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Acute Cholecystitis andEmergency Common Bile Duct Exploration
https://t.me/medicina_free
TG13: updated Tokyo guidelines for the management of acute cholangitis and cholecystitis. J
Hepatobiliary Pancreat Sci. 2013;20(1):1–7. https://doi.org/10.1007/s00534- 012- 0566- y.
9. Yokoe M, Hata J, Takada T, Strasberg SM, Asbun HJ, Wakabayashi G, Kozaka K, Endo
I, Deziel DJ, Miura F, Okamoto K, Hwang TL, Huang WS, Ker CG, Chen MF, Han HS,
Yoon YS, Choi IS, Yoon DS, Noguchi Y, Shikata S, Ukai T, Higuchi R, Gabata T, Mori Y,
Iwashita Y, Hibi T, Jagannath P, Jonas E, Liau KH, Dervenis C, Gouma DJ, Cherqui D, Belli
G, Garden OJ, Giménez ME, de Santibañes E, Suzuki K, Umezawa A, Supe AN, Pitt HA,
Singh H, Chan ACW, Lau WY, Teoh AYB, Honda G, Sugioka A, Asai K, Gomi H, Itoi T,
Kiriyama S, Yoshida M, Mayumi T, Matsumura N, Tokumura H, Kitano S, Hirata K, Inui K,
Sumiyama Y, Yamamoto M.Tokyo guidelines 2018: diagnostic criteria and severity grading of
acute cholecystitis (with videos). J Hepatobiliary Pancreat Sci. 2018;25(1):41–54. https://doi.
org/10.1002/jhbp.515.
10. Ansaloni L, Pisano M, Coccolini F, Peitzmann AB, Fingerhut A, Catena F, Agresta F, Allegri
A, Bailey I, Balogh ZJ, Bendinelli C, Bif W, Bonavina L, Borzellino G, Brunetti F, Burlew
CC, Camapanelli G, Campanile FC, Ceresoli M, Chiara O, Civil I, Coimbra R, De Moya M,
Di Saverio S, Fraga GP, Gupta S, Kashuk J, Kelly MD, Koka V, Jeekel H, Lati R, Leppaniemi
A, Maier RV, Marzi I, Moore F, Piazzalunga D, Sakakushev B, Sartelli M, Scalea T, Stahel
PF, Taviloglu K, Tugnoli G, Uraneus S, Velmahos GC, Wani I, Weber DG, Viale P, Sugrue M,
Ivatury R, Kluger Y, Gurusamy KS, Moore EE. 2016 WSES guidelines on acute calculous
cholecystitis. World J Emerg Surg. 2016;11:25. https://doi.org/10.1186/s13017- 016- 0082- 5.
11. Pisano M, Allievi N, Gurusamy K, Borzellino G, Cimbanassi S, Boerna D, Coccolini F, Tufo
A, Di Martino M, Leung J, Sartelli M, Ceresoli M, Maier RV, Poiasina E, De Angelis N,
Magnone S, Fugazzola P, Paolillo C, Coimbra R, Di Saverio S, De Simone B, Weber DG,
Sakakushev BE, Lucianetti A, Kirkpatrick AW, Fraga GP, Wani I, Bif WL, Chiara O, AbuZidan F, Moore EE, Leppäniemi A, Kluger Y, Catena F, Ansaloni L. 2020 World Society of
Emergency Surgery updated guidelines for the diagnosis and treatment of acute calculus cholecystitis. World J Emerg Surg. 2020;15(1):61. https://doi.org/10.1186/s13017- 020- 00336- x.
12. Naidu K, Beenen E, Gananadha S, Mosse C.The yield of fever, inammatory markers and
ultrasound in the diagnosis of acute cholecystitis: a validation of the 2013 Tokyo guidelines.
World J Surg. 2016;40(12):2892–7. https://doi.org/10.1007/s00268- 016- 3660- 5.
13. Kiewiet JJ, Leeuwenburgh MM, Bipat S, Bossuyt PM, Stoker J, Boermeester MA.A systematic review and meta-analysis of diagnostic performance of imaging in acute cholecystitis.
Radiology. 2012;264(3):708–20. https://doi.org/10.1148/radiol.12111561.
14. Fuks D, Mouly C, Robert B, Hajji H, Yzet T, Regimbeau JM. Acute cholecystitis: preoperative CT can help the surgeon consider conversion from laparoscopic to open cholecystectomy.
