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Wound Care
By :Dr Gopikrishna .B .J
Asst Professor
Dept of P.G.Studies in Shalyatantra
S.D.M.C.A, Hassan
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Anatomy of Skin
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Skin: structure and functionLargest organ of the body
Primary function is protective
Composed of several layersOuter Epidermis and Stratum Corneum
Dermis, containing the capillary network
Subcutaneous layer (hypodermis, adiposelayer)
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Thickness varies from a thin membrane atinternal flexures (e.g. elbows), to thicker at
the soles of the feet which bearconsiderable pressures
Hair follicles, sebaceous glands, and sweatglands pass through the epidermis, but
arise from the dermal layer
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Definition
A cut or break in the continuity of anytissue, caused by injury or operation
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Classification of wounds
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According to their nature :Abrasion
Contusion
Incision
Laceration
Open
Penetrating
Puncture
Septic etc
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According to the
number of skin layers involved:
Superficial
Involves only the epidermisPartial Thickness
Involves the epidermis and the dermis
Full ThicknessInvolves the epidermis, dermis, fat, fascia andexposes bone
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According to contamination
Clean - (non traumatic)
Clean contaminated
Contaminated
Dirty
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According to Grading by tissue Involvement
Grade I non-blanchable erythema of intact skin.Discoloration of the skin, warmth, oedema,
induration or hardness may also be used asindicators in people with dark skin.
Grade II partial-thickness skin loss involving
epidermis, dermis or both.The ulcer is superficialand presents clinically as an abrasion or blister.
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Grade III full thickness skin loss involving damage ornecrosis of subcutaneous tissue that may extend downto but not through underlying fascia
Grade IV extensive destruction, tissue necrosis ordamage to muscle, bone or supporting structures withor without full thickness skin loss.
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The ways in which wounds heal
Three basic classifications exist:Healing by primary intention
Two opposed surfaces of a clean, incised wound
(no significant degree of tissue loss) are held together.
Healing takes place from the internal layers outwardsHealing by secondary Intention
If there is significant tissue loss in the formation of the
wound, healing will begin by the production of
granulation tissue wound base and walls.Delayed primary healing
If there is high infection risk patient is given antibiotics
and closure is delayed for a few days e.g. bites
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Wound healing
All wounds heal following a specific sequence of phaseswhich may overlap
The process of wound healing depends on the type of
tissue which has been damaged and the nature of tissuedisruption
The phases are:
Inflammatory phaseProliferative phase
Remodelling or maturation phase
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The healing process
Day 0 5The healing response starts at the moment ofinjury the clotting cascade is initiated
This is a protective tissue response to stem blood
lossThe inflammatory phase is characterised by heat,swelling, redness, pain and loss of function at thewound site
Early (haemostasis)Late (phagocytosis)
This phase is short lived in the absence ofinfection or contamination
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Granulation
Day 3 14
Characterised by the formation of granulation tissue
in the woundGranulation tissue consists of a combination ofcellular elements including:
Fibroblasts, inflammatory cells, new capillaries
embedded in a loose extra-cellular collagenmatrix, fibronectin and hyularonic acid
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AngiogenesisCollagen first detected at day 3 and rapidlyincreases for approx. 3 weeks, then moregradually for the next 3 months
Fibroplasia (fibroblast proliferation andsynthetic activity) continues in parallel withre-vascularisation
Endothelial cells from the side of venulesclosest to the wound begin to migrate inresponse to angiogenic stimuli (angiogenesis)forming capillary buds, then loops
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EpithelialisationThe epidermis immediately adjacent to thewound edge begins to thicken within 24hrs
after injuryIn approximated incised wounds re-
epithelialisation is usually complete within48hrs.
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MaturationCan last up to 2 years
New collagen forms, changing the shape of
the wound and increasing the tensile strengthScar tissue, however is only ever approx. 50-80% as strong as the original tissue
During the remodelling process there is agradual reduction in cellularity and vascularityof the reparative tissue
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ContractionOnly undesirable where it leads tounacceptable tissue distortion and an
unsatisfactory cosmetic result
Wound contraction usually begins fromday 5 and is complete at approx. day 12
- 15
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Moist wound healingBasic concept is that the presence of exudatewill provide an environment that stimulates
healingExudate contains:Lysosomal enzymes, WBCs, Lymphokines, growthfactors..
