Non-opioid
- also referred to as non-narcotic, peripheral, mild & antipyretic
agents
Opioids
- also called narcotic, central or strong agents
Nonopioids
Nonopiod drugs are used to
treat mild to moderate pain.
Classification
Nonopiods are classified into
three categories:
Salicylates
Aspirin is one of these
types, used to treat mild to moderate pain, inflammation, fever, arthritis
and reduce blood clotting. Aspirin is one of the oldest drugs and is
highly effective.
Nonsteroidial anti-inflammatory
drugs (NSAIDs)
NSAIDs are used to
treat pain and are similar to aspirin in the mechanism of action, pharmacological
effects, and adverse reactions. NSAIDs are available in nonprescription
& prescription strengths. They are also used to treat rheumatoid
arthritis, osteoarthritis, dysmenorrhea, and additional inflammatory
diseases.
Acetaminophen
Acetaminophen is used
to treat pain such as headaches, dental pain, dysmenorrhea, myalgias,
neuralgias and fever particularly in patients who cannot take aspirin.
It does not effect the cardiovascular or respiratory systems and does
not increase bleeding time or cause GI bleeding.
The table below lists some
of the pharmacologic effects and potential adverse effects of these drugs:
Analgesia:
aspirin is used to reduce mild to moderate pain
Antipyretic:
aspirin is used to lower body temperate & treat a fever by
causing peripheral vasodilation and sweating. Does not reduce
body temperature below normal (98.6°F)
Antiinflammatory:
Reduces pain, redness & swelling of inflamed areas by inhibition
of prostaglandin synthesis, vasodilation and increasing capillary
permeability
Anticoagulation:
Reduces blood clotting by inhibition of prostaglandin synthesis.
Small doses are used to prevent recurrence of strokes and myocardial
infarctions.
Pharmacokinetics:
Aspirin is rapidly absorbed from the stomach &
small intestine, then widely distributed to most body tissues. Metabolized
in the liver, then excreted by the kidneys.
Mechanism:
Works by blocking prostaglandin synthesis in the peripheral nerves
& the hypothalamus portion of the brain.
GI:
increased GI ulceration & bleeding
Bleeding:
prolonged bleeding time due to aspirin binding to platelets, reducing
platelet adhesiveness
Allergy:
symptoms ranging from mild rash to anaphylactic shock (Occurs
in about 0.2 to 0.9% of the population)
Analgesia:
NSAIDs are used to reduce mild to moderate pain.
Antipyretic:
NSAIDs are used to lower body temperate & treat a fever by
causing peripheral vasodilation and sweating.
Antiinflammatory:
Reduces pain, redness & swelling of inflamed areas by inhibition
of prostaglandin synthesis, vasodilation and increasing capillary
permeability.
Anticoagulation:
Reduces blood clotting by inhibition of prostaglandin synthesis.
Small doses are used to prevent recurrence of strokes and myocardial
infarctions
Pharmacokinetics:
NSAIDs absorbed from the stomach & small intestine,
then widely distributed to most body tissues. Metabolized in the
liver, then excreted by the kidneys.
Mechanism:
Works by blocking prostaglandin synthesis in the peripheral nerves
& the hypothalamus portion of the brain.
Analgesia:
acetaminophen is used to reduce mild to moderate pain.
Antipyretic:
acetaminophen is used to lower body temperate & treat a fever
by causing peripheral vasodilation and sweating. Does not reduce
body temperature below normal (98.6°F)
Pharmacokinetics:
Acetaminophen is absorbed from the stomach &
small intestine, then distributed to body tissues. Metabolized in
the liver, then excreted by the kidneys.
Mechanism:
Exact mechanism not known, but believed to work in the CNS, not
the peripheral nervous system.
Very few adverse
reactions. Does not cause GI irritation & bleeding.
Extremely high
doses over long time periods may lead to hepatoxicity and nephrotoxicity.
The word opiod refers to a
morphine-like compound that affects the opiod receptors, thereby reducing
pain sensation.
Usefulness
Narcotic or opiod drugs are
used to treat moderate to severe pain that does not respond to nonopiod
drugs. They are used in the following ways:
preoperatively, to...
reduce anxiety
reduce the amount of
general anesthesia used
produce analgesia
in some cough preparations
in some strong antidiarrheal
treatments
Classification
Opiods are classified into
three categories based on their opiate receptor activity:
Opiod Agonist
Used to treat moderate to severe pain. Morphine is considered the prototype.
Mixed Opiod Angonist
Used to treat moderate to severe pain. Not commonly used in dentistry.
Physical dependence to Buprenorphine is low and withdrawal is mild.
Opiod Antagonist
Used to counteract the pharmacologic and reverse reactions of opiod
agonists and mixed angonists and in the management of overdoses.
Opiods have similar actions
and reactions, so the chart below summarizes these effects for all three
categories of opiods (agonist, mixed angonist, antagonist):
Opioid class
Pharmacologic effects
Adverse effects
Agonist:
Codeine
Hydrocodone
Hydromorphone
Meperidine
Morphine
Oxycodone
Mixed agonist:
Buprenorphine
Antagonist:
Nalbuphine
Nalorphine
Naloxone
Pentazcine
Sedation:
produces sedation at therapeutic doses
Euphoria:
may decrease anxiety, increase relaxation and
a feeling of well being
Dysphoria:
some patients experience feelings of irritability
&/or anxiety
Cough Suppression:
can decrease coughing. Used in some cough medications
GI Effect:
causes decrease in propulsive contractions &
motility, may lead to constipation
Respiration:
reduces the rate & depth of respiration, this
effect is dose dependent.
Pharmacokinetics:
Opiods are absorbed when administered intramuscularly,
orally, subcutaneously, intravenously, nasally, & transdermally.
The onset of action is quick, with analgesic response occurring
30 to 40 minutes. Opiods are metabolized in the liver and excreted
through the kidneys. They do cross the placental barrier.
Mechanism:
Bind to receptors along the pain-analgesia pathway of the central
nervous system, inhibiting pain sensations.
Adverse reactions
are proportional to the dose of the opiod drug.
Some effects
include:
nausea &
vomiting
constipation
xerostomia
miosis (pupil
constriction)
release
of histamine causing itching, and urinary retention.
Other adverse
reactions:
Respiratory
depression:
reduces the rate & depth of respiration, which may cause vasodilation
and increase intracranial pressure. Do not
use for head injury patients.
Allergic
Reactions:
the most common allergic reactions are itching & rashes. Nausea
& vomiting are often typical side effects & not true allergic
reactions.