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Feasibility of 24 h continuous-infusion cefiderocol administered by elastomeric pump in attaining an aggressive PK/PD target in the treatment of NDM-producing Klebsiella pneumoniae otomastoiditis

2025/04/29 by Stella Babich, Pier Giorgio Cojutti, Milo Gatti +3 · 1 voice · 1 citation
Engineering · Medicine · #Antibiotics Pharmacokinetics and Efficacy #Intravenous Infusion Technology and Safety #Nosocomial Infections in ICU

paper · pdf · doi:10.1093/jacamr/dlaf066

openalex publication_date 2025/04/29 · openalex created_date 2025/05/06 · openalex updated_date 2026/07/29

Abstract

Abstract Objectives Cefiderocol has emerged as a key treatment for managing MDR infections, and its time-dependent pharmacodynamics are optimized by prolonged infusion to maintain time above the MIC (T > MIC). Whereas recent stability studies have shown cefiderocol remains stable up to 72 h in elastomeric pumps, its use in 24 h continuous infusions (CIs) for outpatient parenteral antibiotic therapy (OPAT) is undocumented. This case highlights its suitability for 24 h CI via elastomeric pumps in an OPAT setting, supported by therapeutic drug monitoring (TDM) to ensure optimal treatment efficacy. Patient/case description A 31-year-old male developed right-sided otomastoiditis caused by Klebsiella pneumoniae producing New Delhi MBL (NDM). Given the resistance profile and the need for prolonged therapy, cefiderocol was initiated at a daily dose of 6 g, administered by 24 h CI using an elastomeric pump. TDM was performed on Days 17 and 45 to assess plasma concentrations. Results TDM confirmed steady-state concentrations (Css 25.2–28.1 mg/L), achieving optimal pharmacokinetic/pharmacodynamic (PK/PD) target attainment such as 100% T > 4–6 MIC (free [f]Css/MIC 10.58–11.80). Significant clinical improvement avoided the need for planned surgery, with no adverse events reported from the venous catheter, antibiotic therapy or elastomeric pump. Conclusions This approach underscores the feasibility and efficacy of cefiderocol administered by 24 h CI by means of an elastomeric pump and supported by real-time TDM in achieving an aggressive PK/PD target for the treatment of otomastoiditis due to NDM-producing K. pneumoniae.

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