NeuroCheck Flashcards

(44 cards)

1
Q

How would you check for meningitis in an infant

A

Check for a full or bulging anterior fontanelle (Sign of raised ICP)

check fontanelle when calm and in supine and upright positions

this usually closes at 13 months

between 4 and 24 months

Also for petechial or purpuric rash

temp

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2
Q

What should septic work up of a febrile unwell infant include

A

full blood examination

blood sugar level

lactate and C-reactive protein at baseline

blood culture

urine microscopy, culture and sensitivities.

+/- Lumbar puncture +/- chest xray

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3
Q

IF a prehospital dose of antibiotic is required for an infant with ?meningitis what would you give

A

Current Australian guidelines suggest use of either ceftriaxone 50 mg/kg (for children >1 month of age) or benzylpenicillin 60 mg/kg

GIVE ceftx if delay in sending child in to hospital as ben pen can sometimes be ineffective against neisseria

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4
Q

Would you give dexamethasone in a child with ?meningitis

A

current guidelines suggest that in children aged >2 months with a high clinical suspicion of meningitis, dexamethasone (0.15 mg/kg IV) could be considered.12,22 Dexamethasone should be given 15 minutes prior to parenteral antibiotics or within one hour of the first antibiotic dose.12

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5
Q

Most common causes of infant meningitis

A

Strep pneumo

Neisseria meningitidis

Haemophilus Influenze type B

Ecoli and group B strep less common

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6
Q

IF you’re in a rural area and infant needs transfer who do you contact?

A

EMergency Paediatric retrieval service

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7
Q

If CSF comes back with gram pos dipplococuss how does that change mx

A

likely strep pneumo

ADD VANC IV

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8
Q

Ongoing seizures in an infant

A

phenytoin 20 mg/kg Loading

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9
Q

History questions when considering headaches associated with ?raised ICP

A

Is the headache worse on getting up from lying down or with postural change?

Are there associated symptoms of tinnitus?

Is there associated nausea and sometimes (projectile) vomiting?

The visual symptoms can also be a result of raised ICP placing pressure on the optic nerve. Relevant questions include:

Is the visual obscuration transient (as reported by Irene)?

Is there horizontal diplopia (may be intermittent)?

Is the vision blurred?31,32

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10
Q
A

Papilloedema

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11
Q

Differential diagnosis for papilloedema

A

intracranial mass

venous malformation (especially dural venous sinus thrombosis)

idiopathic intracranial hypertension (IIH)

malignant hypertension

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12
Q
A
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13
Q
A
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14
Q

Why might you get a sixth nerve palsy in Raised ICP

A

False localising

Compression of CN6 as it enters the midbrain, caused by raised ICP, results in the abduction deficit seen. It is important to remember the cause is compression rather than ischaemia as in an ischaemic CN6 palsy.

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15
Q

IF worried about raised ICP and eye issues - what investigations?

A

Neuroimaging, ideally magnetic resonance imaging (MRI) with magnetic resonance venography (MRV), would help to identify any intracranial lesion including a dural venous sinus thrombosis. In the absence of an MRI, computed tomography (CT) with CT venography (CTV) are sufficient. Following neuroimaging to exclude an intracranial lesion, a lumbar puncture to measure opening cerebrospinal fluid (CSF) pressure is required.

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16
Q

Risk factors for Idiopathic ICH

A

Irene has several risk factors in her presentation that are commonly seen in a diagnosis of IIH including:

>90% of cases are women of childbearing age

recent or longstanding weight gain

certain medications (eg COCP, vitamin A derivatives, withdrawal from corticosteroids, lithium, tetracyclines

