Type
Porous structure
Examples
Type I
Macroporous (> 75 µ)
Marlexa, Proleneb Trelexc
Type II
Microporous (< 10 µ in at least one direction)
ePTFE, Dual-Meshd
Type III
Macro and microporous
PTFEd, Mersileneb
Surgiproe
Type IV
Submicronic pore size
Silastic sheeting, Celgardf
Polypropylene material is one of the most commonly used synthetic meshes. It is nonabsorbable and popular for its macroporous structure. It is advantageous because of better fibrovascular ingrowth and immune cell penetration. It also leads to stronger scar formation, creating a more durable apposition with the fascial edge [5]. These meshes create a stiff scar due to the lack of pliability. This can be useful to cover large defects of the abdominal wall where there is little support. The macroporous structure also allows for neutrophil and macrophage migration into the mesh, thereby allowing clearance of bacteria [1, 4]. More common complications include mesh extrusion or erosion into bowel.
PTFE/ePTFE (Gore-Tex, W.L. Gore, Newark, DE) is another nonabsorbable mesh. It is stronger than polypropylene but also flexible. The expansion process of PTFE creates a material that is relatively inert when implanted. The small pore size accounts for a minimal foreign body reaction compared to polypropylene and accounts for its advantages and disadvantages [5]. There is less risk of the mesh erosion through the skin or viscera due to its microporous structure and can be placed directly over the exposed bowel. The small pore size does predispose this implant to seroma formation, as this fluid cannot adequately egress through the mesh. Similarly, formation of fluid can increase the risk of abdominal compartment syndrome [6] . It also allows smaller bacteria (1 µ in size) to migrate into the mesh but does not allow entry of inflammatory cells, such as macrophages (greater than 50 µ). This, along with the lack of fibrovascular ingrowth, predisposes the implant to infection , which would ultimately mandate mesh removal.
Alternative options include polyglactin-based meshes (e.g., Vicryl, Ethicon; Dexon, Davis & Geck, Sugarland, TX) which are absorbable. Their primary advantage is use as a temporary solution in grossly contaminated wounds. Polyglactin-based options retain their strength in the short term, have a decreased risk of fistula formation, and allow fluid drainage. They are usually not used for long-term or permanent reinforcement as a result of progressive loss in tensile strength over time.
Composite meshes (e.g., Vypro I/II, Ultrapro, Proceed, Ethicon, Somerville, NJ; Sepramesh and Composix, Bard, Murray Hill, NJ) are also available for repair of abdominal wall defects. The primary advantage of composite meshes is that one side of the mesh prevents adhesions to adjacent bowel, while the other provides strength and support to the abdominal wall. These meshes offer a great option for the abdominal wound with exposed viscera; however, the anti-adhesive layer can develop marginal breakdown, leading to adhesions. Also, the permanent materials in these prostheses can become infected if bacterial seeding occurs.
The major drawbacks to the use of synthetic mesh are infection and seroma formation. Seroma formation is common and is usually the result of extensive dissection and creation of dead space. Seromas of the abdominal wall are typically managed with observation; however, if drainage is necessary, it is imperative to obtain a fluid culture. Observed in large series of laparoscopic ventral hernia repair experience, aspiration of seromas has the risk of introducing bacteria, resulting in infection and the recurrence of the hernia. Usually, expectant management is all that is required. Hematomas can also occur and are treated in the same fashion. Hematomas require treatment if actively bleeding, expanding, or infected.
Infection is the most feared complication and usually necessitates prosthetic explantation. This is most commonly due to surgical wound infection that tracks the underlying mesh, resulting ultimately in mesh extrusion. Every attempt should be made to cover the mesh with well-vascularized tissue to decrease the incidence of these complications.
Biologic Mesh
Biologic mesh materials are derived from human or animal tissue. Human dura, dermis, muscle, fascia, small intestine submucosa, porcine dermis, amniotic membranes, and pericardium have all been used in the past as a biologic mesh prosthetic. Chemical treatments are used to minimize associated foreign body reaction. They are incorporated into native tissue by the host inflammatory cascade and continue to undergo remodeling over time. Less concern for complications has been noted even when placing these materials in infected fields or with inadvertent enterotomies or serosal injury. As previously mentioned, routine use of biologic mesh is still difficult to justify, given their high cost and the lack of long-term data. Still, they are an excellent option in complicated abdominal wall defects.
AlloDerm (Lifecell, Branchburg, NJ) and Allomax (Bard, Murray Hill, NJ) are two of the most popular biologic regenerative tissue matrices which consist of non-cross-linked human dermal collagen matrices. The dermal matrix is treated with sodium chloride and sodium deoxycholate to remove living cells, leaving behind extracellular matrix. Acellular human dermis has numerous applications, ranging from incisional and ventral hernia repairs to abdominal and chest wall reconstruction. It is advantageous because of its rapid vascularization, allowing complete incorporation to occur in as little as 4 weeks. Additionally, the large pore size allows fluid to flow freely, consequently decreasing the risk of seroma or increasing intra-abdominal pressure.
