30 Equine Chemical Restraint & Analgesia

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Questions and Answers

In equine field procedures, what is the most critical differentiating factor when deciding between standing sedation and general anesthesia (GA)?

  • The economic constraints of the equine practice and client budget.
  • The preference of the veterinarian regarding personal workload and personnel required.
  • The availability of specialized equipment for recumbent recovery.
  • The primary goal of minimizing patient mortality risk associated with recovery. (correct)

Which scenario most accurately represents a clinical situation where standing sedation would be distinctly advantageous over general anesthesia in equine practice?

  • Conducting a prolonged and invasive arthroscopic procedure in a referral hospital setting.
  • Performing a complex colic surgery requiring full muscle relaxation and controlled ventilation.
  • Performing a castration on a young, healthy colt in a well-equipped surgical suite.
  • Managing a laceration repair in a fractious horse in a remote field location with limited assistance. (correct)

When selecting a sedative protocol for an equine patient undergoing a field procedure, which of the following considerations is paramount in ensuring both efficacy and regulatory compliance?

  • The ease of administration and rapid onset of action to expedite the procedure.
  • The personal preference of the veterinarian based on familiarity with specific sedative agents.
  • The potential for drug residues and adherence to regulations set by equine sport governing bodies. (correct)
  • The cost-effectiveness of the chosen sedative drugs to minimize client expenses.

Considering the principles of drug administration in equine sedation, why is intravenous (IV) catheter placement particularly emphasized when planning for a continuous rate infusion (CRI) of sedatives?

<p>To maintain consistent drug plasma concentrations and facilitate quick adjustments in infusion rates. (B)</p> Signup and view all the answers

Which of the following best explains why intramuscular (IM) administration of sedatives in horses may result in less predictable effects compared to intravenous (IV) administration?

<p>Variability in muscle blood flow and drug absorption rates from IM injection sites. (D)</p> Signup and view all the answers

Alpha-2 adrenergic agonists like xylazine and detomidine are frequently combined with opioids in equine sedation protocols. What is the primary rationale for this combination?

<p>To improve the quality of sedation and provide synergistic analgesia. (B)</p> Signup and view all the answers

Why are alpha-2 adrenergic agonists generally not recommended for sedation in foals less than 14 days old or in very sick foals?

<p>Due to potential for severe cardiovascular depression and paradoxical bradycardia. (A)</p> Signup and view all the answers

What is the most significant cardiovascular effect of alpha-2 adrenergic agonists in horses that necessitates careful monitoring during sedation?

<p>Initial hypertension followed by a more prolonged hypotensive phase and decreased cardiac output. (B)</p> Signup and view all the answers

Inadvertent intracarotid injection of alpha-2 adrenergic agonists in horses can lead to severe neurological signs. Which of the following best describes the primary concern associated with this complication?

<p>Excitement, disorientation, ataxia, collapse, and potentially seizures due to direct brain exposure. (B)</p> Signup and view all the answers

While atipamezole is considered a more selective alpha-2 adrenergic antagonist, its use for reversing xylazine or detomidine in horses is often reserved for emergency situations. What is the primary limiting factor for its routine use?

<p>Potential for severe side effects such as agitation, stress response, and fatalities. (A)</p> Signup and view all the answers

Acepromazine, a phenothiazine tranquilizer, is often used in equine practice. What is the primary mechanism of action that explains its tranquilizing effects?

<p>Blockade of dopamine receptors in the basal ganglia and limbic system. (A)</p> Signup and view all the answers

Why is acepromazine contraindicated or used with extreme caution in stallions intended for breeding purposes?

<p>It can cause irreversible penile prolapse due to relaxation of the retractor penis muscle. (B)</p> Signup and view all the answers

Acepromazine is known to cause vasodilation. While this can be beneficial in some contexts, in which of the following clinical scenarios would this vasodilatory effect be most undesirable and potentially harmful?

<p>In a horse with a low packed cell volume (PCV) or active bleeding. (A)</p> Signup and view all the answers

Benzodiazepines like diazepam and midazolam are often used in equine medicine. What is their primary mechanism of action in producing sedation and muscle relaxation?

