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BIOLOGICAL THERAPIES
MARIA FE SALVADOR-NAVARRETE, MD.
Medication-Induced Movement
Disorders
 neuroleptic-related movement disorders are:
 parkinsonism
 acute dystonia
 and acute akathisia
 Neuroleptic malignant syndrome
 Neuroleptic-induced tardive dyskinesia
Neuroleptic-Induced Parkinsonism
 Diagnosis, Signs, and Symptoms
 Symptoms :stiffness (lead pipe rigidity),
 cogwheel rigidity,
 shuffling gait,
 stooped posture,
 and drooling.
 The pill-rolling tremoR is rare
 coarse tremor similar to essential tremor
 rabbit syndrome,
 perioral tremor occur late in the course of treatment.
 Epidemiology
 Parkinsonian adverse effects occur in about
15 percent of patients who are treated with
antipsychotics, usually within 5 to 90 days of
the initiation of treatment.
 Etiology
 Neuroleptic-induced parkinsonism is caused
by the blockade of dopamine type 2 (D2)
receptors in the caudate at the termination of
the nigrostriatal dopamine neurons
 All antipsychotics can cause the symptoms,
especially high-potency drugs with low levels
of anticholinergic activity
 (e.g., trifluoperazine [Stelazine]).
 Chlorpromazine (Thorazine) and thioridazine
(Mellaril) are not likely to be involved.
 (e.g., aripiprazole [Abilify], olanzapine
[Zyprexa], and quetiapine [Seroquel]) are less
likely to cause parkinsonism.
 Differential Diagnosis
 Included in the differential diagnosis are
idiopathic parkinsonism,
 other organic causes of parkinsonism,
 and depression, which can also be associated
with parkinsonian symptoms.
Treatment
 Parkinsonism can be treated with
anticholinergic agents, benztropine
(Cogentin), amantadine (Symmetrel), or
diphenhydramine (Benadryl)
Neuroleptic-Induced Acute Dystonia
 Diagnosis, Signs, and Symptoms
 Dystonias are brief or prolonged contractions
of muscles that result in obviously
 abnormal movements or postures,
 including oculogyric crises,
 tongue protrusion,
 trismus, torticollis,
 laryngeal–pharyngeal dystonias,
 and dystonic postures of the limbs and trunk
 Other dystonias include blepharospasm and
 glossopharyngeal dystonia;
 >>> dysarthria, dysphagia, and even difficulty in
breathing, which can cause cyanosis.
 Children :
 opisthotonos,
 scoliosis,
 lordosis,
 writhing movements.
 Dystonia can be painful and frightening
 Etiology
 Although it is most common with
intramuscular doses of high-potency
antipsychotics, dystonia can occur with any
antipsychotic.
 The mechanism of action is thought to be
dopaminergic hyperactivity in the basal
ganglia that occurs when central nervous
system (CNS) levels of the antipsychotic drug
begin to fall between doses.
 Differential Diagnosis
 The differential diagnosis includes seizures
and tardive dyskinesia.
 Course and Prognosis
 Dystonia can fluctuate spontaneously and
respond to reassurance, so that the clinician
acquires the false impression that the
movement is hysterical or completely under
conscious control.
 Treatment
 Prophylaxis with anticholinergics or related
drugs (Table 36.2-2)
 Treatment with intramuscular anticholinergics
or intravenous or intramuscular
diphenhydramine (50 mg) almost always relieves
the symptoms.
 Diazepam (Valium) (10 mg intravenously),
 amobarbital (Amytal),
 caffeine sodium benzoate, and hypnosis have
also been reported to be effective.
Neuroleptic-Induced Acute Akathisia
 Diagnosis, Signs, and Symptoms
 Akathisia
 Examples include a sense of anxiety, inability to relax,
jitteriness, pacing, rocking motions while sitting, and rapid
alternation of sitting and standing.
 Akathisia has been associated with the use of a wide range
of psychiatric drugs, including antipsychotics,
antidepressants, and sympathomimetics.
 Once akathisia is recognized and diagnosed, the
antipsychotic dose should be reduced to the minimal
effective level.
 Akathisia may be associated with a poor treatment
outcome.
 Treatment
 Three basic steps in the treatment of akathisia
 reducing medication dosage,
 attempting treatment with appropriate drugs,
 considering changing the neuroleptic.
 The most efficacious drugs are β-adrenergic receptor
antagonists,
