Approach ConsiderationsOnce a pressure injury (pressure ulcer) has developed, immediate treatment is required. Commonly used treatments over the years have included innovative mattresses, ointments, creams, solutions, dressings, ultrasonography (US), ultraviolet (UV) heat lamps, sugar, and surgery. In choosing a treatment strategy, consideration should be given to the stage of the wound and the purpose of the treatment (eg, protection, moisture, or removal of necrotic tissue). An algorithm for assessment and treatment is available. [52, 71, 72] Show
General principles of wound assessment and treatment are as follows:
With thorough and comprehensive medical management, many pressure injuries may heal completely without the need for surgical intervention. Successful medical management of these injuries relies on the following key principles:
If surgical reconstruction of a pressure injury is indicated, it cannot be emphasized too strongly that medical management must be optimized before reconstruction is attempted; otherwise, reconstruction is doomed to failure. That is, spasticity must be controlled, nutritional status must be optimized, and the wound must be clean and free of infection. If there is significant fecal soiling into the injury, diverting colostomy should be considered before reconstruction. If there is a urethral fistula, it should be diverted and healed before reconstruction. Wound reconstruction can be considered once the bacterial load has been sufficiently minimized to reduce the risk of infectious complications. Furthermore, the patient’s social situation and nutritional status must be optimized (albumin level >3.5 g/mL) to reduce the risk of an adverse outcome. Because the complication rate after pressure injury reconstruction can be extremely high, patients who are poor surgical candidates in general should not undergo this procedure. Those who do not have a proper support network and a pressure-release bed at home also are not good candidates for pressure injury reconstruction, because of the risk of recurrence or other complications. Patients who do not comply with nonoperative measures used to promote healing by secondary intention are poor reconstruction candidates as well. Treatment options of unproven efficacy that are currently being studied include hyperbaric oxygen therapy, electrotherapy, growth factors, and negative-pressure wound therapy (NPWT). Initial studies of electrotherapy seem promising, and topical application of the recombinant human growth factor becaplermin has been approved for use in patients with diabetic neuropathic ulcers of the lower extremity. However, not enough evidence is available to permit these treatments to be recommended for the treatment of pressure injuries. Discharge planning begins early in the hospital stay and requires an interdisciplinary approach. Knowledge of available resources facilitates smooth transitions through all levels of care. With more care being conducted in the home environment, education of the patient and caregiver in preventing and treating pressure injuries becomes increasingly important. Various methods can be used to facilitate the educational process, including charts, diagrams, photographs, and videos. This comprehensive approach can positively influence outcome. [72] As a final note, some consideration should be given to the ethics of treating pressure injuries. For some individuals with pressure injuries, such as acutely hospitalized patients with a recoverable illness, aggressive treatment, as outlined in this article, is certainly indicated. For other persons, however, such as chronically or terminally ill patients with long-standing or recurrent ulceration, aggressive treatment may not be in their best interests. In such instances, the wishes of the patient or the patient’s family should be weighed carefully. It may prove to be the case that the patient’s interests are better served by providing medical care and maintaining patient comfort than by instituting major invasive procedures. In March 2015, the American College of Physicians (ACP) published clinical practice guidelines for risk assessment, prevention, and treatment of pressure ulcers (see Guidelines). [73, 74] General Measures for Optimizing Medical StatusSpasticity should be controlled pharmacologically with medications such as diazepam, baclofen, or dantrolene sodium. Patients with spasticity refractory to medication may be candidates for neurosurgical ablation. Flexion contractures may also be relieved surgically. Nutritional status should be evaluated and optimized to ensure adequate intake of calories, proteins, and vitamins. [75] Malnutrition is one of the few reversible contributing factors for pressure injuries, and establishing adequate caloric intake has been shown to improve healing of these lesions. In a review of six clinical studies aimed at examining the effect of oral nutritional supplementation (ONS) enriched with arginine, vitamin C, and zinc in pressure ulcer care, ONS was found to have positive effects on pressure injury healing and potentially to reduce the risk of developing these injuries. [34, 76] Implementation of more invasive methods of nutrient delivery becomes an ethical issue and must be weighed against the complications of such delivery. Goals of nutritional support should include adequate protein intake and the establishment of a positive nitrogen balance, with 1.0-2.0 g/kg/day being recommended for patients with pressure injuries. Other important considerations include cessation of smoking, adequate pain control, maintenance of adequate blood volume, and correction of anemia, the primary aims of which are to prevent vasoconstriction in the wound and to optimizing the oxygen-carrying capacity of the blood. The wound and surrounding intact skin must be kept clean and free of urine and feces through frequent inspection and cleansing. Appropriate evaluation of urinary or fecal incontinence is complex but must be performed thoroughly. Potentially reversible causes should be identified and treated. Urinary incontinence secondary to urinary tract infection (UTI) should be treated with antibiotics. Fecal incontinence secondary to diarrhea may be related to an infectious cause (eg Clostridium difficilepseudomembranous colitis) that resolves with appropriate antibiotics. Manual disimpaction and the addition of stool bulking agents to the diet may relieve overflow fecal incontinence. Urinary or fecal incontinence with no treatable cause may be minimized by establishing a bowel and bladder regimen. Constipating agents and a low residue diet also may be helpful. Diapers and incontinence pads may be useful absorbing moisture away from the surface of the skin, provided that they are checked regularly and changed when soiled. If used inappropriately, these products may actually aggravate maceration and result in dermatitis. A bladder catheter or (in males) a condom catheter may be used to control urinary incontinence. In very severe cases involving chronic stool contamination, surgical diversion should be considered. Bacterial contamination must be assessed and treated appropriately. Differentiation of infection from simple contamination through tissue biopsy (see Workup) helps ensure that antibiotics are used judiciously (ie, only in cases of actual