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ULTRAVIOLET RADIATION (UVR)
ULTRAVIOLET RADIATION (UVR)
INTRODUCTION, PRODUCTION, PHYSIOLOGICAL,
THERAPEUTIC, INDICATION, CONTRAINDICATION,
PRECAUTION & DANGERS.
INTRODUCTION
INTRODUCTION
VISIBLE LIGHT X-RAY
REGION
VISIBLE LIGHT X-RAY
REGION
VISIBLE LIGHT X-RAY
REGION
Ultraviolet radiation (UVR) covers a small part
of electromagnetic spectrum lying between the
violet end of the VISIBLE LIGHT and X-RAY
REGION.
INTRODUCTION
INTRODUCTION
INVISIBLE
UVR are INVISIBLE to the human eyes.
SUN
Natural source of UVR is SUN.
CHEMICAL CHANGES
UVR provoke CHEMICAL CHANGES &
not simply heat at sites where they
are absorbed.
INTRODUCTION
INTRODUCTION
The radiations introduced to the tissues
through 1.subcutaneous tissue, 2.hair
follicles, and 3.sebaceous glands.
GENERALIZED RESPONSE TO UVR
EXPOSURE
GENERALIZED RESPONSE TO UVR
EXPOSURE
1.
2.
3.
4.
5.
6.
7.
UVB)
Sunburn (UVB) / Erythema ( Reddening of the
skin)
Tanning of the skin / Pigmentation
Decrease in sensitivity of the skin (Increased
Epidermal thickness)
UVA)
Premature aging of the skin (UVA)
UVB)
Skin cancer (UVB)
UVB)
Exposure to the eye causes photokeratitis
(UVB)
Photosynthesis of vitamin D
THE PHYSICAL BEHAVIOR OF UVR
THE PHYSICAL BEHAVIOR OF UVR
1. Reflection
2. Refraction
3. Absorption
4. Penetration
TYPES OF UVR
TYPES OF UVR
1. UVA (Long UV) – 400 – 315nm. {penetrates to
dermis, Responsible for development of slow natural
tan}
2. UVB (medium UV, erythemal UV) –
315 – 280nm. {Produces new pigment formation,
sunburn, Vitamin D synthesis. Responsible for
inducing skin cancer}
3. UVC (short UV, germicidal UV) –
280 – 100nm {Does not reach the surface of the earth}
UVR GENERATORS
UVR GENERATORS
1. High pressure mercury vapor
lamp – Air cooled.
2. High pressure mercury vapor
lamp – Water cooled ( Kromayer
lamp).
3. Fluorescent lamps
PRODUCTION OF UVR
PRODUCTION OF UVR
QUARTZ BURNER TUBE
argon
gas and mercury under
reduced pressure
QUARTZ BURNER TUBE
argon
gas and mercury under
reduced pressure
QUARTZ BURNER TUBE
argon
gas and mercury under
reduced pressure
QUARTZ BURNER TUBE
argon
gas and mercury under
reduced pressure
QUARTZ BURNER TUBE
argon
gas and mercury under
reduced pressure
The therapeutic UVR are
produced by mercury vapour
lamp which consists of a
QUARTZ BURNER TUBE
evacuated from air and
containing traces of argon
gas and mercury under
reduced pressure.
An electrode is inserted at
each end of burner tube. The
current is applied to the
electrodes, the mercury
vapour and the passage of
electrons through the vapour
establishes the UVR.
UVR LAMPS
UVR LAMPS
ULTRA-VIOLET APPARATUS
ULTRA-VIOLET APPARATUS
The UV apparatus is grouped as follows:
GENERALISED SKIN CONDITIONS AS ACNE AND
PSORIASIS.
GENERALISED SKIN CONDITIONS AS ACNE AND
PSORIASIS.
GENERALISED SKIN CONDITIONS AS ACNE AND
PSORIASIS.
1- Air-cooled lamps: Hanovia Alpine Sun
Lamp, {High pressure vapour lamps}wavelength
253nm (short wavelength) used in treatment of
GENERALISED SKIN CONDITIONS AS ACNE AND
PSORIASIS.
Emit ultraviolet, infrared, and
visible light
UVR produced falls within UV-B
range
Mainly used to produce
erythema and accompanying
photochemical reactions
TRIDYMITE FORMATION
TRIDYMITE FORMATION
TRIDYMITE.
The heat produced inside the Burner or Quartz
tube causes some of it to change to another
form of silica called TRIDYMITE.
OPAQUE
Tridymite is OPAQUE to UVR. So output of the
rays tends to FALL.
variable resistance
A variable resistance is included in the burner
circuit to increase the potential difference
across the burner & intensity of the current.
OZONE FORMATION
OZONE FORMATION
250nm
OZONE
250nm
OZONE
The photochemical action of UVR shorter
than 250nm in wavelength on
atmospheric oxygen is to form OZONE.
Ozone is a toxic gas for inhalation & partly
prevented by good ventilation.
Levels of ozone can be detected by smell.
ULTRA-VIOLET APPARATUS
ULTRA-VIOLET APPARATUS
Water-cooled lamps:
UVA and UVB
pressure areas ulcers
sinuses
UVA and UVB
pressure areas ulcers
sinuses
UVA and UVB
pressure areas ulcers
sinuses
UVA and UVB
pressure areas ulcers
sinuses
Kromayer lamp, wavelength at 366nm
give both UVA and UVB, used for treating
localised lesions as pressure areas, ulcers,
and sinuses in open areas.
It is a water cooled mercury vapor lamp.
Eliminates the danger of an IRR burn.
ULTRA-VIOLET APPARATUS
ULTRA-VIOLET APPARATUS
The distilled water is circulated in the jacket.
The purpose of which is to absorb the IRR.
After the use of the lamp, the water circulation
should be continued for 5min after the burner is
switched off in order to cool the lamp.
Tap water has the disadvantage, that it contains
SALTS & OTHER IMPURITES which may deposit
on the quartz window.
CARE OF MERCURY VAPOR LAMP
CARE OF MERCURY VAPOR LAMP
1.
2.
3.
4.
5.
6.
It must be kept dry.
It should not be turned on & off more
frequently.
After 1000hrs of use the burner must be
renewed.
The burner of an air cooled lamp should be
cleaned regularly with absolute alcohol.
The burner should not be touched with fingers.
After every 8hrs of use the distilled water
should be renewed.
ADVANTAGE & DISADVANTAGE
OF MERCURY VAPOR LAMP
ADVANTAGE & DISADVANTAGE
OF MERCURY VAPOR LAMP
It used for GENERAL UV
IRRADIATION.
The spectrum contains a
large proportion of short UVR
which are undesirable for the
general treatment.
UVR APPARATUS
UVR APPARATUS
FLUORESCENT TUBES:
The modern treatment methods often require
the use of Long UV without short UV.
So to meet this criteria the fluorescent tubes are
used.
These are similar to the tubes used for lighting.
FLUORESCENT TUBES
FLUORESCENT TUBES
Each tube is about 120cms long.
It is made of a type of glass which allows long
UV to pass.
The output proportion of this is mainly of Long
UV, Few IRR & some Short UV.
It is mainly used for General Irradiation for
individual or in Group.
THERAKTIN TUNNEL
THERAKTIN TUNNEL
Theraktin lamp consists of a number of fluorescent
tubes each with a parabolic reflector incorporated into
a semicircular tunnel.
