Literature DB >> 35435264

Clinical symptoms, diagnosis, treatment, and outcome of COVID-19-associated encephalitis: A systematic review of case reports and case series.

Maryam Koupaei1, Negar Shadab Mehr2, Mohamad Hosein Mohamadi2, Arezoo Asadi3,4, Sajjad Abbasimoghaddam2, Amirhosein Shekartabar2, Mohsen Heidary5,6, Fazlollah Shokri7.   

Abstract

INTRODUCTION: Since COVID-19 outbreak, various studies mentioned the occurrence of neurological disorders. Of these, encephalitis is known as a critical neurological complication in COVID-19 patients. Numerous case reports and case series have found encephalitis in relation to COVID-19, which have not been systematically reviewed. This study aims to evaluate the clinical symptoms, diagnosis, treatment, and outcome of COVID-19-associated encephalitis.
METHODS: We used the Pubmed/Medline, Embase, and Web of Science databases to search for reports on COVID-19-associated encephalitis from January 1, 2019, to March 7, 2021. The irrelevant studies were excluded based on screening and further evaluation. Then, the information relating diagnosis, treatment, clinical manifestations, comorbidities, and outcome was extracted and evaluated.
RESULTS: From 4455 initial studies, 45 articles met our criteria and were selected for further evaluation. Included publications reported an overall number of 53 COVID-19-related encephalitis cases. MRI showed hyperintensity of brain regions including white matter (44.68%), temporal lobe (17.02%), and thalamus (12.76%). Also, brain CT scan revealed the hypodensity of the white matter (17.14%) and cerebral hemorrhages/hemorrhagic foci (11.42%) as the most frequent findings. The IV methylprednisolone/oral prednisone (36.11%), IV immunoglobulin (27.77%), and acyclovir (16.66%) were more preferred for COVID-19 patients with encephalitis. From the 46 patients, 13 (28.26%) patients were died in the hospital.
CONCLUSION: In this systematic review, characteristics of COVID-19-associated encephalitis including clinical symptoms, diagnosis, treatment, and outcome were described. COVID-19-associated encephalitis can accompany with other neurological symptoms and involve different brain. Although majority of encephalitis condition are reversible, but it can lead to life-threatening status. Therefore, further investigation of COVID-19-associated encephalitis is required.
© 2022 The Authors. Journal of Clinical Laboratory Analysis published by Wiley Periodicals LLC.

Entities:  

Keywords:  COVID-19; SARS-CoV-2; encephalitis; systematic review

Mesh:

Year:  2022        PMID: 35435264      PMCID: PMC9102669          DOI: 10.1002/jcla.24426

Source DB:  PubMed          Journal:  J Clin Lab Anal        ISSN: 0887-8013            Impact factor:   3.124


INTRODUCTION

Humans have been struggling with the COVID‐19 epidemic for nearly 2 years. As of early August 2020, more than 17.5 million cases of COVID‐19 were identified in 188 countries, including 680,000 deaths. The disease that often has respiratory symptoms but sometimes also has extrapulmonary manifestations such as neurological symptoms. On average, neurological symptoms appear three weeks after respiratory symptoms. Less common clinical manifestations of COVID‐19 include headache, brain status alteration, chest pain, abdominal pain, diarrhea, and nausea. Nervous manifestations can range from a mild nervous agitation to severe encephalitis. The roll of central nervous system in SARS‐CoV‐2 epidemic has been determined. Ischemic stroke, central nervous system (CNS) inflammation, encephalopathy, and myelitis are common clinical manifestations of the CNS in COVID‐19 patients. Encephalitis means inflammation of the brain, which is mainly caused by the autoimmune process and/or the viral infection. Encephalitis is one of the main and devastating complications associated with CNS. In previous epidemics, MERS‐CoV and SARS‐CoV viruses have caused brain complications such as polyneuropathy, ischemic stroke, encephalitis, and brain status change in patients with Middle East respiratory syndrome coronavirus and severe acute respiratory syndrome coronavirus. , Several case reports and case series have reported the patients with COVID‐19‐associated encephalitis, which in some cases have been fatal. , , The pooled mortality rate from COVID‐19‐associated encephalitis is reported to be 13.4%. In a multicenter study by Pilotto et al. in Italy, 25 out of 45 people with encephalitis tested positive for SARS‐CoV‐2. They found that there is a wide range of clinical manifestations in patients and the response to treatment depends on the specific CNS manifestations. Due to the importance of encephalitis in COVID‐19 patients and the risk of death for them, it is necessary to conduct a detailed systematic review on this study. Therefore, the aim of this study was to evaluate the clinical symptoms, diagnosis, treatment, and outcome of COVID‐19‐associated encephalitis.

MATERIALS AND METHODS

This systematic review was performed according to “Preferred Reporting Items for Systematic Reviews and Meta‐Analyses” (PRISMA) statement.

Search strategy

We used Pubmed/Medline, Embase, and Web of Science databases for this literature. The articles included were only those published in English from January 1, 2019, to March 7, 2021. The search keywords used were “encephalitis,” “brain,” “neurologic,” “COVID‐19,” “severe acute respiratory syndrome coronavirus 2,” “SARS‐CoV‐2,” “2019‐nCoV,” “nCoV disease,” “coronavirus disease‐19,” “2019 novel coronavirus,” and “Wuhan pneumonia.”

Inclusion/exclusion criteria

Case reports and case series reporting encephalitis in patients with COVID‐19 were included. These studies met the following inclusion criteria: (i) COVID‐19 patients were confirmed and diagnosed with RT‐PCR as suggested by WHO; (ii) the raw data for clinical symptoms, diagnosis, treatment, and outcome of COVID‐19‐associated encephalitis were addressed. Studies without enough data, review article, modelling study, commentary, correspondence, editorial, guideline, and news were excluded. All potentially relevant articles were then screened for eligibility. Two reviewers independently screened the records by title, abstract, and full texts to exclude those not related to the current study.

Data collection

The extracted data included first author name; country where the study was conducted; year of publication; type of study; number of patients investigated; distribution of age and sex in the population; diagnosis methods; data for clinical, radiological, and laboratory findings; therapy, and the patient outcome.

