1165. Comparing Patient Risk Factors, Sequence Type, and Resistance Loci Identification Approaches for Predicting Antibiotic Resistance in Escherichia coli Bloodstream Infections
Bibliographic record
Abstract
Abstract Background To improve the adequacy of empiric antibiotic therapy, an important predictor of clinical outcome, rapid diagnostic tests of antibiotic resistance are increasingly being developed that identify the presence or absence of antibiotic resistance genes/Loci. Few approaches have utilized other sources of predictive information, which could be identified in shorter time periods, including patient epidemiologic risk factors for antibiotic resistance and markers of lineage (e.g., sequence type). Methods Using a dataset of 414 Escherichia coli isolated from separate episodes of bacteremia at a single academic institution in Toronto, Canada between 2010 and 2015, we compared the potential predictive ability of three approaches (epidemiologic, sequence type, and gene identification) for classifying antibiotic resistance to three commonly used classes of broad-spectrum antibiotic therapy (third-generation cephalosporins, fluoroquinolones, and aminoglycosides). We used logistic regression models with binary predictor variables to generate model receiver operating characteristic curves. Predictive discrimination was measured using apparent and corrected (bootstrapped) area under the curves (AUCs). Results Using two simple epidemiologic risk factors (prior antibiotic exposure and recent prior Gram-negative susceptibility), modest predictive discrimination was achieved (AUCs 0.65–0.74). Sequence type demonstrated strong discrimination (AUCs 0.84–0.94) across all three antibiotic classes. Epidemiologic risk factors significantly improved sequence-type prediction for cephalosporins and aminoglycosides (P < 0.05). Gene identification approaches provided the highest degree of discrimination (AUCs 0.73–0.99), with no statistically significant benefit of adding epidemiologic predictors. Conclusion Rapid identification of sequence type, or other lineage-based classification, could produce excellent discrimination of antibiotic resistance, and may be improved by incorporating readily available epidemiologic predictors. Disclosures All authors: No reported disclosures.
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How this classification was reachedexpand
Full frame distilled prediction
Teacher imitationNot calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.
Codex and Gemma teacher scores by category
| Category | Codex | Gemma |
|---|---|---|
| Metaresearch | 0.000 | 0.001 |
| Meta-epidemiology (narrow) | 0.000 | 0.000 |
| Meta-epidemiology (broad) | 0.000 | 0.000 |
| Bibliometrics | 0.000 | 0.000 |
| Science and technology studies | 0.001 | 0.000 |
| Scholarly communication | 0.000 | 0.000 |
| Open science | 0.000 | 0.000 |
| Research integrity | 0.000 | 0.000 |
| Insufficient payload (model declined to judge) | 0.000 | 0.000 |
Machine scores (provisional)
The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.
Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.
score_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from itClassification
machine, unvalidatedMachine predicted; a candidate call from one teacher head, not a consensus.
How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".