CHAPTER OBJECTIVES
At the end of this chapter, the learner will be able to:
Explain the cellular and tissue effects of negative pressure wound therapy and link these effects to wound healing.
Describe the components of negative pressure wound therapy systems and their functions.
Describe the indications for negative pressure wound therapy in wound management.
Identify precautions and contraindications for the use of negative pressure wound therapy and develop adaptation strategies.
Describe continuous and intermittent modes of negative pressure wound therapy and the advantages/disadvantages of both.
Describe the basic steps involved in the application of negative pressure wound therapy systems.
Negative pressure wound therapy (NPWT), also known as topical negative pressure therapy (TNP),1,2 and negative pressure wound care (NPWC),3 were first documented as an adjunct treatment for open wounds in the early 1990s.2 By 2004 this active therapy was reported as standard of care for a variety of diagnoses in modern wound management.1 Through the application of a closed wound dressing and attached suction, NPWT applies controlled, subatmospheric pressure to open wounds and has been shown to provide the following benefits for wound healing:
Promotion of moist wound healing4
Reduction of edema and interstitial fluid1,4,5
Approximation of wound edges4,9
Stimulation of granulation tissue formation9,10
Reduction in bacterial load9,11
Reduction in the frequency of dressing changes12
Since its acceptance into evidence-based wound management, NPWT has been utilized to treat a wide variety of acute and chronic wounds13 including acute traumatic and surgical2,14 wounds healing by primary and secondary intention; burns15,16; and chronic wounds associated with venous insufficiency,3,13 diabetes,3,10,17,18 and pressure.19 Events such as the devastating 2010 earthquake in Haiti15 and war in the Middle East15,20,21 have also shown how the benefits of NPWT can positively influence limb salvage rates and decrease morbidity and mortality in mass casualty and high-energy injury situations.
A NPWT system consists of a pump unit that provides suction, a wound filler that transfers negative pressure to the wound bed and allows flow of fluids from the wound, a transparent occlusive sheet that covers the wound filler and creates an airtight seal, and flexible tubing that delivers suction and serves as a conduit for removal of drainage and wound debris.22 Wound fluids are collected in a disposable container that is attached to the pump (FIGURE 15-1). TABLE 15-1 further describes NPWT components.
FIGURE 15-1
Negative pressure wound therapy The fluids are suctioned from the wound, through the foam, into an attached tube and into an air tight disposable canister. Although every system has its own unique characteristics, the basic functions of removing interstitial edema, stimulation cell proliferation, and reducing wound size are the same.
Suction device | Different sizes based on inpatient vs outpatient use Powered by electricity or battery (SnaP system is spring powered)23,24 Reusable or single use and disposable Programmable for different parameters Alarms for full canister, leak, interrupted suction, low battery |
Wound filler | Foam: black, white, green, reticulated open-cell with through holes (ROCF-CC) Gauze: antimicrobial gauze dressing (AMD) |
Occlusive sheet cover | Semipermeable film or sheeting cut to size |
Tubing | Delivers suction and serves as conduit for fluid removal Additional tubing utilized for instillation therapy |
Collection canister | Size varies depending on suction device Single use, disposable Changed when full without necessitating a dressing change Disposed into red biohazard container |
The first commercially available NPWT device marketed in the United States as a wound healing device25 was the Vacuum Assisted Closure or V.A.C. (Kinetic Concepts, Inc (KCI), San Antonio, TX). The initial V.A.C. device was a somewhat bulky, electrically powered unit designed primarily for inpatient use.25 A smaller, portable, battery-operated unit was designed later for use in the outpatient setting.3,16 Over the past few years, an explosion in NPWT interest and development has occurred and now multiple vendors offer relatively silent NPWT devices in various sizes that are reusable, recyclable, or disposable; some units are specially designed for specific types of wounds (see TABLE 15-2 for partial vendor list). Increased healing, portability, and ease of management can result in decreased length of hospital stay, faster return to function,26 cost savings,27 and improved quality of life.
