Chapter 18: Wound management
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Source: Royal Marsden NHS Foundation Trust ([92]).
Source: Adapted from Bale and Jones ([7]), ConvaTec ([14]), Hampton and Collins ([43]), Hess ([47]).
Source: Adapted from Skórkowska‐Telichowska et al. ([95]), Vowden and Vowden ([110]).
Related theory
Wound assessment
There are many frameworks available to aid a systematic approach to wound assessment (Flanagan [32]), though individually none are considered optimal (Greatrex‐White and Moxey [36]).
The ‘TIME’ (tissue, infection/inflammation, moisture balance and edge of wound) acronym was developed in 2002 by an international group of wound care experts to provide a systematic approach to wound assessment and wound bed preparation (Dowsett and Ayello [26], Leaper et al. [61], Werdin et al. [114]) (Table 18.1).
Table 18.1 TIME principles for wound bed preparation
Clinical observations | Proposed pathophysiology | Wound bed preparation: clinical actions | Effect on wound bed of preparation actions | Clinical outcomes | |
---|---|---|---|---|---|
Tissue (non‐viable or viable) | T | Defective matrix and cell debris impair healing | Debridement (episodic or continuous) | Restoration of wound bed and functional extracellular matrix proteins | Viable wound bed |
Infection or inflammation | I |
High bacterial counts or prolonged inflammation
↑ Inflammatory cytokines
↑ Protease activity
↓ Growth factor activity | Remove infected foci with topical/systemic antimicrobials, anti‐inflammatories or protease inhibition |
Low bacteria counts or controlled inflammation
↓ Inflammatory cytokines
↓ Protease activity
↑ Growth factor activity | Bacterial balance and reduced inflammation |
Moisture imbalance | M | Desiccation slows epithelial cell migration and causes maceration of wound margin |
Identify root cause
Apply moisture‐balancing dressings, compression therapy or negative pressure wound therapy (NWPT) |
Restored epithelial cell migration
Desiccation avoided
Oedema (excessive fluid) controlled
Maceration avoided | Moisture balance |
Edge of wound (non‐advancing or undermined) | E |
Non‐migrating keratinocytes
Non‐responsive wound cells and abnormalities in extracellular matrix or abnormal protease activity |
Reassess cause or consider corrective therapies
Debridement
Skin grafts
Biological agents
Adjunctive therapies |
Migrating keratocytes and responsive wound cells
Restoration of appropriate protease profile | Advancing edge of wound |
Wound bed preparation (WBP) is a concept used to guide clinicians to focus on identifying and proactively addressing local barriers to wound healing in order to adequately ‘prepare’ the wound environment for healing (Kamolz and Wild [57]).
Goals of care should be determined early in the assessment process as full healing may not be the intention in fungating wounds or wounds at end of life. The underlying cause of the wound should be assessed, with a focus on details such as location, size and depth (Baranoski and Ayello [8]). The wound should be assessed each time a dressing is applied or if it gives cause for concern. The aim of assessing the wound is to determine the extent of healing and establish which treatment will best provide the ideal environment for healing. Regular wound photography provides a useful cumulative timeline of healing observation, but patient consent should always be gained (Baranoski and Ayello [8]). Figure 18.5 is an example of a wound assessment chart.
Factors that affect wound healing
The rate of wound healing varies depending on the general health, age and mobility of the individual; the location of the wound; the degree of tissue damage; and the treatment applied. It is necessary when assessing and treating a wound that all potential detrimental factors are addressed and minimized, where possible, in order to provide the optimum systemic, local and external conditions for healing.
Factors that may delay healing include disease, poor nutritional state, infection, body mass (Hess [47]) and medications such as chemotherapeutic drugs and steroids (Guo and DiPietro [38]) (Table 18.2). Lifestyle factors such as smoking, alcohol consumption and stress (Guo and DiPietro [38], McDaniel and Browning [67]) can also affect wound healing. Other influences relate to the local microenvironment of the wound, including temperature, pH, humidity, air gas composition, oxygen tension, blood supply, inflammation and the presence of non‐viable tissue (Hess [47], Storch and Rice [100]). Whether this influence is positive or negative may depend on the stage of wound healing that has been reached. Other important considerations are external variables such as continuing trauma or the presence of foreign bodies.
