Complex Regional Pain Syndrome Flashcards

1
Q

What is CRPS?

A
  • A type of chronic pain syndrome previously referred to as Shoulder Hand Syndrome and Reflex Sympathetic Dystrophy
  • In 1993 the International Association for the Study of Pain proposed a name change to CRPS
  • Name change suggested because the term Reflex Sympathetic Dystrophy implied that the sympathetic nervous system was the primary cause. But not all patients with CRPS have sympathetic symptoms
  • Involves several physiological and psychological systems
  • Process is progressive without intervention
  • Impacts women 3x more than men of which 65% are between ages of 30-55 - average age is 40. Smokers are at higher risk
  • Autonomic Nervous System is not under voluntary control
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2
Q

What is the prevalence and risk factors for CRPS?

A
  • Hx of distal radius fracture. Taking 500 mgs of vitamin C a day could reduce chances
  • Hx of peripheral nerve injury (Type 2)
  • Individuals with other inflammatory disorders including DM, RA, fibromyalgia
  • CRPS in UE is more common than in LE
  • In 90% of the cases there was some sort of trauma that occurred that triggered a response
  • The median nerve has a lot of autonomic fibers and is more prone to develop CRPS
  • 10% unknown etiology
  • Children can get CRPS (usually over the age of 5) and it is more common in the LE
  • Children under the age of 5 and the elderly rarely get CRPS
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3
Q

What is hypertrichosis?

A
  • Abnormal hair growth that occurs in response to an irritated cutaneous nerve
  • This response alone does not mean a person has CRPS but signals that a nerve was compressed and there might be sensitivity and numbness
  • Hair will eventually fall off
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4
Q

What are the general symptoms of CRPS?

A
  • Symptoms vary from person to person
  • Prolonged or excessive pain out of proportion to injury
  • Continuous throbbing pain
  • Sensation of burning, stinging, tingling, numbness, squeezing
  • Sensitivity to heat or cold
  • Swelling
  • Changes in skin temperature - sweaty or cold at times and temperature varies. Extremities may be either hot or cold and there is often a difference between involved and uninvolved extremities
  • Changes in skin texture, which may become tender, thin or shiny in the affected area
  • Atrophy
  • CRPS starts distally and can cross and migrate
  • Some people might not experience pain
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5
Q

What are common symptoms of CRPS?

A
  • Inflammation that is usually associated with stiffness
  • Skin color changes
  • Abnormal hair growth or atrophy of hair and nails
  • Spasms in blood vessels and muscles of extremities
  • Osteopenia
  • Insomnia/emotional disturbance
  • Dystonia/motor planning difficulty
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6
Q

What is hyperpathia?

A
  • An umbrella term for abnormal painful reactions to a stimulus
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7
Q

What is allodynia?

A
  • Pain in specific dermatome distribution that is a result of a stimulus that is not normally painful. Pain with touch and movement
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8
Q

What is hyperaglesia?

A
  • An increased sensitivity to pain that may be caused by damage to nociceptors or peripheral nerves. More extreme than allodynia
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9
Q

What is hyperesthesia?

A
  • A condition that involves an abnormal increase in sensitive stimuli of the senses (hearing, touch, taste, etc.). Increased touch sensitivity is known as tactile hyperesthesia and an increased sound sensitivity is known as auditory hyperesthesia
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10
Q

What is the autonomic term vasomotor?

A
  • Dilation (red and swollen) and constriction of blood vessels (blue and stiff)
  • As CRPS progresses, vasodilation turns to vasoconstriction
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11
Q

What is the autonomic term sudomotor?

A
  • Autonomic function associated with the sweat glands

- Lotion is important for people who do not sweat

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12
Q

What is the autonomic term trophic?

A
  • Changes in tissues, due to loss/reduction of nerve and/or blood supply (muscle atrophy, increased nail growth - hypertrichosis, changes in nails, increased hair growth)
  • Muscle atrophy generally results because people do not want to move if they are in pain
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13
Q

What is the role of the parasympathetic system?

A
  • Rest and digest
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14
Q

What is the role of the sympathetic system?

A
  • Fight or flight
  • Increase in blood flow, heightened sensitivity, dilation of pupils, sweating
  • We are preparing to engage in a fight or flight or run away
  • Not all people with CRPS have sympathetic components
  • Old theory was that the sympathetic nervous system would kick into overdrive and not calm down. We now know that it is much more complicated than that and not all individuals have a sympathetic component
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15
Q

What are the two types of CRPS?

A
  • Type I: Occurs after an illness or injury that did not directly damage the peripheral nerves of the affected limb. Ex: CRPS can occur with removal of gall bladder
  • Type II: there is an identifiable peripheral nerve injury

*both types have phases

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16
Q

What are the grades/stages of CRPS?

