Evidence map›Paper›PMID 42560604›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2026

Renal safety of amikacin compared with ceftriaxone in patients treated for urinary tract infection: an observational cohort study.

Iris Zohar, Dvir Melloul, Baruch Satra-Shenes, Orna Schwartz, Debby Ben David, Yasmin Maor

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Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Iris ZoharInfectious Disease Unit, Edith Wolfson Medical Center, Holon, 5822012, Israel. irisz@wmc.gov.il.
Dvir MelloulGray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Baruch Satra-ShenesGray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Orna SchwartzMicrobiology Laboratory, Edith Wolfson Medical Center, Holon, Israel.
Debby Ben DavidGray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Yasmin MaorInfectious Disease Unit, Edith Wolfson Medical Center, Holon, 5822012, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAminoglycosides are broad-spectrum antibiotics commonly used as monotherapy for urinary tract infections (UTIs). However, their use is often limited by concerns regarding nephrotoxicity. We compared the renal safety of amikacin with ceftriaxone in patients treated for UTI with or without bloodstream infection.

methodsWe conducted a single-center retrospective cohort study including adult patients hospitalized between April 2018 and March 2022 who received amikacin or ceftriaxone for UTI for 3-10 days. Patients were matched 1:1 according to age, duration of therapy, and baseline renal function. The primary outcome was acute kidney injury (AKI), defined according to KDIGO criteria. Analyses included Kaplan-Meier time-to-event analysis, propensity score-adjusted Cox regression, and multivariable logistic regression. Alternative etiologies for AKI were also assessed.

resultsA total of 138 matched pairs were included. Overall, 15 patients (5.4%) developed AKI: 9 (6.5%) in the amikacin group and 6 (4.3%) in the ceftriaxone group (P = 0.597), and Kaplan-Meier analysis likewise showed no difference between groups (log-rank P = 0.962). In propensity score-adjusted analysis of the total cohort, amikacin was not associated with increased risk of AKI (aHR 1.305, 95% CI 0.448-3.802, P = 0.626). Independent risk factors for AKI included institutional residence, higher Charlson comorbidity index, and bloodstream infection. Most AKI cases were mild and had alternative explanations.

conclusionsIn this matched cohort, amikacin was not associated with a higher risk of AKI compared with ceftriaxone. These findings suggest that, in selected patients, amikacin may represent a safe carbapenem-sparing option. Further studies are needed to confirm these findings.

Indexed as

Acute kidney injuryAmikacinAntimicrobial stewardshipCeftriaxoneNephrotoxicity

Identifiers

PMID42560604

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