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COMPLICATIONS 451
of the proximal colon that is beyond the size of any available stent. Rectal anastomoses are best suited for stenting because of their size, diameter, and access. However, the stent can cause tenesmus if any part of it is 5 cm or less from the anal verge.
Fibrin glue (combined thrombin and brinogen) or other types of nonbiologic glues have been used during anastomosis creation and for leaks and stulas. Despite the early success showing an 85% heal­ing rate of anal stulae, recent studies have failed to replicate these numbers. It has also been shown that brin glues are less eective in treating rectal complications compared with other areas such as the esophagus. Fibrin glue has a 25% to 33% success rate as a single agent for treating rectal anastomotic complications. e two benets in using brin glue are the speed and ease of application and the fact that it will not prevent the use of any other method if it fails.
It is sometimes possible to reapproximate a so anastomotic staple line that has separated less than 1 cm, using clips or sutures. Beginning at each end of the separation and moving to the middle to place the clips reduces tension on the closure. e cost of this closure is almost prohibitive when multiple clips are used. e endoscopist also requires experience and extraordinary skill to be successful. 

TRANSANAL REPAIR TECHNIQUES

Transanal repair techniques are best used in chronic leaks or stu­las with minimal inammation or infection. E-VAC therapy could potentially be used to provide resolution of inammation and infec­tion and thus allow for earlier and more eective treatment with transanal repair.
Leaks located in the distal rectum can be amenable to repair through an open transanal approach. Leaks located more proximally in the rectum have the potential to be repaired though transanal min­imally invasive surgery for persons experienced with the technique. Simple suturing is prone to fail even for small defects with minimal inammation.
Expanding the small opening of a long-standing, almost chronic leak in the posterior area of a very distal rectal anastomosis to uncover a large presacral sinus, known as “unroong or marsupializa­tion,” permits better drainage and healing that can result in complete resolution of the sinus in a few months through re-epithelialization. “Laying open” can be performed endoscopically using an Olympus triple-lumen needle knife (Olympus, Hamburg, Germany), or with the proctoscope and the laparoscopic electrocautery scissors. Our preferred method is to use a laparoscopic Endo-GIA stapling device, and we have achieved good results. e stapling device is placed through an anoscope in the anus. e thin anvil arm of the Endo­GIA device is inserted through the opening of the leak, and the staple cartridge arm is le within the rectal lumen. e resulting staple lines provide hemostasis and provide “marsupialization” by sealing the edges of the chronic stula and exposing the chronic abscess cavity to the rectal lumen. is becomes a pseudo-diverticulum from the back of the rectum, which eventually becomes epithelialized and part of the rectal wall.
Flap advancement can be used for any anastomotic stula near the anal verge. e repair involves excising the stula opening and mobi­lizing the adjacent tissues, allowing for the approximation of healthy tissues without tension. All of these transanal techniques will need proximal diversion to have any chance of success. 

TURNBULL-CUTAIT PULL THROUGH

Sometimes a surgeon will be faced with a rectal anastomosis that has not healed with use of other modalities and appears to be unsal­vageable. Repeat surgery to resect a low rectal anastomosis asso­ciated with chronic inammation can interrupt locally derived neovascularization and may be associated with undue tension on the new coloanal anastomosis. e combination of poor blood
supply and tension can easily result in a leak. e use of a Turnbull­Cutait pull through of the le colon can eliminate these risks. is technique requires adequate mobilization of the le and transverse colon to allow the bowel to be pulled though the short rectal stump. e mucosa of the rectal stump is stripped to the dentate line and the bowel is pulled through the anus to leave 7 to 10 cm hanging out. A 34 F mushroom catheter, which is long enough to drain the colon above the pelvic oor and bulky enough to passively remain above the pelvic oor, is secured within the lumen of the bowel using an encircling umbilical tape around the portion of the colon pulled through the anal canal. e catheter hangs out of the anus and is placed to closed drainage. e externalized bowel is wrapped with Betadine-soaked Kerlix and continually kept moist with fresh Betadine for 7 days. On day 7 the patient is taken back to the operat­ing room and the external segment of bowel is amputated. A hand­sewn, coloanal anastomosis is then created at the dentate line or the top of the cu of rectal mucosa. e downside of the Turnbull­Cutait procedure is the poor function that oen follows closure of the diverting stoma. 

SUMMARY

A surgeon working with GI anastomoses must be familiar with a broad range of options to diagnose and manage leaks. Until we have a perfect way to prevent leaks, the true skill of the GI sur­geon is the ability to salvage a failed anastomosis in an imperfect biologic system. As techniques of endoscopic closure, placement of stents, vacuum-assisted dressing with an intraluminal sponge, and transanal suture techniques improve with time and experi­ence, the need for a large operative procedure to rescue anasto­moses will diminish. Even so, adherence to surgical principles in the management of intra-abdominal sepsis is particularly impor­tant. In the future, early diagnosis or detection of an impending leak may allow intraluminal treatment before the complications of contamination occur.

