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Acute Pain after Surgery:
Lessons Learned from the Last Decade
Stephan A Schug
Anaesthesiology & Pain Medicine
University of Western Australia
Royal Perth Hospital
Disclosure
The Anaesthesiology Unit of the University of
Western Australia, but not Professor Schug
personally, has received research and travel funding
and speaking and consulting honoraria from Eli Lilly,
bioCSL/Seqirus, Grunenthal, Indivior, Janssen,
Mundipharma, Pfizer, Phosphagenics and
iXBiopharma within the last 5 years.
http://www.iasp-pain.org/GlobalYear
http://fpm.anzca.edu.au/
Resources/Publications
APM:SE 4th edition
Endnote library: 8,598 references
Pages: 647
Key Messages: 669
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZA
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZA
Opioids – the Good
 Opioids are very effective analgesics
 Opioids are necessary to provide pain relief in many
situations linked to severe pain:
– postoperative
– after severe trauma
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZA
Opioids – the Bad
 Opioids are often associated with adverse events including:
– Opioid-Induced Ventilatory Impairment
– Nausea and vomiting
– Constipation
– Urinary retention
– Sedation
– Confusion or agitation
– Rash, itching, hives
– Opioid-Induced Hyperalgesia
Opioid-related AEs increase length of stay and costs
Oderda GM, et al. J Pain Symptom Manage. 2003;25:276-83. TJ et al. Anesth Analg. 2004;98:1665-73.
What Can We Do About
Adverse Effects of Postoperative Opioids?
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Acute Pain Management:
Scientific Evidence 4th edition 2015
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Effects of Parecoxib/Valdecoxib with PCA
Morphine in Laparoscopic Cholecystectomy
Gan TJ, et al. Acta Anaesthesiol Scand 2004;48:1194
Risk of
1 CME*
p<0.01 for all results
*Clinically meaningful events caused by opioid symptom distress
–29.2%
–32.7% –34.4%
–31.0%
0
–5
–10
–15
–20
–25
–30
–35
Opioid
dose
Mean brief
pain inventory
severity
Opioid
symptom
distress score
Change(%)
12
American Pain Society,
American Society of Regional Anesthesia and Pain Medicine,
and the American Society of Anesthesiologists
“The panel recommends that clinicians
offer multimodal analgesia,
or the use of a variety of analgesic
medications and techniques combined
with nonpharmacological interventions,
for the treatment of postoperative pain
in children and adults
(strong recommendation, high-quality
evidence).”
Note: Exact components of effective multimodal care will vary depending on the
patient, setting, and surgical procedure.
Chou R, et al. J Pain. 2016;17:131-57.
Multimodal Analgesia
Adapted from Julius D, Basbaum A. Nature
2001;413:203-10.
Peripheral and Central Sensitisation
Leads to Pain Amplification
Normal
pain response
Sensitised
pain response
Injury
X
HYPERALGESIA
Stimulus intensity
Pain intensity
for stimulus X
normal pain
response
Pain intensity
for stimulus X
sensitised
pain response
ALLODYNIA
Painintensity
10
8
6
4
2
0
14Adapted from: Gottschalk A, Smith DS. Am Fam Physician. 2001;63:1979-84.
Anti-hyperalgesic Therapy:
Opioid-Sparing
~30%
reduction
Opioid
Opioid
Painintensity
10
8
6
4
2
0
X
Stimulus intensity
Anti-
hyper
algesic
Normal
pain
response
Sensitised
pain response
Partially desensitised
pain response
15
Adapted from: Gottschalk A, Smith DS. Am Fam Physician. 2001;63:1979-84.
Zhao et al, J Pain Symp Manag 2004;28:35
Scientific Evidence:
Multimodal Analgesia*
 There is Level I evidence for the effectiveness of the following
components of multimodal analgesia:
– Regional anaesthesia (peripheral and epidural)
– Paracetamol
– NSAIDs/Coxibs
– Alpha-2-Delta Ligands
– Systemic Local Anaesthetics (lignocaine)
– NMDA Receptor antagonists (ketamine, magnesium)
– Alpha-2 Agonists (clonidine/dexmedetomidine)
– [Corticosteroids (dexamethasone)]
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Practical Conclusions:
Multimodal Analgesia*
 Regional anaesthesia techniques should be used whenever possible
 In practical terms current routine use for systemic analgesia should
include:
– Paracetamol
– COX-2 inhibitors/nsNSAIDs (if no renal contraindications)
– Alpha-2-Delta Agonists (single preoperative dose)
 In selected patients
– Low-dose ketamine (opioid tolerant, neuropathic pain)
– Systemic local anaesthetics (bowel surgery?)
– Alpha-2 agonists (agitation? withdrawal?)
17Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Chronification of Pain
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Chronification of Pain
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Acute Pain Management:
Scientific Evidence 4th edition 2015
22.Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
Procedure Specific Postoperative Pain Management (PROSPECT). Available from: http://www.postoppain.org. Accessed June 2017.
Procedure Specific Postoperative Pain Management (PROSPECT). Available from: http://www.postoppain.org. Accessed June 2017.
Procedure Specific Postoperative Pain Management (PROSPECT). Available from: http://www.postoppain.org. Accessed June 2017.