The wavelength between 290 and 350nm (UVA long)
used in treating affecting large areas.
THERAKTIN TUNNEL
THERAKTIN TUNNEL
This provides an even irradiation to patients.
It allows treatment of the whole body in 2
halves.
2 IRR elements are included in order to keep the
patient warm during treatment.
All of the lamps should be positioned at least
18’’ from the patient
PENETRATION OF THE UV RAYS
PENETRATION OF THE UV RAYS
UVA – Dermis level.
UVB – Deep Epidermis
PHYSIOLOGICAL EFFECTS OF UVR
PHYSIOLOGICAL EFFECTS OF UVR
1.
2.
The UVR physiological effects may
be divided into 2 groups;
Local – Effects which produced
locally in the area.
General – Results from a
widespread Irradiation.
LOCAL EFFECTS OF UVR
LOCAL EFFECTS OF UVR
1. ERYTHEMA – It is reddening of the skin.
First observable effect of UV Irradiation.
TRIPLE RESPONSE.
It cause chemical action which result in
IRRITATION & DESTRUCTION of cells. This
causes liberation of “H”-substance which
produce the TRIPLE RESPONSE.
The erythema is regarded as an inflammatory
reaction stimulated by the UVR.
TRIPLE RESPONSE
TRIPLE RESPONSE
1. Dilation of capillaries – H-substance
2. Dilation of arterioles – Axon reflex
3. Exudation of fluids into the tissues –
Increased permeability of the capillary walls.
2. PIGMENTATION / TANNING
2. PIGMENTATION / TANNING
MELANOCYTE & ACCELERATES
MELANIN PIGMENT
MELANOCYTE & ACCELERATES
MELANIN PIGMENT
MELANOCYTE & ACCELERATES
MELANIN PIGMENT
It is thought that the UVR stimulates
MELANOCYTE & ACCELERATES the
production of MELANIN PIGMENT.
Pigmentation commonly follows an
erythemal reaction.
It varies with the dosage of UVR & the
different individuals.
2. PIGMENTATION / TANNING
2. PIGMENTATION / TANNING
PRE-EXISTING
melanin
PRE-EXISTING
melanin
Sometimes immediate tanning occurs as
a result of effects of PRE-EXISTING
melanin. This may occur within minutes of
exposure.
Sun / Carbon arc Brown color
Mercury Vapor lamp Grayish
REDUCES
The pigmentation REDUCES the
penetration of UVB.
3. THICKENING OF EPIDERMIS
3. THICKENING OF EPIDERMIS
UVR provokes an increased
reproduction of KERATINOCYTES.
This leads to thickening of epidermis
which acts does acts a PROTECTION
AGAINST THE RAYS.
So longer doses are required to repeat
an ERYTHEMAL reaction.
4. DESQUAMATION / PEELING
4. DESQUAMATION / PEELING
It is the CASTING OFF of dead cells
from the surface of the skin.
The desquamation is proportional to
the intensity of the erythema.
The peeling results in REDUCTION /
LOSS OF THE INCREASED
RESISTANCE TO THE RAYS.
5. ANTIBIOTIC EFFECT
5. ANTIBIOTIC EFFECT
Destructive effects of ultraviolet
radiation include the
destruction of viruses, bacteria,
and other small organisms on
the skin surface such as FUNGI
commonly found in wounds.
(effect of UVB).
B. GENERAL EFFECTS OF UVR
B. GENERAL EFFECTS OF UVR
1. Vitamin D Production
7-Dehydrocholestrol
Vitamin – D chemical reaction.
7-Dehydrocholestrol
Vitamin – D chemical reaction.
7-Dehydrocholestrol
Vitamin – D chemical reaction.
7-Dehydrocholestrol
Vitamin – D chemical reaction.
In the presence of UVB, converts 7-Dehydrocholestrol into
Vitamin – D through chemical reaction.
absorption of calcium
and phosphorous
absorption of calcium
and phosphorous
Vitamin D is required to assist in the absorption of calcium
and phosphorous from the intestine to blood stream.
2- THE ESOPHYLACTIC EFFECT
2- THE ESOPHYLACTIC EFFECT
General UVA Irradiation
reticulo - endothelial system
Stimulation of reticulo - endothelial system
ANTIBODIES
Ingest bacteria & produce ANTIBODIES
against
BACTERIA & TOXINS
BACTERIA & TOXINS.
So the resistance of the body to infection
is increased & this being known as
ESOPHYLACTIC EFFECT.
3. GENERAL TONIC EFECT
3. GENERAL TONIC EFECT
Its being claimed that because of General
UV Irradiation has a
GENERAL TONIC EFFECT,
GENERAL TONIC EFFECT,
APPETITIE & SLEEP BEING IMPROVED
APPETITIE & SLEEP BEING IMPROVED
NERVOUSNESS & IRRITABILITY
DECREASED
NERVOUSNESS & IRRITABILITY
DECREASED
NERVOUSNESS & IRRITABILITY
DECREASED
THERAPEUTIC EFFECTS OF UVR
THERAPEUTIC EFFECTS OF UVR
The principle therapeutic uses of UVR are
of SKIN DISEASES
PSORIASIS:-
1. PSORIASIS:-
THICK PINK / RED
SILVERY SCALES.
THICK PINK / RED
SILVERY SCALES.
THICK PINK / RED
SILVERY SCALES.
It is a skin condition which presents localized
THICK PINK / RED plaques, sharply
demarcated & covered with SILVERY SCALES.
decrease the DNA synthesis in the cells of the
skin & to improve the skin condition
decrease the DNA synthesis in the cells of the
skin & to improve the skin condition
decrease the DNA synthesis in the cells of the
skin & to improve the skin condition
In this state the aim of UVR irradiation is to
decrease the DNA synthesis in the cells of the
skin & to improve the skin condition
HEALTHY & PSORIASIS SKIN
HEALTHY & PSORIASIS SKIN
2. ACNE VULGARIS
2. ACNE VULGARIS
PUSTULES, PAPULES blocking of
sebaceous pores & hair follicles affecting mainly the
face, chest & back.
PUSTULES, PAPULES blocking of
sebaceous pores & hair follicles affecting mainly the
face, chest & back.
PUSTULES, PAPULES blocking of
sebaceous pores & hair follicles affecting mainly the
face, chest & back.
PUSTULES, PAPULES blocking of
sebaceous pores & hair follicles affecting mainly the
face, chest & back.
PUSTULES, PAPULES blocking of
sebaceous pores & hair follicles affecting mainly the
face, chest & back.
Acne is also a skin condition which presents
PUSTULES, PAPULES formed by blocking of
sebaceous pores & hair follicles affecting mainly the
face, chest & back.
disfiguring
& serious distress.
disfiguring
& serious distress.
The more severe & long lasting forms cause disfiguring
& serious distress.
desquamation to open
Using UVR is aiming to produce desquamation to open
the blocked pores and hair follicles.
E2 dose is given to the face, chest and neck.
3. ECZEMA
3. ECZEMA
INFLAMMATORY RESPONSE
It is an INFLAMMATORY RESPONSE
in the skin associated with OEDEMA.
ITCHING
REDNESS, SCALING, VESCILES
ITCHING
REDNESS, SCALING, VESCILES
The patient suffers marked ITCHING
with REDNESS, SCALING, VESCILES &
exudation of serum on the skin.
(Sub
acute & Chronic stage)
(Sub
acute & Chronic stage)
A mild UVR treatment will help. (Sub
acute & Chronic stage)
4. CHRONIC INFECTION & INFECTED WOUNDS
4. CHRONIC INFECTION & INFECTED WOUNDS
1.
2.
3.
Infected wounds such as
ULCERS
ULCERS
PRESSURE SORES
PRESSURE SORES
SURGICAL INCISIONS
SURGICAL INCISIONS are often treated with HIGH
DOSES of UVR.
remove the (SLOUGH) infected material
promote repair.
remove the (SLOUGH) infected material
promote repair.
remove the (SLOUGH) infected material
promote repair.
The aim of UVR irradiation is to destroy the surface
bacteria, remove the (SLOUGH) infected material &
promote repair.
E3 dose
E3 dose is sufficient, the dose is may be given daily
and is not being applied to normal skin.
PRESSURE AREAS
PRESSURE AREAS
5. VITILIGO
5. VITILIGO
MELANOCYTES
MELANOCYTES
It is a condition in which destruction of
MELANOCYTES in local areas causes WHITE
PATCHES to appear on the skin.
Both UVA & UVB stimulate melanocyte activity.
UVA seems to provoke a DARKER & LONGER
LASTING TANNING.
more THICKENNING.
UVB provokes more THICKENNING.
6. NON – INFECTED WOUNDS
6. NON – INFECTED WOUNDS
GROWTH of GRANULATION
TISSUE & SPEED UP REPAIR
GROWTH of GRANULATION
TISSUE & SPEED UP REPAIR
GROWTH of GRANULATION
TISSUE & SPEED UP REPAIR
The aim of UVR is to stimulate the
GROWTH of GRANULATION
TISSUE & SPEED UP REPAIR.
UVA stimulates GROWTH.
Venous / Arterial ulcers.
Example for non infected wounds
are – Venous / Arterial ulcers.
7. COUNTER IRRITATION
7. COUNTER IRRITATION
It is used to produce a strong
counter irritation effect over the
site of DEEP SEATED PAIN.
E4 dose
mask
of pain .
E4 dose
mask
of pain .
E4 dose
mask
of pain .
E4 dose is given to cause
discomfort and producing mask
of pain .
INDICATIONS FOR UVR
INDICATIONS FOR UVR
DERMATOLOGICAL CONDITIONS
1. DERMATOLOGICAL CONDITIONS – Psoriasis,
Acne, Sub acute & Chronic Eczema.
Calcium / Phosphorus disease
2. Calcium / Phosphorus disease –
Osteomalacia
Non pulmonary tuberculosis
3. Non pulmonary tuberculosis
Local Ulceration
4. Local Ulceration – Ulcers, Pressure sores,
Surgical incision
INDICATIONS FOR UVR
INDICATIONS FOR UVR
Upper respiratory condition
management
Upper respiratory condition
management
5. Upper respiratory condition
management – Common Cold.
6. Counter Irritant Effect.
CONTRAINDICATION OF UVR
CONTRAINDICATION OF UVR
Pulmonary Tuberculosis
1. Pulmonary Tuberculosis
Severe cardiac disturbances
2. Severe cardiac disturbances
Systemic Lupus Erythematosis
3. Systemic Lupus Erythematosis
Severe Diabetes
4. Severe Diabetes
Dermatological Conditions
5. Dermatological Conditions
CONTRAINDICATION OF UVR
CONTRAINDICATION OF UVR
Known Photosensitivity.
6. Known Photosensitivity.
Photosensitizing medication.
7. Photosensitizing medication.
Deep x – Ray therapy.
8. Deep x – Ray therapy.
Acute Febrile illness
9. Acute Febrile illness
10. Recent skin grafts.
CONTRAINDICATION OF UVR
CONTRAINDICATION OF UVR
Porphyrias
Porphyrias
Pellagra
Pellagra
Sarcoidosis
Sarcoidosis
Xeroderma pigmentosum
Xeroderma pigmentosum
Acute psoriasis
Acute psoriasis
Renal and hepatic
insufficiencies
Renal and hepatic
insufficiencies
Renal and hepatic
insufficiencies
Hyperthyroidism
Hyperthyroidism
Generalized dermatitis
Generalized dermatitis
Advanced arteriosclerosis
Advanced arteriosclerosis
Acute eczema
Acute eczema
Herpes simplex
Herpes simplex
Hypersensitivity to
sunlight
Hypersensitivity to
sunlight
Hypersensitivity to
sunlight
DANGERS
DANGERS
Shock
1. Shock
Eyes
2. Eyes - UVR may produce conjunctivitis,
iritis or cataract.
Over Dosage
3. Over Dosage – UVR burn can occur.
Mainly E4 reaction
Ozone
4. Ozone – Important to ensure adequate
Ventilation in the area.
SAFETY PRECAUTIONS AGAINST
SUNLIGHT(UVR)
SAFETY PRECAUTIONS AGAINST
SUNLIGHT(UVR)
1. Eyes protection.
2. SKIN DAMAGE / TANNING PROTECTION
2. SKIN DAMAGE / TANNING PROTECTION
Sunscreen doesn’t offer 100% protection.
Sunscreen doesn’t offer 100% protection.
Sunscreen doesn’t offer 100% protection.
SPF(Sun Protection Factor) 30+ sunscreen
blocks 96% of UV; SPF 15+ blocks out 93%.
SPF(Sun Protection Factor) 30+ sunscreen
blocks 96% of UV; SPF 15+ blocks out 93%.
SPF(Sun Protection Factor) 30+ sunscreen
blocks 96% of UV; SPF 15+ blocks out 93%.
SPF(Sun Protection Factor) 30+ sunscreen
blocks 96% of UV; SPF 15+ blocks out 93%.
In addition to sunscreen, wear a hat,
sunglasses, more clothing, and seek
shade.
In addition to sunscreen, wear a hat,
sunglasses, more clothing, and seek
shade.
In addition to sunscreen, wear a hat,
sunglasses, more clothing, and seek
shade.
In addition to sunscreen, wear a hat,
sunglasses, more clothing, and seek
shade.
In addition to sunscreen, wear a hat,
sunglasses, more clothing, and seek
shade.
PROTECTIVE CLOTHING
PROTECTIVE CLOTHING
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
Most cotton and cotton/
polyester fabrics protect against
95% of UV, but are less effective
if wet, faded, or aged.
TEST DOSE & DETERMINIG MED
TEST DOSE & DETERMINIG MED
(ERYTHEMAL)
(ERYTHEMAL)
It is used to assess the individual patients
(ERYTHEMAL) reaction to uvr irradiation.
MED (MINIMAL
ERYTHEMAL DOSE)
MED (MINIMAL
ERYTHEMAL DOSE)
The basis for any calculation of any UVR
dosage is the MED (MINIMAL
ERYTHEMAL DOSE)
the response of
erythema
the response of
erythema
This MED refers to the response of
erythema for the dose to be given
TEST DOSE CONT….
TEST DOSE CONT….
MED DETERMINE EXPOSURE
TIME
MED DETERMINE EXPOSURE
TIME
MED DETERMINE EXPOSURE
TIME
MED DETERMINE EXPOSURE
TIME
MED DETERMINE EXPOSURE
TIME
The patient must understand that the purpose of the
MED test is to DETERMINE just how much EXPOSURE
TIME is necessary based on their skin sensitivity.
