Exam 2: Lecture 8: Pre-Medications Flashcards

(157 cards)

1
Q

Why do we premedicate animals for surgery?

A
  • Easier handling of patient
  • Lower does of induction and maintenence drugs (Prolems with pulmonary and cardaic issues if we use too much)
  • Pre-emptive analgesia
  • Smooter recovery period
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2
Q

T/F: You can induce an unsedated horse?

A

False!!!

NEVER induce an unsedated horse

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3
Q

What are the benefits of premedication?

A
  • Effective premed = lower amount of drug needed later
    (Minimum alveolar concentration sparing effect for inhalent anesthetics)
  • Synergistic effects from combining drugs produces better results than a single drug alone
  • Decreases cost because lower amounts of induction and maintenance drug used
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4
Q

The theory of pre-emptive or preventative analgesia is???

A

Reduces the amont of anesthestics required to produce a surgical plane of anesthesia

  • Stabilize the maintence of anesthesia
  • Reduced the amount of analgesics required intra-operatively and post-operatively
  • Decreases overall patient morbidity associated with surgeyr and anesthesia
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5
Q

What is the goal of anaglesia?

A

Presurgical and postsurgical analgesia

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6
Q

What does part A described?

A

Surgical and post-surgical afferent input

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7
Q

What does part B described?

A

Post-surgical analgesia

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8
Q

What does part C described?

A

Pre-surgical analgesia

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9
Q

What does part D described?

A

Pre-surgical and post-surgical analgesia

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10
Q

Which Administration technique is preferred?

IM, SQ, IV

A

IV and IM is preferred over SQ

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11
Q

This type of medication administration is typically given in more anxious or fractious patients to facilitate IV catheter placement

A

IM

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12
Q

This type of medication administration is typically given if the patient already has a catheter, the dose can usually be lowered due to more immediae onset and greater degree of effect

A

IV

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13
Q

The following are examples of which administration type?

  • Lumbar epaxial muscles on either side of the dorsal spinous processes
  • Semimembranous and Semitendinosus
  • Quadricpes femoris muscle
  • Cervical epaxial muscles
  • LA patients: Know the landmarks for the “Triangle” area to inject
A

IM site injections

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14
Q

On the pelvic limb what important structure should be avoided

A

Sciatic nerve

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15
Q

What are the 5 commonly used drug classes for premedication

A
  • Anticholinergic
  • Phenothiazines
  • Alpha 2 agonists
  • Benzodiazepines
  • Opioids
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16
Q

Which class of premedication is described as:

  • NOT routinely included in the premedication unless high vagal time is currently suspected or a pediatric patient
A

Anticholinergics

  • prefer to give them only as required during anesthesia
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17
Q

Which anticholinergic drug is able to cross the blood brain barrier and placenta, but limited ability of glycopyrrolate to cross

A

Atropine

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18
Q

Which anticholinergic causes pupil dilation
- impairs vision and may lead to poor recovery in some species (EX: cats)

A

atropine

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19
Q

__________ in high doses inhibit urinary and GI motility

  • use cautiously in horses and cattle because colic and rumen stasis may occur
A

Anticholinergics

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20
Q

What is the duration of action for Atropine

A

Varies by dose and species

  • About 60-90 minutes
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21
Q

How should you administer atropine

A

IV, IM, SQ

in emergency it can be given via endotracheal tube

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22
Q

What is the effect of Atropine

A

Increased heart rate and blood pressure

  • decreases salivary and bronchial secretions
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23
Q

What is the duration of action for Glycopyrrolate

A

Longer than atropine

  • around 2 to 3 hours
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24
Q

How can Glycopyrrolate be administered?

