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Anesthesia
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Solubility of Anesthetic Gases
The anesthetic gasses has different physicochemical characteristics that determine their actions and safety of administration. The solubility refers the way that the gas dissolves in liquids and solids; is a primary factor in the rate of uptake, distribution within the body and defines the rapidity of induction and recovery, the relative effect of changes in ventilation and circulation on alveolar and arterial tension, and anaesthetic potency. In other words, the solubility is the primary determinant of the speed of anesthetic induction and recovery.
The currently used anesthetic produce a dose-dependent decrease in cardiac output, blood pressure and depression of the central nervous system. The newer agents are all relatively insoluble. Desflurane in the least soluble agent.
Inspired anaesthetic gases are diluted by other gases (Oxygen, Nitrogen and Carbon Dioxide) in the patient’s lung. Agents with relatively low blood/gas solubility (such as isoflurane and sevoflurane) will have slower removal from the alveoli than agents with higher solubility (halothane).
Blood gas solubility of some inhalation anesthetics (37o C):
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Desflurane: 0.42
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Halothane: 2.54
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Isoflurane 1.46
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Sevoflurane 0.68
References:
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Veterinary Anesthesia and Analgesia. The Fifth Edition of Lumb and Jones. Wiley Blackwell. 2015.
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Anaesthetic Solubility in Blood and Tissue: Values and Significance. 1964. Brit. J. Anaesth.
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BSAVA Manual of Canine and Feline Anaesthesia and Analgesia. 2nd ed. British Small Animal Veterinary Association. 2007. ​
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Anesthetic Approaches for Canine Spay-Neuter Procedures
Canine castration and ovariohysterectomy/ovariectomy surgeries are linked to variable pain intensity contingent upon the degree of surgical trauma.
Devising effective anesthetic strategies for spay-neuter programs necessitates a comprehensive perspective, encompassing patient volume, procedural intricacies, and medication interactions. The goal is to achieve a balanced anesthesia, finely tuned by crafting a precise blend of analgesic and anxiolytic agents along with inhalant anesthesia. This orchestration ensures pain alleviation, stress reduction, muscle relaxation, and controlled central nervous system depression culminating in unconsciousness.
Analgesic Agents: A judicious fusion of opioids, NSAIDs, and alpha-2 adrenergic agonists ensures meticulous pain management. Multimodal analgesia, synergizing diverse agents, significantly enhances pain control.
Anxiolytics: Integrating tranquilizers (e.g., midazolam, diazepam) and alpha-2 adrenergic agonists mitigates stress, enhancing patient comfort when combined with analgesic interventions.
Inhalant Anesthesia: Overreliance on mask induction is cautioned against due to inconsistent loss of consciousness, heightened stress, and increased aspiration risk. While chamber induction is rarely warranted, it may be considered in exceptional cases. Regular mask maintenance, relevant for specific procedures, necessitates vigilant monitoring and protocol adjustments to minimize risks such as bronchial irritation and gas contamination.
Airway Management: Prudent airway management involving facemasks, endotracheal tubes, or supraglottic airway devices is pivotal. Proficiency and constant vigilance are vital to prevent complications.
Perioperative Thermoregulation: Maintaining patient normothermia is crucial to avoid hypothermia-related complications. Strategies like prewarming, minimizing contact with cold surfaces, and effective insulation techniques are recommended.
Tailoring anesthetic protocols meticulously to each patient's unique characteristics and requirements, and judiciously combining agents, ensures optimal pain control, stress mitigation, and safe anesthesia induction.
Canine and Feline Castration Protocol
Preoperative:
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Analgesia: Opioid administration.
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Sedation: Benzodiazepines (midazolam or diazepam at 0.25–0.4mg/kg IM); intravenous administration of diazepam is recommended due to the painful nature of IM administration; alpha2 adrenoceptor agonist.
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Induction of Anesthesia: A combination of intravenous propofol (3–5 mg/kg), ketamine (3–5 mg/kg) with diazepam or midazolam (0.25 mg/kg), or alfaxalone (1–2 mg/kg); or intramuscular administration of alpha2 adrenoceptor agonist along with ketamine (3–5 mg/kg) or tiletamine/zolazepam (3–4 mg/kg).
