Download Local anesthetics and additives

Survey
yes no Was this document useful for you?
   Thank you for your participation!

* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project

Document related concepts

Neuropharmacology wikipedia , lookup

Pharmacokinetics wikipedia , lookup

Psychopharmacology wikipedia , lookup

Pharmacognosy wikipedia , lookup

Bad Pharma wikipedia , lookup

Theralizumab wikipedia , lookup

Neuropsychopharmacology wikipedia , lookup

Dydrogesterone wikipedia , lookup

Bilastine wikipedia , lookup

Transcript
Should we mix local
anesthetics and additives?
Matthias Desmet MD
az│groeninge
ESRA Winterweek 2017
Why would we use additives?
• Benefit of sISB up to 6 hours with motion and up to 8 hours in rest.
• No benefits after 8 hours.
• More pain between 16 and 24 hours.
• Similar pain after 24 hours.
Abdallah et al. Anesth and Analg 2015
Bingham et al. RAPM 2012
Additives?
Additives?
• Dexamethasone
• Dexmedetomidine
Dexamethasone
Long acting, potent glucocorticoid.
Henzi, Anesth Analg 2000
Waldron, BJA 2013
Dexmedetomidine?
Abdallah et al. BJA 2013
Mechanism of action?
Ideal route of administration?
Yimaz et al. RAPM 2012
Buvanendran et al. RAPM 2016
Desmet et al. BJA 2013
Rahangdale et al. Anesth and Analg 2014
Fredrickson et al. RAPM 2013
Dawson et al. Anaesth 2015
Rosenfeld et al Anaesth 2016
Abdallah et al. RAPM 2015
Alternatives for perineural DXM?
• 5 studies (n= 509) showed no difference.
• 2 studies (n = 188) in favour of perineural DXM.
• Where is the meta-analysis when you need it…
If there is any difference, the clinical impact is probably small…
Jaeger P et al. BJA 2016
“Importantly, the physician is free to use any drug for
off-label indications as long as the use is based on
sound clinical judgment and reasonable scientific
rationale.”
Neal J et al. RAPM 2009
Safety of IV DXM?
• Isolated sensory neurons of rats. (n = 16)
• Exposure to different combo’s of LA and additives.
• Measure cell death.
Williams BA et al RAPM 2011
High dose DXM
In vivo evaluation of Bupi/MDZ/Clonidine/Buprenorphine/DXM.
Results:
1) No neurobehavioural changes.
2) No changes in the sciatic nerve, DRG or dorsal and ventral
nerve roots.
Williams et al Pain Medicine 2015
• “No histopathological changes”
• Changes were caused by:
1. Local manipulation/trauma/injection.
2. Tissue handling and manipulation.
3. Isolated/suspected spontaneous changes with no
relationship to the study drug.
Williams B et al, Pain Medicine 2015
What about intraneural DXM?
Superiority of perineural DXM?
Ma et al. Neuroscience 2010
Superiority of perineural DXM?
An et al. PLOS ONE 2015
Mechanism of action: dexmedetomidine
• Limited evidence for local vasoconstrictor effect.
• No evidence for α receptor mediated effect.
• Evidence for inhibition of the Ih- current.
Nishikawa et al. Anesthesiol 1990
Kopacz et al. Anesthesiol 2001
Kroin et al. Anesthesiol 2004
Brummett C et al. Anesthesiol 2011
Brummett et al.
Anesthesiol 2011
240 min
150 min
Brummett et al. RAPM 2010
Andersen et al. Anesthesiology 2017
Abdallah et al. Anesthesiol 2015
Safety of dexmedetomidine?
• Longstanding experience with clonidine.
• No clinical reports on dexmedetomidine for peripheral nerve blocks.
• Little evidence for a neurotoxic potential.
Zhang et al. PLOS one 2013
Very high doses of DEX (28-40µg/kg)
did not cause perineural inflammation.
Less perineural inflammation in the
DEX-BUPI group than in BUPI group.
Take home message
Perineural administration of DXM should not be
preferred based on current literature.
Perineural administration of DEX seems
reasonable based on current literature.