Miscellaneous Flashcards

1
Q

Carpal tunnel syndrome - definition

A
  • Most common entrapment neuropathy (prevalence about 1 in 25)
  • compression of the median nerve in the carpal tunnel. Typical symptoms include numbness and tingling mainly in the thumb/index/middle and half of ring finger, aching and pain in the anterior wrist and forearm, and clumsiness in the hand.
  • raised pressure within the carpal tunnel and ischaemia of the median nerve
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2
Q

CTS - clinical features

A
  • RF: ge over 30 years, female sex, high BMI
  • numbness of hand(s) (Dominant hand is usually the first and worst affected)
  • night-time worsening (Waking up with paraesthesias/ pain in hand/wrist, and shaking the hand to relieve)
  • numbness in median nerve distribution (Should be sparing of thenar eminence and ulnar/radial area)
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3
Q

Components of the carpal tunnel

A
  • flexor digitorum profundus (four tendons)
  • flexor digitorum superficialis (four tendons)
  • flexor pollicis longus (one tendon)
  • Median nerve
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4
Q

CTS - investigations

A
  • EMG = focal slowing of conduction velocity in the median sensory nerves across the carpal tunnel
  • negative Hoffman’s sign (flick middle finger, watch for flexion of index/ thumb = UMN lesion) can distinguish
    from degenerative cervical myelopathy as CTS is LMN
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5
Q

CTS - management

A
  • Wrist splints worn every night for 1 month.
  • Activities that particularly provoke symptoms should be limited or modified.
  • consider NSAIDs for pain
  • corticosteroid injection
  • surgical decompression (flexor retinaculum division)
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6
Q

Meningitis - viral

A

Viral meningitis is the most common cause of aseptic meningitis. Causative agents include human enteroviruses (most commonly), HSV, mumps, arboviruses such as West Nile, HIV, and (rarely) influenza. However, it is typically self-limiting without serious sequelae.

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7
Q

Viral meningitis - features

A
- RF: infants and young children, older people, young adults, and exposure to insect vectors, unvaccinated for mumps
headache
nausea and vomiting
photophobia
neck stiffness
fever
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8
Q

Meningitis - bacterial

A

Bacterial meningitis is rare but serious. Streptococcus pneumoniae , Haemophilus influenzae type b (Hib), and Neisseria meningitidis are the predominant causative pathogens in both adults and children.

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9
Q

Bacterial meningitis - risk factors

A
  • age ≤5 years or ≥65 years
  • crowding, exposure to pathogens
  • non-immunised infants
  • immunodeficiency, asplenia or hyposplenia
  • cranial anatomical defects
  • ventriculoperitoneal shunt
  • cancer
  • HIV/AIDS
  • cochlear implants
  • sickle cell disease
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10
Q

Bacterial meningitis - features

A
headache
neck stiffness (+ nuchal rigidity - resistance to passive neck flexion
fever
altered mental status, confusion
photophobia
vomiting
seizures
infants: hypothermia, irritability, lethargy, poor feedings, apnoea, high-pitched cry
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11
Q

Meningitis - what signs could be seen O/E?

A
  • rash (in both but more common in viral)

More common in bacterial:

  • Kernig’s sign (severe stiffness of the hamstrings causes an inability to straighten the leg when the hip is flexed to 90 degrees)
  • Brudzinski’s sign (Severe neck stiffness causes a patient’s hips and knees to flex when the neck is flexed)
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12
Q

Bacterial meningitis - investigations

A
  • LP for CSF count = CSF pleocytosis, with WBC count >10⁹/L, predominance of polymorphonuclear leukocytes aka NEUTROPHILS
  • CSF protein = usually elevated (>0.5 g/L).
  • CSF glucose: low = is <45 mg/dL (2.5 mmol/L), or <40% of simultaneously measured serum glucose
  • CSF gram stain reveals organism in 80% cases
  • CSF culture
  • antigen detection in CSF (eg Neisseria meningitidis)
  • blood culture
  • FBC = leukocytosis, anaemia, thrombocytopenia
  • serum CRP = high
  • serum electrolytes, glucose = acidosis, low Ca/Mg, or hyper/hypoglycaemia
  • coagulation profile (PT, INR, activated PTT, fibrinogen, fibrin degradation products) = evidence of DIC (prolonged thrombin time, elevated fibrin degradation products or D-dimer, low fibrinogen or antithrombin)
  • CT head = normal or raised ICP
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13
Q

Viral meningitis - investigations

A
  • CSF microscopy = WBC count >5 cells/mm^3. Lymphocytosis
  • CSF gram stain and culture both negative
  • CSF protein normal or mildly elevated
  • CSF glucose usually normal
  • CT/MRI head = normal or raised ICP. exclude brain abscess and encephalitis (HSV-1 encephalitis normally causes lesions in temporal lobe)
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14
Q

Meningitis - initial management

A
  • LP usually performed before antibiotic administration
  • If the patient is very ill, is immunocompromised, or has received prior Abx, empirical antibiotic Tx is justified
  • need to cover group B streptococci, Listeria , and coliforms
  • local protocols and guidelines should be consulted for selection of antibiotic therapy
  • 1st line Abx normally Cefotaxime IV
  • adjunct dexamethasone (evidence that reduces hearing loss and neurological sequelae) - reduce ICP
  • A diagnosis of viral meningitis will allow antibiotics to be stopped
  • Amoxicillin (or ampicillin) if listeria is suspected
  • Aciclovir - pts with confusion/meningoencephalitis (need to cover for HSV and VZV)
  • elderly: combine vancomycin + ceftriaxone + ampicillin
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15
Q