Radiology. 2012;263(1):128–38. https://doi.org/10.1148/radiol.12110460.
15. Bates DD, LeBedis CA, Soto JA, Gupta A. Use of magnetic resonance in pancreaticobiliary
emergencies. Magn Reson Imaging Clin N Am. 2016;24(2):433–48. https://doi.org/10.1016/j.
mric.2015.11.010.
16. Watanabe Y, Nagayama M, Okumura A, Amoh Y, Katsube T, Suga T, Koyama S, Nakatani K,
Dodo Y.MR imaging of acute biliary disorders. Radiographics. 2007;27(2):477–95. https://
doi.org/10.1148/rg.272055148.
17. Pinto A, Reginelli A, Cagini L, Coppolino F, Stabile Ianora AA, Bracale R, Giganti M,
Romano L. Accuracy of ultrasonography in the diagnosis of acute calculous cholecystitis: review of the literature. Crit Ultrasound J. 2013;5 Suppl 1(Suppl 1):S11. https://doi.
org/10.1186/2036- 7902- 5- S1- S11.
18. Changphaisarnkul P, Saengruang-Orn S, Boonya-Asadorn T.The diagnosis of acute cholecystitis: sensitivity of sonography, cholescintigraphy and computed tomography. J Med Assoc
Thail. 2015;98(8):812–9.
19. Paul Wright G, Stilwell K, Johnson J, Hefty MT, Chung MH. Predicting length of stay and
conversion to open cholecystectomy for acute cholecystitis using the 2013 Tokyo guidelines in
a US population. J Hepatobiliary Pancreat Sci. 2015;22(11):795–801. https://doi.org/10.1002/
jhbp.284.
65

66
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20. Ambe PC, Christ H, Wassenberg D.Does the Tokyo guidelines predict the extent of gallbladder inammation in patients with acute cholecystitis? A single center retrospective analysis.
BMC Gastroenterol. 2015;15:142. https://doi.org/10.1186/s12876- 015- 0365- 4.
21. Yokoe M, Takada T, Hwang TL, Endo I, Akazawa K, Miura F, Mayumi T, Mori R, Chen MF,
Jan YY, Ker CG, Wang HP, Itoi T, Gomi H, Kiriyama S, Wada K, Yamaue H, Miyazaki M,
Yamamoto M. Descriptive review of acute cholecystitis: Japan-Taiwan collaborative epidemiological study. J Hepatobiliary Pancreat Sci. 2017;24(6):319–28. https://doi.org/10.1002/
jhbp.450.
22. Endo I, Takada T, Hwang TL, Akazawa K, Mori R, Miura F, Yokoe M, Itoi T, Gomi H, Chen
MF, Jan YY, Ker CG, Wang HP, Kiriyama S, Wada K, Yamaue H, Miyazaki M, Yamamoto
M. Optimal treatment strategy for acute cholecystitis based on predictive factors: JapanTaiwan multicenter cohort study. J Hepatobiliary Pancreat Sci. 2017;24(6):346–61. https://doi.
org/10.1002/jhbp.456.
23. Cheng WC, Chiu YC, Chuang CH, Chen CY. Assessing clinical outcomes of patients with
acute calculous cholecystitis in addition to the Tokyo grading: a retrospective study. Kaohsiung
J Med Sci. 2014;30(9):459–65. https://doi.org/10.1016/j.kjms.2014.05.005.
24. Kamalapurkar D, Pang TC, Siriwardhane M, Hollands M, Johnston E, Pleass H, Richardson
A, Lam VW.Index cholecystectomy in grade II and III acute calculous cholecystitis is feasible
and safe. ANZ J Surg. 2015;85(11):854–9. https://doi.org/10.1111/ans.12986.
25. Amirthalingam V, Low JK, Woon W, Shelat V.Tokyo guidelines 2013 may be too restrictive
and patients with moderate and severe acute cholecystitis can be managed by early cholecystectomy too. Surg Endosc. 2017;31(7):2892–900. https://doi.org/10.1007/s00464- 016- 5300- 4.
26. Csendes A, Burdiles P, Diaz JC, Maluenda F, Korn O, Vallejo E, Csendes P. Prevalence
of common bile duct stones according to the increasing number of risk factors present.
A prospective study employing routinely intraoperative cholangiography in 477 cases.
Hepatogastroenterology. 1998;45(23):1415–21.
27. Ko CW, Lee SP.Epidemiology and natural history of common bile duct stones and prediction of disease. Gastrointest Endosc. 2002;56(6 Suppl):S165–9. https://doi.org/10.1067/
mge.2002.129005.
28. Ahn KS, Yoon YS, Han HS, Cho JY. Use of liver function tests as rst-line diagnostic
tools for predicting common bile duct stones in acute cholecystitis patients. World J Surg.
2016;40(8):1925–31. https://doi.org/10.1007/s00268- 016- 3517- y.
29. Gurusamy KS, Giljaca V, Takwoingi Y, Higgie D, Poropat G, Štimac D, Davidson
BR.Ultrasound versus liver function tests for diagnosis of common bile duct stones. Cochrane
Database Syst Rev. 2015;2015(2):CD011548. https://doi.org/10.1002/14651858.CD011548.
30. Boys JA, Doorly MG, Zehetner J, Dhanireddy KK, Senagore AJ.Can ultrasound common bile
duct diameter predict common bile duct stones in the setting of acute cholecystitis? Am J Surg.
2014;207(3):432–5; discussion 435. https://doi.org/10.1016/j.amjsurg.2013.10.014.
31. ASGE Standards of Practice Committee, Maple JT, Ben-Menachem T, Anderson MA,
Appalaneni V, Banerjee S, Cash BD, Fisher L, Harrison ME, Fanelli RD, Fukami N, Ikenberry
SO, Jain R, Khan K, Krinsky ML, Strohmeyer L, Dominitz JA.The role of endoscopy in the
evaluation of suspected choledocholithiasis. Gastrointest Endosc. 2010;71(1):1–9. https://doi.
org/10.1016/j.gie.2009.09.041.
32. Barkun AN, Barkun JS, Fried GM, Ghitulescu G, Steinmetz O, Pham C, Meakins JL,
Goresky CA.Useful predictors of bile duct stones in patients undergoing laparoscopic cholecystectomy. McGill Gallstone Treatment Group. Ann Surg. 1994;220(1):32–9. https://doi.
org/10.1097/00000658- 199407000- 00006.
33. Cronan JJ.US diagnosis of choledocholithiasis: a reappraisal. Radiology. 1986;161(1):133–4.
https://doi.org/10.1148/radiology.161.1.3532178.
34. Bose SM, Mazumdar A, Prakash VS, Kocher R, Katariya S, Pathak CM.Evaluation of the
predictors of choledocholithiasis: comparative analysis of clinical, biochemical, radiological, radionuclear, and intraoperative parameters. Surg Today. 2001;31(2):117–22. https://doi.
org/10.1007/s005950170194.
S. Frassini et al.

Acute Cholecystitis andEmergency Common Bile Duct Exploration
https://t.me/medicina_free
35. Abboud PA, Malet PF, Berlin JA, Staroscik R, Cabana MD, Clarke JR, Shea JA, Schwartz JS,
Williams SV.Predictors of common bile duct stones prior to cholecystectomy: a meta- analysis.
Gastrointest Endosc. 1996;44(4):450–5. https://doi.org/10.1016/s0016- 5107(96)70098- 6.
36. Dasari BV, Tan CJ, Gurusamy KS, Martin DJ, Kirk G, McKie L, Diamond T, Taylor
MA.Surgical versus endoscopic treatment of bile duct stones. Cochrane Database Syst Rev.
2013;2013(12):CD003327. https://doi.org/10.1002/14651858.CD003327.pub4.
37. Christensen M, Matzen P, Schulze S, Rosenberg J.Complications of ERCP: a prospective study.
Gastrointest Endosc. 2004;60(5):721–31. https://doi.org/10.1016/s0016- 5107(04)02169- 8.
38. Wang B, Liu Z, Lü Y, Zhao S, Chen L. A meta-analysis of preoperative versus intraoperative endoscopic sphincterotomy in patients with gallbladder and suspected common bile duct
stones. Zhonghua Yi Xue Za Zhi. 2015;95(18):1425–9.
39. De U. Evolution of cholecystectomy: a tribute to Carl August Langenbuch. Indian J Surg.
2004;66:97–100.
