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NEGATIVE PRESSUE WOUND THERAPY
SKIN SUBSTITUES
DR MANO ANANTH AB
PG IN PLASTIC AND RECONSTRUCTIVE SURGERY
CHENGALPATTU MEDICAL COLLEGE
NPWT
Use of a porous
sponge within the
wound, covered by an
airtight occlusive
dressing to which
vaccum is applied
HISTORY
In 1550 BC
• Eber papyrus – ‘cupping’
• Curcurbita - fruit shell
To create suction
• Heat the air in cup  cooled suction
• Hole in the cup  suction applied  closed with
wax
• Applied over intact skin
• In 1000 BC - china
• In 400 BC - Hippocrates – structural problems
HISTORY - CUPPING
• CUPPING DEVICE – Animal horn, bamboo, wood,
copper, bronze, pottery and glass.
Chinese cupping
• ‘’realign and balance the flow of one’s vital
energy or life force known as chi along meridians
,which are influence point for internal organs’’
HISTORY - CUPPING
• Wet cupping
Skin is scraped or puntured for the
toxins to escape
Cupping massage –
• Specialised slave is applied pulls
with large massage cupping glass
with round edges in slow even
movements
• For soft tissue only
• local blood flow stimulation
HISTORY- PHYSIOLOGY
Early 1890s - Prof. August Bier of Germany
• Hyperemic treatment
• In intact skin
• Inducing benefical inflammation against invasion
In 1908 Drs willey mayer , victos schmieden
• First documented apparatus – specially designed
suction glass
• Subatmospheric pressure to skin wound
HISTORY
• Bier assistant – Dr.E.klapp – patented –
KLAPP CUP – local inflamamtion and abscess
• JUNOD’S BOOT Victor T Junod ( 1809-1881 )
Airtight case  air is exhausted
HISTORY
• 1952 German patent
• Absorbent tampons – natural sponge, rubber
sponge, foam rubber,cellulose sponge ,gauze,
cotton
• 1971 Atmos fritzsching patent use of vaccum
pump, cathetor cannula for intermittent
suction
• 1986-1991 – Russians – kremlin papers – on
open wounds
HISTORY
• In 1997 – VAC - vaccum assisted closure –
kinetic concepts.inc (KCI)
• Application of subatmospheric pressure
• Polyurethane sponge – 48 hours
• 2004 – KREMLIN KIT – Blue sky medical
SCIENCE OF NPWT
IDEAL GAS LAWS
• Boyle’s law
• Poiseuille’s law
BOYLE’S LAW
P V = k T
• V – volume of gas
• T - temperature
• P – pressure exerted in a closed environment
• K - Constant
• At constant temperature , volume is indirectly
proportional to pressure
• Decreased volume  increased pressure
POISEUILLE’S LAW
• Calculation of the rate at which an
incompressbile viscous fluid flows through an
cylindrical pipe
• Flow = internal diameter / viscosity ( contact
layer )
• Increased viscosity  decreased flow
• Increased diameter increased flow
• Pump should be placed at the patient level
PATHOPHYSIOLOGY
P – hydrostatic pressure  - oncotic pressure
Kf – filitration coefficent - reflection coefficient
Intesitital fluid
Capillaries PC
Pif
𝐽𝑉 = 𝑘𝑓 𝑃𝑐 − 𝑃𝑖𝑓 −  ( 𝑐 − 𝑖𝑓)
c
if
PATHOPHYSIOLOGY
• Negative pressure  physical force of
compression against the blood vessels(
starling forces )
• Prevent fluid from leaking out
• Pushing fluid back to capillaries of the tissues
that already leaked
PATHOPHYSIOLOGY
Regulating inflammation
 Removal of exudates - edema
• Reduce lactic acid – anaerobic
metabolism ( responsible for
inflammation and sequelae )
• Decreased pain
• Overall decrease INDURATION
PATHOPHYSIOLOGY – HYPEREMIC THEORY
Hyperemic
Changes in
microcirulation
Normal
oxidation
reduction
Normal pH
(Normal or
weak
alkaline)
Detrimental
for
microbes
Increased
lymphocytes
Phagocytosis Autolytic
debridement
PATHOPHYSIOLOGY
Suction and compression deforms cells
Changes in expression of IEG genes
Increased cellular proliferation and
protein synthesis
Dynamic neutrophilic reaction , prevent
denaturation of collagen
