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Moderator : Dr Alok Basu Roy
Presenter: Dr Saurabh Kakkar

 Postoperative pain, especially when poorly
controlled, results in harmful acute effects and
chronic effects
 Widespread recognition of the under treatment of
acute pain by clinicians, economists, and health
policy experts has led to the development of a
national clinical practice guideline for management
of acute pain by a agency of U.S.
Introduction
 Anesthesiologists have developed the concept of
acute postoperative pain services application of
evidence based practice to acute postoperative pain,
and creation of innovative approaches to acute pain
medicine
 Anesthesiologists functions as a “perioperative
physician” consultant, and therapist throughout an
institution, as well as a highly skilled expert in the
operating room
 Postoperative pain management should be tailored
to the needs of special populations who may have
different anatomic, physiologic, pharmacologic, or
psychosocial issues
 Surgery produces tissue injury with consequent
release of histamine and inflammatory mediators
 Release of inflammatory mediators activates
peripheral nociceptors, which initiate transduction
and transmission of nociceptive information to the
central nervous system
 Noxious stimuli are transduced by peripheral
nociceptors and transmitted by A-delta and C nerve
fibers from peripheral visceral and somatic sites to
the dorsal horn of the spinal cord, where integration
of peripheral nociceptive and descending
modulatory input occurs
Pain pathway
 Some impulses pass to the ventral and ventrolateral
horns to initiate segmental (spinal) reflex responses,
which may be associated with increased skeletal
muscle tone, inhibition of phrenic nerve function, or
even decreased gastrointestinal motility
 Others are transmitted to higher centers through the
spinothalamic and spinoreticular tracts, where they
induce supra segmental and cortical responses to
ultimately produce the perception of and affective
component of pain
 Continuous release of inflammatory mediators
causes Sensitization of peripheral nociceptors may
occur and is marked by a decreased threshold for
activation, increased rate of discharge with
activation, and increased rate of basal discharge

 Intense noxious input from the periphery may also
result in central sensitization ( hypersensitivity) and
hyperexcitability.
 Nociception is a dynamic process (i.e.,
neuroplasticity) with multiple points of modulation.
 Persistent noxious input may result in relatively
rapid neuronal sensitization and possibly persistent
pain
 The intensity of acute postoperative pain is a
significant predictor of chronic postoperative pain

 Patient dis-satisfaction
 Decreased Respiratory function
 Myocardial ischemia
 Sodium and water retention
 Increased catabolic state
 Postoperative hypercoagulable state
 Immunosuppression
 Poor wound healing
 Prolonged paralytic ileus
Acute effects of postoperative pain

 Delayed recovery
 Inability to participate in rehabilitation
 Chronic postsurgical pain ( CPSP )
 Financial expenses
Chronic effects of postoperative pain

 Previously called “ preemptive analgesia ”
 It refers to an analgesic intervention that preceded a
surgical injury and was more effective in relieving
acute postoperative pain than the same treatment
following surgery
 The rationale for preemptive analgesia was based on
the inhibition of the development of central
sensitization
 An intervention administered before the surgical
incision is not preventative if it is incomplete or
insufficient
Preventive Analgesia

Principles of a multimodal strategy include:
 Control of postoperative pain to allow early mobilization
 early enteral nutrition
 education, and attenuation of the perioperative stress response
through the use of regional anesthetic techniques
 combination of analgesic drugs (i.e., multimodal analgesia)
The multimodal approach integrates the most recent data and
techniques from surgery, anesthesiology, nociceptive neurobiology,
and pain treatment, making it an extension of clinical pathways
(Enhanced Recovery After Surgery, or ERAS) or fast tracks
MULTIMODAL APPROACH TO
PERIOPERATIVE RECOVERY

 Systemic
1. Opioid analgesics
2. Non-opioid analgesics
 Regional
1. Neuraxial techniques
2. Peripheral techniques
Treatment Methods

 Cornerstone for postoperative pain treatment
 Opioids may be administered by the subcutaneous,
transcutaneous, transmucosal, or intramuscular
route, oral and intravenous
 Prescribed on an as-needed (PRN) basis
 Intravenous Patient-Controlled Analgesia (PCA)
Opioids

 PCA optimizes delivery of analgesic opioids and
minimizes the effects of pharmacokinetic and
pharmacodynamic variability in individual patients
 When pain is experienced, analgesic medication is
self-administered, and when pain is reduced
 PCA device can be programmed for several
variables, including the demand (bolus) dose,
lockout interval, and background infusion
Intravenous Patient-Controlled
Analgesia


