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Mesh Sutured Repairs of Abdominal Wall Defects

Lanier, Steven T. MD; Dumanian, Gregory A. MD; Jordan, Sumanas W. MD, PhD; Miller, Kyle R. MD; Ali, Nada A.; Stock, Stuart R. PhD

Plastic and Reconstructive Surgery – Global Open: September 2016 - Volume 4 - Issue 9 - p e1060
doi: 10.1097/GOX.0000000000001060
Original Article
United States
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Background: A new closure technique is introduced, which uses strips of macroporous polypropylene mesh as a suture for closure of abdominal wall defects due to failures of standard sutures and difficulties with planar meshes.

Methods: Strips of macroporous polypropylene mesh of 2 cm width were passed through the abdominal wall and tied as simple interrupted sutures. The surgical technique and surgical outcomes are presented.

Results: One hundred and seven patients underwent a mesh sutured abdominal wall closure. Seventy-six patients had preoperative hernias, and the mean hernia width by CT scan for those with scans was 9.1 cm. Forty-nine surgical fields were clean-contaminated, contaminated, or dirty. Five patients had infections within the first 30 days. Only one knot was removed as an office procedure. Mean follow-up at 234 days revealed 4 recurrent hernias.

Conclusions: Mesh sutured repairs reliably appose tissue under tension using concepts of force distribution and resistance to suture pull-through. The technique reduces the amount of foreign material required in comparison to sheet meshes, and avoids the shortcomings of monofilament sutures. Mesh sutured closures seem to be tolerant of bacterial contamination with low hernia recurrence rates and have replaced our routine use of mesh sheets and bioprosthetic grafts.

From the *Division of Plastic Surgery, Department of Surgery, and Department of Cell and Molecular Biology, Northwestern Feinberg School of Medicine, Chicago, Ill.

Received for publication June 21, 2016; accepted August 8, 2016.

Supported by internal funding. The use of the advanced photon source for measurement of mesh suture area was supported by the US Department of Energy, Office of Science, Office of Basic Energy Sciences, under contract number DE-AC02-06CH11357.

Disclosure: Dr. Dumanian has financial interest and is an officer of the Advanced Suture Co. and the Mesh Suture Co. He could potentially benefit from the outcomes of this research. Neither of the other authors has any financial disclosures. The Article Processing Charge was paid for by the Division of Plastic Surgery, Northwestern Feinberg School of Medicine.

Supplemental digital content is available for this article. Clickable URL citations appear in the text.

Gregory Dumanian, MD, 675 N. St. Clair, Suite 19-250, Chicago, IL 60611., E-mail: gdumania@nm.org

This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially.

All high-tension internal surgical closures require that the ultimate tensile strength (UTS) of the repair remains greater than the forces applied. Otherwise, changes at the suture/tissue interface (STI) will lead to acute or chronic suture pull-through and surgical failure. For the abdominal wall, prophylactic flat meshes have been shown to improve outcomes of laparotomy closures and hernia repairs.1,2 Unfortunately, flat planar meshes have their own drawbacks, including increased time for placement, increased foreign material, increased tissue dissection, pain, infection, and cost.

Planar meshes reduce hernia formation by improving the UTS of the repair and by better distributing forces at the STI.3 Yet, all these theoretic benefits of planar meshes could be achieved with a better-designed suture. Based on preclinical studies that demonstrate decreased suture pull-through and increased early tensile strength for a novel designed mesh suture,4,5 presented is a series of “mesh sutured” repairs where a strip of planar mesh is introduced through either side of the abdominal wall with a sharp instrument and simply tied as a suture. This off-label use of a planar mesh has shown great efficiency and efficacy for both simple and complex abdominal wall closures.

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METHODS

Determination of Mesh Size and the Number of Knots Required

Mid-weight, macroporous, uncoated polypropylene mesh (PROLENE Soft Prolene Mesh, Ethicon, Somerville, N.J.) of size 12 × 14 inches (30.5 × 35.6 cm) was cut along the blue lines into strips to mimic the UTS of a number 1 polypropylene suture. Based on tensometry data, a 18–20-mm-wide mesh strip tied with a single square knot had no knot failures and an UTS just above that of the target suture strength. An additional throw was added to the square knot for security of these patients.

