Bioactive adrenomedullin in sepsis patients in the emergency department is associated with mortality, organ failure and admission to intensive care.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2022
Historique:
received: 24 11 2021
accepted: 08 04 2022
entrez: 28 4 2022
pubmed: 29 4 2022
medline: 3 5 2022
Statut: epublish

Résumé

Adrenomedullin is a vasoactive hormone with potentially prognostic and therapeutic value, which mainly has been investigated in intensive care unit (ICU) settings. The triaging in the emergency department (ED) of patients to the right level of care is crucial for patient outcome. The primary aim of this study was to investigate the association of bioactive adrenomedullin (bio-ADM) with mortality among sepsis patients in the ED. Secondary aims were to investigate the association of bio-ADM with multiple organ failure (MOF), ICU admission and ED discharge. In this prospective observational cohort study, adult sepsis patients in the ED (2013-2015) had blood samples collected for later batch analysis of bio-ADM. Odds ratios (OR) with 95% confidence interval (CI) for bio-ADM were calculated. Bio-ADM in 594 sepsis patients was analyzed of whom 51 died within 28 days (8.6%), 34 developed severe MOF, 27 were ICU admitted and 67 were discharged from the ED. The median (interquartile range) bio-ADM was 36 (26-56) and 63 (42-132) pg/mL among survivors and non-survivors, respectively, 81 (56-156) pg/mL for patients with severe MOF and 77 (42-133) pg/mL for ICU admitted patients. Each log-2 increment of bio-ADM conferred an OR of 2.30 (95% CI 1.74-3.04) for mortality, the adjusted OR was 2.39 (95% CI 1.69-3.39). The area under the receiver operating characteristic curve of a prognostic mortality model based on demographics and biomarkers increased from 0.80 to 0.86 (p = 0.02) when bio-ADM was added. Increasing bio-ADM was associated with severe MOF, ICU admission and ED discharge with adjusted ORs of 3.30 (95% CI 2.13-5.11), 1.75 (95% CI 1.11-2.77) and 0.46 (95% CI 0.32-0.68), respectively. Bio-ADM in sepsis patients in the ED is associated with mortality, severe MOF, ICU admission and ED discharge, and may be of clinical importance for triage of sepsis patients in the ED.

Sections du résumé

BACKGROUND
Adrenomedullin is a vasoactive hormone with potentially prognostic and therapeutic value, which mainly has been investigated in intensive care unit (ICU) settings. The triaging in the emergency department (ED) of patients to the right level of care is crucial for patient outcome.
OBJECTIVES
The primary aim of this study was to investigate the association of bioactive adrenomedullin (bio-ADM) with mortality among sepsis patients in the ED. Secondary aims were to investigate the association of bio-ADM with multiple organ failure (MOF), ICU admission and ED discharge.
METHODS
In this prospective observational cohort study, adult sepsis patients in the ED (2013-2015) had blood samples collected for later batch analysis of bio-ADM. Odds ratios (OR) with 95% confidence interval (CI) for bio-ADM were calculated.
RESULTS
Bio-ADM in 594 sepsis patients was analyzed of whom 51 died within 28 days (8.6%), 34 developed severe MOF, 27 were ICU admitted and 67 were discharged from the ED. The median (interquartile range) bio-ADM was 36 (26-56) and 63 (42-132) pg/mL among survivors and non-survivors, respectively, 81 (56-156) pg/mL for patients with severe MOF and 77 (42-133) pg/mL for ICU admitted patients. Each log-2 increment of bio-ADM conferred an OR of 2.30 (95% CI 1.74-3.04) for mortality, the adjusted OR was 2.39 (95% CI 1.69-3.39). The area under the receiver operating characteristic curve of a prognostic mortality model based on demographics and biomarkers increased from 0.80 to 0.86 (p = 0.02) when bio-ADM was added. Increasing bio-ADM was associated with severe MOF, ICU admission and ED discharge with adjusted ORs of 3.30 (95% CI 2.13-5.11), 1.75 (95% CI 1.11-2.77) and 0.46 (95% CI 0.32-0.68), respectively.
CONCLUSION
Bio-ADM in sepsis patients in the ED is associated with mortality, severe MOF, ICU admission and ED discharge, and may be of clinical importance for triage of sepsis patients in the ED.

Identifiants

pubmed: 35482727
doi: 10.1371/journal.pone.0267497
pii: PONE-D-21-37270
pmc: PMC9049572
doi:

Substances chimiques

Adrenomedullin 148498-78-6

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0267497

Subventions

Organisme : European Research Council
ID : 885003
Pays : International

Déclaration de conflit d'intérêts

I have read the journal’s policy and the authors of this manuscript have the following competing interests: OM is listed as an inventor on a patent on bio-ADM in dementia prediction. SphingoTec GmbH is the owner of the patent. JS is employed by SphingoTec GmbH, the manufacturer of the bio-ADM assay. Bio-ADM was analysed free of charge by SphingoTec GmbH, Neuendorfstrasse 15A, Hennigsdorf, Germany. OL, MR, KB and HF have declared no competing interests. The competing interests have no influence on the restrictions on sharing data we are bound to. However, due to ethical and legal restrictions related to the Swedish Biobanks in Medical Care Act (2002:297) and the Personal Data Act (1998:204) regarding deposition of data, data are not publicly published but available upon request via the authors.

