1. Pain Management
Aola H. Al Duhaim RN, BScN
Pain Management CNC
AolaH.Duhaim@kfsh.med.sa
Pediatrics
2. The IASP defines Pain as:
“An unpleasant sensory and emotional experience
associated with actual or potential tissue damage, or
described in terms of such damage“
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3. The IASP defines Pain as:
"Pain is whatever the experiencing person says it is and
exists whenever he says it does."
Margo McCaffery
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4. PAIN
▫ Motivates us to withdraw from damaging or
potentially damaging situations.
▫ Protect the damaged body part while it heals, and
avoid those situations in the future.
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6. Children are at Risk of Inadequate Pain
Management
▫ Age-Related Factors
Neurobiological
Physiological
Psychological
▫ Misconceptions
Inadequate analgesia
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7. Developmental Neurobiology
• Sensory fibers are abundant by 20 weeks
• Functional spinal reflex is present by 19 weeks
• Connection to the thalamus are present by 20 weeks
Lee SJ, Ralston H, Drey EA, Partridge J, Rosen MA. Fetal Pain: A Systematic
Multidisciplinary Review of the Evidence.
JAMA. 2005;294(8):947-954
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8. Developmental Neurobiology
• Connection to the subplate neurons are present by 17
weeks e` intensive differentiation by 25 weeks
• Mature thalamocortical projections not present till
29-30 weeks
Lee SJ, Ralston H, Drey EA, Partridge J, Rosen MA. Fetal Pain: A Systematic
Multidisciplinary Review of the Evidence.
JAMA. 2005;294(8):947-954
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9. NOW well accepted by Neuroscientists and Pain Specialists that..
The nervous system is sufficiently developed before birth.
Children experience pain from birth onward
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10. NOW well accepted by Neuroscientists and Pain Specialists that..
Infants and young children may experience a greater
neural response more pain sensation and pain-related
distress
The impact of painful experience on the young
long-term effects can occur
i.e. lowered pain tolerance
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11. Physiological Changes
• CNS (BBB)
• Liver ( Hepatic blood flow Vs.
Immaturity)
• Protein Bindings (Albumin Vs.
AAG)
• Kidney (Protein load ,
Excretion Capability)
• Volume of distribution (water
Vs. Fat compartments)
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13. Cognitive Factors
• Understanding the pain source
• Ability to understand what happen
• Expectation regarding the quality or strength of pain
• Previous experience
• Knowledge of pain control strategies
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14. Behavioral Factors
• Distress responses (child and family)
▫ May initiate, maintain or exacerbate a child’s
pain.
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16. Developmental Stages
Neonate
up to 1 mth
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17. Misconceptions
• The myth that infants and children do not feel pain, or
suffer less from it than adults.
• Lack of routine pain assessment in children.
• Lack of knowledge regarding newer modalities and
proper dosing strategies for the use of analgesics in
children.
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The American Academy of Pediatrics and
the American Pain Society
18. • Fears of respiratory depression or other adverse effects
of analgesic medications.
• The belief that preventing pain in children takes too
much time and effort.
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The American Academy of Pediatrics and
the American Pain Society
Misconceptions
19. Classification of Pain
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20. Sharp & well localized.
Reproduce by touching &
moving the affected area
Somatic1-Nociceptive
Noxious stimulation of
specific pain receptors
Thermal, Mechanical or
Chemical
Deep or Superficial
Stretch, Inflammation &
Ischemia
Poorly localized, cramping,
colicky in nature & may feel like
vague deep ache
21. 2-Non-Nociceptive
within PNS / CNS
Nerve cell dysfunction.
No specific receptors for pain
Neuropathic
AKA: Pinched/ Trapped Nerve
Degeneration, Pressure,
Inflammation ..
it becomes electrically unstable,
firing off signals randomly
Sympathatic
Over-Activity of Sympathetic
Nervous System, and CNS/ PNS
More Commonly After Fractures or
Soft Tissue Injuries
may lead to Complex Regional
Pain Syndrome (CRPS).
Partially Sensitive to:
Paracetamol
NSAIDs
Opioids.
