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Delirium, also referred to as "acute confusional state" or "acute brain syndrome," is a condition of severe confusion and rapid changes in brain function.
An acute medical condition.
Common in UK critical care patients.
Serious adverse outcomes.
Bedside diagnosis.
Maybe the first sign of a new infection.
Pathological, not psychological.
A guideline for discontinuing antiepileptic drugs in seizure-free patients – ...Dr. Rafael Higashi
Aula apresentada por Dr. Rafael Higashi, médico neurologista sobre quando retirar droga antiepilética. A guideline for discontinuing antiepileptic drugs in seizure-free patients – Summary Statement
Medication-induced movement disorder (Extra-Pyramidal Side Effects, EPSE) occurs due to treatment with antipsychotic medications. It can also be defined as physical symptoms, including tremor, slurred speech, akathesia, dystonia, anxiety, distress, paranoia, and bradyphrenia, that are primarily associated with improper dosing of or unusual reactions to neuroleptic (antipsychotic) medications.
Though they are commonly caused by the typical antipsychotics, but can also be caused by the atypical.
The adverse consequences of these syndromes can be minimized by vigilant clinicians who systematically examine patients at risk for these disorders and who manage them properly when discovered.
The best management is, of course, prevention, which starts with the judicious prescription of neuroleptics, and an awareness of the potential for certain nonpsychiatric medications to cause the same movement disorders.
Neuroreceptor Modulation Will Deliver Many Different Flavors
1. Neuroreceptor
Modulation Will
Deliver Many
Different Flavors
Denise H. Rhoney, Pharm.D., FCCP, FCCM
Associate Professor
Eugene Applebaum College of Pharmacy & Health Sciences
Wayne State University
Detroit, Michigan
2. What is Delirium?
Otherwise known as ICU psychosis, acute brain
dysfunction, acute confusional state, toxic‐metabolic
encephalopathy, post‐op confusional state, organic brain
syndrome
Complex neurobehavioral syndrome caused by the
transient disruption of normal neuronal activity
Clinically characterized by :
Acute confusion, fluctuating mental status, inattention,
disorganized thinking, altered levels of consciousness
3. ICU Delirium Facts
60% to 80% of ventilated patients
develop delirium
20% to 50% of lower severity ICU
patients develop delirium
3 times higher risk of death by 6
months
$15k to $25k higher hospital costs
Estimated national $4 to $16 billion
associated costs
5 fewer ventilator free days (days alive Ely EW ICM 2001;27:1892‐900
and off vent), adjusted P=0.03 Ely EW JAMA 2001;286,2703‐2710
Ely EW CCM 2001;29,1370‐79
9 times higher incidence of cognitive McNicoll L, JAGS 2003;51:591‐98
impairment at hospital discharge, adj. Ely EW et al, JAMA 2004;291‐1753‐1762
P=0.002 Milbrandt E et al, Crit Care Med 2004;32:955‐962
Lin et al, Crit Care Med 2004;32:2254‐59
4. Delirium Subtypes*
Characteristic Hyperactive Hypoactive
% in ICU 0‐6% 43.5‐94%
Level of Consciousness Hyperalert/vigilant, distractibility Lethargy, alertness, inattention
Cognition Diffuse deficits, speech Diffuse deficits, slow speech/quiet
loud/rapid/disorganized,
disorientation
Perceptual disturbances Hallucination/delusions None
Physiologic Low‐voltage fast EEG, or normal Slow/diffuse EEG, cerebral
cerebral metabolic activity metabolic activity
Behaviors Psychomotor activity, restless, psychomotor activity, apathetic,
combative, mood liability stimuli response
Possible etiology BZD w/drawal, ETOH/drug BZD intoxication, hepatic
w/drawal, drug intoxication encephalopathy, hypoxia, metabolic
disturbance
Outcome Best Worst
*64% ICU patients with mixed forms
5. Overview of Acute Brain
Dysfunction
Normal & consistent Elderly patients show signs of ICU patients subjected to
connectivity between grey matter atrophy in PPC, medical and
posterior parietal cortex (PPC), MTL and PFC pharmacological challenges
dorsal prefrontal cortex (PFC), that disrupt normal CNS
& medial temporal/ Functional connectivity connectivity and weaken
hippocampal region (MTL) – remains intact but strength of functional links between
circuit is innervated & connections is no longer these cortical regions
maintained by ascending robust
reticular activating system
(ARAS) in the brainstem Gunther ML et al. Medical Hypotheses 2007;69:1179‐1182
6. Neuroimaging Studies
Delirium results in significant hypoperfusion in several brain
regions (frontal, temporal, and subcortical regions)
Critically ill patients with delirium (61% with abnormalities)
Significant ventricular enlargement
Generalized atrophy
Focal lesions in frontal and parietal regions
White matter lesions/hyperintensities
Cortical and subcortical lesions
Fong TG et al. J Gerontol A Biol Sci Med Sci 2007;61A:1294‐9.
