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11 Perforated Diverticulitis: Laparoscopic Lavage andDrainage
127
Despite the initial enthusiasm regarding the use of LLD as a less invasive and morbid alternative to HP, more recent studies have challenged its presumed superi­ority relative to other surgical approaches. Nevertheless in our experience at Texas Endosurgery Institute, in carefully selected patients, LLD has proven to be a safe alternative, decreasing morbidity and mortality, avoiding stoma formation, and improving patient’s health immediately. The overall costs are decreased, and the diseased colon segment can be laparoscopically resected in a non-emergent fashion. Surgical therapy tailored to the patient appears appropriate.

References

1. Parks TG.Natural history of diverticular disease of colon. Clin Gastroenterol. 1975;4:53–69.
2. Morris CR, Harvey IM, Stebbings WS, Hart AR.Incidence of perforated diverticulitis and risk
factors for death in a UK population. Br JSurg. 2008;95:876–81.
3. Vermeulen J, Gosselink MP, Hop WCJ, Lange JF, Coene PPLO, Van de Harst E, Weidema WF,
Mannaerts GHH.Hospital mortality after emergency surgery for perforated diverticulitis. Ned Tijdschr Geneeskd. 2009;153:1209–14.
4. Mayo WJ, Wilson LB, Grifn HZ.Acquired diverticulitis of the large intestine. Surg Gynecol
Obstet. 1907;5:8–15.
5. Judd ES, Pollack LW.Diverticulitis of the colon. Ann Surg. 1924;80:425–38.
6. Lockhart Mummery JP.Late results of diverticulitis. Lancet. 1938;2:1401–4.
7. Smithwick RH. Experiences with the surgical management of diverticulitis of the sigmoid.
Ann Surg. 1942;115:969–83.
8. Jacobson MA, Young LS.New developments in the treatment of gram-negative bacteremia.
West JMed. 1986;144:185–94.
9. Stawicki SP, Brooks A, Bilski T, Scaff D, Gupta R, Schwab CW.The concept of damage con-
trol: extending the paradigm to emergency general surgery. Injury. 2008;39(1):93–101.
10. Miller PR, Chang MC, Hoth JJ, Holmes JH, Meredith JW.Colonic resection in the setting of
damage control laparotomy: is delayed anastomosis safe? Am Surg. 2007;73(6):606–9.
11. Bretagnol F, Pautrat K, Mor C, Benchellal Z, Huten N, De Calan L.Emergency laparoscopic
management of perforated sigmoid diverticulitis: a promising alternative to more radical pro­cedures. JAm Coll Surg. 2008;2006:654–7.
12. Liang S, Russek K, Franklin ME Jr. Damage control strategy for management of perforated
diverticulitis with generalized peritonitis: laparoscopic lavage and drainage vs. laparoscopic Hartmann’s procedure. Surg Endosc. 2012;26:2835–42.
13. Cirocchi R, Trastulli S, Vettoretto N, Milani D, Cavaliere D, Renzi C, Adamenko O, Desiderio
J, Burattini MF, Parisi A, Arezzo A, Fingerhut A.Laparoscopic peritoneal lavage: a denitive treatment for diverticular peritonitis or a “bridge” to elective laparoscopic sigmoidectomy? A systematic review. Medicine. 2015;94(1):e334.
14. Angenete E, Thornell A, Burcharth J, Pommergaard H-C, Skullman S, Bisgaard T, Jess P,
Läckberg Z, Matthiessen P, Heath J, Rosenberg J, Haglind E.Laparoscopic lavage is feasible and safe for the treatment of perforated diverticulitis with purulent peritonitis the rst results from the randomized controlled trial DILALA.Ann Surg. 2016;263(1):117.
15. Galbraith N, Carter JV, Netz U, Yang D, Fry DE, McCafferty M, Galandiuk S.Laparoscopic
lavage in the management of perforated diverticulitis: a contemporary meta-analysis. JGastrointest Surg. 2017;21:1491.
