Skip to main content

WSES Guidelines for the management of acute left sided colonic diverticulitis in the emergency setting

Abstract

Acute left sided colonic diverticulitis is one of the most common clinical conditions encountered by surgeons in acute setting. A World Society of Emergency Surgery (WSES) Consensus Conference on acute diverticulitis was held during the 3rd World Congress of the WSES in Jerusalem, Israel, on July 7th, 2015. During this consensus conference the guidelines for the management of acute left sided colonic diverticulitis in the emergency setting were presented and discussed. This document represents the executive summary of the final guidelines approved by the consensus conference.

Background

Acute left sided colonic diverticulosis is common in Western countries, however its prevalence is increasing throughout the world, probably because of changes in lifestyle [1]. Although left sided colonic diverticulosis is more common amongst elderly patients, a dramatic rise of its incidence has been seen in the younger age groups in recent years [2]. Data from Western populations suggest that up to one fifth of patients with acute diverticulitis are under the age of 50 years of age [35]. Recent evidence suggests that lifetime risk of developing acute left sided colonic diverticulitis (ALCD) is only about 4 % among patients with diverticulosis [6].

ALCD is a common problem encountered by surgeons in the acute setting. It encompasses a variety of conditions, ranging from localized diverticular inflammation to perforation and fecal peritonitis. Daily decisions in the diagnosis and treatment of acute diverticulitis generally depend on clinicians’ personal preferences rather than evidence-based medicine. There is generally a lack of well conducted randomized clinical trials in ALCD and a large amount of evidence in the literature is low quality and conflicting.

Methods

A World Society of Emergency Surgery (WSES) working group published in 2015 a proposal for a new CT based classification for ALCD [7]. This has been extended and developed into guidelines for the management of acute diverticulitis in an emergency setting. A literature search, using the PubMed database, was performed without restriction of time or type of manuscript. The search was limited to English language publications. The final grade of recommendation was performed by using the Grades of Recommendation, Assessment, Development, and Evaluation (GRADE) system (Table 1) [8, 9].

Table 1 Grading of recommendations from Guyatt and colleagues [8, 9]

A World Society of Emergency Surgery (WSES) Consensus Conference on acute diverticulitis was held during the 3rd World Congress of the WSES in Jerusalem, Israel, on July 7th, 2015. During this consensus conference the guidelines were presented and debated. This document represents the executive summary of the final guidelines approved by the consensus conference.

Results

Classification systems

ALCD ranges in severity from uncomplicated inflammatory diverticulitis to complicated diverticulitis (abscess formation or perforation). For the past three decades, the Hinchey classification has been the most commonly used classification for complicated ALCD in international literature [10].

Based on the surgical findings of abscesses and peritonitis, Hinchey et al. classified the severity of acute diverticulitis into four grades:

  • Stage 1 Pericolic abscess

  • Stage 2 Pelvic, intra-abdominal, or retroperitoneal abscess

  • Stage 3 Generalized purulent peritonitis

  • Stage 4 Generalized fecal peritonitis

The management of ALCD has recently changed dramatically in recent years, due to better radiological imaging and availability of non-surgical treatment options. Computer tomography (CT) imaging has become a primary diagnostic tool in the diagnosis and staging of patients with acute diverticulitis and more detailed information provided by CT scans led to several modifications of the Hinchey classification [4, 1117]. For example, in 1989 Neff et al. presented a new classification based on CT findings. It consisted of five stages, ranging from radiological diagnosis of uncomplicated AD (Stage 0) to pneumoperitoneum with abundant free liquid (Stage 4) [11]:

  • Stage 0 Uncomplicated diverticulitis; Diverticula, thickening of the wall, increased density of the pericolic fat

  • Stage 1 Locally complicated with local abscess

  • Stage 2 Complicated with pelvic abscess;

  • Stage 3 Complicated with distant abscess

  • Stage 4 Complicated with other distant complications

In 1997, Sher et al. [12] introduced a modification of Hinchey classification. This classification divided abscesses into pericolic abscesses (stage I), distant abscesses amendable for percutaneous drainage (stage IIa), and complex abscesses associated with a possible fistula (stage IIb). This classification implied the use of new treatment strategies, such as CT-guided percutaneous drainage of abscesses.

