Evidence map›Paper›PMID 41720900›Full record

ArticleScientific reports2026

Synergistic effects of meropenem, amikacin, and ciprofloxacin against carbapenem resistant Pseudomonas aeruginosa isolates.

Zahra Fooladfar, Abolfazl Rafati Zomorodi, Mohammad Hassan Parvizi Mashhadi, Elahe Meftah, Seyed Reza Abdipour Mehrian, Mohammad Motamedifar, Ali Amanati

Abstract read
In one paragraph

Article in Scientific reports, 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
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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

7 authors.

Zahra FooladfarDepartment of Bacteriology & Virology, School of Medicine, Shiraz University of Medical Science, Shiraz, Iran.
Abolfazl Rafati ZomorodiDepartment of Bacteriology & Virology, School of Medicine, Shiraz University of Medical Science, Shiraz, Iran.
Mohammad Hassan Parvizi MashhadiDepartment of Bacteriology & Virology, School of Medicine, Shiraz University of Medical Science, Shiraz, Iran.
Elahe MeftahClinical Research Development Center, Amir Oncology Teaching Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Seyed Reza Abdipour MehrianClinical Research Development Center, Amir Oncology Teaching Hospital, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammad MotamedifarHIV/AIDS Research Center, Institute of Health, Shiraz University of Medical Sciences, Zand St., P.O. Box: 71348-14336, Shiraz, Iran. motamedm@sums.ac.ir.ORCID http://orcid.org/0000-0003-4993-4034
Ali AmanatiClinical Research Development Center, Amir Oncology Teaching Hospital, Shiraz University of Medical Sciences, Shiraz, Iran. dr.amanati14@gmail.com.ORCID http://orcid.org/0000-0001-9173-2853

Funding

Vice-Chancellor for Research at Shiraz University of Medical Sciences IR.SUMS.REC.01 27785
6 · The paper itself

Abstract

Healthcare-associated infections (HAIs) caused by carbapenem-resistant Pseudomonas aeruginosa (CRPA) are considered a major problem in hospitals due to their resistance to the most effective classes of antibiotics. The aim of the present study was to determine the antimicrobial susceptibility patterns of P. aeruginosa isolates from clinical specimens, and the combination effect of meropenem, amikacin, and ciprofloxacin against CRPA isolates. This cross-sectional study analyzed 70 P. aeruginosa isolates collected from hospitalized patients between August and November 2023. Antimicrobial susceptibility testing was performed on all isolates, and carbapenemase production was assessed in CRPA isolates. Five carbapenemase genes (blaIMP, blaVIM, blaKPC, blaSIM, and blaOXA-48) were screened. Meropenem minimum inhibitory concentrations (MICs) were determined via microbroth dilution method, and synergistic effects of meropenem, amikacin, and ciprofloxacin were evaluated using a three-dimensional checkerboard method. The highest resistance was to colistin 52/70 (74.3%), followed by cefotaxime 33/70 (47.1%) and tobramycin 28/70 (40%). Conversely, the lowest resistance was for aztreonam 19/70 (27.1%); 26/70 (37.1%) of isolates were CRPA. The frequency of genes blaIMP and blaOXA-48 were 4/70 (5.7%) and 1/70 (1.4%) in P. aeruginosa isolates, respectively; blaKPC, blaVIM, and blaSIM were not detected. The three-dimensional checkerboard method was established on 8 selected non-susceptible carbapenem P. aeruginosa isolates and the synergistic effect was recorded for 5 of these tested isolates. This study presents a positive correlation between CRPA and multidrug resistance (MDR), including resistance to all tested antibiotics. However, synergistic effects observed in vitro with meropenem, amikacin, and ciprofloxacin combinations suggest that combination therapy holds promise for treating these infections.

Indexed as

AmikacinAnti-Bacterial AgentsCiprofloxacinMeropenemPseudomonas aeruginosaBacterial Proteinsbeta-LactamasesCarbapenemsCross-Sectional StudiesDrug Resistance, Multiple, BacterialDrug SynergismHumansMicrobial Sensitivity TestsPseudomonas InfectionsAmikacinAnti-Bacterial AgentsBacterial Proteinsbeta-LactamasescarbapenemaseCarbapenemsCiprofloxacinMeropenemCarbapenem-resistantCheckerboardCombination therapyMulti-drug resistantP. aeruginosa

Identifiers

PMID41720900
PMCPMC13021908

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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.