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. Author manuscript; available in PMC: 2021 Mar 1.
Published in final edited form as: Transfusion. 2020 Mar;60(Suppl 2):S17–S37. doi: 10.1111/trf.15715

TABLE 13.

Severe donor-related adverse events and rate by type of collection method in the United States, 2015 and 2017

Number of severe donor-related adverse events* Reaction rate

Year Collection type Donor age Blood centers Hospitals Combined (95% CI) Blood centers Hospitals Combined
2017 Whole blood collections All Donors 11,078 951 12,029 (9251–14,807) 1:896 1:525 1:867 (0.12%)
 18 years and younger 3663 241 3904 (2681–5127)
 Older than 18 years 7415 709 8125 (6065–10,184)
Apheresis collections All Donors 2498 88 2585 (2072–3098) 1:937 1:1037 1:940 (0.11%)
 18 years and younger 244 4 248 (113–384)
 Older than 18 years 2253 84 2337 (1676–2998)
All collections All donors 13,576 1038 14,614 (11,664–17,564) 1:903 1:568 1:880 (0.11%)
2015 Whole blood collections (manual, all donors) 11,996 2275 14,271 (9036–19,507) 1:854 1:237 1:756 (0.13)
Apheresis collections (automated, all donors) 3335 156 3491 (1088–5894) 1:786 1:752 1:784 (0.13)
All collections (all donors) 15,331 2431 17,762 (10,744–24,779) 1:839 1:270 1:762 (0.13)
*

Severe donor-related adverse events were defined as events occurring in donors attributed to the donation process that include, for example, major allergic reaction, arterial puncture, loss of consciousness of a minute or more, loss of consciousness with injury, nerve irritation, etc.

The total number of collections was 12,855,000 in 2017 and 13,526,000 in 2015.