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. 2022 Mar 9;15(3):e246922. doi: 10.1136/bcr-2021-246922

Table 1.

Tabulation of laboratory parameters

Laboratory parameters Values in unit (normal range) on admission Values in unit (normal range) 7 weeks later
Haemoglobin 73 g/L (130–180) 102 g/L (130–180)
Mean Corpuscular Volume 90.6 fL (83–101) 93.4 fL (83–101)
Mean Corpuscular Haemoglobin Concentration 33.3 g/dL (31.5–34.5) 33 g/dL (31.5–34.5)
White cell count 11.6×109 /L (4–10) 7.63×109 /L (4–10)
Platelets 292×103 /µL (150–400) 280×103 /µL (150–400)
aPTT 78.7 s (25.4–38.4) 27.1 s (25.4–38.4)
Prothrombin time (PT) 13.1 s (9.62–12.18) 10.6 s (9.62–12.18)
International normalised ratio 1.26 0.97
Creatinine 134 umol/L (45–84)
Serum albumin 31 g/L (35–52)
Carcinoembryonic antigen 6.2 ng/mL (<3)
Carbohydrate antigen (CA 19–9) <2 U/mL (<37)
Alpha fetoprotein 1.5 ng/mL (<9)
Prostate-specific antigen 9.234 ng/mL (<4)
Antinuclear antibodies Negative
Beta-hCG (human chorionic gonadotropin) 2.1 IU/L (<5)
C reactive protein 8.8 mg/L (<5)
Total iron binding capacity 41.4 umol/L
Serum iron 7.6 umol/L
Unsaturated iron-binding capacity 33.8 umol/L
Serum vitamin B12 level 103 pmol/L (133–675)
Serum folate level 12.9 nmol/L (>14.93)
Peripheral blood film Anaemia with increased reticulocytes possibly secondary to underlying bleeding/blood loss. No evidence of haemolysis was seen. White blood cell changes suggest infection or inflammation.
FVIII assay 6.7% (50–150) 365.1% (50–150)
FVIII inhibitor 7.5 BU <0.5 BU
Factor IX assay 114.7% (86.4–128.4)

aPTT, activated partial thromboplastin time; FVIII, factor VIII.