Table 1.
Method | Advantage | Disadvantage | Comments |
---|---|---|---|
Broth dilution | Well-standardised | Time-consuming | Quantitative ** |
Harmonised | Individual mistakes | ||
Commercially available tests are easy to perform | |||
Agar Dilution | Well-standardised | Time-consuming | Quantitative |
Suitable for testing a large number of isolates | Limited concentration of antimicrobial agents | Possible automation in part | |
Disk diffusion | Simple to perform | Time-consuming | Qualitative * |
Low cost | No MIC value | ||
Simple and fast interpretation | The inability for some antibiotics to be tested | ||
The high number of test antibiotics per test | |||
High flexibility in antibiotic selection | |||
Detection of resistance patterns | |||
Mass use and the possibility of automatisation | |||
A number of a different use (AST, identification, screening, etc.) | |||
Detection of heteroresistant population or contamination | |||
Gradient test | Convenient and flexible | Relatively expensive | Quantitative |
Simple to perform | Relatively long incubation | ||
Does not require expertise | |||
Detection of resistance patterns | |||
Automated systems | Simple to perform | Relatively expensive | Semi-quantitative *** |
Chromogenic media | Mass use and the possibility of automatisation | Not completely susceptible and specific | Qualitative with no interpretation criteria (S, I, R) |
Simple to perform | Time-consuming | ||
Simple and fast interpretation | Limited spectra or single antibiotic | ||
Relatively expensive | |||
Screening only or required confirmatory identification | |||
No MIC value | |||
MALDI-TOF MS | Rapid turnaround time | High cost of the MALDI-TOF MS | |
Simple to perform | Need further optimisation for each species and antibiotic combination | ||
Low sample volume requirements | No MIC value | ||
Low per-sample costs | |||
Genetic methods | Rapid | Limited spectra | Qualitative |
Highly accurate | Limited throughput | Semi-quantitative | |
Sensitive | High cost | ||
Reproducible | |||
Increased ability to detect slow-growing or non-cultivable organisms | |||
Genomic methods | Highly accurate | High cost | Qualitative |
Sensitive | Time-consuming | ||
Increased ability to detect slow-growing or non-cultivable organisms | Challenging interpretation of results |
* Qualitative; results are expressed as susceptible (S), susceptible, increased exposure (I), or resistant (R) based on established criteria from EUCAST. ** Quantitative; results are expressed as minimal inhibitory concentration (MIC) for each drug. Susceptibility reports should include interpretation of MIC, such as S, I, or R. *** Semi-quantitative; results are expressed as MIC using three to four antimicrobial dilutions for each drug. Precise MIC values cannot be established if the MIC falls below or above the three to four dilutions used in the test panel. Susceptibility reports include interpretation of breakpoint MIC as S, I, or R. MALDI-TOF MS—matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.