Abstract

BackgroundVancomycin, the first line antibiotic for methicillin-resistant Staphylococcus aureus (MRSA) bacteremia, is often administered inappropriately when MIC is greater than 2 µg/mL, including ‘susceptible’ strains. This study assessed the discordance of vancomycin minimum inhibitory concentration (MIC) for methicillin-resistant Staphylococcus aureus (MRSA).MethodsIn total, 229 MRSA isolates from blood cultures collected between 2009 and 2015 at a tertiary hospital in Taiwan were examined. The MICs of vancomycin were measured using Vitek 2, E-test, and standard broth microdilution at the level of 2 µg/mL.ResultsThe geometric mean of the MICs of hospital-acquired MRSA was higher than that of community-acquired MRSA (P < 0.001), with the exact agreement rates (with broth microdilution) at 2 µg/mL being 53.6% in Vitek 2 and 86.7% in E-test. Overall, E-test (98.1%) had more categorical accordance than did Vitek 2 (94.0%; P = 0.026). Vitek 2 had a tendency to overestimate MRSA in high-MIC isolates, whereas E-test inclined underestimation in low-MIC isolates. Surprisingly, the discordance rates of MRSA vancomycin MICs were higher in hospital-acquired isolates (13.3%–17.0%) than in community-acquired isolates (6.2%–7.0%).ConclusionThe Infectious Diseases Society of America recommends the use of alternative antimicrobial agents when vancomycin MIC is ≥ 2 µg/mL; in this study, only 53.6% of the isolates tested using Vitek 2 showed a high MIC in the broth microdilution method. Accurate identification of the resistance profile is a key component of antimicrobial stewardship programs. Therefore, to reduce inappropriate antibiotic use and mitigate the emergence of resistant strains, we recommend using complementary tests such as E-test or Broth microdilution to verify the MIC before administering second-line antibiotics.Strengths(1) We compared the categorical agreement between different methods measuring MRSA MICs level. (2) Physicians should incorporate this information and consider a complementary test to verify the appropriateness of the decision of shifting vancomycin to second-line antibiotic treatment to improve patients’ prognosis. (3) MRSA-vancomycin MICs at a cutoff of 2 µg/mL obtained using Vitek II exhibited a higher sensitivity level and negative predictive value than those obtained using E-test in the prediction of categorical agreement with standard broth microdilution.Limitation(1) Our research was based on a single hospital-based study. (2) The MRSA strains in this study were stored for more than 12 months after isolation. (3) We did not collect information on clinical prognosis.

Highlights

  • Staphylococcus aureus is a common bacterium and opportunistic pathogen that thrives on skin and mucosal surfaces, and often can cause a range of mild to severe infections if it enters the body through breaks in these surfaces

  • This study focused on a cross comparison of the minimum inhibitory concentration (MIC) of invasive methicillin-resistant Staphylococcus aureus (MRSA) initially detected with Vitek II

  • Previous studies have stated that E-tests over estimated high vancomycin MICs and Vitek II might fail to detect vancomycin MIC elevation (Swenson et al, 2009; Bloomgren & Laible, 2013; Tomczak et al, 2013), our results revealed that the E-test derived MICs were highly consistent with those provided by broth microdilution

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Summary

Introduction

Staphylococcus aureus is a common bacterium and opportunistic pathogen that thrives on skin and mucosal surfaces, and often can cause a range of mild to severe infections if it enters the body through breaks in these surfaces. This pathogen has been building up resistance to conventional penicillins because of the widely inappropriate use of penicillin. The Infectious Diseases Society of America recommends the use of alternative antimicrobial agents when vancomycin MIC is ≥ 2 μg/mL; in this study, only 53.6% of the isolates tested using Vitek 2 showed a high MIC in the broth microdilution method. To reduce inappropriate antibiotic use and mitigate the emergence of resistant strains, we recommend using complementary

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