Introduction and General Principles

Introduction

The optimal soft tissue characteristics required for coverage of defects involving the upper and lower extremity vary according to the site and location of the defect. Characteristics of interest include pliability, durability, sensibility, the ability to cover large surface areas with minimal thickness, and cosmetic appearance. These features allow the best functional outcome, maximally protect the vital structures of the extremity, and optimize the esthetic result. Consideration of donor-site morbidity and minimal disruption of local vasculature becomes more critical when considering the functional restoration of the extremity. Although soft tissue defects can occur from a variety of conditions (trauma, tumor, or infection), soft tissue coverage remains a vital operative intervention that protects underlying vital structures, such as nerves, tendons, blood vessels, and bone; preserves the integrity and continuity of musculoskeletal structures; prevents functional disability; and promotes an acceptable esthetic result. Techniques include primary wound closure, delayed primary wound closure, skin grafting, local random flaps, axial pattern flaps, island adipofascial and fasciocutaneous flaps, muscle or myocutaneous pedicled flaps, and microvascular free-tissue transfer, or free flaps. Optimal choices depend on the extent of the defect and available soft tissue donor sites.

Reconstructive Ladder and Elevator

The concept of the “reconstructive ladder,” or choosing the simplest closure or coverage option available, has been at the forefront of soft tissue reconstruction since its description by Mathes and Nahai in 1982 and assists the surgeon in choosing the best coverage option. However, this approach assumes the coverage technique as the important outcome of interest and may not optimize the reconstruction plan or the functional result in more complex cases. When this is the case, it may be prudent to choose the more complex option to facilitate the reconstruction plan and functional outcome. This paradigm has been described as the “reconstructive elevator.”

Key Points: The Reconstructive Elevator

Moving from bottom to top:

  • Free flap

  • Pedicled flap

  • Local fasciocutaneous flap

  • Skin graft

  • Primary closure

  • Wound care

Initial Evaluation

The detailed patient assessment is critical to the success of any soft tissue repair or reconstruction. The general condition of the patient and the ability to withstand reconstruction must be carefully determined. Included in this analysis is the causative aspect of the defect. In cases of trauma, the antecedent injuries need to be factored; the mechanism of injury, the degree of energy imparted to the soft tissues, and the presence of contamination will significantly affect the surgical plan. A quick analysis of the clinical problem with a template of reconstructive choices is an important and essential step at this point. Ensuring treatment will occur in the correct facility, with the appropriate resources and expertise emphasizing a multidisciplinary approach to care, will ensure the optimum outcome.

The typical approach used by plastic and reconstructive surgeons is to devise a patient-specific surgical plan that includes contingencies for every possible extent or type of defect. This is particularly important in extensive trauma, wherein the final defect after required tissue débridement may be quite different than anticipated. An algorithm, or list of options, for soft tissue reconstruction is often useful and will help the surgeon organize the surgical plan, but in the end, all plans must take a customized approach to the patient. A reconstructive management strategy is based on the evaluation of the defect and the patient's specific functional needs. The mechanism of injury, the location and extent of the wound, tissue viability, contamination, and exposure of vital structures are all critical considerations. A plan for concurrent acute and definitive fracture care must be coordinated with the trauma team and within the scope of wound care.

Most reconstructive surgeons favor immediate reconstruction, except when the defect demands a delay. In high-energy injury patterns, in cases of infection, or in heavily contaminated wounds, it may be necessary to delay definitive wound closure or coverage until an adequate, multistaged evaluation and débridement may be performed. Vacuum-assisted closure (VAC) dressings have improved the treatment of open wounds and may allow some additional delay in flap reconstruction without expectation of further morbidity. However, the general trend supported by the literature remains to cover tissue as soon as the injured patient and limb are optimized, even if this extends past the 72-hour window proposed by Godina.

