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PEDIATRIC PROCEDURAL
SEDATION
Murtuza Ghiya
Specialty Registrar,
Emergency medicine,
Bedford Hospital, NHS trust
ANY PAINFUL EXPERIENCES?
• Children of all ages feel pain
Contents
1. Developmental attributes –age wise
2. Principles of sedation
3. Anxiolysis
4. Local anesthesia
5. Procedural sedation
6. Combinations
7. Post sedation monitoring
DEVELOPMENTAL ATTRIBUTES
Newborn & Infant
( 0 TO 9 MONTHS)
• Pain affects neuro-development
• No Abstraction
• Unable to conceptualize cause and effect,
outcome and benefit
• No concept of time- no anticipation-no
anxiety
• No stranger anxiety
Toddler
(AGES 10 TO 36 MONTHS)
• Stranger anxiety
• Lack of temporal abstraction
• Parental presence and even participation -laps
or arms
• Involve the toddler in decision making
School-aged
(AGES 4 TO 10 YEARS)
• Can conceptualize time (abstraction)
• "Magical thinking"
• Physical restraint may be challenging
Pre-adolescence & Adolescence
(AGES 11 TO 18 YEARS)
• Physical modesty is extreme.
• Cry or even fight.
• Physical restraint is difficult and inappropriate.
PRINCIPLES OF SEDATION
ANXIOLYSIS
Child- parent -child
Non pharmacologic Anxiolysis
• Parental presence---Toddlers/school aged
• Adolescents --- certain history/examination
without parents
• Distraction-(younger children)
picture books, stories , music.
• Distraction-(older children)
video distraction "virtual reality" glasses.
Pharmacologic anxiolysis
• Midazolam - relatively short duration of action
• For anxiolysis, - 0.5 milligram/kg PO
• Onset -20 min
• Flavoured oral suspension
(injectable form - mixed with flavored syrup/beverage)
• The IV - can also be given nasally at 0.2 mg/kg, local
nasal irritation.
• When IV access is already being used for other
reasons.
• 0.05 to 0.1 milligram/kg IV
• Adverse effects- (higher dose) respiratory
depression
• Self-limited. May consider antidote-
F*u*ma*****
LOCAL ANESTHESIA
Topical anesthetics
• Pain of IV catheterization/ wound preparation
• Eutectic mixture of prilocaine + lidocaine - cream
• Onset-30 min
• Absorption is minimal, non toxic- even when applied to
open wounds
• For maximum skin absorption, apply beneath occlusive
dressings such as Tegaderm
Injectable Local Anesthetics
• Lidocaine
• Slow injection with a small-gauge needle
• Sodium bicarbonate 1:4
• When practical, regional blocks better.
PROCEDURAL SEDATION
Oral sucrose 25%
• Newborns and infants
• Pacifier dipped into the solution just before
the procedure.
• Procedures such as LP ,IV line, or during IM
immunization injections.
Indications for procedural sedation
• Eg- ?
Pre Requisites
• Develop your own repertoire
• Keep crash cart ready.
• Written informed consent
( state the alternative option of no sedation!)
• Ideal setting-
1 physician - sedation and airway
+
1physician- performing the procedure
Where to draw the line?
• Category III or higher may not be candidates
for elective procedural sedation in the ED
The Pediatric Sedation Research
Consortium
• “no correlation between fasting status and the
incidence of aspiration or other untoward
outcomes in procedural sedation performed
outside the operating room.”
• Vomiting- more common -typically occurring
in the recovery phase of sedation.
• Consider pre treatment using ondansetron.
• In the ED, the theoretic risk of aspiration vs
against the need for sedation
Propofol
Etomidate
ketamine
• Safe and effective in children
• 2nd most commonly used
• "threshold dose” all or none--- for sedation only
and not for analgesia
• >90% children-adequately sedated @ 1.5 mg/kg
ketamine
• Dose 1-2 mg/kg I.V
• Onset 1-2 minutes
• Duration- 10-12 minutes
ketamine vs propofol
KETAMINE PROPOFOL
Effective sedation +++ ++
Respiratory depression - ++
Hypotension - ++
Need for additional opioid - +
Abolishment of reflexes - ++
Fentanyl
Combinations
• Always preferable.
• To achieve the triad of
Sedation --- Analgesia--- Anxiolysis
• To avoid undue s/e of a single agent.
