Table 1.

Demographic and clinical characteristics of 77 individuals identified in VAERS without reported platelet disorders with suspected de novo ITP following SARS-CoV-2 immunization

Characteristic Mean ± SD, median [IQR], or n (%)No available for analysis
Age  63 ± 19.7 76 
Gender   
 ≤50 years old Men 3 (15) 20 
 Women 17 (85)  
 >50 years old Men 28 (50) 56 
 Women 28 (50)  
Vaccine type Moderna 37 (48) 77 
 Pfizer-BioNTech 40 (52)  
No. of doses received prior to presentation 1
51 (77.3)
15 (22.7) 
66 
Days to symptom onset  8 [3.2-13]
Range 0-38 
74 
Symptoms at presentation* Mucocutaneous bleeding 42 (73.7) 57 
 Genitourinary bleeding 6 (10.5)  
 Gastrointestinal bleeding 5 (6.9)  
 Central nervous system bleeding 1 (1.8)  
 Bleeding reported but not specified 2 (3.5)  
 No bleeding reported 6 (10.5)  
Platelet count at presentation  3 [1-9]
Range 0-47 
73 
≤10 × 109/L 58 (79.4)  
History of autoimmune disease other than ITP Any autoimmune disease 22 (31.9) 69 
Hypothyroidism† 13 (18.8)  
Rheumatologic 4 (5.8)  
Dermatologic 2 (2.9)  
Gastrointestinal 1 (1.4)  
Antiphospholipid syndrome‡ 1 (1.4)  
Multiple sclerosis 1 (1.4)  
Treatment Any combination of steroids, IVIG, and platelet transfusion 21 (44.7) 46 
Steroids only 16 (34)  
Platelet transfusion only 3 (8.5)  
IVIG only 1 (2.1)  
TPO-RA, IVIG, +/− platelet transfusion, steroid 3 (6.4)  
Rituximab, steroids, IVIG, platelet transfusion 1 (2.1)  
Vincristine, IVIG, rituximab, TPO-RA, +/− platelet transfusion, steroid 1 (2.1)  
Response to therapy Yes 26 (92.9) 28 
No 2 (7.1)  
Best known response 30-50 × 109/L 3 (11.5) 26 
50-100 × 109/L 7 (26.9)  
100-150 × 109/L 3 (11.5)  
Normalization§ 6 (23.1)  
Improvementǁ 7 (26.9)  
Time to platelet count >30 × 109 cells/L <3 d of treatment 9 (81.8) 11 
Characteristic Mean ± SD, median [IQR], or n (%)No available for analysis
Age  63 ± 19.7 76 
Gender   
 ≤50 years old Men 3 (15) 20 
 Women 17 (85)  
 >50 years old Men 28 (50) 56 
 Women 28 (50)  
Vaccine type Moderna 37 (48) 77 
 Pfizer-BioNTech 40 (52)  
No. of doses received prior to presentation 1
51 (77.3)
15 (22.7) 
66 
Days to symptom onset  8 [3.2-13]
Range 0-38 
74 
Symptoms at presentation* Mucocutaneous bleeding 42 (73.7) 57 
 Genitourinary bleeding 6 (10.5)  
 Gastrointestinal bleeding 5 (6.9)  
 Central nervous system bleeding 1 (1.8)  
 Bleeding reported but not specified 2 (3.5)  
 No bleeding reported 6 (10.5)  
Platelet count at presentation  3 [1-9]
Range 0-47 
73 
≤10 × 109/L 58 (79.4)  
History of autoimmune disease other than ITP Any autoimmune disease 22 (31.9) 69 
Hypothyroidism† 13 (18.8)  
Rheumatologic 4 (5.8)  
Dermatologic 2 (2.9)  
Gastrointestinal 1 (1.4)  
Antiphospholipid syndrome‡ 1 (1.4)  
Multiple sclerosis 1 (1.4)  
Treatment Any combination of steroids, IVIG, and platelet transfusion 21 (44.7) 46 
Steroids only 16 (34)  
Platelet transfusion only 3 (8.5)  
IVIG only 1 (2.1)  
TPO-RA, IVIG, +/− platelet transfusion, steroid 3 (6.4)  
Rituximab, steroids, IVIG, platelet transfusion 1 (2.1)  
Vincristine, IVIG, rituximab, TPO-RA, +/− platelet transfusion, steroid 1 (2.1)  
Response to therapy Yes 26 (92.9) 28 
No 2 (7.1)  
Best known response 30-50 × 109/L 3 (11.5) 26 
50-100 × 109/L 7 (26.9)  
100-150 × 109/L 3 (11.5)  
Normalization§ 6 (23.1)  
Improvementǁ 7 (26.9)  
Time to platelet count >30 × 109 cells/L <3 d of treatment 9 (81.8) 11 
*

More than 1 site of bleeding reported in some cases, excludes 1 patient with CNS bleeding whose thrombocytopenia resolved with platelet transfusion only and the index patient who did not present with but later developed CNS bleeding.

Includes 1 person with “antithyroglobulin antibody.”

Antiphospholipid syndrome in the same patient with other rheumatologic conditions.

§

Platelet count ≥150 x109/L or described as “platelets normalized.”

ǁ

No platelet count provided but described as “improved” or “resolved.”

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