Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:
Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_890_Библиотеки_им_академика_М_И_Перельмана.pdf
Скачиваний:
0
Добавлен:
31.08.2026
Размер:
33 Мб
Скачать
4 Diverticulitis: Beyond the Basics
53
Fig. 4.2 Pelvic abscess (Hinchey II) with foci of free air
resolution and do not require percutaneous drainage or repet­itive CT scans (especially if the patient is clinically respond­ing with decrease in pain, fever, and leukocytosis) (Fig. 4.2 ) [ 48 ]. Combined series have shown that initial treatment with antibiotics (with or without percutaneous drainage) is suc­cessful in 30–56 % of patients [ 49 ]. Percutaneous drainage was initially used as a bridge to surgery; patients underwent drainage, sepsis resolved, and surgery was then performed electively [ 50 ]. Currently, percutaneous drainage is also used as defi nitive therapy, and some patients may not have further symptoms following successful resolution of the abscess. The decision to perform subsequent resection may therefore be made on an individual basis, recognizing patients with abscess have more severe diverticulitis and are more likely to require surgery. In rare cases, laparoscopic drainage may be performed if there is no radiologic window to drain an abscess (Video 4.1 ). The location of the abscess has been shown to help determine the clinical course, as those patients with more distant abscesses (i.e., Hinchey stage II) are more likely to require resection than patients with pericolic abscess. In a cohort of 465 patients, 73 patients (17 %) had an abscess, of which 45 patients had a pericolic abscess and 28 patients had a pelvic abscess. A larger number of patients with pelvic abscess (71 %) required surgery compared to those with pericolic abscess (51 %) [ 51 ].
Perforated Diverticulitis with Purulent or Feculent Peritonitis
Key Concept : The traditional therapy of mandatory colonic resection with or without diversion for perforated diverticu­litis continues to evolve with the development of improved
imaging , antibiotic success , endoscopic techniques , and implementation of laparoscopic lavage .
The optimal treatment for perforated diverticulitis and associated peritonitis continues to evolve. Options include Hartmann resection, sigmoid resection with primary anasto­mosis (in selected patients), sigmoid resection and primary anastomosis with proximal diversion, on-table lavage with primary anastomosis, and laparoscopic lavage without resec­tion. Hartmann resection remains one of the most common operations performed for perforated diverticulitis but has a number of drawbacks. Approximately 30 % of patients never undergo reversal of the stoma [ 52 , 53 ]. In addition, the oper- ation has considerable morbidity and a reported mortality of up to 18.8 % [ 54 ]. Over the years, a number of other options have been advocated. Fibrin glue with suture repair and omental patching of the perforation has been reported [ 55 ]. Two studies (both underpowered) looked at the role of defunctioning the diseased segment with suture of the perfo­ration and proximal diversion versus resection and had dif­ferent conclusions [ 56 , 57 ]. The role of on-table lavage in approaching patients with colonic emergencies has largely fallen out of favor since the need for bowel preparation has been challenged by a number of reviews [ 58 ]. A systematic review of 569 cases in 50 studies suggested that primary anastomosis with or without diversion was “safe in certain patients with peritonitis” but noted a mortality of 9.9 % and an anastomotic leak rate of 13.9 % [ 54 ].
In approaching the patient with perforated diverticuli­tis, it is important to distinguish between patients who have evidence of peritonitis on physical examination and those patients who have CT fi ndings consistent with perforation but no objective fi ndings of toxicity. While many surgeons trained in the 1970s or 1980s were taught that the fi nding of free air on a chest x-ray or KUB was an absolute indi­cation for surgery, the fi ndings of free air on CT imaging do not necessarily translate into similar recommendations. Dharmarajan and coworkers evaluated CT fi ndings of perfo­rated diverticulitis and devised a grading system based on the amount and location of abnormal air, which may assist with clinical decision-making [ 59 ]. While a grading system is a useful adjunct, I personally rely more heavily on the clinical status of the patient and base my initial strategy on the physi­cal examination fi ndings more than the CT fi ndings alone.
There has recently been a renewed interest in the role of laparoscopic lavage without resection for patients with per­forated diverticulitis and associated purulent peritonitis. In 1996, O’Sullivan and colleagues reported 8 patients with perforated diverticulitis and purulent peritonitis who under­went a laparoscopic lavage [ 60 ]. No resection of the sigmoid colon was performed, and patients were subsequently treated with intravenous antibiotics. At a follow-up of 12–48 months, no patient required subsequent resection, and no patient required an emergent colostomy. Based on these initial encouraging results, a prospective multi-institutional trial
54
P. L . R ob er ts
was subsequently performed of 100 patients with perforated diverticulitis who underwent laparoscopic lavage [
61 ]. The
median age was 62.5 years, and patients were followed for 36 months. The procedure was performed with an umbilical, suprapubic, and right lower quadrant ports, and patients were lavaged with 4 l of fl uid or lavaged until the returns were clear. Eight out of the 100 patients were noted to have fecal peritonitis and were converted to an open procedure and underwent resection and stoma. Of the 92 patients who were managed with laparoscopic lavage, no patient required sub­sequent resection for diverticulitis at a median follow-up of 36 months. There was an overall 4 % morbidity and 3 % mortality rate for the cohort. Two patients developed a pelvic abscess and required drainage, while 2 patients presented with a subsequent attack of diverticulitis. The authors con­cluded that laparoscopic lavage was a reasonable alternative with low mortality and low morbidity, particularly when compared with Hartmann resection. Furthermore, they sug­gested that elective resection, even in this group of patients who presented with perforation, was probably unnecessary and that readmission was uncommon.
Currently, the role of laparoscopic lavage continues to evolve in the treatment of patients with perforated diver­ticulitis and associated purulent peritonitis. A number of additional small series have been reported, including a recent review article evaluating 12 nonrandomized studies encompassing 301 patients with a mean age of 57 years [ 62 ]. Although the majority of patients in these combined series had Hinchey III classifi cation (i.e., purulent peritonitis), 25 % of patients had Hinchey II disease. In the Myers series, 25 % of patients also had Hinchey II disease, suggesting that some of these patients could potentially have been treated with bowel rest and antibiotics alone, along with subsequent per­cutaneous drainage for those patients developing abscesses [ 61 ]. In this combined series, the conversion rate was 4.9 %, while the mean complication rate was 18.9 % and mortality was 0.25 %. Subsequent resection was performed in 51 % of patients, and the majority of the resections were laparo­scopic. In the future, we need to identify those patients who may optimally be treated by lavage. Further classifi cation of the degree of peritonitis either by the Mannheim peritonitis index or the peritonitis severity score may help to further defi ne the optimal candidate for lavage. Similarly, the need for subsequent resection has not been defi ned. In the Afshar series, the majority of patients who underwent elective resection did so because of surgeon preference [ 62 ]. It goes without saying that colonoscopic evaluation of the colon is important in patients to exclude a diagnosis of perforated colon cancer.
