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UnknownNCT05960383

Molecular vs Conventional Microbiologic Diagnosis for Infections in Lung Transplantation

Comparison Between Rapid Molecular Technique BioFire Pneumonia Panel Filmarray and Conventional Culture-based Methods in the Microbiologic Diagnosis on Bronchoalveolar Lavage Fluid of Lung Transplant Patients

Status
Unknown
Phase
Study type
Observational
Enrollment
53 (estimated)
Sponsor
Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The goal of this prospective study is to compare rapid molecular technique BioFire Pneumonia Panel Filmarray and conventional culture-based methods in the microbiologic diagnosis on bronchoalveolar lavage of lung transplant patients. The main questions it aims to answer are: * determine the microbiological concordance between molecular diagnostic and conventional culture techniques on donor's bronchoalveolar lavage before lung transplantation * determine the microbiological concordance between molecular diagnostic and conventional culture techniques on recipient's bronchoalveolar lavage, performed 72 hours after lung transplantation * determine the microbiological concordance between molecular diagnostic and conventional culture techniques in detecting molecular resistance patterns * determine the difference in time to microbiological results between molecular diagnostic and conventional culture techniques * determine time to clinical decision based on molecular diagnostic techniques compared to conventional culture techniques

Detailed description

Molecular assays that detect bacterial organisms by nucleic acid sequences rather than culture have the potential to improve time to diagnosis for lower respiratory tract infections. However, their performance characteristics are unknown in lung transplant recipients. PNEUMOARRAY is a prospective study, including all patients aged \>18 years that undergo lung transplantation from September 2022, at IRCCS Fondazione Cà Granda Policlinico in Milan. Patients who do not meet inclusion criteria are excluded from this study. A fibro-bronchoscopy (FBS) with bronchoalveolar lavage (BAL) is performed, according to clinical practice, both on lungs donor and recipient. Donor's BAL is collected before graft transplantation, while BAL on lung transplant recipient is performed 72 hours after transplantation. On each BAL sample, both of lung donor and recipient, molecular diagnostic and culture exam are performed. The goal of this prospective study is to compare rapid molecular technique BioFire Pneumonia Panel Filamarray and conventional culture-based methods in the microbiological diagnosis on bronchoalveolar lavage of lung transplant patients. The primary outcome is: -determine the microbiological concordance between molecular diagnostic and conventional culture techniques on donor's bronchoalveolar lavage before lung transplantation Secondary outcomes are: * determine the microbiological concordance between molecular diagnostic and conventional culture techniques on recipient's bronchoalveolar lavage, performed 72 hours after lung transplantation * determine the microbiological concordance between molecular diagnostic and conventional culture techniques in detecting molecular resistance patterns * determine the difference in time to microbiological results between molecular diagnostic and conventional culture techniques * determine time to clinical decision based on molecular diagnostic techniques compared to conventional culture techniques Sample size for statistical significance includes 53 patients. For the majority of bacteria and fungi, microbiological culture from BAL remains the gold standard for diagnosis, but cultures are limited by long turnaround time and decreased sensitivity in patients that have received empiric anti-infective therapy. In this setting, fast microbiological diagnosis may be crucial to begin targeted antimicrobial therapy/prophylaxis and identify genes encoding resistance, in order to administer targeted therapy and to reduce antimicrobial resistance.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTBioFire Pneumonia Panel PlusAssessment of sensbility and specificity of BioFire Pneumonia Panel Plus in lung transplantation

Timeline

Start date
2023-02-02
Primary completion
2023-10-31
Completion
2024-11-01
First posted
2023-07-25
Last updated
2023-07-25

Locations

1 site across 1 country: Italy

Regulatory

Source: ClinicalTrials.gov record NCT05960383. Inclusion in this directory is not an endorsement.