Transcript Physiology of Skin Grafts
Physiology of Skin Grafts
SKIN:
Physiology & Function
• Epidermis: – protective barrier (against mechanical damage, microbe invasion, & water loss) – high regenerative capacity – Producer of skin appendages (hair, nails, sweat & sebaceous glands)
SKIN:
Physiology & Function
• Dermis: – mechanical strength (collagen & elastin) – Barrier to microbe invasion – Sensation (point, temp, pressure, proprioception) – Thermoregulation (vasomotor activity of blood vessels and sweat gland activity)
SKIN:
Physiology & Function
• • • • Immunological surveillance Most skin is thin, hair-bearing, has sebaceous glands Skin of palms/soles/flexor surface of digits is thick, not hair-bearing, no sebaceous glands Vascular supply confined to dermis
SKIN:
Anatomy
SKIN:
Anatomy
Skin Grafts:
Classification
• Full thickness skin grafts: • - epidermis & full thickness of dermis Split skin graft: - epidermis & a variable proportion of dermis - thin, intermediate or thick
Skin Grafts: SSG
Skin Grafts:
Classification
Autografts
Isografts
Allografts
Xenografts
Skin Grafts:
“Process of Take”
• • • Vascularity of donor site Tolerance to ischaemia Metabolic activity of the graft
Skin Grafts:
“Process of Take”
• 4 Phases: – Fibrin adhesion – Plasmatic imbibition – Revascularization: Inosculation & capillary ingrowth – Remodelling: Revascularization & fibrous attachment in restoring normal histological architecture
Skin Grafts:
“Process of Take”
• Plasmatic Imbibition: – Initially graft ischaemic (24 – 48 hrs) – Fibrin adhesion – Imbibition allows the graft to survive this period – ? Important for nutrition of graft – ? Stops drying out
Skin Grafts:
“Process of Take”
• Inosculation & capillary ingrowth: – At 48 hrs – Through fibrin layer – Capillary buds from recipient bed contact graft vessels – Open channels (neo-vascularization) pink graft
Skin Grafts:
“Process of Take”
• Revascularization & fibrous attachment: – Connection of graft & host vessels via anastomoses (inosculation) – Formation of new vascular channels by invasion of graft (neovascularisation) – – Combination of old & new vessels (revascularisation) Fibroblast proliferation: conversion of fibrin adhesion fibrous tissue attachment (anchorage within 4 days)
Skin Grafts:
“Process of Take”
Skin Graft Take: Epidermis
Days 0 – 4 Histological changes Epithelium doubles; crusting, scaling of epidermis; swelling of nuclei & cytoplasm; epithelial cell migration to surface; mitosis of follicular & granular cells ++ mitotic activity in SSG not FTSG 3 4 – 8 Week 4 Proliferation & thickening of epithelium (up to 7x) desquamation Epidermis returned to normal thickness
Skin Graft Take: Epidermis
Day 4 10 Histochemical changes Increased RNA in basal cells, indicating protein synthesis RNA returns to normal
Skin Graft Take: Dermis
• Fibrous component:
Collagen Elastin Hyalinized early and progressively replaced with new fibres by 6 weeks; Turned over 3-4X faster than normal skin.
Accounts for resilience; Days 3-7 fragment; Replaced 4-6 weeks.
Extracellular matrix Proteins direct the behaviour of keratinocytes; Communication between keratinocytes & fibroblasts.
Skin Graft Take: Dermis
• Appendages: - sweating dependent on no. of transplanted sweat glands & degree of sympathetic reinnervation; will sweat like recipient site in FTSG only - sebaceous gland activity mostly in thicker grafts: SSG usually dry & shiny - hair grows from FTSG if well taken with no complications
Skin Graft Healing
• • • • Initially white then pinkens with new blood supply Lymphatic drainage by day 6 Collagen replacement from day 7 to week 6 Vascular remodelling for months
Skin Graft Healing
• Contraction: - shrinks immediately due to elastic recoil: 40%; medium SSG 20%; thin SSG 10%.
- secondary contracture as heals: - FTSG remains same size after above shrinkage; - SSG will contract as much as possible; - more dermis = less contraction - ? Due to myofibroblasts – FTSG
Skin Graft Healing
• Reinnervation: – from margins to bed; – 4/52 to 2 years; – Depends on graft thickness and bed; – Uneventful healing leads to near normal 2PD; – Cold sensitivity can be a problem.
Skin Graft Expansion
• • • Based on principle that wounds reepithelialized from the periphery Expansion provides larger areas from which epithelium can grow Larger areas can be covered with less skin
Skin Graft Expansion
• Meshing - covers large area - easier to contour - fluid can drain through holes - cosmetic results less than ideal - various mesh ratio
Skin Graft Survival
• • • • • • Meticulous technique Atraumatic graft handling Well vascularized bed Haemostasis Immobilization No proximal constricting bandages
Skin Graft Failure
• • • • • • • • • • Haematoma Infection Seroma Mobility Inappropriate bed Dependency Arterial insufficiency Venous congestion Lymphatic stasis Technical – upside-down