Final Exam Flashcards

1
Q

The first-line for general immunosuppression is typically

A

High dose glucocorticoids

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2
Q

This drug is ~7-8x more potent than Prednisone

A

Dexamethasone

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3
Q

Side effects from steroids

A

PU, PD, and panting

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4
Q

May be used as adjunctive therapy (to reduce amount of glucocorticoid needed) or as solitary therapy for certain diseases.

A

Other immunosuppressive drugs

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5
Q

Targets for immunosuppressive drug action

A

Antimetabolites and T-cell inhibitors

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6
Q

Impair nucleic acid synthesis (DNA) particularly in rapidly dividing
immune cells, and can block signaling on T-cells

A

Antimetabolites

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7
Q

This antimetabolite is given orally and should not be used in cats due to toxicity in the liver and bone marrow

A

Azathioprine

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8
Q

This antimetabolite is less commonly used, given orally, and often reserved for immune disease unresponsiveness to other therapies

A

Mycophenolate mofetil

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9
Q

This antimetabolite is often started with prednisone for difficult immune diseases

A

Azathioprine

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10
Q

This antimetabolite is administered orally and has relatively few side effects

A

Leflunomide

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11
Q

T-cell inhibitors

A

Cyclosporine and Tacrolimus topical

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12
Q

Atopica, Neoral, and Sandimmune are all bioequivalent

A

FALSE, Sandimmune isn’t bioequivalent to the other two

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13
Q

Topical used in management of dermatologic dz and

perianal fistulas.

A

Tacrolimus topical

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14
Q

A polypeptide that blocks cyclophilin/calcineurin which reduces T-cell activation & response, inhibits production of various cytokines to alter function of other WBCs.

A

Cyclosporine

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15
Q

Used topically on eye to treat keratoconjunctivitis sicca (KCS), used systemically to treat perianal fistules, or as an adjunct with glucocorticoids for other immune diseases

A

Cyclosporine

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16
Q

Tacrolimus topical has a slightly different target than Cyclosporine but essentially the same mechanism of action

A

TRUE

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17
Q

Have a relatively more narrow therapeutic index than other drugs and may require special handling

A

Cancer chemotherapy drugs

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18
Q

When handling chemo should you wear protective equipment?

A

Yes. Gloves, mask, gown

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19
Q

Where the cancer started

A

Primary cancer

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20
Q

Foci of cancerous cells distant from the original neoplasm

A

Metastases or “mets”

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21
Q

Is it possible to find mets without knowing where the primary cancer is?

A

Yep

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22
Q

Complete eradication of the cancer

A

Cure

  • Although this is sometimes possible, it is rarely the goal of therapy in veterinary oncology.
  • Cures often involve extremely aggressive treatment protocols
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23
Q

Decrease in or disappearance of signs and symptoms of cancer

A

Remission

  • Can be partial or complete
  • May be undetectable by available tests but it is not gone completely
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24
Q

Treatment aimed at preserving the quality of life of the patient without specific focus on prolongation of life

A

Palliative care

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25
Q

Palliative care when the decision has been made to cease life- extending treatment and the patient’s further life expectancy is short

A

Hospice care

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26
Q

Drug that is capable of causing tissue necrosis when extravasated

A

Vesicant

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27
Q

Administration of the drug outside of the blood vessel

A

Extravasation

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28
Q

What does BAG stand for and which do we not worry about as much in veterinary medicine?

A

Bone marrow, Alopecia, GI

We don’t really worry about alopecia

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29
Q

Most common of the adverse effects of chemo dugs

A

Gastrointestinal signs

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30
Q

Are antiemetics used before or during treatment when nausea is expected?

A

Yes

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31
Q

Lowest neutrophil count

A

Nadir

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32
Q

If neutropenia is severe what do you do?

A

Prophylactic antibiotics may be started

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33
Q

What kinds of dogs show more hair loss?

A

Dogs with continuously growing coats (poodles, terriers, Old English sheepdogs)

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34
Q

How do cats demonstrate alopecia?

A

Whiskers may fall out

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35
Q

Systemic adverse event that can be life-threatening and occurs
when there is a high tumor burden and treatment causes massive cell death and release of intracellular substances from the dying cancer cells

A

Acute tumor lysis syndrome

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36
Q

To reduce resistance developing in the cancer cell population and minimize toxicity to the patient

A

Multi-drug chemotherapy protocol

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37
Q

Differs from traditional protocols in that lower doses of drugs are given over longer periods of time

A

Metronomic chemotherapy

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38
Q

Dilation of the pupil

A

Mydriasis

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39
Q

Constriction of the pupil

A

Miosis

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40
Q

Most common reasons for using ophthalmic drugs

A
Dilation/constriction of the pupil
Decrease aqueous fluid production or IOP
Increase tear production
Decrease inflammation
Treat infection
Analgesia
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41
Q

What route of administration would you use to reach the anterior portion of the eye?

