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Quinolone Resistance in Bloodstream Isolates of Escherichia Coli

Information source: University of Pittsburgh
Information obtained from ClinicalTrials.gov on February 12, 2009
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Bacterial Infections

Phase: N/A

Status: Recruiting

Sponsored by: University of Pittsburgh

Official(s) and/or principal investigator(s):
David L Paterson, MD, Principal Investigator, Affiliation: University of Pittsburgh

Overall contact:
David L Paterson, MD, Phone: 412-648-6401, Email: patersond@dom.pitt.edu

Summary

This proposed study aims to document the risk factors for quinolone resistance in bloodstream isolates of E. coli. Additionally, the adequacy of empiric antibiotic therapy for E. coli

bloodstream infections will be assessed. Finally, outcome will be recorded - this is

all-cause mortality at 28 days from the time of the first positive blood culture. Hypothesis: Ciprofloxacin resistant strains are associated with admission from nursing home and with prior quinolone use.

Clinical Details

Official title: Quinolone Resistance in Bloodstream Isolates of Escherichia Coli

Study design: Cohort, Retrospective

Detailed description: The following information will be collected: age, sex, occupation, hospital location at the time of positive culture (ER, medical ward, ICU etc), date of positive culture, prior hospitalization, receipt of outpatient dialysis, home care or other regular medical care (eg, outpatient chemotherapy), presence of invasive devices, receipt of antibiotics, including their type and whether they were adequate for the resistance profile of the organism, prior positive microbiologic cultures, time and location of positive cultures, underlying diseases and severity of illness, presence of urinary or intravascular devices, recent immunomodulative therapies or radiation therapy, physical exam findings, laboratory and radiographical data, antimicrobial usage within 30 days of onset of the infection, microbiological data and resistance patterns, choice of antibiotics once organism identified, bacteriological outcomes, laboratory results, demographic information, medications, clinical outcome,gender, height, weight, ethnicity, and past medical history. We will collect information retrospectively.

Eligibility

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion Criteria:

Clinical information is collected by chart review of "case" and "control" patients.

A "case A" patient is defined as follows:

- One or more blood cultures are positive for E. coli. The organism is ciprofloxacin

resistant.

A "case B" patient is defined as follows:

- One or more blood cultures are positive for E. coli. The organism is ciprofloxacin

susceptible. Additionally, 4 controls who are in hospital at the same time as cases will be selected for each case.

Exclusion Criteria:

- If they do not meet inclusion criteria

Locations and Contacts

David L Paterson, MD, Phone: 412-648-6401, Email: patersond@dom.pitt.edu

University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania 15213, United States; Recruiting
David L Paterson, MD, Phone: 412-648-6401, Email: patersond@dom.pitt.edu
Diana Lynn Pakstis, RN, BSN, Phone: 412-648-6553, Email: pakstisdl@dom.pitt.edu
Yohei Doi, MD, Sub-Investigator
David L Paterson, MD, Principal Investigator
Additional Information

Starting date: March 2007
Last updated: October 3, 2008

Page last updated: February 12, 2009

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