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Clinical Trials/NCT04657185
NCT04657185
Completed
Not Applicable

Reducing Perioperative S. Aureus Transmission Via Use of an Evidence-Based, Multimodal Program Driven by an Innovative Software Platform (OR PathTrac)

Georgetown University1 site in 1 country804 target enrollmentJuly 15, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
S. Aureus Transmission
Sponsor
Georgetown University
Enrollment
804
Locations
1
Primary Endpoint
within-case S. aureus transmission
Status
Completed
Last Updated
7 months ago

Overview

Brief Summary

Healthcare-associated infections (HAIs) occur frequently and are associated with patient harm. It is important that healthcare facilities take the necessary steps to prevent the spread of resistant bacteria. ESKAPE bacteria (Enterococcus, S. aureus, Klebsiella, Acinetobacter, Pseudomonas, and Enterobacter spp.) are particularly pathogenic. Isolation of these pathogens from intraoperative reservoirs has been associated with postoperative infection development (i.e. surgical site infections). This project involves implementation of a software platform and bacterial collection system (OR PathTrac) that leverages the epidemiology of intraoperative bacterial transmission to guide dynamic, prospective improvements in perioperative infection control measures. The investigators will assess the effectiveness of OR PathTrac feedback in optimizing an evidence-based, multifaceted, perioperative infection control program.

Detailed Description

Our objective was to analyze the impact of surveillance feedback optimization of a multifaceted, perioperative infection control program on S. aureus transmission and SSIs. A multifaceted infection control program was implemented over 8 months (November 2018 to June 2019). A prospective cohort impact study was then conducted over 8 months (July 2019 to March 2020) to compare the incidence of within-case S. aureus transmission (primary outcome) and surgical site infection (secondary outcome) before (4.5 months) and after (3.5 months) implementation of surveillance feedback.

Registry
clinicaltrials.gov
Start Date
July 15, 2019
End Date
March 20, 2020
Last Updated
7 months ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Adult patients requiring anesthesia and intravenous catheter placement.

Exclusion Criteria

  • Pediatric patients, without requirement of anesthesia and/or intravenous catheter placement.

Outcomes

Primary Outcomes

within-case S. aureus transmission

Time Frame: From patient entry into the operating room until case end, up to 6 hours

S. aureus transmission events detected within a surgical case

Secondary Outcomes

  • surgical site infection(Up to 90 days following surgery)

Study Sites (1)

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