Sbordone R et al. Brain Inj 1998;12:505‐12.
7. Risk Factors for Delirium
Predisposing Host Factors Critical Illness Factors Iatrogenic Factors
Age Acidosis Few social interactions
APOE4 polymorphism Anemia Frequent nursing care
Cognitive impairment CNS pathology Immobilization
Depression Electrolyte disturbances Medications
Stroke History Endocrine derangement Oversedation
Vision/hearing impairment Fever Poorly controlled pain
Hepatic Failure Sleep disturbances
High severity of illness
Hypoperfusion
Hypotension
Hypoxia/anoxia
Infection/sepsis
Malnutrition
Metabolic disturbances
Respiratory failure
Shock
Trauma
8. Risk of Delirium with Commonly
Administered Drugs
High Risk
Opioids (particularly meperidine & morphine)
Antiparkinsonian agents
Antidepressants (particularly anticholinergic agents)
Benzodiazepines
Corticosteroids
Medium Risk
Alpha‐blockers
Beta‐blockers
NSAIDS
Low Risk
ACE‐I
H2 antagonists
Calcium channel blockers
Anticonvulsants
Maldonado JR. Crit Care Clin 2008;24:789‐856.
10. Theories on the Development of
Delirium
Oxygen deprivation hypothesis
Neurotransmitter hypothesis
Large neutral amino acid hypothesis
Neuronal aging hypothesis
Cellular‐signaling hypothesis
Physiologic stress hypothesis
Inflammatory hypothesis
Genetic Factors
Cortisol & HPA disruption
Disruption in circadian rhythm
Disruption in thalamic gating
11. Hypotheses of Delirium
Large neutral amino acid hypothesis
Neurotransmitter hypothesis
Oxygen deprivation hypothesis
Inflammatory hypothesis
Figueroa‐Ramos MI et al. Intensive Care Med 2009;35:781‐795
13. Acetylcholine & Delirium
Decreased ACh synthesis and release
Ach is an important neuromodulator of cortical and hippocampal
neuronal function
Widespread dysfunction of arousal seen in delirium correlates well
with the blockade of the muscarininc cholinergic system
Low levels of ACh described in plasma and CSF of patients with
delirium
Higher levels of serum anticholinergic activity (SAA) have been
associated with increase likelihood of delirium in surgical and
medical inpatients
Detectable SAA levels have been reported even in patients with
delirium who were not exposed to anticholinergic agents
Flacker et al. J Gerontol A Biol Sci Med Sci 2001; Mach et al. J Am Geriatr Sco 1995; Mulsant et al. Arch Gen Psychiatry 2003.
14. Acetylcholine & Delirium
Potential contributing
mechanisms
Aging
Dementia & other “organic
brain injury”
Hypoxia ACh production
anticholinergic activity
Drugs
Endogenous anticholinergic
substances
Central cholinergic pathways overlap with locations of
neuroimaging abnormalities
Hshieh TT et al. J Gerontol A Biol Sci Med Sci 2008; 63:764‐72
16. Dopamine & Delirium
Enhanced central dopaminergic activity
DA agonists cause delirium
DA antagonists treat delirium
Follows an inverted U‐shaped curve
Lack of dopamine = Parkinsonian symptoms
Excess dopamine = psychosis
D2 receptor density declines with age and correlates with frontal cognitive
test scores
DA transporter gene allele A9 is more prevalent in alcoholics with
withdrawal delirium and seizures
DA agonists cause EEG slowing
DA release is increased in hypoxia (while ACh is decreased)
Dopaminergic blockade can be used to reduce hypoxic damage in hippocampus
Trzepacz PT. Sem Clin Neuropsychiatry 2000;5:132‐148.
