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The use of heated metal to treat wounds and control bleeding was the origin of the thermal “cautery”.
Electrically generated heat , “electrocautery” was first introduced by Claude Paquelin in 1875.
Walter de Keating –Hart coined the term “fulgarisation”
Doyen introduced the term “electrocoagulation”
W Clarke defined the term electrodessication
William Bovie is considered the father of modern electrosurgical unit. He developed it in 1926.
The term “electrosurgery” is a general term to describe all the different procedures employing electrically generated heat.
The heat may be generated using either galvanic heat or A.C.
THE BASIC PHYSICS OF ELECTROSURGERY IS TO BOOST THE VOLTAGE AND FREQUENCY WHILE DECREASING THE
AMPERAGE OF ALTERNATING CURRENT FROM THE STANDARD WALL OUTLET. An occilating electromagnetic wave is generated, which
is either a damped or undamped sine wave. This is passed onto the lesion producing molecular movements, leading to friction and
heat production. Heat is also generated through the electric field of the tissue itself and the sum total provides the desired tissue
destruction .
THE TYPE OF SINE WAVE GENERATED DETERMINES THE TYPE OF TISSUE DESTRUCTION .
INDICATIONS :
BENIGN: Warts, acrochordons, molluscum contagiosum, milia, DPN, Small epidermal nevi, seborrheic keratoses, freckles, senile
lentigens, mucosal and sebaceous cyst, vascular lesions ( telangiectasias, spider angioma, cherry angioma, small hemangioma,
venous lakes, angiofibromas, pyogenic granloma), syringomas, trichoepithelioma, xanthelesma, xanthoma, rhinophyma, nevus
sebaceous.
CONTRAINDICATIONS :
ABSOLUTE : KELOIDAL TENDENCY, INFECTIONS OVER THE LESION, CARDIAC PATIENTS ESPECIALLY WITH PACE MAKERS.
RELATIVE : Petit mal epilepsy, Hepatitis B, HIV infection.
1. ELECTROFULGARISATION:
Here superficial tissue is charred by sparks without actually touching the tissue. Long thick sparks are created by
DAMPED SINE WAVES OF LOW AMPERAGE ( 1-2 on the dial) AND HIGH VOLTAGE. The electrode is kept at a small distance ( 2-3
mm) from the lesion and the current is given for a short burst of 2-3 sec at each site. The tissue destruction is rapid with cell
dehydration and necrosis. Verruca plana, milia and DPN are treated in this way. Advantages ---- prevents deeper tissue
destruction. Disadvantage ---- there is risk of damage to the perilesional area. This is countered by the use of epilation needle
electrodes. It is not effective for dermal lesions.
2. ELECTRODESICCATION : here the lesion is touched with the electrode. The bursts of current are of longer duration( 2-4 sec)
and the current intensity is slightly increased to create short fine sparks . THE END POINT IS WHERE THE LESION SHRIVELS
UP AND LIGHTENS IN COLOR. The tissue destruction is deeper and involves superficial mummification and necrosis of cells
after initial dehydration. Thrombosis of minute blood vessels also occur. Larger lesions tend to bubble when there is
separation of the DEJ. The lesion is then removed with a gauze piece, curetted or cut at the base with a pair of scissors. The
lesions usually treated by this method are ---- seborrheic keratoses, pyogenic granuloma, verruca vulgaris, condyloma
acuminate, keratoacanthomas, acrochordons, molluscum contagiosum, xanthomas, xanthelesma, sebaceous hyperplasia,
spider angioma.
Advantages : minimal scarring an defective hemostasis. Disadvantage : the depth cannot be well controlled ---- recurrence is
possible.
3. ELECTROCOAGULATION:
Deeper tissue destruction occurs by this process. The lesion may or may not be touched depending on the depth of
destruction required. Here short thick sparks are created due to DAMPED OR PARTIALLY RECTIFIED SINE WAVES OF HIGH
AMPERAGE BUT LOW VOLTAGE. Due to high current, the dispersive plate is needed. The tissue destruction involves deep necrosis
and coagulation with a hyalinized appearance. Thrombosis of midsized vessels ( 1-2 mm) also occurs. THE RESULTANT TISSUE
APPEARS WHITE AND HOMAGENIZED WITHOUT CHARRING
The primary use is to destroy recurrent verruca vulgaris, trichoepitheliomas, telangiectasias, small BCC and SCC, nail
matrix coagulation in ingrown toe nails.
4. ELECTROSECTION :
This technique cuts the tissue. It requires solid state current with dispersive plate. A high amperage, low voltage current
is used to create RECTIFIED SINE WAVE. There is simultaneous hemostasis due to vessel coagulation. There is grater tissue
destruction with delayed healing due to poor vascularity.
PRECAUTIONS:
INFLAMMABLE STERILIZATION PRODUCTS LIKE SPIRIT AND ALCOHOL MAY BURN ON PASSAGE OF THE SPARK ----
SHOULD BE AVOIDED.
ADEQUATE EXHAUST FACILITIES ARE NEEDED TO EVACUATE SMOKE FUMES
FACE MASK
GLOVES
CHECK ALL CONNECTIONS AND WIRES TO ELIMINATE LOOSE CONNECTIONS THAT MAY CAUSE SHORT CIRCUITS,
ELECTRIC SHOCKS AND FIRE HAZARDS.
POSTOPERATIVE CARE: antibiotic creams. For bigger lesions --- dressing that is changed at 24 hours and then again after 5-7 days.
COMPLICATIONS: Pain, bleeding, secondary infection, sacrring, post inflammatory hypo- or hyper- pigmentation, hypertrophic scar or
keloid.
CRYOSURGERY
DEFINITION : It is a branch of therapeutics that makes use of local freezing for the controlled destruction or removal of living tissues.
CRYOGEN: It is a substance used for cryosurgery. LIQIUD NITROGEN IS THE COLDEST REFRINGENT AND IS THE CRYOGEN OF CHOICE
FOR DERMATOLOGICAL CRYOSURGERY. IT IS THE ONLY CRYOGEN ADVOCATED FOR MALIGNANT SKIN LESIONS.
SALT ICE = -20 DEGREE C
CARBON DIOXIDE SLUSH = -20 DEGREE C
FLUOROCARBONS = -30 DEGREE C
NITROUS OXIDE = -75 DEGREE C
CARBON DIOXIDE SNOW = -79 DEGREE C
LIQUID NITROGEN = -20 DEGREE C ( swab); -196 DEGREE C ( spray)
DIFFERENTIAL SENSITIVITY OF CELLS : There is a minimum temperature below which cells die. In the skin, this is generally around -30
to -40 degree C. cells and tissue sensitivity to sub zero temperature are as follows :
1. melanocytes = -4 to -8 degree C
2. squamous cells = -20 degree C
3. dermal CT and fibroblasts = -30 to -40 degree C
SHAPE OF CRYOLESION: The shape of the cryolesion is hemispherical as the ice front advances from the surface downwards.The
depth of freeze approximates the radius of the flat surface of the frozen hemisphere.
EQUIPMENT FOR CRYOSURGERY : These vary depending on the cryogen used. The equipment of the liquid nitrogen cryo is given ----
(a) Cryocans --- where the LN is stored. Capacities vary from 1-60L. these are vacuum insulated containers.
(b) Withdrawal devices --- these are used to transfer the LN to the cryosurgical unit.
(c) Cryosurgical unit --- these are of the following types
(1) hand held unit --- these units can only be used for the spray technique. The tank is of 500 ml. there is an instant on/off
switch. They have screw on brass tips of 3 diameters --- 0.375mm, 0.5mm and 1 mm resp.
(2) Table top unit --- this is a compact unit with a built in pyrometer that moniters the temp of the tissue being frozen which is a
necessity while treating malignant tumours. The unit has both spray as well as probe facilities. A variety of TIPS ( cones,
probes) can be attached. There are 2 storage cans of 1 litre capacity. The advantages of this unit over the hand held unit are
----
the spray steam continuea unabated for a longer time. Therefore it can be used for prolonged continous or
intermittent treatment.
It allows for regulation of the volume of the nitrogen spray
Excellent for the treatment of malignant lesions
Can be used to treat intraoral/ vaginal/ anal/ rectal lesion as long as probes are available.
The disadvantages include ----
Costly
Large quantity of LN is needed at each sitting.
INDICATIONS:
BENIGN LESIONS ------- warts, molluscum, cystic acne, acne scars, keloid, pyogenic granuloma, acrochordons, seborrheic keratoses,
mucoid cyst
MALIGNANT LESIONS ---- BCC, SCC, basal cell nevus syndrome, lentigo maligna, lentigo maligna melanoma. Tumors less suitable for
cryosurgery are those that are large ( over 2 cm in diameter), recurrent tumors of the feet or lower legs or those with a
histopathological diagnosis of morphemic or mixed type of BCC.
CONTRAINDICATION :
Agammaglobulinemia
Cold intolerance
Cold urticaria
Cryoglobulinemia
Cryofibrinogenemia
Raynaud’s disease
Pyoderma gangrenosum
Collagen vascular and autoimmune diseases
Concurrent treatment with immunosuppressives.
Patients with renal dialysis
Multiple myeloma
PRE-PROCEDURE STEPS :
Photographs
A biopsy to confirm the diagnosis in case of malignant and premalignant conditions
Explanation of the procedure to the patient and obtaining a written informed consent.
Analgesics may be given 1-2 hours before the procedure.
There is also a spray technique using cones or cylinders ---- it is known as restricted spray technique. The advantage is
that the spray is concentrated and its lateral spread is restricted. The technique also gives a very rapid rate of fall of temperature
and is therefore more destructive. This technique is useful in sites such as eyelids, inner canthi where lateral spread is to be
restricted.
Liquid nitrogen is poured from the storage container to the spray unit slowly, using a funnel, until the unit is filled upto 2 inches from
the brim. After the lid is screwed back, one should wait for 3-4 min for the pressure to build up. The appropriate spray tip is selected(
the one that sparay swithin the borders of the lesion). For single short freeze, no LA is needed but if the lesion is large and requires
more freeze time then local anaesthesia is needed. The periphery of the lesion is marked and a rim of normal tissue is included
(benign, 1-2mm; premalignant, 3-5mm; malignant, 5-10mm) is included. K-Y jelly is applied to the lesion. The spray tip is held 1 cm
away and a steady spray of liquid nitrogen is directed at the centre of the marked lesion. The ice field gradually extends upto the
edge of the circle, the freeze time commences once solid ice is formed over the marked area. The spray is adjusted so as to maintain
an ice ball of constant ice and for the required period ( 5-30 sec; normally not more than 30 sec). the lesion is allowed to thaw
gradually. Thaw time is usually double of the freeze time. If a second freeze is required, the lesion should be allowed to thaw
completely before re-freezing. The skin should be palpated to check for the disappearance of the firmness (ice) from the tissue.
3. cryoprobe technique----
cryo probes vary in size from 1 cm to several cm in diameter. A probe suitable to the lesion to be treated is
selected and is pre cooled before application to the surface of the lesion. Its probe tip is applied firmly to the lesion and
cooling is commenced. The probe is allowed to thaw sufficiently before removing it from the treatment site. A repeat
cycle, if required, should be commenced after allowing the lesion to thaw completely.
FOLLOW UP : The patient is asked to follow up after 10-15 days to assess the lesion or earlier if a large blister or
secondary infection develop. THE PROCEDURE CAN BE REPEATED AFTER 3 WEEKS IF REQUIRED.
COMPLICATIONS :
IMMEDIATE ---- pain, headache, edema ( at sites of lax skin), hemorrhage, blister formation and syncope.
DELAYED ---- hemorrhage, post operative infection, granulation tissue formation, pseudoepitheliomatous hyperplasia,
hyperpigmentation, milia, hypertrophic scar, atrophy, hair loss, nerve damage/ paresthesia ( usually temporary).
ADVANTAGES :
Patients of all ages can be treated even those at poor risk for surgery and GA.
It is a OPD procedure
Multiple tumors can be treated at the same time.
Complications are rare and the cosmetic results are excellent.
Cure rate is high in properly selected cases.
Lesions on sites with poor skin mobility that are difficult to excise can be frozen with impunity
Pre-irradiated lesions can also be treated by cryo.
DISADVANTAGES :
DISCOMFORT during the procedure
Post operative edema can be significant
post operative pigmentary changes can occur.