Evidence map›Paper›PMID 24625747›Full record

Observational studyPloS one2014

Risk factors and outcomes stratified by severity of acute kidney injury in malaria.

Kavitha Saravu, Kumar Rishikesh, Chirag R Parikh

Abstract readObservational Study
In one paragraph

Observational study in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 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.

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

21 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Clinical spectrum and complications ofMalariaWorld journal · 2025
    Article
  5. Article
  6. Article
  7. Review
  8. Recurrence inF1000Research · 2022
    Article
  9. Clinical and Laboratory Features Associated with Acute Kidney Injury in Severe Malaria.Indian journal of critical care medicine : peer-reviewed, official publication of Indian Society of Critical Care Medicine · 2018
    Article
  10. Article
  11. Article
  12. Article
  13. Kidney involvement in malaria: an update.Revista do Instituto de Medicina Tropical de Sao Paulo · 2017
    Review
  14. Therapeutic Assessment of Primaquine for Radical Cure ofThe Korean journal of parasitology · 2016
    Observational
  15. Acute Kidney Injury in Western Countries.Kidney diseases (Basel, Switzerland) · 2016
    Review
  16. Acute Kidney Injury in Asia.Kidney diseases (Basel, Switzerland) · 2016
    Review
  17. A Clinical Study of Acute Kidney Injury in Tropical Acute Febrile Illness.Journal of clinical and diagnostic research : JCDR · 2016
    Article
  18. Article
  19. Article
  20. 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

3 authors.

Kavitha SaravuDepartment of Medicine, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Kumar RishikeshDepartment of Medicine, Kasturba Medical College, Manipal University, Manipal, Karnataka, India.
Chirag R ParikhSection of Nephrology, Yale University School of Medicine, VA CT Healthcare System, and the Program of Applied Translational Research, New Haven, Connecticut, United States of America.

Funding

Mentoring Program for Translational and Patient Oriented Research in AKIK24DK090203 · NIDDK · YALE UNIVERSITY · PI PARIKH, CHIRAG R · 2012 to 2016
$896k
NIDDK NIH HHS K24 DK090203NIDDK NIH HHS K24DK090203
6 · The paper itself

Abstract

Severe acute kidney injury (AKI) is known to have prognostic value for in-hospital outcomes in malaria. However, little is known about the association of AKI of lesser severity with malarial risk factors and outcomes--and such a gap is becoming increasingly relevant with the upsurge in the incidence of AKI due to Plasmodium falciparum malaria and Plasmodium vivax malaria over the last decade. We aimed to identify risk factors of AKI in malaria and assessed in-hospital outcomes stratified by severity of AKI. We performed an observational study of 1,191 hospitalized malaria patients enrolled between 2007 and 2011 in a tertiary care academic center in India. Patients were categorized based on peak serum creatinine into one of three groups: no AKI (<1.6 mg/dL), mild AKI (1.6-3.0 mg/dL), and severe AKI (>3 mg/dL). Plasmodium vivax was the predominant species (61.41%), followed by Plasmodium falciparum (36.41%) and mixed infections with both the species (2.18%). Mild and severe AKI were detected in 12% and 5.6% of patients, respectively. Mild AKI due to Plasmodium vivax (49%) and Plasmodium falciparum (48.5%) was distributed relatively equally within the sample population; however, cases of severe AKI due to Plasmodium falciparum (80%) and Plasmodium vivax (13%) was significantly different (P<0.001). On history and physical examination, risk factors for AKI were age, absence of fever, higher heart rate, lower diastolic blood pressure, icterus, and hepatomegaly. The only laboratory parameter associated with risk of AKI on multivariate analysis was direct bilirubin. Patients with mild and severe AKI had greater organ complications, supportive requirements, longer duration of hospital stay and in-hospital mortality in a dose-dependent relationship, than patients with no AKI. Mild AKI is associated with significant (P<0.05) morbidity compared to no AKI, and future studies should assess strategies for early diagnosis of AKI and prevent AKI progression.

Indexed as

Acute Kidney InjuryAdultCohort StudiesDisease ProgressionFemaleHospitalizationHumansIndiaMalaria, FalciparumMalaria, VivaxMaleMiddle AgedPlasmodium falciparumPlasmodium vivaxPrognosisRetrospective Studies

Identifiers

PMID24625747
PMCPMC3953079

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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.