Wound Preparation for Soft Tissue Coverage

A healthy wound bed begins with the meticulous and complete surgical removal of foreign material, infection, and devitalized tissue. Chronic wounds should be converted to acute wounds to promote healing. In acute injury, wounds must be extended past the zone of injury to ensure that complete treatment and effective débridement are accomplished. Judicious use of lavage may help remove foreign matter, but care must be taken not to extend the zone of contamination by forcing debris into the surrounding tissue. Use of a tourniquet early in the case is important to best visualize all contaminants and devitalized tissue and avoid injury to vital structures such as nerves and blood vessels. The tourniquet should be released before closure or dressing application to confirm removal of all devascularized tissue and to ensure adequate hemostasis.

A systematic approach to wound débridement achieves the best results, and sharp débridement is the cornerstone of this surgical technique. Excision of all devitalized tissue to a healthy tissue margin, instead of a “wait-and-see” approach to suspect tissue, will limit persistent contamination and infection. All nonviable or suspect tissue is sharply débrided from the wound until a healthy margin of viable tissue is achieved. Every effort to preserve nerves and blood vessels crossing the zone of injury is made, and if they are transected, these structures are carefully tagged with dyed monofilament suture and documented in the operative records so that they may be more easily visualized during later wound débridement or reconstructive efforts.

Identification of nonviable tissue remains a challenge, and there is no substitute for experience. Knowledge of anatomy and local blood supply is paramount in this endeavor because overly aggressive débridement within muscle compartments may devascularize previously viable tissue. Tendon débridement must be carefully considered due to the potential loss of function. Tendons are also easily desiccated, especially if overlying paratenon or sheath is missing. Injured blood vessels or nerves must be carefully assessed for primary or delayed repair or grafting. Smaller sensory nerve branches may not be amenable to salvage, and if so, we like to pull traction on the proximal end, cut sharply, and allow retraction into the soft tissues. If the stump cannot be retracted, we make every effort to bury it in muscle. Local soft tissues should be used to cover exposed tendons, nerves, and vessels to prevent further injury.

Devascularized bone fragments must be removed from the wound bed, with the exception of substantial articular fragments, which should be retained in an attempt to preserve the articular surface. Curettes, rongeurs, and burs are useful to check for punctate bleeding indicative of healthy bone that should be preserved. Culture of any contaminated or osteolytic bone will help guide antibiotic selection.

Strict hemostasis is critical to prevent hematoma and limit further infection and morbidity caused by blood loss. Suture ligatures and surgical clips should be used for larger vessels, Bovie or bipolar cautery for smaller vessels. The braided suture is typically avoided when possible to avoid harboring bacteria. Judicious use of a tourniquet is helpful to identify and control large bleeding vessels and includes release to assess hemostasis before closure, grafting, or dressing application. Adjunctive topical hemostatic agents are available and have been used successfully in some of our most severely war-injured patients. Lavage is important for removing foreign debris and lowering bacterial counts. Gravity or bulb irrigation is considered the standard, whereas pulsatile lavage can further damage delicate tissues, exacerbating the potential for adhesions and functional loss.

Negative-pressure wound therapy dressings are a great advance in the treatment of wounds not amenable to primary closure. The V.A.C. Therapy dressing is commonly used to manage large wounds from high-energy injuries. It continues to débride wounds, reducing edema and local bacterial counts while promoting the growth of healthy granulation tissue. It also eliminates the need for multiple daily dressing changes, thereby reducing the patient's discomfort and nursing staff workload. It is prudent to limit the exposure of blood vessels, nerves, or tendons to the wound VAC and try to rotate available local tissue to provide coverage before placement of the wound VAC.

Eliminating contamination and infection is essential to successful wound treatment. In addition to appropriate broad-spectrum antibiotic use, there are many different options available that can be tailored to the clinical or surgical situation to provide local infection control. Antibiotic bead pouches or fracture spacers have been used effectively to provide local infection control in cases of wounds with associated high-energy fracture patterns. With comminution and bone loss, soft tissue space can be maintained for future reconstruction and enhanced mechanical stability provided. In a highly resistant bacterial infection, silver-impregnated films, colloidal materials, wound VAC sponges, and distillation solutions are additional options for the surgeon and have been used with great frequency at our institution. For extremely large wounds with highly resistant bacterial colonization or infection that are not amenable to wound VAC treatment, mafenide acetate (Sulfamylon) or Dakin's soaked wet-to-dry dressings have proven effective and resulted in successful wound closure. Infectious disease specialty assistance is recommended in such cases.