Quality assessment

We used the case reports/case series appraisal checklist supplied by the Joanna Briggs Institute (JBI) to evaluate the quality of the studies.

RESULTS

Study selection and general characteristics

As shown in Figure 1, at the first screening, 4455 papers were retrieved. In the second phase, after removing duplicates, 2171 papers remained. These papers were screened by title and abstract, and 119 were selected for detailed full‐text evaluation. Applying the criteria to the full‐text documents, 45 articles were eligible for inclusion in the systematic review. The results of various studies including participants’ clinical manifestations, comorbidities, diagnosis, treatment, and outcome are reported in Tables 1 and 2. Moreover, a summary of the case report and case series findings are reported in Table 3.
FIGURE 1

Flow diagram detailing review process and study selection

TABLE 1

Characteristics of the case series studies

First authorCountryPublished timeNo. of patientsMedian age (years)Male/femaleEncephalitis diagnosis methodCT resultsMRI resultsSpecial encephalitis treatmentSARS‐CoV‐2 diagnosis methodCOVID‐19 treatmentClinical manifestationsSARS‐CoV‐2 diagnosis in CSF sampleComorbiditiesOutcomes
Lopes CCB 32 BrazilDecember 20202501M, 1F2 brain CT scan, 2 brain MRI, 2 EEG2 bilateral lesions in the centrum semiovale/1 focal lesions in globus pallidus and internal capsule/1 signal abnormalities in the white matter, including corpus callosum2 multifocal hyperintensity in centrum semiovale, 1 lesions in the cerebellar white matter and globus pallidusNM2 RT‐PCR1 hydroxychloroquine2 fever, 2 RS, 1 renal failure, 2 delayed awakening after sedation withdrawal, 2 DC, 1 coma, 1 four‐limb weakness2 negative2 hypertension, 1 diabetes, 1 obesity, 1 smoking1 death, 1 partial recovery
Kihira S 33 USAOctober 2020548.63M, 2FMRI, head CT, EEG5 unremarkable5 hyperintensity in the white matter, 3 confluent diffusion restriction in the cerebral white matter, 2 hyperintensity in the splenium of corpus callosum/1 scattered frontoparietal hyperintensity/1 microhemorrhages in corpus callosum/1 intraventricular hemorrhage1 plasma exchange5 RT‐PCRNM1 myocardial infarction, 2 fever, 5 RS, 3 acute renal failure, 1 cardiogenic shock, 1 abdominal pain, 1 cardiac arrest, 1 nausea, 1 vomiting, 1 chills, 5 AMS, 1 focal seizures, 1 lower limbs paralysis3 negative, 1 NP, 1 NM1 Hypertension, 1 diabetes mellitus type 2, 1 pyelonephritis, 1 gestation, 1 obesityNM
Barreto‐Acevedo E 34 PeruJune, 2020250.51M, 1FMRI, CSF analysis, brain tomography2 unremarkable1unremarkable, 1 NPDexamethasoneRT‐PCR, serological testNM2 fever, 2 chills, 1 malaise, 1 headache, 2 AMS, 2 seizuresNP1 obesity1death, 1 transferred to other hospital
Delorme C 35 FranceAugust 2020466.752M, 2F

Brain MRI, CSF analysis, brain

FDG‐PET/CT imaging, EEG

4 NP

1 unremarkable/1 non‐specific

Hyperintensity of the white matter/1 right T2 orbitofrontal

Hyperintensity

3 IV immunoglobulin, 3 IV corticosteroids4 RT‐PCRNM4 cognitive impairment, 2 cerebellar syndrome, 1 myoclonus, 1 psychiatric symptoms, 4 fever, 3 RS, 2 anosmia, 1 ageusia, 1 diarrhea, 2 fatigue, 2 agitation, 1 psychomotor slowing, 1 convulsive status, 1 apraxia, 1 dysexecutive syndrome4 negative1 temporal lobe epilepsy (hippocampal sclerosis), 1 diabetes mellitus type2, 1 hypertension4 discharged
TABLE 2

