Cargando…

5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study

OBJECTIVE: The frequency and implications of an elevated cardiac troponin (4(th) or 5(th) generation TnT) in patients outside of the emergency department or presenting with non-cardiac conditions is unclear. METHODS: Consecutive patients aged 18 years or older admitted for a primary non-cardiac cond...

Descripción completa

Detalles Bibliográficos
Autores principales: Gupta, Vedant, Paranzino, Marc, Alnabelsi, Talal, Ayoub, Karam, Eason, Joshua, Mullis, Andin, Kotter, John R., Parks, Andrew, May, Levi, Nerusu, Sethabhisha, Dai, Chen, Cleland, Daniel, Leung, Steve Wah, Sorrell, Vincent Leigh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872231/
https://www.ncbi.nlm.nih.gov/pubmed/33561174
http://dx.doi.org/10.1371/journal.pone.0246332
_version_ 1783649146898481152
author Gupta, Vedant
Paranzino, Marc
Alnabelsi, Talal
Ayoub, Karam
Eason, Joshua
Mullis, Andin
Kotter, John R.
Parks, Andrew
May, Levi
Nerusu, Sethabhisha
Dai, Chen
Cleland, Daniel
Leung, Steve Wah
Sorrell, Vincent Leigh
author_facet Gupta, Vedant
Paranzino, Marc
Alnabelsi, Talal
Ayoub, Karam
Eason, Joshua
Mullis, Andin
Kotter, John R.
Parks, Andrew
May, Levi
Nerusu, Sethabhisha
Dai, Chen
Cleland, Daniel
Leung, Steve Wah
Sorrell, Vincent Leigh
author_sort Gupta, Vedant
collection PubMed
description OBJECTIVE: The frequency and implications of an elevated cardiac troponin (4(th) or 5(th) generation TnT) in patients outside of the emergency department or presenting with non-cardiac conditions is unclear. METHODS: Consecutive patients aged 18 years or older admitted for a primary non-cardiac condition who had the 4(th) generation TnT drawn had the 5(th) generation TnT run on the residual blood sample. Primary and secondary outcomes were all-cause mortality (ACM) and major adverse cardiovascular events (MACE) respectively at 1 year. RESULTS: 918 patients were included (mean age 59.8 years, 55% male) in the cohort. 69% had elevated 5(th) generation TnT while 46% had elevated 4(th) generation TnT. 5(th) generation TnT was more sensitive and less specific than 4(th) generation TnT in predicting both ACM and MACE. The sensitivities for the 5(th) generation TnT assay were 85% for ACM and 90% for MACE rates, compared to 65% and 70% respectively for the 4(th) generation assay. 5(th) generation TnT positive patients that were missed by 4(th) generation TnT had a higher risk of ACM (27.5%) than patients with both assays negative (27.5% vs 11.1%, p<0.001), but lower than patients who had both assay positive (42.1%). MACE rates were not better stratified using the 5(th) generation TnT assay. CONCLUSIONS: In patients admitted for a non-cardiac condition, 5(th) generation TnT is more sensitive although less specific in predicting MACE and ACM. 5(th) generation TnT identifies an intermediate risk group for ACM previously missed with the 4(th) generation assay.
format Online
Article
Text
id pubmed-7872231
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-78722312021-02-19 5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study Gupta, Vedant Paranzino, Marc Alnabelsi, Talal Ayoub, Karam Eason, Joshua Mullis, Andin Kotter, John R. Parks, Andrew May, Levi Nerusu, Sethabhisha Dai, Chen Cleland, Daniel Leung, Steve Wah Sorrell, Vincent Leigh PLoS One Research Article OBJECTIVE: The frequency and implications of an elevated cardiac troponin (4(th) or 5(th) generation TnT) in patients outside of the emergency department or presenting with non-cardiac conditions is unclear. METHODS: Consecutive patients aged 18 years or older admitted for a primary non-cardiac condition who had the 4(th) generation TnT drawn had the 5(th) generation TnT run on the residual blood sample. Primary and secondary outcomes were all-cause mortality (ACM) and major adverse cardiovascular events (MACE) respectively at 1 year. RESULTS: 918 patients were included (mean age 59.8 years, 55% male) in the cohort. 69% had elevated 5(th) generation TnT while 46% had elevated 4(th) generation TnT. 5(th) generation TnT was more sensitive and less specific than 4(th) generation TnT in predicting both ACM and MACE. The sensitivities for the 5(th) generation TnT assay were 85% for ACM and 90% for MACE rates, compared to 65% and 70% respectively for the 4(th) generation assay. 5(th) generation TnT positive patients that were missed by 4(th) generation TnT had a higher risk of ACM (27.5%) than patients with both assays negative (27.5% vs 11.1%, p<0.001), but lower than patients who had both assay positive (42.1%). MACE rates were not better stratified using the 5(th) generation TnT assay. CONCLUSIONS: In patients admitted for a non-cardiac condition, 5(th) generation TnT is more sensitive although less specific in predicting MACE and ACM. 5(th) generation TnT identifies an intermediate risk group for ACM previously missed with the 4(th) generation assay. Public Library of Science 2021-02-09 /pmc/articles/PMC7872231/ /pubmed/33561174 http://dx.doi.org/10.1371/journal.pone.0246332 Text en © 2021 Gupta et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gupta, Vedant
Paranzino, Marc
Alnabelsi, Talal
Ayoub, Karam
Eason, Joshua
Mullis, Andin
Kotter, John R.
Parks, Andrew
May, Levi
Nerusu, Sethabhisha
Dai, Chen
Cleland, Daniel
Leung, Steve Wah
Sorrell, Vincent Leigh
5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study
title 5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study
title_full 5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study
title_fullStr 5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study
title_full_unstemmed 5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study
title_short 5(th) generation vs 4(th) generation troponin T in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: A cohort study
title_sort 5(th) generation vs 4(th) generation troponin t in predicting major adverse cardiovascular events and all-cause mortality in patients hospitalized for non-cardiac indications: a cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7872231/
https://www.ncbi.nlm.nih.gov/pubmed/33561174
http://dx.doi.org/10.1371/journal.pone.0246332
work_keys_str_mv AT guptavedant 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT paranzinomarc 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT alnabelsitalal 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT ayoubkaram 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT easonjoshua 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT mullisandin 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT kotterjohnr 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT parksandrew 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT maylevi 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT nerususethabhisha 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT daichen 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT clelanddaniel 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT leungstevewah 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy
AT sorrellvincentleigh 5thgenerationvs4thgenerationtroponintinpredictingmajoradversecardiovasculareventsandallcausemortalityinpatientshospitalizedfornoncardiacindicationsacohortstudy