Degenerarion  Restoration phase
SUMMARY
• Increase blood flow in existing vessels
• Promote angioneogeneis  granulation tissue
• Bring oxygen, nutrients and new growth factors
• Removes edema
• Maintain moist wound
• Compression effect
• Kills bacteria
• Prevent denaturation of collagen
PATHOPHYSIOLOGY – MILLER TECHNIQUE
• Non contact method
Physiological principle
• Every action has an equal and opposite reaction to
maintain homeostasis
• Eg: Bowel ,ureter , diaphragm, cardiac contraction
and relaxation
• Negative pressure – need complete relaxation to
rejuvenate
METHOD
• Current gauze dressing change every 24-72
hours
• Pressure (- 70 to – 125 mmHg )
• Suction duration varies in different studies
CONTRAINDICATIONS
• Malignancy
• Ischemic wounds
• Badly infected wound with inadequate
debridement
IDEAL
• Doesn’t degrade
• Allow real time visualization
• Ability to maintain seal in various conditions
• Support skin during sweating and being
friable
FUTURE
• Visual data
• Numericals about wound drainage
• Status of dressing
• Chemical profile
• Functional parameter of pump
SKIN SUBSTITUTE
SKIN SUBSTITUTE
• Replace the function of skin
• To close the wound
• Eliminate pain and promote wound healing
• Eliminate the need for SSG
• Provide epidermal and dermal analogues
TYPES
Component
• Cellular (cultured )
• Acellular
Source
• Human ( Auto / Allogenic )
• Non human
Xenograft – Bovine, procine, murine
• Synthetic
• Combined
TYPES
Layer to be subtituted
• Epidermal
• Dermal
• Dermoepidermal
Duration
• Temporary -
• Permanent
DURATION
TEMPORARY
SINGLE
NATURAL
MINOTIC
MBRANE
POTATO PEEL
SYNTHETIC
POLMER SHEET,
FOAM, SPRAY
DOUBLE LAYER
TRANSCYTE
DURABLE
EPIDERMAL
EPICELL
DERMAL
DERMAL MATRIX
ALLODERM
KOLLAGEN
BIOBRANE
TRANSYTE CHITODERM
DERMOEPIDERMAL
ORCEL APLIGRAF
INTEGRA LASER SKIN
HYALOGRAFT
HISTORY
• 1975 – Rheinwald and Green – composite
Isolated epidermal keratinocytes,
cultured invitro with mouse fibroblast
 large sheet of cultured epithelium
• 1981 – 0’ connor – Autologous keratinocyte
sheets
SKIN SUBSTITUTES
EPIDERMAL
• Epicell ( Epidermal )
• My skin ( Epidermal )
• Cryoskin ( Epidermal )
• Laser skin ( Epidermal )
• Aminiotic membrane
• Potato peel
DERMAL
• Alloderm ( dermal)
• Biobrane ( dermal )
• Dermagraft ( dermal)
• Chitoderm ( dermal )
• Transcyte ( dermal )
COMPOUND
• Hyalograft/ hyalomatric
PA ( compound )
• Integra ( compound )
• Apligraf ( compound )
• Orcel ( compound )
EPIDERMAL SUBSTITUTES
EPICELL
• Epidermal / cellular
• Deep dermal / full thickness burns
• Life saving – mortality ( 90 % vs 37.5 % )
• TSA > 30%
• Keratinocyte from uninjured skin cultured (16-21days )
• 2-8 cell layer / multiple 10000 times
• Contain murine cells  risk of infection ( patient should not
donate )
Petroleum gauze
Cultured keratinocytes + murine cells 2-8 cell layers
MY SKIN
• Autologous
• Cell suspension delivered as spray
• Keratinocytes with sillicone support and
acrylic plasma polymer layer
CRYOSKIN
• Similar – allogenic
• Stored in vapour phase of liquid nitrogen
LASER SKIN
• Proliferation of keratinocytes
• Biocompatibility
• Scleroderma ulcer
• Deep burns
• Good graft take LASER MICRO PERFORATED
HA + BIOMATERIAL SCAFFOLD + KERATINOCYTES
DERMAL SUBSTITUES
BIOBRANE
• Acellular, dermal substitute
• Composite , temporary cover, nylon with collagen peptides
• Protective cover for meshed autografts
• Partial thickenness burns, C/I – Full thickness burns
Thin silcone membrane
Nylon mesh + collagen peptides
Type 1 procine Collagen coating
BIOBRANE
DERMAGRAFT
• Dermal substitute
• Collagen matrix growth factors, protein
GAGs
• DFU - Early cases , heals in 12 weeks
Non porous collagen ge
Bioabsorable polyglactin scaffold + fibroblast+ECM
CHITOSAN
• Polysaccharide – outer skeleton of shell fish
• Self adhesive dressing pad
• Burns, abrasions, bed sore
• Haemostasis – non specific binding with cell
membrane
• Antibacterial
Chitosan
Polyurethane
Polyvinyl
alcohol
TRANSCYTE
• Temporary / Dermal substitute
• Mid dermal / partial thickeness bubrns
• Better than conventional
• Synthetic / bilayered
• Contains collagen, GAGs ,growth factors
Thin silicone layer
Knitted nylon scaffold + stem cell
HYALOGRAFT / HYALOMATRIX PA
• Hyalouronic acid esterification + benzyl
alcohol
• Forms – meshes, non woven textiles,
perforated membrane
Outer silicone layer – PA type
HA + benzyl alcohol + fibroblast / keratinocytes
DERMO-EPIDERMAL SUBSTITUES
APLIGRAF
• Cellular / allograft / bilayered / shelf life 10 days
• Stored in polyethylene, agarose nutrient medium
• Fibroblast/ keratinocytes from neonate foreskin cultured
• Fibroblast seeded in collagen sponge ( 6 days )
• Produce human matrix layer
• Later kerantinocytes seeded on day 6 ( 4days incubation )
• Incubated in air 10 days - maturation
Cultured Fibroblast + collagen sponge
Polyurethane
Epidermal layer – cultured keratinocytes
INTEGRA
• Gold standard for dermal substitute therapy
• Bovine type 1 collagen copolymer with GAG
• Long shelf life
• 15-20 days  Neodermis
• Low immunogenic
• Better cosmetic with less scarring
Epidermal - Polysiloxane layer
Bovine type 1 collagen+ dermal chrondroin sulfate
ORCEL
• Dermo – epidermal
• Cellular / allograft
• Provide cytokine / growth factors
• Dystrophic epidermlysis bullosa
• Full / Partial thickness
• Reduce scarring
• Condition wound for grafting
Non porous collagen ge
Cultured keratinocytes
Cultured fibroblast + bovine 1 collagen sponge
INTEGRA AND HYALOMATRIX
Integra
• Colour
• Elastoproperty
• Better cosmesis
Hyalomatrix
• Hydration
• Transepidermal
regulation
• ECM regulation
• Neoangiogenesis
IDEAL SUBSTITUE
IDEAL SUBSTITUE
FUTURE
• Nanoscaffold
• Gene modified skin substitute
• Foetal wound heals without scarring 
Scarless healing
THANK YOU

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NPWT AND SKIN SUBSTITUTES 2.pptx

  • 1. NEGATIVE PRESSUE WOUND THERAPY SKIN SUBSTITUES DR MANO ANANTH AB PG IN PLASTIC AND RECONSTRUCTIVE SURGERY CHENGALPATTU MEDICAL COLLEGE
  • 2. NPWT Use of a porous sponge within the wound, covered by an airtight occlusive dressing to which vaccum is applied
  • 3. HISTORY In 1550 BC • Eber papyrus – ‘cupping’ • Curcurbita - fruit shell To create suction • Heat the air in cup  cooled suction • Hole in the cup  suction applied  closed with wax • Applied over intact skin • In 1000 BC - china • In 400 BC - Hippocrates – structural problems
  • 4. HISTORY - CUPPING • CUPPING DEVICE – Animal horn, bamboo, wood, copper, bronze, pottery and glass. Chinese cupping • ‘’realign and balance the flow of one’s vital energy or life force known as chi along meridians ,which are influence point for internal organs’’
  • 5. HISTORY - CUPPING • Wet cupping Skin is scraped or puntured for the toxins to escape Cupping massage – • Specialised slave is applied pulls with large massage cupping glass with round edges in slow even movements • For soft tissue only • local blood flow stimulation
  • 6. HISTORY- PHYSIOLOGY Early 1890s - Prof. August Bier of Germany • Hyperemic treatment • In intact skin • Inducing benefical inflammation against invasion In 1908 Drs willey mayer , victos schmieden • First documented apparatus – specially designed suction glass • Subatmospheric pressure to skin wound
  • 7. HISTORY • Bier assistant – Dr.E.klapp – patented – KLAPP CUP – local inflamamtion and abscess • JUNOD’S BOOT Victor T Junod ( 1809-1881 ) Airtight case  air is exhausted
  • 8.
