Evidence map›Paper›PMID 42683513›Full record

ArticleThe Journal of antimicrobial chemotherapy2026

Acute kidney injury in Staphylococcus aureus bacteraemia: a multicentre cohort study of incidence, timing, recovery and associations with antibiotic treatment.

F S Sinkeler, I J E Kouijzer, N G L Jager, J Ten Oever, E Leegwater, J Gisolf, D Reuling, Z M Spoel, M P M Hensgens, R J Brüggemann

Abstract readMulticenter Study
In one paragraph

Article in The Journal of antimicrobial chemotherapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

F S SinkelerDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-5019-0549
I J E KouijzerDepartment of Internal Medicine and Radboudumc Community for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.
N G L JagerDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-4524-9892
J Ten OeverDepartment of Internal Medicine and Radboudumc Community for Infectious Diseases, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0003-2397-0125
E LeegwaterDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.
J GisolfDepartment of Internal Medicine, Rijnstate Hospital, Arnhem, The Netherlands.
D ReulingDepartment of Internal Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
Z M SpoelDepartment of Internal Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
M P M HensgensDepartment of Internal Medicine, University Medical Center Utrecht, Utrecht, The Netherlands.
R J BrüggemannDepartment of Pharmacy, Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0002-7618-725X

Funding

ZonMw 10140022110014
6 · The paper itself

Abstract

BACKGROUND AND

objectivesStaphylococcus aureus bacteraemia (SAB) is associated with high mortality and frequent complications, including acute kidney injury (AKI). Although flucloxacillin has been associated with higher AKI rates than cefazolin, the clinical characteristics of AKI, including severity, timing, recovery and the potential influence of dosing, remain unclear.

methodsWe conducted a retrospective multicentre cohort study across three hospitals in the Netherlands, including adults with SAB treated with cefazolin or flucloxacillin. AKI incidence and severity were compared using adjusted regression analyses. Time-to-event and cumulative incidence analyses were used to evaluate AKI timing and renal recovery. Among flucloxacillin-treated patients, the association between initial dose and AKI was evaluated.

resultsAmong 1408 patients, 483 (34.3%) developed AKI. Most AKI episodes occurred early after index blood culture (median 1.3 days), and recovery within 30 days decreased with increasing AKI severity (81.7% in Stage 1 versus 50.5% in Stage 3). AKI occurred more frequently among patients treated with flucloxacillin than cefazolin (466/1324 [35.2%] versus 17/84 [20.2%], P = 0.004). After multivariable adjustment, flucloxacillin remained associated with higher AKI risk (adjusted OR 2.37, 95% CI 1.30-4.55). Among patients with AKI, severity distribution did not differ between treatments (P = 0.599). Initial flucloxacillin dose was not associated with AKI occurrence, timing or severity.

conclusionsFlucloxacillin was associated with increased AKI risk compared with cefazolin, with most AKI episodes occurring early after index blood culture and recovery decreasing with increasing AKI severity. Lower flucloxacillin doses were not associated with reduced AKI risk, suggesting that dose reduction alone may not mitigate flucloxacillin-associated nephrotoxicity.

Indexed as

Acute Kidney InjuryAnti-Bacterial AgentsBacteremiaStaphylococcal InfectionsAdultAgedAged, 80 and overCefazolinFemaleFirst Generation CephalosporinsFloxacillinHumansIncidenceMaleMiddle AgedNetherlandsAnti-Bacterial AgentsCefazolinFirst Generation CephalosporinsFloxacillin

Identifiers

PMID42683513
PMCPMC13535221

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.