<p>Facilitation of GABA's inhibitory neurotransmitter actions in the CNS. (D)</p> Signup and view all the answers

Why is midazolam often preferred over diazepam for intramuscular (IM) administration in horses, even though intravenous (IV) route is generally preferred for both?

<p>Midazolam is water-soluble and less likely to cause injection site irritation or pain than diazepam. (C)</p> Signup and view all the answers

Flumazenil is the antagonist for benzodiazepines. In what clinical scenario would the use of flumazenil be most critically indicated in an equine patient?

<p>To manage paradoxical excitation or prolonged sedation following midazolam administration. (A)</p> Signup and view all the answers

Opioids like butorphanol, morphine, and hydromorphone are used in equine analgesia. What is a common side effect associated with opioid use in horses, particularly when administered as a sole agent?

<p>Restlessness, agitation, and increased sympathetic nervous system activity. (B)</p> Signup and view all the answers

Local anesthetics like lidocaine and mepivacaine are sodium channel blockers. Why is their efficacy often reduced in inflamed tissues?

<p>The acidic environment of inflamed tissues impairs the ionization and nerve penetration of local anesthetics. (A)</p> Signup and view all the answers

When performing an epidural injection for analgesia in a horse, what is the anatomical landmark used to locate the correct intervertebral space for needle insertion?

<p>Between coccygeal vertebrae 1 and 2 (Co1-Co2). (C)</p> Signup and view all the answers

Why is the maximum volume of local anesthetic containing lidocaine or mepivacaine limited to 10mL in equine epidural analgesia, while larger volumes (20-40mL) can be used when not combined with sodium channel blockers?

<p>To minimize the risk of cranial diffusion of local anesthetic and potential hindlimb weakness or ataxia. (B)</p> Signup and view all the answers

In managing a horse with colic, xylazine is often chosen as a first-line sedative and analgesic. What is the most significant limitation of using xylazine alone for colic pain management that necessitates considering additional analgesic strategies?

<p>Its limited analgesic efficacy, particularly for severe visceral pain associated with colic. (C)</p> Signup and view all the answers

For choke management in horses, positioning the head as ventral as possible is recommended. What is the primary physiological rationale behind this positioning?

<p>To decrease the risk of aspiration pneumonia by promoting drainage of esophageal contents. (A)</p> Signup and view all the answers

In managing lacerations in horses, a combination of sedation, analgesia, and anti-inflammatory medication is often employed. What is the primary benefit of including an anti-inflammatory agent like phenylbutazone or flunixin meglumine in this protocol?

<p>To provide preemptive analgesia and reduce post-operative pain and inflammation. (D)</p> Signup and view all the answers

When performing a standing joint lavage in a horse, why might a combination of xylazine and butorphanol be preferred over detomidine and butorphanol in certain clinical situations?

<p>Xylazine has a faster onset of action than detomidine, allowing for quicker procedural initiation. (A)</p> Signup and view all the answers

In cast placement for equine limbs, the primary goal of sedation is to ensure the horse stands quietly for 30-40 minutes. Why is detomidine often chosen as the sedative agent in this scenario?

<p>Detomidine offers a longer duration of sedation compared to xylazine, minimizing the need for redosing. (B)</p> Signup and view all the answers

For standing enucleation in horses, a combination of xylazine, hydromorphone, and local anesthesia is recommended. What is the specific rationale for including hydromorphone in this protocol?

<p>To provide potent systemic analgesia to manage the intense pain associated with eye removal. (A)</p> Signup and view all the answers

In laparoscopic ovariectomy in horses, epidural analgesia is often used in addition to sedation and local anesthesia. What is the primary advantage of epidural analgesia in this procedure?

<p>To block pain transmission from the surgical site, reducing systemic analgesic requirements. (A)</p> Signup and view all the answers

In the example pain management protocol for extreme laminitis, several medications are listed. What is the primary rationale for including pentoxifylline in the treatment regimen for laminitis?

<p>To improve digital blood flow and microcirculation, counteracting the vasoconstrictive processes in laminitis. (B)</p> Signup and view all the answers

Gabapentin is included in the example pain management protocol for extreme laminitis. What is the primary mechanism by which gabapentin provides analgesia, particularly in chronic pain conditions like laminitis?

