Chapter 8 Pt 5 Flashcards
what is Parkinson’s Disease
an idiopathic, progressive neurodegenerative disease characterized by depletion of DOPAMINE in the BASAL GANGLIA
put o 75% of patients with PD meet criteria for major NCD, typically late in the course of the disease
what are the clinical manifestations of PD
rigidity, resting tremor, bradykinesia, and postural instability
cognitive manifestations consist of executive dysfunction and visuospatial impairments
depression, anxiety, personality changes, and apathy are common
psychotic symptoms may result from disease itself or medications
how is PD diagnosed
requires presence of BRADYKINESIA and either TREMOR or RIGIDITY
what is required for PD diagnosis
BRADYKINESIA
what is good supporting information that the diagnosis is PD
asymmetry of motor symptoms and favorable response to dopaminergic therapy support the diagnosis
mild or major NCD is attributable to PD if
COGNTIVE DECLINE APPEARS AFTER THE ONSET OF MOTOR SYMPTOMS and no other underlying etiology is identified
how is PD treated
CARBIDOPA-LEVODOPA and/or DOPAMIE AGONISTS
cholinesterase inhibitors are used to treat cognitive symptoms and may also ameliorate some of the neuropsychiatric symptoms (hallucinations)
psychotic symptoms may respond to decrease in dopamine agonsits
what are the preferred mediations for treatment of psychotic symptoms in PD not responsive to dose reduction
QUEITAPINE and CLOZAPINE
symptoms of parkinson’s can be exacerbated by what medications
antipsychotics
what is Prion Disease
form of subacute spongiform encephalopathy caused by proteinaceous infectious particles (prions)
most cases occur sporadically
up to 15% are familial (autosomal DOMINANT)
what is the most common prion disease
CREUTZFELDT JAKOB disease
what are clinical manifestations of prion disease
RAPIDLY PROGRESSIVE cognitive decline
difficulties with CONCENTRATION, MEMORY, and JUDGEMENT occur early
more than 90% of patients have MYOCLONUS (often provoked by startle)
depression, apathy, and hypersonic are also common
basal ganglia and cerebellar dysfunction: ATAXIA, NYSTAGMUS, HYPOKINESIA
rapidly progressive cognitive decline and MYOCLONUS suggests
CJD
how is prion disease diagnosed
biopsy of brain tissue or autopsy
probably CJD diagnosis: RAPID PROGRESSION of cognitive decline at least 2: -MYOCOLONUS -visual or cerebellar signs -pyramidal or extrapyramidal sings -akinetic mutism
what are supportive findings of prion disease
periodic SHARP WAVE COMPLEXES on EEG
CSP positive for 14-3-3 proteins
lesions in PUTAMEN or CAUDATE nucleus on MRI