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Physical Characterization

A small rectangle of size 0.3 × 0.98 cm of the same polypropylene mesh underwent synchrotron microcomputed tomography (microCT) at station 2-BM at the Advanced Photon Source, Argonne National Laboratory, Argonne, Ill.6 One thousand one hundred and eighty slices were imported into ImageJ with a BoneJ plugin,7 an open source image analysis software, for determination of surface area.

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Clinical Experience

Inclusion Criteria

The decision to perform a mesh sutured repair was made by the senior surgeon (GAD) based on a relative contraindication to the use of sheet mesh including the added time needed for placement, contamination, and/or a lack of a posterior sheath for avoidance of intraperitoneal mesh placement against bowel. For nonmidline and small defects, mesh sutured repairs were performed to avoid the surgical difficulties required for placement of a planar mesh and due to the known failure rates with standard suture closures. Patients were educated preoperatively about the risks and benefits of sutures, meshes, and mesh strips used as sutures.

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Surgical Technique

Subcutaneous tissue was elevated off of the abdominal wall to achieve a 1-cm bite of unscarred abdominal wall spaced 1 cm from each other (Fig. 1) for the interrupted closure. A sharp surgical snap is used to pierce the abdominal wall, with care made to minimize the size of the hole (See video, Supplemental Digital Content, a sharp hemostat is used to pierce the abdominal wall approximately 1 cm from the newly debrided edge of the rectus muscle. The mesh strip is then pulled through the substance of the abdominal wall and then tied like a suture with 3 throws to close the defect, http://links.lww.com/PRSGO/A265). Use of cautery to touch the fascia at the site of the entry point lessens the force required to pierce the abdominal wall. Anterior components release with perforator preservation is performed for larger defects (Figs. 2–5).8 Flank defects are generally closed in two layers, approximating the transversus abdominis and internal oblique in the first row, followed by apposition of the external oblique in the second row. Several strips are placed and are snapped long. Tension on all these strips approximates the abdominal wall to facilitate knot tying. A suction drain is required in the subcutaneous tissue and is removed when <20 cm3 per day.

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Analysis of Outcomes

A comprehensive retrospective institutional review board–approved review was performed for all patients who underwent a mesh sutured repair and who had 30-day follow-up for this retrospective review. The widest separation of the medial aspect of the rectus muscles was recorded for midline defects for hernia size. Operative reports were reviewed for indications for a mesh sutured repair and the CDC wound classification9 and Ventral Hernia Working Group (VHWG)10 category. Surgical site occurrence (SSO) is defined as any surgical site infection (SSI), seroma, hematoma, delayed wound healing, enterocutaneous fistula, reoperation, or dehiscence. SSI was defined as a clinical diagnosis of wound infection based on the appearance of wound erythema, drainage, and need for postoperative antibiotics. Seroma was defined as any appreciable subcutaneous fluid collection in the postoperative period that was opened to accelerate healing and not treated with antibiotics. All medical complications requiring an intervention and readmission or reoperation within 30 days were recorded. Hernia recurrence was assessed by physical examination by a physician, routine surveillance of CT scan, and in 4 patients by telephone interview. Length of follow-up was defined as the time from surgery to the last documented abdominal wall examination as described above.

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RESULTS

Surface Area

The surface area of a number 1 polypropylene suture (0.4 mm in diameter) for a 1-cm length is calculated to be 0.126 cm2 (SA = length × diameter × π). Using microCT, the surface area of a 1-cm length of a 20-mm-wide mesh strip was measured to be 4.31 cm2, for a 34-fold increase.

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Clinical Results

Patient Cohort Description

One hundred and fifteen consecutive patients underwent mesh sutured closures of the abdominal wall without an underlying planar mesh, and 107 had at least 30-day follow-up. The prime indication for use of mesh strips is a contaminated midline closure (Table 1). For the 76 patients with documented preoperative hernias, the average midline rectus muscle separation for the 41 available CT scans was 9.1 ± 5.5 cm (range 2–21 cm).