A

Topical

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42
Q

What route of administration would you use to reach the posterior portion of the eye?

A

Systemic

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43
Q

Give one drop at a time and then wait ____ and then give the next drop

A

5 minutes

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44
Q

Pupil dilation and constriction are controlled by the actions of

A

The PSNS and SNS

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45
Q

Direct acting parasympathomimetic, causes miosis that lasts about 2-6 hours, commonly used to localize parasympathetic lesions to the iris sphincter.

A

Pilocarpine

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46
Q

Pilocarpine is used to treat glaucoma and dry eye that is due to neurogenic causes.

A

FALSE. Uncommonly used to treat either

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47
Q

Indirect acting parasympathomimetics that increase uveoscleral drainage for up to 48 hours

A

Demecarium and Physostigmine

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48
Q

Indirect acting parasympathomimetic uncommonly used as a glaucoma preventative

A

Demecarium

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49
Q

Indirect acting parasympathomimetic that readily crosses the BBB

A

Physostigmine

-Not commonly used systemically, be cautious of the amount of systemic absorption in small patients

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50
Q

Indirect acting parasympathomimetic that causes miosis that lasts for a long time (>12 hours)

A

Echothiophate

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51
Q

Will cause paralysis of the iris sphincter muscle and ciliary body – leading to potent mydriasis

A

Blocking the PSNS

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52
Q

Direct acting parasympatholytic that causes mydriasis and cycloplegia. Onset of ~1hr which can last 120+ hours

A

Atropine

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53
Q

Direct acting parasympatholytic that basically acts the SAME way as Atropine but has a faster onset (~15-30 mins) and shorter duration (~3-12 hours)

A

Tropicamide

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54
Q

Used as a mydriatic/cycloplegic to reduce pain associated with uveitis and may be used to break up/prevent synechiae when there is inflammation of the eye

A

Atropine

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55
Q

Cycloplegia is a major issue in what species?

A

Horses

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56
Q

What can be the issue with giving atropine to cats?

A

Bitter taste

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57
Q

Tropicamide is less bitter than atropine but still may cause hypersalivation in cats

A

TRUE

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58
Q

Atropine and Tropicamide should be used in primary glaucoma

A

Figgity figgity FALSE

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59
Q

These drugs also cause decreased production of aqueous humor (by reducing cAMP levels) and are sometimes used for that purpose as adjunct therapy in the management of glaucoma

A

Adrenergic agents

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60
Q

Direct acting a1 agonist that will cause mydriasis in the dog but can take some time to do so and is not very effective for pupil dilation in cats, horses, or cattle. It is used perioperatively for some surgeries to reduce local bleeding (vasoconstriction) and used sometimes in the diagnosis and localization of sympathetic lesions.

A

Phenylephrine

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61
Q

Nonselective beta-adrenergic antagonist thought to inhibit cAMP production leading to decreased aqueous humor formation, though there may also be some effect on Na/K/ATPase which also
reduces aqueous production. Often used in the chronic management of glaucoma. May cause miosis but not potent. Bradycardia could be seen if there is sufficient systemic absorption

A

Timolol

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62
Q

These block the carbonic anhydrase enzyme which results in decreased formatin of bicarbonate in the non-pigmented ciliary epithelium

A

Carbonic anhydrase inhibitors

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63
Q

Can be used topically or systemically in the management of glaucoma, however topical usage will reduce the potential for systemic adverse effects.

A

Carbonic anhydrase inhibitors

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64
Q

This CAI is effective in dogs and cats (less so in horses). It may cause more stinging than brinzolamide

A

Dorzolamide

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65
Q

This CAI is not effective in cats

A

Brinzolamide

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66
Q

These agents are analogs of Prostaglandin F which very selectively stimulate Prostaglandin F receptors in the eye to increase uveoscleral outflow of aqueous which reduces IOP. Very potent in reducing IOP in dogs but have questionable efficacy in cats and horses. Qork rapidly (within 30-120 minutes) and are synergistic with other anti-glaucoma medications. Adverse effects include miosis, so they should not be used in anterior lens luxation. Prostaglandins may exacerbate ocular inflammation.

A

Prostaglandin analogs

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67
Q

The most commonly used prostaglandin analog

A

Latanoprost

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68
Q

Most commonly needed to treat KCS and some immune-mediated corneal diseases

A

Immunosuppression of the eye

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69
Q

Typically the ‘first line’ for treatment of chronic immune-mediated ophthalmic diseases. Act by inhibiting T-lymphocytes. Longterm (or lifelong) therapy may be necessary. Accumulate in the corneal stroma and also penetrate the conjunctiva to be taken up into the lacrimal gland. Cause local immunosuppression so are contraindicated in the face of active infection. Avoid repeated contact with skin (of the person administrating the drug).