Proper patient education should be given:-
Proper patient education should be given:-
Wear Goggles
1. Wear Goggles
Observe & monitor the skin condition
2. Observe & monitor the skin condition
3. Keep skin moisture following exposure to UVR
Pigmentation changes are to be expected & are a
normal response.
Pigmentation changes are to be expected & are a
normal response.
4. Pigmentation changes are to be expected & are a
normal response.
Prolonged & repeated exposure leads to premature
aging.
Prolonged & repeated exposure leads to premature
aging.
5. Prolonged & repeated exposure leads to premature
aging.
STEPS TO DETERMINE TEST DOSE / SKIN TEST
STEPS TO DETERMINE TEST DOSE / SKIN TEST
1. The area chosen for the test is of importance.
Because the patient is to inspect at regular intervals
a convenient, visible site is essential.
Because the patient is to inspect at regular intervals
a convenient, visible site is essential.
2. Because the patient is to inspect at regular intervals
a convenient, visible site is essential.
It should be clear of skin disease.
3. It should be clear of skin disease.
The FLEXOR SURFACE of the FOREARM is the most
usual site.(Other sites are – Abdomen, Medial aspect
of arm / thigh)
The FLEXOR SURFACE of the FOREARM is the most
usual site.(Other sites are – Abdomen, Medial aspect
of arm / thigh)
The FLEXOR SURFACE of the FOREARM is the most
usual site.(Other sites are – Abdomen, Medial aspect
of arm / thigh)
4. The FLEXOR SURFACE of the FOREARM is the most
usual site.(Other sites are – Abdomen, Medial aspect
of arm / thigh)
5. The selected site should be cleaned with soap &
water to remove surface grease.
6. Cover the patient other areas leaving only the
forearm exposed to UVR.
STEPS TO DETERMINE TEST DOSE / SKIN TEST
STEPS TO DETERMINE TEST DOSE / SKIN TEST
7. Three to Five holes of at least 2cm² &
1cm apart are cut in a piece of lint/paper/
cardboard is taken for irradiation of UVR
along with a slide cover – to pull up to
reveal one opening at a time.
STEPS TO DETERMINE TEST DOSE / SKIN TEST
STEPS TO DETERMINE TEST DOSE / SKIN TEST
8. This cutting is fixed to the forearm with adhesive
plaster.
IDENTIFICATION OF THE ERYTHEMA EASIER
9. The cuttings are of different sizes & shapes in-order
to make IDENTIFICATION OF THE ERYTHEMA EASIER
for the patient.
10. Allow the lamp to warm up according to the
manufacturer instructions.
11. Place the lamp PERPENDICULAR to the area being
tested (Forearm) & a DISTANCE of 60 to 90cms from
the site.
12. Expose the 1st opening for 30sec, then expose the
2nd opening for another 30sec & go on till the last
opening
STEPS TO DETERMINE TEST DOSE / SKIN TEST
STEPS TO DETERMINE TEST DOSE / SKIN TEST
13. So the 1st opening would receive the longest
exposure time & the last opening would receive the
least amount of exposure time.
14. Switch off the lamp
15. Instruct the patient to MONITOR the forearm every
2hrs & note which opening or shape appeared pink /
red first & when it faded / disappeared.
16. The patient is also given a card similar to the
opening to make a note.
MINIMAL ERYTHEMAL DOSE
MINIMAL ERYTHEMAL DOSE
It is a slight reddening
(erythema) of the skin
which takes from 6 – 8hrs
to develop & which is still
just visible at 24hrs.
DESCRIPTION OF DEGREES OF ERYTHEMA
DESCRIPTION OF DEGREES OF ERYTHEMA
Degree
of
Erythem
a
Latent
period
In
HRS
Appearance
color
Duration
of
Erythema
Skin
Oedema
Skin
discomfort
Desquam
ation of
skin
Relation
to
E1 Dose
E1 6-8 Mildly pink <24hrs None None None E1
E2 4-6 Definite Pink
Red. Blanches
on Pressure
2 Days None Slight
Soreness,
Irritation
Powder
y
2.5% of
E1
E3 2-4 Very red, Does
not blanch on
pressure
3-5 Days Some Hot &
Painful
In thin
Sheets
5% of
E1
E4 <2 Angry Red A Week Blister Very
Painful
Thick
Sheets
10% of
E1
DOSAGE
DOSAGE
a)
b)
c)
d)
The skin response to UVR depends on;
1. The quantity of UVR energy applied to unit area of
the skin.(Depends on);
The output of lamp – Make, Type, Aging
Distance between the lamp & the skin – Inverse
square law
Angle at which radiations fall on the skin – cosine law
Time for which radiations are applied
2. The sensitivity of the skin
CALCULATION OF DOSAGE
CALCULATION OF DOSAGE
E1/MED is the basic of UV calculation
which is determined for each individual
patient by performing a skin test.
From this point all other doses of UVR
can be calculated.
E2 = 2½ x E1
E3 = 5 x E1
E4 = 10 x E1
CALCULATION OF DOSAGE
CALCULATION OF DOSAGE
EXAMPLE:
If the E1 dose of the patient is 25sec, calculate
the E3 dose?
E1 dose = 25sec
E3 dose = 5 x E1
E3 dose = 5 x 25 = 125sec
CALCULATION OF NEW DOSE
CALCULATION OF NEW DOSE
The dose at different distances from the lamp
to skin can be calculated by formula;
NEWDOSE = OLD DOSE X NEW DISTANCE²
OLD DISTANCE ²
PROGRESSION OF DOSAGE
PROGRESSION OF DOSAGE
An exposure to UVR should not be repeated until the
erythema caused by a previous dose has faded.
Thickening of the epidermis
Necessary to increase the exposure in order to repeat the
erythemal reaction at each successive dose
Doses are progressed as follows:
To repeat an E1 25% of the preceding dose is added
To repeat an E2 50% of the preceding dose is added
To repeat an E3 75% of the preceding dose is added
To repeat an E4 100% of the preceding dose is added
PROGRESSION OF DOSAGE
PROGRESSION OF DOSAGE
Examples of progression of dosage
If E1 is 30sec, find the second progression (P2E1)?
E1= 30sec
P1(Day one progression)E1 = E1 + 25% of E1 = 30
+30/4 = 30 + 7.5 =37.5sec
P2(Day two progression) E1 = P1E1 + 25% of P1E1 =
37.5 +37.5/4 = 46.9sec
P2E1 = 47sec
SELECTION OF DOSAGE LEVEL
SELECTION OF DOSAGE LEVEL
1. An E1/MED – Given to the total body area
(Whole body)
2. An E2 - May not be given to up to 20% of total
body area
3. An E3 – May not be given to up to 250cm² of
normal skin
4. An E4 – May only be given to an area up to
25cm² of normal skin.
FREQUENCY OF UVR TREATMENT
FREQUENCY OF UVR TREATMENT
1. An E1 / MED may be given DAILY
2. An E2 – Should be given every second day
3. An E3 – Should be given every 3 or 4th day (Twice
Weekly)
4. An E4 – may only be given once a week or even
once a fortnight.
N.B. when treating non-skin areas such as pressure
areas or ulcers, all doses may be given daily as there is
no erythema reaction produced.
