Rosen & Barkin's 5-Minute Emergency Medicine Consult (510 page)

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Authors: Jeffrey J. Schaider,Adam Z. Barkin,Roger M. Barkin,Philip Shayne,Richard E. Wolfe,Stephen R. Hayden,Peter Rosen

Tags: #Medical, #Emergency Medicine

BOOK: Rosen & Barkin's 5-Minute Emergency Medicine Consult
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See Also (Topic, Algorithm, Electronic Media Element)
  • Phimosis
  • Priapism
CODES
ICD9

605 Redundant prepuce and phimosis

ICD10

N47.2 Paraphimosis

PARKINSON DISEASE
Adam Z. Barkin
BASICS
DESCRIPTION
  • Gradual progressive neurologic disorder of middle or late life
  • Degeneration of dopaminergic neurons in the substantia nigra
  • Development of Lewy bodies in the residual dopaminergic neurons
  • Accelerated cortical atrophy
  • Can begin unilaterally, but generalizes to symmetric
  • Affects 1% of people >60 yr; 4% >80 yr
  • May have symptoms 20 yr prior to diagnosis
    • Nonspecific:
      • Fatigue
      • Constipation
      • Hyposomia
ETIOLOGY
  • Sporadic or idiopathic
  • Disorders presenting with parkinsonism:
    • Drug induced:
      • Parkinsonism-hyperpyrexia syndrome (dopaminergic drug withdrawal)
      • Amphotericin B
      • Chemotherapeutic drugs
      • Neuroleptic treatment induced
    • Toxins:
      • Carbon monoxide
      • Methanol
      • Cyanide
      • Organophosphate poisoning
      • 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine
    • Brain lesions:
      • Basal ganglia stroke
      • Midbrain lesions
      • Hydrocephalus
    • Infections:
      • Mycoplasma
      • Viral encephalitis
    • Other:
      • Central pontine myelinosis
      • Encephalitis lethargica (autoantibodies against basal ganglia antigens)
DIAGNOSIS
SIGNS AND SYMPTOMS
  • Nonmotor vs. motor symptoms:
    • Nonmotor:
      • Orthostatic hypotension
      • Constipation
      • Delayed gastric emptying
      • Dysphagia
      • Pain sensory dysfunction
      • Depression
      • Hallucinations
      • Dementia
      • Sleep disorders
  • Motor symptoms:
    • “Pill-rolling” resting tremor
    • “Cog-wheel” rigidity due to increased muscular tone
    • Stooped posture and instability of posture
    • Bradykinesia: Extreme slowness in movement
    • “Masked face” appearance
History
  • Sudden change in baseline motor function or mental status:
    • May be the only indication of systemic disease such as infection
  • Noncompliance (sudden withdrawal) of dopaminergic medications can lead to parkinsonism-hyperpyrexia syndrome:
    • Rigidity, pyrexia, reduced consciousness
    • Complications:
      • Acute renal failure
      • Venothrombosis
      • Disseminated intravascular coagulation
      • Rhabdomyolysis
      • Autonomic instability
Physical-Exam
  • Cog-wheel rigidity:
    • Jerking movements when a muscle is passively stretched
  • Stooped posture
  • Pill-rolling tremor
ESSENTIAL WORKUP
  • History is of primary importance:
    • Diagnosis is made based on clinical findings
  • Important historical information includes:
    • Onset of symptom, whether gradual or sudden
    • History of potential causes of a Parkinson-like syndrome
    • Patients with established Parkinson disease (PD):
      • Sudden change in baseline motor function
      • Change in mental status
      • Should prompt workup for infectious process
DIAGNOSIS TESTS & NTERPRETATION
Lab
  • No specific or recommended lab studies necessary to confirm the diagnosis
  • Disorders presenting as PD may require directed lab studies as appropriate for suspected cause
  • Directed labs if suspect parkinsonism-hyperpyrexia syndrome
Imaging
  • CT and MRI are not required to diagnose PD but are often elements of evaluation for dementia
  • CXR may be indicated for any signs of respiratory tract infection
DIFFERENTIAL DIAGNOSIS
  • Benign familial tremor
  • Major depression
  • Wilson disease
  • Huntington disease
  • Alzheimer disease
  • Creutzfeldt–Jakob disease
  • Carbon monoxide poisoning
  • B
    12
    deficiency
  • Hydrocephalus
  • Multi-infarct dementia
  • Essential tremor disorders
  • Hypothyroidism
  • Dementia with Lewy bodies
TREATMENT
ED TREATMENT/PROCEDURES
  • Treatment with antiparkinsonian medications can be initiated in the ED to alleviate symptoms
  • Consultation with neurology for recommended medication regimens and ongoing support and monitoring is prudent
  • For patients with mild disease, no medication may be required
  • For moderate disease, anticholinergic medications and dopaminergic medications should be used
  • Treat underlying infection, if present
  • Treat parkinsonism-hyperpyrexia syndrome:
    • Replace levodopa or bromocriptine
    • Supportive
    • Treat complications
MEDICATION
  • PD:
    • Amantadine: 100 mg BID
      • Stimulates dopamine release
    • Benztropine: 0.5–1 mg TID
      • Anticholinergic
      • Limited use in tremor-dominant PD
    • Carbidopa/levodopa: 25/100 mg TID
      • Carbidopa lessens peripheral side effects and increased levodopa CNS bioavailability
      • Levadopa is direct precursor to dopamine
    • Entacapone: 200 mg PO BID–QID
      • Adjunct therapy; should be administered concomitantly with carbidopa/levodopa
      • Increases CNS levadopa bioavailability
    • MAO inhibitors
      • May be used in mild disease as first-line therapy
    • Selegiline: 5 mg qam and noon
    • Rasagiline: 1–2 mg QD
    • Dopamine agonists:
      • Pramipexole: 0.5–1.5 mg PO TID
      • Ropinirole: 3–6 mg PO TID
      • Apomorphine: 0.2–0.6 mL SQ PRN
  • Parkinsonism-hyperpyrexia syndrome:
    • Levodopa: 50–100 mg IV over 3 hr
    • Bromocriptine: 7.5–15 mg PO TID
First Line

Carbidopa/levodopa

FOLLOW-UP
DISPOSITION
Admission Criteria
  • Patients with previously diagnosed Parkinson with infections, trauma, cardiovascular emergencies, cerebrovascular emergencies, GI emergencies, electrolyte disturbances, altered mental status, or other medical problems
  • Depression with intent to do self-harm
  • Confirm diagnosis and levodopa responsiveness
  • Medication complications (parkinsonism-hyperpyrexia syndrome)
  • Management of motor fluctuations and dyskinesias
  • Inability to go home secondary to elder abuse
  • Complications from deep brain stimulation devices (e.g., headache, infection, mental status change)
  • Failure to thrive

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