A

Cyclosporine

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70
Q

Has the same mechanism but possibly different receptor sites than Cyclosporine and sometimes works from some patients non-responsive to Cyclosporine therapy. Generally reserved as a second-line of therapy.

A

Tacrolimus

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71
Q

Inflammation in the anterior portion of the eye can be reduced with the use of

A

Glucocorticoids or NSAIDs

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72
Q

Provide more potent anti-
inflammatory effects than NSAIDs, however they also are more likely to impair healing and immune response to infection. Should NOT be used in the face of active infection or corneal ulcers. Use with caution in cats who may have chronic herpesvirus infx

A

Glucocorticoids

-commonly used agents: prednisolone acetate, dexamethasone sodium phosphate and hydrocortisone

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73
Q

Penetrates into the anterior chamber and so is better for treating anterior uveitis

A

Prednisolone acetate

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74
Q

Does not penetrate as well and so may be better for treating corneal inflammation

A

Dexamethasone sodium phosphate

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75
Q

Commonly combined in ‘triple antibiotic’ mixtures

A

Hydrocortisone

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76
Q

These drugs work through inhibition of COX-2 but may have some anti-COX-1 activity as wel. Used to treat ocular inflammation, particularly in situations where glucocorticoids are contraindicated.

A

NSAIDs

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77
Q

Two commonly used topical ophthalmic NSAIDs

A

Flurbiprofen and Diclofenac

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78
Q

Rare anaphylactic reaction in some cats to

A

Polymyxin B or Bacitracin

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79
Q

Topical ophthalmic antiviral agent

A

Gancyclovir

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80
Q

Systemic ophthalmic antiviral agent

A

Famcyclovir

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81
Q

Ophthalmic antifungal agent

A

Natamycin

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82
Q

Ophthalmic topical anesthetic, typically used to decrease corneal sensation to allow diagnostic evaluation.

A

Proparacaine

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83
Q

Inhibitor of appetite

A

Serotonin (5-HT1)

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84
Q

Stimulants of appetite

A

Norepinephrine (alpha-2)
Dopamine (D1 receptors)
GABA (by inhibiting the satiety center)

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85
Q

These drugs work by stimulating GABA which inhibits the satiety center to increase appetite, more effective in cats than dogs, generally useful for short term only, and most common side effect is sedation

A

Benzodiazepines (Diazepam, Midazolam)

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86
Q

Diazepam is typically given IV and Midazolam is given IM

A

TRUE

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87
Q

Oral use of this drug can cause idiosyncratic hepatotoxicity in cats

A

Diazepam

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88
Q

Appetite stimulation is observed at sub-hypnotic doses though the mechanism is not well understood but may involved stimulation of GABA and inhibition of 5-HT1. Given IV, provides a very short term increase in appetite.

A

Propofol

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89
Q

Repeated doses of this drug in cats can cause oxidative RBC injury and Heinz body anemia has been observed when it is used daily for >5 days

A

Propofol

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90
Q

Inhibit the satiety center by blocking 5-HT1 receptors

A

Serotonin antagonists

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91
Q

This appetite stimulant is effective in cats, not so much in dogs. Used orally, well absorbed, generally takes 2-3 days to see a response. Most common side effect is sedation.

A

Cyproheptadine

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92
Q

This appetite stimulant is a tricyclic antidepressant that blocks both 5-HT1 and 5-HT2 receptors and also increases NE
centrally. Used in dogs more than cats.

A

Mirtazapine

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93
Q

Drugs that induce emesis

A

Emetics

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94
Q

Drugs that suppress emesis

A

Antiemetics

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95
Q

Dogs have fewer Dopamine and Histamine receptors in the CRTZ, but more alpha-2 and serotonin receptors.

A

FALSE, cats

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96
Q

Receptors in the CRTZ that can stimulate vomiting

A

Serotonin (5-HT3)
Adrenergic (alpha-2)
Dopamine (D2)
Metabolic (toxins)

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97
Q

Most common peripherally acting emetic

A

Hydrogen peroxide 3%

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98
Q

Should you use Hydrogen Peroxide in cats?

A

Hell nah, higher risk of mucosal damage

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99
Q

Cause direct irritation to the oropharynx and gastric lining leading to stimulation of the emetic center and vomiting.

A

Peripherally acting emetics

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100
Q

Stimulate the vomiting center and tend to be more effective than peripheral emetics. Ideally used with toxin ingestion and vomiting needs to occur several times.

