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
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