16. Vennix S, Musters GD, Mulder IM, Swank HA, Consten EC, Belgers EH, van Geloven AA,
Gerhards MF, Govaert MJ, van Grevenstein WM, Hoofwijk AG, Kruyt PM, Nienhuijs SW, Boermeester MA, Vermeulen J, van Dieren S, Lange JF, Bemelman WA.Laparoscopic peri­toneal lavage or sigmoidectomy for perforated diverticulitis with purulent peritonitis: a multi­center, parallel-group, randomized, open-label trail. Lancet. 2015;386:1289–77.
128
17. Agresta F, etal. Laparoscopic approach to acute abdomen from the Consensus Development
Conference of the Società Italiana di Chirurgia Endoscopica e nuove tecnologie (SICE), Associazione Chirurghi Ospedalieri Italiani (ACOI), Società Italiana di Chirurgia (SIC), Società Italiana di Chirurgia d’Urgenza e del Trauma (SICUT), Società Italiana di Chirurgia nell’Ospedalità Privata (SICOP), and the European Association for Endoscopic Surgery (EAES). Surg Endosc. 2012;26(8):2134–64.
18. Chabok A, Pahlman L, Hjern F, Haapaniemi S, Smedh K, AVOD Study Group. Randomized
clinical trial of antibiotics in acute uncomplicated diverticulitis. Br JSurg. 2012;99:532–9.
19. Feingold D, Steele SR, Lee S, Kaiser A, Boushey R, Buie WD, Rafferty JF.Practice param-
eters for the treatment of sigmoid diverticulitis. Dis Colon Rectum. 2014;57(3):284–94.
20. Mahmoud NN, Riddle EW. Minimally invasive surgery for complicated diverticulitis.
JGastrointest Surg. 2017;21:731–8.
M.E. Franklin Jr. and M.A. Hernández
Perforated Diverticulitis: What Are theOptions forResection?
FrançoisLetarte andCarlJ.Brown

Introduction

Diverticulosis typically involves the sigmoid colon and occurs in 50% of people aged over 50years and up to 80% in those aged over 80 [1]. The vast majority of patients with colonic diverticulosis are asymptomatic, whereas 10–25% will develop at least a single episode of diverticulitis [2–4]. In these patients, 10–33% will even­tually need surgical intervention [2, 5, 6] and only 1% of patients with diverticulosis will require surgery [7]. Of all admitted patients with a diagnosis of acute diverticu­litis, 10–20% will require surgical treatment [8]. Urgent indications for surgery in patients with diverticulitis include obstruction, hemorrhage, failure of medical man­agement, and free perforation. In this chapter, we will only consider options and issues related to the last two.
In essence, all presentations of diverticulitis are secondary to perforation of diverticula. However, most are microperforations that are walled off by adjacent organs or omentum. Free perforation necessitating urgent surgery is uncommon and is the indication to undergo emergent surgery in less than 25% of patients with acute complicated diverticulitis [7]. Rodkey and Welch [8] reviewed the indications for surgery in a series of 688 patients with acute diverticulitis: perforation with local peritonitis or pelvic abscess in 32.3%, generalized peritonitis in 14.6%, pain in
13.4%, obstruction in 10.9%, pericolic abscess in 10.9%, stula in 9.7%, and bleed­ing in 8.2%. Free perforation following diverticulitis is especially common and lethal in immunosuppressed patients [9, 10].
12
F. Letarte • C.J. Brown (*) Department of Surgery, St. Paul’s Hospital, University of British Columbia, Vancouver, BC, Canada e-mail: etarte@gmail.com; cbrown@providencehealth.bc.ca
© Springer International Publishing AG 2018 C.M. Schlachta, P. Sylla (eds.), Current Common Dilemmas in Colorectal Surgery,
https://doi.org/10.1007/978-3-319-70117-2_12
129
130
F. Letarte and C.J. Brown

Classification

Hughes was the rst to present a practical clinical classication of diverticulitis based on the operative ndings [11]. He divided patients according to the severity of their peritoneal contamination. Hinchey rened this classication into the widely adopted four-stage classication of presentations of diverticulitis [12]. In this clas­sication, most patients treated by surgery for acute perforation are stage III or IV, representing generalized purulent and fecal peritonitis, respectively (Table 12.1). More recently, Killingback proposed a more complicated classication that differ­entiates abscess, perforation, and peritonitis into subclassications [10].
