Detomidine

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Detomidine.png

A sedative and analgesic medication used in veterinary medicine


CaptionSynonyms
Detomidine
Drug Information
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Detomidine is a sedative and analgesic medication primarily used in veterinary medicine. It is commonly administered to horses and other large animals to facilitate handling, diagnostic procedures, and minor surgical interventions. Detomidine is classified as an alpha-2 adrenergic agonist, which means it works by stimulating alpha-2 receptors in the central nervous system, leading to sedation and pain relief.

Mechanism of Action[edit | edit source]

Detomidine exerts its effects by binding to alpha-2 adrenergic receptors in the brain and spinal cord. This binding inhibits the release of norepinephrine, a neurotransmitter involved in arousal and alertness, resulting in sedation and analgesia. The drug also has muscle relaxant properties, making it useful for various veterinary procedures.

Uses[edit | edit source]

Detomidine is used in veterinary medicine for:

  • Sedation during diagnostic procedures such as radiography and endoscopy.
  • Pain relief during minor surgical procedures.
  • Facilitating the handling of fractious or difficult animals.
  • Pre-anesthetic medication to reduce the required dose of general anesthesia.

Administration[edit | edit source]

Detomidine is typically administered via intravenous (IV) or intramuscular (IM) injection. The dosage and route of administration depend on the species, size, and condition of the animal. It is important to follow veterinary guidelines and recommendations when using detomidine to ensure safety and efficacy.

Side Effects[edit | edit source]

Common side effects of detomidine include:

  • Bradycardia (slow heart rate)
  • Hypotension (low blood pressure)
  • Respiratory depression
  • Sweating in horses
  • Ataxia (loss of coordination)

Precautions[edit | edit source]

Detomidine should be used with caution in animals with pre-existing cardiovascular or respiratory conditions. It is also important to monitor animals closely during and after administration to manage any adverse effects promptly.

See Also[edit | edit source]

References[edit | edit source]


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