Evidence map›Paper›PMID 42581256›Full record

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

Ampicillin/ceftriaxone vs. β-lactam/aminoglycoside combination therapy for Enterococcus faecalis infective endocarditis: a systematic review and meta-analysis.

Yui Sugimoto, Ryosuke Sasaki, Mayu Tominaga, Ryuka Hirai, Takayuki Mihara, Rina Shimamura, Maiko Yoshikawa, Shintaro Ikegami, Sora Shimada, Ayu Tsubouchi and 5 more

Abstract read
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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.

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

15 authors.

Yui Sugimoto *Division of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Ryosuke Sasaki *Division of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Mayu Tominaga *Division of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Ryuka Hirai *Division of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Takayuki MiharaDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Rina ShimamuraDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Maiko YoshikawaDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Shintaro IkegamiDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Sora ShimadaDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Ayu TsubouchiDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Yuko OkamotoDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Yuki IgarashiDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan. igarashi-yk@keio.jp.ORCID https://orcid.org/0009-0002-1936-910X
Yuki EnokiDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.
Kazuaki TaguchiBiomedical and Health Sciences, Hiroshima University, Hiroshima, Japan.
Kazuaki MatsumotoDivision of Pharmacodynamics, Keio University Faculty of Pharmacy, 1-5- 30 Shibakoen, Minato-ku, Tokyo, 105-8512, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnterococcus faecalis infective endocarditis (EFIE) remains a formidable infection requiring prolonged antimicrobial therapy. Although β-lactam/aminoglycoside (BL + AG) combination therapy has long been regarded as the standard treatment, AG-associated toxicities pose a major clinical dilemma. Recently, dual β-lactam therapy with ampicillin/ceftriaxone (A + C) has become an established treatment option. This systematic review and meta-analysis aimed to compare the efficacy and safety of A + C versus BL + AG therapy in patients with EFIE.

methodsA literature search was conducted using PubMed, the Cochrane Library, Web of Science, and ClinicalTrials.gov. Clinical studies comparing A + C versus BL + AG for EFIE were included. Primary outcomes were mortality and relapse rates. Secondary outcomes included overall adverse events, renal adverse events, ototoxicity/vestibular toxicity, skin rash, Clostridioides difficile diarrhea, and regimen changes or discontinuation. Pooled ORs and 95% CIs were estimated utilizing random-effects models.

resultsSix studies involving 619 patients with EFIE were included. Cumulative mortality (OR 1.10, 95% CI: 0.73-1.65) and relapse rates (OR 1.08, 95% CI: 0.39-3.01) did not differ significantly between A + C and BL + AG. However, A + C was associated with significantly lower incidences of total adverse events (OR 0.20, 95% CI: 0.08-0.53), renal adverse events (OR 0.34, 95% CI: 0.19-0.58), ototoxicity/vestibular toxicity (OR 0.07, 95% CI: 0.01-0.37), and antibiotic regimen change (OR 0.20, 95% CI: 0.10-0.39) or discontinuation (OR 0.17, 95% CI: 0.05-0.56).

conclusionA + C therapy was associated with a more favorable safety profile than BL + AG therapy, with no significant differences in efficacy, mortality, or relapse in patients with EFIE. These findings support the use of A + C as an important therapeutic option for patients at increased risk of AG-associated toxicity.

Indexed as

AminoglycosideAmpicillinCeftriaxoneEnterococcus faecalis infective endocarditisMeta-analysis

Identifiers

PMID42581256

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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.