Most cases of perforated diverticulitis will be walled off by adjacent structures preventing free perforation and generalized peritonitis (Hinchey I/II) and resolve with antibiotics and bowel rest. Rarely, purulent peritonitis may arise following a progressive leak from a diverticulum or presumed rupture of a previously contained perforation. In rare cases, patients initially presenting with early-stage diverticulitis will develop free perforation and generalized fecal peritonitis. This scenario is asso­ciated with a very high mortality rate [13–16].
The Hinchey classication system is used to determine both treatment and prog­nosis. Haglund etal. [5] conrmed the impact of free perforation on outcomes; in their series, patients experienced 33% surgical mortality in the presence of free perforation compared to a 3% mortality rate when only acute inammation was present. Other reports have also shown that both localized peritonitis and abscess are associated with lower mortality when compared to diffuse fecal or purulent peritonitis [12, 17, 18].
Table 12.1 Clinical classication of complicated diverticulitis based on operative ndings
Classication Hughes [11] Stage I Local peritonitis
Hinchey [12] Stage I Pericolic abscess or phlegmon
Killingback [10] Stage I Abscess
Stage
Stage II Local pericolic or pelvic abscess Stage III General peritonitis due to ruptured pericolic or pelvic abscess Stage IV General peritonitis due to free perforation of the colon
Stage II Pelvic, intraabdominal, or retroperitoneal abscess Stage III Generalized purulent peritonitis Stage IV Generalized fecal peritonitis
a Peridiverticular b Mesenteric c Pericolic (pelvic) Stage II Perforation a Free b Concealed Stage III Gangrenous sigmoiditis Stage IV Peritonitis a Serous, purulent or fecal b Local, pelvic or generalized
Description
12 Perforated Diverticulitis: What Are theOptions forResection?
131
Indications forSurgery
As previously described, we consider two scenarios that require surgery for perfo­rated diverticulitis. The rst indication includes patients who present with general­ized peritonitis due to free perforation. Typically, these patients present with diffuse peritonitis, tachycardia, hypotension, and free air on x-ray and/or CT scan. The decision to operate is not usually difcult. The second indication includes patients who fail to respond to non-operative management. Most will be patients with a phlegmon or abscess with persistent fevers, leukocytosis, tachycardia, pain and ten­derness on examination despite intravenous antibiotics, bowel rest, and uid resus­citation. It is important to note that most patients with evidence of “perforation” on CT imaging may present with localized peritonitis and non-operative management can safely be attempted. Free air will often result from the initial microperforation that is quickly contained by the adjacent structures, preventing free perforation and generalized peritonitis in most cases.
Surgical Management ofPerforated Diverticulitis
The main objective of surgical resection for perforated diverticulitis is to eliminate the source of ongoing sepsis as quickly and safely as possible. Laparoscopic lavage has been proposed as an alternative to resection, and this option is discussed in detail in a different chapter.
Limitations oftheAvailable Evidence
The current literature on the management of perforated diverticulitis consists mostly of case series and retrospective reports increasing the risk for bias. Another concern is the lack of consistent classication of diverticular disease that can lead to comparison of patients with different severity of disease. Most studies do not specify precisely the extent of peritonitis (i.e., localized vs. purulent vs. feculent peritonitis). The authors also compare series from different eras where there are numerous confounding factors inuencing patient outcomes (e.g., antibiotic use, improvements in perioperative care). Hence, their conclusions and recommendations should be interpreted with caution.
Historic Management
In the early-mid twentieth century, the recommendation for patients presenting with perforated diverticulitis was a three-stage procedure: an initial transverse loop colostomy and drainage, followed 3 to 6months later by a subsequent resection, and nally, closure of the loop colostomy [19, 20]. This procedure has largely been abandoned in favor of either the Hartmann’s procedure or resection with primary anastomosis with or without proximal diversion. In 1984, Krukowski and Matheson
132
F. Letarte and C.J. Brown
reviewed the world literature on emergency surgery for diverticular disease compli­cated by generalized peritonitis [14]. They demonstrated a clear advantage in terms of mortality and morbidity after resection of the diseased segment rather than per­forming an operation where the colon was retained. Their review included 1282 patients from 57 publications. The mortality rates in operations where the colon was resected ranged 6.1–12.2%. When the diseased segment was diverted but not resected, mortality was 25.7–28.1%. The authors recommended that segmental resection should be performed. While the three-stage procedure has been aban­doned, there continues to be debate on which surgical procedure to choose when facing perforated diverticulitis. We will review the controversies and highlight the circumstances when each may be applied.
