objectives what is a physical agent modality? - asht · pdf filewhat is a physical agent...
TRANSCRIPT
Hand Therapy Review CourseUC Irvine Medical Center
Orange, CAFebruary 24-26, 2017
Physical Agent Modalities for the Hand TherapistAlessia DiGennaro Kerner, OTR/L, CHT
Hand Therapy Review CourseUC Irvine Medical Center
Orange, CAFebruary 24‐26, 2017
Physical Agent Modalities for the Hand Therapist
Alessia DiGennaro Kerner, OTR/L, CHT
Objectives
1. Understand physiologic changes with modalities.
2. Review procedures, contraindications and precautions of each modality.
3. Objectively assess the efficacy of PAMs.
What is a Physical Agent Modality?
Procedures and interventions that are systematically applied
to modify specific client factors when neurological, musculoskeletal,
or skin conditions are present that may be limiting
occupational performance. (Bracciano, 2008)
What Can Modalities Affect?Pain
Blood & Lymphatic Flow
Tissue Healing
Nerve Function
Tissue Extensibility
Edema & Inflammation
Muscle Excitability
Metabolic Changes
Modality TypesThermotherapy &
Application of electrical current
Methods of Energy Transfer
Conduction Thermal transfer between two surfaces by direct contact
Hot/Cold PacksParaffin
Convection Transfer of heat by movement of a medium
FludiotherapyWhirlpool
Conversion Energy converted to heat in the tissues by friction
UltrasoundDiathermy
Radiation Direct transfer of energy without a medium
LaserUV
Evaporation Absorption of energy by conversion from liquid to vapor
Spray & StretchSweating
Superficial Thermal Modalities
Hot packs
Paraffin
Fluidotherapy
Hydrotherapy
Cryotherapy
Physiological Effects of Heat
Reduces pain
Decreases muscle guarding, spasms and protective posturing
Improves connective tissue extensibility
Improves tissue healing
Ranges of Superficial Heat
• 98.6F (37.5C)Normal temperature of tissue
• 98–101F (37 – 38.5 C)
Mild heat
• 101–103F (38.5 – 40 C)
Moderate
• 104-113F (40 – 45C) (Feels very hot)
Vigorous: Therapeutic range
• +113°
Potential Tissue Damage
Effectiveness of Heat
Benefits of heat depend upon
Type
Duration
Depth
Temperature
Stretch
Contraindications for Heat
Impaired sensation
Vascular compromise or disease
Diabetes with impaired circulation
Acute injury or inflammation
Vascular instability
Skin graft, Replant
Malignancy/Cancer
Recent or potential hemorrhage
Precautions for Heat
Poor thermoregulation
Poor sensation
Edema
Impaired cognition
Impaired speech/language
Cardiac conditions
Rheumatoid Arthritis
Hot Packs
Conduction
H2O in tank: 165°- 170°F
Penetrates 1-2 cm.
6-8 towel layers
Commercial terry cloth equals 4 layers
Temperature remains elevated 45-60 min.
Treatment time 10-20 min.
Hot PacksAdvantages
InexpensiveEasy set upPassive stretchLarge tx areaHome program
DisadvantagesStatic positionObserve skinBurnsHeavyPoorly conform
Electric heating pads
ThermaCare heat wraps
Rice or flax packs
Portable Heating Options
Paraffin
Conduction
Low specific heat
Circumferential heating
113º-129º F
Treatment 10-20 min
Dip or immersion
ParaffinAdvantages
Soothing/lubricatingHighly conformingElevateCost effectiveHome program
DisadvantagesMessyCross contaminationRestock materialsOpen wound
Precautions with Paraffin
Do not apply to: Open wounds
Burned tissue
Insensate areas
Otherwise same as with other heat
modalities
Fluidotherapy
Convection
Warm-up prior to use
112-118 F
Corn cob particles
Treatment 10-20 min
Fluidotherapy
Advantages
AROM or PROM
Adjustable temperature
Adjustable agitation
Desensitization
Disadvantages
Semi-dependent position
Expensive
One patient treated/time
Respiratory irritation
HydrotherapyConvection
Temp 91 degrees
Treatment 10-20 min
AdvantagesLubricates dry skinCleansing effectDressing removalAROM
DisadvantagesDependent positionTank sterilizationAdditives cytotoxic
Due to disadvantages of whirlpool, pulsed lavage with suction is often preferred for wound care
Cryotherapy Physiological Effects of Cryotherapy
Decrease inflammation &/or edema
Pain modulation
Decrease guarding &muscle spasms
Cameron 2009
Cryotherapy
Ice packs
Cold packs
Vapocoolant sprays
Ice probes
Cold compression units
Contraindications for Cold
Diminished sensation
Compromised vascular system Replants
New graft/flap
Diabetics with compromised sensation
Peripheral Vascular Disease
Very young/elderly
Open wounds
Cold UrticariaA histamine response that causes
raised red areas (hives) as a localized response
Systemic Urticaria: facial flushing, ↑ blood pressure, ↑ heart rate, light headed
Contraindications for Cold
Raynaud’s PhenomenonCyanosis, pallor, redness following exposure to cold
Associated with autoimmune conditions such as RA and Lupus.
