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Anesthesia / Drugs

In document RykuPrep Study Guide (Page 43-50)

 With younger patients, you must be concerned about hypoglycemia and hypotension.  Until oxygen pressures reach < 60mmHg, there is little change in oxygen saturation.

o Oxygen pressure of 60 mmHg means there is 90% oxygen saturation. Below 60 mmHg, oxygen saturation declines rapidly.

 Adrenergic receptors are stimulated by epinephrine and norepinephrine.

o Alpha-1 & Alpha-2 adrenergic receptors are sympathetic receptors located on the arteries. They increase blood pressure by constricting arteries, which causes bradycardia.

o Beta-1 adrenergic receptors are in the heart and increase heart rate & contractility. o Beta-2 adrenergic receptors are in the lungs and smooth muscle. They dilate

bronchioles (let more air in lungs) and dilate skeletal muscles (to get more muscle blood flow).

 Blood pressure is the force of the blood pushing against the arteries. o Vasodilators decrease blood pressure.

 Vasoconstrictors increase blood pressure.

o Hypotension is systolic pressure less than 80mmHg & mean pressure less than 60 mmHg.

 Treat hypotension by decreasing anesthetic gas, fluid boluses, and atropine / glycopyrrolate.

 Can use dopamine (an alpha agonist) or norepinephrine CRIs to raise blood pressure.

 Normal end-tidal CO2 is 35 – 40 cmH20.

o Best way to decrease CO2 is to increase ventilation. Can manually do this or

decrease anesthetic gas.  Cardiopulmonary arrest:

o Under anesthesia, you have ~50% chance of return of spontaneous circulation (complete survival rate).

 Under other circumstances, you have ~5% chance.

o The purpose of chest compressions and giving breaths is to maintain blood flow until you can get epinephrine into the body.

 Chest compressions by themselves are unlikely to return spontaneous circulation.

o Signs of cardiopulmonary arrest include:

 Lack of cardiac activity (no heart rate or blood pressure)  Apnea (lack of breathing)

 Centrally fixed eye with mydriasis o What to do with cardiopulmonary arrest:

 Turn off anesthetic gas and any other depressants (opioid CRIs, etc.)  Give shock dose bolus of fluids.

 Ensure that airway is maintained by endotracheal tube (palpate larynx or use laryngoscopre).

 Give 10 breaths per minute.

 Give cardiac compressions (120 compressions per minute). 

 Purpose of external cardiac massage is to deliver oxygen and epinephrine to the heart and periphery.

 Give 1 – 2 doses of low dose of epinephrine (0.01 mg/kg).  Give a high dose of epinephrine (0.1 mg/kg) after that.

 Epinephrine has alpha and beta adrenergic effects. It directly increases heart rate, heart contractility, and blood pressure. It decreases total peripheral resistance.

 Can give atropine if you suspect the arrest is due to vagal stimulation.  Open the chest at 4th intercostal space after five minutes of unsuccessful

compressions for intra-thoracic cardiac compressions.  Compress apex to base (reverse milking).  All anesthetic drugs diminish thermoregulation.

o Never use electric blankets because they burn animals.

o Cold temperature decreases coagulation, decrease leukocyte function, and causes peripheral vasoconstriction (hyperperfusion).

o Low temperatures lower the MAC of anesthetic gases, thus decreasing the required amount of gas.

 Small, young, cachectic patients are at risk for hypoglycemia during surgery. o Can cause sympathetic hyperactivity.

 Guaifenesin is a centrally-acting muscle relaxant with an unknown mechanism. o Succinylcholine is a depolarizing neuromuscular blocking agent.

o Atracurium is a non-depolarizing neuromuscular blocking agent.  Premedication:

o Premedication is administration of drugs prior to anesthetic induction.

o Reduces apprehension, facilitates handling, enhancing peri-operative analgesia, and minimizing adverse effects of anesthetic drugs.

o Acepromazine

 This is a phenothiazine.

 Tranquilizer that is a dopamine antagonist.

 Commonly given with an opioid for neuroleptanalgesia (a state of minimal responsiveness).

 Major side effect is hypotension by being an alpha-1 antagonist. This is offset by benefits in healthy animals, but don’t use in hypovolemic patients.

 Also decreases seizure threshold and platelet function. o Only decreases seizure threshold IV at higher doses.  Causes splenic dilation, decreased hemoglobin concentration, and

decreased hematocrit.

o Don’t use acepromazine with splenic masses.

 This can be reversed with the alpha-agonist phenylephrine, which has no cardiac effects.

