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J. Blank and M. I. Goldblatt
inguinal ligament to the iliopubic tract, an aponeurotic band overlying the superior pubic ramus (blue line, Fig.3.2). The iliopubic tract also connects the ASIS to the pubic tubercle; it is connected to the inguinal ligament medially by Cooper’s liga­ment (yellow line, Fig.3.2) [10, 11]. The internal and external rings refer to the open- ings of the inguinal canal, through which the spermatic cord structures pass (green line, Fig.3.2). The internal ring is visible on laparoscopy at the inferior portion of the eld. It is formed by a hiatus in the transversalis fascia [9]. The external ring is not visible in the laparoscopic view; it is formed by a hiatus in the external oblique apo­neurosis [9].
There are two triangular portions of the inguinal region that deserve special attention. The “triangle of pain” contains the lateral femoral cutaneous nerve, the femoral branch of the genitofemoral femoral, and the femoral nerves [9]. This tri­angle is bounded superiorly by the inguinal ligament, inferomedially by the sper­matic cord, and laterally by the iliac crest [11]. Placement of staples or tacks in this area may predispose the patient to chronic pain or paresthesias in the inguinal region, testicle, or thigh [1, 10]. The “triangle of doom” contains the external iliac vessels and the deep circumex iliac vein. This triangle is bounded by the vas def­erens medially and the spermatic vessels laterally and may cause signicant hemor­rhage if violated [1, 11].
The three types of hernias that may be encountered in the inguinal region are indirect, direct, and femoral hernias. Often, these are indistinguishable on preopera­tive physical exam. Indirect hernias run with the spermatic cord and are found lat­eral to the inferior epigastric vessels (polygon, Fig.3.2). Large indirect hernias may extend into the scrotum. Direct hernias protrude through Hesselbach’s triangle, a triangle superior to the inguinal ligament and medial to the epigastric vessels, which forms the “oor” of an open inguinal hernia repair (Fig. 3.3; circle, Fig. 3.2). Femoral hernias occur inferior to the inguinal ligament within the femoral canal, medial to the femoral artery and vein [9, 11].
Indirect, direct, and femoral hernias all begin within the myopectineal orice, rst described in 1956 by Fruchaud [12]. This is a weakness in the transversalis fascia that is bounded by internal oblique and transverse abdominal muscles superi­orly, the iliopsoas muscle laterally, and the rectus muscle medially [13]. The region
Fig. 3.3 Direct right inguinal hernia repair, with Cooper’s ligament (yellow line), inferior epigastric vessels (buried in fat, under red line), and direct hernia medial to the epigastric vessels, in the white circle. Med medial, Sup supercial, Lat lateral
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is divided in half by the inguinal ligament and contains the ve major nerves of the region: the genital and femoral branches of the genitofemoral nerve, the femoral nerve, and the anterior and lateral femoral cutaneous nerves, from medial to lateral [14]. This region also contains the femoral vessels, as well as the round ligament in women and the spermatic cord in men [13].
Access tothePreperitoneal/Intraperitoneal Space: Laparoscopic Dissection
Access to the preperitoneal space for a totally extraperitoneal (TEP) or the intraperi­toneal space for a transabdominal preperitoneal (TAPP) approach differs. We will rst describe preperitoneal access in the TEP approach. Three laparoscopic ports are placed in the midline: one 10-mm or 12-mm port directly below the umbilicus and two 5-mm infraumbilical ports (Fig.3.1a). Local anesthetic (the authors prefer a 50:50 mix of 0.5% bupivacaine and 1% lidocaine with epinephrine) is inltrated in the patient’s skin inferior to the umbilicus. The 10-mm/12-mm port incision is then made just inferior to the umbilicus, and the subcutaneous tissues are dissected down to the fascia. A 1-cm horizontal incision is made in the anterior rectus sheath, just off midline and ipsilateral to the inguinal hernia (the authors prefer the left side in bilateral inguinal hernias). The anterior rectus sheath is opened to expose the underlying rectus muscle, which is retracted anteriorly and laterally with an S-retractor.
