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132 Cards in this Set

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CNS effects of dissociative anesthetics

seizures, increased cerebral blood flow/intracranial pressure, emergence delirium/hallucinations

CV effects of dissociative anesthetics

indirect: increase catecholamines --> tachycardia (predominate unless depleted)




direct: myocardial depressant

resp effects of dissociative anesthetics

bronchodilation, maintenance of pharyngeal/laryngeal reflexes

MOA of etomidate

enhances the affinity of inhibitory NT GABA at the GABA-A receptor

how is etomidate metabolized?

hydrolyzed by hepatic microsomal enzymes and plasma esterases

main clinical use of etomidate

used in patients w/ cardiac disease, or in patients that require stable CV function due to other concurrent diseases

effects of propylene glycol in etomidate

hemolysis

endocrine effects of etomidate

adrenocortical suppression

neurosteroid induction agent

alfaxalone

MOA of alfaxalone

enhances GABA-mediated neurodepression (...think propofol, etomidate, barbiturates)

How is alfaxalone metabolized/excreted?

metabolized by hepatic glucuronidases - metabolized more slowly in cats

important side effects of alfaxalone

dose-dependent cardioresp depression

MOA of barbiturates

decreases rate of dissociation of GABA from GABA-A receptor




directly opens Cl- channel --> hyperpolarization

CNS effects of barbiturates

vasoconstriction, decreased cerebral blood flow --> decrease intracranial pressure




decreased cerebral metabolic oxygen requirement

CV effects of barbiturates

minimal decreases in BP w/ healthy patients; profound hypotension in hypovolemic pts




myocardial depression, arrhythmias

resp effects of barbiturates

resp depression

effects of administering barbiturates outside the vein

sloughing of the tissue, pain

pros and cons of inhalant inductions

pros: aggressive animals that can't be handled, pets w/ severe liver disease, used in some wildlife/exotics




cons: can't get rapid control of airway, stressful for animal, creates excitement phase w/o premed --> lose control of airway --> vomit/regurg

opioid inductions common in which patients...

critically ill, highly unstable

TIVA

- total intravenous anesthesia




- method of inducing and maintaining general anesthesia exclusively by IV administered drugs

advantages of TIVA

- better recovery profile


- portable delivery system (i.e. syringe pump)


- less operating room pollution (no waste gases)

disadvantages of TIVA

- cost prohibitive


- availability of suitable drugs and delivery systems


- can't reliably monitor plasma concentration of drugs like ET inhalant agent monitoring

uses of TIVA

- GA


- day surgery


- supplement to locoregional anesthetic


- sedation for diagnostic/therapeutic procedures

disadvantages of repeat bolus TIVA

peaks and troughs in drug concentration - can see toxic effects or under-dosing

disadvantages of CRI TIVA

delay to peak effect




need loading dose




decrease in concentration at transition from loading dose to maintenance (due to drug redistribution)

target controlled infusion

aims to achieve predicted target blood concentration based on population pharmacokinetic studies




actual concentrations achieved may be greater/less than selected target, but provides closest approximation of blood concentration of drug for a patient

propofol in TIVA

- rapidly metabolized w/ minimal accumulation


- smooth recovery and less CV depression than isoflurane


- has been co-infused w/: fentanyl, morphine, remifentanil, dexmed, ketamine...


- can see abnormal motor activity in dogs, Heinz body anemia in cats

fentanyl CRI

single injection can be used for short-duration analgesia during anesthesia

nicotinic synapses

pre-synaptic cell: motor neuron


post-synaptic cell: muscle cell




ACh synthesized/released by nerve cell binds to nicotinic receptors on muscle cell. conformation change allows Na+ ions into muscle cell --> membrane depolarization --> muscle contraction




ACh in cleft is hydrolyzed by AChE. Na+ channel closes.

MOA of non-depolarizing neuromuscular blockers

competitive antagonists




bind to nicotinic ACh receptors and prevent ACh from interacting w/ the receptor

reversal of nondepolarizing NM blockers

are not hydrolyzed by AChE - redistribute, metabolized and excreted




can be reversed by increasing the amount of ACh at the synapse... giving an AChE inhibitor




ACETYLCHOLINE CAN HAVE FATAL EFFECTS ON HEART; give w/ atropine/glycopyrrolate to prevent bradycardia

edrophonium, neostigmine

AChE inhibitors, reverse non-depolarizing neuromuscular blockers

depolarizing neuromuscular blockers

nicotinic receptor agonists




bind to receptor and generate AP, produce contraction but do not release from the receptor; cell cannot repolarize, produces paralysis

reversal of depolarizing neuromuscular blocks

broken down in plasma by pseudocholinesterase enzymes




no pharmocologic reversal agents

indications for using neuromuscular blockers

- improvement of surgical field


- prevent coughing during intubation/OLV


- reducing fractures


- intraocular sx


- C-section (don't cross the placenta)


- reduce the volume of inhalants needed


- rapid sequence induction

cons of neuromuscular blockers

- paralysis


- patient can't breathe (have to breathe for them)


- can't move in response to pain


- no hypnotic or analgesic properties (in people, awareness under anesthesia reported more w/ NMBAs)

what is residual paralysis?

presence of undetected weakness after anesthesia




residual weakness increases risks of aspiration, airway obstruction, hypoxia




risks of residual paralysis increased by residual effects of anesthetic agents, hypothermia




monitor with ENS - paralyzed nerves don't respond to stimulation

succinylcholine

depolarizing NMBA

benzylisoquinolones

non-depolarizing NMBAs




i.e. atracurium, cisatracurium, etc.




can release histamine --> tachycardia, hypotension, bronchospasm




extra-hepatic metabolism

steroidal NMBAs

non-depolarizing NMBAs




i.e. vecuronium, rocuronium




vagolytic - inhibits vagus n.




hepatic metabolism, renal excretion

Hoffman elimination

spontaneous nonenzymatic chemical breakdown that occurs at physiological pH and temperature, independent of renal and hepatic metabolism




occurs w/ atracurium

important functions of CV system

deliver oxygen from lungs to tissues




remove CO2 from tissues and deliver to lung




transfer heat




deliver hormones, nutrients




remove metabolic waste

causes of hypothermia under anesthesia

decreased muscle activity




vasodilation of peripheral vasculature




depression of thermoregulatory centers in CNS




(usu. cold in OR, heat lost from open body cavities, etc.)

basal metabolic oxygen requirement

~10mL/kg/min

mixed venous oxygen

measure of the global balance between supply and demand of oxygen




decreases when: oxygen demand increases OR oxygen supply decreases




mixed venous oxygen content under normal circumstances = ~15mL/dL

arterial oxygen content

under normal circumstances ~20mL/dL

oxygen delivery eqn

oxygen delivery = cardiac output x oxygen content of arterial blood

cardiac output eqn

cardiac output = stroke volume x heart rate




cardiac output = pressure drop/vascular resistance





oxygen content eqn

oxygen content = oxygen on hemoglobin + oxygen in simple solution

CV concerns in pediatric and geriatric patients

more susceptible to CV depression

thermoreg. concerns in pediatric and geriatric patients

hypothermia

anesthetic concerns - sighthounds

altered pharmacokinetics of barbiturates - less fat for drugs to redistribute to leads to prolonged recoveries

anesthetic concerns - brachycephalic breeds

- difficult to visualize rima glottidis



- hypoplastic trachea limits size of endotracheal tube that can be passed



- airway anatomy increases risk of airway obstruction on extubation

anesthetic concerns - toy breeds, pediatrics

hypoglycemia

anesthetic concerns - boxers

bradycardia and hypotension following acepromazine (tx: fluid bolus, atropine)

anesthetic concerns - large/giant breeds

assume subclinical dilated cardiomyopathy - can result in arrhythmias under anesthesia

fasting time in adults? in pediatrics/toy breeds?

adults: usu. fast after midnight, but 6-8 hrs depending on previous meal




peds/toy: 1-2 hrs ONLY (monitor BG)

why do you need venous access during anesthetic procedures?

- fluid therapy




- ER venous access

preoxygenation

administration of oxygen prior to induction/intubation




increases functional residual capacity in case of apnea/hypoxia during induction

brachycephalic upper airway syndrome

stenotic nares


elongated soft palate


everted laryngeal saccules


redundant pharyngeal tissue


hypoplastic trachea

assessing depth of anesthesia

too light: globe is central, jaw tone is tight, palpebral reflex present




adequate: rotated globe




too deep: globe is central, jaw tone is slack, palpebral reflex absent

monitoring equipment

LOOK AT YOUR PATIENT!!


stethoscope


pulse ox


capnograph


blood pressure


electrocardiography


temperature


glucometer (peds)

complications of equine anesthesia

- behavior




- size




- thoraco-abdominal anatomy

normal resp rate of horse

~14 breaths per min

normal tidal volume of horse

10-15 ml/kg

dead space of horse

vd/vt ~60%

implications of large dead space volume

rapid shallow breathing is ineffective




ventilator settings should be at low breaths per minute w/ large tidal volumes

resp problems w/ horses under anesthesia

- can generate enough inspiratory pressure to cause pulmonary edema or collapse airways




