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Emergence of Resistance in Intestinal Microflora During Carbapenem Treatments

Emergence of Resistance in Intestinal Microflora During Carbapenem Treatments

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01703299
Acronym
ERIC
Enrollment
35
Registered
2012-10-10
Start date
2012-10-31
Completion date
2014-03-31
Last updated
2015-05-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Carbapenem-induced Resistance

Keywords

imipenem, ertapenem, resistance, commensal flora

Brief summary

The use of carbapenems, very broad spectrum antibiotics of last resort, is becoming more common due to the increased prevalence in the hospital and community of extended spectrum β-lactamase (ESBL) producing gram-negative bacilli (GNB), including CTX-M type, which are resistant to all other β-lactam antibiotics. Meanwhile, it creates a selective pressure towards emergence of strains which are also resistant to carbapenems, placing patients in a catastrophic situation of therapeutic dead-end. A better understanding of the mechanisms of emergence of BGN resistant to carbapenems is necessary to optimize their use and undertake preventive measures to preserve their effectiveness. The aim of the study is to evaluate and describe the emergence of carbapenem-induced resistant GNB in patient intestinal microflora.

Detailed description

The use of carbapenems, very broad spectrum antibiotics of last resort, is becoming more common due to the increased prevalence in the hospital and community of extended spectrum β-lactamase (ESBL) producing gram-negative bacilli (GNB), including CTX-M type, which are resistant to all other β-lactam antibiotics. Meanwhile, it creates a selective pressure towards emergence of strains which are also resistant to carbapenems, placing patients in a catastrophic situation of therapeutic dead-end. A better understanding of the mechanisms of emergence of BGN resistant to carbapenems is necessary to optimize their use and undertake preventive measures to preserve their effectiveness. Hypotheses: Carbapenems induce in treated patients the emergence of resistant GNB in intestinal flora and have an impact on colonization resistance of the gut microbiota. Primary objective: To determine the frequency of emergence of carbapenems resistant GNB in the intestinal flora at the end of a treatment by imipenem or ertapenem. Secondary objective(s): * Assess the presence of carbapenem resistant GNB in the intestinal flora before treatment. * Evaluate the presence and / or persistence of carbapenem resistant GNB in the intestinal flora on day 3 of treatment, and 15 days and 1 month after the end of treatment. * Determine the molecular mechanisms of resistance of strains of interest. * Describe the gastrointestinal tract colonization by non-commensal microorganisms before and after treatment (impact on colonization resistance). * Describe the characteristics of patients with emergence of resistance compared to patients who do not. * Proper conservation of stool of 10 patients for metagenomic and/or metatranscriptomic analysis of changes in the intestinal flora. Primary endpoint: Presence of carbapenem resistant GNB in the stool at the end of treatment in patients who did not before, after culture on selective media. Secondary endpoints: * Presence of carbapenem resistant GNB in stools before treatment, at day 3 and 15 days and 1 month after stopping treatment, after culture on selective media. * PCR and sequencing of resistance genes from strains of interest. * Colonization of the digestive tract by non-commensal microorganisms before and after treatment. * Characteristics of patients with or without emergence of resistance.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age\> or = 18 years old * hospitalized * initiating a treatment by imipenem or ertapenem- * faeces harvested before the beginning of treatment * written informed consent from the patient or from a relative if the patient is incapable of expressing his/her consent * reachable by phone after hospitalization (only for patients able to express their consent).

Exclusion criteria

: * hospitalized in intensive care unit * concomitant antibiotic treatment (except aminosid or vancomycin for less than 4 days). Secondary

Design outcomes

Primary

MeasureTime frameDescription
presence of carbapenem-resistant gram-negative bacteria at the end of carbapenem treatment in faeces of patients who were free of carbapenem-resistant gram-negative bacteria before the beginning of treatmentat the end of carbapenem treatment period which usually lasts between 2 and 15 daysfaecal bacterial growth on selective culture media

Secondary

MeasureTime frameDescription
presence of carbapenem-resistant gram-negative bacteria in patient faeces before carbapenem treatment, at day 3 of carbapenem treatment and at day 15 et day 30 after the end of carbapenem treatmentbefore, at day 3 of carbapenem treatment and at day 15 and day 30 after the end of carbapenem treatmentfaecal bacterial growth on selective culture media

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 10, 2026