TY - JOUR
T1 - Low-dose corticosteroid treatment in septic shock
T2 - A propensity-matching study
AU - Funk, Duane
AU - Doucette, Steven
AU - Pisipati, Amarnath
AU - Dodek, Peter
AU - Marshall, John C.
AU - Kumar, Anand
AU - Arabi, Yaseen
AU - Dellinger, Phillip
AU - Dial, Sandra
AU - Ellis, Paul
AU - Feinstein, Daniel
AU - Gurka, Dave
AU - Guzman, Jose
AU - Keenan, Sean
AU - Kramer, Andreas
AU - Kumar, Aseem
AU - Lapinsky, Stephen
AU - Laporta, Denny
AU - Laupland, Kevin
AU - Light, Bruce
AU - Maki, Dennis
AU - Martinka, Greg
AU - Memish, Ziad
AU - Mirzanejad, Yazdan
AU - Parrillo, Joseph E.
AU - Patel, Gourang
AU - Penner, Charles
AU - Roberts, Dan
AU - Ronald, John
AU - Simon, Dave
AU - Sharma, Sat
AU - Al Shirawi, Nehad
AU - Wood, Gordon
AU - Wood, Kenneth E.
AU - Zanotti, Sergio
N1 - Publisher Copyright:
Copyright © 2014 by the Society of Critical Care Medicine and Lippincott Williams & Wilkins.
PY - 2014
Y1 - 2014
N2 - Objective: Given conflicting data and current guidelines, low-dose corticosteroids are often used in the treatment of septic shock. To evaluate the therapeutic benefit of early low-dose corticosteroid in patients with septic shock. Design: Retrospective, multicenter, propensity-matched cohort study. Setting: ICUs of 28 academic and community hospitals in three countries between 1996 and 2007. Subjects: Six thousand six hundred sixty-three eligible patients with septic shock of whom 1,838 received IV low-dose corticosteroid treatment within 48 hours of the diagnosis of septic shock and were matched to a comparable group who did not receive low-dose corticosteroid. Measurements and Main Results: The primary outcome was 30-day mortality. Mortality analyses were stratified by severity of illness (Acute Physiology and Chronic Health Evaluation II quartile). Using a Cox proportional hazards model, corticosteroid therapy was associated with similar 30-day mortality when compared with the matched control cohort (652/1,838 [35.5%] vs 641/1,838 [34.9%]; hazard ratio, 0.98; 95% CI, 0.88-1.10; p = 0.77). In the subgroup of patients with the Acute Physiology and Chronic Health Evaluation II score quartile more than or equal to 30, low-dose corticosteroid was associated with lower mortality (232/461 [50.6%] vs 251/450 [55.8%]; hazard ratio, 0.81; 95% CI, 0.68-0.97; p = 0.02). In logistic regression models, corticosteroid therapy was not associated with reductions in ICU (556/1,838 [30.3%] vs 558/1,838 [30.4%]; odds ratio, 0.99; 95% CI, 0.86-1.15; p = 0.94) or hospital mortality (797/1,838 [43.4%] vs 773/1,838 [42.1%]; odds ratio, 1.05; 95% CI, 0.93-1.20; p = 0.42). Similarly, there were no significant differences in ventilator-(median and interquartile range, 13 [0-25] vs 15 [0-25]; p = 0.8) and pressor/inotrope-free days (median and interquartile range, 25 [3-27] vs 24 [2-28]; p = 0.63) up to 30 days between groups. Conclusion: Early administration of low-dose corticosteroid is not associated with decreased mortality when it is administered to unselected patients with septic shock. A beneficial effect of low-dose corticosteroid on mortality may exist in patients with the highest severity of illness. Future trials of low-dose corticosteroid in septic shock should consider restricting the study population to this cohort.
AB - Objective: Given conflicting data and current guidelines, low-dose corticosteroids are often used in the treatment of septic shock. To evaluate the therapeutic benefit of early low-dose corticosteroid in patients with septic shock. Design: Retrospective, multicenter, propensity-matched cohort study. Setting: ICUs of 28 academic and community hospitals in three countries between 1996 and 2007. Subjects: Six thousand six hundred sixty-three eligible patients with septic shock of whom 1,838 received IV low-dose corticosteroid treatment within 48 hours of the diagnosis of septic shock and were matched to a comparable group who did not receive low-dose corticosteroid. Measurements and Main Results: The primary outcome was 30-day mortality. Mortality analyses were stratified by severity of illness (Acute Physiology and Chronic Health Evaluation II quartile). Using a Cox proportional hazards model, corticosteroid therapy was associated with similar 30-day mortality when compared with the matched control cohort (652/1,838 [35.5%] vs 641/1,838 [34.9%]; hazard ratio, 0.98; 95% CI, 0.88-1.10; p = 0.77). In the subgroup of patients with the Acute Physiology and Chronic Health Evaluation II score quartile more than or equal to 30, low-dose corticosteroid was associated with lower mortality (232/461 [50.6%] vs 251/450 [55.8%]; hazard ratio, 0.81; 95% CI, 0.68-0.97; p = 0.02). In logistic regression models, corticosteroid therapy was not associated with reductions in ICU (556/1,838 [30.3%] vs 558/1,838 [30.4%]; odds ratio, 0.99; 95% CI, 0.86-1.15; p = 0.94) or hospital mortality (797/1,838 [43.4%] vs 773/1,838 [42.1%]; odds ratio, 1.05; 95% CI, 0.93-1.20; p = 0.42). Similarly, there were no significant differences in ventilator-(median and interquartile range, 13 [0-25] vs 15 [0-25]; p = 0.8) and pressor/inotrope-free days (median and interquartile range, 25 [3-27] vs 24 [2-28]; p = 0.63) up to 30 days between groups. Conclusion: Early administration of low-dose corticosteroid is not associated with decreased mortality when it is administered to unselected patients with septic shock. A beneficial effect of low-dose corticosteroid on mortality may exist in patients with the highest severity of illness. Future trials of low-dose corticosteroid in septic shock should consider restricting the study population to this cohort.
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U2 - 10.1097/CCM.0000000000000518
DO - 10.1097/CCM.0000000000000518
M3 - Article
C2 - 25072758
AN - SCOPUS:84922019928
SN - 0090-3493
VL - 42
SP - 2333
EP - 2341
JO - Critical care medicine
JF - Critical care medicine
IS - 11
ER -