More Sensitive to:
•Anti-Depressants
•Anti-Convulsants
•Anti-Arrhythmics
•NMDAAntagonists
•Topical Capsaicin may be helpful
22. Acute Pain:
• More common
• Begins suddenly
• Sharp in quality
• Serves as a warning of disease/threat
• Caused by ..
▫ Procedures
▫ Surgery
▫ Broken bones
▫ Dental work
▫ Burns or cuts
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23. Chronic Pain:
• Longer than 3-6 months
• Despite the fact that an injury has healed
• Pain signals remain active in the nervous system for
weeks, months, or years.
Such as:
• Cancer pain
• Arthritis pain
• Neurogenic pain (pain resulting from damage to nerves)
• Psychogenic pain (pain not due to past disease or injury or any visible sign
of damage inside)
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24. Breakthrough pain:
A sudden Flare-up of pain that “break through” the
around the clock medication used for persistent pain.
Up to 86% of the patients
3 – 30 min & require different Tx.
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25. Overtreatment
Increased around the clock
medication
Increased side Effects
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26. BTP Medications may not act
quickly enough
Patient suffer pain up to 30 min
or more
Undertreatment
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27. Quick onset BTP medication
Last as long as the BTP (30min)
Easily used
Has manageable Side Effects
PreferredTreatment
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28. Why Should we Treat Pain?
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30. When ..?
• On admission
• After any known pain- producing event
• With each new report of pain
• Routinely at regular intervals
• After intervention
▫ at appropriate time (e.g. 15-30 min P` IV , 1 hr P` PO);
Follow-up assessment is crucial
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31. • To assess pain adequately we must consider..
▫ The developmental stage
▫ Age
▫ Experience
▫ Family Culture/Belief
▫ Language
▫ Severity of Illness
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32. Neonates and Infants
▫ They communicate distress by crying
▫ Should involve the parents
Notice changes in the infant not obvious to the health care
provider
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33. Neonates and Infants
Observational pain scales (unable to verbalize)
These scales, though essential, also respond to distress
from causes other than pain, such as hunger, fear or
anxiety
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34. Preschool and School Age Children
Simple self-report scales using facial expressions or
small objects
To allow more accurately description of their pain
intensity.
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38. Observational Pain Scales
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FLACC 2M – 3 Y
39. King Fahad Specialist Hospital
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2- Poker Chip Scale “pieces of hurt,”
1- Oucher Scale (ethnic versions) well accepted in children over 6 years of age
40. King Fahad Specialist Hospital
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3- Wong-Baker
Faces Scale (free to
use)
(available in 30 languages)4-
5- VAS , NRS
8 years and older
without difficulty
41. Pain Assessment in Pediatrics
Adult Pediatrics
Pain
Fear
Pain receptors are the same in the pediatric patient compared to the adult.
But Children do have increased fear and anxiety.
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42. Pain control must be based on scientific fact, not on
personal beliefs or opinions
Optimal pain management is the right of all patients
and the responsibility of all health professionals
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43. Treatment should include
▫ Pharmacological - Appropriate Multi-Modal
▫ Non-Pharmacological
▫ Sympathetic Nerve Blocks – as needed
▫ Intensive Rehabilitation
Occupational and Physiotherapy.
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45. • Special Considerations in Treating Infants and
Children.
• Although most of the major organ systems in infants
are well developed at birth, their functional maturity
is often delayed.
• In the first months:
▫ These systems rapidly mature similar to adults before 3
months of age.
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46. Multi-Modal Medications
• Inhibition of peripheral inflammatory response
to tissue injury (NSAIDs)
• Blocking the pain receptors (Opioids)
• Neural blockade of transmission of pain
impulses (Regional Tech./Neuraxial blocks)
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47. Multi-Modal Medications
• Prevention of “Central Sensitization” before
tissue injury (Preemptive analgesia)
• Prevention & treatment of anxiety accompanying
acute pain.
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48. Preemptive analgesia
• Treatment that ..
▫ Starts before surgery
▫ Prevent the establishment of Central Sensitization
caused by Injury/Inflammatory responses.
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50. Drugs used for pain management
• Non-Steroidal Anti-Inflammatory Drugs (NSAIDS)
• Acetaminophen
• Opioids
• Adjuvant
• Others
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51. Analgesics (Opioids/L.A)
Most are conjugated in the liver.