A number of guidelines have been refi ned to include a state­ment on lavage. The European Association for Endoscopic Surgery consensus statement of laparoscopy for abdominal
emergencies states that “colon resection remains the gold standard, but laparoscopic lavage and drainage may be con­sidered in some selected patients” [ 16 ]. The Association of Coloproctology of Great Britain and Ireland states that “lap­aroscopic lavage may play a role in some patients with acute diverticulitis. Whilst this is an alternative to resection in the acute setting for some patients, it is not certain whether it is an acute alternative to delayed resection” [ 12 ]. At the present time, I use laparoscopic lavage selectively in otherwise fi t patients with perforated diverticulitis. In the concept of the calculated risk, we as the surgeons “make the calculations,” and the patients “incur the potential risk.” I do not generally recommend lavage to unstable patients or those with a num­ber of other associated comorbidities.
Reoperative Surgery for Diverticular Disease
Key Concept : Reoperative surgery entails unique technical and decision - making challenges that need to be considered both prior to and at the time of surgery to optimize outcomes .
Reoperation for complicated diverticular disease occurs for two main reasons: as a planned procedure to restore intes­tinal continuity after resection, stoma, and Hartmann closure of the rectum and as an unplanned procedure to treat com­plications or unanticipated events after initial resection and primary anastomosis. The latter occurrence is mainly due to anastomotic leakage but may occur from fi stula, abscess, or stricture at the anastomosis. This section discusses considerations prior to reoperative surgery including anat­omy, timing of reoperation, anatomic considerations, preop­erative preparation, conduct of the operation, and outcome.
Reoperative Surgery After Hartmann Resection
The Hartmann resection was fi rst described by Henri Hartmann for the treatment of rectal cancer in which he described two patients presenting with obstruction in whom he resected the tumor and closed the “superior part of the rectum and left it in the peritoneum without disturbing the pelvic fl oor” [ 63 ]. The procedure quickly became the proce- dure of choice for the majority of patients who underwent emergency surgery for perforated diverticulitis in the second half of the twentieth century, replacing the three-stage proce­dure of initial colostomy, subsequent resection, and fi nally colostomy takedown that was advocated by Lockhart­Mummery [ 64 , 65 ]. Of note, Hartmann believed that reversal of the Hartmann procedure should not be attempted. Currently, Hartmann takedown still has signifi cant morbidity and mortality and a relatively low reversal rate. Unfortunately, the risk of needing to return to the operating room for a repeat stoma remains high.
4 Diverticulitis: Beyond the Basics
55
Timing
After Hartmann resection for perforated diverticulitis, most patients are eager to proceed as soon as possible with rever­sal of the colostomy. In contrast to patients who may be chronically ill with infl ammatory bowel disease for years prior to resection, these patients often had never been ill before and had never anticipated leaving the hospital with a stoma after treatment for diverticulitis. Surgery for Hartmann reversal may be undertaken early (<3 months from initial surgery) or late (>3 months from initial surgery). There are advocates of each approach [
6670 ]. Proceeding with
Hartmann takedown close to the time of initial surgery has several disadvantages, predominantly due to adhesions and the acute infl ammatory response after initial surgery which may lead to a diffi cult dissection, potential enterotomies, and diffi culty with identifi cation of the Hartmann stump. While waiting for at least 3 months will presumably allow the patient suffi cient time to heal and facilitate identifi cation of the Hartmann stump, waiting longer may make identifi cation of the stump more diffi cult secondary to fi brosis. The two approaches (waiting less than 3 months vs. greater than 3 months) have not been assessed in a randomized trial. My approach has been to wait for 3 months prior to Hartmann takedown. Waiting for this time period ideally reduces the diffi culty and potential complications from adhesions.
Preoperative Preparation
General preoperative assessment of the patient should routinely be performed. Nutritional status is optimized. Cardiopulmonary disease is identifi ed and evaluated. Reoperative pelvic surgery is associated with a high risk of thromboembolic complications, and patients are admin­istered appropriate prophylaxis. Although increasing evi­dence suggests that mechanical bowel preparation is not necessary, I believe that it is preferable in reoperative sur­gery to minimize spillage in case the bowel is entered. Preoperative intravenous antibiotics are administered, although there is little evidence to support additional dosing.
Preoperative Imaging
For patients >50 years old who have not had prior colonic evaluation, a colonoscopy or barium enema should be per­formed. Prior to planning Hartmann takedown, my prefer­ence is to perform a barium enema through the stoma and a Gastrografi n enema through the rectum. The Gastrografi n enema is particularly useful as it gives an assessment of the length and confi guration of the rectal segment and gives an assessment of any residual sigmoid colon and/or diverticula
4.3 ). Many patients have undergone the initial resec-
(Fig. tion by another surgeon; at times, because of intraoperative factors, a substantial amount of sigmoid colon is left in place. The road map of the specifi c anatomy is better deter-
Fig. 4.3 Gastrografi n enema shows residual sigmoid colon and diverticula
mined by a Gastrografi n study than by a fl exible sigmoidos­copy, although both can be performed. These procedures are also helpful to evacuate retained fecal residue. Scybala retained in the rectum from the original Hartmann resection should be evacuated at this time or with distal rectal wash­out at the time of surgery to facilitate placement of a sizer and subsequently the EEA stapler. Even with a washout at the time of colostomy takedown, this may be diffi cult to accomplish.