40. Schmidt M, Søndenaa K, Vetrhus M, Berhane T, Eide GE.Long-term follow-up of a randomized controlled trial of observation versus surgery for acute cholecystitis: non-operative management is an option in some patients. Scand J Gastroenterol. 2011;46(10):1257–62. https://
doi.org/10.3109/00365521.2011.598548.
41. Charlson ME, Carrozzino D, Guidi J, Patierno C. Charlson comorbidity index: a critical review of clinimetric properties. Psychother Psychosom. 2022;91(1):8–35. https://doi.
org/10.1159/000521288.
42. Sundararajan V, Henderson T, Perry C, Muggivan A, Quan H, Ghali WA.New ICD-10 version of the Charlson comorbidity index predicted in-hospital mortality. J Clin Epidemiol.
2004;57(12):1288–94. https://doi.org/10.1016/j.jclinepi.2004.03.012.
43. https://www.asahq.org/standards- and- guidelines/asa- physical- status- classication- system
44. Catena F, Ansaloni L, Bianchi E, Di Saverio S, Coccolini F, Vallicelli C, Lazzareschi D, Sartelli
M, Amaduzzi A, Amaduzz A, Pinna AD.The ACTIVE (acute cholecystitis trial invasive versus endoscopic) study: multicenter randomized, double-blind, controlled trial of laparoscopic
versus open surgery for acute cholecystitis. Hepatogastroenterology. 2013;60(127):1552–6.
45. Johansson M, Thune A, Nelvin L, Stiernstam M, Westman B, Lundell L.Randomized clinical
trial of open versus laparoscopic cholecystectomy in the treatment of acute cholecystitis. Br J
Surg. 2005;92(1):44–9. https://doi.org/10.1002/bjs.4836.
46. Hussain A.Difcult laparoscopic cholecystectomy: current evidence and strategies of management. Surg Laparosc Endosc Percutan Tech. 2011;21(4):211–7. https://doi.org/10.1097/
SLE.0b013e318220f1b1.
47. Coccolini F, Catena F, Pisano M, Gheza F, Fagiuoli S, Di Saverio S, Leandro G, Montori
G, Ceresoli M, Corbella D, Sartelli M, Sugrue M, Ansaloni L.Open versus laparoscopic
cholecystectomy in acute cholecystitis. Systematic review and meta-analysis. Int J Surg.
2015;18:196–204. https://doi.org/10.1016/j.ijsu.2015.04.083.
48. Pisano M, Ceresoli M, Cimbanassi S, Gurusamy K, Coccolini F, Borzellino G, Costa G,
Allievi N, Amato B, Boerma D, Calcagno P, Campanati L, Campanile FC, Casati A, Chiara O,
Crucitti A, di Saverio S, Filauro M, Gabrielli F, Guttadauro A, Kluger Y, Magnone S, Merli C,
Poiasina E, Puzziello A, Sartelli M, Catena F, Ansaloni L. 2017 WSES and SICG guidelines on
acute calculous cholecystitis in elderly population. World J Emerg Surg. 2019;14:10. https://
doi.org/10.1186/s13017- 019- 0224- 7.
49. Gutt CN, Encke J, Köninger J, Harnoss JC, Weigand K, Kipfmüller K, Schunter O, Götze T,
Golling MT, Menges M, Klar E, Feilhauer K, Zoller WG, Ridwelski K, Ackmann S, Baron A,
Schön MR, Seitz HK, Daniel D, Stremmel W, Büchler MW.Acute cholecystitis: early versus
delayed cholecystectomy, a multicenter randomized trial (ACDC study, NCT00447304). Ann
Surg. 2013;258(3):385–93. https://doi.org/10.1097/SLA.0b013e3182a1599b.
50. Pucher PH, Brunt LM, Davies N, Linsk A, Munshi A, Rodriguez HA, Fingerhut A, Fanelli RD,
Asbun H, Aggarwal R, SAGES Safe Cholecystectomy Task Force. Outcome trends and safety
measures after 30 years of laparoscopic cholecystectomy: a systematic review and pooled
data analysis. Surg Endosc. 2018;32(5):2175–83. https://doi.org/10.1007/s00464- 017- 5974- 2.