A

Centrally acting emetics

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101
Q

Stimulates dopamine receptors in the CRTZ, can be used by all routes (including conjunctival sac), more effective in dogs (efficacy ~10% in cats), overdose can cause respiratory depression but can be reversed by Naloxone

A

Apomorphine

102
Q

Alpha-2 agonists, more effective emetics in cats because they have fewer dopamine receptors but more alpha-2 receptors than dogs.

A

Xylazine or Dexmedetomidine

103
Q

Labeled for prevention of motion sickness in dogs (oral) and treatment of acute vomiting in dogs (oral or SC) and cats (SC). The injection stings, can be reduced by refrigeration.

A

Maropitant citrate

104
Q

Dopamine antagonist that also blocks 5-HT3 receptors (at higher doses) and is also a prokinetic. Generally more potent than other dopamine antagonists like the Phenothizines and is used more commonly. Antagonizes apomorphine induced emesis.

A

Metoclopramide

105
Q

Act on serotonin receptors centrally and peripherally, initially used for chemotherapy related nausea, more potent than Metoclopramide, most commonly given as an injectable but oral formulations are available.

A

Ondansetron

106
Q

The original H2 blocker, has a lower potency than others in this group (H2 blockers) and duration of action may be less. Does not have an effect on GI motility. Also, it inhibits hepatic microsomal enzymes therefore a significant number of drug-drug interactions.

A

Cimetidine

107
Q

This H2 blocker is more potent than Cimetidine and in canines it acts as a mild prokinetic. Microsomal enzyme inhibition is far less than with Cimetidine so fewer clinically relevant interactions.

A

Ranitidine

108
Q

This H2 blocker has a similar potency and possibly slightly longer duration than Ranitidine. Does not have any effect on GI motility. Very few drug-drug interactions.

A

Famotidine

109
Q

More potent than H2 blocker class, raise gastric pH by irreversibly inhibiting the H+/K+/ATPase proton pump which results in decreased hydrochloric acid production

A

Proton Pump Inhibitors

110
Q

PPI used orally. Prilosec (human formulation) and Gastrogard (equine formulation)

A

Omeprazole

111
Q

A prostaglandin analog. Increases mucus and sodium bicarbonate secretion, stimulates epithelialization of the mucosa and mucosal blood flow resulting in ulcer healing (COX-1). Used orally to treat NSAID induced gastric ulcers.

A

Misoprostol

112
Q

A sucrose-aluminum compound, given orally. Binds to the ulcer site and protects it against acid, pepsin and bile. Requires and acidic environment to bind to mucosa. May also stimulate protective prostaglandins and antioxidants and increase mucosal blood flow. Poorly absorbed, acts locally, and has few side effects.

A

Sucralfate

113
Q

Timing of dosing is important with this drug. It can impair the absorption of other drugs so it’s recommended to wait 2 hours after administration before giving other oral medications.

A

Sucralfate

114
Q

Oral antacids

A

Aluminum, Magnesium and Calcium salts

115
Q

Inactivates pepsin and binds to bile salts, may stimulate prostaglandins

A

Aluminum hydroxide

116
Q

All levels of the GIT are muscular and move

A

True

117
Q

Movement of the gut wall

A

Motility

118
Q

Time it takes for material to get from point A to point B within the GIT

A

Transit time

119
Q

Increased GI motility

A

Acetylcholine (parasympathetic)
Serotonin (5-HT3)
Peptides (motilin)

120
Q

Decreased GI motility

A

Norepinephrine (sympathetic)
Dopamine (suppresses Ach)
Endorphins (opioids)

121
Q

It stimulates gastric motility and relaxes the pyloric sphincter (improved gastric emptying), peristalsis in the duodenum and jejunum (improved intestinal transit time) as well as increasing LES pressure. It has minimal effect on colonic motility. Commonly used in small animals. Relatively short duration of action

A

Metoclopramide

122
Q

5-HT4 receptor agonist in enteric neurons to indirectly increase parasympathetic input. Also block dopamine, but to a lesser extent than metoclopramide does. Available by compounding and has a prokinetic effect on all parts of the GI tract, including the colon in equines. It is often used to treat megacolon in cats. Does not stimulate GI secretions.

A

Cisapide

123
Q

H2 receptor antagonist and also has some cholinergic activity – most clinically apparent in the canine. Stimulate GI motility, increase LES tone and gastric emptying, and increase intestinal and colonic motility.

A

Ranitidine

124
Q

Used in humans and has been investigated in equines for reducing postoperative ileus.

A

Lidocaine

125
Q

Diarrhea is associated with hypomotility

A

False, hypermotility

126
Q

These opioid drugs work on central and peripheral opioid receptors to inhibit propulsive motility, increase segmental motility, decrease intestinal secretion and inhibit the defecation reflex. Used in acute and sometimes chronic, nonspecific diarrhea. Should NOT be used in diarrhea due to bacterial causes.

