Rapid De-escalation of Anti-MRSA Therapy Guided by S. Aureus Nares Screening in Case of Pneumonia

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Bari Aldo Moro

About this trial

The current IDSA/ATS guidelines recommend Linezolid and Vancomycin for MRSA coverage in hospitalized patients with pneumonia, which is common clinical practice in Italy. However, a nasal PCR-assay for MRSA has a high negative predictive value and can facilitate rapid antibiotic de-escalation, thereby avoiding unnecessary anti-MRSA treatments. The indiscriminate use of these drugs has contributed to the emergence of resistant S. aureus strains and has led to significant adverse effects, without providing any survival benefits. Additionally, it has increased hospital stays and associated costs. The proposed study aims to use this diagnostic tool to shorten empirical anti-MRSA treatment duration in pneumonia patients, focusing on reducing antimicrobial therapy days while measuring in-hospital mortality, length of stay and adverse drug event incidence.

Eligibility criteria

Qualifiers

Subjects 18 years or older.

Patients hospitalized at the Azienda Consorziale Policlinico di Bari;

Clinical diagnosis of CAP/HAP/VAP;

Commitment by the prescribing physician to set an anti-MRSA antibiotic therapy in empirical

Disqualifiers

Febrile neutropenia or severe immunodeficiency;

Chronic airway infection (eg cystic fibrosis);

Suspect of extrapulmonary infection by MRSA

Refusal by the patient or legal guardian;

Trial design

Treatments tested in this trial

  • MRSA nasal swab based de-escalation

Treatment groups

76 Participants
are divided into 2 treatment groups

Sponsors and collaborators