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. 2017 Jan 31;2017(1):CD008075. doi: 10.1002/14651858.CD008075.pub3

Cole 2001.

Methods Country:  Australia
Setting: tertiary‐centre ICU
Time frame: unclear
Cross‐over RCT
Intention‐to‐treat analysis: yes
Follow‐up period: 2 days
Lost to follow‐up: none
Participants No. of participants randomized: 11
No. of participants analysed: 11
Mean age: 63.1
Male, no. (%): 8/11 (73)
Inclusion criteria
Septic shock (criteria of bone)
Established ARF secondary to septic shock (with oliguria or anuria)
Established need for RRT
Recognized source of sepsis that had been treated with antibiotics and surgical drainage of source if necessary
 
Exclusion criteria
ESRD
AIDS
Life expectancy < 6 months
Withdrawal of therapy possible
Interventions Treatment intervention
HVHF
8‐Hour session
Filter: 1.6 m2 AN 69
Blood flow: 300 mL/min; ultrafiltrate flow: 100 mL/min
Lactate buffered replacement fluid: one‐third delivered pre‐filter, two‐thirds post‐filter
 
Control intervention
CVVH
8‐Hour session
Filter: 1.2 m2 AN 69 polyacrylonitrile
Blood flow: 200 mL/min; ultrafiltrate flow: 1 L/h
Lactate buffered replacement fluid delivered pre‐filter
 
MAP to be maintained at > 70 mmHg throughout
Outcomes Mean arterial pressure and norepinephrine dose
Notes Funding source: Austin & Repatriation Medical Centre Anaesthesia and Intensive Care Trust Fund and Hospal Pty Ltd
No conflicts of interest declared
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk Random sequence generation by computer programme
Allocation concealment (selection bias) Low risk Sealed opaque envelopes
Blinding of participants and personnel (performance bias) 
 All outcomes Low risk Not possible to blind personnel to allocated treatment, although considered to be at low risk
Blinding of outcome assessment (detection bias) 
 All outcomes Unclear risk Not stated as for whom or how outcome assessment was made
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No missing outcome data
Selective reporting (reporting bias) Low risk Protocol available and predefined outcomes reported
Other bias Low risk Appears to be free of other sources of bias