Faro 1988.
Methods | Design: randomised double‐blinded No. eligible: not stated No. randomised: 114 No. analysed: 100 Drop‐outs/withdrawals: 14 (5 in vaginal group had abdominal surgery, 1 had operation cancelled, 6 received additional antibiotics, 2 received inappropriate doses) Years of recruitment: not stated Setting: centre not stated but study took place in the United States |
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Participants | Inclusion criteria: women scheduled for elective vaginal hysterectomy. Exclusion criteria: not stated Age: mean 32 to 33 years Type of hysterectomy: vaginal | |
Interventions | Treatment 1: 4 grams mezlocillin Treatment 2: 2 grams cefoxitin Route: IV Single/multiple doses: multiple Timing of doses: first dose within 1 hour of surgery, second dose on return from recovery room, and third dose 6 hours later |
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Outcomes | Postoperative infection, early and early + late Pelvic infection Need for therapeutic antibiotics Length of hospital stay Follow‐up: 6 weeks |
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Funding | Miles Laboratories | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | "Computer‐generated ... schedule" |
Allocation concealment (selection bias) | Unclear risk | Method not described |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Described as double‐blind ‐ no details given |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Imbalance in proportions of exclusion (10 vs 4) but reasons for exclusion not stated by treatment group |
Selective reporting (reporting bias) | Unclear risk | Insufficient information to make a conclusive judgement |
Other bias | Unclear risk | Insufficient information to make a conclusive judgement |