Contraindications for Cold
CryoglobulinemiaTissue ischemia occurs with Application of cold secondary to an abnormal blood protein turning into a gel.
Associated with:Autoimmune conditions Chronic liver disease Multiple melanomaInfection
Paroxysmal Cold Hemoglobinuria(PCH)
Hemoglobin released from damaged RBC and lysed RBC can be seen in urine, leading
to subsequent anemia.
Therapeutic Application of Cryotherapy
Most Treatments range: 23°– 32 F
Responses to coldStage I Cold 1 - 3 minutesStage II Burning 3 - 5 minutesStage III Aching 5 - 7 minutesStage IV Numbness 7+ minutes
**General timeline, varies with tissue/patient
Cold Packs Conduction
Silica gel stored at 23 F
Moist towel enhances effectiveness
Penetrates 1-2 cm
AdvantagesEasy to useLarge tx areaHome program
DisadvantagesConform poorlyObserve skin changes
Ice Massage
Vigorous cooling
Effective for small areas
Small paper cup or popsicle stick
Cryocup
Treatment 3-5 min
Burning aching numbness
Ice Massage
AdvantagesCools quicklyEasy to applyMonitor skin changesHome ProgramInexpensive
DisadvantagesPatient toleranceMessyCovers small area
Cold Compression Units
Circulated cold water
Pneumatic pressure
Acute injuries
Conformity issues
Temperature adjustable
Cold Vapocoolant Spray “Spray and stretch”
Evaporation
Trigger point, referred pain & acupressure
Method:Place muscle on stretchSpray at 30°angle2 feet from skin6 sweeps parallel to mm. fiber10 cm. per second
Ultrasound
Ultrasound
Sound wave that produces changes in tissues
Electrical energy converts to mechanical (sound) energy
Mechanical pressure waves cause vibrating molecules to bump into adjacent molecules, transferring energy from one to another
A chain reaction continues though a material until the energy is dissipated
Ultrasound TransducerTransducer = “Sound head”
Contains a crystal that converts electrical energy into high frequency sound waves by expanding and contracting, called Piezoelectric effect
The machine often has interchangeable sound headsDifferent sizes
Different frequencies1 MHz or 3 MHz
Google, 4/1/13
Relates to:Area of the transducer from which the US energy radiates
Vibration is not uniform so the ERA is typically smaller than the total area of the sound head
Treatment area should not exceed 2x the ERA
ERA can be found on stickeron ultrasound cord
Effective Radiating Area Beam Non-uniformity Ratio
Relates to:Ratio of peak power and average power output
Lower BNR = More comfortable
Regulations 6:1 or less
Hot spots
Ultrasound Parameters
Frequency
Spatial Average Intensity
Duty Cycle
Duration ofTreatment
Relates to: Depth of penetration
Expressed in MHz
1 MHz heats 2-5 cm.“Deep, slower to get warm”
3 MHz heats 1-2 cm.“Hot, fast and shallow”
Frequency
Spatial Average IntensityRelates to:Magnitude of the force in a sound wave
Expressed as W/cm²
Greater intensity = greater temperature increase with continuous ultrasound setting
No specific guidelines on selecting intensity
Devices allow for up to 3.0 W/cm2, usually .25-2.0 W/cm2
Turning up the power (intensity) simply sends more energy to the same depth.” (Knight, 2007)
Duty CycleRelates to: Proportion of total treatment time US is on
Expressed as a percentage or ratio
Continuous100% Thermal Modality
Pulsed10%, 20% or 50%Non-thermal Modality
Application of UltrasoundFull contact with skin
Sound head parallel with skin
Constant movement of sound head(2-5 cm/sec)
Overlap strokes (1/2 of ERA)
Absorption of UltrasoundEnergy penetrates tissue that is high in water content.
