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26 Robotic Ventral andIncisional Hernia Repair: Management ofAdverse Events
421
post- operative period while recovering in the hospital are taken, including pharma­cologic prophylaxis with subcutaneous Heparin or low-molecular weight Heparin (Lovenox), along with mechanical prophylaxis with sequential compression devices and frequent ambulation. If the surgery is planned to be ambulatory, then post-operative pharmacologic DVT prophylaxis is not indicated unless, again, if the patient has a prior history of DVT and/or PE [18]. In fact, large studies have already demonstrated that robotic ventral hernia repair is associated with shorter length of stay and complication rates, where DVT and PE do not play a signicant role [19].
Hospital-acquired pneumonia (HAP) has also been studied as a possible adverse event following minimally invasive ventral or incisional hernia repair, including the robotic approach. The literature results vary, but a recent study showed higher rates of pneumonia in patients who underwent robotic ventral hernia repair compared to those who had the procedure with laparoscopic techniques. However, after control­ling for confounding variables, there was no signicant difference [20]. Part of the reason may be that the patients who are selected to undergo a robotic repair tend to be of more advanced age and with a higher American Society of Anesthesiologists (ASA) classication, which puts them at a higher risk for pneumonia. Aspiration precautions in this patient population are essential. On the other hand, the use of incentive spirometry on robotic ventral or incisional hernia repair patients is part of the fundamental principles of postoperative recovery, both in the hospital and at home, to counteract the effects of atelectasis and prevent pneumonia.
Finally, the discussion of adverse events during or after robotic ventral or inci­sional hernia repair cannot be complete without an analysis of system malfunction. This topic has been a very important one for the Food and Drug Administration (FDA) for several years since the robotic platform was approved in the United States. At least in the urology international literature, possible malfunction mecha­nisms during urologic robotic procedures have included the arm system, the optical system, the power system with the connector, endoscopic instruments, and the soft­ware itself [21]. The most important lesson is the proper training of the surgical team to manage the malfunction in a timely fashion and, if not possible, to convert to a traditional laparoscopic approach if possible before considering conversion to open. In either case, patient safety is at the forefront of any action taken in the oper­ating room.
In the American literature, a very large retrospective series of 14years of data has revealed some important lessons, as well, specically pertaining to the surgical specialties that utilize the robot more often. These specialties, including gynecol­ogy, urology, and general surgery, exhibit lower rates of mortality, injuries, and conversions to open compared to those specialties where the robotic platform is not frequently used, such as cardiothoracic surgery and otolaryngology. System mal­function was also studied in terms of adverse events dealing with the components of the platform, including burnt or broken pieces of instruments falling into the patient, electrical arcing, unintended operation of instruments, system errors, and problems with the visual system. The procedure was interrupted to restart the system some­times, while other times the procedure was rescheduled when critical portions were
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A. M. Gonzalez and R. J. Oviedo
not performed. Education is of paramount importance, both for the surgical team and for the industry, so that adverse events are reported properly and dealt with as soon as they occur [22].
To summarize, robotic ventral and incisional hernia repair has become one of the most frequently performed minimally invasive procedures for general surgeons in the last few years, with the development of advanced techniques for abdominal wall reconstruction that go beyond a traditional laparoscopic intraperitoneal onlay mesh (IPOM) repair. These advanced techniques expand to the realm of intracorporeal primary closure of the hernia, preperitoneal or extraperitoneal mesh implantation, with or without posterior component separation via the transversus abdominis release (TAR) approach. Patients who were traditionally not considered for minimal access surgery are being offered a robotic repair, with successful outcomes and low rates of complications, including recurrence. Adverse events do and will continue to occur, but their incidence can be lowered with the use of meticulous technique espe­cially during adhesiolysis and enterolysis, the primary repair of the defect, the implantation of the mesh in the selected plane, and the adherence to sound surgical principles just as it is done during open surgery. Constant awareness and knowledge of possible system malfunction scenarios and potential injuries to the patient must always be mastered by the entire team to achieve the highest standards of quality and patient safety.

References

1. Warren JA, Love M.Incisional hernia repair– minimally invasive approaches. Surg Clin N
Am. 2018;98:537–59. https://doi.org/10.1016/j.suc.2018.01008
2. Bensley RP, etal. Risk of late-onset adhesions and incisional hernia repairs after surgery. J Am
Coll Surg. 2013;216(6):1159–116812. https://doi.org/10.1016/j.jamcollsurg.2013.01.060.
3. Prabhu AS, etal. Laparoscopic vs robotic Intraperitoneal mesh repair for incisional hernia: an
Americas hernia society quality collaborative analysis. J Am Coll Surg. 2017;225(2):285–93.
4. Li J, Ji Z, Zhang W, Li L.The comparison of lightweight mesh and standard mesh in incisional
hernia repair with the open sublay technique: the results of a meta-analysis. Surg Laparosc Endosc Percutan Tech. 2015;25:238–44.
5. Darehzereshki A, et al. Biologic versus nonbiologic mesh in ventral hernia repair: a sys-
tematic review and meta-analysis. World J Surg. 2014;38:40–50. https://doi.org/10.1007/
s00268-013-2232-1.
6. Kennedy M, etal. Robotic TAPP ventral hernia repair: early lessons learned at an inner city
safety net hospital. JSLS. 2018;22(1):e2017.00070. https://doi.org/10.4293/JSLS.2017.00070.
7. Sharma A, Chowbey P, Kantharla NS, Baijal M, Soni V, Khullar R.Previously implanted intra-
peritoneal mesh increases morbidity during re-laparoscopy: a retrospective, case-matched cohort study. Hernia. 2018;22:343–51. https://doi.org/10.1007/s10029-017-1686-8
8. Haitian Z, et al. Totally extraperitoneal laparoscopic hernioplasty – the optimal surgical
approach. Surg Laparosc Endosc Percutan Tech. 2009;19(6):501–5.
9. Williams SB, Greenspon J, Young HA, Orkin BA. Small bowel obstruction: conserva-
tive vs surgical management. Dis Colon Rectum. 2005;48:1140–6. https://doi.org/10.1007/
s10350-004-0882-7.
10. Carbonell AM, et al. Reducing length of stay using a robotic-assisted approach for ret-
romuscular ventral hernia repair. Ann Surg. 2018;267(2):210–7. https://doi.org/10.1097/
SLA.0000000000002244.
26 Robotic Ventral andIncisional Hernia Repair: Management ofAdverse Events
11. Chou R, etal. Guidelines on the management of postoperative pain: a clinical practice perspec-
tive from the American pain society, the American Society of Regional Anesthesia and Pain Medicine, and the American Society of Anesthesiologists’ Committee on Regional Anesthesia, Executive Committee, and Administrative Council. J Pain. 2016;17(2):131–57.
12. Boerboom SL, etal. Preperitoneal bupivacaine inltration reduces postoperative opioid con-
sumption, acute pain, and chronic postsurgical pain after bariatric surgery: a randomized con­trolled trial. Obes Surg. 2018;28(10):3102–10.
13. Tayar C, Karoui M, Cherqui D, Fagniez PL. Robot-assisted laparoscopic mesh repair
of incisional hernias with exclusive intracorporeal suturing: a pilot study. Surg Endosc. 2007;21:1786–9. https://doi.org/10.1007/s00464-007-9247-3.
14. Lindmark M, Strigard K, Lowenmark T, Dahlstrand U, Gunnarsson U.Risk factors for surgi-
cal complications in ventral hernia repair. World J Surg. 2018;42(11):3528–36.
15. Oviedo RJ, Robertson JC, Desai AS.Robotic ventral hernia repair and endoscopic component
separation: outcomes. JSLS. 2017;21(3):e2017.00055.
16. Oviedo RJ, Brownstein NC, Smith SL, Robertson JC, Nair-Collins S.First 200 robotic general
surgery cases in a community hospital: a retrospective cohort study. World J Surg Surgical Res. 2018;1:1034.
