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. 2013 Aug 19;3:27. doi: 10.1186/2110-5820-3-27

Table 1.

Comparison of selected randomized, controlled trials assessing the effects of therapeutic interventions on sepsis-related mortality between 2001 and 2013

1st author and year of publication Therapeutic intervention assessed (inclusion time window) Mortality rate in control arm (%) Impact on mortality Impact on adverse events Effect of studied therapy*
Rivers 2001 [2]
Early goal guided therapy (As soon as possible)
49.2
Decreased mortality
No difference
Better
Bernard 2001 [3]
Drotrecogin alfa (24 h)
30.8
Decreased mortality
Serious bleeding event
Annane 2002 [6]
Hydrocortisone + fludrocortisone (3 h)
63
Decreased mortality
No difference
Cruz 2009 [7]
Polymyxin B hemoperfusion (6 h)
53
Decreased mortality
Cartridge clotting Hypotension and tachycardia
 
Warren 2001 [8]
Antithrombin III (6 h)
38.7
No difference
No difference
No difference
Reinhart 2004 [9]
Extracorporeal endotoxin adsorber (24 h)
26
 
No difference
Heinrich 2006 [10]
IG-MA enriched Ig** (not available)
28.2
 
Not available
Annane 2007 [12]
Norepinephrine plus dobutamine (24 h)
34
 
No difference
Russel 2008 [14]
Vasopressin (24 h)
39
 
No difference
Ranieri 2012 [1]
Drotrecogin alfa (24 h)
24.2
 
No difference
Opal 2013 [15]
Eritoran (12 h)
26.9
 
No difference
 
Lopez 2004 [16]
NO synthase inhibitor LNMA (72 h)
49
Increased mortality
Low cardiac output
Worse
Abraham 2005 [11]
Drotrecogin alfa (48 h)
17
No difference
Bleeding events
Brunkhorst 2008 [17]
Insulin/pentastarch (12 h)
26
No difference
Hypoglycemia
Renal failure
Coagulopathy
Sprung 2008 [18]
Hydrocortisone (72 h)
31.5
No difference
Increased infections events
Stephens 2008 [13]
G-CSF*** (24 h)
25
No difference
Higher rate of new organ failure
Patel 2010 [19]
Dopamine Early goal guided therapy
43
No difference
Arrhythmias
Annane 2010 [20]
Corticosteroid/Insulin (not available)
45.8
No difference
Superinfection
Hypoglycemia
Perner 2012 [21] 6% HES 130/0.42 (24 h) 43 Increased mortality Not available  

The selected trials were categorized in three groups depending on whether the effect of the studied intervention on mortality and/or serious adverse events was “better”: studied intervention leading to a significant reduction in mortality; “not different”: similar impact of the studied intervention on mortality and no severe adverse events; “worse”: studied intervention leading to a significant increase in mortality and/or to a significant increase in serious adverse events.

*Statistically significant difference vs. control arm: **neutropenic patients; ***granulocyte colony-stimulating factor.