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17
Q

Management of Idiopathic ICH

A

acetozalmide via neurologist

Weight reuction

Opthalmology referral for monitoring of vision

neurology – commencement of acetazolamide initially in tolerated doses up to 1 g daily to control symptoms and reduce production of CSF. Acetazolamide is a carbonic anhydrase inhibitor that can reduce CSF production. Various trials have shown improvements in symptoms and visual function with maximally tolerated doses of acetazolamide (maximum 4 g/day). A neurologist may prescribe topiramate; however, there are ocular side effects so this is not first-line treatment.35

ophthalmology – documentation of optic nerve function including vision and visual fields. Figure 3 shows a typical visual field in this case (enlarged blind spot). Optic nerve function requires monitoring for worsening, should medical treatment not effectively reduce CSF pressure.

allied health – gradual weight loss is an important aspect of treating IIH; it must be done in an appropriate and safe manner. A dietitian and/or counsellor may assist patients to achieve weight loss.

The general practitioner’s (GP) role is to oversee specialist management, as patients with IIH will initially present to their GPs for follow-up on discharge from hospital.

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18
Q

What other management is there for refractory raised ICH

A

Intracranial shunt

and optic nerve sheath fenestration

19
Q

Red flags in headache

A

New onset, specific setting. New headache in the setting of cancer (metastases), human immunodeficiency virus infection (opportunistic infection), postmanipulation or trauma of the neck, or associated with mild head trauma in the elderly (subdural haematoma)

New headache that is persistent

Focal signs or symptoms (other than the typical visual or sensory aura of migraine)

Headache with focal neurological signs that precede or outlast the headache (the rare exception is hemiplegic migraine)

Headache that is progressive (may suggest a mass lesion)

Headache of sudden onset (may indicate a bleed either into the subarachnoid space or the cerebral parenchyma)

Headache with rash (may indicate meningococcal meningitis or Lyme disease)

Persistent unilateral temple headache in adult life (may indicate cranial arteritis)

Headache with a raised erythrocyte sedimentation rate (may be an indication of cranial arteritis, collagen disease or systemic infection)

Headache with papilloedema (raises the suspicion of raised intracranial pressure due to a mass lesion or benign intracranial hypertension)

Nonmigraine headaches in pregnancy or postpartum (cerebral vein thrombosis can occur during or just after pregnancy)

Headache triggered by cough or straining (may be an indication of either a mass lesion or a subarachnoid bleed)

Headache clearly triggered by changes in posture (may indicate low cerebrospinal fluid [CSF] pressure, for instance due to spontaneous CSF leak)

Headache associated with pressing visual disturbances (may indicate conditions such as glaucoma or optic neuritis)

Headaches that have primary characteristics, but with unusual features

20
Q

Common DDx of headache

A

Primary or tension-type headaches are the most common causes of headaches. Other causes of headaches by decreasing frequency include migraines, head trauma, idiopathic stabbing headaches, exertional headache, vascular disorders, intra-cranial haemorrhage or brain tumours.41

21
Q

What history questions in headache

A

headache characteristics, timing, constancy, aggravating factors, associated nausea and vomiting, severity and history of any prior headaches.

A history of associated symptoms is important, including other neurological symptoms, seizures, recent falls/trauma, constitutional symptoms, as well as previous medical, family and surgical history

22
Q

Examination in headache

A
  1. Vital signs (BP)
  2. Fundoscopy (pappilloedema)
  3. Cranial nerve examination
  4. Peripheral nerve examination
23
Q

Brain tumour headache symptoms

A

is one that starts in early morning before the patient rises from bed and disappears soon after the patient gets up. The headache is often initially mild but can become progressively more frequent, severe and of longer duration. However, only a small proportion (17%) of patients present with this symptom.42 According to lifetime prevalence studies, only a minority (0.7%) of headaches in patients presenting to general practice are caused by brain tumours.43

The presenting symptoms related to a glioma are determined by the tumour’s size, location and rate of growth. The usual presenting symptoms of glioblastoma multiforme (GBM) include a short duration of increased intracranial pressure (headache, nausea, vomiting) and/or focal neurological symptoms that reflect the tumour. Presenting symptoms, and the proportion of presenting patients, are headaches (19–34%), hemiparesis (14–41%), seizures (17–31%), cognitive deficits (15–22%), speech deficits (6–32%), visual disturbance (3–15%), ataxia (9%) and cranial nerve deficits (9%).42