17. Gonzalez AM, Romero RJ, Seetharamaiah R, Gallas M, Lamoureux J, Rabaza JR.Laparoscopic
ventral hernia repair with primary closure versus no primary closure of the defect: potential benets of the robotic technology. Int J Med Robot. 2015;11:120–5. https://doi.org/10.1002/
rcs.1605.
18. Gonzalez A, etal. Robotic-assisted ventral hernia repair: a multicenter evaluation of clinical
outcomes. Surg Endosc. 2017;31:1342–9. https://doi.org/10.1007/s00464-016-5118-0.
19. Beekman R, Crowther M, Farrokhyar F, Birch DW.Practice patterns for deep vein thrombosis
prophylaxis in minimal-access surgery. Can J Surg. 2006;49(3):197–202.
20. Altieri MS, Yang J, Xu J, Talamini M, Pryor A, Telem DA.Outcomes after robotic ventral
hernia repair: a study of 21,565 patients in the state of NewYork. Am Surg. 2018;84(6):902–8.
21. Coakley KM, etal. A nationwide evaluation of robotic ventral hernia surgery. Am J Surg.
2017;214:1158–63. https://doi.org/10.1016/j.amjsurg.2017.08.022.
22. Chen CC, etal. Malfunction of the da Vinci robotic system in urology. Int J Urol. 2012;19:736–
40. https://doi.org/10.1111/j.1442-2042.2012.03010.x.
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Incisional Hernia inOncologic Surgery
27
JohnM.Lyons III
The past 50years has seen major changes in the eld of cancer surgery. Where pre­viously, radical surgery was thought to be a prerequisite for cure, modern cancer surgeons understand that radicality can be superuous; and bigger procedures do not always lead to better cancer outcomes. Today, preoperative surgical evaluation considers technology, multimodal therapy, and minimally invasive techniques. While great advances in multimodal cancer treatment have been realized, surgery remains the mainstay of treatment for most solid organ intra-abdominal malignan­cies. Rather than replacing surgery as a treatment modality, systemic therapy has, in many cases, enabled surgeons to expand their services to patients previously consid­ered unresectable.
A good example is colorectal liver metastasis. Previously, very conservative cri­teria limited resectability only to those with unilobar, small volume, liver-only dis­ease in whom a very wide margin could be achieved. However, liver surgery has become safer in the past 30years [1]. This fact as well as advances in portal vein embolization, ablation techniques, and multi stage hepatectomy has led to an increase in the number of complex resections [2]. Moreover, pre-operative chemo­therapy has the ability convert select patients with advanced disease to a resectable status [3]. Preoperative “conversion therapy” is now discussed regularly in patients with locally advanced pancreas cancer, gastric cancer, and several other solid organ malignancies [4, 5]. A similar trend has been seen in the management of primary and secondary peritoneal malignancies. Once thought to be a futile endeavor, now select patients with good functional status and low volume peritoneal disease are offered large cytoreductive surgeries with concomitant administration of intra­operative chemotherapy routinely.
J. M. Lyons III (*) Our Lady of the Lake Physician Group, Baton Rouge, LA, USA
Louisiana State University Health Sciences Center, New Orleans, LA, USA e-mail: John.lyons@fmolhs.org
© Springer Nature Switzerland AG 2019 K. A. LeBlanc (ed.), Robotic Assisted Hernia Repair,
https://doi.org/10.1007/978-3-030-23025-8_27
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While our ability to support these patients through complex oncologic resections has improved greatly, postoperative incisional hernia (IH) remains a source of major morbidity. About 1/3 of patients with postoperative IH will have symptoms of pain/ discomfort, obstruction, or limitations of activity which can translate into worse physical and social functioning, general health perception, and overall lower body image [6, 7]. An estimated 17% of these patients present with incarceration or stran­gulation necessitating an urgent or emergent operation [8]. Moreover, the incidence of these defects appears to be rising as does the cost of repairs with a recent estimate of over $3 billion per year [9, 10].
Several technical and patient-related factors have been identied as predictive of postoperative IH.These include obesity, poor glycemic control, smoking, loss of domain, surgical site infection [11]. This chapter reviews several risk factors associ­ated with the development of postoperative IH, focusing on those which have unique signicance or prevalence in the cancer patient.
27.1 Size oftheIncision
The choice of incision in abdominal surgery depends on adequacy of exposure, previous abdominal incisions, body habitus, the anticipated pathology, and surgeon preference. Traditional (open) approaches to cancer surgery include midline, para­median, transverse, and oblique incisions.
The midline incision is the most commonly used in abdominal surgery as it is the simplest and provides adequate exposure to practically all four quadrants [12]. It is rapid to open and close; it is usually bloodless; and no muscle bers are divided. However, IH is a major problem following midline incision with rates ranging up to 20% [13].
The paramedian incision may be an alternative to the midline incision. It is usu­ally made by incising the skin down to the anterior rectus sheath over its the middle third. The rectus muscle is dissected free from its anterior and medial attachments and mobilized laterally to expose the posterior sheath, which is then incised longi­tudinally. The rectus muscle is not divided and its blood supply and innervation is maintained so that it bolsters the closure of the posterior and anterior sheaths at the conclusion of the case [14]. One of the challenges in evaluating this incision is that not all paramedian incisions are the same. Some groups using a medial paramedian (closer to the midline) have shown rates of IH very similar to those of a midline laparotomy [15, 16]. However, other groups using the lateral paramedian incision have seen virtually no incisional hernias [17]. Cahalane etal. combined prospective data from several series using the lateral paramedian incision and observed hernias in only four of 1203 (0.33%) cases at 1year, without a single dehiscence [17]. Thus, the closer the fascial incision is to the midline, the less effective the paramedian incision is in the prevention of IH.In addition, the paramedian incision tends to be more limiting and more time-consuming than the midline incision.
Transverse and/or oblique incisions are associated with fewer IH, and some have suggested less respiratory compromise, less overall morbidity than midline
27 Incisional Hernia inOncologic Surgery
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incisions [18, 19]. However, similar exposure constraints limit the utility of these approaches to cases with a very narrow focus.
The eld of minimally invasive surgery has grown considerably since the report of the rst laparoscopic appendectomy by Dr. Kurt Semm in the early 1980s [20]. Since that time, it has been applied to several types of oncologic resection; however the most comprehensive and thorough analysis of minimally invasive oncologic resection has been in the arena of colorectal surgery. The rst laparoscopic colecto­mies were performed in the early 1990s [21]. While these early cases demonstrated technical feasibility, concerns regarding adequacy of lymph node staging, the effect of abdominal insufation on tumor dissemination, and the risk of trocar site implants made the oncologic merits of laparoscopy less certain. To address these oncologic concerns, several randomized controlled trials were conducted comparing laparo­scopic to open colon resections [2225]. In general, laparoscopy was found to have lower blood loss, less need for narcotics, quicker return of bowel function. Moreover, they all demonstrated oncologic equivalency with regard to survival and recurrence in long-term follow-up. The range of laparoscopic procedures has now expanded to include resection for gastric cancer, esophageal cancer, gynecologic cancer, as well as prostate and bladder cancer [2629]. Minimally invasive pancreatic and liver resection surgery is also being evaluated [30, 31].
Incisional hernia rates following laparoscopic and open surgery have been com­pared by many. A retrospective analysis of 1057 colectomies (289 laparoscopic, 768 open) performed in a single British training center focused exclusively on patients with colorectal cancer [32]. The primary outcome was incidence of IH relative to surgical approach. They found the overall incidence of IH was 14.8% and noted no signicant difference between the open and laparoscopic technique (14.4% vs. 15.9%, p=0.566). These ndings were corroborated by a larger British registry study looking at IH incidence in colorectal cancer patients [33]. However, this is contrary to data obtained from the Danish Colorectal Cancer Group and the Dutch National Patient Registry which did show a difference in IH incidence favoring laparoscopy (5.3% vs.
7.3%, p<0.001) [34]. In general, the published rates of IH after laparoscopy vary greatly in non-randomized studies likely reecting different methods of IH detection (some using radiology, other using only clinical examination) and varying length of follow up. Two of the randomized multicenter trials designed to assess oncological outcome did not detect a decrease in IH after laparoscopic access, although a trend in favor of laparoscopy was seen in follow-up of the CLASICC trial [35, 36]. Kossler-Ebs etal., performed a meta-analysis on 24 randomized controlled trials com­paring IH rates after laparoscopic versus open surgery for all indications [37]. This included analysis of 3490 patients. The authors found that IH was signicantly reduced among patients whose surgery was completely laparoscopic (4.3% vs. 10.1%, p=0.0002). However, this difference was not observed in the subgroup of patients having “laparoscopic assisted” surgery with the hernia incidence at the extraction site comparable to that of open surgical approaches (5.5% vs. 7.8%, p=0.31).
Proponents of robotic-assisted surgery have suggested that the rate of IH is lower than that of typical laparoscopy because the robotic technique enables the use of smaller port incision sites and wristed instruments which promote less direct tissue
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trauma [38]. To date, there are few series reporting IH rates following robotic abdominal surgery; and most of these reports are small, single institutional series. However, data that do exist suggest that the reduction in IH following robotic sur­gery is negligible. One single-institution retrospective review of 259 patients under­going a robotic colorectal surgery from 2009 to 2014 found the overall IH rate to be
5.8% [39]—a rate similar to that reported by several laparoscopic series [40, 41]. A relatively recent study from the Memorial Sloan Kettering Cancer Center compared IH rates among patients who had undergone laparoscopic versus robotic right col­ectomy for colon cancer [42]. The clinical and demographic characteristics between the two groups were similar except that patients in the laparoscopic group had more advanced stage on average. Overall complication rates between the two groups were similar as was the incidence of IH.The rate of IH development was 22% and 17% (p=0.39) for the laparoscopic and robotic groups, respectively.

27.2 Obesity

Obesity is a critical world health problem. A 2005 pooled analysis indicated that 937 million adults are overweight, and 396 million are obese. Taken together this means that approximately 1/3 of the world population is considered either over­weight or obese; and if that trend continues, the incidence of overweight and obese people worldwide is projected to reach approximately 58% by 2030 [43]. The phys­iologic relationship between obesity and oncogenesis is complex, but the biological mechanisms that have received most attention include insulin, insulin-like growth factors, sex hormones, and adipokines. Briey, in the obese patient, insulin resis­tance develops as a metabolic adaptation to increased levels of circulating free fatty acids released from intra-abdominal adipose tissue. This is compensated by increased pancreatic insulin secretion. This chronic hyperinsulinemia has been linked to oncogenesis in several types of cancers [44].
The link between obesity and cancer has been demonstrated in numerous clinical studies as well [45]. In 2002, the International Agency for Research on Cancer (IARC) concluded that there is adequate evidence of an association between obesity and several cancers including colon, postmenopausal breast, endometrial, kidney, and esophageal [46]. In 2009, a collaborative analysis of 57 prospective studies was reported evaluating the relationship between body mass index (BMI) and cause spe­cic mortality evaluating over 900,000 patients [47]. These authors found that for every increase in BMI by 5kg/m
Obesity is also a major risk factor for the development of incisional hernias. This is likely because of the increased abdominal wall tension observed in obese patients. According to Laplace’s law, abdominal wall tension is directly related to the radius of the abdomen and intra-abdominal pressure, and studies have conrmed a direct correlation between obesity and increased intra-abdominal pressure [48, 49]. In consideration of these pathophysiological mechanisms, central obesity plays a very strong role in IH development. Some have contended that rather than central obesity or BMI, the degree of visceral adiposity is a better predictor of IH in cancer patients.
2
, all cancer mortality increased by 10%.
