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dc.contributor.authorOttestad, William Arne
dc.contributor.authorRognes, Ingrid Nygren
dc.contributor.authorPischke, Søren
dc.contributor.authorMollnes, Tom Eirik
dc.contributor.authorAndersson, Ulf
dc.contributor.authorEken, Torsten
dc.date.accessioned2020-02-10T15:18:41Z
dc.date.available2020-02-10T15:18:41Z
dc.date.created2019-09-09T14:43:14Z
dc.date.issued2019
dc.identifier.citationCritical Care Medicine. 2019, 47 (8), e614-e622.nb_NO
dc.identifier.issn0090-3493
dc.identifier.urihttp://hdl.handle.net/11250/2640864
dc.description.abstractObjectives: The causal role of the prototype alarmin high mobility group box 1 protein in systemic inflammation and remote organ injury after trauma and shock is established in animal models but not in humans. Our aim was therefore to determine high mobility group box 1 protein concentration kinetics with high time resolution during the first hours after trauma in individual patients and investigate the association with outcome. Design: Prospective single-center observational study. Setting: University hospital Level I trauma center. Patients: Convenience recruitment of 136 trauma patients. Interventions: None. Measurements and Main Results: Total plasma high mobility group box 1 protein levels were analyzed with enzyme-linked immunosorbent assay in repeated samples. Relationships between predefined predictor variables and outcome were examined in multivariable linear regression models. Ventilator-free days was used as primary outcome measure. Two distinct high mobility group box 1 protein release phases were identified. An initial exponential decay phase with half-life 26 minutes was not correlated with outcome. In contrast, a second high mobility group box 1 protein wave peaking 3–6 hours after trauma in the most severely injured and physiologically deranged patients was consistently the most important predictor of outcome in our multivariable models, rendering all other predictor variables insignificant except for smaller contributions from age and sex, and of admission base excess for maximal creatinine concentration. Conclusions: High mobility group box 1 protein was released in two consecutive phases. Only the second high mobility group box 1 protein wave was a significant predictor of outcome. Patients with a high high mobility group box 1 protein concentration between 3 and 6 hours after trauma might hypothetically benefit from high mobility group box 1 protein-specific antagonist therapy.nb_NO
dc.language.isoengnb_NO
dc.publisherLippincott, Williams & Wilkinsnb_NO
dc.titleBiphasic release of the alarmin high mobility group box 1 protein early after trauma predicts poor clinical outcomenb_NO
dc.typeJournal articlenb_NO
dc.typePeer reviewednb_NO
dc.description.versionacceptedVersionnb_NO
dc.source.pagenumbere614-e622nb_NO
dc.source.volume47nb_NO
dc.source.journalCritical Care Medicinenb_NO
dc.source.issue8nb_NO
dc.identifier.doi10.1097/CCM.0000000000003800
dc.identifier.cristin1722898
dc.description.localcode© 2019. This is the authors' accepted and refereed manuscript to the chapter. Locked until 31.8.2020 due to copyright restrictions. The final authenticated version is available online at: http://dx.doi.org/10.1097/CCM.0000000000003800nb_NO
cristin.unitcode194,65,15,0
cristin.unitnameInstitutt for klinisk og molekylær medisin
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextpreprint
cristin.qualitycode2


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