67

68
https://t.me/medicina_free
51. van Dijk AH, de Reuver PR, Tasma TN, van Dieren S, Hugh TJ, Boermeester MA.Systematic
review of antibiotic treatment for acute calculous cholecystitis. Br J Surg. 2016;103(7):797–811.
https://doi.org/10.1002/bjs.10146.
52. Loozen CS, van Santvoort HC, van Duijvendijk P, Besselink MG, Gouma DJ, Nieuwenhuijzen
GA, Kelder JC, Donkervoort SC, van Geloven AA, Kruyt PM, Roos D, Kortram K,
Kornmann VN, Pronk A, van der Peet DL, Crolla RM, van Ramshorst B, Bollen TL,
Boerma D. Laparoscopic cholecystectomy versus percutaneous catheter drainage for acute
cholecystitis in high risk patients (CHOCOLATE): multicentre randomised clinical trial.
BMJ. 2018;363:k3965. https://doi.org/10.1136/bmj.k3965.
53. Teoh AYB, Kitano M, Itoi T, Pérez-Miranda M, Ogura T, Chan SM, Serna-Higuera C,
Omoto S, Torres-Yuste R, Tsuichiya T, Wong KT, Leung CH, Chiu PWY, Ng EKW, Lau
JYW. Endosonography-guided gallbladder drainage versus percutaneous cholecystostomy in
very high-risk surgical patients with acute cholecystitis: an international randomised multicentre controlled superiority trial (DRAC 1). Gut. 2020;69(6):1085–91. https://doi.org/10.1136/
gutjnl- 2019- 319996.
54. Sartelli M, Catena F, Ansaloni L, Coccolini F, Corbella D, Moore EE, Malangoni M, Velmahos
G, Coimbra R, Koike K, Leppaniemi A, Bif W, Balogh Z, Bendinelli C, Gupta S, Kluger Y,
Agresta F, Di Saverio S, Tugnoli G, Jovine E, Ordonez CA, Whelan JF, Fraga GP, Gomes CA,
Pereira GA, Yuan KC, Bala M, Peev MP, Ben-Ishay O, Cui Y, Marwah S, Zachariah S, Wani
I, Rangarajan M, Sakakushev B, Kong V, Ahmed A, Abbas A, Gonsaga RA, Guercioni G,
Vettoretto N, Poiasina E, Díaz-Nieto R, Massalou D, Skrovina M, Gerych I, Augustin G, Kenig
J, Khokha V, Tranà C, Kok KY, Mere AC, Lee JG, Hong SK, Lohse HA, Ghnnam W, Verni
A, Lohsiriwat V, Siribumrungwong B, El Zalabany T, Tavares A, Baiocchi G, Das K, Jarry J,
Zida M, Sato N, Murata K, Shoko T, Irahara T, Hamedelneel AO, Naidoo N, Adesunkanmi
AR, Kobe Y, Ishii W, Oka K, Izawa Y, Hamid H, Khan I, Attri A, Sharma R, Sanjuan J, Badiel
M, Barnabé R.Complicated intra-abdominal infections worldwide: the denitive data of the
CIAOW study. World J Emerg Surg. 2014;9:37. https://doi.org/10.1186/1749- 7922- 9- 37.
S. Frassini et al.

Acute Colonic Diverticulitis
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DarioTartaglia, FedericoCoccolini, AlessioMazzoni,
ValerioGenovese, CamillaCremonini, EnricoCicuttin,
andMassimoChiarugi
1 Percutaneous Drainage
Diverticulitis may occur with a pericolic or distant abscess in the pelvis: pericolic in
1B and pelvic distant from the colon in grade 2 according to Wasvary’s modied
Hinchey’s classication [1]. The size of the abscess is the mainstream for proper
treatment. The intravenous administration of large-spectrum antibiotics could be
associated with the need to place percutaneous drainage, mainly in case of larger
abscesses. The exact size cutoff in which one should apply for percutaneous drainage has been a topic of debate for a long time, and nowadays, we still do not have a
denitive answer. Since the early 2000s, the cutoff value diameter for amenability
of the percutaneous abscess has progressively been reduced from 5 to 3cm [2, 3].
Abscesses under 3cm can be treated with IV, broad-spectrum antibiotics that cover
Gram-negative and anaerobic bacteria. This medical approach could lead to a resolution in more than 80% of cases.
