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
18 The Failed Anastomosis
303
94. Bretagnol F, Panis Y, Rullier E, et al. Rectal cancer surgery with or without bowel preparation: the French GRECCAR III multicenter single-blinded randomized trial. Ann Surg. 2010;252:863–8.
95. Abbas MA. Anastomotic leak: should we continue to accept the risks? Dis Colon Rectum. 2010;53(6):859–60.
96. Kelly H, Hurdon E. The vermiform appendix and its diseases. Philadelphia: WB Saunders and Company; 1905.
97. Kudszus S, Roesel C, Schachtrupp A, Hoer JJ. Intraoperative laser fl uorescence angiography in colorectal surgery: a noninvasive analysis to reduce the rate of anastomotic leakage. Langenbecks Arch Surg. 2010;395(8):1025–30.
98. Yalin R, Aktan AO, Yegen C, et al. Importance of testing stapled rectal anastomoses with air. Eur J Surg. 1993;159(1):49–51.
99. Wheeler JM, Gilbert JM. Controlled intraoperative water testing of left-sided colorectal anastomoses: are ileostomies avoidable? Ann R Coll Surg Engl. 1999;81:105–8.
100. Schmidt O, Merkel S, Hohenberger W. Anastomotic leakage after low rectal stapler anastomosis: signifi cance of intraoperative anas­tomotic testing. Eur J Surg Oncol. 2003;29(3):239–43.
101. Griffen FD, Knight CD, Whitaker JM, et al. The double stapling technique for low anterior resection. Ann Surg. 1990;211: 745–52.
102. Li VK, Wexner SD, Pulido N, et al. Use of routine intraoperative endoscopy in elective laparoscopic colorectal surgery: can it fur­ther avoid anastomotic failure? Surg Endosc. 2009;23(11): 2459–65.
103. Chen CW, Chen MJ, Yeh YS, Tsai HL, Chang YT, Wang JY. Intraoperative anastomotic dye test signifi cantly decreases inci­dence of anastomotic leaks in patients undergoing resection for rectal cancer. Tech Coloproctol. 2013;17:579–83.
104. Gurjar SV, Forshaw MJ, Ahktar N, Stewart M, Parker MC. Indwelling trans-anastomotic rectal tubes in colorectal surgery: a survey of usage in UK and Ireland. Colorectal Dis. 2007;9: 47–51.
105. Morks AN, Havenga K, Ploeg RJ. Can intraluminal devices pre­vent or reduce colorectal anastomotic leakage: a review. World J Gastroenterol. 2011;17(40):4461–9.
106. Bulow S, Bulut O, Christensen IJ, Harling H, Rectal Stent Study Group. Transanal stent in anterior resection does not prevent anas­tomotic leakage. Colorectal Dis. 2006;8(6):494–6.
107. Ravo B. The intracolonic bypass procedure. Int J Colorectal Dis. 1987;2(1):38–42.
108. Ye F, Wang D, Xu X, Liu F, Lin J. Use of intracolonic bypass secured by a biodegradable anastomotic ring to protect the low rectal anastomosis. Dis Colon Rectum. 2008;51:109–15.
109. Masoomi H, Luo R, Mills S, Carmichael JC, Senagore AJ, Stamos MJ. Compression anastomosis ring device in colorectal anastomo­sis: a review of 1,180 patients. Am J Surg. 2013;205(4):447–51.
110. Fajardo AD, Chun J, Stewart D, Safar B, Fleshman JW. 1.5:1 meshed AlloDerm bolsters for stapled rectal anastomoses does not provide any advantage in anastomotic strength in a porcine model. Surg Innov. 2011;18(1):21–8.
111. Fajardo AD, Amador-Ortiz C, Chun J, Stewart D, Fleshman JW. Evaluation of bioabsorbable seamguard for staple line reinforce­ment in stapled rectal anastomoses. Surg Innov. 2012;19(3):288–94.
112. Stamou KM, Menenakos E, Dardamanis D, et al. Prospective comparative study of the effi cacy of staple-line reinforcement in laparoscopic sleeve gastrectomy. Surg Endosc. 2011;25(11): 3526–30.
113. Thornton M, Joshi H, Vimalachandran C, et al. Management and outcome of colorectal anastomotic leaks. Int J Colorectal Dis. 2011;26(3):313–20.
114. Sutton CD, Marshall LJ, Williams N, Berry DP, Thomas WM, Kelly MJ. Colo-rectal anastomotic leakage often masquerades as a cardiac complication. Colorectal Dis. 2004;6(1):21–2.
115. Bellows CF, Webber LS, Albo D, Awad S, Berger DH. Early pre­dictors of anastomotic leaks after colectomy. Tech Coloproctol. 2009;13(1):41–7.
116. Almeida AB, Faria G, Moreira H, Pinto-de-Sousa J, Correia-da­Silva P, Maia JC. Elevated serum C-reactive protein as a predic­tive factor for anastomotic leakage in colorectal surgery. Int J Surg. 2012;10(2):87–91.
117. Welsch T, Muller SA, Ulrich A, et al. C-reactive protein as early predictor for infectious postoperative complications in rectal sur­gery. Int J Colorectal Dis. 2007;22:1499–507.
118. Korner H, Nielsen HJ, Soreide JA, Nedrebo BS, Soreide K, Knapp JC. Diagnostic accuracy of C-reactive protein for intraabdominal infections after colorectal resections. J Gastrointest Surg. 2009;13(9):1599–606.
