Académique Documents
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SYLLABUS
PRACTICALS-
Surgical instruments and equipment. Operation theatre routines. Surgical
pack:
Preparation, sterilization and handling. Familiarisation with suture materials,
surgical
knots, suture patterns and their use. Familiarisation to live
surgery haemostatsis.
COURSE OVERVIEW
• History of surgery
• Classification
• General surgery principles
• Pre and post-operative considerations
• History and Development of Veterinary Surgery
Module-1 =
HISTORY OF ANAESTHESIA
Classification of surgery-
DEFINITION
FUNCTIONS OF A SURGEON
TENETS OF HALSTED
HISTORY
PREPARATION OF PATIENT
DAY OF OPERATION
LOCATION
PLANNING
MAINTENANCE OF RECORDS
POST-OPERATIVE MEDICATION
POST-OPERATIVE DIET
• Oral intake of food and fluid is restricted for 12-24 hours after
major operation.
• Liquid diet should be given at second day.
• Semisolid food should be given from forth day.
• Solid food should be given after 8th day of operation.
• Food must be free from fat and some vitamins, enzymes should
be added.
POST-OPERATIVE EXCERCISE
POST-OPERATIVE DRESSING
FOLLOWED BY CHECK UP
Module – 2 =
ASEPSIS, ANTISEPSIS & THEIR APPLICATIONS IN VETY.
SURGERY.
TERMINOLOGY
THERMAL
Points to be considered
Methods
FILTRATION
RADIATION
CHEMICAL AGENT
• An ideal chemical agent should have following
properties o kill all pathogenic microorganism
o work effectively in short period of time o
exert residual action
o not corrode, dry or stain
o be stable, odorless, non toxic
o be effective in presence of organic matter
o not be inactivated by other concurrently used chemicals
Alcohol
Aldehyde
) Formaldehyde
PREOPERATIVE CONSIDERATIONS
THE OWNER
SURGICAL RISK
• These are
o Evaluation of operative risk
o Recognition and correction of preoperative deficits
o Prevention of intra-operative and postoperative complication
before they develop
o Resuscitation and after care of surgical patient
SURGICAL JUDGEMENT
Module -3
DEFINITION
CLASSIFICATION
PATHOPHYSIOLOGY OF SHOCK
SYMPTOMS OF SHOCK
TREATMENT
MODULE-4=
HAEMORRHAGE
CLASSIFICATION
External haemorrhage
Internal haemorrhage
Depending on the time of occurrence
Depending on the source of haemorrhage
o External haemorrhage occurs from open wounds or cut wounds
that is visible on the outside of the body
o Example
▪ Epistaxis – bleeding from nose.
▪ Haematuria: Blood in urine.
▪ Haematemesis- vomiting fresh blood .
▪ Haemoptysis – coughing up blood from the lungs .
▪ Melena - presence of blood in faeces.
o Internal haemorrhage is bleeding occurring inside the body . It
may be caused by high blood pressure (by causing blood vessel
rupture) or other forms of injury, especially high speed
deceleration occurring during an automobile accident , which can
cause organ rupture. When blood is collected in a newly formed
cavity called as Haematoma.
o Example:
▪ Haemometra - haemorrhage into uterus
▪ Haemopleura - haemorrhage into pleural cavity
▪ Haemoperitoneum - haemorrhage into peritoneal cavity
▪ Haematocele - haemorrhage in to tunica vaginalis
▪ Haemarthrosis - haemorrhage into a joint
▪ Haematomyelia - haemorrhage into spinal cord
▪ Petechiae - Pinpoint haemorrhages on skin and subcutis
▪ Ecchymosis - haemorrhagic spots on skin and
subcutis. o Depending on the time of occurrence
▪ Primary haemorrhage occurs immediately after injury.
▪ Reactionary haemorrhage occurs within 24hours after the
primary bleeding has been arrested due to mechanical
disturbance of clot in vessel or due to slipping of the
ligature.
▪ Secondary haemorrhage occurs after about a week or more
due to septic disintegration of clot or due to sloughing of
portion of vessel because of a septic or gangrenous lesion.
o Depending on the source of haemorrhage: Arterial, Venous
and Capillary
ETIOLOGY
SYMPTOMS
Methods of haemostasis
FLUID INFUSION
Fluids
During anaemia
• If the PCV less than 20% blood transfusion is indicated and if the serum
protein is less than 3 to 3.5 g/dl further volume replacement is done
using plasma or synthetic colloidal is administered.
• Blood volume is calculated as 8 to 10% of the body weight in dogs (45%
cells and 55% plasma) and 6% in cats(36% cells and 64% plasma).
• Blood transfusion is indicated in dogs whose preanaesthetic
haemtocrit is less than 30 to 34% and in cats less than 25 to 29%.
• If the blood loss is more than 10% during surgery blood transfusion
is necessary.
• Blood and plasma transfusion is done based on the following formula.
o Amount of donor blood needed (ml) = Recipient blood
volume in ml x ((Desired PCV - Patient PCV) / PCV of donar
blood)
o Amount of donor plasma needed (ml) = Recipient
plasma volume in ml x ((Desired TSP - Patient TSP) / TSP of
donar blood)
• Indications
o To maintain plasma volume in uncomplicated
anaesthetized cases.
o To replace deficits in dehydration
o To restore interstitial fluid status
o To promote diuresis
• Disadvantages
o Large volume of administration coupled with migration
into interstitial spaces may result in oedema
o Produce haemodilution in anaemic
• Indications
o Expansion of plasma volume
o Used in the intial treatment of shock
o Administered intraoperatively during cardiac surgery
o To prevent tissue oedema from the conventional therapy
o These agents increase the plasma volume; cardiac output and
improves the blood pressure. They increase the myocardial
contractility
o Improve the microcirculatory blood flow by decreasing the
systemic vascular resistance, lowering the blood viscosity and
reducing the size of the endothelial cells.
• Disadvantages
o Induce hypernatraemia, hyperchloraemia,
hypdokalaemia, hypermolarity and metabolic acidosis
o May induce mild cellular dehydration
o Uncontrolled bleeding will become worsen due to the
rapid increase in blood pressure.
• Indications
o Hypoproteinemia and hypoalbuminemia
o Blood loss
o Hypovolemia
o Sepsis
o Persistent hypotension
o Does not cross the capillary walls hence will have sustained effect
o No risk of transmission of infectious diseases as compared
with plasma and less expensive
• Disadvantages
o Induce pulmonary oedema in patients with permeable capillaries
o May induce circulatory over load
o May induce coagulation disorders due to dilution of platelets,
precipitation of coagulation factors, increased fibrinolytic activity
and decreased functional von willebrand factor.
Module -6
ABSCESS -- DEFINITION
PARTS OF AN ABSCESS
CLASSIFICATION OF ABSCESS
ETIOLOGY OF ABSCESS
ACUTE ABSCESS
Symptoms
TREATMENT
TUMORS (Neoplasm)
• The term neoplasm is a Greek word used primarily for new formations or new
growths.
• Tumour may be defined as “an abnormal mass of tissue, the growth of which
extends uncontrolled, in comparison to the normal tissue and persists in the
same excess even after cessation of the stimuli which evoked the change.”
TYPES OF TUMOR
Benign Malignant
Grow slowly Grow rapidly
Locally grow to great size Create metastases
Don’t invade the neighboring tissue Invade and destroy neighboring tissues.
Usually do not return after surgical removal Recurrence after surgical removal
INCIDENCE
VARIETIES OF TUMORS
Tissue of origin Name of tumor Cell type
Mesenchymal Fibroma Fibrous connective
Tumors tissue
Chondroma Cartilaginous tissue
Osteoma Bony tissue
Odontoma Tooth substances
Myoma muscular tissue
Myxoma Cardiac skeleton
Lipoma Adipose tissue
Neuroma Nerve cells and fibers
Leiomyoma Smooth muscle
Rhabdomyoma Skeletal tissue
Haemangioma Blood vessels
Meningioma Meninges
Teratoma Germ cells
Epithelial tumors Papilloma Skin or mucous
membrane
Adenoma Glandular epithelium
Basal cell tumour Basal cell of skin
Hepatocellur adenoma Hepatocytes
Glomus tumour Melanocytes
Blood cells Non-Hodgkin lymphoma and Hodgkin Lymphoid cells
lymphoma
Leukemia Hematopoietic cells
DIAGNOSIS
TREATMENT
CYST
DIAGNOSIS
• Cysts are generally non-inflammatory in nature and develop slowly with well
defined periphery.
• On palpation fluid filled cyst fluctuates uniformly while cysts with solid mass
fluctuates en-masse.
TREATMENT
• Puncture and evacuate the contents of cyst and inject an irritant solution like Tr.
iodine to destroy the smooth lining membrane and setting up inflammation.
• Use of setton to drain cyst is a good practice.
• Surgical excision of the cyst is the preferred option. Intact cyst is carefully
dissected and removed from the surrounding tissue in possible cases.
DIFFERENTIAL DIAGNOSIS
• Cyst
o Slow in development as compared to an abscess.
o Soft and fluctuates uniformly, but not hard at periphery.
o No inflammatory symptoms.
o No pain sensation.
• Haematoma
o Forms due to coagulation of blood or serum.
o Doughy on palpation and forms immediately following an injury.
o Does not point like an abscess.
o No pain sensation.
• Hernia
o History of recent injury and swelling.
o Hernial ring can be palpated.
• Tumour
o Uniformly hard in consistency.
o Exploratory puncture with needle may reveal
blood. o No pain sensation.
o Does not point like an abscess.
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MODULE-7
NECROSIS
• Necrosis means death of tissue in the body. This occurs when enough blood
is not supplied to the tissue, whether from injury, radiation, or chemicals.
• Necrosis is not reversible.
CLASSIFICATION
• Avascular necrosis is a disease resulting from the temporary or permanent loss
of the blood supply to the bones. Without blood, the bone tissue dies and
causes the bone to collapse. This disease also is known as osteonecrosis,
aseptic necrosis, and ischemic bone necrosis
• Coagulative necrosis is typically seen in hypoxic environments (e.g.
myocardial infarction , infarct of the spleen ).
• Liquefactive necrosis is usually associated with cellular destruction and
pus formation (e.g. pneumonia ).
• Haemorrhagic necrosis is due to blockage of the venous drainage of an
organ or tissue (e.g. in testicular torsion ).
• Caseous necrosis is a specific form of coagulation necrosis typically caused
by mycobacteria (e.g. tuberculosis ).
• Fatty necrosis results from the action of lipases on fatty tissues (e.g. acute
pancreatitis , mammary tissue necrosis).
• Fibrinoid necrosis is caused by immune -mediated vascular damage. It is
marked by deposition of fibrin -like proteinaceous material in arterial walls.
ETIOLOGY
GANGRENE
ETIOLOGY
• The main factors in gangrene are loss of blood supply, and later invasion of the
part by micro-organisms.
• Gangrene may be caused by:
o Direct damage to tissues which include:
▪ Mechanical compression or interference with blood and
nerve supply to a part of the body or an organ while lying on
a hard floor. Example: bed-sores; sit-fast.
▪ Physical agents like application of heat and cold. Example: burns,
frost-bite.
▪ Action of acids, alkali and other chemicals producing dry
gangrene and moist gangrene.
▪ Impaction of intestine in the hernial ring and infestation with
pathogenic microbes especially with anaerobic infection.
o Indirect changes in tissues due to cardiac, venous, arterial or
nervous affections like:
▪ Ergot intoxication, which causes spasmodic narrowing
of arterioles and leads to dry gangrene of extremities. It
is commonly seen in feet of cattle.
▪ Diabetic gangrene narrows arteries and sugar in tissues, favours
bacterial growth.
▪ Senile gangrene i.e. arteriosclerosis in old age, which
narrows lumen of blood vessels.
• Extremities like legs, ears, tail, wattle and combs. It is mostly due to freezing
or ergot poisoning.
• Mammary gland: Staphylococcal mastitis produces necrosis due to toxins or
thrombosis of mammary vessels.
• Involvement of lung due to wrong drenching of medicines, improper passage
of stomach tube or severe lung infection.
• Intestines in equines are commonly involved either with infarction due to
verminous thrombosis of anterior mesenteric artery; or due to acute,
local passive hyperaemia produced by intestinal torsion, volvulus or
intussusceptions.
DIAGNOSIS
TREATMENT
ULCER
• An ulcer is a localised defect in the continuity of an epithelial surface without
any tendency to heal.
• It is usually associated with an inflamed base of granulation tissue with or
without necrotic slough.
• The majority is chronically inflamed; the slough at their base
represents inadequate drainage.
• Acutely inflamed ulcers may have an outer rim of cellulitis.
• Ulcer must be differentiated from erosion which is an epithelial defect with
loss of superficial layers, but the basal layers are intact.
CLASSIFICATION
ETIOLOGY
• Cattle: yoke
• Horse: saddle place, elbow, limbs.
• Dog: root of tail, tip of ears, and cornea of eye.
SYMPTOMS
• The edge of ulcer may be raised or in level with the surrounding skin
and rugged.
• The center of the lesion may be flat or concave, and may show necrotic spots.
• Granulations are pale or blue in colour depending upon the form.
• The discharge may be serous, purulent or grayish.
TREATMENT
CLASSIFICATION
CAUSES
• Thermal injuries
o Direct heat
o Flame
o Scalding
• Electrical burns
o Electrical cord
exposure o Lightning
Chemical burns
• Injuries caused by chemicals like strong acids and alkalis, solvents, petroleum
distillates and hot tars are referred to as chemical burns.
• The chemical produces localized necrosis of skin and deeper tissues with which
it comes in contact.
• The degree of tissue destruction depends on the strength of the chemical and
the duration of contact.
• Chemical causes local coagulation of proteins and necrosis.
CLINICAL SIGNS
Thermal burns
Electrical burns
• No pain
• Well-circumscribed cold, blood less, pale yellow lesion.
Chemical burns
TREATMENT
o Drugs like gentian violet, picric acid, acriflavin and tannic acid should
not be used as far as possible as they delay the healing process
by damaging the living cells.
o Analgesic should be given to reduce pain.
o Hypovolemic shock and acidosis are to be prevented by supplementation
of large quantities of fluid (Dextrose 5%) including 4%
sodium bicarbonate.
o The treatment in chemical burns should include washing with lots of
plain water and neutralization of the offending chemicals. Acids can be
neutralized with 2-3% solution of sodium carbonate or milk, while alkali
with 2% vinegar, citric or boric acid. Finally soothing ointment like
olive oil may be applied. If shock occurs, keep the animal warm
with heating pads or hot water bottles and a blanket of heavy coat. A
burn patient (pet) should be provided with ample warm fluids to
drink and this may be given in the form of milk or glucose water.
FROST BITE
• Frost bite is injury of tissues due to the action of a low temperature on them.
• The condition is rare in animals because they can withstand cold
temperature due to their hairy coats and will instinctively seek shelter from
inclement weather.
• Udder and teats are commonly frozen in cows during exercise on frosty winter
days. Besides the prepuce, penis and scrotum in horses, snout of pig, comb and
wattles of birds, tip of the ear and scrotum of dogs, tail and distal extremities
in other animals are commonly affected.
• It usually occurs in a low temperature but it can also ensue in prolonged
action of wet moderate above zero temperature (3-7ºc) since heat conductance
of the skin is increased and heat emission is intensified by it.