 Initiate multimodal analgesic techniques
– Minimise use of opioids
– Maximise use of non-opioid agents
– Use regional anaesthesia whenever possible
• Superior to opioids, especially in orthopaedic
patients
 Use evidence-based, procedure-specific pain management
guidelines where available
– http://fpm.anzca.edu.au/Resources/Publications
– http://www.jpain.org/article/S1526-5900(15)00995-5/pdf
– http://www.postoppain.org
Conclusions
26

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Acute pain after surgery - lessons learned from the last decade - Stephan Schug - SSAI2017

  • 1. Acute Pain after Surgery: Lessons Learned from the Last Decade Stephan A Schug Anaesthesiology & Pain Medicine University of Western Australia Royal Perth Hospital
  • 2. Disclosure The Anaesthesiology Unit of the University of Western Australia, but not Professor Schug personally, has received research and travel funding and speaking and consulting honoraria from Eli Lilly, bioCSL/Seqirus, Grunenthal, Indivior, Janssen, Mundipharma, Pfizer, Phosphagenics and iXBiopharma within the last 5 years.
  • 5. APM:SE 4th edition Endnote library: 8,598 references Pages: 647 Key Messages: 669 Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZA
  • 6. Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZA
  • 7. Opioids – the Good  Opioids are very effective analgesics  Opioids are necessary to provide pain relief in many situations linked to severe pain: – postoperative – after severe trauma Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZA
  • 8. Opioids – the Bad  Opioids are often associated with adverse events including: – Opioid-Induced Ventilatory Impairment – Nausea and vomiting – Constipation – Urinary retention – Sedation – Confusion or agitation – Rash, itching, hives – Opioid-Induced Hyperalgesia Opioid-related AEs increase length of stay and costs Oderda GM, et al. J Pain Symptom Manage. 2003;25:276-83. TJ et al. Anesth Analg. 2004;98:1665-73.
  • 9. What Can We Do About Adverse Effects of Postoperative Opioids? Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 10. Acute Pain Management: Scientific Evidence 4th edition 2015 Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 11. Effects of Parecoxib/Valdecoxib with PCA Morphine in Laparoscopic Cholecystectomy Gan TJ, et al. Acta Anaesthesiol Scand 2004;48:1194 Risk of 1 CME* p<0.01 for all results *Clinically meaningful events caused by opioid symptom distress –29.2% –32.7% –34.4% –31.0% 0 –5 –10 –15 –20 –25 –30 –35 Opioid dose Mean brief pain inventory severity Opioid symptom distress score Change(%)
  • 12. 12 American Pain Society, American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists “The panel recommends that clinicians offer multimodal analgesia, or the use of a variety of analgesic medications and techniques combined with nonpharmacological interventions, for the treatment of postoperative pain in children and adults (strong recommendation, high-quality evidence).” Note: Exact components of effective multimodal care will vary depending on the patient, setting, and surgical procedure. Chou R, et al. J Pain. 2016;17:131-57.
  • 13. Multimodal Analgesia Adapted from Julius D, Basbaum A. Nature 2001;413:203-10.
  • 14. Peripheral and Central Sensitisation Leads to Pain Amplification Normal pain response Sensitised pain response Injury X HYPERALGESIA Stimulus intensity Pain intensity for stimulus X normal pain response Pain intensity for stimulus X sensitised pain response ALLODYNIA Painintensity 10 8 6 4 2 0 14Adapted from: Gottschalk A, Smith DS. Am Fam Physician. 2001;63:1979-84.
  • 15. Anti-hyperalgesic Therapy: Opioid-Sparing ~30% reduction Opioid Opioid Painintensity 10 8 6 4 2 0 X Stimulus intensity Anti- hyper algesic Normal pain response Sensitised pain response Partially desensitised pain response 15 Adapted from: Gottschalk A, Smith DS. Am Fam Physician. 2001;63:1979-84. Zhao et al, J Pain Symp Manag 2004;28:35
  • 16. Scientific Evidence: Multimodal Analgesia*  There is Level I evidence for the effectiveness of the following components of multimodal analgesia: – Regional anaesthesia (peripheral and epidural) – Paracetamol – NSAIDs/Coxibs – Alpha-2-Delta Ligands – Systemic Local Anaesthetics (lignocaine) – NMDA Receptor antagonists (ketamine, magnesium) – Alpha-2 Agonists (clonidine/dexmedetomidine) – [Corticosteroids (dexamethasone)] Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 17. Practical Conclusions: Multimodal Analgesia*  Regional anaesthesia techniques should be used whenever possible  In practical terms current routine use for systemic analgesia should include: – Paracetamol – COX-2 inhibitors/nsNSAIDs (if no renal contraindications) – Alpha-2-Delta Agonists (single preoperative dose)  In selected patients – Low-dose ketamine (opioid tolerant, neuropathic pain) – Systemic local anaesthetics (bowel surgery?) – Alpha-2 agonists (agitation? withdrawal?) 17Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 18. Chronification of Pain Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 19. Chronification of Pain Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 20. Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 21.
  • 22. Acute Pain Management: Scientific Evidence 4th edition 2015 22.Schug et al. Acute Pain Management: Scientific Evidence 4th edition ANZCA&FPMANZCA
  • 23. Procedure Specific Postoperative Pain Management (PROSPECT). Available from: http://www.postoppain.org. Accessed June 2017.
  • 24. Procedure Specific Postoperative Pain Management (PROSPECT). Available from: http://www.postoppain.org. Accessed June 2017.
  • 25. Procedure Specific Postoperative Pain Management (PROSPECT). Available from: http://www.postoppain.org. Accessed June 2017.
  • 26.  Initiate multimodal analgesic techniques – Minimise use of opioids – Maximise use of non-opioid agents – Use regional anaesthesia whenever possible • Superior to opioids, especially in orthopaedic patients  Use evidence-based, procedure-specific pain management guidelines where available – http://fpm.anzca.edu.au/Resources/Publications – http://www.jpain.org/article/S1526-5900(15)00995-5/pdf – http://www.postoppain.org Conclusions 26