regional anesthesia pharmacology and therapeutics

19
Regional Anesthesia Pharmacology and Therapeutics Edwin Perez, MD, BS, High School Director-Acute Pain Newark Beth Israel (not the one in New York :(

Upload: dr-edwin-perez

Post on 08-Jan-2017

299 views

Category:

Health & Medicine


0 download

TRANSCRIPT

Page 1: Regional Anesthesia Pharmacology and Therapeutics

Regional Anesthesia Pharmacology and

TherapeuticsEdwin Perez, MD, BS, High School

Director-Acute PainNewark Beth Israel

(not the one in New York :(

Page 2: Regional Anesthesia Pharmacology and Therapeutics

Objectives

Types-Amides vs EstersSpread of LocalPharmacokineticsUse of VasoconstrictorsToxicity

Page 3: Regional Anesthesia Pharmacology and Therapeutics

Objectives

key points about all blocks in generalwhen to use themrisks/benefitsultrasound versus landmark/stim techniqueLAST

Page 4: Regional Anesthesia Pharmacology and Therapeutics

Amides And Esters

All local Anesthetics (LA) have a hydrocarbon chain connected to a lipophilic portion. This is done by either an ester (-CO-) bond or amine (-HNC-) bond. amides are metabolized in liveresters are metabolized in plasma by

pseudocholinesterase

Page 5: Regional Anesthesia Pharmacology and Therapeutics

Rule of iEsters AmIdesprocaine lIdocainechloroprocaine bupIvacainetetracaine mepIvacainecocaine ropIvacaine

Page 6: Regional Anesthesia Pharmacology and Therapeutics

Do you have any allergies?

Extremely unlikely-1% of ADR are caused by Local anestheticsMost likely seeing systemic toxicityesters are the culprit more than amides-think PABAwhen linked to amides usually due to preservative-methylparaben

Page 7: Regional Anesthesia Pharmacology and Therapeutics

Max single-shot doseEsters-

procaine-1000mg in 70kg malechloroprocaine-800mg in 70kg male 1000mg in 70kg male w/epi

tetracaine-20mg in 70kg maleAmides

Lidocaine- 3 or 5mg/kg depending on epiBupivacaine/Ropivacaine 3mg/kg

Page 8: Regional Anesthesia Pharmacology and Therapeutics

Spread (rules are different for peripheral)

Page 9: Regional Anesthesia Pharmacology and Therapeutics

Pharmacology 101:its gotta get inside

LA bind to sodium channels on the inside of the channel

They also obstruct the outsidemaintains them in inactivated-closed state

Page 10: Regional Anesthesia Pharmacology and Therapeutics

Pharmacokinetics

pKa of local anesthetics makes them such that only 0.5% is already in a nonionized form.It must be nonionized to cross (abscess)Intrinsic vasodilator-lidocaineesters safer except in pseudocholinesterase deficiency

Page 11: Regional Anesthesia Pharmacology and Therapeutics

Toxicity

1) #1 casue is accidental intravascular placement

2) Then from absorptionintercostal>caudal>epidural> sciatic

Page 12: Regional Anesthesia Pharmacology and Therapeutics

CNSScale of effects

A) AnalgesiaB) Lightheadedness, tinnitus, numb tongueC) SeizuresD) ComaE) Then cardiovascular depression

Page 13: Regional Anesthesia Pharmacology and Therapeutics

Cardiac

Hypotensionincreased P-R and wide QRSarrythmiabupivacaine is fast in/slow out

Page 14: Regional Anesthesia Pharmacology and Therapeutics

Other effectsTRICauda equina syndrome

Page 15: Regional Anesthesia Pharmacology and Therapeutics

Why BlocksSignificant improvement in analgesia

Significant improvement in patient satisfaction

Sometimes decreased LOS

Decreased opioid requirements by 50% or more

Page 16: Regional Anesthesia Pharmacology and Therapeutics

BlocksChronic vs Acute Pain Blocks (diag vs ther)contraindicationsperipheral blocks only work on peripheryblock effect timesnerve sparing and the compartment syndrome situationadjuvant therapy (fem/sciatic controversy)how long do blocks actually last

Page 17: Regional Anesthesia Pharmacology and Therapeutics

LAST Rectus Sheath Block

Page 18: Regional Anesthesia Pharmacology and Therapeutics

Checklist for Treatment of Local Anesthetic Systemic Toxicity

The Pharmacologic Treatment of Local Anesthetic Systemic Toxicity (LAST) is Different from Other Cardiac Arrest Scenarios❑ Get Help ❑ Initial Focus❑ Airway management: ventilate with 100% oxygen ❑ Seizures uppression: benzodiazepines are preferred; AVOID propofolin patients having signs of cardiovascular instability ❑ Alert the nearest facility having cardiopulmonary bypass capability❑ Management of Cardiac Arrhythmias ❑ Basic and Advanced Cardiac Life Support (ACLS) will requireadjustment of medications and perhaps prolonged effort❑ AVOID vasopressin, calcium channel blockers, beta blockers, or local anesthetic❑ REDUCE individual epinephrine doses to <1 mcg/kg ❑ Lipid Emulsion (20%) Therapy (values in parenthesis are for 70kg patient)❑ Bolus 1.5 mL/kg (lean body mass) intravenously over 1 minute (~100mL)❑ Continuous infusion 0.25 mL/kg/min (~18 mL/min; adjust by roller clamp)❑ Repeat bolus once or twice for persistent cardiovascular collapse❑ Double the infusion rate to 0.5 mL/kg/min if blood pressure remains low❑ Continue infusion for at least10 minutes after attaining circulatory stability❑ Recommended upper limit: Approximately 10 mL/kg lipid emulsion over the first 30 minutes❑ Post LAST events at www.lipidrescue.org and report use of lipid to www.lipidregistry.org

Page 19: Regional Anesthesia Pharmacology and Therapeutics

BibliographyDang, Charles;The value of adding sciatic block to continuous femoral block for analgesia after total knee replacement; Regional Anesthesia and Pain Medicine; Volume 30, Issue 2, March–April 2005, Pages 128–133

Benzon, Honorio, Essentials of Pain Medicine and Regional Anesthesia, 2005

Neal, Joseph;ASRA Practice Advisory on Local Anesthetic Systemic Toxicity; Regional Anesthesia & Pain Medicine; March/April 2010; Vol 35 Issue 2; pp152-161

Stoelting, Robert; Basics of Anesthesia; 2000