Anesthestic Agents & Adjuncts_Preanesthestics_NN
Anesthetic Agents and Adjuncts
Preanesthetics
Purpose of preanesthetics: Prepare the animal for anesthesia, ensuring a smoother induction and recovery process.
Neuroleptanalgesia
Definition: A profound state of sedation and analgesia induced by simultaneous administration of an opioid and a tranquilizer.
Opioids:
Morphine
Buprenorphine
Butorphanol
Hydromorphone
Tranquilizers:
Acepromazine
Diazepam
Midazolam
Xylazine
Dexmedetomidine
Use of Neuroleptanalgesics
Sedation for minor procedures.
Induction of general anesthesia, particularly in dogs.
Not recommended for young, healthy dogs and cats.
Preanesthetic Medications
Objectives:
Calm or sedate an excited animal.
Minimize adverse drug effects.
Reduce the dose of concurrent drugs.
Ensure smoother anesthetic induction and recovery.
Provide analgesia and muscle relaxation.
Route of Administration for Preanesthetic Medications
Affects onset of action and duration of effects:
Subcutaneous (SC): Slowest onset, longest duration.
Intramuscular (IM): Faster onset, shorter duration.
Intravenous (IV): Fastest onset, shortest duration.
Preanesthetic Anticholinergics
Definition: Parasympatholytic drugs that block acetylcholine.
Functions:
Prevent and treat bradycardia.
Decrease salivary secretions.
Common Agents:
Atropine (fast onset, short peak, short duration).
Glycopyrrolate (slower onset, longer peak, longer duration).
Anticholinergic Effects
CNS: Limited effect.
Cardiovascular: Prevents bradycardia.
Secretions: Decreases production.
Eyes: Causes mydriasis and corneal drying.
Respiratory: Bronchodilation.
Adverse Effects of Anticholinergics
Cardiac arrhythmia; contraindicated in animals with elevated heart rates or cardiac diseases.
Temporary bradycardia (Atropine).
Thickened respiratory and salivary secretions; may lead to airway blockage.
Inhibition of intestinal peristalsis; may lead to colic in horses or bloat in ruminants.
Tranquilizers and Sedatives
Main categories include:
Phenothiazines
Benzodiazepines
Alpha2-adrenoceptor agonists
Alpha2-antagonists.
Phenothiazines: Acepromazine Maleate
Also known as acepromazine or "ace".
Used for preanesthetic sedation; decreases the necessary dose of general anesthetic.
Facilitates induction and recovery; can combine with opioids.
Approved for use in horses, dogs, and cats; administered IV or IM.
No reversal agent available; metabolized by the liver; crosses the placenta slowly.
Effects of Acepromazine
CNS: Calming, reluctance to move; less pronounced sedation in cats.
Cardiovascular: Peripheral vasodilation, leading to hypotension, increased heart rate, and hypothermia.
Respiratory: Worsens the depressive effect of other drugs.
Gastrointestinal: Antiemetic effect and decreases allergic response.
Adverse Effects of Acepromazine
CNS: Reduced seizure threshold, potential for aggression or excitement.
Cardiovascular: Dose-dependent hypotension and penile prolapse in large animals.
Hematologic: Decreased packed cell volume (PCV) possibly from splenic engorgement.
Precaution: Avoid in animals undergoing allergy testing.
Special Considerations for Acepromazine
Adjust dose based on needle placement.
Increased potency and duration in geriatrics, neonates, and debilitated animals.
Breed considerations: caution particularly in Australian Shepherds, Boxers, Greyhounds, and Terriers.
Benzodiazepines
Controlled substances with rapid onset and short duration. Common benzodiazepines include:
Diazepam
Zolazepam
Midazolam.
Effects of Benzodiazepines
CNS: Effective calming and anticlimactic only in old or ill patients; minimal sedation or analgesia.
Anticonvulsant effect: Useful for animals having seizures.
Cardiovascular and respiratory safety: High margin of safety; minimal effects noted.
Skeletal muscle relaxation: Can potentiate effects of general anesthetics; appetite stimulation in cats and ruminants.
Adverse Effects of Benzodiazepines
CNS: Disorientation and excitement in young, healthy dogs; dysphoria and aggression in cats.
Motor Effects: Muscle fasciculations in horses and ataxia in large animals.