In 2002 Ambrosetti et al. [13] classified diverticulitis into severe or moderate disease. In this classification, the CT scan determined the grade of severity guiding the physician in the treatment of acute complications. Moderate diverticulitis was defined by wall thickening of ≥ 5 mm and signs of inflammation of pericolic fat. Severe diverticulitis was defined by wall thickening accompanied by abscess formation, extraluminal air or extraluminal contrast leak:

  • Moderate diverticulitis Localized sigmoid wall thickening

  • Pericolic fat stranding

  • Severe diverticulitisAbscess

  • Extraluminal air

  • Extraluminal contrast

In 2005 Kaiser et al. [14] modified Hinchey classification according to specific CT findings:

  • Stage 0 mild clinical diverticulitis

  • Stage 1a confined pericolic inflammation,

  • Stage 1b confined pericolic abscess

  • Stage 2 pelvic or distant intra-abdominal abscess

  • Stage 3 generalized purulent peritonitis

  • Stage 4 fecal peritonitis at presentation.

In 2013 Mora Lopez et al. proposed [15] a modification of the previous Neff classification dividing Neff stage 1 into stage 1 a (localized pneumoperitoneum in the form of air bubbles) and 1 b abscess (<4 cm):

  • Stage 0 Uncomplicated diverticulitis. Diverticula, thickening of the wall, increased density of the pericolic fat

  • Stage 1 Locally complicated diverticulitis

  • Stage 1a Localized pneumoperitoneum in the form of air bubbles

  • Stage 1b Abscess (<4 cm)

  • Stage 2 Complicated diverticulitis with pelvic abscess. Abscess > 4 cm in pelvis

  • Stage 3 Complicated diverticulitis with distant abscess. Abscess in abdominal cavity (outside pelvis)

  • Stage 4 Complicated diverticulitis with other distant complications. Abundant pneumoperitoneum and/or intra-abdominal free liquid

Recently Sallinen at al. [16] published an interesting retrospective study of patients treated for diverticulitis, setting the stage for the treatment of acute diverticulitis based on clinical, radiologic and physiologic parameters. They included 5 stages:

  • Stage 1 Uncomplicated diverticulitis

  • Stage 2 Complicated diverticulitis with small abscess (<6 cm)

  • Stage 3 Complicated diverticulitis with large abscess (≥6 cm) or distant intraperitoneal or retroperitoneal air

  • Stage 4 Generalized peritonitis without organ dysfunction

  • Stage 5 Generalized peritonitis with organ dysfunction

Finally a proposal for a CT guided classification of left colon acute diverticulitis was published in 2015 by the WSES acute diverticulitis working group [7]. It is a simple classification system of acute diverticulitis based on CT scan findings. It may guide clinicians in the management of acute diverticulitis and may be universally accepted for day to day practice. The WSES classification divides acute diverticulitis into 2 groups: uncomplicated and complicated.

In the event of uncomplicated acute diverticulitis, the infection does not extend to the peritoneum. In the event of complicated acute diverticulitis, the infectious process proceeds beyond the colon. Complicated acute diverticulitis is divided into 4 stages, based on the extension of the infectious process:

Uncomplicated

  • Stage 0 Diverticula, thickening of the colonic wall or increased density of the pericolic fat

  • Complicated

  • Stage 1a Pericolic air bubbles or little pericolic fluid without abscess (within 5 cm from inflamed bowel segment)

  • Stage 1b Abscess ≤ 4 cm

  • Stage 2a Abscess > 4 cm

  • Stage 2b Distant air (>5 cm from inflamed bowel segment)

  • Stage 3 Diffuse fluid without distant free air (no hole in colon)

  • Stage 4 Diffuse fluid with distant free air (persistent hole in colon)

Diagnosis

  1. 1)

    An accurate assessment of the patients using clinical signs, laboratory inflammation markers and radiological findings is recommended to identify the best treatment for each patient with ALCD (Recommendation 1 C).

  2. 2)

    The clinical diagnosis of ALCD alone is not sufficiently accurate for patients with suspected diverticulitis (Recommendation 1 C).

  3. 3)

    Pain in the lower left abdomen on physical examination and C-reactive protein (CRP) 50 mg/l or more suggests a diagnosis of ALCD (Recommendation 1 C).

Clinical findings of patients having ALCD include acute pain or tenderness in the left lower quadrant which may be associated with increased inflammatory markers including C-reactive protein (CRP) and white blood cell count (WBC). Clinical diagnosis of ALCD usually lacks accuracy. In a prospective analysis [17] conducted on 802 consecutive patients that presented with abdominal pain to the emergency department, positive and negative predictive values of clinical diagnosis were 0.65 and 0.98 respectively. Additional cross-sectional imaging had a positive and negative predictive value of more 0.95 and 0.99 respectively. Additional radiology examinations improved the diagnostic accuracy in 37 % of the patients, but changed the management in only 7 %. Ultrasound and CT had superior diagnostic accuracy, however these examinations rarely changed the initial management proposal.

