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. 2022 Jun 16;40(33):4788–4795. doi: 10.1016/j.vaccine.2022.06.014

Table 1.

Clinical and laboratory features of case series.

Variable Alive
Deceased
All cases
(*3 cases without outcome information)
Age-yr
Median 45.5 (IQR 19.3) 37 (IQR 18) 41 (IQR 21.3)
Range 23–75 28–86 23–86
Total 16 19 38*3
Sex n/total (%)
Female 12/16 (75%) 10/20 (50%) 24/39 (61.5%)
Male 4/16 (25%) 10/20 (50%) 15/39 (38.5%)
Total 16 20 39
Days from vaccination
to symptoms*1
Median 9 (IQR 8) 8 (IQR 3) 8 (IQR 6)
Range 0–37 0–11 0–37
Total 13 20 36*4
Days since onset of
VITT symptoms and
hospital admission
Median 0 (IQR 5) 4 (IQR 6) 3 (IQR 7)
Range 0–8 0–12 0–12
Total 8 19 29*5
Platelet count
– per µL
Median 46,500 (IQR 49,500) 23,000 (IQR 35,500) 34,000 (IQR 45,000)
Range 2,000–147,000 8,000–113,000 2,000–147,000
Total 16 20 39
D-dimer (FEU)
Median 10,700 (IQR 18,560) 41,000 (IQR 87,845) 19,235 (IQR 33,356)
Range 1,119–40,800 4,000–128,000 1,119–128,000
Total 12 13 28*6
Anti-PF4 Elisa*2
Positive 6 12 18
Negative 8 1 12
Total 14 13 30*7

*1 interval between vaccine and symptoms (assuming the date of the dose applied closely to event onset).

*2 nine results were not available.

*3 one without age information.

*4 this information was not available in 3 cases.

*5 this information was not available in 10 cases.

*6 this information was not available in 11 cases.

*7 this information was not available in 09 cases.