Table 1

Table 1

Over 40% of patients were ASA 3 or above (Table 2). Almost 10% of patients had a prior or concurrent prosthetic mesh infection. Nonsterile surgical fields (CDC Class 2 and above) were present in 49 patients (Figs. 6–10), and these patients had an average transverse separation of their rectus muscles of 10.2 cm for those with CT scans. Of the patients treated, 28% were VHWG 2, 38% grade 3, and 6% grade 4 (Table 3). There were 30 cases with preexisting wounds or stomas at the time of surgery, and 17 cases with entry into the gastrointestinal or genitourinary tract. Ten patients had closure of an acute abdominal wall dehiscence. One-fourth of the patients underwent components releases.

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Table 2

Table 2

Table 3

Table 3

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Clinical Outcomes

Follow-up ranges from 30 to 1043 days, with an average follow-up of 234 days and a median follow-up of 178 days. As 9 patients did not have full thickness defects, hernia rates were calculated for the remaining 98 patients. Four of these 98 patients went on to develop an incisional hernia (4.1%). One patient had a recurrence after repair of an umbilical hernia. Two patients with full midline closures were found each to have a single 1-cm asymptomatic defect by surveillance CT scan (but not on physical examination). The fourth patient with diabetes, obesity, and a 14.8-cm hernia underwent a colostomy takedown early in the study. After the colostomy takedown and components release, her midline was closed with a sequence of a mesh strip followed by two interrupted 0-polypropylene sutures repeated for the length of the midline defect (in this series of patients, she was the only patient treated in this manner, whereas 4 others had alternating sutures and mesh strips). At the time of her hernia rerepair, an unusual surgical finding of hernia defects interspersed with well-approximated abdominal wall segments were noted. Biopsy of the joined areas of abdominal wall revealed the presence of the mesh strips still holding the rectus muscles in apposition (Table 4).

Table 4

Table 4

SSO occurred in 8 patients (17%), with the most common postoperative complication being a seroma treated in the office with drainage in 11 (10.3%), whereas 30-day SSI was 4.6%. Three hematomas and two infections required operative treatment of the subcutaneous tissues, and there were no deep infections or fistulas. Nine patients were readmitted within 30 days. Only one knot located at the bottom of a seroma cavity was excised in the office, and no other mesh sutures have required early or late removal. Excluding CDC 1 clean cases, SSO was 22% and SSI was 6.1%.

Two patients died, one from a ruptured bladder and amyloid-induced heart failure and the other on high-dose steroids from sepsis after a colostomy takedown. Neither patient was included in our outcomes as they did not reach a 30-day follow-up (Figs. 11–15).

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DISCUSSION

Small-diameter sutures concentrate force and pressure at the STI, leading to acute or chronic suture pull-through and surgical failure.11 Many materials have been implanted in an attempt to achieve a reliable high-tension closure including silver wire,12 dermal autograft strips,13 and collagen ribbon.14 The spacing of sutures to avoid tearing has intensely investigated.15 However, the problem may actually be the 3000-year-old suture design of a flexible linear thread that concentrates forces at the STI to achieve tissue apposition. Stagnant progress in the hernia repair field16 and a failure rate of suture repairs of incisional hernias of 63% at 10 years17 perhaps is explained by this reliance on the standard suture design for tissue approximation.