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Maintenance of Anesthesia: Inhalation anesthesia or propofol, alfaxalone, or ketamine (1/3 or 1/2 of initial dose) to effect; endotracheal intubation is recommended. Venous access is advised.
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Local Anesthetic Techniques: Employ intra-testicular and incisional blocks.
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Postoperative Analgesia: Administer NSAID.
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Protocol without Controlled Drugs: Administer a combination of NSAID and alpha2 adrenoceptor agonist, optionally supplemented with tramadol (2–5 mg/kg IM).
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Protocol with Limited Analgesic Availability: Employ alpha2 adrenoceptor agonist, optionally combined with NSAID. Intravenous or inhalant agents for induction and maintenance of anesthesia are recommended. Employ intra-testicular and incisional blocks for local anesthesia. Administer postoperative NSAID.
Feline and Canine Ovariohysterectomy.
A comprehensive approach to ovariohysterectomy is recommended to enhance analgesia at both ovarian and uterine surgical sites. The protocol involves the following steps:
Preoperative:
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Analgesia: Administer an opioid for preoperative pain management.
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Sedation: Employ benzodiazepines or an alpha2 adrenoceptor agonist for sedation.
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Induction of Anesthesia: Choose between intravenous propofol (3–5 mg/kg), ketamine (3–5 mg/kg) combined with diazepam/midazolam (0.25 mg/kg), or alfaxalone (1–2 mg/kg); alternatively, use an intramuscular combination of alpha2 adrenoceptor agonist and ketamine (5.0–7.5 mg/kg) or tiletamine/zolazepam (3–4 mg/kg).
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Maintenance of Anesthesia: Employ inhalation anesthesia, or adjust propofol, alfaxolone, or ketamine (1/3 or 1/2 of initial dose) to effect. Ensure venous access and apply local anesthesia via incisional and intraperitoneal/ovarium ligament blocks.
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Postoperative Analgesia: Administer NSAID for effective pain management.
Castration Procedures for Local Anesthesia (Felines and Canines) Step-by-Step Instructions:
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Choose the desired local anesthetic. Calculate the lower dosage range, which is 1 mg/kg (for cats) or 2 mg/kg (for dogs) of bupivacaine, ropivacaine, or 4 mg/kg (for cats) and 6 mg/kg (for dogs) of lidocaine.
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Conduct a preliminary surgical scrub around the testicles and the incision site, either scrotal (for cats) or prescrotal (for dogs).
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Insert a 22-gauge needle into the testicle's center, aiming the needle tip toward the spermatic cord.
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Aspirate and inject half of the calculated volume into each testicle, or inject until the testicle becomes turgid, whichever occurs first.
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The drug migrates along the spermatic cord, delivering pain relief for cord and vessel surgical manipulation.
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For incision-related pain relief:
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a. For cats: Continue infiltration as the needle exits the testicular body, targeting the skin and subcutaneous tissue.
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b. For dogs: Administer local anesthetic in the skin and subcutaneous tissue at the incision site.
While bupivacaine or ropivacaine offer longer duration than lidocaine, some practitioners lean towards lidocaine due to its higher safety margin if inadvertently administered IV, especially considering the testicles' vascularity. Thus, personal comfort with the drugs guides the final choice for this block.
Indications for Local anesthesia in Feline and Canine Ovariohysterectomies Step-by-Step Instructions:
(This approach may prove more efficacious than mesovarium block, as it provides analgesia at both ovarian and uterine surgical sites.)
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Choose and calculate the full dose of a local anesthetic, such as:
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Lidocaine (cats: 2–4 mg/kg, dogs: 4–6 mg/kg)
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Bupivacaine (cats: 1 mg/kg, dogs: 2 mg/kg)
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Ropivacaine (cats: 1 mg/kg, dogs: 2 mg/kg)
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If necessary, dilute the drug with saline; the total volume must be at least 0.4–0.6 mL/kg to lavage the entire abdominal cavity.
