| Literature DB >> 34483649 |
Samad Shams Vahdati1, Alireza Ala1, Dara Rahmanpour2, Elyar Sadeghi-Hokmabadi3, Fateme Tahmasbi2.
Abstract
BACKGROUND: Neurological involvements of COVID-19 are one of the most reported manifestations of this infection. This study aims to systematically review the previous systematic reviews which addressed the neurological manifestations of the COVID-19 infection.Entities:
Keywords: COVID-19; Corona virus disease 2019; Neurological manifestations; Neurology; Systematic review
Year: 2021 PMID: 34483649 PMCID: PMC8401342 DOI: 10.1186/s41983-021-00366-5
Source DB: PubMed Journal: Egypt J Neurol Psychiatr Neurosurg ISSN: 1110-1083
Fig. 1Search results and selection of studies for systematic review according to the PRISMA flowchart
Fig. 2The quality of included studies according to the AMSTAR-2
The characteristics of included systematic reviews regarding the general manifestations of COVID-19 infection
| Authors | Origin | Type | Quality | Number of included studies | Types of included studies | Assessing the quality of included studies | Searched databases | Main results |
|---|---|---|---|---|---|---|---|---|
| 1. Whittaker et al. 2020 [ | UK | Systematic review | Critically Low | 31 | Cohort, case report, cross-sectional, case–control | None | Pubmed, Embase, Scopus, Google Scholar, Cochrane Library, Ovid | Headache and anosmia were the most common neurological manifestations of SARS-CoV-2 in hospitalized patients. Less common symptoms include seizure, stroke and isolated cases of GBS1 |
| 2. Wang et al. 2020 [ | China | Systematic review + meta-analysis | Critically Low | 41 | Case series, case report, cross-sectional, case–control, letters | NIH2 quality assessment tool | Pubmed, Embase, Scopus, medRxiv, bioRvix | The most common manifestationswere fatigue, anorexia, dyspnea/shortness of breath, and malaise. The common specific neurological symptoms included OGD3, especially in mild cases. GBS and acute inflammation of the brain, spinal cord, and meninges |
| 3. Chen et al. 2020 [ | Germany | Systematic review | Moderate | 92 | Cohort, case series, case report, case–control, letters | 1. Criteria for diagnosis of Covid-192. Laboratory confirmation method 3. The respiratory specimens used for testing | Pubmed, medRxiv, bioRxiv, Three Chinese databases | Headache, dizziness, taste and smell dysfunctions, and impaired consciousness were the most frequently described neurological symptoms |
| 4. Neishaboori et al. 2020 [ | Iran | Systematic review + meta-analysis | Moderate | 7 | Cohort, case series, case–control | NHLBI4 quality assessment tool | Pubmed, Embase, Scopus, Web of Science | The most common type of CNS5 complications included encephalopathy and acute cerebrovascular disease |
| 5. Di Carlo et al. 2020 [ | Italy | Systematic review | Moderate | 19 | Cohort, case series, case report, case–control | Modified NOS6 | Pubmed, Embase | Headache, dizziness, OGD were reported in patients, three studies reported radiological confirmed acute cerebrovascular disease |
| 6. Asadi-Pooya et al. 2020 [ | Iran | Systematic review | Critically Low | 8 | Cohort, case series, case report | None | Pubmed, Scopus | Nonspecific neurological symptoms, such as confusion and headache were reported in COVID-19 patients. A few patients also showed more specific manifestations, such as seizure or cerebrovascular problems |
| 7. Nepal et al. 2020 [ | Nepal | Systematic review | Critically Low | 37 | Cohort, case series, case report, case–control | None | Pubmed, Google Scholar, Chinese National Knowledge Infrastructure, Research square, medRxiv, Social Science Research Network, and ChinaXiv | The most commonly reported neurological manifestations of COVID-19 weremyalgia, headache, altered sensorium and OGD. Uncommonly, COVID-19 can also present with CNS manifestations such as ischemic stroke, intracerebral hemorrhage, encephalo-myelitis, and acute myelitis, PNS7 manifestations such as GBS and Bell’s palsy, and skeletal muscle manifestations such as rhabdomyolysis are also reported |
| 8. Taherifard et al. 2020 [ | Iran | Systematic review | Critically Low | 22 | Case series, case report | None | Pubmed, Scopus, Web of Science | The virus seemed to affect both PNS and CNS. The most frequently reported neurological complication was acute ischemic cerebrovascular accident, followed by GBS syndrome |