Intraoperative Considerations
Patient Positioning
Anticipate a long procedure and pad the patient’s bony promi­nences accordingly. The patient may be placed in lithotomy position in Lloyd Davies, Allen, or Yellowfi n stirrups. Care should be taken to avoid pressure on the peroneal nerves and the hips. Overall, my preferred position is aimed to have symmetric hip extension, knee fl exion, and thigh abduction. Extreme hip extension beyond 60° can occasionally lead to femoral nerve palsies if a self-retaining retractor is positioned against the extended extremity. The perineum should be hang­ing slightly over the table to ensure easy passage of the EEA stapler. Rectal washout can be performed and a mushroom catheter left in the rectum if desired to facilitate identifi ca­tion of the Hartmann pouch. A proctoscope and/or sizer may also be used intraoperatively to identify the pouch. The vagina should also be included in the prep. Alternatively, my prefer­ence is to position the patient supine on a split leg table with the legs abducted. The split leg table avoids potential diffi culties
56
P. L . R ob er ts
with long-standing lithotomy position including nerve injuries and compartment syndrome. Once again, care must be taken to ensure that the patient is positioned far enough down on the table that access to the anus (to pass the EEA stapler) can be achieved. A beanbag with the arms tucked at the sides can be helpful to ensure the patient does not slip cephalad on the table, especially when in steep Trendelenburg position.
Approach to the Procedure
The procedure may be undertaken by a laparoscopic or open approach. Adhesions encountered from previous surgery or prior infection may make a laparoscopic approach impossi­ble. The extent and degree of adhesions may be diffi cult to predict; on occasion much less severe adhesions are encoun­tered than anticipated, and the procedure progresses quite smoothly. Alternatively, with extensive adhesions, bowel injury may occur when attempting to enter the peritoneal cavity. A reasonable approach is the use of a “peek port” which entails entering the abdomen through a small incision and assessing the degree of adhesions [ 71 ]. The laparoscopic equipment is not opened until the feasibility of a laparo­scopic hand-assisted approach is determined. Alternatively, a port can also be placed away from the site of the previous surgery to assess the degree of adhesions and the feasibility of a straight laparoscopic approach.
Exposure and Lighting
The importance of having adequate exposure and lighting cannot be overestimated with reoperative surgery. If an open approach is used, the incision should extend to the symphysis pubis. Cephalad extension of the midline incision may be needed if splenic fl exure mobilization is needed. Operating between the patient’s legs provides optimal visualization of the splenic fl exure as does rotation of the table to a left-side­ up position.
Adequate OR lighting, a headlight, and/or lighted pelvic retractors are helpful. A self-retaining retractor with bladder blade is also used. Straight blade (Wylie renal vein or St. Mark’s) and curved (Deaver) retractors are available, with the former being more helpful for deep pelvic dissection, which is on occasion necessary to free up the Hartmann stump. Care must be taken to avoid placing these retractors on the drapes and causing a fi re.
Initial Dissection
The initial dissection is focused on lysing all small bowel adhesions in the pelvis to be able to identify the Hartmann pouch. Ultimately, in the majority of cases, all small bowel adhesions from the ligament of Treitz to the ileocecal valve are lysed to be able to mobilize the colostomy and bring the proximal colon down to the pelvis without tension. The pel­vic dissection associated with a prior Hartmann resection may be challenging secondary to dense adhesions and the
inability to distinguish a plane suitable for dissection. It is advisable to lyse the fi lmy small bowel adhesions fi rst and then attack the more diffi cult adhesions. With few excep­tions, there are small bowel and/or omental adhesions to the top of the Hartmann pouch. Dense adhesions often occur to the top of the Hartmann pouch, and encountering staple material is an indication of proximity to this structure. If extremely dense adhesions are encountered, hydrodissection or infi ltration of the fused area with saline with a small­gauge needle may be helpful [ 72 ]. The appendix can also be drawn down into the pelvis toward the Hartmann and may occasionally lead the surgeon to believe he or she has encountered the right ureter. The left ovary and tube, in par­ticular, may be fused with the top of the Hartmann pouch. Bleeding from the pelvic wall may often occur from entering the fallopian tubes or a branch of the ovarian vessels.
The ureters should be identifi ed, and the surgeon should be aware that they may be in an unanticipated position, par­ticularly drawn in more medially, after prior surgery. Ureteral stents may be used in selected cases with prior severe pelvic sepsis or unclear anatomy. Stents do not prevent ureteral injury but facilitate the recognition of such injury. I selec­tively use stents in patients with hydronephrosis or a large amount of retroperitoneal infl ammation. The vagina may be adherent to the rectum and dissection facilitated by placing a fi nger in the vagina to identify the proper planes.
The colostomy is mobilized by incising the mucocutane­ous junction and trying to preserve all the mesenteric attach­ments. Injection with saline or local anesthetic around the mucocutaneous junction circumferentially may facilitate dissection. The stoma is resected and fresh bowel used for the intended anastomosis. Once the stoma is mobilized, the surgeon can generally assess whether there is adequate length for a tension-free anastomosis. Additional length is facilitated by a number of maneuvers including division of the lateral colonic attachments, takedown of the splenic fl ex­ure, division of the inferior mesenteric artery at the takeoff of the aorta, and division of the inferior mesenteric vein at the inferior border of the pancreas. Alternatively, further length can be achieved by mobilizing the rectum further distally and essentially bringing the Hartmann pouch up to the proxi­mal bowel. Once complete mobilization of the proximal colon is performed and adhesiolysis is completed, the small bowel and colon can be packed into the upper abdomen.
Identifi cation and Mobilization of the Hartmann Pouch
Once the small bowel is mobilized, the top of the Hartmann pouch can be identifi ed. Some surgeons mark the top of the pouch with long suture material to facilitate identifi cation. I have not found this to be helpful and have found that inser­tion of a proctoscope or fl exible sigmoidoscope facilitates identifi cation of the Hartmann pouch. The staple line of the Hartmann is identifi ed, and the length of the pouch is usually
4 Diverticulitis: Beyond the Basics
57
longer than anticipated, even if it is located below the pelvic brim. If the staple line is adherent to the presacral fascia, it is generally safe to commence the dissection in the posterior midline, thus avoiding the ureters and the iliac vessels. It is not uncommon for the superior rectal artery to be left intact, and placing a Babcock clamp on the end of the Hartmann pouch and applying cephalad traction facilitate identifi cation of the mesentery and straightening of the rectum. My prac­tice is to mobilize and dissect out the Hartmann pouch at least to the mid- to proximal rectum. This is generally neces­sary to “straighten out the rectum,” which often times has a concertina-like confi guration following Hartmann resection. If this is not done, it is often diffi cult to guide the EEA stapler per anum to the top of the Hartmann pouch. Once the Hartmann pouch is mobilized, a small sizer is placed per rec­tum to ensure that this passes easily to the area of the intended anastomosis. In those patients who have had signifi cant sep­sis or in those who have had a long-standing Hartmann pouch, further mobilization may be needed. We have found that in women further dissection is often needed in the ante­rior cul-de-sac as the mid-rectum tends to angulate and adhere to the uterus. Despite further mobilization, some patients may still have a fairly fi brotic pelvis (in which the rectum is intrinsically normal but the surrounding tissues are fi brotic enough that it is impossible to pass a sizer). In this case, an EEA-stapled anastomosis may not be feasible and a handsewn anastomosis preferable. The top of the intended site of anastomosis is then re-resected and the integrity of the rectum tested by fi lling the pelvis with saline and insuffl ating the Hartmann pouch.
