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. 2021 Sep 28;78(11):1–10. doi: 10.1001/jamaneurol.2021.3619

Table 1. Details of SARS-CoV-2 Vaccination, Previous COVID-19 Infection, and Thrombocytopenia.

Variable Group, No./total No. (%)
TTS (n = 78) No TTS (n = 38)
SARS-CoV-2 vaccinea
ChAdOx1 nCov-19 76/78 (97)b 20/38 (53)
Ad26.COV2.S 1/78 (1) 0
BNT162b2 1/78 (1) 15/38 (40)c
mRNA-1273 0 1/38 (3)
CoronaVac 0 2/38 (5)
Time from vaccination to CVST symptom onset, median (IQR), dd 9 (7-10) 7 (3-16)
Previous COVID-19 infection 1/72 (1) 4/36 (11)
Confirmede 0 4/36 (11)
Suspected 1/72 (1) 0
Thrombocytopenia details
Platelet count at admission, median (IQR), ×103/μL 45 (25-71) 272 (224-319)
Platelet count nadir, median (IQR), ×103/μL 30 (14-53)f NA
Positive for PF4 antibodies 63/69 (91)g NA
Positive findings on platelet activation assays 36/36 (100) NA
Positive for antiphospholipid antibodies 8/56 (14)h 0i

Abbreviations: CVST, cerebral venous sinus thrombosis; NA, not applicable; TTS, thrombosis with thrombocytopenia syndrome.

SI conversion factor: To convert platelet count to ×109 per liter, multiply by 1.

a

In the ChAdOx1 nCov-19 group, 29 different vaccine batch numbers could be identified among 53 patients; in the BNT162b2 group, 9 different batch numbers among 10 patients; and in the CoronaVac group, 1 batch number in 1 patient.

b

One patient developed CVST with TTS after the second ChAdOx1 nCov-19 vaccination; PF4 antibodies were not tested in this patient.

c

Nine patients developed CVST without TTS after the second BNT162b2 vaccination.

d

Data for 1 patient was missing in each group.

e

Positive findings on nucleic acid amplification test.

f

Data missing for 11 patients.

g

Of the 6 patients who tested negative for PF4 antibodies, 3 were tested with an enzyme-linked immunosorbent assay and 3 with a rapid test.

h

Not performed in 22 patients.

i

Not performed in 9 patients.