Publications by authors named "Biba Stanton"

Article Synopsis
  • - Functional Neurological Symptom Disorder (FNSD) involves neurological-like symptoms without a clear neurological cause, and the mechanisms behind it are complex and not fully understood.
  • - A study tested the use of remote monitoring technologies (RMT) on 17 individuals with FNS and 17 healthy controls to track symptoms, daily events, and physiological data, finding that those with FNS reported higher levels of negative emotions, pain, and sleep issues.
  • - Results indicate that daily stressors and negative feelings significantly impact FNS severity, suggesting that addressing emotional responses could help those with FNS, and calls for larger studies to explore these findings further.
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Introduction: Advances have been made in understanding the aetiology of functional neurological disorder (FND); however, its pathophysiological mechanisms have not been definitively demonstrated. Evidence suggests interacting roles for altered emotional processing and interoception, elevated autonomic arousal, and dissociation, but there is limited evidence demonstrating their causal influence on specific FND symptoms. Our superordinate aim is to elucidate potentially shared and distinct aetiological factors and mechanisms in two common FND subtypes, functional seizures (FS) and functional motor symptoms (FMS).

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Objective: This study examined etiological factors and symptom triggers of functional motor symptoms (FMS) or functional seizures (FS) and assessed potential relationships with relevant clinical features (i.e., functional symptoms, quality of life, and general functioning).

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CSF-venous fistulas (CVFs) are increasingly recognised as a cause of spontaneous intracranial hypotension. They may present atypically including with brain sagging pseudo-dementia. Cervical CVFs are rare and their management can be difficult due to associated eloquent nerve roots.

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Background: Progressive multifocal leukoencephalopathy (PML) is a rare demyelinating disease due to a lytic infection of oligodendrocytes caused by John Cunningham polyoma virus (JCV) infection. Idiopathic CD4+ T-cell lymphocytopenia (ICL) is a very rare cause of PML.

Methods: We present an individual with PML secondary to ICL treated with 3 doses of pembrolizumab, a Programmed-Death-1 Immune Checkpoint Inhibitor following with complete resolution of symptoms and conduct a review of the literature.

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Article Synopsis
  • The study investigated how highly arousing emotional stimuli affect functional neurological symptoms (FNS) in individuals with functional neurological disorder (FND) compared to healthy controls, focusing on the relationship between emotional response and autonomic reactivity.
  • Results showed that FND participants reported higher FNS after viewing negative images, particularly when viewing them passively, and physiological measures, such as skin conductance and heart rate, correlated with those symptom ratings.
  • The findings suggest that emotional events may influence FNS through autonomic responses rather than changes in subjective feelings, with cognitive detachment potentially playing a moderating role; more research is needed to explore the neural mechanisms involved.
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In neurological practice, we take pride in accurate diagnosis and using neuroscience to develop novel disease-modifying therapies, but we sometimes neglect symptom management and the treatment of distress. Most patients with neurological disorders report that their mental health needs are not being met. Of the many forms of psychological therapy, cognitive behavioural therapy (CBT) is the most likely to be available to our patients.

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Article Synopsis
  • The study evaluated neurocognitive functioning in individuals with functional motor symptoms (FMS) and functional seizures (FS) compared to healthy controls, focusing on attention, executive function, social cognition, and metacognitive accuracy.
  • Results indicated no significant differences in objective cognitive tests between the two groups, but the FMS/FS group showed faster reaction times on an emotional task and reported more cognitive complaints in daily life.
  • The findings highlight a disconnect between subjective self-reports of cognitive issues and actual performance on cognitive assessments in the FMS/FS group, potentially influenced by associated factors like depression and psychological symptoms.
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Article Synopsis
  • The study investigated interoception (awareness of internal body states) in individuals with functional motor symptoms (FMS) and seizures (FS) compared to healthy controls (HC), focusing on measures of accuracy and insight.* -
  • Results showed no significant differences in interoceptive accuracy or confidence between the two groups, but those with FMS/FS scored lower on certain awareness subscales related to not being distracted and trusting bodily signals.* -
  • Impaired interoceptive accuracy might not be central to FMS/FS; instead, a lack of insight and altered body awareness could play a role in the severity and impact of symptoms, suggesting that reduced self-evaluation certainty contributes to the disorder's development
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Hypertrophic pachymeningitis is a rare disorder of the dura mater of the spine or brain. It can be caused by inflammatory, infective or neoplastic conditions or can be idiopathic. We report a man with hypertrophic pachymeningitis and bilateral chronic subdural haematoma caused by IgG4-related disease.