Characteristics of case report studies

First authorCountryPublished timeAge (years)SexEncephalitis diagnosis methodCT resultsMRI resultsSpecial encephalitis treatmentSARS‐CoV‐2 diagnosis methodCOVID‐19 treatmentClinical manifestationsSARS‐CoV‐2 diagnosis in CSF sampleComorbiditiesOutcomes
Kumar N 36 IndiaOctober 202035MHead CTHypodensities in both thalami and left caudate nucleusNPPropofol infusion, mannitol, IV methylprednisoloneRT‐PCRHydroxychloroquine, azithromycin, IV amoxicillin‐clavulanic acidFever, vomiting, DCNPInvasive meningiomaDeath
Novi G 37 ItalySeptember 202064FBrain and spine MRI, CSF analysisNPMultiple enhancing lesions of the brain, bilateral optic nerve enhancementIV methylprednisolone, prednisoneRT‐PCR, antibody testingIV immunoglobulinRS, anosmia, ageusia, visual impairment, behavioral changes, headache, hyperreflexiaPositiveVitiligo, hypertension, monoclonal gammopathyDischarged
Ayuso LL 38 SpainSeptember 202072FBrain MRI, immunoblot analysisNPHyperintensity in cerebellum, contrast enhancement on the floor of the fourth ventricleIV methylprednisolone, prednisoneRT‐PCR, chest CTHydroxychloroquine, azithromycin, ceftriaxonePsychiatric symptoms, fever, AMS, dizziness, visual impairment, unsteadiness, cerebellar signsNPHypertension, hyperlipidemia, smoking, depressionDischarged
Khan Z 39 USANovember 202030MHead CTOpacifications of paranasal sinuses, hypodensity of the white matterHyperintensity in the white matter of cerebral hemispheresAcyclovirRT‐PCR, chest CTyNMSeizure, DC, behavioral changes, myoclonus, AMS, psychiatric symptomsNPObesityStill hospitalized
Westhoff TH 40 GermanyJuly 202069MBrain MRI, CSF analysisNPLinear meningeal enhancement/hyperintensity in the white matterNMRT‐PCR, chest CTHydroxychloroquineFever, RS, diarrhea, pancreas and kidney allograft dysfunction, seizure, hemi‐neglect, fatiguePositiveImmunosuppressionDischarged
Kamal YM 41 United Arab EmirateSeptember 202031MCSF analysis, head CT, brain MRIBilateral hypodensities in the external capsules, the insular cortex and white matter of the frontal lobesBilateral diffusion restriction in the temporal and frontal lobes/bilateral hyperintensity in the temporal lobe cortexIV acyclovir sodiumRT‐PCRChloroquine, lopinavir–ritonavirBehavioral changes, AMS, agitation, drowsinessPositiveNoneDischarged
Rebeiz T 21 USASeptember 2020NMMCSF analysis, brain MRISubarachnoid hemorrhage within the mesial parietal region/nonspecific hypo‐attenuation in the splenium of the corpus callosumDiffusion restriction and hyperintensity of the corpus callosum, left thalamus and frontal cortexAcyclovir, ceftriaxone, vancomycinRT‐PCRNMBehavioral changes, fever, AMS, psychiatric symptomsNPNoneDeath
Zoghi A 42 IranJune 202021MCSF analysis, brain and cervical MRINPHyperintensity in the internal capsule, cerebral peduncles, pons and the corpus callosumIV vancomycin, meropenem, acyclovirChest CT, antibody testingPlasma exchangeAnorexia, vomiting, food intolerance, malaise, lower limbs paralysis, weakness, urinary retention, drowsinessNegativeNoneNM
Moriguchi T 9 JapanMay 202024MBrain MRINPHyperintensity along the wall of right lateral ventricle, right temporal lobe and hippocampus, slight hippocampus atrophyIV ceftriaxone, vancomycin, acyclovir, steroidsChest CT, RT‐PCRFavipiravirFatigue, fever, headache, RS, seizure, unconsciousnessPositiveNMStill hospitalized
Haqiqi A 43 United kingdomJanuary 202156MHead CT, brain MRI, CSF analysisDiffuse hypodensity of the white matter/multiple bilateral white matter hemorrhagic foci involving the corpus callosumHyperintensity of the white matter/diffuse hemosiderin staining throughout the white matter and the corpus callosum/some cystic hemorrhagic areas within both cerebral hemispheresNoneRT‐PCRSupportive careRS, acute kidney injury, DCNegativeHypertension, chronic kidney disease, hypercholesterolemia, asthma, obesityDischarged
Pizzanelli C 44 ItalyJanuary 202174FBrain MRI, total body PET/TCUnremarkableHyperintensity in the temporal lobes, mild hippocampal thickeningIV methylprednisolone, oral prednisoloneChest CT, RT‐PCRRemdesevir, dexamethasoneFever, RS, seizure, AMS, oral automatism, weakness, ideo‐motor slowingNegativeNoneDischarged
Al Mazrouei SS 1 United Arab EmiratesSeptember 202043MHead CT, brain MRIHypodensity of bilateral thalamiHyperintensity in the frontal lobes, insula, thalamus and globus pallidusNMRT‐PCR, Chest CTNMFever, RS, weakness, fatigue, DCNPDiabetes mellitus type2Death
Sirous R 2 USAAugust 202050MMRI, magnetic resonance angiography, magnetic resonance venographyMild cerebral generalized parenchymal volume loss with sulcal enlargementCerebral edema with mass effect, downward cerebellar tonsillar herniation/compression and displacement of the brainstem and 4th ventricleNMRT‐PCRIV hydroxychloroquineFatigue, headache, nausea, vomiting, lethargy, AMSNPNoneDeath
Mardani M 45 IranJuly 202064FCSF analysisUnremarkableNPNMRT‐PCR, CSF analysisIV ceftriaxone, clindamycin, hydroxychloroquine, lopinavir/ritonavirRS, weakness, DCPositiveHypertension, ischemic heart disease, metastatic colorectal cancerNM
Vandervorst F 46 BelgiumJuly 202029MBrain MRIUnremarkableHyperintensity of the left temporal cortex/mild gyral expansionNMRT‐PCR, chest CTIV acyclovir, hydroxychloroquineWeakness, RS, anorexia, Anosmia, ageusia, AMS, short‐term memory deficits, psychiatric symptomsNegativeNoneDischarged
Freire‐Álvarez E 31 SpainOctober 202039MBrain MRIUnremarkableHyperintensity at the cortical and subcortical right frontal regions, right thalamus and mammalary body, temporal lobes and cerebral pedunclesIV immunoglobulin, tocilizumabRT‐PCR, chest CTLopinavir/ritonavir, subcutaneous interferon beta‐1bFatigue, DC, malaise, fever, AMS, headache, drowsiness, minimal stiff neck, language disorder, paraphasiaNegativeNMClinical improvement, Still hospitalized
Parsons T 47 GermanyMay 202051FBrain MRI, EEGNPHyperintensities in the white matterMethylprednisolone, IV ImmunoglobulinRT‐PCR, chest CTNMRS, fever, vomiting, unresponsiveness, flaccid musclesNegativeNMNM
Al‐olama M 48 United Arab EmiratesMay 202036MBrain CT, CT angiographyHematoma in the right frontal lobe with surrounding edema/extracerebral hemorrhage/cortical swelling/bilateral supratentorial leptomeningeal increased enhancementNPNMPCRNMFever, RS, headache, body pain, diarrhea, vomiting, drowsiness, AMSNPNoneStill hospitalized