Table 18.2 Factors that may delay wound healing
Factor | Action |
---|---|
Extrinsic factors | |
Cold | Any drop in temperature delays healing by up to 4 hours |
Excessive heat | Temperature over 30°C reduces tensile strength and causes vasoconstriction |
Chronic excessive exudate | Wounds should not be too wet or too dry (see moisture imbalance in Table 18.1) |
Poor dressing application and techniques | Delays may be caused by:
|
Poor surgical technique | Prolonged operating time, and inappropriate use of diathermy and drains can lead to haematomas and infection |
Intrinsic factors | |
Age | The elderly have a thinning of the dermis and underlying structural support for the wound (i.e. less moisture and subcutaneous fat); the metabolic process and circulation also slow with age |
Medical and general health conditions | Diabetes, cardiopulmonary disease, hypovolaemic shock, rheumatoid arthritis, anaemia and obesity can delay healing |
Malnutrition or protein–energy malnutrition | Malnutrition can cause generally poor healing, decreased tensile strength, and higher risk of wound dehiscence and infection; low serum albumin causes oedema |
Psychosocial factors | Alcohol and smoking (carbon monoxide affects the blood vessels and circulation of oxygen), poor mobility, stress, isolation, anxiety and altered body image can delay healing |
Drugs | Steroids, non‐steroidal anti‐inflammatories, anti‐inflammatories, immunosuppressants and cytotoxic chemotherapy can delay wound healing |
Improving the blood flow to the wound bed will increase the availability of nutrients, oxygen, active cells and growth factors within the wound environment (Collier [13]). This may be achieved, if appropriate, through consideration of revascularization approaches or advanced therapies (Atkin et al. [6]).
Tissue (viable or non‐viable)
Non‐viable tissue in the wound bed will delay healing (Gray et al. [35]). Accurately identifying the different types of tissue in the wound bed by using the wound healing continuum (Figure 18.6) can guide the clinician to implement the correct actions and treatment plan to promote healing (Ousey and Cook [83]).
Debridement of devitalized tissue
Debridement is an essential component of wound bed preparation (Atkin [5]) and should be considered following a holistic patient assessment (Nazarko [76]). Debridement may not always be appropriate (McFarland and Smith [68]), for example in patients with clotting disorders, malignancy or ischaemic limbs, or in the palliative care environment (Wounds UK [119]).
The aim of debridement is to:
- remove necrosis, slough, eschar, sources of inflammation or infection, exudate, serocrusts, hyperkeratosis, pus, haematomas, foreign bodies, debris and bone fragments
- decrease odour, excess moisture and risk of infection
- stimulate wound edges and epithelialization
- improve quality of life (Strohal et al. [102]).
Non‐viable tissue and debris in a wound can:
- act as a physical barrier to healing
- impede normal extracellular matrix formation, angiogenesis, granulation and epidermal resurfacing
- reduce the effectiveness of topical preparations, such as antimicrobials
- mask or mimic signs of infection
- serve as a source of nutrients for bacteria
- contribute to overproduction of inflammatory cytokines, which can promote a septic response
- prevent the practitioner from gaining an accurate picture of tissue destruction and inhibit correct assessment of the wound
- lead to overproduction of exudate and odour (Wounds UK [119]).
Informed consent must be obtained before debridement. The healthcare professional must provide the patient with information regarding the methods of debridement available; this will include the predicted benefits and associated risks involved (Strohal et al. [102]).
There are many different approaches to wound debridement (Table 18.3). Various factors will inform the most appropriate method of debridement for a particular wound, such as suitability to the patient, type of wound, treatment aims, anatomical location and degree of debridement required (Madhok et al. [64]).