Using logistic regression analysis, Lameris et al. [18] in 2010, developed a clinical decision rule for diagnosis of diverticulitis, based on 3 criteria: direct tenderness in the left lower quadrant, 2) CRP > 50 mg/l and 3) absence of vomiting. Of 126 clinically suspected patients enrolled in this prospective study, 30 patients had all 3 features (24 %), of whom 29 had a final diagnosis of acute diverticulitis (97 %; 95 % CI: 83 %-99 %). Of the 96 patients without all 3 features, 45 (47 %) did not have diverticulitis. In a quarter of patients with suspected diverticulitis, the diagnosis could be made clinically based on a combination of the three criteria.

Andeweg et al. in 2011 [19], using retrospective data from 287 patients, developed a clinical scoring system for the diagnosis of ALCD that had a diagnostic accuracy of 86 %. It was based on the independent predictors of ALCD and included patients’ age, one or more previous episodes, localization of symptoms in the lower left abdomen, aggravation of pain on movement, the absence of vomiting, localization of abdominal tenderness in the lower left abdomen, and C-reactive protein 50 or more.

CRP has been identified as a useful biomarker of inflammation and it may be useful in the prediction of the clinical severity of acute diverticulitis as demonstrated by several recent studies [2022]. To investigate the value of C-reactive protein (CRP) and of other laboratory parameters of the patients in the prediction of the clinical severity of acute diverticulitis a retrospective study was published in 2014 [20]. A CRP cutoff value of 170 mg/L significantly discriminated severe from mild diverticulitis (87.5 % sensitivity, 91.1 % specificity, area under the curve 0.942, P < 0.00001). The author concluded that CRP is a useful tool in the prediction of the clinical severity of acute diverticulitis. A mild episode is very likely in patients with CRP less than 170 mg/L. Those with higher CRP values have a greater probability of undergoing surgery or radiological drainage.

In another study, the diagnostic value of serological infection markers and body temperature in discriminating complicated from uncomplicated diverticulitis was assessed [21]. A total of 426 patients were included in this study of which 364 (85 %) presented with uncomplicated and 62 (15 %) with complicated diverticulitis. Only CRP was of sufficient diagnostic value (area under the curve 0.715). The median CRP in patients with complicated diverticulitis was significantly higher than in patients with uncomplicated disease (224 mg/l, range 99–284 vs 87 mg/l, range 48–151). Patients with a CRP of 25 mg/l had a 15 % chance of having complicated diverticulitis. This increased from 23 % at a CRP value of 100 mg/l to 47 % for 250 mg/l or higher. The optimal threshold was reached at 175 mg/l with a positive predictive value of 36 %, negative predictive value of 92 %, sensitivity of 61 % and a specificity of 82 %.

Recently Makela et al. [22] published a study which compared the CRP values of 350 patients who presented first time with symptoms of acute diverticulitis with the CT findings and clinical parameters by means of both univariate and multivariate analyses. CRP cut-off value of 149.5 mg/l significantly discriminated acute uncomplicated diverticulitis from complicated diverticulitis (specificity 65 %, sensitivity 85 %, area under the curve 0.811, p = 0.0001). In multivariate analysis, a CRP value over 150 mg/l and old age were independent risk factors for acute complicated diverticulitis. The mean CRP value was significantly higher in the patients who died (mean CRP of 207) than in those who survived (mean CRP of 139). In addition, a CRP value over 150 mg/l and free abdominal fluid in CT were independent variables predicting postoperative mortality. The study confirmed that CRP is useful for the predicting the severity of acute diverticulitis on admission. The authors concluded that patients with a CRP value higher than 150 mg/l have an increased risk of complicated diverticulitis and should always undergo a CT examination.

  1. 4)

    Computed tomography (CT) scan of the abdomen and pelvis is indicated for all patients with suspected ALCD. It has high sensitivity and specificity and can assess the severity of diverticulitis guiding clinicians in planning treatment (Recommendation 1 C).

  2. 5)

    Ultrasound (US) may be a useful alternative in the initial evaluation of patients with suspected ALCD. It has wide availability and easy accessibility. It may have satisfactory sensitivity and specificity when performed by an expert operator. A step-up approach with CT performed after an inconclusive or negative US may be a safe approach for patients suspected of acute diverticulitis (Recommendation 1 C).