| 9. Ghannam et al. 2020 [ | USA | Systematic review | Moderate | 42 | Case series, case report | JBI8 Critical Appraisal Tool | Pubmed, Ovid Medline | COVID-19 patients demonstrated cerebrovascular insults, neuromuscular disorders, and encephalitis or encephalopathy |
| 10. Abdullahi et al. 2020 [ | Nigeria | Systematic review + meta-analysis | Moderate | 60 | Cohort, case series, case report, cross-sectional, case–control | Modified McMaster critical review form | Pubmed, Embase, Google Scholar, Web of Science | The most common type of neurological and musculoskeletal manifestations were as followed: OGD, myalgia, headache, back pain, dizziness, acute cerebrovascular disease and impaired consciousness |
| 11. Cagnazzo et al. 2020 [ | France | Systematic review | Moderate | 39 | Case series, case–control | Modified NOS | Pubmed, Embase, Scopus | Headache, muscle injury, psychiatric involvement, impaired consciousness, OGD, acute cerebrovascular events and dizziness were the most frequently reported neurological manifestations. Less common ones were ischemic stroke, cranial nerve impairment, nerve root and plexus disorders, epilepsy, and hemorrhagic stroke |
| 12. Collantes et al. 2020 [ | Philippines | Systematic review + meta-analysis | High | 35 | Cohort, case series, case report, case–control | Murad tool | Pubmed, Embase, Scopus, WHO database | The most common type of neurological involvements were headache, dizziness, headache and dizziness, nausea, vomiting, nausea and vomiting, confusion and myalgia. The most common neurological complication associated with COVID-19 was vascular disorders; others included encephalopathy, encephalitis, oculomotor nerve palsy, isolated sudden-onset anosmia, GBS, and Miller–Fisher syndrome |
| 13. Orrù et al. 2020 [ | Italy | Systematic review | Critically Low | 87 | Cohort, case report, case–control, in-press articles | None | Pubmed, Scopus | OGD, ischemic/hemorrhagic stroke, meningoencephalitis and encephalopathy, including acute necrotizing encephalopathy were commonly associated with COVID-19; PNS involvements included, GBS and Miller Fisher syndromes |
| 14. Favas et al. 2020 [ | India | Systematic review + meta-analysis | High | 212 | Cohort, experimental, case report, cross-sectional, case–control, letters | NOS, CONSORT9 | Pubmed, Embase, Scopus, Google Scholar, Cochrane Library, Web of Science, WHO database, EBSCO, Clinicaltrial.gov | OGD, myalgia, headache, dizziness, and syncope are reported in COVID-19. Ischemic stroke, followed by hemorrhagic stroke, and cerebral venous thrombosis were also reported |
| 15. Munhoz et al. 2020 [ | Brazil | Systematic review | Critically Low | 43 | Cohort, experimental, case series, case report, case–control | None | Pubmed, LILACS | Non-specific symptoms, such as hyposmia and myalgia, to more complex and life-threatening conditions, such as cerebrovascular diseases, encephalopathies, and GBS are associated with COVID-19 infection |
| 16. Romoli et al. 2020 [ | Italy, Austria, Zurich, Switzerland | Systematic review | Moderate | 27 | Cohort, case series, case report, cross-sectional, case–control | NOS | Pubmed, Embase, Google Scholar, medRxiv, ChinaXiv | Cases of OGD, GBS, Miller-Fisher syndrome, cranial neuropathy, meningitis, encephalitis, and various other conditions were linked to COVID-19 |
| 17. Pinzon et al. 2020 [ | Indonesia | Systematic review + meta-analysis | Moderate | 33 | Cohort, experimental, case report, ross-sectional, case–control | The Oxford CEBM12 | Pubmed | Myalgia was the most common, neurologic symptom of COVID-19, followed by headache, dizziness; nausea with or without vomiting; concurrent cerebrovascular disease; and impaired consciousness |
| 18. Chua et al. 2020 [ | Singapore | Systematic review + meta-analysis | Critically Low | 48 | Cohort, case series, case report, cross-sectional, case–control, letters, rapid comments | None | Pubmed, Google Scholar | Stroke is the most frequently reported neurological manifestation in COVID-19 and has the highest mortality rate. Other manifestations included GBS and variants, meningitis, encephalitis, encephalopathy, myelitis and seizures |
| 19. Scoppettuolo et al. 2020 [ | Switzerland, Belgium | Systematic review | Critically Low | 42 | Case series, case report | None | Pubmed, Scopus, Cochrane Library | Neurological complications of SARS-CoV-2 are mainly related to OGD, cerebrovascular disease and PINS10 are rare |