On the other hand, larger abscesses might be evacuated with US- or CT-guided
percutaneous drainage (Figs.1 and 2). The choice to use US or CT as guidance
depends on the abscess location: for instance, supercial ones could be easily
chased by ultrasound. Therefore, CT scan represents the preferred method of evacuation [4]. However, this procedure is not free of risks: it has been shown that it is
D. Tartaglia (*)
Emergency Surgery Unit and Trauma Center, University Hospital of Pisa, Pisa, Italy
Emergency Surgery Unit and Trauma Center, Cisanello Hospital, University of Pisa,
Pisa, Italy
e-mail: dario.tartaglia@unipi.it
F. Coccolini · A. Mazzoni · V. Genovese · C. Cremonini · E. Cicuttin · M. Chiarugi
Emergency Surgery Unit and Trauma Center, University Hospital of Pisa, Pisa, Italy
e-mail: federico.coccolini@unipi.it; massimo.chiarugi@unipi.it
© The Author(s), under exclusive license to Springer Nature Switzerland AG 2023
F. Coccolini et al. (eds.), Mini-invasive Approach in Acute Care Surgery,
Hot Topics in Acute Care Surgery and Trauma,
https://doi.org/10.1007/978-3-031-39001-2_7
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Fig. 1 A CT scan with
contrast showing a large
pelvic collections along the
left paracolic gutter
Fig. 2 The pericolic
abscess treated with a
percutaneous “pig-tail”
drain
D. Tartaglia et al.
related to 3% of complications, mainly constituted by visceral injuries rather than
vascular ones.
Furthermore, it has been established that 57% of patients develop a stulous
communication to the colon, subsequently to drain placement. Moreover, these
patients had longer procedure times and larger abscess sizes. Conversely, female sex

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71
ab
Fig. 3 A 10cm pelvic abscess with an air level inside. (a, b) The abscess treated with a percutane-
ous drain. For the presence of enteric material from the drain and the worsening of the patient’s
clinical condition, a sigmoid resection was performed
and higher BMI may represent protective factors against the development of intestinal stulous communications [5].
The more the diameter increases, the higher is the risk of failure to control source
infection in the percutaneous draining [6]. The presence of signicant comorbidities, ASA (American Society of Anesthesiologists) score 4, elevated values of
Charlson Comorbidity Index, and immunosuppression state represent other factors
of risk of PCD failure [7, 8].
The recurrence rate after percutaneous drainage is about 25% [3]. Also, in these
cases, abscesses larger than 5cm have an increased risk of recurrence [9].
Although the best treatment for larger abscesses is still not dened, we can
assume that PCD must be almost always considered as the rst choice in nonperitonitis patients. In fact, acute surgery is related to a high rate of postoperative
complications, permanent stoma, and short-term mortality (up to 12%).
Surgery is mandatory in case of PCD failure, a patient’s clinical worsening, and
hemodynamical instability. A cutoff size of 5cm is predictive for the need for emergency surgery within 30days from the presentation (Fig.3) [10].
In their retrospective study on 105 patients undergoing CT-guided abscess drainage, Raman etal. showed that 57% of patients presented a post-procedural stula.
An 85% required surgical intervention, 83% of them with minimally invasive surgery. Interestingly, they found that men’s gender, lower BMIs, current tobacco
users, higher ASA class, and larger abscess on initial presentation were related to
stulous communication [11].
In conclusion, PCD could be a valuable tool in patients with diverticular abscess
without signs of peritonitis. However, it might not be resolutive in larger abscesses
and clinically compromised cases. Therefore, if the procedure fails, surgery must be
advocated.

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D. Tartaglia et al.