119. Noble F, Curtis N, Harris S, et al. Risk assessment using a novel score to predict anastomotic leak and major complications after oesophageal resection. J Gastrointest Surg. 2012;16(6):1083–95.
120. den Dulk M, Noter SL, Hendriks ER, et al. Improved diagnosis and treatment of anastomotic leakage after colorectal surgery. Eur J Surg Oncol. 2009;35(4):420–6.
121. Phitayakorn R, Delaney CP, Reynolds HL, et al. Standardized algorithms for management of anastomotic leaks and related abdominal and pelvic abscesses after colorectal surgery. World J Surg. 2008;32(6):1147–56.
122. Smith JJ, et al. The national bowel cancer audit project 2007. London: Association of Coloproctology of Great Britain and Ireland; 2007. p. 63–4.
123. Rahbari NN, Weitz J, Hohenberger W, et al. Defi nition and grad­ing of anastomotic leakage following anterior resection of the rec­tum: a proposal by the international study group of rectal cancer. Surgery. 2010;147(3):339–51.
124. Lim M, Akhtar S, Sasapu K, et al. Clinical and subclinical leaks after low colorectal anastomosis: a clinical and radiologic study. Dis Colon Rectum. 2006;49(10):1611–9.
125. van Ruler O, Mahler CW, Boer KR, et al. Comparison of on­demand vs. planned relaparotomy strategy in patients with severe peritonitis: a randomized trial. JAMA. 2007;298(8):865–72.
126. Koperna T, Schulz F. Relaparotomy in peritonitis: prognosis and treatment of patients with persisting intraabdominal infection. World J Surg. 2000;24(1):32–7.
127. Ruttinger D, Kuppinger D, Holzwimmer M, et al. Acute prognosis of critically ill patients with secondary peritonitis: the impact of the number of surgical revisions, and of the duration of surgical therapy. Am J Surg. 2012;204(1):28–36.
128. Lamme B, Boermeester MA, Reitsma JB, Mahler CW, Obertop H, Gouma DJ. Meta-analysis of relaparotomy for secondary peritonitis. Br J Surg. 2002;89(12):1516–24.
129. Person B, Dorfman T, Bahouth H, Osman A, Assalia A, Kluger Y. Abbreviated emergency laparotomy in the non-trauma setting. World J Emerg Surg. 2009;4:41.
130. Hedrick TL, Sawyer RG, Foley EF, Friel CM. Anastomotic leak and the loop ileostomy: friend or foe? Dis Colon Rectum. 2006;49(8):1167–76.
131. Damrauer SM, Bordeianou L, Berger D. Contained anastomotic leaks after colorectal surgery: are we too slow to act? Arch Surg. 2009;144(4):333–8.
132. Fraccalvieri D, Biondo S, Saez J, et al. Management of colorectal anastomotic leakage: differences between salvage and anasto­motic takedown. Am J Surg. 2012;204(5):671–6.
133. Verlaan T, Bartels SA, van Berge Henegouwen MI, Tanis PJ, Fockens P, Bemelman WA. Early, minimally invasive closure of anastomotic leaks: a new concept. Colorectal Dis. 2011;13 Suppl 7:18–22.
134. Whitlow CB, Opelka FG, Gathright Jr JB, Beck DE. Treatment of colorectal and ileoanal anastomotic sinuses. Dis Colon Rectum. 1997;40(7):760–3.
304
N. Smallwood et al.
135. van Koperen PJ, van der Zaag ES, Omloo JM, Slors JF, Bemelman WA. The persisting presacral sinus after anastomotic leakage fol­lowing anterior resection or restorative proctocolectomy. Colorectal Dis. 2011;13:26–9.
136. Cleary RK, Pomerantz RA, Lampman RM. Colon and rectal inju­ries. Dis Colon Rectum. 2006;49(8):1203–22.
137. Hallbook O, Sjodahl R. Anastomotic leakage and functional out­come after anterior resection of the rectum. Br J Surg. 1996; 83:60–2.
138. Ricciardi R, Roberts PL, Marcello PW, et al. Anastomotic leak testing after colorectal resection: what are the data? Arch Surg. 2009;144(5):407–11.
139. Iesalnieks I, Kilger A, Glass H, et al. Intraabdominal septic com­plications following bowel resection for Crohn’s disease: detri­mental infl uence on long-term outcome. Int J Colorectal Dis. 2008;23(12):1167–74.
140. Gutierrez A, Lee H, Sands BE. Outcome of surgical versus percu­taneous drainage of abdominal and pelvic abscesses in Crohn’s disease. Am J Gastroenterol. 2006;101(10):2283–9.
141. Nagell CF, Holte K. Treatment of anastomotic leakage after rectal resection with transrectal vacuum-assisted drainage (VAC). A method for rapid control of pelvic sepsis and healing. Int J Colorectal Dis. 2006;21(7):657–60.
142. Weidenhagen R, Gruetzner KU, Wiecken T, Spelsberg F, Jauch KW. Endoscopic vacuum-assisted closure of anastomotic leakage following anterior resection of the rectum: a new method. Surg Endosc. 2008;22(8):1818–25.
143. van Koperen PJ, van Berge Henegouwen MI, Rosman C, et al. The Dutch multicenter experience of the endo-sponge treatment for anastomotic leakage after colorectal surgery. Surg Endosc. 2009;23(6):1379–83.
144. Arezzo A, Miegge A, Garbarini A, Morino M. Endoluminal vac­uum therapy for anastomotic leaks after rectal surgery. Tech Coloproctol. 2010;14(3):279–81.
145. Weidenhagen R, Wiecken F, Spelsberg K, Jauch W. User’s report. Available at:
doc_index.html?med_id=1000007687
146. Lippert E, Klebl FH, Schweller F, et al. Fibrin glue in the endo­scopic treatment of fi stulae and anastomotic leakages of the gas­trointestinal tract. Int J Colorectal Dis. 2011;26(3): 303–11.
147. Gisbertz SS, Sosef MN, Festen S, Gerhards MF. Treatment of fi s­tulas in ano with fi brin glue. Dig Surg. 2005;22(1–2):91–4.
148. Freeman RK, Ascioti AJ, Wozniak TC. Postoperative esophageal leak management with the polyfl ex esophageal stent. J Thorac Cardiovasc Surg. 2007;133:333–8.
149. Freeman RK, Van Woerkom JM, Ascioti AJ. Esophageal stent placement for the treatment of iatrogenic intrathoracic esophageal perforation. Ann Thorac Surg. 2007;83:2003–8.
150. Amrani L, Menard C, Berdah S, et al. From iatrogenic digestive perforation to complete anastomotic disunion: endoscopic stent­ing as a new concept of stent-guided regeneration and re­epithelialization. Gastrointest Endosc. 2009;69(7):1282–7.
151. DiMaio CJ, Dorfman MP, Gardner GJ, et al. Covered esophageal self-expandable metal stents in the nonoperative management of postoperative colorectal anastomotic leaks. Gastrointest Endosc. 2012;76(2):431–5.
www.aesculap.extranet.bbraun.com/public/frame_
. Accessed 9 Feb 2013.
152. Song H-Y, Kim JH, Kim KR, et al. Malignant rectal obstruction within 5 cm of the anal verge: is there a role for expandable metal­lic stent placement? Gastrointest Endosc. 2008;68:713–20.
153. Gornals JB, Golda T, Soriano A. Stent-in-stent technique for removal of a metal stent embedded in the colon wall by using a fully covered, self-expandable metal esophageal stent (with video). Gastrointest Endosc. 2012;76(3):695–6.
154. Blumetti J, Chaudry V, Prasad L, Abcarian H. Delayed transanal repair of persistent coloanal anastomotic leak in diverted patients after resection for rectal cancer. Colorectal Dis. 2012;14(10):1238–41.
155. Zhou JL, Shen B. Endoscopic needle knife therapy for anasto­motic leakage following anterior resection for rectal cancer. Colorectal Dis. 2012;14(6):e365–6.
156. Stewart BT, Stitz RW. Marsupialization of presacral collections with the use of an endoscopic stapler. Dis Colon Rectum. 1999;42:264–5.
157. Fleshman JW, McLeod RS, Cohen Z, Stern H. Improved results following the use of an advancement technique in the treatment of ileoanal anastomotic complications. Int J Colorectal Dis. 1988; 3:161–5.
158. Pitel S, Lefevre JH, Tiret E, Chafai N, Parc Y. Redo coloanal anas­tomosis: a retrospective study of 66 patients. Ann Surg. 2012;256(5):806–10; discussion 810–1.
159. Lefevre JH, Bretagnol F, Maggiori L, Ferron M, Alves A, Panis Y. Redo surgery for failed colorectal or coloanal anastomosis: a valu­able surgical challenge. Surgery. 2011;149(1):65–71.
160. Bannura GC, Cumsille MA, Barrera AE, Contreras JP, Melo CL, Soto DC. Predictive factors of stenosis after stapled colorectal anastomosis: prospective analysis of 179 consecutive patients. World J Surg. 2004;28(9):921–5.
161. Nguyen-Tang T, Huber O, Gervaz P, Dumonceau JM. Long-term quality of life after endoscopic dilation of strictured colorectal or colocolonic anastomoses. Surg Endosc. 2008;22(7):1660–6.
162. Kim PH, Song HY, Park JH, Kim JH, Na HK, Lee YJ. Safe and effective treatment of colorectal anastomotic stricture using a well-defi ned balloon dilation protocol. J Vasc Interv Radiol. 2012;23(5):675–80.
163. Polese L, Vecchiato M, Frigo AC, et al. Risk factors for colorectal anastomotic stenoses and their impact on quality of life: what are the lessons to learn? Colorectal Dis. 2012;14(3):e124–8.
164. Nieponice A, McGrath K, Qureshi I, et al. An extracellular matrix scaffold for esophageal stricture prevention after circumferential EMR. Gastrointest Endosc. 2009;69(2):289–96.
165. Schlegel RD, Dehni N, Parc R, et al. Results of reoperations in colorectal anastomotic strictures. Dis Colon Rectum. 2001;44: 1464–8.
166. Perez Roldan F, Gonzalez Carro P, Villafanez Garcia MC, et al. Usefulness of biodegradable polydioxanone stents in the treat­ment of postsurgical colorectal strictures and fi stulas. Endoscopy. 2012;44(3):297–300.
167. Curcio G, Spada M, di Francesco F, et al. Completely obstructed colorectal anastomosis: a new non-electrosurgical endoscopic approach before balloon dilatation. World J Gastroenterol. 2010;16(37):4751–4.
168. McKee R, Pricolo VE. Stapled revision of complete colorectal anastomotic obstruction. Am J Surg. 2008;195(4):526–7.

