When and How to Use MIC in Clinical Practice?

Abstract

Bacterial resistance to antibiotics continues to be a global public health problem. The choice of the most effective antibiotic and the use of an adapted dose in the initial phase of the infection are essential to limit the emergence of resistance. This will depend on (i) the isolated bacteria and its resistance profile, (ii) the pharmacodynamic (PD) profile of the antibiotic used and its level of toxicity, (iii) the site of infection, and (iv) the pharmacokinetic (PK) profile of the patient. In order to take account of both parameters to optimize the administered treatment, a minimal inhibitory concentration (MIC) determination associated with therapeutic drug monitoring (TDM) and their combined interpretation are required. The objective of this narrative review is thus to suggest microbiological, pharmacological, and/or clinical situations for which this approach could be useful. Regarding the microbiological aspect, such as the detection of antibiotic resistance and its level, the preservation of broad-spectrum β-lactams is particularly discussed. PK-PD profiles are relevant for difficult-to-reach infections and specific populations such as intensive care patients, cystic fibrosis patients, obese, or elderly patients. Finally, MIC and TDM are tools available to clinicians, who should not hesitate to use them to manage their patients.

Keywords: PK/PD parameters; TDM-guided dosing adjustment; clinical practice; microbiology; minimal inhibitory concentration; pharmacology.

Figure 1

Microbiological, pharmacological, and clinical situations where an interpretation of the antibiotic concentration in relation to the MIC determination would be useful. TDM: therapeutic drug monitoring; MIC: minimal inhibitory concentration; ESBL: extended spectrum β-lactamase; MDR: multidrug-resistant.