A

Iv, IM, SQ

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25
What is the effects of Glycopyrrolate
Increases heart rate and blood pressure - Decreases salivary and bronchial secretions
26
Side effects of Anticholinergics include?
- Hot (as a horse) - Dry (as a bone) - Blind (as a bat) - Red (as a beat) - Mad (as a hatter)
27
EXTRA
28
EXTRA
29
Following IV injection of _____, an initial increase in vagal tone may occur and a transient decreased heart rate or heart block can occur. This is followed by the expected increae in heart rate
Atropine
30
What is recommended when giving Atropine
Recommended giving 1/2 atropine dose IV and then the rest IM or SQ
31
______ is less likely to cause an inital increase in vagal tone compared to atropine
Glycopyrrolate
32
What is the MOA for Phenothiazines (EX: acepromazine)
Dopamine (D1 and D2) receptor antagonist in the CNS - **acts like a straight jacket: looks calm and relaxed, but internally may be anxious** SAME
33
Which drug is most commonly used for its tranqilizing and antimetic effects
Acepromazine
34
T/F: Acepromazine relives anxiety, which is why its a good tranq
FALSE!!! - it does not relieve anxiety
35
What is the duration for Acepromazine given IV
Peak effect around 15 min.
36
What is the duration for Acepromazine given IM
Peak effect around 30 min
37
T/F: Acepromazine has a long lasting effect (4-8 hours) and has no reversal agent
TRUE!!!!
38
T/F: Acepromazine has some muscle relaxation and analgesia effects
FALSE!!! Acepromazine has some muscle relaxation, but no analgesic effect
39
_______ works synergestically with analgesic drugs, so the dose can be lowered and still achieve the desired sedative effect
Acepromazine
40
What is the dose dependent MAC of Acepromazine
around 30-40%
41
Which drug has anti-histamine effects, so avoid using prior to skin testing for allergies
Acepromazine Also has - Anti-nausea effect - Anti-arrythmic properties - Altered thermoregulation (decreases body temp when used)
42
FITB: Acepromazine: a-1 adrenergic blockade = vasodilation = ? - subsequent Epinephrine administration may cause a paradoxial drop in blood pressure (B2 effect) because alpha receptors are blocked
Hypotension
43
_________ causes anti-sympathetic effects due to decreased mobilization of catecholamines centrally and peripherally
Acepromazine
44
Which drug is histrocially not used in epipletic patients because it was thought to lower the seizure threshold. This is controversial because recent literature has not found an association btw the two
Acepromazine
45
Avoid using Acepromazine in what type of situations?
- Fractious or agressive patients or those with high anxiety - Liver disease or portocaval shunts - Valubale breeding stallions due to potential for paraphimosis (inability to retract the penis) - Von Willebrands disease or other clotting disorders - Shock or cardiovascular disease
46
What effect does Acepromazine have on Van Willebrands disease or other clotting disorders?
Acepromazine decreases platelet aggregation
47
what does Acepromazine do to pt's with shock or cardiovascular disease
Reduced PCV due to splenic sequestrations of RBC's
48
What drug has the following effects on boxers or short nosed dogs - Spontaneous fainting or syncope may occur due to sinoatrial block caused by excessive vagal tone - A low dose may be considered or it can be avoided if possible - Atropine may help prevent these effects
Acepromazine
49
What drug class has the following effects: - Overally effect in the patient is sedation - muscle relaxation - analgesia
Alpha 2 adrenoreceptors agonists
50
Xylazine, detomidine, romifidine, medetomidine, and dexmedetomidine are part of what drug class
Alpha 2 adrenoreceptors agonists
51
What are the physiologic effects of Alpha 2 adrenoreceptors agonists
- Sedation - Bradycardia - decreased tachycardia - Anti-shivering - Vasoconstriction - Vasodilation - Dieuresis - Analgesia
52
__________ are transmembrane G-protein coupled receptors located on pre and post synaptic sites on nerve and cell membranes in the brain, spinal cord, and periphery
Alpha 2 receptors
53
MOA of Alpha 2 adrenoreceptors agonists
Produces CNS depression by stimulation of pre and post synpatic A2 adrenoreceptors in the CNS and periphery = Decreased NE release and reduces ascending nociceptive input = decrease in CNS sympathetic outflow and decrease in ciruclating catecholamines
54
What are the 4 types of Adrenergic receptors
- Alpha 1 - Alpha 2 - Beta 1 - Beta 2
55
What type of Adrenergic receptor is described as: - Vasoconstriction - increased peripheral resistance ( blood flow) - Increased blood pressure - Mydriasis - Increased closure bladder sphincters
Alpha 1
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What type of Adrenergic receptor is described as: - Inhibits NE release - Inhibits AcH release - Inhibits Insulin release
