrob Chemoth 45: 329–335.
[43]  Al-Kofide H, Zaghloul I, Al-Naim L (2010) Pharmacokinetics of vancomycin in adult cancer patients. J Oncol Pharm Pract 16: 245–250.
[44]  Badran EF, Shamayleh A, Irshaid YM (2011) Pharmacokinetics of vancomycin in neonates admitted to the neonatology unit at the Jordan University Hospital. Int J Clin Pharmacol Ther 49: 252–257.
[45]  Golestaneh L, Gofran A, Mokrzycki MH, Chen JL (2009) Removal of vancomycin in sustained low-efficiency dialysis (SLED): a need for better surveillance and dosing. Clin Nephrol 72: 286–291.
[46]  Dolton M, Xu H, Cheong E, Maitz P, Kennedy P, et al. (2010) Vancomycin pharmacokinetics in patients with severe burn injuries. Burns 36: 469–476.

Full-Text

Contact Us

service@oalib.com

QQ:3279437679

WhatsApp +8615387084133