19. GABA & Delirium
Predominant inhibitory
neurotransmitter in CNS
in hepatic encephalopathy and
benzodiazepine use
sedative/alcohol withdrawal
Flumazenil has improved hypoactive
delirium in cirrhotic patients
Oversedation with GABAergic agents
has been found to be a risk factor for
transitioning to delirium and
prolonged mechanical ventilation
Maldonado JR. Crit Care Clin 2008;24:789‐856.
Pandharipande P et al. Anesthesiology 2006; 104:21‐6
20. GABA & Delirium
GABAergic agents contribute to the development of
delirium via various possible mechanisms
Interfering with physiologic sleep patterns
Interfering with central cholinergeric function causing
centrally mediated acetylcholine deficient state
Disrupting circadian rhythm of melatonin release
Enhancing NMDA‐induced neuronal damage
Disrupting thalamic gating function leading to sensory
overload and hyperarousal
Maldonado JR. Crit Care Clin 2008;24:789‐856.
21. Other Neurotransmitters & Delirium
Serotonin:
Most abundant neurotransmitter in the brainstem, its synthesis and
release depends on its precursor tryptophan
Increased and decreased serotonin levels are both associated with
development of delirium
Cerebral serotonin is increased in hepatic encephalopathy, septic delirium
and serotonin syndrome
Histamine:
HA1 & HA2 alter the polarity of hippocampal neurons
Pharmacological antagonism of HA1 and HA2 causes delirium
Both excess and deficiency of HA may be related to delirium
H2 Blockers cimetidine, ranitidine may cause cognitive dysfunction and
delirium in elderly
Maldonado JR. Crit Care Clin 2008;24:789‐856.
22. Other Neurotransmitters & Delirium
Norepinephrine:
Plays important role in modulating attention, anxiety & mood
Enhanced central noradrengergic activity ( NE)
Acute NE release due to hypoxia leads to further neuronal injury and worsening
delirium
Cortisol release with injury may lead to further NE release and activity
Up‐regulation of NE receptors due to chronic GABA suppression
Dexmedetomidine has been shown to decrease NE conc. by up to 90%
Significantly decreased incidence of delirium associated with Dex compared to
midazolam
Glutamate:
Enhanced glutamate activity leading to neuronal injury via activation of NMDA
receptors
Metabolized by glutamate decarboxylase into GABA
DA may enhance GLU‐mediated injury
Hshieh TT et al. J Gerontol A Biol Sci Med Sci 2008; 63:764‐72 Engelhard K et al. Anesth Analg 2003;96:524‐31
Maldonado JR. Crit Care Clin 2008;24:789‐856 Riker R et al JAMA 2009;301:489‐99
23. Interaction Between
Neurotransmitters
Hshieh TT et al. J Gerontol A Biol Sci Med Sci 2008; 63:764‐72
24. Medications, alcohol withdrawal Medications, medical illness
Ach (-) Benzodiazepine and alcohol withdrawal
Ach (+)
Medications, Stroke
D(+)
Benzodiazepine, hepatic failure
Cytokine Excess
GABA (+)
5HT (+)
GLU (+)
Medications, substance withdrawal
Hepatic failure, alcohol withdrawal
5HT (-)
Cortisol excess
Tryptophan depletion
Glucocorticosteroids, Cushing’s syndrome
Surgical Illness, medical illness
Maldonado JR. Crit Care Clin 2008;24:789‐856.
26. Summary
Firm understanding of pathophysiology of delirium
remains elusive despite improvements in diagnosis and
treatment
Neurotransmitter imbalance along with a number of other
hypotheses have been implicated in the development of
delirium
Understanding cellular response to critical illness,
including neurotransmitter activity and neuroreceptor
expression, may lead to innovative diagnostic and
treatment modalities