Morphine

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Morphine In Dogs & Cats: Uses, Dosage and Side Effects

Morphine In Dogs & Cats: Uses, Dosage and Side Effects

Overview

  • Analgesia is mediated by the mu-opioid receptor.

Uses of Morphine

  • Management of moderate to severe pain in the perioperative period.
  • Morphine can be given as a constant rate infusion to provide analgesia intraoperatively and in the postoperative period.
  • Incorporation into sedative and pre-anaesthetic medication protocols to provide improved sedation and analgesia.
  • Preservative-free morphine can be administered into the epidural space where it will provide analgesia for up to 24 hours.
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Dose of Morphine in Dogs and Cats

Dogs:

Analgesia:

  • a dose of 0.5 mg/kg i.v., i.m. q2h is required to produce analgesia in experimental models.
  • Pain should be assessed frequently and the dose adjusted based on the requirement for analgesia.
  • Continuous rate infusion: 0.15–0.2 mg/kg/h i.v.

Epidural morphine (use Duramorph as it is preservative-free):

  • 0.1–0.2 mg/kg diluted with 0.26 ml/kg of sterile saline (up to a total maximum volume of 6 ml in all dogs).
  • There is a latent period of 30–60 minutes following epidural administration;
    duration of action is 18–24 hours.

Cats:

Analgesia:

  • 0.1–0.4 mg/kg i.v., i.m. q3–4h.
  • Pain should be assessed frequently and the dose adjusted based on the requirement for analgesia.
  • Continuous rate infusions of morphine have not been widely evaluated in cats.

Epidural morphine:

  • dose as for dogs.

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Side Effects of Morphine in Dogs and Cats

  • Morphine can cause respiratory depression, although this is unlikely when used
    at clinical doses in awake cats and dogs.
  • Respiratory depression may occur when given i.v. during general anaesthesia due to increased depth of anaesthesia.
  • Vomiting is common after morphine administration and it causes constriction of GI sphincters (such as the pyloric sphincter) and may cause a reduction in GI motility when given over a long period.
  • Morphine crosses the placenta and may exert sedative effects in neonates born to bitches treated prior to parturition.
  • Severe adverse effects can be treated with naloxone.

Contraindications of Morphine in Dogs and Cats

  • No information is available.

Some Notes:

  • Other CNS depressants (e.g. anaesthetics, antihistamines, barbiturates, phenothiazines, tranquillizers) may cause increased CNS or respiratory depression when used
    concurrently with narcotic analgesics.
  • The utilisation of methadone is recommended above morphine as the authorised substitute for administering single or repeated bolus doses to canines and felines.
  • The increased accessibility of data pertaining to the pharmacological properties and administration of morphine via continuous rate infusion may provide a rationale for prioritising its utilisation above methadone in this particular mode of drug delivery.
  • Morphine serves as the benchmark opioid against which all other opioids are measured.
  • It offers significant pain relief and is a fundamental component of analgesic treatments following surgical procedures in human patients.
  • In canines, the medication has a brief period of efficacy and necessitates repeated administration in order to achieve desired outcomes.
  • Constant rate infusions (CRIs) can also be employed as a means to address this particular constraint.
  • The length of action in felines has not been thoroughly assessed; nonetheless, it seems to have a duration of action ranging from 3 to 4 hours.
  • Accumulation is a probable outcome following the administration of repeated doses over an extended period of time. This phenomenon may enable a reduction in dosage or an extension of the dosing interval. When administered intravenously at a rapid rate, morphine induces the release of histamine.
  • It is recommended to dilute the drug and administer it intravenously at a gradual rate.
  • Administering morphine to animals prior to surgery who are not experiencing pain often leads to vomiting.
  • It is advisable to avoid using morphine in cases where vomiting is prohibited, such as in animals with elevated intraocular pressure.
  • Transient excitation can potentially manifest when intravenous administration of morphine is administered.
  • The utilisation of oral morphine in feline and canine patients is infrequent due to its high first-pass metabolism, resulting in a diminished plasma concentration after to oral administration.
  • It is imperative to monitor respiratory function in anaesthetized patients who are administered morphine.
  • The response to opioids exhibits variability across individual patients, thereby necessitating the assessment of pain following their delivery.
  • The metabolism of morphine takes place in the liver, and those with poor liver function may experience a lengthened duration of its effects.
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