Evidence map›Paper›PMID 28062207›Full record

ArticleThe American journal of emergency medicine2017

Cardiometabolic biomarkers are predictors of readmission and death in patients hospitalized for acute dyspnea.

Nathalie Lund, Klas Gränsbo, Camilla Wernersson, Olle Melander

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Article in The American journal of emergency medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Nathalie LundSkåne University Hospital Malmö, Clinical Research Centre, Malmoe, Sweden. Electronic address: nathalie.lund@med.lu.se.
Klas GränsboSkåne University Hospital Malmö, Clinical Research Centre CRC, Malmoe, Sweden.
Camilla WernerssonSkåne University Hospital Malmö, Clinical Research Centre CRC, Malmoe, Sweden.
Olle MelanderSkåne University Hospital Malmö, Clinical Research Centre CRC, Malmoe, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcute dyspnea affects a large heterogeneous patient group with high mortality and readmission rates. PURPOSE: To investigate if cardiometabolic biomarkers and clinical characteristics predict readmission and death in patients hospitalized for acute dyspnea.

methods65 dyspnea patients at a general internal medicine ward were followed for six months. The combined endpoint was readmission or death. MEASUREMENTS AND

resultsCardiometabolic biomarkers at admission were related to the endpoint in Cox proportional hazard models (adjusted for sex, age, oxygen saturation, respiratory rate and C-reactive protein (CRP)). The biomarkers tissue-type plasminogen activator (tPA), prolactin (PRL), tumor necrosis factor receptor superfamily member 6 (FAS) and C-C motif chemokine 3 (CCL3) were independently and significantly related to the endpoint and combined into a biomarker risk score (BRS). Each SD increment of the BRS conferred a hazard ratio (HR) of 2.13 (1.39-3.27) P=0.001. The top vs bottom tertile of the BRS conferred a HR of 4.75 (1.93-11.68) P=0.001. Dyspnea severity was also associated with worse outcome, HR=3.43 (1.28-9.20) P=0.014. However, when mutually adjusted the BRS remained significant (P=0.004) whereas dyspnea severity was not. The BRS was related to the endpoint among patients with mild to moderate dyspnea (P=0.016) but not among those with severe dyspnea.

conclusionA score of tPA, PRL, FAS and CCL3 predicts 6-month death and readmission in patients hospitalized for acute dyspnea and may prove useful to optimize length of stay and follow-up. Although the BRS outweighs dyspnea severity in prediction of the endpoint, its prognostic role is strongest in mild-moderate dyspnea.

Indexed as

HospitalizationMortalityAgedAged, 80 and overBiomarkersChemokine CCL3Dyspneafas ReceptorFemaleHumansMalePatient ReadmissionPrognosisProlactinProportional Hazards ModelsRetrospective StudiesBiomarkersCCL3 protein, humanChemokine CCL3FAS protein, humanfas ReceptorProlactinTissue Plasminogen Activatoracute dyspneabiomarkerPrognosisrisk score

Identifiers

PMID28062207
PMCPMC5754318

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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.