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Effect of Antibiotic Rotation in the ICU on the Prevalence of Antibiotic Resistant Gram-negative Colonisation

The SATURN Consortium, Impact of Specific Antibiotic Therapies on the Prevalence of hUman Host ResistaNt Bacteria. Workpackage 2: The SATURN ICU-trial.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01293071
Acronym
SATURN
Enrollment
10000
Registered
2011-02-10
Start date
2011-01-31
Completion date
2014-01-31
Last updated
2015-12-02

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

Conditions

Infections

Keywords

Antibiotic rotation, Cycling, Mixing, Gram-negative, EU, Multi center, Multi Centre, Cluster randomized trial, Cross over

Brief summary

The SATURN ICU-trial studies the effect of antibiotic rotation on the prevalence of antibiotic resistant Gram-negative colonisation.

Detailed description

Antibiotic rotation has been previously studied with varied results. The theory behind antibiotic rotation is that intermittently changing antibiotic classes will reduce the ecological selective pressure that drives the emergence of antibiotic resistance. This study compares the effect of 2 types of antibiotic rotation on Gram-negative colonisation in the ICU and also compares both interventions with standard care. The two interventions apply to the empiric treatment and are: 1) fast rotation, i.e. every other patient another class and 2) slow rotation, i.e. every other 1.5month another preferred class for empiric Gram-negative antibiotic therapy.

Interventions

OTHERAntibiotic rotation

Rotation of antibiotic classes as specific preferred antibiotic class to be used for empiric treatment of ICU acquired infections.

Sponsors

UMC Utrecht
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* There are at least 8 beds, with an average bed-occupancy of 80%; all of which have capacity for mechanical ventilation. * The ICU can adhere to the selected antibiotics for empiric treatment of infections. * There is an operational digital patient-information system, from which data can be extracted and delivered in a pre-defined format. Specifically an automated process for digital data-collection regarding microbiological culture-results (from swabs and bacteraemias), antibiotic prescription and patient demographics and illness severity-scores. * Colonization with ESBL or resistance for any of the antibiotic groups is endemic, with proportions of ICU-acquired bacteraemias used as a proxy. Therefore, the investigators prefer proportions of AMRB infection in the period 2008-2009 to be: ESBL resistance among GNB 1 to 10% Piperacillin/Tazobactam among GNB 1 to10% Carbapenem resistance among Klebsiella Pneumoniae less than 5% * Have the ability of at least one dedicated Infection Control HCW available for 0,2fte, for patient monitoring, compliance monitoring and instruction of HCWs regarding interventions. In the following this person will be called Research-Nurse or RN. * Can store screening-cultures at -70ºC * Can facilitate transport through a UMCU courier. * There is written approval for the study from the institution's IRB with a waiver for patient informed consent. * A signature page is signed by the daily management of the candidate-ICU by both ICU physician and director and the ICU nursing-director and presented to the UMCU, indicating willingness to enroll the candidate-ICU in the study.

Exclusion criteria

ICUs planning to introduce, during the SATURN trial period, any major diagnostic- or intervention program that will affect AMRB ecology\* * Burn units; due to the specific nature of the care provided and the patients admitted. * Cardiothoracic surgery units; because of the expected small number of patients admitted for three days or more. * Paediatric and neonatal ICUs.

Design outcomes

Primary

MeasureTime frame
Mean prevalence of ICU patients colonised with antimicrobial resistant Gram-negative pathogensMonthly point-prevalence screening of all ICU patients

Secondary

MeasureTime frame
AMRB acquisition incidence, measured as status conversion from noncolonized to colonized during admission at ICU per 100 patients.2011-2013
ICU-acquired bacteraemia rate with AMRB (expressed as the rate of ICU-acquired bacteraemia per 1000 patient-days)2011-2013
Overall length of ICU-stay hospital-stay and percentage of in-hospital mortality of the total admitted ICU-population.2011-2013
Effectiveness of empirical treatment of ICU-acquired bacteraemia, expressed as proportion of bacteraemia for which appropriate antibiotics are administered within 24 hours with antibiotics that the specific pathogens is susceptible for.2011-2013

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026