Table 2.
First author or trial name | CCP arm, N | Control arm, N | Control | Clinical status: severity of COVID-19 | Transfusion-related adverse events | Mortality related to transfusion of CCP |
---|---|---|---|---|---|---|
PLACID Trial19 | 227 | 224 | Standard of care | Moderate WHO scale 4-5 | 3 transfusion-related events with CCP | 3 deaths reported as possibly related to transfusion of CCP |
AlQahtani20 | 20 | 20 | Standard of care | Moderate WHO scale 4-6 | No transfusion-related events reported | N/A |
Avendano-Sola31 | 38 | 43 | Standard of care | Moderate WHO scale 4-6 | 2 transfusion-related events with CCP | N/A |
CONCOR-1 Study Group13 | 614 | 307 | Standard of care | Moderate to severe WHO scale 4-6 | 35 transfusion-related events in the CCP cohort: 4 were life-threatening (2 TACO, I possible TRALI, 1 TAD) | N/A |
Bennet-Guerrerro21 | 59 | 15 | Nonimmune plasma | Moderate to severe WHO scale 4-7* | 1 transfusion-related event in CCP group and 0 in control group | N/A |
REMAP-CAP Investigators26 | 1084 | 916 | Standard of care | Moderate to severe WHO scale 4-7* | 32/1075 (3.0%) with ≥ 1 serious adverse event in the CCP group vs 12/905 (1.3%) in the control group | N/A |
Gharbharan22 | 43 | 43 | Standard of care | Moderate to severe WHO scale 4-7* | No SAEs reported with CCP | N/A |
Hamdy30 | 15 | 15 | Standard of care | Moderate to severe WHO scale 4-6 | No transfusion-related events reported | N/A |
RECOVERY Trial26 | 5795 | 5763 | Standard of care | Moderate to severe WHO scale 4-7* | 13 transfusion-related events in CCP cohort reported to SHOT: 9 pulmonary reactions (not TRALI); 4 serious febrile, allergic or hypotensive reactions; 16 severe allergic reactions reported within 72 h of randomization in CCP cohort and 2 in control group. | 3 deaths reported in CCP cohort that may have been related to transfusion |
Kirenga27 | 69 | 67 | Standard of care | Moderate to severe WHO scale 4-6 | 3 adverse events were judged definitively related, and 3 were judged possibly related to plasma transfusion. | |
SIREN-C3PO Investigators35 | 257 | 254 | Normal saline | Mild WHO scale 2-3 | Transfusion-related adverse events occurred more frequently in CCP arm and dyspnea was more frequent in placebo arm. | N/A |
CAPSID Trial28 | 53 | 52 | Standard of care | Moderate to severe WHO scale 4-7 | No significant difference was seen in the frequency or grade of adverse events when comparing the CCP and standard of care arms. | N/A |
Li23 | 52 | 51 | Standard of care | Moderate to severe WHO scale 4-7* | 2 transfusion-related events with CCP | N/A |
Libster33 | 80 | 80 | Normal saline | Asymptomatic to mild WHO scale 1-2 | No transfusion-related events reported in CCP or control cohorts. | N/A |
O’Donnell24 | 150 | 73 | Nonimmune plasma | Moderate to severe WHO scale 4-9 | 4 events definitely or probably related to transfusion occurred in CCP cohort; 3 events definitely or probably related to transfusion occurred in control group | N/A |
PlasmAr Study Group29 | 228 | 105 | Normal Saline | Moderate to severe WHO scale 4-6 | 11 transfusion-related events reported for CCP cohort; 2 transfusion-related events reported in control group | N/A |
Joyner50 | 20 000 | N/A | N/A | Moderate to severe WHO scale 4-7* | Events reported as possibly or definitely related to transfusion: 36 TACO; 21 TRALI; 21 severe allergic | 10 events within 4 h of CCP transfusion, all reported as possibly related |
TACO, transfusion-associated circulatory overload; TAD, transfusion-associated dyspnea; TRALI, transfusion-related acute lung injury.
Information was not available to distinguish between WHO scale categories 7 and 9.