US passes through to deeper tissues
Fat, blood
Energy is absorbed well, into dense tissue that are high in protein.
Tissues heat up
Ligament, Tendon, Fascia, Joint capsule, scar tissue
Absorption dependent on coupling medium. Ultrasound gel: 96%Ultrasound lotion: 90%Betamethasone (.05%) in ultrasound gel: 88%
Physiological Effects of Thermal Ultrasound
Increase extensibility in collagen-rich tissues
Decrease joint stiffness
Decrease spasm
Decrease pain
Promote tissue healing
Temperature Increases with Thermal Ultrasound
Continuous treatment at1W/cm² & 1MHz = ↑ by 0.36°F (0.2°C) per minute1W/cm² & 3MHz = ↑ 1.6°F (0.9°C) per minute
So… to get a tissue temp increase of 5°F (3°C) it would take
5 minutes at 3MHz10-15 minutes at 1MHz
Knight, 2007
Tissue temperature changes and benefits last for approximately 4 minutes after treatment ends.
Stretch during or immediately afterward for best benefits.
Physiological Effects of Non-thermal Ultrasound
Decrease inflammation
Increase cell membrane permeability
Stimulate tissue regeneration (soft tissue & bone)
Increase fibroblastic activity
Synthesize collagen– increases tensile strength
Generally associated with pulsed US
20% for most research
Contraindications for Ultrasound
Insufficient circulation, thrombophlebitis or DVT
Malignant tumors & cancer
Pregnancy
Acute infection May use 24 hours after antibiotics are started
Joint cement or plastic components
Psoriasis
Children (over growth plates)
Over CNS tissue, eyes, reproductive organs, electronic implants
Precautions for UltrasoundAcute inflammation
Impaired cognition
Decreased/lack of sensation
Fractures Specific devices deliver very low dose US: 0.15 W/cm2; at 20%, 15-20 minutes
PVD: Be careful with thermal US
Can go over metal implants if sound head is kept moving and patient has normal sensation
Phonophoresis
Related to:The application of therapeutic US toassist in the diffusion of medication throughthe skin
Increase permeability of stratum corneum.
Ultrasound absorption lessened with medication in coupling medium. May decrease benefits of ultrasound.
Drug is more concentrated in treatment area but does become systemic.
Medications Used in Phonophoresis
Local Analgesics: Lidocaine, Lidex, Theragesic cream
Local Anti-inflammatory medications: Hydrocortisone or Dexamethasone
Non-steroidal medications: Salicylates
1.Need prescription for medication used with phono2.Need to use a coupling medium with phono3.Pre-heating area with a hot-pack or thermal ultrasound beforemay enhance penetration 4.Suggested treatment parameters:
3 MHz frequency, continuous, 0.5-.75 W/cm²for 5-10 minutes
Contraindications for Phonophoresis
Check for allergy to medication being used
Same as contraindications to ultrasound
Electrotherapy
Electrotherapy BasicsRelates to:Flow or movement of ions or electrons via electrical current
Produces chemical, mechanical,thermal and magnetic changes in stimulated tissues
Electrical current flow takes pathof least resistance. Moves from high (cathode) to low (anode) electron concentration
Electrotherapy uses direct current, alternating current and pulsed current to delivery therapeutic benefit
Direct CurrentUnidirectional - continuous flow of particles in one direction
Used for iontophoresis, wound healing, stimulation for denervated muscles
Alternating Current
Bi-directional – continuous flow of charged particles
Symmetrical or asymmetrical
Used for IFC & Russian stimulation
Pulsed CurrentNon-continuous flow of AC delivered in a series of pulses which last < 1 sec. before next series of pulses.