 NSAID’S :
 Inhibition of cyclooxygenase (COX) and synthesis of
prostaglandins
 COX-1 is constitutive and COX-2 is inducible
 COX-1 participates in platelet aggregation, hemostasis,
and gastric mucosal protection, whereas COX-2
participates in pain, inflammation, and fever
 provide effective analgesia for mild to moderate pain
 side effects include decreased hemostasis, renal
dysfunction, and gastrointestinal hemorrhage
 Diclofenac, Acetaminophen , Ketorolac
Non - Opioids

 Gabapentanoids
 Gabapentin and pregabalin, antiepileptic drugs
 used in the treatment of neuropathic pain
 interact with calcium channel α2-δ ligands to inhibit
calcium influx and subsequent release of excitatory
neurotransmitters
 meta-analysis demonstrated use of pregabalin was
associated with a decrease in opioid consumption and
opioid-related side effects, but no difference in pain
intensity
 perioperative administration of gabapentin and
pregabalin may reduce the incidence of CPSP
Non - Opioids

 Ketamine
 Traditionally recognized as an intraoperatively
anesthetic induction agent
 Small analgesic dose ketamine can facilitate
postoperative analgesia because of its NMDA-
antagonistic properties, which may be important in
attenuating central sensitization and opioid tolerance
 can be administered orally, intravenously,
subcutaneously, or intramuscularly
Non - Opioids


 Single-Dose Neuraxial Opioids
 Administration of a single dose of opioid may be
efficacious as a sole or adjuvant analgesic drug when
administered intrathecally or epidurally
 One of the most important factors in determining the
clinical pharmacology for a particular opioid is its
degree of lipophilicity
 Continuous Epidural Analgesia
 Analgesia delivered through an indwelling epidural
catheter is a safe and effective method for
management of acute postoperative pain
REGIONAL ANALGESIC TECHNIQUES


DRUG INTRATHECAL
SINGLE DOSE
EPIDURAL
SINGLE DOSE
EPIDURAL
CONTINUOUS
INFUSION
FENTANYL 5 – 25 µg 50 – 100 µg 25 – 100 µg/hr
MORPHINE 0.1 – 0.3 µg 1 – 5 µg 0.1 – 0.2 µg/hr
REGIONAL ANALGESIC TECHNIQUES

 Local anesthetics
 Opioids
 Local anesthetics + Opioids
 Adjuvants – Clonidine , Ketamine , Dexmedtomidine
Analgesic drugs for regional
techniques


 Hypotension
 Motor block
 Pruritus
 Respiratory depression
 Nausea and vomiting
 Urinary retention
 Migration of catheter
Side Effects of Neuraxial Analgesic
Drugs

Patient Controlled Epidural Analgesia

 Reduction in mortality and morbidity
 Postoperative thoracic epidural analgesia can facilitate
return of gastrointestinal motility without contributing to
anastomotic bowel dehiscence
 Preserving postoperative pulmonary function through
providing superior analgesia and thus reducing splinting
behavior and attenuating the spinal reflex inhibition of
diaphragmatic function
 Decreases the incidence of postoperative myocardial
infarction by attenuating the stress response and
hypercoagulability
Benefits of Epidural Analgesia

 Epidural hematoma
 Epidural abscess
 Infections like meningitis
 Intrathecal or intravascular migration
Risks With Epidural Analgesia

 Analgesia superior to that with systemic opioids
 Brachial plexus, Lumbar plexus, Femoral, Sciatic-
popliteal, and Scalp nerve blocks
 one-time injection used primarily for intraoperative
anesthesia
 Continuous infusions of local anesthetics is
administered through peripheral nerve catheters
 Techniques like nerve stimulation, ultrasound
guidance, and paresthesia elicitation are used
Peripheral Regional Analgesia

 Paravertebral blocks
 Intercostal blocks
 Transversus abdominis plane blocks
 Interpleural (intrapleural) analgesia
 Cryoanalgesia
 Intra – articular analgesia
Nonepidural Analgesia

 Transcutaneous electrical nerve stimulation (TENS)
 Acupuncture
 Exercise/activity
 Psychological approaches
 All of these approaches to postoperative pain are
relatively safe, noninvasive, and devoid of the
systemic side effects seen with other analgesic
treatment options
Non – Pharmacological techniques