American Medical Products | extriCARE, VENTURI™ Compact (portable)
SVED Wound Rx System
|
DeRoyal | PRO-III and PRO-II (portable)
|
Genadyne Biotechnologies | XLR8 (portable)
XLRS plus (hospital and home care)
UNO (single-use system) |
Cardinal Health | SVED (portable)
|
Kinetic Corporation, Inc (KCI), an Acelity Company | V.A.C. Ulta and V.A.C. Instill (instillation option)
|
Medela, Inc | Invia Liberty (portable, inpatient, or outpatient use)
|
Mölnlycke Health Care | Avance (portable, inpatient, or outpatient use)
|
Premco Medical Systems, Inc | PMS-800 and PMS-800V (portable, inpatient, and outpatient use)
|
Smith and Nephew, Inc | Renasys EZ Plus (inpatient use)
|
Spiracure, Inc | SnaP Wound Care System (portable, single use)
|
Talley Group Ltd | Venturi Avanti (inpatient or outpatient use)
|
NPWT promotes wound healing primarily through removal of wound fluid, mechanical stimulation of cells, facilitation of wound contraction, and occlusion of the wound from environmental contaminants. As fluid is suctioned from the wound, interstitial edema is reduced. Inflammatory mediators and bacteria are removed along with tissue fluids, thereby reducing wound inflammation and facilitating progression to the proliferative healing phase. Mechanical stimulation at both the tissue (macrostrain) and cellular (microstrain) levels28 encourages increased cellular proliferation, granulation tissue formation, and wound contraction.14,29 The occlusive covering maintains a moist wound healing environment and an airtight seal that is vital in sustaining negative pressure.1,5,14,30 Despite differences in size and shape, all NPWT devices basically offer the same benefits, and selection of a device may depend on the patient’s medical coverage. Most devices offer several options for “tailoring”22 NPWT to each patient need so that optimal care can usually be achieved regardless of specific vendor. CASE STUDY
INTRODUCTION
LS is a 59-year-old male referred for wound care of the left hand. He was admitted to the hospital with an infected bite on the dorsal hand that required extensive surgical debridement, which was performed the day before the initial consultation for wound care (FIGURE 15-2).
DISCUSSION QUESTIONS
What medical information would you need from the patient’s chart to determine if NPWT is indicated?
What wound characteristics would determine if NPWT is indicated?
NPWT has several documented effects at the cellular and tissue levels. Due to the close, interrelated nature of these effects, cellular and tissue changes associated with NPWT are discussed together and presented in the following main categories: occlusion, cellular deformation, fluid removal, circulation, contraction, and bioburden (TABLE 15-3).
Occlusion | |
Cellular deformation | |
Removal of fluid | |
Circulation |
|
Contraction |
|
Bioburden |
|
The benefits of moist wound healing have been well established.1,5,14,30 Since NPWT requires an airtight seal in order to maintain suction, all devices require that an occlusive dressing be applied over the open wound site. As long as the seal is maintained, a moist wound environment is created. NPWT dressings are changed every 48–72 hours; thus, exposure of the wound to air (which can decrease wound bed moisture and temperature, and subsequently slow down the healing process) is reduced and the moist wound environment preserved.
The suction force associated with NPWT causes mechanical deformation of cells.2,14,33 Referred to as microstrain13,15,28 or simply strain,33 the stretching force creates changes within the cells that result in increased release of growth factors and cytokines associated with cellular proliferation.9,13 Increased cellular division and migration of macrophages, lymphocytes, and fibroblasts are also facilitated.13,14,33 Mechanical deformation caused by negative pressure results in increased angiogenesis and granulation tissue formation and is one of the most significant effects of NPWT.1,33 DeFranzo et al.37 demonstrated that in healthy, noninfected wounds, newly formed granulation tissue is routinely present within 48 hours after NPWT is initiated.