Pelvic Bleeding

Amit Merchea and Bruce G. Wolff
Key Points
• Intraoperative presacral hemorrhage is a rare but potentially lethal complication.
• Most frequently, hemorrhage can be controlled by simple local means such as compression, electro­cautery, or ligation.
• In laparoscopic cases, if control cannot be achieved, conversion to an open procedure should be expedi­tious and defi nitive.
• Surgeons should have an algorithm for treating bleeding that they and their operative team are com­fortable enacting quickly and defi nitively.
1 9
potential sites of hemorrhage include the presacral space, iliac vasculature, retroprostatic or retrovaginal region, and gluteal vessels.
Presacral venous bleeding has a reported incidence in the literature of 3–9 % [ 1 , 2 ]. The presacral venous plexus is covered by the presacral and pelvic fascia over the anterior sacrum. It is formed by two lateral sacral veins, the middle sacral vein, and many communicating veins. These ulti­mately communicate with the internal vertebral venous sys­tem via the basivertebral veins, which may be large-caliber and high-pressure vessels (Fig. 19.1 ) [ 3 , 4 ]. It has been dem- onstrated that the adventitia of the presacral veins is adherent to the periosteum of the sacrum where the veins enter the sacral foramina – these areas are particularly vulnerable to tearing [ 5 ]. Mobilization of the rectum during proctectomy is

Introduction

Key Concept: Hemorrhage is rare, but can be life- threatening. It is imperative to know the anatomy, remain calm, be metic­ulous, and know when to call for help.
Hemorrhage during pelvic surgery is a rare but potentially life-threatening phenomenon. The internal iliac (hypogas­tric) arteries supply the majority of blood fl ow to the pelvis. This vessel divides into anterior and posterior branches, with the anterior division providing the majority of the vascular supply to the pelvis and the posterior division largely providing collateral circulation. Areas of the pelvis that are
A. Merchea , MD Division of Colon and Rectal Surgery , Department of Surgery, College of Medicine, Mayo Clinic , 4500 San Pablo Rd, Jacksonville , FL 32224 , USA e-mail: merchea.amit@mayo.edu
B. G. Wolff , MD ( Division of Colon and Rectal Surgery, Department of Surgery , College of Medicine, Mayo Clinic , 200 First Street SW , Rochester , MN 55904 , USA e-mail: wolff.bruce@mayo.edu
*)
presacral fascia is breached, signifi cant hemorrhage may ensue from the underlying presacral venous plexus or basi­vertebral veins [ 2 , 4 ]. When the basivertebral veins are injured, these may retract into the sacral foramen making control diffi cult. Moreover, in the lithotomy position, the hydrostatic pressure in the sacral veins can be signifi cantly higher than that of the inferior vena cava – thus increasing the potential rate of hemorrhage [ 46 ]. One must remember that it is very rarely necessary to violate the presacral fascia or to dissect upon the surface of the sacrum. Another caveat is careful placement of sutures in the presacral fascia during rectal rectopexy. During rectopexy, the presacral fascia is exposed and sutures are placed through this into the underly­ing periosteum. If bleeding is noticed with placement of these sutures, one can tie these down in an effort to ligate the injured vessel.
The overall incidence of vascular injury during pelvic operations is low (~1–2.3 per 100,000) [ planes are often readily apparent in the normal patient; how­ever, body habitus, previous surgery, large tumors, infl am­mation, radiation, and other factors may alter them and make these planes more diffi cult to discern. Adequate preoperative preparation, complete understanding of anatomic relations
7 , 8 ]. Dissection
S.R. Steele et al. (eds.), Complexities in Colorectal Surgery, DOI 10.1007/978-1-4614-9022-7_19, © Springer Science+Business Media New York 2014
305
306
A. Merchea and B.G. Wolff
Fig. 19.1 The presacral venous plexus with communicating veins and basivertebral veins (With permission from Mayo Foundation for Medical Education and Research. All rights reserved)
Certain other patient factors may portend an increased risk of intraoperative hemorrhage. The re-operative pelvis requires a number of particular considerations. The surgeon must realize that anatomy may be altered or displaced sec­ondary to adhesions and fi xation of structures, including vas­culature. Large, vascular tumors may pose a signifi cant challenge for the surgeon [
9 ]. Preoperative planning and
potential coil embolization in these cases may temper the risk of intraoperative hemorrhage during resection. An intra­lesional resection may even be necessary in large tumors that may distort the anatomy , although in cases of malig­nancy this would be oncologically inappropriate [ 10 ].
Preoperative radiotherapy can increase the risk of bleeding compared to non-radiated cases [ 11 ]. Radiation therapy can lead to fi brosis and scarring, making identifi cation of, and dissection in, appropriate tissue planes diffi cult. Tissues may become fi xed and immobile, increasing the risk of inadvertent injury.
Limited literature exists concerning the characteristics and management of operative vascular injury. Oderich et al. have published a retrospective review spanning 18 years from the Mayo Clinic examining iatrogenic operative inju­ries of the abdominal and pelvic venous system. Of the 44 venous injuries identifi ed, 30 involved the pelvic vasculature (most commonly, the external iliac vein). Perioperative mor­tality was 18 %, all attributed to the venous injury [ 7 ].

Prevention

within the pelvis, along with meticulous surgical technique and appropriate exposure, is essential to limit the risk of pel­vic hemorrhage.