Discuss
• Midaz + fentanyl
• Midaz + morphine
• Fentanyl + propofol
• Propofol + ketamine
• Ketamine + midaz
• Etomidate + propofol
Postsedation monitoring and recovery
• Immediately post-procedure---removal of
painful stimulus
• Paradoxical over sedation and respiratory
depression
• Despite ketamine + ondansetron, nausea and
vomiting may occur
Discharge criteria
1. Stable serial vital signs, including blood
pressure and pulse oximetry.
2. Return to pre-sedation mental status;
3. Ability to sit unaided
Written Discharge Advice
• Watch for vomiting
• Abnormal somnolence
• Restrict activities to bare minimum
Conclusions
• Break the cycle
• Approach changes as age changes
• Never ignore neonatal pain
• Different drugs for different procedures
• Rational drug combinations
• ? Ketamine underused
• Vomiting common complication
• Lets put a smile on the face
THANK YOU
SUCROSE
MALLAMPATTI- SUPINE VS SITTING
LET EMLA
EMLA
• A concern with EMLA is the risk of systemic absorption; however, absorption is
minimal and should not produce toxic plasma levels with routine dosing, even
when applied to open wounds.[4]
• When applied to the skin, an anesthetic response occurs within 45 to 60 minutes
and lasts for one to two hours after removal. Additionally, the site of application
can affect the duration of analgesia; areas with increased vasculature can increase
drug clearance.[3]
• , and the manufacturer recommends the following: age 0-3 months or < 5 kg
should receive 1 g over 10 cm2 skin for up to 1 hour; age 3-12 months and > 5 kg
should receive 2 g over 20 cm2 skin for up to 4 hours; age 1-6 years and > 10 kg
should receive 10 g over 100 cm2 skin for up to 4 hours; and age 7-12 years and >
20 kg should receive 20 g over 200 cm2 skin for up 4 hours.[4]
• For maximum skin absorption, EMLA should be applied beneath occlusive
dressings such as Tegaderm.[5]
• Because of the risk of methemoglobinemia, EMLA use should be avoided in
neonates with a gestational age of less than 37 weeks and in infants under the age
of 1 year who are receiving concomitant therapy with agents such as phenytoin or
acetaminophen.[4]
Dosing for EMLA is age- and weight-
based
• < 5 kg should receive 1 g over 10 cm2 skin
• > 5 kg should receive 2 g over 20 cm2 skin
• > 10 kg should receive 10 g over 100 cm2 skin
• > 20 kg should receive 20 g over 200 cm2 skin
for up 4 hours.[4]
Flumazenil
• Usual Pediatric Dose for Reversal of Sedation
• IV:
Infants and Children:
Benzodiazepine reversal when used in conscious sedation or general anesthesia:
Initial dose: 0.01 mg/kg (maximum dose: 0.2 mg) given over 15 seconds; may repeat 0.01 mg/kg
(maximum dose: 0.2 mg) after 45 seconds, and then every minute to a maximum total cumulative
dose of 0.05 mg/kg or 1 mg, whichever is lower; usual total dose: 0.08 to 1 mg (mean: 0.65 mg)
Management of benzodiazepine overdose: Minimal information available; initial dose: 0.01 mg/kg
(maximum dose: 0.2 mg) with repeat doses of 0.01 mg/kg (maximum dose: 0.2 mg) given every
minute to a maximum total cumulative dose of 1 mg; as an alternative to repeat bolus doses, follow
up continuous infusions of 0.005 to 0.01 mg/kg/hour have been used; further studies are needed.
• Usual Pediatric Dose for Benzodiazepine Overdose
• 1 to 17 years:
Initial dose: 0.01 mg/kg IV over 15 seconds.
Repeat doses: 0.01 mg/kg given over 15 seconds; may repeat 0.01 mg/kg after 45 seconds, then
every minute to a maximum total cumulative dose of 0.05 mg/kg.
Continuous IV infusion: 0.005 to 0.01 mg/kg/hr was used in a premature neonate (gestational age:
32 weeks) exposed to high doses of diazepam intrapartum.
Myoclonus, benzodiazepine induced: IV: 0.078 mg/kg once was effective in a single full-term
neonate who was receiving continuous infusion midazolam
• Why is pethidine c/I in paediatric
• Tramadol in pediatrics?
• Mechanism of analgesia for sucrose?
• Pics- pierre robin syndrome, trisomy 21
• Stranger anxiety at?
• Toddler?
• Amnestic
• Guided imagery
• Flumazenil dose
• LET- topical vs mucous membrane.
• Eutectic?
