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An adaptive function*
An unpleasant sensory and emotional* experience
associated with actual or potential tissue damage, or
described in terms of such damage. (IASP)
Influenced by anxiety, depression expectation and other
factors.
COMMON CONDITIONS:
o Arthritis
o Persistent neck/back pain
o Neuralgias
o Peripheral neuropathies
o Peripheral vascular disease
o Chronic regional pain syndrome (CRPS -1, -2, -NOS)
o Hyperesthesia
o Myofascial pain syndrome
o Fibromyalgia syndrome
o Phantom limb pain
o Cancer
o Postoperative pain
o Spinal stenosis
Correlates with the prevalence of the conditions
Back pain affects ~75 % of most industrialized nations
Intermediate-stage cancer 40 % of pts
Advanced cancer 60-80% of pts
o Both
Widespread pain that covers half of the body (R or L half, upper or
lower half) plus axial skeleton
> 3 mos
11/18 tender points
Muscular pain
> 18 y/o
women> men
Prevalence increases with age
May be from physical trauma or viral infection
Pathology
1. Phantom limb
2. MS
3. Malignant
Physical
Psychological
Environmental
Workers Compensation
Litigation
AFFECTIVE
o Depression
o Anxiety
o Anger
COGNITIVE
LEARNING
o Operant Learning
o Fear of Movement
Pain beliefs and Coping
Anxiety and Fear Avoidance
Catastrophizing
Depression and Grieving
Nonorganic Findings
Stress
Personality Disorders
Social Support
How do we feel pain?
By: Jamie
Transduction (receptor
activation)
Transmission
Modulation
Perception
Peripheral free nerve endings that
responds to noxious stimuli and
result in perception of pain
Found in:
o Interstitial Tissues -> mechanical,
thermal, & chemical stimulation
o Vessel Walls -> same, plus constriction
and dilation of the vessels
ThermalNociceptor
Mechanical Nociceptor
Polymodal Nociceptor
A-delta fiber -> Fast, myelinated, localized
o Stimulus: pinprick, heat
o Sensation: sharp, pricking, burning,
dermatomal
C fiber -> slow, unmyelinated, poorly
localized
o Stimulus: tissue damage
o Sensation: slow, dull, crawling, sclerotomal
Spinothalamic Tract
Spinoreticular Tract
Spinomesencephalic
Tract
GateControl Theory
Descending Pain
Modulation System
Substantia Gelatinosa contains
ascending gating mechanism to
block nociceptive impulses from
leaving the dorsal horn of the spinal
cord
Two Descending Pain Modulation
System
o Action of Neurotransmitters
Serotonin, Dopamine, Norepinephrine,
Substance P
o Mediated by Neuromodulators
Enkephalin, B-endorphin
Quilang, Cris Michael S.
Idiopathic.
.
Idiopathic pala, uwi na tayo
Considered early as Somatic Manifestation of Affective
Disorder(Mood Disorder).
But further research show that FMS pain is causing
depression.
Affective FMSCausing
Dysfunction Affective
Causing FMS. Vs. Dysfunction.
Skeletal muscles have FMS have low levels of
shown abnormalities energy due to lower
that cause pain. than normal ATP values
although others argue in the blood.
that it is due to Chronic Prolonged work will
Deconditioning caused proceed to an
by FMS anaerobic respiration
which cause to
increase lactic acid
production .
Dysfunctions in the Hypothalamic-Pituitary-Adrenal axis,
Sympathoadrenal gland, and Hypothalamic-Pituitary growth
hormone axis.
Causing hormonal imbalances which leads to the disruption
in the Homeostasis. (e.g. Dizziness and lightheadedness
due to Orthostatic hypotension; dysregulated blood
pressure, High sympathetic activity at night, dysregulated
circadian rhythm, etc.)
These are probably directly related or secondary causes of
FMS.
Serotonin (5-HT) and Substance P were the primary
neurotransmitters that play a role for FMS
Activated type A
and C fiber
afferent neurons
release substance
P into the spinal
cord dorsal horn.
Substance P can
contact with the
neurokinin-1
receptors and
facilitate
nociception.
Production of
Serotonin from
Raphe nuclei from
the brainstem.
Serotonin inhibits
production of
Substance P.
Dysfunction to the
Production of
Serotonin in the
brainstem is the
most likely
Pathophysiology for
FMS.
By: Rosalin, Cristina Veronica A.
Section: BSPT 4-2
FMS has striking similarities to
chronic fatigue syndrome (CFS)
Diagnostic criteria for CFS focuses
on fatigue, whereas the criteria for
FMS focuses on pain, the two most
prominent symptoms of these
syndromes.
Studies have shown that CFS and
FMS are characterized by greater
similarities than differences and
involve both the central and
peripheral nervous systems as well
as the body tissues themselves*
A thorough hx, physical examination and appropriate selected
laboratory or imaging studies can usually differentiate FM
from connective tissue or other systemic dses.
o Chronic (>3 mos), widespread pain
Fatigue, tenderness, depression/anxiety, nonrestorative sleep, cognitive
difficulties (the so called fibrofog), and fxnal impairment
1. Tricyclic anti-depressants
- Have been adopted for use in the treatment of fibromyalgia
because of their ability to boost levels of the brain neurochemical
serotonin (usually deficient in FM patients) and to control pain
and promote sleep.