There are clinical studies which have shownthat wounds maintained in a moistenvironment have lower infection rates andheal more quickly
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Factors affecting wound healingLocal Factors
1. Infection
2. Presence of necrotic tissue
3. Poor blood supply
4. Venous or lymph stasis
5. Tissue tension
6. Haematoma
7. Large defect or poor opposition
8. Recurrent trauma
9. X-Ray irradiated area
10. Wounds over joint & back
11. Underlying diseases like osteomyelitis & malignancy
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Complications of wound healing1. Implantation cysts
2. Painful scars
3. Cicatrisation
4. Keloid formation
5. Neoplasia
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Practical considerations
The cause of the wound
Underlying disease processesCurrent health status
Medication
Acute or chronic?Attitude to the wound
Availability of care
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Healing requirementsIdentification of the hindrance to healing
Adequate nutritional statusAdequate perfusion and oxygenation
High quality, research-based patient andwound management
Correction of the underlying cause of theproblem
Disease management
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Wound assessment
WOUND ASSESSMENT
Lab tests:TcPO2 Size, depth
& location
Wound bed:
necrosis granulation
Surrounding skin:colour, moisture,
Wound edge
Odour orexudate
Signs ofinfection
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Clinical appearance
Slough (yellow)
Necrotic tissue (black)Infected tissue (green)
Granulating tissue (red)
Epithelialising (pink)
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Sloughy wound Aim: to liquefy slough and
aid its removal
Dead cells accumulated in
exudate
Prepare wound bed for
granulation
Assess wound depth and
exudate levels Hydrogels, hydrocolloids,
alginates and hydrofibre
dressings
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Necrotic wound Aims: to debride and
remove eschar
Provide the rightenvironment forautolysis
Assess wound depthand
exudate levels
Hydrogels, hydrocolloid
dressings
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Infected wound Aims: reduce exudate,
odour and promote
healing Clinical signs of
infection
Swab wound systemicantibiotics
Treat symptomatically:exudate and odourcontrol
Change dressings daily
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Granulating wound Aims: support
granulation, protectnew tissue, keep moist
Assess depth andexudate levels
Moist wound surface non-adherent dressing
Treat over-granulation
Hydrocolloids, foams,alginates
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Wound characteristicsExudate
Odour
Condition oftissue withinthe wound
Condition ofthesurroundingskin
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The surrounding skin
Eczema
Psoriasis
Maceration/excoriation
due to exudate or
bowel contents
Self-inflicted damage
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Dressing choice
The purpose of
dressings:
To aid debridement
To remove excessexudate
To control bleeding
To protect a wound
To support healing
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The ideal dressing
A dressing that
Creates the optimum
Environment
Wound debridement
Wound cleansing
Alternative therapies
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Dressing choice
Non-adherent wound contact materials
Films
HydrogelsHydrofibre dressings
Hydrocolloids
Foams
Alginates
Miscellaneous
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Wound CleansingThe aims of wound cleansing are
to remove any foreign matter
such as gravel or soil, to remove any
loose surface debris such as necrotic
tissue and remove any remnants of
the previous dressing.