S u g g e S t e d R e a d i n g

Alves A, Panis Y, Trancart D, etal. Factors associated with clinically signi-
cant anastomotic leakage aer large bowel resection: multivariate analysis of 707 patients. World J Surg. 2002;26(4):499–502.
Blumetti J, Chaudhry V, Cintron JR, etal. Management of anastomotic leak:
lessons learned from a large colon and rectal surgery training program. World J Surg. 2014;38(4):985–991.
den Dulk M, Noter SL, Hendriks ER, etal. Improved diagnosis and treat-
ment of anastomotic leakage aer colorectal surgery. Eur J Surg Oncol. 2009;35:420–426.
Fraccalvieri D, Biondo S, Saez J, etal. Management of colorectal anastomotic
leakage: dierences between salvage and anastomotic takedown. Am J Surg. 2012;204(5):671–676.
Hirst N, Tiernan J, Millner P, Jayne D. Systematic review of methods to pre-
dict and detect anastomotic leakage in colorectal surgery. Colorectal Dis. 2014;16(2):95–109.
Nagell CF, Holte K. Treatment of anastomotic leakage after rectal resec-
tion with transrectal vacuum-assisted drainage (VAC). A method for rapid control of pelvic sepsis and healing. Int J Colorectal Dis. 2006;21(7):657–660.
Phitayakorn R, Delaney CP, Reynolds HL, etal. Standardized algorithms for
management of anastomotic leaks and related abdominal and pelvic ab­scesses aer colorectal surgery. World J Surg. 2008;32(6):1147–1156.
Snijders HS, Wouters MW, van Leersum NJ, etal. Meta-analysis of the risk
for anastomotic leakage, the postoperative mortality caused by leak­age in relation to the overall postoperative mortality. Eur J Surg Oncol. 2012;38:1013–1019.
ornton M, Joshi H, Vimalachandran C, etal. Management and outcome of
colorectal anastomotic leaks. Int J Colorectal Dis. 2011;26:313–320.
Weidenhagen R, Gruetzner KU, Wiecken T, etal. Endoscopic vacuum-
assisted closure of anastomotic leakage following anterior resection of the rectum: a new method. Surg Endosc. 2008;22:1818–1825.

C  C
Rhodri J. Codd and Peter M. Sagar

INTRODUCTION

Colonoscopy remains the gold standard for colonic investigation. It is a sensitive diagnostic tool and provides a nonsurgical approach for the removal of colonic and rectal polyps. However, colonoscopy is invasive. It can be a challenging procedure to perform and is associ­ated with infrequent but potentially serious complications. Most of these complications occur aer therapeutic procedures have been performed. Potential complications are listed in Box 86-1.
Adverse events can occur before, during, or aer a procedure. Postprocedure complications can occur immediately, within days, or sometimes years aer the procedure (e.g., a stricture related to previous endoscopic mucosal resection). Knowledge of the potential complications together with early recognition and appropriate man­agement of the situation will help improve patient outcomes. 

RISK MANAGEMENT

Perhaps the most important aspect of colonoscopy is minimizing risk for the patient, which starts with a targeted history that includes cardiac and respiratory risk factors, history of renal impairment, the presence of diabetes or bleeding disorders, drug history (particularly antiplatelet and anticoagulant agents), and a history of allergies. e patient’s comorbidities are balanced against the possible benets of colonoscopy to determine whether the procedure should be per­formed at all. Comorbidities also inuence choice of bowel prepara­tion (renal function status) and the depth and duration of conscious sedation (respiratory function).
Although the skill and experience of each colonoscopist varies, every colonoscopy should be performed or supervised by an endos­copist with adequate training as dened by the various supervising societies. e complication rate is highest for inexperienced colonos­copists who have performed a low volume of procedures. e risk of complications can be up to three times higher aer a polypectomy performed by a “low-volume” colonoscopist (i.e., an endoscopist who has experience with 1 to 141 colonoscopies) when compared with a “high-volume” colonoscopist (i.e., an endoscopist who has experience with 379 to 1225 colonoscopies). Inherent in the better outcome of experienced endoscopists is experience and knowledge of the equipment, including the electrocautery generator and the various adjuncts. A poorly functioning scope and lack of familiar­ity with equipment will place the patient at an unnecessary risk. It is also important that colonoscopists be aware of their own limitations because overambition may lead to adverse events. As the complex­ity of polypectomy increases, the risk of complications also increases. Using lower risk procedures when appropriate, or referring patients
BOX 86-1: Potential Complications
Bowel preparation complications Sedation complications Hemorrhage Perforation Diastatic serosal tears Bacteremia Vasovagal reex Postcolonoscopy distension Splenic trauma Cardiac events Missed disease Death
to “high-volume” endoscopists, can reduce the risk of perforation and gastrointestinal bleeding.
In this chapter we will concentrate on the management of two potentially life-threatening and surgically important complications of colonoscopy: perforation and hemorrhage. 