Newborns, and especially premature infants, have
delayed maturation of the enzyme systems involved
in drug conjugation
▫ Several of these hepatic enzyme systems mature at varying
rates over the first 6 months of life.
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52. Analgesics (Opioids/L.A)
Glomerular filtration rates :
▫ Diminished in the first week of life, especially in premature
infants
▫ but sufficiently mature to clear medications and metabolites
by 2 weeks of age.
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53. Analgesics (Opioids/L.A)
Newborns
have a higher percentage of body weight as water and
less as fat
Water soluble drugs often have larger volumes of
distribution.
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54. Analgesics (Opioids/L.A)
Newborns
• Have reduced plasma concentrations of both albumin
and alpha-1 acid glycoprotein
may lead to higher concentrations of unbound drug (active), and
thereby greater drug effect or drug toxicity.
• Have diminished ventilatory responses to hypoxemia
and hypercarbia - especially premature infants
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55. Acetaminophen
• Excellent safe profile and lack of significant side
effects
• commonly used
• mild to moderate pain,
• often combined with opioid (for more severe pain)
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56. Acetaminophen
• Can results in Hepatotoxicity
• Infants and children produce high levels of GSH as a
part of hepatic growth may provide some
protection
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57. Acetaminophen
• Still acetaminophen toxicity are highest in pediatric
patients.
▫ Analysis of Poison Control Center data, FDA adverse
event reports, and clinical trial reports indicate that
therapeutic doses of <75 mg/kg daily are safe with
respect to hepatotoxicity.
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58. NSAIDs
• Pharmacodynamics and pharmacokinetics are not
much different than in adults.
• Potential for GI, renal and other toxicities exist
but less than in adults.
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60. Patient Controlled Analgesia
• Widely used for postoperative pain relief
• Appropriate preoperative teaching and
encouragement
• As young as 6 to 7 years of age can independently
use the PCA
• 4 and 6, however, require encouragement from their
parents and nurses
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61. Local Anesthetics and Regional Anesthesia
• Topical Anesthetics (EMLA)
• provide pain relief prior to needle-stick
procedures
• requires 30 to 60 minutes to become fully
effective after application.
• must be applied in a thick layer
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62. EMLA
• Clinical trials have shown effectiveness of EMLA in
reducing the pain or distress of a number of common
pediatric procedures including:
▫ venous cannulation
▫ Venipuncture
▫ lumbar puncture,
▫ Circumcision
▫ urethral meatotomy
▫ Immunizations
▫ dermatologic procedures … etc.
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64. Comfort Methods:
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Repositioning
Singing
or soft music
Gentle stroking
Rocking with the child
in a rocking chair
65. Swaddling
Comfort Methods:
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Watching a movie
Reading a book
Other methods used at home
to comfort the child
66. Psychological strategies:
For children undergoing repeated painful procedures,
cognitive-behavioral therapy
▫ decrease anxiety and distress
▫ help children master a distressing situation.
▫ take time to learn and master
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67. Psychological strategies:
• Distraction techniques
▫ divert attention away from painful stimuli
• positive incentive techniques
▫ provide a small reward (e.g., stickers or prizes)
Decrease anxiety but not adequate as the sole means of
pain relief.
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68. Persistent Pain in Children
• Children with chronic medical disease can
experience:
▫ a significant amount of pain associated with both their
underlying disease and the procedures that are performed to
treat it.
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69. Persistent Pain in Children
• Children with chronic medical disease can
experience:
▫ They deserve not only access to adequate pain medication,
but also psychological support to help them continue to
learn and grow as they should.