Technical Considerations
The extent of resection is determined intraoperatively based on the quality of the tis­sues and should include the entire thickened contracted segment, including the inammatory process. Proximal and distal margins should be healthy colon and rec­tum. The most important factor to prevent recurrence of diverticulitis is to extend the distal margin of resection to the proximal rectum to create a colorectal anastomosis.
Thaler etal. examined the impact of surgery-related variables on recurrence rate after sigmoid resection for diverticulitis [21]. The level of the anastomosis was the only predictor of recurrence; patients with colosigmoid anastomosis had a recur­rence rate fourfold higher than patients with colorectal anastomosis (2.8% vs.
12.5%, p=0.033). Similarly, Benn etal. in a series of 501 patients reported a diver­ticulitis recurrence rate that was doubled in patients whom the distal margin used in the anastomosis was the sigmoid colon rather than the rectum (6.7% vs. 12.5%) [22]. In both series, the segment harboring diverticulitis was in the sigmoid colon.
In cases where the diseased colonic segment is proximal to a healthy sigmoid, it is likely safe to proceed with a colo-colonic anastomosis as long as the entire thick­ened segment is removed. While there are no comparative studies supporting this approach, it is clear that removing all colonic diverticula en bloc is not advisable in patients with diverticulitis. While it is not necessary to remove all diverticula­bearing colon, efforts should be made to avoid including diverticula in the anasto­mosis to decrease the risk of leak.
It is not clear whether effort should be made to preserve the inferior mesenteric artery and its branches. The rationale behind preserving this artery is that it may improve blood supply to the distal aspect of the anastomosis and, hence, reduce the risk of anastomotic leakage. A retrospective review of 130 patients with diverticuli­tis who underwent elective resection, where the primary outcome was to evaluate the impact of inferior mesenteric artery (IMA) or superior rectal artery (SRA) pres­ervation with respect to anastomotic leak rates, showed that preservation of the major vascular pedicle was not associated with improved outcomes [23]. However, a randomized controlled study looking at 86 patients undergoing sigmoidectomy for complicated diverticular disease observed a lower clinical leak rate when preserving the SRA (2% vs. 7%, p=0.03) [24]. Of note, the authors used liberal denitions of
12 Perforated Diverticulitis: What Are theOptions forResection?
133
leak that may not represent actual or clinically signicant anastomotic leaks and may have inuenced the results.
While the evidence is marginal, it appears that preservation of the IMA may be benecial. However, the diagnosis of diverticulitis is often in doubt at the time of emergency surgery, as there is a possibility of undiagnosed cancer. Bacon etal. [25] found an underlying carcinoma in 7.7% of 351 patients undergoing elective resec­tion for diverticulitis. In cases of emergent colectomy for presumed diverticulitis, two series report 20–25% rates of unexpected underlying carcinoma [26, 27]. While our experience more closely reects cancer incidence similar to those reported by Bacon etal., we believe that patients having emergency surgery where endoscopic exclusion of a malignancy is not possible should undergo an oncologic resection including high ligation of the IMA.
Hartmann’s Vs. Primary Anastomosis
Hartmann’s procedure, consisting of sigmoid resection, terminal colostomy, and closure of the rectal stump, is the easiest, fastest, and safest operation to clear the sepsis-inducing segment of the colon and avoid the risk of anastomotic leak. The disadvantages of interval colostomy include rectal stump leak, stoma complica­tions, and long hospital stay. Most importantly, intestinal reconstruction can be quite challenging and is associated with a signicant risk of complications, with observed morbidity of up to 40% [28]. Data from large administrative database studies show that more than a third of patients never undergo Hartmann reversal and that the number increases up to 70% when patients are aged over 77years [29, 30]. These factors make a primary colorectal anastomosis an enticing alternative.