HEMORRHAGE

Hemorrhage is a rare complication of diagnostic colonoscopy because clinically signicant bleeding from mucosal biopsy sites is uncom­mon. However, hemorrhage is the most common complication asso­ciated with endoscopic polypectomy. Hemorrhage can be dened as acute blood loss aer a polypectomy that is severe enough to mandate admission to the hospital.
Steps Prior to Colonoscopy
It is important to ascertain whether the patient has a history of a bleeding disorder or is undergoing anticoagulant or antiplatelet ther­apy. Use of anticoagulant and antiplatelet agents should be stopped for a sucient period before a polypectomy is performed. A compre­hensive guide to the management of anticoagulant and antiplatelet therapy in patients undergoing endoscopic procedures is available in a document published by the working party for the British Society of Gastroenterology (see Suggested Reading).
e patient and his or her family need to be warned about the possibility of postpolypectomy bleeding. Patients should not travel to areas remote from medical care for the next 2 weeks. 
452
COMPLICATIONS 453
Risk Factors for Bleeding
Postpolypectomy bleeding rates between 0.16% and 6.1% have been reported. Factors associated with an increased risk of bleeding include patient age (elderly persons have a higher risk), size of the polyp, location of the polyp (right colonic polyps have a higher risk of bleeding), number and structure of the polyps (sessile and thick­stalked polyps are more likely to bleed) and the use of anticoagulant drugs. Some series report bleeding rates aer polypectomy of up to 10% for large (>2 cm) right-sided colonic polyps. In addition to these factors, the type of diathermy setting can aect the risk of postpol­ypectomy bleeding. e use of pure-cut diathermy is associated with a higher rate of immediate bleeding, whereas blend and coagulation diathermy settings are associated with lower rates of hemorrhage.
Prevention of Bleeding
e European Society of Gastrointestinal Endoscopy has con­cluded that the placement of detachable loop ligating devices for large pedunculated polyps and the submucosal injection of diluted (1:10,000) epinephrine for sessile polyps are eective strategies to reduce postpolypectomy bleeding. e ecacy of other measures, including endoclip placement and argon plasma coagulation, has not been proven. A helpful strategy in a high-risk patient with multiple polyps is to remove the largest polyp and leave the others, so that if bleeding occurs, the site is already known. 
Treatment of Bleeding
Hemorrhage sometimes occurs despite adequate risk assessment and good technique. In this situation, it is important to have an appro­priate management strategy. A suggested approach is summarized in
Figure 86-1. Bleeding can occur immediately or can be delayed up
to 30 days aer the procedure. In most cases of immediate hemor­rhage, it is possible to treat the bleeding endoscopically. A working
knowledge of endoscopic hemostatic techniques is important, and use of a combination of these techniques can be helpful.
Injection of epinephrine (a 1:10,000 solution) via a exible injec­tor needle causes vasoconstriction and controls most bleeding. e aim is to form a bleb of the solution at the site of bleeding by injection into the submucosal plane. Injection of several milliliters around the bleeding site may be necessary to achieve the desired eect.
Should bleeding occur aer removal of a pedunculated polyp, hemo­stasis is achieved by snaring the stalk and holding it for at least 5 minutes. Some snares are detachable and can be le in situ. Repeat transection of the base of the polyp is not recommended because this maneuver can make regrasping of the base impossible should the bleeding continue. Hemoclips are safe to use to treat immediate bleeding. However, accurate placement is sometimes dicult, and multiple clips are oen required.
Methods of direct-contact thermal treatment including the use of a heater probe, electrocautery, and argon plasma coagulation can be useful in the treatment of hemorrhage. Although these techniques carry a risk of perforation, short bursts of light contact without exces­sive pressure will reduce the likelihood of perforation.
When endoscopic techniques prove unsuccessful in achieving hemostasis, decisions must be made about further management. e volume and ow of bleeding should be estimated and the like­lihood of spontaneous cessation should be assessed at colonoscopy. Should the ow of blood be brisk and continuous, then appropriate resuscitation with blood products is oen necessary. Angiographic transarterial embolization can be successful in achieving hemosta­sis. However, patients must be stable enough to be transferred to the radiology department and must be aware of the signicant risk (approximately 11%) of colonic ischemia requiring colectomy.
Surgery is a last resort. A laparoscopic approach is appropriate and preferable to open surgery. In cases of immediate postpolypectomy bleeding, the site of hemorrhage is usually known. is knowledge can allow a segmental colonic resection and primary anastomosis because the colon should be clean aer the bowel preparation used for the patient’s colonoscopy. In unusual cases, depending on the availability of angiography, a subtotal colectomy may be required
Immediate Hemorrhage
Assess site of bleeding
Endoscopic Treatment
Injection of epinephrine 1 in 10,000 sol
If possible direct pressure with sling
± Hemoclip application
± Direct contact thermal treatment
If unsuccessful consider CT angiography with embolization
If unsuccessful consider segmental resection/subtotal colectomy
FIGURE 86-1 Algorithm for postcolonoscopy bleeding. C T, Computed tomography.
n
Delayed Hemorrhage
If small volume and patient stable can
watch and closely monitor
or
Early colonoscopy/CT angiography to identify site of bleeding and treat
If brisk bleeding or patient unstable consider on table colonoscopy ± laparoscopy/laparotomy
*In all cases, patients must be closely monitored and resuscitated with blood products when appropriate.
CompliCations of ColonosCopy454
when delayed hemorrhage occurs or if uncertainty exists about the site of bleeding. On-table colonoscopy can be helpful in facilitating potential endoscopic control of hemorrhage or can identify the site of bleeding and allow segmental colonic resection.
Delayed bleeding oen can be managed expectantly if the volumes of blood are relatively small and the patient is hemodynamically sta­ble. However, should the bleeding be more profuse, then colonoscopy has a role. In this situation, it may be safer to perform colonoscopy in an operating room with an anesthetist and blood products available in the event that the patient requires an emergency laparotomy. Usually a bowel preparation can be administered at the same time that resus­citation is occurring, although repeat scoping of an unprepared colon can be performed. e site of bleeding is oen marked by an adherent clot, which must be removed by irrigation before hemostasis can be obtained. Adrenalin injection, clips, or coagulation can be used. 

