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Akathisia
SUMMARIZED BY: ADE WIJAYA, MD
Lohr, J. B., Eidt, C. A., Alfaraj, A. A., & Soliman, M. A. (2015). The clinical challenges of akathisia. CNS spectrums, 20(S1), 1-16.
Outline:
• Introduction
• Subtype
• Etiology
• Risk factors
• Differential diagnosis
• Pathophysiology
• Assestment
• Treatment
• Summary
Introduction
• Coined by the Czechoslovakian neuropsychiatrist, Ladislav Hascovecin 1901
• Psychiatric  movement disorder
• A sensorimotor disorder
• Extrapyramidal
Subtype by Duration
Acute
• < 1 weeks
subacute
• > 1 weeks and < several months
Chronic
• Several months
Other Subtypes
• 2 weeks after discontinuation of antipsychotics
• Symptoms disappear after 6 weeksWithdrawal
• Occurs late in the treatment course ( > 3 months)
• May emerge after drugs discontinuation or dose reduction
• Reduce its severity by increasing the dose
• Persist for months and years
Tardive
• No sensory component
• Psychiatric conditionpseudoakathisia
Bing-Siccard •Parkinson’s disease (PD)
•Post-encephalitic parkinsonism
Etiology
• Drug-induced akathisia
• Antipsychotics
• Antidepressants
• Other drugs
• Akathisia in parkinsonian condition
• Spontaneous akathisia
Antipsychotic-induced Akathisia
• First-generation antipsychotics
• 8–76% of treated patients
• Lower incidence in 2nd generation antipsychotics
Antidepressant-induced Akathisia
• SSRI
• Azithromycin
• Calcium channel blockers,
• Lithium,
• Anti-dopaminergic anti-emetics (such as prochlorperazine and metaclopramide)
• Dopamine-depleting agents (reserpine and tetrabenazine)
• Recreational drugs:
- gamma-hydroxybutyrate (GHB)
- methamphetamine
- 3,4-methylenedioxymethamphetamine (MDMA, ecstasy)
- cocaine
Other drugs
Akathisia in parkinsonian condition
• Parkinson disease
• Post-encephalitic parkinsonism,
• Cortico-basal degeneration (CBD)
• Multiple system atrophy (MSA)
• L-Dopo related
Risk Factors for Drug-Induced Akathisia
• Schizophrenia
• Bipolar disorder
• Higher dose
• Rapid dose increase
• Traumatic brain injury
• Cancer
• Iron deficiency
• Advance age
• Female
Differential Diagnosis
• Anxiety
• Agitation with medical conditions
• Psychomotor agitation
• Tics and Tourette disorder
• Antipsychotic-induced tardive dyskinesia
• Antipsychotic-induced dystonia
• Antipsychotic-induced parkinsonian tremor
• RLS and PLMD
Pathophysiology
• Blockade of mesocortical dopaminergic pathways
• Generalized reduction in dopamine in the brain  increase noradrenergic activity
Assestment
• Clinical observation and patient report
• Barnes Akathisia Rating Scale (BARS)
Treatment
• Treatment aimed at the cause
• Reduce or switch medications, observe until 6 weeks (due to withdrawal akathisia)
• Correct Fe in iron deficiency
• Anticholinergic drugs (such as biperiden, trihexyphenidyl, and benztropine)
• Beta-blockers (such as propranolol and metoprolol)
• Serotonin 5-HT2A antagonists (such as mianserin, mirtazapine, and cyproheptadine)
• Vitamin B6, n-acetylcysteine, tetrabenazine, and benzodiazepine
• Piracetam, buspirone, opiates, clonidine, bromocriptine, amantadine
Summary
1. Akathisia is a complex, confusing, and under-recognized problem that causes considerable
suffering
2. Sensorimotor movement disorder
3. EPS
4. Treatment aimed at the cause
Akathisia

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Akathisia

  • 1. Akathisia SUMMARIZED BY: ADE WIJAYA, MD Lohr, J. B., Eidt, C. A., Alfaraj, A. A., & Soliman, M. A. (2015). The clinical challenges of akathisia. CNS spectrums, 20(S1), 1-16.
  • 2. Outline: • Introduction • Subtype • Etiology • Risk factors • Differential diagnosis • Pathophysiology • Assestment • Treatment • Summary
  • 3. Introduction • Coined by the Czechoslovakian neuropsychiatrist, Ladislav Hascovecin 1901 • Psychiatric  movement disorder • A sensorimotor disorder • Extrapyramidal
  • 4. Subtype by Duration Acute • < 1 weeks subacute • > 1 weeks and < several months Chronic • Several months
  • 5. Other Subtypes • 2 weeks after discontinuation of antipsychotics • Symptoms disappear after 6 weeksWithdrawal • Occurs late in the treatment course ( > 3 months) • May emerge after drugs discontinuation or dose reduction • Reduce its severity by increasing the dose • Persist for months and years Tardive • No sensory component • Psychiatric conditionpseudoakathisia Bing-Siccard •Parkinson’s disease (PD) •Post-encephalitic parkinsonism
  • 6. Etiology • Drug-induced akathisia • Antipsychotics • Antidepressants • Other drugs • Akathisia in parkinsonian condition • Spontaneous akathisia
  • 7. Antipsychotic-induced Akathisia • First-generation antipsychotics • 8–76% of treated patients • Lower incidence in 2nd generation antipsychotics Antidepressant-induced Akathisia • SSRI
  • 8. • Azithromycin • Calcium channel blockers, • Lithium, • Anti-dopaminergic anti-emetics (such as prochlorperazine and metaclopramide) • Dopamine-depleting agents (reserpine and tetrabenazine) • Recreational drugs: - gamma-hydroxybutyrate (GHB) - methamphetamine - 3,4-methylenedioxymethamphetamine (MDMA, ecstasy) - cocaine Other drugs
  • 9. Akathisia in parkinsonian condition • Parkinson disease • Post-encephalitic parkinsonism, • Cortico-basal degeneration (CBD) • Multiple system atrophy (MSA) • L-Dopo related
  • 10. Risk Factors for Drug-Induced Akathisia • Schizophrenia • Bipolar disorder • Higher dose • Rapid dose increase • Traumatic brain injury • Cancer • Iron deficiency • Advance age • Female
  • 11.
  • 12. Differential Diagnosis • Anxiety • Agitation with medical conditions • Psychomotor agitation • Tics and Tourette disorder • Antipsychotic-induced tardive dyskinesia • Antipsychotic-induced dystonia • Antipsychotic-induced parkinsonian tremor • RLS and PLMD
  • 13. Pathophysiology • Blockade of mesocortical dopaminergic pathways • Generalized reduction in dopamine in the brain  increase noradrenergic activity Assestment • Clinical observation and patient report • Barnes Akathisia Rating Scale (BARS)
  • 14.
  • 15. Treatment • Treatment aimed at the cause • Reduce or switch medications, observe until 6 weeks (due to withdrawal akathisia) • Correct Fe in iron deficiency • Anticholinergic drugs (such as biperiden, trihexyphenidyl, and benztropine) • Beta-blockers (such as propranolol and metoprolol) • Serotonin 5-HT2A antagonists (such as mianserin, mirtazapine, and cyproheptadine) • Vitamin B6, n-acetylcysteine, tetrabenazine, and benzodiazepine • Piracetam, buspirone, opiates, clonidine, bromocriptine, amantadine
  • 16. Summary 1. Akathisia is a complex, confusing, and under-recognized problem that causes considerable suffering 2. Sensorimotor movement disorder 3. EPS 4. Treatment aimed at the cause