A dissecting balloon is then placed in the preperitoneal space posterior to the rectus muscle and anterior to the posterior rectus sheath. The surgeon’s nger may be used to develop a tunnel in the preperitoneal space prior to inserting the dissect­ing balloon [1]. The dissecting balloon is inserted to the pubic symphysis and inated. For unilateral hernia repair, the assistant places pressure on the contralat­eral lower quadrant to prevent unnecessary tissue dissection (or a unilateral balloon may be used), and the balloon is gradually inated under direct laparoscopic vision. For bilateral hernia repair, the dissecting balloon is fully inated under direct lapa­roscopic vision to open the preperitoneal space bilaterally. Care must be taken to ensure that the balloon is dissecting posterior to the epigastric vessels. If the balloon begins to dissect between the rectus muscle and the epigastric vessels, ination is halted, the balloon is removed, and the dissection is performed manually.
After deation, the dissecting balloon is removed, and a 10-mm or 12-mm Hasson trocar is placed in the same incision. The preperitoneal space is then insuf­ated to 12mmHg pressure. This insufation pressure is lower than that required for a TAPP repair to avoid barotrauma to the peritoneum. The two 5-mm trocars are then placed in the midline under direct vision, one trocar two ngerbreadths below the umbilicus and one trocar ve ngerbreadths below the umbilicus. Alternatively, some surgeons prefer their trocars closer to the pubic symphysis [8]. The dissection is initially carried out in a medial to lateral fashion. A laparoscopic Kittner or blunt dissecting forceps is used to remove the loose areolar tissue from the pubic symphy­sis and Cooper’s ligament, and gentle dissection proceeds laterally toward the
28
J. Blank and M. I. Goldblatt
ASIS.Care is taken to ensure that the epigastric vessels remain anterior. In some patients, the transversalis fascia continues inferiorly, and the plane posterior to the transversalis fascia must be created starting inferiorly near the cord structures.
Once at the ASIS, the dissection is carried medially toward the internal ring, which is skeletonized using blunt dissection to reveal the structures of the spermatic cord: the vas deferens, pampiniform venous plexus, autonomic nerve bers, and testicular artery. An indirect hernia or a cord lipoma may be found running with the cord structures into the internal ring; this may be reduced with gentle traction, and the peritoneum should be pushed posteriorly. A large indirect hernia sac can be divided just distal to the internal ring and the remainder of the sac left in situ to avoid trauma to the spermatic cord [1].
Dissection continues medially, where a direct inguinal hernia may be seen supe­rior to the inguinal ligament, within Hesselbach’s triangle. This triangle is formed by the inguinal ligament inferiorly, the inferior epigastric vessels laterally, and the lateral edge of the rectus sheath medially. Hernias found in this region may be gen­tly reduced with a laparoscopic Kittner or blunt graspers. A femoral hernia may also be visualized inferior to Hesselbach’s triangle and may be reduced by the same technique. There is typically lymphatic tissue medial to the external iliac vein, which should not be mistaken for a femoral hernia.
The dissection is now complete, and the following structures are clearly visu­alized: the pubic symphysis or tubercle medially; the ASIS laterally; the skele­tonized internal ring with the vas deferens entering medially and the spermatic vessels entering laterally; the epigastric vessels approximately halfway between the pubic tubercle and ASIS, overlying the anterior abdominal wall; and the peritoneum posteriorly. At this point, the surgeon may proceed with mesh placement.
Access to the peritoneal cavity for a TAPP approach begins with inltration of local anesthetic as above and placement of an optical trocar or Hasson trocar just inferior to the umbilicus into the peritoneal cavity. The abdomen is insufated to 15mmHg pressure, and the abdominal contents are inspected for visceral injury or other diseases. The patient may be placed in Trendelenburg position to allow the bowel to fall cephalad out of the pelvis to aid in visualization of the inguinal region [1]. Two additional 5-mm trocars are then placed under direct vision in the right and left mid-abdomen, along the mid-clavicular line (Fig.3.1b).