PERFORATION

Perforation can be dened as the evidence of air, luminal contents, or instrumentation outside the gastrointestinal tract. In general, the incidence of postcolonoscopic perforation is low, with rates rang­ing from 0.1% to 0.6%. erapeutic procedures are associated with a higher risk of perforation when compared with diagnostic colonos­copy alone.
In the United Kingdom, the National Health Service bowel cancer screening program quality assurance guidelines suggest perforation rates of less than 1 in 1000 cases for diagnostic colonoscopy and less than 1 in 500 cases aer polypectomy.
Causes of Perforation
A perforation during diagnostic colonoscopy can be caused in sev­eral ways, the most common of which is the use of excessive force when pushing through the tip of the colonoscope. Other mechanisms include the use of manipulation such as the dangerous blind “slide­by” technique, aggressive resolution of sigmoid loops, and excessive force along the antimesenteric border associated with looping of the scope. Overinsuation of the colon also can result in perforation as a result of barotrauma.
Sometimes clues exist to an increased potential for perforation. For instance, in patients with severe inammation or acute angulation of the colon associated with adhesions from previous surgery, particular care should be taken not to use excessive force. In patients with diverticular disease, the endoscopist also should take special care not to inadvertently push the scope through a diverticulum, mistaking it for the lumen, and thereby perforating the colon. e risk for perforation also exists when the colon is weak, such as in the setting of ischemic or Crohn colitis. Scoping should be performed carefully in such patients, and the colonos­copist must be ready to retreat if the colon seems too fragile.
erapeutic procedures carry a particular risk of perforation. e risk is increased aer removal of sessile polyps, particularly if the polyp is large and right sided. Technique is important to avoid excessive risk of perforation. e endoscopist should be careful not to include any bowel wall within the snare during polypectomy and not to use prolonged electrocautery that can result in thermal necrosis and a transmural burn. Two centimeters is the maximum polyp diameter that should be drawn into the snare. Appropriate use of electrocautery is of particular importance when removing right­sided polyps because of the relative thinness of the colonic wall. 
Diagnosis of Perforation
When a perforation happens, early diagnosis is essential. Perfora­tion may be obvious during the procedure when intra-abdominal fat or viscera can be seen through the scope, but in many cases the
symptoms and signs are more subtle. Other signs of perforation that may be noted during the procedure include irreducible abdominal distension, a sudden inability to maintain insuation of the colonic lumen, or a sudden increase in patient discomfort.
Apart from persistence of the abdominal distension, immediate postprocedure signs may be subtle. e presentation of peritonitis may be delayed because the patient usually has undergone bowel preparation, and the degree of contamination is therefore minimal. Localized or generalized peritonitis may take time to develop and in many cases will not occur at all. Similarly, fever, leukocytosis, and other signs of sepsis can take hours or days to develop.
In the event of any suspicion of a perforation, a plain abdominal and erect chest radiograph will likely show evidence of free or retro­peritoneal air. e amount of free air may bear little relationship to the clinical picture and should not be used as a marker of severity. In patients with “benign pneumoperitoneum,” radiologic evidence of free gas is recognized in an asymptomatic patient aer colonoscopy; this condition has been identied in 1 of 100 consecutive abdominal radiographs. One likely mechanism is a pneumatic serosal split as a result of the use of air as an insuating gas and a tight sigmoid pre­venting distal decompression, which causes distention of the proxi­mal colon and splitting of the serosa. Gas can escape the bowel, but no frank perforation exists. e presence of postcolonoscopy free intraperitoneal air does not mandate surgical exploration. Nonopera­tive management, which usually consists of close observation under the care of gastroenterologists and surgeons, is successful in many patients. Patients initially should take nothing by mouth in case sur­gical intervention becomes necessary. Intravenous uids and broad­spectrum intravenous antibiotics should be administered, including adequate anaerobic coverage. Close monitoring and regular surgical review is required to identify any evidence of deterioration, which may be an indication for surgery.
e ndings at colonoscopy can be helpful in determining the risk of fecal peritonitis and the need for surgery. e adequacy of bowel preparation can provide clues as to the risk of immediate fecal soiling. If the bowel has been well prepared and is clean, the immediate risk is lower than in a patient with poor bowel preparation and liquid stool within the colon. e latter patient is more likely to require surgical intervention aer an iatrogenic perforation because spillage of feces into the peritoneal cavity is more likely.
Should the colonoscopist identify intraperitoneal viscera or fat during the procedure, then an operation is warranted, because the defect will be sizeable and will not heal with conservative measures alone. Endoscopic closure of iatrogenic perforations of the colon using endoclips has been reported in the literature. However, these studies are mainly small case series or case reports, and attempting endoscopic closure would depend on the prior experience and skill of the endoscopist involved. 
Management of Perforation
In patients with generalized peritonitis and sepsis, decision making is easy because surgery is usually warranted. Similarly, patients who are asymptomatic oen can be managed conservatively. However, some patients have more subtle signs such as localized peritonitis, a low­grade fever, tachycardia, and/or leukocytosis (postpolypectomy syn­drome). ese patients may respond to bowel rest and intravenous antibiotics but require very close monitoring for any deterioration that would warrant surgery.
Should surgery be necessary, preoperative localization of the per­foration operatively may be desirable. Usually the likely site is obvious from the colonoscopy report and from the early symptoms, but if the patient underwent multiple polypectomies, the site of interest may be unclear. In this situation, a water-soluble enema may be requested but should not delay surgical treatment.
Traditionally, patients requiring surgical intervention for iatro­genic colonic perforation would undergo laparotomy with either
If perforation noted at colonoscopy, then assess adequacy of bowel preparation and size of defect
Consider endoclip if endoscopist is appropriately trained
Early postprocedure patient assessment— history, examination, plain films ± CT
COMPLICATIONS 455
Asymptomatic or mild symptoms
Closely monitor
NBM, IV fluid, broad spectrum antibiotics
FIGURE 86-2 Perforation management algorithm. C T, Computed tomography; NBM, nothing by mouth.
Localized peritonitis
(Postpolypectomy Syndrome)
Consider nonsurgical approach with regular reassessment and a low threshold to proceed to surgery if deterioration
suture repair of the defect or colonic resection. A proportion of patients will require formation of a stoma in the form of a defunction­ing loop ileostomy or an end colostomy (Hartmann procedure). In recent years, it has been recognized that patients can be safely treated laparoscopically aer colonoscopic perforation. is approach is pre­ferred because patients can benet from minimally invasive surgery while undergoing either suture repair with washout and drainage or segmental colonic resection. A well-prepared colon with minimal fecal soiling should allow safe suture repair and drainage or seg­mental resection with primary anastomosis. In a small proportion of patients, clinical reasons for avoiding primary anastomosis may exist. If signicant fecal soiling, perioperative instability, or major comor­bidity is present, the risk of anastomotic leakage may be deemed too high and colonic diversion is preferred. Restorative surgery can then be considered once the patient has recovered from the acute event.
A management algorithm for patients with colonic perforation aer a colonoscopy is provided in Figure 86-2. is algorithm should be considered a guide and not a denitive management strategy because ultimately each case is dierent and the surgeon should adopt an indi­vidualized approach to patients with iatrogenic colonic perforation.