Risk Factors for Major Bleeding

Key Concept: Appropriately and completely evaluate the patient preoperatively and attempt to anticipate and plan for patients that may have an increased risk of bleeding.
The patient must be appropriately screened and examined preoperatively. Among the goals of this evaluation is to iden­tify any comorbid condition that may infl uence the operative outcome. Within the context of bleeding, the patient must be screened in terms of their hematologic system – in particular, examining for any acquired or congenital coagulopathy (from inherited/acquired platelet disorders, factor defi ciency, organ dysfunction, medications, etc.). In addition to a complete med­ication administration history, any prior kidney or liver dys­function or malnutrition may impact the body’s ability to form clot. Routine coagulation studies should be carried out prior to any procedure with the potential for blood loss. If a patient has an identifi ed coagulation disorder, perioperative management of this may be best managed in concert with a hematologist.
Key Concept: Maintain adequate exposure (do not compro-
mise safety for cosmesis) and have meticulous surgical technique.
Secondary to preoperative patient preparation, operative conduct is important in preventing hemorrhage. Adequate exposure and meticulous surgical dissection are essential. For open operations, a generous incision should be made to adequately visualize the anatomy. Laparoscopic or robotic approaches may improve visualization and dissection, par­ticularly in a narrow pelvis, but control of hemorrhage once it occurs may be technically challenging.
Fundamental surgical principles of tension and counter­tension facilitate the identifi cation and dissection in avascular planes. Eight avascular planes and spaces within the pelvis have been previously described (Table 19.1 ) [ 12 ]. Dissection
Table 19.1 Avascular planes and potential spaces of the pelvis
Retropubic space Vesicovaginal space Rectovaginal space Retrorectal space Pararectal spaces (two) Paravesical spaces (two)
19 Pelvic Bleeding
307
Fig. 19.2 The eight avascular planes of the pelvis (With permission from Mayo Foundation for Medical Education and Research. All rights reserved)
within these spaces can be expeditious and is generally safe (Fig. 19.2 ). When performing proctectomy, bluntly dissecting the posterior mesorectum from the sacrum with one’s hand has been reported to be a common cause of presacral venous trauma and, in general, should be avoided [ 4 ].

