{"id":4153,"date":"2022-04-10T19:23:20","date_gmt":"2022-04-10T19:23:20","guid":{"rendered":"http:\/\/wp.cov19longhaulfoundation.org\/?p=4153"},"modified":"2022-04-10T19:23:20","modified_gmt":"2022-04-10T19:23:20","slug":"spectrum-of-neurological-complications-following-covid-19-vaccination","status":"publish","type":"post","link":"https:\/\/cov19longhaulfoundation.org\/?p=4153","title":{"rendered":"Spectrum of neurological complications following COVID-19 vaccination"},"content":{"rendered":"\n<p>Authors:  <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Garg%20RK%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=34719776\">Ravindra Kumar Garg<\/a><sup>1<\/sup>&nbsp;and&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/?term=Paliwal%20VK%5BAuthor%5D&amp;cauthor=true&amp;cauthor_uid=34719776\">Vimal Kumar Paliwal<\/a><sup>2<\/sup>    <a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#\">Neuro  <\/a>2022; 43(1): 3\u201340.Published online 2021 Oct 31.&nbsp;doi:&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/dx.doi.org\/10.1007%2Fs10072-021-05662-9\" target=\"_blank\">10.1007\/s10072-021-05662-9<\/a>PMCID:&nbsp;PMC8557950PMID:&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pubmed\/34719776\">34719776<\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Abs1title\">Abstract<\/h2>\n\n\n\n<p id=\"Par1\">COVID-19 vaccines have brought us a ray of hope to effectively fight against deadly pandemic of COVID-19 and hope to save lives. Many vaccines have been granted emergency use authorizations by many countries. Post-authorization, a wide spectrum of neurological complications is continuously being reported following COVID-19 vaccination. Neurological adverse events following vaccination are generally mild and transient, like fever and chills, headache, fatigue, myalgia and arthralgia, or local injection site effects like swelling, redness, or pain. The most devastating neurological post-vaccination complication is cerebral venous sinus thrombosis. Cerebral venous sinus is frequently reported in females of childbearing age, generally following adenovector-based vaccination. Another major neurological complication of concern is Bell\u2019s palsy that was reported dominantly following mRNA vaccine administration. Acute transverse myelitis, acute disseminated encephalomyelitis, and acute demyelinating polyneuropathy are other unexpected neurological adverse events that occur as result of phenomenon of molecular mimicry. Reactivation of herpes zoster in many persons, following administration of mRNA vaccines, has been also recorded. Considering the enormity of recent COVID-19-vaccinated population, the number of serious neurological events is miniscule. Large collaborative prospective studies are needed to prove or disprove causal association between vaccine and neurological adverse events occurring vaccination.<\/p>\n\n\n\n<p id=\"Par2\">SARS-CoV-2 is a novel coronavirus that can rapidly affect human beings and can result in coronavirus disease (COVID-19). COVID-19 is dominantly characterized by lung damage and hypoxia. The first case of COVID-19, in Wuhan, China, was reported on December 8, 2019. Later, the World Health Organization announced COVID-19 as a worldwide health emergency, on January 30, 2020. On March 11, 2020, COVID-19 was declared a pandemic. As per the latest World Health Organization report, there were 196,553,009 confirmed cases as on August 1, 2021 along with 4,200,412 deaths [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR1\">1<\/a>].<\/p>\n\n\n\n<p id=\"Par3\">Early this year, COVID-19 vaccines has brought a ray of hope to effectively fight against this deadly pandemic and save precious human lives. Currently, four major vaccine types are being used. These vaccine types include viral vector-based vaccines, COVID-19 mRNA-based vaccines, inactivated or attenuated virus vaccine, and protein-based vaccines. In viral vector-based vaccines, adenovirus is used to deliver a part of SARS-COV-2 genome to human cells. Human cells use this genetic material to produce SARS-COV-2 spike protein. Human body recognizes this protein to start a defensive response. The mRNA-based vaccines consist of SARS-COV-2 RNA. Once introduced, genetic material helps in making SARS-COV-2-specific protein. This protein is recognized by human body to start defensive immune reaction. In inactivated or attenuated vaccines, killed or attenuated SARS-COV-2 virus triggers immune response. Protein-based vaccines use the spike protein or its fragments for inciting immune response. These COVID-19 vaccines have received emergency approvals in different countries for human use [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR2\">2<\/a>].&nbsp;As per the latest World Health Organization report,&nbsp;until August 1, 2021, globally, a total of&nbsp;3,839,816,037 COVID-19 vaccine doses&nbsp;have been globally administered [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR1\">1<\/a>].<\/p>\n\n\n\n<p id=\"Par4\">In fact, all kinds of vaccines are associated with the risk of&nbsp;several serious neurological&nbsp;complications, like acute disseminated encephalomyelitis, transverse myelitis, aseptic meningitis, Guillain-Barr\u00e9 syndrome, macrophagic myofasciitis, and myositis. Influenza vaccine has been found associated with narcolepsy in young persons. Several pathogenic mechanisms, like molecular mimicry, direct neurotoxicity, and aberrant immune reactions, have been ascribed to explain these vaccines associated with neurological complications [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR3\">3<\/a>].&nbsp;Even COVID-19 vaccines are not free from neurological complications. In this article, we have focused on the neurological complications following COVID-19 vaccination that were reported after their emergency use authorizations.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec1title\">Search strategy<\/h2>\n\n\n\n<p id=\"Par5\">We reviewed available data regarding neurological complications (post-authorization) described following the World Health Organization\u2013approved COVID-19 vaccination. We classified COVID-19 vaccination associated with neurological complications in two broad groups: (1) common but mild and (2) rare but severe. We searched PubMed, Google, and Google Scholar databases using the keywords \u201cCOVID\u201019\u201d or \u201cSARS\u2010CoV\u20102\u201d and \u201cvaccination\u201d or \u201cvaccine,\u201d to identify all published reports on neurological complications of COVID\u201019 vaccines. We in this review&nbsp;will focus on spectrum of published neurological adverse events following COVID-19 vaccination. Last search was done on August 1, 2021.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec2title\">Mild neurological events<\/h2>\n\n\n\n<p id=\"Par6\">Neurological adverse events following COVID-19 vaccination are generally mild and transient, like fever\/chills, headache, fatigue, myalgia and arthralgia, or local injection site effects like swelling, redness, or pain. These mild neurological symptoms are common following administration of all kinds of COVID-19 vaccines.<\/p>\n\n\n\n<p id=\"Par7\">Anxiety-related events, like feeling of syncope and\/or dizziness, are particularly common. For example, Centers for Disease Control and Prevention, in a report published on April 30, 2021, recorded 64 anxiety-related events (syncope in 17) among 8,624 Janssen COVID-19 vaccine recipients. None of the event was labeled as serious [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR4\">4<\/a>].<\/p>\n\n\n\n<p id=\"Par8\">In Mexico (data available in form of preprint) among 704 003 subjects who received first doses of the Pfizer-BioNTech mRNA COVID-19 vaccine, 6536 adverse events following immunization were recorded. Among those, 4258 (65%) had at least one neurologic manifestation, mostly (99.6%) mild and transient. These events included headache (62\u00b72%), transient sensory symptoms (3\u00b75%), and weakness (1%). In this study, there were only 17 serious adverse events, seizures (7), functional syndromes (4), Guillain-Barr\u00e9 syndrome (3), and transverse myelitis (2) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR5\">5<\/a>].<\/p>\n\n\n\n<p id=\"Par9\">In South Korea, Kim and co-workers collected data of post-vaccination adverse events following first dose of adenovirus vector vaccine ChAdOx1 nCoV-19 (1,403 subjects) and mRNA vaccine BNT162b2&nbsp;(80 subjects) vaccinations. Data were collected daily for 7&nbsp;days after vaccination. Authors noted that 91% of adenovirus-vectored vaccine and 53% of mRNA vaccine recipients had mild adverse reactions, like injection-site pain, myalgia, fatigue, headache, and fever [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR6\">6<\/a>].&nbsp;A mobile-based survey among healthcare workers (265 respondents) who received both doses of the BNT162b2 mRNA vaccine was conducted. The most common adverse effects were muscle ache, fatigue, headache, chills, and fever. Adverse reactions were higher after the second dose compared with that after the first dose [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR7\">7<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec3title\">Headache<\/h3>\n\n\n\n<p id=\"Par10\">Headache is one of the most frequent mild neurological complaints reported by a large number of COVID-19 vaccine recipients, soon after they receive vaccine.<\/p>\n\n\n\n<p id=\"Par11\">A review of headache characteristic noted that among 2464 participants, headache begun 14.5\u2009\u00b1\u200921.6&nbsp;h after AstraZeneca adenovirus vector vaccine COVID-19 vaccination and persisted for 16.3\u2009\u00b1\u200930.4&nbsp;h. Headaches, in majority, were moderate to severe in intensity and generally localized to frontal region. Common accompanying symptoms were fatigue, chills, exhaustion, and fever [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR8\">8<\/a>].&nbsp;In a multicenter observational cohort study, G\u00f6bel et al. recorded clinical characteristic of headache occurring after the mRNA BNT162b2 mRNA COVID-19 vaccination. Generally, headache started 18.0\u2009\u00b1\u200927.0&nbsp;h after vaccination and persisted for 14.2\u2009\u00b1\u200921.3&nbsp;h. In majority, the headaches were bifrontal or temporal, dull aching character and were moderate to severe in intensity. The common accompanying symptoms were fatigue,&nbsp;exhaustion, and muscle pain [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR8\">8<\/a>].<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec4title\">Severe neurological adverse events<\/h2>\n\n\n\n<p id=\"Par12\">Serious adverse reaction following immunization is defined as a post-vaccination event that are either life-threatening, requires hospitalization, or result in severe disability. The World Health Organization listed Guillain-Barr\u00e9 syndrome, seizures, anaphylaxis, syncope, encephalitis, thrombocytopenia, vasculitis, and Bell\u2019s palsy as serious neurologic adverse events. Instances of serious adverse&nbsp;events following COVID-19 vaccinations&nbsp;are continuously pouring in the current scientific literature and are source of vaccine hesitancy in many persons [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR9\">9<\/a>] (Fig.&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/figure\/Fig1\/\">1<\/a>).<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/figure\/Fig1\/\"><\/a><\/p>\n\n\n\n<figure class=\"wp-block-image is-resized is-style-default\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/bin\/10072_2021_5662_Fig1_HTML.jpg\" alt=\"An external file that holds a picture, illustration, etc.\nObject name is 10072_2021_5662_Fig1_HTML.jpg\" width=\"562\" height=\"306\" title=\"Click on image to zoom\"\/><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/figure\/Fig1\/\"><\/a><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/core\/lw\/2.0\/html\/tileshop_pmc\/tileshop_pmc_inline.html?title=Click%20on%20image%20to%20zoom&amp;p=PMC3&amp;id=8557950_10072_2021_5662_Fig1_HTML.jpg\"><\/a><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/figure\/Fig1\/\">Fig. 1<\/a><\/p>\n\n\n\n<p id=\"__p1\">A flow diagram depicts the spectrum of severe neurological complications following COVID-19 vaccinations (ADEM, acute disseminated encephalomyelitis; CVST, cerebral venous sinus thrombosis; LETM, longitudinally extensive transverse myelitis; MS, multiple sclerosis; NMOSD, neuromyelitis optica spectrum disorders; PRES, posterior reversible encephalopathy syndrome; TIA, transient ischemic attacks)<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec5title\">Functional neurological disorders<\/h3>\n\n\n\n<p id=\"Par13\">Functional neurological disorders are triggered by physical\/emotional stress following an injury, medical illness, a surgery, or vaccination. Functional neurological disorders often remain misdiagnosed despite extensive workup.