Key result
Nonadherence to IDSA antibiotic guidelines is linked to ~34% higher SSI risk, driven by incorrect choice.
Why the study?
Surgical site infections persist despite adherence to SCIP antibiotic timing metrics, raising the question of whether nonadherence to comprehensive IDSA antibiotic metrics is associated with surgical site infections.
Does nonadherence to IDSA-defined antibiotic metrics increase surgical site infections in adults undergoing noncardiac surgery?
Does nonadherence to IDSA-defined antibiotic metrics increase surgical site infections in adults undergoing noncardiac surgery?
Nonadherence to comprehensive IDSA perioperative antibiotic guidelines, particularly regarding antibiotic choice and intraoperative redosing, is common and significantly associated with increased surgical site infections in noncardiac surgery.
May prompt quality initiatives on IDSA antibiotic choice and redosing; leaves open causal effects on SSIs.
Importance Despite nearly universal adherence to the Surgical Care Improvement Project (SCIP), surgical site infections (SSIs) persist. Compared with SCIP, which largely focuses on antibiotic timing, the Infectious Diseases Society of America (IDSA) guidelines provide a more comprehensive framework of antibiotic metrics, including procedure-specific antibiotic selection, weight-adjusted dosing, timing of the first dose, and appropriate redosing. Objective To assess whether nonadherence to each antibiotic administration metric of IDSA guidelines is associated with SSIs. Design, Setting, and Participants In this nationwide, multicenter, cross-sectional study, patients aged 18 years or older who underwent noncardiac surgeries involving a skin incision between January 1, 2014, and August 31, 2022, were included from merged data of the Multicenter Perioperative Outcomes Group, National Surgical Quality Improvement Program, and Michigan Surgical Quality Collaborative registries. Analyses were conducted between July 2, 2024, and April 24, 2025. Exposure Nonadherence to IDSA-defined antibiotic metrics. Main Outcomes and Measures The primary end point was SSI, defined as any superficial, deep tissue, or organ-space infection as recorded in the National Surgical Quality Improvement Program and Michigan Surgical Quality Collaborative registries. The association of nonadherence to IDSA guidelines (both overall and individually) was examined using hierarchical generalized linear mixed models. Results Of 134 413 eligible surgical cases, a total of 119 236 patients (mean [SD] age, 56.2 [15.9] years; 58.1% women) from 37 institutions met the inclusion criteria, among whom 6796 (5.7%) had incomplete covariate data. Failure to adhere to any IDSA metric was common in 26.1% of cases, with individual nonadherence rates as follows: 13.3% for antibiotic choice, 9.0% for weight-adjusted dosing, 3.0% for timing relative to incision, and 4.8% for correct intraoperative redosing interval. Overall, SSIs occurred in 4.4% of cases. After adjusted analysis, guideline-nonadherent antibiotic administration was significantly associated with SSIs (relative risk [RR], 1.34 [95% CI, 1.26-1.43]). Nonadherence to antibiotic choice (RR, 1.43 [95% CI, 1.33-1.53]) and failure to appropriately redose intraoperatively (RR, 1.12 [95% CI, 1.02-1.24]) were significantly associated with SSIs. Conclusions and Relevance This cross-sectional study found that IDSA guideline nonadherence, including incorrect antibiotic choice and missed intraoperative redosing, was common and associated with increased SSI risk, despite high adherence to SCIP timing metrics. Improving adherence to IDSA-recommended antibiotic selection and redosing may meaningfully reduce SSIs.
No takes yet. Share an insight, caveat, or question.
Bardia et al. (2026) studied this question. Nonadherence to IDSA antibiotic guidelines increased surgical site infection risk by 34%, especially incorrect choice (RR 1.43) and missed intraoperative redosing (RR 1.12).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: