Application of therapeutic drug monitoring to the treatment of bacterial central nervous system infection: a scoping review

Author:

Arkell Paul1,Wilson Richard1234ORCID,Watkins Killian1,Antcliffe David B156,Gilchrist Mark124,Wilson Mark7,Rawson Timothy M12,Holmes Alison123

Affiliation:

1. Department of Infectious Disease, Centre for Antimicrobial Optimisation, Imperial College London , Hammersmith Hospital, Du Cane Road , UK

2. Department of Infectious Disease, National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance, Imperial College London, Hammersmith Campus , Du Cane Road , UK

3. Department of Pharmacology and Therapeutics, Institute of Systems, Molecular and Integrative Biology, University of Liverpool , Liverpool L69 3BX , UK

4. Department of Pharmacy, Imperial College Healthcare NHS Trust, St Mary's Hospital , Praed Street, London W2 1NY , UK

5. Department of Anaesthesia and Critical Care, Imperial College Healthcare NHS Trust, St Mary’s Hospital , Praed Street, London W2 1NY , UK

6. Division of Anaesthesia, Pain and Critical Care Medicine, Imperial College London , South Kensington Campus, London SW7 2AZ , UK

7. Department of Neurosurgery, Imperial College Healthcare NHS Trust, St Mary’s Hospital , Praed Street, London W2 1NY , UK

Abstract

Abstract Background Bacterial central nervous system (CNS) infection is challenging to treat and carries high risk of recurrence, morbidity, and mortality. Low CNS penetration of antibiotics may contribute to poor clinical outcomes from bacterial CNS infections. The current application of therapeutic drug monitoring (TDM) to management of bacterial CNS infection was reviewed. Methods Studies were included if they described adults treated for a suspected/confirmed bacterial CNS infection and had antibiotic drug concentration(s) determined that affected individual treatment. Results One-hundred-and-thirty-six citations were retrieved. Seventeen manuscripts were included describing management of 68 patients. TDM for vancomycin (58/68) and the beta-lactams (29/68) was most common. Timing of clinical sampling varied widely between studies and across different antibiotics. Methods for setting individual PK-PD targets, determining parameters and making treatment changes varied widely and were sometimes unclear. Discussion Despite increasing observational data showing low CNS penetration of various antibiotics, there are few clinical studies describing practical implementation of TDM in management of CNS infection. Lack of consensus around clinically relevant CSF PK-PD targets and protocols for dose-adjustment may contribute. Standardised investigation of TDM as a tool to improve treatment is required, especially as innovative drug concentration-sensing and PK-PD modelling technologies are emerging. Data generated at different centres offering TDM should be open access and aggregated to enrich understanding and optimize application.

Funder

Department of Health

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology,Microbiology (medical)

Reference39 articles.

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