A
  • Grade 1: algodystrophy (disruption of bone growth combined with sympathetic symptoms)
  • Grade 2: sympathetic dystrophy without pain
  • Grade 3: sympathetic maintained pain
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17
Q

What are the time frames/stages of CRPS?

A
  • Acute Phase: first 3 months
  • Subacute Phase: 3 more months
  • Chronic Phase: 6 months and onward
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18
Q

How is CRPS evaluated and identified?

A
  • Early dx of CRPS is of utmost importance. The sooner proper treatment is delivered, the better the outcome
  • The medical community is not often trained to spot early signs of CRPS
  • Patient often gets “labeled” as being a malingerer, magnifier, or having psychological issues
  • Mechanism of injury: usually follows some type of trauma such as a fracture, sharp force injury, surgery, infections, heart problems, and cumulative trauma disorders. Insult may be quite mild in nature
  • May spread in 70%, only 8% are systemic
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19
Q

What are the International Association for The Study of Pain (IASP) criteria for evaluating CRPS?

A
  • Presence of inciting noxious event or prolonged immobilization
  • Continuing pain, allodynia, or hyperaglesia which is disproportionate to any inciting event
  • Edema, changes in the skin, blood flow or abnormal sudomotor activity in the region of pain
  • The diagnosis is excluded by the existence of a condition that would otherwise account for the degree of pain and dysfunction
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20
Q

What are therapeutic ways to identify CRPS?

A
  • Through history of health, mechanism of injury, and post injury care
  • Pain threshold evaluation: McGill Pain Questionnaire and Visual Analog Scale
  • Clinical observations including movement and assessment of skin color, nails, and possible atrophy
  • Semmes Weinstein Monofilament testing because light touch can be perceived as being painful
    • The presence of pain associated with light touch (2.83) is abnormal
  • Neuromusculoskeletal evaluation including: ROM, sensation, fine/gross motor control. Muscle testing if pain is limited or not present
  • Bone scans can also detect osteopenia
  • Comparing the temperature of one extremity to another
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21
Q

What are diagnostic tests that can detect CRPS?

A
  • 3 phase bone scan to evaluate vascular profusion
  • Monitoring digital pulp temperature
  • X-rays used to evaluate regional osteopenia - intervenous contrast is used. Regular radio graphs are usually only 60% accurate
  • Thermography is imaging that can be useful in diagnosing CRPS. CRPS can be associated with abnormal skin temperature regulation, often described as a “hot” or “cold” feeling of the skin
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22
Q

How severe can CRPS be?

A
  • Pain is primary complaint and often out of proportion with the nature of the original trauma
  • On the McGills scale it is rated as 42/50 - worse than child birth (32) and amputation of a digit (39)
23
Q

What is the clinical presentation of CRPS Stage I?

A
  • First 3 months
  • Increased hair and nail growth
  • Changes in sweating
  • Increased pain
  • Skin becomes thin and dry
  • Color changes to red, area becomes warm and swollen, but can quickly become cold
  • Allodynia (non-painful stimuli evokes pain)
  • Hyperalgesia (painful stimuli evokes more intense pain than usual)
24
Q

What is the clinical presentation of CRPS Stage II?

A
  • 3-6 months
  • Decreased hair growth
  • Swelling that can spread
  • Stiffness
  • Appearance
  • Joints thicken
  • Muscles atrophy
25
Q

What is the clinical presentation of CRPS Stage III?

A
  • 6 months or longer
  • Changes are irreversible at this stage
  • Severely limited mobility of affected area
  • Contractures of the muscles and tendons that flex the joints
  • Muscle wasting
26
Q

What are statistics of recovering from CRPS?

A
  • 80% of those who receive treatment within the first year will have significant improvements
27
Q

What are OT and PT interventions for treating CRPS?

A
  • Modalities: fluidotherapy is ok as long as temperature is monitored. No ice packs or heat packs.
  • Exercise
  • Edema control, massage, pressure garments (e.g. flexion gloves can be helpful because they have rubberbands to distract fingers and break reflex loop)
  • Stress loading (e.g. weight bearing into a scrub brush)
  • Desensitization
  • Functional activities
  • Imagery and relaxation
  • Mirror box
  • CPM: continual passive motion machines as tolerated
  • Splinting is controversial
28
Q

What should an OT evaluation include for someone who might have CRPS?