SENSITIZATION / SENSITIZING DRUGS
SENSITIZATION / SENSITIZING DRUGS
A number of drugs & some foods in a few
patients are known to sensitize patients to the
effects of UVR.
Commonly seen sensitizing groups are;
1. psoralens - Sensitizer
2. Sulphonamides - Antibiotic
3. Phenothiazine – Tranquilizer
4. Barbiturates
5. Gold therapy
6. Aspirin & Derivatives

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ultra violet.pdf

  • 1. ULTRAVIOLET RADIATION (UVR) ULTRAVIOLET RADIATION (UVR) INTRODUCTION, PRODUCTION, PHYSIOLOGICAL, THERAPEUTIC, INDICATION, CONTRAINDICATION, PRECAUTION & DANGERS.
  • 2. INTRODUCTION INTRODUCTION VISIBLE LIGHT X-RAY REGION VISIBLE LIGHT X-RAY REGION VISIBLE LIGHT X-RAY REGION Ultraviolet radiation (UVR) covers a small part of electromagnetic spectrum lying between the violet end of the VISIBLE LIGHT and X-RAY REGION.
  • 3. INTRODUCTION INTRODUCTION INVISIBLE UVR are INVISIBLE to the human eyes. SUN Natural source of UVR is SUN. CHEMICAL CHANGES UVR provoke CHEMICAL CHANGES & not simply heat at sites where they are absorbed.
  • 4. INTRODUCTION INTRODUCTION The radiations introduced to the tissues through 1.subcutaneous tissue, 2.hair follicles, and 3.sebaceous glands.
  • 5. GENERALIZED RESPONSE TO UVR EXPOSURE GENERALIZED RESPONSE TO UVR EXPOSURE 1. 2. 3. 4. 5. 6. 7. UVB) Sunburn (UVB) / Erythema ( Reddening of the skin) Tanning of the skin / Pigmentation Decrease in sensitivity of the skin (Increased Epidermal thickness) UVA) Premature aging of the skin (UVA) UVB) Skin cancer (UVB) UVB) Exposure to the eye causes photokeratitis (UVB) Photosynthesis of vitamin D
  • 6. THE PHYSICAL BEHAVIOR OF UVR THE PHYSICAL BEHAVIOR OF UVR 1. Reflection 2. Refraction 3. Absorption 4. Penetration
  • 7. TYPES OF UVR TYPES OF UVR 1. UVA (Long UV) – 400 – 315nm. {penetrates to dermis, Responsible for development of slow natural tan} 2. UVB (medium UV, erythemal UV) – 315 – 280nm. {Produces new pigment formation, sunburn, Vitamin D synthesis. Responsible for inducing skin cancer} 3. UVC (short UV, germicidal UV) – 280 – 100nm {Does not reach the surface of the earth}
  • 8.
  • 9. UVR GENERATORS UVR GENERATORS 1. High pressure mercury vapor lamp – Air cooled. 2. High pressure mercury vapor lamp – Water cooled ( Kromayer lamp). 3. Fluorescent lamps
  • 10. PRODUCTION OF UVR PRODUCTION OF UVR QUARTZ BURNER TUBE argon gas and mercury under reduced pressure QUARTZ BURNER TUBE argon gas and mercury under reduced pressure QUARTZ BURNER TUBE argon gas and mercury under reduced pressure QUARTZ BURNER TUBE argon gas and mercury under reduced pressure QUARTZ BURNER TUBE argon gas and mercury under reduced pressure The therapeutic UVR are produced by mercury vapour lamp which consists of a QUARTZ BURNER TUBE evacuated from air and containing traces of argon gas and mercury under reduced pressure. An electrode is inserted at each end of burner tube. The current is applied to the electrodes, the mercury vapour and the passage of electrons through the vapour establishes the UVR.
  • 12. ULTRA-VIOLET APPARATUS ULTRA-VIOLET APPARATUS The UV apparatus is grouped as follows: GENERALISED SKIN CONDITIONS AS ACNE AND PSORIASIS. GENERALISED SKIN CONDITIONS AS ACNE AND PSORIASIS. GENERALISED SKIN CONDITIONS AS ACNE AND PSORIASIS. 1- Air-cooled lamps: Hanovia Alpine Sun Lamp, {High pressure vapour lamps}wavelength 253nm (short wavelength) used in treatment of GENERALISED SKIN CONDITIONS AS ACNE AND PSORIASIS.
  • 13. Emit ultraviolet, infrared, and visible light UVR produced falls within UV-B range Mainly used to produce erythema and accompanying photochemical reactions
  • 14. TRIDYMITE FORMATION TRIDYMITE FORMATION TRIDYMITE. The heat produced inside the Burner or Quartz tube causes some of it to change to another form of silica called TRIDYMITE. OPAQUE Tridymite is OPAQUE to UVR. So output of the rays tends to FALL. variable resistance A variable resistance is included in the burner circuit to increase the potential difference across the burner & intensity of the current.
  • 15. OZONE FORMATION OZONE FORMATION 250nm OZONE 250nm OZONE The photochemical action of UVR shorter than 250nm in wavelength on atmospheric oxygen is to form OZONE. Ozone is a toxic gas for inhalation & partly prevented by good ventilation. Levels of ozone can be detected by smell.
  • 16. ULTRA-VIOLET APPARATUS ULTRA-VIOLET APPARATUS Water-cooled lamps: UVA and UVB pressure areas ulcers sinuses UVA and UVB pressure areas ulcers sinuses UVA and UVB pressure areas ulcers sinuses UVA and UVB pressure areas ulcers sinuses Kromayer lamp, wavelength at 366nm give both UVA and UVB, used for treating localised lesions as pressure areas, ulcers, and sinuses in open areas. It is a water cooled mercury vapor lamp. Eliminates the danger of an IRR burn.
  • 17. ULTRA-VIOLET APPARATUS ULTRA-VIOLET APPARATUS The distilled water is circulated in the jacket. The purpose of which is to absorb the IRR. After the use of the lamp, the water circulation should be continued for 5min after the burner is switched off in order to cool the lamp. Tap water has the disadvantage, that it contains SALTS & OTHER IMPURITES which may deposit on the quartz window.
  • 18. CARE OF MERCURY VAPOR LAMP CARE OF MERCURY VAPOR LAMP 1. 2. 3. 4. 5. 6. It must be kept dry. It should not be turned on & off more frequently. After 1000hrs of use the burner must be renewed. The burner of an air cooled lamp should be cleaned regularly with absolute alcohol. The burner should not be touched with fingers. After every 8hrs of use the distilled water should be renewed.
  • 19. ADVANTAGE & DISADVANTAGE OF MERCURY VAPOR LAMP ADVANTAGE & DISADVANTAGE OF MERCURY VAPOR LAMP It used for GENERAL UV IRRADIATION. The spectrum contains a large proportion of short UVR which are undesirable for the general treatment.
  • 20. UVR APPARATUS UVR APPARATUS FLUORESCENT TUBES: The modern treatment methods often require the use of Long UV without short UV. So to meet this criteria the fluorescent tubes are used. These are similar to the tubes used for lighting.
  • 21. FLUORESCENT TUBES FLUORESCENT TUBES Each tube is about 120cms long. It is made of a type of glass which allows long UV to pass. The output proportion of this is mainly of Long UV, Few IRR & some Short UV. It is mainly used for General Irradiation for individual or in Group.