infection) and, ideally, helps minimize the development of resistant species. Antibiotics also are indicated when accompanying osteomyelitis, cellulitis, bacteremia, or sepsis is present. A system of assessing wound healing must be in place to facilitate continuity of care among the various health care providers involved in the care of the patient. This often includes serial photography, detailed descriptions of the wound, and measurement of wound dimensions. Pressure ReductionThe first step in healing a pressure injury is determination of the cause (ie, pressure, friction, or shear). [5, 77, 78] Turning and repositioning the patient remains the cornerstone of prevention and treatment through pressure relief. Patients who are capable of shifting their weight every 10 minutes should be encouraged to do so. Repositioning should be performed every 2 hours, even in the presence of a specialty surface or bed. Patients who are bedbound should be positioned at a 30° angle when lying on their side to minimize pressure over the ischial tuberosity and greater trochanter. Efforts should be made to avoid sliding the patient over a surface to prevent shear forces and friction. Patients who develop a pressure injury while sitting should be placed on bed rest with frequent repositioning. Pressure reduction may be achieved through the use of specialized support surfaces for bedding and wheelchairs that can keep tissue pressures below 32 mm Hg (the standard threshold value for evaluating support surfaces). [79, 80, 81, 82, 83] In theory, reduction of tissue pressures below capillary filling pressures should allow adequate tissue perfusion. Various different types of specialized support surfaces are available (see Table 1 below). Table 1. Advantages and Disadvantages of Specialized Support Surfaces (Open Table in a new window)
These support surfaces may be divided into dynamic systems, which require an energy source to alternate pressure points, and static systems, which rely on redistribution of pressure over a large surface area and do not require an energy source. Each device may be further described as either pressure-reducing or pressure-relieving. Pressure-relieving devices consistently reduce pressure below capillary closing pressure; pressure-reducing devices keep pressures lower than standard hospital beds but not consistently below capillary closing pressure. These pressure-relief surfaces are often heavy, expensive, and difficult to clean, and they require ongoing maintenance to ensure proper function. In addition, they must be used properly to be effective. The patient’s head and shoulders should be only minimally elevated on one pillow or a foam wedge to reduce shear forces and prevent the patient from “bottoming out” or having the sacrum or ischial tuberosities resting on the bed frame. In a comparative study, two different cushions to prevent heel pressure injuries were investigated: a wedge-shaped, bed-wide, viscoelastic foam cushion and an ordinary pillow. [84] The patients using the wedge-shaped cushion had a decreased incidence of heel pressure injuries, and the probability of remain free of pressure injuries remained higher. To date, relatively few clinical trials have been performed to evaluate the effectiveness of specialized support surfaces. Those that have been published have mostly been based on evaluation of tissue interface pressure, which is the force per unit area that acts perpendicularly between the body and the support surface and serves as an approximation of capillary closing pressure. [79, 80, 85, 81, 86, 87, 88, 89, 82, 83, 51] Clinical trials for prevention and treatment of pressure injuries have been performed on air-fluidized and low-air loss beds. [50, 90, 91, 92] Although there is evidence that all of these surfaces can help prevent or treat pressure injuries can be prevented or improved, no data suggest that one support surface consistently performs better than all others in all circumstances. [50, 91, 93, 94, 95, 96] Therefore, patients should be actively treated on an individual basis to reduce specific risk factors. A systematic review concluded that special foam mattresses designed to prevent pressure injuries were generally more effective than standard mattresses in patients at risk. [97] Organizations might consider the use of pressure-relief devices for high-risk patients in the operating room because this is associated with a reduction in the postoperative incidence of pressure injuries. An updated systematic study not only confirmed the benefit of higher-specification foam mattresses but also suggested that sheepskin overlays were beneficial as well. [98] One of the trials included in this analysis determined that alternating-pressure mattresses may be more cost effective than alternating-pressure overlays; a further update confirmed this determination. [99] Several studies found only limited evidence when higher-technology products were compared. [100, 97] Selection of a support surface should be based on the patient’s management plan, his or her risk factors for developing pressure injuries, and the cost of obtaining and servicing the device. [85, 101] A dynamic management plan for each individual should include discontinuing the use of a support surface when it is determined that the patient is no longer at risk for developing pressure injuries. [50, 93, 94, 102, 103] Any individual thought to be at risk for developing pressure injuriesshould be placed on a pressure-reducing device (eg, foam, static air, alternating air, gel, or water) when lying in bed to relieve pressure on the heels. [104, 102, 105, 106, 107, 108] For persons who use a wheelchair, pressure-reducing devices of foam, gel, air, or a combination of these materials should be used. [109, 86, 110, 111, 112] Pressure-reducing devices should be used in addition to standard nursing care. [4, 113, 114] The Agency for Healthcare Policy and Research (AHCPR) Pressure Ulcer Panel has developed guidelines for managing existing pressure ulcers (see Guidelines). [104, 26, 115, 116, 117, 91, 93, 96, 118, 10, 50, 118, 119] Wound ManagementDébridement and debriding agentsThe purpose of wound débridement is to remove all materials that promote infection, delay granulation, and impede healing, including necrotic tissue, eschar, and slough (ie, the stringy yellow, green, or gray nonviable debris in an ulcer). Accurate injury staging cannot be accomplished until necrotic tissue is removed. [120] The following three débridement procedures are commonly used:
Povidone-iodine solution can be used to debride infected wounds. Although the effervescent action of hydrogen peroxide results in wound débridement, it is not recommended for frequent or long-term use in pressure injuries, because it indiscriminately removes necrotic material and fragile granulation tissue and because it and other cleansing agents have been found to be toxic to fibroblasts. [124, 125, 121] Once débridement has been completed and clean granulation tissue has been established, the use of debriding agents should be discontinued, and the site should be kept clean and moist. [125] Solutions for wound cleansingThe major purpose of cleansing the wound is to decrease its bioburden and facilitate healing. [71, 124] When no germicidal action is required, normal saline is used. Saline solution should also be used as a rinse after other solutions are used to irrigate the wound and minimize fluid shifts within newly forming tissue. Normal saline solution can reduce the drying effects that some irrigants may have on tissue. [71, 126] Povidone-iodine is useful against bacteria, spores, fungi, and viruses. Dilution is recommended, and this agent should be discontinued when granulation occurs. [71] Laboratory data demonstrate that povidone-iodine is toxic to fibroblasts in vitro, a finding that has theoretical implications for wound healing. Because povidone-iodine can affect thyroid function, it could be contraindicated for some patients. [126] Acetic acid (0.5%) is specifically effective against Pseudomonas aeruginosa, a particularly difficult and common organism in fungating lesions. Acetic acid can change the color of tissue and can mask potential superinfection. Rinsing with normal saline also is recommended. [126] Sodium hypochlorite (2.5%) has some germicidal activity but is primarily used to debride necrotic tissue. Before it is used, zinc oxide should be placed around the edges of the wound to reduce the amount of irritation. [71] After cleansing with sodium hypochlorite, normal saline should be used as a rinse. [126] A multitude of cleansing agents are on the market, but none has been shown to be more efficacious than the others, and expert opinion still favors normal saline. [121] Wound dressingsThe choice of wound dressings varies with the state of the wound, the goal being to achieve a clean, healing wound with granulation tissue. A stage 1 pressure injury may not require any dressing. For more advanced injuries, various dressing options are available (see Table 2 below). Table 2. Key Performance Characteristics of Major Wound Dressing Types (Open Table in a new window)
Hydrocolloid dressings form an occlusive barrier over the wound while maintaining a moist wound environment and preventing bacterial contamination. A gel is formed when wound exudate comes in contact with the dressing. This gel can have fibrillolytic properties that enhance wound healing, protect against secondary infection, and insulate the wound from contaminants. [52, 127] Hydrocolloids help prevent friction and shear and may be used in stage 1, 2, 3, and some stage 4 pressure injuries with minimal exudate and no necrotic tissue. Gel dressings are available in sheet form, in granules, and as liquid gel. All forms of gel dressings keep the wound surface moist as long as they are not allowed to dehydrate. Some gel dressings provide limited to moderate absorption, some provide insulation, and some provide protection against bacterial invasion. All gel dressings allow atraumatic removal. [121, 52, 128] Transparent adhesive dressings are semipermeable and occlusive. They allow gaseous exchange and transfer of water vapor from the skin and prevent maceration of healthy skin around the wound. In addition, they are nonabsorptive, reduce secondary infection, and allow atraumatic removal. These dressings minimize friction and shear and may be used in shallow stage 1, 2, and 3 pressure injuries with minimal exudate and no necrotic tissue; however, they do not work well on patients who are diaphoretic or have wounds with significant exudation. [52] Alginate dressings are semiocclusive, highly absorbent, and easy to use. [129, 130] They are natural, sterile, nonwoven dressings derived from brown seaweed. Alginate forms a gel when it comes into contact with wound drainage, and may be used in light to heavily draining stage 2, 3, and 4 injuries. It may be used in both infected and noninfected wounds [129] ; however, it should not be applied to dry or minimally draining wounds, as it can cause dehydration and delay wound healing. Wounds with surface debris or fibrinous exudate may be mechanically debrided with wet-to-dry dressings incorporating normal saline or enzymatically debrided with collagenase. Wounds with a high level of bacterial contamination may benefit from wound irrigation. It has been shown that irrigation by low-pressure pulsatile lavage therapy with saline is more effective than continuous saline irrigation in decreasing bacterial loads within wounds. [131] Vacuum-assisted closure (VAC) sponges conform to the wound surface by suction and stimulate wound contracture while removing exudate and edema. Daily whirlpool therapy or pulse lavage therapy may be used to irrigate and mechanically debride the wound. The choice of dressings is not as important as their appropriate application. The following points should be kept in mind:
Antimicrobials and antibioticsAntibiotic creams such as silver sulfadiazine may be applied to wounds to decrease bacterial load. Silver sulfadiazine has an excellent antimicrobial spectrum of activity, low toxicity, ease of application, and minimal pain. It inhibits DNA replication and modification of the cell membrane of Staphylococcus aureus; Escherichia coli; Candida albicans; Klebsiella, Pseudomonas, and Proteus species; and Enterobacteriaceae. Mafenide, an antimicrobial agent that is bacteriostatic to many gram-positive and gram-negative organisms, including Pseudomonas aeruginosa, can penetrate an eschar and promote autolytic softening of the eschar prior to débridement. Evaluation of a patient with an infected wound should follow an algorithmic approach. The following questions should be asked:
The adverse effects of antibiotics are well known, and those that impede wound healing should be considered and counteracted. Antibiotic resistance is a major concern. Therefore, when antibiotic therapy is ordered, the wound care specialist must be alert to detect signs of antibiotic resistance, and he or she must be attentive to the results of the laboratory data, especially culture and sensitivity results. Patients who are immunocompromised or have impaired chemotaxis resulting in bacterial overgrowth or candidiasis need concomitant treatment with selected antimycotic or antifungal agents. Other considerations in prescribing an antibiotic include the patient’s length of hospital stay, the availability of home health services and infusion services, the influence of the pharmacy and therapeutics committee, the hospital’s formulary, and the influence of the payer’s approval of prescription benefits. Other wound treatmentsA wide variety of additional therapeutic methods are being evaluated for the treatment of chronic wounds, specifically for pressure injury management. [132] These include electrotherapy, [133, 134] application of growth factors, [135, 136, 137, 57] and preventive use of free radical scavengers and special drug delivery systems. [138, 139, 140] The recombinant human platelet-derived growth factor becaplermin has been approved by the US Food and Drug Administration (FDA) for the treatment of lower-extremity diabetic neuropathic ulcers that extend into the subcutaneous tissue or beyond. Studies are underway to explore the possibility of expanding its approved indications to include other wounds. Other growth factors also are being evaluated for use in human clinical settings. Another potentially promising treatment option is NPWT using VAC. [141, 142, 143] NPWT enhances wound healing by reducing edema, increasing the rate of granulation tissue formation, and stimulating circulation. Increased blood flow translates into a reduction in the bacterial load (removal of interstitial tissue) and delivery of infection-fighting leukocytes. [144] The following are general indications for NPWT [145] :
