Evidence map›Paper›PMID 26571483›Full record

ArticleNephron2015

Categories of Hospital-Associated Acute Kidney Injury: Time Course of Changes in Serum Creatinine Values.

David G Warnock, T Clark Powell, John P Donnelly, Henry E Wang

Open access · bronzeAbstract read
In one paragraph

Article in Nephron, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 2 syntheses or guidelines pooled it, 10 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. UAB-UCSD O'Brien Center for Acute Kidney Injury Research.American journal of physiology. Renal physiology · 2021
    Review
  6. Article
  7. Article
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

4 authors at 2 institutions in 2 countries.

David G WarnockDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Ala., USA.
T Clark Powell
John P Donnelly
Henry E Wang
University of Alabama at Birmingham · USGeneral Department of Preventive Medicine · VN

Funding

UAB-UCSD O'Brien Core Center for Acute Kidney Injury ResearchP30DK079337 · NIDDK · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI AGARWAL, ANUPAM · 2008 to 2022
$18.3M
UAB Health Services Research (HSR) Training ProgramT32HS013852 · AHRQ · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI LEVITAN, EMILY B, MUGAVERO, MICHAEL J · 2003 to 2024
$8.0M
Risk Factors for Sepsis in the CommunityR01NR012726 · NINR · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI WANG, HENRY E. · 2011 to 2015
$2.6M
AHRQ HHS T32 HS013852AHRQ HHS T32-HS013852NIDDK NIH HHS P30 DK079337NINR NIH HHS R01 NR012726NINR NIH HHS R01-NR012726
6 · The paper itself

Abstract

unlabelledHospital-associated acute kidney injury (HA-AKI) is associated with increased inpatient mortality. Our objective was to categorize HA-AKI based on the timing of minimum and peak inpatient serum creatinine (sCr) and describe the association with inpatient mortality. MATERIALS AND

methodsThis study is a retrospective analysis of an administrative data set for adults admitted to a single medical center for over 4 years. Changes and timing of the minimum and peak sCr were used to define HA-AKI categories.

resultsPeak creatinine followed minimum creatinine for HA-AKI, and preceded the minimum value for transient HA-AKI (THA-AKI). A subset of patients developed HA-AKI after recovering from THA-AKI. Multivariable Cox regression analyses examined the association between these categories and 28-day inpatient mortality, adjusting for age, sex, race, Charlson comorbidity index, baseline kidney function, AKI recovery and renal replacement therapy. There were 50,601 patients included in the analyses, and 29,996 (59%) did not have AKI. There were 2,440 deaths; HA-AKI had a 2.24-fold (95% CI 1.99-2.51) increased risk, while THA-AKI group (12,101) had a 1.23-fold (95% CI 1.09-1.40) increased risk for inpatient mortality. THA-AKI patients who recovered and then developed HA-AKI had the same mortality risk as THA-AKI (1.27-fold [95% CI 1.07-1.51]) but longer hospitalization and less recovery from AKI.

conclusionsRisk of short-term inpatient mortality is associated with AKI, and this risk is attenuated with recovery of kidney function in the hospital. Systematic surveillance with repeated inpatient sCr values is needed to assess the short- and long-term consequences of HA-AKI.

Indexed as

Acute Kidney InjuryAdultAgedCreatinineFemaleHospitalsHumansMaleMiddle AgedProportional Hazards ModelsRetrospective StudiesCreatinine

Identifiers

PMID26571483
PMCPMC4698143
OpenAlexW2196598261

What OpenQuestion holds

Textmetadata
LicenceTDM
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.