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Traditional methods:
Swabbing with cotton wool
Antiseptic solution
Dry dressings
Daily change of dressing/woundinspection
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Lotions and potions
Hypochlorites
Hydrogen peroxide
Chlorhexidine
ProflavineSaline 0.9%
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Saline 0.9%The only completely safe cleansing
agentSafe to use with wound management
products
Sachets, plastic containers and
aerosols for easy irrigation
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Necrotic woundsAim: to debride and remove eschar
Masks the full extent of the wound
Provide the right environment forautolysis
Assess wound depth and exudate
levels
Hydrogels, hydrocolloids, alginates,hydrofibre dressings
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Sloughy woundsAim: to liquefy slough and aid its
removal
Dead cells accumulated in exudate
Prepare wound bed for granulation
Assess wound depth and exudate levels
Hydrogels, hydrocolloids, alginates andhydrofibre dressings
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Infected wounds
Aim: reduce exudate, odour and promote
healing
Clinical signs of infectionSwab wound systemic antibiotics
Treat symptomatically: exudate and
odour controlChange dressings daily
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Granulating wounds
Aim: support granulation, protect new
tissue, keep moist
Assess depth and exudate levels
Moist wound surface non-adherent
dressing
Treat overgranulation
Hydrocolloids, foams, alginates
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Epith
elialising wounds
Aims: to provide suitable
conditions for re-surfacingN.A. ultra, films, hydrocolloids
Disturb as little as possible
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Film dressings
Semi-permeable primary or secondary
dressingsClear polyurethane coated with adhesive
Conformable, resistant to shear and tear
Do not absorb exudate
Examples: Tegaderm, Op-site.
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HydrocolloidsPectin, gelatin, carboxymethylcellulose and
elastomers
Environment for autolysis to debride sloughy or
necrotic wounds
Occlusive --> hypoxic environment to
encourage angiogenesisWaterproof
Different presentations e.g. Urgotul
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Foam dressings
Advanced polymer technology
Non-adherent wound contact layerHighly absorptive
Semi-permeable
Various typesAdhesive and non-adhesive
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Hydrogels
Sheets or gels
Starch and polyacrylamide (94% water)Low exudate, shallow wounds
Re-hydrates necrotic tissue
Secondary dressing needed
May cause skin maceration
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Alginates
Seaweed dressings
Form a gel over the woundModerate to high exudate wounds
Easily removed
Can cause pain
Help to debride a wound
Different presentations
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Tissue Viability
Documenting wound care
Potential for litigation
Good staff communicationContinuity of care
To assess progress or deterioration
Should be factual not subjectiveWound assessment charts
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Patient assessment parameters
Nutritional status
Level of mobilityMental attitude (compliance)
Dressing tolerance
Age
Metabolic disease
Vascular insufficiency
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Is the wound acute or chronic?
Post-operative?
Healing or non-healing?
Underlying cause?
Infected or colonised?Skin problems around the wound?
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Assessment parametersCause
Wound classification
Depth of the woundShape and size
The amount of exudate
The position of the woundThe clinical appearance
The environment of care
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Innovations in Wound Management
Biosurgery (LarvalTherapy)
VAC therapy
Warmth
Laser therapy
Leeches
MySkin
Tenderwet
Dispersion therapy
Hydrofibre dressings
Long-term usedressings
Natural skin
Growth hormones
Hyaluronic acid dressing
Myskin
Xelma
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Biosurgery(Larval therapy)
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Luciliasericata (greenbottles)
Ingestbacteriawhich are
destroyed in theirgutWide range ofinfected wounds
Removes slough and malodour
Bred assterile larvae
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2mm long special dressingtechnique
Sleeves or bags
Numbers needed
Removal
Reassessment
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Associated problems
Potentially infected larvae
Allergic reactionTickling sensation
Ethical issues
Aesthetic issues
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VAC Therapy
Provides a moist environment
Prevents bacterial activity
Evacuates excess exudate
Kills anaerobic bacteria in the woundbed
Controls odour
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Negative pressure suction drainage Not a new idea as surgeons have employed drainage
methods for years
The difference: the application
of topical negative sub-
atmospheric pressure
across the surface of the
wound
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Chronic non-healing wounds:
Pressure ulcers
Venous/arterial ulcers Diabetic ulcers
Sub-acute non-healing wounds
Dehisced surgical woundsAcute and traumatic wounds Meshed flaps and grafts Graft and flap donor sites
Indications
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Contraindications Fistula of unknown source
Opening into a body cavity
Vulnerable body organs (protect) Malignancy
Necrotic tissue with eschar
Untreated osteomyelitis
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Recommended regime Negative pressure
50-75mmHg split-skin graft, leg ulcer
125mmHg all other wounds Cycle
continuous for 48 hours then intermittentpressure
wound assessment determines cycle
Dressing changes
4-5 days (every 48 hours if infected)
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Success will depend on:
Wound selection Type of foam dressing
The degree of negative pressure
The duration of treatment
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Laser therapy
Little evidence of faster healing
Needs expert handling
May increase tensile strength
Costly
Time-consuming
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Hydrofibre dressingAquacel hydrofibre, non-woven
hydrocolloid dressing
Forms a non-sticky gelVery absorbent
Moist environment
Needs secondary dressing
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Long-term use dressingsMepitel, Omniderm, TegaporeNon-adherent
Allow passage of exudate into asecondary dressing
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Urgotul hydrocolloid andpetroleum jelly
Promogran collagen and cellulose it interferes with substances
(proteases) in the wound thatprevent it healing
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Natural skin
Vivoderm, Dermagraft, Apligraf
Expensive but cost-effective
Reduce need for skin grafts
Useful for diabetic ulcers
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Growth hormones
Proteins that direct biological
processesChronic wound deficiency
Messengers
Under research
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XelmaWhat is Xelma extracellular matrix protein?Xelma consists of amelogenin proteins, a thickening
agent propylene glycol alginate (PGA) and water.Xelma has been proven to improve healing in hard toheal ulcers.What is Xelma for?Xelma is a medical device for treatment of hard-to-
heal ulcers, primarily venous leg ulcers. It is indicatedfor use with standard compression therapy of non-infected wounds.
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XelmaHow is Xelma different from other therapies?Xelma is the first product containing extracellular matrixprotein, amelogenin, which temporarily replaces thedamaged extracellular matrix proteins in the hard-to-healwounds in order to restore wound healing.
How does Xelma work?When applied to the wound bed Xelma provides atemporary extracellular matrix protein for cell attachment.This creates favourable conditions for wound healing by
restoring vital cell functions including proliferation,migration and production of growth factors and essentialextracellular matrix proteins. Restoration of the cellularand biochemical balance is facilitated in the hard-to-healwound, which will promote granulation tissue formationand normal wound healing.
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Myskin
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Myskin case studiesPatient Profile
Mrs B 68 years oldMedical ConditionTwo chronic non-healing pressure ulcers.
The Patient
After receiving a burn to her leg Mrs Bwas left with scar tissue causing her footto become deformed. Pressure ulcersdeveloped from her corrective footwear and despiteconventional treatment they remained unhealed for threeyears. Mrs B was also awaiting surgery to correct her footwhich was not possible until the ulcers had healed.
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MyskinEvaluationMrs B has undergone three skin grafts along with conventionaltreatment all of which have failed to heal the ulcers. Mrs B was thenreferred for treatment with Myskin.For Myskin treatment, a thin biopsy (approximately 0.6mm thick,2cmx2cm) of skin is taken from the thigh area and transported to thelaboratory in sterile saline solution. The biopsy is treated with adigestive enzyme overnight. The following day the keratinocytes areisolated from the dermal/epidermal junction, multiplied in cell cultureand stored in liquid nitrogen until they are needed.Three days before dressings are required, keratinocytes are thawed andcultured on a 5cm silicone disc. These discs have a patented surfacelayer that encourages keratinocytes, to transfer from the dressing to
the wound bed and promote re-epithelialization. This cell transferprocess takes about four days after which the Myskin dressing can beremoved and a standard dressing applied.
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MyskinMrs B attended the clinic for the once weekly dressing applications which, after
four days, were removed and replaced with a standard dressing.Twenty twoweeks after the firstMyskin dressing was applied one ulcer had healed
completely and the second healed after forty five weeks.BothUlcers Healed
OutcomeAfter two applications Mrs B experienced a significant reduction in pain and oncethe ulcers had completely healed Mrs B was referred back to the orthopaedicteam. She has since had her foot deformity corrected with no complications postoperatively. Mrs B has now resumed activities which she previously enjoyed such
as swimming and has been on holiday.Due to the severity, location and age of the ulcers it was necessary for Mrs B tohave several more applications of myskin than usually required. It has beenfound that up to twelve applications are usually needed to heal a chronic woundalthough the number of applications may vary between patients.