 although anticholinergic drugs, benzodiazepines,
 and cyproheptadine (Periactin) may benefit some patients.
 In some cases of akathisia, no treatment seems to be
effective.
Neuroleptic-Induced Tardive
Dyskinesia
 Diagnosis, Signs, and Symptoms
 Tardive dyskinesia is a delayed effect of
antipsychotics;
 it rarely occurs until after 6 months of treatment.
 The disorder consists of abnormal,
 involuntary, irregular choreoathetoid
movements of the muscles of the head, limbs,
and trunk.
 The severity of the movements ranges from
minimal—often missed by patients and their
families—to grossly incapacitating.
 Perioral movements are the most common and include
darting, twisting, and protruding movements of the
tongue; chewing and lateral jaw movements; lip puckering;
and facial grimacing.
 Finger movements and hand clenching are also common.
 Torticollis, retrocollis, trunk twisting, and pelvic thrusting
occur in severe cases.
 In the most serious cases, patients may have breathing and
swallowing irregularities that result in aerophagia,
belching, and grunting.
 Respiratory dyskinesia has also been reported. Dyskinesia is
exacerbated by stress and disappears during sleep.
 Treatment
 The three basic approaches to tardive
dyskinesia are prevention, diagnosis, and
management.
 Clozapine is the only antipsychotic to have
minimal risk of tardive dyskinesia, and can
even help improve preexisting symptoms of
tardive dyskinesia.
Neuroleptic Malignant
Syndrome
 Diagnosis, Signs, and Symptoms
 Neuroleptic malignant syndrome is a life-
threatening complication
 The motor and behavioral symptoms include
 muscular rigidity and dystonia, akinesia, mutism,
obtundation, and agitation.
 The autonomic symptoms include high fever,
sweating, and increased pulse and blood pressure.
 Laboratory :increased white blood cell count and
increased levels of creatinine phosphokinase, liver
enzymes, plasma myoglobin, and myoglobinuria,
occasionally associated with renal failure.
 Treatment
 In addition to supportive medical treatment, the most commonly
used medications for the condition are dantrolene (Dantrium)
and bromocriptine (Parlodel), although amantadine (Symmetrel)
is sometimes used.
 Bromocriptine and amantadine pose direct DRA effects and may
serve to overcome the antipsychotic-induced dopamine receptor
blockade.
 The lowest effective dosage of the antipsychotic drug should be
used to reduce the chance of neuroleptic malignant syndrome.
 Antipsychotic drugs with anticholinergic effects seem less likely
to cause neuroleptic malignant syndrome (Table 36.2-4).
Electroconvulsive therapy (ECT) has been used successfully and is
preferred by some clinicians.
Medication-Induced Postural
Tremor
 Diagnosis, Signs, and Symptoms
 Tremor is a rhythmic alteration in movement
that is usually faster than one beat per
second.
 Etiology
 Whereas all the above diagnoses specifically
include an association with a neuroleptic, a
range of psychiatric medications can produce
tremor—most notably, lithium,
antidepressants, and valproate (Depakene).
 Treatment
 The treatment involves four principles:
 The lowest possible dose of the psychiatric drug
should be taken.
 Patients should minimize caffeine consumption.
 The psychiatric drug should be taken at bedtime
to minimize the amount of daytime tremor.
 β-adrenergic receptor antagonists (e.g.,
propranolol [Inderal]) can be given to treat drug-
induced tremors.
 Other Movement Disorders
 Nocturnal Myoclonus
 Nocturnal myoclonus consists of highly
stereotyped, abrupt contractions of certain
leg muscles during sleep. Patients lack any
subjective awareness of the leg jerks.
 Restless Leg Syndrome
 In restless leg syndrome, persons feel deep
sensations of creeping inside the calves
whenever sitting or lying down.The
dysesthesias are rarely painful, but are
agonizingly relentless and cause an almost
irresistible urge to move the legs; thus, this
syndrome interferes with sleep and with
falling asleep.
 Hyperthermic Syndromes
 All the medication-induced movement
disorders may be associated with
hyperthermia.Table 36.2-5 lists the various
conditions associated with hyperthermia