Radiological imaging techniques that are used for diagnosing acute diverticulitis in the emergency setting are computed tomography (CT) and ultrasound (US). CT imaging is becoming by now the gold standard in the diagnosis and staging of patients with ALCD. CT imaging with intravenous contrast has excellent sensitivity and specificity [2325]. CT findings in patients with ALCD may include diverticulosis with associated colon wall thickening, fat stranding, phlegmon, extraluminal gas, abscess formation or intra-abdominal diffuse fluid. CT imaging can go beyond accurate diagnosis of ALCD; CT criteria may be also used to determine the grade of severity and may drive treatment planning of patients [7]. US is a real-time dynamic examination with wide availability and easy accessibility [26] and may be useful in diagnosing and managing critically ill patients who cannot be moved to CT. Its limitations include operator-dependency, poor assessment in obese patients, difficulty in the detection of free air and deeply located abscesses [27].

A systematic review and meta-analysis of studies [28] that reported diagnostic accuracy of the clinical diagnosis and diagnostic modalities in patients with suspected diverticulitis was published in 2014. Summary sensitivity estimates for US were 90 % (95 % CI: 76-98 %) versus 95 % (95 % CI: 91-97 %) for CT (p = 0.86). Summary specificity estimates for US were 90 % (95 % CI: 86-94 %) versus 96 % (95 % CI: 90-100 %) for CT (p = 0.04).

Although CT is the most sensitive imaging investigation for patients with suspected acute diverticulitis, a step-up approach with CT performed after an inconclusive or negative US, has been proposed as safe and alternative approach for patients with suspected acute diverticulitis [28, 29]. Magnetic resonance imaging, which is not constrained by the operator dependency limitation of ultrasound [30, 31], until now is difficult to perform at the emergency department.

Immunocompromised patients

  1. 6)

    Immunosuppression can increase the complication rate in patients with ALCD. Elective sigmoid resection after an episode of ALCD should be recommended in immunocompromised patients (Recommendation 1 C).

Immunocompromised patients, including patients with kidney failure, organ transplant patients and patients using corticosteroids are at increased risk to have complicated diverticulitis requiring emergency surgery [3235]. Immunocompromised patients may fail standard, nonoperative treatment. As such, most of these patients require urgent surgical intervention, and this is associated with a significantly higher mortality rate [36].

A recent study by Biondo et al. [37] analyzed the relationship between the different causes of immunosuppression (IMS) and diverticulitis. Immunocompromised patients were divided in 5 groups according to the causes of IMS: group I, chronic corticosteroid therapy; group II, transplant patients; group III, malignant neoplasm disease; group IV, chronic renal failure; group V, others immunosuppressant treatment. The rate of emergency surgery was high (39.3 %). It was needed more frequently in group I. Overall, postoperative mortality was of 31.6 % and recurrence rate after successful nonoperative management occurred in 30 patients (27.8 %).

Treatment of uncomplicated acute diverticulitis

  1. 7)

    Antimicrobial therapy can be avoided in immunocompetent patients with uncomplicated diverticulitis without systemic manifestations of infection (Recommendation 1 A).

  2. 8)

    If patients need antimicrobial therapy, oral administration may be acceptable (Recommendation 1 B).

The utility of antimicrobial therapy in acute uncomplicated diverticulitis has been a point of controversy in the international medical community. In the last few years several studies demonstrated that antimicrobial treatment was not superior to withholding antibiotic therapy in patients with mild unperforated diverticulitis, in terms of clinical resolution [38].

The current consensus is that uncomplicated diverticulitis may be a self-limiting condition in which local host defenses’ can manage the bacterial inflammation without antibiotics in immunocompetent patients. In this context antibiotics may, therefore, not be necessary in the treatment of uncomplicated disease.

A multi-centre randomized trial involving ten surgical departments in Sweden and one in Iceland recruited 623 patients with computed tomography-verified acute uncomplicated left-sided diverticulitis was published in 2012 by Chabok et al. [39]. Patients were randomized to treatment with (314 patients) or without (309 patients) antibiotics. Antibiotic treatment for acute uncomplicated diverticulitis neither accelerated recovery nor prevented complications or recurrence. It should therefore be reserved for the treatment of complicated diverticulitis.

A recent prospective single-arm study analyzed [40] the safety and efficacy of symptomatic (nonantibiotic) treatment for CT-proven uncomplicated diverticulitis during a 30-day follow-up period. Overall, 161 patients were included in the study, and 153 (95 %) completed the 30-day follow-up. A total of 14 (9 %) patients had pericolic air. Altogether, 140 (87 %) patients were treated as outpatients, and 4 (3 %) of them were admitted to the hospital during the follow-up. None of the patients developed complicated diverticulitis or required surgery, but, 2 days (median) after inclusion, antibiotics were given to 14 (9 %, 6 orally, 8 intravenously) patients.