Alpha 2
57
What type of Adrenergic receptor is described as: - Increased HR - Increased lipolysis - Increased myocardial contractility - Increased Renin
Beta 1
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What type of Adrenergic receptor is described as: - Vasodilation - Decreased peripheral resistance - Bronchodilation - Increased Glycogenolysis (muscle and liver) - Increased Glucagon release - Relaxes uterine smooth muscle
Beta 2
59
With A1 is there more NE or E
NE
60
With A2 is there more NE or E
E
61
With B1 is there more NE or E
NE = E (same amount of both)
62
With B2 is there more NE or E
Way more E than NE
63
How can Alpha 2 adrenoreceptor agonist be administered
can be given IV, IM, buccally and by epidural route
64
Which adrenergic receptor selectively determines the amount of cardiovascular effects due to A1 stimulation
A2
65
Alpha 2 adrenoreceptors agonists are reversible with the use of _____ (Ex: yohimbine, tolazoline, and atipamezole)
A2 adrenoreceptors antgonists
66
What are the cardiovascular effects of Alpha 2 adrenoreceptors agonists
induced bradycardia due to - increased systemic vascular resitance (SVR) in the periphery - Decreased sympathetic tone due to decreased NE outflow in the CNS
67
Which drug can increase cardiac sensitivity to catecholamine induced arrythmias during halothane anesthesia
Xylazine
68
Which drug class?? Cardiac output decreases due to decreased HR and increased vascular resistance - PCV increase = MM pale + gray because hearder to get O2 to tissues
Alpha 2 adrenoreceptors agonists
69
Should you use an anticholinergic when giving an alpha 2 agonists?
NOT generally recommened to give together as a premed
70
If you are really concerned about the level of bradycardia in a patient that received an A2 agonists, then consider the following steps?
1. determine the patients BP 2. Check with surgeon (has stimulation started) 3. How long since drugs were given - if BP is low and it has been 30-45 min since a2 agonist admistration and surgical stimulation is either not helping or going to take a while to begin - consider the administering anticholinergic IM or SQ - Lidocaine could be considered instead - Reversal with atipamezole (IM) +/- anticholinergic
71
What are the behavioral effects of an Alpha 2 adrenoreceptors agonists
- agression after administration is reported in horses - If patient is very nervous or excited, it may show an inadequate response, strartle when touched or a loud noise occurs
72
What are the respiratory effects of a pt given Alpha 2 adrenoreceptors agonists
- Hypoventilation or apnea due to respiratory center depression - Decrease sensitivity to increased PCO2 in the respiratory center - Horses and brachycephalic animals are prone to stridor and dyspnea from upper airway obstruction - Sneezing/ itchy nose noted occasionally in donkeys
73
What are the GI and renal effects of Alpha 2 adrenoreceptors agonists
- Decreased gastric acid secretions and GI motality - May cause vomiting in dogs and cats - Swallowing refles obtunded - **Excellent analgesic for treating GI pain** - Suppresses insulin release = hyperglycemia and glucosuria - Reduces hepatic blood flow and rate of metabolism - Inhibits anti-diuretic hormone and increases release of atrial natriuretic factor = diuresis with increased sodium and water excretion
74
With Xylazine, what is important to be aware of?
2 different concentrations for small animals and ruminants
75
What is the duration of Xylazine
Fast onset within 1-5 minutes and effects lasts 20-40 minutes after IV injection
76
Which drug may induce premature delivery in cattle due to oxytocin like effects
Xylazine
77
How can Detomidine be administered
IM or IV there is a gel form that can be given sublingually to horses
78
What is the duration of Detomidine
Onset of action is slightly longer than xylazine - Effects lasts 90-120 minutes - dose depenedent and route dependent
79
What is the duration of Romifidine
Effects lasts 45 to 90 minutes (up to 2 hours) after IV injection
80
Which drug is generally thought to produce less ataxia than xylazine, so it became popular for use in dentals and other standing procedures
Romifidine
81
Which drug can be reveresed with Atipamezole
Dexmedetomidine
82
What is the duration of Dexmedetomidine
Quick onset after IV administration (1-3 minutes) and IM administration (5-10 minutes). Trasmucosal takes longer (30-60 minutes) - effects lasts 90-120 minutes
83
Which drug has an onset in about 10 minutes afer IM injection and even faster if given IV
Medetomidine
84
Which drugs analgesia lasts about 30 minutes, but sedation can lasts up to 2 hours
Medetomidine
85
How can you reverse Medetomidine
Atipamezole
86
When you use Zenalpha what should you always do?
decrease the dose when you use
87
