Real-world experience of therapeutic drug monitoring and PK/PD achievement of ceftaroline administered by different infusion regimens in patients with confirmed infections caused by Gram-positive bacteria

Author:

Fresán Daniel1,Luque Sonia234,Benítez-Cano Adela5ORCID,Sorlí Luisa3467,Montero María Milagro3467ORCID,De-Antonio Marta2,Vega Victoria8,Roberts Jason A9101112ORCID,Horcajada Juan P3467,Grau Santiago2347

Affiliation:

1. Pharmacy Department, Hospital Universitario de Navarra , Pamplona , Spain

2. Pharmacy Department, Hospital del Mar, Parc de Salut Mar , Barcelona , Spain

3. Infectious Pathology and Antimicrobials Research Group (IPAR), Institut Hospital del Mar d’Investigacions Mèdiques (IMIM) , Barcelona , Spain

4. CIBERINFEC, ISCIII-CIBER de Enfermedades Infecciosas, Instituto de Salud Carlos III , Av. de Monforte de Lemos, 5 , Madrid 28029, Spain

5. Department of Anaesthesiology and Surgical Intensive Care, Hospital del Mar, Parc de Salut Mar , Barcelona , Spain

6. Infectious Diseases Department, Hospital del Mar, Parc de Salut Mar , Barcelona , Spain

7. Department of Medicine and Life Sciences (MELIS), Universitat Pompeu Fabra , Barcelona , Spain

8. Analytical Department, Laboratori de Referència de Catalunya , Barcelona , Spain

9. University of Queensland Centre for Clinical Research, Faculty of Medicine, The University of Queensland , Brisbane , Australia

10. Herston Infectious Diseases Institute (HeIDI), Metro North Health , Brisbane , Australia

11. Departments of Pharmacy and Intensive Care Medicine, Royal Brisbane and Women’s Hospital , Brisbane , Australia

12. Division of Anaesthesiology Critical Care Emergency and Pain Medicine, Nîmes University Hospital, University of Montpellier , Nîmes , France

Abstract

Abstract Background Ceftaroline is a novel cephalosporin active against MDR Gram-positive (GP) bacteria. For β-lactam antibiotics, such as ceftaroline, prolonged infusions and therapeutic drug monitoring (TDM) are used for dosage optimization based on their pharmacokinetics/pharmacodynamics (PK/PD). Objectives To describe our experience with TDM and PK/PD target attainment of ceftaroline administered by intermittent and prolonged infusion in a cohort of patients with MDR-GP bacterial infections. Methods Patients treated with ceftaroline administered by continuous (24 h), extended (3 h/6 h) and intermittent infusion (1 h) and undergoing TDM of plasma concentrations were included. A 100%fT>4×MIC was the pre-specified PK/PD target and 100%fT>10×MIC was considered overexposure. Dose recommendations were made based on TDM results and each patient’s clinical condition. Results Twelve patients [83.3% male, median age of 73 (38–83) years] were included. Nine patients (75%) achieved 100%fT>4×MIC, all under prolonged infusions. In one patient, the 100%fT was >10×MIC but no toxicity was observed. Based on TDM results, initial doses were recommended to be maintained in eight patients, decreased in three and increased in one. Conclusions The administration of ceftaroline by prolonged infusion together with TDM may be a useful strategy for achieving the desired PK/PD target in these patients. However, more studies evaluating the relationship between PK/PD attainment and clinical outcomes are needed.

Publisher

Oxford University Press (OUP)

Subject

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

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