Evidence map›Paper›PMID 36186791›Full record

ArticleFrontiers in medicine2022

Morphogenetic dispositions for variability in acute kidney injury after cardiac surgery: Pilot study.

Radmila Karan, Natasa Kovačević-Kostić, Bratislav Kirćanski, Jelena Čumić, Duško Terzić, Vladimir Milićević, Vojislav Velinović, Miloš Velinović, Biljana Obrenović-Kirćanski

Abstract read
In one paragraph

Article in Frontiers in medicine, 2022. 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

9 authors.

Radmila KaranFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Natasa Kovačević-KostićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Bratislav KirćanskiFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Jelena ČumićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Duško TerzićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Vladimir MilićevićClinic for Cardiac Surgery, Clinical Center of Serbia, Belgrade, Serbia.
Vojislav VelinovićClinic for Cardiology, Clinical Center of Serbia, Belgrade, Serbia.
Miloš VelinovićFaculty of Medicine, University of Belgrade, Belgrade, Serbia.
Biljana Obrenović-KirćanskiFaculty of Medicine, University of Belgrade, Belgrade, Serbia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The aim of our study was to evaluate the degree of genetic homozygosity in cardiac surgical patients with postoperative acute kidney injury (AKI), compared to the subgroup without postoperative AKI, as well as to evaluate antropomorpho-genetic variability in cardiac surgical patients with regard to the presence and severity degree of AKI. Materials and methods: The prospective cohort study included an analysis of 138 eligible coronary artery disease (CAD) surgical patients that were screened consecutively. The tested group was divided into three subgroups according to RIFLE criteria: Subgroup NoAKI ( Results: Comparing subgroups NoAKI and risk, four ORHTs were significantly more frequent in the risk subgroup. Comparing subgroups NoAKI and injury, nine ORHTs were significantly more frequent in the injury subgroup; while comparing the injury subgroup and risk, five ORHTs were significantly more frequent in injury than in the risk subgroup. Results also showed a significant increase in the mean value of ORHTs for the injury subgroup compared to NoAKI subgroup ( Conclusion: Our findings pointed to the higher degree of recessive homozygosity and decreased variability in AKI patients vs. NoAKI individuals, thus presumably facilitating the development and severity degree expression of AKI in patients after cardiac surgery.

Indexed as

acute kidney injurycardiac surgerycoronary artery diseaseobservable recessive human traitsvariability

Identifiers

PMID36186791
PMCPMC9523005

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.