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DELIRIUM
WHAT IS IN THIS PRESENTATION:
 Why do we need to know about delirium?
 What is delirium?
 D/D with respect to psychiatry
 How to prevent delirium?
 Diagnosis and assessment
 Treatment
WHY DO WE NEED TO KNOW ABOUT
DELIRIUM?
WHY DO WE NEED TO KNOW ABOUT DELIRIUM?
 Delirium is common
 Delirium is associated with increased complications
 Delirium is often unrecognized
 Delirium is preventable
WHAT IS DELIRIUM?
WHAT IS DELIRIUM?
• Acute confusional state
• Constellation of symptoms
• Widespread disruption of higher cortical function
• Acute onset and fluctuating course
• Three core domains:
- cognitive with disproportionate impairment of attention
- circadian disturbance (sleep wake cycle, motor alterations)
- disturbances of higher level of thinking(comprehension, language,
thinking process)
CORE FEATURES & ASSOCIATED FEATURES
Core features:
• Features that are almost invariably present
• Disturbances of - attention
- memory
- orientation
- language
- thought process
- sleep-wake cycle
Meagher et al 2007 BJP
CORE FEATURES & ASSOCIATED FEATURES
Associated features:
• Features that are more variable in presentation
• Psychotic symptoms
• Affective disturbances
• Different motoric profiles
Meagher et al 2007 BJP
IMPAIRMENT OF CONSCIOUSNESS
 Universal, fluctuating
 Barely perceptible dulling of awareness to profound coma
 Worsen at night, with fatigue, decreased environmental stimuli
 Failure to be selective -----------distractible
 Failure to mobilize & sustain attention -------impaired attention
 Inability to shift attention------------perseveration
 Minor degree---vague malaise, feelings of uncertainity, difficulties in
judging passage of time, focusing attention, neglect of appearance,
episode of incontinence
 Severe degree----too slow in responding, loses thread in conversation,
attention to outside events hard to arouse and sustain, drowsy
RECENT WORKS
• Disorder of global cognition
• Prominent disturbance of attention
• Disorientation is least frequent core symptom
• Cognition & language are not as fluctuant as previously
described
• Subsyndromal , resolving , persisting delirium
Meagher et al BJP 2012 & BJP 2007
PREDISPOSING OR VULNERABILITY FACTORS
Demographics
Older age
Male gender
Cognitive status
Dementia
Cognitive impairment
History of delirium
Depression
Functional status
Functional dependence
Immobility
Poor activity level
History of falls
Sensory impairment
Vision impairment
Hearing impairment
Decreased Intake
Dehydration
Malnutrition
Drugs
Multiple psychoactive drugs
High number of drugs
Alcohol abuse
Medical Comorbidity
High severity of illness
High level of comorbidity
Chronic renal or hepatic disease
Previous stroke
Neurologic disease
Metabolic derangements
Fracture or trauma
Terminal illness
HIV infection
Inouye SK. NEJM 2006;354:1157-65
PRECIPITATING FACTORS OR INSULTS
Drugs
Sedative hypnotics
Narcotics
Anticholinergic drugs
Polypharmacy
Alcohol or drug withdrawal
Primary neurological diseases
Stroke, particularly nondominant hemispheric
Intracranial bleed
Meningitis/encephalitis
Environmental
Intensive care unit admission
Physical restraint use
Bladder catheter use
High number of procedures
Pain
Emotional stress
Prolonged sleep deprivation
Intercurrent illnesses
Infections
Iatrogenic complications
Severe acute illness
Hypoxia
Shock
Fever/hypothermia
Anemia
Dehydration
Poor nutritional status
Low serum albumin
Metabolic derangements (e.g., electrolytes,
glucose, acid-base)
Surgery
Orthopedic surgery
Cardiac surgery
Duration of cardiopulmonary bypass
Non-cardiac surgery
Inouye SK. NEJM 2006;354:1157-65
Risk Factors
Predisposing
Precipitating
Comorbidities
·Diabetes
·MI
·Etc…
Perioperative
Drugs
·Anesthetics
· Opioids
· Benzodiazepines
·Etc…
URGENT RECOGNITION:
 Wernicke’s
 Hypoxia
 Hypoglycemia
 Hypertensive encephalopathy
 Intracerebral hemorrhage
 Meningitis/encephalitis
 Poisoning/medications
ETIOLOGIES -“ I WATCH DEATH “
• I = Infection
• W = Withdrawal
• A = Acute Metabolic
• T = Trauma
• C = CNS Pathology
• H = Hypoxia
• D = Deficiencies
(especially vitamin)
• E = Endocrinopathies
• A = Acute Vascular
• T = Toxins
• H = Heavy metals
Flacker JM. J Gerontol Biol Sci 1999;54:B239-46
DIFFERENTIAL DIAGNOSIS IN
PSYCHIATRY
DIFF DELIRIUM & PSYCHIATRIC DISORDER
• Clouded consciousness or decreased level of alertness
• Disorientation
• Acuity of onset and course- serial mental status exams can
help demonstrate this
• Age >40 without prior psych history
• Presence of risk factors for delirium, recent medical illness or
treatment
DELIRIUM V/S SCHIZOPHRENIA
• Onset of schizophrenia is rarely after 50.