The removal of interstitial wound fluid is a significant factor associated with NPWT.1,5,14 Removal of edema associated with acute injury and trauma facilitates oxygen and nutrient diffusion34 as well as decreased inflammation as inflammatory mediators are removed with wound fluid.1,2 It has been well documented that chronic wound fluid is detrimental to wound healing1,35,36,41 and due to its unique method of fluid removal, NPWT is especially beneficial in the treatment of chronic wounds.37 Studies conducted by Labanaris42 and Dini et al.13 show that NPWT induces proliferation of lymph vessels and suggest that this aids in quick reduction of wound fluid especially in the first 4 days of treatment. Dini et al.13 also demonstrated that NPWT encouraged opening of collapsed lymph vessel lumens in chronic venous insufficiency wounds. In many cases, tissue edema can be significantly resolved within 3–5 days, thereby facilitating reduction of wound surface area fairly quickly.37
Local circulation is improved with NPWT6,7,8,14,28,33 through the combined benefits of cellular deformation and fluid removal. In an animal study, Borgquist8 demonstrated improved blood flow at 1.0 and 2.5 cm from the wound edge with the application of negative pressure. Conversely, it has been shown that due to compression of tissues, blood flow is actually decreased at the superficial wound edge and may extend as far as 0.5 cm from the wound edge indicating that NPWT may create a gradient of blood flow changes.6,7,34 Researchers believe hypoperfusion at the wound edge acts as a stimulus for angiogenesis and is therefore seen as a beneficial effect of NPWT.6,34 NPWT-induced hypoperfusion may not, however, be beneficial in situations where blood flow is already significantly compromised; further decreases in blood flow could result in ischemia and tissue necrosis. In this case, the use of lower negative pressures would be appropriate so that compression of tissue at the wound edge is reduced.8 Also, when wound edge blood flow is a concern, intermittent NPWT may be more appropriate than continuous therapy since the on/off cycles provide decompression or rest periods that may decrease the risk of ischemia.7 (Intermittent and continuous therapy are discussed in more detail in the section on Parameters.) In all cases, since the amount of wound edge compression is pressure dependent, it is recommended that the lowest effective pressure be used in order to decrease potential complications with hypoperfusion.22
Studies support that the centripetal1 pulling or suction force of NPWT assists in approximating wound edges and with wound contraction.14,32 This action, referred to as “macrostrain,”9,15,28 combined with reductions in localized tissue edema via fluid removal, effectively reduces the wound surface area. Additionally, wound edge macrostrain has been shown to mechanically stimulate larger cytoskeleton structures within granulation tissue, resulting in increased cellular proliferation.1,14,28
The exact method of how NPWT affects bacterial load remains unclear.9,15,20,22,32 A study conducted by Weed et al.39 showed wound closure with NPWT even in the presence of 106 bacteria. Other studies have demonstrated improved healing although bacteria levels actually increased during NPWT use.32 It appears that NPWT positively affects wound bioburden through all of the mechanisms discussed above.43 Some of the newer NPWT units provide for the instillation of topical solutions as another mechanism of combating bacteria. Overall, NPWT is just one component in a treatment strategy for highly contaminated or infected wounds14,17,33 and should be combined with other standard therapies, including sharp/surgical debridement, systemic antibiotics, irrigation with pulsed lavage with suction (see Chapter 17, Pulsed Lavage with Suction), and topical antibacterials.32 In 2009, a multidisciplinary expert panel stressed this point by identifying prerequisite recommendations regarding the use of NPWT on infected wounds. These recommendations include the following: the patient is free of systemic signs of infection, necrotic tissue is debrided and abscesses are drained, and perfusion is adequate for healing (TABLE 15-4 and FIGURES 15-3 and 15-4).44
FIGURE 15-4
Wound not appropriate for NPWT Although this wound has been surgically debrided and is an appropriate shape for NPWT, the amount of necrotic tissue and lack of angiogenesis at the edges indicate that there is insufficient perfusion (or blood supply) for the wound to heal. Therefore, it is inappropriate for NPWT.
