Webert 2008.
Methods | Randomised controlled trial | |
Participants | 60 adult participants with acute leukaemia were randomly allocated to 1 of 2 groups:
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Interventions |
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Outcomes | Transfusions, bleeding risk, 30‐day mortality provided by authors | |
Notes | ‐ | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Low risk | Sequence generation was computer‐generated. |
Allocation concealment (selection bias) | Low risk | Allocation was internet‐based and central. |
Blinding of participants and personnel (performance bias) All outcomes | Unclear risk | Participants and clinicians were not blinded. |
Blinding of outcome assessment (detection bias) All outcomes | Low risk | Outcomes were assessed blinded. |
Incomplete outcome data (attrition bias) All outcomes | Low risk | There were no missing data. |
Selective reporting (reporting bias) | Low risk | No reporting bias was apparent. |
Other bias | Low risk | No other biases were apparent. |
Abbreviations
ACS = acute coronary syndrome ARDS = acute respiratory distress syndrome CARE = Cardiac Anesthesia Risk Evaluation DSMB = Data Safety Monitoring Board GI = gastrointestinal Hb = haemoglobin Hct = haematocrit ICU = intensive care unit IHD = ischaemic heart disease M/F = male/female PLTs = platelets RBC = red blood cells SD = standard deviation TKA = total knee arthroplasty