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. 2017 Feb 9;2017(2):CD003543. doi: 10.1002/14651858.CD003543.pub4

Chan 2011.

Methods STUDY DESIGN: ITS
Risk of Bias: MEDIUM
Participants PROVIDERS: all physicians in the hospital
 PARTICIPANTS: all patients
 CLINICAL PROBLEM: use of restricted antibiotics (amikacin, 3rd‐ and 4th‐generation cephalosporins, carbapenems, fluoroquinolones, glycopeptides, and piperacillin/tazobactam)
 SETTING: 1 university hospital in Taiwan
Interventions FORMAT, Interventions: educational outreach by review and recommend change; restrictive ‐ expert approval required plus review and make change
Intervention Functions: education, enablement, persuasion, restriction
 DELIVERER: AMT
 COMPARISON: usual care
 DESIRED CHANGE: decrease excessive
Outcomes PRESCRIBING: Choice: DDD/1000 OBD of restricted antibiotics
MICROBIAL: isolation rates Clostridium difficile, MRSA, and multidrug‐resistant gram‐negative bacteria
Notes ADDITIONAL DATA: no response from authors to request for additional data
FINANCIAL SUPPORT: Funding: Chang Gung Memorial Hospital (Taoyuan, Taiwan) (grant CMRPG340236). Competing Interests: none declared
Microbial Risk of Bias: HIGH (case definition clear, planned intervention but no data about infection control)
Risk of bias
Bias Authors' judgement Support for judgement
Intervention independent (ITS) ? Low risk States in discussion that biggest limitation was lack of external controls, but that is common to all ITS studies.
Analysed appropriately (ITS) ? Low risk Re‐analysed
Shape of effect pre‐specified (ITS) ? Low risk Point of analysis was point of intervention.
Unlikely to affect data collection (ITS) ? Unclear risk DDD data from pharmacy computer, the same pre‐ and postintervention
Knowledge of the allocation adequately prevented(ITS)? Low risk DDD data from pharmacy computer, the same pre‐ and postintervention
Incomplete outcome data addressed (ITS) ? Low risk DDD data from pharmacy computer, the same pre‐ and postintervention
Free of selected reporting (ITS) ? Low risk DDD data from pharmacy computer, the same pre‐ and postintervention
Free of other bias (ITS) ? Low risk > 1 year data pre‐ and postintervention