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I.5 Pediatric Delirium PPT 2017

This document discusses pediatric delirium, including its definition, prevalence in pediatric intensive care units, risk factors, clinical characteristics of different subtypes, etiology, diagnosis, treatment approaches, and potential long-term sequelae. Key points include that pediatric delirium affects 20-30% of critically ill children, has high morbidity and mortality, and treatment involves a focus on minimizing risk factors and using low doses of medications like benzodiazepines and antipsychotics gradually over time based on individual response and scales.

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100% found this document useful (1 vote)
364 views26 pages

I.5 Pediatric Delirium PPT 2017

This document discusses pediatric delirium, including its definition, prevalence in pediatric intensive care units, risk factors, clinical characteristics of different subtypes, etiology, diagnosis, treatment approaches, and potential long-term sequelae. Key points include that pediatric delirium affects 20-30% of critically ill children, has high morbidity and mortality, and treatment involves a focus on minimizing risk factors and using low doses of medications like benzodiazepines and antipsychotics gradually over time based on individual response and scales.

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Ptrc Lbr Lp
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© © All Rights Reserved
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PSYCHIATRY & PEDIATRICS

Chapter I.5

Pediatric
Delirium:
A Practical
Approach

Jan N M Schieveld, Erwin


Ista, Hennie Knoester &
Marja L Molag
DEPRESSION IN CHILDREN AND
ADOLESCENTS

Adapted by Julie Chilton


The “IACAPAP Textbook of Child and Adolescent Mental Health” is available at the
IACAPAP website http://iacapap.org/iacapap-textbook-of-child-and-adolescent-
mental-health

Please note that this book and its companion PowerPoint are:
· Free and no registration is required to read or download it
· This is an open-access publication under the Creative Commons Attribution Non-
commercial License. According to this, use, distribution and reproduction in any
medium are allowed without prior permission provided the original work is
properly cited and the use is non-commercial.
• The Basics
• Epidemiology
• Clinical
Characteristics
• Etiology
• Diagnosis
• Treatment
• Sequelae
• acute confusional state
• toxic psychosis
• ICU psychosis
• organic psychosyndrome
• encephalopathy
• First described in 1935
• Underrecognized and
underdescribed until
1991
• Awareness increasing in
last few years
• More publications
lately Paul Eugen Bleuler

• More research needed


• Latin de-lira (out of the track)
• Neurocognitive disorder due to a somatic illness
or its treatment
• One of several brain reactions to illness:
– Sickness behavior
– Fever
– Epilepsy
– Catatonia
– Delirium
– Refractory agitation
– Coma
– Disturbance of attention*/awareness
– Changes in cognition
– Develops quickly and fluctuates
– Typically worse in evening
– Likely result of medical condition or treatment
– Excludes coma

*attention is the first to be lost and the last back


• Etiologically nonspecific organic cerebral
syndrome with disturbances of:
– Consciousness and attention
– Perception
– Thinking
– Memory
– Psychomotor behavior
– Emotion
– Sleep-wake schedule
• Variable duration and severity
• High prevalence
• 10-30% of general hospital patients
• Up to 80% in intensive care
• In adults, associated with increased:
– Length of stay
– Morbidity
– Mortality
• In elderly, associated with:
– Faster cognitive decline
– Loss of independence
– Increased mortality x 1 year
• Most important predictor of proximity of death in
elderly and oncology patients of any age
• 20-30% of critically ill children
• A worldwide problem in PICU’s*
• Risk factors include:
– Younger age
– Severity of underlying illness
– Number of medications
– Diagnostic tools used
– General ward vs intensive
Zbigniew J Lipowski
care unit
– Developmental delay
– Previous episode
PICU: Pediatric intensive care unit
• Can be benign or non-benign
• 2 types of benign delirium:
– Emergence delirium/agitation
• Immediate postoperative period
• After anesthesia withdrawal
• Short-lived~ 30-45 minutes
• Resolves completely
– Common/general practice delirium
• With infections, fevers
• Confusion
• Waxing/waning course
• Worse at night
• Resolves within 2-3 days
• If persistent, or already present in the morning, it requires
emergency medical evaluation
• Hyperactive
– Agitation
– Irritability
– Increased motor activity

• Hypoactive:
– Apathetic
– Uninterested

• Mixed
• 6 year old boy with asthma attack
• Intubated and sedated in ICU
• After extubation on day 3:
– Confused and anxious
– Hallucinations of flying objects and monsters
– Verbally aggressive
– Diagnosed with delirium and treated with
lorazepam and IV haloperidol
– Improved after 24 hours
• 3 year old girl mechanically ventilated for 6 days
after tracheal surgery
• Sedated with midazolam, ketamine,
dexmedetomidine, levomepromazine,
dexamethasone, and morphine
• Everything tapered for extubation and morphine
switched to methadone
• Day after extubation became:
– Agitated and disoriented
– Unable to focus attention
– Then apathetic and unresponsive
– 21 points on the CAP-D
*MG Wise in Textbook of Neuropsychiatry (1987)
• Eye contact with parents?
• Purposeful actions?
• Aware of surroundings?
• Restless?
• Inconsolable?
• Underactive?
• Increased response latency?
• “This is NOW not my child anymore!” (comment
by parents, family)
1. Developing somatic complications?

2. Medication change?

3. Physical discomfort?
• Minimize risk factors:
– Repeated orientation
– Early mobilization
– Noise reduction
– Non-pharmacologic sleep management
– Day-night rhythm
– Single room
• Preventive administration not recommended
• Consider for:
– Anxiety, agitation, hallucinations, sleep
• Monitor drug-drug interactions
• Weigh risks and benefits
• Same medications used in adults and children
– Benzodiazepine withdrawal benzodiazepines and clonidine
– Opiate withdrawal clonidine and methadone
• Recommendations based on consensus not evidence
– IV and PO haloperidol (EKG if risk factors)
– PO risperidone
– adverse effects: dystonia, oculogyric crisis, akathisia, hyperpyrexia
• Start low and go slow
• Scales 3 times a day
• Wean gradually
EXAMPLE

• Using repeated loading doses (starting low & going slow) try
to find a therapeutic response after 1 or 2 hours, or in the
first 24 hours, and the duration of it.
• Then calculate, based on these data, a maintenance dosage
for the next 24 hours (divided in 3 doses).
• The maintenance dosages suggested are only indicative.
• Preventive administration not recommended
• No studies
• No consensus
• No studies on delirium
• Increased length of hospital stay
• Large increase in hospital costs
• Increased mortality
• PTSD symptoms
• Delusional memories
• Cognitive problems after intensive care unit stays
– Hypoxia
– Hypoperfusion
– Infection
– Trauma
• Neurotoxicity in animal studies
– Benzodiazepines
– Opioids
– Anesthetics

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