A
  • History
  • Observe the body part (e.g. skin color, texture, temperature)
  • Edema (take photos, measure, Volumeter)
  • Assess pain
  • Assess sensation
  • Assess grip (this is usually significantly affected due to proprioceptive dysfunction)
  • Check for skin atrophy and document changes during therapy
    • Dry, scaly, shiny
    • Hair grows in course clumps and then thins
  • Nails are more brittle and grow faster
  • Sweaty or goose flesh/bumps
  • Mottled, red or blue appearance
  • Vasomotor changes
    • Sensations of warmth or coolness without even touching the patient
    • Changes in skin color from white mottled to red or blue
    • Changes in color and pain triggered by changes in room temperature
  • Movement
    • Difficulty initiating movement, reports stiffness, tremors
    • Dystonia (i.e. abnormal posturing, involuntary jerking, painful postures)
    • Cramps/muscle spasms
  • Weakness
  • Slow movement
  • Coordination, dexterity, functional use during daily living skills
  • Atrophy due to disuse
29
Q

What is the MCP Squeeze Test?

A
  • Grasp the MCP heads and lightly squeeze

- Test is positive if patient pulls away

30
Q

What is the drop and swipe test?

A
  • Part 1: alcohol swab package is opened and squeezed till alcohol drops on the affected limb. In 10-60 seconds ask the patient what they feel. If pain dramatically increases the patient is experiencing thermal hyperalgesia. But if patient reports that it feels cold/cool then it is a normal response and not thermal hyperalgesia
  • Part 2: swipe the alcohol pad lightly over the affected area. If patient responds with increased pain or withdraws the limb or tells you to stop, then they are experiencing mechanical hyperalgesia
  • Most patients with CRPS experience both thermal and mechanical hyperalgesia
31
Q

What are examples of OT goals when working with someone that has CRPS?

A
  • Minimize edema
  • Normalize sensation
  • Increase flexibility, ROM, coordination
  • Promote normal positioning
  • Decrease muscle guarding
  • Increase functional use to increase independence
  • Educate patient on the pain cycle, medications, and pain management
  • Normal use of affected area
  • Facilitate movement (cornerstone of treatment). The person will not cause harm by moving
32
Q

What are interventions that are contraindicated with most CRPS cases?

A
  • PROM. Once the person does not have pain then PROM can be performed. Do not want to trigger an inflammatory response
  • Avoid joint mobilization
  • Avoid splinting and casting to immobilize area
33
Q

What is Watson Carlson Stress Loading?

A
  • Scrub and carry (promotes compression and distraction)
  • Dystrophile: a devise that is used to measure the amount of weight bearing a person can perform
  • The goal is to bear as much weight as possible through the affected extremity. It is common for pain and swelling to increase slightly in the first few days of protocol. But positive results are usually observed within the first week of treatment
  • Begin with 3 minutes/3 times a day and progress to 10-15 minutes/3 times a day
  • Carry: the patient is asked to carry an object weighing 1-2 pounds during the day. This causes a distraction force on the limb
  • This approach increases the large fiber afferent impulses and in turn helps relieve pain
34
Q

What are examples of stress loading activities?

A
  • Scrubbing a plywood board while in the quadruped position. Scrub for 3-5 minutes every 2 hours and work up to 10 minutes every 2 hours
  • Carry a weighted bag in the affected hand. Grade up the weight as quickly as possible according to level of tolerance
  • Functional activities: washing windows, wiping counters, ironing, scrubbing bath tile, carrying groceries, sanding wood
35
Q

Why is functional activity important to incorporate when treating CRPS?

A
  • Prevents atrophy of disuse
  • Daily activities can be performed at home
  • Craft activities can be performed in the clinic
  • Each activity will encourage the patient to view their hand as a functional part of their body
36
Q

What is maladaptive cortical remapping?

A
  • Disorganization of the cortical representation of the affected limb results in pain and dysfunction
  • The homunculus becomes disorganized and then there is an altered view and perception of the person’s body
37
Q

What is brain smudging?

A
  • Mapping in the brain can change dramatically because the brain may sense trouble. It then recruits neighboring cells and that part of the brain becomes disinhibited
  • Can occur anywhere in the body because it can be a useful defense mechanism
  • Educate to take away fear that brain used to make pathway
  • Graded activity (thinking about movement to actually movement)
  • Exploring with different textures

*Good cortical remapping involves experienced based learning!

38
Q

What is Phase I of Graded Motor Imagery?

A
  • Phase I: laterality or the discrimination of the left from the right with accuracy and speed
  • This can be done by having the patient find their affected hand on every page of a book/magazine
  • Patient has to be able to establish right from left in order to do Graded Motor Imagery
39
Q

What happens to laterality in patients with CRPS?

A
  • Laterality is lost. The brain tunes out the affected limb
  • The average time for someone to distinguish right from left is 2.4 seconds
  • For someone with CRPS, it takes twice as long (average of 4.7 seconds)
  • Treatment is focused on accuracy and not speed when identifying body part
40
Q

What techniques are used during Phase I of Guided Motor Imagery?