Patient is free of most systemic signs of gross infection. Necrotic tissue is debrided and abscesses are drained. Wound has adequate perfusion. |
TABLE 15-5 provides a list of wound etiologies for which NPWT is indicated (FIGURES 15-5 to 15-12). The cellular and tissue effects need to be considered for each indication in order to obtain optimal patient outcomes and for future problem solving.
FIGURE 15-5
Abdominal incisional wound on a patient who has had a Whipple procedure for chronic pancreatitis The erythema on the periwound skin is a result of the copious drainage that has been coming from the wound. This wound is indicated for NPWT to promote granulation and closure, as well as to manage exudate and allow the skin to recover.
FIGURE 15-6
Abdominal wound with the NPWT in place NPWT is applied to the wound in FIGURE 15-5 with a layer of Vaseline gauze under the adhesive drape to further protect the inflamed skin and to help minimize pain when the drape is removed. Also note the Chariker–Jeter or mesentery approach of applying the suction tube into the foam. This method is recommended for high-output wounds, small or narrow wounds where the round track pad may press on surrounding tissue, or gauze-filled wounds.
FIGURE 15-11
Traumatic wound on the lower extremity is prepared for NPWT application by placing white foam over exposed bone, non-adhesive mesh over muscle, and Xeroform strips over the edges These strategies minimize both pain and damage to existing structures and new granulation tissue when the dressing is removed.
Acute surgical and traumatic | Meshed grafts and flaps1,2,19,45 Wounds in need of additional physical stabilization37 Fasciotomies performed for compartment syndrome9,32 Full-thickness wounds with or without exposed structures or hardware prior to grafting, primary or secondary intention closure1,35 Over at-risk surgical incisions48,49 Deep partial- and full-thickness burns2,50 Traumatic amputations and deep lacerations Over dermal substitutes (Integra, Integra Sciences Corp, Plainsboro, NJ) and bioengineered skin substitutes (Apligraf, Organogenesis, Inc, Canton, MA)51 |
Chronic | Debrided neuropathic wounds and open amputation sites associated with diabetes1,37,52 Stage III and IV pressure ulcers37,53 Wounds associated with venous insufficiency3,13 Wounds associated with arterial insufficiency—with caution8,19 Palliative care1 |
Evidence supports the use of NPWT for most acute surgical wounds14 and for traumatic2,37 wounds (especially those with exposed bone, tendon,1,27,45 or hardware1) that require increased granulation prior to surgical closure or grafting. One exception to acute surgical wounds is an abdominal wound with thin tissue protecting any part of the gastric system in which case the negative pressure may increase the risk of enterocutaneous fistula formation. Due to the cellular and tissue effects of NPWT, placement over a new split-thickness skin graft (STSG) has been shown to increase graft “take” through edema reduction and graft stabilization2,32 and is indeed considered by some as the standard of care for high-risk STSGs.2 When treatment is initiated and the wound filler compresses, NPWT can assist with stabilization or splinting of the wound site. DeFranzo and colleagues37 also found that NPWT utilized in complicated traumatic lower extremity, ankle, and foot injuries allowed patients to be more mobile sooner than with other dressings due to the increased stabilization. In mass casualty or battlefield situations, NPWT is used to stabilize and protect large open wounds until patients can be transported to advanced facilities for appropriate care.15,20,32
NPWT application over suture lines improves wound integrity by maintaining wound edge approximation and decreasing periwound tension, thereby decreasing the risk of dehiscence in high-risk patients.48,49,54 Disposable, 7-day NPWT units, such as Prevena (Prevena Incision Management System, KCI USA, an Acelity Company, San Antonio, TX) are available specifically for use with surgical incisions (FIGURE 15-13). NPWT may also be indicated for full-thickness burns after debridement of nonviable tissue has been performed.9,50 However, guidelines developed by an expert panel in 2010 recommended that the decision to use NPWT on full-thickness burns should only be made by a burn specialist (refer to Chapter 10 for more discussion about treatment of burns).50 Application of NPWT to deep partial thickness burns may prevent progression of tissue damage due to improved circulation and edema reduction.50
FIGURE 15-13
NPWT for surgical incisions The Prevena Incision Management System is a small NPWT unit that is placed over surgical incisions to help prevent dehiscence and surgical site infection. The disposable unit has a 45-mL canister and a peel-and-stick foam pad. It is applied over a clean surgical incision and left in place for the duration of the battery life. (PrevenaTM Incision Management System; Courtesy of KCI Licensing, Inc, an Acelity Company, 2013.)