CAUSES
CLINICAL SIGNS
TREATMENT
DRUGS
MODULE-8: WOUND –
AND TREATMENT
Learning objectives
CLASSIFICATION OF WOUND
Open wounds
SYMPTOMS OF WOUND
HAEMOSTASIS
INFLAMMATORY PHASE
• The second phase of wound healing i.e. the inflammatory phase lasts
for 1-3 days in uninfected wounds.
o Classic signs include the following:
▪ Redness (rubor)
▪ Swelling (tumor)
▪ Pain ( dolor)
▪ Heat (calor)
▪ Loss of function (function laesa)
o Process
▪ The inflammatory response increases vascular
permeability, resulting in migration of neutrophils and
monocytes into the surrounding tissue. The neutrophils
engulf debris and microorganisms, providing the first line
of defense against infection. Neutrophil migration ceases
after the first few days post-injury if the wound is not
contaminated. If this acute inflammatory phase persists,
due to wound hypoxia, infection, nutritional deficiencies,
medication use, or other factors related to the patient’s
immune response, it can interfere with the late
inflammatory phase.
▪ In the late inflammatory phase, monocytes converted in the
tissue to macrophages, which digest and kill bacterial
pathogens, scavenge tissue debris and destroy remaining
neutrophils. Macrophages begin the transition from wound
inflammation to wound repair by secreting a variety of
chemotactic and growth factors that stimulate cell migration,
proliferation, and formation of the tissue matrix.
PROLIFERATIVE PHASE
Local factors
Systemic factors
Medication
Systemic diseases
LOCAL FACTORS
SYSTEMIC FACTORS
SYSTEMIC DISEASES
• Local pain/tenderness
• Local swelling/oedema
• Increased exudate
• Frank pus
• Wound breakdown
• Pyrexia
• Delayed healing
• Change in appearance of granulation tissue
• Bridging of epithelial tissue
• Abnormal smell
MANAGEMENT OF WOUNDS
Contaminated wound
• Presence of:
o Foreign bodies
o Debris e.g. slough, residue from hydrocolloid
dressings o Purulent exudate i.e. infection
EQUIPMENT
• Clean basin - basin for this purpose must be washed with soapy water,
rinsed and dried before use.
• Warm tap water is required otherwise cold water may reduce the
temperature of the wound surface to a degree where cell mitosis will not
recommence for up to 4 hours.
• Gauze / soft wash cloth: Contaminated wound, where possible,
immerse and clean. Otherwise, the soaked wash cloth must be
squeezed over it allowing the water to wash over it. Non-fiber shedding
gauze should be used where foreign bodies remain. This is not a routine
practice as it redistributes bacteria, is painful and causes trauma to
healing cells
• Disposable gloves (clean but not sterile)
o The following procedures should be meticulously adhered:
▪ A sterile gauze pad should be placed over the wound
followed by shaving the surrounding skin and finally,
cleaning the edges of wound with a detergent soap and
water.
▪ The surrounding area should be draped with a sterile one.
▪ The wound area should be prepared for surgical
debridement by gentle irrigation with lukewarm isotonic
saline solution.
▪ Devitalized and ragged skin edges, nonviable and
heavily contaminated tissues should be removed.
▪ Again the wound area should be exposed by gentle traction
and carefully irrigated.
▪ After cleansing, dry surrounding skin but not the
wound itself.
▪ The operative field should be again prepared by
placing sterile gauze over the wound and redraping the
surrounding area.
▪ Capillary and venous oozing should be controlled by gentle
pressure and ligating blood vessels if necessary.
▪ Wound closure should be done either by suture without
drainage or placing a small rubber drain into the depths
of the wound and other end in the skin margin.
▪ The wound may be loosely packed with petrolatum-
impregnated gauze and sutured at a later date (delayed
primary closure).
• reflex status, integument, location of the lesion and weight of the animal.