Table 18.3 Common debridement methods
Debridement method | Mechanisms of action | Advantages of this method | Disadvantages of this method | Who can implement this method? | How can this method be used? |
---|---|---|---|---|---|
Autolytic | A naturally occurring process in which the body's own enzymes and moisture rehydrate, soften and liquify hard eschar and slough |
Least invasive method
Can be used before or between other methods of debridement | Slow, increasing the potential for infection and maceration | Any qualified nurse | Apply appropriate dressings (e.g. hydrogel or semi‐occlusive) to achieve a moist wound healing environment |
Mechanical | Physical disruption and removal of non‐viable tissue from the wound bed |
Can be used on devitalized tissues
Quick and easy
Can disturb biofilms
Patients can self‐ administer under supervision |
Not suitable for use on hard, dry eschar
Not suitable for already painful wounds | Any qualified nurse | Employ single‐use mechanical wound debridement product (e.g. monofilament pad or wipe) indicated in local wound dressings formulary |
Bio‐surgical (larvae) | Larvae quickly remove devitalized tissue from the wound; they are available loose or in a ‘bagged’ dressing | Highly selective and rapid |
Costs higher than autolytic/mechanical methods but treatment time is short
Exercise caution with anticoagulants |
Any qualified nurse with appropriate training or a specialist practitioner | Order and apply larvae as per local guidelines; seek specialist guidance if needed |
Sharp | Removal of dead or devitalized tissue using a scalpel, curette, scissors and/or forceps to just above the viable tissue level |
Selective and quick
Analgesia not normally required
Works best on harder eschar that can be grasped with forceps
Can be used at the bedside or in a clinic |
Practitioners must be able to distinguish tissue types and understand anatomy as the procedure carries a risk of damage to blood vessels, nerves and tendons
Not as effective on soft, adherent slough
Does not result in total debridement of all non‐viable tissue | Skilled practitioner (podiatrist or specialist nurse) with specialist training | Refer to specialist |
Surgical | Excision or wider resection of non‐viable tissue, including the removal of healthy tissue from the wound margins, until a bleeding wound bed is achieved | Selective and best used on large areas where rapid removal of devitalized tissue is required |
Anaesthetic is usually required
Higher costs related to theatre time | Must be performed by a surgeon, podiatrist or specialist nurse with appropriate training in the operating theatre | Refer to specialist |
Source: Adapted from Vowden and Vowden ([111]).
Inflammation and infection (or bacterial burden)
It is generally agreed that all chronic wounds harbour a variety of bacteria to some degree. As many chronic wounds fail to advance further than the inflammation phase of wound healing (Harries et al. [45]), their clinical presentation can often be mistaken for wound infection (Hampton [42]).
There are several stages in the continuum of wound infection: contamination, colonization, local infection, spreading infection and systemic infection (IWII [52]). The virulence of the infection involves a complex interaction between the individual and the condition of the wound (Butcher [12]). When a wound becomes infected, it displays the characteristic signs of heat,
redness, swelling/inflammation, pain, increased exudate and malodour. The patient may also develop generalized pyrexia.
Clinicians must respond rapidly if a patient with a wound demonstrates signs of potentially fatal infection, including a systemic inflammatory response, sepsis, extensive tissue necrosis, gas gangrene or necrotizing fasciitis (Copeland‐Halperin et al. [17], IWII [52]). An essential role within wound management is therefore reducing bacterial burden, and many dressings are impregnated with antimicrobial compounds, such as silver, iodine or honey (Butcher [12]) (see Table 18.4). There is supporting evidence for the use of silver and other antimicrobials in reducing colonization and increasing healing rates (Leaper [60]). However, topical antimicrobials can be ineffective in the presence of biofilms (Percival [84]). Topical antibiotics are generally not advocated as they may increase bacterial resistance, and the use of antimicrobials prophylactically is controversial (Butcher [12], Cutting [20]).