Unidirectional or bi-directional
Physiological Effects of Electrotherapy
Pain reduction
Stimulate tissue healing
Reduce edema
Facilitates muscle contraction
Strengthen motor patterns
Electrotherapy Terms
Charge
Resistance/Impedance
Amplitude
Duration
Frequency
Ramp
D Lingle 2013
Charge
Cathode: negative pole; attracts (+)
Anode: positive pole; attracts (-)
Cations: positive ions
Anions: negative ions
D. Lingle 2013
Resistance/Impedance
Relates to:Opposition to the flow of charged particles
Skin impedance offers resistance to current flow
Resistance varies throughout the body depending upon:
Water content, blood flow, patient activity or position, conducting medium
Decrease resistance by keeping patient & electrodes hydrated, and clean
D. Lingle 2013
Pulse Amplitude“Intensity”
Relates to:Maximal current (voltage) achieved in a monophasic pulse or in each phase of a biphasic pulse
Measured in milliamps (mA)
Needs to be strong enough fortherapeutic benefit
Peak Amplitude = Highest point of pulse
Devices have full adjustability of these settings
Pulse Duration“Pulse width”
Relates to:Time period that current is “on”
Interval between beginning and end of all phases of pulse
Expressed in milliseconds
Generally set between 200 & 400 milliseconds
Devices have full adjustability of these settings
Pulse Frequency“Pulse Rate”
Relates to:Pulses per second
Expressed as pps Pulses per second (pulsed current) Beats per second (interferential current) Cycles per second (alternating current)
Typical NMES setting is between 35-50 pps
Ramp
Relates to:Gradual increase in theintensity of a musclecontraction
On/Off CycleRelates to:
Periods of electrical stim versus periods of no stim
Expressed as a ratioOn Time
Typically 8-12 secondsOff time
Typically 10 – 50 seconds
On/Off Ratio
1:1, 1:2, 1:3, …
Example
1:5 = 8 seconds on, 40 sec off
Or 10 seconds on, 50 sec. off D Lingle 2013
ElectrodesSkin & hair
Coupling agent
1/2 diameter of electrode spacing
Electrode size
Muscle sizeSmall muscle: Monopolar placement Small electrode over motor point, slightly large
electrode elsewhereLarge muscle: Bipolar placement 2 electrodes of same size over proximal & distal
muscle
Electrode Placement
Superficial musculature = close together
Deeper musculature = farther apart
Areas of decreased skin resistance
Trigger points, motor points & acupuncture points are frequently close together.
Direct: electrodes are placed directly on the painful site.
Contiguous (bracketed): electrodes are placed around the painful tissues.
Proximal to painful areas
Parallel to pain, linear or crossed
Over path of peripheral nerve
Dermatome: At SC nerve root and distal end of dermatome
Electrode Placement Neuromuscular Electrical Stimulation
NMESStimulation of innervated muscle to restore muscle function:
Muscle strengthening
Spasm & spasticity reduction
Prevent disuse atrophy
Enhancement of ROM
Muscle reeducation
Neuromuscular Electrical Stimulation
Fast-twitch fibers
Immobilization atrophy = large, fast twitch fibers
Normal AROM = small, slow twitch fibers
Combine with functional task or active motion
Treatment TimeFrequency and duration of treatment depend on goals
StrengtheningNeed 10 – 15 strong contractions per treatmentDuty cycle 1:5 →1:3 delivered 1-3 times per day
Ramp up 2 sec., 6 sec. on, ramp down 2 sec. = 10 sec.
50 seconds off
Total treatment time = 10-15 minutes
EnduranceDuty cycle 1:3, Ramp up/down 1-2 sec., Time 30+ min., 1x/day
Interferential CurrentIFC
Pain & edema control
Quadripolar
Electrode placement so currents intersect
“Beat” creates therapeuticeffect
Interferential Current
Example:
Channel 1 = 4000Hz Channel 2 = 4100Hz
“Beat” = 100Hz
Interferential Current
Quadripolar (“True- Interferential)
Pre-modulated IFC
Interferential CurrentPain control
Low beat frequency (1-10 Hz)
Intensity: moderate sensory to motor level
Theory: Release of opiates
Higher burst frequency (80-150 Hz) affects widest range of receptors but duration of pain reduction is thought to be less
Intensity: Strong sensory level
Edema Reduction
Medium beat frequencies (15 Hz) may reduce edema by activating musculoskeletal pumping action.