S u g g e S t e d R e a d i n g S

Chukmaitov A, Bradley CJ, Dahman B, et al. Association of polypectomy
techniques, endoscopist volume, and facility type with colonoscopy com-
plications. Gastrointest Endosc. 2013;77:436–446.
Generalized peritonitis or significant sepsis
Laparoscopy/laparotomy ± suture repair or colonic segmental resection
Consider stoma formation, depending on the status of the patient, the degree of contamination, and the health of the bowel
Gatto NM, Frucht H, Sundararajan V, etal. Risk of perforation aer colo-
noscopy and sigmoidoscopy: a population based study. J Natl Cancer Inst.
2006;95:230–236. Grupka MJ, Benson J. Endoscopic clipping. J Dig Dis. 2008;9:72–78. Kapetanos D, Beltsis A, Chatzimavroudis G, Katsinelos P. Postpolypectomy
bleeding: incidence, risk factors, prevention, and management. Surg Lapa-
rosc Endosc Percutan Tech. 2012;22:102–107. Kim HS, Kim TI, Kim WH, etal. Risk factors for immediate postpolypec-
tomy bleeding of the colon: a multicenter study. Am J Gastroenterol.
2006;101:1333–1341. Rabeneck L, Paszat LF, Hilsden RJ, etal. Bleeding and perforation aer outpa-
tient colonoscopy and their risk factors in usual clinical practice. Gastro-
enterology. 2008;135:1899–1906. Rotholtz NA, Laporte M, Lencinas S, etal. Laparoscopic approach to colonic
perforation due to colonoscopy. World J Surg. 2010;34(8):1949–1953. Rutter MD, Chilton A. Quality assurance guidelines for colonoscopy. NHS
BCSP Publication. 2011;6:24. Sivak MV Jr., ed. In: Gastroenterologic Endoscopy. 2nd ed. Philadelphia:
Saunders; 2000. Tytgat GNJ, Classen M, Waye JD, Nakazawa S, eds. Practice of erapeutic
Endoscopy. 2nd ed. London: Saunders; 2000. Veitch AM, Baglin TP, Gershlick AH, etal. Guidelines for the management of
anticoagulant and antiplatelet therapy in patients undergoing endoscopic
procedures. Gut. 2008;57:1322–1329. Way e J D, Lewis BS, Yessayan S. Colonoscopy: a prospective report of compli-
cations. J Clin Gastroenterol. 1992;15:347–351.

M  H  P S
John H. Marks and Grace A. Montenegro

INTRODUCTION

Pelvic dissection is inherent to the management of many rectal, uro­logic, and gynecologic conditions, and operating deep in the pel­vis requires an intimate knowledge of the anatomy of this region. Whether performed in an open, laparoscopic, or robotic manner, surgery must be precise to avoid violating cancer planes and to pre­vent nerve damage and pelvic bleeding. e greatest challenges are posed by reoperative pelvic surgery and surgery in the presence of pelvic inammation or bulky ultra-low rectal cancers, or when exten­sive pelvic brosis and obliteration of planes is present as a result of recurrent tumors or treatment with radiation.
Presacral hemorrhage is one of the most feared complications of pelvic surgery. An incidence of 9.4% and a mortality of 4.3% have been reported. When discussing the prevention and management of hemorrhage that occurs during pelvic surgery, it is helpful to outline the relevant anatomy, as well as the principles of pelvic bleeding and tactics for controlling it. 

PERTINENT ANATOMY

e pelvis is a bony and muscular cone, bounded posteriorly by the sacrum and coccyx and the piriformis and coccygeal muscles; ante­riorly by parts of obturator internus, levator ani and the pubic bone; laterally by the ilium and ischium, obturator internus, and superior part of levator ani; and inferiorly by the levator ani muscles. e pel­vis contains the rectum, distal sigmoid colon, bladder, and distal ure­ters, as well as ovaries, fallopian tubes, uterus and vagina in women and seminal vesicles, ductus deferentes, ejaculatory ducts, and pros­tate in men.
e taeniae coli coalesce to form a complete longitudinal muscle coat of the rectum as the sigmoid terminates. e rectum lacks epi­ploic appendices, haustrae, and a well-dened mesentery. e poste­rior rectal wall lies in the sacral hollow and is entirely extraperitoneal, whereas the upper rectum is invested by peritoneum anteriorly and laterally and the middle third only anteriorly. e lower third of the rectum is entirely extraperitoneal because the anterior peritoneal reection is found at 7.5 to 5.0 cm from the anal verge in women and at 9.0 to 7.0 cm from the anal verge in men. Anteriorly, the rectum is in close proximity to the cervix and posterior vagina in women and is closely related to the prostate, seminal vesicles, and bladder in men. It is separated from these structures by the fascia of Denonvilliers. e fascia propria of the rectum is an extension of the parietal endopelvic fascia that lines the oor and walls of the pelvis and encloses rectum, adipose tissue, and blood and lymphatic vessels. It is more obvious laterally and posteriorly. e lateral ligaments of the rectum contain connective tissue and nerves and, in 25% of patients, branches of the middle rectal artery. It is important to note that the middle rectal arteries and pelvic plexus run underneath the lateral ligaments. e
456
presacral fascia covers the concavity of the sacrum and coccyx, and the presacral nerves, middle sacral artery, and presacral veins run behind it (Fig. 87-1).
During posterior rectal dissection, it is important to keep in the avascular plane between fascia propria of the rectum and the pre­sacral fascia, anterior to the hypogastric nerves. Dissection deep to the presacral fascia can cause life-threatening venous bleeding. e venous plexus is particularly at risk deep in the presacral hollow when, in taking the dissection posteriorly down to the pelvic oor, the surgeon does not recognize the anterior curve of the sacrum and enters the presacral veins. e presacral venous plexus is formed by the two lateral sacral veins, the middle sacral vein, and communicat­ing veins (Fig. 87-2). ese veins have no valves and communicate via the basivertebral veins in the internal vertebral venous system. e adventitia of the basivertebral veins is xed to the sacral periosteum at the margins of the sacral foramina mainly at the level of S3-S4. In the lithotomy position, presacral veins can reach hydrostatic pres­sures up to three times the normal pressure of the inferior vena cava. Retraction of the cut end of the vein into a sacral foramen also can be a problem when the presacral fascia is violated, preventing control by simple tie or suture ligation.
e visceral pelvic fascia of Denonvilliers is a fascial layer that separates the extraperitoneal rectum anteriorly from the prostate and seminal vesicles or vagina. e mesorectal plane represents the continuation of the same plane of posterior and lateral dissection of the rectum. is natural anatomic plane is located between the pari­etal and visceral pelvic fascia and is the embryologic basis of a total mesorectal dissection (Fig. 87-3). Sharp and precise dissection in this plane should be bloodless. Bleeding should raise the question of an improper plane of dissection. Blunt dissection, particularly with a hand in the presacral space, runs the risk of tearing the mesentery and avulsing vessels, causing both bleeding and an inadequate total mesorectal excision.
Just above its bifurcation, the aorta gives rise to the middle sacral artery. e analogous middle sacral vein drains into the le common iliac vein. e internal iliac arteries represent the main arterial supply to the pelvis through posterior and anterior trunks. On the viscera, these arteries anastomose with each other, providing collateral circu­lation between the le and right sides of the pelvis. e veins corre­spond to the branches of the artery. e posterior trunk is composed of the iliolumbar, lateral sacral, and superior gluteal arteries. e lat­eral sacral artery supplies the vertebral contents and enters the rst and or second anterior sacral foramen. e superior gluteal artery courses posteriorly and leaves the pelvis through the greater sciatic foramen. e anterior trunk of the internal iliac artery is long when compared with the posterior trunk and is closely related to the lateral pelvic wall.
e rst branch of the anterior trunk is the obturator artery. It extends forward along the pelvic wall against the fascia over the obturator muscle and leaves the pelvis via the obturator canal. e
COMPLICATIONS 457
PSVS
l
nerve
Nervi erigente
Fascia propria of rectum
Seminal vesicles
Fascia of Denonvilliers
Middle rectal artery
Lateral ligament
Presacral fascia
Presacral veins
FIGURE 87-1 Presacral fascia. (From Church JM, et al. The surgical anatomy of the rectum--a review with particular relevance to the hazards of rectal mobili-
Bladder
Pelvic plexus
Pelvic wall
Rectum
Mesorectum
Superior rectal artery
Hypogastric
sation. Int J Colorect Dis. 1987;2:158-166.)
MSV
Rectum
Sacral nerve S3
Visceral pelvic fascia
Parietal pelvic fascia
IIV
S2TVT LSV
BVV
FIGURE 87-2 Presacral venous plexus.
FIGURE 87-3 Mesorectal plane.
BVV
IVVS
Bladder
Hypogastric nerve
Internal iliac artery
Middle hemorrhoida artery
Piriformis muscle
Hypogastric nerve plexus
S3
ManageMent of HeMorrHage during Pelvic Surgery458
vein, and nerve in pudendal
anal sphincter
Anal canal
Rectum
umbilical artery is the second branch. It runs parallel to or just above the pelvic brim and turns onto the anterior abdominal wall lateral to the bladder. e inferior vesical artery is typically the next branch and supplies the bladder. e middle hemorrhoidal artery is also a branch of the internal iliac anterior trunk; however, it is present in only 10% to 60% of dissections and has variable con­tribution to the rectal blood supply. It traverses the pelvis on the superior aspect of the levator ani. It does not travel directly through lateral stalks, but its branches may run through them (Fig. 87-4). e middle hemorrhoidal artery reaches the lower third of the rec­tum anterolaterally, close to the level of the pelvic oor and deep to the levator fascia. It is prone to be injured during low anterior resection, when anterolateral dissection of the rectum is performed close to the pelvic oor and the prostate and seminal vesicles or upper part of the vagina are being separated from it. e anterior trunk of the internal iliac nally bifurcates into the inferior gluteal and pudendal arteries. e internal pudendal courses down on the anterior surface of the sacral plexus. e pudendal vessels then send branches medially to the pelvic oor, anal sphincters (inferior hem­orrhoidal artery), and genitalia.
e superior hemorrhoidal artery is the direct continuation of the inferior mesenteric artery. It divides within the mesorectum at the level of S3 into descending right and le branches to the rectum. Within the submucosa of the rectum, these branches run straight downward to supply the lower rectum and anal canal. As these branches reach the rectal columns, they condense into capillary plexi in locations corresponding to internal hemorrhoidal groups, right posterior, right anterior, and le lateral positions. 