Table 18.4 Dressing groups (refer to the manufacturers’ recommendations with regard to individual products)
Dressings | Description | Advantages | Disadvantages |
---|---|---|---|
Activated charcoal | Contains a layer of activated charcoal that traps and reduces odour‐causing molecules | Easy to apply as either a primary or secondary dressing; can be combined with another dressing with absorbency | Need to obtain a good seal to prevent leakage of odour; some dressings lose effectiveness when wetc18-note-0001 |
Adhesive island | A low‐adherent, absorbent pad located centrally on an adhesive backing | Quick and easy to apply; protects the suture line from contamination and absorbs exudate and blood | Only suitable for light exudate; some can cause skin damage (excoriation, blistering) if applied incorrectly |
Alginates | A textile fibre dressing derived from seaweed; the soft woven fibres gel as they absorb exudate and promote autolytic debridement; available as a sheet, ribbon or packing | Suitable for moderate to heavy exudate; can be used on infected wounds; have haemostatic properties for bleeding wounds | Cannot be used on dry wounds or wounds with hard necrotic tissue (eschar); sometimes a mild burning or ‘drawing’ sensation is reported on applicationc18-note-0001 |
Antimicrobials (e.g. iodine, silver or honey) | Available as a primary or secondary layer and available topically (i.e. cream) | Suitable for chronic wounds with heavy exudate that need protection from bacterial contamination by providing a broad range of antimicrobial activities; can reduce or prevent infection | Sometimes sensitivity occurs with the use of silver and some skin staining can occur; instructions vary with products and dressings are expensive; evidence base for use is controversial and needs to be monitoredc18-note-0001 |
Capillary wound dressings | Composed of 100% polyester filament outer layers and a 65% polyester and 35% cotton woven inner layer; the outer layer draws exudate, interstitial fluid and necrotic tissue into the inner layer via a capillary action | Suitable for light to heavy exudate; debride necrotic tissue; protect and insulate the wound; maintain a moist environment and prevent maceration; encourage development of granulation tissue; can be cut to any shape and are available in large rolls; can be used as a wick to drain sinus and cavity wounds | Can be hard to cut and have limited conformability to fit into wounds; cannot be used where there is the risk of bleeding due to the ‘drawing’ action and resultant increase in blood flow to the wound bed |
Foams | Produced in a variety of forms, most being constructed of polyurethane foam; may have one or more layers | Suitable for use with open, exuding wounds; highly absorbent and non‐adherent, and maintains a warm, moist wound bed; available for low to high exudates; available as non‐adhesive and adhesive borders, which can negate the need for securing device | May be difficult to use in wounds with deep tracts and need a combined approach with an alginate or hydrofibre |
Hydrocolloid | Usually consists of a base material containing gelatine, pectin and carboxymethylcellulose combined with adhesives and polymers; the base material may be bonded to either a semi‐permeable film or a film plus polyurethane foam; some have a border | Suitable for acute and chronic wounds with low to no exudate; provides a moist wound environment; promotes wound debridement; provides thermal insulation; waterproof and provides a barrier to micro‐organisms; easy to use; does not require secondary dressing | May release degradation products into the wound; strong odour produced as dressing interacts with exudate; not suitable for infected or dry wounds, or wounds with high exudate levels |
Hydrofibre | Same consistency as hydrocolloid but in a soft woven sheet; has extra absorbency | Forms a soft, hydrophilic, gas‐permeable gel on contact with the wound and manages exudate while preventing maceration of the wound edge; easy to remove without trauma to the wound bed | Does not have haemostatic property of alginates; not suitable for dry woundsc18-note-0001 |
Hydrogels | Contains 17.5–90% water, depending on the product; available as a gel or solid sheet; aids vertical exudate wicking | Suitable for light exudate wounds; donate fluid to dry necrotic tissue; can reduce pain and are cooling; low trauma at dressing changes; can be used as carriers for drugs | Cool the wound surface; use with caution in infected wounds; can cause peri‐wound maceration due to leakage if too much gel is applied or the wound has moderate to heavy exudatec18-note-0001 |
Primary wound contact layer | Most are silicone based; applied directly to the wound bed | Conformable; non‐adherent so can reduce trauma and pain on dressing change; some can reduce moisture loss; can be used with negative pressure wound therapy (NPWT) | Requires a secondary dressing |
Semi‐permeable films | Polyurethane film with a hypoallergenic acrylic adhesive; they have a variety of application methods, often consisting of a plastic or cardboard carrier | Only suitable for shallow, superficial wounds; suitable for prophylactic use against friction damage; useful as a retention dressing; allow passage of water vapour; allow monitoring of the wound | Not suitable for exuding wounds; possibility of adhesive trauma if removed incorrectly; can macerate, slip or leak |
Skin barrier film |
Alcohol‐free liquid polymer that forms a protective film on the skin | Non‐cytotoxic; does not sting if applied to raw areas of skin; high wash‐off resistance; protects the skin from body fluids, friction and shear and the effects of adhesive products | Requires good manual dexterity to apply; may cause skin warming on application |
a | Requires a secondary dressing. |
Immunosuppressed patients, diabetic patients and those on systemic steroid therapy may not present with the classic signs of infection. Instead, they may experience delayed healing, breakdown of the wound, presence of friable granulation tissue that bleeds easily, formation of an epithelial tissue bridge over the wound, increased production of exudate, malodour and increased pain.