• Auditory hallucinations are much more common than visual
hallucinations
• Memory is grossly intact and disorientation is rare
• Speech is not dysarthric
• No wide fluctuations over the course of a day
• Thought content and abnormal perceptions are related
• In delirium, thought and perception are influenced by
immediate environment
MOOD DISORDER V/S DELIRIUM
• Mood disorders manifest persistent rather than labile mood
with more gradual onset
• In mania the patient can be very agitated however cognitive
performance is not usually as impaired
• Flight of ideas usually have some thread of coherence unlike
simple distractibility
• Disorientation is unusual in mania
DELIRIUM V/S DEMENTIA
Delirium Dementia
Impaired memory +++ +++
Impaired thinking +++ +++
Clouding of consciousness +++ -
Major attention deficit +++ +
Fluctuation of course/day +++ +
Disorientation +++ ++
Vivid perceptual dbn ++ +
Incoherent speech ++ +
Disrupt sleep/wake cycle ++ +
Nocturnal exacerbation ++ +
Acute/subacute onset ++ -
Impaired judgement ++ +++
DELIRIUM IS PREVENTABLE
PREVENTING DELIRIUM
• Yale delirium prevention trial
• Designed to counteract iatrogenic influences leading to
delirium in the hospital
• Multicomponent intervention strategy targeted at 6 delirium
risk factors
SIGNIFICANCE OF DELIRIUM PREVENTION TRIAL
• First demonstration of delirium as a preventable medical
condition
• Targeted multicomponent strategy works
• Significant reduction in risk of delirium and total delirium days,
without significant effect on delirium severity or recurrence
• Primary prevention of delirium likely to be most effective
treatment strategy
• Effectiveness and cost-effectiveness of the program has been
demonstrated in multiple studies
YALE DELIRIUM PREVENTION PROGRAM
• Cognitive impairment
• Sleep deprivation
• Immobilization
• Vision impairment
• Hearing impairment
• Dehydration
• Reality orientation
• Sleep enhancement
protocol
• Early mobilization
• Vision aids, adaptive eqp.
