Methods |
Randomised clinical trial |
Participants |
Participants older than 18 years of age who had haematemesis or melena, or both (due to upper GI bleeding)
|
Interventions |
The restrictive transfusion group was transfused for haemoglobin < 7 g/dL, and the liberal transfusion group was transfused when Hg was < 9 g/dL. In both groups, 1 unit of RBCs was transfused initially. |
Outcomes |
Death at 45 days |
Notes |
‐ |
Risk of bias |
Bias |
Authors' judgement |
Support for judgement |
Random sequence generation (selection bias) |
Low risk |
Random sequence generation was computer generated. |
Allocation concealment (selection bias) |
Low risk |
The trial used sealed consecutively numbered, opaque envelopes. |
Blinding of participants and personnel (performance bias)
All outcomes |
Unclear risk |
Clinicians and participants were not blinded. |
Blinding of outcome assessment (detection bias)
All outcomes |
Low risk |
Mortality was the primary outcome. Assessors of other outcomes were not documented to be blinded. |
Incomplete outcome data (attrition bias)
All outcomes |
Low risk |
The trial had good follow up. |
Selective reporting (reporting bias) |
Low risk |
Reporting was complete. |
Other bias |
Low risk |
No other biases were apparent. |