- lungs collapse from position, lack of muscle tone --> atelectesis




- increased V/Q mismatch than in SA




- need to breathe for horses under anesthesia - IPPV helps w/ oxygenation/delivery of inhalants

normal HR in horse

30-45 beats per minute

normal aterial BP in horse

130/90, MAP 100

CV considerations in horses under anesthesia

- I-II degree heart blocks are common/non-pathologic




- atrial fib is most common arrhythmia




- maintain MAP >70 to perfuse muscle, avoid rhabdomyolysis

GIT considerations in horses under anesthesia

- auscult GIT before sedation




- fasting >12 hrs decreases fermentation while anesthetized, decreases abdominal distention

fasting period in a horse

>12 hours

commonly used sedatives for horses

xylazine


detomidine


romifidine


dexmed




(less severe CV effects than in cats/dogs)

agent used to co-induce w/ ketamine

benzodiazepines




(poor sedatives alone, provide muscle relaxation)

use of opioids in horses

often combined to augment sedation




mu agonists - better analgesia, concerned w/ ileus (usu small doses don't cause colic)




mixed agonists - less analgesia, less pronounced side effects

induction agents in horses

can use inhalants in neonates




ketamine/benzo combo in adults

concerns w/ inhalants in horses

hypotension more common/severe than in cats/dogs - use other drug to decrease MAC (ketamine, lidocaine, detomidine)

"triple drip"

guaifenesin, ketamine, xylazine




adequate for short procedures




common for field procedures

complications w/ recovery in horses

- horses become excited/scared




- ataxic




- fractures, airway obstruction

nerve block for celiotomy in a ruminant

inverted L or paravertebral

nerve block for claw amputation in ruminant

intravenous regional

nerve block for dehorning in ruminant

zygomaticotemporal

nerve block for obstetrical procedures in ruminants

caudal epidural blocks

sedation in ruminants

xylazine in cattle (@ much lower doses than horses)


sheep and goats VERY sensitive. sheep prone to pulmonary edema.


normal alpha-2 side effects (bradycardia, hyper- and hypotension, hyperglycemia, thermoregulation inhibition)


reverse w/ yohimbine

sedation in small ruminants

benzodiazepines +/- other anesthetic drugs

fasting period in adult ruminants

18-24 hrs off feed. 6-8 hrs off water


(shorter in sm ruminants)

fasting period in neonatal ruminants

miss one milk feeding

induction of anesthesia in ruminants

agents: thiopental, ketamine, propofol, guiafenesin




keep head elevated to reduce aspiration until tube is inserted/cuff is inflated

access to jugular vein in camelids

- in middle of neck: skin is thick and transverse vertebral processes, muscles overlie the vein




- can usually access cranially, but must avoid carotid a.

sedation in pigs

alpha-2 + opiate + ketamine usu most effective; volume of injectate should be minimal




IM injections in neck (avoid meat spots)




they will bite you

catheterization in pigs

can place catheter in ear vein once sedated

complications w/ intubation in pigs

long, narrow buccal cavity


tortuous oro-pharyngo-laryngo-tracheal pathway


small larynx




can rupture trachea causing pneumomediastinum and pneumothorax

malignant hyperthermia

heritable disease in swine, causing complications under anesthesia




caused by uncoupling of metabolic pathways




dx: increasing body temp, muscle rigidity


tx: stop anesthesia, whole body cooling, dantrolene

what do you do immediately after inserting the endotracheal tube?

provide oxygen

to ensure the patient has not arrested after intubation palpate the...

pulse, apex beat

why do you auscult both sides of the chest after induction/intubation?

to make sure both lungs are being adequately ventilated, and that the endotracheal tube has not been inserted too far into a bronchus

when is it appropriate to extubate a normal cat/dog? a brachycephalic cat/dog?

when the pt has coughed/swallowed several times in a short period




when the pt is actively rejecting the tube - gagging, coughing strongly

what do you look for or do immediately after extubation?

check resp rate/effort


check pulse ox on room oxygen


TPR, assess for pain

if a pt is having a rough recovery, what do you do?

assess pain vs delirium




pain - try an opioid bolus


delirium - can re-sedate the patient (ace, dexmed)

effects of increased abdominal pressure on anesthesia

- decreases venous return


- reduces FRC


- increases risk of hypoxia

physiologic changes during pregnancy affecting anesthesia

- increased abdominal pressure


- progesterone decreases esophageal tone


- dilutional anemia


- risk of hemorrhage (increased blood supply to the uterus)


