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 |