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Right after making the incision or upon completing the abdominal procedure (before closing the incision), gently instill the local anesthetic into the peritoneal cavity through the incision.
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Proceed with the incision closure, allowing the local anesthetic to remain within the abdomen.
Administering abdominal lavage immediately post-incision may enhance effectiveness (preemptive analgesia), but caution is needed to prevent absorption by blood-sponges. The objective is to retain the drug within the abdomen; therefore, lavage just prior to closure could be more efficient.
​
REFERENCES:
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Griffin, B. The Association of Shelter Veterinarians 2016 Veterinary Medical Care Guidelines for Spay-Neuter Programs. JAVMA, Vol 249, No. 2. 2016.
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Mathews, K. WSAVA Guidelines for Recognition, Assessment and Treatment of Pain. JSAP, Vol 55, Issues 6. 2014.
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Grubb, T. 2020 AAHA Anesthesia and Monitoring Guidelines for Dogs and Cats. Veterinary Practice Guidelines. J Am Anim Hosp Assoc, 56. 2020.
​
RECOMMENDED LINKS:
Spay / Neuter Programs. Association of Shelter Veterinarians.
AAHA Guidelines. 2020 AAHA Anesthesia and Monitoring Guidelines for Dogs and Cats.
​
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Dexmedetomidine
Pharmacology:
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Dexmedetomidine is an α2-adrenergic receptor agonist.
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It is the dextrorotatory enantiomer of medetomidine, about twice as potent.
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Dexmedetomidine is highly specific for α2 receptors, leading to CNS depression, analgesia, peripheral vasoconstriction, bradycardia, respiratory depression, and more.
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It has varying effects on intestinal muscle tone, blanched mucous membranes, and can cause prolonged hypertension.
Pharmacokinetics:
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In dogs (IM administration), it has 60% bioavailability, reaching peak levels in about 35 minutes.
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Volume of distribution is 0.9 L/kg, with an elimination half-life of 40-50 minutes.
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It's metabolized in the liver and eliminated primarily in urine and feces.
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In cats (IM administration), peak levels occur in about 15 minutes.
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Volume of distribution is 2.2 L/kg, with an elimination half-life of approximately 1 hour.
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Metabolites are primarily eliminated in urine and feces.
Adverse Effects:
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Adverse effects include bradycardia, vasoconstriction, muscle tremors, transient hypertension, reduced tear production, AV blocks, decreased respiration, hypothermia, urination, vomiting, hyperglycemia, and pain on IM injection.
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Rare effects may include prolonged sedation, paradoxical excitation, hypersensitivity, pulmonary edema, apnea, and circulatory failure.
Clinical Applications:
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Dexmedetomidine can be administered intranasally and has been effective in reducing stress in dogs.
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It is commonly used as a sole sedative or in combination with opioids for general anesthesia or improving sedation quality.
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Administering it epidurally or as a constant-rate infusion extends the duration of local regional blocks.
Contraindications/Precautions:
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Cardiovascular diseases, including valvular regurgitation or arrhythmias, are contraindications.
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Bradyarrhythmias are frequent and may require treatment with anticholinergics or lidocaine.
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Dexmedetomidine is contraindicated in patients with renal insufficiencies, anuria, or a blocked urinary system.
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Avoid use in geriatric, pregnant, pediatric, sick, or debilitated patients.
Practical Notes:
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Patients may experience transient hyperglycemia after administration.
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Provide a quiet, darkened room with minimal stimulus.
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Monitor patients and have reversal agents like atipamezole available.
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Vasoconstriction may affect mucous membrane color and pulse oximetry.
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Low doses are suitable for premedication in cats with HCM.
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Dexmedetomidine is more likely to cause vomiting in cats compared to xylazine; consider maropitant for premedication.
Dexmedetomidine Doses:
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Intranasal: A study showed that 0.02 mg/kg dexmedetomidine produced effective sedation in dogs.
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Oral transmucosal (OTM, buccal) administration in cats: Dexmedetomidine at 40 micrograms/kg appears to give similar levels as IM administration.
