| 'Risk of bias' assessment of Ahn 2020 | |||
| Domain | Assessed outcomes | Authors' judgement | Support for judgement |
| Representative study group (selection bias) | Not available | High | 2 participants only |
| Outcome detectors blinded to intervention (detection bias) | Adverse events | High | Not blinded, awareness of intervention can bias assessment of subjective outcomes |
| Complete outcome assessment/follow‐up (attrition bias) | Adverse events | Low | Assessed and reported for both cases |
| Well‐defined study group (reporting bias) | Not available | Low | Population and intervention are well described |
| Well‐defined outcome (reporting bias) | Adverse events | High | No adverse reaction occurred after the administration of convalescent plasma in both cases. Observation period not reported |
| Well‐defined risk estimates (analyses) | Adverse events | Not applicable | No analyses performed |
| Important prognostic factors or follow‐up taken adequately into account (confounding) | Not available | High | Not adjusted for confounding factors |