When wounds are associated with fractures in the acute setting, provisional stabilization should be attempted to maintain soft tissue space, prevent mechanical agitation of the surrounding tissues, and optimize pain control when definitive fixation is not advisable. In general, external fixators and Kirschner wires are preferred acutely with conversion to definitive fixation as indicated by the injury, especially in the setting of high-energy injuries, such as blast injuries, when large amounts of debris are forced into the wounds with tremendous energy and the level of contamination is typically higher than that seen in most blunt open trauma.

For highly contaminated wounds, or when there is a concern for viability in critical areas or structures, repeat operative débridement should be planned every 24 to 36 hours until a healthy, vascularized soft tissue bed is achieved.

Pearls and Pitfalls

Wound Coverage Treatment Pitfalls

  • Inadequate clinical and surgical resources for proper treatment

  • Failure to recognize and optimize host factors

  • Failure to recognize and treat vascular compromise

  • Inadequate debridement

  • Failure to recognize and treat infection

  • Wound closure with excessive tension

  • Inadequate soft tissue rest

  • Prominent bone or hardware

Negative-Pressure Wound Therapy

Negative-pressure wound therapy (NPWT) was first introduced to North America in 1997. Since the US military combat operations in 2001, NPWT has become an integral tool in the treatment of open wounds. The goal of NPWT is to stabilize a wound for ultimate primary or secondary soft tissue coverage. Indications include acute or chronic wounds after a thorough débridement; temporary coverage of fasciotomy sites; wound infection; open fracture; exposed bone, joint, or hardware; or closed surgical wounds. Contraindications include wounds involving a tumor, exposed neurovascular structures, anastomoses, wounds overlaying thoracoabdominal organs, or wounds with significant necrotic tissue.

NPWT has many potential benefits to wound care, including the stabilization of wounds during serial débridement, removal of gross exudate, decreasing the likelihood of infection in open fractures, wound contraction, reduction of dead space, increasing the microvascularity of the wound, and improving the wound environment by stimulating granulation in preparation for ultimate coverage. Mechanotransduction precipitated by the NPWT upregulates specific intracellular gene expression, leading to cellular mitosis and subsequent granulation tissue formation and wound contraction. This process may be further supplemented with a graduated closure technique, or “Jacob's ladder.” Vessel loops may be crisscrossed over the sponge, which rests on top of the open wound. The elastic loop is maintained at the wound edge with staples. With mild tension, the elastic loop is tightened, and the wound edges are held in slight proximity via a corset effect. This loop may be tightened as swelling of the limb recedes.

Duration of therapy before wound coverage is not uniform and has been reported from a few days to a year. However, NPWT may have a particular benefit in the setting of split-thickness skin grafts (STSGs). A systematic review compiling 653 patients from five cohort studies and seven randomized controlled trials evaluated STSGs with and without NPWT as a bolster for 5 to 8 days. Those treated with NPWT had a significantly higher rate of graft take and a lower reoperation rate. NPWT as a bolster for STSG also has been shown to improve the qualitative appearance of the graft compared with a standard bolster.

After a methodical débridement in the appropriate setting, an NPWT vacuum may be applied. First, the wound is packed with a sponge, which should not overlap the wound edges. The wound is then covered with an impermeable adhesive plastic barrier. It is imperative that the wound edges are clean and dry to ensure a proper seal. Next, a small port is cut into the central portion of the plastic adhesive over the sponge. The distal adhesive end of the suction tubing is placed over the small portal. Additional plastic adhesive may be placed over the connection for the security of the suction tubing. The suction tubing is connected to the suction canister and mechanical pump. The pump is turned on to continuous pressure at 125 mm Hg. One should visualize the sponge suck down and run a seal check on the vacuum before applying a dressing over the wound.

