# P-868. Creation of a Novel OUD-Specific Antibiogram

**Authors:** Zachary Nichols, Matthew Pettengill, Nathaniel Hurwitz, Bryan Hess, Carolyn Kramer, Elizabeth Novick, John Zurlo, Rebecca Jaffe, Nikhil Seval

PMC · DOI: 10.1093/ofid/ofaf695.1076 · Open Forum Infectious Diseases · 2026-01-11

## TL;DR

This study created a new antibiogram for people with opioid use disorder, showing significant differences in antibiotic susceptibility compared to the general population.

## Contribution

The novel contribution is the creation of an OUD-specific antibiogram revealing distinct microbial resistance patterns.

## Key findings

- OUD patients showed significantly lower susceptibility to TMX-SMX in MSSA isolates compared to non-OUD patients.
- E. coli isolates from non-OUD patients exhibited higher resistance to ampicillin, ampicillin-sulbactam, and TMP-SMX than OUD isolates.
- OUD patients accounted for 32% of S. pyogenes isolates despite being a smaller portion of the overall population.

## Abstract

People who inject drugs are host to a clinically distinct microbial ecology given the population’s high pathogen burden and repeated, incomplete antibiotic exposures. Syndromic antibiograms have a potential utility in this population, and have not to our knowledge been used in patients with opioid use disorder (OUD) and may inform clinically relevant practice changes.OUD Antibiogram TableThe completed antibiogram table comparing the OUD population we identified with the general institutional population.Hospitalizations for Substance Use-Associated Infections in Philadelphia, 2010-2021Citywide hospitalization trends for skin and soft tissue infection and bacteremia in patients with substance use disorder show clear upward trajectories.

OUD Antibiogram Table

The completed antibiogram table comparing the OUD population we identified with the general institutional population.

Hospitalizations for Substance Use-Associated Infections in Philadelphia, 2010-2021

Citywide hospitalization trends for skin and soft tissue infection and bacteremia in patients with substance use disorder show clear upward trajectories.

We conducted a retrospective study of adults (≥18 years) admitted to Thomas Jefferson University Hospital or Jefferson Methodist Hospital during 2022-2023. Persons with OUD were identified by presence of OUD ICD diagnoses (F11.x ICD10 codes) and a positive fentanyl urine test, and positive cultures were included. Patients under 18 were excluded. Patient records were identified through EPIC and cross-referenced with Clinical Microbiology Laboratory data. We analyzed susceptibility patterns for common injection-related organisms (if ≥30 isolates present) and compared them with institutional antibiogram data after removing the OUD population.Detections in Overdose Decedents' Toxicology TestsThe prevalence of benzodiazepines versus xylazine in post-mortem toxicology in Philadelphia, showing xylazine's growing market share.

Detections in Overdose Decedents' Toxicology Tests

The prevalence of benzodiazepines versus xylazine in post-mortem toxicology in Philadelphia, showing xylazine's growing market share.

1807 patients met OUD criteria over the two-year period. Susceptibility data was obtained for Staphylococcus aureus, Streptococcus pyogenes, Pseudomonas aeruginosa, Proteus mirabilis, E. coli for both the OUD group and total group, and an antibiogram was created as per institutional protocol. Cochran–Mantel–Haenszel testing showed a significant dependence (p=2.35e-8) between OUD and susceptibility when controlling for antibiotic-organism pairs. TMX-SMX susceptibility amongst MSSA isolates was 97% (non-OUD) versus 92% (OUD)(p=.012), and amongst MRSA isolates was 85% (non-OUD) versus 80% (OUD)(p=.087). Significantly increased resistance patterns were seen amongst E. Coli isolates in the non-OUD cohort versus OUD (ampicillin-sulbactam 57% vs 43%, p=.006; TMP-SMX 72% vs 62%, p=.012, ampicillin 48% vs 3%, p=.004). 32% of all S. pyogenes isolates for the given culture sites were from persons with OUD.

A novel customized antibiogram that showed statistically and clinically significant differences in antibiotic susceptibility rates in the inpatient population with chart-identified OUD and identified valuable population level infection prevalence data.

All Authors: No reported disclosures

## Linked entities

- **Chemicals:** fentanyl (PubChem CID 3345), xylazine (PubChem CID 5707), ampicillin (PubChem CID 6249), sulbactam (PubChem CID 130313), TMP-SMX (PubChem CID 5578)
- **Diseases:** Staphylococcus aureus infection (MONDO:0005545), E. coli infection (MONDO:0020920)
- **Species:** Staphylococcus aureus (taxon 1280), Streptococcus pyogenes (taxon 1314), Pseudomonas aeruginosa (taxon 287), Proteus mirabilis (taxon 584), Escherichia coli (taxon 562)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12791372/full.md

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Source: https://tomesphere.com/paper/PMC12791372