<p>Modulation of calcium channels and neurotransmitter release, particularly in neuropathic pain pathways. (A)</p> Signup and view all the answers

Omeprazole is listed in the example pain management protocol for extreme laminitis. What is the therapeutic rationale for including omeprazole in this context, considering it is a proton pump inhibitor?

<p>To prevent or treat gastric ulcers, a common complication in horses under stress and receiving NSAIDs. (A)</p> Signup and view all the answers

Acetaminophen is included in the multimodal pain management for extreme laminitis. What is the presumed primary analgesic mechanism of acetaminophen in horses?

<p>Central inhibition of COX enzymes, particularly COX-3, and modulation of descending serotonergic pathways. (A)</p> Signup and view all the answers

Fentanyl patches are utilized in the example laminitis pain management. What is the main advantage of using a transdermal fentanyl patch in managing chronic pain compared to intermittent bolus opioid injections?

<p>Transdermal patches deliver a continuous and sustained release of fentanyl, maintaining stable plasma drug levels. (C)</p> Signup and view all the answers

Domperidone is included in the laminitis pain management protocol. What is the intended pharmacological action of domperidone in this specific context?

<p>To inhibit prolactin secretion, which may have indirect benefits in managing certain endocrine aspects of laminitis. (D)</p> Signup and view all the answers

Phenylbutazone is a cornerstone NSAID used in equine medicine and is included in the example laminitis protocol and for laceration and joint lavage management. What is a major limitation or significant side effect associated with chronic or high-dose phenylbutazone use in horses?

<p>Gastrointestinal ulceration, particularly gastric and right dorsal colitis. (D)</p> Signup and view all the answers

In the context of equine sedation and analgesia, what does 'CRI' stand for, and what is its primary advantage over bolus administration for certain procedures?

<p>Continuous Rate Infusion; advantage is sustained drug plasma concentrations and effect. (C)</p> Signup and view all the answers

Considering the principles of equine anesthesia, what is 'MAC' an abbreviation for in the context of inhalant anesthetics, and what does it clinically represent?

<p>Minimum Alveolar Concentration; represents the potency of an inhalant anesthetic. (D)</p> Signup and view all the answers

What is the significance of 'dorm gel' mentioned in the context of alpha-2 agonists administration in horses?

<p>It refers to a specific formulation of detomidine for oral transmucosal administration. (A)</p> Signup and view all the answers

Considering the principles of drug administration in equine sedation, why is achieving a quiet environment particularly emphasized to optimize the effects of sedative medications?

<p>To reduce endogenous catecholamine release, which can antagonize the effects of sedatives, especially alpha-2 agonists. (B)</p> Signup and view all the answers

A horse sedated with detomidine exhibits a transient period of hypertension immediately following administration, which is then followed by hypotension and bradycardia. What is the most critical physiological concern arising directly from the initial hypertensive phase in this scenario?

<p>Transient increase in myocardial oxygen demand in a potentially compromised cardiovascular system, exacerbating pre-existing conditions. (A)</p> Signup and view all the answers

In a stallion intended for breeding, the use of acepromazine is approached with extreme caution primarily due to its potential to induce which of the following irreversible complications?

<p>Persistent penile prolapse and subsequent paraphimosis leading to tissue damage and potential loss of breeding soundness. (A)</p> Signup and view all the answers

When performing epidural analgesia in horses using a combination of lidocaine and xylazine, the maximum recommended volume is limited to 10mL, significantly less than volumes permissible with xylazine alone. What is the primary rationale for this volume restriction when lidocaine is included?

<p>Lidocaine's local anesthetic properties significantly increase the risk of cranial diffusion and subsequent hindlimb weakness or recumbency at higher volumes. (D)</p> Signup and view all the answers

In managing a horse with severe colic pain requiring sedation and analgesia for examination, detomidine and butorphanol are chosen. Considering the limitations of this drug combination in managing severe visceral pain, which of the following best describes the most significant clinical challenge that may necessitate additional analgesic strategies?

<p>The ceiling effect of butorphanol's analgesic efficacy, potentially insufficient to manage extreme visceral pain from severe colic effectively. (B)</p> Signup and view all the answers

Flashcards

Standing Sedation

Outlines the advantages and disadvantages of keeping a horse standing during sedation.