| 20. Tsai et al. 2020 [ | Taiwan | Systematic review + meta-analysis | Critically Low | 79 | Case series, case report | None | Pubmed, Embase, Cochrane Library | OGD, myalgia, headache, acute cerebral vascular disease, dizziness, altered mental status, seizure, encephalitis, neuralgia, ataxia, GBS, Miller Fisher syndrome, intracerebral hemorrhage, polyneuritis cranialis, and dystonic posture were demonstrated in COVID-19 patients |
| 21. Ibrahim 2020 [ | Egypt | Systematic review | Critically Low | 20 | Cohort, experimental, case series, case report, cross-sectional | None | Pubmed, Scopus, Cochrane Library, clinicaltrials.gov | CNS symptoms was more common compared to the PNS. Headache was the most common neurological symptoms in regard to number of patients, meanwhile dizziness had the highest incidence |
1. GBS: Guillain–Barré syndrome, 2. NIH: National Institutes of Health, 3. OGD: Olfactory and Gustatory Disorder, 4. NHLBI: National Heart, Lung, and Blood Institute, 5. CNS: central nervous system, 6. NOS: Newcastle–Ottawa Scale, 7. PNS: Peripheral Nervous System, 8. JBI: Joanna Briggs Institute, 9. CONSORT: Consolidated Standards of Reporting Trials, 10. PINS: Post-infection Neurological Syndrome. P value < 0.05 was considered to be statistically significant
Characteristics of included systematic reviews regarding stroke in COVID-19 infection
| Authors | Origin | Type | Quality | Number of included studies | Types of included studies | Assessing the quality of included studies | Searched databases | Main results |
|---|---|---|---|---|---|---|---|---|
| 1. Valencia-Enciso et al. 2020 [ | Colombia | Systematic review | Moderate | 47 | Cohort, case series, case report, case–control | NOS | Pubmed, Scopus | A positive correlation seemed to exist between COVID-19 severity and temporality of stroke |
| 2. Fraiman et al. 2020 [ | South Korea | Systematic review | Critically Low | 80 | Not mentioned | None | Pubmed | Cerebrovascular events, especially ischemic stroke, were a common neurological manifestation in COVID-19 patients |
| 3. Lee et al. 2020 [ | Malaysia | Systematic review + meta-analysis | Moderate | 28 | Cohort, case series, case report | STROBE2 | Pubmed, Medline, Cinhal | Stroke is an uncommon symptom in COVID-19 patients, but can be prognostic factor and an indicator of the severity of the infection |
| 4. Bhatia et al. 2020 [ | India | Systematic review | Moderate | 30 | Cohort, case series, case report | Oxford CEBM3 critical appraisal tool | Pubmed, Embase, Scopus | COVID-19 is associated with higher mortality rates in stroke patients |
| 5. Wijeratne et al. 2020 [ | Australia | Systematic review | Low | 18 | Cohort, case series, case report, case–control, reviews | None | Pubmed, Embase, Cochrane Library, Medline, Cinhal, Ovid | Neutrophil–Lymphocyte ratio at time admission is associated with the duration before onset of clinical features of AIS3 |
| 6. Fridman et al. 2020 [ | Canada | Systematic review + meta-analysis | Low | 10 | Not mentioned | None | Pubmed, medRxiv, bioRxiv, Research Square search engines | The mortality of Stroke in COVID-19 patients is associated with age, comorbidities and the severity of the infection |
| 7. Yamakawa et al. 2020 [ | USA | Systematic review + meta-analysis | Moderate | 26 | Cohort, case series, case report, case–control | Assessment of risk of bias in prevalence studies | Pubmed, Embase, | The frequency of detected stroke in hospitalized patients was associated with age and other stroke risk factors |
| 8. Katsanos et al. [ | Greece | Systematic review + meta-analysis | High | 18 | Cohort | NOS | Pubmed, Scopus | COVID-19 infection is associated with an increased risk of ischemic stroke, especially cryptogenic stroke; in addition to an increased risk of mortality |
| 9. Tan et al. 2020 [ | Singapore | Systematic review + meta-analysis | Moderate | 39 | Cohort, case series, case report | NOS, JBI5 tool | Pubmed, Embase | AIS is associated with COVID-19 infection with a high mortality rate |
| 10. Nannoni et al. 2020 [ | UK | Systematic review + meta-analysis | Moderate | 61 | Cohort, case series, case report, case–control, letters | NOS | Pubmed, Scopus, MedRxiv | Acute cerebrovascular events are associated with the severity of the disease and pre-existing vascular risk factors in COVID-19 patients |
| 11. Fatima et al. 2020 [ | USA | Systematic review | Moderate | 6 | Cohort, case series, case report | GRADE6, Cochrane Collaboration’s tool | Pubmed, Embase, Scopus, Google Scholar, Cochrane Library, Medline | Stroke is associated with COVID-19 infection in patients with underlying risk factors including hypertension |
