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Multicenter Study
. 2010;14(3):R102.
doi: 10.1186/cc9044. Epub 2010 Jun 3.

Global utilization of low-dose corticosteroids in severe sepsis and septic shock: a report from the PROGRESS registry

Affiliations
Multicenter Study

Global utilization of low-dose corticosteroids in severe sepsis and septic shock: a report from the PROGRESS registry

Richard Beale et al. Crit Care. 2010.

Abstract

Introduction: The benefits and use of low-dose corticosteroids (LDCs) in severe sepsis and septic shock remain controversial. Surviving sepsis campaign guidelines suggest LDC use for septic shock patients poorly responsive to fluid resuscitation and vasopressor therapy. Their use is suspected to be wide-spread, but paucity of data regarding global practice exists. The purpose of this study was to compare baseline characteristics and clinical outcomes of patients treated or not treated with LDC from the international PROGRESS (PROmoting Global Research Excellence in Severe Sepsis) cohort study of severe sepsis.

Methods: Patients enrolled in the PROGRESS registry were evaluated for use of vasopressor and LDC (equivalent or lesser potency to hydrocortisone 50 mg six-hourly plus 50 microg 9-alpha-fludrocortisone) for treatment of severe sepsis at any time in intensive care units (ICUs). Baseline characteristics and hospital mortality were analyzed, and logistic regression techniques used to develop propensity score and outcome models adjusted for baseline imbalances between groups.

Results: A total of 8,968 patients with severe sepsis and sufficient data for analysis were studied. A total of 79.8% (7,160/8,968) of patients received vasopressors, and 34.0% (3,051/8,968) of patients received LDC. Regional use of LDC was highest in Europe (51.1%) and lowest in Asia (21.6%). Country use was highest in Brazil (62.9%) and lowest in Malaysia (9.0%). A total of 14.2% of patients on LDC were not receiving any vasopressor therapy. LDC patients were older, had more co-morbidities and higher disease severity scores. Patients receiving LDC spent longer in ICU than patients who did not (median of 12 versus 8 days; P <0.001). Overall hospital mortality rates were greater in the LDC than in the non-LDC group (58.0% versus 43.0%; P <0.001). After adjusting for baseline imbalances, in all mortality models (with vasopressor use), a consistent association remained between LDC and hospital mortality (odds ratios varying from 1.30 to 1.47).

Conclusions: Widespread use of LDC for the treatment of severe sepsis with significant regional and country variation exists. In this study, 14.2% of patients received LDC despite the absence of evidence of shock. Hospital mortality was higher in the LDC group and remained higher after adjustment for key determinates of mortality.

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Figures

Figure 1
Figure 1
Patient disposition. Patients were enrolled from December 2002 until December 2005 in 37 countries at 276 sites. There were 12,570 adult patients with severe sepsis entered into the PROGRESS database of which 8,968 were used for this sub-study. LDC, Low-Dose Corticosteroids; HDC, High-Dose Corticosteroids.
Figure 2
Figure 2
Comparison of within-region mortality. N, the number of patients within the region, and the % of LDC represents the percentage of low-dose corticosteroid use within the region.
Figure 3
Figure 3
Temporal pattern of low-dose corticosteroid use over time. N, the number of patients in the quartiles.

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