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. Author manuscript; available in PMC: 2014 Jul 1.
Published in final edited form as: J Trauma Acute Care Surg. 2013 Jul;75(1 0 1):S3–S8. doi: 10.1097/TA.0b013e31828fa3a0

Table 1.

PROMMTT site characteristics

Site Waiver of
Consent?		 Number of
patients
enrolled in
PROMMTT		 IRB approved
residual blood
collection		 Number (%) of
patients from
whom
discarded
blood samples
were collected		 Number (%)
patients with at
least one
sample
analyzed
1 Yes 308 Yes 173 (56.2%) 170 (98.3%)
2 Yes 138 Yes 21 (15.2%) 21 (100%)
3 Yes 61 Yes 1 (1.6%) 1 (100%)
4 Yes 128 Yes 6 (4.7%) 6 (100%)
5 Yes 143 Yes 0 0
6 Yes 110 No 0 0
7 Yes 107 No1 0 25
8 No 121 No 0 0
9 Yes 101 No 0 0
10 Yes 28 Yes 13 (46.4%) 12 (92.3%)
1

Site 7 was approved to collect timed blood samples under a separate protocol, and results were shared with PROMMTT