A

Diphenoxylate and Loperamide

127
Q

This anti-diarrheal opioid has a faster onset, longer duration of action and greater efficacy

A

Loperamide

128
Q

This anti-diarrheal opioid crosses the BBB and thus has more side effects

A

Diphenoxylate

129
Q

These compounds are not absorbed systemically, they coat and protect the GI mucosa or physically bind with toxic compounds locally in the gut lumen.

A

GI protectants and adsorbents

130
Q

Commonly used nonspecific GI protectants/coating agents

A

Magnesium trisilicate and hydrated aluminum silicate

131
Q

A special adsorbent use frequently in toxicosis. Comes with or without sorbitol

A

Activated charcoal

132
Q

Possesses antimicrobial, anti-secretory and anti-inflammatory processes. Can cause toxicity in cats. Use of this drug will turn the patient’s stool very dark.

A

Bismuth subsalicylate

133
Q

These drugs promote defecation by increasing the frequency of defecation or the fecal volume, or by changing the consistency.

A

Laxative and cathartic drugs

134
Q

Acts as mechanical or lubricant laxatives, or fecal softeners. Mineral oil and Laxatone are examples

A

Emollient laxatives

135
Q

These absorb water and swell, stimulating reflexive peristaltic movement in the GIT. Psyllium and prunes are examples

A

Simple bulk laxatives

136
Q

These are nonabsorbed or poorly absorbed compounds that attract water into the intestinal lumen by osmotic pressure and reflexively stimulate peristaltic activity. Sugar alcoholas (sorbitol) and polyethylene glycols (GoLYTELY) are examples

A

Osmotic cathartics

137
Q

These irritate the GI mucosa an stimulate peristaltic activity and increased secretions. Bisacodyl is an example

A

Irritant cathartic

138
Q

This extends the colon and can initiate the defecation reflex, it also introduces fluids to mix with the stool present in the colon. Plain warm water is an example

A

Enemas

139
Q

This type of enema should NOT be used in cats

A

Phosphate-containing enema

risk of toxicity

140
Q

Four steps of the nociception (pain) pathway

A

Transduction (peripheral tissue)
Transmission (via peripheral nerves)
Modulation (in the spinal cord)
Perception (in the brain)

141
Q

Cause reversible blockade of transmission in peripheral nerves or spinal cord, usually to stop pain signals

A

Local anesthetics

142
Q

Most commonly used local anesthetic in veterinary medicine. Used as a LA and also systemically. Banned in Europe for food producing animals. Rapid onset (~5 min) and medium duration (~40-60 min) (longer duration if given with epinephrine). Cats are more sensitive than dogs, sheep may be more sensitive than other livestock.

A

Lidocaine

143
Q

Systemically used as a Class 1B antiarrhythmic, a CRI as an adjunctive analgesic, and as a CRI for GI prokinetic/anti-inflammatory (to treat/prevent post-op ileus in horses)

A

Lidocaine

144
Q

Frequently used LA for local infiltration, nerve blocks, and epidurals. Potent with a slow onset (~20 min), duration up to 8 hours. Most cardiotoxic of the LAs

A

Bupivacaine

145
Q

Used for diagnostic nerve blocks in horses. Similar to lidocaine but less irritating.

A

Mepivacaine

146
Q

Won’t be used as a LA but it is in some Penicillin G preparations. Toxic, can cause CNS stimulation – excitement, seizures. Don’t give IV.

A

Procaine

147
Q

Used topically (ophthalmic formulation), allows for corneal & conjunctival manipulation. Rapid onset (~30s) and short duration (~10-20 min)

A

Proparacaine

148
Q

These prevent inflammation by inhibiting cyclooxygenase (COX) enzymes (and are not steroids)

A

Nonsteroidal anti-inflammatory drugs (NSAIDs)

149
Q

NSAIDs are weak bases

A

N to the O!

They are weak acids

150
Q

Constitutive, physiologic production of prostaglandins that play an important role in normal homeostasis.

A

COX-1

151
Q

Inducible, prostaglandins produced during inflammation.

A

COX-2

152
Q

Involved with GI mucosal maintenance & vasodilation in kidney in response to decreased blood flow.

A

PGE 1

153
Q

For routine analgesia/anti-inflammatory uses which COX is generally preferable?

A

COX-2 selectivity

154
Q

Should you use NSAIDs and steroids together?

A

No! Don’t be stupid, make good choices.

155
Q

Generally good absorption PO or IM. Highly protein bound (95-99%). Provide analgesia whether inflammation present or not.

A

NSAIDs

156
Q

Large animal NSAID. Given PO, IV, IM (?). Labeled only for IV use in cattle, IM in swine. Muscle necrosis has been reported with IM administration, do NOT use IM in equines. Don’t use in small animals. Used more so for visceral pain.