Goodloe TB 49 AlabamaJanuary, 202152MBead CT, EEGUnremarkableUnremarkableVancomycin, ceftriaxone, azithromycin, acyclovirRT‐PCRNMAMS, agitation, feverNPHypertension, diabetes mellitus type2, end‐stage renal disease, coronary artery diseaseDischarged
Sattar SBA 23 USASeptember 202044MBrain MRI, head CT, CSF analysisFew scattered foci of white matter hypo‐attenuationAbnormal medial cortical signals in the bilateral frontal lobesNMRT‐PCR, chest CTHydroxychloroquine, azithromycinFever, RS, seizure, AMS, unresponsivenessPositiveNoneDischarged
Haider A 29 USAMarch 202066MEEG, brain MRIUnremarkableSmall lacunar infarcts and a patchy area of bright signals in the cortical and lateral periventricular regionsTocilizumab, IV immunoglobulin, rituximabRT‐PCRNMSeizure, AMS, behavioral changesNPBenign prostatic hypertrophy, fatty liver disease, hypertensionDischarged
Cariddi LP 50 ItalyJune, 202064FHead CT, brain MRIBilateral hypodensity of the white matter/a small left occipital parenchymal hemorrhageBilateral edema with bilateral occipital foci of subacute hemorrhageNMRT‐PCRHydroxychloroquine, darunavir/cobicistatFever, RS, visual impairment, AMS, drowsiness, reduced tendon reflexesNegativeHypertension, gastroesophageal reflux disease, hyperuricemia, dyslipidemia, obstructive sleep apnea, atrial fibrillationPartial recovery
Sofijanova A 51 Republic of MacedoniaNovember 20209 monthNMHead CT, biochemical blood testEnlargement of the lateral ventricles, with intraventricular masses, internal hydrocephalusNPAnti‐edematous therapyNMCephalosporin, aminoglycoside, antiviral drugRS, convulsive status, fever, DC, vomiting, seizureNPNMTransferred to another hospital
Ghosh R 11 IndiaAugust 202044FBrain MRI, CSF analysisNPT2‐weighted hyperintensity in the parietal lobes with peri‐lesional edemaIV methylprednisoloneRT‐PCRCeftriaxone, vancomycin, acyclovirMyalgia, RS, hypogeusia, hyposmia, AMS, seizure, unconsciousness, reduced tendon refluxes, loss of sphincter controlNPNoneDeath
Pilotto A 52 ItalyAugust, 202060MEEG, brain MRI, CSF analysisUnremarkableUnremarkableMethylprednisoloneRT‐PCR, chest CTRitonavir/lopinavir, hydroxychlroroquineFever, RS, cognitive fluctuations, DC, AMS, behavioral changes, astheniaNegativeNoneDischarged
Azab MA 3 EgyptFebruary, 202189MMRI, post‐mortem biopsyNPHyperintensity near the basal ganglia and thalamiNMSerological testAcyclovir, acetaminophenRash, seizure, tremors, RS, cerebellar signs, fever, headache, dizziness, myalgiaNPNMDeath
Abdi S 53 IranJune, 202058MBrain MRI, CSF analysisNPHyperintensity of the white matter/involvement of cortical and deep gray matter and midbrainIV dexamethasoneRT‐PCR, chest CTNMDrowsiness, gait disturbance, DCNegativeNMDeath
Dharsandiya M 54 IndiaAugust, 202068MHead CT, blood test, CSF analysisAge‐related cortical atrophy (unremarkable)NPMethylprednisolone, tocilizumabRT‐PCR, chest CTAzithromycin, hydroxychloroquine, gamma globulinFever, RS, renal failure, viral sepsis, autonomic disturbance, AMS, seizureNPDiabetes, hypertensionDeath
Babar A 55 USAOctober, 202020FBrain MRI, CSF analysis, EEGUnremarkableUnremarkableMethylprednisoloneRT‐PCRLevofloxacin, acyclovirRS, ageusia, insomnia, Fever, AMS, psychiatric symptomsNegativeObesity, anxietyDischarged
Virhammar J 56 SwedenJune, 202055FHead CT, CSF analysis, EEG, brain MRIHypodensities in the thalami and midbrainHyperintensity in subinsular regions, thalami, and brainstem/involvement of temporal lobes, hippocampi, and cerebral pedunclesIV immunoglobulinRT‐PCR, chest CTAcyclovir, plasma exchangeFever, myalgia, impaired brain stem reflexes, myoclonus, lethargy, DCPositiveNoneDischarged to rehabilitation
Farhadian S 57 USAJune, 202078FBrain MRI, EEG, CSF analysisNPGeneralized atrophy/hyperintensity in white matterNMRT‐PCR, chest CTHydroxychloroquineSeizure like activity, RS, fever, AMSNegativeImmunosuppression due to kidney transplantationDischarged
de Miranda Henriques‐Souza AM 58 BrazilOctober, 202012FBrain and spine MRI, CSF analysisNPBilateral restricted diffusion in the white matter/hyperintensity of the corpus callosumMethylprednisoloneRT‐PCRNMTetraplegia, fever, deep areflexia, skin rash, headache, RS, acute motor weakness, numbnessNegativeNoneDischarged
Afshar H 59 IranAugust 202039FBrain MRINPHyperintensities in bilateral thalami, temporal lobes and ponsIV immunoglobulin, IV methylprednisoloneChest CTMeropene, levofloxacin, linezolide, hydroxychloroqine, atazanavir, IV immunoglobulinFever, myalgia, anorexia, drowsiness, RS, DC, headache, seizureNegativeNoneDischarged
Crosta F 60 ItalyDecember 202079MEEG, brain MRIUnremarkableHyperintensity of the left temporal cortex, with mild gyral expansionNMRT‐PCRClarithromycin, dexamethasoneFever, AMS, anosmia, RS, ageusia, DC, short‐term memory deficits, psychiatric symptomsNPHypertension, diabetes, chronic heart failureDischarged
Sangare A 61 FranceNovember 202056MEEG, brain MRINPHemorrhagic lesions in the pontine tegmentum and subinsular regions, including corpus callosumIV methylprednisolone, plasma exchange with albuminRT‐PCR, chest CTCephalosporin linezolide, trimethoprime‐sulfamethoxazole, meropenem aminosidFever, RS, reversible acute kidney failure, visual impairment, unresponsivenessNegativeHypertensionDischarged
El‐Zein RS 62 USASeptember 202040MEEG, blood tests, CSF analysisUnremarkableUnremarkableIV immunoglobulinSimplexa SARS‐CoV‐2 assayHydroxychloroquineFever, fatigue, AMS, RS, psychiatric symptoms, increased agitationNegativeNoneDischarged
Etemadifar M 4 IranSeptember 202051MHead CT, brain MRIGeneralized brain edema/signs of brain herniationGeneralized brain edema, downward herniation of cerebellar tonsils and brainstem, hyperintensities in bilateral cerebral cortices and corpus striatumNMRT‐PCRHydroxychloroquine, lopinavir/ritonavir, IV acyclovir, IV dexamethasoneHeadache, drowsiness, nausea, vomiting, RS, seizure, cardiac arrest, impaired brain stem reflexesNPHypothyroidism migraineDeath
Peng LV 63 ChinaFebruary, 202190FCSF analysis, physical and neurological examinationUnremarkableNPMannitol and anti‑viral therapy (Ganciclovir)RT‑PCR, Chest CTNMFever, RS, fatigue, unconsciousness, unresponsiveness, increased muscle tensionNegativeCerebral lacunar infarction with no neurological deficits‐ live in a healthcare unitDeath (irrelevant cause)
Hayashi M 10 JapanAugust 202075MNeurological examination, brain MRINPHyperintensity in the splenium of corpus callosumCorticosteroid pulse, meropenemRT‐PCRFavipiravir, corticosteroid pulseUrinary incontinence, diarrhea, DC, cerebellar signs, fever, AMS, tremor, gait disturbanceNP