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Chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) is a disabling long-term condition of unknown cause. The National Institute for Health and Care Excellence (NICE) published a guideline in 2021 that highlighted the seriousness of the condition, but also recommended that graded exercise therapy (GET) should not be used and cognitive-behavioural therapy should only be used to manage symptoms and reduce distress, not to aid recovery. This U-turn in recommendations from the previous 2007 guideline is controversial.

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Functional neurological disorder (FND) can be a difficult diagnosis for patients to understand and for clinicians to explain. The postdiagnostic support that patients with other chronic neurological illnesses normally receive is often not available to patients with FND. Here, we share our experience of how to set up an FND education group, including the content, practical aspects of delivering groups and how to avoid potential pitfalls.

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Article Synopsis
  • Functional neurological disorder (FND) is a common and serious condition that many doctors don’t fully understand.
  • It has been recognized for over 100 years but people with FND still face unfair treatment and discrimination.
  • The text argues that FND is a feminist issue because it often affects women and highlights the need for better education and healthcare for those affected by this disorder.
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Background: Catatonia is a psychomotor syndrome that has a wide range of aetiologies. Determining whether catatonia is due to a medical or psychiatric cause is important for directing treatment but is clinically challenging. We aimed to ascertain the performance of the electroencephalogram (EEG) in determining whether catatonia has a medical or psychiatric cause, conventionally defined.

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Recent observations suggest that autism spectrum disorder (ASD) co-occurs in people with a functional neurological disorder (FND), but little systematic data are available on the relationship between FND and autism. The study aimed to assess the self-reported autistic traits via a standardized questionnaire and the prevalence of previously diagnosed ASD among people with FND and their 1st-degree relatives. We performed a survey of members of the patient organization FNDHope, using a self-completed questionnaire for screening for autistic traits and ASD: the adult autism subthreshold spectrum (AdAS spectrum).

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Psychiatrists often order investigations such as blood tests, neuroimaging and electroencephalograms for their patients. Rationales include ruling out 'organic' causes of psychiatric presentations, providing baseline parameters before starting psychotropic medications, and screening for general cardiometabolic health. Hospital protocols often recommend an extensive panel of blood tests on admission to a psychiatric ward.

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A 53-year-old woman developed subacute onset of upper limb weakness, sensory loss and cerebellar dysfunction. She was known to have human T-lymphotropic virus type 1 (HTLV-1)-associated myelopathy. MR scan of the brain showed extensive T2 hyperintensity within the deep and subcortical white matter, with punctate contrast enhancement.

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Suspected cauda equina syndrome is a common presentation in emergency departments, but most patients (≥70%) have no cauda equina compression on imaging. As neurologists become more involved with 'front door' neurology, referral rates of patients with these symptoms are increasing. A small proportion of patients without structural pathology have other neurological causes: we discuss the differential diagnosis and how to recognise these.

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Recent reports have highlighted rare, and sometimes fatal, cases of cerebral venous sinus thrombosis (CVST) and thrombocytopenia following the Vaxzevria vaccine. An underlying immunological mechanism similar to that of spontaneous heparin-induced thrombocytopenia (HIT) is suspected, with the identification of antibodies to platelet factor-4 (PF4), but without previous heparin exposure. This unusual mechanism has significant implications for the management approach used, which differs from usual treatment of CVST.

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Objectives: Transcranial magnetic stimulation (TMS) has been used therapeutically for functional (conversion) motor symptoms but there is limited evidence for its efficacy and the optimal protocol. We examined the feasibility of a novel randomised controlled trial (RCT) protocol of TMS to treat functional limb weakness.

Design: A double-blind (patient, outcome assessor) two parallel-arm, controlled RCT.

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Background: A 2011 survey of neurologists' attitudes to conversion disorder found a tacit acceptance of the psychological model but significant ambivalence around its relationship to feigning. These issues are under increased scrutiny as the DSM-5 revision removed both the requirement for a psychological formulation and the exclusion of feigning from the diagnostic criteria. Whether those attitudes are shared with psychiatrists is unknown.

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A 22-year-old African woman developed acute behavioural change, against a background of sickle cell disease with strokes requiring a ventriculoperitoneal shunt. She alternated between mutism with prolonged staring and posturing, and a state of agitation with elation and echolalia. Cerebrospinal fluid (CSF) protein was elevated and electroencephalogram showed mild slowing with bitemporal slow and sharp waves.

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Apathy is an under-recognised and underestimated problem for people with chronic neurological disorders. Despite being common and disabling, it is seldom volunteered as a symptom by patients or even their caregivers. Yet apathy undoubtedly has an important impact on caregiver stress, functional disability and quality of life.

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