27 Incisional Hernia inOncologic Surgery
Using pre-operative CT scans, Aquina at el. assessed several radiographic measure­ments of abdominal fat volume in a series of patients undergoing surgery for colorectal cancer. With very good interobserver reliability, they found that visceral fat volume determined by preoperative imaging was more predictive of IH than BMI alone (HR 2.04, 95% CI 1.07–3.91) [50]. In addition, visceral fat is metaboli­cally active and is likely to alter the normal immune function [51]. This alteration has been linked to an increased risk of surgical site infection after colon resection; another independent risk factor for incisional hernia development [52].
429

27.3 Malnutrition

In order to promote healing, the surgical wound mediates the release of amino acids from muscles, gluconeogenesis, and other metabolic responses through afferent nerve bers that perceive pain, inammation, and changes in pH [53]. Successful healing also requires vitamins C, A, and B6 for collagen synthesis and cross-linking and essential fatty acids for cell synthesis. It is an anabolic process that occurs dur­ing a state of postoperative catabolism. Without these substances, wound healing is impaired. Naturally, patients with inadequate nutrition possess a limited supply of nutritional building blocks and not unexpectedly experience poor wound healing. This association between poor nutritional parameters and IH development has been demonstrated by many studies [54, 55]. One of the largest series to demonstrate this comes from the National Surgery Quality Improvement Program (NSQIP). Data from NSQIP (a large, multicenter, risk-adjusted, database) have consistently shown low serum albumin to be a risk factor for IH formation [55].
While malnutrition is not a feature exclusive to cancer patients, cancer has a pro­found impact on patient metabolism [56]. Advanced cancer patients can experience accelerated proteolysis, lipolysis, and diminished muscle protein synthesis [57]. Altered carbohydrate metabolism leads to increased hepatic glucose production and decreased insulin sensitivity. These alterations cause increased energy expenditure, loss of lean body mass, and generalized wasting [58]. The link between cancer-related malnutrition and IH has been noted in clinical studies as well. Researchers from the University of Wisconsin studied 265 patients following cytoreductive surgery for gynecologic malig­nancy [59]. At 1-year follow up, they found that poor nutritional status (preoperative albumin 3g/dL or less) was an independent risk factor for early onset IH development. These nutritional considerations deserve special attention in cancer patients who are undergoing surgery; and taken together, it may explain why several authors have found that just harboring a cancer diagnosis is a risk factor for incisional hernia.

27.4 Immunosuppression

When cancer cells are encountered invivo, the immune system recognizes tumor specic antigens on the surface of cancer cells in a manner similar to the recognition of non-self-pathogens [60]. Innate immune cells, such as NK cells, recognize the
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lack of MHC-I surface molecules on cancer cells, engage in active killing of these cells, and then recruit other inammatory cells through their cytokine production. Recruited monocytes phagocytose tumor cells and then present tumor-associated antigens on their surface which activates a specic cytolytic T cell response that is directed against the tumor. Then, like a pathogen induced immune response, these specic effector T cells clonally expand and travel to the tumor to eradicate it from the body. Over time, selective cancer cells develop the ability to evade the immune system by decreasing their immunogenicity while at the same time promoting a highly immunosuppressive microenvironment that continues to support their own nutrition, angiogenesis and matrix remodeling.
Data from transplant recipients indicate that the immunosuppression is an impor­tant and potentially modiable risk factor for IH formation. Several studies have found variable results but seem to implicate high dose steroids and sirolimus with higher rates of hernia formation [61, 62]. One study from 2002 compared mycophe­nolate mofetil and sirolimus directly and found signicantly more wound complica­tions with sirolimus, a nding supported by a similar study in heart transplant patients [63, 64]. Conversely, another study noted that failure to initiate immuno­suppression therapy following transplantation was associated with a higher risk of hernia formation [65]. However, the decision to withhold immunosuppression fol­lowing transplantation is likely representative of other clinical factors (i.e. delayed graft failure or presence of postoperative infections) that could also likely be risk factors for IH development.
