Jhanji 2010.
Methods | RCT Single centre |
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Participants | 135 patients (3 arms) 45 patients in each arm Elective Gastrointestinal surgery |
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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 |
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Outcomes | Microvascular flow and oxygenation Complications Infections Acute kidney injury Cardiac complications Critical care free days HLOS Hospital mortality |
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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 |