Hemsell 1987.
Methods | Design: randomised blinded No. eligible: not stated No. randomised: 237 No. analysed: 212 Drop‐outs/withdrawals: 25 (18 did not have scheduled surgery, 6 had intraoperative antibiotics, 1 needed antibiotics postoperatively for pneumonia) Years of recruitment: 1983 to 1985 Setting: Parkland Memorial Hospital, Dallas, Texas, USA |
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Participants | Inclusion criteria: women having vaginal hysterectomy Exclusion criteria: antibiotic within previous 3 days, allergy to study drugs Age: 32 to 33 years Type of hysterectomy: vaginal | |
Interventions | Treatment 1: 1 gram cephazolin (first‐generation cephalosporin) Treatment 2: 2 grams cephazolin *Study also compares cephalosporins against each other ‐ data not included Route: IM Single/multiple doses: single Timing of doses: immediately before going to operating theatre |
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Outcomes | Postoperative infection, late and early + late Pelvic infection Postoperative fever Adverse effects (narrative data only) Need for therapeutic antibiotics Hospital length of stay Cost of surgery (data relate only to direct healthcare costs, minus study drugs ‐ data not included in this review) |
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Funding | Eli Lilly and Company | |
Notes | ||
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Computer‐generated |
Allocation concealment (selection bias) | Low risk | Reported that "vials completely wrapped with paper to obscure identification" |
Blinding (performance bias and detection bias) All outcomes | Unclear risk | Probably double‐blinded but no additional details reported on outcome assessor |
Incomplete outcome data (attrition bias) All outcomes | Low risk | Proportions of withdrawals and reasons for withdrawals balanced across groups |
Selective reporting (reporting bias) | Unclear risk | Insufficient information to make a conclusive judgement |
Other bias | Low risk | Baseline demographic characteristics similar between treatment groups |