The following are general contraindications for NPWT [145] :
Principles of Surgical InterventionEven with optimal medical management, many patients require a trip to the operating room for débridement, diversion of the urinary or fecal stream, release of flexion contractures, wound closure, or amputation. Débridement is aimed at removing all devitalized tissue that serves as a reservoir for ongoing bacterial contamination and possible infection. Extensive débridement should be done in the operating room, but minor débridement is commonly performed at the bedside. Although many of these patients are insensate, others are unable to communicate pain sensation. Pain medication should be administered liberally, and vital signs may indicate pain perception. Care should be taken with bedside débridement because wounds may bleed significantly. Urinary or fecal diversion may be necessary to optimize wound healing. Many of these patients are incontinent and their wounds are contaminated with urine and feces daily. Patients with loose stools benefit from constipating agents and a low-residue diet. Release of flexion contractures resulting from spasticity may assist with positioning problems, and amputation may be necessary for a nonhealing wound in a patient who is not a candidate for reconstructive surgery. Reconstruction of a pressure injury is aimed at improvement of patient hygiene and appearance, prevention or resolution of osteomyelitis and sepsis, reduction of fluid and protein loss through the wound, and prevention of future malignancy (Marjolin ulcer). In general, stage 3 and 4 pressure injuries tend to require flap reconstruction. The first step is adequate excision of the injury, including the bursa or lining, surrounding scar tissue, and any heterotopic calcification found. Underlying bone must be adequately debrided to ensure that there is no retained nidus of osteomyelitis. Some evidence in the literature indicates that pulsed lavage can be beneficial in reducing bacterial counts in wounds, and some surgeons routinely use this method after débridement. Once the wound has been appropriately debrided, it may be closed in a variety of ways, depending on the location of the pressure injury, any previous scars or operations, and the surgeon’s individual preference. However, the basic tenets of reconstruction remain the same in all pressure injury reconstructions. Very few pressure injuries can or should be closed primarily after débridement, given the unacceptably high complication rates. A well-vascularized pad of tissue should be placed in the wound, usually a musculocutaneous flap transposed or rotated on a pedicle containing its own blood supply. This also may involve the use of tissue expansion or a free flap with microvascular anastomosis. The goals are to eliminate dead space in the wound, enhance perfusion, decrease tension on the closure, and provide a new source of padding over the bony prominence. Before wound closure, drains should be placed in the bed of the wound. This allows external drainage of any fluid that may accumulate beneath the flap and should help minimize wound complications such as hematoma and seroma. Surgical DébridementOnce the decision has been made to reconstruct, the wound is debrided. It should be noted that débridement of a pressure injury that will be reconstructed is different from débridement of a pressure injury that will be treated conservatively (ie, allowed to heal by secondary intention). Pressure injuries that are treated conservatively are not radically debrided; they need only be debrided of obvious necrotic tissue. For pressure injuries that will be reconstructed, a radical bursectomy is performed to prevent the development of infection or seroma under the flap. This radical bursectomy is technically achieved by placing a methylene blue–moistened sponge in the bursa and excising the pressure injury circumferentially, removing all granulation tissue, even from the wound base (see the image below). Radical bursectomy is performed by placing methylene blue–moistened sponge in bursa and excising pressure ulcer circumferentially, removing all granulation tissue, even from wound base.After the bursectomy, primary closure of the pressure injury is almost always under tension and is therefore doomed to fail if attempted. Other technical points of pressure injury reconstruction include radically removing underlying necrotic bone, padding of the bone stump, filling the dead space with muscle, using a large flap, achieving adequate flap mobilization to avoid tension, and avoiding adjacent flap territories to preserve options to reconstruct other locations. Options for Wound ClosureSeveral options are available for surgical management of pressure injuries, including direct closure, skin grafting, skin flaps, and musculocutaneous flaps. Such management can provide skin coverage as well as soft tissue coverage. Flaps containing muscle provide a physiologic barrier to infection, eliminate dead space in the wound, and improve vascularity. Improved vascularity enhances local oxygen tension, provides extended soft-tissue penetration for antibiotics, and improves total lymphocyte function. [146, 147, 148] The patient should be medically stable and able to benefit from the procedure. The patient should also participate in the decision. The nutritional status of the patient must be considered because good nutritional parameters are required for good wound healing and immune function. Involuntary muscle spasms should be controlled preoperatively with baclofen or diazepam. Factors associated with impaired healing should be corrected preoperatively. Tobacco use and smoking are associated with intrinsic factors that compromise wound healing. [149] For example, carbon monoxide and nicotinic acid are potent vasoconstrictors that increase blood viscosity. [150] These factors predispose tissue to excessive oxidase activity and free radical injury. Under normal conditions, the body is able to handle normal oxidative stress. However, with excessive stress comes increased risk for development of pressure injuries and impaired wound healing. A neutrophil-mediated free radical injury results in excessive oxidase activity, which can cause vascular damage and thrombosis, leading to cell death and tissue destruction. [138, 139, 140] Patient positioning is dictated by the location of the ulcer and the planned reconstruction. Many pressure ulcers occur in the gluteal region and require prone positioning. Most anesthesiologists choose to use general endotracheal anesthesia, particularly if the patient is prone, but ulcer closure may be performed under regional or local anesthesia if necessary. Significant blood loss is possible; accordingly, 2 units of type-specific packed red blood cells should be available during the operation. Arrangements should be made to have a pressure-reducing mattress available for the postoperative period to reduce the risk of immediate recurrence or dehiscence. If urinalysis and urinary culture findings (ie, nitrites, leukocyte esterase) confirm the presence of a urinary tract infection (UTI), appropriate treatment should be provided. Direct closureAlthough direct closure is the simplest approach, pressure injuries considered for surgical treatment are usually too large to be amenable to direct primary closure. Because these wounds are tense as a result of large soft-tissue defects, direct closure can lead to wound defects, excessive wound tension, and a paucity of soft-tissue coverage. Tissue expanders have been used to provide more skin surface and to facilitate closure. [151] Skin graftsSplit-thickness skin grafts can be used to repair shallow defects and pressure injuries, but their main disadvantage is that they provide only a skin barrier. When applied directly to granulating bone, skin grafts quickly erode, thus precluding healing. They also cause scars in the area from which the skin is harvested, and the transplanted skin is never as tough as the original skin. Skin flapsBefore the 1970s, repair using local full-thickness skin flaps was the standard surgical treatment for pressure injuries; today, it is typically employed as an alternative to secondary repair. [152] Local skin flaps have a random vascular supply, and the tissue repair is essentially a redistribution of inadequately perfused tissue rather than a planned revascularization that makes use specific blood vessels. Myocutaneous flapsMyocutaneous (musculocutaneous) flaps are usually the best choice for patients with spinal cord injuries (SCIs) and for those who have a loss of muscle function that does not contribute to a comorbidity. For patients who are ambulatory, the choice is less clear, in that the improved blood supply and reliability of the muscle flap must be balanced against the need to sacrifice functional muscle units. [153, 154, 155] Myocutaneous flaps can help heal osteomyelitis and limit the damage caused by shearing, friction, and pressure. [156, 157, 158] They bring muscle and skin to the area of the defect and are probably as resistant to future pressure injuries as the original skin. Free flapsFree flaps are muscle-type flaps in which the vein and artery are disconnected at the donor site and subsequently reconnected to the vessels at the recipient site with the aid of a microscope. This is the most complex method of wound closure and would be considered only after all other options for reconstruction have been exhausted. In paraplegic patients dependent on their upper body for mobility, the latissimus dorsi would typically be an unacceptable donor for free tissue transfer; however, a portion of the muscle may be used with limited donor site morbidity. A protocol for postoperative care must be followed strictly for free flap survival. [159] Surgical Management of Specific Pressure Injury TypesThe choice of reconstruction approach depends on the location of the pressure injury. Ischial pressure injuryThe ischial location is the most common site of pressure injury in individuals with paraplegia. In the course of excisional débridement in preparation for flap repair of an ischial wound, aggressive resection of the ischial tuberosity may raise the risk of a contralateral ischial pressure injury from increased contralateral pressure. Bilateral ischiectomy increases pressure on the perineum and thus increases the risk of perineal pressure injury. Recurrence of the pressure injury is common in the ischial location. [160] Therefore, the first option for reconstruction of ischial wounds is the gluteal thigh rotation flap, which does not preclude the future use of the inferior portion of the gluteus maximus muscle. [161, 162] The gluteal thigh rotation flap is an axial flap based on the inferior gluteal artery. Both the biceps femoris flap and the hamstring myocutaneous flap transect the inferior gluteal artery. With the gluteal thigh flap, a superiorly based flap is elevated, with its axis being the inferior gluteal artery located between the greater trochanter and the ischial tuberosity (see the image below). With gluteal thigh flap, superiorly based flap is elevated, with inferior gluteal artery located between greater trochanter and ischial tuberosity as its axis.The gluteal thigh rotation flap is raised as a fasciocutaneous flap superiorly to the gluteal crease (see the image below). Gluteal thigh rotation flap is raised as fasciocutaneous flap superiorly to gluteal crease.The gluteal thigh flap may be raised to include the inferior portion of the gluteus maximus. This increases the arc of rotation and allows the flap to be used to reconstruct sacral defects (see the image below). [161] Gluteal thigh flap may be raised to include inferior portion of gluteus maximus, which increases arc of rotation to allow flap also to be used to reconstruct sacral defects.Another popular option for ischial reconstruction, the inferior gluteus maximus myocutaneous flap, limits options for reconstruction of sacral wounds. Bilateral V-Y advancement flaps, inferiorly based random flaps, and superior gluteal myocutaneous flaps are not options for sacral reconstruction if an inferior gluteal myocutaneous flap has been used. Additional options described for ischial reconstruction include the hamstring myocutaneous flap, the biceps femoris myocutaneous flap, the tensor fasciae latae (TFL) flap, the gracilis myocutaneous flap, [160] and the medially based posterior thigh skin flap with or without the biceps femoris. Sacral pressure injurySacral pressure injuries (see the image below) are common in patients who have been on prolonged bed rest. Treatment involves complete excision, including the entire bursa, and conservative ostectomy. Sacral pressure ulcer before and after flap closure.Small sacral pressure injuries can be reconstructed with an inferiorly based skin rotation flap, with or without a superior gluteus maximus myocutaneous flap (see the images below). The use of the random skin rotation flap does not preclude later use of the gluteus maximus. When a random skin rotation flap is used, it is essential to design a large and wide flap with an axis of rotation that permits tension-free closure. Small sacral pressure sores can be reconstructed with the inferior-based skin rotation flap, with or without the superior gluteus maximus myocutaneous flap. Small sacral pressure ulcer reconstructed with inferiorly based skin rotation flap. Small sacral pressure ulcer reconstructed with inferiorly based skin rotation flap.With a superior gluteal myocutaneous flap, a wide skin rotation flap is elevated with the superior portion of the gluteus maximus. Landmarks for the superior gluteal artery on which this flap is based include the posterior superior iliac spine (PSIS) and the ischial tuberosity (see the image below). Landmarks for superior gluteal artery, on which superior gluteus maximus muscle flap is based, include posterior superior iliac spine and ischial tuberosity.The superior and inferior gluteal arteries branch from the internal iliac artery superior and inferior to the piriformis approximately 5 cm from the medial edge of the origin of the gluteus maximus from the sacrococcygeal line (from PSIS to coccyx; see the image below). Superior and inferior gluteal arteries branch from internal iliac superior and inferior arteries to piriformis approximately 5 cm from medial edge of origin of gluteus maximus from sacrococcygeal line.When the superior portion