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. 2022 Sep 16;6(6):e12809. doi: 10.1002/rth2.12809

TABLE 2.

Laboratory results of 169 patients with COVID‐19 on day of sample collection

Laboratory parameter Thrombosis (N = 58) No thrombosis (N = 111) Reference range p value
Coagulation assays, median (range)
PT (s)
UMC Utrecht 14.8 (11.9–20.9) 14.3 (11.7–32.6) 10.0–13.0 0.03
Erasmus MC 13.2 (10.9–18.2) 13.2 (11.5–15.8) 10.9–13.3 0.7
aPTT (s) a
UMC Utrecht 39.0 (27.0–60.0) 35.0 (23.0–105.0) 24.0–34.0 0.2
Erasmus MC 32.0 (20.0–70.0) 25.0 (18.0–73.0) 22.0–32.0 0.3
Fibrinogen (g/L), median (range) 6.7 (1.8–11.9) 5.8 (2.7–10.0) 2.0–4.0 0.1
D‐dimer (mg/L), median (range)
UMC Utrecht 5.9 (0.4–100.0) 1.2 (0.2–34.0) 0.00–0.50 <0.0001
Erasmus MC 3.2 (0.2–15.2) 1.2 (0.3–35.2) 0.00–0.50 0.05
CRP (mg/L), median (range) 154.5 (1.4–480.0) 70 (1.4–432.0) 0–10 <0.0001
Platelet count (×109/L), median (range) 259 (51–842) 283 (96–611) 150–450 0.4
Anti‐FXa levels, b n
<0.50 IU/ml 39 56
0.50–0.99 IU/ml 19 54
1.00–1.39 IU/ml 0 1

Note: Data of PT are missing for 8 patients, aPTT for 46 patients, fibrinogen for 33 patients, D‐dimer for 34 patients, CRP for 2 patients, and platelet count for 4 patients.

Abbreviations: aPTT, activated partial thromboplastin time; CRP, C‐reactive protein; ICU, intensive care unit; PT, prothrombin time.

a

LA‐insensitive aPTT reagent was used.

b

Determined before mixing with normal plasma. Different assays were used for PT, aPTT, and D‐dimer determination, so data for UMC Utrecht and Erasmus MC were separated.