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Pain and Sedation Management PICU.pptx
1. Pain and Sedation management PICU
Dr. Sabona Lemessa (Assistant professor in pediatrics and child health,
JUMC)
8/12/2022
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2. Outline
Introduction
Definition of pain
Classification
Causes of pain in ICU
Effect
Goal of sedation
Assessment
Management principles
Reference
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3. Introduction
The treatment and alleviation of pain is a basic human right that exists
regardless of age.
Hospitalization in general, and admission to the PICU in particular
are frightening and painful experiences to children and their families
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4. Definition
Pain is an unpleasant sensory or emotional experience
associated with actual or potential tissue damage, or
described in terms of such damage (International Association for
the study of Pain: IASP,1979)
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5. Cont…
has two important elements
pain encompasses both peripheral physiologic and central
cognitive/emotional components
may or may not be associated with real tissue damage
may exist in the absence of demonstrable somatic pathology.
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6. Classification
Nociceptive pain:- the result of tissue damage
typically involves bones, joints and soft tissue.
It is further subdivided into somatic & visceral.
Neuropathic pain
arising from abnormal neural activity secondary to disease or injury
of nervous system.
It remains persistent without ongoing disease.
It involves CNS, nerve plexuses, nerve roots or PS.
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7. Causes of pain in ICU
the primary illness, trauma or the disease process
daily nursing procedures- turning, tracheal suctioning and wound care
exacerbated by emotional distress and anxiety which result of
Separation from one's parents and family
being surrounded by unfamiliar people, sleep loss and fragmentation
the fear of pain, loss of control or even death.
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8. Effect of pain
While not specific or sensitive indicators of pain, responses to pain and
stress can include:-
increases in intracranial pressure, heart rate
Increase in respiratory rate, blood pressure, blood glucose
Stress hormones and decreases in oxygen saturation.
Pain can induce agitation, Stress induced secondary injury.
Agitation causing loss of artificial airway or intravenous access
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11. Pain assessment
A patient’s self-report is the single most reliable indicator of pain
In neonates, infants and children aged <3 year
behavioral observational scales
rely on facial expression, motor responses and physiological indices
Children aged 3–8 yr are generally able to use self-reporting techniques
‘faces scales’ using either photographs or drawings of faces
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14. Cont…
Vital sign changes and physiologic indicators are NOT valid indicators of
pain
However, these may be the only indicators of distress in the critically ill
child.
Physiologic indicators-
include diaphoresis, pupil dilation and
processed electroencephalography (i.e. bispectral index).
May be used when patients are sedated and/or muscle-relaxed
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15. Assessment of patients who are heavily sedated or muscle-relaxed
There are no validated pain scales
Patients unable to express pain behaviors will be scored as deeply sedated
or without pain if using behavioral scales.
How to Assess
Search for potential sources of pain and assume pain present if
there is cause for pain
Anticipate and treat pain for procedures, Trial treatment/analgesia
Use physiologic indicators cautiously to prompt further
assessment/treatment
but do not rely on them exclusively
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16. Sedation assessment
COMFORT scale
5 behavioral variables (alertness, facial tension, muscle tone,
agitation and movement) and
3 physiologic variables (PR, respiration, and BP)
State Behavioral Scale (SBS)
defines the sedation-agitation continuum to guide goal-directed
therapy
using a patient’s response to voice, gentle touch, and noxious
stimuli such as suctioning
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17. Summary of recommended sedation assessment tools for critically ill children
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18. Goal of sedation
provide adequate comfort and safety
optimizing patient-ventilator synchrony and
minimizing the risk of delirium and sleep disturbances.
both excessive and inadequate sedation should be avoided
to provide a child with anxiolysis
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19. Management
The most commonly used agents for long-term sedation are
benzodiazepines, opioids and a-agonists
Parenteral drug administration through intravenous access is most
common in the critically ill ICU patient
Enteral administration is not effective
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21. Analgesics with Antipyretic Activity or Nonopioid (“Weaker”) Analgesics
Acetaminophen (paracetamol), salicylate (aspirin), ibuprofen, naproxen and
diclofenac
provide pain relief primarily by blocking peripheral and central prostaglandin
production
The most commonly used nonopioid analgesic remains acetaminophen
(paracetamol).
