Koo 2005.
Methods | Randomised clinical trial | |
Participants | Country: South Korea
Number randomised: 50
Postrandomisation dropouts: not stated
Revised sample size: 50
Average age: 53 years
Women: 14 (28%)
Number of cirrhotics: not stated
Number of major liver resections: 38 (76%)
Number of right hepatectomies: 27 (54%)
Follow‐up (months): until discharge
Further details of methods of liver resection
Inclusion criteria: adults scheduled for elective hepatectomy Exclusion criteria
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Interventions | Participants were randomly assigned to 2 groups. Group 1: clamp‐crush method (n = 25) Group 2: cavitron ultrasonic surgical aspirator (n = 25) | |
Outcomes | The outcomes reported were: proportion of people with any adverse events, operative blood loss, and operating time | |
Notes | — | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Comment: this information was not available. |
Allocation concealment (selection bias) | Unclear risk | Quote: "Randomization was performed by opening a sealed envelope before induction of anaesthesia". Comment: further information on sealed envelope system were not available. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Comment: this information was not available. |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | Comment: this information was not available. |
Incomplete outcome data (attrition bias) All outcomes | Unclear risk | Comment: this information was not available. |
Selective reporting (reporting bias) | High risk | Comment: mortality and morbidity were not reported. |
Vested interest bias | Unclear risk | Comment: this information was not available. |
Other bias | Low risk | Comment: no other bias |