The peritoneum is then scored using cautery or scissors approximately 6–7cm cephalad from the pubic symphysis or 2cm above the superior edge of the hernia defect [1]. The peritoneal ap is created by gently pulling the peritoneum posterior toward the abdominal contents. This is performed in a medial to lateral fashion, from the median umbilical ligament to the ASIS, preserving the medial umbilical ligament to avoid inadvertent bleeding from a remnant umbilical artery [10]. The preperitoneal space is developed using a laparoscopic Kittner or blunt graspers for dissection in the avascular plane between the peritoneum and transversalis fascia [10]. In some patients, the peritoneum does not separate from the transversalis fas­cia, and so in order to dissect laterally, the dissection must go to the pretransversalis
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plane. The surgeon should then identify the previously discussed structures: the pubic tubercle and Cooper’s ligament medially, the ASIS laterally, and the internal ring with the vas deferens and spermatic vessels. Indirect hernias will be visualized with the spermatic cord and may be gently reduced. Direct hernias will again be seen in Hesselbach’s triangle, and femoral hernias will be visible at the femoral canal, inferior to the inguinal ligament. At this point, the surgeon may proceed with mesh placement.
Mesh Placement
A variety of types of mesh may be used for inguinal hernia repairs and will be dis­cussed in later chapters. Regardless of the type of mesh and operative approach, it is imperative that the mesh cover the regions of indirect, direct, and femoral hernias. The authors prefer a 2-cm overlap across the midline and under the pubic symphysis to ensure proper mesh coverage.
The mesh is rolled in a caudal to cranial orientation prior to placement into the preperitoneal space. Once rolled up, the mesh is placed through the 10-mm/12-mm trocar. It is then unrolled in a cranial to caudal fashion, ensuring a 2-cm overlap of the midline, until the most inferior portion of the mesh covers the pubic symphysis (Fig.3.4). The mesh must cover all three potential hernia spaces. A non-adherent mesh may then be secured with tacks to the anterior abdominal wall, taking care to avoid the epigastric vessels and the triangles of doom and pain. Tacks are placed at the medial aspect of the pubic tubercle into Cooper’s ligament. Additional tacks can be placed along the anterior abdominal wall, typically one medially and one later­ally. Absorbable tacks are preferred by the authors. The assistant’s hand may be placed on the abdominal wall to palpate the tacking device and ensure that all tacks are placed superior to the iliopubic tract, to avoid the triangle of pain. Approximately 10mL of 0.5% bupivacaine is then instilled into the eld. The mesh is held in posi­tion and the eld is desufated. If a TAPP approach has been chosen, the perito­neum is now placed over the mesh and stapled or sewn in place.
Fig. 3.4 Left inguinal hernia repair. Unrolling mesh in a cranial to caudal direction, ensuring at least 2-cm overlap of the pubic tubercle. Shown here are Cooper’s ligament (yellow line), spermatic cord (green line), and the pubic tubercle (rectangle). Med medial, Sup supercial, Lat lateral
30
J. Blank and M. I. Goldblatt
Closure
The trocars are removed, and attention is directed to the 10-mm/12-mm trocar site. The fascia is closed using a 0 Vicryl in a gure-of-eight fashion. The skin and the remaining 5-mm port sites are closed using 4-0 Monocryl in a subcuticular fashion, and incisions are covered with Steri-Strips. After sufcient recovery, the patient may be discharged home on the same day.
Complications
Many surgeons still feel that placement of a urinary catheter is paramount to pre­venting bladder injury. This complication is rare, occurring in less than 1% of all laparoscopic inguinal hernia repairs, and is more common in TAPP repairs than TEP repairs [15, 16]. Still, patients who have undergone previous surgery in the space of Retzius are at high risk for bladder injury [1]. An open repair should be seriously considered for these patients. If a bladder injury does occur, it should be repaired anteriorly to prevent mesh placement near the repair [1]. The authors have their patients void immediately before going to the OR and have stopped using urinary catheters, except in those patients with signicant benign prostatic hypertrophy (BPH).
Urinary retention is also a recognized complication of laparoscopic inguinal hernia repair, with a wide variation of incidence (1–22% [17]) in the literature. The use of Foley catheterization has not been extensively studied in this instance, and it is unknown whether this intervention would improve on the rate of post­operative urinary retention. In fact, a retrospective review by Patel and col­leagues [18] suggested that Foley catheter placement may induce urinary retention due to detrusor muscle injury during placement. This study also described signicant variables that inuence the rate of postoperative urinary retention, including age over 50years, bilateral hernia repair, and increased use of postoperative narcotics [18].
