chpater 11 analgesic drugs - week 5 Flashcards

1
Q

analgesics

A

Medications that relieve pain without causing loss of consciousness
“Painkillers”
Opioid analgesics
Adjuvant analgesic drugs

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2
Q

pain

A

An unpleasant sensory and emotional experience associated with actual or potential tissue damage
A personal and individual experience
Whatever the patient says it is
Exists when the patient says it exists

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3
Q

nociception

A

Pain results from stimulation of sensory nerve fibres called nociceptors.
These receptors transmit pain signals from various body regions to the spinal cord and brain.

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4
Q

pain threshold

A

Level of stimulus needed to produce the perception of pain
A measure of the physiological response of the nervous system

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5
Q

pain tolerance

A

The amount of pain a person can endure without it interfering with normal function
Varies from person to person
Subjective response to pain, not a physiological function
Varies by attitude, personality, environment, culture, ethnicity

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6
Q

classication of pain by onset and duration

A

Acute pain
Sudden onset
Limited, has an end
Persistent pain (chronic pain)
Persistent or recurring
Lasts 3 to 6 months
More difficult to treat
Tolerance

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7
Q

classifications of pain

A

Referred
Neuropathic
Phantom
Cancer
Central
Vascular

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8
Q

gate theroy of pain trasmission

A

Most common and well-described theory
Uses the analogy of a gate to describe how impulses from damaged tissues are sensed in the brain
Many current pain management strategies are aimed at altering this system.

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9
Q

four distinct processess of pain

A

Transduction
Transmission
Perception
Modulation

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10
Q

transduction

A

Transformation of stimuli into electrochemical energy
Release of pain-medicating chemicals
Nociceptors

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11
Q

pain transduction

A

Tissue injury causes the release of the following:
Bradykinin
Histamine
Potassium
Prostaglandins
Serotonin
Substance P
These substances stimulate nerve endings, 
starting the pain process.
The nerve impulses enter the spinal cord 
and travel up to the brain.
The point of spinal cord entry or the “gate” is the dorsal horn.
This gate regulates the flow of sensory impulses to the brain
Closing the gate stops the impulses.
If no impulses are transmitted to higher centres in the brain, there is no pain perception.

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12
Q

pain transmission

A

Two types of nociceptor pain fibres:
Large-diameter, A-delta fibres, and small-diameter
C fibres

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13
Q

pain modularion

A

Neural activity that controls pain transmission to neurons
Both peripheral and central nervous systems
Descending pain system
Enkephalins and endorphins

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14
Q

massage

A

Massaging a painful area often reduces the pain.
Large sensory A nerve fibres inhibit impulse transmission
Close the gate

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15
Q

treatment of pain in spceial situations

A

Patient-controlled analgesia (PCA)
Patient comfort versus fear of drug addiction
Opioid tolerance
Use of placebos
Recognizing patients who are opioid tolerant
Breakthrough pain
Synergistic effects

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16
Q

adjuvant drugs

A

Drugs from chemical categories other than opioids
Assist primary drugs in relieving pain
Nonsteroidal anti-inflammatory drugs (NSAIDs)
Antidepressants
Anticonvulsants
Corticosteroids
Example: adjuvant drugs for neuropathic pain
Amitriptyline (antidepressant)
Gabapentin or pregabalin (anticonvulsants)

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17
Q

WHO - three step analgesic ladder

A

Step 1: Nonopioids with or without adjuvant medications after the pain has been identified and assessed. If pain persists or increases, treatment moves to:
Step 2: Opioids with or without nonopioids and with or without adjuvants. If pain persists or increases, management then rises to:
Step 3: Opioids indicated for moderate to severe pain, administered with or without nonopioids or adjuvant medications

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18
Q

opioid drugs

A

Synthetic drugs that bind to the opiate receptors to relieve pain
Mild agonists: codeine, hydrocodone
Strong agonists: morphine, hydromorphone hydrochloride, oxycodone, meperidine, fentanyl, methadone
Meperidine: not recommended for long-term use because of the accumulation of a neurotoxic metabolite, normeperidine, which can cause seizures.

