Evidence map›Paper›PMID 32844151›Full record

ArticleProceedings. IEEE International Conference on Healthcare Informatics2019

Identifying KDIGO Trajectory Phenotypes Associated with Increased Inpatient Mortality.

Taylor D Smith, Victor Ortiz Soriano, Javier A Neyra, Jin Chen

Open access · greenAbstract read
In one paragraph

Article in Proceedings. IEEE International Conference on Healthcare Informatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Electronic Phenotype for Detection, Staging, and Subtyping of Acute Kidney Injury.American journal of kidney diseases : the official journal of the National Kidney Foundation · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. [Artificial intelligence and acute kidney injury].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2024
    Review
  7. Review
  8. Incidence, Outcomes, and Predictors of Subphenotypes of Acute Kidney Injury among Acute Respiratory Distress Syndrome Patients: A Prospective Observational Study.Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine · 2023
    Article
  9. Review
  10. Subphenotypes in acute kidney injury: a narrative review.Critical care (London, England) · 2022
    Review
  11. 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 1 institution in 1 country.

Taylor D SmithDept of Computer Science, University of Kentucky, Lexington, KY USA.
Victor Ortiz SorianoDept of Internal Medicine, University of Kentucky, Lexington, KY USA.
Javier A NeyraDept of Internal Medicine, University of Kentucky, Lexington, KY USA.
Jin ChenInstl for Biomedical Informatics, University of Kentucky, Lexington, KY USA.
University of Kentucky · US

Funding

Kentucky Center for Clinical and Translational ScienceUL1TR001998 · NCATS · UNIVERSITY OF KENTUCKY · PI HARTMANN, KATHERINE E, KERN, PHILIP A · 2016 to 2025
$34.2M
NCATS NIH HHS UL1 TR001998
6 · The paper itself

Abstract

Acute kidney injury (AKI) is a complex systemic syndrome associated with high morbidity and mortality and risk for the subsequent development of renal and non-renal complications. Nearly 50% of patients in the ICU experience AKI. AKI severity is a key metric for evaluating patients risk of hospital mortality. Current AKI stratification is based on absolute changes in Serum Creatinine (SCr) and the maximal increase relative to the patients baseline value. However, such measurement does not consider either the progression or duration of AKI, both of which are associated with adverse outcomes post-AKI. In this article, by leveraging a large volume of SCr temporal variabilities, we present a novel model called Trajectory of Acute Kidney Injury (TAKI) for the identification of AKI trajectory subtypes. Experimental results demonstrate that TAKI is better than the existing trajectory subtyping methods on both the inpatient mortality stratification and the post-7-day AKI progression estimation. With TAKI, it is found that the trend of KDIGO trajectory appears to be more highly associated with inpatient mortality rates than the maximum KDIGO score.

Indexed as

Acute Kidney InjuryDynamic Trajectory AlignmentKDIGO Trajectory Subtyping

Identifiers

PMID32844151
PMCPMC7444813
OpenAlexW2989583073

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.