2 Laparoscopic Peritoneal Lavage
It has been widely described that laparoscopic peritoneal lavage has represented a
potentially viable option for patients with purulent diverticulitis. By itself, the procedure presents quite simple steps: placement of three ports, complete evacuation of
the purulent collection, accurate visualization of the descending colon and sigma,
execution of a hydropneumatic or methylene bleu test to rule out eventual visceral
discontinuity, and nally putting some drains in situ. In the 1990s, several retrospective studies showed very promising results that started a “hot” debate about the
efcacy of this procedure in the treatment of peritonitis due to acute perforated
diverticulitis. The discussion is heavily still going on [12–14]. These rst studies
reported very low rates of morbidity (0–4%), mortality (<2%), reoperation (2–7%),
and diverticulitis recurrence (0–5%) during 12- to 48-month follow-up. As a result,
the conclusions were very optimistic: the laparoscopic peritoneal lavage was considered a safe and effective alternative to traditional surgical resection allowing to
avoid elective colon resection in most cases [14]. However, during the second
decade of this century, the scientic community raised a need to clarify the real
benet deriving from laparoscopic peritoneal lavage. Thus, three randomized studies from northern Europe were conducted: LADIEs, SCANDIV, and DILALA trials
[15–17]. The rst one in chronological order, the LADIEs with the LOLA arm, was
prematurely interrupted because of an exceedingly high rate of complications in
laparoscopic lavage [15]. The Scandinavian SCANDIV study reported a higher
complication rate, short-term morbidity, and mortality in laparoscopic lavage, even
though long-term follow-up showed no differences in severe complications [18].
Furthermore, the authors identied that recurrence of diverticulitis after laparoscopic lavage was more common (21% vs. 4%), often leading to sigmoid resection
(30%). The authors agreed that a higher resection rate must be weighed against the
lower stoma prevalence in laparoscopic lavage, encouraging to take “shared” decisions, considering both short-term and long-term consequences. On the other hand,
the DILALA trial reported better results for laparoscopic lavage, identifying shorter
operative time, and hospital stay with no differences in terms of morbidity and mortality [17]. At the 2-year follow-up, the laparoscopic lavage was associated with a
45% reduced risk of undergoing operations than Hartmann’s. In the study by Kohl
etal., the authors considered the laparoscopic lavage a better option for perforated
diverticulitis with purulent peritonitis than open resection and colostomy [19].
However, an important criticism merging from the literature versus these encouraging results was represented by the very limited number of patients per arm enrolled
in the DILALA: 39in the lavage group and 36in Hartmann’s procedure [20]. A
multicentric prospective international study was conducted in 2018: the LLO Study,
which included 231 patients affected by purulent peritonitis caused by acute diverticulitis. Among 212 patients who underwent lavage, the postoperative morbidity
rate was 33%, the mortality rate was 2%, and the readmission rate was 10%. Overall,
the technique was successful in 172 patients (81%): there were no signs of sepsis
and no need for further surgery during the hospital stay and 60days after discharge.

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Nevertheless, 46 episodes (26.7%) of acute diverticulitis were recorded during the
11-month follow-up [21].
Several meta-analyses have been performed with different results [22–33]. The
difference in the results was due to the variability of the considered studies, the type
of the analysis, and the focused outcomes analyzed. Some reviews concluded that
laparoscopic lavage does not represent a safe approach for purulent diverticular
peritonitis because of the high rate of reoperations (up to 30%), higher rate of postoperative intra-abdominal abscesses, and the relevant risk of not recognizing a carcinoma in almost 10% of patients [24, 25, 27, 29, 34, 35]. Other reviews gave more
prudent conclusions, reporting that laparoscopic lavage can be comparable to sigmoid resection in terms of mortality. At the same time, it is related to a signicantly
higher rate of reoperations and intra-abdominal abscesses [23, 26, 33]. Conversely,
other meta-analyses supported the use of laparoscopic lavage, stating that the procedure may be an effective and safe option for the treatment of patients with purulent diverticular peritonitis; in fact, the lavage is associated with a lower risk of
reoperations within the rst 12months after index surgery, lower hospital costs, and
comparable morbidity and mortality than resections [22, 30, 31].
An important point in favor of the laparoscopic lavage is the reduced risk of
colostomy at 1- and 2-year follow-up, when the procedure is effective [19, 36].
Schultz etal. described a signicantly lower stoma rate in the lavage group than
resection (14% vs. 42%) at the 1-year follow-up of the SCANDIV study. However,
the quality of life did not differ between groups, as laparoscopic lavage was associated with deeper surgical-site infections (32% vs.13%) and more unplanned reoperations (27% vs. 10%) [36]. Kohl etal., instead, reported better results in their
2-year results of the randomized clinical trial DILALA.The lavage group had a
45% reduced risk of undergoing one or more operations, fewer operation rates than
Hartmann’s group, and a more reduced stoma rate (7% vs. 23%). In addition, the
authors did not nd signicant differences in the mean number of readmissions and
mortality [19].