Mild

Alzheimer's disease

Death
Kumar A 64 USANovember 202035FBrain MRI, EEG, CSF analysisUnremarkableHyperintensity in the white matter involving bilateral cerebral pedunclesMethylprednisolone, IV immunoglobulin, plasma exchangeRT‐PCR, serological testsNMAnosmia, ageusia, gait disturbance, neuropathy, weakness, drowsiness, lethargyNegativeGastric bypass surgery, anemiaDischarged to a long‐term care facility
Muccioli L 65 ItalySeptember 202047FEEG, brain MRINPHyperintensity in the white matterTocilizumabChest CT, RT‐PCRNMAsthenia, RS, ageusia, hyposmia, language disturbance, pain in the extremities, fever, AMS, headache, agitationNegativeNoneDischarged
TABLE 3

Summary of the case reports and case series findings

VariablesNo. of studies n/N %
Gender
Male2932/5360.38
Female1921/5339.62
Age
<30 (years old)66/5311.32
31–50 (years old)1618/5333.96
>51 (years old)2529/5354.72
Age/sex
<30 (years old)
Male44/666.67
Female22/633.33
31–50 (years old)
Male1112/1866.67
Female66/1833.33
>51 (years old)
Male1516/2955.17
Female1213/2944.83
Clinical manifestation
Neurological manifestations
Decreased consciousness/unconsciousness1718/5433.33
Behavioral changes66/5411.11
Altered mental status2429/5453.70
Cerebellar signs45/549.25
Seizure1516/5429.62
Agitation56/5411.11
Headache1111/5420.37
Memory deficits22/543.70
Unresponsiveness44/547.40
Convulsive status22/543.70
Cognitive impairment25/549.26
Language disturbance22/543.70
Paraphasia11/541.85
Tremors22/543.70
Lower limbs paralysis22/543.70
Gait disturbance33/545.55
Unsteadiness11/541.85
Hemi‐neglect11/541.85
Impaired brain stem reflexes22/543.70
Pain33/545.55
Coma11/541.85
Apraxia11/541.85
Dysexecutive syndrome11/541.85
Psychomotor slowing11/541.85
Ideo‐motor slowing11/541.85
Oral automatism11/541.85
Neuropathy11/541.85
Reduced tendon reflexes22/543.70
Loss of sphincter control11/541.85
Deep areflexia11/541.85
Psychiatric symptoms
Psychiatric symptoms88/5414.81
General symptoms
Fever3238/5470.37
Vomiting88/5414.81
Nausea33/545.55
Diarrhea44/547.40
Anosmia/hyposmia78/5414.81
Ageusia/dysgeusia88/5414.81
Dizziness22/543.70
Malaise33/545.55
Fatigue89/5416.66
Drowsiness99/5416.66
Weakness/asthenia1010/5418.51
Lethargy33/545.55
Chills23/545.55
Anorexia33/545.55
Food intolerance11/541.85
Insomnia11/541.85
Numbness11/541.85
Neuromuscular symptoms
Myalgia44/547.40
Hyperreflexia11/541.85
Myoclonus33/545.55
Neck stiffness11/541.85
Flaccid muscles11/541.85
Tetraplegia11/541.85
Increased muscle tension11/541.85
Other
Respiratory symptoms3037/5468.51
Visual impairment44/547.40
Renal dysfunction810/5418.51
Cardiac dysfunction24/547.40
Rash22/543.70
Viral sepsis11/541.85
Delayed awakening after sedation12/543.70
Autonomic disturbances11/541.85
Comorbidities
Hypertension1314/4829.16
Diabetes mellitus77/4814.58
Obesity66/4812.50
Neurologic disorders55/4810.41
Cardiologic disorder44/488.33
Dyslipidemia22/484.16
Anemia11/482.08
Psychiatric disorders22/484.16
Renal dysfunction33/486.25
Immunosuppressive state22/484.16
Smoking22/484.16
Hypercholesterolemia11/482.08
Hypothyroidism11/482.08
Vitiligo11/482.08
Monoclonal gammopathy11/482.08
Asthma11/482.08
Colorectal cancer11/482.08
Fatty liver disease11/482.08
Gastroesophageal reflux disease11/482.08
Hyperuricemia11/482.08
Obstructive sleep apnea11/482.08
Benign prostatic hypertrophy11/283.57
Gestation11/205.00
No comorbidities1515/4831.25
Presence of SARS‐CoV‐2 RNA in the CSF sample
Positive77/3420.58
Negative2127/3479.41
SARS‐CoV‐2 diagnosis method
RT‐PCR4049/5392.45
Chest CT2020/5337.73
Serological testing (anti‐SARS‐CoV‐2 antibody)56/5311.32
Simplexa SARS‐CoV‐2 assay11/531.88
Encephalitis diagnosis method
Brain MRI3644/5481.48
Head CT scan1520/5437.03
CSF analysis2125/5446.29
Electroencephalogram1523/5442.59
Total body PET/TC11/541.85
FDG‐PET/CT imaging14/547.40
CT angiogram11/541.85
Magnetic resonance angiography and venography11/541.85
Biochemical blood tests33/545.55
Post‐mortem biopsy11/541.85
Physical and neurological examination22/543.70
Immunoblot analysis11/541.85
Brain tomography11/541.85
Special encephalitis treatment
Dexamethasone23/368.33
Plasma exchange33/368.33
IV methylprednisolone/oral prednisone1313/3636.11
IV immunoglobulin810/3627.77
Corticosteroids24/3611.11
Steroids11/362.77
Propofol infusion11/362.77
Mannitol22/365.55
Acyclovir66/3616.66
Ceftriaxone33/368.33
Vancomycin44/3611.11
Meropenem22/365.55
Tocilizumab44/3611.11
Azithromycin11/362.77
Rituximab11/362.77
Anti‐edematous therapy11/362.77
COVID‐19 treatment
Hydroxychloroquine1515/3050.00
Chloroquine11/303.33
Azithromycin44/3013.33
IV amoxicillin‐clavulanic acid11/303.33
IV immunoglobulin22/306.66
Ceftriaxone33/3010.00
Dexamethasone33/3010.00
Favipiravir22/306.66
Ritonavir/lopinavir55/3016.66
Plasma exchange22/306.66
Remdesevir11/303.33
Clarithromycin11/303.33
Corticosteroid pulse11/303.33
Clindamycin11/303.33
Interferon beta‐1b11/303.33
Darunavir/cobicistat11/303.33
Cephalosporin22/306.66
Aminoglycoside11/303.33
Vancomycin11/303.33
Linezolide22/306.66
Acyclovir66/3020.00
Acetaminophen11/303.33
Gamma globulin11/303.33
Levofloxacin22/306.66
Meropene11/303.33
Atazanavir11/303.33
Trimethoprime‐sulfamethoxazole11/303.33
Meropenem aminosid11/303.33
Outcome
Death1313/4628.26
Discharged2023/4650.00
Discharged to rehabilitation/partial recovery44/468.69
Still hospitalized44/468.69
Transferred to another hospital22/464.34
Brain MRI pattern
Unremarkable66/4712.76
Hyperintensity in the white matter1521/4744.68
Hyperintensity in the corpus callosum56/4712.76
Hyperintensity in the cerebellum33/476.38
Hyperintensity of the thalamus66/4712.76
Hyperintensity in the temporal lobe88/4717.02
Hyperintensity in the frontal lobe55/4710.63
Hyperintensity in the brainstem33/476.38
Hyperintensity in the parietal lobe22/474.25
Hyperintensity along the wall of lateral ventricle11/472.12
Hemorrhagic/microhemrorrhagic areas45/4710.63
Signs of brain edema44/478.51
Confluent diffusion restriction in the white matter24/478.51
Compression and displacement of the brainstem and fourth ventricle11/472.12
Downward cerebellar tonsilar herniation22/474.25
Mild gyral expansion22/474.25
Involvement of cortical and deep gray matter and midbrain11/472.12
Diffuse hemosiderin staining throughout the white matter and corpus callosum11/472.12
Linear meningeal enhancement11/472.12
Contrast enhancement on the floor of the fourth ventricle11/472.12
Bilateral optic nerve enhancement11/472.12
Slight hippocampus atrophy11/472.12
Mild hippocampal thickening11/472.12
Generalized brain atrophy11/472.12
Head CT scan pattern
Unremarkable1520/3557.14
Hypodensity of the white matter66/3517.14
Hypodensity of the thalamus33/358.57
Hypodensity of the corpus callosum22/355.71
Hypodensity in the cerebellum23/358.57
Cerebral hemorrhages/hemorrhagic foci44/3511.42
Brain swelling and edema22/355.71
Brain herniation11/352.85
Opacification of paranasal sinuses11/352.85
Internal hydrocephalus11/352.85
Parenchymal hematoma with surrounding edema11/352.85
Cerebral parenchymal volume loss with sulcal enlargement11/352.85
Enlargement of the lateral ventricles with intraventricular masses11/352.85
Increased supratentorial leptomeningeal enhancement11/352.85
Flow diagram detailing review process and study selection Characteristics of the case series studies Brain MRI, CSF analysis, brain FDG‐PET/CT imaging, EEG 1 unremarkable/1 non‐specific Hyperintensity of the white matter/1 right T2 orbitofrontal Hyperintensity Characteristics of case report studies Mild Alzheimer's disease Summary of the case reports and case series findings

