Evidence map›Paper›PMID 27852290›Full record

ArticleCritical care (London, England)2016

Acute kidney injury subphenotypes based on creatinine trajectory identifies patients at increased risk of death.

Pavan K Bhatraju, Paramita Mukherjee, Cassianne Robinson-Cohen, Grant E O'Keefe, Angela J Frank, Jason D Christie, Nuala J Meyer, Kathleen D Liu, Michael A Matthay, Carolyn S Calfee and 3 more

Registry-linked trialAbstract readMulticenter Study
In one paragraph

Article in Critical care (London, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05247502 (Impact of the Characteristics of Acute Renal Failure in Intensive Care on the Long-term Renal Prognosis), which is not on this map. Cited by 53 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed, 2 pooled it
–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.

NCT05247502 recruitingnot on this mapstarted 2022, after this paper: background citation

Impact of the Characteristics of Acute Renal Failure in Intensive Care on the Long-term Renal Prognosis: Prospective Multicenter Cohort Study

TypeobservationalSponsorUniversity Hospital, Clermont-FerrandRan2022 to 2028Enrolled860ConditionsAcute Kidney Injury, Transient Acute Renal Failure, Persistent Acute Renal FailureArmsData observation
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
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  14. [Clinical sub-phenotypes of acute kidney injury in children and their association with prognosis].Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2025
    Article
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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

13 authors.

Pavan K BhatrajuDivision of Pulmonary and Critical Care Medicine, University of Washington, Harborview Medical Center, 325 9th Avenue, Seattle, WA, 98104, USA. bhatraju@uw.edu.
Paramita MukherjeeKidney Research Institute, University of Washington, Seattle, WA, USA.
Cassianne Robinson-CohenKidney Research Institute, University of Washington, Seattle, WA, USA.
Grant E O'KeefeDepartment of Surgery, University of Washington, Seattle, WA, USA.
Angela J FrankDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Jason D ChristieDivision of Pulmonary, Allergy, and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Nuala J MeyerDivision of Pulmonary, Allergy, and Critical Care, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Kathleen D LiuDepartment of Medicine, University of California, San Francisco, CA, USA.
Michael A MatthayDepartment of Medicine, University of California, San Francisco, CA, USA.
Carolyn S CalfeeDepartment of Medicine, University of California, San Francisco, CA, USA.
David C ChristianiDepartment of Environmental Health, Harvard T.H. Chan School of Public Health, Boston, MA, USA.
Jonathan HimmelfarbKidney Research Institute, University of Washington, Seattle, WA, USA.
Mark M WurfelDivision of Pulmonary and Critical Care Medicine, University of Washington, Harborview Medical Center, 325 9th Avenue, Seattle, WA, 98104, USA.

Funding

RESPIRATORY RESEARCH TRAINING PROGRAMT32HL007287 · NHLBI · UNIVERSITY OF WASHINGTON · PI Kristina Anne Crothers, David J. Horne · 1985 to 2026
$16.7M
MOLECULAR EPIDEMIOLOGY OF ARDSR01HL060710 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI CHRISTIANI, DAVID C · 2000 to 2015
$8.4M
Genetic risks for ALI in ARDSnet and the iSPAAR ConsortiumRC2HL101779 · NHLBI · UNIVERSITY OF WASHINGTON · PI WURFEL, MARK M · 2009 to 2010
$4.7M
Gene Polymorphisms, Inflammation and Outcome from TraumaR01GM066946 · NIGMS · UNIVERSITY OF WASHINGTON · PI O'KEEFE, GRANT E · 2003 to 2007
$1.6M
Identification of Sub-phenotypes of Acute Kidney Injury in the Intensive Care UnitF32DK112532 · NIDDK · UNIVERSITY OF WASHINGTON · PI BHATRAJU, PAVAN KUMAR · 2016 to 2017
$139k
NHLBI NIH HHS R01 HL060710NHLBI NIH HHS RC2 HL101779NHLBI NIH HHS T32 HL007287NIDDK NIH HHS F32 DK112532NIGMS NIH HHS R01 GM066946
6 · The paper itself

Abstract

backgroundAcute kidney injury (AKI) is common among intensive care unit (ICU) patients. AKI is highly heterogeneous, with variable links to poor outcomes. Current approaches to classify AKI severity and identify patients at highest risk for poor outcomes focus on the maximum change in serum creatinine (SCr) values. However, these scores are hampered by the need for a reliable baseline SCr value and the absence of a component differentiating transient from persistent rises in SCr. We hypothesized that identification of resolving or nonresolving AKI subphenotypes based on the early trajectory of SCr values in the ICU would better differentiate patients at risk of hospital mortality.

methodsWe performed a secondary analysis of two prospective studies of ICU patients admitted to a trauma ICU (group 1; n = 1914) or general medical-surgical ICUs (group 2; n = 1867). In group 1, we tested definitions for resolving and nonresolving AKI subphenotypes and selected the definitions resulting in subphenotypes with the greatest separation in risk of death relative to non-AKI controls. We applied this definition to group 2 and tested whether the subphenotypes were independently associated with hospital mortality after adjustment for AKI severity.

resultsAKI occurred in 46% and 69% of patients in groups 1 and 2, respectively. In group 1, a resolving AKI subphenotype (defined as a decrease in SCr of 0.3 mg/dl or 25% from maximum in the first 72 h of study enrollment) was associated with a low risk of death. A nonresolving AKI subphenotype (defined as all AKI cases not meeting the "resolving" definition) was associated with a high risk of death. In group 2, the resolving AKI subphenotype was not associated with increased mortality (relative risk [RR] 0.86, 95% CI 0.63-1.17), whereas the nonresolving AKI subphenotype was associated with higher mortality (RR 1.68, 95% CI 1.15-2.44) even after adjustment for AKI severity stage.

conclusionsThe trajectory of SCr levels identifies AKI subphenotypes with different risks for death, even among AKI cases of similar severity. These AKI subphenotypes might better define the patients at risk for poor outcomes who might benefit from novel interventions.

Indexed as

PhenotypeAcute Kidney InjuryAdolescentAdultAgedBiomarkersCase-Control StudiesCohort StudiesCreatinineFemaleHospital MortalityHumansIntensive Care UnitsMaleMiddle AgedProspective StudiesBiomarkersCreatinineAcute kidney injuryCritical careIntensive care unitMortalitySubphenotypesTrajectory

Identifiers

PMID27852290
PMCPMC5112626

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Registered trials

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.