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Chapter 36 t reg cells
 
Chapter 34 medical stat
Chapter 34 medical statChapter 34 medical stat
Chapter 34 medical stat
 
Chapter 33 isolated tumor cells
Chapter 33 isolated tumor cellsChapter 33 isolated tumor cells
Chapter 33 isolated tumor cells
 
Chapter 32 invasion and metastasis
Chapter 32 invasion and metastasisChapter 32 invasion and metastasis
Chapter 32 invasion and metastasis
 
Chapter 31 genetic counselling
Chapter 31 genetic counsellingChapter 31 genetic counselling
Chapter 31 genetic counselling
 
Chapter 30 febrile neutropenia
Chapter 30 febrile neutropeniaChapter 30 febrile neutropenia
Chapter 30 febrile neutropenia
 
Chapter 29 dendritic cells
Chapter 29 dendritic cellsChapter 29 dendritic cells
Chapter 29 dendritic cells
 
Chapter 28 clincal trials
Chapter 28 clincal trials Chapter 28 clincal trials
Chapter 28 clincal trials
 
Chapter 27 chemotherapy side effects dr lms
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Chapter 26 chemoprevention of cancer
Chapter 26 chemoprevention of cancerChapter 26 chemoprevention of cancer
Chapter 26 chemoprevention of cancer
 
Chapter 25 assessment of clincal responses
Chapter 25 assessment of clincal responsesChapter 25 assessment of clincal responses
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Chapter 24.3 metronomic chemotherapy
Chapter 24.3 metronomic chemotherapyChapter 24.3 metronomic chemotherapy
Chapter 24.3 metronomic chemotherapy
 
Chapter 24.2 lmwh in cancer asso thrombosis
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Chapter 24.1 kinase inhibitors and monoclonal antibodies
Chapter 24.1 kinase inhibitors and monoclonal antibodiesChapter 24.1 kinase inhibitors and monoclonal antibodies
Chapter 24.1 kinase inhibitors and monoclonal antibodies
 
Chapter 24 tyrosine kinase inhibitors
Chapter 24 tyrosine kinase inhibitorsChapter 24 tyrosine kinase inhibitors
Chapter 24 tyrosine kinase inhibitors
 

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Medication-Induced Movement Disorders Guide