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Acute postoperative pain

  • 1. Moderator : Dr Alok Basu Roy Presenter: Dr Saurabh Kakkar
  • 2.   Postoperative pain, especially when poorly controlled, results in harmful acute effects and chronic effects  Widespread recognition of the under treatment of acute pain by clinicians, economists, and health policy experts has led to the development of a national clinical practice guideline for management of acute pain by a agency of U.S. Introduction
  • 3.  Anesthesiologists have developed the concept of acute postoperative pain services application of evidence based practice to acute postoperative pain, and creation of innovative approaches to acute pain medicine  Anesthesiologists functions as a “perioperative physician” consultant, and therapist throughout an institution, as well as a highly skilled expert in the operating room  Postoperative pain management should be tailored to the needs of special populations who may have different anatomic, physiologic, pharmacologic, or psychosocial issues
  • 4.  Surgery produces tissue injury with consequent release of histamine and inflammatory mediators  Release of inflammatory mediators activates peripheral nociceptors, which initiate transduction and transmission of nociceptive information to the central nervous system  Noxious stimuli are transduced by peripheral nociceptors and transmitted by A-delta and C nerve fibers from peripheral visceral and somatic sites to the dorsal horn of the spinal cord, where integration of peripheral nociceptive and descending modulatory input occurs Pain pathway
  • 5.  Some impulses pass to the ventral and ventrolateral horns to initiate segmental (spinal) reflex responses, which may be associated with increased skeletal muscle tone, inhibition of phrenic nerve function, or even decreased gastrointestinal motility  Others are transmitted to higher centers through the spinothalamic and spinoreticular tracts, where they induce supra segmental and cortical responses to ultimately produce the perception of and affective component of pain  Continuous release of inflammatory mediators causes Sensitization of peripheral nociceptors may occur and is marked by a decreased threshold for activation, increased rate of discharge with activation, and increased rate of basal discharge
  • 6.   Intense noxious input from the periphery may also result in central sensitization ( hypersensitivity) and hyperexcitability.  Nociception is a dynamic process (i.e., neuroplasticity) with multiple points of modulation.  Persistent noxious input may result in relatively rapid neuronal sensitization and possibly persistent pain  The intensity of acute postoperative pain is a significant predictor of chronic postoperative pain
  • 7.   Patient dis-satisfaction  Decreased Respiratory function  Myocardial ischemia  Sodium and water retention  Increased catabolic state  Postoperative hypercoagulable state  Immunosuppression  Poor wound healing  Prolonged paralytic ileus Acute effects of postoperative pain
  • 8.   Delayed recovery  Inability to participate in rehabilitation  Chronic postsurgical pain ( CPSP )  Financial expenses Chronic effects of postoperative pain
  • 9.   Previously called “ preemptive analgesia ”  It refers to an analgesic intervention that preceded a surgical injury and was more effective in relieving acute postoperative pain than the same treatment following surgery  The rationale for preemptive analgesia was based on the inhibition of the development of central sensitization  An intervention administered before the surgical incision is not preventative if it is incomplete or insufficient Preventive Analgesia
  • 10.  Principles of a multimodal strategy include:  Control of postoperative pain to allow early mobilization  early enteral nutrition  education, and attenuation of the perioperative stress response through the use of regional anesthetic techniques  combination of analgesic drugs (i.e., multimodal analgesia) The multimodal approach integrates the most recent data and techniques from surgery, anesthesiology, nociceptive neurobiology, and pain treatment, making it an extension of clinical pathways (Enhanced Recovery After Surgery, or ERAS) or fast tracks MULTIMODAL APPROACH TO PERIOPERATIVE RECOVERY
  • 11.   Systemic 1. Opioid analgesics 2. Non-opioid analgesics  Regional 1. Neuraxial techniques 2. Peripheral techniques Treatment Methods
  • 12.   Cornerstone for postoperative pain treatment  Opioids may be administered by the subcutaneous, transcutaneous, transmucosal, or intramuscular route, oral and intravenous  Prescribed on an as-needed (PRN) basis  Intravenous Patient-Controlled Analgesia (PCA) Opioids