However the high mortality associated with sepsis, requires clinicians to maintain a high index of clinical suspicion, in the conditions that predispose to sepsis. WSES expert panel suggests antimicrobial therapy covering Gram negative and anaerobes in patients with radiological documented uncomplicated acute diverticulitis associated with systemic manifestations of infection.

An appropriate antimicrobial regimen administered for an adequate duration has minimal impact on the emergence of antimicrobial resistance [41].

If antimicrobial therapy is necessary oral administration of antibiotics may be equally as effective as intravenous administration.

A randomized controlled trial of oral versus intravenous therapy for clinically diagnosed acute uncomplicated diverticulitis was published in 2009 [42]. Oral and intravenous regimens utilizing ciprofloxacin and metronidazole were compared. There were 41 patients in the oral arm and 38 in the IV arm (n = 79). No patients had to be converted to intravenous antibiotics from the oral group. There was a complete resolution of symptoms in both groups.

In immunocompromised patients antibiotics with a broader-spectrum should be used. No studies have examined the value of dietary restriction or bed rest [43].

  1. 9)

    Outpatient management is suggested for patients with uncomplicated acute diverticulitis, with no comorbidities. These patients should be clinically monitored as outpatients and re-evaluated within 7 days to assess for resolution of the inflammatory processes. Earlier revaluation is necessary if the clinical condition deteriorates (Recommendation 1 B).

Patients with uncomplicated diverticulitis symptoms without significant comorbidities, who are able to take fluids orally and manage themselves at home, can be treated as outpatients. They should be re-evaluated within 7 days. However if the clinical condition deteriorates, re-evaluation should be carried out earlier. Patients with significant comorbidities and unable to take fluids orally should be treated in hospital with intravenous fluid.

Etzioni et al. [44] in 2010 published a retrospective analysis, demonstrating that outpatient treatment was effective for the vast majority (94 %) of patients suffering from acute diverticulitis. A systematic review on outpatient management of acute uncomplicated diverticulitis was recently published in 2014 [45]. Jackson et al. concluded that current evidence suggested that a more progressive, ambulatory-based approach to the majority of cases of acute uncomplicated diverticulitis was justified. Rodríguez-Cerrillo et al. [46] have recently shown that elderly patients with co-morbidities can be safely treated at home avoiding hospital admission.

The DIVER trial [47] has recently demonstrated that outpatient treatment may be safe and effective in selected patients with uncomplicated acute diverticulitis and can reduces the costs without negatively influencing the quality of life of these patients. This multicenter, randomized controlled trial included patients older than 18 years with acute uncomplicated diverticulitis. All the patients underwent abdominal CT. The first dose of antibiotic was given intravenously to all patients in the emergency department and then patients were either admitted to hospital or discharged. Among a total of 132 patients, four patients in those admitted to hospital and three patients in those discharged to home management developed treatment failure (there was no differences between the groups (P = 0.62). The overall health care cost per episode was 3 times less in the outpatient treated group, with significant costs savings of €1124.70 per patient. No differences were observed between the groups in terms of quality of life.

Treatment of localized complicated diverticulitis

  1. 10)

    Patients with CT findings of pericolic air or small fluid collection should be managed by antimicrobial therapy. (Recommendation 1 C).

High mortality associated with sepsis, requires maintaining a high index of clinical suspicion for deterioration and more aggressive management. WSES expert panel routinely recommends antimicrobial therapy in patients with pericolic air or small fluid collection. CT findings of pericolic air in the form of air bubbles or little pericolic fluid without abscess and distant air indicates a complicated acute diverticulitis and antimicrobial therapy should always recommended [7].

Treatment of diverticular abscesses

  1. 11)

    Patients with small diverticular abscesses (<4-5 cm) may be treated by antibiotics alone (Recommendation 1 C).

  2. 12)

    Patients with large abscesses (>4–5 cm) can best be treated by percutaneous drainage combined with antibiotic treatment (Recommendation 1 C).

  3. 13)

    Whenever percutaneous drainage of the abscess is not feasible or not available, based on the clinical conditions patients with large abscesses can be initially treated by antibiotic therapy alone. However careful clinical monitoring is mandatory. (Recommendation 1 C).

Approximately 15–20 % of patients admitted with acute diverticulitis have an abscess on CT scan [48]. The size of 3–6 cm has been generally accepted as (all of low level of evidence), to be a reasonable limit between antimicrobial versus percutaneous drainage in the management of diverticular abscesses [4853]. The size of 4–5 cm may be a reasonable limit between antibiotic treatment alone versus percutaneous drainage combined with antibiotic treatment in the management of diverticular abscesses. Based on the clinical conditions also patients with large abscesses can be initially treated by antibiotic therapy alone. However careful clinical monitoring is mandatory. A CT scan should be repeated if the patient fails to show clinical and laboratory improvement.