<\/p>\n\n\n\n<p id=\"Par14\">After availability of COVID-19 vaccine, many YouTube videos depicted continuous limb and trunk movements and difficulty walking immediately after COVID-19 vaccine administration. These videos were of concern as they&nbsp;were the&nbsp;source of \u201cvaccine hesitancy\u201d [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR10\">10<\/a>].&nbsp;Kim and colleagues reviewed several such social media videos demonstrating motor movements consistent with functional motor symptoms occurring after administration of COVID-19 vaccine. Motor movements were bizarre asynchronous and rapidly variable in frequency and amplitude consistent with functional neurological disorder. The Functional Neurological Disorder Society has lately clarified that movement disorder is consistent with functional in nature. The spread of these videos are important because these functional disorders created concerns for vaccine hesitancy [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR11\">11<\/a>].<\/p>\n\n\n\n<p id=\"Par15\">Several other kinds of functional neurological disorders have also been reported. Butler and colleagues described two young ladies, who presented with functional motor deficits mimicking stroke. Both these patients had variability in weakness and had&nbsp;many non-specific symptoms. A detailed workup and neuroimaging failed to demonstrate any specific abnormality [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR12\">12<\/a>].&nbsp;Ercoli&nbsp;and colleagues described a middle-aged man who, immediately after vaccine administration, reported bilateral facial paralysis along with failure to blink. These manifestations resolved quickly within 40&nbsp;min. Immediately after administration of second dose of vaccine, he complained of respiratory distress and swollen tongue. Again, all these symptoms resolved quickly following treatment with corticosteroids, however, he developed new symptoms in the form of&nbsp;right hemiparesis. Two weeks later, he developed facial hypoesthesia. A detailed workup of the patient failed to demonstrate any abnormality. A diagnosis of functional neurological disorder was, finally, made [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR13\">13<\/a>].<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec6title\">Cerebral vascular events<\/h2>\n\n\n\n<p id=\"Par16\">As a matter of concern, increasing number of reports about adenoviral vector vaccine-induced cerebral vascular adverse events, like cerebral venous thrombosis, arterial stroke, and intracerebral hemorrhage, is getting published in leading medical journals. These reports are alarming as post-vaccination vascular events culminate either in severe disability or death. Vaccine-induced cerebral vascular adverse events are generally associated with severe immune-mediated thrombotic thrombocytopenia. Thrombocytopenia generally clinically manifests within 5 to 30&nbsp;days after administration of adenovirus vector-based vaccines. In post-vaccination thrombotic thrombocytopenia, a picture similar to that of heparin-induced thrombocytopenia is encountered. When heparin binds platelet factor 4, there is generation of antibodies against platelet factor 4. Antibodies against platelet factor 4 result in platelet destruction and trigger the intravascular blood clotting [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR14\">14<\/a>]. The post-mortem examination, in patients with vaccine-induced thrombocytopenia, demonstrated extensive involvement of large venous vessels. Microscopic findings showed vascular thrombotic occlusions occurring in the vessels of multiple body organs along with marked inflammatory infiltration [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR15\">15<\/a>]. The vector-based vaccines contain genetic material of SARS-COV-2 that is capable of encoding the spike glycoprotein. Possibly, leaked genetic material binds to platelet factor 4 that subsequently activates formation of autoantibodies. These autoantibodies destroy platelets [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR16\">16<\/a>,&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR17\">17<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec7title\">Cerebral venous thrombosis<\/h3>\n\n\n\n<p id=\"Par17\">Cerebral venous thrombosis is the one of the most feared devastating COVID-19 vaccine-associated neurological complication. Cerebral venous thrombosis should be suspected in all vaccinated patients, who has persistent headache. Headache is generally unresponsive to the analgesics, and some patients may have focal neurological deficits. Affected patients are generally females of younger ages (Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab1\/\">\u200b(Table1)1<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR18\">18<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR46\">46<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 1<\/h3>\n\n\n\n<p id=\"__p2\">Clinical, magnetic resonance imaging findings, and outcome details of patients who developed cerebral venous sinus thrombosis after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complications<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration of onset after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment given<\/th><\/tr><\/thead><tbody><tr><td>Castelli et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR18\">18<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Italy<\/td><td>50\/M<\/td><td>COVID-19 vaccine AstraZeneca<\/td><td>10&nbsp;days<\/td><td>Severe headache, right hemiparesis, unsteady gait, and visual impairment of 4&nbsp;days Patient needed ICU care and mechanical ventilation<\/td><td>Intra-parenchymal hemorrhage CT angiography\u2009=\u2009left transverse and sigmoid venous sinuses thrombosis<\/td><td>Fibrinogen concentrate (10&nbsp;g total) and platelet (4 units total) a bilateral decompressive craniectomy<\/td><\/tr><tr><td>D\u2019Agostino et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR19\">19<\/a>]&nbsp;<\/td><td>Cerebral venous thrombosis and disseminated intravascular coagulation<\/td><td>Italy<\/td><td>54\/F<\/td><td>The AstraZeneca vaccine<\/td><td>12&nbsp;days<\/td><td>Altered sensorium and hemiparesis Myocardial infarction<\/td><td>Multiple subacute lobar hemorrhages basilar artery thrombosis associated with the superior sagittal sinus thrombosis Bilateral adrenal hemorrhage<\/td><td>Intensive care unit<\/td><\/tr><tr><td>Scully et al. (report of 23 patients) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR20\">20<\/a>]<\/td><td>Thrombocytopenia (23 patients) Cerebral venous thrombosis (13 patients)<\/td><td>London<\/td><td>12&nbsp;years (Median)<\/td><td>ChAdOx1 nCoV-19 vaccine (AstraZeneca)<\/td><td>6 to 24&nbsp;days<\/td><td>13 patients with cerebral venous thrombosis<\/td><td>Not available<\/td><td>Not available<\/td><\/tr><tr><td>Franchini et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR21\">21<\/a>]<\/td><td>Cerebral venous thrombosis<\/td><td>Italy<\/td><td>50\/M<\/td><td>COVID-19 vaccine AstraZeneca<\/td><td>7&nbsp;days<\/td><td>Coma thrombocytopenia<\/td><td>Intra-parenchymal hemorrhage Angiography cerebral venous sinus thrombosis<\/td><td>Intensive care unit<\/td><\/tr><tr><td>Mehta et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR22\">22<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>UK<\/td><td>32\/M<\/td><td>Vaxzevria vaccine<\/td><td>9&nbsp;days<\/td><td>Thunderclap headache Left hemiparesis, left-sided incoordination Thrombocytopenia and rapidly evolving coma<\/td><td>Superior sagittal sinus and cortical vein thrombosis and significant cortical edema with small areas of parenchymal and subarachnoid hemorrhage<\/td><td>Intensive care unit<\/td><\/tr><tr><td>25\/M<\/td><td>Vaxzevria vaccine<\/td><td>6&nbsp;days<\/td><td>Headache hemiparesis, left hemisensory loss Seizures, agitation, decerebrate posturing, reduced GCS Thrombocytopenia<\/td><td>Superior sagittal sinus thrombosis with extension into the cortical veins and hemorrhage in lobar and sub-arachnoid locations<\/td><td>Intensive care unit<\/td><\/tr><tr><td>Bersinger&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR23\">23<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>France<\/td><td>21\/F<\/td><td>ChAdOx1 nCoV-19 vaccine<\/td><td>9&nbsp;days<\/td><td>Headaches, seizures, hemiplegia, expressive aphasia, and no pupillary abnormalities and altered sensorium The platelet count was 61,000 per cubic millimeter<\/td><td>CT of the head showed massive thrombosis in the deep and superficial cerebral veins, thrombosis of the left jugular vein, and left frontoparietal venous hemorrhagic infarction<\/td><td>A selective arterial embolization was performed immediately after decompressive craniectomy IV immunoglobulin Fondaparinux<\/td><\/tr><tr><td>Ramdeny et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR24\">24<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>United Kingdom<\/td><td>54\/M<\/td><td>COVID-19 Vaccine AstraZeneca<\/td><td>21&nbsp;days<\/td><td>Worsening headache, bruising and unilateral right calf swelling Thrombocytopenia D-dimer\u2009=\u200960,000&nbsp;ng\/ml Anti-platelet factor 4<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Intravenous immunoglobulin<\/td><\/tr><tr><td>Zakaria et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR25\">25<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Malaysia<\/td><td>49\/M<\/td><td>First dose of mRNA SARS-CoV-2 vaccine<\/td><td>16&nbsp;days<\/td><td>New onset of mild to moderate headache and giddiness<\/td><td>CT) of the brain showed cordlike hyperattenuation within the left transverse and sigmoid sinus suggestive of cord or dense clot sign CT cerebral venography a long segment-filling defect and empty delta sign within the superior sagittal sinus extending into the torcula Herophili, left transverse sinus, and sigmoid sinus to proximal internal jugular vein<\/td><td>Subcutaneous Clexane improved<\/td><\/tr><tr><td>Ryan et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR26\">26<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Ireland<\/td><td>35\/F<\/td><td>AZD1222 (COVID-19 Vaccine AstraZeneca)<\/td><td>10&nbsp;days<\/td><td>Headache thrombocytopenia bruising and petechiae Antibody to platelet factor 4<\/td><td>MR venogram showed cerebral venous sinus thrombosis<\/td><td>Apixaban<\/td><\/tr><tr><td>Graf et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR27\">27<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Germany<\/td><td>29\/M<\/td><td>ChAdOx1 nCov-19, AstraZeneca<\/td><td>9&nbsp;days<\/td><td>Severe headache and hematemesis thrombocytopenia<\/td><td>Complete thrombosis of the left transverse and sigmoid sinus down to the left proximal jugular vein Temporo-parietal intracranial hemorrhage CT angiography revealed extensive thrombosis of the mesenteric and portal vein<\/td><td>High-dose immunoglobulins Argatroban<\/td><\/tr><tr><td>George et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR28\">28<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>USA<\/td><td>40\/F<\/td><td>ChAdOx1 nCov-19, AstraZeneca<\/td><td>7&nbsp;days<\/td><td>Headache&nbsp;thrombocytopenia Antibody to platelet factor 4<\/td><td>Venous thrombosis involving the left transverse sigmoid sinus and internal jugular vein<\/td><td>A direct thrombin inhibitor (bivalirudin) Intravenous immune globulin (IVIG)<\/td><\/tr><tr><td>Jamme et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR29\">29<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>France<\/td><td>69\/F<\/td><td>First dose of Oxford\u2013AstraZeneca vaccine<\/td><td>11&nbsp;days<\/td><td>Headache associated with behavioral symptoms<\/td><td>Bilateral frontal hemorrhage cerebral venous thrombosis of the left internal jugular vein, sigmoid sinus, and superior sagittal sinus<\/td><td>None<\/td><\/tr><tr><td>Tiede et al. (report of 5 patients) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR30\">30<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Germany<\/td><td>41 and 67&nbsp;years All females<\/td><td>ChAdOx1 COVID-19 vaccine (AZD1222, Vaxzevria)<\/td><td>5 to 11&nbsp;days after first vaccination<\/td><td>Cerebral venous sinus thrombosis (CVST), splanchnic vein thrombosis (SVT), arterial cerebral thromboembolism, and thrombotic microangiopathy thrombocytopenia Autoantibodies against platelet factor 4<\/td><td>Brain hematomas infarcts, presence of thrombi in major vessels<\/td><td>Intravenous immunoglobulin or corticosteroids Argatroban<\/td><\/tr><tr><td>Schulz et al. (report of 45 cases) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR31\">31<\/a>]<\/td><td>Cerebral venous thrombosis<\/td><td>Germany<\/td><td>46.5&nbsp;years (mean)\/35 females<\/td><td>BNT162b2, ChAdOx1, and mRNA-1273<\/td><td>Within 30&nbsp;days of vaccination<\/td><td>Thrombocytopenia in all patients<\/td><td>Cerebral venous thrombosis<\/td><td>Intravenous immunoglobulins, plasmapheresis, corticosteroids, anticoagulants<\/td><\/tr><tr><td>Bourguignon et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR32\">32<\/a>]<\/td><td>A