A New Advancement in Anesthesia. Your clear choice for induction.

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Transcription:

A New Advancement in Anesthesia Your clear choice for induction.

By Kirby Pasloske

When using Alfaxan, patients should be continuously monitored, and facilities for maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available.

Structure O O O Me H Me H Me Me H H H H H HO H Alfaxalone 3- -hydroxy-5- -pregnane-11,20-dione H H O Progesterone 3- -one-pregnane-20-one SMART SAFE VERSATILE PROVEN

The Formulation + + Buffers to ph 7 + Water For Injection = Cyclodextrin Clear, iso-osmolar with the viscosity of water 10 mg ml -1 SMART SAFE VERSATILE PROVEN

Dopamine Glutamate GABA Catecholamines Glycine Serotonin

SMART SAFE VERSATILE PROVEN

When using Alfaxan, patients should be continuously monitored, and facilities for maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available.

Safety Data Type of Study Acute Overdose Margin of Safety Dose multiple of 1X (2 mg/kg) Up to 10X* (20 mg/kg) Up to 5X^ (10 mg/kg) Number of Doses 1 3 over 1 week Type of Study Acute Overdose Margin of Safety Dose multiple of 1X (5 mg/kg) Up to 5X* (25 mg/kg) Up to 5X^ (25 mg/kg) Number of Doses 1 3 over 1 week *some animals required IPPV with room air ^no observable toxicity in blood, tissue and cellular level

Metabolism and Clearance Species Half life (min) Clearance (ml kg -1 min -1 )* 34 60 43 35 *Cardiac Output (HR X SV) = 116 and 146 ml kg -1 min -1 in dog and cat, respectively

No Accumulation CRI - Dog 100 Start Infusion End Infusion Plasma conc. (mg/l) 10 1 Alfaxalone P<0.05 0.1 Alfaxan Infusion rate = 0.07 mg/kg/min 0 20 40 60 80 100 120 140 Time (min)

No Accumulation Repeat Dose Loading Dose @ 5 mg/kg 10 Repeat dose @ 2 mg/kg Alfaxalone Plasma conc. (mg/l) 1 Last Dose P<0.05 0.1 0 30 60 90 120 150 Time (minutes)

Drug Interaction Study Drug Class Anticholinergics Benzodiazepines Opioid pure agonist Opioid mixed agonist/antagonists Example Drug(s) atropine, glycopyrrolate midazolam, diazepam morphine, methadone, hydromorphone, fentanyl butorphanol, buprenorphine Phenothiazines acepromazine Alpha 2 adrenergic agonists medetomidine, dexmedetomidine

Blood Pressure Effect

Respiratory Rate Effect

Accidental Overdose! Cat recovered and sent home next day

When using Alfaxan, patients should be continuously monitored, and facilities for maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available.

Dose Administration When first using Alfaxan, draw up the full dose Divide the dose into 4 equal volumes ¼ dose q 15 seconds and patient chooses the dose Dogs Healthy, Not premedicated* 2 mg/kg Alfaxan administered IV Cats Healthy, Not premedicated* 5 mg/kg Alfaxan administered IV Premedication may alter the dose requirement of Alfaxan Anesthesia can be prolonged by further administration

Duration of Anesthesia 2 mg/kg (1X) IV will produce approximately 5-10 min of anaesthesia (unpremedicated and undisturbed) 5 mg/kg (1X) IV will produce approximately 15-30 min of anaesthesia (unpremedicated and undisturbed)

Anesthetic Potency and Volume Drug Approximate Dose (mg/kg) Potency Approximate Duration of Effect (min) Concentration (mg/ml) Volume IV* (ml) Thiopental 15 10 25 6 Propofol 6 5 10 6 Alfaxalone 2 5 10 2 Etomidate 2 10 2 10 Ketamine + diazepam Tiletamine +zolazepam 10/0.5 15 100/5 2 (1+1) 5/5 (10) 30 50/50 (100) 1 *Dose based on a 10 kg dog

Alfaxan Induction

Recovery from Alfaxan

Versatility That Fits Your Patients Alfaxan is your clear choice for induction in ALL of your patients

Co-Morbidities Co Morbidity Type What s the problem? Author and Forum Okay Elderly Patient Less physiological reserve Lukasik, V (WVC, 2016) Obesity CV, Pulmonary, Type II Diabetes etc. Lukasik, V (WVC, 2016) Liver Disease Metabolism altered Strunin, 1977 (humans) Kidney Disease Clearance decreased Sear JW, 1979 (humans) Lukasik (WVC, 2016) Cardiac Disease (valvular and hypertrophic) Cardiac output, automaticity and perfusion Caulkett, N (IVECCS, 2016) Mama, K (Clinician s Brief, AUG 2016) Diabetes Glucose metabolism Lukasik, V (WVC, 2016) Munoz, K (AVA, Sep, 2016) Status Epilepticus Functional disruption of neuronal APs Gianotti, G (personal communication)

Multiple Attributes Approved for both cats and dogs Compatible with all premedicant drugs Rapid and smooth Induction Excellent muscle relaxation No pain upon injection No tissue irritation Minimal disruption to cardiovascular & pulmonary function Approved for induction and maintenance of anesthesia Wide margin of safety Rapid elimination from the body Safe, consecutive day administration

When using Alfaxan, patients should be continuously monitored, and facilities for maintenance of a patent airway, artificial ventilation, and oxygen supplementation must be immediately available.

Proven Over 15 Years In Market Alfaxan was first manufactured and launched by Jurox in Australia and New Zealand in 2001

Family-owned global animal health company Who is? Dr. John O Brien & Family Veterinary-exclusive products Over 120 small & large animal health products Shipping to over 30 countries FDA compliant manufacturing plant for cgmp Kirby s Office

Proven & Approved for Cats and Dogs Registered in multiple countries & administered to millions of cats and dogs globally. Approved by the VDD, commercially available since 2011. All Alfaxan is manufactured at the same site in Australia

Hospital Support On demand or live Webinar with a Jurox Veterinarian (me) http://www2.jurox.com/alfaxanwebinar http://www2.jurox.com/alfaxanshort http://www2.jurox.com/alfaxanlong http://www2.jurox.com/ca/alfaxan-resource-guide.pdf www.alfaxan.com Timely responses to technical questions and or adverse events kirby.pasloske@jurox.com Customer Service through Central Sales (1-800-387-2522) Pacific Veterinary Sales (1-800-663-6966)

A New Advancement in Anesthesia Your clear choice for induction.