| Methods | Randomised controlled trial | |
| Participants | 838 critically ill patients with euvolemia after initial treatment who had Hb concentrations <9.0 g/dL within 72 hours after admission to the intensive care unit were randomly assigned to 1 of 2 groups:
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| Interventions |
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| Outcomes | Outcomes reported: mortality, length of hospital stay, length of ICU stay, blood usage (units), complications, infection rates, cardiac events, pulmonary oedema, pneumonia | |
| Notes | ||
| Risk of bias | ||
| Bias | Authors’ judgement | Support for judgement |
| Random sequence generation (selection bias) | Low risk | Computer-generated random order |
| Allocation concealment (selection bias) | Unclear risk | Sealed, opaque envelopes prepared by the data-coordinating centre and distributed to each participating institution where they were opened up sequentially to determine the patients treatment assignment. The envelopes were returned periodically to the co-ordinating centre for auditing |
| Blinding (performance bias and detection bias) All outcomes |
Unclear risk | “It was not feasible to mask the assigned transfusion strategy from health care providers” |
| Incomplete outcome data (attrition bias) All outcomes |
Low risk | Intention-to-treat analysis used |
| Selective reporting (reporting bias) | Low risk | - |
| Other bias | Low risk | - |