Performing the Anastomosis
I prefer using the EEA stapler to perform anastomosis after Hartmann resection. The anvil is placed in the proximal bowel. A handsewn purse string is placed, or a purse-string device may be used. A sizer is used to guide through the rectum to the top of the re-resected Hartmann pouch. Occasionally, it is diffi cult to introduce the stapler into the anus, and Khoury and Opelka have reported placement of a Faensler or Chelsea-Eaton anoscope with gradual dilata­tion of the sphincter and placement of the stapler shaft through the anoscope [ 73 ]. The EEA stapler is guided through with the trocar exiting at the top of the Hartmann pouch, the anvil is snugged up and secured, and the stapler is fi red. The instrument is generally removed easily, and the tissue rings are inspected for thickness and integrity. The anastomosis is then tested by occluding the bowel proximally and introducing air through a proctoscope or a fl exible sigmoidoscope [ 74 ].
Alternatives
There is no one single technique to perform an anastomosis after Hartmann takedown, and some ingenuity and employ-
ing other techniques may be necessary. The stapler may not pass up to the top of the rectum because of fi brosis and con­traction, particularly if the patient has been diverted for many years. In this case, there are several alternatives. One option is to perform a handsewn anastomosis. Another option is to introduce the stapler and bring the trocar through the anterior rectal wall, thus performing an end of colon to side of rectum anastomosis [ 73 ]. Further options include employing a double purse-string technique in which a purse string is placed in the proximal colon and the distal end (rec­tum). The stapler is still introduced through the anus. A fi nal technique employs a single purse string in the rectum and placing the stapler through the side of the proximal colon and completing the anastomosis by transecting the end of the colon with a TA stapler.
Abdominal Wall Closure
Following completion of the anastomosis, the abdomen is irrigated and the incision closed. A mass closure technique is superior to layered closure. A continuous abdominal wall closure is associated with a lower risk of abdominal wound dehiscence. Furthermore, a meta-analysis of six randomized controlled trials found that the risk of incisional hernia for­mation was signifi cantly less with a continuous compared with an interrupted closure (regardless of the suture type used) [ 75 ]. The use of resorbable versus non-resorbable sutures results in no difference in dehiscence rates, but higher rates of persistent sinus formation and chronic wound prob­lems occurred with non-resorbable sutures. Optimal primary wound closure is with a mass closure continuous technique with resorbable sutures placed at an interval of 1 cm apart and 1 cm back on the fascia [ 76 ]. Laparoscopic techniques minimize incision length and wound trauma and may be associated with less wound complications.
Reoperation for Sepsis and Anastomotic Complications After Hartmann Takedown
Key Concept : Identifi cation of anastomotic leak through test­ing is an integral part of left - sided anastomosis . For those experiencing a leak requiring operative intervention , decid­ing between proximal diversion alone and resection and diversion depends on the patient ’ s clinical manifestations and the intraoperative fi ndings .
Anastomotic leak is among the most serious potential complications after Hartmann takedown (Fig.
4.4 ). The lack
of a standardized defi nition precludes comparison among units and even a precise incidence of this complication. We have used the United Kingdom (UK) working party defi ni­tion of leakage of gastrointestinal contents or contrast from a surgically constructed anastomosis [
77 ]. In our unit, we have
reviewed 998 left-sided colorectal anastomoses and have noted a clinical leak rate of 4.8 % [
74 ]. Air leak testing was
performed intraoperatively in 825 left colon anastomoses.
58
P. L . R ob er ts
Fig. 4.4 Gastrografi n enema shows a leak at the top of the Hartmann pouch with extravasation ( arrow ) and intraluminal contrast ( arrow ) into small bowel
A clinical leak was noted in 7.7 % of anastomosis with a positive air leak test compared with 3.8 % of anastomosis with a negative air leak test and 8.1 % of all untested anasto­moses ( P < 0.3). The data suggest that air leak testing should be performed in all such anastomosis to allow the surgeon to detect and repair a leak at the time of initial procedure.
Management of anastomotic leak depends on the clini­cal manifestations of the leak and the overall condition of the patient. Anastomotic dehiscence may manifest as peri­tonitis, a colocutaneous fi stula, an associated abscess, or even be relatively asymptomatic. For those patients with generalized peritonitis, urgent exploration is performed after fl uid resuscitation and intravenous antibiotics. Stoma site marking is ideally done preoperatively. Placement in lithotomy position or on a split leg table is helpful in case sigmoidoscopy is needed. The two main intraoperative con­siderations are to leave the anastomosis in place and to divert proximally or to resect the anastomosis and perform a colostomy. In patients with total anastomotic dehiscence, a large defect, or concerns about the viability of the anasto­mosis, resection of the anastomosis is advisable. The distal end is stapled or handsewn, and the proximal colon brought out as a colostomy. Unfortunately, a substantial number of these patients will never undergo colostomy closure.
In selected cases of a small defect and a relatively stable patient, the anastomosis may be left in place and diverted proximally with either a colostomy or ileostomy. A recent meta-analysis suggested that an ileostomy was associated with less stoma-related complications and a lower incidence
of abdominal wall hernias [
78 ]. A concern of such an
approach is leaving a large column of stool, which may then leak through the anastomosis resulting in ongoing pelvic sepsis. If a diverting ileostomy is performed, lavaging the distal bowel or endoscopically evacuating the distal bowel should be considered. An ileostomy may be associated with a high incidence of dehydration and the need for readmis­sion, especially in elderly patients [
79 ].
Chronic sepsis or anastomotic leak may also manifest as a colocutaneous fi stula. A major risk factor for the develop­ment of a colocutaneous fi stula is the anastomosis to the distal sigmoid colon and not the proximal rectum [ 45 ]. While selected cases may heal with good nutritional support and a tincture of time, re-resection of the anastomosis is needed for persistent fi stulas.