 Not reversible and not an analgesic.

 Protects from arrhythmias, is an antiemetic, causes penile protrusion in horses, & is an antihistamine.

 Decreases anesthetic requirements up to 40% (lowers MAC) o Opioids can be used as premedications.

o Alpha-2 agonists: (Xylazine, Medetomidine, & Dexmedetomidine)  Ruminants are more susceptible.

 Analgesics, sedatives, and muscle relaxants  Reversed by yohimbine & atipamezole.

 Can cause bradycardia, AV block, and decrease GI motility. Causes hypertension then hypotension.

 Don’t use in pregnant females because it increases uterine tone.  Inhibit insulin and cause hyperglycemia.

 Inhibits anti-diuretic hormone (ADH), which means they increase diuresis

 Xylazine can be given to cats to vomit.

 Avoid in critically ill and heart failure patients because of cardiovascular effects.

o Benzodiazepines: (Diazepam, Midazolam, & Zolazepam)  Muscle relaxants and anxiolytics

 Are not analgesics  Reverse with Flumazenil

o Anticholinergics: (Glycopyrrolate & Atropine)

 Inhibit parasympathetic innervation; they increase heart rate and cause bronchodilation

 Decrease GI motility, salivation, and bronchial secretions  Cause mydriasis

Opioids:

o Analgesics that are parasympathomimetics (activate parasympathetic system).  Major side effects dysphoria, respiratory depression, sedation, vomiting,

constipation, and bradycardia.

 Decrease the anesthetic requirement (decrease MAC) of isoflurane.  Subcutaneous administration causes more vomiting than other

administrations.

 When combined with acepromazine emesis is inhibited. o Mu-agonists have greater analgesia than kappa-agonists. o Reversed with Naloxone.

o Hydromorphone  Pure agonist o Methadone  Pure agonist o Buprenorphine  Mixed agonist-antagonits o Fentanyl  Pure agonist

 Shortest half-life; normally given as a CRI o Butorphanol  Mixed agonist-antagonists o Morphine  Pure agonist

 Induces histamine release, so don’t use with mast cell tumor patients.  Epidural morphine provides analgesia for at least 12 hours.

o

Tramodol

 Longest acting opoid Induction Agents:

o Propofol:

 An induction anesthetic unrelated to other general anesthetics.  Causes poor analgesia.

 Mechanism of action is unknown.

Causes respiratory depression, increased intraocular pressure, and bradycardia.

 With repeated doses, propofol can cause Heinz body anemia in cats.

 Short duration of action (2 – 5 minutes)  Cleared by the liver.

 Cats usually recover from propofol rapidly and smoothly.  Not a controlled substance.

 No antagonist. o Alfaxalone:

 Neuroactive steroid molecule that binds to GABA receptors (inhibitory neurotransmitter).

 Can cause respiratory depression, but to a lesser degree than propofol.  Provides poor analgesia.

o Benzodiazepines o Ketamine

 Ketamine causes an increase in muscle tone, increased intraocular pressure, and increased sympathetic tone.

Causes tachycardia and should be avoided in cats. That’s because up to 20% of cats have undiagnosed hypertrophic cardiomyopathy, where you want to lower heart rate to improve diastolic filling.  Preserves blood pressure and breathing well. Also provides some

analgesia.

Combined with diazepam, ketamine is a very good induction agent in healthy patients.

 Don’t use in head trauma patients because it will increase intracranial pressure.

Also don’t use in hyperthyroid patients because it can cause thyroid levels to increase.

Don’t use with pheochromocytomas or heart disease because ketamine causes an increase in catecholamines.

 Cleared by kidneys in cats and liver in dogs. o

Thiopental is a barbiturate that can cause cardiac arrhythmias.

 Thiopental is the barbiturate with the shortest onset of action and duration.  Ventricular bigeminy is the most common arrhythmia.

 Thiopental, like acepromazine, causes splenic engorgement.

 Is a strong irritant if it goes perivascular. Treat by diluting the area with saline.

 Not gold standard but can be used effectively and cheaply in healthy patients.

 Don’t use in sighthounds (including Greyhounds) because they don’t metabolize it well.

 Protein-bound, so will get a disproportionately large effect in hyperproteinemic animals.

Inhalant Anesthetics:

o Advantages over injectable anesthetics are minimal metabolism, rapid adjustment, and the ability to give with oxygen.

o Inhalant anesthetics are the most cardiodepressive drugs.

o Inhalant anesthetics are vasodilators, which decrease blood pressure.

o Can cause malignant hyperthermia due to a hypermetabolic state, especially in swine.