Meningitis managment- confirmed viral aetiology

A

For all pathogens except HSV, varicella zoster, CMV:
- supportive care: adequate hydration, antipyretics for fever, anti-emetics if vomiting, analgesia for headaches

  • HSV or varicella zoster = aciclovir or valaciclovir + supportive care
  • CMV = ganciclovir or valganciclovir + supportive
  • recurrent viral meningitis (Mollaret’s meningitis, commonly due to HSV-2): consider antiviral
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16
Q

Bacterial meningitis - management (empirical)

A
  • < 3 month age = cefotaxime + amoxicillin
  • > 3 month to 50 years = ceftriaxone OR cefotaxime
  • > 50 years = cefotaxime + amoxicillin

(pt older than 3 m –> dexamethasone)

  • supportive care = oxygen if symptoms of shock or resp distress, IV fluids, prevention of hypoglycaemia and hyponatraemia, anticonvulsant therapy to control and prevent seizures, vasopressors (e.g. adrenaline) if hypotensive or poor perfusion
  • ppx to ppl that have been in contact with the pt 7 days prior onset: ciprofloxacin
17
Q

Myasthenia gravis - features

A
  • disorder of the post-synaptic membrane at NMJ against the nicotinic acetylcholine receptor (AChR)
  • muscle weakness that increases with exercise (fatigue) and improves on rest. Commonly presents with drooping eyelids, double vision, oropharyngeal and/or appendicular weakness, and shortness of breath.
  • associated with thymoma
  • a/w pernicious anaemia, autoimmune thyroid disorders, rheumatoid, SLE
18
Q

MG - investigations

A
  • single fibre electromyography: high sensitivity (92-100%)
  • Elevated serum acetylcholine receptor antibody titres or muscle-specific tyrosine kinase antibodies are present.
  • CT thorax to exclude thymoma
  • CK normal
19
Q

MG - treatment

A
  • plasma exchange or IV immunoglubulin
  • prednisolone
  • 2nd line: eculizumab or rituximab
20
Q

Lambert-Eaton myasthenic syndrome (LEMS)

A
  • circulating antibodies against voltage-gated calcium channels; these impair neuromuscular transmission by inhibiting release of ach into the synaptic cleft.
  • associated with small-cell lung cancer.
  • Similar to myasthenia gravis but movements IMPROVE with exercise, in MG they get WORSE with exercise
  • insidious and gradual onset of fatigue, weakness, and a dry mouth
  • proximal muscle weakness in hip girdle and thigh muscles; absent or reduced tendon reflexes and dilated, poorly reactive pupils
21
Q

Charcot-Marie-Tooth disease

A
  • hereditary motor and sensory neuropathy (HMSN)
  • CMT 1 and 2 autosomal dominant, CMT 4 recessive
  • CMT 1 affect schwann cell and myelin (demyelinating CMT), while CMT 2 affect axons (axonal CMT)
  • Key features include clumsiness as a child, weak ankles, symmetrical nerve conduction changes (slow conduction and absent sensory responses), and a steppage gait (lifting legs up excessively to clear toes)
  • Pes cavus (high foot arches with hammer toes) and distal atrophy of the hands and legs
  • There may be a history of frequently sprained ankles
  • Foot drop
  • Distal muscle weakness + atrophy
  • Hyporeflexia
22
Q

Somatisation Disorder

A
  • Hx of many physical complaints before the age of 30
  • 4 x pain symptoms ( history of pain in atleast 4 different sites) = 2 x GI symptoms, 1 x sexual symptoms, 1 x pseudoneurological e.g. low coordination/balance
  • symptoms are not faked
  • common features: 1. teenage onset. 2. female
    3. vague or dramatic history. 4. emphasis on suffering
    6. personality or mood disorders 7. substance abuse
23
Q

Conversion disorder

A

Pt presents with a motor or sensory impairment with no organic cause identified during testing (physical manifestation of a psychological problem)

  • unconsciously mimicking symptoms
  • not for conscious external motive
  • inconsistent symptoms and findings
  • Eg stroke-like impairments, pseudoseizures, tremor

In other words, unintentionally mimicks sickness for no external reason

24
Q

Factitious disorder

A
  • faked symptoms (consciously mimicks symptoms)
  • motivation for behavior is to adopt the sick role, and external incentives for behavior are absent

(unlike malingering, where symptoms are faked to get reward eg avoiding work/school)

In other words, intentionally fakes to be sick for no external reason

25
Q

Meningitis - vaccinations

A

Men B = 3 doses -> 2 months, 4 months, 12-13 months

Men C

Men ACWY = meningitis ACWY vaccine has replaced meningitis C for 13-18 year-olds due to an increased incidence of meningitis W. Also to new students (up to the age of 25 years) at university

26
Q

Meningitis - TB and fungal

A

TB

  • CSF: low glucose, high protein
  • mildly raised lymphocytes
  • The Ziehl-Neelsen stain is only 20% sensitive in TB meningitis therefore PCR is sometimes used

Fungal

  • CSF: low glucose, high protein
  • mildly raised lymphocytes