Reoperation for Recurrent Diverticulitis
Key Concept : Re - resection of the prior anastomosis with special attention to the distal and proximal margins , along with ensuring a tension - free anastomosis , is paramount to improving outcomes for reoperative diverticular disease .
Recurrent diverticulitis following sigmoid resection is uncommon. In the patient presenting with abdominal pain following resection for diverticulitis, a thorough investiga­tion should be undertaken to exclude other causes of abdom­inal pain including infl ammatory bowel disease, irritable bowel syndrome, gynecologic disease, adhesive disease, and infectious complications from the initial resection. Recurrent diverticulitis should also be distinguished from poorly char­acterized pain following resection. A recent study of 325 patients who underwent either laparoscopic or open sigmoid resection for diverticulitis noted that 20 % of patients had ongoing functional symptoms [ 80 ]. Munson and colleagues found that 27.2 % of patients following resection for diver­ticular disease continued to have pain [ 81 ]. The most com- mon risk factor associated with recurrent diverticulitis is failure to perform a colorectal anastomosis and performing a colocolic anastomosis with retained distal sigmoid colon as the proximal section margin (Fig. 4.3 ). Although diverticuli- tis may only involve a portion of the sigmoid colon, it is important to resect the sigmoid colon and perform resection to the proximal rectum. The rectum is identifi ed at the level at which the tenia fan out, which is usually at the sacral promontory. In the presence of prior infl ammation, this spot may not be readily apparent, in which case the level of the bowel just below the sacral promontory is a reasonable land­mark. The proximal resection margin is less well established. While it is not necessary to resect all proximal diverticula, the anastomosis should be performed in soft pliable bowel. In the evaluation of the patient with recurrent diverticulitis, it is helpful to obtain prior records, including the pathology report and operative note, to ensure that the diagnosis was indeed diverticulitis and to review specifi c operative details.
4 Diverticulitis: Beyond the Basics
59
Ureteral stents may be considered especially if the original operation was diffi cult, associated with unclear anatomy, or associated with postoperative pelvic sepsis or anastomotic complications. The patient should be prepared for the possi­bility of a temporary stoma, especially if the anastomosis is low. Adequate mobilization of the colon is key, and splenic fl exure mobilization is necessary. If these various maneuvers do not result in suffi cient mobility and allow a tension-free anastomosis, the middle colic vessels on occasion require division with blood supply of the residual colon based on the right and/or ileocolic vessels. Additional approaches such as bringing the right colon through a window in the mesentery or resecting further and bringing the hepatic fl exure down to the rectum may be needed [
82 , 83 ].
The prior anastomosis may also be densely adherent to the presacral fascia. The presacral fascia is a condensation of the parietal endopelvic fascia, and it is important to get into the right plane; otherwise, massive pelvic bleeding may occur from the avalvular presacral veins which com­municate with the basivertebral veins [ 84 ]. The sympa- thetic pelvic nerves run caudad and lateral over the presacral fascia to join the pelvic plexus laterally and are at risk for damage if the plane is not developed and exposed correctly. Depending on the diffi culty of the pelvic dissec-
be necessary.
Reoperative surgery, in general, is challenging, and reop­erative surgery for diverticulitis, specifi cally, is no excep­tion. No one approach can be employed to guarantee success, and the surgeon must have a number of approaches and tech­niques in his or her armamentarium to ensure optimal patient outcome.

Conclusion

Our understanding and treatment of diverticulitis con-
tinue to evolve. Recent trends have shown increased use
of laparoscopic techniques both for elective and emer-
gency surgeries and a trend to primary anastomosis
for both elective and urgent operations [ 85 ]. Although
the literature supports a more conservative approach to
patients with uncomplicated diverticulitis, there has been
a dramatic increase in the frequency of elective surgi-
cal resection for diverticulitis by 38 %. The increase
in elective surgical resection is nine times greater
than the increase in urgent surgical resection, suggest-
ing that clinical practice does not mirror the current
recommendations.
Future investigations should focus on the identifying risk factors for recurrent diverticulitis and optimally iden­tify those patients who require early surgical intervention. Ultimately increased understanding of this common dis­ease will help physicians and surgeons in the prevention and treatment of diverticulitis.

Summary Pearls

Diverticulitis is one of the most common gastrointestinal dis­eases. The trend over the last decade has been toward a greater understanding of the disease that will ultimately result in a more “personalized” approach to the patient. I believe that we will ultimately be able to delineate the natural history of diver­ticular disease and predict the clinical course of disease for an individual patient. In the meantime, you should have a thor­ough understanding of all the factors involved when deciding on a management strategy to ensure optimal outcomes.

References

1. Available at http://hcup.ahrq.gov . Accessed 15 Dec 2012.
2. Salem L, Anaya DA, Flum DR. Temporal changes in the manage­ment of diverticulitis. J Surg Res. 2004;124(2):318–23.
3. Stollman NH, Raskin JB. Diagnosis and management of diverticu­lar disease of the colon in adults. Ad hoc practice parameters com­mittee of the American College of Gastroenterology. Am J Gastroenterol. 1999;94:3110–21.
4. Wong WD, Wexner SD, Lowry A, et al. Practice parameters for the treatment of sigmoid diverticulitis–supporting documentation. The Standards Task Force. The American Society of Colon and Rectal Surgeons. Dis Colon Rectum. 2000;43:290–7.
5. Surgical treatment of diverticulitis. Patient care committee of the Society for Surgery of the Alimentary Tract (SSAT). J Gastrointestinal Surg. 1999;3:212–13.
6. Kohler L, Sauerland L, Neugebauer E. Diagnosis and treatment of diverticular disease: results of a consensus development confer­ence. The Scientifi c Committee of the European Association for Endoscopic Surgery. Surg Endosc. 1999;13:430–6.
7. Salem L, Veenstra D, Sullivan SD, et al. the timing of elective col­ectomy in diverticulitis: a decision analysis. J Am Coll Surg. 2004; 199:904–12.
8. Richards FJ, Hammitt JK. Timing of prophylactic surgery in pre­vention of diverticulitis recurrence: a cost effectiveness analysis. Dig Dis Sci. 2002;57(9):1903–8.
9. Janes S, Meagher A, Frizelle FA. Elective surgery after acute diver­ticulitis. Br J Surg. 2005;92(2):133–42.
10. Chapman J, Davies M, Wolff B, et al. Complicated diverticulitis: is it time to rethink the rules? Ann Surg. 2005;242:576–81; discussion 581–3.