24
Q

What are MEdicare indications for a brain MRI

What are contraindications

A

The permissible Medicare Benefits Schedule indications for brain MRI include unexplained seizure(s) and chronic headache with suspected intracranial pathology.

artificial cardiac pacemakers, metallic foreign body in the eye or joint replacement

MRI is more sensitive than CT

but usually CT head is imaging investigation of choice

25
What are the treatment options for glioblastoma multiforme?
Surgical resection Adjuvant chemo and radiotherapy
26
Advice about prognosis in GBM?
**GBM is an incurable form of brain cancer that generally has a poor prognosis (life expectancy of months to years).42 However, high-grade gliomas are heterogeneous disease**s and there can be variability in the prognosis, which is primarily based on the patient’s age and performance status, the extent of surgical resection and molecular features of the tumour.47,50 In fit, young patients (aged \<70 years) following trimodality treatment (surgery, radiotherapy and chemotherapy), the expected median survival ranges from 14 to 18 months, and a five-year survival of 10–15% has been shown.50 Patients should be encouraged to openly discuss issues such as life expectancy with their treating oncology team It is important to highlight that adjuvant treatment is reasonably well tolerated and can allow the patient to successfully maintain their current function and quality of life for a period of time. Further discussions with the treating oncology team regarding benefits and toxicities of treatment should be encouraged.
27
What is the role of steroids in Brain tunmours
Reduce cerebral oedema relieve intracranial pressure symptoms such as nausea, vomiting and headache. often post adjuvant radiotherapy **Usually dexamethasone 8-16mg/day**
28
Side effects of long term glucorticoid use
**Gastrointestinal** Gastric irritation **Metabolic** Weight gain Glucose intolerance **Skin and connective tissue** Cushingoid appearance Myopathy Easy bruising Osteoporosis/osteopenia **Cardiovascular** Fluid retention Hypertension **Psychiatric** Insomnia Psychosis **Endocrine** Hypoadrenalism
29
What advice do you give someone on long term GCS therapy eg pred or dexa
Toxicity is dose dependent Patients taking steroids longer term should undergo assessment of their **limb power, blood pressure, blood sugar level, lipids, weight and mental health at baseline** and at _regular intervals_.
30
Driving with GBM
A patient with a brain tumour is not fit to hold an unconditional license. Jørgen will be unlikely to return to his previous employment as a truck driver. General practitioners are encouraged to liaise with the treating oncologist or neurosurgeon to provide patients with consistent and accurate guidance regarding driving. ITs patients responsibility to inform the Road traffic authroyity that they have a condition that could affect their driving
31
What are the complications of GBM
1. PSych - psychosocial assistance eg Mental health plan and counsellor 2. HIGH VTE risk - watch for PE's or DVTs 3. Neurocognitive decline - Formal neuropsych assessment if worseing 4. Stress - both for individual and carers 5. Disease progression - affecting function
32
Terminal Glioma - what are main sx
fatigue, nausea, neurological deficits, seizures and immobility.42 Pain is not a major component in the terminal phase of patients with glioma. In consultating with oncology unit consider: early pall care referral community services End of life care discussions
33
A young wonman presents with leg tingling and numbness - history questions
It is important to determine whether there has been any history of **trauma or change in appearance** of her left leg, such as skin rash or swelling. In addition to the sensory changes, it is important to know if she has **weakness** in the leg; any symptoms in the **right leg, arms or cranial nerves**; difficulty with **urination or bowel motions**; or **perineal numbness.** It is also important to enquire about other recent neurological symptoms such as **visual changes, headache, problems with thinking, blackouts or any episodes of transient neurological symptoms in the past such as loss of vision, sensory changes or weakness in the limbs.** It is recommended to enquire about infective symptoms such as f**evers, sweats or weight loss**.
34
DDx of UMN signs and sensory levle
MS or Cord compression - ED ref
35