What two drugs make up Zenalpha and how are they important
Medetomidine (crosses the blood brain barrier) Vatinoxan (Peripheral Alpha 2 antagonist and does not spike BP)
88
What are the 4 main points of Zanalpha
1. Procedural sedation 2. Short onset (5-15min) 3. Short duration (30-45 min) 4. CV stability / parameters maintained at more acceptable levels
89
What drug is typically used to reverse Xylazine
Yohimbine
90
What drug do you avoid using in camelids due to adverse effects?
Tolazoline
91
Which drug has a higher alpha 2 : alpha 1 selectivity so indicated for the reversal of medetomidine and dexmedetomidine
Atipamezole
92
The concentration of ____ was formulated so that the volume of injectate is the same (mL for mL) as the dose of dexmedtomidine given
Atipamezole
93
Atipamezole is always given?
IM - effects seen within 5 mintues - Because it work so fast DONT give IV
94
Which class of drugs has many potential uses such as - Centrally acting muscle relaxants - anti-anxiety effects - Treatment of active seizures - Used during anesthesia
Benzodiazepines
95
What is the MOA of Benzodiazepines
Enhances the activity of the CNS inhibitory neurotransmitter gamma aminobutyric acid (GABA) by binding to a specific site on the GABAa receptor - which opens chloride channels and hyperpolarizes the membrane
96
What are the effects of Benzodiazepines
- Reduces sympathetic output - Minimal Sedation - Muscle relaxation - Antiseizure effects - Minimal cardiovascular and respiratory effects - No analgesia
97
98
Which drug must be formulated in propylene glycol to make drug soluble. So rapid IV administration can cause bradycardia, hypotention or apnea
Diazepam
99
What is the duration of Diazepam
Metabolized in liver and duration of action is 1 to 4 hours - dirty drug
100
What is the paradoxial effect with Diazepam
Paradoxical excitement and aggression can occur
101
Which drug is water insoluble, so do NOT give IM
Diazepam
102
Which drug is water soluble so you can give IM, IV, or via mucus membranes
Midazolam
103
______ is more potent than Diazepam
Midazolam
104
Which drug is metabolized in the liver, but metabolites are inactive (unlike diazpam). So shorter acting with less risk of accumulation
Midazolam
105
T/F: Midazolam is the better choice for sick, debilitated or older patients
true
106
What paradoxial effect may Midazolam have?
Excitement and aggression can occur
107
Which drug is fine for a certain population of patients but dont count on using it for an otherwisw healthy, normal patient
Midazolam
108
What drug causes excitation instead of sedation and now you have to restrain a cat who is both high and aggressive
Midazolam
109
Which drug will rapidly reverse all effects of Benzodiazepines - Expensive - Occasionally needed to reverse sedative and or dysmoprhic effets of benzodiazepines in the recovery period, during CPR or if the liver metabolism is impaired - DO NOT give to an epileptic patient
Flumazenil
110
Which class of drugs are coupled to G protein receptors that ultimately decrease conducatance through calcium channels and open inward potassium channels = hyperpolarization of membranes and decreased propagation of action potentials
Opioids
111
What is MOA of Opioids
Reversible combination with one or more receptors (mu, kappa, and delta) in the brain and spinal cord
112
Where are Opioids metabolized
In the liver and the metabolites of some drugs have analgesic properties
113
What are the CNS effects of Opioids?
- Sedation - Euphoria - Dysphoria
114
Which drug class has respiratory effects inluding - depression of the respiratory center response to hypercapnia and hypoxemia - cough suppression - Panting
Opioids
115
What effects do Opioids have on the cardiovascular system
Bradycardia
116
GI effects of which drugs include - vomiting - defectation - salivation - decreases gastric emptying time - ileus - vomiting is uncommon in painful animals - Morphine is the only opioids to cause these effects
Opioids
117
which species has miosis and which has mydriasis on opioids
Miosis = dogs Mydriasis = cats
118
Which drug has a high affinity for mu receptors, but some affinity for delta and kappa receptors - Hydrophilic compared to other Opioids so longer duration of action than lipophilic Opioids
Morphine
119
Morphine - Can give IV = _______ release and subsequent hypotension
Histamine
120
What is the duration of Morphine
4-6 hours - Dose dependent MAC sparing effect
121
Which drug is semi-synthetic pure mu agonist with similar properties to morphine (EX: hydrophilic)
Hydromorphone
122
Which drug is 5-10x more potent? - Morphine - Hydromorphone
Hydromorphone is more potent
123
Hydromorphone is dose dependent analgesia, so how can it be administered?
IV, IM, SQ - Less likely to vomit if given IV
124
What is the duration of action for Hydromoprhone