BLEEDING

Avoiding pelvic bleeding without compromising the intended sur­gery is always the primary goal, but because of the complex anatomy of the pelvis, bleeding may occur even during procedures performed by the most experienced of surgeons. Preparation for this eventuality is hence the key to containing it. In preoperative planning, one must
consider the challenges of the procedure, disease, and body habitus. Dicult dissections are anticipated in patients with recurrent or bulky tumors, morbid obesity with bulky peritoneal fat, tumors in the distal third of the rectum, and a narrow pelvis in men. Typing and cross-matching of blood should be performed for any pelvic sur­gery. e anesthesiologist should have good venous access prior to the start of the procedure.
When major pelvic bleeding is encountered, several points are important. e need for additional trocars or hands to aid in retrac­tion must be anticipated. Good communication with the operating room sta and the anesthesia team is essential, and extra suction catheters may be necessary. e best initial management is direct pressure, either with a nger, a sponge on a stick, or a pack at the site of bleeding. Once direct pressure is applied, the anesthesia team should be notied of the blood loss and the potential for further loss, and time is required for the loss to be caught up and for further prod­ucts to be made available. Delivery of the specimen with the packing in place should be performed if possible because it allows better visu­alization of the presacral region. 
TACTICS FOR CONTROL OF PELVIC
BLEEDING
Major Vessel Bleeding
Iliac Vessels
Bleeding from the common iliac or internal iliac arteries or veins is usually massive. It may occur in very slim patients in whom dissec­tion is deceptively easy, or very stuck patients in whom absence of tissue planes can hide a vessel. Major arterial bleeding is obvious; major venous bleeding is a rapid welling up of a pool of blood in the surgical eld. Immediate packing and a request for a vascular surgery consultation can be followed by optimizing exposure for the attempt at control. If a vascular surgeon is not available, the bleeding
Superior rectal artery and vein
Sigmoid colon
Rectosigmoid junction
Rectal ampulla
Anorectal junction
Levator ani muscle
Pudendal canal
Anal column
Puborectalis muscle
Internal anal sphincter
Intersphincteric groove (anocutaneous line)
Deep
Superficial
Subcutaneous
FIGURE 87-4 Lateral stalks with pelvic plexus and mid rectal arteries.
Inferior epigastric artery
Obturator artery
Umbilical artery
Inferior vesicle artery
Inferior gluteal artery
Internal pudendal artery
Superior vesicle artery Middle rectal artery
Internal pudendal artery,
canal (in obturator fascia)
Inferior rectal artery
Pectinate (analrectal) line
Zones of external
COMPLICATIONS 459
site is controlled by mobilizing the vessel above and below and apply­ing vascular clamps. e tear or cut is then repaired with a vascular suture. Success depends on recognizing the approximate site of the damage early to facilitate early control of bleeding. 
Minor Vessel Bleeding
Arterial bleeders are easier to control than other sources of bleeding. ey are obvious and can be controlled with suture ligation, hemo­clips, endo ties, or electrocautery. e main challenge involves sutur­ing deep in the pelvis and subsequently tying, when there is a risk of avulsing the vessel. Care must be taken not to pull on the tie as the knot is placed down. Dissection of the feeding artery with liga­tion may be necessary to control arterial hemorrhage. e last resort of packing the pelvis and transporting the patient to interventional radiology for the embolization of internal iliac branches is rarely nec­essary in an elective case; it is an excellent tactic but is generally used in trauma patients and in persons with venous bleeding. 
Presacral Bleeding
Violation of the presacral fascia and release of the venous pool from its high hydrostatic pressure can lead to a life-threatening hemor­rhage. Although prevention of this complication is a far better strat­egy than controlling it, it is imperative for the pelvic surgeon to be armed with techniques for treatment. Communication with the anesthesia team is essential. Blood should be available in the room, and two large-bore intravenous lines should be in place. Decisions regarding a blood warmer and the need for platelets and fresh frozen plasma can be made on an evolving basis depending on the volume of blood loss and the patient’s condition. A second suction device on the operative eld is sometimes helpful. Tragic problems may occur if the surgeon and anesthesiologist are not in close contact and if hypotension is corrected with pressors rather than with volume, or if the surgeon is not told of hemodynamic problems and forges ahead rather than continuing to apply pressure to allow the anesthesia team to catch up with the blood loss.
Pelvic Packing
Packing is always a safe technique when dealing with massive presa­cral bleeding, especially in a patient who is becoming hemodynami­cally unstable. It can be used at the initial time of bleeding in an eort to gain control of the situation denitively, or as a fallback position, with transport to the intensive care unit (ICU) when control of bleed­ing cannot be accomplished. When a decision has been made to leave packs in place for control of bleeding, a return to the operating room for removal of the packs within 24 to 48 hours is required. Although recurrent hemorrhage is a risk at the time of the second look, oen the prolonged pressure of the packs within the pelvis and the opportunity for replacement of blood volume, normalization of coagulation, and correction of patient temperature in the ICU result in a more control­lable situation. orough soaking of the packing before it is removed diminishes the likelihood of displacement of any coagulum with the packing and a resultant resumption of bleeding. A modied packing technique was described by Metzger in which a bowel isolation bag is placed in the presacral space with its neck brought out through a perineal wound. e bag is lled with gauze packing, which can be removed at the bedside 2 to 4 days later, along with the bag. is technique allows the surgeon to observe for any ongoing blood loss. e surface of the bag allows the gauze to tamponade the bleeding, but because it is not adherent, it can be removed without disruption of the clot and rebleeding. e technique does not require a return to the operating room for removal of the packing. However, the need for a separate perineal wound, particularly in patients with a fresh anas­tomosis, is a disadvantage. Other devices that have been described
for tamponade include tissue expanders and saline solution bags. Although avoiding another exposure to anesthetic is a consideration, a return to the operating room may allow better exposure for ensur­ing hemostasis and anastomotic integrity. 
Suture Ligation
Suture ligation has the potential for aggravating rather than control­ling presacral bleeding. Although it can be eective, the needle oen causes further injury to the fragile venous walls. More commonly, the veins are injured as the suture pulls through the walls as they are tied. If suture ligation is used, it is important that the suture includes the presacral fascia, presacral veins, and deep connective tissue. Jiang etal reported that circular suture ligation of the venous plexus in the area with intact presacral fascia that surrounds the bleeding site is an eective, simple technique. By incorporating additional tissue in the suture, the veins are less likely to be injured when the suture is tied. 
Thumbtacks
