Antibiotic Stewardship Program in Pancreatic Surgery: a Multicenter Time Series Analysis (BIOSTEPS).
NCT ID: NCT04199494
Last Updated: 2020-02-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
1200 participants
OBSERVATIONAL
2019-12-16
2022-12-16
Brief Summary
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Objective: To evaluate the useful of an antimicrobial stewardship program and a patient-tailored antibiotic prophylaxis in the reduction of the occurrence of SSI and the inappropriate use of key antibiotics in patients undergoing pancreatic surgery.
Study design: A time series study will be conducted. The antimicrobial stewardship program is shared between three national high-volume centers of pancreatic surgery. Statistical significance and effect size were calculated by segmented regression analysis of interrupted time series of drug use, SSI rate, and costs for 3 years before and after the introduction of the program.
Study population: Patients with an indication for elective pancreatic surgery.
Main study parameters/endpoints: Primary outcome is the reduction of SSI rate. Secondary outcomes are the reduction of the use of the key antibiotics (such as piperacillin/tazobactam and carbapenems), the microbial whole-genome sequencing (WGS) of the carbapenemase-producing Enterobacteriaceae, and the reduction of the treatment costs
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Detailed Description
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Conditions
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Study Design
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OTHER
OTHER
Interventions
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Antibiotic Stewardship Program
The patient do the routinely preoperative lab tests, including the rectal swab (RS). The Antibiotic Stewardship Program (ASP) has been shown to effectively reduce unnecessary antibiotic use and optimize the treatment of infectious diseases. To be successful, multiple aspects should be considered in the ASP. Initially, the infection control specialists will follow the routine activity of each department in order to define what could immediately be improved. Internal antibiotic prophylaxis and therapy guidelines will be defined and shared between groups. The RS, collected at the preoperative testing, is evaluated by the infection control specialist. In case of identification of MDR bacteria, each patient will receive a tailored AP based on the antibiograms of the RS. In any case, the infection control specialist will choose the best solution for the patient avoiding the key antibiotics
Eligibility Criteria
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Inclusion Criteria
* Age ≥ 18 years
* American Society of Anesthesiologists (ASA) score \< 4
* The ability of the subject to understand the character and individual consequences of the clinical trial
* Written informed consent
Exclusion Criteria
* ASA score ≥4
* Immune suppressed patients
* Pregnant women
* Participation in another study with interference of study outcomes
* Impaired mental state or language problems
18 Years
ALL
No
Sponsors
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Agenzia Italiana del Farmaco
OTHER_GOV
Azienda Ospedaliera Universitaria Integrata Verona
OTHER
Responsible Party
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Locations
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AOUI Verona
Verona, , Italy
AOUI Verona
Verona, , Italy
Countries
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Facility Contacts
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Other Identifiers
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TRS 2018-00001695
Identifier Type: -
Identifier Source: org_study_id
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