Professional Documents
Culture Documents
Pain Management
Significance of Pain
Subjective response: only felt by the person
Negative: discomfort
Protective role: warning of potential threat to health
(sometimes a life-threatening condition); prompt for
person to seek medical attention
Pain
- An unpleasant sensory and emotional experience with
actual or potential tissue damage.
- The most common reason for seeking health care.
- The fifth vital sign by the American Pain Society
(2003)
- JCAHO (2005) standards state that pain is assessed
in all patients and that patients have the right to
appropriate assessment and management of pain.
- Pain is whatever a person says it is, existing whenever
the experiencing person says it does (McCaffery &
Pasero, 1999).
- Pain is categorized according to its duration, location,
and etiology.
Types of Pain
Acute pain can be described as lasting from seconds to 6
months
Chronic (persistent) pain is constant or intermittent
pain that persists beyond the expected healing time and
that can seldom be attributed to a specific cause or
injury.
Cancer-related pain
According to Location
(eg, pelvic pain, headache, chest pain). This type of
categorization aids in communication about and
treatment of the pain.
According to Etiology
Burn pain and postherpetic neuralgia are examples of
pain described
Classifications of Pain and Definitions
A. Acute: sudden onset, usually sharp and
localized; less than 6 months; significant of
actual or potential injury to tissues; initiates
flight or fight stress response
1. Somatic: arises from skin, close to surface of
body; sharp or dull; often with nausea and
vomiting
Sleep deprivation
Acute pain
Chronic pain
Depression
Increased disability
Suppression of immune function
Pathophysiology of Pain
involve the peripheral and central nervous systems.
Nociceptors (pain receptors) are free nerve endings in
the skin that respond only to intense, potentially
damaging stimuli. Such stimuli may be mechanical,
thermal, or chemical in nature. The joints, skeletal
muscle, fascia, tendons, and cornea also have
nociceptors that have the potential to transmit stimuli
that produce pain.
Transmission of pain (nociception)
Chemical substances
Past experience
Anxiety
Depression
Culture
Gender
Genetics
Gerontologic considerations
Expectations
The Placebo Effect
meadowsweet,
willow
Acetaminophen Ginkgo and
possibly some of
the abovementioned herbs
Echinacea, kava,
willow,
meadowsweet
Opioids
Valerian, kava,
chamomile
Ginseng
Alfentanil,
fentanyl,
sufentanil
Grapefruit juice
Enhanced risk of
bleeding
Increased potential
for hepatotoxicity
and nephrotoxicity
Increased central
nervous system
depression
Inhibits analgesic
effects
Inhibits the
cytochrome P450
3A4 enzyme in the
liver, blocking
metabolism of the
drug
Name
Morphine
Starting Dose
(milligrams)
Modera Severe
te Pain Pain
3060
(oral)
10
(parenter
al)
Precautions
and
Contraindicati
Comments
ons
Acts as an
Use with
agonist at
caution,
specific opioid especially in
receptors in the elderly
CNS to produce patients, very
analgesia,
ill patients, and
euphoria, and those with
sedation.
respiratory
impairment.
Major risks
include
respiratory
depression,
apnea,
circulatory
depression, and
respiratory
arrest, shock,
and cardiac
Codeine
1530
(oral)
arrest. Obtain
history of
hypersensitivit
y to opioids.
Monitor
patient closely.
If prescribed in
correct dose,
oral
preparations
(MS Contin)
are effective in
treating
moderate and
severe pain.
60 (oral) Acts as an
Many
up to
agonist at
preparations of
360/24 hr specific opioid codeine and the
receptors in the other opioids in
CNS to produce this table are
analgesia,
combinations
euphoria, and with nonopioid
sedation. Is also analgesics.
an antitussive. Caution must
10% of people be used in
lack the enzyme patients with
needed to make impaired
codeine active. ventilation,
Codeine may bronchial
cause more
asthma,
nausea and
increased
constipation perintracranial
unit of
pressure, or
analgesia than impaired liver
other mu
function and in
Propoxyphe 65130
ne (Darvon) (oral)
Hydrocodon 510
e (Vicodin) (oral)
inhibitors. Is
irritating to
tissues with
repeated
intramuscular
injections.
Chronic use
should be
avoided.
Should not be
used for more
than 1 or 2
days.
Weak analgesic; Accumulation
acts as an
of
agonist at
propoxyphene
specific opioid and toxic
receptors in the metabolites
CNS to produce occurs with
analgesia,
repetitive
euphoria, and dosing.
sedation. Many Overdose is
preparations complicated by
include
seizures.
nonopioid
Propoxyphene
analgesics;
is not
biotransformed recommended
to potentially for older adults
toxic metabolite or patients with
(norpropoxphe renal
ne).
impairment.
Most
preparations
are combined
with nonopioid
Tramadol
(Ultram)
50100
(oral)
analgesics.
Unique
Most common
mechanism;
side effects are
analgesia
dizziness,
results from the nausea,
synergy of two constipation,
mechanisms. and
Maximum dose somnolence.
is 400 mg/day. Lowers seizure
threshold.
NSAIDs decrease pain by inhibiting cyclooxygenase, which is the enzyme involved in the
production of prostaglandin.
Nonpharmacologic Interventions
Respiratory depression
Sedation
Constipation
Pruritus