report three patients one had cerebral venous sinus thrombosis<\/td><td>Canada<\/td><td>69\/M<\/td><td>ChAdOx1 nCov-19, AstraZeneca<\/td><td>12&nbsp;days<\/td><td>Diabetes mellitus, hypertension, obstructive sleep apnea, recently diagnosed prostate cancer Headache and confusion left-sided weakness Thrombocytopenia Autoantibodies against platelet factor 4<\/td><td>Right middle cerebral-artery stroke with hemorrhagic transformation Right cerebral transverse and sigmoid sinuses, right internal jugular vein, hepatic vein, and distal lower-limb vein; pulmonary embolism<\/td><td>Intravenous immunoglobulin Plasmapheresis<\/td><\/tr><tr><td>Gattringer et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR33\">33<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Austria<\/td><td>39\/F<\/td><td>The first vaccination with ChAdOx1 nCov-19 (AstraZeneca)<\/td><td>8&nbsp;days<\/td><td>Headache since 2&nbsp;days thrombocytopenia (84\u2009\u00d7\u200910 [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR8\">8<\/a>]\/L)<\/td><td>Left sigmoid\/transverse sinus thrombosis without brain parenchymal involvement<\/td><td>Intravenous immunoglobulin<\/td><\/tr><tr><td>Ikenberg et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR34\">34<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Germany<\/td><td>early 30&nbsp;s\/F<\/td><td>The first dose of ChAdOx1 nCov-19 (AstraZeneca)<\/td><td><\/td><td>Headache Gait ataxia, and amnestic difficulties as well as aphasia Thrombocytopenia of 37 000\/\u00b5L<\/td><td>CVST of the left transverse and sigmoidal sinus with a left-temporal and left-cerebellar intracerebral hemorrhage<\/td><td>Intravenous immunoglobulin argatroban<\/td><\/tr><tr><td>Clark et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR35\">35<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>USA<\/td><td>40\/F<\/td><td>The Ad26.COV2.S (Johnson &amp; Johnson\/ Jansen) vaccine<\/td><td>5&nbsp;days<\/td><td>Worsening headaches thrombocytopenia<\/td><td>Cerebral venous sinus thrombosis involving the left transverse and sigmoid sinuses, extending into the left internal jugular vein<\/td><td>Bivalirudin infusion Intravenous immunoglobulin<\/td><\/tr><tr><td>Bonato et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR36\">36<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Italy<\/td><td>26\/F<\/td><td>ChAdOx1 nCoV-19 vaccine<\/td><td>14&nbsp;days<\/td><td>headache non-responsive to drugs right-sided weakness and visual disturbances rapidly deteriorated with decreased consciousness<\/td><td>Multifocal venous thrombosis with bilateral occlusion of parietal cortical veins, straight sinus, vein of Galen, internal cerebral veins, and inferior sagittal sinus. Right parietal and left frontoparietal lobes an extensive venous infarction with hemorrhagic transformation Platelet-factor 4 (PF4)\u2013heparin IgG antibodies \u2013 elevated thrombocytopenia<\/td><td>Dexamethasone Intravenous immunoglobulin argatroban<\/td><\/tr><tr><td>Wang et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR37\">37<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Taiwan<\/td><td>41\/F<\/td><td>First vaccination with ChAdOx1 nCoV-19<\/td><td>7&nbsp;days<\/td><td>Fever and headache thrombocytopenia positive anti-PF4 antibodies<\/td><td>MR venography revealed cerebral venous sinus thrombosis<\/td><td>Intravenous immunoglobulin<\/td><\/tr><tr><td>Dutta et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR38\">38<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>India<\/td><td>51\/M<\/td><td>First-dose of COVISHIELD<\/td><td>6&nbsp;days<\/td><td>Headache double vision papilledema Platelet count was normal<\/td><td>MR venography revealed thrombosis in superior sagittal sinus and transverse sinus<\/td><td>Low-molecular-weight heparin<\/td><\/tr><tr><td>Aladdin et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR39\">39<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Saudi Arabia<\/td><td>36\/F<\/td><td>First dose of the ChAdOx1 nCoV-19 vaccine<\/td><td>14&nbsp;days<\/td><td>Vomiting and severe headache left upper limb weakness thrombocytopenia Disseminated intravascular coagulation<\/td><td>Brain computed tomography (CT) scan showed superior sagittal thrombosis with thickened cortical veins and bilateral hypodensities in the parietal lobes<\/td><td>Low-molecular-weight heparin ICU care<\/td><\/tr><tr><td>Lavin et al. (a series of 4 patients) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR40\">40<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Ireland<\/td><td>29\/F 38\/M 50\/F 35\/F<\/td><td>Vaxzevria vaccine (ChAdOx1 nCoV-19, AstraZeneca)<\/td><td>10&nbsp;days 16&nbsp;days 23&nbsp;days 14&nbsp;days<\/td><td>Visual disturbance followed by a headache, nausea, vomiting, bruising and petechiae severe thunderclap headache, nausea and vomiting headache, persistent bruising and petechiae all had thrombocytopenia<\/td><td>Dural venous sinus thrombosis in one patient only other had abdominal abnormalities<\/td><td>Intravenous immunoglobulin<\/td><\/tr><tr><td>T\u00f8lb\u00f8ll S\u00f8rensen et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR41\">41<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>UK<\/td><td>30\/F<\/td><td>ChAdOx1 nCoV-19<\/td><td><\/td><td>Headache and general malaise portal vein thrombosis thrombocytopenia and consumption coagulopathy Anti-platelet antibodies were detected<\/td><td>Normal<\/td><td>Tinzaparin<\/td><\/tr><tr><td>Fan et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR42\">42<\/a>]&nbsp;(a series of 3 patients)<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Singapore<\/td><td>54\/M 62\/F 60\/F<\/td><td>BNT162b2 mRNA vaccination<\/td><td>1&nbsp;day 9&nbsp;days 8&nbsp;days<\/td><td>Severe headache and vomiting and acute left hemiparesis Headache and vomiting Right ataxic hemiparesis There was no thrombocytopenia<\/td><td>A large right temporo-parietal lobe intraparenchymal hemorrhage Acute right cerebral bleed involving occipital and temporal lobes associated with subarachnoid hemorrhage Venous infarct in bilateral perirolandic gyri Venogram confirmed cerebral venous sinus thrombosis in all three<\/td><td>Low-molecular-weight heparin decompressive craniectomy<\/td><\/tr><tr><td>Suresh and Petchey&nbsp; [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR43\">43<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>UK<\/td><td>27\/M<\/td><td>ChAdOx1 nCOV-19 vaccine<\/td><td>2&nbsp;days<\/td><td>Worsening headache and new homonymous hemianopia Thrombocytopenia Anti-platelet antibodies were detected<\/td><td>Acute parenchymal bleed with subdural extension CT venogram confirmed significant cerebral venous sinus thrombosis<\/td><td>Dabigatran and intravenous immunoglobulins<\/td><\/tr><tr><td>Dias et al. (a series of 2 patients) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR44\">44<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Portugal<\/td><td>47\/F 67\/F<\/td><td>BNT162b2 mRNA SARS-CoV-2 vaccine<\/td><td>6&nbsp;days 3&nbsp;days<\/td><td>Headache, nausea and photophobia a sudden left motor deficit Sudden right lower limb clonic movements, followed by motor deficit, loss of consciousness and headache There was no thrombocytopenia Anti-platelet antibodies were not detected<\/td><td>MRI with venography revealed thrombosis of superior sagittal, right lateral, transverse, sigmoid sinuses, and jugular vein and left sigmoid sinus, together with right frontal subarachnoid hemorrhage and a cortical venous infarct Brain MRI showed thrombosis of high convexity cortical veins, superior sagittal, right transverse, and sigmoid sinus and jugular vein<\/td><td>Acetazolamide and enoxaparin Levetiracetam 500&nbsp;mg bid and enoxaparin<\/td><\/tr><tr><td>Guan et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR45\">45<\/a>]<\/td><td>Cerebral venous sinus thrombosis<\/td><td>Taiwan<\/td><td>52\/M<\/td><td>The first dose of ChAdOx1 nCov-19 (AstraZeneca)<\/td><td>10&nbsp;days<\/td><td>Nausea and thunderclap headache thrombocytopenia Platelet factor 4 antibodies detected<\/td><td>Hyperdensity of the sinus, including cord sign and dense vein sign at the left transverse and sigmoid sinuses CT venogram revealed CVST at the left transverse sinus and sigmoid sinuses and thrombosis of the left internal jugular vein<\/td><td>Apixaban Outcome not provided<\/td><\/tr><tr><td>Varona et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR46\">46<\/a>]<\/td><td>Cerebral venous sinus thrombosis and primary adrenal insufficiency<\/td><td>Spain<\/td><td>47\/M<\/td><td>Adenoviral (ChAdOx1) vector-based COVID-19 vaccine<\/td><td>10&nbsp;days<\/td><td>Headache, somnolence, and mild confusion Blateral segmentary pulmonary embolism Thrombocytopenia Anti-platelet antibodies were detected<\/td><td>Consistent with cerebral venous thrombosis<\/td><td>Intravenous immunoglobulins and subcutaneous fondaparinux hydrocortisone Patient improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab1\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<p id=\"Par18\">In Europe, since March 2021, cases of cerebral venous thrombosis started pouring in following COVID-19 vaccination, particularly after administration of viral vector based (AstraZeneca ChAdOx1 nCoV-19 and the Johnson and Johnson Ad26. COV2.S) vaccines [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR22\">22<\/a>]. Scully and colleagues recently reported findings of 23 patients, who presented with thrombosis and thrombocytopenia (platelet counts below 10\u2009\u00d7\u2009109\/L). These patients developed thrombosis and thrombocytopenia 6 to 24&nbsp;days after they received the first dose of the viral vector-based vaccines. In a significant observation, authors, in majority of patients, demonstrated the presence of autoantibodies against platelet factor 4. Additionally, D-dimer levels were found elevated [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR20\">20<\/a>].&nbsp;Tiede and co-workers reported five German cases of prothrombotic immune thrombocytopenia after vaccination with viral vector-based vaccine (Vaxzevria). In these patients, acute vascular events clinically manifested as cerebral venous sinus thrombosis, splanchnic vein thrombosis, arterial cerebral thromboembolism, and\/or thrombotic microangiopathy within 2&nbsp;weeks post vaccination. All five patients had low platelet counts and markedly raised D-dimer. In all, autoantibodies against platelet factor 4 were also demonstrated [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR30\">30<\/a>].<\/p>\n\n\n\n<p id=\"Par19\">Potteg\u00e5rd et al. in Denmark and Norway evaluated incidence of arterial events, venous thromboembolism, thrombocytopenia, and bleeding among vaccinated population. The vaccinated cohorts comprised of 148,792 Danish people and 132,472 persons from Norway. All has received their first dose of viral vector-based vaccine (ChAdOx1-S). An excess rate of venous thromboembolism (like cerebral venous thrombosis) was observed among vaccine recipients, within 28&nbsp;days of vaccine administration. Authors estimated an increased rate for venous thromboembolism corresponding to 11 excess events per 100,000 vaccinations with 2.5 excess cerebral venous thrombosis events per 100,000 vaccinations [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR47\">47<\/a>].<\/p>\n\n\n\n<p id=\"Par20\">Krzywicka&nbsp;et al., from the Netherlands, collected data of 213 cases with post-vaccination&nbsp;(187 after adenoviral vector vaccines and 26 after a mRNA vaccine) cerebral venous sinus thrombosis; they noted thrombocytopenia in 107\/187 (57%) post-vaccination&nbsp;cerebral venous sinus thrombosis cases. Thrombocytopenia was not recorded in any of patients, who received an mRNA-based vaccine. Cerebral venous sinus thrombosis after adenoviral vector vaccines carried poorer prognosis. Approximately, 38% (44\/117) patients in adenoviral vector vaccine group died, while in mRNA vaccine group, 20% (2\/10) had died [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR48\">48<\/a>].<\/p>\n\n\n\n<p id=\"Par21\">Recently published National Institute for Health and Care Excellence (NICE) guidelines recommend that the patients with clinical diagnosis of vaccine-induced immune thrombocytopenia and thrombosis should be treated with intravenous administration of human immunoglobulin, at a dose of 1&nbsp;g\/kg. If there is no response or there is further deterioration, second dose of human immunoglobulin should be given. In patients with insufficient response, methylprednisolone 1&nbsp;g intravenously for 3&nbsp;days or dexamethasone 20 to 40&nbsp;mg for 4&nbsp;days can be used [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR49\">49<\/a>].<\/p>\n\n\n\n<p id=\"Par22\">Heparin needs to be avoided, instead alternative anticoagulants like argatroban, bivalirudin, fondaparinux, rivaroxaban, or apixaban should be used for anticoagulation [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR49\">49<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR51\">51<\/a>]. NICE guidelines further recommend that patients with very low platelet count should be treated either alone with a argatroban or a combination of argatroban and platelet transfusion [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR49\">49<\/a>].