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Clinical Trials/NCT06542965
NCT06542965
Completed
Not Applicable

Clinical Characteristics, Risk Factors and Resistance Mechanisms for Bloodstream Infection of Carbapenem-Resistant Proteus Mirabilis

Dokuz Eylul University1 site in 1 country67 target enrollmentJanuary 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Proteus Mirabilis Infection
Sponsor
Dokuz Eylul University
Enrollment
67
Locations
1
Primary Endpoint
Carbapenem Use
Status
Completed
Last Updated
last year

Overview

Brief Summary

This study aims to determine the clinical characteristics, risk factors, and resistance mechanisms of patients with carbapenem-resistant P. mirabilis bacteremia.Patients with P. mirabilis growth in blood culture samples sent to bacteriology laboratory between 2018 and 2021 were retrospectively analyzed. Patients meeting the inclusion criteria were divided into carbapenem-resistant and carbapenem- susceptible groups. The investigators recorded demographic data, clinical features, and laboratory findings. Resistance genes were investigated in carbapenem-resistant isolates using PCR.

Detailed Description

Patients with P. mirabilis growth in blood culture who met the study criteria were divided into two groups as carbapenem susceptible and resistant according to carbapenem antibiogram results. Patients with carbapenem-resistant P. mirabilis (CRPM) growth in blood culture were included in the case group and patients with carbapenem- susceptible P. mirabilis (CSPM) growth in blood culture were included in the control group. Demographic characteristics of the patients, concomitant chronic diseases, Charlson comorbidity index (CCI), hospital and intensive care unit (ICU) hospitalization and number of days in the last year, history and type of invasive intervention in the last three months (surgical-invasive), history of antibiotic use in the last three months and types of antibiotics used (Penicillin, cephalosporin, quinolone, carbapenem, tigecycline, colistin, aminoglycoside), hospitalization unit, total length of hospitalization, sample collection unit, growth result and antibiogram, clinical and laboratory data of the day of growth, sepsis and septic shock evaluated according to systemic inflammatory response syndrome (SIRS) criteria, 30-day mortality and patient outcome information were recorded. Carbapenemase-producing gene regions were investigated by Polymerase Chain Reaction (PCR) in accessible samples of patients with carbapenem-resistant P. mirabilis growth in blood cultures.

Registry
clinicaltrials.gov
Start Date
January 1, 2018
End Date
January 1, 2023
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Cağlar Iirmak

Principal Investigator, Medical Specialists in Infectious Diseases

Dokuz Eylul University

Eligibility Criteria

Inclusion Criteria

  • Inpatients aged 18 years and older
  • P. mirabilis growth in blood cultures

Exclusion Criteria

  • Samples taken in emergency departments, outpatient clinics, day treatment units
  • Recurrent growths of the same patient

Outcomes

Primary Outcomes

Carbapenem Use

Time Frame: 1 year

number of patients using carbapenem before P. mirabilis growth in blood cultures

Presence of chronic disease

Time Frame: 1 year

number of patients with chronic disease

Intensive Care Units

Time Frame: 1 year

number of patients admission in ıntensive care units before P. mirabilis growth in blood cultures

Length of hospital stay

Time Frame: 1 year

Length of hospital stay days

Mortality

Time Frame: 30 days

number of patients who died

Study Sites (1)

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