There is currently no universally agreed‐upon definition of wound infection that can be applied to all wounds (Cutting [20]). The clinical presentation of a wound should lead to the diagnosis of an infection. A wound swab should only be obtained if it is advocated by the clinical picture.
Wound swabs
There has been much debate and discussion as to which technique to use when obtaining a wound swab – the Z technique or the Levine technique (Myers [75]). The Z technique involves moving the swab in a zig‐zag pattern across the wound while rotating the probe to achieve 10 points of contact without touching the edges of the wound. In the Levine technique, a swab is rotated over a 1 cm2 area for 5 seconds with sufficient pressure to extract fluid (Copeland‐Halperin et al. [17]).
The literature highlights that the Levine technique is more accurate when swabbing wounds than the Z technique because it takes samples from both the surface of the wound and the wound tissue due to the application of pressure to extract fluid (Angel et al. [2]). The Z technique has 63% sensitivity and 53% specificity while the Levine technique has 91% sensitivity and 57% specificity (Bonham [9], Stotts [101]), which suggests that the Levine technique is more reliable in determining the organism in acute and chronic wounds when wound swabs are used to collect sample and cultures than the Z technique (Angel et al. [2]).
The procedure of obtaining a wound swab (see Chapter c13: Diagnostic tests) must always be explained to the patient and they must be informed that there may be some discomfort. The Levine technique involves cleansing the wound with normal saline. This will remove any debris on the wound bed. Avoid using antiseptics or antimicrobial agents prior to swabbing as this may influence the results (Reynolds [91]). Rotate the swab over a 1 cm2 area of clean viable tissue with enough pressure to extract fluid from the inner part of the wound (Huang et al. [51], IWII [52]).
Where possible, do not obtain sample from slough, pus or necrotic tissue as this will not provide an accurate profile of the microflora contained within the tissue (Cross [19]). Insert the wound swab into the culture container. Re‐dress the wound after the procedure. Relevant clinical information about the patient and the wound should be provided with the sample, including the wound's aetiology, the anatomical location of the wound, current treatment, and presenting signs and symptoms (Cooper [16]).
Moisture balance
Wound exudate usually performs a useful function by aiding autolytic debridement and providing nutrients to the healing wound bed. It is required in the process of epithelialization, to allow the movement of cells across the surface of the wound (Jones [56]). However, in the presence of excess exudate, the process of wound healing can be adversely affected. This is especially so in chronic wounds, where there is increased proteolytic activity, leading to damage in the wound bed. Matrix metalloproteases are found in exudate, and, when present in chronic exudate, their beneficial properties, such as the provision of essential nutrients for cell metabolism, are hindered. This can be a significant factor in delayed healing (Hampton [42]).
The control of oedema or elevating the affected limb (e.g. in a lower leg wound) undoubtedly helps in the reduction of wound exudate. However, if the methods for achieving these goals are unsuccessful or contraindicated then exudate must be managed through the use of wound management products. These include absorbent wound dressings (e.g. alginates, hydrofibre or foams), non‐adherent primary wound contact layers with a secondary absorbent pad, wound manager bags and negative pressure wound therapy (NPWT) (discussed later in this chapter). NPWT is highly effective in controlling excessive exudate (Probst and Huljev [88]). It is also vital to protect the skin surrounding the wound from maceration by excess exudate and excoriation from corrosive exudate. Useful products for skin protection include alcohol‐free skin barrier films and thin hydrocolloid dressings, which can be cut and used to ‘frame’ the wound edges.
