Evidence map›Paper›PMID 28593401›Full record

ArticleIntensive care medicine2017

External validation of a biomarker and clinical prediction model for hospital mortality in acute respiratory distress syndrome.

Zhiguo Zhao, Nancy Wickersham, Kirsten N Kangelaris, Addison K May, Gordon R Bernard, Michael A Matthay, Carolyn S Calfee, Tatsuki Koyama, Lorraine B Ware

Open access · greenAbstract readValidation Study
In one paragraph

Article in Intensive care medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 41 citations in OpenAlex.

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  17. Refining the Syndrome.Pediatric critical care medicine : a journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies · 2020
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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 at 3 institutions in 1 country.

Zhiguo ZhaoDepartment of Biostatistics, Vanderbilt University, Nashville, TN, USA.
Nancy WickershamDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University, T1218 MCN, 1161 21st Avenue S., Nashville, TN, 37232-2650, USA.
Kirsten N KangelarisDivision of Hospital Medicine, Department of Medicine, University of California San Francisco, San Francisco, CA, USA.
Addison K MayDivision of Trauma and Surgical Critical Care, Vanderbilt University, Nashville, TN, USA.
Gordon R BernardDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University, T1218 MCN, 1161 21st Avenue S., Nashville, TN, 37232-2650, USA.
Michael A MatthayDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Carolyn S CalfeeDepartment of Medicine, University of California San Francisco, San Francisco, CA, USA.
Tatsuki KoyamaDepartment of Biostatistics, Vanderbilt University, Nashville, TN, USA.
Lorraine B WareDivision of Allergy, Pulmonary and Critical Care Medicine, Department of Medicine, Vanderbilt University, T1218 MCN, 1161 21st Avenue S., Nashville, TN, 37232-2650, USA. lorraine.ware@vanderbilt.edu.
Vanderbilt University · USUniversity of California, San Francisco · USUniversity of San Francisco · US

Funding

Resolution of Clinical Lung InjuryR37HL051856 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHAY, MICHAEL A. · 2006 to 2015
$3.9M
Cigarette Smoke Exposure and Acute Lung Injury After Severe Blunt TraumaR01HL110969 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CALFEE, CAROLYN · 2012 to 2016
$1.9M
RESOLUTION OF CLINICAL LUNG INJURYR01HL051856 · NHLBI · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI MATTHAY, MICHAEL A. · 1996 to 2005
$1.7M
Chemokine-related acute lung injury pathogenesis in African-American patientsK23HL116800 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KANGELARIS, KIRSTEN NEUDOERFFER · 2013 to 2017
$876k
Molecular Endotypes of ARDS: Identification, Biology, and Differential Response to TherapyR01HL131621 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI CALFEE, CAROLYN · 2016 to 2017
$806k
Inflammatory and epithelial injury markers for ARDS prognosis:A validation studyR21HL112656 · NHLBI · VANDERBILT UNIVERSITY · PI WARE, LORRAINE B · 2012 to 2013
$228k
NHLBI NIH HHS K23 HL116800NHLBI NIH HHS R01 HL051856NHLBI NIH HHS R01 HL110969NHLBI NIH HHS R01 HL131621NHLBI NIH HHS R21 HL112656NHLBI NIH HHS R37 HL051856
6 · The paper itself

Abstract

purposeMortality prediction in ARDS is important for prognostication and risk stratification. However, no prediction models have been independently validated. A combination of two biomarkers with age and APACHE III was superior in predicting mortality in the NHLBI ARDSNet ALVEOLI trial. We validated this prediction tool in two clinical trials and an observational cohort.

methodsThe validation cohorts included 849 patients from the NHLBI ARDSNet Fluid and Catheter Treatment Trial (FACTT), 144 patients from a clinical trial of sivelestat for ARDS (STRIVE), and 545 ARDS patients from the VALID observational cohort study. To evaluate the performance of the prediction model, the area under the receiver operating characteristic curve (AUC), model discrimination, and calibration were assessed, and recalibration methods were applied.

resultsThe biomarker/clinical prediction model performed well in all cohorts. Performance was better in the clinical trials with an AUC of 0.74 (95% CI 0.70-0.79) in FACTT, compared to 0.72 (95% CI 0.67-0.77) in VALID, a more heterogeneous observational cohort. The AUC was 0.73 (95% CI 0.70-0.76) when FACTT and VALID were combined.

conclusionWe validated a mortality prediction model for ARDS that includes age, APACHE III, surfactant protein D, and interleukin-8 in a variety of clinical settings. Although the model performance as measured by AUC was lower than in the original model derivation cohort, the biomarker/clinical model still performed well and may be useful for risk assessment for clinical trial enrollment, an issue of increasing importance as ARDS mortality declines, and better methods are needed for selection of the most severely ill patients for inclusion.

Indexed as

APACHEHospital MortalityInterleukin-8Pulmonary Surfactant-Associated Protein DRespiratory Distress SyndromeAcute Lung InjuryAdultAgedBiomarkersCohort StudiesFemaleHumansMaleMiddle AgedObservational Studies as TopicRandomized Controlled Trials as TopicBiomarkersInterleukin-8Pulmonary Surfactant-Associated Protein DARDSBiomarkerHospital mortalityPredictionValidation

Identifiers

PMID28593401
PMCPMC5978765
OpenAlexW2621829139

What OpenQuestion holds

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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.