<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec8title\">Arterial events<\/h2>\n\n\n\n<p id=\"Par23\">Several acute arterial events, like arterial thrombosis, intracerebral hemorrhage, transient global amnesia, and spinal artery ischemia, have also been reported following vaccination [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR31\">31<\/a>].<\/p>\n\n\n\n<p id=\"Par24\">Simpson and colleagues, in Scotland, estimated the incidence of vaccine-associated thrombocytopenia and vascular events following administration of first dose of viral vector-based vaccine (ChAdOx1) or mRNA (BNT162b2 Pfizer-BioNTech or mRNA-1273 Moderna) vaccination. First dose of viral vector-based vaccine was associated with small enhanced risk of idiopathic thrombocytopenic purpura; in addition, up to 27&nbsp;days after vaccination, there was possibility of an increased risk for thromboembolic and hemorrhagic events. No such adverse associations were noted with mRNA vaccines [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR52\">52<\/a>]. The reports of COVID-19 vaccine-related intracerebral hemorrhage and ischemic stroke are summarized in Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab2\/\">\u200bTable22<\/a>&nbsp;[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR53\">53<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR61\">61<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 2<\/h3>\n\n\n\n<p id=\"__p3\">Clinical, neuroimaging and outcome details of patients who suffered strokes (other than cerebral venous thrombosis) after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Athyros and Doumas [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR53\">53<\/a>]<\/td><td>Intracerebral hemorrhage<\/td><td>Greece<\/td><td>71\/F<\/td><td>Moderna anti-COVID-19 vaccine<\/td><td>3&nbsp;days<\/td><td>Right hemiplegia, aphasia, agnosia Acute hypertensive crisis<\/td><td>Left basal ganglia hemorrhage<\/td><td>Clonidine, furosemide<\/td><td>Died<\/td><\/tr><tr><td>Bj\u00f8rnstad-Tuveng [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR54\">54<\/a>]<\/td><td>Intracerebral hemorrhage<\/td><td>Norway<\/td><td>Thirties\/F<\/td><td>AstraZeneca\u2019s vaccine ChAdOx1 nCoV-19<\/td><td>9&nbsp;days<\/td><td>Slurred speech, left hemiparesis, and reduced consciousness<\/td><td>Right intracerebral hemorrhage on CT, thrombosis in transverse sinus and pulmonary artery on postmortem<\/td><td>ICU management<\/td><td>Died<\/td><\/tr><tr><td>de M\u00e9lo Silva et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR55\">55<\/a>]<\/td><td>Intracerebral hemorrhage with intraventricular extension<\/td><td>Brazil<\/td><td>57\/F<\/td><td>ChAdOx1 nCoV-19 vaccine<\/td><td>5&nbsp;days<\/td><td>Left hemiparesis, vomiting, and somnolence<\/td><td>A large right deep frontal lobe parenchymal hematoma<\/td><td>ICU management Decompressive craniectomy<\/td><td>Survived with disabilities<\/td><\/tr><tr><td>Bayas et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR56\">56<\/a>]<\/td><td>Bilateral superior ophthalmic vein thrombosis, ischemic stroke, and immune thrombocytopenia<\/td><td>Germany<\/td><td>55\/F<\/td><td>SARS-CoV-2\u2014 ChAdOx1 nCoV-19<\/td><td>10&nbsp;days<\/td><td>Flu-like illness, diplopia, vision loss, a transient, mild, right-sided hemiparesis, and aphasia, focal seizures<\/td><td>MRI showed superior ophthalmic vein thrombosis An MRI showed an ischemic stroke in the left parietal lobe, middle cerebral artery territory, with restricted diffusion<\/td><td>Intravenous dexamethasone Anticoagulants<\/td><td>Improved<\/td><\/tr><tr><td>Al-Mayhani et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR57\">57<\/a>]&nbsp;<\/td><td>Ischemic stroke with thrombocytopenia<\/td><td>London<\/td><td>35\/F 37\/F 43\/F<\/td><td>ChAdOx1 nCoV-19 vaccine ChAdOx1 nCoV-19 vaccine ChAdOx1 nCoV-19 vaccine<\/td><td>11&nbsp;days 12&nbsp;days 21&nbsp;days<\/td><td>Left face, arm, leg weakness and drowsiness Headache, left visual field loss, confusion, left arm weakness Dysphasia<\/td><td>Right middle-cerebral artery infarct Bilateral acute border zone infarcts Left middle-cerebral artery infarct<\/td><td>Decompressive hemicraniectomy Intravenous immunoglobulin Intravenous immunoglobulin<\/td><td>Died Improved Stable<\/td><\/tr><tr><td>Blauenfeldt et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR58\">58<\/a>]<\/td><td>Ischemic stroke<\/td><td>Denmark<\/td><td>60\/M<\/td><td>mRNA-based vaccine BNT162b2 (Pfizer\/BIOTECH)<\/td><td>7&nbsp;days<\/td><td>Bilateral adrenal hemorrhages A massive right sided ischemic stroke Thrombocytopenia Platelet factor 4 (PF\u20104) reactive antibodies<\/td><td>Angiography showed occlusion of the right internal. Carotid artery<\/td><td>Intensive care unit<\/td><td>Palliative care<\/td><\/tr><tr><td>Malik&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR59\">59<\/a>]<\/td><td>transient ischemic attack<\/td><td>USA<\/td><td>43\/F<\/td><td>Johnson and Johnson COVID-19 Ad26.COV2.S vaccination<\/td><td>10&nbsp;days<\/td><td>Headache, fever, body aches, chills, mild dyspnea and light-headedness thrombocytopenia numbness and tingling of her face and right arm<\/td><td>Right internal carotid artery (ICA) thrombus<\/td><td>Fondaparinux<\/td><td>Improved<\/td><\/tr><tr><td>Finsterer and Korn [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR60\">60<\/a>]<\/td><td>Aphasia<\/td><td>Austria<\/td><td>52\/M<\/td><td>The second dose of an mRNA-based SARS-CoV-2 vaccine<\/td><td>7&nbsp;days<\/td><td>Sudden-onset reading difficulty and aphasia motor aphasia with paraphasia<\/td><td>A lobar bleeding in the left temporal lobe<\/td><td>Supportive<\/td><td>Improved<\/td><\/tr><tr><td>Walter et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR61\">61<\/a>]<\/td><td>Ischemic stroke Main stem occlusion of middle cerebral artery<\/td><td>Germany<\/td><td><\/td><td>First dose ChAdOx1 nCov-19 vaccine<\/td><td><\/td><td>acute headache, aphasia, and hemiparesis Platelet count and fibrinogen level were normal<\/td><td>Main stem occlusion of middle cerebral artery A wall-adherent, non-occluding thrombus in the ipsilateral carotid bulb&nbsp;was noted<\/td><td>Within 1&nbsp;h after start of IV thrombolysis<\/td><td>Thrombus dissolved and patient improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab2\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec9title\">Intracerebral hemorrhage<\/h3>\n\n\n\n<p id=\"Par25\">Athyros and Doumas reported a 71-year-old female. who developed intracerebral hemorrhage after she received the first dose of the Moderna mRNA vaccine.<\/p>\n\n\n\n<p id=\"Par26\">On the third post-vaccination day, the patient developed right hemiplegia, aphasia, and agnosia along with accelerated hypertension. Computed tomography revealed a hematoma in the left basal ganglia. On the 9th day, she died [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR53\">53<\/a>].<\/p>\n\n\n\n<p id=\"Par27\">In another report, Bj\u00f8rnstad-Tuveng et al. described a young woman, who had a fatal cerebral event following vaccination with AstraZeneca\u2019s ChAdOx1 nCoV-19 vaccine.&nbsp;She was found to have severe thrombocytopenia. The patient died the next day of the event. Post-mortem examination revealed antibodies against platelet factor 4 and the presence of small thrombi in the transverse sinus, frontal lobe, and pulmonary artery [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR54\">54<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec10title\">Acute ischemic stroke<\/h3>\n\n\n\n<p id=\"Par28\">Bayas and co-workers described a case that presented with superior ophthalmic vein thrombosis, ischemic stroke, and immune thrombocytopenia, after administration of viral vector-based vaccine. Intravenous dexamethasone resulted in marked improvement in platelet count [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR56\">56<\/a>]. Al-Mayhani&nbsp;et al. described three cases of vaccine-induced thrombotic thrombocytopenia, all presented with arterial strokes. Authors opined that young patients with arterial stroke after receiving the COVID-19 vaccine should always be evaluated for vaccine-induced thrombotic thrombocytopenia. Other laboratory tests, like platelet count, D-dimers, fibrinogen level, and testing for platelet factor 4 antibodies, should also be performed [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR57\">57<\/a>].<\/p>\n\n\n\n<p id=\"Par29\">Blauenfeldt&nbsp;et al. described a 60-year-old woman, who presented with intractable abdominal pain, 7&nbsp;days after receiving the adenoviral (ChAdOx1) vector-based COVID-19 vaccine. Abdominal computed tomography revealed bilateral adrenal necrosis. Later, a massive right cerebral infarction, secondary to occlusion of the right internal carotid artery, occurred that led to death of the patient. Blood tests showed thrombocytopenia, elevated in D-dimer and platelet factor 4 antibodies [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR58\">58<\/a>].<\/p>\n\n\n\n<p id=\"Par30\">Many reports of acute brain disorders like encephalopathy, seizures, acute disseminated encephalopathy, neuroleptic malignant syndrome, and post-vaccine encephalitis were described secondary to COVID-19 vaccine. These are summarized in Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab3\/\">\u200bTable33<\/a>&nbsp;[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR62\">62<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR75\">75<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 3<\/h3>\n\n\n\n<p id=\"__p4\">Clinical, neuroimaging and outcome details of patients who presented with an acute brain disorder (other than cerebral venous thrombosis and arterial stroke) after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Baldelli&nbsp;<strong>et al.<\/strong>&nbsp;[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR62\">62<\/a>]<\/td><td>Reversible encephalopathy<\/td><td>Italy<\/td><td>77\/M<\/td><td>The first dose of ChAdOx1 nCoV-19 vaccine (AstraZeneca)<\/td><td>1&nbsp;day<\/td><td>Delirium A significant increase of interleukin (IL)-6 in both CSF and serum<\/td><td>Normal<\/td><td>Corticosteroids<\/td><\/tr><tr><td>Aladdin and Shirah [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR63\">63<\/a>]<\/td><td>New-onset refractory status epilepticus<\/td><td>Saudi Arabia<\/td><td>42\/F<\/td><td>ChAdOx1 nCoV-19 vaccine<\/td><td>10&nbsp;days<\/td><td>Headache and fever first-ever generalized tonic\u2013clonic seizure lorazepam, levetiracetam, and phenytoin failed to control<\/td><td>Increase in the signal on FLAIR images at bilateral hippocampi and insula<\/td><td>Midazolam and propofol Plasma exchange<\/td><td>Improved<\/td><\/tr><tr><td>Ghosh et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR64\">64<\/a>]<\/td><td>Seizures<\/td><td>India<\/td><td>68\/M<\/td><td>Covishield vaccine<\/td><td>4&nbsp;days<\/td><td>Focal onset non-motor seizure<\/td><td>Periventricular&nbsp;leukoaraiosis and cortical atrophy<\/td><td>brivaracetam<\/td><td>Improved<\/td><\/tr><tr><td>Liu et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR65\">65<\/a>]&nbsp;(two cases)<\/td><td>Associated with non-convulsive status epilepticus<\/td><td>USA<\/td><td>86\/F 73\/M<\/td><td>Moderna COVID-19 vaccine<\/td><td>7&nbsp;days 21&nbsp;days<\/td><td>Diastolic dysfunction,&nbsp;chronic kidney disease and diabetes mellitus with acute encephalopathy Acute confusion with visual hallucinations EEG demonstrated non-convulsive focal status epilepticus Acute encephalopathy with non-convulsive status epilepticus<\/td><td>Normal<\/td><td>Antiepileptic therapy and ICU care<\/td><td>Both improved<\/td><\/tr><tr><td>Naharci and Tasc [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR66\">66<\/a>]<\/td><td>Delirium<\/td><td>Turkey<\/td><td>88\/F<\/td><td>first dose of CoronaVac\u2013-an inactivated COVID-19 vaccine<\/td><td><\/td><td>Acute confusion, hallucinations, agitation, and sleep disturbance<\/td><td>None<\/td><td>Haloperidol and trazodone<\/td><td>Improved<\/td><\/tr><tr><td>Salinas&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR67\">67<\/a>]<\/td><td>Transient akathisia<\/td><td>USA<\/td><td>36\/F<\/td><td>Pfizer-BioNTech vaccine<\/td><td>Within 24&nbsp;h of second dose<\/td><td>Restless body syndrome had fever after 5&nbsp;h of motor restlessness resolved after 24&nbsp;h<\/td><td>None<\/td><td>None<\/td><td>Improved<\/td><\/tr><tr><td>Zavala-Jonguitud et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR68\">68<\/a>]<\/td><td>Delirium<\/td><td>Mexico<\/td><td>89\/M<\/td><td>The first dose of BNT162b2 RNA vaccine<\/td><td>24&nbsp;h<\/td><td>Acute confusion, fluctuating attention, anxiety and inversion of the sleep\u2013wake cycle History of type 2 diabetes mellitus, hypertension, stage III\u2010b chronic kidney disease, prostatic hyperplasia<\/td><td>Not done<\/td><td>Quetiapine<\/td><td>Improved<\/td><\/tr><tr><td>Alfishawy et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR69\">69<\/a>]<\/td><td>Neuroleptic malignant syndrome<\/td><td>Kuwait<\/td><td>74\/F<\/td><td>BNT162b2 mRNA COVID-19 vaccine<\/td><td>16&nbsp;days<\/td><td>Old case of dementia and bipolar disorder and was receiving memantine, donepezil, and quetiapine presented with fever, delirium, rigidity, and elevated CPK<\/td><td>Normal<\/td><td>Symptomatic<\/td><td>Improved<\/td><\/tr><tr><td>Ozen Kengngil et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR70\">70<\/a>]<\/td><td>Acute disseminated encephalomyelitis like MRI lesions<\/td><td>Turkey<\/td><td>46\/F<\/td><td>Inactivated SARS-CoV-2 vaccine of Sinovac<\/td><td>1 Month<\/td><td>Seizures, normal examination<\/td><td>T2, FLAIR hyperintensity in thalamus, and corona radiata<\/td><td>Methyl prednisolone<\/td><td>No recurrence of seizures<\/td><\/tr><tr><td>Cao and Ren [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR71\">71<\/a>]<\/td><td>Acute disseminated encephalomyelitis<\/td><td>China<\/td><td>24\/F<\/td><td>SARS-CoV-2 Vaccine (Vero Cell), Inactivated<\/td><td>2&nbsp;weeks<\/td><td>Somnolence and memory&nbsp;decline, MMSE-11 inflammatory changes in CSF<\/td><td>T2\/FLAIR white matter hyperintensity in both temporal lobes<\/td><td>IV immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td><strong>Raknuzzaman et al.