| 12. Siepmann et al. 2021 [ | Germany | Cohort + Systematic review | Critically Low | 2 | Cohort, experimental | Oxford CEBM tool | Pubmed, Embase, Cochrane Library | The severity of COVID-19 infection is associated with an increased risk of acute stroke |
| 13. Szegedi et al. 2020 [ | Germany | Narrative review + Systematic review | Critically Low | 25 | Cohort, case series, case report | None | Pubmed, Scopus | In COVID-19 patients the most common type of stroke was AIS |
1. NOS :Newcastle–Ottawa Scale, 2. STROBE: Strengthening the Reporting of Observational Studies in Epidemiology, 3. CEBM: Centre for Evidence-Based Medicine, 4. AIS: Acute Ischemic Stroke, 5. JBI: Joanna Briggs Institute 6. GRADE: Grading of Recommendations Assessment, Development and Evaluation. P value < 0.05 was considered to be statistically significant
The characteristics of included systematic reviews regarding the olfactory and oral dysfunction of COVID-19 infection
| Authors | Origin | Type | Quality | Number of included studies | Types of included studies | Assessing the quality of included studies | Searched databases | Main results |
|---|---|---|---|---|---|---|---|---|
| 1. Borsetto et al. 2020 [ | Critically Low | Systematic Review + Meta-analysis | UK | 18 | Not mentioned | None | Embase, Scopus, Web of Science, Medline, MedRxiv | The alteration of the sense of smell or taste was estimated 31% in severe and 67% in mild-to-moderate symptomatic patients |
| 2. da Costa et al. 2020 [ | Moderate | Systematic Review | Brazil | 6 | Cohort, cross sectional, case–control | NOS1 | Pubmed, Scopus, Google Scholar, Cochrane library, LILACS2, Science direct | OGD3 occurs at varying intensities and prior to the general symptoms of COVID-19 |
| 3. Samaranayake et al. 2020 [ | Moderate | Systematic Review | United Arab Emirates | 8 | Cohort, cross sectional, case–control | Nine-item checklist for prevalence study | Pubmed, Web of Science, EBSCO | Anosmia and dysgeusia symptoms were present in both ambulatory and hospitalized patients and mild-to-severe cases of COVID-19 |
| 4. Lechner et al. 2020 [ | Critically Low | Systematic Review | UK | 31 | Case series, case reports, cross sectional | None | Pubmed | OGD is indicative of COVID-19 infection and should be implicated in evaluation of healthcare workers |
| 5. Rocke et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | UK | 12 | Case series, cross sectional, case–control | ROBINS‐E | Pubmed, Embase, Cochrane library, HMIC, MedRxiv | There is a significant evidence demonstrating an association between olfactory dysfunction and COVID‐19 |
| 6. Zahra et al. 2020 [ | Moderate | Systematic Review | UK | 23 | Cohort, case series, cross sectional, case–control | NOS | Pubmed, Scopus, Google Scholar, Cochrane library, Medline | Symptoms of anosmia and dysgeusia were frequently reported by COVID-19-positive patients; more commonly in females and in younger patients |
| 7. Fuccillo et al. 2020 [ | Moderate | Systematic Review | Italy | 32 | Cohort, case series, cross sectional | NHLBI4 Assessment Tools, Oxford CEBM5 guide | Pubmed, Embase, Web of Science | Olfactory disorders represent an important clinical characteristic of COVID-19 |
| 8. Hoang et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | Thailand | 14 | Case series, cross sectional, case–control | Modified NOS | Pubmed, Embase, Scopus, Medline OVID | OGD and COVID-19 are associated |
| 9. Tong et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | USA | 10 | Cohort, case series, cross sectional, case–control | The quality assessment checklist for prevalence studies adapted from Hoy et al. | Pubmed, Scopus | OGS are common symptoms in patients with COVID-19 and may be manifested as an early symptoms in the clinical course of the COVID-19 infection |
| 10. Passarelli et al. 2020 [ | Critically Low | Systematic Review | Italy | 5 | Not mentioned | None | Pubmed | Anosmia and ageusia are a significant sign and can be considered as the first manifestation of the infection |
| 11. Agyeman et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | Australia | 24 | Not mentioned | Murad tool | Pubmed, Embase, Medline, MedRxiv | High prevalence of OGD among patients infected with COVID-19 are reported across the literature |
