Willemsen 2010.
Methods | STUDY DESIGN: ITS Risk of Bias: LOW |
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Participants | PROVIDERS: all physicians in the hospital PARTICIPANTS: all patients receiving therapeutic antibiotics CLINICAL PROBLEM: decrease use of ciprofloxacin SETTING: 1 hospital in the Netherlands | |
Interventions | FORMAT: Interventions: educational meetings with dissemination of guidelines; educational outreach by review and recommend change; reminders (physical, newsletter and on all microbiology reports saying that ciprofloxacin should be prescribed on strict indications only) Intervention Functions: education, enablement, environmental restructuring, persuasion DELIVERER: AMT COMPARISON: usual care DESIRED CHANGE: decrease excessive | |
Outcomes | PRESCRIBING: Choice: prescribed daily doses of ciprofloxacin (IV and oral) MICROBIAL: % quionolone‐resistant gram‐negative clinical isolates |
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Notes | FINANCIAL SUPPORT: Funding: Amphia Hospital, Breda/Oosterhout, Netherlands. Competing Interests: none declared ADDITIONAL DATA: no response from authors to request for additional data Microbial Risk of Bias: LOW Case definition infection with quionolone‐resistant gram‐negative bacteria, Planned intervention Low, Other infection control Low, no changes (information in Discussion) |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Intervention independent (ITS) ? | Low risk | |
Analysed appropriately (ITS) ? | Low risk | Segmented regression analysis |
Shape of effect pre‐specified (ITS) ? | Low risk | Point of intervention was point of analysis. |
Unlikely to affect data collection (ITS) ? | Low risk | Outcomes from pharmacy and microbiology computers |
Knowledge of the allocation adequately prevented(ITS)? | Low risk | Outcomes from pharmacy and microbiology computers |
Incomplete outcome data addressed (ITS) ? | Low risk | Outcomes from pharmacy and microbiology computers |
Free of selected reporting (ITS) ? | Low risk | Outcomes from pharmacy and microbiology computers |
Free of other bias (ITS) ? | Low risk | 1 year data pre‐ and postintervention |