Veterinary Anesthesia Severna Park Veterinary Hospital Aug. 6, 2014

Post on 09-Feb-2016

46 views 1 download

description

Veterinary Anesthesia Severna Park Veterinary Hospital Aug. 6, 2014. Rebecca Krimins, DVM, MS Advanced Anesthesia and Pain Management for Animals. Topics. Anesthetic drugs Pre-anesthetic combinations Monitoring a nesthetic depth. Ketamine. - PowerPoint PPT Presentation

Transcript of Veterinary Anesthesia Severna Park Veterinary Hospital Aug. 6, 2014

Veterinary AnesthesiaSeverna Park Veterinary Hospital

Aug. 6, 2014

Rebecca Krimins, DVM, MSAdvanced Anesthesia and Pain

Management for Animals

Topics

• Anesthetic drugs• Pre-anesthetic combinations• Monitoring anesthetic depth

Ketamine

• Dissociative: dissociate the thalamocortic and limbic systemscataleptoid state (eyes open, swallow reflex intact)

• Muscle rigidity• Decreases cardiac contractility• Increase peripheral vascular resistance

decreases cardiac output

Ketamine

• NMDA-antagonistic properties (blocks glutamate)

• Helpful with superficial pain, not useful for deep or chronic pain (poor visceral analgesia)

• Helps prevent sensitization (windup) of nociceptive pathways

Ketamine

• Rapid onset (~ 5 minutes)• Moderate DOA (1-2 hours)• Stimulate sympathetic tone increased HR and BP• Induce salivation and airway secretions• Pain upon IM injection (low pH)• Some dogs show emergence delirium

(uncoordinated movements of head/neck, voacalizations, salivation, agitation)

Ketamine Pre-anesthetic Dosage

• Dogs: 1-3 mg/kg IV, IM, SQ• Cats: 3-10 mg/kg IV, IM, SQ

Ketamine

• CRI dosage for intra-op pain:– 0.5 mg/kg IV bolus– 10 ug/kg/min CRI (lower doses for post-op)

• Apnea in some (but generally is NOT a respiratory depressant)

• Don’t administer with an anticholinergic• Associated with premature ventricular

depolarizations

Tiletamine

• Dissociative• More potent than ketamine (3X), longer DOA• Produces sedation, immobility, amnesia,

analgesia, muscle rigidity• (Zolazepam: similar to diazepam but is water

soluble and more potent; can cause prolonged recovery in cats)

Ketamine/valium andTiletamine/zolazepam

• Different neuroactive agents usedinduce anesthesia with the goal of achieving the highest quality of anesthesia with minimal side effects

• Ketamine/valium– Ketamine 5 mg/kg IV– Diazepam 0.25 mg/kg IV

• Tiletamine/zolazepam: (2-8 mg/kg IV, IM)– DOA: 20 min to one hour– Limited shelf-life after reconstitution– Induction: 1-3 mg/kg IV or 6-8 mg/kg IM

Telazol Difference in Dogs vs Cats

• Dogs: get a tiletamine hangover• Cats: get a zolazepam hangover

Ket/Val (or Telazol) vs Propofol

• Compared to propofol:– Less muscle relaxation– Increased salivation– Increased dysphoria

• Good cardiopulmonary support– HR, CO, BP well maintained

• Short duration

Propofol

• 2,6,-diisopropylphenol• Propofol: soybean oil, glycerol, egg

phosphatide • Propoflo-28: benzyl alcohol• White emulsion: shake thoroughly (don’t mix

with other drugs)• Metabolized by liver, extrahepatic sites of

metabolism

Propofol

• Induction dose: 4-8 mg/kg IV• Microdose under GA: 1-2 mg/kg IV• Titrate to effect• Duration of action: 10-20 minutes• Advantages: rapid induction of GA, rapid

metabolism, rapid emergence from GA, low incidence of nausea/vomiting

Propofol

• Disadvantages– Hypotension and cardiac depression– Respiratory depression– Pain on injection– Heinz body anemia in cats (repeated use)

Dexmedetomidine

• α-2 adrenergic agonist• Properties: sedative-hypnotic, analgesic, muscle

relaxation– Anxiolysis, calming

• Stimulate α2 receptors in braindecreased norepinephrine release

• Dose-dependent CV effects: vasoconstrictionhypertensionreflex bradycardia

Dexmedetomidine

• Dosage: dependent on patient and procedure– IM: 5 ug/kg– IV: 1-2 ug/kg

• Rapid onset (~ 5 minutes)• Moderate duration (~2 hours)• Atipamezole (reversal): – Give same volume as dexmedetomidine IM, SQ, IV

Hydromorphone and Morphine

• Pure mu opioids; excellent analgesics• Both drugs can cause excitement when used

alone, in young, healthy animals• Both drugs will slow heart rate (increased

vagal efferent activity) and cause respiratory depression

• Profound sparing effect with induction and maintenance agents

Hydromorphone vs Morphine• Hydromorphone:

– SQ route associated with vomiting & panting– Doses > 0.1 mg/kg may produce hyperthermia– DOA: 1-4 hours

• Morphine:– Can cause vomiting– Associated with histamine release– Excitement in cats– Metabolites excreted by the kidneys– DOA: 2-4 hours

• Pupil size: miosis and mydriasis– Miosis (dogs)– Mydriasis (cats)

Hydromorphone and Morphine

• Hydromorphone dosages (SQ, IM, IV)– SQ: 0.1 mg/kg (DOA: 1-4 hours)– IV: 0.05 mg/kg (DOA: 1-2 hours)

• Morphine (SQ, IM, IV)– IM: 0.2-0.6 mg/kg– IV: 0.1-0.5 mg/kg

• Naloxone (reversal) 1-10 ug/kg IV– Take 1 ml naloxone, dilute with 9ml saline, titrate 1

ml/min to effect

Pre-anesthetic Combinations

• Think about: – Procedure: surgical vs diagnostic vs other– Level of pain involved in procedure– Duration of procedure– Patient status– How much time do you have

Pre-anesthetic Combinations

• Opioid• +/- benzodiazepine• +/- α2- agonist• +/- phenothiazine• +/- anticholinergic

How to Monitor Anesthetic Depth

• No single parameter tells you how light/deep– Gather all information together (patient, normals,

disease states, drugs, procedure type and duration)

• Must know parameter normals in order to be able to identify abnormals– Temp, pulse, RR, BP– SBP > 140 mmHg = light– SBP < 80 mmHg = deep

How to Monitor Anesthetic Depth

• Interact with patient• Every 5 minutes, check palpebral reflex

(corneal reflex) and jaw tone; position of eye; check for signs of movement, muscle twitching, neck tone

• Maintain body temperature• Vaporizer setting for past 15 minutes = ?

Questions

Email: drkrimins@gmail.com

Advanced Anesthesia and Pain Managementfor Animals

www.aapma.com