• Amplifying devices,
adaptive eqp
• Early recognition & Rx
Risk factor Intervention
DIAGNOSIS AND ASSESSMENT
DIAGNOSIS AND ASSESSMENT
• Delirium is a clinical diagnosis
• History and physical examination
• Mental Status Exam
• Rating Scales-consider on admission
ASSESSMENT INSTRUMENTS
To identify delirium:
• Delirium rating scale – revised 98 ( DRS – R98)
• Confusion assessment method (CAM)
• Delirium symptom interview (DSI)
• Confusion assessment method for ICU (CAM-ICU)
• Intensive care delirium screening checklist (ICDSC)
To assess symptom severity:
• Delirium detection scale (DDS)
• Memorial delirium assessment scale (MDAS)
To test neuropsychological function:
• Cognitive test for delirium (CTD)
DIAGNOSIS AND ASSESSMENT
 Lab tests cannot diagnose delirium but may support
dx
 CBC, CMP, UA, urine tox, TSH, B12, ammonia
 CXR, EKG, LP if indicated
 Neuroimaging
 EEG
 Generalized slowing in delirium, nonspecific
 Triphasic waves in hepatic encephalopathy
 Low voltage fast activity in EtOH or BZD w/d
TREATMENT
TREATING PATIENTS WITH DELIRIUM
Treat underlying causes
 Don’t stop looking after finding one potential cause
• Anticipate in high risk states
• Diagnosis & treatment should occur concurrently
• Regular evaluation of progress is important
• Best managed in hospital setting
TREATING PATIENTS WITH DELIRIUM
• Supportive and environmental measures
- support and orientation
- unambiguous environment
- maintaining competence
• Drug treatment
- antipsychotics
- benzodiazepines
- emerging therapies
• Managing patients after discharge
PROVIDING SUPPORT AND ORIENTATION
 Communicate clearly and concisely; give repeated verbal
reminders of the day, time, location, and identity of key
individuals, such as members of the treatment team and
relatives
 Provide clear signposts to patient's location including a clock,
calendar, chart with the day's schedule
 Have familiar objects
 consistency in staff
 Use television or radio for relaxation and to help the patient
maintain contact with the outside world
 Involve family and caregivers to encourage feelings of security
and orientation
PROVIDING AN UNAMBIGUOUS ENVIRONMENT
 Simplify care area by removing unnecessary objects; allow
adequate space
 between beds
 Consider using single rooms to aid rest and avoid extremes of
sensory experience
 Avoid using medical jargon in patient's presence because it
may encourage paranoia
 Ensure that lighting is adequate; provide a 4060 W night light
to reduce misperceptions
 Control sources of excess noise (such as staff, equipment,
visitors); aim for < 45 decibels in the day and < 20 decibels at
night
 Keep room temperature between 21.1°C to 23.8°C
MAINTAINING COMPETENCE
 Identify and correct sensory impairments
 Encourage self care and participation in treatment
 Treatments to allow maximum periods of uninterrupted sleep
 Maintain activity levels:
-ambulatory patients should walk three times each day;
-nonambulatory patients should undergo a full range of
movements for 15 minutes three times each day
DRUG TREATMENT
• Benefits v/s adverse effects
• Use of psychotropic drugs:
- complicates ongoing assesment of MSE
- impair patient’s ability to understand or co-operate
- greater incidence of falls
• Prescribing often influenced by:
- pressure from relatives
- time constraints
-diff in coomunication between medical & nursing staff
ANTIPSYCHOTICS
• Hyperactive and hypoactive delirium
• Improve cognition
• Rapid onset
• Improvement evident in hours or days
• Superior to benzodiazepines
ANTIPSYCHOTICS
• Chlorpromazine , Haloperidol, Droperidol – similar efficacy
• Atypicals – further research needed
• Haloperidol is preferred:
- fewer active metabolites
- limited anticholinergic side effects
- less sedative & hypotensive effects
- administered by different routes
- EPS *reported incidence is low
*iv administration – EPS less likely
BENZODIAZEPINES
• Can protect or pose risk
• Delirium associated with seizure, withdrawal from alcohol or
sedatives
• Adjunct if antipsychotics are not tolerated
• Lorazepam is preferred
- rapid onset
- short duration of action
- low risk of accumulation
- no major active metabolites
- predictable bioavailability if given i.m.
EMERGING THERAPIES
• Physostigmine – anticholinergic delirium
(hypoxia, hypoglycaemia, drug related, trauma)
• Nicotine replacement treatment – protective?