&nbsp;<\/strong>[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR72\">72<\/a>]<\/td><td>Acute disseminated encephalomyelitis<\/td><td>Bangladesh<\/td><td>55\/M<\/td><td>BNT162b2 mRNA COVID-19 vaccine<\/td><td>3&nbsp;weeks<\/td><td>Delirium followed by loss of consciousness<\/td><td>T2\/FLAIR white matter hyperintensities in periventricular region<\/td><td>Methyl prednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Torrealba-Acosta&nbsp;<strong>et al.&nbsp;<\/strong>[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR73\">73<\/a>]<\/td><td>Acute encephalitis, myoclonus and Sweet syndrome<\/td><td>USA<\/td><td>77\/M<\/td><td>mRNA-1273 vaccine<\/td><td>1&nbsp;day<\/td><td>Confusion, fever and generalized rash; later headache, dizziness and double vision leading to severe encephalopathy Intermittent orofacial movements and upper extremity myoclonus CSF showed increased cells and protein. Skin biopsy showed vasculitis changes<\/td><td>Normal<\/td><td>Methylprednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Vogrig et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR74\">74<\/a>]<\/td><td>Acute disseminated encephalomyelitis<\/td><td>Italy<\/td><td>56\/F<\/td><td>Pfizer-BioMTech COVID-19 vaccine (Comirnaty)<\/td><td>2&nbsp;weeks<\/td><td>Horizontal gaze-evoked&nbsp;nystagmus, Mild weakness on left upper limb, left hemi-ataxic gait<\/td><td>T2\/FLAIR white matter hyperintensity in left&nbsp;cerebellar peduncle prednisone improved FLAIR sequences were observed, the largest in the left centrum semiovale<\/td><td>Prednisone<\/td><td>Improved<\/td><\/tr><tr><td>Zuhorn et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR75\">75<\/a>]<\/td><td>Postvaccinal encephalitis Similar to autoimmune encephalitis<\/td><td>Germany<\/td><td>21\/F<\/td><td>ChAdOx1 nCov-19 vaccine the first dose<\/td><td>5&nbsp;days<\/td><td>Headache and progressive neurological symptoms including attention and concentration difficulties and a seizure CSF lymphocytic pleocytosis EEG slow delta rhythm<\/td><td>Normal<\/td><td>Prednisone<\/td><td>Improved<\/td><\/tr><tr><td>63\/F<\/td><td>ChAdOx1 nCov-19 vaccine<\/td><td>6&nbsp;days<\/td><td>Gait disorder, a vigilance disorder and a twitching all over her body Opsoclonus-myoclonus syndrome CSF lymphocytic pleocytosis EEG slow delta rhythm<\/td><td>Normal<\/td><td>Methylprednisolone<\/td><td>Improved<\/td><\/tr><tr><td>63\/M<\/td><td>ChAdOx1 nCov-19 vaccine<\/td><td>8&nbsp;days<\/td><td>Isolated aphasia and fever CSF lymphocytic pleocytosis EEG normal<\/td><td>Normal<\/td><td>None<\/td><td>Mild improvement despite no treatment<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab3\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec11title\">Encephalopathy<\/h3>\n\n\n\n<p id=\"Par31\">Some patients developed encephalopathy following administration of COVID-19 vaccines. Acute encephalopathy is defined as rapidly evolving disorder of the brain. Acute encephalopathy clinically manifests either with delirium, decreased consciousness, or coma.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec12title\">Delirium<\/h3>\n\n\n\n<p id=\"Par32\">Delirium is characterized with fluctuating disturbance in attention and awareness. Zavala-Jonguitud and P\u00e9rez-Garc\u00eda described an 89-year-old man, who developed delirium after mRNA vaccination. Within 24&nbsp;h, patient developed confusion, fluctuating attention, anxiety, and inversion of the sleep\u2013wake cycle. Patient had many comorbidities (diabetes mellitus, hypertension, and chronic kidney disease). Patient improved after he was treated with quetiapine [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR68\">68<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec13title\">Neuroleptic malignant syndrome<\/h3>\n\n\n\n<p id=\"Par33\">Neuroleptic malignant syndrome&nbsp;is a life-threatening complication of many&nbsp;antipsychotic&nbsp;drugs characterized by fever, altered mental status, muscle rigidity, and autonomic dysfunction. In an isolated report, neuroleptic malignant syndrome, in a 74-year-old female with dementia and bipolar disorder 16&nbsp;days after COVID-19 vaccination, has been described [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR69\">69<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec14title\">Acute disseminated encephalomyelitis<\/h3>\n\n\n\n<p id=\"Par34\">Acute disseminated encephalomyelitis (ADEM) is an acute inflammatory demyelinating disorder of the central nervous system. In the majority, ADEM is a post-infectious entity; in many cases, it even develops after vaccination [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR76\">76<\/a>]. In two cases, acute disseminated encephalomyelitis following COVID-19 vaccination has been reported. In first such case a 46-year-old woman received&nbsp;Sinovac inactivated SARS-CoV-2 vaccine before onset of clinical manifestations. Patient was presented with seizures, and magnetic resonance imaging revealed multiple, discrete T2\/FLAIR periventricular. hyperintense lesions. Patient improved following methylprednisolone treatment [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR70\">70<\/a>] Another patient was a 24-year-old female who presented with encephalopathy along with limb weakness of 1-day duration. Two weeks prior, patient was vaccinated with inactivated SARS-CoV-2 vaccine. Magnetic resonance imaging revealed multiple, discrete T2\/FLAIR hyperintense lesions in the brain. Patient improved following treatment with antiepileptics and intravenous immunoglobulins [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR71\">71<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec15title\">Post-vaccinal encephalitis<\/h3>\n\n\n\n<p id=\"Par35\">Zuhorn et al. reported a case series 3 patients, who presented with post-vaccinal encephalitis, akin to autoimmune encephalitis, 7 to 11&nbsp;days after administration of adenovirus-based ChAdOx1 nCov-19 vaccine. All patients fulfilled the diagnostic criteria for possible autoimmune encephalitis. One interesting case had presented with opsoclonus-myoclonus syndrome. Two patients presented with cognitive decline, seizures, and gait disorder. Neuroimaging did not reveal any abnormality. CSF pleocytosis was noted in all three patients. All patients responded well to corticosteroids [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR75\">75<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec16title\">Transverse myelitis<\/h3>\n\n\n\n<p id=\"Par36\">Acute transverse myelitis is an inflammatory spinal cord disorder that clinically manifests with the paraparesis\/quadriparesis, transverse sensory level, and bowel or bladder dysfunction. Acute transverse myelitis usually is a postinfectious disorder. Magnetic resonance imaging demonstrates T2\/FLAIR hyperintensity extending several spinal cord segments. Autoimmunity via mechanism of molecular mimicry is usually responsible for spinal cord dysfunction. Adenoviral vector-based COVID-19 vaccines are more frequently associated with causation of transverse myelitis. In isolated cases, even inactivated virus vaccine and mRNA-based vaccines had precipitated acute demyelination spinal cord syndromes, like multiple sclerosis and neuromyelitis optica. Reports of myelitis associated with vaccination for SARS-CoV-2 are summarized in Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab4\/\">\u200bTable44<\/a>&nbsp;[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR77\">77<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR83\">83<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 4<\/h3>\n\n\n\n<p id=\"__p5\">Clinical, neuroimaging, and outcome details of patients who presented with spinal cord involvement after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Malhotra et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR77\">77<\/a>]<\/td><td>Transverse myelitis<\/td><td>India<\/td><td>36\/M<\/td><td>Viral-vectored, recombinant ChAdOX1 nCoV-19 Covishield vaccine&nbsp;(AstraZeneca vaccine by Serum Institute of India)<\/td><td>On the 8th post-vaccination day<\/td><td>Abnormal sensations in lower limbs with truncal level<\/td><td>T2-hyperintense lesion in the dorsal aspect of spinal cord at C6 and C7 vertebral levels<\/td><td>Methylprednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Fitzsimmons and Nance [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR78\">78<\/a>]<\/td><td>Transverse myelitis<\/td><td>USA<\/td><td>63\/M<\/td><td>Second dose of the Moderna vaccine<\/td><td>Within 1&nbsp;day<\/td><td>Lower back pain, paresthesia in both feet, and pain in lower extremities difficulty in walking and urinary retention<\/td><td>Increased T2 cord signal seen in the distal spinal cord and conus<\/td><td>Intravenous immunoglobulin and methylprednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Tahir et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR79\">79<\/a>]<\/td><td>Transverse myelitis<\/td><td>USA<\/td><td>44\/F<\/td><td>Ad26.COV2.S (Johnson &amp; Johnson) vaccine<\/td><td>10&nbsp;days<\/td><td>Cervical cord transverse myelopathy CSF increased cells<\/td><td>Increased T2 cord signal seen in the spinal cord extending from the C2-3 segment into the upper thoracic region<\/td><td>Plasma exchange and methylprednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Pagenkopf and S\u00fcdmeyer [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR80\">80<\/a>]<\/td><td>Longitudinally extensive transverse myelitis<\/td><td>Germany<\/td><td>45\/M<\/td><td>First dose COVID-19-vaccine (AZD1222, AstraZeneca)<\/td><td>11&nbsp;days<\/td><td>Thoracic back pain and urinary retention<\/td><td>T2 hyperintense signal of the spinal cord with wide axial and longitudinal extent reaching from C3 to Th2<\/td><td>Prednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Helmchen et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR81\">81<\/a>]<\/td><td>Optic neuritis with longitudinal extensive transverse myelitis in stable multiple sclerosis<\/td><td>Germany<\/td><td>40\/F<\/td><td>Astra Zeneca, COVID19 Vaccine\u00ae; Vaxzevria<\/td><td>2&nbsp;weeks<\/td><td>Blindness paraplegia, with absent tendon reflexes in the legs, incontinence, and a sensory deficit for all qualities below Th5. CSF showed severe pleocytosis and elevated protein<\/td><td>Increased longitudinal centrally located signal intensities throughout the thoracic&nbsp;spinal cord<\/td><td>Corticosteroids and plasmapheresis<\/td><td>Improved<\/td><\/tr><tr><td>Havla et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR82\">82<\/a>]<\/td><td>First manifestation of multiple sclerosis<\/td><td>Germany<\/td><td>28\/F<\/td><td>Pfizer-BioNTech COVID-19 vaccine<\/td><td>6&nbsp;days first dose<\/td><td>Myelitis oligoclonal bands<\/td><td>MRI revealed multiple (&gt;\u200920), partially confluent lesions with spatial dissemination but no gadolinium enhancement. Contrast-enhancing lesion at the T6 level, suggestive of myelitis<\/td><td>Methylprednisolone and plasma exchange<\/td><td>Improved<\/td><\/tr><tr><td>Chen et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR83\">83<\/a>]<\/td><td>Neuromyelitis optica spectrum disorder<\/td><td>China<\/td><td>Middle-aged female<\/td><td>The first dose of inactivated virus vaccine<\/td><td>3&nbsp;days<\/td><td>Dizziness and unsteady walking AQP4-positive<\/td><td>MRI scanning of the brain revealed area postrema and bilateral hypothalamus lesions<\/td><td>Methylprednisolone<\/td><td>Improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab4\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<p id=\"Par37\">Malhotra&nbsp;and colleagues reported a 36-year-old patient, who had short-segment myelitis 21&nbsp;days after first dose of adenoviral vector-based (Oxford\/AstraZeneca, COVISHIELD&#x2122;) vaccine. Patient recovered completely after treatment with methylprednisolone [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR77\">77<\/a>]. Fitzsimmons and Nance reported another patient of acute transverse myelitis following Moderna vaccine (an mRNA vaccine). The 63-year-old patient developed symptoms of acute myelopathy within 24&nbsp;h of vaccination. MRI revealed increased T2 cord signal seen in the distal spinal cord and conus. Patient improved considerably following treatment with methylprednisolone and intravenous immunoglobulin [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR78\">78<\/a>].