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Dexmedetomidine combined with buprenorphine in cats: Used at 20 micrograms/kg for IM administration.
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Dexmedetomidine combined with local anesthetic for regional anesthesia: Used at 0.001 mg/kg.
References:
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Grimm, KA. Veterinary Anesthesia and Analgesia the 5th Edition of Lumb and Jones. 2015.
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Plumb, DC. Plumb’s Veterinary Drug Handbook. 7th edition. Pharma Vet Inc. 2011.
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Shelby, AM. Small Animal Anesthesia Techniques. 2nd ed. Wiley Blackwell. 2023.
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Managing Hypoventilation in Veterinary Anesthesia
Hypoventilation during anesthesia, as outlined by the AAHA guidelines, can be identified by observing respiratory rate and depth, and quantified using capnometry. It can cause hypercarbia and subsequent respiratory acidosis, as well as hypoxemia. To correct hypoventilation, ensure anesthetic depth is not excessive and initiate positive pressure ventilation (PPV) if necessary. Mechanical ventilation can be employed, with care taken to monitor the hemodynamic status, as PPV can impact cardiac output. It's also crucial to recheck blood pressure after starting PPV and adjust ventilator settings based on end-tidal CO2 levels to prevent barotrauma.
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For a comprehensive understanding, please refer directly to the AAHA guidelines
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Isoflurane in Veterinary Medicine: Use, Benefits, and Precautions
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Isoflurane is widely utilized in veterinary anesthesia due to its potent inhalant properties, which allow it to serve as the primary or sole anesthetic agent in various surgical procedures. Its advantages include rapid induction and recovery times, minimal cardiovascular and respiratory depression, and muscle relaxation, making it an ideal choice for a broad range of veterinary patients, including those with cardiovascular compromise.
Isoflurane's minimal alveolar concentration (MAC) in dogs has been extensively studied, providing a basis for dosing and administration guidelines to ensure effective anesthesia while minimizing the risk of overdose or insufficient anesthesia depth. Research indicates that isoflurane MAC can be effectively reduced by adjunctive medications such as lidocaine and dexmedetomidine, which may also confer additional analgesic benefits and reduce the overall isoflurane requirement, potentially decreasing the risk of isoflurane-related complication.
However, there are several considerations and potential complications associated with isoflurane anesthesia. The use of nitrous oxide, for example, can expedite induction but may lead to oxygen dilution and diffusion hypoxia upon discontinuation, necessitating careful monitoring of oxygenation and the administration of pure oxygen post-anesthesia. Additionally, the transfer of nitrous oxide into closed gas spaces within the body can cause expansion and potentially dangerous pressure increases, highlighting the need for cautious use in patients with certain conditions.
Metabolism of isoflurane is primarily through pulmonary exhalation, with minimal liver metabolism, thereby reducing the risk of hepatotoxicity but necessitating effective ventilation and waste gas scavenging systems in the surgical environment to minimize occupational exposure.
Dosing of isoflurane must be carefully managed, considering the individual patient's health status, breed, and the nature of the procedure being performed. The dose is adjusted to achieve the desired depth of anesthesia, with continuous monitoring of vital signs to ensure patient safety.
Precautions with isoflurane use include ensuring proper patient fasting prior to anesthesia to reduce the risk of aspiration, careful monitoring of body temperature, blood pressure, heart rate, and respiratory rate during anesthesia, and the provision of adequate post-anesthetic care to ensure a smooth recovery.
In summary, isoflurane remains a cornerstone of veterinary anesthesia due to its efficacy and safety profile when used appropriately. Veterinary professionals must remain vigilant in monitoring and adjusting anesthesia depth, managing potential complications, and employing adjunctive therapies to enhance analgesia and minimize isoflurane requirements, thereby ensuring optimal outcomes for their patients.
References:
Lidocaine, Dexmedetomidine and Their Combination Reduce Isoflurane Minimum Alveolar Concentration in Dogs. PLOS ONE.
Inhalants Used in Veterinary Anesthesia | IVIS
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