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MANAGEMENT OF
SURGICAL
WOUND
Dr Mohammed Mujtaba
Dept of Gen. Surgery
Sequence of flow
• Normal wound healing
• Types of surgical wound
• Classification of wound closure and healing
• Factors influencing healing of a wound
• General principles of management of wound
• Types of Dressing
• Recent advances
• Wound is defined as a break in normal continuity of a tissue/
endothelium due to exogenous cause.
• Ulcer is defined as a break in normal continuity of a tissue/
endothelium due to endogenous cause.
Normal Wound Healing:
Three phases:
1. Inflammatory phase
2. Proliferative phase
3. Maturational phase
Types of Surgical Wound:
• CLASS I  CLEAN:
• Respiratory , gastrointestinal, genital and urinary tracts not entered
• Uninfected Operative wound
• No break in aseptic technique
• No inflammation is encountered.
• Eg: Breast Surgery, Hernia repair, Joint arthroplasty, Excisions
• CLASS II  CLEAN CONTAMINATED:
• Respiratory, gastrointestinal, genital or urinary tract is entered under
controlled conditions
• No major break in aseptic technique
• No acute inflammation
• No spillage
• Eg: Cholecystectomy ( chronic inflammation), Gastrointestinal procedures,
Gynecological procedures
• CLASS III  CONTAMINATED:
• Acute, non purulent inflammation encountered
• Open, fresh, accidental wounds
• Visible spillage from intestinal tract
• Necrotic tissue without evidence of purulent drainage
• Operations with major break in sterile technique
• Eg: Bowel resection for infarcted and/ or necrotic bowel, Cholecystectomy
with actue inflammation or bile spillage
• CLASS IV  DIRTY:
• Presence of frank pus or abscess
• Perforated viscera
• Fecal contamination
• Old Traumatic wounds with retained devitalized tissue
• Wet gangrene
• Eg: Laparotomy for intraabdominal abscess, Incision and Drainage for infection/
abscess, Ruptured appendicitis, Hollow viscus perforation, Amputation in presence
of infection
Tidy vs Untidy Wounds:
Tidy:
• Incised
• Clean
• Healthy tissues
• Seldom tissue loss
Untidy:
• Crushed or avulsed
• Contaminated
• Devitalised tissue
• Other tissue loss
Classification of Wound closure and Healing:
• Primary Intention:
• Wound edges apposed with suture/ stapler
• Normal healing  Minimal scar
• Secondary Intention:
• Wound left open
• Healing  granulation, contraction and epithelialization
• Increased inflammation and proliferation  Poor scar
• Tertiary intention ( delayed primary intention ):
• Wound initially left open
• Edges later opposed when healing condition is favourable
Factors affecting wound healing:
• Site of wound and Structure involved
• Mechanism : Incision / Crush / Crush avulsion
• Contamination : foreign body / bacteria
• Loss of tissue
• Local factors : Vascular insufficiency / Previous radiation / pressure
• Systemic factors: Malnutrition / Vitamin and mineral deficiencies /
Immunosupression / Smoking
Wound Dressings
The two concepts that are
critical when selecting
appropriate dressings for
wounds are Occlusion and
Absorption.
TYPES OF DRESSING:
1. Non adherent fabrics
2. Absorptive
3. Occlusive
4. Creams, Ointments and Solutions
1. Non adherent fabrics:
• Fine mesh gauze
• Function : Protection, moist
environment
• It has Occlusive and non adherent
properties
• Antibacterial characteristics
• Eg : Scarlet red, Vassiline gauze
2. Absorptive:
• Gauze :
• Wide mesh gauze
• Removes exudates, prevents maceration
• Foams:
• Hydrophobic polyurethane sheets
• Protection, absorption of exudates
• May provoke skin maceration
3. Occlusive:
NON BIOLOGIC:
- A. Films
- B. Hydrocolloids
- C. Alginates
- D. Hydrogels
BIOLOGIC:
- A. Homograft
- B. Xenograft
- C. Amnion
- D. Skin substitues
A. FILMS:
- Clear polyurethane membranes with acrylic adhesives
- Waterproof, permeable to oxygen, carbon dioxide and watervapour
- allows visualization of wound
- nonabsorptive/ leakage/ requires intact skin around wound area
- adhere to the wound bed  exudate accumulation
SABISTON TEXTBOOK OF SURGERY VOL 1
FIRST SOUTH ASIA EDITION
HYDROCOLLOIDS:
- Hydrocolloid matrix ( gelatin, pectin, carboxymethylcellulose)
- Absorbs water from wound exudates  swells  liquefies  moist
gel
- Bulky/ interference with function / cytotoxic / unpleasant odour /
acidic pH at wound site
ALGINATES:
- Cellulose like polysaccharide fibres derived from calcium salt of
alginate ( sea weed )
- Soluble sodium salt in contact with wound exudate  hydrophilic gel
HYDROGELS:
- Polyethylene oxide or carboxymethylcellulose of water
- Rehydrating agents
- Weak mechanical properties  secondary dressing
HOMOGRAFT:
- Derived from genetically unique humans
- Temporary dressing
- Rejected if on wound for prolonged periods
- From cadaver skin
XENOGRAFT:
- Interspecies graft ( eg. Pig skin)
Recent advances in Mx of Wound:
- Hyperbaric oxygen therapy
- NPWT (Negative pressure-assisted wound therapy)
- Tissue engineering
- Growth factors
- Nanoparticles
HYPERBARIC OXYGEN THERAPY :
• Principle : uses oxygen as a drug and the hyperbaric chamber as a delivery system
to increase pO2 at the target area.
• Inhalation of 100 % O2 at 1.9 to 2.5 atm  increases tissue pO2 by upto 10 times
• Higher PaO2  supplies metabolic requirements and Induces synthesis of
endothelia cell NO synthase  angiogenesis / enhance fibroblast and leukocyte
function
Fig: Hyperbaric oxygen therapy chamber
NPWT:
• Negative Pressure- Assisted Wound Therapy
• Removal of chronic edema / Increase in local
blood flow / stimulation of granulation tissue
 endothelial proliferation and angiogenesis
Fig: Schematic diagram NPWT ( Negative Pressure-Assisted Wound Therapy
TISSUE ENGINEERING:
• Bioengineered skin substitues :
• Expansion of patient derived keratinocytes
• Behaves similar to extracellular matrix (ECM)
• Improves wound microenvironment
• Epidermal substitutes:
• Gold standard: Autograft from split-thickness skin grafting / cell line
bioreactor expansion
• Not subject to rejection
• 2- 3 weeks delay to generate enough tissue to cover a defect
• Limitations: well vascularized dermal bed required / low expansion
capabilities / limit of ability to form new tissue
• Gene and Stem cell therapy:
• MAPCs – Multipotent Adult Progenitor cells  self renewing
• MSCs- Mesenchymal Stem Cells  Improved granulation tissue formation
and neovascularization
Advantages/ Disadvantages and Indications of
graft and skin substitues:
Mx of Wound Healing.pptx
Mx of Wound Healing.pptx

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Mx of Wound Healing.pptx

  • 1. MANAGEMENT OF SURGICAL WOUND Dr Mohammed Mujtaba Dept of Gen. Surgery
  • 2. Sequence of flow • Normal wound healing • Types of surgical wound • Classification of wound closure and healing • Factors influencing healing of a wound • General principles of management of wound • Types of Dressing • Recent advances
  • 3. • Wound is defined as a break in normal continuity of a tissue/ endothelium due to exogenous cause. • Ulcer is defined as a break in normal continuity of a tissue/ endothelium due to endogenous cause.
  • 4. Normal Wound Healing: Three phases: 1. Inflammatory phase 2. Proliferative phase 3. Maturational phase
  • 5. Types of Surgical Wound: • CLASS I  CLEAN: • Respiratory , gastrointestinal, genital and urinary tracts not entered • Uninfected Operative wound • No break in aseptic technique • No inflammation is encountered. • Eg: Breast Surgery, Hernia repair, Joint arthroplasty, Excisions
  • 6. • CLASS II  CLEAN CONTAMINATED: • Respiratory, gastrointestinal, genital or urinary tract is entered under controlled conditions • No major break in aseptic technique • No acute inflammation • No spillage • Eg: Cholecystectomy ( chronic inflammation), Gastrointestinal procedures, Gynecological procedures
  • 7. • CLASS III  CONTAMINATED: • Acute, non purulent inflammation encountered • Open, fresh, accidental wounds • Visible spillage from intestinal tract • Necrotic tissue without evidence of purulent drainage • Operations with major break in sterile technique • Eg: Bowel resection for infarcted and/ or necrotic bowel, Cholecystectomy with actue inflammation or bile spillage
  • 8. • CLASS IV  DIRTY: • Presence of frank pus or abscess • Perforated viscera • Fecal contamination • Old Traumatic wounds with retained devitalized tissue • Wet gangrene • Eg: Laparotomy for intraabdominal abscess, Incision and Drainage for infection/ abscess, Ruptured appendicitis, Hollow viscus perforation, Amputation in presence of infection
  • 9.
  • 10. Tidy vs Untidy Wounds: Tidy: • Incised • Clean • Healthy tissues • Seldom tissue loss Untidy: • Crushed or avulsed • Contaminated • Devitalised tissue • Other tissue loss
  • 11. Classification of Wound closure and Healing: • Primary Intention: • Wound edges apposed with suture/ stapler • Normal healing  Minimal scar
  • 12. • Secondary Intention: • Wound left open • Healing  granulation, contraction and epithelialization • Increased inflammation and proliferation  Poor scar
  • 13.
  • 14. • Tertiary intention ( delayed primary intention ): • Wound initially left open • Edges later opposed when healing condition is favourable
  • 15. Factors affecting wound healing: • Site of wound and Structure involved • Mechanism : Incision / Crush / Crush avulsion • Contamination : foreign body / bacteria • Loss of tissue • Local factors : Vascular insufficiency / Previous radiation / pressure • Systemic factors: Malnutrition / Vitamin and mineral deficiencies / Immunosupression / Smoking
  • 16.
  • 17. Wound Dressings The two concepts that are critical when selecting appropriate dressings for wounds are Occlusion and Absorption.
  • 18. TYPES OF DRESSING: 1. Non adherent fabrics 2. Absorptive 3. Occlusive 4. Creams, Ointments and Solutions
  • 19. 1. Non adherent fabrics: • Fine mesh gauze • Function : Protection, moist environment • It has Occlusive and non adherent properties • Antibacterial characteristics • Eg : Scarlet red, Vassiline gauze
  • 20. 2. Absorptive: • Gauze : • Wide mesh gauze • Removes exudates, prevents maceration
  • 21. • Foams: • Hydrophobic polyurethane sheets • Protection, absorption of exudates • May provoke skin maceration
  • 22. 3. Occlusive: NON BIOLOGIC: - A. Films - B. Hydrocolloids - C. Alginates - D. Hydrogels BIOLOGIC: - A. Homograft - B. Xenograft - C. Amnion - D. Skin substitues
  • 23. A. FILMS: - Clear polyurethane membranes with acrylic adhesives - Waterproof, permeable to oxygen, carbon dioxide and watervapour - allows visualization of wound - nonabsorptive/ leakage/ requires intact skin around wound area - adhere to the wound bed  exudate accumulation SABISTON TEXTBOOK OF SURGERY VOL 1 FIRST SOUTH ASIA EDITION
  • 24. HYDROCOLLOIDS: - Hydrocolloid matrix ( gelatin, pectin, carboxymethylcellulose) - Absorbs water from wound exudates  swells  liquefies  moist gel - Bulky/ interference with function / cytotoxic / unpleasant odour / acidic pH at wound site
  • 25. ALGINATES: - Cellulose like polysaccharide fibres derived from calcium salt of alginate ( sea weed ) - Soluble sodium salt in contact with wound exudate  hydrophilic gel
  • 26. HYDROGELS: - Polyethylene oxide or carboxymethylcellulose of water - Rehydrating agents - Weak mechanical properties  secondary dressing
  • 27. HOMOGRAFT: - Derived from genetically unique humans - Temporary dressing - Rejected if on wound for prolonged periods - From cadaver skin XENOGRAFT: - Interspecies graft ( eg. Pig skin)
  • 28. Recent advances in Mx of Wound: - Hyperbaric oxygen therapy - NPWT (Negative pressure-assisted wound therapy) - Tissue engineering - Growth factors - Nanoparticles
  • 29. HYPERBARIC OXYGEN THERAPY : • Principle : uses oxygen as a drug and the hyperbaric chamber as a delivery system to increase pO2 at the target area. • Inhalation of 100 % O2 at 1.9 to 2.5 atm  increases tissue pO2 by upto 10 times • Higher PaO2  supplies metabolic requirements and Induces synthesis of endothelia cell NO synthase  angiogenesis / enhance fibroblast and leukocyte function
  • 30. Fig: Hyperbaric oxygen therapy chamber
  • 31. NPWT: • Negative Pressure- Assisted Wound Therapy • Removal of chronic edema / Increase in local blood flow / stimulation of granulation tissue  endothelial proliferation and angiogenesis
  • 32. Fig: Schematic diagram NPWT ( Negative Pressure-Assisted Wound Therapy
  • 33. TISSUE ENGINEERING: • Bioengineered skin substitues : • Expansion of patient derived keratinocytes • Behaves similar to extracellular matrix (ECM) • Improves wound microenvironment
  • 34. • Epidermal substitutes: • Gold standard: Autograft from split-thickness skin grafting / cell line bioreactor expansion • Not subject to rejection • 2- 3 weeks delay to generate enough tissue to cover a defect • Limitations: well vascularized dermal bed required / low expansion capabilities / limit of ability to form new tissue
  • 35. • Gene and Stem cell therapy: • MAPCs – Multipotent Adult Progenitor cells  self renewing • MSCs- Mesenchymal Stem Cells  Improved granulation tissue formation and neovascularization
  • 36. Advantages/ Disadvantages and Indications of graft and skin substitues: