Infectious Disorders and Neoplasms of CNS Flashcards

1
Q

Describe meningitis

A
  • Inflammation of the meninges of brain & spinal cord secondary to infection
  • Needs to be treated quickly
  • Inflammation can extend to 1st & 2nd layers of cortex & spinal cord
  • Increased chance of tissue infarction, scar tissue formation, which can restrict CSF flow, resulting in hydrocephalus
  • Stretch & pressure on meninges can cause the cardinal sign: headache
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2
Q

Pathogenesis of meninges

A
  • Bacterial & viral infections: Pneumonia, Influenza, Meningococcus, Tuberculosis, Enterviruses, Herpes virus
  • Pathogens invade host mucosal epithelium, multiply in blood stream & cross BBB into CSF
  • CSF offer much less immunity from pathogens due to lack of immune cells
  • Besides inflammation of meninges, neuronal cell death can occur through apoptosis & necrosis
  • White matter injury also occurs secondary to small vessel vasculitis, venous thrombosis & focal ischemia
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3
Q

Clinical manifestations of meningitis

A
  • Primary signs: headache, sudden high fever, stiff neck
  • Other signs: altered mental status, vomiting, focal deficits, loss of appetite, sensitivity to light
  • Positive meningeal signs: Nuchal rigidity, Kernig’s sign, Brudzinski’s sign
  • In severe cases: opisthotonus, seizures, reduced level of consciousness
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4
Q

How to diagnose meningitis

A
  • Lumbar puncture for culture to determine the type of organism involved
  • CT or MRI
  • Time course of onset indicates type of organism
  • Viral meningitis can develop in hrs and bacterial can take 1-2 days
  • Gram staining of bacterial cells for. faster diagnosis of. bacterial meningitis
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5
Q

Treatment of meningitis

A
  • Treated promptly with antibiotics that can cross BBB
  • Steroids like dexamethasone to reduce inflammation
  • Viral meningitis is symptomatic
  • Prognosis of. viral meningitis is excellent, most individuals recover in 1-2 wks
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6
Q

Describe encephalitis

A
  • Acute inflammatory disease of the brain parenchyma caused. by direct viral/bacterial invasion or by hypersensitivity initiated by virus
  • Inflammation primarily in gray matter of CNS
  • Viruses. carried by mosquitoes & ticks are responsible
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7
Q

Causative viruses of encephalitis

A
  • West nile virus
  • Herpes simplex
  • Mycoplasma
  • Protozoa
  • Complication from bacterial meningitis
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8
Q

Clinical manifestations of encephalitis

A
  • Sx depend on etiologic agent & brain area involved
  • Fever, headache, n/v followed by altered mental status (lethargy, confusion, memory disturbances), seizures
  • May be focal signs, hemiparesis, aphasia, sensory deficits, ataxia, chorea, athetosis
  • Infants: irritability, poor appetite
  • Meningeal irritation can cause stiff back, neck
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9
Q

Clinical manifestations of encephalitis from west nile virus

A
  • Fever
  • Headache
  • Stiff neck
  • Photophobia
  • Lesion of anterior horn cells cause paralysis & diminished reflexes
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10
Q

Clinical manifestations of encephalitis from herpes simplex

A
  • Seizures
  • Hallucinations
  • Memory disturbances
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11
Q

Diagnosis and treatment of encephalitis

A
  • Dx depends on detection of IgM antibody in serum or CSF, EEG
  • MRI better than CT
  • Tx depends on infectious agent: Acyclovir improves outcomes from herpes simplex
  • Close supervision of Sx is critical
  • Prognosis depends on infectious agent, recovery from paralysis is variable, depending on degree of motor neuron involvement
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12
Q

Describe primary versus secondary CNS neoplasms

A
  • Primary: develop in brain, spinal cord, or surrounding structures; benign or malignant
  • Secondary: metastatic; spread to CNS from another site such as lung or breast
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13
Q

