Evidence map›Paper›PMID 28353411›Full record

ArticlePathogens and global health2017

Polymyxin-B and vancomycin-associated acute kidney injury in critically ill patients.

Douglas de Sousa Soares, André da Fonte Reis, Geraldo Bezerra da Silva Junior, Tacyano Tavares Leite, Sérgio Luiz Arruda Parente Filho, Carina Vieira de Oliveira Rocha, Elizabeth De Francesco Daher

Abstract read
In one paragraph

Article in Pathogens and global health, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.1field-weighted citation impact, top 14% of its field
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

12 citing papers in PubMed, 25 citations in OpenAlex.

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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 at 3 institutions in 1 country.

Douglas de Sousa Soaresa Department of Internal Medicine, School of Medicine, Post-Graduation Program in Medical Sciences , Federal University of Ceará , Fortaleza , Brazil.
André da Fonte Reisb Division of Nephrology , Fortaleza General Hospital , Fortaleza , Brazil.
Geraldo Bezerra da Silva Juniorc School of Medicine, Post-Graduation Program in Collective Health, Health Sciences Center , University of Fortaleza , Fortaleza , Brazil.
Tacyano Tavares Leitea Department of Internal Medicine, School of Medicine, Post-Graduation Program in Medical Sciences , Federal University of Ceará , Fortaleza , Brazil.
Sérgio Luiz Arruda Parente Filhoa Department of Internal Medicine, School of Medicine, Post-Graduation Program in Medical Sciences , Federal University of Ceará , Fortaleza , Brazil.
Carina Vieira de Oliveira Rochaa Department of Internal Medicine, School of Medicine, Post-Graduation Program in Medical Sciences , Federal University of Ceará , Fortaleza , Brazil.
Elizabeth De Francesco Dahera Department of Internal Medicine, School of Medicine, Post-Graduation Program in Medical Sciences , Federal University of Ceará , Fortaleza , Brazil.
Universidade Federal do Ceará · BRHospital Geral de Fortaleza · BRUniversidade de Fortaleza · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aims to investigate renal toxicities of Polymyxin B and Vancomycin among critically ill patients and risk factors for acute kidney injury (AKI).

methodsThis is a cross-sectional study conducted with patients admitted to an intensive care unit (ICU) of a tertiary hospital in Brazil. Patients were divided into two groups: those who used association of Polymyxin B + Vancomycin (Group I) and those who used only Polymyxin B (Group II). Risk factors for AKI were also analyzed.

resultsA total of 115 patients were included. Mean age was 59.2 ± 16.1 years, and 52.2% were males. Group I presented higher GFR (117.1 ± 70.5 vs. 91.5 ± 50 ml/min/1.73 m², p = 0.02) as well as lower creatinine (0.9 ± 0.82 vs. 1.0 ± 0.59 mg/dL, p = 0.014) and urea (51.8 ± 23.7 vs. 94.5 ± 4.9 mg/dL, p = 0.006) than group II on admission. Group I also manifested significantly higher incidence of AKI than group II (62.7% vs. 28.5%, p = 0.005), even when stratified according to RIFLE criteria ('Risk' 33.9% vs. 10.7%; 'Injury' 10.2% vs. 8.9%; 'Failure' 18.6% vs. 8.9%; p = 0.03). Accumulated Polymyxin B dose > 10 million IU was an independent predictor for AKI (OR = 2.72, 95% CI = 1.13-6.51, p = 0.024).

conclusionsAlthough patients who received Polymyxin B plus vancomycin had more favorable clinical profile and higher previous GFR, they presented a higher AKI incidence than those patients who received Polymyxin B alone. Cumulative Polymyxin B dose > 10 million IU was independently associated to AKI.

Indexed as

Acute Kidney InjuryAdultAgedAnti-Bacterial AgentsBrazilCritical IllnessCross-Sectional StudiesFemaleHumansIncidenceMaleMiddle AgedPolymyxin BRisk FactorsVancomycinAnti-Bacterial AgentsPolymyxin BVancomycinacute kidney injurydrug toxicityPolymyxin Bvancomycin

Identifiers

PMID28353411
PMCPMC5445639
OpenAlexW2603669971

What OpenQuestion holds

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Registered trials

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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.