Controlling Bleeding

Key Concept: Stay calm, have a stepwise algorithm for approaching various bleeding scenarios, and use the tech­niques you are comfortable with.
When a signifi cant vascular injury occurs or brisk bleed­ing is evident, rapid and purposeful action must be taken to achieve control. Fundamental to achieving this is mainte­nance of composure and calm for the surgeon. Equally important is open communication with the anesthesiology team to alert them of signifi cant hemorrhage so that more intensive monitoring can be initiated (hemodynamics, blood loss, urinary output, etc.) and blood products can be acquired from the blood bank. Methods of hemorrhage control include manual compression, electrocautery [ 13 ], vascular ligation, suture repair, use of topical coagulants [ control techniques [
5 ], and radiologic intervention.
Whichever method is utilized, evacuation of blood from the operative fi eld and securing adequate exposure of the bleed­ing site is imperative to accurately identify the source. Caution must be taken to protect vulnerable structures in the
14 , 15 ], damage-
vicinity of the bleeding source as proximal and distal control is achieved, if possible.
The initial maneuver in controlling bleeding is often sim­ple packing of the pelvis with laparotomy sponges . Laparoscopically, a smaller sponge, such as a Ray-Tec, may
be inserted through a 10/12 mm port and used to clear fi eld or tamponade low-volume bleeding. In many cases of low-
pressure, low-volume bleeding, the hemorrhage will readily cease. Clips (or sutures) on visible presacral vessels may be feasible and must be placed on both sides of the vessel. Sometimes further mobilization of the rectum or surrounding
structures is necessary in order to adequately visualize the bleeding point. Other unique and novel techniques have been
described with varying success to halt presacral hemorrhage that could not be stopped with more conventional means (packing, electrocautery, suture ligature, clamping).
Many topical hemostatic agents have been described [
14 ].
In our practice bone wax, gelatin foams (Gelfoam), oxidized cellulose (Surgicel), and thrombin with gelatin (FloSeal) are most commonly used. Bone wax exerts its effect through occlusion of bleeding orifi ces. This is not absorbed by the body and may become a nidus for infection [
16 ]. Gelatin
foams and oxidized cellulose act by providing a matrix for the initiation of coagulation [ 17 , 18 ]. These are best used to control small vessel bleeding and are absorbed by the body within weeks. Thrombin with gelatin requires contact with blood to serve as the source for fi brinogen and can achieve reasonable control of moderate arterial bleeding [ 19 ].
Argon plasma coagulation is another thermal method of coagulation. In this modality, argon gas is ionized and used to deliver thermal energy to tissue adjacent to the probe with limited depth of penetration (2–3 mm). If readily available, this may be an effective tool.
The use of titanium thumbtacks inserted into the bleeding orifi ce of the sacrum has previously been reported (Fig. 19.3 ) [ 4 , 20 ]. These thumbtacks, however, may not be readily available and a rare complication of erosion through the bowel wall has been reported [
21 ]. Harrison et al. [ 22 ]
reported on eight patients with massive bleeding treated with muscle fragment welding technique (Fig.
19.3 ), initially
described by Xu in 1994 [ 23 ]. In this method a segment of rectus abdominis muscle is harvested from the patient’s inci­sion and placed over the bleeding region. Electrocautery on maximum is then applied to a forceps holding the muscle in place to “weld” the bleeding site. In all of these patients, hemostasis was successfully achieved after initial attempts at control via tamponade failed. Remzi et al. [ 24 ] describe securing a patch of harvested rectus abdominis to the bleed­ing point with absorbable sutures. While successful in their reported patients, suturing in a narrow, bleeding pelvis may be technically diffi cult and time consuming.
Other open surgical methods reported include the use of
secured hemostatic sponges [
1 , 15 ], tissue expanders [ 25 ,
308
A. Merchea and B.G. Wolff
a
bc
def
Fig. 19.3 Methods for control of hemorrhage. ( a ) Normal presacral venous plexus anatomy, ( b ) electrocautery, ( c ) suture ligature or clip- ping of transected vessels, ( d ) pelvic packing, ( e ) thumbtacks inserted
26 ], and saline bags [ 27 ]. Van der Vurst et al. [ 1 ] recently described the use of an endoscopic helical tacker to secure a sponge of Surgicel over the bleeding sacrum, thus eliminat­ing the space beneath and providing tamponade. Tissue expanders and saline bags employ the same concept as pack­ing in arresting hemorrhage. Proponents of these methods suggest that advantages include the ability to perfectly fi t the concavity of the sacrum, the ability to increase the hemo­static pressure by increasing the fl uid infused, and the poten­tial ability to remove the devices at bedside, under local procedures [ 27 ]. While each of these alternative methods is reportedly effective, it is of our opinion that the simplest and most expeditious method that the operative team is comfort­able with is initially chosen.
In the event of intractable pelvic hemorrhage, internal iliac artery ligation can increase the likelihood of control by decreasing the mean blood fl ow, mean arterial pressure, and overall pulse pressure within the pelvis [ 28 , 29 ]. Care must be taken to identify the other branches of the iliac system to avoid inadvertent ligation of the common or external iliac arteries and to avoid injury to the hypogastric vein, which is deep and lateral, during ligation of the artery. These vessels
into the sacrum, and ( f ) muscle welding (With permission from Mayo Foundation for Medical Education and Research. All rights reserved)
can be temporarily occluded with vessel loops or atraumatic vascular clamps to determine the level of effectiveness of this maneuver. Ligation does not generally cause pelvic ischemia
because of the extensive collaterals, unless the patient has signifi cant peripheral arterial disease.
As laparoscopic and robotic methods are becoming more prevalent, surgeons must become facile with managing intra­operative complications, including bleeding. Management of this potentially lethal complication can be particularly challenging. Many of the same (or similar) techniques that are used in open approaches can be employed in laparo­scopic operations [ 11 ]. However, if minimally invasive mea- sures at controlling hemorrhage fail, the decision to convert to an open procedure must be made rapidly and without hesitation.
The initial maneuver laparoscopically often employs electrocautery to coagulate small bleeding vessels. Compression of the site with a gauze sponge inserted through one of the trocars can aide in compression, visualization, and exposure. Secondary to this, some authors have described harvesting an omental patch or epiploic fat and subsequently using bipolar cautery to “weld” this over the bleeding site,
19 Pelvic Bleeding
309
much like the rectus abdominis muscle patch. Bovine peri­cardial grafts have also been tacked to the bleeding site by endoscopic helical tackers to achieve tamponade [
11 ].
Finally, argon beam coagulation is an alternative method that may be used [ 30 ]. It must be noted, however, that there should not be signifi cant delay in enacting any of these meth­ods. Not just the surgeon but the operating room staff must all be comfortable with the use of these tools. Given the potential lethality of presacral hemorrhage, surgeon judg­ment is the most important of the available tools – there should be no delay in converting to an open procedure if this is necessary to achieve hemostasis. The key is to minimize the blood loss – after control, set up remedial maneuvers methodically.
Massive, ongoing hemorrhage leads to acidosis, hypother­mia, and coagulopathy – the so-called lethal triad [ 31 ]. In such circumstances the surgeon must consider “bailing out” and resuscitating the patient out of the operating room – par­ticularly when the patient develops ongoing coagulopathy, despite blood product administration [ 5 ]. Originally described in the trauma literature [ 32 , 33 ], the principles of “damage- control surgery” can be applied to other circumstances.
Pelvic packing with later reexploration is one form of damage control. Zama et al. [ 34 ] reported their experience in 93 patients with pelvic packing during abdominoperineal resection or low-anterior resection where packing was kept in place for up to 48 h. No patient in this series required any further intervention after removal of the packs, and there were no intra-abdominal or pelvic infectious complications or rebleeding. Our method of pelvic packing and temporary abdominal closure includes tightly packing multiple lapa­rotomy pads within the pelvis; a sterile plastic drape is placed overlying the bowel to protect it, followed by suction drains and sterile towels. A sterile adhesive, occlusive drape is placed over this and suction applied to the drains. The patient is reexplored once physiologically stabilized in 24–48 h. Should bleeding persist or rebleeding occurs, transcatheter arterial embolization of the bleeding vessel can be attempted.

Summary Pearls

Pelvic and presacral bleeding is a rare and sometimes lethal event. The risk is limited by exquisite anatomic knowledge and careful dissection. However, they can occur and you need to be prepared that this may occur every time you per­form a pelvic dissection. While you, as the surgeon, should have a stepwise algorithm to treat such episodes, you must have the instruments either readily available or nearby. Asking for tacks when no one is aware of where they are is futile. Finally, be comfortable with the techniques they employ, and do not hesitate in seeking assistance of more experienced colleagues, if necessary.

