Wound Care Gopi Sir

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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

    e uvwi : |

    xYs vrq kU uhmcNSl Wiq ||

    x c 1/31

    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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