Advice for patient with MS to reduce risk of relapse
STOP SMOKING (associated with higher risk of relapse and speed of disease progression) General health advice -reduce weight, and exercise Maintain vitamin D within normal range NO evidence to support wahls diet which is a restrictive diet limits legumes, wholegrains, eggs, dairy and processed foods and has been promoted as being beneficial for patients with MS. It is important to tell any patient seeking information regarding the Wahls diet that currently there is insufficient evidence to support any particular restrictive diet in preference to the Australian Healthy Food guidelines, which recommend Australians need to eat more vegetables, legumes and fruit, and fewer cakes, biscuits, chocolate, confectionary and food and drinks high in saturated fat, added sugar and salt.65 Only 5% of Australians consume the recommended amount of vegetables.65
36
A patient with MS is commenced on IV infusions of biologic - what screening
ocrelizumab, is a six-monthly IV infusion performed in a day unit. It is a humanised anti-CD20 monoclonal antibody that depletes B cells that modulate the immune response. Patients are screened prior to starting treatment for **human immunodeficiency virus (HIV), contact with tuberculosis and immunity to hepatitis B virus, measles, mumps, rubella and varicella. MMR is a live attenuated vaccine and is not safe to give to immunocompromised patients. It can be given prior to treatment initiation.** There is no evidence of a higher risk of malignancy in patients treated with ocrelizumab; however, there are data to support this in other chronically immunosuppressed groups such as recipients of solid organ transplants and patients with HIV.66 It is recommended that patients see their general practitioner annually for a **check-up including age-appropriate cancer screening programs such as cervical and breast cancer screening, and a yearly skin check.**66
37
Will MS disease modification therapy reduce initial symptoms? HOw would you treat neuropathic pain
Seyma’s disease-modifying MS treatment, ocrelizumab, will not improve symptoms of MS from previous attacks. **It is used to reduce the relapse rate and disability from MS and prevent new lesions on MRI**.67 The persisting neurological symptoms and signs do not mean her treatment is not working. Given the impact on Seyma’s quality of life, you could consider a treatment for neuropathic pain such as **amitriptyline, gabapentin or pregabalin.** It would be important at this point to screen for symptoms of **depression**, which are often present in patients with chronic pain. Reassurance that things are going well is important, but should both pain and depression require treatment, options include **amitriptyline and venlafaxine.**
38
If someone with MS wants to have a baby? what adivce?
Many MS drugs are contraindicated in pregnancy and needs consultation with her neurologist. Possilby an increased risk of relapse for up to three months post partum. Very small risk of passing on MS The risk to Seyma’s child of developing MS is very low. MS is probably the result of a complex interaction between genes and the environment.70 One Danish study estimated the excess risk from having a first-degree relative with MS as conferring an additional 2.5% lifetime risk.70
39
40
MS and depression correlation and mx?
Depression is very common in patients with MS. The rate is higher than the general population and higher than other chronic illnesses.71 **The lifetime prevalence is estimated to be 50%, with an annual prevalence of 20%**.71 Some evidence indicates there is a higher suicide rate in patients with MS.71 There is limited research to support any specific treatment for depression in patients with MS,72 and it should be **treated by combining both pharmacological and psychological support.**
41
After ceasing ocrelizumab how long should you wait before trying to conceive
6 MONTHS
42
What do different meningitis bugs look like on gram stain
Strep pneumo - gram pos diplocci N. Meningitidis- Gram-negative coccus HIB - gram neg bacillis Group B strep - more often seen in chains but gram pos cocc
43
What should CSF opening pressure be on LP
A lumbar puncture is performed under computed tomography guidance; the reference range for **opening CSF pressure is 21–25 cmH2O.**
44
After treatment what percentage of patients with GBM have at least one ongoing neurological deficit
85%