A

Flunixin Meglumine

157
Q

Used commonly in horses, banned in dairy cattle. Tends to be used for musculoskeletal pain. Give PO or IV but do NOT give IM/SC (very irritating, sloughing/necrosis can be seen). Can mask lameness - withdrawal time may be required for racing animals.

A

Phenylbutazone (“Bute”)

158
Q

Preferential COX-2 NSAIDs

A

Carprofen
Meloxicam
Deracoxib

159
Q

Commonly used in small animal medicine as analgesics and anti-inflammatory agents. Available in a variety of oral options and injectable.

A

Deracoxib

160
Q

Approved for SINGLE injection use in cats

A

Meloxicam

161
Q

Selective COX-2 NSAIDs

A

Firocoxib and Robenacoxib

162
Q

Oral paste for horses, chewable tablets for dogs

A

Firocoxib

163
Q

The first NSAID approved for multiple doses in cats

A

Robenacoxib

164
Q

Generally greater COX-2 selectivity will have fewer adverse effects

A

True dat

165
Q

If changing from NSAID to steroid

A

Sufficient washout period (typically 1-2 weeks)

166
Q

If changing from steroid to NSAID

A

Will need to wean the steroid, then have minimum 1 week washout period

167
Q

If changing between two different NSAIDs

A

Should still have washout – based on half-life or use a conservative default of 1 week.

168
Q

Weak μ agonist (opioid) but also serotonin and NE reuptake inhibitor, M1 antagonist . Generally used as an oral analgesic. May lower seizure threshold, avoid in epileptic patients.

A

Tramadol

169
Q

NMDA antagonist sometimes used as an adjunctive analgesic in small animals. Also an oral drug.

A

Amantadine

170
Q

Sometimes used for control on neuropathic pain. MoA involves altering calcium influx in neuronal cells. May cause sedation/ataxia, frequent dosing required. Do not use human oral liquid in dogs (contains Xylitol)

A

Gabapentin

171
Q

Anti-inflammatory & chondroprotective agents. Generally low toxicity, efficacy not always proven.

A

Glucosamine chondroitin
Polysulfated glycosaminoglycans (PSGAGs)
Pentosan polysulfate
Omega-3 fatty acids

172
Q

Induces a state of behavioral change wherein anxiety is relieved and the patient is relaxed although aware of their surroundings.

A

Tranquilizer

173
Q

Induces a state characterized by CNS depression and

drowsiness, decreased awareness of surroundings.

A

Sedative

174
Q

Induces sleep

A

Hypnotic

175
Q

Induces stupor bordering on general anesthesia

A

Narcotic

176
Q

Loss of sensation in a circumscribed body area.

A

Local/Regional anesthesia

177
Q

Drug-induced unconsciousness characterized by controlled, reversible depression of the CNS with analgesia. The patient cannot be aroused. Sensory, motor and autonomic reflexes are reduced.

A

General anesthesia

178
Q

Drugs that dissociate the thalamocortic and limbic systems resulting in a catatonic state where the eyes remain open and swallowing reflexes remain functional. Skeletal muscles maintain tone.

A

Dissociative anesthesia

179
Q

Main inhibitory neurotransmitter

A

GABA

180
Q

Ryanodine receptor antagonist, inhibits calcium release from the SER to cause muscle relaxation - does not generally affect respiratory muscles. Used for treatment of malignant hyperthermia primarily. Injectable is not compatible with saline of D5W.

A

Dantrolene

181
Q

Centrally acting muscle relaxant (on the spinal cord) labeled for use in equines, used off-label in cattle. Used as an injectable, typically as a 5% solution for IV infusion. Onset of action is ~2 min and duration of action is 10-20 min. Depresses nerve impulses in the spinal cord, brainstem, and subcortical areas of the brain to cause centrally mediated generalized muscle relaxation, sedation +/- analgesia.

A

Guaifenesin (GG/GGE)

182
Q

If >10% solution is used thrombophlebitis and/or hemolysis can be seen.

A

Guaifenesin (GG/GGE)

cattle are more sensitive to hemolysis than horses

183
Q

Centrally acting muscle relaxant, chemically similar to Guaifenesin - works on the spinal cord. Approved for dogs, cats and horses. Generally not used with anesthesia, typically used to reduce muscle spasms. Adjunct therapy for medical management of IVDD and supportive therapy for tremorgenic toxicoses.

A

Methocarbamol

184
Q

Used primarily in veterinary medicine for sedation but a few drugs in the class are more suitable for other indications. Drugs in this class work primarily as dopamine receptor antagonists.

A

Phenothiazines

185
Q

Good sedation, moderate muscle relaxation, NO analgesia, and hypotension is a potential effect.

