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Clinical Trials/NCT04011657
NCT04011657
Completed
Not Applicable

Effective Antimicrobial StewaRdship StrategIES (ARIES): Cluster-randomized Trial of a Computerized Decision Support System Versus Antibiotic Prospective Review and Feedback in Antimicrobial Stewardship

Tan Tock Seng Hospital1 site in 1 country1,257 target enrollmentMarch 1, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Infection, Bacterial
Sponsor
Tan Tock Seng Hospital
Enrollment
1257
Locations
1
Primary Endpoint
30-day mortality
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

Background Prospective review and feedback (PRF) of antibiotic prescriptions is a labor-intensive core strategy of antimicrobial stewardship (AMS). The investigators hypothesized that a computerized decision support system (CDSS) providing recommendations for antibiotics, investigations and referrals would reduce the requirement for PRF without causing harm.

Methods A parallel-group, 1:1 block-cluster randomized, cross-over study was conducted in 32 medical and surgical wards from March to August 2017. The intervention arm comprised voluntary use of CDSS at first prescription of piperacillin-tazobactam or a carbapenem, while the control arm was compulsory CDSS. PRF was continued for both arms. Primary outcome was 30-day mortality.

Detailed Description

Increasing antimicrobial resistance due to inappropriate antimicrobial use is a global concern. Multi-disciplinary antimicrobial stewardship teams have become an integral part of the response to this issue. Through prospective review of antibiotic prescriptions and feedback (PRF) to healthcare providers, antimicrobial stewardship has been shown to improve clinical response, reduce adverse effects and mortality. However, this strategy is labor-intensive to implement and skilled healthcare workers are an expensive and scarce resource. Antibiotic computerized decision support systems (CDSS) have been used to facilitate these processes and may circumvent the limitations of lack of manpower. In previous studies, CDSS led to increased susceptibility of Pseudomonas aeruginosa to imipenem and Enterobacteriaceae to gentamicin and ciprofloxacin, and an overall reduction in broad-spectrum antibiotic use. CDSS could improve clinical outcomes. Currently, there are limited studies comparing the combined effects of these two strategies. At Tan Tock Seng Hospital, a university teaching hospital in Singapore, antimicrobial stewardship has focused on PRF by a multi-disciplinary team since 2009. This team reviews piperacillin-tazobactam and carbapenem orders against hospital antibiotic guidelines from day two of antibiotic prescription. In March 2010, we implemented CDSS triggered at the point of antibiotic ordering and compulsory for the prescriber to review. Prescribers are free to accept or reject the CDSS recommendations. While PRF and CDSS are performed following the same institutional guidelines, there may be differences in physicians' acceptance of recommendations and the accessibility to recommendations between these two interventions. In previous studies, PRF recommendations had an acceptance of 60-70% while compulsory CDSS was 40%. The investigators hypothesized that compulsory CDSS and PRF would improve clinical outcomes compared with voluntary CDSS and PRF, and compulsory CDSS would improve appropriate antibiotic practice and reduce the requirement for subsequent PRF.

Registry
clinicaltrials.gov
Start Date
March 1, 2017
End Date
February 28, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Tan Tock Seng Hospital
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients who are started on the 1st episode of piperacillin-tazobactam or carbapenem during the study period.
  • Medical and surgical wards

Exclusion Criteria

  • Intensive care unit (ICU), high dependency and step-down care wards

Outcomes

Primary Outcomes

30-day mortality

Time Frame: Follow-up up to 30 days from the start date of the first episode of piperacillin-tazobactam or carbapenem use

Death at 30 days

Secondary Outcomes

  • 30-day readmission(Readmissions 30 days after the cessation of first episode of piperacillin-tazobactam or carbapenem use)
  • 7-day clinical response(Follow-up up to 7 days from the date of the first episode of piperacillin-tazobactam or carbapenem use)
  • Diarrhea this admission(From the start date from the first episode of piperacillin-tazobactam or carbapenem use until the discharge date or up to 6 months whichever occurred earlier)
  • Appropriateness of antibiotics(It is assessed only once at the point of the first episode of piperacillin-tazobactam or carbapenem use in the index admission. It is only assessed once till discharge or up to 6 months)
  • Index antibiotic days of therapy,(From the start date of the first episode of piperacillin-tazobactam or carbapenem use to the end date of this antibiotic which is followed up till discharge or up to 6 months.)
  • length of stay(It is assessed from the date of admission till the date of discharge or up to 6 months)
  • 6-months incidence of multi-drug resistant organisms(up to 6 months (Clinical cultures only))
  • Gross hospitalization costs(Gross hospitalization costs incured from date of admission till date of discharge or up to 6 months)
  • 30-day re-infection(Re-start of piperacilin-tazobactam or carbapenem 30 days after the cessation of first episode of piperacillin-tazobactam or carbapenem use)

Study Sites (1)

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