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19
Q

opioid ceiling effect

A

Drug reaches a maximum analgesic effect.
Analgesia does not improve, even with higher doses.
Codeine phosphate
Pentazocine
Nalbuphine

20
Q

agonists (opioid anagesics) mechanism of action

A

Bind to an opioid pain receptor in the brain
Cause an analgesic response (reduction of pain sensation)

21
Q

agonists-antagonists(opioid anagesics) mechanism of action

A

Bind to a pain receptor
Cause a weaker pain response than full agonists
Also called partial agonists or mixed agonists

22
Q

antagonists(opioid anagesics) mechanism of action

A

Reverse the effects of these drugs on pain receptors
Bind to a pain receptor and exert no response
Also known as competitive antagonists

23
Q

equianalgesia

A

Ability to provide equivalent pain relief by calculating dosages of different drugs or routes of administration that provide comparable analgesia
Examples: morphine, hydromorphone, oxycodone, hydrocodone bitartrate, fentanyl
Continuous release vs. immediate release formulations

24
Q

Opioid Analgesics:
Indications

A

Mainly used to alleviate moderate to severe pain
Often first line agents analgesic in immediate post operative setting
Often given with adjuvant analgesic drugs to assist primary drugs with pain relief
Balanced anaesthesia
Opioids are also used for:
Cough centre suppression
Treatment of diarrhea

25
Q

Opioid Analgesics: 
Contraindications

A

Known drug allergy
Severe asthma
Use with extreme caution in patients with the following:
Respiratory insufficiency
Elevated intracranial pressure
Morbid obesity or sleep apnea
Paralytic ileus
Pregnancy

26
Q

Opioid Analgesics: 
Adverse Effects

A

Central nervous system (CNS) depression
Leads to respiratory depression
Most serious adverse effect
Nausea, vomiting, constipation, biliary tract spasm
Urinary retention
Hypotension, palpitations, flushing
Itching, rash, wheal formation
Pinpoint pupils indicating a possible overdose

27
Q

Opioids: Opioid Tolerance

A

A common physiological result of chronic opioid treatment
State of adaptation
Result: larger dose is required to maintain the same level of analgesia

28
Q

Opioids: Physical Dependence

A

Physiological adaptation of the body to the presence of an opioid
Opioid tolerance and physical dependence are expected with long-term opioid treatment and should not be confused with psychological dependence (addiction).

29
Q

Opioids: Psychological Dependence

A

Addiction: a pattern of compulsive drug use characterized by a continued craving for an opioid and the need to use the opioid for effects other than pain relief

30
Q

Opioid Analgesics: 
Toxicity and Management of Overdose

A

Naloxone hydrochloride
Naltrexone (ReVia®)
Regardless of withdrawal symptoms, when a patient experiences severe respiratory depression, an opioid antagonist should be given.

31
Q


Toxicity and Management
 of Overdose


A

Opioid withdrawal or opioid abstinence syndrome
Occur in 2 weeks in opioid-naïve patients
Gradual dosage reduction after chronic opioid use

32
Q

Opioid Analgesics: Interactions

A

Alcohol
Antihistamines
Barbiturates
Benzodiazepines
Promethazine
Monoamine oxidase inhibitors
Others

33
Q

Codeine Sulphate

A

Codeine sulphate
Natural opiate alkaloid (Schedule I) obtained from opium
Less effective
Ceiling effect
More commonly used as an antitussive drug
Gastrointestinal (GI) disturbance

34
Q

Codeine Sulphate

A

Codeine sulphate
Natural opiate alkaloid (Schedule I) obtained from opium
Less effective
Ceiling effect
More commonly used as an antitussive drug
Gastrointestinal (GI) disturbance

35
Q

Fentanyl

A

Synthetic opioid (Schedule I) used to treat moderate to severe pain
Parenteral injections, transdermal patches (Duragesic Mat®), sublingual effervescent tablet (Fentora®)

36
Q

Dilaudid

A

Hydromorphone (Dilaudid®): very potent opioid analgesic; Schedule I drug
1 mg of intravenous (IV) or intramuscular (IM) hydromorphone is equivalent to 7 mg of morphine.