  • 1. BIOLOGICAL THERAPIES MARIA FE SALVADOR-NAVARRETE, MD.
  • 2. Medication-Induced Movement Disorders  neuroleptic-related movement disorders are:  parkinsonism  acute dystonia  and acute akathisia  Neuroleptic malignant syndrome  Neuroleptic-induced tardive dyskinesia
  • 3. Neuroleptic-Induced Parkinsonism  Diagnosis, Signs, and Symptoms  Symptoms :stiffness (lead pipe rigidity),  cogwheel rigidity,  shuffling gait,  stooped posture,  and drooling.  The pill-rolling tremoR is rare  coarse tremor similar to essential tremor  rabbit syndrome,  perioral tremor occur late in the course of treatment.
  • 4.  Epidemiology  Parkinsonian adverse effects occur in about 15 percent of patients who are treated with antipsychotics, usually within 5 to 90 days of the initiation of treatment.
  • 5.  Etiology  Neuroleptic-induced parkinsonism is caused by the blockade of dopamine type 2 (D2) receptors in the caudate at the termination of the nigrostriatal dopamine neurons
  • 6.  All antipsychotics can cause the symptoms, especially high-potency drugs with low levels of anticholinergic activity  (e.g., trifluoperazine [Stelazine]).  Chlorpromazine (Thorazine) and thioridazine (Mellaril) are not likely to be involved.  (e.g., aripiprazole [Abilify], olanzapine [Zyprexa], and quetiapine [Seroquel]) are less likely to cause parkinsonism.
  • 7.  Differential Diagnosis  Included in the differential diagnosis are idiopathic parkinsonism,  other organic causes of parkinsonism,  and depression, which can also be associated with parkinsonian symptoms.
  • 8. Treatment  Parkinsonism can be treated with anticholinergic agents, benztropine (Cogentin), amantadine (Symmetrel), or diphenhydramine (Benadryl)
  • 9. Neuroleptic-Induced Acute Dystonia  Diagnosis, Signs, and Symptoms  Dystonias are brief or prolonged contractions of muscles that result in obviously  abnormal movements or postures,  including oculogyric crises,  tongue protrusion,  trismus, torticollis,  laryngeal–pharyngeal dystonias,  and dystonic postures of the limbs and trunk
  • 10.  Other dystonias include blepharospasm and  glossopharyngeal dystonia;  >>> dysarthria, dysphagia, and even difficulty in breathing, which can cause cyanosis.  Children :  opisthotonos,  scoliosis,  lordosis,  writhing movements.  Dystonia can be painful and frightening
  • 11.  Etiology  Although it is most common with intramuscular doses of high-potency antipsychotics, dystonia can occur with any antipsychotic.  The mechanism of action is thought to be dopaminergic hyperactivity in the basal ganglia that occurs when central nervous system (CNS) levels of the antipsychotic drug begin to fall between doses.
  • 12.  Differential Diagnosis  The differential diagnosis includes seizures and tardive dyskinesia.  Course and Prognosis  Dystonia can fluctuate spontaneously and respond to reassurance, so that the clinician acquires the false impression that the movement is hysterical or completely under conscious control.
  • 13.  Treatment  Prophylaxis with anticholinergics or related drugs (Table 36.2-2)  Treatment with intramuscular anticholinergics or intravenous or intramuscular diphenhydramine (50 mg) almost always relieves the symptoms.  Diazepam (Valium) (10 mg intravenously),  amobarbital (Amytal),  caffeine sodium benzoate, and hypnosis have also been reported to be effective.
  • 14. Neuroleptic-Induced Acute Akathisia  Diagnosis, Signs, and Symptoms  Akathisia  Examples include a sense of anxiety, inability to relax, jitteriness, pacing, rocking motions while sitting, and rapid alternation of sitting and standing.  Akathisia has been associated with the use of a wide range of psychiatric drugs, including antipsychotics, antidepressants, and sympathomimetics.  Once akathisia is recognized and diagnosed, the antipsychotic dose should be reduced to the minimal effective level.  Akathisia may be associated with a poor treatment outcome.
  • 15.  Treatment  Three basic steps in the treatment of akathisia  reducing medication dosage,  attempting treatment with appropriate drugs,  considering changing the neuroleptic.  The most efficacious drugs are β-adrenergic receptor antagonists,  although anticholinergic drugs, benzodiazepines,  and cyproheptadine (Periactin) may benefit some patients.  In some cases of akathisia, no treatment seems to be effective.
  • 16. Neuroleptic-Induced Tardive Dyskinesia  Diagnosis, Signs, and Symptoms  Tardive dyskinesia is a delayed effect of antipsychotics;  it rarely occurs until after 6 months of treatment.  The disorder consists of abnormal,  involuntary, irregular choreoathetoid movements of the muscles of the head, limbs, and trunk.  The severity of the movements ranges from minimal—often missed by patients and their families—to grossly incapacitating.
  • 17.  Perioral movements are the most common and include darting, twisting, and protruding movements of the tongue; chewing and lateral jaw movements; lip puckering; and facial grimacing.  Finger movements and hand clenching are also common.  Torticollis, retrocollis, trunk twisting, and pelvic thrusting occur in severe cases.  In the most serious cases, patients may have breathing and swallowing irregularities that result in aerophagia, belching, and grunting.  Respiratory dyskinesia has also been reported. Dyskinesia is exacerbated by stress and disappears during sleep.
  • 18.  Treatment  The three basic approaches to tardive dyskinesia are prevention, diagnosis, and management.  Clozapine is the only antipsychotic to have minimal risk of tardive dyskinesia, and can even help improve preexisting symptoms of tardive dyskinesia.
  • 19. Neuroleptic Malignant Syndrome  Diagnosis, Signs, and Symptoms  Neuroleptic malignant syndrome is a life- threatening complication  The motor and behavioral symptoms include  muscular rigidity and dystonia, akinesia, mutism, obtundation, and agitation.  The autonomic symptoms include high fever, sweating, and increased pulse and blood pressure.  Laboratory :increased white blood cell count and increased levels of creatinine phosphokinase, liver enzymes, plasma myoglobin, and myoglobinuria, occasionally associated with renal failure.
  • 20.  Treatment  In addition to supportive medical treatment, the most commonly used medications for the condition are dantrolene (Dantrium) and bromocriptine (Parlodel), although amantadine (Symmetrel) is sometimes used.  Bromocriptine and amantadine pose direct DRA effects and may serve to overcome the antipsychotic-induced dopamine receptor blockade.  The lowest effective dosage of the antipsychotic drug should be used to reduce the chance of neuroleptic malignant syndrome.  Antipsychotic drugs with anticholinergic effects seem less likely to cause neuroleptic malignant syndrome (Table 36.2-4). Electroconvulsive therapy (ECT) has been used successfully and is preferred by some clinicians.
  • 21. Medication-Induced Postural Tremor  Diagnosis, Signs, and Symptoms  Tremor is a rhythmic alteration in movement that is usually faster than one beat per second.
  • 22.  Etiology  Whereas all the above diagnoses specifically include an association with a neuroleptic, a range of psychiatric medications can produce tremor—most notably, lithium, antidepressants, and valproate (Depakene).
  • 23.  Treatment  The treatment involves four principles:  The lowest possible dose of the psychiatric drug should be taken.  Patients should minimize caffeine consumption.  The psychiatric drug should be taken at bedtime to minimize the amount of daytime tremor.  β-adrenergic receptor antagonists (e.g., propranolol [Inderal]) can be given to treat drug- induced tremors.
  • 24.  Other Movement Disorders  Nocturnal Myoclonus  Nocturnal myoclonus consists of highly stereotyped, abrupt contractions of certain leg muscles during sleep. Patients lack any subjective awareness of the leg jerks.
  • 25.  Restless Leg Syndrome  In restless leg syndrome, persons feel deep sensations of creeping inside the calves whenever sitting or lying down.The dysesthesias are rarely painful, but are agonizingly relentless and cause an almost irresistible urge to move the legs; thus, this syndrome interferes with sleep and with falling asleep.
  • 26.  Hyperthermic Syndromes  All the medication-induced movement disorders may be associated with hyperthermia.Table 36.2-5 lists the various conditions associated with hyperthermia