• Nurse maids elbow
• Mallampati – adult vs paeds– Cormack Lehane
• Intranasal midaz
• Fenta repiratory depression

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Pediatric procedural sedation.pptx

  • 1. PEDIATRIC PROCEDURAL SEDATION Murtuza Ghiya Specialty Registrar, Emergency medicine, Bedford Hospital, NHS trust
  • 3. • Children of all ages feel pain
  • 4. Contents 1. Developmental attributes –age wise 2. Principles of sedation 3. Anxiolysis 4. Local anesthesia 5. Procedural sedation 6. Combinations 7. Post sedation monitoring
  • 6. Newborn & Infant ( 0 TO 9 MONTHS) • Pain affects neuro-development • No Abstraction • Unable to conceptualize cause and effect, outcome and benefit • No concept of time- no anticipation-no anxiety • No stranger anxiety
  • 7. Toddler (AGES 10 TO 36 MONTHS) • Stranger anxiety • Lack of temporal abstraction • Parental presence and even participation -laps or arms • Involve the toddler in decision making
  • 8. School-aged (AGES 4 TO 10 YEARS) • Can conceptualize time (abstraction) • "Magical thinking" • Physical restraint may be challenging
  • 9. Pre-adolescence & Adolescence (AGES 11 TO 18 YEARS) • Physical modesty is extreme. • Cry or even fight. • Physical restraint is difficult and inappropriate.
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  • 16. Non pharmacologic Anxiolysis • Parental presence---Toddlers/school aged • Adolescents --- certain history/examination without parents • Distraction-(younger children) picture books, stories , music. • Distraction-(older children) video distraction "virtual reality" glasses.
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  • 18. Pharmacologic anxiolysis • Midazolam - relatively short duration of action • For anxiolysis, - 0.5 milligram/kg PO • Onset -20 min • Flavoured oral suspension (injectable form - mixed with flavored syrup/beverage) • The IV - can also be given nasally at 0.2 mg/kg, local nasal irritation.
  • 19. • When IV access is already being used for other reasons. • 0.05 to 0.1 milligram/kg IV • Adverse effects- (higher dose) respiratory depression • Self-limited. May consider antidote- F*u*ma*****
  • 21. Topical anesthetics • Pain of IV catheterization/ wound preparation • Eutectic mixture of prilocaine + lidocaine - cream • Onset-30 min • Absorption is minimal, non toxic- even when applied to open wounds • For maximum skin absorption, apply beneath occlusive dressings such as Tegaderm
  • 22. Injectable Local Anesthetics • Lidocaine • Slow injection with a small-gauge needle • Sodium bicarbonate 1:4 • When practical, regional blocks better.
  • 24. Oral sucrose 25% • Newborns and infants • Pacifier dipped into the solution just before the procedure. • Procedures such as LP ,IV line, or during IM immunization injections.
  • 25. Indications for procedural sedation • Eg- ?
  • 26. Pre Requisites • Develop your own repertoire • Keep crash cart ready. • Written informed consent ( state the alternative option of no sedation!) • Ideal setting- 1 physician - sedation and airway + 1physician- performing the procedure
  • 27. Where to draw the line?
  • 28. • Category III or higher may not be candidates for elective procedural sedation in the ED
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  • 31. The Pediatric Sedation Research Consortium • “no correlation between fasting status and the incidence of aspiration or other untoward outcomes in procedural sedation performed outside the operating room.”
  • 32. • Vomiting- more common -typically occurring in the recovery phase of sedation. • Consider pre treatment using ondansetron. • In the ED, the theoretic risk of aspiration vs against the need for sedation
  • 35. ketamine • Safe and effective in children • 2nd most commonly used • "threshold dose” all or none--- for sedation only and not for analgesia • >90% children-adequately sedated @ 1.5 mg/kg
  • 36. ketamine • Dose 1-2 mg/kg I.V • Onset 1-2 minutes • Duration- 10-12 minutes
  • 37. ketamine vs propofol KETAMINE PROPOFOL Effective sedation +++ ++ Respiratory depression - ++ Hypotension - ++ Need for additional opioid - + Abolishment of reflexes - ++
  • 39. Combinations • Always preferable. • To achieve the triad of Sedation --- Analgesia--- Anxiolysis • To avoid undue s/e of a single agent.
