Project start date: 01-May-2020 Project end date: 30-Apr-2022
Neurological complications of COVID-19
Acute neurological syndrome, as defined below, in patients with evidence of suspected or proven COVID-19
Study website: https://www.coronerve.com/Specific research question:
- What are the demographic, clinical, laboratory and radiological features of patients presenting with acute neurological syndromes during or following coronavirus infection?
- What treatments do they receive?
- What are their outcomes?
Aims
We will use the extensive network of neurologists who submit data to the British Paediatric Neurological Surveillance Unit (BPNSU) to identify cases of acute neurological syndromes associated with COVID-19, through direct infection and para-infectious or post-infectious presentations in the UK.
Objectives
i. To determine the demographic, clinical, laboratory and radiographic features of patients presenting with acute neurological syndromes during or within 6 weeks of virologically proven coronavirus infection
ii. To determine the proportion receiving immune and associated therapies and what these are.
iii. To determine the clinical outcomes of patients which each neurological syndrome relative to baseline features and treatments received.
Lead Investigator:
Dr Rachel Kneen (as part of the CoroNerve Study Group)
Consultant Paediatric Neurologist and Honorary Senior Clinical Lecturer
Institute of Infection and Global Health,
University of Liverpool
Alder Hey Children’s NHS Foundation Trust
Additional investigators:
The CoroNerve Study Group: Dr Benedict D Michael, Dr Rhys H Thomas, Dr Ian Galea, Dr Ara Varatharaj, Dr Mark Ellul, and Professor Sarah Pett.
The CoroNerve Steering Committee: Dr Nicholas WS Davies, Dr Hadi Manji, Dr Michael Zandi, Dr Laura Benjamin, Professor Tom Solomon, Dr Jonathan Coles, and Dr Ava Easton.
- Age range for cases: 0-18 years
- Proven COVID-19: Confirmed by polymerase chain reaction from clinical samples (sputum, nasal/throat swab, bronchioalveolar lavage, cerebrospinal fluid) or serology and/or vaccination
- Probably COVID-19: Chest radiograph compatible and clinical suspicion and/or vaccination, but not meeting ‘proven’ criteria
- Possible COVID-19: Clinical suspicion of COVID-19 but not meeting above criteria
- Delirium (e.g. metabolic disturbance, iatrogenic)
- Encephalopathy attributable to fever/sepsis
- Encephalopathy attributable to hypoxia-ischaemia
- Posterior reversible encephalopathy syndrome (PRES)
- Malignant cerebral oedema
- Mild encephalopathy with a reversible splenial lesion (MERS)
- Acute infantile encephalopathy predominantly affecting the frontal lobes (AIEF)
- Encephalopathy: other
- Viral encephalitis Due to SARS-CoV-2 (CSF or tissue positive by PCR or intrathecal antibody synthesis) Other viral pathogen (e.g. CSF PCR positive Herpes simplex virus) Acute Disseminated Encephalomyelitis (ADEM)- by MRI criteria Acute Necrotising Encephalitis- by MRI criteria Acute Haemorrhagic Leukoencephalopathy- by MRI criteria
- Limbic encephalitis Antibody-mediated encephalitis (recognised antibody in serum or CSF) Aetiology unknown
- Encephalitis: other
- Aseptic meningitis Viral meningitis due to SARS-CoV-2 Other proven viral meningitis Pathogen unknown
- Meningitis: other
- Meningoencephalitis (if encephalopathy present)
- Multiple sclerosis
- Neuromyelitis Optic-Spectrum Disorder Positive for Aquaporin-4 antibodies Positive for anti-MOG antibodies No antibodies identified
- Central demyelination: other
- Acute ataxia
- Cerebellar syndrome: other
- Direct viral myelitis SARS-CoV-2 positive PCR in CSF and/or intrathecal antibody synthesis Other pathogen (e.g. varicella zoster)
- Para/post-viral myelitis SARS-CoV2 negative PCR in CSF and/or no intrathecal antibody synthesis
- Acute flaccid myelitis (lower motor neurone signs e.g. flaccid, areflexic limb[s] without sensory signs)
- Myelitis: other Free text