Describe paraneoplastic syndromes versus leptomeningeal carcinoma

A
  • Paraneoplastic: may. occur bc of remote effects or indirect effects on CNS from cancer elsewhere in body
  • Leptomeningeal Carcinoma: when cancer metastasizes to pia &. arachnoid with multiple lesions in meninges & CSF pathways
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14
Q

Diagnosis and treatment of CNS neoplasms

A
  • Dx is devastating to patient & family
  • Difficult decisions about treatment options & QOL issues add stress
  • Caregiving & financial struggles are. frequently encountered
  • Situation is improving with dramatic new advances in radiologic imaging, neurosurgery, adjuvant therapy
  • At present ~50% of patients with CNS tumors can be successfully treated & have excellent long term prognosis
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15
Q

Effects of CNS neoplasms

A
  • Most primary malignant tumors are locally invasive & cause significant morbidity & mortality
  • Early effects: displacement of Brian or spinal cord tissue or blockage of CSF circulation causing increased ICP
  • Tumor grows -> compression increases -> specific neurologic deficits
  • As tumor progresses symptoms of brain tumors may range from minimal (lethargy) to marked (paralysis)
  • Primary CNS tumors do not usually metastasize outside CSN due to lack of CNS lymphatic system to transport cancer cells
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16
Q

Initial signs of a CNS neoplasms

A
  • Headache: tension type and migraine most common
  • Changes in mental status
  • Behavioral changes
  • Papilledema, swelling in optic disc
  • ~20-50% adults develop seizure activity: may be the first sign of tumor in them
17
Q

Clinical manifestations of CNS neoplasms

A
  • Headache
  • Visual changes
  • Nausea
  • Vomiting
  • Cognitive changes
  • Lethargy
  • Behavioral changes
  • Seizures
  • Syncope
  • Weakness
  • Hemiparesis, hemiplegia
  • Apraxia
  • Cortical sensory deficits
  • Sensory impairments
  • Cranial nerve palsies
  • Aphasia
  • Facial numbness
  • Hearing disturbances
  • Anosmia
  • Swallowing difficulties
  • Paralysis of outward gaze
  • Papilledema
  • Incoordination
  • Ataxia
  • In children: diastases of cranial sutures & enlarging head size
18
Q

How to diagnose of CNS neoplasms

A
  • Clinical examination & imaging
  • MRI more informative than CT
19
Q

Medical treatment of CNS neoplasms

A
  • Surgical removal of tumor
  • Radiation therapy
  • Chemotherapy
  • Hormonal therapy
  • Immunotherapy
20
Q

CNS neoplasms implications for PT

A
  • Cluster of symptoms indicating. possible tumor: headache, N/V, lethargy, etc, and progression of symptoms despite physical therapy interventions
  • Will require immediate referral to physician
21
Q

CNS neoplasms implications for PT in acute post-op rehab

A
  • Knowledge of different tumors for treatment planning, goal setting, pt/family education
  • Knowledge of complications from surgery, radiation, chemotherapy and be able to adjust interventions
  • Management of increases ICP: shunt, elevation of head to 20-30º, neck in neutral, avoid extreme hip/knee flexion
  • Patient education to observe status of drainage in shunt, precautions to avoid coughing, sneezing, or blowing nose, check body temp. is normal
  • ROM may be started is medically stable to minimize risk of DVT
22
Q

CNS neoplasms implications for PT in subacute & ambulatory rehab

A
  • Continue monitoring required vital signs, neurologic changes, and adverse effects
  • No heat or cold to irradiated. areas for several wks after Tx until skin has healed
  • Strength & endurance training, functional mobility, balance, gait training, AD requirements. depending on impairments
  • Good outcomes with interval training
  • Avoid exercises that increase ICP like vigorous resistive exercises or isometrics
  • Outcome measure: Karnofsky scale
23
Q

CPG for cancer patients

A
  • Goal of 150 min of mod-intensity aerobic exercise over 3-5 days & resistance training at least 2 days per wk
  • Resistance sessions involve 8-10 muscle groups, 8-10 reps. 2 sets for 2-3 days/wk
  • Pre-exercise assessment recommended
  • When possible it’s recommended cancer patients exercise in a group