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1 risk of reoperation for bleeding or need for blood product transfusion.
2 tients (69%), and 28 patients (67%) required blood product transfusion.
3 ed growth factor support, and three required blood product transfusions.
4 , continuous veno-venous hemofiltration, and blood product transfusions.
5 nt has reduced intraoperative blood loss and blood product transfusions.
6 iated with major blood loss and the need for blood product transfusions.
7 2% vs. 2.4%, p = 0.002), had higher rates of blood product transfusions (13.1% vs. 3.1%, p < 0.0001),
8 ump CABG, significantly reduced the rates of blood-product transfusion (50.7% vs. 63.3%; relative ris
9 4%; P=0.96) or requirement for postoperative blood product transfusion (adjusted OR, 1.17; 95% CI, 0.
10 irus infection that presumably resulted from blood product transfusions administered before the intro
11 s is likely related to the administration of blood product transfusion after the onset of fulminant h
12 ndrome continues to be supportive care, with blood product transfusion and antibiotics for infectious
13 nal shock, maternal requirement of allogenic blood product transfusion and lower gestational age were
14 and related physician orders, demographics, blood products transfusion, and outcomes were collected
15 ntly, Jehovah's Witness patients, who refuse blood product transfusion, are usually excluded from liv
18 ostatic reoperation and the requirements for blood product transfusions during and after off-pump cor
19 et count), and its use may avoid unnecessary blood product transfusion in patients with cirrhosis and
23 rs such as total parenteral nutrition (TPN), blood product transfusions, invasive procedures, central
24 tality (odds ratio, 0.40; P=0.017), need for blood product transfusion (odds ratio, 0.74; P=0.009), m
27 military combat causalities in Afghanistan, blood product transfusion prehospital or within minutes
28 n the incidence of hemostatic reexploration, blood product transfusion rates, morbidity, and mortalit
30 ocol, all subjects in the SOC group received blood product transfusions versus 5 in the TEG group (10
31 No significant clinical bleeding events or blood product transfusions were observed in this trial.
32 Pugh B: 26; C: 58) without overt bleeding or blood-product transfusion were prospectively evaluated w
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