Successful use of NPWT has been documented for ulcers associated with pressure,1,37,53 venous insufficiency,14 and diabetes1 as well as chronic wounds related to reconstructive surgery29 and exposure to radiation.19 NPWT can also be effective in palliative care of terminal patients with highly exudating malignant wounds by reducing odor, controlling drainage, and decreasing dressing changes (FIGURE 15-14).1 NPWT in the presence of arterial insufficiency requires caution due to wound and periwound hypoperfusion as previously discussed.6,8,34 CLINICAL CONSIDERATION
Toe and forefoot amputation sites after vascular reconstruction need careful monitoring to ensure that perfusion is adequate for healing, otherwise the pressure may occlude superficial capillaries and result in tissue necrosis.
FIGURE 15-14
Palliative care NPWT dressing on a large upper back wound where a malignant tumor was excised. The patient is on hospice, and the dressing is used to manage drainage, minimize pain, minimize dressing changes, and optimize quality of life for both patient and family members during end-of-life care.
NPWT has been used on patients of all ages including neonates and the elderly.26 Evidence documenting NPWT use on the very young stresses the need for special consideration regarding patient size and weight as neonates, infants, and children are more susceptible to dehydration.26 In pediatrics, pressure settings range from 50 to 125 mmHg and are dependent on age, wound etiology, and location.26 In 2009, Baharestani and expert colleagues26 published detailed best practice guidelines for the use of NPWT in pediatric patients (TABLES 15-6 to 15-8) and providers engaged in pediatric wound management are advised to follow these guidelines. Dehydration can also be an issue for elderly patients and fluid levels should be monitored closely in patients with high-output wounds. Physicians should be notified if two collection canisters are filled within a 24-hour period.19
Negative Pressure Setting (mmHg) | |||
Wound Type/Condition | Newborn/Infant (Birth–2 Years) | Child (>2–12 Years) | Adolescent (>12–21 Years) |
Sternal | −50 to −75 continuous | −50 to −75 continuous | −50 to −75 continuous |
Omphalocele/gastroschisis | −50 to −75 continuous | ||
Enterocutaneous fistula | −50 to −75 continuous | −75 to −125 continuous | −75 continuous |
Abdominal compartment syndrome | −50 to −75 continuous | −50 to −125 continuous | −75 to −125 continuous |
Spinal | −50 to −75 continuous | −75 to −100 continuous | −75 to −125 continuous |
Pilonidal disease | −50 to −75 continuous | −50 to −125 continuous | −75 to −125 continuous |
Pressure ulcer | −50 to −75 continuous | −75 to −125 continuous | −75 to −125 continuous |
Extremity wounds | −50 to −75 continuous | −75 to −100 continuous | −75 to −125 continuous |
Fasciotomy wounds | −50 to −75 continuous | −75 to −100 continuous | −75 to −125 continuous |
Burns | −50 to −75 continuous | −75 to −125 continuous | −75 to −125 continuous |
Postgraft wounds | −50 to −75 continuous | −75 to −100 continuous | −75 to −125 Continuous |
Precautions | |
Spinal cord injury | Discontinue NPWT/ROCF to help minimize sensory stimulation |
Bradycardia | Do not place dressing in proximity to the vagus nerve |
Periwound tissue protection | Protect fragile/friable periwound skin with additional drape, thin hydrocolloid, or other transparent film Repetitively applying and removing drapes may lead to stripping of periwound skin Do not allow foam to overlap onto intact skin |
Temperature | Closely monitor and maintain temperature |