Compared to other biologic prostheses, acellular dermal matrix has been shown to have lower rates of hernia recurrence , seroma, and wound infection. Local wound care resolves most cases of dermal matrix exposure and wounds usually heal by secondary intention. FlexHD (Ethicon, Somerville, NJ), a less commonly used acellular dermal matrix, is another available product. In contrast to early versions of Alloderm and Allomax, FlexHD does not require refrigeration and is readily available for instant use.
Surgisis (Cook Medical, Bloomington, IN) is made of porcine small intestinal submucosa. Historically, it was used for arterial bypass, ACL repair, and bladder slings. It is available in a perforated and non-perforated form. The perforated version facilitates vascular ingrowth, but is also more adhesiogenic as compared to the non-perforated alternative. Surgisis has a tensile strength greater than two times the strength of native tissue and has been shown to have almost five times the strength 2 years after repair [7]. Other studies did show higher rates of infection when it was used in highly contaminated wounds or in critically ill patients. Surgisis is an excellent choice in clean-contaminated cases where surgeons would prefer to avoid a synthetic mesh.
Permacol (Covidien Surgical, Mansfield, MA) is an acellular porcine dermis which is decellularized and chemically cross-linked to inhibit breakdown of the collagen matrix. It creates less foreign body reaction than Surgisis and the collagen is resistant to degradation. Small case series supports its use in infected areas with contamination; however, there is little long-term outcome data. XenMatrix (Bard, Murray Hill, NJ) is another porcine dermis-derived biologic mesh and is not cross-linked (Bard Davol). The lack of cross-linking may contribute to the high rates of infiltration and remodeling in this material when compared to Permacol. In contrast to human-derived dermis options, Permacol appears relatively more rigid.
Technique
Options for the placement of mesh include an underlay, an inlay, or an onlay technique. Though several approaches are feasible, evidence has shown that technique is one of the primary factors driving hernia recurrence . While intraperitoneal placement has been described, it is preferable to avoid mesh contact with bowel if possible.
The underlay technique is defined as an intraperitoneal placement of the prosthesis (Fig. 6.1). This is the preferable method of placement because intra-abdominal pressure will push the prosthetic against the rectus abdominis and its overlying fascia. In addition, there is a large amount of surface area in contact between the mesh and the fascia [8]. As a result, we believe the underlay technique has the lowest incidence of recurrent herniation. It also has the lowest rate of infection and wound breakdown due to the greater soft tissue protection from skin flora and environmental contaminants.
Fig. 6.1
Underlay placement of dermal matrix
Inlay placement is defined as a bridge of prosthetic mesh between the edges of the rectus fascia (retrorectus and preperitoneal). This method usually has an unacceptably high incidence of recurrent hernia (up to 75 %) [9]. This is likely due to a small total contact area between the mesh and fascia, which leads to a weaker repair.
Onlay is placement of the mesh superficial to the fascial repair. There is less fibrovascular infiltration of the mesh in this position, and it is closer to the skin, making this method the most likely to have wound complications. The onlay technique requires dissection in the subcutaneous plane which may lead to seroma formation (Fig. 6.2). Furthermore, division of blood supply to the overlying skin can lead to skin necrosis, breakdown, and subsequent prosthetic infection . However, the onlay technique does avoid the risk of visceral adhesion formation or more importantly bowel erosion and fistula formation.
Fig. 6.2
Onlay placement of dermal matrix
Vacuum-Assisted Closure
Vacuum-assisted closure (VAC) or negative pressure wound therapy (NPWT) is a commonly used technique in the management of open abdominal wounds. Negative pressure is applied to a wound through a sponge system usually at a pressure of − 125 mmHg. The VAC has great success if infection is controlled, necrotic tissue is debrided, and bacterial counts are minimized. Gross infection, presence of necrotic tissue, and residual neoplasia are contraindications to the use of VAC therapy.
The VAC can remove a large amount of fluid in a short period of time. This allows for faster and improved wound healing as tissue edema decreases and soft tissue perfusion increases. Research has shown stimulation of granulation tissue and fibrovascular ingrowth allowing for better wound healing and a favorable wound bed, should a skin graft be needed for wound coverage. Bacterial counts are significantly decreased with VAC therapy, which greatly assists wound closure. VAC therapy also limits repeated operative interventions and allows wounds to be temporized, while optimizing patients for definitive surgery [10].
Tissue Expansion
In the presence of significantly large soft tissue defects in the abdominal wall, tissue expanders are a viable option for reconstruction (Fig. 6.3). Hollow prosthetics are implanted into soft tissue and gradually filled with saline to produce tissue recruitment and growth overlying the expander. They help recruit and provide autologous tissue that is well vascularized and has adequate innervation, which is ideal for abdominal wall reconstruction .
Fig. 6.3
a–c Use of tissue expansion in the closure of an abdominal wall defect. Final result is shown in c
The major drawback to tissue expansion is the long period of time required for expansion and patient discomfort during the expansion period. Additionally, it is frequently inconvenient, as the expander must be placed overlying firm areas such as the chest wall, the iliac crest, or the lumbar fascia. Furthermore, expanders have a propensity to become infected, especially in an already compromised abdominal wound. This technique is not frequently used and should be considered only when options are limited or tissue defects are substantial [11].