The available comparative data are mostly observational studies suggesting pri­mary anastomosis (PRA), and Hartmann’s procedure (HP) is associated with similar outcomes in terms of morbidity and mortality. However, these studies are marred by considerable selection bias, where younger, healthier patients tend to be managed with a restorative approach. Abbas etal. reviewed this literature comparing the safety and feasibility of PRA compared to HP for patients with acute complicated diverticu­litis [31]. Eighteen studies including 884 patients were included in the review, none of which were randomized controlled trials. When compared to HP, PRA was associated with lower mortality rate (9% vs. 19%) and similar postoperative morbidity rates (29% vs. 33.4%). He found an anastomotic leak rate of 5.5% in the PRA patients compared to 8% in the HP patients. Constantinides et al. conducted a prospective study to assess adverse events following PRA versus HP for complicated diverticular disease [32]. Over a 12-month period across 42 centers in Great Britain, data were collected for 248 patients who underwent PRA and 167 patients who underwent HP.After adjusting for risk factors for selection of patients for a non-restorative pro­cedure, HP was found to be associated with similar 30-day mortality (OR 1.76, p = 0.223), increased surgical complications (OR 1.90, p = 0.025), and increased overall medical complications (OR 2.08, p = 0.026) when compared to PRA.Constantinides also published a second systematic review comparing PRA and HP [33]. It included 963 patients (57% PRA and 43% HP) from 15 studies. Overall
134
F. Letarte and C.J. Brown
mortality was signicantly reduced with PRA (4.9% vs. 15.1%; OR 0.41). Subgroup analyses were performed, and PRA was associated with decreased mortality when trials were matched for emergency operations (6.4% vs. 15.6%; OR 0.44). However, when trials were matched for severity of peritonitis of Hinchey III or IV, there was no signicant difference in mortality (14.1% vs. 14.4%, OR= 0.85) (see Table12.2). Salem etal. also conducted a systematic review on the topic. Their paper included 1051 patients undergoing HP and 569 patients undergoing PRA.Mortality rates were, respectively, 19.6% for HP and 9.9% for PRA.However, no subgroup analyses were performed. A study by Aydin, one of the largest single institution retrospective reviews, aimed to assess the likelihood of Hartmann versus primary anastomosis in patients with perforated diverticulitis. They described a diverticulitis disease propen­sity score which showed that the strongest predictors of Hartmann’s procedure were urgent or emergent cases, BMI over 30, Manheim peritonitis index of 10 and over, immunosuppression, and Hinchey grade III or IV [36]. These factors have also been recognized in other studies as predictors of end- colostomy formation, including a pro­spective study showing an association between higher Manheim peritonitis index and likelihood of end colostomy [34, 35, 37]. A more recent systematic review and meta­analysis addressing the treatment of Hinchey III and IV diverticulitis found compa­rable mortality between patients undergoing primary anastomosis versus Hartmann’s procedure [38]. Marked heterogeneity and potential for selection bias once again limit the interpretation of the results as well as the possibility to draw any conclusion.
A single small randomized trial has tried to address the issue of selection bias [39]. Oberkoer etal. randomized 64 patients with Hinchey III and IV diverticulitis to HP or PRA.The study was discontinued early as an interim safety analysis showed HP to be associated with signicantly more serious complications when compared to ileos­tomy reversal. The majority of patients included were Hinchey stage III diverticulitis. There was no signicant difference in terms of mortality and morbidity between the two groups, but stoma reversal was signicantly higher in the primary anastomosis group. PRA was also associated with shorter hospital stay and lower in-hospital costs.
The Dutch Diverticular Disease (3D) Collaborative Study group started the Ladies trial in 2010in an effort to answer two important questions. The rst, com­paring laparoscopic lavage with sigmoidectomy for purulent perforated diverticuli­tis, was stopped early by the data safety monitoring committee and is discussed in another chapter. In the DIVA arm (perforated DIVerticulitis: sigmoid resection with or without Anastomosis), patients randomized to resection were then randomized to either HP or PRA [40]. The results of this trial are still pending, but this will provide more clarity for surgeons.