Vascular injury usually involves the inferior epigastric and spermatic vessels, as well as the iliac veins, and is more common in TEP than TAPP [1, 16, 19, 20].The overall incidence of vascular injury during laparoscopic inguinal hernia repair is low, at 0–3% [16, 19, 20]. The use of a Hasson trocar for entrance into the abdomen as well as identication of vascular landmarks may help decrease the incidence of these injuries [1]. Aberrant vasculature, specically the corona mortis, may also be injured during dissection (Fig. 3.5). This vascular anomaly may be present as a branch of the external iliac artery or the inferior epigastric artery and passes over the pubic tubercle on the way to the obturator region [11]. The corona mortis is present in approximately 15–40% of cases [20].
Chronic nerve pain is a common complaint after both open and laparoscopic inguinal hernia repair. Patients may complain of burning pain or numbness to the
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Fig. 3.5 Aberrant branch of the obturator artery, the corona mortis (black line), connects the inferior epigastric artery (red line) to the obturator artery. The external iliac artery is deep to the operative eld but shown here for reference. Again shown are Cooper’s ligament (yellow line), the spermatic cord (green line), and the iliopubic tract (blue line)
31
inguinal region, testicle, or thigh. Delayed onset of symptoms usually signies a self-limiting condition. However, if symptoms occur in the recovery room, imme­diate return and re-exploration should be considered, especially if tacks were used [1]. Violation of the triangle of pain greatly increases the risk of chronic nerve pain.
Recurrence of inguinal hernia after both open and laparoscopic repair is another recognized complication. A meta-analysis of over 6000 patients who underwent either open or laparoscopic inguinal hernia repair found a signicantly increased risk of recurrence for laparoscopic inguinal hernia repair (RR=2.06). Subgroup analysis revealed no difference between TAPP and open inguinal hernia repairs, but TEP repairs were associated with a signicantly increased risk of recurrence when compared to open (RR=3.72) [21]. Another meta-analysis conrms these results, with a recurrence rate of 2.7% for open repairs and 5.5% for laparoscopic repairs [22]. Many surgeons agree that the learning curve for TEP repairs is high and the number of cases to achieve mastery may be over 250.
Conclusion
We have presented our preferred operative technique for laparoscopic TEP and
TAPP inguinal hernia repairs. Laparoscopic inguinal hernia repair is a viable
alternative to open inguinal hernia repair, and the complex anatomy of the region
requires intraoperative vigilance in order to avoid morbidity and mortality for
our patients.
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J. Blank and M. I. Goldblatt
References
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neal (TAPP) and totally extraperitoneal (TEP) repairs. In: Scott-Conner CEH, editor. Chassin’s operative strategy in general surgery. NewYork: Springer; 2014.
2. Bathla L, Fitzgibbons RJ. Chapter 8B. Perspective on hernias: laparoscopic inguinal hernia
repair. In: Zinner MJ, Ashley SW, editors. Maingot’s abdominal operations, 12e. NewYork: The McGraw-Hill Companies; 2013.
3. Koch A, Edwards A, Haapaniemi S, Nordin P, Kald A.Prospective evaluation of 6895 groin
hernia repairs in women. Br J Surg. 2005;92(12):1553–8.
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FA.Transabdominal preperitoneal versus totally extraperitoneal repair of inguinal hernia: a meta-analysis of randomized studies. Am J Surg. 2013;206(2):245–52.
5. Krishna A, Misra MC, Bansal VK, Kumar S, Rajeshwari S, Chabra A.Laparoscopic
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6. Bansal VK, Misra MC, Babu D, Victor J, Kumar S, Sagar R, Rajeshwari S, Krishna A, Rewari
V.A prospective, randomized comparison of long-term outcomes: chronic groin pain and qual­ity of life following totally extraperitoneal (TEP) and transabdominal preperitoneal (TAPP) laparoscopic inguinal hernia repair. Surg Endosc. 2013;27(7):2373–82.
7. Richardson WS, Hamad GG, Stefanidis D, Guidelines Committee SAGES.SAGES VTE pro-
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(TEP). In: Zollinger’s Atlas of surgical operations, 10e. NewYork: McGraw-Hill Education;
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9. J.P. Wagner, Brunicardi, F.C., Amid, P.K., & Chen, D.C. (2014). Inguinal hernias. In F.C.