A retrospective study assessing the effectiveness of antibiotics as sole initial therapy in patients with large diverticular abscess was published in 2015 by Elagili et al. [54]. Thirty-two patients were treated with antibiotics alone because of either technically impossible percutaneous drainage or surgeon preference, while 114 underwent percutaneous drainage. Urgent surgery was required in 8 patients with persistent symptoms during treatment with antibiotics alone (25 %) and in 21 patients (18 %) after initial percutaneous drainage (p = 0.21). Patients treated with antibiotics had a significantly smaller abscess diameter (5.9 vs. 7.1 cm, p = 0.001) and shorter interval from initial treatment to sigmoidectomy (mean 50 vs. 80 days, p = 0.02). The Charlson comorbidity index, initial treatment failure rates, postoperative mortality, overall morbidity, length of hospital stay during treatments, and overall and permanent stoma rates were comparable in the two groups. Postoperative complications following antibiotics alone were significantly less severe than after percutaneous drainage based on the Clavien-Dindo classification (p = 0.04).

In patient displaying an appropriate clinical improvement, drainage catheter can be removed when the output has ceased and the patient has improved clinically. In doubtful cases a fistulogram can be performed with water-soluble contrast via the percutaneous drainage catheter prior to drain removal. If no identifiable cavity remains the catheter should be removed.

  1. 14)

    In patients with diverticular abscesses treated conservatively early colonic evaluation (4–6 weeks) should be planned (Recommendation 1 C).

  2. 15)

    In patients with CT-proven uncomplicated diverticulitis treated conservatively (without other risk factors) early follow-up colonoscopy is not required. Patients aged 50 years or older should participate in colorectal cancer screening programs (Recommendation 1 C).

Colonic localized abscess is an uncommon but possible presentation of colon cancer, and it may mimic complicated diverticular disease [55, 56]. It has been demonstrated that the risk of malignancy after a CT-proven uncomplicated diverticulitis is low and in the absence of other indications, routine colonoscopy may not be necessary. A systematic review investigating the rate of colorectal cancer (CRC) found by colonoscopy after an episode of uncomplicated diverticulitis was published in 2014 [57]. Nine studies met the inclusion criteria and included a total number of 2,490 patients with uncomplicated diverticulitis. Subsequent colonoscopy after an episode of uncomplicated diverticulitis was performed in 1,468 patients (59 %). Seventeen patients were diagnosed with CRC, having a prevalence of 1.16 % (95 % confidence interval 0.72-1.9 % for CRC). Hyperplastic polyps were seen in 156 patients (10.6 %), low-grade adenoma in 90 patients (6.1 %), and advanced adenoma was reported in 32 patients (2.2 %). The results of this review demonstrates that unless colonoscopy is regarded for screening in individuals aged 50 years and older, routine colonoscopy in the absence of other clinical signs of CRC is not required in patients following an episode of acute uncomplicated diverticulitis.

Another systematic review and meta-analysis on the role of routine colonic evaluation after radiologically confirmed acute diverticulitis was published in 2014 [58]. Eleven studies from 7 countries were included in the analysis. Among 1970 patients, cancer was only found in 22 (0.01 %) cases.

The risk of malignancy after a radiologically proven episode of acute uncomplicated diverticulitis was low. Patients with complicated diverticulitis had a significant risk of colorectal cancer at subsequent colonic evaluation.

A retrospective study of 633 patients with acute diverticulitis diagnosed by CT was published in 2014 [59]. Of 663, 97 underwent emergency resection, whereas 536 were treated conservatively, 394 of whom underwent colonoscopy. The findings showed 17 cancers (2.7 %) in patients with an initial diagnosis of acute diverticulitis. As shown by CT, 16 cancer patients (94 %) had abscess, whereas one patient had pericolic extraluminal air but no abscess. Of the patients with abscess, 11.4 % had cancer mimicking acute diverticulitis. No cancer was found in the patients with uncomplicated diverticulitis.

Treatment of diffuse peritonitis

Although most patients hospitalized for acute diverticulitis can be managed by non-operative treatment, up to 25 % may require urgent operative intervention [60]. Patients with diffuse peritonitis are typically critical ill patients and require prompt fluid resuscitation, antibiotic administration, and surgery without delay.

Although the absolute prevalence of perforated diverticulitis complicated by generalized peritonitis is low, it has a significant postoperative mortality, regardless of selected surgical strategy.