  • 40. Discuss • Midaz + fentanyl • Midaz + morphine • Fentanyl + propofol • Propofol + ketamine • Ketamine + midaz • Etomidate + propofol
  • 41. Postsedation monitoring and recovery • Immediately post-procedure---removal of painful stimulus • Paradoxical over sedation and respiratory depression • Despite ketamine + ondansetron, nausea and vomiting may occur
  • 42. Discharge criteria 1. Stable serial vital signs, including blood pressure and pulse oximetry. 2. Return to pre-sedation mental status; 3. Ability to sit unaided
  • 43. Written Discharge Advice • Watch for vomiting • Abnormal somnolence • Restrict activities to bare minimum
  • 44. Conclusions • Break the cycle • Approach changes as age changes • Never ignore neonatal pain • Different drugs for different procedures • Rational drug combinations • ? Ketamine underused • Vomiting common complication • Lets put a smile on the face
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  • 53. EMLA • A concern with EMLA is the risk of systemic absorption; however, absorption is minimal and should not produce toxic plasma levels with routine dosing, even when applied to open wounds.[4] • When applied to the skin, an anesthetic response occurs within 45 to 60 minutes and lasts for one to two hours after removal. Additionally, the site of application can affect the duration of analgesia; areas with increased vasculature can increase drug clearance.[3] • , and the manufacturer recommends the following: age 0-3 months or < 5 kg should receive 1 g over 10 cm2 skin for up to 1 hour; age 3-12 months and > 5 kg should receive 2 g over 20 cm2 skin for up to 4 hours; age 1-6 years and > 10 kg should receive 10 g over 100 cm2 skin for up to 4 hours; and age 7-12 years and > 20 kg should receive 20 g over 200 cm2 skin for up 4 hours.[4] • For maximum skin absorption, EMLA should be applied beneath occlusive dressings such as Tegaderm.[5] • Because of the risk of methemoglobinemia, EMLA use should be avoided in neonates with a gestational age of less than 37 weeks and in infants under the age of 1 year who are receiving concomitant therapy with agents such as phenytoin or acetaminophen.[4]
  • 54. Dosing for EMLA is age- and weight- based • < 5 kg should receive 1 g over 10 cm2 skin • > 5 kg should receive 2 g over 20 cm2 skin • > 10 kg should receive 10 g over 100 cm2 skin • > 20 kg should receive 20 g over 200 cm2 skin for up 4 hours.[4]
  • 55. Flumazenil • Usual Pediatric Dose for Reversal of Sedation • IV: Infants and Children: Benzodiazepine reversal when used in conscious sedation or general anesthesia: Initial dose: 0.01 mg/kg (maximum dose: 0.2 mg) given over 15 seconds; may repeat 0.01 mg/kg (maximum dose: 0.2 mg) after 45 seconds, and then every minute to a maximum total cumulative dose of 0.05 mg/kg or 1 mg, whichever is lower; usual total dose: 0.08 to 1 mg (mean: 0.65 mg) Management of benzodiazepine overdose: Minimal information available; initial dose: 0.01 mg/kg (maximum dose: 0.2 mg) with repeat doses of 0.01 mg/kg (maximum dose: 0.2 mg) given every minute to a maximum total cumulative dose of 1 mg; as an alternative to repeat bolus doses, follow up continuous infusions of 0.005 to 0.01 mg/kg/hour have been used; further studies are needed. • Usual Pediatric Dose for Benzodiazepine Overdose • 1 to 17 years: Initial dose: 0.01 mg/kg IV over 15 seconds. Repeat doses: 0.01 mg/kg given over 15 seconds; may repeat 0.01 mg/kg after 45 seconds, then every minute to a maximum total cumulative dose of 0.05 mg/kg. Continuous IV infusion: 0.005 to 0.01 mg/kg/hr was used in a premature neonate (gestational age: 32 weeks) exposed to high doses of diazepam intrapartum. Myoclonus, benzodiazepine induced: IV: 0.078 mg/kg once was effective in a single full-term neonate who was receiving continuous infusion midazolam
  • 56. • Why is pethidine c/I in paediatric • Tramadol in pediatrics? • Mechanism of analgesia for sucrose? • Pics- pierre robin syndrome, trisomy 21 • Stranger anxiety at? • Toddler? • Amnestic • Guided imagery • Flumazenil dose • LET- topical vs mucous membrane. • Eutectic? • Nurse maids elbow • Mallampati – adult vs paeds– Cormack Lehane • Intranasal midaz • Fenta repiratory depression

Notes de l'éditeur

  1. Buccal only for convulsions
  2. Flumazenil- available
  3. Apply and send to riverbank EMLA contains lidocaine 2.5% and prilocaine 2.5% as an oil-in-water emulsion
  4. What is the problem with malampatti in ED
  5. Similar to propofol in that the protective airway reflexes may be significantly reduced
  6. if sleeping, we should be able to easily awaken the patient to pre-sedation mental status.