Evidence map›Paper›PMID 35287608›Full record

ArticleBMC pediatrics2022

Clinical course of neonatal acute kidney injury: multi-center prospective cohort study.

O C Pantoja-Gómez, S Realpe, Ginna Cabra-Bautista, J M Restrepo, O L Prado, A M Velasco, G E Martínez, S Leal, A Vallejo, Jose Andrés Calvache

Abstract read
In one paragraph

Article in BMC pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Gut microbiota and neonatal acute kidney injury biomarkers.Pediatric nephrology (Berlin, Germany) · 2023
    Review
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.

O C Pantoja-GómezDepartamento de Pediatría, Universidad del Cauca, Popayán, Colombia. opantojag@unicauca.edu.co.
S RealpeDepartamento de Pediatría, Universidad del Cauca, Popayán, Colombia.
Ginna Cabra-BautistaDepartamento de Pediatría, Universidad del Cauca, Popayán, Colombia.
J M RestrepoServicio de Nefrología Pediátrica, Fundación Valle del Lili, Cali, Colombia.
O L PradoDepartamento de Pediatría, Universidad del Cauca, Popayán, Colombia.
A M VelascoDepartamento de Pediatría, Universidad del Cauca, Popayán, Colombia.
G E MartínezDepartamento de Pediatría, Universidad del Cauca, Popayán, Colombia.
S LealHospital Susana López de Valencia, Popayán, Colombia.
A VallejoHospital Universitario San Jose, Popayán, Colombia.
Jose Andrés CalvacheDepartamento de Anestesiología, Universidad del Cauca, Popayán, Colombia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeonatal acute kidney injury (AKI) has been associated with unfavorable outcomes, including increased mortality. We aimed to describe the clinical course and outcomes during the first 7 days after diagnosis in newborns with AKI in three neonatal intensive care units in Popayán-Colombia.

methodsMulti-center prospective cohort study conducted between June 2019 and December 2020 in three NICUs after ethical approval. We included newborns between 2 and 28 days of life, first diagnosed with AKI using the KDIGO classification modified for newborns which consider increased serum creatinine values over baseline values as well as urine output over time in hours or both. Patients with chromosomal abnormalities, major kidney malformations, and complex congenital heart disease were excluded. Patients were followed for up to 7 days after diagnosis and the maximum KDIGO stage, recovery of kidney function, need for renal replacement therapy and cumulative incidence of death were evaluated.

resultsOver the 18 months of the study, 4132 newborns were admitted to the NICUs, and 93 patients (2.25, 95% CI 1.82-2.75%) developed neonatal AKI. 59.1% of the newborns were premature and there were no differences in severity according to gestational age. During follow-up, the maximum KDIGO was 64.5% for AKI-stage 1, 11.8% for AKI-stage 2, and 23.7% for AKI-stage 3. Kidney function recovery was higher in AKI-stage 1 patients vs. AKI-severe (AKI-stage 2 and 3) (95% vs. 48.5%). Five patients (5.4%) received renal replacement therapy and 15 died (16.1%), four in AKI-stage 1 vs. 11 in AKI-severe (6.7% vs 33.3%).

conclusionsNewborns admitted to the NICUs can develop AKI regardless of gestational age, and it is more frequent between the second and ninth days of life. More patients whit AKI-stage 1 recover and die less than those in a severe stage.

Indexed as

Acute Kidney InjuryHumansIncidenceInfant, NewbornIntensive Care Units, NeonatalProspective StudiesRenal Replacement TherapyRetrospective StudiesRisk FactorsAcute kidney injuryInfant, NewbornIntensive care units, NeonatalKDIGOMortalityRenal replacement therapy

Identifiers

PMID35287608
PMCPMC8920800

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LicenceCC BY
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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.