A critical issue may be the CT presence of distant free air without diffuse fluids (fluids in 2 or >2 abdominal quadrants) because distant pneumoperitoneum is pathognomonic for sigmoid perforation even in absence of CT findings of diffuse peritoneal fluid.

  1. 16)

    Patients with CT findings of distant air without diffuse fluid may be treated by conservative treatment in selected cases. However, there is a risk of treatment failure and emergency surgery may be required. Careful monitoring is mandatory. A CT scan should be repeated early on the basis of the clinical and laboratory evaluation (Recommendation 1 C).

  2. 17)

    If the conservative treatment fails in patients with distant air without diffuse fluid, surgical resection and anastomosis with or without stoma or Hartmann resection is suggested according to the patient clinical conditions and comorbidities (Recommendation 1 B).

Although CT findings of distant free air (a known predictor of failure of non-operative treatment [25]), Dharmarajan et al. [61] described a high success rate for non-operative management in patients with acute diverticulitis and a pneumoperitoneum, excluding those with hemodynamic instability. Sallinen et al. [62] reported results of non-operative management in patients with CT verified extra-luminal air. The study showed that non operative treatment was feasible therapy only for hemodynamic stable patients with pericolic extraluminal air or with small amount of distant intraperitoneal air in the absence of clinical diffuse peritonitis or fluid in the fossa Douglas. Occurrence of large amount of distant intraperitoneal air or distant retroperitoneal air even in the absence of clinical generalised peritonitis was associated with high failure rate (57 %–60 %) of non-operative management. Moreover nearly 60 % patients with distant intraperitoneal air were primary treated by surgery.

Highly selected group of patients at this stage may be treated by conservative treatment. However it may be associated with failure and a careful clinical and CT monitoring is mandatory [7]. Suggested intervention for patients at this stage should be surgical resection and anastomosis with or without stoma in stable patients without co-morbidities and Hartmann resection in unstable patients or in patients with multiple co-morbidities [7].

  1. 18)

    Laparoscopic peritoneal lavage and drainage should not be considered the treatment of choice in patients with generalized peritonitis. (Recommendation 1 A).

A conservative approach using laparoscopic peritoneal lavage and drainage has been debated in recent years as an alternative to colonic resection [63]. It can potentially avoid a stoma in patients with diffuse peritonitis. It consists of the laparoscopic aspiration of pus followed by abdominal lavage and the placement of abdominal drains, which remain for many days after the procedure.

In 2013 a Dutch retrospective analysis of 38 patients [64] treated by laparoscopic lavage was published highlighting some doubts about this procedure to treat critically ill patients. In seven patients laparoscopic lavage did not control abdominal sepsis, two died of multiple organ failure and five required further surgical interventions (three Hartmann resection, one diverting stoma and one perforation closure). One of these died from aspiration and the remaining four experienced prolonged complicated recovery. Multiple co-morbidities, immunosuppression, a high CRP level and/or a high Mannheim Peritonitis Index were also predictors of a high risk of failure. The authors concluded that patient selection was of utmost importance and identification of an overt sigmoid perforation is of critical importance.

Great debate is still open on this topic, mainly due to the discrepancy and sometime disappointing results of the latest prospective trials such as SCANDIV, Ladies, and DILALA trials [6567]

In 2014 the first results from the randomized controlled trial DILALA were published [65]. Initial diagnostic laparoscopy showing Hinchey III disease was followed by randomization between laparoscopic lavage and colon resection and stoma. Morbidity and mortality after laparoscopic lavage did not differ when compared with the Hartmann procedure. Laparoscopic lavage resulted in shorter operating time, shorter time in the recovery unit, and shorter hospital stay with the avoidance of a stoma. In this trial, laparoscopic lavage as treatment for patients with perforated diverticulitis Hinchey III disease was feasible and safe in the short-term.

In 2015 the results of SCANDV study were published [66]. Among patients with likely perforated diverticulitis and undergoing emergency surgery, the use of laparoscopic lavage vs primary resection did not reduce severe postoperative complications and led to worse outcomes in secondary end points. These findings do not support laparoscopic lavage for treatment of perforated diverticulitis. In the same year, the result of LADIES Study was published. This showed that laparoscopic lavage was not superior to sigmoidectomy for the treatment of purulent perforated diverticulitis [67].

  1. 19)

    Hartmann resection is still advised for managing diffuse peritonitis in critically ill patients and in patients with multiple comorbidities. However in clinically stable patients with no co-morbidities primary resection with anastomosis with or without a diverting stoma may be performed (Recommendation 1 B).