  • 22. THERAKTIN TUNNEL THERAKTIN TUNNEL Theraktin lamp consists of a number of fluorescent tubes each with a parabolic reflector incorporated into a semicircular tunnel. The wavelength between 290 and 350nm (UVA long) used in treating affecting large areas.
  • 23. THERAKTIN TUNNEL THERAKTIN TUNNEL This provides an even irradiation to patients. It allows treatment of the whole body in 2 halves. 2 IRR elements are included in order to keep the patient warm during treatment. All of the lamps should be positioned at least 18’’ from the patient
  • 24. PENETRATION OF THE UV RAYS PENETRATION OF THE UV RAYS UVA – Dermis level. UVB – Deep Epidermis
  • 25. PHYSIOLOGICAL EFFECTS OF UVR PHYSIOLOGICAL EFFECTS OF UVR 1. 2. The UVR physiological effects may be divided into 2 groups; Local – Effects which produced locally in the area. General – Results from a widespread Irradiation.
  • 26. LOCAL EFFECTS OF UVR LOCAL EFFECTS OF UVR 1. ERYTHEMA – It is reddening of the skin. First observable effect of UV Irradiation. TRIPLE RESPONSE. It cause chemical action which result in IRRITATION & DESTRUCTION of cells. This causes liberation of “H”-substance which produce the TRIPLE RESPONSE. The erythema is regarded as an inflammatory reaction stimulated by the UVR.
  • 27. TRIPLE RESPONSE TRIPLE RESPONSE 1. Dilation of capillaries – H-substance 2. Dilation of arterioles – Axon reflex 3. Exudation of fluids into the tissues – Increased permeability of the capillary walls.
  • 28. 2. PIGMENTATION / TANNING 2. PIGMENTATION / TANNING MELANOCYTE & ACCELERATES MELANIN PIGMENT MELANOCYTE & ACCELERATES MELANIN PIGMENT MELANOCYTE & ACCELERATES MELANIN PIGMENT It is thought that the UVR stimulates MELANOCYTE & ACCELERATES the production of MELANIN PIGMENT. Pigmentation commonly follows an erythemal reaction. It varies with the dosage of UVR & the different individuals.
  • 29.
  • 30. 2. PIGMENTATION / TANNING 2. PIGMENTATION / TANNING PRE-EXISTING melanin PRE-EXISTING melanin Sometimes immediate tanning occurs as a result of effects of PRE-EXISTING melanin. This may occur within minutes of exposure. Sun / Carbon arc Brown color Mercury Vapor lamp Grayish REDUCES The pigmentation REDUCES the penetration of UVB.
  • 31. 3. THICKENING OF EPIDERMIS 3. THICKENING OF EPIDERMIS UVR provokes an increased reproduction of KERATINOCYTES. This leads to thickening of epidermis which acts does acts a PROTECTION AGAINST THE RAYS. So longer doses are required to repeat an ERYTHEMAL reaction.
  • 32. 4. DESQUAMATION / PEELING 4. DESQUAMATION / PEELING It is the CASTING OFF of dead cells from the surface of the skin. The desquamation is proportional to the intensity of the erythema. The peeling results in REDUCTION / LOSS OF THE INCREASED RESISTANCE TO THE RAYS.
  • 33. 5. ANTIBIOTIC EFFECT 5. ANTIBIOTIC EFFECT Destructive effects of ultraviolet radiation include the destruction of viruses, bacteria, and other small organisms on the skin surface such as FUNGI commonly found in wounds. (effect of UVB).
  • 34. B. GENERAL EFFECTS OF UVR B. GENERAL EFFECTS OF UVR 1. Vitamin D Production 7-Dehydrocholestrol Vitamin – D chemical reaction. 7-Dehydrocholestrol Vitamin – D chemical reaction. 7-Dehydrocholestrol Vitamin – D chemical reaction. 7-Dehydrocholestrol Vitamin – D chemical reaction. In the presence of UVB, converts 7-Dehydrocholestrol into Vitamin – D through chemical reaction. absorption of calcium and phosphorous absorption of calcium and phosphorous Vitamin D is required to assist in the absorption of calcium and phosphorous from the intestine to blood stream.
  • 35. 2- THE ESOPHYLACTIC EFFECT 2- THE ESOPHYLACTIC EFFECT General UVA Irradiation reticulo - endothelial system Stimulation of reticulo - endothelial system ANTIBODIES Ingest bacteria & produce ANTIBODIES against BACTERIA & TOXINS BACTERIA & TOXINS. So the resistance of the body to infection is increased & this being known as ESOPHYLACTIC EFFECT.
  • 36. 3. GENERAL TONIC EFECT 3. GENERAL TONIC EFECT Its being claimed that because of General UV Irradiation has a GENERAL TONIC EFFECT, GENERAL TONIC EFFECT, APPETITIE & SLEEP BEING IMPROVED APPETITIE & SLEEP BEING IMPROVED NERVOUSNESS & IRRITABILITY DECREASED NERVOUSNESS & IRRITABILITY DECREASED NERVOUSNESS & IRRITABILITY DECREASED
  • 37. THERAPEUTIC EFFECTS OF UVR THERAPEUTIC EFFECTS OF UVR The principle therapeutic uses of UVR are of SKIN DISEASES PSORIASIS:- 1. PSORIASIS:- THICK PINK / RED SILVERY SCALES. THICK PINK / RED SILVERY SCALES. THICK PINK / RED SILVERY SCALES. It is a skin condition which presents localized THICK PINK / RED plaques, sharply demarcated & covered with SILVERY SCALES. decrease the DNA synthesis in the cells of the skin & to improve the skin condition decrease the DNA synthesis in the cells of the skin & to improve the skin condition decrease the DNA synthesis in the cells of the skin & to improve the skin condition In this state the aim of UVR irradiation is to decrease the DNA synthesis in the cells of the skin & to improve the skin condition
  • 38. HEALTHY & PSORIASIS SKIN HEALTHY & PSORIASIS SKIN
  • 39. 2. ACNE VULGARIS 2. ACNE VULGARIS PUSTULES, PAPULES blocking of sebaceous pores & hair follicles affecting mainly the face, chest & back. PUSTULES, PAPULES blocking of sebaceous pores & hair follicles affecting mainly the face, chest & back. PUSTULES, PAPULES blocking of sebaceous pores & hair follicles affecting mainly the face, chest & back. PUSTULES, PAPULES blocking of sebaceous pores & hair follicles affecting mainly the face, chest & back. PUSTULES, PAPULES blocking of sebaceous pores & hair follicles affecting mainly the face, chest & back. Acne is also a skin condition which presents PUSTULES, PAPULES formed by blocking of sebaceous pores & hair follicles affecting mainly the face, chest & back. disfiguring & serious distress. disfiguring & serious distress. The more severe & long lasting forms cause disfiguring & serious distress. desquamation to open Using UVR is aiming to produce desquamation to open the blocked pores and hair follicles. E2 dose is given to the face, chest and neck.