Références

Intensive Care Med. 2012 Oct;38(10):1647-53
pubmed: 22777516
News Physiol Sci. 1999 Dec;14:255-259
pubmed: 11390861
BMJ Open. 2019 Feb 22;8(11):e020337
pubmed: 30798282
Lancet. 2007 Oct 20;370(9596):1453-7
pubmed: 18064739
Eur J Heart Fail. 2019 Jun;21(6):732-743
pubmed: 30843353
Endothelium. 2007 Nov-Dec;14(6):345-51
pubmed: 18080871
J Clin Med. 2020 Apr 22;9(4):
pubmed: 32331426
Endocr Rev. 2000 Apr;21(2):138-67
pubmed: 10782362
J Appl Lab Med. 2017 Sep 1;2(2):222-233
pubmed: 32630976
Intern Emerg Med. 2022 Mar;17(2):541-550
pubmed: 34173962
Br J Clin Pharmacol. 2018 Sep;84(9):2129-2141
pubmed: 29856470
Crit Care. 2020 Nov 4;24(1):636
pubmed: 33148300
Eur J Endocrinol. 2012 Dec;167(6):847-53
pubmed: 23002189
BMC Infect Dis. 2012 Aug 08;12:184
pubmed: 22874067
Biochem Biophys Res Commun. 1993 Apr 30;192(2):553-60
pubmed: 8387282
Am J Emerg Med. 2016 Feb;34(2):257-62
pubmed: 26577429
Clin Chem. 2005 Oct;51(10):1823-9
pubmed: 16099941
Curr Med Chem. 2007;14(15):1689-99
pubmed: 17584073
Crit Care Med. 2018 Jun;46(6):997-1000
pubmed: 29767636
Crit Care. 2019 Feb 8;23(1):40
pubmed: 30736862
Expert Rev Mol Diagn. 2021 Apr;21(4):397-404
pubmed: 33736553
Chest. 2017 Aug;152(2):312-320
pubmed: 28411114
Intensive Care Med. 2007 Apr;33(4):703-10
pubmed: 17318497
Shock. 2018 Aug;50(2):132-140
pubmed: 29324626
Crit Care. 2019 Oct 29;23(1):335
pubmed: 31665092
Crit Care. 2018 Dec 21;22(1):354
pubmed: 30583748
Invest Clin. 2016 Mar;57(1):66-76
pubmed: 27382803
Crit Care Med. 2020 Jan;48(1):49-55
pubmed: 31625979
Crit Care. 2014 Feb 17;18(1):R34
pubmed: 24533868
Intensive Care Med. 2021 Nov;47(11):1284-1294
pubmed: 34605947
Open Heart. 2019 Jul 3;6(2):e001048
pubmed: 31354956
Crit Care. 2005;9(6):R816-24
pubmed: 16356231
Crit Care Med. 2013 Feb;41(2):580-637
pubmed: 23353941
Crit Care. 2016 Jun 09;20(1):178
pubmed: 27282767
Br J Anaesth. 2007 Dec;99(6):830-6
pubmed: 17962242
Ann Lab Med. 2019 Sep;39(5):454-463
pubmed: 31037864
Intensive Care Med. 2009 Nov;35(11):1859-67
pubmed: 19662382
Crit Care. 2015 Oct 29;19:377
pubmed: 26511878
Eur J Pharmacol. 2015 Oct 5;764:140-148
pubmed: 26144371
Biometrics. 1988 Sep;44(3):837-45
pubmed: 3203132
Circ Res. 2002 Oct 4;91(7):618-25
pubmed: 12364390
Crit Care. 2019 May 31;23(1):196
pubmed: 31151462
J Leukoc Biol. 2006 Aug;80(2):237-44
pubmed: 16769769
Clin Chem Lab Med. 2021 Jan 14;59(6):1165-1176
pubmed: 33554514
Eur J Heart Fail. 2019 Feb;21(2):163-171
pubmed: 30592365
Hypertension. 2001 May;37(5):1279-84
pubmed: 11358941
Biomolecules. 2020 Aug 11;10(8):
pubmed: 32796765
Eur J Heart Fail. 2018 Sep;20(9):1363-1365
pubmed: 29932477

Auteurs

Oscar H M Lundberg (OHM)

Department of Clinical Sciences, Anaesthesiology and Intensive Care, Medical Faculty, Lund University, Lund, Sweden.
Department of Intensive and Perioperative Care, Skåne University Hospital, Malmö, Sweden.

Mari Rosenqvist (M)

Department of Clinical Sciences, Medical Faculty, Lund University, Malmö, Sweden.
Department of Infectious Diseases, Skåne University Hospital, Malmö, Sweden.

Kevin Bronton (K)

Department of Clinical Sciences, Medical Faculty, Lund University, Malmö, Sweden.
Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden.

Janin Schulte (J)

SphingoTec GmbH, Hennigsdorf, Germany.

Hans Friberg (H)

Department of Clinical Sciences, Anaesthesiology and Intensive Care, Medical Faculty, Lund University, Lund, Sweden.
Department of Intensive and Perioperative Care, Skåne University Hospital, Malmö, Sweden.

Olle Melander (O)

Department of Clinical Sciences, Medical Faculty, Lund University, Malmö, Sweden.
Department of Infectious Diseases, Skåne University Hospital, Malmö, Sweden.
Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden.

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