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1 2%) received plasma, and 394 (5.3%) received cryoprecipitate.
2 Plasma from 4 patients with type I VWD was cryoprecipitated.
3 mortality was lowest in the tranexamic acid/cryoprecipitate (11.6%) and tranexamic acid (18.2%) grou
4 examic acid (18.2%) groups compared with the cryoprecipitate (21.4%) and no tranexamic acid/cryopreci
6 plasma, 9.6 +/- 4.9 U vs. 4.9 +/- 3.6 U; and cryoprecipitate, 4.3 +/- 3.6 U vs. 2.2 +/- 3.5 U; p < 0.
7 rozen plasma (4.8 versus 3.1 U, P<0.03), and cryoprecipitate (9.9 versus 5.4 U, P<0.002) than patient
8 nd more aggressive use of plasma, platelets, cryoprecipitate and coagulation factor isolates, decreas
10 complex with fibrin by gel chromatography of cryoprecipitates and then separated from the fibrin eith
12 anti-Fas antibody, normal plasma depleted of cryoprecipitate, and low concentrations (< or = 0.1 micr
13 y use of platelets, fresh frozen plasma, and cryoprecipitate; and adjusting for country produced resu
14 en-carrying capacity; platelets, plasma, and cryoprecipitate are intended to facilitate hemostasis th
15 ned with a multiple myeloma serum containing cryoprecipitates, but multiple myeloma sera without cryo
17 on develop detectable serum cryoglobulins or cryoprecipitates (CP), although most do not show clinica
18 otease is present in fresh-frozen plasma, in cryoprecipitate-depleted plasma (cryosupernatant), and i
23 arly, patients given aprotinin received more cryoprecipitate in the intensive care unit (7.3 versus 3
27 an [SD], 23.0 [19.2]) and no tranexamic acid/cryoprecipitate (mean [SD], 21.2 [18.5]) (P < .001) grou
28 (mean [SD], 28.3 [15.7]) and tranexamic acid/cryoprecipitate (mean [SD], 26 [14.9]) groups compared w
29 Injury severity scores were highest in the cryoprecipitate (mean [SD], 28.3 [15.7]) and tranexamic
30 following groups: tranexamic acid (n = 148), cryoprecipitate (n = 168), tranexamic acid/cryoprecipita
31 , cryoprecipitate (n = 168), tranexamic acid/cryoprecipitate (n = 258), and no tranexamic acid/cryopr
33 Fibrinogen therapy can be administered with cryoprecipitate or fibrinogen concentrates, and clinical
34 onvirally inactivated factor concentrates or cryoprecipitates prepared from local blood donors was co
35 cipitates, but multiple myeloma sera without cryoprecipitates presented no problem in the EIA system.
36 egativity to HHV-6 (P=0.034), intraoperative cryoprecipitate requirements greater than the 75th perce
37 plasma (RR, 0.37; 95% CI, 0.21 to 0.64), and cryoprecipitate (RR:0.06; 95% CI, 0.02 to 0.22) were low
38 as well as risk of packed red blood cell and cryoprecipitate transfusions after coronary artery bypas
40 ts (3 vs. 1.6, p =0.0004), and the number of cryoprecipitate units (2.4 vs. 1.2, p =.04) transfused a
41 ty to proteolysis of the VWF in the VWF-rich cryoprecipitate was assessed by incubation with a normal
42 n requirements of packed red blood cells and cryoprecipitate was higher in the patients with severe m
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