Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/12872
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dc.contributor.authorNgaosuwan K.
dc.contributor.authorOunchokdee K.
dc.contributor.authorChalermchai T.
dc.date.accessioned2021-04-05T03:21:43Z-
dc.date.available2021-04-05T03:21:43Z-
dc.date.issued2018
dc.identifier.issn10732322
dc.identifier.other2-s2.0-85051031361
dc.identifier.urihttps://ir.swu.ac.th/jspui/handle/123456789/12872-
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85051031361&doi=10.1097%2fSHK.0000000000001061&partnerID=40&md5=38344b0773047b0f1858ecffea3e6187
dc.description.abstractBackground: The current international guideline recommended 200 mg/day of hydrocortisone intravenously to treat septic shock. However, a subsequent study on cortisol metabolism actually showed an increase in cortisol level during sepsis. Hence, the smaller hydrocortisone dose of 100 mg/day might be sufficient and reduce steroid-associated complications. We aimed to compare the clinical outcomes of minimized hydrocortisone dose of 100mg to the currently recommended dose in the treatment of septic shock patients. Methods: A double-blinded randomized controlled trial included 80 septic shock patients with hemodynamic instability despite fluid and vasopressive therapy. Participants were divided equally into two groups to treat with 100 mg/day or 200 mg/day of hydrocortisone, then stepwise down titrated and discontinued on day 8. The outcome of interest was the hyperglycemic rate. Vital status, time to shock reversal, superinfection and gastrointestinal bleeding rates were also compared. Results: Patients with 100mg hydrocortisone had significantly lower hyperglycemic rate compared with 200 mg, 63.9% versus 86.5% (the adjusted hazard ratio [HR], 0.08; 95% confidence interval [CI], 0.02-0.41, P=0.002). Time to shock reversal was shorter in patients with 100mg hydrocortisone, 2 days vs. 4 days, P=0.031. The 28-day mortality rate when adjusted for Simplified Acute Physiology Score II showed no significant difference (HR, 0.68; 95% CI, 0.37-1.24, P=0.209). The reinfection and gastrointestinal bleeding rates were comparable between groups. Conclusion: Minimized daily hydrocortisone dosage of 100mg could lower the occurrence of hyperglycemia without increasing mortality in septic shock, compared with the currently recommended dosage of 200 mg/day. Copyright © 2017 by the Shock Society.
dc.subjectdopamine
dc.subjectepinephrine
dc.subjectglucose
dc.subjecthydrocortisone sodium succinate
dc.subjectnoradrenalin
dc.subjecthydrocortisone
dc.subjectadult
dc.subjectArticle
dc.subjectclinical outcome
dc.subjectcontrolled study
dc.subjectdouble blind procedure
dc.subjectdrug dose reduction
dc.subjectdrug dose titration
dc.subjectdrug fatality
dc.subjectdrug withdrawal
dc.subjectfemale
dc.subjectfluid therapy
dc.subjectgastrointestinal hemorrhage
dc.subjectglucose blood level
dc.subjecthuman
dc.subjecthyperglycemia
dc.subjectmajor clinical study
dc.subjectmale
dc.subjectmortality rate
dc.subjectoutcome assessment
dc.subjectparallel design
dc.subjectrandomized controlled trial
dc.subjectrecommended drug dose
dc.subjectseptic shock
dc.subjectSimplified Acute Physiology Score
dc.subjectsuperinfection
dc.subjectaged
dc.subjectblood
dc.subjectcomplication
dc.subjectdisease free survival
dc.subjectgastrointestinal hemorrhage
dc.subjecthyperglycemia
dc.subjectmiddle aged
dc.subjectmortality
dc.subjectsurvival rate
dc.subjecttime factor
dc.subjectvery elderly
dc.subjectAged
dc.subjectAged, 80 and over
dc.subjectDisease-Free Survival
dc.subjectDouble-Blind Method
dc.subjectFemale
dc.subjectGastrointestinal Hemorrhage
dc.subjectHumans
dc.subjectHydrocortisone
dc.subjectHyperglycemia
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectShock, Septic
dc.subjectSurvival Rate
dc.subjectTime Factors
dc.titleClinical outcomes of minimized hydrocortisone dosage of 100mg/day on lower occurrence of hyperglycemia in septic shock patients
dc.typeArticle
dc.rights.holderScopus
dc.identifier.bibliograpycitationShock. Vol 50, No.3 (2018), p.280-285
dc.identifier.doi10.1097/SHK.0000000000001061
Appears in Collections:Scopus 1983-2021

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