Unlike aspirin and the NSAIDs, acetaminophen works primarily centrally (COX
III) and
has minimal, if any, anti-inflammatory activity
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22. Opioid Analgesics
The opioids most commonly used In the management of pain are μ
agonists
morphine, meperidine, methadone, codeine, oxycodone and the fentanyl
In the PICU, fentanyl and morphine are the most commonly utilized
opioids
Produce delayed gastric emptying, decreased intestinal peristalsis, and
urinary retention
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25. Iatrogenic withdrawal syndrome assessment in infants and children
Prolonged administration of opioids and/or benzodiazepines may induce
drug tolerance and physiological dependency
Due to Abrupt discontinuation or (too rapid) weaning
after >=5days of continuous infusion, >=10days in intermittent
bolus
The onset of withdrawal can occur after 1 up to 48 h after tapering
off or discontinuation
An estimated 10–34 % of all PICU patients are at risk of IWS
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26. Manifestation
Neurologic: irritability, anxiety, tremors, clonus, yawning, sneezing,
delirium, seizures, hallucinations, and mydriasis
Gastroenteric: feeding intolerance with vomiting, diarrhea,
uncoordinated sucking
Activation of sympathetic nervous system: tachycardia,
hypertension, tachypnea, sweating, fever, and cough
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30. Cont…
Tolerance is defined as “decreasing clinical effects of a drug after
prolonged exposure to it”.
Physical dependence is defined as the “physiologic and biochemical
adaptation of neurons such that
removing a drug precipitates withdrawal or
An abstinence syndrome”
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31. Cont…
To prevent or delay tolerance:
Titrate opioids to adequate pain management; adjust to minimum
effective dose
Regularly reassess if continued use needed
Use longer acting opioids, like methadone, for persistent pain
Consider daily interruption of sedatives
Gradually wean patients at risk
Consider a methadone weaning protocol or the addition of clonidine
or alternatives.
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32. Sleep in the PICU
Promoting sleep can be considered a PICU pain management
Intervention
Disruptions of sleep
Noise, Light
Analgesics/sedatives, Mechanical ventilation
Nursing care/procedures,
Post-traumatic stress (pain from trauma/burn)
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33. Cont…
Recommendations
Decrease noise < 45 dB
Promote day/night rhythm
Daylight, Family presence
Cluster care/ minimize nighttime interruptions
PICU patients are at risk for sleep loss/disruption, which may
contribute to delayed healing and poor pain tolerance.
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34. DELIRIUM IN THE PICU
o Characterized by an acute onset and fluctuating course with reduced
awareness
o impairments in attention and
o changes in cognition (memory deficits, language disturbances,
hallucinations)
o all in combination with a pathophysiologic cause
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35. Cont…
Develops over hours to days
Fluctuates in severity
Higher rate in patients with longer PICU length of stay
Risk factors:
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37. Delirium management
Preventive measures:
o Promote daily routine, caregiver interaction during day
o Promote uninterrupted sleep
o Offer a familiar environment (e.g. favorite toys)
o Cluster care to minimize interruptions
o Conduct regular delirium screening
o Assess and manage pain
o Consistent assessment/management of pain may decrease
risk and severity of delirium
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38. Preventing adverse effects of PICU hospitalization
Strategies to reduce pain
Identify painful events that can be eliminated or reduced
Use developmentally appropriate pharmacological and
biobehavioral
approaches for painful procedures
Ensure adequate analgesia if pain identified or likely
Incorporate multi-modal analgesia
Balance needs for analgesia and sedation
Address sources of non-pain related distress
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39. Reference
Sapna R. Kudchadkar, R. Blaine Easley, Kenneth M. Brady, Myron Yaster,
Pain and Sedation Management, pediatric ICU 5th edition.
Sean Barnes, MD, MBA,* Myron Yaster, MD,† Sapna R. Kudchadkar, MD,
on Pediatric Sedation Management, Department of Anesthesiology &
Critical Care Medicine, Johns Hopkins University School of Medicine,
MAY 2016.
Stephen D. Playfor MD, Consultant Paediatric Intensivist, Royal
Manchester Children’s, on Analgesia and sedation in critically ill children,
Volume 8 Number 3 2008.
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40. Pain is a more terrible lord of mankind than even death itself.
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Editor's Notes
Search for potential reasons for pain
• Review the patient’s clinical condition. Are there any problems or
diagnoses that commonly cause pain? If so, assume pain is present
and treat it.
