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P-1688. Differences in Guideline-Concordant Antibiotic Prescribing Based on Age, Sex, Race, and Ethnicity for the Management of Inpatients with Community-Acquired Bacterial Pneumonia (CABP) due to Pseudomonas aeruginosa: a Retrospective Cohort Analysis of the All of Us Database

Corbyn M. Gilmore, Adriana Vargus, Christopher R Frei

Open Forum Infectious Diseases, 2025

119 participants

Abstract

Abstract Background This is one of the first studies to evaluate health disparities in antibiotic prescribing for inpatients with community-acquired bacterial pneumonia (CABP) from Pseudomonas aeruginosa.Table 1. Patient Baseline Characteristics, by Guideline-Concordant and Discordant Antibiotics * Bold italics indicates statistically significant findings. + Some groups contain non-exact participant counts to prevent displaying any participant count that is less than 20 and to comply with the All of Us data and statistic dissemination policy. Methods Inpatients with CABP due to P. aeruginosa (SNOMED: 41381004) were identified in the All of Us database (2016-2022). Patients with treatment settings other than inpatient, other pathogens, and other pneumonia types were excluded. Patients were grouped by age, sex, race, and ethnicity. The proportion of patients prescribed guideline-concordant and guideline-discordant anti-pseudomonal antibiotics (GCAB and GDAB) were compared with chi-square. GCAB (2019 IDSA/ATS CABP guidelines), were: aztreonam, cefepime, ceftazidime, imipenem, meropenem, and piperacillin-tazobactam. Significant associations between patient characteristics and prescribing (p < 0.05) were assessed using multivariate logistic regression, with subgroup as the independent variable, anti-pseudomonal prescribing as the dependent variable, and divergent baseline characteristics as confounders. Odds ratios (OR) and 95% confidence intervals (95% CI) for receipt of GCAB…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 119 participants or records.

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