# Adverse Events Comparison of Double Beta-Lactam Combinations for Bloodstream Infections: Ampicillin plus Ceftriaxone and Ampicillin/Cloxacillin

**Authors:** Kazuhiro Ishikawa, Daiki Kobayashi, Nobuyoshi Mori

PMC · DOI: 10.3390/antibiotics13080696 · Antibiotics · 2024-07-25

## TL;DR

This study compares the safety of different beta-lactam antibiotic combinations for treating bloodstream infections, finding that one combination increases the risk of kidney injury.

## Contribution

The study provides new evidence on the adverse event profiles of double beta-lactam combinations in bacteremia treatment.

## Key findings

- ABPC/MCIPC treatment was associated with a higher risk of acute kidney injury compared to ABPC alone.
- ABPC + CTRX showed no significant increase in adverse events compared to ABPC alone.
- Propensity score matching confirmed the increased AKI risk with ABPC/MCIPC.

## Abstract

In Japan, only ampicillin/cloxacillin (ABPC/MCIPC) is available as an anti-staphylococcal penicillin-based treatment for Staphylococcus aureus bacteremia. However, the incidence of adverse events associated with double beta-lactam administration remains unknown. Therefore, we investigated the adverse events of double beta-lactam administration in patients with bacteremia. Adult patients (≥18 years) with bacteremia treated with ABPC, ABPC + ceftriaxone (CTRX), or ABPC/MCIPC were retrospectively analyzed. The primary outcome of this study was the incidence of adverse events such as acute kidney injury, liver dysfunction, and myelosuppression. Chi-square tests and t-tests were used for bivariate analysis. Propensity score (PS) matching was conducted to adjust for confounding factors. We included 277 ABPC-, 57 ABPC + CTRX-, and 43 ABPC/MCIPC-treated patients. Significant differences were noted in age, number of male patients, proportion of patients with qSOFA score ≥2, incidence of chronic kidney disease, treatment duration, mechanical ventilation use, vasopressor use, and proportion of patients with acute kidney injury (AKI) KDIGO grade ≥2. Further, a significant difference was observed between ABPC and ABPC/MCIPC, with a hazard ratio of 1.83 in AKI. In the PS-matched cohort, AKI incidence associated with ABPC/MCIPC was significantly higher than that associated with ABPC. ABPC + CTRX may be safe, whereas ABPC/MCIPC presents a higher risk of AKI and may not be suitable.

## Linked entities

- **Chemicals:** ampicillin (PubChem CID 6249), ceftriaxone (PubChem CID 5479530), cloxacillin (PubChem CID 6098)
- **Diseases:** acute kidney injury (MONDO:0002492), chronic kidney disease (MONDO:0005300)
- **Species:** Staphylococcus aureus (taxon 1280)

## Full-text entities

- **Diseases:** liver dysfunction (MESH:D017093), bacteremia (MESH:D016470), Bloodstream Infections (MESH:D018805), chronic kidney disease (MESH:D051436), AKI (MESH:D058186)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC11350733/full.md

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Source: https://tomesphere.com/paper/PMC11350733