Abstract

Drug monitoring is one strategy of antibiotic stewardship to face antimicrobial resistance. This strategy could have a determinant role in critically ill patients treated with carbapenems to overcome pharmacokinetic variability, reduce the risk of subtherapeutic dosage or toxicity, and reduce the risks inherent to treatment. However, the effectiveness of therapeutic drug monitoring (TDM) is unknown. This paper aims to identify TDM effectiveness in critically ill patients treated with carbapenems. English and ClinicalTrials.gov databases were searched to identify relevant studies evaluating carbapenem TDM. Randomized controlled trials (RCTs) and comparative cohort studies were selected for inclusion if they compared carbapenem TDM to standard care in adult critically ill or sepsis/septic shock patients. The primary outcome was mortality. Secondary outcomes included morbidity, clinical cure, microbiological eradication, antimicrobial resistance, drug-related side effects, and achievement of target plasma concentrations. Overall, performing carbapenem TDM was not associated with a decrease in mortality. However, it could be evidence for a relationship with clinical cure as well as target attainment. Some studies found favorable outcomes related to clinical and microbiological responses, such as lower procalcitonin levels at the end of the monitored therapy compared to standard care. For the primary and secondary outcomes analyzed, strong evidence was not identified, which could be due to the size, risk of bias, and design of selected studies.

Highlights

  • It is of great importance to know the concentration of the antibiotic, which must be higher than the minimum effective concentration (MEC) for a favorable clinical outcome for the patient [1] to avoid antibioticresistant bacteria [2]

  • The aim of benefits this review is to identify in critically ill patients not clear

  • Tool fo and its application has been limited to a few antibiotics with PK features that increase the risk of clinical failure and toxicity, like vancomycin and aminoglycosides [31,32]. βLactam and, carbapenem therapeutic drug monitoring (TDM) have not been widely investigated because of the wide therapeutic index (TI) associated with these antibiotics

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Summary

Introduction

The measurement of the concentration of drugs in fluids such as plasma, serum, or blood in patients at specific intervals is called therapeutic drug monitoring (TDM) [3,4]. There are several indications to perform TDM, such as drugs with a narrow therapeutic index (NTI), high variability or unpredictability between drug dose and plasma concentration, situations where there is knowledge of the clinical effect and/or toxicity related to concentration, adverse effects defined by overdose or insufficient dose, and availability of equipment and personnel for the processing and interpretation of the results of TDM [1,7,8]. NTI is used to identify those drugs where small differences in dose or blood concentration may lead to dependence, therapeutic failure, or side effects. According to the World Health Organization (WHO), drugs that require TDM are anticonvulsants, antiarrhythmics, immunosuppressants, and antibiotics (fluoroquinolones, lipopeptides, glycopeptides, and β-lactams, among many others) [4]

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