Advantages of Standing Sedation

Mortality risk, cost, and personnel needed are reduced with this method.

Disadvantages of Standing Sedation

Less ideal surgical conditions, more movement, ataxia, insufficient analgesia, increased risk to personnel and asepsis is more difficult to maintain

Considerations for Sedation

The type of procedure, temperament, facilities, and medical conditions helps to determine the need for sedation and/or analgesia.

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Routes of Administration

IM, IV CRI, epidural

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Principles of Drug Administration

Drug effects are optimal in a quiet environment with adequate time for the drug to take effect.

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Bolus IV

The primary mode of sedation, solo or in combination. Common combos: Xylazine/butorphanol, detomidine/butorphanol, xylazine/acepromazine

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Continuous Rate Infusion (CRI)

Typically used for long term pain management or during surgical procedures to maintain a even sedative effect

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CRI Pain Management

long term pain management (laminitis, septic joint, orthopedic pain, colic): Detomidine, Lidocaine, Ketamine, Xylazine/butorphanol, Xylazine/morphine / ketamine, Medetomidine / morphine, Xylazine/ lidocaine

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Epidural Site

Between coccygeal vertebrae 1 and 2 (or 2-3)

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Epidural Needle Size

18G 1.5" needle

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Epidural Drugs

Lidocaine, mepivocaine, mepivocaine or lidociane/xylazine or detomidine, detomidine/morphine

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Epidural Volume

Maximum volume of lidocaine =7 ml

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Epidural Total Volume

10 ml with lidocaine or mepivacaine (risk of cranial diffusion and loss of use of hindlimbs). Larger volume without sodium channel blockers (20-40mls)

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Drug Costs

Acepromazine, Xylazine, Detomidine, Detomidine gel, Butorphanol, Morphine and Hydromorphone

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α2-Adrenoreceptor Agonists

activation of α2-Adrenoreceptors on locus coeruleus in pons of brainstem. This drug is the most common sedative class used in horses

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Route and Effects of α2-Adrenoreceptor Agonists

Administered IV, IM, transmucosal (dorm gel), CRI. Provides reliable sedation, analgesia, and muscle relaxation and increased sensitivity to touch

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Duration of Action - A2 Agonists

Xylazine-20-60 minutes. Detomidine- 45-120 minutes

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Side Effects - A2 Agonists

Hypertension, hypotension, decreased cardiac output, decreased heart rate, usually minor unless combined with other drugs and may change laryngeal function

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A2 Agonist Reversal

Atipamezole (most selective). Use only in emergency situations, dose to effect. Can lead to severe agitation, stress response, and fatalities

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Phenothiazines

MOA: blocks dopamine receptors in basal ganglia and limbic system. Provides tranquilizing effect, has no potent sedative or analgesic effect

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Side Effects of Phenylthiazines

Increase digital blood flow to help with laminitis, but can cause protrusion of the penis from sheath.

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Administration of Phenylthiazines

Administered PO, IM, IV. Peak effects PO: 1 hour. IM: 20-40 minutes. IV: 10-30 minutes. No safe antagonists are available for horses

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Phenothiazines Cardiovascular Effects

Arterial hypotension, +/- HR effects, decrease PCV (splenic relaxation, RBC sequestration), do not use in horses with low PCV or bleeding disorders

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Benzodiazepines

MOA: facilitates the actions of y-aminobutyric acid (GABA), inhibitory neurotransmitter in CNS. Causes muscle relaxation, anxiolytic, hypnotic, anticonvulsive and no analgesia

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Benzodiazepines in horses

Use has unreliable sedation, causes severe ataxia and muscle relaxation

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Benzodiazepines Administration

Administered IV preferred, IM only as last resort and only use midazolam. Antagonist: Flumazenil

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Opioids

Act via various opioid receptors. Administered IV, IM, epidural. Effects action is variable but often used in combination with other sedatives

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Opioids Side Effects

Side effects: restlessness, agitation, increased sympathetic activation, ataxia, ileus. Excitatory effects less common when used with other sedatives

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Sodium Channel Blockers

Local nerve blocks-Wounds, arthrocentesis/synovial lavage

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Effect Duration - Sodium Channel Blockers

