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. 2012 Nov 14;2012(11):CD004082. doi: 10.1002/14651858.CD004082.pub5

Jhanji 2010.

Methods RCT
Single centre
Participants 135 patients (3 arms)
45 patients in each arm
Elective
Gastrointestinal surgery
Interventions Postoperative
3 arms to the study (arm‐1 CVP group fluid optimisation according to CVP, arm‐2 SV fluid optimization according to SV, third arm had fluids and continuous dopexamine infusion)
LidCO
Goals = SV
Outcomes Microvascular flow and oxygenation
Complications
Infections
Acute kidney injury
Cardiac complications
Critical care free days
HLOS
Hospital mortality
Notes The 3rd arm with continuous dopexamine infusion is not included in the analysis as the control group was not matched
Risk of bias
Bias Authors' judgement Support for judgement
Random sequence generation (selection bias) Low risk "Participants were randomly allocated to one of three treatment groups by computer‐generated random sequence in blocks of nine"
Allocation concealment (selection bias) Low risk "The study group allocations were placed in serially numbered opaque envelopes"
Blinding of participants and personnel (performance bias) 
 All outcomes Unclear risk "Only the member of the research team who delivered the intervention was aware of the study group allocation"
Blinding of outcome assessment (detection bias) 
 All outcomes Low risk "Clinical outcomes data for each patient were collected by a member of the research team who was unaware of study group allocation"
Incomplete outcome data (attrition bias) 
 All outcomes Low risk No missing outcome data
Selective reporting (reporting bias) Low risk Published report includes all expected outcomes
Other bias Unclear risk Study was supported by pharmaceutical company