Thrombocytopenia and thrombosis have been reported following vaccination with the
ChAdOx1 nCoV-19 (AstraZeneca) vaccine, an adenoviral vector COVID-19 (coronavirus
disease 2019) vaccine.[1]
[2]
[3]
[4]
[5] Previous cases of vaccine-induced immune thrombotic thrombocytopenia (VITT) have
been reported with symptom onset between 5 to 30 days postvaccination, typically with
severe thrombocytopenia, unusual thromboses, high mortality, and platelet-activating
antibodies against platelet factor 4 (PF4) despite no previous exposure to heparin.[1]
[2]
[3] Here we report two patients with VITT presenting as lower limb venous thrombosis
(one with concurrent pulmonary embolism) and mild thrombocytopenia. One had a late
presentation 31 days postvaccination. Both patients were shown to have platelet-activating
antibodies in a PF4-dependent serotonin-release assay (SRA).
Case 1
A 68-year-old male received his first dose of ChAdOx1 nCoV-19 vaccine (day 0). On
day 31, he noted left leg swelling and erythema. Two days later he presented to an
urgent care center with clinical evidence of left lower limb deep-vein thrombosis
(DVT). The D-dimer was >20 mg/L (reference range: <0.5 mg/L); the platelet count was
116 × 109/L (reference range: 150–400 × 109/L); the patient's usual platelet count was 200 × 109/L ([Fig. 1A]). He was started on apixaban 10 mg twice-daily as an outpatient; the next day, Doppler
ultrasound demonstrated extensive left lower limb DVT involving the mid-superficial
femoral vein and extending into the popliteal vein and its trifurcation. He continued
apixaban at home, with no bleeding. At follow-up outpatient assessment (day 37), his
left leg swelling was reduced; the D-dimer had decreased to 6.1 mg/L. At this time,
the polyspecific PF4/polyanion enzyme immunoassay (EIA; Immucor, Dartmouth, Canada)
was positive (1.020 optical density [OD] units; reference range: <0.400), as were
two immunoglobulin G (IgG)-specific EIAs (PF4/heparin [PF4/H][6] and PF4 alone [see the figure legend for the method]), with >50% inhibition with
high heparin (100 IU/mL); patient serum induced serotonin release in the presence
of PF4 ([Fig. 1A], inset). On day 39, leg swelling had further improved; the D-dimer was 5.6 mg/L
and the platelet count was 160 × 109/L. Given the persistent relative thrombocytopenia and positive VITT serology, he
received 85 g of intravenous immune globulin (IVIG) (1 g/kg dose [weight: 85 kg; height:
191 cm]), with a second dose 24 hours later. His platelet count rose (peak: 234 × 109/L) and the D-dimer progressively decreased. At last assessment on day 147, he remained
well, without signs or symptoms of pulmonary embolism or cerebral venous thrombosis
(CVT); however, he continues to have mild thrombocytopenia and elevated D-dimer levels
despite having received a third dose of IVIG on day 72.
Fig. 1 Clinical course of two patients with vaccine-induced immune thrombotic thrombocytopenia
(VITT) with venous thromboembolism and mild thrombocytopenia. For both patients, the
baseline (“pre”) platelet count represents the mean value of three (patient 1) or
two (patient 2) previous platelet count values. “Day 0” indicates the date of vaccination.
The inset shows the detailed results of testing for VITT antibodies. Three EIAs are
shown: polyspecific (IgGAM) EIA with PF4/polyvinyl sulfonate as the target antigen,
as well as two “in-house” IgG-specific EIAs with PF4/heparin (PF4/H) and PF4 alone
as target antigens. The IgG-specific EIA used to detect antibodies specific to PF4
alone was modified from a published method,[6] whereby PF4 alone (60 µg/mL), rather than PF4/heparin complexes, was coated onto
the plates, prior to addition of patient sample. +High heparin indicates EIA performed
with 100 IU/mL heparin. For both patients, EIA reactivity remained positive post-IVIG,
whereas the platelet activation assays became negative. (A) Patient 1: treatment with high-dose intravenous IVIG was associated with a transient
increase in the platelet count (peak, 5 days post-initiation). The patient had no
recurrence of thrombosis (last follow-up, day 147). (B) Patient 2: treatment with high-dose IVIG was associated with a transient increase
in the platelet count (peak platelet count, 9 days after initiating IVIG). The patient
had no recurrence of thrombosis (last follow-up, day 138). IV.3 is the name of the
Fc receptor-blocking monoclonal antibody used to demonstrate Fc receptor-dependent
platelet activation. DVT, deep-vein thrombosis; EIA, enzyme immunoassay; IgG, immunoglobulin
G; IU, international units; IVIG, immune globulin; OD, optical density; PF4, platelet
factor 4; PF4/H, platelet factor 4/heparin; PVS, polyvinyl sulfonate; VITT, vaccine-induced
immune thrombotic thrombocytopenia; VTE, venous thromboembolism.