11. Rafferty J, Shellito P, Hyman NH, Buie WD, Standards commit­tee of American Society of Colon and Rectal Surgeons. Practice parameters for sigmoid diverticulitis. Dis Colon Rectum. 2006; 49(7):939–44.
12. Fozard JB, Armitage NC, Schofi eld JB, Jones OM, Association of Coloproctology of Great Britain and Ireland. ACPGBI position statement on elective resection for diverticulitis. Colorectal Dis. 2011;13 Suppl 3:1–11.
13. Parks TG. Natural history of diverticular disease of the colon: a review of 521 cases. BMJ. 1969;4:639–45.
14. Makela J, Vuolio S, Kiviniemi H, et al. Natural history of diverticu­lar disease; when to operate? Dis Colon Rectum. 1998;41:1523–8.
15. Makela JT, Kiviniemi HO, Laitinen ST. Spectrum of disease and outcome among patients with acute diverticulitis. Dig Surg. 2010;27(3):190–6.
16. Broderick-Villa G, Burchette FJ, Collin JC, Abbas MA, et al. Hospitalization for acute diverticulitis does not mandate routine elective colectomy. Arch Surg. 2005;140:576–81.
60
P. L . R ob er ts
17. Shaikh S, Kurkowski ZH. Outcome of a conservative policy for managing acute sigmoid diverticulitis. Br J Surg. 2007;94:876–9.
18. Hall JF, Roberts PL, Ricciardi R, Read T, Scheirey C, Wald C, et al. Long-term follow-up after an initial episode of diverticuli­tis: what are the predictors of recurrence? Dis Colon Rectum. 2011;54(3):283–8.
19. Chautems RC, Ambrosetti P, Ludwig A, et al. Long term follow-up after the fi rst acute episode of sigmoid diverticulitis; is surgery mandatory? A prospective study of 118 patients. Dis Colon Rectum. 2002;49:939–44.
20. Haglund U, Hellberg R, Johnson C, et al. Complicated diverticular disease of the sigmoid colon. An Analysis of short and long term outcome in 293 patients. Ann Chir Gynaecol. 1970;68:41–6.
21. Eglinton T, Nguyen T, Raniga S, Dixon L, Dobbs B, Frizelle FA. Patterns of recurrence in patients with acute diverticulitis. Br J Surg. 2010;97(6):952–7.
22. Chapman JR, Dozois EJ, Wolff BG, Gullerud RE, Larson DR. Diverticulitis; a progressive disease? Do multiple recurrences pre­dict less favorable outcomes? Ann Surg. 2006;243(6):876–80; dis­cussion 880–3.
23. Anaya DA, Flum DR. Risk of emergency colectomy and colostomy in patients with diverticular disease. Arch Surg. 2005;140(7):681–5.
24. Klarenbeek BR, Samuels M, van der Wal MA, van der Peet DL, Meijerink WF, Cuesta MA. Indications for elective sigmoid resec­tion in diverticular disease. Ann Surg. 2010;251(4):670–4.
25. Boostrom SY, Wolff BG, Cima RR, Merchea A, Dozois EJ, Larson DW. Uncomplicated diverticulitis, more complicated than we thought. J Gastrointest Surg. 2012;16:1744–9.
26. Ambrosetti P, Grossholz M, Becker C, Terrier F, Morel P. Computed tomography in acute left colonic diverticulitis. Br J Surg. 1997;84:532–4.
27. Poletti PA, Platon A, Rutschmann O, Kinkel K, Nyikus V, Ghiorghui S, Morel P, et al. Acute left colonic diverticulitis; can CT fi ndings be used to predict recurrence? Am J Roentgenol. 2004;182(5):1159065.
28. Hall JF, Roberts PL, Ricciardi R, Read TE, Marcello PW, Schoetz DJ. The Lahey Score; a simple score to predict the need for early surgical intervention for diverticulitis. In: Presented at the American College of Surgeons, 2012.
29. Benn PL, Wolff BG, Ilstrup DM. Level of anastomosis and recur­rent colonic diverticulitis. Am J Surg. 1986;151:269–71.
30. Thaler K, Baig MK, Berho M, et al. Determinants of recurrence after sigmoid resection for uncomplicated diverticulitis. Dis Colon Rectum. 2003;46(3):385–8.
31. Carlson RM, Roberts PL, Hall JF, Marcello PW, Read TE, Ricciardi R. Is routine splenic fl exure mobilization during anterior resection always necessary. In: Presented at the American Society of Colon and Rectal Surgeons Annual meeting, San Antonio, 2012.
32. Schauer PR, Ramos R, Ghiatas AA, et al. Virulent diverticular dis­ease in young obese men. Am J Surg. 1992;164:443–6.
33. Ouriel K, Schwartz SI. Diverticular disease in the young patients. Surg Gynecol Obstet. 1983;16:1–5.
34. Acousta JA, Grebene ML, Doberneck RC, et al. Colonic diver­ticular disease in patients 40 years old or younger. Am Surg. 1992;58:605–7.
35. Janes S, Meagher A, Faragher IG, Shedda S, Frizelle FA. The place of elective surgery following acute diverticulitis in young patients: when is surgery indicated? An analysis of the literature. Dis Colon Rectum. 2009;52(5):1008–16.
36. Vignati PV, Welch JP, Cohen JL. Long-term management of diver­ticulitis in young patients. Dis Colon Rectum. 1995;38:627–9.
37. Hall JF, Roberts PL, Ricciardi R, Marcello PW, Scheirey C, Wald C, et al. Colonic diverticulitis: does age predict severity of disease on CT imaging. Dis Colon Rectum. 2010;53(2):121–5.
38. Etzioni DA, Cannom RR, Ault GT, Beart Jr RW, Kaiser AM. Diverticulitis in California from 1995 to 2006; increased rates of treatment for younger patients. Am Surg. 2009;75(10):981–5.
39. Russ AJ, Obma KL, Rajamanickam V, Wan Y, Heise CP, Foley EF, et al. Laparoscopy improves short-term outcomes after surgery for diverticular disease. Gastroenterology. 2010;138(7):2267–74.
40. Klarenbeek BR, Veenhof A, Bergamaschi R, van der Peet DL, van den Broek WT, de Lange ES, et al. Laparoscopic sigmoid resection for diverticulitis decreases major morbidity rates: a randomized control trial; short term results of the Sigma Trial. Ann Surg. 2009;249(1):39–44.