References

1. van der Vurst TJ, Bodegom ME, Rakic S. Tamponade of presacral hemorrhage with hemostatic sponges fi xed to the sacrum with endoscopic helical tackers: report of two cases. Dis Colon Rectum. 2004;47(9):1550–3 [Case Reports].
2. Pollard CW, Nivatvongs S, Rojanasakul A, Ilstrup DM. Carcinoma of the rectum. Profi les of intraoperative and early postoperative complications. Dis Colon Rectum. 1994;37(9):866–74.
3. Baque P, Karimdjee B, Iannelli A, Benizri E, Rahili A, Benchimol D, et al. Anatomy of the presacral venous plexus: implications for rectal surgery. Surg Radiol Anat. 2004;26(5):355–8.
4. Wang QY, Shi WJ, Zhao YR, Zhou WQ, He ZR. New concepts in severe presacral hemorrhage during proctectomy. Arch Surg. 1985;120(9):1013–20.
5. McPartland KJ, Hyman NH. Damage control: what is its role in colorectal surgery? Dis Colon Rectum. 2003;46(7):981–6 [Review].
6. Hill AD, Menzies-Gow N, Darzi A. Methods of controlling presa­cral bleeding. J Am Coll Surg. 1994;178(2):183–4.
7. Oderich GS, Panneton JM, Hofer J, Bower TC, Cherry Jr KJ, Sullivan T, et al. Iatrogenic operative injuries of abdominal and pelvic veins: a potentially lethal complication. J Vasc Surg. 2004;39(5):931–6.
8. Nehler MR, Taylor Jr LM, Porter JM. Iatrogenic vascular trauma. Semin Vasc Surg. 1998;11(4):283–93 [Review].
9. Glasgow SC, Birnbaum EH, Lowney JK, Fleshman JW, Kodner IJ, Mutch DG, et al. Retrorectal tumors: a diagnostic and therapeutic challenge. Dis Colon Rectum. 2005;48(8):1581–7.
10. Dozois EJ, Malireddy KK, Bower TC, Stanson AW, Sim FH. Management of a retrorectal lipomatous hemangiopericytoma by preoperative vascular embolization and a multidisciplinary surgical team: report of a case. Dis Colon Rectum. 2009;52(5):1017–20 [Case Reports].
11. D’Ambra L, Berti S, Bonfante P, Bianchi C, Gianquinto D, Falco E. Hemostatic step-by-step procedure to control presacral bleeding during laparoscopic total mesorectal excision. World J Surg. 2009;33(4):812–5.
12. Gostout BS, Cliby WA, Podratz KC. Prevention and management of acute intraoperative bleeding. Clin Obstet Gynecol. 2002; 45(2):481–91 [Review].
13. Filippakis GM, Leandros M, Albanopoulos K, Genetzakis M, Lagoudianakis E, Pararas N, et al. The use of spray electrocautery to control presacral bleeding: a report of four cases. Am Surg. 2007;73(4):410–3.
14. Achneck HE, Sileshi B, Jamiolkowski RM, Albala DM, Shapiro ML, Lawson JH. A comprehensive review of topical hemostatic agents: effi cacy and recommendations for use. Ann Surg. 2010;251(2):217–28 [Research Support, Non-U.S. Gov’t Review].
15. Zhang CH, Song XM, He YL, Han F, Wang L, Xu JB, et al. Use of absorbable hemostatic gauze with medical adhesive is effective for achieving hemostasis in presacral hemorrhage. Am J Surg. 2012;203(4):e5–8.
16. Johnson P, Fromm D. Effects of bone wax on bacterial clearance. Surgery. 1981;89(2):206–9 [Research Support, U.S. Gov’t, P.H.S.].
17. Wilkinson HA, Baker S, Rosenfeld S. Gelfoam paste in experimen­tal laminectomy and cranial trephination: hemostasis and bone healing. J Neurosurg. 1981;54(5):664–7.
18. Frantz VK. Absorbable cotton, paper and gauze: (oxidized cellu­lose). Ann Surg. 1943;118(1):116–26.
19. Germanos S, Bolanis I, Saedon M, Baratsis S. Control of presacral venous bleeding during rectal surgery. Am J Surg. 2010;200(2): e33–5.
20. Nivatvongs S, Fang DT. The use of thumbtacks to stop massive presacral hemorrhage. Dis Colon Rectum. 1986;29(9):589–90.
21. Critchley AC, Holtham SJ. An unusual case of chronic anal pain–a pin in the bum? Ann R Coll Surg Engl. 2010;92(6):W27–8 [Case Reports].
310
A. Merchea and B.G. Wolff
22. Harrison JL, Hooks VH, Pearl RK, Cheape JD, Lawrence MA, Orsay CP, et al. Muscle fragment welding for control of massive presacral bleeding during rectal mobilization: a review of eight cases. Dis Colon Rectum. 2003;46(8):1115–7.
23. Xu J, Lin J. Control of presacral hemorrhage with electrocautery through a muscle fragment pressed on the bleeding vein. J Am Coll Surg. 1994;179(3):351–2.
24. Remzi FH, Oncel M, Fazio VW. Muscle tamponade to control pre­sacral venous bleeding: report of two cases. Dis Colon Rectum. 2002;45(8):1109–11 [Case Reports].
25. Cosman BC, Lackides GA, Fisher DP, Eskenazi LB. Use of tissue expander for tamponade of presacral hemorrhage. Report of a case. Dis Colon Rectum. 1994;37(7):723–6 [Case Reports].
26. Braley SC, Schneider PD, Bold RJ, Goodnight Jr JE, Khatri VP. Controlled tamponade of severe presacral venous hemorrhage: use of a breast implant sizer. Dis Colon Rectum. 2002;45(1):140–2 [Case Reports].
27. Ng X, Chiou W, Chang S. Controlling a presacral hemorrhage by using a saline bag: report of a case. Dis Colon Rectum. 2008; 51(6):972–4 [Case Reports].
28. Burchell RC. Physiology of internal iliac artery ligation. J Obstet Gynaecol Br Commonw. 1968;75(6):642–51.
29. Tomacruz RS, Bristow RE, Montz FJ. Management of pelvic hem­orrhage. Surg Clin North Am. 2001;81(4):925–48.
30. Kandeel A, Meguid A, Hawasli A. Controlling diffi cult pelvic bleeding with argon beam coagulator during laparoscopic ultra low anterior resection. Surg Laparosc Endosc Percutan Tech. 2011;21(1):e21–3.
31. Moore EE, Burch JM, Franciose RJ, Offner PJ, Biffl WL. Staged physiologic restoration and damage control surgery. World J Surg. 1998;22(12):1184–90; discussion 90–1.
32. Shapiro MB, Jenkins DH, Schwab CW, Rotondo MF. Damage con­trol: collective review. J Trauma. 2000;49(5):969–78.
33. Stone HH, Strom PR, Mullins RJ. Management of the major coagu­lopathy with onset during laparotomy. Ann Surg. 1983;197(5): 532–5.
34. Zama N, Fazio VW, Jagelman DG, Lavery IC, Weakley FL, Church JM. Effi cacy of pelvic packing in maintaining hemostasis after rectal excision for cancer. Dis Colon Rectum. 1988;31(12): 923–8.
Part IV
Anorectal Disease