Since no strong evidence is available to allow for general guidelines, surgeons must weigh the benets of primary anastomosis versus the risks linked to anasto­motic failure and longer operating times. In clinical practice, the decision to per­form primary anastomosis should be individualized to each patient, and surgeons should ask themselves if the patient could withstand and survive an anastomotic leak. Presence of any one of the parameters including hemodynamic instability, acidosis, acute organ failure, and any signicant comorbidity such as diabetes, mal­nutrition, chronic end-stage organ failure, or immunosuppression should prompt the
OutcomeMortality comperison in diverticular disease
Stud or
02 Mortality - diverticular diseas Drumm [24] Gregg [26]
]1
U
52 K Alenis [21]
]1
Hold [27]
]1
Peoples [30]
]1 Medina [29] Sarin [33]
83
Saccomani [32]
74
]1 Wedel [35]
19 G Schiling [36] Blair [22]
41
]2
Regenet [31]
]2
Subtot
Total events: 27 (PRA), 63 (Hartman’s procedure)
Test Test
03 Mortality - diverticular disease and emergency operations only
Hold [27]
]1
Saccomani [32]
77
]1
G
]2
Schiling [36]
]2
Blair [22]
]2
Regenet [31]
]2
Subtot
Total events: 17 (PRA), 39 (Hartman’s procedure)
Test Test
05 Mo Drumm [24]
Medina [29]
]1
G
Schiling [36]
]2
Regenet [31]
]2
Subtot Total events: 11 (PRA), 16 (Hartman’s procedure) Test Test
07 Mortality - diverticular disease and abscess/peritonitis Drumm [24] U
53 Alanis [21]
]1 Hold [27] Peoples [30]
]1 Medina [29] Wedel [35]
11
]1 G
]2 Schiling [36]
]2 Blair [22]
41
]2 Regenet [31]
]2 Subtot Total events: 23 (PRA), 58 (Hartman’s procedure)
Test for heterogeneity: Ch Test
Modified from Constantinides et al. systematic review [33]
12 Perforated Diverticulitis: What Are theOptions forResection?
Table 12.2 Mortality comparing PRA vs. HP
135
y
sub category
nderwood [34] 0/61/1 ourtesis [28] 1/23 0/10 2.80 1.40 [0.05, 37.33] 1988
oozsen [25] 5/32 6/28 12.880.68 [0.18, 2.53] 2001
al (95% Cl)547 416100.000.41 [0.22, 0.77]
for heterogeneity: Chi2 = 20.10, df = 14 (P = 0.13), I2 = 30.4% for overall effect: Z = 2.77 (P = 0.006)
oozsen [25] 5/32 6/28 21.660.69 [0.18, 2.53
al (95% Cl)230 250 100.00 0.44 [0.24, 0.83]
for heterogeneity: Chi2 = 4.53, df = 5 (P = 0.48), I2 = 0% for overall effect: Z = 2.55 (P = 0.01)
rtality - diverticular disease and Hinchey >2
oozsen [25] 5/32 6/28 38.770.68 [0.18, 2.53] 2001
al (95% Cl)78111 100.00 0.85 [0.36, 2.01]
for heterogeneity: Chi2 = 2.43, df = 4 (P = 0.66), I2 = 0% for overall effect: Z = 0.38 (P = 0.71)
nderwood [34] 0/61/1
oozsen [25] 5/32 6/28 14.910.68 [0.18, 2.53
al (95% Cl)444 366100.000.43 [0.21, 0.85]
for overall effect: Z = 2.41 (P = 0.02)
PRA
n/N
e
2/31/5 2.85 8.00 [0.31, 206.37] 1984 0/35 2/25 3.15 0.13 [0.01, 2.88
1/34 4/26 5.50 0.17 [0.02, 1.59 4/99 9/76 14.25 0.31 [0.09, 1.06 2/11 8/43 8.69 0.97 [0.18, 5.40 0/31/3 2.37 0.24 [0.01, 8.62] 1991 2/19 0/ 1/26 3/ 2/1837/3
1/13 4/42 5.38 0.79 [0.08, 7.78] 2001 3/33 13/6 3/27 4/33 9.75 0.91 [0.18, 4.45
4/99 9/76 23.950.31 [0.09, 1.06 1/26 3/
1/13 4/42 9.05 0.79 [0.08, 7.78 3/33 13/64 21.200.39 [0.10, 1.49 3/27 4/33 16.390.91 [0.18, 4.45
2/31/5 8.58 8.00 [0.31, 206.37] 1984
0/31/3 7.12 0.24 [0.01, 8.62
