| Methods | Randomised controlled trial | |
| Participants | 25 patients were studied prospectively following acute injury and haemorrhage. These patients were randomised to 1 of 2 groups:
|
|
| Interventions |
NB: all patients had sustained a Class III or Class IV haemorrhage and had clinical signs of shock (systolic blood pressure < 90 torr, heart rate >100 bpm or urine output < 20 ml/hr) before entry into the study. Patients were resuscitated according to the clinical protocol of the centre first using crystalloid to re-establish organ perfusion and haemodynamic stability and then giving sufficient packed red cells to achieve a Hct close to 30%. Patients were studied twice a day for 3 days after the period of haemorrhagic shock |
|
| Outcomes | Outcomes reported: RBC consumption (units), cardiopulmonary parameters: pulmonary capillary wedge pressure (PCWP), intrapulmonary shunt, tissue oxygenation/perfusion, oxygen consumption/delivery, arterial and venous O2 saturations, arterial and venous O2 contents, cardiac index (CI), heart rate, systemic vascular resistance, left ventricular stroke work index | |
| Notes | ||
| Risk Of Bias | ||
| Bias | Author’ judgement | Support for judgement |
| Random sequence generation (selection bias) | Unclear risk | No information |
| Allocation concealment (selection bias) | Unclear risk | No information |
| Blinding (performance bias and detection bias) All outcomes |
Unclear risk | No information |
| Incomplete outcome data (attrition bias) All outcomes |
Low risk | Appears to have been complete |
| Selective reporting (reporting bias) | Unclear risk | - |
| Other bias | Low risk | - |