Walsh 1983.
Methods | Design: randomized controlled study Withdrawals: 0 Setting: single centre, UK Sample size: 21 |
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Participants | 3 arms included in the trial, with 7 participants in each. Arms were given lactated Ringer's solution, 5% dextrose, and normal saline. Only 2 arms were included for analysis (N = 14). Age (mean): Hartmann's 55/normal saline 50 years Gender (M/F): not reported ASA grade: not reported Surgery type: elective cholecystectomy Surgery duration (mean): not reported Anaesthesia type: general |
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Interventions |
Intervention n = 7 Buffered arm ‐ Hartmann's solution Control n = 7 Non‐buffered arm ‐ normal saline 6 mL/kg/h Co‐interventions: none |
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Outcomes | Estimated blood loss measured intraoperatively | |
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) | Low risk | Methods of randomization unclear |
Allocation concealment (selection bias) | High risk | Allocation concealment not mentioned |
Blinding of participants and personnel (performance bias) All outcomes | High risk | Blinding not mentioned |
Blinding of outcome assessment (detection bias) All outcomes | High risk | Blinding not mentioned |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | No withdrawals |
Selective reporting (reporting bias) | Low risk | No evidence of selection bias. All proposed outcome measures adequately reported |
Other bias | Low risk | No other information given |