Cytotoxic chemotherapy has long been known to affect the immune system. Most cytotoxic agents work by indiscriminant interference with the proliferation of rapidly dividing cells. This causes a major suppressive effect on the cellular media­tors of both humoral and cell-mediated immunity during treatment. In addition, some have demonstrated diminished levels of immune parameters persisting for up to 12months following cessation of treatment suggesting a more extended immuno­logical effect than has previously been considered [66]. The relationship between chemotherapy and IH has been discussed in the literature. While some authors have found postoperative chemotherapy to be a risk for IH formation, Nilson etal., and others observed that preoperative, but not postoperative chemotherapy, was associ­ated with IH [6769]. They also noted that longer duration (>6cycles) of preopera­tive chemotherapy was predictive of IH formation, and that the greatest risk factor observed was the administration of bevacizumab. This anti-VEGF agent has long been associated with impaired healing and has been implicated by others in the formation of postoperative IH [67].

27.5 Age

The median age of a new cancer diagnosis is in the United States is 66, and over 75% of patients with cancer are older than 55 [70]. Between 1982 and 2003, the population older than 65 doubled, and the population older than 85 quadrupled [71]. As a result, seniors with cancer are more frequently referred to surgeons for
27 Incisional Hernia inOncologic Surgery
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consideration of resection. Aging is associated with decline in functional reserve as well as physiologic changes in major organs that may affect the ability to heal from surgical procedures. Several authors have demonstrated age to be a signicant risk for the development of postoperative IH [13, 72]. Itatsu etal., studied this in a pro­spective observation of over 4000 patients who underwent abdominal surgery from November 2009 to February 2011 [69]. They noted an estimated incidence of IH to be 10.3% at 2years. Moreover, in multivariable analysis, increasing age by 10year interval (HR-1.3, 1.6 to 1.45) was found to be an independent risk factor for the development of IH.

27.6 Special Considerations: Cytoreductive Surgery

Surgical cytoreduction with hyperthermic intraperitoneal chemotherapy (HIPEC) is a strategy used to treat primary and secondary peritoneal malignancies. The rst descriptions of cytoreductive surgery were in the 1930s when Dr. JV Meigs described tumor debulking surgery for ovarian cancer theorizing that reducing mac­roscopic disease would improve symptoms [73]. Phase 1 trials were eventually con­ducted in the 1980s [74]; and through work conducted by Sugarbaker and others, guidelines regarding patient selection, technical feasibility, in adequacy of cytore­duction have been assembled [75].
Current indications exist for gynecologic, colorectal, appendiceal, and primary peritoneal neoplasms. The technique involves stripping disease from the perito­neum and visceral organs and leaving minimal residual tumor volume within the abdomen. Following surgery, a heated chemotherapy perfusate is administered intraoperatively into the abdomen to cover all peritoneal surfaces. Intraperitoneal chemotherapy allows a high local concentration of cytotoxic drugs to target any microscopic residual tumor volume [76]. Patients undergoing these procedures can experience signicant morbidity and mortality, up to 52% and 5.8% in some series [76]. More common sources of morbidity include stula formation, abscess, anas­tomotic leakage, and signicant abdominal wall complications as well. Valle etal. reported an increased risk of abdominal wall infection in patients with colorectal surgery undergoing HIPEC [77]. This was attributed to longer operative time, intra­operative contamination during enteric resections, and treatment-related immuno­suppression. In 2017, Struller etal., described the abdominal wall morbidity of 271 patients undergoing HIPEC at a single European comprehensive cancer center [78]. They noted an abdominal wall rupture rate of 4% which they acknowledged as ele­vated, but they also noted an IH incidence of only 7%. They felt that this rate was low secondary to shorter follow up. Risk factors for these complications included age, cardiopulmonary comorbidities, and certain histiotypes including pseudomyx­oma and mesothelioma.
Several reconstructive strategies have been undertaken to mitigate the degree of abdominal wall morbidity that is experienced postoperatively. Scholer et al. described their experience using a combination of biologic mesh, component sepa­ration, and rectus abdominis myocutaneous ap to reconstruct HIPEC patients