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70. SUMMARY
• The pediatric nervous system is fully developed and
able to respond to Nociceptive stimuli even in pre-
term neonates
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71. SUMMARY
• Pain can have lasting physiological and
developmental consequences if not appropriately
managed
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72. SUMMARY
• Regular pain assessment is fundamental to good pain
management but is often poorly performed
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73. SUMMARY
• A variety of pain assessment tools are available and
should be utilized according to a patient’s age and
developmental stage
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74. SUMMARY
• Multi-modal therapy is appropriate for managing all
forms of pediatric pain and should utilize
combinations of local anesthetic, paracetamol,
NSAIDs and opioids as appropriate
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75. SUMMARY
• Adequate monitoring, safety equipment and
resuscitation skills are needed to safely manage
patients requiring combinations of sedation and
analgesia for painful procedures
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76. SUMMARY
• The pharmacokinetic and pharmacodynamic profile
of commonly used analgesics can be variable
depending on the age and development
King Fahad Specialist Hospital
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الـتخـصـصي فـهـد الـمـلـك مــسـتــشـفى
الــدمـام
77. THANK YOU
Aola H. Al Duhaim RN, BScN
Pain Management CNC
AolaH.Duhaim@kfsh.med.sa
King Fahad Specialist Hospital
Dammam
الـتخـصـصي فـهـد الـمـلـك مــسـتــشـفى
الــدمـام
Editor's Notes
1- Tissue damage
2- Activation of the PNS
3- Activation of CNS @ the Spinal cord level
4- Transmission of Pain signal to the brain and reaction
The blood–brain barrier (BBB) is a highly selective permeability barrier that separates the circulating blood from the brain extracellular fluid (BECF) in the central nervous system (CNS). The blood–brain barrier is formed by capillary endothelial cells, which are connected by tight junctions with an extremely high electrical resistivity of at least 0.1 Ω⋅m.[1] The blood–brain barrier allows the passage of water, some gases, and lipid soluble molecules by passive diffusion, as well as the selective transport of molecules such as glucose and amino acids that are crucial to neural function. On the other hand, the blood–brain barrier may prevent the entry of lipophilic, potentialneurotoxins by way of an active transport mechanism mediated by P-glycoprotein. Astrocytes are necessary to create the blood–brain barrier. A small number of regions in the brain, including the circumventricular organs (CVOs), do not have a blood–brain barrier.
Neonates and infants have a lower AAG concentration in serum as compared with adults; therefore, their free fraction of local anaesthetics is increased accordingly. This has important clinical implications since, at least at steady state, the toxic effects of local anaesthetics are directly related to the free (unbound) drug concentration
After injection into the epidural space, absorption into the bloodstream follows a biphasic process. The buffering properties of the epidural space are important and prevent a rapid rise in concentration. In infants and children, the epidural space seems to protect patients in a similar manner. Moreover, it has been observed that the peak plasma concentration (Cmax) of ropivacaine is delayed in infants and children when compared with adults. The time to Cmax decreases from 90–120 minutes in infants aged less than 6 months to 30 minutes in children aged more than 8 years. This delay in Cmax may also be related to the lower clearance observed in younger patients. Local anaesthetics are metabolised by cytochrome P450 (CYP). The main CYP isoforms involved are CYP3A4 for lidocaine and bupivacaine and CYP1A2 for ropivacaine. CYP3A4 is not mature at birth but is partly replaced by CYP3A7. The intrinsic clearance of bupivacaine is only one-third of that in adults at 1 month of age, and two-thirds at 6 months. CYP1A2 is not fully mature before the age of 3 years. Indeed, the clearance of ropivacaine does not reach its maximum before the age of 5 years. However, at birth this clearance is not as low as expected, and ropivacaine may be used even in younger patients.
NMDA Antagonists are a class of anesthetics that work to antagonize, or inhibit the action of, the N-Methyl-D-aspartate receptor (NMDAR). They are used as anesthetics for animals and for humans; the state of anesthesia they induce is referred to as dissociative anesthesia. There is evidence that NMDA receptor antagonists can cause a certain type of neurotoxicity or brain damage referred to as Olney's Lesions in rodents, although such damage has never been conclusively observed in primates likehumans. Recent research conducted on primates suggests that, while very consistent and long-term ketamine use may be neurotoxic, acute use is not.[1][2]
Several synthetic opioids function additionally as NMDAR-antagonists, such as pethidine, methadone, dextropropoxyphene, tramadol and ketobemidone.
Some NMDA receptor antagonists, such as ketamine, dextromethorphan (DXM), phencyclidine (PCP), Methoxetamine (MXE), and nitrous oxide (N2O), are popular recreational drugs used for their dissociative, hallucinogenic, and euphoriant properties. When used recreationally, they are classified as dissociative drugs.
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