A

Phenothiazines

186
Q

Epinephrine stimulates α1, α2, β1 and β2 so if α1 is blocked then β2 mediated vasodilation is unopposed leading to hypotension. What is this called?

A

Epinephrine reversal

187
Q

Dogs with ABCB1 gene mutation may have a decreased response and shorter duration of effect with phenothiazines.

A

False. They have a pronounced response with a longer duration of effect.

188
Q

Phenothiazines have a low oral availability in dogs (~20%)

A

True

189
Q

The most important phenothiazine for the purposes of sedation. Frequently used along with opioids for restraint or anesthetic premedication. Hypotension is the predominant adverse effect, boxers are particularly sensitive to the CV effects and is not approved for use in food animals.

A

Acepromazine

190
Q

Acepromazine provides analgesia

A

False - provides NONE

191
Q

Potentiate GABA receptors. Bind to and activate benzodiazepine binding site on GABAa receptors to cause hyperpolarization of neurons.

A

Benzodiazepines

192
Q

Mild sedation (can potentiate other drugs), good muscle relaxation, NO analgesia, minimal cardiorespiratory effects at normal doses. Used as an anxiolytic, an anticonvulsant, and an appetite stimulant.

A

Benzodiazepines

193
Q

Prototypical benzodiazepine. High amount of propylene glycol so it should not be given IM (causes pain). Commonly used in anesthetic premedication or induction, also used for control of seizures (not chronic management). Avoid oral use in cats.

A

Diazepam

194
Q

IM version of diazepam

A

Midazolam

195
Q

Human approved benzodiazepine. Has a longer duration of action and hasn’t been associated with hepatic necrosis when given orally to cats.

A

Alprazolam

196
Q

Zolazepam

A

Benzodiazepine

197
Q

Reversal agent for benzodiazepines as a class.

A

Flumazenil

Not common that we need to reverse these drugs

198
Q

Commonly used in both large and small animal veterinary medicine. Act by agonizing a2 adrenergic and nonadregenergic receptors.

A

Alpha-2 agonists

199
Q

Very good sedation, good muscle relaxation, MILD analgesia, biphasic CV effects, mild respiratory depression (more issues in sheep) and can be used as an emetic in cats.

A

Alpha-2 agonists

200
Q

Humans can experience profound hypotension if inadvertently exposed to veterinary alpha-2 agonist drugs

A

True

201
Q

Ruminants are more sensitive than small animals, equines and swine are the least sensitive.

A

Xylazine

202
Q

Most commonly used alpha-2 agonist for small animals.

A

Dexmedetomidine

203
Q

Used in equines and cattle. Available as a sublingual gel for horses. May produce less profound sedation and be more suitable for standing procedures in large animals.

A

Detomidine and Romifidine

204
Q

Used to reverse the effects of alpha-2 agonists. Reversal with reverse ALL of the effects, including analgesia.

A

Alpha-2 antagonist

205
Q

The antagonist should be roughly matched to the agonist used.

A

True

206
Q

Less selective for a2:a1 and used when needed for reversal of xylazine

A

Yohimbine

207
Q

Highly selective for a2:a1 and is used to reverse dexmedetomidine

A

Atipamezole

208
Q

Agonists at opioid receptors (anything that can be displaced by naloxone)

A

Opioid

209
Q

Naturally occurring drugs (alkaloids) extracted from opium

A

Opiates

210
Q

Stupor bordering on general anesthesia

A

Narcosis

211
Q

Combination of a sedative with an analgesic (opioid) which results in synergistic effects

A

Neuroleptanalgesia

212
Q

Activate μ-opioid receptors completely

A

Full μ agonists

213
Q

Activate some opioid receptors, but not completely

A

Partial agonists

214
Q

Activate some opioid receptors and block others

A

Mixed agonist-antagonists

215
Q

Block all opioid receptors

A

Full antagonists

216
Q

Not a lot of sedation by themselves, not a lot of muscle relaxation, GREAT analgesia, respiratory depression effect.

A

Opioid agonists

217
Q

Excitation, sweating, rigidity, coma, and seizures

A

Serotonin syndrome

218
Q

Prototypical analgesic, onset 5-15 mins and last several hours, used in epidurals. Risk of histamine release, especially in dogs with IV use.

A

Morphine - full μ agonist

219
Q

Less histamine release, used IV in place of morphine, similar onset and duration as morphine

A

Hydromorphone - full μ agonist

220
Q

Potent, onset ~ 1 min and lasts ~30mins so suitable for CRI administration, available as a transdermal

A

Fentanyl - full μ agonist

221
Q

Very potent (4000-10,000x morphine). Used in wildlife, specialized training required and must have antagonists on-hand

A

Carfentanil/Etorphine - full μ agonist

222
Q

Semisynthetic partial μ agonist, will not see as much analgesia as a full μ agonist. Less apparent negative effects. Slower onset (~45 mins) and longer duration (up to 8 hours in cats) than morphine. More useful than other opioids for at-home analgesia, especially in cats where other options are limited.