Time to Effect 5-10 minutes. Duration of Effect 60-180 minutes. Efficacy decreased in inflamed tissue

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Colic Workup: First Choice drug

Xylazine (150-200mg, 0.3-0.4mg/kg IV). Should last 45-60 minutes

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Colic Workup: Second Choice drug

Detomidine (5-10mg, 0.01-0.02 mg/kg IV) + butorphanol (5-10mg 0.01-0.02 mg/kg IV)

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Choke Sedation

Head as ventral as possible to decrease aspiration and increase drainage. Detomidine (0.01-0.02mg/kg IV) + butorphanol (0.01-0.02mg/kg IV)

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Laceration Treatment

Administer Detomidine and Butorphanol combo while using anti-inflammatory to treat Lacerations

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Standing Joint Procedure

Use Detomidine or Xylazine with Butorphanol while also using anti-inflammatory and local analgesia like mepivicaine

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Cast Placement Procedure

Use Detomidine with or without Butorphanol while maintaing stillness for the procedure

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Standing Enucleation

Xylazine and Hydromorphone Combo for Sedation, While also Using Local & Systemic Alagesia

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Laparoscopic Ovariectomy

Use Detomindine, Sedation (bolus or CRI), Local Alagesia (Carbocaine) + Sedation + Analgesia Epirdural

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Study Notes

  • Equine field chemical restraint and analgesia is the topic
  • Haileigh Avellar, DVM, MS, DACVS-LA, is the author
  • Given for VCS 881 Clinical Pharmacology
  • Presentation Date is April 15, 2025

Objectives

  • Outline advantages and disadvantages of standing sedation
  • Develop a sedation protocol for basic medical or surgical procedures
  • Understand mechanisms, routes, and side effects of commonly used sedatives in equine patients
  • Doses provided are for record keeping only, not for testing

Standing Sedation vs. GA

  • Standing sedation has decreased risk of mortality and decreased cost
  • Standing sedation requires decreased personnel
  • Standing sedation may result in less than ideal surgical conditions, more movement, and ataxia
  • Standing sedation may provide insufficient analgesia, increased risk to personnel, and makes asepsis more difficult to maintain

First Considerations

  • Considerations include the type of procedure, temperament of the horse, and surgical facilities
  • Any pre-existing medical conditions should also be considered
  • Determine whether sedation, analgesia, or both are required

Other considerations- Drug Selection

  • Additional considerations include route of administration, such as IM, IV, CRI, or epidural
  • Other factor include onset time, duration of effect, side effects, other drug properties, and cost of drugs
  • Record keeping requirements and drug residues USEF, AQHA, Racing, and FEI, should also be considered

Principles of Drug Administration

  • Best drug effects occur in quiet patients and in a quiet environment with adequate time for effect
  • IM administration has a longer onset time, requires higher doses, and can produce less predictable effects than IV
  • Bolus injections and redosing are most common
  • CRI can be advantageous for prolonged procedures when using a loading dose
  • Placing an IV catheter provides quick access, which is required for CRI

Cost of Drugs

  • Acepromazine 50ml costs $35/bottle as of January 2024
  • Xylazine 50 ml costs $50/bottle
  • Detomidine 20 ml costs $500/bottle or $25/ml as of January 2024
  • Detomidine gel costs $24/tube as of January 2024
  • Butorphanol 50 ml costs $648 ($13/ml)
  • Morphine 500 mg is $$$, and not generally available
  • Hydromorphone 20 ml costs $102/bottle

α2-Adrenoreceptor Agonists

  • α2-Adrenoreceptor Agonists include: Xylazine, Detomidine, and Romifidine
  • The MOA for α2-Adrenoreceptor Agonists is activation of α2-Adrenoreceptors on the locus coeruleus in the pons of the brainstem
  • α2-Adrenoreceptor Agonists are the most commonly used class of sedatives in horses
  • The route of administration is IV, IM, transmucosal (dorm gel), and CRI
  • α2-Adrenoreceptor Agonists provide reliable sedation, analgesia, and muscle relaxation
  • Increased sensitivity to touch may result
  • These are often combined with opioids to improve quality of sedation or decreased touch stimulation with opioids
  • α2-Adrenoreceptor Agonists use is not recommended in foals less than 14 days old or in very sick foals

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