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Table 2 Blood cell count and standard coagulation tests

From: Impact of fibrinogen concentrate alone or with prothrombin complex concentrate (+/− fresh frozen plasma) on plasma fibrinogen level and fibrin-based clot strength (FIBTEM) in major trauma: a retrospective study

 

FC group

FC–PCC group

FC–PCC–FFP group

p-value

 

n

 

n

 

n

  

Hemoglobin (g/dL)

       

ER

85

12.8 (11.2–13.9)

63

11.1 (8.8–12.7)

9

8.4 (6.5–11.6)

<0.0001

ICU

70

8.8 (7.8 9.9)

44

9.3 (8.1–10.2)

9

8.0 (7.1–10.0)

0.20

24h

81

8.8 (7.8 9.9)

51

9.3 (8.1–10.2)

4

8.0 (7.1–10.0)

0.27

Platelet count (x 10 9 /L)

       

ER

85

210 (176–251)

63

181 (141–215)

9

203 (162–295)

0.041

ICU

54

148 (108–179)

41

104 (65–126)

7

58 (35–88)

<0.0001

24h

80

122 (95–162)

51

90 (63–111)

4

58 (37–75)

<0.0001

PT (seconds)

       

ER

83

14.6 (13.4–15.8)

63

17.0 (15.3–19.3)

9

22.0 (17.7–27.9)

<0.0001

ICU

34

17.5 (15.5–19.6)

31

21.0 (17.1–24.3)

7

28.6 (26.6–44.1)

<0.0001

24h

70

16.2 (15.2–17.8)

48

16.7 (15.6–18.0)

4

16.6 (16.1–16.7)

0.49

aPTT (seconds)

       

ER

82

28.8 (26.0–31.7)

62

33.2 (28.0–43.5)

9

48.8 (35.3–96.5)

<0.0001

ICU

42

32.7 (29.9–36.4)

31

46.9 (36.5–54.7)

8

180.0 (89.7–180.0)

<0.0001

24h

77

37.7 (33.6–40.4)

49

40.2 (37.2–46.7)

4

45.5 (38.2–49.6)

0.0003

Fibrinogen (mg/dL)

       

ER

79

198 (156–225)

60

151 (112–199)

9

95 (83–161)

<0.0001

ICU

41

188 (147–219)

32

162 (129–203)

8

119 (82–142)

0.0034

24h

76

266 (236–309)

49

274 (222–316)

4

269 (240–298)

0.96

  1. Data are presented as median (interquartile range) or percentage of patients. p-values are derived from the ANOVA; significance level p < 0.05.
  2. aPTT, activated partial thrombin time; PT, prothrombin time.
  3. FC group, patients receiving fibrinogen concentrate only; FC–PCC group, patients receiving fibrinogen concentrate and prothrombin complex concentrate; FC–PCC–FFP group, patients receiving fibrinogen concentrate, prothrombin complex concentrate and fresh frozen plasma.
  4. Results were obtained at the following timepoints: upon admission to the emergency room (ER), admission to the intensive care unit (ICU) and 24 hours (24h) after ER admission; n = number of patients with available data.