 Treat with Dantrolene.

o Less potent & higher MAC = slower induction and recovery.

o Lower mean alveolar concentration (MAC) means increased potency.  Desflurane has the highest MAC & Isoflurane has the lowest MAC. o

Sevoflurane

 Smoother induction.

 Medium potency (less than isoflurane & more than desoflurane)

 Produces breakdown product called Compound A which may cause renal damage. o Desflurane  Least potent o Isoflurane  Most potent o Halothane

 Highly metabolized by the liver

 Makes myocardium more susceptible to catecholamine-induced arrhythmias.

 Can cause malignant hyperthermia. o

Nitrous Oxide

 Cannot be used by itself for clinical anesthesia because of its high MAC. 

 Azathioprine is an immune-suppressive drug not normally used in cats because of bone marrow suppression.

 Prednisone should not be used with infection because it will suppress the immune system. o Cats and horses get prednisolone.

o Steroids also have anti-insulin effects (can cause diabetes), joint problems, skin disorders, and renal disorders.

 Cyclophosphamide is an immune-suppressive drug.

 Ketoconazole can cause hepatotoxicity, anorexia, vomiting, diarrhea, and adrenal insufficiency.

 Ivermectin stimulates GABA, an inhibitory neurotransmitter. o Ivermectin is active against mites, nematodes, and ticks.

 Not active against trematodes (flukes). 

 Praziquantel only treats tapeworms.

Penicillins (Penicillin, Ampicillin, Amoxacillin) work by inhibiting formation of peptidoglycan cross-links in bacterial cell walls.

o Effective against gram + and anaerobic bacteria.

o Can combine with beta-lactamase inhibitors such as clavulanic acid to extend spectrum of activity.

o NEVER give procaine penicillin intravenously; it causes CNS toxicity.  Cephalosporins (Cephalexin, Cefazolin, Ceftiofur) work by inhibiting formation of

peptidoglycan cross-links in bacterial cell walls.

o Later generations effective against gram +, gram -, & anaerobic bacteria.  Vancomycin works by interfering with cell wall synthesis.

o Effective against gram + bacteria. o Use against resistant bacteria only.

Aminoglycosides (Gentamycin, Neomycin, Amikacin) work by binding to the 30s ribosomal subunit, which interferes with protein synthesis.

o Effective against gram - bacteria. o Nephrotoxic & ototoxic

o Poorly absorbed by feline intestinal tract.

Tetracyclines (Tetracycline and Doxycycline) work by binding to the 30s ribosomal subunit, which interferes with protein synthesis.

o Effective against gram +, gram -, & anaerobic bacteria. Also effective against Ehrlichial, Anaplasmal, and Rickettsial bacteria.

o Nephrotoxic and will discolor teeth in puppies.

Chloramphenicol works by binding to the 50s ribosomal subunit, which interferes with protein synthesis.

o Effective against gram -, gram +, & anaerobic bacteria. o Causes bone marrow depression in humans.

o Forbidden in food animals.

Lincosamides (Lincomycin, Clindamycin) work by binding to the 50s ribosomal subunit, which interferes with protein synthesis.

o Effective against gram + & anerobic bacteria. o Do not use in horses.

Macrolides (Erythromycin, Azithromycin, Clarithromycin) work by binding to the 50s ribosomal subunit, which interferes with protein synthesis.

o Effective against gram + & anaerobic bacteria.  Metronidazole works be breaking apart DNA.

o Effective against anaerobic bacteria & protozoa. o Can have neurologic side effects.

Rifampin works by inhibiting RNA polymerase. o Effective against gram + bacteria.

o Mainly used against Rhodococcus equi in foals.

Fluoroquinolones (Enrofloxacin, Ciprofloxacin) work by inhibiting DNA gyrase. o Effective against gram - bacteria.

Trimethoprim-sulfamethoxazole (also known as TMS) works by interfering with folate metabolism.

o Effective against gram +, gram -, & anaerobic bacteria.

Bacteria

 On bacterial culture & sensitivity reports, oxacillin indicates methicillin resistance.  Streptococcus & Staphylococcus are gram + cocci.

Clostridium are anaerobes.

Nocardia & Actinomyces are gram-positive filamentous rods.

o Actinomyces is a normal flora of the mouth and orpharynx.Klebsiella is a gram-negative encapsulated facultative anaerobic rod.

In document RykuPrep Study Guide (Page 43-50)

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