Brunicardi, D.K. Andersen, T.R. Billiar, D.L. Dunn, J.G. Hunter, J.B. Matthews, & R.E. Pollock (Eds.), Schwartz’s principles of surgery, 10e. NewYork: McGraw-Hill Education.
10. Ellison EC, Zollinger RM. Repair of inguinal hernia, laparoscopic transabdominal preperi-
toneal (TAPP). In: Zollinger’s Atlas of surgical operations, 10e. New York: McGraw-Hill Education; 2016.
11. Ellison EC, Zollinger RM.Laparoscopic anatomy of the inguinal region. In: Zollinger’s Atlas
of surgical operations, 10e. NewYork: McGraw-Hill Education; 2016.
12. Fruchaud H.Anatomie chirurgicale des hernies de l’aine. Doin, Paris, 299–303 and 336–342;
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13. Kang JS, Qiao F, Nie L, Wang Y, He SW, Wu B. Preperitoneal femoral hernioplasty: an
“umbrella” technique. Hernia. 2015;19(5):805–8.
14. Bathla L, Fitzgibbons RJ Jr. Perspective on hernias: laparoscopic inguinal hernia repair. In:
Zinner MJ, Ashley SW, editors. Maingot’s abdominal operations, 12e. NewYork: McGraw­Hill; 2013.
15. Kocot A, Gerharz EW, Riedmiller H.Urological complications of laparoscopic inguinal hernia
repair: a case series. Hernia. 2011;15(5):583–6.
16. McCormack K, Wake B, Perez J, Fraser C, Cook J, McIntosh E, etal. Laparoscopic surgery
for inguinal hernia repair: systematic review of effectiveness and economic evaluation. Health Technol Assess. 2005;9(14):1–203, iii–iv.
17. Sivasankaran MV, Pham T, Divino CM.Incidence and risk factors for urinary retention follow-
ing laparoscopic inguinal hernia repair. Am J Surg. 2014;207(2):288–92.
18. Patel JA, Kaufman AS, Howard RS, Rodriguez CJ, Jessie EM.Risk factors for urinary reten-
tion after laparoscopic inguinal hernia repairs. Surg Endosc. 2015;29(11):3140–5.
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19. Sharma D, Yadav K, Hazrah P, Borgharia S, Lal R, Thomas S.Prospective randomized trial
comparing laparoscopic transabdominal preperitoneal (TAPP) and laparoscopic totally extra peritoneal (TEP) approach for bilateral inguinal hernias. Int J Surg. 2015;22:110–7.
20. Moreno-Egea A, Paredes PG, Perello JM, Campillo-Soto A, Baena EG, Munoz JR, Aguayo-
Albasini JL.Vascular injury by tacks during totally extraperitoneal endoscopic inguinal her­nioplasty. Surg Laparosc Endosc Percutan Tech. 2010;20(3):e129–31.
21. O’Reilly EA, Burke JP, O’Connell PR. A meta-analysis of surgical morbidity and recur-
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and other open nonmesh techniques for inguinal hernia repair: a meta-analysis of randomized controlled trials. Surg Endosc. 2005;19(5):605–15.
Hernia Materials: Fundamentals ofProsthetic Characteristics
CoreyR.Deeken andSpencerP.Lake
For nearly 80 years, biomaterials have been utilized to reinforce hernia repairs, beginning with silver and tantalum meshes in the early 1940s [1, 2] and progressing to permanent synthetic polymer meshes in the late 1950s [3]. In more recent years, advancements in biomaterial technology have led to rapid expansion of this eld with nearly 150 hernia repair materials now available [4]. This seemingly ever­expanding array of biomaterials has recently been classied by our group in a hier­archical fashion (Fig. 4.1) [4] that better reects the nuances of recent designs compared to previous classication schemes [5, 6].