- progesterone decreases MAC


- decreased vascular resistance

anesthetic factors that affect intracranial pressure

vomiting/coughing


increased central venous pressure


hypercapnia


hypoxemia


inhalant anesthetics


ketamine


severe hypertension

Cushing's reflex

cerebral perfusion pressure = MAP - ICP




as ICP increases, blood pressure must increase to perfuse the brain. vasoconstriction increases BP, but produces reflex bradycardia

anesthetic concerns in diabetic pts

hyperglycemia


iatrogenic hypoglycemia


slow gastric emptying time


cardiac autonomic neuropathy


possible renal disease


DKA

problems associated with acidosis

increased incidence of arrhythmias


decreased cardiac function


decreased effect of catecholamines


increased risk of morbidity/mortality

fasting small mammals

- unnecessary in sm mammals that don't vomit


- can be detrimental to the GIT in some species - i.e. rabbits, g. pigs


- can lead to dehydration, hypoglycemia


- should be done cautiously in pregnant animals


- can be difficult in animals that hide food in cheek pouches, or practice coprophagy

methods of ferret restraint

scruffing, wrapping in a towel, tiny ferret muzzles

methods of rabbit restraint

scruffing, wrapping in a towel


always restrain/support pelvic limbs and prevent rabbits from kicking back legs and fracturing vertebral column

methods of rodent restraint

scruffing, cup them in your hand, tapered plastic film tubes (pastry bags), purpose designed devices




avoid picking them up by their tails

sites for blood collection in ferrets

jugular, cephalic v., lateral saphenous v., cranial vena cava

sites for blood collection in mice/rats

retroorbital venous plexus, superficial temporal v., tail vein

atropinases

circulate in rabbit plasma, cause atropine to have unpredictable effects on heart rate

breathing system used in sm mammal anesthesia

most need non-rebreathing systems




(larger rabbits may be big enough for a pediatric rebreathing circuit)

features of rabbit upper airway that make intubation difficult

epiglottis is dorsal to soft palate, must be retracted ventrally


butterfly shaped epiglottis


mouth doesn't open wide


larynx is caudal and ventral to angle of the mandible

methods of rabbit intubation

blind - listen for airflow, use capnograph


visualize w/ laryngoscope, otoscope, endoscope


retrograde


nasotracheal

palatal ostium

connection between oropharynx and pharynx in chinchillas and g. pigs.




is highly vascular and prone to trauma/hemorrhage during intubation

ways to intubate rats/mice

w/ otoscope and guide wire


w/ fiberoptic endoscope

V-gel

supraglottic device manufactured for rabbits

sustained-release opioid used in sm mammals

buprenorphine

porphyrin staining

can be a sign of pain/stress in rats




pigment produced by Harderian gland in the orbit can be seen around eyes, nose and front paws

signs of pain in sm mammals

changes in activity level, hunching, decreased e/d, decreased urination/defecation, reduced grooming, changes in temperament, vocalizations, tachycardia, tachypnea

challenges of anesthetizing zoo/wildlife

often no hx/pre-anesthetic exam/diagnostics


limited knowledge of pharmacology, physiology


less than ideal environmental conditions


stressful, dangerous inductions


challenging to provide appropriate supportive care, monitoring

human safety risks assoc. w/ zoo/wildlife capture/immobilization

animal can physically injure humans


transmission of zoonotic diseases


drugs


environmental conditions


capture techniques

ways to prevent human injuries

have a plan! communicate!


understand the species


familiarize w/ the environment


handle drugs carefully, w/ a buddy


have antagonists readily available


wear PPE


know where the ER facilities are


only use firearms/drug delivery systems if trained

factors to account for when selecting free-ranging wild animal immobilization environment

temperature


light conditions


terrain


non-target animals


equipment needed


capture technique

qualities of an ideal immobilization agent

small volume needed


acts quickly


reversible


produces hypnosis


versatile


stable


high margin of safety for animal


safe for human handler

dangerous high and low body temps

high: 41C (105.8F)


low: 35C (95F)

prevention of hyperthermia in immobilized wildlife

avoid capture during hot ambient temps


provide shade


do not pursue animals for more than 2-5 mins


limit stress


limit physical restraint

treatment of hyperthermia in immobilized wildlife

active cooling with fluids, antagonize anesthetic agents, oxygen supplementation

treatment of rumen tympany/bloat in immobilized wild ruminants

position in sternal recumbency w/ neck extended


elevate cranial end of body


pass orogastric tube


trocarize


pharmacologic antagonism

capture myopathy

most common in ungulates




due to massive discharge of the sympathetic nervous system




four recognized forms




similar to exertional rhabdomyolysis in humans