Pearls and Pitfalls

Negative-Pressure Wound Therapy

  • NPWT is not a substitute for a thorough wound débridement.

  • After application, the NPWT dressing should be changed at bedside or in the operating room every 2 to 5 days.

  • Suction pressure of 125 mm Hg is optimal to increase microvascularity, but lower pressures have provided satisfactory results.

  • A complete seal may be difficult near burns or external fixation pins. For these cases, sterile hydrocolloid gel may help secure a seal. In addition, Ioban (3M, Maplewood, MN) may be wrapped over the wound.

  • Try to minimize the time from wound coverage with adhesive plastic to the trial of the seal. A wound may secrete fluid, which can affect the seal and would then require reapplication of the plastic adhesive to reseal the edges.

  • NPWT may be used as a bolster after application of an STSG, which may serve to remove exudate and reduce hematoma formation.

  • A rash secondary to mechanical irritation may occur in 2% to 5% of patients. This typically resolves within 48 hours of discontinuation of NPWT.

Wound Coverage Types

Skin Grafts

Full-Thickness Skin Graft

Full-thickness skin grafts, by definition, remove the entire epidermis and dermis of the affected area, requiring primary closure. Advantages of full-thickness skin grafts are reduced graft contracture and enhanced durability. For this reason, they are typically employed in the hand. Disadvantages include limitations in recipient-site coverage.

For upper extremity wounds, the graft may be harvested from the hypothenar region of the hand, the medial aspect of the arm, the palmar wrist crease, or the groin. The donor is typically raised in an ellipse fashion and defatted as the graft is sharply elevated. An abundance of fat on the raised graft may serve as a barrier to vascularization. However, if the fat is removed too aggressively, it is possible to turn the full-thickness skin graft into an STSG, which may introduce a higher likelihood of graft contracture. Once elevated and inset with absorbable suture, the graft is bolstered in a tie-over fashion and covered with a dressing, and the joint is immobilized for 2 weeks. After de-epithelization, the graft should have similar color, texture, and elasticity to the surrounding tissue.

Split-Thickness Skin Graft

STSGs are a good coverage option for simple wounds that cannot be closed primarily and have a healthy wound bed. By definition, STSGs remove the epidermis but only partially harvest the dermis, allowing for regeneration of epidermis at the harvest site. The thickness of the graft will determine the potential of graft contraction, with thinner grafts contracting more and thicker grafts contracting less. This thinner graft may be advantageous when the wound condition dictates contracture to a smaller wound; conversely, a thicker graft may be preferred when wound contracture is not desired, such as crossing a joint. In a healthy wound bed, STSGs are reliable and can be meshed to cover a larger area than that harvested from the donor site.

An STSG can be harvested with a knife then fenestrated or raised with a commercial dermatome. The region that is to be harvested is shaved preoperatively if necessary. Sterile mineral oil is then applied to the harvest site. The skin is held under tension, and a dermatome is applied to the skin at a 45-degree angle with steady downward pressure. Once the desired length of graft is obtained, the graft may be meshed on the back table. The graft will have to be less than 0.015 inches thick to fit into the graft mesher. Meshing the graft will allow for increased graft excursion, potentially reducing the likelihood of hematoma formation, and allow for more rapid epithelization. A bolster should be applied and may consist of either NPWT or a traditional tie-over bolster. The bolster should remain in place for at least 5 to 7 days. The region should be immobilized for up to 2 weeks to minimize graft shear. Although an STSG will cover and stabilize a wound, the graft will not appear exactly similar to the surrounding dermis, may contract, and will be insensate. However, a cosmetic donor site with limited morbidity can be expected even when a large volume of skin graft is required.