| 12. Pang et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | Singapore | 19 | Cohort, case series, cross sectional, case–control | The risk of bias tool for prevalence studies by Hoy et al. | Pubmed | Patient-reported olfactory dysfunction is a highly specific manifestation of COVID-19 |
| 13. Hajikhani et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | Iran | 15 | Not mentioned | JBI6 tool | Pubmed, Embase, Web of Science | OGD in patients with confirmed COVID-19 have a high prevalence |
| 14. Sedaghat et al. 2020 [ | Critically Low | Systematic Review | USA | 6 | Not mentioned | None | Pubmed, Embase, Web of Science | OGD is highly common in the course of COVID-19 infection and patients may experience sudden-onset of smell alteration as the first symptom |
| 15. Chi et al. 2020 [ | Low | Systematic Review + Meta-analysis | China | 12 | Not mentioned | None | Pubmed, Embase, Cochrane library, Cumulative Index to Nursing and Allied Health Literature, National Digital Library of Theses and Dissertations in Taiwan database, Art Image Indexing Service on the Internet Database (Chinese database) | OGD is associated with COVID-19 infection and in some patients is the first symptom of the infection |
| 16. Giorli et al. 2020 [ | Critically Low | Systematic Review + Meta-analysis | Italy | 11 | Cohort, cross sectional, case–control | None | Pubmed, Scopus, Web of Science | New onset olfactory dysfunction is associated with COVID-19, anosmia is more frequent in non-hospitalized COVID-19 patients than in hospitalized ones |
| 17. Ibekwe et al. 2020 [ | Moderate | Systematic Review + Meta-analysis | Nigeria | 32 | Cohort, cross sectional, case–control | JBI tool | Pubmed, Embase, Google Scholar, Web of Science | The prevalence of smell and taste loss among COVID-19 patients was high globally |
| 18. Chung et al. 2020 [ | Critically Low | Cohort + Systematic Review | China | 23 | Cohort, experimental, case series, case reports | None | Pubmed | COVID-19-related smell disturbance can be severe and prolonged and may be the only symptom |
| 19. Printza et al. 2020 [ | Critically Low | Systematic Review | Greece | 24 | Cohort, case series, cross sectional, case–control | None | Pubmed, Cochrane library, MedRxiv | Anosmia is more prevalent in COVID-19 patients than in patients suffering from other respiratory infections or controls |
1. NOS: Newcastle–Ottawa Scale, 2. LILACS: Latin American and Caribbean Health Sciences Literature; 3. OGD: Olfactory and Gustatory Dysfunctions; 4. NHLBI: National Heart, Lung, and Blood Institute; 5. CEBM: Center for Evidence-Based Medicine; 6. JBI: Joanna Briggs Institute
The characteristics of the included systematic reviews regarding Guillen-Barre syndrome in COVID-19 infection
| Authors | Origin | Type | Quality | Number of included studies | Types of included studies | Assessing the quality of included studies | Searched databases | Main results |
|---|---|---|---|---|---|---|---|---|
| 1. Carrillo-Larco et al. 2020 [ | Europe | Systematic review | Critically low | 8 | Case series, case report | None | Embase, Scopus, Web of Science, Global Health, Medline, MedRvix | Basic evidence suggests that GBS1 occurs after COVID-19 onset |
| 2. Gittermann et al. 2020 [ | Chile | Systematic review | Low | 24 | Case series, case report | NHLBI2 tool | Pubmed, Cochrane Library, Science Direct, Medline, WHO search tool | There seem to be a strong association between the GBS and Covid-19 which differs in presentations, including the severity of the GBS manifestations |
| 3. Uncini et al. 2020 [ | Europe | Systematic review | Critically low | 33 | Case series, case report | None | Pubmed | Classical GBS is presented in Covid-19 patients |
| 4. Hasan et al. 2020 [ | Bangladesh | Systematic review + meta-analysis | Low | 45 | Case series, case report, cross sectional | JBI3 tool | Pubmed, Web of Science, Cochrane Library, Web of Science | An association exists between classic GBS and Covid-19. These manifestations are responsive to GBS standard treatments |
| 5. Abu-Rumeileh et al. 2020 [ | Germany | Systematic review | Critically low | 52 | Case series, case report, reviews with case reports, reviews, letters, original article, point of view, and brief report | None | Pubmed, Google Scholar | COVID-19-associated GBS seems to share most features of classic post-infectious GBS with possibly the same immune-mediated pathogenetic mechanisms |
1. GBS: Guillain-Barré Syndrome; 2. NHLBI: National Heart, Lung, and Blood Institute; 3. JBI: Joanna Briggs Institute