<\/p>\n\n\n\n<p id=\"Par38\">Earlier, in phase III trial of Oxford\/AstraZeneca vaccine, 2 patients had developed transverse myelitis. One of the case of transverse myelitis was reported 14&nbsp;days after booster vaccination. The expert committee considered that this case was the most likely an idiopathic, short segment transverse myelitis. The second case was reported 68&nbsp;days post-vaccination. Experts believed that in this case, transverse myelitis was not likely to be associated with vaccination. This patient was earlier diagnosed as a case of multiple sclerosis [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR84\">84<\/a>,&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR85\">85<\/a>].<\/p>\n\n\n\n<p id=\"Par39\">The pathogenesis of acute transverse myelitis following COVID-19 vaccination remains unknown. Possibly, SARS-CoV-2 antigens present in the COVID-19 vaccine or its adenovirus adjuvant induce immunological reaction in the spinal cord. The occurrence of 3 reported acute transverse myelitis adverse effects among 11,636 participants in the vaccine trials was considered high and a cause of concern [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR86\">86<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec17title\">Bell\u2019s palsy<\/h3>\n\n\n\n<p id=\"Par40\">Several cases of Bell\u2019s palsy have occurred following COVID-19 vaccination. (Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab5\/\">\u200b(Table5)5<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR87\">87<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR95\">95<\/a>]. The instances of Bell\u2019s palsy are most often associated with mRNA vaccines [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR96\">96<\/a>]. Vaccine-associated Bell\u2019s palsy generally responds very well to the oral corticosteroids. The exact pathogenesis remains speculative.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 5<\/h3>\n\n\n\n<p id=\"__p6\">Summary of reported patients, who suffered from Bell\u2019s palsy after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Shemer et al. (a report of 9 cases) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR87\">87<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Israel<\/td><td>35\u201386 (<em>M<\/em>\u2009=\u20095 and&nbsp;<em>F<\/em>\u2009=\u20094)<\/td><td>BNT162b2 SARS-CoV-2 vaccine<\/td><td>4\u201330&nbsp;days after first dose 3 received 2nd dose<\/td><td>Acute facial weakness One had herpes zoster ophthalmicus and herpes zoster oticus<\/td><td>None<\/td><td>Corticosteroids<\/td><td>Not given<\/td><\/tr><tr><td>Repajic et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR88\">88<\/a>]<\/td><td>Bell&#8217;s palsy<\/td><td>USA<\/td><td>57\/F<\/td><td>Pfizer-BioNTech COVID-19 A messenger RNA (mRNA) vaccine<\/td><td>36&nbsp;h after second dose<\/td><td>3 previous episodes of Bell\u2019s palsy ageusia Facial weakness<\/td><td>None<\/td><td>Prednisone<\/td><td>Improved<\/td><\/tr><tr><td>Colella&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR89\">89<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Italy<\/td><td>37\/M<\/td><td>mRNA vaccine BNT162b2<\/td><td>5&nbsp;days after first dose<\/td><td>Acute facial weakness<\/td><td>Not done<\/td><td>Corticosteroids<\/td><td>Improved<\/td><\/tr><tr><td>Martin-Villares et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR90\">90<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Spain<\/td><td>34\/F<\/td><td>Moderna COVID-19 vaccine<\/td><td>2&nbsp;days<\/td><td>Grade III facial palsy She developed a right Bell\u2019s palsy in 2012 during pregnancy (5th month)<\/td><td>None<\/td><td>Corticosteroids<\/td><td>Improved<\/td><\/tr><tr><td>Nishizawa et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR91\">91<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Japan<\/td><td>62\/F<\/td><td>Ad26.COV2.S vaccination<\/td><td>20&nbsp;days<\/td><td>House-Brackmann score 4 Bell\u2019s Palsy<\/td><td>Normal<\/td><td>None<\/td><td>None<\/td><\/tr><tr><td>G\u00f3mez de Terreros et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR92\">92<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Spain<\/td><td>50\/M<\/td><td>Pfizer-BNT162b2 mRNA vaccine<\/td><td>9&nbsp;days<\/td><td>Muscle weakness on the left side of his face<\/td><td>Normal<\/td><td>Corticosteroids<\/td><td>Improved<\/td><\/tr><tr><td>Burrows&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR93\">93<\/a>]<\/td><td>Sequential contralateral facial nerve palsies<\/td><td>UK<\/td><td><\/td><td>First and second doses of the Pfizer-BioNTech COVID-19 vaccine<\/td><td>Right palsy, 5&nbsp;h Left palsy after 2&nbsp;days<\/td><td>Two discrete contralateral episodes of Bell\u2019s palsy<\/td><td>Normal<\/td><td>Prednisolone<\/td><td>Improved both the time<\/td><\/tr><tr><td>Obermann&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR94\">94<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Germany<\/td><td>21\/F<\/td><td>First dose of SARS-CoV-2 mRNA vaccine Comirnaty (BNT162b2, BioNTech\/Pfizer)<\/td><td>2&nbsp;day<\/td><td>Facial muscle paralysis SARS-CoV-2 antibodies were present in blood and CSF<\/td><td>Normal<\/td><td>Prednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Iftikhar et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR95\">95<\/a>]<\/td><td>Bell\u2019s palsy<\/td><td>Qatar<\/td><td>36\/M<\/td><td>Second dose of the mRNA-1273&nbsp;vaccine<\/td><td>1&nbsp;day<\/td><td>Facial palsy<\/td><td>Normal<\/td><td>Prednisolone<\/td><td>Improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab5\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<p id=\"Par41\">In a case\u2013control study, Shemer&nbsp;et al. compared clinical parameters of patients with Bell\u2019s palsy following mRNA vaccination with that of patients with Bell\u2019s palsy without vaccination. Out of 37 patients, 21 had received vaccination. Bell\u2019s palsy developed within 2&nbsp;weeks following first dose of COVID-19 vaccination. There was no difference in any of the clinical parameter between vaccinated or unvaccinated groups [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR97\">97<\/a>].<\/p>\n\n\n\n<p id=\"Par42\">Earlier, in the Pfizer-BioNTech clinical trial, which included 44,000 participants, 4 people had Bell\u2019s palsy. No case of Bell\u2019s palsy was reported in the placebo arm. In the Moderna trial, which included 30,400 participants, 3 vaccine recipients reported Bell\u2019s palsy. One person was in the placebo arm [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR98\">98<\/a>]. An article, published in&nbsp;the Lancet, analyzed the combined phase 3 data of Pfizer and Moderna trials and noted that the rate of Bell\u2019s palsy was higher than expected [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR98\">98<\/a>].<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec18title\">Other cranial nerve involvement<\/h2>\n\n\n\n<p id=\"Par43\">In isolated instances, mRNA vaccines were found associated with olfactory dysfunction and sixth cranial nerve palsy (Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab6\/\">\u200b(Table6)6<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR99\">99<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR104\">104<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 6<\/h3>\n\n\n\n<p id=\"__p7\">Summary of reported patients, who suffered from cranial nerve involvement (other than Bell\u2019s palsy) after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Konstantinidis et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR99\">99<\/a>] Report of 2 patients<\/td><td>Olfactory dysfunction<\/td><td>Greece<\/td><td>Both female<\/td><td>Pfizer-BioNTech BNT162b2<\/td><td>3 and 5&nbsp;days after second dose<\/td><td>Hyposmia after their second dose<\/td><td>None<\/td><td>Olfactory training<\/td><td>Improved<\/td><\/tr><tr><td>Keir et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR100\">100<\/a>]<\/td><td>Phantosmia<\/td><td>USA<\/td><td>57\/F<\/td><td>Pfizer-BioNTech COVID-19 vaccination Second dose<\/td><td>None<\/td><td>Feeling weak, fatigued, with random episodes of \u2018\u2018smelling smoke\u2019\u2019 associated with hyposmia<\/td><td>Postcontrast CT demonstrates faint enhancement left olfactory tract MRI enhancement of the left greater than right olfactory bulb and bilateral olfactory tracts<\/td><td>None<\/td><td>None<\/td><\/tr><tr><td>Reyes-Capo et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR101\">101<\/a>]<\/td><td>Acute abducens nerve palsy<\/td><td>USA<\/td><td>59\/F<\/td><td>Pfizer-BioNTech COVID-19 vaccine<\/td><td>2&nbsp;days<\/td><td>Fever for 1&nbsp;day followed by diplopia<\/td><td>Normal MRI of brain and orbits<\/td><td>Not available<\/td><td>Sensory-motor examination remained unchanged in recent follow-up<\/td><\/tr><tr><td>Parrino et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR102\">102<\/a>]<\/td><td>Tinnitus<\/td><td>Italy<\/td><td>37\/F 63\/ 30\/M<\/td><td>BNT162b2 mRNA-vaccine<\/td><td>7-h first dose 20&nbsp;h 7&nbsp;days<\/td><td>Sudden unilateral tinnitus<\/td><td>Normal MRI<\/td><td>Corticosteroids, in two<\/td><td>Improved all<\/td><\/tr><tr><td>Tseng&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR103\">103<\/a>&nbsp;] PMID:&nbsp;<strong>34,297,133<\/strong><\/td><td>Reversible tinnitus and cochleopathy<\/td><td>Taiwan<\/td><td>32\/M<\/td><td>First dosage of the AstraZeneca COVID-19 vaccine<\/td><td>5&nbsp;h<\/td><td>High-pitch tinnitus and disturbed the normal hearing high fever with chills and myalgia<\/td><td>Not done<\/td><td>Corticosteroids<\/td><td>Improved<\/td><\/tr><tr><td>Narasimhalu&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR104\">104<\/a>]<\/td><td>Trigeminal and cervical radiculitis<\/td><td>Singapore<\/td><td>52\/F<\/td><td>Pfizer-BioNTech vaccination (tozinameran)<\/td><td>3&nbsp;h first dose<\/td><td>Numbness, swelling and pain over the left face and neck<\/td><td>MRI of trigeminal nerve revealed thickening and perineural sheath enhancement of the V3 segment of the left trigeminal nerve The MRI of the cervical spine revealed spondylotic changes<\/td><td>Pregabalin<\/td><td>Improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab6\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec19title\">Olfactory dysfunction<\/h3>\n\n\n\n<p id=\"Par44\">Olfactory dysfunction is the most frequent neurological complication of COVID-19. Konstantinidis and colleagues reported two cases of smell impairment after second dose of the BioNTechBNT162b2 vaccine (Pfizer) administration [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR51\">51<\/a>].<\/p>\n\n\n\n<p id=\"Par45\">Keir and colleagues reported phantosmia following administration of Pfizer COVID-19 vaccine. Patient complained of constantly \u201csmelling smoke\u201d and headaches.&nbsp;MRI of brain of the patient showed enhancement of the olfactory bulbs and bilateral olfactory tracts [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR100\">100<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec20title\">Abducens nerve palsy<\/h3>\n\n\n\n<p id=\"Par46\">Reyes-Capo et al. reported a 59-year-old lady, who presented with an abducen nerve palsy 2&nbsp;days post-vaccination (Pfizer-BioNTech mRNA vaccine). Neuroimaging in this patient was normal..