Impact of a TDM-guided ECPA Program for Optimizing Pharmacodynamic Target Attainment of Continuous Infusion Beta-lactam-based Regimen

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna

About this trial

Previous studies have clearly demonstrated a significant impact of optimised antibiotic therapy based on a TDM-guided approach in reducing the clinical and microbiological failure rate and in improving the achievement of an optimal pharmacokinetic/pharmacodynamic target. However, no study has yet evaluated this aspect in the specific scenario of liver transplant patients with documented infections with Gram-negative pathogens.

Eligibility criteria

Qualifiers

adult OLT recipients (age ≥ 18 years);

documented Gram-negative infections occurring in the first 90 days after transplantation;

treatment with beta-lactam based-regimens;

signed informed consent.

Disqualifiers

patients receiving beta-lactam-based regimens for less than 48 hours;

patients with isolation of a Gram-negative resistant to all available beta-lactam classes;

patients on palliative care and/or not resuscitation order.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

No trial groups listed