The long-term strength of an abdominal wall closure is important, as a number of hernias occur >1 year after closure.18 The strength of any repair is the sum of the physical construct and the scar of biologic healing. Humans have been assessed to encapsulate rather than to incorporate foreign materials than other species,19 and a mesh sutured repair uses this response to its advantage. The authors hypothesize that the mesh suture creates a magnified foreign body response because of its increased surface area in comparison to standard suture. The surface area of a 20-mm-wide mesh strip is over 34 times the surface area of a number 1 polypropylene suture. It is believed that a persistent foreign body response and associated scar formation will be important for the long-term strength of the closure. Experimental evidence shows that the foreign body response recedes when the foreign body disappears,20,21 and this may explain why abdominal wall scars after laparotomy and closure with absorbable sutures are only 70% as strong as unscarred linea alba.22 Foreign body-induced scar from implanted polypropylene23 is localized to the site of abdominal wall closure and magnified by the high surface area. Our hernia recurrence rate of <4% at the early mean follow-up time of 234 days is encouraging and is much less than expected, when compared to a cohort of similarly complex sutured repairs performed by the senior author.24 This ability is attributed to reliably suture wide abdominal defects (and avoid planar mesh) due to this magnified foreign body response, as these strips had the tensile strength of standard number one polypropylene sutures. Numerous types of defects were closed with or without components releases, relying on the distribution of forces to limit or avoid pull-through. The results are similar to that described for polypropylene “bands” that are introduced from semilunar line to semilunar line to close a midline defect, but were not tied to themselves to create a knot.25 Efficacy of the mesh strips is most dramatically demonstrated in the 49 repairs CDC grades 2–4. Only one patient had a hernia in these complex cases despite an average transverse hernia width of 10.2 cm. The remaining 48 patients maintained unscarred tissue planes for a later planar mesh closure if necessary.

The safety of mesh sutured repairs can be assessed with comparisons to both sutured closures of the abdominal wall and planar mesh hernia repairs in contaminated fields. The SSI rate of 4.6% for the entire cohort is less than a recent meta-analysis for sutured ventral hernia closures of 6.6%.26 The SSI rate of 6.1% for the 49 contaminated and clean-contaminated closures compares favorably to a 14–15% 30-day SSI rate in 2 recent studies of nonsterile planar mesh repairs27,28 Of the 31 closures not done for hernias, 10 were for fascial dehiscence after laparotomy—a situation regarded to be challenging with high failure rates.29 Mesh sutured repairs employ far less foreign material and require less tissue dissection than do planar mesh repairs. The fact that the majority of the prosthetic material is incorporated and thus located within tissue, as opposed to lying on its surface as do planar meshes, most probably is protective against infection. There is a minimal contact of the mesh strip with the bowel unlike intra-abdominal meshes. Finally, the authors feel that the physical attributes of the mesh are extremely important. Biomaterials with pores >1 mm generate the most biocompatible tissue response.30 Resistance to infection is evidenced by several patients with exposed mesh strips who healed with local wound care. The polypropylene filaments used in this particular mesh are measured by microCT to be 0.14 mm in diameter, and this compares to 0.4 mm for number 1 polypropylene. There may be a threshold in humans for the ability of a narrow filament foreign body to be cleared of surface bacteria, with the thinner the better. We have observed that small-diameter sutures (3-0 and smaller) do not form deep stitch abscesses, and we question whether the exceedingly low infection rate of intravascular stents despite episodes of transient bacteremia31 is due to the thin size of the metal filaments (0.08 mm) rather than their material composition.

Another issue for tissue tolerance is the physical characteristics of the mesh strip knots. Mesh strips are predominantly air and therefore the filaments collapse when tied to produce a small knot. Unlike the knots of solid sutures, the knots of mesh sutures still maintain an element of porosity (confirmed by microCT) that permit tissue incorporation, and may explain only a single knot being removed in this series.

Our enthusiasm for this technique is tempered by the relatively short follow-up. Categorization of results is difficult considering the varied types of defects closed with this technique. Although the passage of mesh strips with the aid of a sharp clamp is clumsy, a mesh suture with an attached needle is in development. Despite the lack of an attached needle, in our hands, a mesh sutured repair is both versatile and fast, in addition to avoiding the placement of a planar mesh with its required tissue dissection. These repairs avoid the sizeable costs associated with the bioprosthetic meshes often encouraged for use in contaminated situations. Long-term studies incorporating safety, efficacy, and cost will determine the proper place for this new abdominal wall closure technique and are underway.

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ACKNOWLEDGMENT

The authors thank Dr. Carmen Soriano for her assistance.

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Copyright © 2016 The Authors. Published by Wolters Kluwer Health, Inc. on behalf of the American Society of Plastic Surgeons. All rights reserved.