4-6 hours (for acute surgical pain, lasts about 3-4 hours)
125
When giving hydromorphone, which animals are reported to present with hyperthermia.
Cats - but occurs with other Opioids
126
Which drug is a synthetic pure mu agonist that is 100x more potent than morphine
Fentanyl
127
What is the duration of Fentanyl
Fast onset (1-2 min) and short duration (around 30 min) due to lipophilicity - Given IV bolus, followed by a continiouse rate infusion
128
Which drug is half as potent as Fentanyl
Remifentanil
129
Which drug is unique because it is metabolized by nonspecific esterases that occur in the body (mainly skeletal muscle). This leads to clinical advantage of extremly rapid clearence rate that is not dependent on liver or kidney function
Remifentanil
130
Which drug requires a CRI due to rapid clearence. Recovery occurs 3-7 minutes after discontinuation of CRi, so could be useful in situations in which intense analgesia is nedded for a short time period
Remifentanil
131
Which drug is a synthetic pure mu agonist with similar potency to morphine, but causes less sedation and more dysphoria
Methadone
132
Which drug is least likely of a u-agonist opioids to cause vomiting
Methadone
133
Methadone is a ______ receptor antagonist and _______ reuptake inhibitor, which could improve analgesia and help prevent development of tolerance
NMDA serotonin
134
What is the duration of Methadone
2-6 hours
135
What is one of the most used opioids?
Butorphanol
136
Which drug is a mixed agonist - antagonist (agonist at kappa receptor and parial mu receptor against OR considered an antagonist at mu)
Butorphanol
137
Which drug is used for mild to moderate visceral pain, that is not effective for severe or orthopedic / dental pain
Butorphanol
138
Which drug has mild sedation and anti-tussive effects; less respiratory depression than pure mu agonist "celling effect"
Butorphanol
139
What is the duration of Butorphanol
30 min to 2 hours
140
Which drug can be used to reverse sedative or respiratory effects of pure mu agonist
Butorphanol
141
Which drug is a partial mu agonist and an antagonist at kappa receptors
Buprenorphine
142
Which drug is not adequate for severe pain + does not provide much analgesia
Buprenorphine
143
Buprenorphine has a higher receptor affinity and can displace ___________ agonist, and makes it difficult to antagonize
Pure mu
144
In order to cause a response similar to full mu agonist, ________must occupy a higher number of receptors
Buprenorphine
145
What is the duration for Buprenorphine
Long duration of action (4-8 hours, maybe 12 hours depending on dose), but slower onset of about 30 minutes to an hour after IV administration
146
How can Buprenorphine be administered
IV, IM and some SQ but can also be given via oral transmucosal route in cats
147
Simbadol is a brand of which drug that is for SQ injectable use in cats for 24 hour duration of surgical pain control
Buprenorphine injection
148
T/F: Simadol is FDA approved in cats?
true
149
Which drug was approved for use by the FDA in 2022 to help with post-op pain control up to 4 days in cats - adminsiter transdermally - risk of accidental exposure, so wear gloves to apply
Transdermal buprenorphine
150
Which drug is used to reverse pure mu and mixed agonist/antagonists (ex: butorphanol) because it has a high affinity for mu and kappa receptors but no intrinsic activity
Naloxone
151
What is the duration of Naloxone
Rapid onset (1-2 min) and lasts 30-60 min
152
Extra
153
What is the term for A state of CNS depression and analgesia produced by the combination of a tranquilizer or sedative and analgesic drug
Neuroleptanalgesia - The patient may or may not remain conscious * Useful for premedication or for short medical or surgical procedures * Be aware that bradycardia and respiratory depression can occur * Typically, the dose of each drug can be lowered due to synergism
154
The follow are examples of? * Acepromazine + opioid * Benzodiazepine + opioid * Alpha2-agonist + opioid * Example: 20 mcg/kg Dexmedetomidine + 0.2 mg/kg Butorphanol + 5 mg/kg ketamine IM produces heavy sedation to anesthesia in cats having castration performed (this is called “Kitty Magic” in some practices) * For dental or standing procedure in a horse: detomidine 40 mcg/kg IV + morphine 0.3 mg/kg IV
Neuroleptanalgesia
155
Do we have to be careful providing Anesthesia for obese or normal sized pt's
Obese
156
Opioids and propofol may depress ventilation or cause apnea so monitor _____, atrial blood gases and be ready to provide ______ while giving anesthesia for obese patient
ETCO2 ventilation - Continue oxygen in recovery and keep intubated until patient can maintain airway - reduce volume of drugs given via epidural route
157
Avoid what type of agonist if possible to due cardiovascular depression while giving anesthesia for obese patient
A2 agonists