Case 2
A 55-year-old male received his ChAdOx1 nCoV-19 vaccine (day 0). From day 8 to day
11, he experienced an intermittent, bitemporal headache (7/10 severity) that was pulsatile
in nature, without focal neurologic deficits. On day 11, he experienced dyspnea on
exertion and cough; his respiratory symptoms worsened over the next few days. On day
15, he experienced small-volume hemoptysis (without other bleeding) and attended the
emergency department. The platelet count was 103 × 109/L; the patient's usual platelet count was 265 × 109/L ([Fig. 1B]). His D-dimer was >20 mg/L. Contrast tomography (CT) imaging of his chest demonstrated
bilateral pulmonary emboli with evidence of saddle embolism. There were no echocardiographic
findings of right heart strain and he was hemodynamically stable. Doppler ultrasound
showed a left lower limb DVT, with partially occlusive thrombus in the distal superficial
femoral vein extending into the popliteal vein. CT venography of his brain did not
show CVT. He was admitted to a hospital and initiated on rivaroxaban 15 mg twice-daily
on day 16. Following the first two doses of anticoagulation, IVIG was started empirically
given the clinical suspicion for VITT. He received 100 g IVIG (1 g/kg dose [weight:
100 kg; height: 179 cm]) daily for 2 days, on days 17 and 18. The screening polyspecific
PF4/polyanion EIA was positive (2.554 OD units) as were two IgG-specific EIAs (PF4/H
and PF4 alone), with >50% inhibition with high heparin; patient serum induced serotonin
release in the presence of PF4 ([Fig. 1B], inset). After two doses of IVIG, his platelet count rose quickly (peak: 488 × 109/L). He was discharged home on rivaroxaban. Serial D-dimer measurements showed progressive
decline and he remained clinically well (last follow up, day 138).
For both patients, repeat serological testing post-IVIG showed persistent reactivity
in all three EIAs, but negative platelet activation assays ([Fig. 1A, B], insets).
Discussion
We present two patients with confirmed VITT who had mild thrombocytopenia, demonstrating
that VITT can occur on a spectrum of severity. For the first patient, the onset of
symptoms began 31 days post-ChAdOx1 nCoV-19 vaccination, which is later than most
other reports.[1]
[2]
[3]
[4]
[5] The patient clinically improved with initial treatment with direct oral anticoagulant
(DOAC) alone. This case illustrates that VITT should be considered—and can present
clinically—more than 30 days following ChAdOx1 nCoV-19 vaccination. Current guidelines[7]
[8] suggest considering VITT when thrombosis occurs up to day 28 postvaccination; however,
delayed symptom onset occurred in our case. The second patient presented within the
typically cited window postvaccination, and also responded well to DOAC with additional
IVIG. Although the ultimate outcome was favorable, he presented with pulmonary embolism,
a potentially fatal thrombotic event. Despite both patients having marked elevations
in D-dimer (>20 mg/L), they had only mild thrombocytopenia.
Similar to heparin-induced thrombocytopenia (HIT), VITT can present with a range of
thrombocytopenia, and should still be considered even if the platelet count is above
100 × 109/L. Our patients' platelet count falls were ∼40% (patient 1) and ∼60% (patient 2)
from their usual baseline values. Approximately 10 to 20% of patients with HIT have
platelet count nadirs that are >100 × 109/L,[9] and VITT cases with mild thrombocytopenia have been reported.[1]
[3]
[10] Although there have been several reports of patients with severe VITT, we observed
two patients, presenting within a few days of one another at one hospital, both with
lower limb venous thrombosis and mild thrombocytopenia, both with overall good outcomes.
Although we administered high-dose IVIG to both patients, we acknowledge that favorable
outcomes may have occurred even without this treatment. However, the natural history
of VITT remains undefined, and given the life-threatening nature of this novel prothrombotic
disorder, de-escalation of platelet and coagulation activation by high-dose IVIG is
an important treatment consideration.[11] High-dose IVIG has demonstrated clinical benefit[1]
[2]
[3]
[4]
[11]
[12] in the management of VITT and is considered in current guidelines and expert consensus
to be an important up-front treatment.[7]
[13]
[14] Both patients' post-IVIG serum reverted to a negative PF4-enhanced SRA despite persisting
EIA reactivity ([Fig. 1A, B], insets). These data support a recent report[11] indicating that the mechanism of action of IVIG is competitive inhibition of VITT
antibody-mediated platelet activation at the level of the platelet Fc receptors, without
affecting binding of VITT antibodies to the (recently identified[15]) PF4 antigen target. Our cases thus further support the efficacy of IVIG in correcting
thrombocytopenia and reducing hypercoagulability in VITT.