41. Ridgway PF, Latif A, Shabbir J, Ofriokuma F, Hurley MJ, Evoy D, et al. Randomized controlled trial of oral vs intravenous therapy for the clinically diagnosed acute uncomplicated diverticulitis. Colorectal Dis. 2009;11(9):941–6.
42. Etzioni DA, Chiu VY, Cannom RR, Burchette RJ, Haigh PI, Abbas MA. Outpatient treatment of acute diverticulitis and predictors of failure. Dis Colon Rectum. 2010;53(6):861–5.
43. Hjern F, Josephson T, Altman D, Holmstrom B, Mellgren A, Pollack J, et al. Conservative treatment of acute colonic diver­ticulitis; are antibiotics always mandatory? Scan J Gastroenterol. 2007;42(1):41–7.
44. Gatta L, Vakil N, Vaira D, Pilotto A, Curlo M, Comparato G, Leandro G, et al. Effi cacy of 5-ASA in the treatment of colonic diverticular disease. J Clin Gastroenerol. 2010;44(2):113–6.
45. Fazio VW, Church JM, Jagelman DG. Colocutaneous fi stulas com­plicated diverticulitis. Dis Colon Rectum. 1987;30(2):89–94.
46. Ricciardi R, Baxter NN, Read TE, Marcello PW, Hall J, Roberts PL. Is the decline in the surgical treatment for diverticulitis associ­ated with an increase in complicated diverticulitis? Dis Colon Rectum. 2009;52(9):1558–63.
47. Hinchey EJ, Schaal PG, Richards GK. Treatment of perforated diverticular disease of the colon. Adv Surg. 1978;12:85–109.
48. Siewert B, Tye G, Kruskal J, et al. Impact of CT-guided drainage in the treatment of diverticular abscess: size matters. AJR Am J Roentgenol. 2006;186:680–6.
49. Soumain S, Thomas S, Mohan PP, Khan N, Khan Z, Raju T. Management of Hinchey II diverticulitis. World J Gastroenterol. 2008;14(47):7163–9.
50. Saini S, Mueller PR, Wittenberg J, Butch RJ, Rodkey GV, Welch CE. Percutaneous drainage of diverticular abscess. An adjunct to surgical therapy. Arch Surg. 1986;121(4):475–8.
51. Ambrosetti P, Chautems R, Soravia C, et al. Long-term outcome of mesocolic and pelvic diverticular abscesses: a prospective study of 73 cases. Dis Colon Rectum. 2005;48:787–91.
52. Seetharam S, Paige J, Horgan PG. Impact of socioeconomic depri­vation and primary pathology on rate of reversal of Hartmann’s procedure. Am J Surg. 2003;186:154–7.
53. Maggard MA, Zingmond D, O’Connell JB, Ko CY. What propor­tion of patients with an ostomy (for diverticulitis) get reversed? Am Surg. 2004;70(10):928–31.
54. Salem L, Flum DR. Primary anastomosis or Hartmann’s procedures for patients with diverticular peritonitis? A Systematic review. Dis Colon Rectum. 2004;47:1953–64.
55. Karoui M, Champault A, Pautrat K, Valleur P, Cherqui D, Champault G. Laparoscopic peritoneal lavage or primary anas­tomosis with defunctioning stoma for Hinchey 3 complicated diverticulitis: results of a comparative study. Dis Colon Rectum. 2009;52(4):609–15.
56. Krukowski ZH, Matheson NA. Emergency surgery for diverticular disease complicated by generalized and faecal peritonitis; a review. Br J Surg. 1984;71(12):921–7.
57. Zeitoun G, Laurent A, Rouffet F, Hay J, Fingerhut A, Paquet J, Pellon G, et al. Multicentre, randomized clinical trial of primary versus secondary sigmoid resection in generalized peritonitis com­plicating sigmoid diverticulitis. Br J Surg. 2000;87(10):1366–74.
58. Slim K, Vicaut E, Launay-Savary MV, et al. Updated systemic review and meta-analysis of randomized clinical trials on the role of mechanical bowel preparation before colorectal surgery. Ann Surg. 2009;249(2):203–9.
4 Diverticulitis: Beyond the Basics
61
59. Dharmarajan S, Hunt SR, Birnbaum EH, Fleshman JW, Mutch MG. The effi cacy of nonoperative management of acute complicated diverticulitis. Dis Colon Rectum. 2011;54(6):663–71.
60. O’Sullivan GC, Murphy D, O’Brien MG, Ireland A. Laparoscopic management of generalized peritonitis due to perforated colonic diverticula. Am J Surg. 1996;171(4):432–4.
61. Myers E, Hurley M, O’Sullivan GC, Kavanagh D, Wilson I, Winter DC. Laparoscopic peritoneal lavage for generalized peritonitis due to perforated diverticulitis. Br J Surg. 2008;95(1):97–101.
62. Afshar S, Kurer MA. Laparoscopic peritoneal lavage for perforated sigmoid diverticulitis. Colorectal Dis. 2012;14920:135–42.
63. Hartmann H. Nouveau procede d’ablation des cancers de la partie terminale du colon pelvien. Congres Francais de Chirugia. 1923;30:2241. Cited by: Corman ML. Classic articles in colonic and rectal surgery. Dis Colon Rectum. 1984;27:273.
64. Lockhart-Mummery JP. Late results in diverticulitis. Lancet. 1938;2:1401–2.
65. Smithwick RH. Experiences with surgical management of diver­ticulitis of sigmoid. Ann Surg. 1942;15:969–85.
66. Albarran SA, Shimoens C, Van de Winkel N, et al. Restoration of digestive continuity after Hartmann’s procedure: ASA score is a predictive factor for risk of postoperative complications. Acta Chir Belg. 2009;109:714–9.
67. Khan AL, Ah-See AK, Crofts TJ, et al. Reversal of Hartmann’s colostomy. J R Coll Surg Edinb. 1994;39:239–42.
68. Keck JO, Collopy BT, Ryan PJ, et al. Reversal of Hartmann’s pro­cedure: effect of timing and technique on ease and safety. Dis Colon Rectum. 1994;37:243–8.
69. Fleming FJ, Gillen P. Reversal of Hartmann’s procedure following acute diverticulitis: is timing everything? Int J Colorectal Dis. 2009;24:1219–25.
70. Salem L, Anaya DA, Roberts KE, et al. Hartmann’s colectomy and reversal in diverticulitis: a population-level assessment. Dis Colon Rectum. 2005;48:988–95.