In the Deeken & Lake Mesh Classication System [4], hernia repair materials are rst grouped according to the composition of the underlying structural scaffold material, forming three broad groups: permanent synthetic polymers, resorbable polymers, and biological tissue-derived materials (Fig.4.1). Hernia repair materials are then further subdivided based on the presence of a coating, barrier layer, or rein­forcing material. Coatings and barriers are used to minimize tissue attachment by separating the abdominal viscera from the mesh when utilized in the intraperitoneal position. Coatings are applied to the surface of the individual mesh bers and do not span across the pores of the mesh, while a barrier layer is applied continuously across the surface of the mesh, spanning the pores and creating a distinct layer. Barrier layers are additionally characterized as composite or noncomposite. Composite barrier layers are constructed of a distinct anti-adhesion layer that is
4
C. R. Deeken (*) Covalent Bio, LLC, St. Louis, MO, USA e-mail: deekenc@covalentbiollc.com
S. P. Lake Department of Mechanical Engineering and Materials Science, Washington University, St. Louis, MO, USA e-mail: lake.s@wustl.edu
© Society of American Gastrointestinal and Endoscopic Surgeons (SAGES) 2019 S. S. Davis Jr. et al. (eds.), The SAGES Manual of Hernia Surgery,
https://doi.org/10.1007/978-3-319-78411-3_4
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eB
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C. R. Deeken and S. P. Lake
Bare
PP
PET
PTFE
PVDF
Permanent
Synthetic
Barriers &
Coatings
Permanent
Barrier
Permanent
Coating
Resorbable
Barrier
Resorbable
Coating
Biological
Tissue Barrier
Reinforced ReinforcedBar
Resorbable
Fibers
P4HB
Silk
PGA
PLGA
TMC
Resorbable
Synthetic
Barriers &
Coatings
Resorbable
Barrier
Biological
Tissue-Derived
Barriers &
are
Coatings
Non-crosslinked
Crosslinked
HumanPorcineBovineOvine
Antimicrobial
Permanent
Fibers
Permanent
Barrier
Resorbable
Fibers
Resorbable
Barrier
Fig. 4.1 Deeken & Lake Mesh Classication System hierarchy encompassing three main catego­ries that are further distinguished by the presence, type, and composition of complementary barri­ers, coatings, or reinforcing materials. Terms of Use: This gure was adapted from the original gure licensed under a Creative Commons Attribution 4.0 License (https://creativecommons.org/
licenses/by/4.0/) attributed to Corey Deeken and Spencer Lake. The original version can be found
here: https://doi.org/10.1016/j.jmbbm.2017.05.008. The content of the gure is reprinted with minor modications to the original work [4]
sewn or vacuum-pressed onto the structural mesh component. Noncomposite barri­ers are formed from a single sheet of scaffold material that possesses side-specic features: anti-adhesive (e.g., smooth surface or smaller pores) or tissue attachment properties on the sides of the biomaterial intended to be placed in contact with the viscera and the abdominal wall, respectively. Reinforcing materials, which can be permanent or resorbable, are often included to optimize initial mechanical support of the defect and facilitate handling during implantation. To date, both permanent synthetic and biological tissue-derived scaffold designs have incorporated reinforc­ing materials, creating many unique combinations in which part or all of the scaf­fold resorbs over time, gradually transferring the load back to the host tissue in the process.
The rst broad category of hernia repair materials in the Deeken & Lake Mesh Classication System [4] consists of permanent synthetic polymers such as poly­propylene (PP), polyester (PET), polytetrauoroethylene (PTFE), polyvinylidene uoride (PVDF), and various combinations of these polymers (Table4.1). Many of the products in this category are available as bare meshes, without coatings, barri­ers, or reinforcements (Table4.1, column 1). However, several designs contain anti­adhesion barriers that may be classied as permanent, resorbable, or biological tissue derived. These barriers are further subdivided into noncomposite or compos­ite barriers (Table4.1, column 2). In the permanent barrier, noncomposite group, the anti-adhesion barriers of all current designs are comprised of expanded PTFE (ePTFE). In the permanent barrier, composite group, the anti-adhesion barriers of all current designs are also comprised of ePTFE, except for one design comprised of silicone (Surgimesh
®
XB, Aspide/BG Medical, Barrington, IL). In the permanent coating group, the anti-adhesion coatings of all current designs are comprised of titanium (TIMESH product line, Biomet Biologics/GfE Med. GmbH).