of the gluteus maximus muscle is used as a flap, it is elevated in a lateral-to-medial direction to keep from injuring the superior gluteal artery, which can be difficult to identify from the medial direction because of the inflammation and scarring associated with the sacral pressure injury. The insertion of the superior portion of the gluteus maximus is the iliotibial tract; this insertion is released. When superior portion of gluteus maximus is used as flap, it is elevated in lateral-to-medial direction to avoid injury to superior gluteal artery. Insertion of superior portion of gluteus maximus into iliotibial tract is released. Harvesting entire length of muscle may be necessary to allow rotation or turnover into defect without tension.The superior gluteal artery is only 4 cm long, which limits the rotation of the muscle. Thus, harvesting the entire length of the muscle may be necessary to allow for rotation or turnover into the defect without tension. Larger sacral pressure injuries require the use of bilateral flaps such as bilateral V-Y myocutaneous advancement flaps (see the first image below). V-Y flaps can be based on the superior, inferior, or entire gluteus maximus, depending on the location of the pressure injury (see the second image below). Larger sacral ulcers require use of bilateral flaps, such as bilateral V-Y advancement flaps. V-Y flaps can be based superiorly or inferiorly or on entire gluteus maximus.The V should be fashioned wide enough and long enough to permit closure as a Y without tension. The medial edge of the origin of the gluteus maximus is elevated in a medial-to-lateral direction for approximately 4 cm because the superior and inferior gluteal arteries enter the gluteus maximus 5 cm from its origin. Release of the gluteal muscle insertion laterally is important for medial advancement and tension-free approximation of the muscles medially. Inflamed fibrous tissue along the medial muscle edge can be preserved and used to hold sutures for midline muscle approximation. Another option for sacral reconstruction is the transverse lumbosacral flap. [163] Trochanteric pressure injuryTrochanteric pressure injuries are less common and are typically associated with minimal skin loss. Excisional debridement of these injuries in preparation for flap repair involves resection of the entire bursa and greater trochanter of the femur. The first option for reconstruction of trochanteric pressure injuries is the TFL flap, a myocutaneous flap based on the lateral femoral circumflex artery. [164] The TFL is 13 cm long, 3 cm wide, and 2 cm thick, and it originates from the anterior superior iliac spine (ASIS) and the iliac crest and inserts into the iliotibial tract. The skin paddle is harvested in a width of 10 cm and designed over the muscle along an axis from the ASIS to the lateral tibial condyle (see the image below). Skin paddle is harvested 10 cm in width and designed over muscle along axis from anterior superior iliac spine to lateral tibial condyle.The inferior limit of the cutaneous territory can be extended to 6 cm above the knee and 25-35 cm in length (see the image below). The lateral femoral circumflex artery can be found approximately 6-8 cm inferior to the ASIS. In patients with lumbar lesions, a sensate TFL flap can be designed to include the T12 dermatome by fashioning the flap to include the area 6 cm posterior to the ASIS. Inferior limit of cutaneous territory can be extended to 6 cm above knee and 25-35 cm in length. Lateral femoral circumflex artery can be found approximately 6-8 cm inferior to anterior superior iliac spine.Other described modifications of the TFL flap include the retroposition V-Y flap and the bipedicled TFL flap. Other options for trochanteric pressure injury reconstruction include the vastus lateralis myocutaneous flap, the gluteal thigh flap, and the anterior thigh flap. Multiple pressure injuriesMultiple pressure injuries may be observed in the same patient. Reconstruction of multiple injuries may require the use of a total thigh flap (see the image below). The total thigh flap is a long and formidable operation that typically involves the transfusion of 6-20 units of blood. It should be reserved for use as a salvage procedure when other attempts have been unsuccessful. Patients who have undergone a unilateral total thigh flap can sit a wheelchair (see image below). Patient required reconstruction of extremely large pressure ulcer with fillet total thigh flap procedure.Postoperative CareIn terms of the ultimate success or failure of pressure injury reconstruction, the work done in the operating room is only the first step. Once a pressure injury has been successfully closed, appropriate postoperative care must be initiated to encourage wound healing and to reduce the risk of complications such as recurrence. From the time of transfer from the operating table to the air-fluid bed, care must be exercised to prevent shearing and tension across the flap repair. Patients are positioned flat in the air-fluid bed for 4 weeks. After 4 weeks, the patient can be placed carefully into a semisitting position. At 6 weeks after surgery, the patient begins sitting, initially for only 10 minutes at a time. After these sitting periods, the flap should be evaluated for discoloration and wound edge separation. Over 2 weeks, the sitting periods are increased in 10-minute increments until they reach 2 hours. Patients are taught to lift themselves to relieve pressure for 10 seconds every 10 minutes. Skin care must be performed daily. This involves careful inspection of all skin surfaces to identify areas of impending breakdown before the breakdown occurs. (An often overlooked detail is to remove compression stockings and inspect the heels.) Skin should be washed with soap and water and completely dried. Moisture should not be allowed to accumulate on the skin or in clothing or bedding, nor should the skin be allowed to become overly dry and scaly. Skin moisturizers are useful to maintain the appropriate level of moisture at the skin surface. Patients may benefit from transfer to a subacute or rehabilitation facility after wound closure. This allows them to receive ongoing education, observation, and rehabilitative therapies before returning to their usual place of residence. ComplicationsComplications as a result of reconstructive surgery are, unfortunately, considerable. Such complications include the following:
With the use of well-vascularized flaps, flap necrosis is infrequent. Treatment of patients with pressure injuries involves several perioperative considerations to minimize the risk of adverse outcomes of the reconstruction, as follows:
Even with close adherence to these guidelines, pressure injury recurrence rates are high. In caring for patients with chronic pressure ulcers, it is essential to plan flap procedures carefully and provide social resources unstintingly to reduce the high risk of adverse outcomes in this complication-prone population. ActivityAfter successful wound closure, ambulatory patients should be out of bed with assistance as soon as possible. More strenuous physical activity should be delayed for approximately 6 weeks. In patients with ischial tuberosity pressure injuries, sitting may be resumed 6 weeks after a healed wound is achieved. Sitting may be gradually reintroduced over several weeks, and detailed guidelines have been published. Because of the extremely high pressures generated over the ischial tuberosities during sitting, wheelchair patients should lift themselves out of their seat or rock back in the chair every 15 minutes. These recommendations regarding the resumption of activity vary according to the clinical situation and are implemented at the discretion of the treating physician. PreventionAlthough in principle, pressure injuries are preventable and should not occur, they continue to be among the most pervasive and perplexing problems encountered in the treatment of persons who are ill, recovering from illness, or functionally impaired. In 2016, the Wound, Ostomy and Continence Nurses Society (WOCN) issued guidelines for the prevention and management of pressure ulcers (injuries). [165] (See Guidelines.) In 2017, the WOCN Society issued an updated position statement on the topic of avoidable and unavoidable pressure ulcers (injuries). [166] This statement defined unavoidable pressure ulcers as those that develop even though the patient's clinical condition and pressure ulcer risk factors were properly evaluated and interventions consistent with patient needs, management goals, and standards of practice were implemented, monitored, and revised as appropriate. To the extent that prevention is achievable, it is the optimal form of treatment. Prevention of pressure ulcers has two main components: identification of patients at risk and interventions designed to reduce the risk. Identification of patients at riskVarious approaches to the identification of persons at risk for the formation of pressure injuries have been tested. A person who uses a wheelchair, is in bed for most of the day, or has impaired ability to reposition the body should be assessed for additional factors that increase risk of pressure injuries. General physical and mental condition, nutritional status, activity level, mobility, and degree of bowel and bladder control are all known to affect this risk. [51, 167, 122, 113] A simple clinical prediction rule based on five patient characteristics may help identify patients who are at increased risk for pressure injury development and thus in need of preventive measures. Detection of a stage 2 or worse pressure injury during admission to the hospital is directly related to the following independent predictors of pressure injuries [168] :
A systematic assessment of pressure injury risk can be accomplished by using a assessment tool such as the Braden scale or the Norton scale (see Table 3 below). No information is currently available to suggest that adaptations of these risk assessment tools or the assessment of any single risk factor or a combination of risk factors predicts risk as well as the overall scores obtained with these tools. [169, 170] Table 3. Norton and Braden Scales for Assessing Pressure Ulcer Risk (Open Table in a new window)
In 1992, the Agency for Health Care Policy and Research (AHCPR), now known as the Agency for Healthcare Research and Quality (AHRQ), developed guidelines for the prediction and prevention of pressure ulcers in adults. [9] In 1994, these guidelines were followed by guidelines for the treatment of these lesions. [121] According to the AHPCR prevention guidelines, risk assessment should include the following [9] :
Prime candidates for pressure ulcers include the following [9] :
Secondary factors include the following [9] :
The WOCN Society has also issued guidelines on preventing pressure injuries (see Guidelines). [165] Interventions for minimizing riskEffective prevention of pressure injuries depends on a comprehensive care plan that includes strategies and practices aimed at reducing or eliminating the risk of these injuries. Elements of such a plan may include the following:
All interventions should be monitored and documented. Specific details that are required include who should provide the care, how often it should be provided, and the supplies and equipment needed. How the care is to be undertaken should be individualized, written down, and readily available. Results of the interventions and the care being rendered should be documented. To ensure continuity, documentation of the plan of care should be clear, concise, and accessible to every caregiver. Patient education is also essential. In a study assessing the results of a long-term acute care hospital’s program to reduce the occurrence of pressure injuries, the hospital traced its apparently above-average ulcer prevalence rates to the lack of wound care professionals, methods for consistently documenting prevention and wound data, and an interdisciplinary wound care team approach. [173] By addressing these issues, the hospital was able to reduce the prevalence of facility-acquired pressure injuries from 41% to an average of 4.2% over a 12-month period. ConsultationsA multidisciplinary approach can yield maximal benefit. Neurosurgery, urology, plastic surgery, orthopedic surgery, and general surgery consultations all may be indicated in a given case. Rehabilitation medicine specialists, social workers, and psychologists or psychiatrists may work with geriatricians and internists to improve the patient’s health, attitude, support structure, and living environment. Plastic surgeons perform most pressure injury reconstructions; a plastic surgery consultation is appropriate with any complex or chronic wound. Long-Term MonitoringFollow-up should be performed every 3 weeks for the first several months. The interval may then be increased to every 6 months and then yearly. Early issues include suture removal, drain removal, and when to allow the patient to exercise or sit up. Concise documented measurement of the wound healing process contributes to efficient management. The most common method of monitoring the healing of pressure injuries utilizes photography and diagrams. [57] Another method is to measure the volume (volumetrics) and the dimensions of the pressure injury wound (eg, by using a measured amount of saline to infer the volume of the wound). Sophisticated radiographic techniques are available for this purpose as well, but they are too expensive for routine use. Once healing is complete, long periods of uninterrupted pressure must be avoided. Patients must be repositioned frequently, either by their own efforts or with help from their support group. Seated patients with upper-extremity function should lift themselves from their wheelchair for at least 10 seconds every 10-15 minutes. Patients in bed should be repositioned at least every 2 hours. Pressure dispersion, through the application of specialized support surfaces on beds and wheelchairs, should be extended through the wound healing period and into the outpatient setting if available and tolerated by the patient. This is an adjunct to the alternating of weightbearing surfaces and maintains low pressures on the tissues at all times. Control of spasticity and maintenance of adequate nutrition also must be continued into the outpatient setting to prevent recurrence. After they return home, patients may benefit from visits from a home health care organization. Such visits may ease the transition and ensure that pressure avoidance strategies are adapted to the home and continued over the long term.
