Evidence map›Paper›PMID 23566734›Full record

ArticleJournal of critical care2013

Improving risk classification of critical illness with biomarkers: a simulation study.

Christopher W Seymour, Colin R Cooke, Zheyu Wang, Kathleen F Kerr, Donald M Yealy, Derek C Angus, Thomas D Rea, Jeremy M Kahn, Margaret S Pepe

Abstract read
In one paragraph

Article in Journal of critical care, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–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

13 citing papers in PubMed.

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  4. The Copenhagen Triage Algorithm: a randomized controlled trial.Scandinavian journal of trauma, resuscitation and emergency medicine · 2016
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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

9 authors.

Christopher W SeymourDepartments of Critical Care and Emergency Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; The Clinical Research, Investigation, and Systems Modeling of Acute Illness (CRISMA) Center, Department of Critical Care, Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA. Electronic address: seymourcw@upmc.edu.
Colin R Cooke
Zheyu Wang
Kathleen F Kerr
Donald M Yealy
Derek C Angus
Thomas D Rea
Jeremy M Kahn
Margaret S Pepe

Funding

Institute for Translational Health Science (KL2)KL2RR025015 · NCRR · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2007 to 2011
$9.3M
Statistical Methods for Medical Tests and BiomarkersR01GM054438 · NIGMS · UNIVERSITY OF WASHINGTON · PI PEPE, MARGARET S. · 1996 to 2015
$4.7M
Considerations of covariates in biomarker studiesR01CA129934 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI PEPE, MARGARET S. · 2007 to 2010
$845k
Pre-hospital identification of high-risk sepsisK23GM104022 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SEYMOUR, CHRISTOPHER WARREN · 2013 to 2016
$674k
NCI NIH HHS CA129934NCI NIH HHS R01 CA129934NCRR NIH HHS KL2 RR025015NIGMS NIH HHS GM054438NIGMS NIH HHS K23 GM104022NIGMS NIH HHS K23GM104022NIGMS NIH HHS R01 GM054438
6 · The paper itself

Abstract

purposeOptimal triage of patients at risk for critical illness requires accurate risk prediction, yet few data on the performance criteria required of a potential biomarker to be clinically useful exists. MATERIALS AND

methodsWe studied an adult cohort of nonarrest, nontrauma emergency medical services encounters transported to a hospital from 2002 to 2006. We simulated hypothetical biomarkers increasingly associated with critical illness during hospitalization and determined the biomarker strength and sample size necessary to improve risk classification beyond a best clinical model.

resultsOf 57,647 encounters, 3121 (5.4%) were hospitalized with critical illness and 54,526 (94.6%) without critical illness. The addition of a moderate-strength biomarker (odds ratio, 3.0, for critical illness) to a clinical model improved discrimination (c statistic, 0.85 vs 0.8; P<.01) and reclassification (net reclassification improvement, 0.15; 95% confidence interval, 0.13-0.18) and increased the proportion of cases in the highest-risk category by +8.6% (95% confidence interval, 7.5%-10.8%). Introducing correlation between the biomarker and physiological variables in the clinical risk score did not modify the results. Statistically significant changes in net reclassification required a sample size of at least 1000 subjects.

conclusionsClinical models for triage of critical illness could be significantly improved by incorporating biomarkers, yet substantial sample sizes and biomarker strength may be required.

Indexed as

BiomarkersTriageCritical IllnessEmergency Service, HospitalHumansRisk AssessmentBiomarkersBiomarkerReclassificationSample sizeSimulation

Identifiers

PMID23566734
PMCPMC3707977

What OpenQuestion holds

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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.