A
  • Diaphragmatic breathing
  • Meditation
  • Guided imagery
  • Biofeedback
41
Q

What is Phase II of Graded Motor Imagery?

A
  • Imagining the extremity performing motion: static > dynamic > while doing a task

This phase provides brain mapping opportunities without moving the affected extremity

Ask the patient what activities they want to be able to perform with their affected hand to guide therapy

42
Q

What is Phase III of Graded Motor Imagery?

A
  • Mirror Therapy
  • The mirror conveys visual stimuli to the brain while observing the unaffected extremity
  • Principle states affected limb can be stimulated by visual cues originating from the opposite side of the body
  • This phase can only be done if the pain is not reproduced
43
Q

What is the order of Mirror Box therapy?

A
  • Static observation > observe motion of non-affected extremity using mirror > bilateral motion using mirror
44
Q

What components make edema management successful?

A
  • Elevation
  • Diaphragmatic breathing
  • Patient can perform edema retrograde massage
  • Gentle compression garment. Use caution and only for short periods of time because they tend to irritate and can cause pain and swelling
45
Q

What techniques make sensory discrimination successful?

A
  • Identifying objects in hand
  • Tactile discrimination and desensitization
  • Sharp vs dull
  • Graphesthesia training: writing a number or letter on the patient’s affected area
  • Restore and normalize proprioception
  • Desensitization = patient is in control
46
Q

What type of exercise should be incorporated with people who have CRPS?

A
  • Gentle AROM as tolerated
  • PROM can be performed once the client can tolerate without the systemic response
  • Strengthening in later stages as edema and stiffness decrease
  • If there is any increased pain or edema then it is a sign that the intervention was too forceful or aggressive
  • Exercise should be performed every hour
47
Q

What types of interventions/equipment/tools are successful in identifying movement disorders (dystonia and neglect) with CRPS?

A
  • Proprioceptive Neuromuscular Facilitation (PNF)
  • Stationary bike
  • UBE
  • Chinese meridian balls
  • Functional tasks
  • Yoga
  • Tai chi
  • Dance
48
Q

What is transcutaneous electrical nerve stimulators (TENS)?

A
  • Functional Electrical Stimulation used to decrease pain, edema, and increase muscle strength
  • Sends superficial signal to the brain that travels faster than pain signals and causes a “traffic jam” of signals to allow movement
49
Q

What are heat/cold modalities that can be used with CRPS?

A
  • Moist heat: can increase tissue extensibility if followed by exercise. Do NOT use in Stage I
  • Whilrpool: have the patient perform exercises while their hand is under water for 10 minutes maximum
  • Fluidotherapy
  • Paraffin: only used in late stages of CRPS. Used in conjunction with passive stretch to increase joint mobility
50
Q

What is a low level laser light?

A
  • Preliminary studies are encouraging low level laser light to reduce CRPS pain
  • It stimulates healing and relieves pain without side effects
51
Q

Why should splints be used with caution when treating CRPS?

A
  • Splints immobilize joints and that can increase CRPS
  • But splints might be important to prevent joint contractures
  • May have to build up splint wear time

Examples of splints used for CRPS: traction glove and resting hand splint

52
Q

When are pharmacologic interventions used to treat CRPS?

A
  • Rarely used in isolation but usually in combination with therapy and adaptive modalities
  • Although pain medications are often prescribed, they are not affective in alleviating neurogenic pain
  • Increase intake of trytophan. This is found in low fat foods and is a precursor to Seratonin
  • Nutrition should be addressed. Decrease caffeine and alcohol intake. Reduce intake of foods high in tyrosine (e.g. cheese, soy, beef) which is an amino acid precursor to adrenaline
53
Q

What are stellate ganglion nerve blocks?

A
  • When performed correctly by an anesthesiologist, it causes drooping/ptosis of the eyelid
  • Patient must go to therapy immediately following the injection and must perform movement/exercises throughout the day
  • Patients usually receive a series of 5 to 6 injections
  • Blocks relieve pain and enable more effective therapy, improve mood, and improve level of activity
  • The stellate ganglion is a cluster of sympathetic nerves at the back of the neck and they can become overactive in CRPS
54
Q

What are surgical interventions used to treat CRPS?

A
  • Decompression: used if a nerve is compressed (e.g. carpal tunnel syndrome)
  • Sympathectomy: operation rarely used to divide the sympathetic nerves in patients - controversial
  • Spinal cord stimulation or intrathecal drug pumps: pain medications are injected continuously into the space around the spinal cord
  • Deep brain stimulation and electrotherapy: are therapies used but new therapies are emerging