Very few studies focused on comparing laparoscopic peritoneal lavage versus
laparoscopic sigmoidectomy in complicated acute diverticulitis. A multicentric
study by Catry etal. enrolled 40 patients with purulent diverticular peritonitis and
compared 15 laparoscopic peritoneal lavages versus 25 sigmoidectomies. In the latter group, only four were treated with a laparoscopic approach. 40% of laparoscopic
lavage patients required reoperation for peritonitis (26.6%), intra-abdominal bleeding (13.3%), intra-abdominal abscess (7%), ileus (7%), and wound infections (7%).
For these reasons, the authors concluded that laparoscopic lavage is associated with
a high risk of failure in daily practice. Consequently, laparoscopic sigmoidectomy
should be the primary option for treating purulent diverticular peritonitis [37]. In a
multicenter study led by our Institution, 66 patients with a pelvic abscess not amenable to conservative management or with purulent diverticular peritonitis were
enrolled: 28 (42%) underwent laparoscopic lavage and 38 (58%) underwent laparoscopic sigmoidectomy. The authors found that the failure to achieve source control
and the need to return to the operating room were more frequent in laparoscopic
lavage (29.6% vs. 2.6% and 18.5% vs. 0, respectively). Furthermore, diverticular

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recurrence was signicantly higher in the lavage group (27.3% vs. 0%). As a result,
the authors concluded that laparoscopic lavage for perforated diverticulitis carries a
high risk of failure in daily practice [38].
Laparoscopic lavage is cheaper than colonic resection. In the Swedish DILALA
trial, clinical effectiveness and resource use were derived from the 43 patients randomized in the laparoscopic lavage group and the remaining 40 treated with
Hartmann’s procedure. In the laparoscopic lavage group, the authors found a mean
discount per patient of almost €9000 at the short-term analysis (rst 12months) and
almost €19,794 at the long-term analysis. So far, they concluded that the signicant
cost reduction, the safeness, and the efcacy of laparoscopic lavage make the procedure eligible for a routinary use for the treatment of complicated diverticular
peritonitis [39]. Quite similar results were obtained by Vennixet al. in their economic evaluation of the randomized LOLA (LaparOscopicLAvage) arm of the
Ladies trial. They demonstrated that total medical costs for lavage were lower
(almost €3500) at 12months, although surgical interventions may increase costs.
The same was for the long-term results, where lavage was associated with a reduced
cost of almost € 6377. It must be said that stoma reversal operations can also get
costs increased in the Hartmann’s procedure group. However, considering the failure in carrying on the LOLA arm in the LADIES study due to an unacceptable too
much high rate of postoperative complications, the authors were more prudent in
exalting the lavage.
The positions about laparoscopic lavage from the major international surgical
societies’ guidelines are very different. The recent guidelines from the World
Society of Emergency Surgery state: We suggest performing laparoscopic perito-
neal lavage and drainage only in very selected patients with generalized peritonitis.
It is not considered as the rst line treatment in patients with peritonitis from acute
colonic diverticulitis, notwithstanding weak recommendation [40]. The European
Association for Endoscopic Surgery (EAES) and Society of American
Gastrointestinal and Endoscopic Surgeons (SAGES) guidelines on acute diverticulitis management recommend that: Lavage should be considered in selected Hinchey
III patients by surgeons with appropriate expertise and the ability to closely watch
for and manage complications; the lower stoma rate should be weighed against the
higher risk of complications and re-intervention. Also, in this case, recommenda-
tions were weak [41]. Recently, the European Society of Coloproctology guidelines
stated more straightforwardly: Laparoscopic lavage is feasible in selected patients
with Hinchey III peritonitis. Alternatively, resection is recommended [42]. The 2020
American Society of Colon and Rectal Surgeons Guidelines for the management of
left-sided colonic diverticulitis recommends colectomy for both feculent and purulent peritonitis, stating that In patients with purulent peritonitis, colectomy is pre-
ferred over laparoscopic lavage. Laparoscopic lavage is associated with higher
rates of secondary intervention in comparison with colectomy [43]. Interestingly,
the Japanese guidelines for diverticular disease management did neither consider
the laparoscopic lavage [44].
Briey, we could conclude that laparoscopic peritoneal lavage is feasible in
patients with purulent diverticulitis. Still, it should be reserved only in very selected
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