Edge non‐advancement
Wound treatment planning
Clinicians must select appropriate dressings based on the tissue types in the wound bed, the treatment aims and the most suitable dressing properties. Based on the wound healing continuum, Figure 18.7 is an example dressing selection guide for wounds healing by secondary intention. It provides guidance on choice of products and their desired properties in relation to the tissue types in the wound bed, treatment aims and moisture levels. Where complete healing is the main aim, the clinician should use products that will create the optimal wound bed environment, ensuring the wound progresses through the wound healing continuum and subsequently completes the four phases of wound healing.
Caution must be exercised when considering hydrating wounds on the foot and/or at the end of life. Specialist referral may be required.
Principles of dressing a wound
With the exception of wounds where the main aim is to manage and improve symptoms, such as in malignant wounds or wounds at end of life, an ideal wound dressing must be capable of fulfilling the following functions:
- creates a moist, clean, warm environment
- provides hydration if the wound is dry or desiccated
- absorbs and adequately manages excess exudate
- provides protection to the peri‐wound area
- allows for gaseous exchange
- is impermeable to micro‐organisms
- is free of toxic or irritating particles
- does not shed particles or fibres
- can conform to the wound surface and anatomical location
- causes minimal pain and epidermal stripping during application and removal
- does not compromise the patient's religious or ethical beliefs
- is easy to use
- is cost‐effective (Boyer [10], Skórkowska‐Telichowska et al. [95], Sood et al. [98]).
Clinicians must be aware of the components of the wound care products used (Table 18.4). Dressings containing ingredients derived from animals, such as collagen and honey, may not be acceptable to patients from some faith, ethnic or ethical groups, such as Hindu, Islam, Sikhism or vegan (Eriksson et al. [30], Sood et al. [98]).
Principles of cleansing a wound
The aim of wound cleansing is to help create the optimum local conditions for wound healing (Lloyd Jones [63]). Wound cleansing takes into consideration the wound bed, wound margins and peri‐wound skin as all are central to successful healing (Kamolz and Wild [57]).
Wound cleansing can be considered ritualistic, non‐evidence‐based and often carried out unnecessarily (Lloyd Jones [63]). There is no robust evidence to suggest that routine cleansing of wounds expedites healing or reduces infection (Fernandez and Griffiths [31]). If a wound appears clean with little exudate, the clinician must consider the benefits and risks of cleansing the wound (McLain and Moore [72]).
When a wound bed is exposed to temperatures below core body temperature (36–38°C) or above 42°C, cellular activity is reduced, resulting in delayed wound healing (McGuiness et al. [69]). It can take 3 hours or longer for the wound to return to normal temperature (McKirdy [71]). Clinicians should consider warming cleansing solutions before use (HSE [50]).
Cleansing technique
Although swabbing wounds with soaked gauze swabs may be effective in removing foreign bodies from the surface of a wound, irrigation is the preferred technique as it is less damaging to new, fragile granulating tissue (Hall [41], McLain and Moore [72], Watret and Armitage [113]) and the potential of shedding gauze fibres into the wound is avoided (Wolcott and Fletcher [118]). Showering (at least 48 hours post‐operatively) or immersing limbs may also be considered for those with chronic wounds located on the lower extremities (McLain and Moore [72]).
Cleansing solutions
Current evidence suggests that there is no significant difference in healing or infection rates between wounds cleansed with tap water (of drinkable quality) or 0.9% sodium chloride (Fernandez and Griffiths [31], Hall [41]). NICE ([81]) recommends using 0.9% sodium chloride for wound cleansing for 48 hours post‐operatively. Wolcott and Fletcher ([118]) repeat concerns that plumbing in healthcare facilities may be colonized with microbes, predominantly those of the genus Pseudomonas.
Where clinically indicated, there is evidence to support the use of modern, low‐toxicity antimicrobial wound cleansing solutions such as polyhexamethylene biguanide (PHMB) or octenidine dihydrochloride in the reduction of wound microbial bio‐burden (Andriessen and Eberlein [1], Butcher [12], Cutting and Westgate [21]).