  • 40. 3. ECZEMA 3. ECZEMA INFLAMMATORY RESPONSE It is an INFLAMMATORY RESPONSE in the skin associated with OEDEMA. ITCHING REDNESS, SCALING, VESCILES ITCHING REDNESS, SCALING, VESCILES The patient suffers marked ITCHING with REDNESS, SCALING, VESCILES & exudation of serum on the skin. (Sub acute & Chronic stage) (Sub acute & Chronic stage) A mild UVR treatment will help. (Sub acute & Chronic stage)
  • 41. 4. CHRONIC INFECTION & INFECTED WOUNDS 4. CHRONIC INFECTION & INFECTED WOUNDS 1. 2. 3. Infected wounds such as ULCERS ULCERS PRESSURE SORES PRESSURE SORES SURGICAL INCISIONS SURGICAL INCISIONS are often treated with HIGH DOSES of UVR. remove the (SLOUGH) infected material promote repair. remove the (SLOUGH) infected material promote repair. remove the (SLOUGH) infected material promote repair. The aim of UVR irradiation is to destroy the surface bacteria, remove the (SLOUGH) infected material & promote repair. E3 dose E3 dose is sufficient, the dose is may be given daily and is not being applied to normal skin.
  • 43. 5. VITILIGO 5. VITILIGO MELANOCYTES MELANOCYTES It is a condition in which destruction of MELANOCYTES in local areas causes WHITE PATCHES to appear on the skin. Both UVA & UVB stimulate melanocyte activity. UVA seems to provoke a DARKER & LONGER LASTING TANNING. more THICKENNING. UVB provokes more THICKENNING.
  • 44. 6. NON – INFECTED WOUNDS 6. NON – INFECTED WOUNDS GROWTH of GRANULATION TISSUE & SPEED UP REPAIR GROWTH of GRANULATION TISSUE & SPEED UP REPAIR GROWTH of GRANULATION TISSUE & SPEED UP REPAIR The aim of UVR is to stimulate the GROWTH of GRANULATION TISSUE & SPEED UP REPAIR. UVA stimulates GROWTH. Venous / Arterial ulcers. Example for non infected wounds are – Venous / Arterial ulcers.
  • 45. 7. COUNTER IRRITATION 7. COUNTER IRRITATION It is used to produce a strong counter irritation effect over the site of DEEP SEATED PAIN. E4 dose mask of pain . E4 dose mask of pain . E4 dose mask of pain . E4 dose is given to cause discomfort and producing mask of pain .
  • 46. INDICATIONS FOR UVR INDICATIONS FOR UVR DERMATOLOGICAL CONDITIONS 1. DERMATOLOGICAL CONDITIONS – Psoriasis, Acne, Sub acute & Chronic Eczema. Calcium / Phosphorus disease 2. Calcium / Phosphorus disease – Osteomalacia Non pulmonary tuberculosis 3. Non pulmonary tuberculosis Local Ulceration 4. Local Ulceration – Ulcers, Pressure sores, Surgical incision
  • 47. INDICATIONS FOR UVR INDICATIONS FOR UVR Upper respiratory condition management Upper respiratory condition management 5. Upper respiratory condition management – Common Cold. 6. Counter Irritant Effect.
  • 48. CONTRAINDICATION OF UVR CONTRAINDICATION OF UVR Pulmonary Tuberculosis 1. Pulmonary Tuberculosis Severe cardiac disturbances 2. Severe cardiac disturbances Systemic Lupus Erythematosis 3. Systemic Lupus Erythematosis Severe Diabetes 4. Severe Diabetes Dermatological Conditions 5. Dermatological Conditions
  • 49. CONTRAINDICATION OF UVR CONTRAINDICATION OF UVR Known Photosensitivity. 6. Known Photosensitivity. Photosensitizing medication. 7. Photosensitizing medication. Deep x – Ray therapy. 8. Deep x – Ray therapy. Acute Febrile illness 9. Acute Febrile illness 10. Recent skin grafts.
  • 50. CONTRAINDICATION OF UVR CONTRAINDICATION OF UVR Porphyrias Porphyrias Pellagra Pellagra Sarcoidosis Sarcoidosis Xeroderma pigmentosum Xeroderma pigmentosum Acute psoriasis Acute psoriasis Renal and hepatic insufficiencies Renal and hepatic insufficiencies Renal and hepatic insufficiencies Hyperthyroidism Hyperthyroidism Generalized dermatitis Generalized dermatitis Advanced arteriosclerosis Advanced arteriosclerosis Acute eczema Acute eczema Herpes simplex Herpes simplex Hypersensitivity to sunlight Hypersensitivity to sunlight Hypersensitivity to sunlight
  • 51. DANGERS DANGERS Shock 1. Shock Eyes 2. Eyes - UVR may produce conjunctivitis, iritis or cataract. Over Dosage 3. Over Dosage – UVR burn can occur. Mainly E4 reaction Ozone 4. Ozone – Important to ensure adequate Ventilation in the area.
  • 52. SAFETY PRECAUTIONS AGAINST SUNLIGHT(UVR) SAFETY PRECAUTIONS AGAINST SUNLIGHT(UVR) 1. Eyes protection.
  • 53. 2. SKIN DAMAGE / TANNING PROTECTION 2. SKIN DAMAGE / TANNING PROTECTION Sunscreen doesn’t offer 100% protection. Sunscreen doesn’t offer 100% protection. Sunscreen doesn’t offer 100% protection. SPF(Sun Protection Factor) 30+ sunscreen blocks 96% of UV; SPF 15+ blocks out 93%. SPF(Sun Protection Factor) 30+ sunscreen blocks 96% of UV; SPF 15+ blocks out 93%. SPF(Sun Protection Factor) 30+ sunscreen blocks 96% of UV; SPF 15+ blocks out 93%. SPF(Sun Protection Factor) 30+ sunscreen blocks 96% of UV; SPF 15+ blocks out 93%. In addition to sunscreen, wear a hat, sunglasses, more clothing, and seek shade. In addition to sunscreen, wear a hat, sunglasses, more clothing, and seek shade. In addition to sunscreen, wear a hat, sunglasses, more clothing, and seek shade. In addition to sunscreen, wear a hat, sunglasses, more clothing, and seek shade. In addition to sunscreen, wear a hat, sunglasses, more clothing, and seek shade.
  • 54. PROTECTIVE CLOTHING PROTECTIVE CLOTHING Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged. Most cotton and cotton/ polyester fabrics protect against 95% of UV, but are less effective if wet, faded, or aged.
  • 55. TEST DOSE & DETERMINIG MED TEST DOSE & DETERMINIG MED (ERYTHEMAL) (ERYTHEMAL) It is used to assess the individual patients (ERYTHEMAL) reaction to uvr irradiation. MED (MINIMAL ERYTHEMAL DOSE) MED (MINIMAL ERYTHEMAL DOSE) The basis for any calculation of any UVR dosage is the MED (MINIMAL ERYTHEMAL DOSE) the response of erythema the response of erythema This MED refers to the response of erythema for the dose to be given
  • 56. TEST DOSE CONT…. TEST DOSE CONT…. MED DETERMINE EXPOSURE TIME MED DETERMINE EXPOSURE TIME MED DETERMINE EXPOSURE TIME MED DETERMINE EXPOSURE TIME MED DETERMINE EXPOSURE TIME The patient must understand that the purpose of the MED test is to DETERMINE just how much EXPOSURE TIME is necessary based on their skin sensitivity. Proper patient education should be given:- Proper patient education should be given:- Wear Goggles 1. Wear Goggles Observe & monitor the skin condition 2. Observe & monitor the skin condition 3. Keep skin moisture following exposure to UVR Pigmentation changes are to be expected & are a normal response. Pigmentation changes are to be expected & are a normal response. 4. Pigmentation changes are to be expected & are a normal response. Prolonged & repeated exposure leads to premature aging. Prolonged & repeated exposure leads to premature aging. 5. Prolonged & repeated exposure leads to premature aging.