37
Q

Methadone Hydrochloride

A

Synthetic opioid analgesic (Schedule I)
Opioid of choice for detoxification treatment of opioid addicts in methadone maintenance programs
Renewed interest in the use of methadone for chronic (e.g., neuropathic) and cancer-related pain
Prolonged half-life of the drug: cause of unintentional overdoses and deaths
Cardiac dysrhythmias

38
Q

Morphine Sulphate

A

Naturally occurring alkaloid derived from the opium poppy
Drug prototype for all opioid drugs; Schedule I controlled substance
Indication: severe pain
Oral, injectable, and rectal dosage forms; also extended-release forms

39
Q

Naloxone Hydrochloride (Narcan®)

A

Pure opioid antagonist
Drug of choice for the complete or partial reversal of opioid-induced respiratory depression
Indicated in cases of suspected acute opioid overdose
Failure of the drug to significantly reverse the effects of the presumed opioid overdose indicates that the condition may not be related to opioid overdose.

40
Q

Nonopioid Analgesics:
Acetaminophen (Tylenol®)

A

Analgesic and antipyretic effects
Little to no anti-inflammatory effects
Available over the counter (OTC) and in combination products with opioids

41
Q

Acetaminophen: Mechanism 
of Action

A

Similar to that of salicylates
Blocks pain impulses peripherally by inhibiting prostaglandin synthesis

42
Q

Acetaminophen: Indications

A

Mild to moderate pain
Fever
Inability to take aspirin products

43
Q

Acetaminophen dosage

A

Maximum daily dose for healthy adults is 4 g/day, but Health Canada is considering lowering*
2 000 mg for older adults and those with liver disease
Inadvertent excessive doses may occur when different combination drug products are taken together.
Be aware of the acetaminophen content of all medications taken by the patient (OTC and prescription).

*Note: As of the date of writing of this text, Health Canada had not yet made this decision.

44
Q

Acetaminophen: Contraindications and Interactions

A

Should not be taken in the presence of following:
Drug allergy
Liver dysfunction
Possible liver failure
G6PD deficiency
Dangerous interactions may occur if taken with alcohol or other drugs that are hepatotoxic.

45
Q

Acetaminophen: Toxicity and Managing Overdose

A

Even though available OTC, lethal when overdosed
Overdose, whether intentional or resulting from chronic unintentional misuse, causes hepatic necrosis: hepatotoxicity.
Long-term ingestion of large doses also causes nephropathy.
Recommended antidote: acetylcysteine regimen

46
Q

Analgesics:
Nursing Implications

A

Before beginning therapy, perform a thorough history regarding allergies and use of other medications, including alcohol, health history, and medical history.
Obtain baseline vital signs, intake and output.
Assess for potential contraindications and drug interactions.
Perform a thorough pain assessment, including pain intensity and character, onset, location, description, precipitating and relieving factors, type, remedies, and other pain treatments.
Level of pain is now considered a “fifth vital sign.”
Rate pain on a 0–10 or similar scale.
Be sure to medicate patients before the pain becomes severe, so as to provide adequate analgesia and pain control.
Pain management includes pharmacological and nonpharmacological approaches; be sure to include other interventions as indicated.
Patients should not take other medications or OTC preparations without checking with their physicians.
Instruct patients to notify physician about signs of allergic reaction or adverse effects.

47
Q

Opioid Analgesics:
Nursing Implications

A

Oral forms should be taken with food to minimize gastric upset.
Ensure safety measures, such as keeping side rails up, to prevent injury.
Withhold dose and contact physician if there is a decline in the patient’s condition or if vital signs are abnormal, especially if respiratory rate is less than 10 breaths/min.
Check dosages carefully.
Follow proper administration guidelines for IM injections, including site rotation.
Follow proper guidelines for IV administration, including dilution, rate of administration, etc.

Constipation is a common adverse effect and 
may be prevented with adequate fluid and 
fibre intake.
Instruct patients to follow directions for administration carefully and to keep a record of their pain experience and response to treatments.
Patients should be instructed to change positions slowly to prevent possible orthostatic hypotension.
Monitor for adverse effects
Contact physician immediately if the patient’s vital signs change, condition declines, or pain continues.
Respiratory depression may be manifested by a respiratory rate of less than 10 breaths/min, dyspnea, diminished breath sounds, or shallow breathing.
Monitor for therapeutic effects.
Decreased perception of pain
Decreased severity of pain
Increased periods of comfort
Improved activities of daily living, appetite, and sense of well-being
Decreased fever (acetaminophen)