Precautions: Administer Diazepam IV slowly; avoid oral Diazepam in cats due to risk of liver failure.
Use of Benzodiazepines
Diazepam: Not water-soluble; do not mix with water-soluble drugs; don’t store in plastic. Commonly paired with ketamine for anesthesia induction in small mammals and horses.
Midazolam: Water-soluble; can be administered IM or SC; good sedative for swine, ferrets, rabbits, and birds.
Zolazepam: Available as a component of Telazol®.
Alpha2-Adrenoceptor Agonists
Noncontrolled agents providing sedation, analgesia, and muscle relaxation for various species.
Administered IM or IV before minor surgical procedures.
Effects are readily reversed with alpha2-antagonists.
Key Alpha2-Agonists
Xylazine, Dexmedetomidine, Detomidine, Romifidine: Used primarily in large animals like horses.
Functionality of Alpha2-Agonists
Stimulates sympathetic nervous system (SNS) receptors, decreasing norepinephrine release, which leads to decreased response in the "fight-or-flight" scenarios.
Effects include sedation, analgesia, bradycardia, hypotension, and hypothermia with a rapid onset lasting 1-2 hours.
Effects of Alpha2-Agonists
CNS: Dose-dependent sedation.
Cardiovascular: Initial vasoconstriction and hypertension followed by decreased cardiac output.
Respiratory: Potentially significant depressant effect.
Additional: Muscle relaxation, vomiting, temporary hyperglycemia, hypothermia.
Adverse Effects of Alpha2-Agonists
CNS: Behavioral changes vary per species.
Cardiovascular: May see bradycardia and hypotension; concurrent administration with other drugs can magnify effects.
Gastrointestinal Issues: Can also lead to bloat in dogs and cattle or salivation/regurgitation in cattle.
Caution with Alpha2-Agonists
Monitor closely, especially in geriatric, diabetic, pregnant, pediatric, or ill patients. Administer anticholinergics beforehand to mitigate effects.
Alpha2-Antagonists
Functionality: Reverse all effects of alpha2-agonists, correcting analgesia and sedation.
Adverse effects of overdose: Neurological (excitement), cardiovascular (hypotension), gastrointestinal (salivation).
Specific Alpha2-Antagonists
Tolazoline: Nonspecific antagonist for ruminants.
Yohimbine: Used in dogs, cats, horses; species-dependent dose ratio.
Atipamezole: Specific antagonist for dexmedetomidine; faster recovery for cats compared to dogs.
Opioids
Derivatives of opium classified into agonists, partial agonists, and antagonists used to provide analgesia and sedation, especially during anesthetic induction.
Commonly Used Opioids
Agonists: Morphine, hydromorphone, fentanyl.
Partial agonist: Buprenorphine.
Agonist-antagonists: Butorphanol and nalbuphine.
Antagonists: Naloxone, etorphine.
Opioid Pharmacodynamics
Mimic endogenous opioids affecting pain pathways in the CNS via mu, kappa, and delta receptors.
Each type provides varying effectiveness based on receptor interaction.
Effects of Opioids
CNS: Vary significantly based on species with potential for sedation or stimulation.
Analgesia: Most effective with pure agonists for severe pain during premedication for surgery.
Cardiovascular effects typically lead to bradycardia; respiratory depression occurs in more sensitive patients.
Other Effects of Opioids
Behavioral effects such as miosis in dogs and mydriasis in cats, alongside temperature variations and sweating.
Adverse Effects of Opioids
CNS responses of anxiety or disorientation, cardiovascular effects leading to marked bradycardia, respiratory issues including decreased oxygen levels, and potential GI complications.
Other Adverse Effects of Opioids
Risk of physical dependence and dermal reactions; significant drug interactions exist.
Use of Opioids
Employed as preanesthetic agents either alone or alongside tranquilizers and anticholinergics for effective analgesia.
Opioid Antagonists
Function to reverse the effects of opioids responsible for CNS and respiratory depression, facilitating recovery in sedated patients.
Naloxone Hydrochloride: Commonly used with rapid effect for reversal of sedation in various animals.
Effects of Opioid Antagonists
Quick reversal of opioid effects with minimal adverse reactions; however, rapid cessation can induce withdrawal symptoms.
Use of Opioid Antagonists
Primarily in emergencies for overdose situations, reviving neonates from C-section anesthesia if the dam received opioids.