71. Read TE, Salgado J, Ferraro D, et al. “Peek port”: a novel approach for avoiding conversion in laparoscopic colectomy. Surg Endosc. 2009;23(3):477–81.
72. Worsey MJ, Fazio VW. Reoperative Pelvic Surgery. In: Yeo CJ, Dempsey DT, Klein AS, Pemberton JH, Peters JH, editors.
Shackelford’s Surgery of the Alimentary Tract. 6th ed. Philadelphia: Saunders/Elsevier; 2007. p. 2409–18.
73. Khoury DA, Opelka FG. Anoscopic-assisted insertion of end-to­end anastomosing staplers. Dis Colon Rectum. 1995;38:533–4.
74. Ricciardi R, Roberts PL, Marcello PW, Hall JF, Read TE, Schoetz DJ. Anastomotic leak testing after colorectal resection: what are the data? Arch Surg. 2009;144(5):407–11.
75. Hodgson NC. The search for an ideal method of abdominal fascial closure: a meta-analysis. Ann Surg. 2000;231(3):436–42.
76. Ceydeli A, Rucinski J, Wise L. Finding the best abdominal clo­sure: an evidence-based review of the literature. Curr Surg. 2005;62(2):220–5.
77. Bruce J, Krukowski ZH, Al-Khairy G, Russell EM, Park KG. Systematic review of the defi nition and measurement of anastomotic leak after gastrointestinal surgery. Br J Surg. 2001;88(9):1157–68.
78. Tilney HS, Sains PS, Lovegrove RE, et al. Comparison of outcomes following ileostomy versus colostomy for defunctioning colorectal anastomoses. World J Surg. 2007;31:1141–5.
79. Hayden DM, Pinzon MC, Francescatti AB, Edquist SC, Malczewski MR, Jolley JM. Hospital readmission for fl uid and electrolyte abnor­malities following ileostomy construction. Preventable or unpredict­able. J Gastrointest Surg. 2013;17:298–303. Epub 2012 Nov 29.
80. Levack MM, Savitt LF, Berger DL, Shellito PC, Hodin RA, Rattner DW, et al. Sigmoidectomy syndrome? Patients’ perspectives on the functional outcomes following surgery for diverticulitis. Dis Colon Rectum. 2012;55(1):10–7.
81. Munson KD, Hensien MA, Jacob LN, et al. Diverticulitis-a com­prehensive follow-up. Dis Colon Rectum. 1996;39:318–22.
82. Le TH, Gathright Jr JB. Reconstitution of intestinal continuity after extended left colectomy. Dis Colon Rectum. 1993;36:197–8.
83. Beck DE. Intraoperative anastomotic challenges. In: Whitlow CB, Beck DE, Margolin DA, Hicks TC, Timmcke AE, editors. Improved outcomes in colon and Rectal Surgery. London: Informa Healthcare;
2010. p. 33–55.
84. Qinyao W, Wejiin S, Youren Z, et al. New concepts in severe presacral hemorrhage during proctectomy. Arch Surg. 1985;120:1013–20.
85. Masoomi H, Buchberg BS, Magno C, Mills SD, Stamos MJ. Trends in diverticulitis management in the United States from 2002 to
2007. Arch Surg. 2011;146(4):400–6.

Carcinomatosis: Cytoreduction and Heated Intraperitoneal Chemotherapy (HIPEC) Versus Palliation

Björn L. D. M. Brücher , Avital Itzhak , Anton Bilchik , Aviram Nissan , and Alexander Stojadinovic
5
Abbreviations
BMI Body mass index CC score Completeness of cytoreduction score CDSS Clinical decision support systems CRC Colorectal cancer CRS Cytoreductive surgery CT Computed tomography CTR-1 Copper transport protein-1
B. L. D. M. Brücher , MD, PhD, FRCS (Engl), FACS (*) Department of Surgery , Bon Secours Cancer Institute , Richmond , VA , USA
INCORE = International Consortium of Research of the Theodor­Billroth- Academy e-mail: b-bruecher@gmx.de
A. Itzhak , MD, FACS Department of Surgery , Bon Secours Cancer Institute , Richmond , VA , USA
Uniformed Services University of the Health Sciences , Bethesda , MD , USA
A. Bilchik , MD, PhD, FACS Department of Surgery , John Wayne Cancer Institute , Santa Monica , CA , USA
A. Nissan , MD, FACS Department of Surgery , Hadassah-Hebrew University , Jerusalem , Israel
United States Military Cancer Institute , Bethesda , MD , USA
A. Stojadinovic , MD, FACS Department of Surgery , Bon Secours Cancer Institute , Richmond , VA , USA
Uniformed Services University of the Health Sciences , Bethesda , MD , USA
United States Military Cancer Institute , Bethesda , MD , USA
®
, Richmond , VA , Germany-Israel-Serbia-USA
DPAM Disseminated peritoneal adenomucinosis EPIC Early postoperative IP chemotherapy HIPEC Hyperthermic intraperitoneal Chemotherapy ICU Intensive care unit IV Intravenous NCCTG North Central Cancer Treatment Group OR Operating room PC Peritoneal carcinomatosis PCI Peritoneal cancer index PSM Peritoneal surface malignancy QOL Quality of life RCT Randomized controlled trial TPN Total parenteral nutrition
Contributing Author Declaration We certify that all individuals who qualify as authors have been listed; each author has participated in one or more of the following areas: con­ception and design of this work, the acquisition and/or analysis of data, the writing and/or critical revision of the document, and supervision of this cooperative research effort. All contributing authors approve of the submission of this version of the manuscript and assert that the docu­ment represents valid work. If information derived from another source was used in this manuscript, we obtained all necessary approvals to use it and made appropriate acknowledgements in the document. All con­tributing authors take public responsibility for this work.
Disclaimer The views expressed in this manuscript are those of the authors and do not refl ect the offi cial policy of the Department of the Army, the Department of Defense, or the US Government.
Copyright Protection One of the contributing authors are military service members (or employees of the US Government: AS), and this work was prepared as part of their offi cial duties. Title 17 U.S.C. 105 provides the “Copyright protection under this title is not available for any work of the United States Government.” Title 17 U.S.C. 101 defi nes a US Government work as a work prepared by a military service member or employee of the US Government as part of that person’s offi cial duties.
S.R. Steele et al. (eds.), Complexities in Colorectal Surgery, DOI 10.1007/978-1-4614-9022-7_5, © Springer Science+Business Media New York 2014
63