  • 57. STEPS TO DETERMINE TEST DOSE / SKIN TEST STEPS TO DETERMINE TEST DOSE / SKIN TEST 1. The area chosen for the test is of importance. Because the patient is to inspect at regular intervals a convenient, visible site is essential. Because the patient is to inspect at regular intervals a convenient, visible site is essential. 2. Because the patient is to inspect at regular intervals a convenient, visible site is essential. It should be clear of skin disease. 3. It should be clear of skin disease. The FLEXOR SURFACE of the FOREARM is the most usual site.(Other sites are – Abdomen, Medial aspect of arm / thigh) The FLEXOR SURFACE of the FOREARM is the most usual site.(Other sites are – Abdomen, Medial aspect of arm / thigh) The FLEXOR SURFACE of the FOREARM is the most usual site.(Other sites are – Abdomen, Medial aspect of arm / thigh) 4. The FLEXOR SURFACE of the FOREARM is the most usual site.(Other sites are – Abdomen, Medial aspect of arm / thigh) 5. The selected site should be cleaned with soap & water to remove surface grease. 6. Cover the patient other areas leaving only the forearm exposed to UVR.
  • 58. STEPS TO DETERMINE TEST DOSE / SKIN TEST STEPS TO DETERMINE TEST DOSE / SKIN TEST 7. Three to Five holes of at least 2cm² & 1cm apart are cut in a piece of lint/paper/ cardboard is taken for irradiation of UVR along with a slide cover – to pull up to reveal one opening at a time.
  • 59. STEPS TO DETERMINE TEST DOSE / SKIN TEST STEPS TO DETERMINE TEST DOSE / SKIN TEST 8. This cutting is fixed to the forearm with adhesive plaster. IDENTIFICATION OF THE ERYTHEMA EASIER 9. The cuttings are of different sizes & shapes in-order to make IDENTIFICATION OF THE ERYTHEMA EASIER for the patient. 10. Allow the lamp to warm up according to the manufacturer instructions. 11. Place the lamp PERPENDICULAR to the area being tested (Forearm) & a DISTANCE of 60 to 90cms from the site. 12. Expose the 1st opening for 30sec, then expose the 2nd opening for another 30sec & go on till the last opening
  • 60. STEPS TO DETERMINE TEST DOSE / SKIN TEST STEPS TO DETERMINE TEST DOSE / SKIN TEST 13. So the 1st opening would receive the longest exposure time & the last opening would receive the least amount of exposure time. 14. Switch off the lamp 15. Instruct the patient to MONITOR the forearm every 2hrs & note which opening or shape appeared pink / red first & when it faded / disappeared. 16. The patient is also given a card similar to the opening to make a note.
  • 61. MINIMAL ERYTHEMAL DOSE MINIMAL ERYTHEMAL DOSE It is a slight reddening (erythema) of the skin which takes from 6 – 8hrs to develop & which is still just visible at 24hrs.
  • 62. DESCRIPTION OF DEGREES OF ERYTHEMA DESCRIPTION OF DEGREES OF ERYTHEMA Degree of Erythem a Latent period In HRS Appearance color Duration of Erythema Skin Oedema Skin discomfort Desquam ation of skin Relation to E1 Dose E1 6-8 Mildly pink <24hrs None None None E1 E2 4-6 Definite Pink Red. Blanches on Pressure 2 Days None Slight Soreness, Irritation Powder y 2.5% of E1 E3 2-4 Very red, Does not blanch on pressure 3-5 Days Some Hot & Painful In thin Sheets 5% of E1 E4 <2 Angry Red A Week Blister Very Painful Thick Sheets 10% of E1
  • 63. DOSAGE DOSAGE a) b) c) d) The skin response to UVR depends on; 1. The quantity of UVR energy applied to unit area of the skin.(Depends on); The output of lamp – Make, Type, Aging Distance between the lamp & the skin – Inverse square law Angle at which radiations fall on the skin – cosine law Time for which radiations are applied 2. The sensitivity of the skin
  • 64. CALCULATION OF DOSAGE CALCULATION OF DOSAGE E1/MED is the basic of UV calculation which is determined for each individual patient by performing a skin test. From this point all other doses of UVR can be calculated. E2 = 2½ x E1 E3 = 5 x E1 E4 = 10 x E1
  • 65. CALCULATION OF DOSAGE CALCULATION OF DOSAGE EXAMPLE: If the E1 dose of the patient is 25sec, calculate the E3 dose? E1 dose = 25sec E3 dose = 5 x E1 E3 dose = 5 x 25 = 125sec
  • 66. CALCULATION OF NEW DOSE CALCULATION OF NEW DOSE The dose at different distances from the lamp to skin can be calculated by formula; NEWDOSE = OLD DOSE X NEW DISTANCE² OLD DISTANCE ²
  • 67. PROGRESSION OF DOSAGE PROGRESSION OF DOSAGE An exposure to UVR should not be repeated until the erythema caused by a previous dose has faded. Thickening of the epidermis Necessary to increase the exposure in order to repeat the erythemal reaction at each successive dose Doses are progressed as follows: To repeat an E1 25% of the preceding dose is added To repeat an E2 50% of the preceding dose is added To repeat an E3 75% of the preceding dose is added To repeat an E4 100% of the preceding dose is added
  • 68. PROGRESSION OF DOSAGE PROGRESSION OF DOSAGE Examples of progression of dosage If E1 is 30sec, find the second progression (P2E1)? E1= 30sec P1(Day one progression)E1 = E1 + 25% of E1 = 30 +30/4 = 30 + 7.5 =37.5sec P2(Day two progression) E1 = P1E1 + 25% of P1E1 = 37.5 +37.5/4 = 46.9sec P2E1 = 47sec
  • 69. SELECTION OF DOSAGE LEVEL SELECTION OF DOSAGE LEVEL 1. An E1/MED – Given to the total body area (Whole body) 2. An E2 - May not be given to up to 20% of total body area 3. An E3 – May not be given to up to 250cm² of normal skin 4. An E4 – May only be given to an area up to 25cm² of normal skin.
  • 70. FREQUENCY OF UVR TREATMENT FREQUENCY OF UVR TREATMENT 1. An E1 / MED may be given DAILY 2. An E2 – Should be given every second day 3. An E3 – Should be given every 3 or 4th day (Twice Weekly) 4. An E4 – may only be given once a week or even once a fortnight. N.B. when treating non-skin areas such as pressure areas or ulcers, all doses may be given daily as there is no erythema reaction produced.
  • 71. SENSITIZATION / SENSITIZING DRUGS SENSITIZATION / SENSITIZING DRUGS A number of drugs & some foods in a few patients are known to sensitize patients to the effects of UVR. Commonly seen sensitizing groups are; 1. psoralens - Sensitizer 2. Sulphonamides - Antibiotic 3. Phenothiazine – Tranquilizer 4. Barbiturates 5. Gold therapy 6. Aspirin & Derivatives