Evidence map›Paper›PMID 26963914›Full record

Trial reportPloS one2016

Pediatric in-Hospital Death from Infectious Disease in Uganda: Derivation of Clinical Prediction Models.

Nasim Lowlaavar, Charles P Larson, Elias Kumbakumba, Guohai Zhou, J Mark Ansermino, Joel Singer, Niranjan Kissoon, Hubert Wong, Andrew Ndamira, Jerome Kabakyenga and 2 more

Abstract readClinical TrialMulticenter Study
In one paragraph

Trial report in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 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

11 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Pooled it
  4. Review
  5. Article
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  11. Observational
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

12 authors.

Nasim LowlaavarDepartment of Anesthesiology, Pharmacology, & Therapeutics, University of British Columbia, Vancouver, Canada.
Charles P LarsonCenter for International Child Health, BC Children's Hospital, Child and Family Research Institute, Vancouver, Canada.
Elias KumbakumbaDepartment of Pediatrics, Mbarara University of Science and Technology, Mbarara, Uganda.
Guohai ZhouDepartment of Statistics, University of British Columbia, Vancouver, Canada.
J Mark AnserminoDepartment of Anesthesiology, Pharmacology, & Therapeutics, University of British Columbia, Vancouver, Canada.
Joel SingerSchool of Population and Public Health, University of British Columbia, Vancouver, Canada.
Niranjan KissoonDepartment of Pediatrics, BC Children's Hospital and University of British Columbia, Vancouver, Canada.
Hubert WongSchool of Population and Public Health, University of British Columbia, Vancouver, Canada.
Andrew NdamiraDepartment of Pediatrics, Mbarara University of Science and Technology, Mbarara, Uganda.
Jerome KabakyengaMaternal, Newborn and Child Health Institute, Mbarara University of Science and Technology, Mbarara, Uganda.
Julius KiwanukaDepartment of Pediatrics, Mbarara University of Science and Technology, Mbarara, Uganda.
Matthew O WiensSchool of Population and Public Health, University of British Columbia, Vancouver, Canada.

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

backgroundPediatric hospital mortality from infectious diseases in resource constrained countries remains unacceptably high. Improved methods of risk-stratification can assist in referral decision making and resource allocation. The purpose of this study was to create prediction models for in-hospital mortality among children admitted with suspected infectious diseases.

methodsThis two-site prospective observational study enrolled children between 6 months and 5 years admitted with a proven or suspected infection. Baseline clinical and laboratory variables were collected on enrolled children. The primary outcome was death during admission. Stepwise logistic regression minimizing Akaike's information criterion was used to identify the most promising multivariate models. The final model was chosen based on parsimony.

results1307 children were enrolled consecutively, and 65 (5%) of whom died during their admission. Malaria, pneumonia and gastroenteritis were diagnosed in 50%, 31% and 8% of children, respectively. The primary model included an abnormal Blantyre coma scale, HIV and weight-for-age z-score. This model had an area under the curve (AUC) of 0.85 (95% CI, 0.80-0.89) with a sensitivity and specificity of 83% and 76%, respectively. The positive and negative predictive values were 15% and 99%, respectively. Two alternate models with similar performance characteristics were developed withholding HIV and weight-for-age z-score, for use when these variables are not available.

conclusionsRisk stratification of children admitted with infectious diseases can be calculated based on several easily measured variables. Risk stratification at admission can be used for allocation of scarce human and physical resources and to guide referral among children admitted to lower level health facilities.

Indexed as

Hospital MortalityHospitals, PediatricModels, BiologicalChild, PreschoolFemaleGastroenteritisHumansInfantMalariaMalePneumoniaPredictive Value of TestsUganda

Identifiers

PMID26963914
PMCPMC4786260

What OpenQuestion holds

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LicenceCC BY
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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.