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ANTIBIOTICS
di i
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Indications
1.Contaminated wound
2.Areas of marginal viability
3.Wounds involving joints, openfractures
4.All human bite wounds
5.Most animal bite wounds
6.Generally, wounds > 12hr. old
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SPECIALWOUNDS
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Bite Wounds
High risk of infection with involvement of
bones, joints, tendons, vessels, nervesPuncture wounds (difficult to irrigate anddecontaminate)
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Dog Bites
75% involve the extremities
Most dog bites in children involve an extremitySevere facial lacerations involve the cheeks andlips as they try to "kiss the doggie
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Closure
Dog bites scalp, face, trunk, proximal
extremities may be closed if superficial
Human bites never close primarily(delay 48 72hr.)
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Puncture Wounds
Never close
Irrigate drain, if necessaryFoot shoe on or barefoot?
Increased infection risk if shoe on
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Abscesses
Incise, drain, irrigate, loosely pack withIodoform gauzeReturn at 24 hrs. for irrigation fresh packReturn at 48 hrs. for pack removal andhealing by granulation
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New onset DM may present with abscessAntibiotics may be indicated in
addition to I&D
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Nail / Nail Bed Injury
Subungual hematoma, < 40 % nail area,nail bed injury unlikely, but distal phalanxfx. Might be presentTreatment: Battery cautery to make
drainage hole in nail, irrigate with 25ga.needle and 1% lidocaineNail Bed - requires surgical repair
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Foreign Bodies
Inert (glass, metal), may leaveunremoved if necessaryOrganic (wood), must be removed
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VamanaEix qx vT i MT
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xYs vrq kU uhmcNSl Wiq ||
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Wound with hypergranulation,shothahaving predominance of kapha, blackishor reddish wounds vamana is beneficial.
VIRECHANA
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VIRECHANA
Wounds afflicted by Vata &
predominance of Pitta Dosha
Situated in Madhyama & Adhoshaka of the body
Non healing wounds, chronic wounds
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SIRAVYDHANA
Vrana which is predominant of Pitta andRakta
In Margavarana conditions,raktamokshanais advised
Indicated in shothayuktha, kathina,shyama, aruna rakta and vedanayuktavrana with vishalamoola.
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In pitta pradhanacondition raktha
mokshana can bedone with jalauka
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LEKHANA
Should be done in Kathina(hard), thick &rolled margins of vrana and in hard &raised granulated surface
KASHAYA
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KASHAYA
Kashaya should be used for shodhana, in
wound having foul smell, Kledayukta, Picchila,
Shodhana kashaya drugs are Shankhini,Ankhotha, Karaveera, Sumana, Suvarchala &
Aragvadhadhi gana
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KALKA
Kalka should be used for Shodhana in highlyinfected wound, foul smell, & when all
the Doshas are involved (vata & kapha)
Drugs are Haratala, Pippali, Maricha, Shunthi,
Sphatika.
SARPI
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SARPI
In Pittaja Vrana symptoms are Daha & paka,the drug are used Karpasa Phala SiddhaGhrita
TAILA
In Kaphaja Vrana if wound is UtsannaMamsa, Ruksha, Alpasravayukta the drugs tobe used Sarshapa + Tila Taila
RASAKRIYA
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RASAKRIYA
An indurated ulcer, not responding to Taila should
be purified with a dually prepared Rasakriya.
Shodhana Rasakriya - Brihati,Kantakari,Haritala, Manashila
The drugs are Salasaraadi Gana, Patola, Triphala.
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AVACHOORNA
Medhayuktha, superficial wound, foul smell
conditions choorna is used for Shodhana
Drugs are Kaseesa, Saindava, Vacha,
Rajanidwaya
UTSADANA
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UTSADANA
Utsanna mridu mamsa Kasisa
& Madhu
DARUNIKARANA
Mridu mamsa Dhava,Priyangu,Ashoka etc Avachoornana.
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C l i
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ConclusionWound care is complex
There are no easy solutions
Evidence is needed of efficacy
and cost-effectiveness
Correction of the underlying causativefactors is essential
Key principles must be adhered to withregard to basic patient and wound
assessment
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