McFarlane 1994.
Methods | Design: randomized controlled trial Withdrawals: none Setting: single centre (UK) Sample size: 30 |
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Participants | Age (mean): 57/54 years Gender (M/F): not described ASA grade: I or II Surgery type: major elective hepatobiliary or pancreatic surgery Surgery duration (mean): 3.3/3.7 hours Anaesthesia type: general |
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Interventions |
Intervention n = 15 Buffered arm ‐ Plasmalyte 148 infusion 15 mL/kg/h Control n = 30 Non‐buffered arm ‐ normal saline infusion 15 mL/kg/h Rate adjusted in response to clinical state, but not according to a clinical protocol Co‐interventions: all fluids warmed |
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Outcomes | Blood loss (mL/kg) mean and SD, chloride, bicarbonate, base excess, PaCO2, lactate up to 24 hours postoperatively | |
Notes | Funding source: not disclosed Declarations of interest: none disclosed |
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Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Randomization method not clear |
Allocation concealment (selection bias) | High risk | No evidence of allocation concealment |
Blinding of participants and personnel (performance bias) All outcomes | High risk | No evidence of blinding |
Blinding of outcome assessment (detection bias) All outcomes | High risk | No evidence of blinding |
Incomplete outcome data (attrition bias) All outcomes | Low risk | All outcome data complete |
Selective reporting (reporting bias) | Low risk | No evidence of selection bias. All proposed outcome measures adequately reported |
Other bias | Low risk | No other information forthcoming |