  • 9. HISTORY • 1952 German patent • Absorbent tampons – natural sponge, rubber sponge, foam rubber,cellulose sponge ,gauze, cotton • 1971 Atmos fritzsching patent use of vaccum pump, cathetor cannula for intermittent suction • 1986-1991 – Russians – kremlin papers – on open wounds
  • 10. HISTORY • In 1997 – VAC - vaccum assisted closure – kinetic concepts.inc (KCI) • Application of subatmospheric pressure • Polyurethane sponge – 48 hours • 2004 – KREMLIN KIT – Blue sky medical
  • 11.
  • 12. SCIENCE OF NPWT IDEAL GAS LAWS • Boyle’s law • Poiseuille’s law
  • 13. BOYLE’S LAW P V = k T • V – volume of gas • T - temperature • P – pressure exerted in a closed environment • K - Constant • At constant temperature , volume is indirectly proportional to pressure • Decreased volume  increased pressure
  • 14. POISEUILLE’S LAW • Calculation of the rate at which an incompressbile viscous fluid flows through an cylindrical pipe • Flow = internal diameter / viscosity ( contact layer ) • Increased viscosity  decreased flow • Increased diameter increased flow • Pump should be placed at the patient level
  • 15. PATHOPHYSIOLOGY P – hydrostatic pressure  - oncotic pressure Kf – filitration coefficent - reflection coefficient Intesitital fluid Capillaries PC Pif 𝐽𝑉 = 𝑘𝑓 𝑃𝑐 − 𝑃𝑖𝑓 −  ( 𝑐 − 𝑖𝑓) c if
  • 16.
  • 17. PATHOPHYSIOLOGY • Negative pressure  physical force of compression against the blood vessels( starling forces ) • Prevent fluid from leaking out • Pushing fluid back to capillaries of the tissues that already leaked
  • 18. PATHOPHYSIOLOGY Regulating inflammation  Removal of exudates - edema • Reduce lactic acid – anaerobic metabolism ( responsible for inflammation and sequelae ) • Decreased pain • Overall decrease INDURATION
  • 19. PATHOPHYSIOLOGY – HYPEREMIC THEORY Hyperemic Changes in microcirulation Normal oxidation reduction Normal pH (Normal or weak alkaline) Detrimental for microbes Increased lymphocytes Phagocytosis Autolytic debridement
  • 20. PATHOPHYSIOLOGY Suction and compression deforms cells Changes in expression of IEG genes Increased cellular proliferation and protein synthesis Dynamic neutrophilic reaction , prevent denaturation of collagen Degenerarion  Restoration phase
  • 21. SUMMARY • Increase blood flow in existing vessels • Promote angioneogeneis  granulation tissue • Bring oxygen, nutrients and new growth factors • Removes edema • Maintain moist wound • Compression effect • Kills bacteria • Prevent denaturation of collagen
  • 22.
  • 23. PATHOPHYSIOLOGY – MILLER TECHNIQUE • Non contact method Physiological principle • Every action has an equal and opposite reaction to maintain homeostasis • Eg: Bowel ,ureter , diaphragm, cardiac contraction and relaxation • Negative pressure – need complete relaxation to rejuvenate
  • 24. METHOD • Current gauze dressing change every 24-72 hours • Pressure (- 70 to – 125 mmHg ) • Suction duration varies in different studies
  • 25. CONTRAINDICATIONS • Malignancy • Ischemic wounds • Badly infected wound with inadequate debridement
  • 26. IDEAL • Doesn’t degrade • Allow real time visualization • Ability to maintain seal in various conditions • Support skin during sweating and being friable
  • 27. FUTURE • Visual data • Numericals about wound drainage • Status of dressing • Chemical profile • Functional parameter of pump
  • 29.
  • 30.