Study population

From a total of 45 studies, 53 patients with COVID‐19‐associated encephalitis were enrolled from 18 countries. Forty‐one (93.18%) studies were case reports and 4 (6.82%) were case series. The most significant number of studies was conducted in the USA (n = 10), followed by Italy (n = 6) and Iran (n = 5).

Demographic data

Demographic information of the individuals with COVID‐19‐associated encephalitis can be found in Tables 1 and 2. The patients were 21 female and 32 male with mean age of 52.12 years ranged between 9 months and 89 years. The highest incidence of COVID‐19‐associated encephalitis was observed in people over 50 years of age (54.72%).

Diagnostic methods

COVID‐19 was most often diagnosed by RT‐PCR (92.45%) and chest CT (37.73%). In addition, serological tests (11.32%) and simplexa assay (1.88%) were used to detect SARS‐CoV‐2 virus (Table 3). Brain MRI (81.48%), CSF analysis (46.29%), electroencephalography (42.59%), and head CT (37.03%) were the most frequently used methods to diagnose encephalitis (Table 3). The most common brain MRI patterns were hyperintensity in the white matter (44.68%), hyperintensity in the temporal lobe (17.02%), and hyperintensity of the thalamus (12.76%). In addition, hypodensity of the white matter (17.14%) and cerebral hemorrhages/hemorrhagic foci (11.42%) were the most common head CT scan patterns.

Clinical manifestations

Clinical manifestations were reported in five categories including (A) neurological manifestations such as altered mental status (53.70%), decreased consciousness/unconsciousness (33.33%), and seizure (29.62%); (B) psychiatric symptoms (14.81%); (C) general symptoms such as fever (70.37%), headache (20.37%), weakness/asthenia (18.51%), and drowsiness (16.66%); (D) neuromuscular symptoms such as myalgia (7.40%), myoclonus (5.55%); and (E) other clinical manifestation such as respiratory symptoms (68.51%), renal dysfunction (18.51%), and visual impairment (7.40%).

Comorbidities

The most common comorbidities were hypertension (29.16%), diabetes mellitus (14.58%), obesity (12.50%), and neurologic disorders (10.41%). The less common comorbidities were anemia (2.08%), hypercholesterolemia (2.08%), hypothyroidism (2.08%), vitiligo (2.08%), and asthma (2.08%).

Treatment options

A wide range of treatment options was used to treat COVID‐19. The most common of which were hydroxychloroquine (50%), acyclovir (20%), and ritonavir/lopinavir (16.66%), respectively. Common encephalitis treatment modalities included IV methylprednisolone/oral prednisone (36.11%), IV immunoglobulin (27.77%), acyclovir (16.66%). In Table 3, we summarize all of the drugs used.

Outcomes

In total, 58.69% of the patients with COVID‐19‐associated encephalitis discharged and 13.05% of them were still hospitalized. The pooled mortality rate of these patients was 28.26%.

Risk of bias assessment

The results of the critical appraisal (JBI checklist) of included studies are summarized in Table S1. Overall, 45 articles were identified as having a low risk of bias (quality assessment score >7).

DISCUSSION

Encephalitis is one of the specific neurological manifestations of COVID‐19 that can cause severe damage to the patient. In this study, we reviewed case series and case reports to evaluate the clinical symptoms, diagnosis, treatment, and outcome of COVID‐19‐associated encephalitis. The patients with COVID‐19‐associated encephalitis can show encephalitis weeks after the onset of symptoms of COVID‐19 or to have symptoms of COVID‐19 and encephalitis at the same time. Our study indicated that the clinical manifestations in patients with COVID‐19‐associated encephalitis can be both central nervous system symptoms (i.e., headache, dizziness, and impaired consciousness) and peripheral nervous system symptoms (i.e., hypogeusia, hyposmia, etc.). The most common symptoms were related to altered mental status (53.7%), decreased consciousness/unconsciousness (33.3%), and seizure (29.6%). These results were consistent with a systematic review performed by Siow et al. They also reported that decreased level of consciousness (77.1%), alter in mental state (72.3%), and seizures (38.2%) were the most common symptoms in patients with COVID‐19‐associated encephalitis. Correia et al. conducted a systematic review on the neurological manifestations of patients with COVID‐19. The rate of altered consciousness in their study was reported to be 11.2%. The difference in the results of their study with us could be due to differences in the time frame of each study and the number of patients admitted. Furthermore, headache (20.37%) and weakness/asthenia (18.51%) were other clinical symptoms of COVID‐19‐associated encephalitis in the present study. Correia et al. and Siow et al. reported headache rates of 16.8% and 27.3%, respectively. In this study, myalgia (7.4%) was the most frequent neuromuscular symptom. The prevalence of myalgia in a meta‐analysis done by Li et al. was 35.8%. Fever (70.37%) and respiratory failure (68.51%) were the most common symptoms of COVID‐19 in our evaluation. Heidary et al. achieved the same results in their study. They reported that clinical symptoms of COVID‐19 included coughing (81.3%), fever (62.8%), and dyspnea (60%). Also, Koupaei et al. demonstrated that the COVID‐19 patients mostly suffered from fever (78.8%), cough (63.7%), and respiratory distress (22.6%). So far, several cases of COVID‐19‐associated encephalitis have been reported in people who did not have symptoms of COVID‐19. The presence of asymptomatic people with encephalitis recommends that performing the diagnostic tests is necessary to prevent the spread of the disease. , On the contrary, CNS involvement is similar in the SARS‐CoV‐2, SARS‐CoV, and MERS‐CoV viruses. Thus, it is recommended that more sensitive and specific tests be performed. In this study, the most common methods used to diagnose encephalitis were MRI (81.48%), CSF analysis (46.29%), electroencephalogram (42.59%), and head CT scan (37.03%). Among the analysis performed on CSF, only 79.41% were positive and showed the presence of viral RNA. This may be due to the mechanism of encephalitis that the virus has not entered CSF and cannot be detected. Moreover, in the early stages of the disease, CSF may have a normal level and cause a false‐negative result. The most common MRI findings included hyperintensity in the white matter, hyperintensity in the temporal lobe, and hyperintensity in the corpus callosum, respectively. Although the CT findings of patients with COVID‐19‐associated encephalitis usually are not remarkable, our study showed that the most findings are hypodensity of the white matter (17.14%) and cerebral hemorrhages/hemorrhagic foci (11.42%). Probably, some of the signs in the imaging are related to the subcortical white matter hyperintensities and microbleeds in the deep gray nuclei caused by underlying diseases. The association between underlying diseases such as hypertension, diabetes, chronic obstructive pulmonary disease (COPD), cardiovascular disease, and cerebrovascular disease has been identified with COVID‐19. People with the above underlying diseases are more likely than others to develop COVID‐19 and the severity of the disease. In the present study, patients with COVID‐19‐associated encephalitis had a higher percentage of hypertension (29.16%) and diabetes mellitus (14.58%). Angiotensin‐converting enzyme 2 (ACE2), the receptor for SARS‐CoV‐2, is abundant in various organs. Diabetes can increase the serum ACE2. Thus, it is not surprising that diabetes is a common comorbidity in patients with COVID‐19‐associated encephalitis. In this study, COVID‐19‐associated encephalitis was more common in people over 50 years of age (54.72%). It seems that elderly people with several underlying diseases are less able to physiological rearrangement, which makes them more prone to encephalitis. Although various treatments have been used to treat COVID‐19‐associated encephalitis, none of them can be used with certainty. At the time of the COVID‐19 epidemic, physicians should suspect SARS‐CoV‐2 as a differentiating factor when certain diseases and neurological symptoms occur. Our survey showed that IV methylprednisolone/oral prednisone (36.11%), IV immunoglobulin (27.77%), and acyclovir (16.66%) were the common treatment options to treat encephalitis. The healing role of IV immunoglobulin in severe cases of COVID‐19 has been confirmed in several studies. , , , There are some limitations in this study. First, only case reports and case series were enrolled in this systematic review. Thus, the existence of publication bias should be considered. Second, since our search was limited to articles published in English, some relevant articles in other languages have missed. Third, some studies lacked sufficient data.

