Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/11635
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dc.contributor.authorSuzuki, Satoshien
dc.contributor.authorEgi, Moritokien
dc.contributor.authorSchneider, Antoine Gen
dc.contributor.authorBellomo, Rinaldoen
dc.contributor.authorHart, Graeme Ken
dc.contributor.authorHegarty, Colinen
dc.date.accessioned2015-05-16T01:15:07Z
dc.date.available2015-05-16T01:15:07Z
dc.date.issued2012-12-21en
dc.identifier.citationJournal of Critical Care 2012; 28(4): 536.e9-19en
dc.identifier.govdoc23265292en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/11635en
dc.description.abstractThe aim of this study was to assess the association of phosphate concentration with key clinical outcomes in a heterogeneous cohort of critically ill patients.This was a retrospective observational study at a general intensive care unit (ICU) of an Australian university teaching hospital enrolling 2730 adult critically ill patients.We studied 10504 phosphate measurements with a mean value of 1.17 mmol/L (measurements every 28.8 hours on average). Hyperphosphatemia (inorganic phosphate [iP] concentration > 1.4 mmol/L) occurred in 45% and hypophosphatemia (iP ≤ 0.6 mmol/L) in 20%. Among patients without any episodes of hyperphosphatemia, patients with at least 1 episode of hypophosphatemia had a higher ICU mortality than those without hypophosphatemia (P = .004). In addition, ICU nonsurvivors had lower minimum phosphate concentrations than did survivors (P = .009). Similar results were seen for hospital mortality. However, on multivariable logistic regression analysis, hypophosphatemia was not independently associated with ICU mortality (adjusted odds ratio, 0.86 [95% confidence interval, 0.66-1.10]; P = .24) and hospital mortality (odds ratio, 0.89 [0.73-1.07]; P = .21). Even when different cutoff points were used for hypophosphatemia (iP ≤ 0.5, 0.4, 0.3, or 0.2 mmol/L), hypophosphatemia was not an independent risk factor for ICU and hospital morality. In addition, timing of onset and duration of hypophosphatemia were not independent risk factor for ICU and hospital mortality.Hypophosphatemia behaves like a general marker of illness severity and not as an independent predictor of ICU or in-hospital mortality in critically ill patients.en
dc.language.isoenen
dc.subject.otherCritical illnessen
dc.subject.otherHypophosphatemiaen
dc.subject.otherInorganic phosphateen
dc.subject.otherIntensive care uniten
dc.subject.otherMortalityen
dc.subject.otherAgeden
dc.subject.otherChi-Square Distributionen
dc.subject.otherCritical Illness.mortalityen
dc.subject.otherFemaleen
dc.subject.otherHospital Mortalityen
dc.subject.otherHumansen
dc.subject.otherHypophosphatemia.mortalityen
dc.subject.otherIntensive Care Unitsen
dc.subject.otherLogistic Modelsen
dc.subject.otherMaleen
dc.subject.otherMiddle Ageden
dc.subject.otherRetrospective Studiesen
dc.subject.otherRisk Factorsen
dc.subject.otherStatistics, Nonparametricen
dc.subject.otherSurvival Rateen
dc.titleHypophosphatemia in critically ill patients.en
dc.typeJournal Articleen
dc.identifier.journaltitleJournal of Critical Careen
dc.identifier.affiliationDepartment of Intensive Care, Austin Hospital, Melbourne, Victoria, Australiaen
dc.identifier.doi10.1016/j.jcrc.2012.10.011en
dc.description.pages536.e9-19en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/23265292en
dc.type.austinJournal Articleen
local.name.researcherBellomo, Rinaldo
item.languageiso639-1en-
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
crisitem.author.deptIntensive Care-
crisitem.author.deptData Analytics Research and Evaluation (DARE) Centre-
crisitem.author.deptIntensive Care-
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