A

Buprenorphine

223
Q

Synthetic κ agonist and μ antagonist. Approved as analgesic in cats, dogs, and horses and as antitussive in dogs. One of the more commonly used opioids in equine, used in SA to ‘partially’ reverse a full mu agonist.

A

Butorphanol

224
Q

Used to reverse the effects of opioids

A

Pure antagonists

225
Q

Competitive receptor antagonist used for reversal of opioid-
induced adverse effects. Rapid onset (minutes) and short duration (1-2h) - repeated doses may be needed until the opioid is gone. Will reverse the analgesic effects as well!

A

Naloxone

226
Q

Semisynthetic opioid, used orally as an antitussive. Human formulations may contain other drugs.

A

Hydrocodone

227
Q

Pros of injectable anesthetics

A

Rapid onset of anesthesia
Rapid control of the airway
IM injection may be possible Minimal equipment

228
Q

Cons of injectable anesthetics

A

Minimal control over waking Controlled substances

229
Q

What kind of a state do dissociative anesthetics produce?

A

Catatonic

230
Q

A barbiturate that is an IV anesthetic induction agent but not in North America because of ethical issues

A

Thipoental

231
Q

IV or oral barbiturate used to control refractory seizures or in seizure management. Sometimes used as a mild sedative.

A

Phenobarbital

232
Q

Barbiturate used primarily for euthanasia. Can be used to manage refractory seizures

A

Pentobarbital

233
Q

These potentiate GAGA, creating a dose-dependent CNS depression, and offer full anesthesia, moderate muscle relaxation, NO analgesia. Side effects can be apnea, hypotension and arrhythmias.

A

Barbiturates

234
Q

Full anesthesia, good muscle relaxation, NO analgesia. Side effects: respiratory depression, hypotension, and apnea on induction. Also used as an anticonvulsant. Will cause myotonia on induction.

A

Propofol

235
Q

Emulsion containing egg lecithin and soybean oil. One of the few white liquids than can go IV. Once opened must be discarded within 24h.

A

Propoflo

236
Q

Benzyl alcohol preservative. Once opened stable at room temp for 28 days. Not labeled for cats.

A

Propoflo 28

237
Q

Given IV only. Metabolism is rapid, allowing for repeated dosing/CRI. Widely distributed to all tissues (lipid soluble drug).

A

Propofol

238
Q

Neurosteroid which is an analog of progesterone. Does NOT bind to usual steroid receptors. Has similar pharmacokinetics to Propofol.

A

Alfaxalone

239
Q

It exists. It’s great for cardiac patients - for less stable cardiac patients because it has minimal CV or resp suppressant effects.. Can’t be used as a CRI because it causes adrenal suppression and contains a lot of propylene glycol.

A

Etomidate

240
Q

NMDA receptor channel blocker, inhibits activation by glutamate.

A

Dissociative anesthetics

241
Q

Major dissociative anesthetic

A

Ketamine

242
Q

Clinical manifestation of abnormal electrical activity in the brain

A

Seizure

243
Q

Seizures that occur intermittently over months to years

A

Epilepsy

244
Q

Seizures lasting 5min or longer, 2 or more discrete seizures without full recovery of consciousness in between.

A

Status epilepticus

245
Q

2 or more seizures over minutes to hours with full recovery in between

A

Cluster seizures

246
Q

First line for stopping a seizure because of high lipophilicty and rapid brain penetration. The most commonly used drug in this class to do so?

A

Benzodiazepines – Diazepam

247
Q

Potentiates GABA receptors. Long-acting barbiturate; controlled drug. Cytochrome p450 induction. Best choice drug for dogs and cat.

A

Phenobarbital

248
Q

A salt/chemical available as a powder with an unknown MOA but raises seizure threshold by competing with Cl- transport. Must use loading dose or it will take 8-9 weeks to reach effective levels. Avoid in cats (asthma) and not metabolized by liver – good for patients with hepatopathies.

A

Bromide

249
Q

Pyrrolidine derivative with an unknown MOA. Can be used as primary AED or add-on. Very safe with few side effects but expensive.

A

Levetiracetam

250
Q

Sulfonamide-base, dogs on enzyme inducers require 2x dosage, rapid CNS penetration, tolerance may develop.

A

Zonisamide

251
Q

Sympathetic GABA analog. Potentiates GABA; blocks Na channels. Usually used as an add-on, frequent dosing, oral solution contains xylitol (toxic in dogs) and sedation/ataxia with high doses.

A

Gabapentin