Hemorrhoidal Disease: Postoperative Complications

Stefan D. Holubar and David E. Rivadeneira
Key Points
• In the United States, governmental and medical society recommendations suggest that Americans should ingest at least 25 g of dietary fi ber (12 serv­ings of fruits and/or vegetables per day). Many patients fi nd this a diffi cult-to- obtain goal and is the basis for recommendations for supplemental solu­ble fi ber to allow soft, bulky stool, which minimizes hemorrhoidal tissue trauma.
• When considering any operative approach to inter­nal hemorrhoidal disease, proper patient selection is the crucial fi rst step in avoiding complications. A complex interplay of factors such as age, gender, continence, comorbidities, and expected survival all play an important role in deciding on the optimal treatment.
• Despite the degree to which hemorrhoidal disease impacts patients’ lives, surgeons and patients must be aware that postoperative complications may result in permanent quality of life consequences.
S. D. Holubar , MD, MS, FACS Section of Colon and Rectal Surgery , Dartmouth-Hitchcock Medical Center, Geisel School of Medicine at Dartmouth, The Dartmouth Institute for Health Policy Research , One Medical Center Drive, Level 4C , Lebanon , NH 03756 , USA e-mail: stefan.holubar@dartmouth.edu , http://www.dhmc.org
D. E. Rivadeneira , MD, MBA, FACS, FASCRS ( Division of Colorectal Surgery , Huntington and Southside Hospitals Northshore/LIJ Health System , Hofstra University School of Medicine, 755 New York Avenue, Suite 108 , Huntington , NY 11743 , USA e-mail: drivadeneira@nshs.edu, http://www.drdavidrivadeneira.com
*)
2 0

The Hemorrhoidal Consult

Key Concept: When patients are referred to you with symp­toms due to hemorrhoids, it is not hemorrhoidal pathology until you make the diagnosis.
“Hemorrhoids” are without a doubt the most common indication for referral to a colorectal surgeon. Due to several factors ranging from lack of experience to lack of a complete examination, you will often fi nd that less than half of the patients referred for that indication actually have hemor­rhoidal disease and only a minority (~10 %) of which will require intervention more than lifestyle modifi cation [ 1 , 2 ]. While this is more likely a refl ection of improper training, it serves notice that you are the expert and need to be very familiar with anorectal anatomy and pathology. Given that half of the population of the United States over 50 are esti­mated to have hemorrhoidal bleeding at some point, likely due in part to lack of dietary fi ber in the Western diet, the magnitude of the problem for both colorectal surgeons and as a public health concern should not be underestimated [ 3 ].
When approaching the hemorrhoidal consultation, one of the fi rst things you as the consultant should consider is the patient’s age. Aging results in physiologic changes that include pelvic fl oor laxity and constipation but also bring about a more sedentary lifestyle and the need for medica­tions that can lead to excess straining. Similarly, patient gen­der has important implications. For females this includes a thorough gynecologic history focusing on prolonged labor, number of vaginal deliveries, episiotomies, and lacerations, as these can impact surgical decision-making and may con­tribute to otherwise avoidable complications. For example, a female patient with grade 3 hemorrhoids who had a previous third- or fourth-degree laceration may have an attenuated rectovaginal septum (Fig. ings, you may choose to perform a hemorrhoidectomy rather than a pexy, due to the risk of an iatrogenic rectovaginal
20.1 ). Depending on your fi nd-
S.R. Steele et al. (eds.), Complexities in Colorectal Surgery, DOI 10.1007/978-1-4614-9022-7_20, © Springer Science+Business Media New York 2014
313