1/13 4/42 16.200.79 [0.08, 7.78
3/27 4/33 29.330.91 [0.18, 4.45
2/31/5 3.30 8.00 [0.31, 206.37] 1984
1/34 4/26 6.37 0.17 [0.02, 1.59 4/99 9/76 16.490.31 [0.09, 1.06] 1990 2/11 8/43 10.050.97 [0.18, 5.40 0/31/3 2.74 0.24 [0.01, 8.62] 1991 2/1837/3
1/13 4/42 6.23 0.79 [0.08, 7.78 3/33 13/6 3/27 4/33 11.280.91 [0.18, 4.45
i2 = 15.26, df = 10 (P = 0.12), I 2 = 34.5%
Hartmann’s
Procedure
n/N
OR (random)
95% Cl
Weight%OR (random)
.720.74 [0.03, 20.81] 1984
.032.43 [0.10, 56.39] 1991 .610.05 [0.00, 0.65 .410.04 [0.01, 0.19] 1997
2.61 0.39 [0.10, 1.49
.750.05 [0.00, 0.65
.150.74 [0.03, 20.81] 1984
0.89 0.04 [0.01, 0.19
4.59 0.39 [0.10, 1.49
95% Cl Year
984
989 990 990
993
002 003
990 993 001 001 002 003
991
001
003
989
990
997 001 001 002 003
136
F. Letarte and C.J. Brown
operating surgeon to strongly consider end colostomy. Diffuse peritonitis, either purulent or feculent, is often considered as a strong contraindication for primary anastomosis. However, it is our opinion that select young patients, hemodynami­cally stable with healthy tissues and without any signicant comorbidities, could undergo safely primary anastomosis even in the presence of diffuse peritonitis. Diverting loop ileostomy should be strongly considered in any of the cases.
Damage Control Surgery forPerforated Diverticulitis
Initially described for patients with major abdominal injuries, indications for damage control surgery (DCS) have expanded to include patients with severe peritonitis and instability [41–43]. DCS for perforated diverticulitis has been reported as an alterna­tive treatment strategy by several authors [7, 44–49]. DCS for perforated diverticuli­tis involves a three-stage approach: stage I, an abbreviated initial operative procedure with temporary abdominal closure; stage II, continued resuscitation and manage­ment of physiologic and acid–base derangements; and stage III, denitive treatment and closure. This alternative approach allows for rapid source control and patient resuscitation in the intensive care, postponing the decision on the denitive surgical resolution to a semi-elective setting in a hemodynamically stable patient. In a series by Kafka-Ritsch et al. [46], they achieved a low mortality rate (9.8%), and most patients were discharged with their colon reconstructed (77% overall, 50% for fecal peritonitis). All of this despite a median Manheim peritonitis index of 26 and a high rate of severe comorbidities (Table12.3). This alternative concept should be taken into consideration before choosing to perform a Hartmann’s procedure in patients presenting with extensive peritonitis from perforated diverticulitis.
Table 12.3 Outcomes of damage control surgery for complicated diverticulitis
Study Sohn etal. [42] N 18 19
Kafka-Ritsch etal. [46]
Finlay etal. [43] N Not applicable 14
Outcomes
Postoperative complication rate
Mortality 11% 10.5% Primary anastomosis 22.2% 78.9% N Not applicable 51 Postoperative complication
rate Mortality 9.8% Primary anastomosis 76%
Postoperative complication rate
Mortality 7.1% Primary anastomosis 85.7%
Primary denitive surgery
39% 32%
Damage control surgery
Not available
Not available