- Common tricyclics include:
- Elavil (Amitriptyline) Pamelor (Nortriptyline) Sinequan (Doxepin)
Desyrel (Trazadone)
- Side effects: dry mouth, drowsiness, morning hangover,
constipation, weight gain, and sometimes anxiety. Because of
their sedating qualities, tricyclics are usually taken at bedtime.
2. Muscle relaxants
- Decrease pain in fibromyalgia patients by minimizing muscle
spasms and muscle pain. Because of their sedating qualities, they
also help to increase sleep and are usually taken at bedtime.
- Typically used muscle relaxants are:
- Flexeril (cyclobenzaprine hydrochloride) Norflex (orphenadrine
citrate) Soma (carisoprodol) Skelaxin (metaxalone) Robaxin
(methocarbamol)
- Side Effects: drowsiness, dry mouth, constipation, headache, and
heart palpitations
3.Selective Serotonin and Norepinephrine Reuptake Inhibitors (SSNRIs)
- Increase the activity of chemicals called serotonin and norepinephrine
in the brain.
- Examples of SSNRIs:
- Effexor XR (venlafaxine hydrochloride) and two drugs approved by the
U.S. Food and Drug Administration (FDA) for the treatment of
fibromyalgia: Cymbalta (duloxetine) and Savella (milnacipran).
4. Anti-convulsant medications
- Relief of neuropathic pain in fibromyalgia patients (i.e., burning and
electric shock-like feelings in the extremities). If tolerated, these
medications can help relieve nerve irritation.
- Examples of anti-convulsants are:
- Neurontin (gabapentin) Lyrica (pregabalin) Depakote (divalproex)
Dilantin (phenytoin) Tegretol (carbamazepine)
- Side effects: sedation, dry mouth, and dizziness
RESEARCH
Newer FDA- licensed drugs the two SSNRIs duloxetine (Cymbalta) and
milnacipran (Savella) and the anti-epileptic drug, pregabalin (Lyrica)
Patients with unstable hypertension or chronic liver disease should use
duloxetine or milnacipran with caution.
When depression is co-morbid with fibromyalgia, individuals taking milnacipran
or duloxetine should be monitored for suicidal thoughts or signs of aggression.
When gastrointestinal issues like dyspepsia or irri- table bowel syndrome are
present in a patient, pregabalin might be the best drug choice.
FM patients who also have tension or migraine headaches need to keep an
eye on the severity of head- aches when either duloxetine or milnacipran is
taken.
FM patients with chronic heart failure or obesity should use pregabalin with
caution. In addition, the neurocognitive side effects of pregabalin such as
confu- sion, disturbed attention, and euphoric mood might dictate limited use
in patients with severe fibro fog.
5. Sleep medicines
- Used to treat insomnia and other sleep disorders. By improving sleep, it is
also possible to decrease pain and achieve better daytime functioning.
- Examples of commonly prescribed drugs include the central nervous system
depressants Ambien (zolpidem tartrate) and Sonata (zaleplon). These drugs
can be habit-forming and are therefore usually prescribed for short periods
of time.
- A new product, Lunesta (eszopiclone), is one of the generation of sleep aids
like Ambien which helps people to fall asleep without the next day hangover
characteristic of older-generation sleep drugs.
6. Benzodiazepines
- Very sedating and usually taken at bedtime, are sometimes used to help
patients feel calmer and cope with pain more effectively.
- They include the following:
Klonopin (clonazepam) Valium (diazepam) Restoril (temazapam) Xanax
(alprazolam).
MYOFASCIAL PAIN SYNDROME
Analgesics, Non-steroidal anti-inflammatory drugs, Muscle
relaxants and Tricyclic antidepressants, anxiolytics and
anticonvulsants
Non-steroidal anti-inflammatory drugs (NSAIDs) and other
analgesics usually provide moderate symptomatic relief.
Tricyclic antidepressant drugs, which modulate pain at the central
level, are often of benefit, especially in those patients with an
associated sleep disturbance.
Tizanidine (a muscle relaxant which also ameliorates pain by
activating a2-adrenergic receptors) is often a useful adjunct in
difficult-to-treat myofascial pain syndromes.
Diazepam is also recommended for the relaxation of reflex
spasms and the management of anxiety in MPS patients
o Graded exercise
As tolerated then progressed
o Postural exercise
Improve posture and body mechanics, decrease
muscle imbalance and decrease stress on
musculoskeletal structures
o Aerobic conditioning
Counteract deconditioning
o Balance and proprioceptive training
Pain
Massage
Relax muscles
Diaphragmatic breathing
Yoga, Tai Chi, or Qigong
heat, cold, ultrasound, laser, traction, or
TENS
Fibromyalgia Myofascial Pain