Literature DB >> 34001390

The importance of recognizing cerebral venous thrombosis following anti-COVID-19 vaccination.

Alfonso Ciccone1, Bruno Zanotti2.   

Abstract

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Year:  2021        PMID: 34001390      PMCID: PMC8108377          DOI: 10.1016/j.ejim.2021.05.006

Source DB:  PubMed          Journal:  Eur J Intern Med        ISSN: 0953-6205            Impact factor:   7.749


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To the Editor. In March 2021, the reporting of cases of thrombosis post-COVID-19 vaccine AstraZeneca raised safety concerns and determined the temporary suspension of vaccinations in some countries in Europe [1]. On the 18th of March, EMA published its preliminary review of cases concluding that “the benefit of the vaccine in combating the still widespread threat of COVID-19 (which itself results in clotting problems and may be fatal) continue to outweigh the risk of side effects” [2]. On the same day, a one-week campaign was launched in Italy through the secretariat of the Hospital Neurosciences Society (SNO) to gather all cases of cerebral venous thrombosis within one month of anti-COVID-19 vaccine administration. The purpose of this campaign is to identify, through an exhaustive collection of post-COVID-19 vaccine cerebral venous thrombosis cases, a common pattern among demographic, clinical, laboratory and risk factors, to support a possible causal link between COVID-19 vaccine and cerebral thrombosis. The most remarkable findings of the cases observed (Table 1 ) are early platelet consumption (82%), extra-cerebral thrombosis (73%) and poor outcome (only one patient without neurological deficit) with high mortality (45%), compared to expected mortality of less than 5% in patients with cerebral sinus thrombosis not exposed to the COVID-19 vaccine [3]. Clinical manifestation appeared during the first 11 days after the vaccination.
Table 1

Characteristics of patients with cerebral vein thrombosis following COVID-19 vaccine. We considered the day of vaccination as day 0.

Patient No.SexAge (yrs)Type of vaccineRisk factorsOnset of neurological symptomsCerebral vein involvedType of cerebral damageExtracerebral thrombosisNo. of platelets (*103/uL)I.N.R, aPTT ratioD-Dimer (ng/mL)TreatmentsOutcome
upon first admission to the hospital
1M50AstraZeneca, first doseSmokerHeadache on day 7Superior sagittal, left straight and sigmoid sinuses, gulf of the jugular veinMassive brain hemorrhage with trans-tentorial herniationPulmonary embolism151.19,0.88>10000S.c. enoxaparin, i.v. mannitol, craniectomyDeath on day 13
2F42AstraZeneca, first doseMutation factor IIHeadache, fever on day 0Superior sagittal, right straight and sigmoid sinuses, gulf of the jugular veinBrain hemorrhagic infarctionSuprahepatic vein591,31,0.931458S.c. enoxaparin, i.v. mannitol, thrombectomy, craniectomy.In a coma on day 23
3F55Pfizer, second doseObesityHeadache on day 1Right straight and sigmoid sinuses, jugular veinBrain hemorrhageSuspected pulmonary embolism591.330.839000S.c. enoxaparinDeath on day 5
4F32AstraZeneca, first doseThrombocytopenia in infancy with brain hemorrhage, oral contraceptiveHeadache, orbital bruising, abdominal pain and fever, on day 1Left straight and sigmoid sinusesCerebella hemorrhagic infarction with tonsillar herniationEpigastric and periuterin veins thrombosis, renal infarction301.28,1.1411332Fondaparinux, metil-prednisolonDeath on day 24
5F35AstraZeneca, first doseOral contraceptiveHeadache, nausea and vomiting on day 6Superior sagittal, right straight and sigmoid sinusesBrain hemorrhagic infarction with and midline shiftPortal and mesenteric veins441.030.86>8000I.v. mannitol, i.v. metil-prednisolon, i.v. fresh plasma, c.c. enoxaparin, plasmapheresisIn a coma on day 13
6F51AstraZeneca, first doseHeterozygosis for factor V Leiden and MTHFRHeadache, vomiting and drowsiness on day 10Left straight and sigmoid sinuses, jugular vein, Galeno and internal cerebral veinsBilateral deep brain hemorrhagic infarction with brain swellingPelvic district.501.140.83,35200I.v. remifentanil and noradrenalin, ventriculostomyDeath on day 13
7M64AstraZeneca, first doseSinusitisHeadache and vomiting on day 4inferior sagittal, anterior part of the superior sagittal, left straight and sigmoid sinusesNoneNone187NA,1.032500S.c. enoxaparinNo neurological deficit on day 20
8F40AstraZeneca, first doseAnamnestic spontaneous abortionHeadache on day 5Inferior sagittal, left straight and sigmoid sinuses and jugular veinBrain hemorrhagic infarctionBrain hemorrhagic infarction401.060.82,27546S.c. fondaparinuxAphasia and right hemiparesis on day 15
9F49AstraZeneca, first doseContraceptive vaginal ring, migraine with auraHeadache on day 11Left straight and sigmoid sinuses, jugular veinBrain hemorrhagic infarction with swellingNone2780.960.7314700S.c. enoxaparin, i.v. mannitolSignificant disability at day 20
10F54AstraZeneca, first doseNoneHeadache and vomiting on day 2Superior sagittal sinus, Galen vein.Brain hemorrhagic infarction, subarachnoid hemorrhage, brainstem infarction and swellingAortic arch, thoracic aorta, portal, suprahepatic, right coronary, pulmonary and basilar arteries131.30.8378254S.c. enoxaparin, s.c. fondaparinux, desametasoneDeath on day 15
11F55AstraZeneca, first doseNoneHeadache and fever on day 6Left jugular veinCerebellar hemorrhagic infarction with swellingPulmonary thromboembolism, portal vein and inferior cava311.340.92,>10000S.c. fondaparinux, i.v. metil-prednisolone, i.v. mannitol, craniectomyIn a coma on day 25
Characteristics of patients with cerebral vein thrombosis following COVID-19 vaccine. We considered the day of vaccination as day 0. These issues led to speculation that COVID-19 vaccine might determine cerebral venous thrombosis due to an immune thrombocytopenia [4] as described in SARS-CoV-2 infection, through molecular mimicry between virus and platelet antigens [5]. Similarly, after vaccination, the antibodies produced against the spike proteins might cross-react with specific antigens expressed on the platelet surface. The reason why such a chain of events sporadically occurs remains obscure. Therefore, cerebral venous thrombosis after COVID-19 vaccination can be the first manifestation of a much more complex disorder mimicking heparin-induced thrombocytopenia. An inclusive awareness of the clinical and laboratory features of these events plays a crucial role in the early identification of patients at their first clinical manifestation, in order to undertake all the possible measures to prevent the dramatic consequences of immune thrombocytopenia. Although from these case series there is no evidence of any predisposing conditions to identify patients at risk, the widespread knowledge of this possible severe adverse event of COVID-19 vaccination is already a valid prevention strategy.

Declaration of Competing Interest

None.
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