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

Liebowitz 2008.

Methods STUDY DESIGN: ITS
Risk of Bias: LOW
Participants PROVIDERS: all physicians in the hospital
 PARTICIPANTS: all patients in the hospital
CLINICAL PROBLEM: incidences of MRSA
SETTING: 1 general hospital in the UK
Interventions FORMAT: Intervention: educational meetings with dissemination of guideline; reminders, verbal on rounds
Intervention Function: education, persuasion
DELIVERER: AMT
COMPARISON: usual care
DESIRED CHANGE: reduce inappropriate
Outcomes PRESCRIBING: Choice: DDDs per 1000 OBD each month
MICROBIAL: Episodes of MRSA blood isolates per 1000 OBD each month
Notes FINANCIAL SUPPORT: Funding: unrestricted educational grant from Wyeth. Competing Interests: LDL received honoraria for lectures from Bayer and Bard.
ADDITIONAL DATA: no response from authors to request for additional data
Microbial ROB HIGH; case definition Low, planned intervention Low, other infection control High, no information about infection control other than screening for MRSA
Risk of bias
Bias Authors' judgement Support for judgement
Intervention independent (ITS) ? Low risk 18 months' pre‐ and 15 months' postintervention data
Analysed appropriately (ITS) ? Low risk Segmented regresssion analysis
Shape of effect pre‐specified (ITS) ? Low risk Point of analysis is point of intervention.
Unlikely to affect data collection (ITS) ? Low risk Pharmacy data used pre‐ and postintervention.
Knowledge of the allocation adequately prevented(ITS)? Low risk Pharmacy data used pre‐ and postintervention.
Incomplete outcome data addressed (ITS) ? Low risk Pharmacy data used pre‐ and postintervention.
Free of selected reporting (ITS) ? Low risk Pharmacy data used pre‐ and postintervention.
Free of other bias (ITS) ? Low risk > 1 year data pre‐ and postintervention