It may inhibit sympathetic activity assisting with fluid drainage.(Goats, GC, 2009)
High Volt Pulsed CurrentHVPC
Prevention of edema in acute inflammatory stage Use cathode as the active electrode, and anode as
dispersive
Intensity below motor threshold
Tissue healing Cathode or anode is the active electrode placed at
the wound
Intensity comfortable sensory stimulation
High Volt Pulsed CurrentWaveform: twin peaked monophasic pulsed current
Pulse duration: fixed within unit
Frequency: 1 – 120 Hz
Amplitude: to patient tolerance
Active electrode is usually smaller than the dispersive
Polarity: positive or negative
Russian Stimulation
Used for muscle strengthening
Medium frequency, AC, bursts to elicit tetanic contraction
10 sec. on, 50 sec. off for 10 min.
Variable evidence of it’s effectiveness
Transcutaneous Electrical Stimulation
TENSUsed to modulate pain perception
Pulsed current
Modulation TENS units have modulations built in to decrease
accommodation Waveform parameters such as frequency, duration and
intensity, are periodically changed to decrease the chances of accommodating to the stimulation, which make it less effective.
Michlovitz 2012
Pain Control Theories Related to TENS
Gate Control Theory (Melzak and Wall 1965)
When an electrical current is applied to a painful area, transmission of the perception of pain via small diameter, slow, “C” fibers to the brain is inhibited by the activity of the large diameter, fast conducting, “A” proprioceptive sensory nerve fibers
This closes the gate to the pain perception to the brain
Application: Conventional (High Frequency) TENS
Pain Control Theories Related to TENS
Endorphin Release Theory or Opiate-Mediated Control Theory
The brain can secrete analgesic substances such as endorphins (endogenous opiates) that act on the CNS & PNS to modulate pain and provide a sense of well-being
Application: Low Frequency TENS & Brief Noxious level TENS
Conventional vs. High Rate TENS
High pulse frequency (90-150 pps)
Short (low) pulse duration (50-100 msec)
Intensity: comfortable, Sensory level (tingling)
Length of treatment: 20-60 min
(+) Fast pain relief (-) short carryover
Gate theory
“Accupuncture-like” TENS
Low pulse frequency (2-10 pps)
Long pulse duration 160 - 400 msec.
Intensity: Motor level (visible muscle twitches)
Length of treatment: 20-45+ minutes
Longer relief of pain (possibly 2 – 6 hrs)
Often used for non-acute pain
Possible method of action:
release of endorphins
ElectroacupunctureNoxious, Brief & Intense TENS
High pulse frequency: > 100 pps
Long pulse duration: (300-1000 msec)
Intensity: strong motor level to uncomfortable
Length of Treatment : brief, just a few min.
Possible method of action:
through the release of endorphins (& possibly blocking pain perception)
Used prior to painful activity
High level of analgesia is achieved for a short period of time
Contraindications to Electrical Stimulation
Demand cardiac pacemakers
Indwelling stimulators
Trunk of pregnant patient
Carotid sinus/artery
Eyes
Unstable fractures
Active TB
Cancer
Peripheral Vascular disease
Hx seizures
Peripheral nerve disease
Infections
Rapid fatigue syndromes
Precautions for Electrical Stimulation
Areas of decreased sensation
Excessive Adipose tissue
Unhealed incisions
Cardiac conditions
Bony prominence
Impaired cognition
Pt. unable to provide feedback
Over growth plates
Skin irritations to electricity or gels
When driving or operating machinery
Iontophoresis
The delivery of ions into the body for therapeutic purposes using an electrical current; transcutaneously via passive absorption over time
IontophoresisDirect current
Electrically charged electrode will repel a similarly charged ion
(+) ions placed under (+) electrode
(-) ions under (-) electrode
Delivery electrode contains medication
Non-delivery or return electrode opposite polarity
D. Lingle 2013
Coulomb’s law in electrophysics states that:
Like charges repel and opposite charges attract
Positively charged ions (cations) will be repelled from the positive pole
Negatively charged ions (anions) will be repelled from the negative pole
Before Using Iontophoresis!