Author Chief Editor John Geibel, MD, MSc, DSc, AGAF Vice Chair and Professor, Department of Surgery, Section of Gastrointestinal Medicine, Professor, Department of Cellular and Molecular Physiology, Yale University School of Medicine; Director of Surgical Research, Department of Surgery, Yale-New Haven Hospital; American Gastroenterological Association Fellow; Fellow of the Royal Society of Medicine John Geibel, MD, MSc, DSc, AGAF is a member of the following medical societies: American Gastroenterological Association, American Physiological Society, American Society of Nephrology, Association for Academic Surgery, International Society of Nephrology, New York Academy of Sciences, Society for Surgery of the Alimentary Tract Disclosure: Nothing to disclose. Acknowledgements Kat Kolaski, MD Assistant Professor, Departments of Orthopedic Surgery and Pediatrics, Wake Forest University School of Medicine Kat Kolaski, MD is a member of the following medical societies: American Academy for Cerebral Palsy and Developmental Medicine and American Academy of Physical Medicine and Rehabilitation Disclosure: Nothing to disclose. Consuelo T Lorenzo, MD Physiatrist, Department of Physical Medicine and Rehabilitation, Alegent Health Immanuel Rehabilitation Center Consuelo T Lorenzo, MD is a member of the following medical societies: American Academy of Physical Medicine and Rehabilitation Disclosure: Nothing to disclose. Joseph A Molnar, MD, PhD, FACS Director, Wound Care Center, Associate Director of Burn Unit, Associate Professor, Department of Plastic and Reconstructive Surgery, Wake Forest University School of Medicine Joseph A Molnar, MD, PhD, FACS is a member of the following medical societies: American Association of Plastic Surgeons, American Burn Association, American College of Surgeons, American Medical Association, American Society for Parenteral and Enteral Nutrition, American Society of Plastic Surgeons, North Carolina Medical Society, Peripheral Nerve Society, Undersea and Hyperbaric Medical Society, and Wound Healing Society Disclosure: Abbott Laboratories Honoraria Speaking and teaching; Clincal Cell Culture Grant/research funds Co-investigator; KCI, Inc Wake Forest University receives royalties Other Michael Neumeister, MD, FRCSC, FRCSC, FACS Chairman, Professor, Division of Plastic Surgery, Director of Hand/Microsurgery Fellowship Program, Chief of Microsurgery and Research, Institute of Plastic and Reconstructive Surgery, Southern Illinois University School of Medicine Michael Neumeister, MD, FRCSC, FRCSC, FACS is a member of the following medical societies: American Association for Hand Surgery, American Association of Plastic Surgeons, American Burn Association, American College of Surgeons, American Medical Association, American Society for Reconstructive Microsurgery, American Society for Surgery of the Hand, American Society of Plastic Surgeons, Association of Academic Chairmen of Plastic Surgery, CanadianSocietyofPlastic Surgeons, Illinois State Medical Society, Illinois State Medical Society, Ontario Medical Association, Plastic Surgery Research Council, Royal College of Physicians and Surgeons of Canada, and Society of University Surgeons Disclosure: Nothing to disclose. Adrian Popescu, MD Research Fellow, Department of Physical Medicine and Rehabilitation, University of Pennsylvania School of Medicine Disclosure: Nothing to disclose. Patrick J Potter, MD, FRCP(C) Associate Professor, Department of Physical Medicine and Rehabilitation, University of Western Ontario School of Medicine; Consulting Staff, Department of Physical Medicine and Rehabilitation, St Joseph's Health Care Centre Patrick J Potter, MD, FRCP(C) is a member of the following medical societies: American Paraplegia Society, Canadian Association of Physical Medicine and Rehabilitation, Canadian Medical Association, College of Physicians and Surgeons of Ontario, Ontario Medical Association, and Royal College of Physicians and Surgeons of Canada Disclosure: Nothing to disclose. Don R Revis Jr, MD Consulting Staff, Department of Surgery, Division of Plastic and Reconstructive Surgery, University of Florida College of Medicine Don R Revis Jr, MD is a member of the following medical societies: American College of Surgeons, American Medical Association, American Society for Aesthetic Plastic Surgery, and American Society of Plastic Surgeons Disclosure: Nothing to disclose. Richard Salcido, MD Chairman, Erdman Professor of Rehabilitation, Department of Physical Medicine and Rehabilitation, University of Pennsylvania School of Medicine Richard Salcido, MD is a member of the following medical societies: American Academy of Pain Medicine, American Academy of Physical Medicine and Rehabilitation, American College of Physician Executives, American Medical Association, and American Paraplegia Society Disclosure: Nothing to disclose. Wayne Karl Stadelmann, MD Stadelmann Plastic Surgery, PC Wayne Karl Stadelmann, MD is a member of the following medical societies: Alpha Omega Alpha, American College of Surgeons, American Society of Plastic Surgeons, New Hampshire Medical Society, Northeastern Society of Plastic Surgeons, and Phi Beta Kappa Disclosure: Nothing to disclose. Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference Disclosure: Medscape Salary Employment Bradon J Wilhelmi, MD Professor and Endowed Leonard J Weiner, MD, Chair of Plastic Surgery, Residency Program Director, University of Louisville School of Medicine Bradon J Wilhelmi, MD is a member of the following medical societies: Alpha Omega Alpha, American Association for Hand Surgery, American Association of Clinical Anatomists, American Association of Plastic Surgeons, American Burn Association, American College of Surgeons, American Society for Aesthetic Plastic Surgery, American Society for Reconstructive Microsurgery, American Society for Surgery of the Hand, American Society of Plastic Surgeons,Association for Surgical Education, Plastic Surgery Research Council, and Wound Healing Society Disclosure: Nothing to disclose. Acknowledgments The authors and editors of Medscape Reference gratefully acknowledge the contributions of Steve Jenkins in the Department of Physical Medicine and Rehabilitation at the University of Kentucky for his significant editorial assistance in preparing this article. Dr Richard Salcido acknowledges that his studies cited in this article are supported by the National Heart, Lung and Blood Institute, the National Institutes of Health grant P01HL36552-07, the National Center for Medical Rehabilitation Research grant R01HD31426-01, the Paralyzed What dressing is used for a Stage 2 pressure ulcer?Currently, hydrocolloid dressings are widely used in individuals with Category/Stage II pressure ulcers. They are also used as primary dressings in the management of Category/Stage III and IV pressure ulcers that are healing well and have become shallow.
What is the best treatment for a Stage 2 pressure ulcer?Stage II pressure sores should be cleaned with a salt water (saline) rinse to remove loose, dead tissue. Or, your provider may recommend a specific cleanser. Do not use hydrogen peroxide or iodine cleansers. They can damage the skin.
What type of dressing should a nurse use on a stage I pressure ulcer?Wound dressings for a grade 1 pressure ulcer should be simple and offer protection without risking any further skin damage, especially if the patient is sliding down the bed or chair causing the dressing to 'ruck'. A film dressing or a thin hydrocolloid would be appropriate to protect the wound area.
What kind of dressing is good for pressure sores?hydrocolloid dressings – contain a gel that encourages the growth of new skin cells in the ulcer, while keeping the surrounding healthy skin dry. other dressing types – such as foams, films, hydrofibres/gelling fibres, gels and antimicrobial (antibiotic) dressings may also be used.
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