<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec21title\">Otologic manifestations<\/h3>\n\n\n\n<p id=\"Par47\">A variety of otologic manifestations has been noted following COVID-19 vaccination. Parrino and colleagues described three patients with sudden unilateral tinnitus following BNT162b2 mRNA vaccine administration. Tinnitus rapidly resolved in 2 cases. Wichova and colleagues in a retrospective review recorded 30 patients, who either had significantly exacerbated otologic symptoms or had a new symptom after getting mRNA vaccine. Post-vaccination otologic manifestations included hearing loss with tinnitus, dizziness, or with vertigo. In some patients, with Meni\u00e8re&#8217;s disease or autoimmune inner ear disease, vaccine led to exacerbation of the pre-existing otologic symptoms [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR102\">102<\/a>,<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR105\">105<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec22title\">Acute vision loss<\/h3>\n\n\n\n<p id=\"Par48\">Santovito and Pinna reported an unusual patient, who developed acute visual impairment following the 2nd dose of the Pfizer-BioNTech COVID-19 vaccine. Prior to visual symptoms, patient experienced unilateral headache. He also reported mild confusion, asthenia, and profound nausea. His symptoms got relieved after taking analgesics. Possibly, patient had an acute attack of migraine with aura that got precipitated by the vaccine [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR106\">106<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec23title\">Guillain-Barr\u00e9 syndrome<\/h3>\n\n\n\n<p id=\"Par49\">Guillain-Barr\u00e9 syndrome is a post-infectious disorder of peripheral nerve manifesting with lower motor neuron type of sensory-motor quadriparesis. Acute motor weakness is frequently preceded by an antecedent microbial infection. There are numerous reports indicating that COVID-19 infection can trigger Guillain-Barr\u00e9 syndrome.&nbsp;The US Food and Drug Administration has recently expressed its concern regarding a possible association between the Johnson and Johnson COVID-19 vaccine with Guillain-Barr\u00e9 syndrome [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR107\">107<\/a>].<\/p>\n\n\n\n<p id=\"Par50\">After emergency use approvals, all kinds of COVID-19 vaccines were found associated with Guillain-Barr\u00e9 syndrome. Adenovector-based vaccines were more frequently associated with Guillain-Barr\u00e9 syndrome. Earlier, in phase 3 trial of Johnson and Johnson adenovirus vector-based COVID-19 vaccine, 2 patients developed Guillain-Barr\u00e9 syndrome. One patient belonged to vaccine group and other to placebo group. Both patients had Guillain-Barr\u00e9 syndrome within 2&nbsp;weeks of&nbsp;receiving injections. The Guillain-Barr\u00e9 syndrome in the vaccine arm was preceded by chills, nausea, diarrhea, and myalgia [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR108\">108<\/a>,&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR109\">109<\/a>].<\/p>\n\n\n\n<p id=\"Par51\">Post-vaccination Guillain-Barr\u00e9 syndrome generally affects older adults within 2&nbsp;weeks of vaccine administration. Clinical presentation is similar to acute demyelinating neuropathy; nerve conduction studies show demyelinating pattern, and CSF examination shows cyto-albuminic dissociation. Many patients present only with facial diplegia. Response to immunotherapy is generally good. (Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab7\/\">\u200b(Table7)7<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR110\">110<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR126\">126<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 7<\/h3>\n\n\n\n<p id=\"__p8\">Summary of reported patients, who developed an acute peripheral nerve disorder after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Waheed et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR110\">110<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>USA<\/td><td>82\/F<\/td><td>Pfizer-BioNTech COVID-19 A messenger RNA (mRNA) vaccine<\/td><td>2&nbsp;weeks<\/td><td>Areflexic paraparesis with distal sensory loss CSF showed albuminocytologic dissociation<\/td><td>enhancement of cauda equina nerve roots<\/td><td>IV immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>M\u00e1rquez Loza et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR111\">111<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>USA<\/td><td>60\/F<\/td><td>Johnson &amp; Johnson, d26.COV2.S, a recombinant adenovirus serotype 26 (Ad26) vector vaccine<\/td><td>2&nbsp;weeks<\/td><td>Ophthalmoplegia, facial diplegia and Areflexic quadriparesis CSF showed albuminocytologic dissociation<\/td><td>Enhancement of cauda equina nerve roots<\/td><td>IV immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>Patel et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR112\">112<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>UK<\/td><td>37\/M<\/td><td>COVID-19 ChAdOx1 vaccine adenovirus-vectored vaccine Oxford AstraZeneca<\/td><td>2&nbsp;weeks<\/td><td>Symmetrical, progressive ascending muscle weakness areflexic bilaterally in the lower limbs<\/td><td>Cauda equina nerve root enhancement<\/td><td>Intravenous immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>Razok et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR113\">113<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>Qatar<\/td><td>73\/M<\/td><td>Pfizer-BioNTech COVID-19 vaccine<\/td><td>20&nbsp;days Second dose<\/td><td>Acute bilateral lower limb weakness<\/td><td>None<\/td><td>IVIG<\/td><td>Improved<\/td><\/tr><tr><td>Ogbebor et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR114\">114<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>US<\/td><td>86\/3F<\/td><td>Pfizer-BioNTech COVID-19 vaccine<\/td><td>1&nbsp;day<\/td><td>Weakness in her bilateral lower extremities and by day 6, she could no longer walk CSF\u2009=\u2009a protein 162&nbsp;mg\/dL and glucose (49&nbsp;mg\/dL)<\/td><td>None<\/td><td>Intravenous immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>Finsterer&nbsp; [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR115\">115<\/a>]<\/td><td>Exacerbating Guillain-Barr\u00e9 syndrome<\/td><td>Austria<\/td><td>32\/M<\/td><td>A vector-based COVID-19 vaccine<\/td><td>8&nbsp;days<\/td><td>Paresthesia&nbsp;and dysphagia bilateral frontal and nuchal headache<\/td><td>None<\/td><td>Intravenous immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>Marammatom&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR116\">116<\/a>] Report of 7 cases<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>India<\/td><td><\/td><td>ChAdOx1-S\/nCoV-19 adenovector-based vaccine<\/td><td>Within 2&nbsp;weeks of the first dose<\/td><td>All patients progressed to areflexic quadriplegia 2 cases required mechanical ventilation All 7 cases had bilateral facial paresis Four patients (57%) also developed other cranial neuropathies (4th and 5th<sup>)<\/sup><\/td><td>In two patients, MRI brain and spine were normal<\/td><td>Intravenous immunoglobulin<\/td><td>One recovered Rest six still bed bound<\/td><\/tr><tr><td>Allen et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR117\">117<\/a>] Report of 4 cases<\/td><td>Guillain-Barr\u00e9 syndrome variant<\/td><td>UK<\/td><td>20\u201357 all males<\/td><td>Oxford-AstraZeneca SARS-CoV2 vaccine<\/td><td>Within 3&nbsp;weeks<\/td><td>Facial weakness in 1 facial diplegia in 3 areflexic quadriparesis in 1 Cyto-albuminic dissociation in all<\/td><td>MRI of the brain and whole spine with contrast showed enhancement of the facial nerve within the right internal auditory canal<\/td><td>Intravenous immunoglobulin, oral steroids, or no treatment<\/td><td>All improved<\/td><\/tr><tr><td>Kohli et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR118\">118<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>India<\/td><td>71\/M<\/td><td>Covishield, AstraZeneca, University of Oxford<\/td><td>6&nbsp;days<\/td><td>Areflexic quadriparesis with bulbar palsy NCV- demyelinating pattern<\/td><td>None<\/td><td>Intravenous immunoglobulin and mechanical ventilation<\/td><td>Improved<\/td><\/tr><tr><td>Azam et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR119\">119<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>UK<\/td><td>67\/M<\/td><td>The first dose of the AstraZeneca COVID-19<\/td><td>15&nbsp;days<\/td><td>Areflexic quadriparesis with facial diplegiaNCV- demyelinating pattern<\/td><td>Normal<\/td><td>Intravenous immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>Hasan&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR120\">120<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>UK<\/td><td>62\/F<\/td><td>First dose of the Oxford\/AstraZeneca COVID-19 vaccine<\/td><td><\/td><td>Weakness of bilateral lower limbs preceded by paresthesia and numbness a flaccid-type paraplegia NCV- demyelinating pattern CSF-albumin-cytological dissociation<\/td><td>Normal<\/td><td>Intravenous immunoglobulin<\/td><td>The patient remains in the ICU<\/td><\/tr><tr><td>Theuriet et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR121\">121<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>France<\/td><td>72\/M<\/td><td>First dose of ChAdOx1 nCoV-19 vaccine (VaxZevria\/Oxford-AstraZeneca)<\/td><td>3&nbsp;weeks<\/td><td>Areflexic quadriparesis with facial diplegia NCV- demyelinating pattern<\/td><td>None<\/td><td>Intravenous immunoglobulin<\/td><td>The patient remains in the ICU<\/td><\/tr><tr><td>Bonifacio et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR122\">122<\/a>] (A series of 5 cases)<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>UK<\/td><td>43\/M 51&nbsp;M 53\/M 66\/m 71\/f<\/td><td>Vaxzevria AstraZeneca, University of Oxford COVID-19 vaccine<\/td><td>11&nbsp;days 7&nbsp;days 7&nbsp;days 8&nbsp;days 12&nbsp;days<\/td><td>Bilateral facial weakness with paresthesia variant of Guillain-Barr\u00e9 syndrome NCV- demyelinating pattern in 4 patients<\/td><td>Bilateral contrast enhancement along whole facial nerve in 3 patients<\/td><td>Intravenous immunoglobulin Was given in 2 patients<\/td><td>All improved<\/td><\/tr><tr><td>Nasuelli&nbsp;et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR123\">123<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>Italy<\/td><td>59\/M<\/td><td>ChAdOx1 nCoV-19 vaccine<\/td><td>10&nbsp;days<\/td><td>Areflexic quadriparesis with facial diplegia NCV- demyelinating pattern in 4 patients CSF-albumin-cytological dissociation<\/td><td>Normal<\/td><td>Intravenous immunoglobulin<\/td><td>Improved<\/td><\/tr><tr><td>Jain et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR124\">124<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>USA<\/td><td>65\/F<\/td><td>Ad26.COV2.S (Johnson &amp; Johnson) vaccine<\/td><td>19&nbsp;days<\/td><td>Facial diplegia<\/td><td>Normal<\/td><td>Intravenous immunoglobulin And plasmapheresis<\/td><td>Improved<\/td><\/tr><tr><td>McKean and Chircop [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR125\">125<\/a>]<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>Malta<\/td><td>48\/M<\/td><td>Vaxzevria AstraZeneca, University of Oxford COVID-19 vaccine First dose<\/td><td>10&nbsp;days<\/td><td>Facial diplegia and severe back pain ascending paresthesia and bilateral progressive areflexic lower limb weakness. CSF-albumin-cytological dissociation NCV multifocal sensorimotor demyelinating polyneuropathy<\/td><td>Normal<\/td><td>Intravenous immunoglobulin and oral prednisolone<\/td><td>Improved<\/td><\/tr><tr><td>Bonifacio et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR126\">126<\/a>] (a report of 5 cases)<\/td><td>Guillain-Barr\u00e9 syndrome<\/td><td>UK<\/td><td><\/td><td><\/td><td><\/td><td><\/td><td><\/td><td><\/td><td><\/td><\/tr><tr><td>Waheed et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR127\">127<\/a>]<\/td><td>Small fiber neuropathy<\/td><td>USA<\/td><td>57\/F<\/td><td>Pfizer-BioNTech COVID-19 A messenger RNA (mRNA) vaccine (Second dose)<\/td><td>Subacute onset<\/td><td>Intense burning dysesthesias in the feet gradually spreading to the calves and minimally into the hands (Nerve biopsy proved small fiber neuropathy)<\/td><td>None<\/td><td>Gabapentin<\/td><td>Symptomatic improvement<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab7\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<p id=\"Par52\">Proposed pathogenesis of Guillain-Barr\u00e9 syndrome&nbsp;is an autoantibody-mediated immunological damage of peripheral nerves via mechanism of molecular mimicry between structural components of peripheral nerves and the microorganism. Lately, several cases of Guillain-Barr\u00e9 syndrome&nbsp;following COVID-19 vaccination have also been reported.<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec24title\">Small fiber neuropathy<\/h3>\n\n\n\n<p id=\"Par53\">Waheed et al. described a 57-year-old female, who presented with painful neuropathy following administration of the mRNA COVID-19 vaccine. Patient subacutely presented with intense peripheral burning sensations. Electrodiagnostic studies were normal. Skin biopsy proved small fiber neuropathy. Patient responded to gabapentin.(Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab7\/\">\u200bgabapentin.(Table7)7<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR127\">127<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec25title\">Parsonage-Turner syndrome<\/h3>\n\n\n\n<p id=\"Par54\">Parsonage-Turner syndrome or neuralgic amyotrophy is clinically manifested with acute unilateral shoulder pain followed by brachial plexopathy. Parsonage-Turner syndrome is usually triggered by any infection, surgery, or rarely vaccination. In many reports, Parsonage-Turner syndrome has been described following COVID-19 vaccination.(Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab8\/\">\u200bvaccination.