Effect of Treatment With Low Doses of Hydrocortisone and Fludrocortisone on Mortality in Patients With Septic Shock
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- 21 August 2002
- journal article
- clinical trial
- Published by American Medical Association (AMA) in JAMA
- Vol. 288 (7) , 862-871
- https://doi.org/10.1001/jama.288.7.862
Abstract
Research from JAMA — Effect of Treatment With Low Doses of Hydrocortisone and Fludrocortisone on Mortality in Patients With Septic Shock — ContextSeptic shock may be associated with relative adrenal insufficiency. Thus, a replacement therapy of low doses of corticosteroids has been proposed to treat septic shock.ObjectiveTo assess whether low doses of corticosteroids improve 28-day survival in patients with septic shock and relative adrenal insufficiency.Design and SettingPlacebo-controlled, randomized, double-blind, parallel-group trial performed in 19 intensive care units in France from October 9, 1995, to February 23, 1999.PatientsThree hundred adult patients who fulfilled usual criteria for septic shock were enrolled after undergoing a short corticotropin test.InterventionPatients were randomly assigned to receive either hydrocortisone (50-mg intravenous bolus every 6 hours) and fludrocortisone (50-µg tablet once daily) (n = 151) or matching placebos (n = 149) for 7 days.Main Outcome MeasureTwenty-eight-day survival distribution in patients with relative adrenal insufficiency (nonresponders to the corticotropin test).ResultsOne patient from the corticosteroid group was excluded from analyses because of consent withdrawal. There were 229 nonresponders to the corticotropin test (placebo, 115; corticosteroids, 114) and 70 responders to the corticotropin test (placebo, 34; corticosteroids, 36). In nonresponders, there were 73 deaths (63%) in the placebo group and 60 deaths (53%) in the corticosteroid group (hazard ratio, 0.67; 95% confidence interval, 0.47-0.95; P = .02). Vasopressor therapy was withdrawn within 28 days in 46 patients (40%) in the placebo group and in 65 patients (57%) in the corticosteroid group (hazard ratio, 1.91; 95% confidence interval, 1.29-2.84; P = .001). There was no significant difference between groups in responders. Adverse events rates were similar in the 2 groups.ConclusionIn our trial, a 7-day treatment with low doses of hydrocortisone and fludrocortisone significantly reduced the risk of death in patients with septic shock and relative adrenal insufficiency without increasing adverse events.Keywords
This publication has 22 references indexed in Scilit:
- Adrenal Insufficiency1Published by Elsevier ,2007
- Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of careCritical Care Medicine, 2001
- Effect of hydrocortisone on phenylephrine– mean arterial pressure dose-response relationship in septic shockClinical Pharmacology & Therapeutics, 2000
- A 3-Level Prognostic Classification in Septic Shock Based on Cortisol Levels and Cortisol Response to CorticotropinJAMA, 2000
- Treating Patients with Severe SepsisNew England Journal of Medicine, 1999
- An Historical Review of Glucocorticoid Treatment in Sepsis. Disease Pathophysiology and the Design of Treatment InvestigationSepsis, 1999
- Impaired pressor sensitivity to noradrenaline in septic shock patients with and without impaired adrenal function reserveBritish Journal of Clinical Pharmacology, 1998
- Reversal of late septic shock with supraphysiologic doses of hydrocortisoneCritical Care Medicine, 1998
- Corticosteroid Therapy in Severe IllnessNew England Journal of Medicine, 1997
- Cortisol response to corticotropin and survival in septic shockThe Lancet, 1991