Literature DB >> 20556772

Teicoplanin versus vancomycin for proven or suspected infection.

Alexandre B Cavalcanti1, Anderson R Goncalves, Claudia S Almeida, Diogo Dg Bugano, Eliezer Silva.   

Abstract

BACKGROUND: Vancomycin and teicoplanin are commonly used to treat gram-positive infections, particularly those caused by methicillin-resistant Staphylococcus aureus (MRSA). There is uncertainty regarding the effects of teicoplanin compared to vancomycin on kidney function with some previous studies suggesting teicoplanin is less nephrotoxic than vancomycin.
OBJECTIVES: To investigate the efficacy and safety of vancomycin versus teicoplanin in patients with proven or suspected infection. SEARCH STRATEGY: We searched the Cochrane Renal Group's Specialised Register, CENTRAL, MEDLINE, EMBASE, reference lists of nephrology textbooks, review articles with relevant studies and sent letters seeking information about unpublished or incomplete studies to investigators involved in previous studies. SELECTION CRITERIA: We searched for randomised controlled trials (RCTs) in any language comparing teicoplanin to vancomycin for patients with proven or suspected infection. DATA COLLECTION AND ANALYSIS: Two authors independently evaluated methodological quality and extracted data using standardised data extraction forms. Study investigators were contacted for information not available in the original manuscripts. Random effects model was used to estimate the pooled risk ratio (RR) with 95% confidence interval (CI). MAIN
RESULTS: We included 24 studies (2,610 patients) in this review. Teicoplanin reduced the risk of nephrotoxicity compared to vancomycin (RR 0.66, 95% CI 0.48 to 0.90).The effects of teicoplanin or vancomycin were similar for clinical cure (RR 1.03, 95% CI 0.98 to 1.08), microbiological cure (RR 0.98, 95% CI 0.93 to 1.03) and mortality (RR 1.02, 95% CI 0.79 to1.30). Six studies reported no cases of acute kidney injury (AKI) needing dialysis. Adverse events were less frequent with teicoplanin including cutaneous rash (RR 0.57, 95% CI 0.35 to 0.92), red man syndrome (RR 0.21, 95% CI 0.08 to 0.59) and total adverse events (RR 0.73, 95% CI 0.53 to 1.00). A lower risk of nephrotoxicity with teicoplanin was observed in patients either with (RR 0.51, 95% CI 0.30 to 0.88) or without aminoglycosides (RR 0.31, 95% 0.07 to 1.50), and also when vancomycin dosing was guided by serum levels (RR 0.22, 95% CI 0.10 to 0.52). AUTHORS'
CONCLUSIONS: Teicoplanin and vancomycin are both effective in treating those with proven or suspected infection; however the incidence of adverse effects including nephrotoxicity was lower with teicoplanin. There were no cases of AKI needing dialysis. It remains unclear whether the differential effect on kidney function should influence which antibiotic be prescribed, although it may be reasonable to consider teicoplanin for patients at higher risk for AKI needing dialysis.

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Year:  2010        PMID: 20556772     DOI: 10.1002/14651858.CD007022.pub2

Source DB:  PubMed          Journal:  Cochrane Database Syst Rev        ISSN: 1361-6137


  29 in total

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Review 2.  [Antibiotic dosing for renal function disorders and continuous renal replacement therapy].

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3.  Improving Clinical Outcomes in Patients With Methicillin-Sensitive Staphylococcus aureus Bacteremia and Reported Penicillin Allergy.

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Review 4.  Vancomycin and the Risk of AKI: A Systematic Review and Meta-Analysis.

Authors:  Abhisekh Sinha Ray; Ammar Haikal; Kassem A Hammoud; Alan S L Yu
Journal:  Clin J Am Soc Nephrol       Date:  2016-11-28       Impact factor: 8.237

5.  Population Pharmacokinetics of Teicoplanin in Preterm and Term Neonates: Is It Time for a New Dosing Regimen?

Authors:  A Kontou; K Sarafidis; O Begou; H G Gika; A Tsiligiannis; K Ogungbenro; A Dokoumetzidis; E Agakidou; E Roilides
Journal:  Antimicrob Agents Chemother       Date:  2020-03-24       Impact factor: 5.191

Review 6.  Total Syntheses of Vancomycin-Related Glycopeptide Antibiotics and Key Analogues.

Authors:  Akinori Okano; Nicholas A Isley; Dale L Boger
Journal:  Chem Rev       Date:  2017-04-24       Impact factor: 60.622

7.  Population pharmacokinetics and pharmacodynamics of teicoplanin in neonates: making better use of C-reactive protein to deliver individualized therapy.

Authors:  V Ramos-Martín; M N Neely; P McGowan; S Siner; K Padmore; M Peak; M W Beresford; M A Turner; S Paulus; W W Hope
Journal:  J Antimicrob Chemother       Date:  2016-08-19       Impact factor: 5.790

8.  Multicenter prospective observational study of the comparative efficacy and safety of vancomycin versus teicoplanin in patients with health care-associated methicillin-resistant Staphylococcus aureus bacteremia.

Authors:  Young Kyung Yoon; Dae Won Park; Jang Wook Sohn; Hyo Youl Kim; Yeon-Sook Kim; Chang-Seop Lee; Mi Suk Lee; Seong-Yeol Ryu; Hee-Chang Jang; Young Ju Choi; Cheol-In Kang; Hee Jung Choi; Seung Soon Lee; Shin Woo Kim; Sang Il Kim; Eu Suk Kim; Jeong Yeon Kim; Kyung Sook Yang; Kyong Ran Peck; Min Ja Kim
Journal:  Antimicrob Agents Chemother       Date:  2013-10-28       Impact factor: 5.191

9.  Therapeutic drug concentrations of teicoplanin in clinical settings.

Authors:  So-Yun Nah; Jae Hyoung Im; Jin Yeob Yeo; Ji-Hyeon Baek; Cheol-Woo Kim; Moon-Seok Nam; Hye-Kyung Lee; Moon-Hyun Chung; Jin-Soo Lee
Journal:  Infect Chemother       Date:  2014-03-21

10.  Risk factors for failure of outpatient parenteral antibiotic therapy (OPAT) in infective endocarditis.

Authors:  Christopher J A Duncan; David A Barr; Antonia Ho; Emma Sharp; Lindsay Semple; R Andrew Seaton
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