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. 2022 Jul 21;140(3):196–207. doi: 10.1182/blood.2021012248

Table 2.

Adverse events related to transfusion of COVID-19 convalescent plasma

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.