- Direct due to:
- SARS-CoV-2 SARS-CoV-2 positive PCR in CSF and/or intrathecal antibody synthesis
- Other pathogen (e.g. enterovirus)
- Guillain-Barre syndrome (Ascending sensory-motor flaccid, paralysis – typically areflexic)
- Miller-Fisher syndrome (Ophthalmoplegia, ataxia, and areflexia)
- Guillain-Barre syndrome and variants: other Free text
- Neuropathy attributable to critical illness (e.g. prolonged ITU admission)
- Peripheral neuropathy: other
- Myopathy attributable to critical illness (e.g. prolonged ITU admission)
- Rhabdomyolysis (e.g. CK >5 times the upper limit of normal and/or acute renal failure)
- Myositis: other
- Transient ischaemic attack (symptoms/signs 24 hours)
- Ischaemic stroke - large artery (on neuroimaging)
- Ischaemic stroke – lacunar (on neuroimaging)
- Cerebral haemorrhage (on neuroimaging)
- Sub-arachnoid haemorrhage (on neuroimaging)
- Cerebral vasculitis (angiographic beading and/or inflammation in CSF and/or clinical suspicion)
- Cerebral vein / sinus thrombosis (on neuroimaging)
- Cerebrovascular: other Free text
- Convulsive status epilepticus (30minutes of continuous convulsive seizures or repeated seizures without complete recovery between)
- Non-convulsive status epilepticus (>30minutes of continuous subtle motor signs or electroencephalographic evidence seizures or repeated clinical/EEG evidence without complete recovery between)
- New-onset refractory status epilepticus (as above lasting 1-2 days continuously)
- Hyperkinetic Choreathetosis (writhing movements) Ballismus (large amplitude brief movements)
- Hypokinetic Parkinsonism (rigidity, bradykinesia, pill-rolling rest tremor)
- Dystonia Tremor (other than rest tremor)
- Movement Disorder: other
- Narcolepsy
- Other central hypersomnia
- Parasomnias Circadian rhythm sleep-wake disorder
- Sleep Disorder: other
- Psychosis
- Major depression
- Mania
- Anxiety
- Obsessive-compulsive or related syndrome
- Tics
- Catatonia
- Impulse control syndrome
- Neurocognitive (dementia-like) syndrome
- Personality change
- Apathy
- Chronic fatigue
- Post-traumatic stress disorder
- Functional neurological disorder
- Other dissociative syndromes
- Psychiatric syndromes: other
- Myasthenia gravis (e.g. neurophysiological evidence of decremental responses, jitter on single-fibre, and/or acetylcholine receptor/MUSK antibody positive)
- Lambert-Eaton syndrome (e.g. neurophysiological evidence of incremental responses and/or voltage-gated calcium channel antibody positive)
- Neuromuscular junction syndromes: other
- Locked in syndrome
- Bulbar/pseudobulbar palsies
- Eye movement disorder / nystagmus
- Vertigo
- Neurogenic ECG changes / cardiac arrythmia
- Unexplained coma
- Central apnoea
- Brainstem syndromes: other
No evidence of active or recent COVID-19 Infection. BACKGROUND:
Para- and post-viral acute neurological syndromes are an important and treatable cause of significant neurological morbidity and mortality. However, evidence in the literature is limited to case reports and very small case series, and there remain many answered questions including which anti-inflammatory therapy to give to which patients. During the 2009/2010 H1N1 (swine flu) pandemic we identified many cases of severe neurological complications including Acute Necrotising Encephalopathy (ANE) and Acute Leucoencephalopathy through the BPNSU and British Neurological Surveillance Unit (BNSU). Recently some have identified cases of severe acute CNS inflammatory syndromes associated with the novel COVID-19 strain. However, epidemiological and clinical data are not known. Additionally, it is unclear if the COVID-19 strain accounts for a significant proportion of these. These data are needed to direct future studies and public health programmes.Parallel studies are underway through the Association of British Neurologists, the British Association os Stroke Physicians, the Royal College of Psychiatrists, and key partners.