• Anticipate and treat pain caused by procedures.
Rule out other conditions such as constipation or infection. Be sure the
patient is dry, warm or cool enough, positioned in a comfortable way,
and that other basic needs are met.
Try to obtain self-report
• Attempts should first be made to obtain self-report from all patients,
even if it’s a simple “yes/no.” It may be possible to obtain a selfreport
from patients with intellectual disabilities and those who are
critically ill.
Observe behaviors (use validated tools)
• Be vigilant for subtle behavioral changes; remember that behavioral
changes do not translate to a pain intensity rating, but should raise
suspicion of the presence of pain.
Ask others who know the child well (parent or caregiver reports)
• Ask others (surrogate reporting), if the child is in pain. Those who
know a patient best can help identify specific behaviors that indicate
pain for this individual.
Trial a treatment (consider an analgesic)
If pain is likely, attempt an analgesic trial and look for changes in
behavior or other signs of improvement.
Vital sign changes
• Usually reflect stress response; therefore they are not specific or
sensitive to pain
• Inconsistent across patients
• Inconsistent during single patient observations
• Some PICU patients lack ability to exhibit some vital sign changes due
to medical condition and/or treatments. Example: a child with
congenital heart disease with conduction abnormality, pacemaker,
and/or cardiovascular medications
Physiologic indicators
There is not sufficient evidence to support using vital signs or other
physiologic indicators to assess pain. There is high inter-individual
variability in vital sign data.
Proposed physiologic indicators include diaphoresis, pupil dilation, and
processed electroencephalography (i.e. bispectral index).
Pupillary dilation may indicate inadequate analgesia (Gelinas et al., 2014;
Luckett & Hays, 2013). Like vital signs, pupil dilation is NOT specific for
pain and pupils can be constricted with severe pain.
Processed electroencephalography, such as bispectral index (BIS), may
be used when patients are sedated and/or muscle-relaxed. BIS values are
subject to artifact from clinical conditions and medical devices, and
therefore, are NOT recommended for monitoring pain
Morphine is a long-acting opioid analgesic with important age-dependent
pharmacokinetics. Large doses of morphine (0.5-2 mg/kg), combined with N2 O
provide adequate analgesia for painful procedures. Equivalent doses of morphine
per kilogram are associated with higher blood levels in neonates than in older
children, with plasma concentrations approximating 3 times those of adults.
Morphine exhibits a longer elimination half-life (14 hr) in young children than in
adults (2 hr). The immature blood-brain barrier of neonates is more permeable to
morphine. Morphine is often associated with hypotension and bronchospasm
from histamine release and should be used with caution in children with asthma.
Morphine has renally excreted active metabolites and is relatively
contraindicated in renal failure. Because of morphine's prolonged duration of
action and cardiorespiratory side effects, the fentanyl class of synthetic opioids
has increased in popularity for perioperative analgesia.
Prolonged use may cause hemodynamic collapse, bradycardia, metabolic
acidosis, cardiac failure, rhabdomyolysis, hyperlipidemia, profound shock, and
death (propofol infusion syndrome)
Symptoms reach their peak within 72 hours and
include abdominal cramps, vomiting, diarrhea, tachycardia, hypertension, diaphoresis, restlessness
insomnia, movement disorders, reversible neurologic abnormalities, and seizures
Gradual weaning (e.g. 10 -20% decline in dose every day or every-other day).
Its incidence in the PICU is highly variable. In
Spain, it affects 50% of the patients who have a continuous
infusion of sedoanalgesia for 48hours, increasing to more than
80% when infusion lasts more than 5 days.[7] In other countries,
the incidence of the IWS is similar, reaching 50% in patients with
infusions of more than 24hours of duration, and an increase from
80% to 100% when exceeding 5 days of treatment.[7–10]
Regarding the IWS signs and symptoms, these vary depending
on the drug and patient characteristics, such as age, cognitive
status, etc. The most common manifestations are at breathing
level (tachypnoea), gastrointestinal (nausea, vomiting, diarrhea),
nervous system (sweating, tachycardia, mydriasis), and motor
level (tremors, abnormal movements, hyperreflexivity, hypertonia).[
1,8] In addition, it is worth noting that opioid abstinence
originates more superficial movement disorders and gastrointestinal
disorders, as opposed to the withdrawal of BZD.[11]