Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock
- PMID: 12186604
- DOI: 10.1001/jama.288.7.862
Effect of treatment with low doses of hydrocortisone and fludrocortisone on mortality in patients with septic shock
Erratum in
- JAMA. 2008 Oct 8;300(14):1652. Chaumet-Riffaut, Philippe [corrected to Chaumet-Riffaud, Philippe]
Abstract
Context: Septic shock may be associated with relative adrenal insufficiency. Thus, a replacement therapy of low doses of corticosteroids has been proposed to treat septic shock.
Objective: To assess whether low doses of corticosteroids improve 28-day survival in patients with septic shock and relative adrenal insufficiency.
Design and setting: Placebo-controlled, randomized, double-blind, parallel-group trial performed in 19 intensive care units in France from October 9, 1995, to February 23, 1999.
Patients: Three hundred adult patients who fulfilled usual criteria for septic shock were enrolled after undergoing a short corticotropin test.
Intervention: Patients were randomly assigned to receive either hydrocortisone (50-mg intravenous bolus every 6 hours) and fludrocortisone (50- micro g tablet once daily) (n = 151) or matching placebos (n = 149) for 7 days.
Main outcome measure: Twenty-eight-day survival distribution in patients with relative adrenal insufficiency (nonresponders to the corticotropin test).
Results: One 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 Vasopressor therapy was withdrawn within 28 days in 46 patients (40%) in the placebo group and in 65 patients (57%) in the corticosteroid group (hazard ratio, 1.91; 95% confidence interval,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.
Conclusion: In 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.
Comment in
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Corticosteroids and septic shock.JAMA. 2002 Aug 21;288(7):886-7. doi: 10.1001/jama.288.7.886. JAMA. 2002. PMID: 12186608 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):43; author reply 43-4. doi: 10.1001/jama.289.1.43-a. JAMA. 2003. PMID: 12503964 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):42; author reply 43-4. doi: 10.1001/jama.289.1.42-b. JAMA. 2003. PMID: 12503965 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):42; author reply 43-4. doi: 10.1001/jama.289.1.42-a. JAMA. 2003. PMID: 12503966 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):41; author reply 43-4. doi: 10.1001/jama.289.1.41-c. JAMA. 2003. PMID: 12503967 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):41-2; author reply 43-4. doi: 10.1001/jama.289.1.41-d. JAMA. 2003. PMID: 12503968 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):41; author reply 43-4. doi: 10.1001/jama.289.1.41-b. JAMA. 2003. PMID: 12503969 No abstract available.
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Corticosteroids for patients with septic shock.JAMA. 2003 Jan 1;289(1):41; author reply 43-4. doi: 10.1001/jama.289.1.41-a. JAMA. 2003. PMID: 12503970 No abstract available.
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Hydrocortisone and fludrocortisone improved 28-day survival in septic shock and adrenal insufficiency.ACP J Club. 2003 Mar-Apr;138(2):44. ACP J Club. 2003. PMID: 12614129 No abstract available.
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Paresis following mechanical ventilation.JAMA. 2003 Apr 2;289(13):1634; author reply 1634-5. doi: 10.1001/jama.289.13.1634-b. JAMA. 2003. PMID: 12672726 No abstract available.
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