• Pimozide –potent calcium antagonist
- delirium ass with hypercalcemia
• Trazadone & Mianserin ( 5HT 2 antagonist)
• Light therapy
OUTCOME OF DELIRIUM
40%
25%
35%
Recovery Permanent Cognitive Impairment Mortality
MANAGING AFTER DISCHARGE
• Many patients dicharged before full resolution
• Delirium may persists for weeks or even months
• Risk of new diagnosis of dementia increased at least threefold
• Problems in attention may persist
• Prevent further episodes
- address risk factors
- correct sensory impairments
• Look for psychological sequalae
- depression
- PTSD
• Follow up - must
THANK YOU
“Knowing is not enough;
we must apply.
Willing is not enough;
we must do.”
- Goethe

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Delirium - an overview

  • 2. WHAT IS IN THIS PRESENTATION:  Why do we need to know about delirium?  What is delirium?  D/D with respect to psychiatry  How to prevent delirium?  Diagnosis and assessment  Treatment
  • 3. WHY DO WE NEED TO KNOW ABOUT DELIRIUM?
  • 4. WHY DO WE NEED TO KNOW ABOUT DELIRIUM?  Delirium is common  Delirium is associated with increased complications  Delirium is often unrecognized  Delirium is preventable
  • 6. WHAT IS DELIRIUM? • Acute confusional state • Constellation of symptoms • Widespread disruption of higher cortical function • Acute onset and fluctuating course • Three core domains: - cognitive with disproportionate impairment of attention - circadian disturbance (sleep wake cycle, motor alterations) - disturbances of higher level of thinking(comprehension, language, thinking process)
  • 7. CORE FEATURES & ASSOCIATED FEATURES Core features: • Features that are almost invariably present • Disturbances of - attention - memory - orientation - language - thought process - sleep-wake cycle Meagher et al 2007 BJP
  • 8. CORE FEATURES & ASSOCIATED FEATURES Associated features: • Features that are more variable in presentation • Psychotic symptoms • Affective disturbances • Different motoric profiles Meagher et al 2007 BJP
  • 9. IMPAIRMENT OF CONSCIOUSNESS  Universal, fluctuating  Barely perceptible dulling of awareness to profound coma  Worsen at night, with fatigue, decreased environmental stimuli  Failure to be selective -----------distractible  Failure to mobilize & sustain attention -------impaired attention  Inability to shift attention------------perseveration  Minor degree---vague malaise, feelings of uncertainity, difficulties in judging passage of time, focusing attention, neglect of appearance, episode of incontinence  Severe degree----too slow in responding, loses thread in conversation, attention to outside events hard to arouse and sustain, drowsy
  • 10. RECENT WORKS • Disorder of global cognition • Prominent disturbance of attention • Disorientation is least frequent core symptom • Cognition & language are not as fluctuant as previously described • Subsyndromal , resolving , persisting delirium Meagher et al BJP 2012 & BJP 2007
  • 11. PREDISPOSING OR VULNERABILITY FACTORS Demographics Older age Male gender Cognitive status Dementia Cognitive impairment History of delirium Depression Functional status Functional dependence Immobility Poor activity level History of falls Sensory impairment Vision impairment Hearing impairment Decreased Intake Dehydration Malnutrition Drugs Multiple psychoactive drugs High number of drugs Alcohol abuse Medical Comorbidity High severity of illness High level of comorbidity Chronic renal or hepatic disease Previous stroke Neurologic disease Metabolic derangements Fracture or trauma Terminal illness HIV infection Inouye SK. NEJM 2006;354:1157-65
  • 12. PRECIPITATING FACTORS OR INSULTS Drugs Sedative hypnotics Narcotics Anticholinergic drugs Polypharmacy Alcohol or drug withdrawal Primary neurological diseases Stroke, particularly nondominant hemispheric Intracranial bleed Meningitis/encephalitis Environmental Intensive care unit admission Physical restraint use Bladder catheter use High number of procedures Pain Emotional stress Prolonged sleep deprivation Intercurrent illnesses Infections Iatrogenic complications Severe acute illness Hypoxia Shock Fever/hypothermia Anemia Dehydration Poor nutritional status Low serum albumin Metabolic derangements (e.g., electrolytes, glucose, acid-base) Surgery Orthopedic surgery Cardiac surgery Duration of cardiopulmonary bypass Non-cardiac surgery Inouye SK. NEJM 2006;354:1157-65