  • 13.   PCA optimizes delivery of analgesic opioids and minimizes the effects of pharmacokinetic and pharmacodynamic variability in individual patients  When pain is experienced, analgesic medication is self-administered, and when pain is reduced  PCA device can be programmed for several variables, including the demand (bolus) dose, lockout interval, and background infusion Intravenous Patient-Controlled Analgesia
  • 14.
  • 15.   NSAID’S :  Inhibition of cyclooxygenase (COX) and synthesis of prostaglandins  COX-1 is constitutive and COX-2 is inducible  COX-1 participates in platelet aggregation, hemostasis, and gastric mucosal protection, whereas COX-2 participates in pain, inflammation, and fever  provide effective analgesia for mild to moderate pain  side effects include decreased hemostasis, renal dysfunction, and gastrointestinal hemorrhage  Diclofenac, Acetaminophen , Ketorolac Non - Opioids
  • 16.   Gabapentanoids  Gabapentin and pregabalin, antiepileptic drugs  used in the treatment of neuropathic pain  interact with calcium channel α2-δ ligands to inhibit calcium influx and subsequent release of excitatory neurotransmitters  meta-analysis demonstrated use of pregabalin was associated with a decrease in opioid consumption and opioid-related side effects, but no difference in pain intensity  perioperative administration of gabapentin and pregabalin may reduce the incidence of CPSP Non - Opioids
  • 17.   Ketamine  Traditionally recognized as an intraoperatively anesthetic induction agent  Small analgesic dose ketamine can facilitate postoperative analgesia because of its NMDA- antagonistic properties, which may be important in attenuating central sensitization and opioid tolerance  can be administered orally, intravenously, subcutaneously, or intramuscularly Non - Opioids
  • 18.
  • 19.   Single-Dose Neuraxial Opioids  Administration of a single dose of opioid may be efficacious as a sole or adjuvant analgesic drug when administered intrathecally or epidurally  One of the most important factors in determining the clinical pharmacology for a particular opioid is its degree of lipophilicity  Continuous Epidural Analgesia  Analgesia delivered through an indwelling epidural catheter is a safe and effective method for management of acute postoperative pain REGIONAL ANALGESIC TECHNIQUES
  • 20.
  • 21.  DRUG INTRATHECAL SINGLE DOSE EPIDURAL SINGLE DOSE EPIDURAL CONTINUOUS INFUSION FENTANYL 5 – 25 µg 50 – 100 µg 25 – 100 µg/hr MORPHINE 0.1 – 0.3 µg 1 – 5 µg 0.1 – 0.2 µg/hr REGIONAL ANALGESIC TECHNIQUES
  • 22.   Local anesthetics  Opioids  Local anesthetics + Opioids  Adjuvants – Clonidine , Ketamine , Dexmedtomidine Analgesic drugs for regional techniques
  • 23.
  • 24.   Hypotension  Motor block  Pruritus  Respiratory depression  Nausea and vomiting  Urinary retention  Migration of catheter Side Effects of Neuraxial Analgesic Drugs
  • 26.   Reduction in mortality and morbidity  Postoperative thoracic epidural analgesia can facilitate return of gastrointestinal motility without contributing to anastomotic bowel dehiscence  Preserving postoperative pulmonary function through providing superior analgesia and thus reducing splinting behavior and attenuating the spinal reflex inhibition of diaphragmatic function  Decreases the incidence of postoperative myocardial infarction by attenuating the stress response and hypercoagulability Benefits of Epidural Analgesia
  • 27.   Epidural hematoma  Epidural abscess  Infections like meningitis  Intrathecal or intravascular migration Risks With Epidural Analgesia
  • 28.   Analgesia superior to that with systemic opioids  Brachial plexus, Lumbar plexus, Femoral, Sciatic- popliteal, and Scalp nerve blocks  one-time injection used primarily for intraoperative anesthesia  Continuous infusions of local anesthetics is administered through peripheral nerve catheters  Techniques like nerve stimulation, ultrasound guidance, and paresthesia elicitation are used Peripheral Regional Analgesia
  • 29.   Paravertebral blocks  Intercostal blocks  Transversus abdominis plane blocks  Interpleural (intrapleural) analgesia  Cryoanalgesia  Intra – articular analgesia Nonepidural Analgesia
  • 30.   Transcutaneous electrical nerve stimulation (TENS)  Acupuncture  Exercise/activity  Psychological approaches  All of these approaches to postoperative pain are relatively safe, noninvasive, and devoid of the systemic side effects seen with other analgesic treatment options Non – Pharmacological techniques
  • 31.