Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/45955
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dc.contributor.authorPreiser, Jean Charlesen_US
dc.contributor.authorDevos, Philippeen_US
dc.contributor.authorRuiz-Santana, Sergioen_US
dc.contributor.authorMélot, Christianen_US
dc.contributor.authorAnnane, Djillalien_US
dc.contributor.authorGroeneveld, Johanen_US
dc.contributor.authorIapichino, Gaetanoen_US
dc.contributor.authorLeverve, Xavieren_US
dc.contributor.authorNitenberg, Gérarden_US
dc.contributor.authorSinger, Pierreen_US
dc.contributor.authorWernerman, Janen_US
dc.contributor.authorJoannidis, Michaelen_US
dc.contributor.authorStecher, Adelaen_US
dc.contributor.authorChioléro, Renéen_US
dc.date.accessioned2018-11-23T00:10:28Z-
dc.date.available2018-11-23T00:10:28Z-
dc.date.issued2009en_US
dc.identifier.issn0342-4642en_US
dc.identifier.urihttp://hdl.handle.net/10553/45955-
dc.description.abstractAn optimal target for glucose control in ICU patients remains unclear. This prospective randomized controlled trial compared the effects on ICU mortality of intensive insulin therapy (IIT) with an intermediate glucose control.Adult patients admitted to the 21 participating medico-surgical ICUs were randomized to group 1 (target BG 7.8-10.0 mmol/L) or to group 2 (target BG 4.4-6.1 mmol/L).While the required sample size was 1,750 per group, the trial was stopped early due to a high rate of unintended protocol violations. From 1,101 admissions, the outcomes of 542 patients assigned to group 1 and 536 of group 2 were analysed. The groups were well balanced. BG levels averaged in group 1 8.0 mmol/L (IQR 7.1-9.0) (median of all values) and 7.7 mmol/L (IQR 6.7-8.8) (median of morning BG) versus 6.5 mmol/L (IQR 6.0-7.2) and 6.1 mmol/L (IQR 5.5-6.8) for group 2 (p < 0.0001 for both comparisons). The percentage of patients treated with insulin averaged 66.2 and 96.3%, respectively. Proportion of time spent in target BG was similar, averaging 39.5% and 45.1% (median (IQR) 34.3 (18.5-50.0) and 39.3 (26.2-53.6)%) in the groups 1 and 2, respectively. The rate of hypoglycaemia was higher in the group 2 (8.7%) than in group 1 (2.7%, p < 0.0001). ICU mortality was similar in the two groups (15.3 vs. 17.2%).In this prematurely stopped and therefore underpowered study, there was a lack of clinical benefit of intensive insulin therapy (target 4.4-6.1 mmol/L), associated with an increased incidence of hypoglycaemia, as compared to a 7.8-10.0 mmol/L target.en_US
dc.languageengen_US
dc.relation.ispartofIntensive Care Medicineen_US
dc.sourceIntensive Care Medicine [ISSN 0342-4642], v. 35, p. 1738-1748en_US
dc.subject32 Ciencias médicasen_US
dc.subject3201 Ciencias clínicasen_US
dc.subject.otherCritically-Ill Patientsen_US
dc.subject.otherHospital Mortalityen_US
dc.subject.otherInfusion Protocolen_US
dc.subject.otherHyperglycemiaen_US
dc.subject.otherImplementationen_US
dc.subject.otherHypoglycemiaen_US
dc.subject.otherManagementen_US
dc.subject.otherSeverityen_US
dc.subject.otherFailureen_US
dc.subject.otherSurgeryen_US
dc.titleA prospective randomised multi-centre controlled trial on tight glucose control by intensive insulin therapy in adult intensive care units: The Glucontrol studyen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s00134-009-1585-2en_US
dc.identifier.scopus72249083789-
dc.identifier.isi000270171900014-
dc.contributor.authorscopusid7005853172-
dc.contributor.authorscopusid7005945993-
dc.contributor.authorscopusid55518542700-
dc.contributor.authorscopusid25959227200-
dc.contributor.authorscopusid7006490729-
dc.contributor.authorscopusid56230616500-
dc.contributor.authorscopusid7102499389-
dc.contributor.authorscopusid7005993180-
dc.contributor.authorscopusid7006151978-
dc.contributor.authorscopusid7005692454-
dc.contributor.authorscopusid7401840755-
dc.contributor.authorscopusid7005970260-
dc.contributor.authorscopusid7003527036-
dc.contributor.authorscopusid35485734300-
dc.contributor.authorscopusid7005548420-
dc.description.lastpage1748en_US
dc.description.firstpage1738en_US
dc.relation.volume35en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid99622-
dc.contributor.daisngid3413114-
dc.contributor.daisngid839958-
dc.contributor.daisngid64195-
dc.contributor.daisngid29165-
dc.contributor.daisngid861026-
dc.contributor.daisngid189083-
dc.contributor.daisngid87023-
dc.contributor.daisngid13540903-
dc.contributor.daisngid187810-
dc.contributor.daisngid61721-
dc.contributor.daisngid70172-
dc.contributor.daisngid6004361-
dc.contributor.daisngid6218065-
dc.description.numberofpages11en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Preiser, JC-
dc.contributor.wosstandardWOS:Devos, P-
dc.contributor.wosstandardWOS:Ruiz-Santana, S-
dc.contributor.wosstandardWOS:Melot, C-
dc.contributor.wosstandardWOS:Annane, D-
dc.contributor.wosstandardWOS:Groeneveld, J-
dc.contributor.wosstandardWOS:Iapichino, G-
dc.contributor.wosstandardWOS:Leverve, X-
dc.contributor.wosstandardWOS:Nitenberg, G-
dc.contributor.wosstandardWOS:Singer, P-
dc.contributor.wosstandardWOS:Wernerman, J-
dc.contributor.wosstandardWOS:Joannidis, M-
dc.contributor.wosstandardWOS:Stecher, A-
dc.contributor.wosstandardWOS:Chiolero, R-
dc.date.coverdateOctubre 2009en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.jcr5,168
dc.description.jcrqQ1
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Grupo de investigaciones infecciosas, nutricionales e inflamatorias en pacientes hospitalarios / Study Group on infectious, nutritional and inflammatory diseases in hospitalized patients-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0003-3927-3236-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameRuiz Santana, Sergio-
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