  • 14. URGENT RECOGNITION:  Wernicke’s  Hypoxia  Hypoglycemia  Hypertensive encephalopathy  Intracerebral hemorrhage  Meningitis/encephalitis  Poisoning/medications
  • 15. ETIOLOGIES -“ I WATCH DEATH “ • I = Infection • W = Withdrawal • A = Acute Metabolic • T = Trauma • C = CNS Pathology • H = Hypoxia • D = Deficiencies (especially vitamin) • E = Endocrinopathies • A = Acute Vascular • T = Toxins • H = Heavy metals
  • 16. Flacker JM. J Gerontol Biol Sci 1999;54:B239-46
  • 18. DIFF DELIRIUM & PSYCHIATRIC DISORDER • Clouded consciousness or decreased level of alertness • Disorientation • Acuity of onset and course- serial mental status exams can help demonstrate this • Age >40 without prior psych history • Presence of risk factors for delirium, recent medical illness or treatment
  • 19. DELIRIUM V/S SCHIZOPHRENIA • Onset of schizophrenia is rarely after 50. • Auditory hallucinations are much more common than visual hallucinations • Memory is grossly intact and disorientation is rare • Speech is not dysarthric • No wide fluctuations over the course of a day • Thought content and abnormal perceptions are related • In delirium, thought and perception are influenced by immediate environment
  • 20. MOOD DISORDER V/S DELIRIUM • Mood disorders manifest persistent rather than labile mood with more gradual onset • In mania the patient can be very agitated however cognitive performance is not usually as impaired • Flight of ideas usually have some thread of coherence unlike simple distractibility • Disorientation is unusual in mania
  • 21. DELIRIUM V/S DEMENTIA Delirium Dementia Impaired memory +++ +++ Impaired thinking +++ +++ Clouding of consciousness +++ - Major attention deficit +++ + Fluctuation of course/day +++ + Disorientation +++ ++ Vivid perceptual dbn ++ + Incoherent speech ++ + Disrupt sleep/wake cycle ++ + Nocturnal exacerbation ++ + Acute/subacute onset ++ - Impaired judgement ++ +++
  • 23. PREVENTING DELIRIUM • Yale delirium prevention trial • Designed to counteract iatrogenic influences leading to delirium in the hospital • Multicomponent intervention strategy targeted at 6 delirium risk factors
  • 24. SIGNIFICANCE OF DELIRIUM PREVENTION TRIAL • First demonstration of delirium as a preventable medical condition • Targeted multicomponent strategy works • Significant reduction in risk of delirium and total delirium days, without significant effect on delirium severity or recurrence • Primary prevention of delirium likely to be most effective treatment strategy • Effectiveness and cost-effectiveness of the program has been demonstrated in multiple studies
  • 25. YALE DELIRIUM PREVENTION PROGRAM • Cognitive impairment • Sleep deprivation • Immobilization • Vision impairment • Hearing impairment • Dehydration • Reality orientation • Sleep enhancement protocol • Early mobilization • Vision aids, adaptive eqp. • Amplifying devices, adaptive eqp • Early recognition & Rx Risk factor Intervention
  • 27. DIAGNOSIS AND ASSESSMENT • Delirium is a clinical diagnosis • History and physical examination • Mental Status Exam • Rating Scales-consider on admission
  • 28. ASSESSMENT INSTRUMENTS To identify delirium: • Delirium rating scale – revised 98 ( DRS – R98) • Confusion assessment method (CAM) • Delirium symptom interview (DSI) • Confusion assessment method for ICU (CAM-ICU) • Intensive care delirium screening checklist (ICDSC) To assess symptom severity: • Delirium detection scale (DDS) • Memorial delirium assessment scale (MDAS) To test neuropsychological function: • Cognitive test for delirium (CTD)
  • 29. DIAGNOSIS AND ASSESSMENT  Lab tests cannot diagnose delirium but may support dx  CBC, CMP, UA, urine tox, TSH, B12, ammonia  CXR, EKG, LP if indicated  Neuroimaging  EEG  Generalized slowing in delirium, nonspecific  Triphasic waves in hepatic encephalopathy  Low voltage fast activity in EtOH or BZD w/d