Sterile stainless steel or titanium thumbtacks can be placed directly into a sacral foramen containing a bleeding presacral vein. is approach allows direct pressure but avoids the risk of venous injury that can occur with sutures. Although it is occasionally helpful, sig­nicant limitations to this approach exist. umbtacks cannot be applied to bleeding points originating from sacral neural foramen or near vital structures such as the ureters. umbtacks are also ineec­tive in cases of diuse bleeding. Additionally, authors of some case reports have described thumbtack displacement, resulting in chronic pain and anastomotic disruption (Fig. 87-5).
Wang etal described the use of a titanium table xation staple with a cancellous bone gra at the site of bleeding in the sacrum. e staple has four superne spiral spikes for xation and can vary in size to t the size of the bleeding hole. e stapler has a specic driver and hammer to make xation easy.
A less traumatic technique sometimes used to apply permanent pressure for presacral hemorrhage control is the application of bone wax. is technique is only helpful in very limited bleeding situa­tions. Pressure with wax without coagulation in the presence of dif­fuse presacral bleeding will not be successful. 
Muscle Fragment Welding
e muscle fragment welding technique involves the use of a 1.5- to
2.0-cm square segment of rectus abdominis muscle harvested from the incision and held in place with forceps over the bleeding area while vigorous suctioning is implemented to expose the presacral eld. Electrocautery at a high setting (100 Hz) is applied to the for­ceps and transmitted to the muscle fragment to weld it to the bleeding site. Although the muscle fragment or coagulum may fall free from the site, the source of the bleeding is welded closed. An advantage of this technique is that no additional equipment is required and no for­eign bodies are le in place for later removal. e rectus abdominis muscle also can be used to control presacral bleeding. A 4 × 2 × 1 cm piece of rectus is harvested as a free ap and sewn over the bleeding area to tamponade the bleeding. Although no additional equipment is necessary for this procedure, the need to suture the rectus in place may in itself prompt further bleeding. 
Bipolar Electrocautery
Electrocautery combined with forceps can be used for localized pel­vic bleeding. It may not be successful in cases of diuse hemorrhage, even with higher cautery settings. Filippakis etal described the use of spray electrocautery to control presacral bleeding. e spray setting for monopolar electrocautery generates a direct current that operates between 200 kHz and 3.3 MHz, well above the range at which neuro­muscular stimulation could occur. Tissue fulguration is achieved by
Ureter
Obturator artery
Ductus deferens
Prostatic plexus
Dorsal nerve of peni
c
Perinea nerve
Sympathetic
Umbilical artery
Vesical plexus
s
Lumbar sympathetic ganglia
ManageMent of HeMorrHage during Pelvic Surgery460
Hemostasis Step-by-Step Technique
trunk and ganglia
Hypogastric plexus
Hypogastric nerve
Sacral plexus
Pelvic splanchnic nerves
Pudendal nerve
Inferior hypogastric plexus
Inferior
l
rectal nerve
D’Ambra et al described a hemostatic step-by-step technique that utilizes local compression of the bleeding site with tampon gauze or an absorbable knitted fabric hemostat (Tabotamp, Ethi­con, Somerville, N.J.). When bleeding does not stop, an epiploic appendage or omental scrap is localized and ablated by coagulat­ing the pedicle with bipolar forceps and using it as a plug on the tip of the grasping forceps. The plug is placed on the bleeding site and monopolar coagulation is applied with use of electrified dissecting forceps through interposed grasping forceps. This tech­nique leads to progressive liquefaction of the fatty scrap but pre­vents the underlying presacral venous structure from tearing and aids in denatured protein clotting of vessels, resulting in stable hemostasis.
A third step is used if the fatty scrap does not work. A small scrap of bovine pericardium gra is tacked to the bleeding site by endo­scopic helicoidal protack. e biologic step was only used in two of seven cases in which presacral hemorrhage was managed. Hemostatic gauze, a collagen-like natural substance created from chemically treated cellulose, is approved for use in China and has been described to help control bleeding from open wounds and body cavities. Upon contact with blood, the gauze expands to three to four times its size and converts into a gel. It then dissolves into saline and glucose over a period of 1 to 2 weeks. 
Hemostatic Agents
Ureter
Hypogastric nerve
FIGURE 87-5 Pelvic nerves.
Superior hypogastric plexus
Sacral nerve root
Inferior hypogastri plexus
using electrical arcs. e sparks jump from the electrode across the air gap to the tissue, which causes clotting of blood and destruction of tissue with no cutting eect. e benet of this approach is that with the arcing, the coagulum is not formed and pulled o by the cautery as it is moved. e correct method to achieve fulguration when using coagulation is to hold the tip of the active electrode slightly above the target tissue at a 90-degree angle. is technique can eectively reach and coagulate nonvisible bleeding points when bleeding originates from basivertebral veins that pass through the sacral foramen. e use of the argon beam coagulator to control presacral bleeding during an ultra-low anterior resection has also been described. e equip­ment, operated with a “point and shoot” method, does not require additional training to use and works easily in connes of a narrow pelvis during laparoscopic surgery. For this method to be eective, however, the operative eld must be dry, and therefore ample, well­directed suction is needed. 
Mechanical Hemostatic Agents
Mechanical hemostatic agents include porcine gelatin (Gelfoam and Gelfoam Plus [Pharmacia and Upjohn Co., New York, N.Y.] and Surgifoam [Ethicon]), cellulose (Surgicel and Surgicel Nu­Knit [Ethicon]), bovine collagen (Avitene sheets and Ultrafoam collagen sponges [Davol Inc., Warwick, R.I.]), and polysaccharide spheres (Arista [Davol Inc.]). These agents integrate an absorb­able sponge, foam, pad, or other material with a topical hemo­static agent that is then applied to the affected area. They form a matrix at the site of bleeding, activating the extrinsic clotting pathway and allowing clotting to occur. These agents rely on fibrin production to achieve hemostasis; therefore, they are only appro­priate for patients with an intact coagulation cascade. Bovine col­lagen and polysaccharide spheres are the most effective; porcine gelatins have improved efficacy when used with topical thrombin. Typically these agents are suited for capillary, venous, or small arterial bleeding. 
Active Hemostatic Agents
Active hemostatic agents include bovine thrombin (Thrombin­JMI [GenTrac, Inc., Middleton, Wisc.]), recombinant thrombin (Recothrom [ZymoGenetics, Inc., Seattle, Wash.]), and pooled human plasma thrombin (Evithrom [OMRIX Biopharmaceu­ticals, Ltd., Somerville, N.J.]). These agents are topical throm­bins that stimulate fibrinogen at the bleeding site to produce a fibrin clot; therefore, circulating fibrinogen is necessary. Active hemostatic agents can be used effectively in patients with coagu­lation systems that are impaired. They are applied via pump or spray kits or delivered via a saturated absorbable gelatin sponge directly to the site of bleeding. Bovine thrombin is the most common and least expensive active hemostat used in the United States today. It is stored at room temperature and comes in pow­der form that is easily reconstituted with saline solution when needed for use. Active hemostatic agents are suited for small capillary and venous bleeding. Pooled human plasma throm­bin is contraindicated in patients with a human blood product allergy.