  • 31. SKIN SUBSTITUTE • Replace the function of skin • To close the wound • Eliminate pain and promote wound healing • Eliminate the need for SSG • Provide epidermal and dermal analogues
  • 32. TYPES Component • Cellular (cultured ) • Acellular Source • Human ( Auto / Allogenic ) • Non human Xenograft – Bovine, procine, murine • Synthetic • Combined
  • 33. TYPES Layer to be subtituted • Epidermal • Dermal • Dermoepidermal Duration • Temporary - • Permanent
  • 34. DURATION TEMPORARY SINGLE NATURAL MINOTIC MBRANE POTATO PEEL SYNTHETIC POLMER SHEET, FOAM, SPRAY DOUBLE LAYER TRANSCYTE DURABLE EPIDERMAL EPICELL DERMAL DERMAL MATRIX ALLODERM KOLLAGEN BIOBRANE TRANSYTE CHITODERM DERMOEPIDERMAL ORCEL APLIGRAF INTEGRA LASER SKIN HYALOGRAFT
  • 35. HISTORY • 1975 – Rheinwald and Green – composite Isolated epidermal keratinocytes, cultured invitro with mouse fibroblast  large sheet of cultured epithelium • 1981 – 0’ connor – Autologous keratinocyte sheets
  • 36. SKIN SUBSTITUTES EPIDERMAL • Epicell ( Epidermal ) • My skin ( Epidermal ) • Cryoskin ( Epidermal ) • Laser skin ( Epidermal ) • Aminiotic membrane • Potato peel DERMAL • Alloderm ( dermal) • Biobrane ( dermal ) • Dermagraft ( dermal) • Chitoderm ( dermal ) • Transcyte ( dermal ) COMPOUND • Hyalograft/ hyalomatric PA ( compound ) • Integra ( compound ) • Apligraf ( compound ) • Orcel ( compound )
  • 38. EPICELL • Epidermal / cellular • Deep dermal / full thickness burns • Life saving – mortality ( 90 % vs 37.5 % ) • TSA > 30% • Keratinocyte from uninjured skin cultured (16-21days ) • 2-8 cell layer / multiple 10000 times • Contain murine cells  risk of infection ( patient should not donate ) Petroleum gauze Cultured keratinocytes + murine cells 2-8 cell layers
  • 39. MY SKIN • Autologous • Cell suspension delivered as spray • Keratinocytes with sillicone support and acrylic plasma polymer layer CRYOSKIN • Similar – allogenic • Stored in vapour phase of liquid nitrogen
  • 40. LASER SKIN • Proliferation of keratinocytes • Biocompatibility • Scleroderma ulcer • Deep burns • Good graft take LASER MICRO PERFORATED HA + BIOMATERIAL SCAFFOLD + KERATINOCYTES
  • 42. BIOBRANE • Acellular, dermal substitute • Composite , temporary cover, nylon with collagen peptides • Protective cover for meshed autografts • Partial thickenness burns, C/I – Full thickness burns Thin silcone membrane Nylon mesh + collagen peptides Type 1 procine Collagen coating
  • 44. DERMAGRAFT • Dermal substitute • Collagen matrix growth factors, protein GAGs • DFU - Early cases , heals in 12 weeks Non porous collagen ge Bioabsorable polyglactin scaffold + fibroblast+ECM
  • 45. CHITOSAN • Polysaccharide – outer skeleton of shell fish • Self adhesive dressing pad • Burns, abrasions, bed sore • Haemostasis – non specific binding with cell membrane • Antibacterial Chitosan Polyurethane Polyvinyl alcohol
  • 46. TRANSCYTE • Temporary / Dermal substitute • Mid dermal / partial thickeness bubrns • Better than conventional • Synthetic / bilayered • Contains collagen, GAGs ,growth factors Thin silicone layer Knitted nylon scaffold + stem cell
  • 47. HYALOGRAFT / HYALOMATRIX PA • Hyalouronic acid esterification + benzyl alcohol • Forms – meshes, non woven textiles, perforated membrane Outer silicone layer – PA type HA + benzyl alcohol + fibroblast / keratinocytes
  • 49. APLIGRAF • Cellular / allograft / bilayered / shelf life 10 days • Stored in polyethylene, agarose nutrient medium • Fibroblast/ keratinocytes from neonate foreskin cultured • Fibroblast seeded in collagen sponge ( 6 days ) • Produce human matrix layer • Later kerantinocytes seeded on day 6 ( 4days incubation ) • Incubated in air 10 days - maturation Cultured Fibroblast + collagen sponge Polyurethane Epidermal layer – cultured keratinocytes
  • 50.
  • 51. INTEGRA • Gold standard for dermal substitute therapy • Bovine type 1 collagen copolymer with GAG • Long shelf life • 15-20 days  Neodermis • Low immunogenic • Better cosmetic with less scarring Epidermal - Polysiloxane layer Bovine type 1 collagen+ dermal chrondroin sulfate
  • 52. ORCEL • Dermo – epidermal • Cellular / allograft • Provide cytokine / growth factors • Dystrophic epidermlysis bullosa • Full / Partial thickness • Reduce scarring • Condition wound for grafting Non porous collagen ge Cultured keratinocytes Cultured fibroblast + bovine 1 collagen sponge
  • 53. INTEGRA AND HYALOMATRIX Integra • Colour • Elastoproperty • Better cosmesis Hyalomatrix • Hydration • Transepidermal regulation • ECM regulation • Neoangiogenesis
  • 56. FUTURE • Nanoscaffold • Gene modified skin substitute • Foetal wound heals without scarring  Scarless healing