  • 31. TREATING PATIENTS WITH DELIRIUM Treat underlying causes  Don’t stop looking after finding one potential cause • Anticipate in high risk states • Diagnosis & treatment should occur concurrently • Regular evaluation of progress is important • Best managed in hospital setting
  • 32. TREATING PATIENTS WITH DELIRIUM • Supportive and environmental measures - support and orientation - unambiguous environment - maintaining competence • Drug treatment - antipsychotics - benzodiazepines - emerging therapies • Managing patients after discharge
  • 33. PROVIDING SUPPORT AND ORIENTATION  Communicate clearly and concisely; give repeated verbal reminders of the day, time, location, and identity of key individuals, such as members of the treatment team and relatives  Provide clear signposts to patient's location including a clock, calendar, chart with the day's schedule  Have familiar objects  consistency in staff  Use television or radio for relaxation and to help the patient maintain contact with the outside world  Involve family and caregivers to encourage feelings of security and orientation
  • 34. PROVIDING AN UNAMBIGUOUS ENVIRONMENT  Simplify care area by removing unnecessary objects; allow adequate space  between beds  Consider using single rooms to aid rest and avoid extremes of sensory experience  Avoid using medical jargon in patient's presence because it may encourage paranoia  Ensure that lighting is adequate; provide a 4060 W night light to reduce misperceptions  Control sources of excess noise (such as staff, equipment, visitors); aim for < 45 decibels in the day and < 20 decibels at night  Keep room temperature between 21.1°C to 23.8°C
  • 35. MAINTAINING COMPETENCE  Identify and correct sensory impairments  Encourage self care and participation in treatment  Treatments to allow maximum periods of uninterrupted sleep  Maintain activity levels: -ambulatory patients should walk three times each day; -nonambulatory patients should undergo a full range of movements for 15 minutes three times each day
  • 36. DRUG TREATMENT • Benefits v/s adverse effects • Use of psychotropic drugs: - complicates ongoing assesment of MSE - impair patient’s ability to understand or co-operate - greater incidence of falls • Prescribing often influenced by: - pressure from relatives - time constraints -diff in coomunication between medical & nursing staff
  • 37. ANTIPSYCHOTICS • Hyperactive and hypoactive delirium • Improve cognition • Rapid onset • Improvement evident in hours or days • Superior to benzodiazepines
  • 38. ANTIPSYCHOTICS • Chlorpromazine , Haloperidol, Droperidol – similar efficacy • Atypicals – further research needed • Haloperidol is preferred: - fewer active metabolites - limited anticholinergic side effects - less sedative & hypotensive effects - administered by different routes - EPS *reported incidence is low *iv administration – EPS less likely
  • 39. BENZODIAZEPINES • Can protect or pose risk • Delirium associated with seizure, withdrawal from alcohol or sedatives • Adjunct if antipsychotics are not tolerated • Lorazepam is preferred - rapid onset - short duration of action - low risk of accumulation - no major active metabolites - predictable bioavailability if given i.m.
  • 40. EMERGING THERAPIES • Physostigmine – anticholinergic delirium (hypoxia, hypoglycaemia, drug related, trauma) • Nicotine replacement treatment – protective? • Pimozide –potent calcium antagonist - delirium ass with hypercalcemia • Trazadone & Mianserin ( 5HT 2 antagonist) • Light therapy
  • 41. OUTCOME OF DELIRIUM 40% 25% 35% Recovery Permanent Cognitive Impairment Mortality
  • 42. MANAGING AFTER DISCHARGE • Many patients dicharged before full resolution • Delirium may persists for weeks or even months • Risk of new diagnosis of dementia increased at least threefold • Problems in attention may persist • Prevent further episodes - address risk factors - correct sensory impairments • Look for psychological sequalae - depression - PTSD • Follow up - must
  • 43. THANK YOU “Knowing is not enough; we must apply. Willing is not enough; we must do.” - Goethe