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Aurora Pop-Vicas et al
Fig. 1. Flowchart of study selection from the literature review. *Studies included obstetric-gynecological surgeries other than hysterectomy. Abbreviation: SSI, surgical site infection.
surgeries other than hysterectomy in 95 of 798 patients enrolled (12%). Clinical outcomes for this study were reported based on randomized antimicrobial drug arm, but they were not stratified by type of surgery performed. Meta-analyses with and outside this study showed no significant differences in results. We, therefore, chose to retain this study into our final analysis because of its relatively large sample size and because the majority (88%) of the patients underwent abdominal hysterectomy.
Antimicrobial prophylaxis characteristics
There was significant clinical heterogeneity among studies regarding antimicrobial prophylaxis choice and dosing, with anti- microbials administered in varying doses, either as a single pre- operative dose in some studies, or as additional postoperative doses within first 48 hours of surgery in others (Table 1). None of the studies specified whether antimicrobial dosing was adjusted based on patient’s weight/body mass index and/or renal clearance, although 2 studies did specify antimicrobial redosing intraopera- tively for extensive blood loss or surgery duration>3hours.20,24
Clinical outcome definitions and reporting
Definitions and reporting for the clinical outcome of our interest, SSI, were generally consistent between studies. They included the
following terms: surgical wound infection, vaginal cuff infection, postoperative vaginal wound infection, infected pelvic abscess or hematoma, pelvic infection requiring parenteral antimicrobial therapy, abdominal wound infection, pelvic cellulitis. We also included the following phrases: “any surgical wound which drained purulent or serous material, together with or without positive cultures” and “pelvic infection, defined as fever plus ≥1of the following: purulent drainage from the vaginal cuff, abdominal pain with rebound tenderness and/or guarding, localized ten- derness with a tender adnexal mass on bimanual palpation, or bacteremia with or without hypotension” (Table 1).
Study quality and risk of bias
Details related to randomization, such as the randomization sequence for treatment allocation, and details related to treatment concealment and blinding were not reported in 5 studies,17,19,21–23 and were not present in 3 studies,18,20,24 rendering 8 studies at indeterminate and high risk of bias, respectively. An intention-to- treat analysis was performed in only 1 study.25 Table 3 shows details related to risk of bias for the studies included in the sys- tematic review and meta-analysis. As shown by the funnel plot in Figure 2, publication bias was
not present, and the Egger test of the intercept lacked statistical significance (P=.11).
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