Dolecek 2009.

Methods	Randomised controlled trial, randomised according to computer‐generated randomisation list
Participants	56 patients with severe sepsis. Patients were included if they were 18 years or older and developed severe sepsis. Exclusion criteria: severe coagulopathy, pregnant, cardiac failure, acute renal failure, aortal aneurysm, severe aortal regurgitation or dysrhythmia
Interventions	1) 20% Albumin (n = 30) 2) 6% HES (n = 26)
Outcomes	Death Haemodynamic variables
Notes	Follow‐up 28 days
Risk of bias
Bias	Authors' judgement	Support for judgement
Allocation concealment (selection bias)	Low risk	Sealed opaque sequentially numbered envelopes (information obtained from authors)