Need to obtain a prescription from the treating physician for medication used with iontophoresis
Therapeutic Effects of Iontophoresis
Dependent upon medication selected, but include:
Decrease Inflammation (acute and chronic)
Decrease Pain
Soft tissue de-mineralization (calcium deposits)
Promote Wound healing
Decrease Scar tissue/adhesions
Decrease Hyperhidrosis
Medications Used with Iontophoresis
ION POLARITY PURPOSE
Dexamethasone (-) Decrease inflammation
(tendonitis, tendonosis)
Acetic Acid (-) Helps dissolve Calcium deposits
Iodine (-) Decrease scar tissue
Lidocaine (+) Decrease local pain
Tap Water (+) (-)Switch halfway
thru tx.
Decrease hyperhidrosis
(sweaty palms/soles of feet)
Dosage with Iontophoresis
Inflammatory conditions: 4.0 mA/10 minutes
Treatment time may vary depending on patient tolerance (common 2.0 mA/20min.)
Scar formation: intensity 4.0 mA/20 min.
Number of treatment sessions: generally 6 treatments, no more frequent than every 2 days
Some skin reaction is common due to DC current
Manipulating Dosage with Iontophoresis
40 mA minutes = 4.0 mA X 10 minutes
40 mA minutes = 3.0 mA X 13.3 minutes
40 mA minutes = 2.0 mA X 20 minutes
40 mA minutes = 1.0 mA X 40 minutes
40 milliamp minute treatment can be broken down into any of the following:
Contraindications with Iontophoresis
Damaged skin/open skin lesions
Known sensitivity or allergy to therapeutic ions
Moderate to severe sensory impairment
Acute injury if bleeding still occurring
Fresh scars
Over electronic implants
Over area of exposed metal
Cardiac Pacemakers: demand type
Pregnancy: first trimester
Cancer or history of cancer
Precautions with Iontophoresis
Poor contact between electrode and skin
Patient tolerance to treatment
Matching polarity of ion with correct electrode
Inspect skin for reaction from previous iontophoresis treatment
Intermittent Pneumatic Compression Pump
Edema reduction for subacute and chronic edema (not acute edema)
Applies pressure to assist with venous and lymphatic drainage
Never set pressure greater than 10mmHg below diastolic blood pressure Generally 30-50 mmHg in UE
On/off generally 3:1
Treatment time 45-60 min
Intermittent Pneumatic Compression Pump
Precautions
Impaired sensation
Impaired communication or cognition
Controlled HTN
Cancer in the area
Stroke or TIA
Areas of superficial nerves
Contraindications
Pulmonary edema
CHF
DVT
Uncontrolled HTN
Obstructed venous or lymphatic return
Post arterial re-vascularization or repair
Skin infection
Unhealed fx
Things to Remember…
Inspect skin: Prior to, during & after treatment
Determine cognitive status
Check sensory status in treatment area
Combine heat and stretch when indicated
Objective measurements…
Assessing Effectiveness of Modalities
PainNumeric Pain Rating Scale (NPRS)Visual Analog Scale (VAS)
EdemaMeasure circumference or volume
ROMMeasure with goniometer
Muscle GuardingObserve
Strength/Motor FunctionGrip, pinch, MMT
FunctionObserve ADL/IADL, Patient rated evalsJebsen hand, etc.
Scar/Tissue HealingMeasure pliability, Wound assessments
Documenting Modalities& Setting Treatment Plans
Documentation of modalities should allow any therapist to step in and complete a treatment without difficulty.
Parameters: Location, duration, equipment used, & treatment response (objective improvements)
Be a researcher… write objective treatment goals for the use of PAMs and reassess patient status frequently to evaluate the benefits of PAMs.
Continue using PAMs only when you notice a therapeutic benefit!!!
ReferencesBracciano A,(2008), Physical Agent Modalities: Theory and Application for the Occupational Therapist, Slack Inc.
Cameron, M, (2009), Physical Agents in Rehabilitation: From Research to Practice, Saunders Elsevier.
Fedorczyck , J, (2012) The Use of Physical Agents in Hand Therapy, ASHT Hand Therapy Review Course.
Knight, KL, Draper, DO, (2007), Therapeutic Modalities: The Art and Science With Clinical Activities Manual, Lippincott Williams & Wilkins.
Bellew, JW, Michlovitz, S, Nolan, TP, (2016) Modalities for Therapeutic Intervention, F A Davis.
ASHT Test Prep book 3rd edition
Contact Information