Wound Type/Condition | Black (Polyurethane) Foam | White (Polyvinylalcohol) Foam | Silver (Polyurethane) Foam |
Sternal | X | X | X |
Omphalocele/gastroschisis | X | ||
Enterocutaneous fistula | X | X | |
Abdominal compartment syndrome | X | ||
Spinal | X | X | X |
Pilonidal disease | X | X | |
Pressure ulcer | X | X | |
Extremity wounds | X | X | |
Fasciotomy wounds | X | X | |
Burns | X | X | |
Postgraft placement | X | X |
Precautions and contraindications for NPWT are listed in TABLE 15-9. Wounds with low-level vascular compromise may benefit from NPWT and in this situation, research supports the use of intermittent mode therapy at lower pressure levels to reduce the risk of ischemia and ischemic pain.6,7,8,22,34,44 In 2004, Banwell and Musgrave1 reported that NPWT showed no benefit for wounds with significant ischemia. This was reported again in 2012 by McCallon55 who stated that NPWT was ineffective on wounds with significant proximal arterial occlusion. NPWT has the potential to increase wound ischemia leading to further tissue necrosis and ischemic pain,27 therefore initiation of treatment is deferred until blood flow is restored by revascularization surgery or endovascular procedures. If blood supply remains marginal, treatment is deferred until signs of granulation appear at the wound edges indicating there is sufficient oxygenation to support angiogenesis. Signs of oxygenation are especially important if there is necrotic tissue in the wound that needs to be debrided before initiation of NPWT.
Precautions | Anticoagulants19 Low platelet count Nonenteric and unexplored fistulas19,44 Over named structures (bone, tendon, organs, vessels, etc.); requires placement of several layers of barrier dressing15 or use of white foam Monitor for bleeding49 Avoid circumferential occlusive sheeting application due to increased risk of ischemia49 Monitor skin condition when dressing placed over bony prominences or prominent hardware due to compression37,49 Debride sharp edges of exposed bone prior to application to protect soft tissues during compression44 Notify physician if drainage in collection canister is sanguineous, is filled with drainage in 1 hour, or if more than two canisters are filled within a 24-hour period19 |
Contraindications | Wounds with more than 30% slough, necrotic tissue1 Gross infection with or without frank pus,57,58 or sepsis57 Malignancy in treatment area19 except in cases of palliative care1 Lack of hemostasis56 Blood dyscrasia57 such as with leukemia or hemophilia Directly over exposed vessels, bypass grafts, organs, or other named structures57 Ischemic wounds with significant proximal occlusion1,55 Intermittent not used over grafting due to high potential for graft disruption32 No suction devices/pumps in MRI, HBOT, or close to flammable anesthetics (see specific vendor specifications)55 Any wound that shows a negative response to initial treatment |
A study by Jung et al. reinforced the caution that is necessary with patients who have compromised vascularity, especially those with diabetes. TcPO2 measurements were taken on the dorsal foot of patients with diabetes before, during, and after application of −125 mmHg negative pressure with polyurethane foam. A significant decrease in surface TcPO2 occurred during treatment (84%) and after discontinuation of therapy (40.3%). The rationale for this decrease was the presence of vasculopathy that affects both the macro- and microcirculation associated with diabetes. Their results suggest that minimal compression of the foam is recommended when applying NPWT to the diabetic foot ulcer, and as stated above, NPWT should be applied after successful revascularization.59