(Table8)8<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR128\">128<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR130\">130<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 8<\/h3>\n\n\n\n<p id=\"__p11\">Summary of reported patients, who developed neuralgic amyotrophy after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Mahajan et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR128\">128<\/a>]<\/td><td>Parsonage-Turner syndrome<\/td><td>USA<\/td><td>50\/M<\/td><td>COVID-19 BNT162b2 vaccination<\/td><td>7&nbsp;days<\/td><td>Sudden onset of severe left periscapular pain&nbsp;after first dose One week after the second dose, the patient developed left hand grip and left wrist extension weakness. Electromyography showed decreased motor unit recruitment<\/td><td>Normal<\/td><td>Corticosteroids<\/td><td>Improved<\/td><\/tr><tr><td>Diaz-Segarra et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR129\">129<\/a>]<\/td><td>Painless idiopathic neuralgic amyotrophy<\/td><td>USA<\/td><td>35\/F<\/td><td>Pfizer-BioNTech COVID-19 vaccine<\/td><td>9&nbsp;days<\/td><td>New-onset painless left arm weakness, numbness, and paresthesias<\/td><td>Cervical spine computed tomography showed mild degenerative changes without foraminal narrowing<\/td><td>High-dose prednisone<\/td><td>Improved<\/td><\/tr><tr><td>Antonio Crespo Burillo et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR130\">130<\/a>]<\/td><td>Parsonage-Turner syndrome<\/td><td>Spain<\/td><td>38\/M<\/td><td>Vaxzevria (AstraZeneca)<\/td><td>4&nbsp;days<\/td><td>Shoulder and arm pain Electrophysiology suggested brachial plexopathy<\/td><td>MRI of the shoulder revealed a mild left subacromial tendinopathy<\/td><td>Methylprednisolone<\/td><td>Improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab8\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec26title\">Herpes zoster<\/h3>\n\n\n\n<p id=\"Par55\">Herpes zoster occurs following reactivation of varicella&nbsp;zoster&nbsp;virus. Patients with herpes zoster present with the classic maculopapular rash, which is unilateral, confined to a single dermatome. The rash disappears in 7 to 10&nbsp;days. Postherpetic neuralgia is the frequent complication of herpes zoster, which is noted in 1 in 5 patients.&nbsp;McMahon and co-workers recorded 414 cutaneous reactions to mRNA COVID-19 vaccines, and 5 (1.9%) were diagnosed with herpes zoster [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR131\">131<\/a>]. Other types of COVID-19 vaccines are infrequently associated with post-vaccination reactivation of herpes zoster. It has been suggested that vaccine-induced immunomodulation, resulting in dysregulation of T cell function, is responsible for reactivation of herpes zoster virus [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR132\">132<\/a>,&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR133\">133<\/a>]. Reports of herpes zoster reactivation after vaccine against SARS-CoV-2 are summarized in Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab9\/\">\u200bTable99<\/a>&nbsp;[<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR134\">134<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR142\">142<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 9<\/h3>\n\n\n\n<p id=\"__p12\">Summary of reported patients, who developed Herpes zoster after vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Tessas and Kluger [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR134\">134<\/a>]<\/td><td>Herpes zoster<\/td><td>Finland<\/td><td>44\/M<\/td><td>BNT162b2 mRNA COVID-19 vaccine<\/td><td>7&nbsp;days<\/td><td>Herpetiform vesicular and erythematous rash on the left upper back<\/td><td>None<\/td><td>Oral valacyclovir<\/td><td>Improved<\/td><\/tr><tr><td>Rodr\u00edguez-Jim\u00e9nez et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR135\">135<\/a>]&nbsp;A report of 5 cases<\/td><td>Herpes zoster<\/td><td>Spain<\/td><td>39\u201358 F\u2009=\u20093<\/td><td>BNT162b2 mRNA COVID-19vaccine (Pfizer)<\/td><td>1\u201316 (4 less than 7&nbsp;days)<\/td><td>Painful herpetiform dermatomal rash<\/td><td>None<\/td><td>None<\/td><td>None<\/td><\/tr><tr><td>Eid et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR136\">136<\/a>]<\/td><td>Herpes zoster<\/td><td>Lebanon<\/td><td>79\/M<\/td><td>mRNA COVID vaccine<\/td><td>6&nbsp;days<\/td><td>Painful herpetiform dermatomal rash<\/td><td>None<\/td><td>Antiviral treatment<\/td><td>Improved<\/td><\/tr><tr><td>Bostan and Yalici-Armagan [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR137\">137<\/a>]<\/td><td>Herpes zoster<\/td><td>Turkey<\/td><td>78\/M<\/td><td>Inactivated COVID-19 vaccine<\/td><td><\/td><td>Erythematous, painful, and pruritic lesions on chest<\/td><td><\/td><td><\/td><td><\/td><\/tr><tr><td>Furer et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR138\">138<\/a>]&nbsp;(a report of 6 cases)<\/td><td>Herpes zoster<\/td><td>Israel<\/td><td>36\u201361 All females<\/td><td>BNT162b2 mRNA vaccination<\/td><td>3 -14&nbsp;days<\/td><td>All had autoimmune inflammatory rheumatic diseases Herpes zoster ophthalmicus in one Truncal herpes zoster in others<\/td><td>Not done<\/td><td>NA<\/td><td>NA<\/td><\/tr><tr><td>Aksu and \u00d6zt\u00fcrk et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR139\">139<\/a>]<\/td><td>Herpes zoster<\/td><td>Turkey<\/td><td>68\/M<\/td><td>The inactivated COVID-19 vaccine<\/td><td>5&nbsp;days<\/td><td>multiple pinheaded vesicular lesions upon an erythematous base occupying an area on his right mammary region and back corresponding to T3\u2013T5 dermatomes<\/td><td>Not done<\/td><td>Valacyclovir paracetamol<\/td><td>Improved<\/td><\/tr><tr><td>Chiu et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR140\">140<\/a>]&nbsp;(a report of 3 cases)<\/td><td>Herpes zoster<\/td><td>Taiwan<\/td><td>71\/M 46\/M 42\/M<\/td><td>Pfizer-BNT162b2 mRNA and Moderna mRNA-1273<\/td><td>2&nbsp;days 7&nbsp;days 2&nbsp;days<\/td><td>Erythematous papules and vesicle in dermatomal pattern<\/td><td>Not done<\/td><td>Oral acyclovir<\/td><td>All improved<\/td><\/tr><tr><td>Alpalh\u00e3o and Filipe et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR141\">141<\/a>]&nbsp;(a report of 4 cases)<\/td><td>Herpes zoster<\/td><td>Portugal<\/td><td>NA<\/td><td>Pfizer\u2019s Comirnaty&#x2122; vaccine AstraZeneca Vaxzevria&#x2122; vaccine<\/td><td>3\u20136&nbsp;days<\/td><td>Erythematous papules and vesicle in dermatomal pattern<\/td><td>Not done<\/td><td>Valacyclovir<\/td><td>All improved<\/td><\/tr><tr><td>Channa et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR142\">142<\/a>]<\/td><td>Herpes zoster<\/td><td>USA<\/td><td>81\/M<\/td><td>mRNA-1273 (Moderna) Covid-19 vaccine<\/td><td>3&nbsp;days<\/td><td>A dermatomal rash<\/td><td>Not done<\/td><td>Not available<\/td><td>Not available<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab9\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"Sec27title\">Myositis and rhabdomyolysis<\/h3>\n\n\n\n<p id=\"Par56\">There are reports, which have indicated that COVID-19 vaccines have potential to damage the skeletal muscles as well (Table&nbsp;<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab10\/\">\u200b(Table10)10<\/a>) [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR143\">143<\/a>\u2013<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR147\">147<\/a>]. Tan and colleagues described a patient with a known carnitine palmitoyltransferase-II deficiency disorder, who developed fever, vomiting, shortness of breath, frank haematuria, myalgia and muscle weakness within four hours of receiving AstraZeneca COVID-19 vaccine [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR143\">143<\/a>]. Theodorou and colleagues described a 56-year-old woman who, 8&nbsp;days after a second dose of vaccine administration, developed severe left upper arm pain along restricted shoulder movements. Her serum creatine kinase was elevated suggesting skeletal muscle damage. MRI revealed severely edematous deltoid muscles. Contrast-enhanced imaging demonstrated enhancement of deltoid muscles suggestive of myositis [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR146\">146<\/a>].<\/p>\n\n\n\n<h3 class=\"wp-block-heading\">Table 10<\/h3>\n\n\n\n<p id=\"__p13\">Summary of reported patients, who developed an acute muscular disorder following vaccination against SARS-CoV-2<\/p>\n\n\n\n<figure class=\"wp-block-table is-style-regular\"><table><thead><tr><th>Reference<\/th><th>Neurological complication<\/th><th>Country<\/th><th>Age\/sex<\/th><th>Vaccine type<\/th><th>Duration after vaccination<\/th><th>Clinical features<\/th><th>Neuroimaging<\/th><th>Treatment<\/th><th>Outcome<\/th><\/tr><\/thead><tbody><tr><td>Tan et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR143\">143<\/a>]<\/td><td>Rhabdomyolysis in a patient with Carnitine palmitoyltransferase II deficiency<\/td><td>UK<\/td><td>27\/M<\/td><td>COVID-19 vaccine AstraZeneca<\/td><td>5&nbsp;h<\/td><td>Fever, vomiting, shortness of breath, frank hematuria, and myalgia CK concentration of 105,000 U\/L and deranged liver function tests (ALT 300 U\/L and AST 1496 U\/L)<\/td><td>None<\/td><td>Continuous intravenous dextrose 10% and a high carbohydrate diet<\/td><td>Improved<\/td><\/tr><tr><td>Mack et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR144\">144<\/a>]<\/td><td>Rhabdomyolysis<\/td><td>USA<\/td><td>80\/M<\/td><td>Second dose of Moderna COVID-19 vaccine<\/td><td>2&nbsp;days<\/td><td>Generalized body aches, nausea, and vomiting elevated CK<\/td><td>None<\/td><td>IV fluids<\/td><td>Improved<\/td><\/tr><tr><td>Nassar et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR145\">145<\/a>]<\/td><td>Rhabdomyolysis<\/td><td>USA<\/td><td>21\/M<\/td><td>First Pfizer\/BioNTech COVID-19 vaccine<\/td><td>1&nbsp;day<\/td><td>Severe back pain with radiation to his left lateral thigh Creatinine phosphokinase (CPK) level more than 22,000 U\/L<\/td><td>Normal<\/td><td>IV fluids<\/td><td>Improved<\/td><\/tr><tr><td>Theodorou et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR146\">146<\/a>]<\/td><td>Myositis<\/td><td>Greece<\/td><td>56\/F<\/td><td>Modified mRNA COVID-19 vaccine<\/td><td>8&nbsp;days after second dose<\/td><td>There was tenderness over the deltoid muscle, guarding, and decreased abduction of the shoulder and arm along with elevated CPK<\/td><td>On MRI, the deltoid muscle was edematous. On contrast enhancement, muscle exhibited enhancement indicating inflammation<\/td><td>Symptomatic<\/td><td>Improved<\/td><\/tr><tr><td>Godoy et al. [<a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/#CR147\">147<\/a>]<\/td><td>Myositis ossificans<\/td><td>Brazil<\/td><td>51\/M<\/td><td><\/td><td>3&nbsp;months<\/td><td>Right upper arm pain, soreness and palpable mass<\/td><td>Intramuscular nodule n the proximal fibers of the brachii muscle with perilesional muscle edema One week later, CT showed a hypoattenuating intramuscular nodule with internal calcifications<\/td><td>NSAIDs<\/td><td>Improved<\/td><\/tr><\/tbody><\/table><\/figure>\n\n\n\n<p><a href=\"https:\/\/www.ncbi.nlm.nih.gov\/pmc\/articles\/PMC8557950\/table\/Tab10\/?report=objectonly\">Open in a separate window<\/a><\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Sec28title\">Conclusion<\/h2>\n\n\n\n<p id=\"Par57\">Post-authorization, a wide spectrum of serious neurological complications has been reported following COVID-19 vaccination. The most devastating neurological complication is cerebral venous sinus thrombosis that has been reported in females of childbearing age following adenovector-based vaccines. Another major neurological complication of concern is Bell\u2019s palsy that was reported dominantly following mRNA vaccine administration. Transverse myelitis, acute disseminated encephalomyelitis, and Guillain-Barr\u00e9 syndrome are other severe unexpected post-vaccination complications that can occur as result of molecular mimicry and subsequent neuronal damage. Most of other serious neurological complications are reported in either in form of isolated case reports or small cases series. A causal association of these adverse events is controversial; large collaborative prospective studies are needed to prove causality.<\/p>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"Bib1title\">References<\/h2>\n\n\n\n<p>1.&nbsp;World Health Organization. 12 January 2021. WHO Coronavirus (COVID-19) Dashboard. &amp;It; The World Health Organization&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/covid19.who.int\/\" target=\"_blank\">https:\/\/covid19.who.int\/<\/a>. Accessed 1 Aug&nbsp;2021.<\/p>\n\n\n\n<p>2.&nbsp;Jeff Craven. 10 June 2021. COVID-19 vaccine tracker. &amp;It;&nbsp;<a rel=\"noreferrer noopener\" href=\"https:\/\/www.raps.org\/news-and-articles\/news-articles\/2020\/3\/covid-19-vaccine-tracker\/\" target=\"_blank\">https:\/\/www.raps.org\/news-and-articles\/news-articles\/2020\/3\/covid-19-vaccine-tracker<\/a>. Accessed 16 June 2021.<\/p>\n\n\n\n<p>3.&nbsp;Piyasirisilp S, Hemachudha T. 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