Clinical Trial Summary
Duration of therapy in severe infections has a high impact in term of compliance, adverse
events, and costs but also in term of antibiotic pressure on selection of multidrug-resistant
pathogens. In this context, many advancements have been obtained for an early diagnosis of IE
with a strict selection of criteria for surgery. Moreover, the use in antibiotic regimen of
new drugs with peculiar PK/PD characteristics, as a quick bactericidal action, also for IE
was not accompanied to a revaluation of duration of antibiotic treatment. On this basis, US
and European guidelines recommend a 6-week duration of antibiotic treatment for IE due to
enterococcal species.
AIM 1: To evaluate a 4-week duration of antibiotic therapy versus a 6-week duration according
to international guidelines.
AIM 2: Second aim is to evaluate the PK/PD of antimicrobials in relation to the probability
of target attainment (PTA) of optimal exposure against enterococci.
AIM 3: Finally, we will analyze the bactericidal activities of antibiotic combinations used
in patients with IE and the survival of the subgroup of patients who underwent surgery.
Open-label, multicenter, randomized, non-inferiority trial to be conducted in a 3-year
period. The institutional review board at each site will approve the protocol, and all
patients or their authorized representatives will provide written informed consent. Eligible
patients will be 18 years of age or older with a documented IE due to enterococcal strains,
according to the modified Duke criteria.
63 patients in each of the two arms. The study will be conducted at Italian sites. Data on
demographic characteristics, comorbidities, antibiotic and concomitant therapies will be
collected. Baseline treatments will be defined according to the patients' pharmacological
history. IE will be defined according to modified Duke criteria. Antibiotic treatment,
indications and timing of surgery will be based on the 2015 American Heart Association and
European Society of Cardiology guidelines.
Blood samples for determining antibiotic concentrations of ampicillin, gentamicin,
vancomycin, daptomycin and linezolid will be collected at predetermined times in order to
allow estimation of PK/PD.
Randomization:
1. 4-week duration of antibiotic therapy
2. standard 6-week duration of antibiotic therapy The intention-to-treat population (ITT)
will include all randomized patients. The modified intention-to-treat population (mITT)
will include all randomized patients receiving at least one dose of study medication.
The clinically evaluable (CE) population will include ITT patients demonstrating
sufficient adherence to study protocol.
Primary endpoint: non-inferiority of a 4-week course in terms of outcome at 60 days.
Secondary endpoints: microbiological eradication, pharmacological concentrations of
antibiotic regimens, patients undergoing surgery, duration of therapy according with
resistance profile of enterococcal species.