Dermal Substitutes

The past several decades have seen significant research and interest in dermal substitutes for a variety of applications, including burns, nail bed reconstruction, complex wounds, coverage of donor-site defects of flaps, degloving injuries, after oncologic resection, in congenital correction, and in heavily contaminated war wounds after staged débridements. Perhaps the most commonly reported dermal substitute for wound coverage is Integra (Integra Life Sciences, Plainsboro, NJ), an acellular bilaminate membrane composed of cross-linked bovine tendon collagen and chondroitin-6-sulfate. Integra is most commonly used in a meshed bilayer construct with the addition of a silicone layer to prevent desiccation. Dermal substitutes such as Integra are easy to use or apply, limit donor-site morbidity, are readily available, and have a proven track record in burn patients and complex extremity wounds ( Box 19.1 ). One prospective trial analyzed 18 patients with bilateral dorsal hand wounds; one hand received STSG alone, and the other received one-stage dermal substitute and STSG. Although there was no difference in graft survival, the dermal substitute cohort had improved range of motion and superior skin quality (Vancouver Burn Skin Score). In addition, in a retrospective review of patients with severe burns, those treated with Integra had an average length of stay 40% shorter than those treated with skin grafting alone.

Box 19.1
Advantages and Disadvantages of Dermal Substitute Utilization

Advantages

  • Ease of use

  • Unlimited quantity

  • Limit donor-site morbidity

  • Reduce necessity for rotational or pedicle flaps in soft tissue loss of the finger, hand, and wrist

  • Improved range of motion after STSG

  • Improved quality of skin after STSG

Disadvantages

  • Cost

  • Requires a second procedure

  • Risk of infection under silicone layer

  • Silicone dislodgement and desiccation

In many cases, use of Integra has eliminated the need for complex flap reconstruction and its associated morbidity. Coupled with a split-thickness or full-thickness skin graft, usually performed 14 to 21 days after initial application, Integra has provided reliable coverage of complex wounds with exposed muscle, tendon, and even bone. However, successful coverage has not been proven with application directly over the fracture. The disadvantages of dermal substitutes are the financial cost of the implant and the inherent lack of antimicrobial properties, prompting the use of additional antimicrobial dressings that may increase cost. NPWT is now commonly used with Integra application and may accelerate healing and time to skin graft placement. In addition to primary coverage of complex wounds, Integra has been used to decrease donor-site morbidity in flap surgery by providing a more supple, durable coverage. Integra has also been used effectively to provide durable coverage of amputation stumps that allow functional prosthetic usage.

Random-Pattern Flaps

By definition, random skin flaps have no named blood vessels and rely on the subdermal vascular plexus for perfusion. This limits the geometry of the flap, requiring that the length of the flap be no more than twice the base of the flap to ensure flap blood flow. Longer flap geometries have been described, but flap viability may be compromised, and when this occurs, it will be at the distal extent of the flap. This type of flap requires mobile skin, and the donor defect can usually be closed, although the addition of a Z-plasty may be required.

Axial-Pattern Flaps

Axial-pattern flaps are fasciocutaneous flaps designed around a named artery and vein. The groin flap is a classic example of this flap, designed around the circumflex scapular artery and vein. Axial-pattern flaps have the advantage of supplying a much larger flap than random-pattern flaps, and due to a larger, more robust vascular system, they can be converted to free flaps if required.

Island-Pattern Flaps

Island-pattern flaps are similar to axial-pattern flaps, in that the flap is supplied by a named artery and venous outflow. However, as the name would imply, island flaps can be separated completely from the harvest site and transposed somewhat distantly on its named arteriovenous pedicle. The advantage is usually ease of flap harvest and inset. The disadvantage is the potential loss of a named artery supplying distant structures. Common examples include the radial forearm flap in the upper extremity and the reverse sural artery flap in the lower extremity. Island-pattern flaps may be fasciocutaneous, involving the skin and fascia, or adipofascial flaps, preserving the skin at the donor site.

Perforator Flap

Perforator flaps are fasciocutaneous flaps that derive their blood supply from intramuscular and intermuscular septal perforators from the deep vascular arterial system. The most common example of this type of flap is the anterolateral thigh flap. Perforator flaps can be pedicled or used as free flaps. Propeller flaps are a subgroup of perforator flaps, defined as perforator flaps that are islanded and rotated into a defect. These flaps have seen increased popularity in the reconstruction of small soft tissue defects in the upper and lower extremity.

Free Flap

By definition, a free flap is harvested, its blood supply is divided, and then it is reanastomosed to an arteriovenous supply at the flap recipient site, usually requiring microsurgical techniques. A free flap, or free tissue, is usually classified by its blood supply. A free flap can include skin, fascial and subcutaneous fat, muscle, bone, or combinations of any tissue type based on its blood supply. Muscle flaps, such as the latissimus dorsi muscle flap, continue to be commonly employed in reconstructive surgery. Muscle flaps have the advantage of covering large defects and filling three-dimensional volume defects, but they may not be the best coverage option when staged reconstructive procedures, such as tendon or nerve reconstruction procedures, are anticipated. Because of these limitations, fasciocutaneous and adipofascial flaps based on large named arteriovenous pedicles, or even smaller flaps based on smaller perforator vessels, have recently gained popularity among reconstructive surgeons.

Soft Tissue Reconstruction of the Upper Extremity

Surgical Planning

Selecting the optimal reconstructive option depends heavily on the location of the defect. For simplification, the following algorithmic approach divides the upper extremity into five anatomic zones: shoulder, arm (within 6 to 8 cm from elbow), elbow (including lower 6 to 8 cm of arm), forearm, and hand. Specific flaps, as shown in Table 19.1 , can effectively reconstruct each anatomic region.

Table 19.1
Options for Soft Tissue Reconstruction of the Upper Extremity by Location
Simple Wound (No Exposed Bone, Tendons, or Neurovascular Structures)
    • Use split-thickness skin grafting in the arm and forearm

    • Use full-thickness skin graft for the palmar hand and digits

    • Can use dermal substitutes to increase thickness and durability of graft

Complex Wounds (Exposed Bone, Tendons, or Neurovascular Structures) Shoulder
    • Scapular/parascapular flap

    • Latissimus dorsi muscle flap

    • Free flap

Brachium/Arm
    • Latissimus dorsi muscle flap

    • Pectoralis muscle flap

    • Free flap

Elbow
    • Radial forearm flap

    • Lateral arm flap

    • Latissimus dorsi muscle flap

    • Anconeus muscle flap

    • Free flap

Forearm
    • Groin flap

    • Free flap

Wrist and Hand
    • Reverse radial forearm flap

    • Posterior interosseous artery flap

    • Dorsal metacarpal artery flap

    • Groin flap

    • Fillet flap

    • Free flap

A defect that involves bone, blood vessels, and/or nerves will need a careful assessment and stepwise treatment plan. Reconstruction typically involves skeletal fixation as the starting point. All vascular repairs typically require autologous grafts. Determination for acute repair versus delayed reconstruction of any nerve or tendon injuries must be determined before definitive wound closure or coverage.

Intuitively, the lack of local available soft tissue generally precludes a simple reconstruction method. However, certain anatomic areas are easier to reconstruct with fasciocutaneous flaps, which provide durable coverage. These areas include the shoulder, limited defects on the dorsal elbow, or even in the cubital fossa. In certain situations when there is a healthy, well-vascularized soft tissue bed comprising healthy muscle or even paratenon, a simple skin graft may be an easy reconstructive strategy. Of course, the long-term problems with graft contractures and lack of durability, usually due to thin, insensate coverage, adversely affect the outcome.

Understanding the vascular roadmap becomes essential to upper extremity reconstruction in two critical ways: (1) identification of donor vessels and (2) understanding the impact of sacrificing a vessel for flap anastomoses. Methods of assessing vascular integrity include a simple physical examination of the pulses, an Allen test (using Doppler ultrasound confirmation both preoperative and intraoperatively), and, when needed, an angiogram or a magnetic resonance angiogram (MRA) if available. More recently, indocyanine green fluorescence angiography used in the SPY imaging system has gained increasing interest and use for flap design and intraoperative and postoperative flap assessment. Further work is ongoing to define its role as a reliable tool for the surgeon.

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