CONCLUSION

In this systematic review, various aspects of COVID‐19‐associated encephalitis including clinical symptoms, diagnosis, treatment, and outcome were studied. COVID‐19‐associated encephalitis is one of the complications of SARS‐CoV‐2, which may accompany with other neurological symptoms and make the patient's condition worse. It usually occur in severe cases and can increase the mortality rate. Thus, it is recommended to pay special attention to neurological symptoms during the COVID‐19 epidemic. Lack of proper attention causes problems such as delay in COVID‐19 diagnosis, virus transmission, and increased mortality. Therefore, further studies on COVID‐19‐associated encephalitis are suggested.

CONFLICT OF INTEREST

The authors declare that they have no competing interests.

AUTHORS’ CONTRIBUTION

Maryam Koupaei, Negar Shadabmehr, Mohamad Hosein Mohamadi, Arezoo Asadi, Sajjad Abasi Moghadam, Amirhosein Shekartabar, Mohsen Heidary, and Fazlollah Shokri contributed in revising and final approval of the version to be published. All the authors agreed and confirmed the study for publication. Table S1 Click here for additional data file.
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Review 1.  Encephalopathy in patients with COVID-19: A review.

Authors:  Ravindra Kumar Garg; Vimal Kumar Paliwal; Ankit Gupta
Journal:  J Med Virol       Date:  2020-07-11       Impact factor: 2.327

2.  A case of possible atypical demyelinating event of the central nervous system following COVID-19.

Authors:  Anahita Zoghi; Mahtab Ramezani; Mehrdad Roozbeh; Ilad Alavi Darazam; Mohammad Ali Sahraian
Journal:  Mult Scler Relat Disord       Date:  2020-06-24       Impact factor: 4.339

3.  Autoimmune limbic encephalitis related to SARS-CoV-2 infection: Case-report and review of the literature.

Authors:  Chiara Pizzanelli; Chiara Milano; Silvia Canovetti; Enrico Tagliaferri; Francesco Turco; Stefano Verdenelli; Lorenzo Nesti; Marta Franchi; Enrica Bonanni; Francesco Menichetti; Duccio Volterrani; Mirco Cosottini; Gabriele Siciliano
Journal:  Brain Behav Immun Health       Date:  2021-01-24

4.  SARS-CoV-2 associated viral encephalitis with mortality outcome.

Authors:  Mohammed A Azab; Ahmed Y Azzam
Journal:  Interdiscip Neurosurg       Date:  2021-02-25

Review 5.  COVID-19 in HIV-positive patients: A systematic review of case reports and case series.

Authors:  Mohsen Heidary; Arezoo Asadi; Negar Noorbakhsh; Shirin Dashtbin; Parisa Asadollahi; Atieh Dranbandi; Tahereh Navidifar; Roya Ghanavati
Journal:  J Clin Lab Anal       Date:  2022-02-20       Impact factor: 3.124

6.  Encephalitis as a clinical manifestation of COVID-19.

Authors:  Mingxiang Ye; Yi Ren; Tangfeng Lv
Journal:  Brain Behav Immun       Date:  2020-04-10       Impact factor: 7.217

7.  COVID-19-related encephalopathy: a case series with brain FDG-positron-emission tomography/computed tomography findings.

Authors:  C Delorme; O Paccoud; A Kas; A Hesters; S Bombois; P Shambrook; A Boullet; D Doukhi; L Le Guennec; N Godefroy; R Maatoug; P Fossati; B Millet; V Navarro; G Bruneteau; S Demeret; V Pourcher
Journal:  Eur J Neurol       Date:  2020-09-22       Impact factor: 6.288

8.  Delayed SARS-COV-2 leukoencephalopathy without Severe Hypoxia.

Authors:  Arooshi Kumar; Anlys Olivera; Nancy Mueller; Jonathan Howard; Ariane Lewis
Journal:  J Neurol Sci       Date:  2020-09-18       Impact factor: 3.181

9.  SARS-CoV-2-Associated Acute Hemorrhagic, Necrotizing Encephalitis (AHNE) Presenting with Cognitive Impairment in a 44-Year-Old Woman without Comorbidities: A Case Report.

Authors:  Ritwik Ghosh; Souvik Dubey; Josef Finsterer; Subham Chatterjee; Biman Kanti Ray
Journal:  Am J Case Rep       Date:  2020-08-16
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1.  Comparison of clinical, radiological and laboratory findings in discharged and dead patients with COVID-19.

Authors:  Mahbobe Jafari; Maryam Akbari; Maryam Navidkia; Shirin Dashtbin; Seyede Faezeh Mousavi; Mohsen Heidary; Saeed Khoshnood
Journal:  Vacunas       Date:  2022-06-01

Review 2.  Clinical symptoms, diagnosis, treatment, and outcome of COVID-19-associated encephalitis: A systematic review of case reports and case series.

Authors:  Maryam Koupaei; Negar Shadab Mehr; Mohamad Hosein Mohamadi; Arezoo Asadi; Sajjad Abbasimoghaddam; Amirhosein Shekartabar; Mohsen Heidary; Fazlollah Shokri
Journal:  J Clin Lab Anal       Date:  2022-04-18       Impact factor: 3.124

Review 3.  A Comprehensive Review of the Protein Subunit Vaccines Against COVID-19.

Authors:  Mohsen Heidary; Vahab Hassan Kaviar; Maryam Shirani; Roya Ghanavati; Moloudsadat Motahar; Mohammad Sholeh; Hossein Ghahramanpour; Saeed Khoshnood
Journal:  Front Microbiol       Date:  2022-07-14       Impact factor: 6.064

4.  Evaluating the characteristics of patients with SARS-CoV-2 infection admitted during COVID-19 peaks: A single-center study.

Authors:  Seyede Faezeh Mousavi; Mohammadamin Ebrahimi; Seyed Amirhosein Ahmadpour Moghaddam; Narges Moafi; Mahbobe Jafari; Ayoub Tavakolian; Mohsen Heidary
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5. 

Authors:  Fazlollah Shokri; Saeed Rezapoor; Masoud Najafi; Mohsen Asadi; Mohammad Karimi Alavije; Moussa Abolhassani; Mohammad Hossein Moieneddin; Amir Muhammad Ashrafi; Narges Gholipour; Parisa Naderi; Jamshid Yazdani Charati; Reza Alizadeh-Navaei; Majid Saeedi; Mohsen Heidary; Mostafa Rostamnezhad
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