Hartmann resection has been considered the procedure of choice in patients with generalized peritonitis and remains a safe technique for emergency colectomy in diverticular peritonitis, especially in critically ill patients and in patients with multiple co-morbidities. However restoration of bowel continuity after a Hartmann procedure has been associated with significant morbidity [68]. Many patients cannot undergo reversal surgery due to comorbidities; therefore, they remain with a permanent stoma [69].

Common use of Hartmann’s resection in treating diverticular perforation worldwide is confirmed by a recent Australian study analyzing administrative data of patients with acute diverticulitis admitted, from 2009 to 2013, in eight tertiary referral centres with specialist colorectal services [70]. Among 2829 emergency admissions for AD across 4 years in eight hospitals, 724 were for complicated acute diverticulitis. The emergency operative intervention rate was 10.4 %, with one third of the admissions for complicated diverticulitis having an operation. Hartmann's procedure was the most commonly performed emergency operation, accounting for 72 % of resections.

Another population-based retrospective cohort study using administrative discharge data, conducted in Ontario (Canada) was published in 2014 [71]. Among 18,543 patients hospitalized with a first episode of diverticulitis, from 2002 to 2012, 3873 underwent emergency surgery. The use of laparoscopy increased (9 % to 18 %, p <0.001), whereas the use of the Hartmann’s procedure remained unchanged (64 %) and was the most frequently used urgent operative approach in patients with complicated AD.

In recent years, some authors have reported the role of primary resection and anastomosis with or without a diverting stoma, in the treatment of diverticulitis, even in the presence of diffuse peritonitis [72]. The decision regarding the surgical choice in patients with diffuse peritonitis is generally left to the judgment of the surgeon, who takes into account the clinical condition and the comorbidities of the patient. Studies comparing mortality and morbidity of Hartmann’s procedure versus primary anastomosis did not show any significant differences. However, most studies had relevant selection bias as demonstrated by four systematic reviews [7376].

A comparison of primary resection and anastomosis (PRA) with or without defunctioning stoma to Hartmann's procedure (HP) as the optimal operative strategy for patients presenting with Hinchey stage III-IV, was published by Constantinides et al. [76]. A total of 135 PRA, 126 primary anastomoses with defunctioning stoma (PADS), and 6619 Hartmann's procedures (HP) were considered in the study. Morbidity and mortality was 55 % and 30 % for PRA, 40 % and 25 % for PADS, and 35 % and 20 % for HP. Stomas remained permanent in 27 % of HP and in 8 % of PADS. The authors concluded that primary anastomosis with defunctioning stoma may be the optimal strategy for selected patients with diverticular peritonitis and may represent a good compromise between postoperative adverse events, long-term quality of life and risk of permanent stoma.

A small randomized trial of primary anastomosis with ileostomy vs Hartmann’s procedure in patients with diffuse diverticular peritonitis was published by Oberkofler et al. in 2012 [77]. Sixty-two patients with acute left-sided colonic perforation (Hinchey III and IV) from 4 centers were randomized to Hartmann procedure (n = 30) and to primary anastomoses with diverting ileostomy (n = 32). A planned stoma reversal operation was performed after 3 months in both groups. The study reported no difference in initial mortality and morbidity (mortality 13 % vs 9 % and morbidity 67 % vs 75 % in Hartmann procedure vs primary anastomosis), but a reduction in length of stay, lower costs, fewer serious complications and greater stoma reversal rates in the primary anastomosis group.

  1. 20)

    Emergency laparoscopic sigmoidectomy for the treatment of perforated diverticulitis with generalised peritonitis is feasible in selected patients provided they are handled by experienced hands (Recommendation 2 C).

Laparoscopic sigmoidectomy for diverticulitis has initially been confined to the elective setting however in stable patients, laparoscopic sigmoidectomy may be feasible in purulent and fecal diverticular peritonitis in the emergency setting. In 2015 a systematic review on laparoscopic sigmoidectomy for diverticulitis in the emergency setting was published [78].

The review included 4 case series and one cohort study (total of 104 patients) out of 1,706 references. Hartmann's procedure (HP) was performed in 84 patients and primary anastomosis in 20. The mean operating time varied between 115 and 200 min. The conversion rate varied from 0 to 19 %. The mean length of hospital stay ranged between 6 and 16 days. Surgical re-intervention was necessary in 2 patients. In 20 patients operated upon without defunctioning ileostomy, no anastomotic leakage was reported. Three patients died during the postoperative period. Stoma reversal after HP was performed in 60 out of 79 evaluable patients (76 %).

These guidelines are limited by the low quality evidence which showed that emergency laparoscopic sigmoidectomy for the treatment of perforated diverticulitis with generalised peritonitis is feasible. These studies occurred in selected patients and in experienced units and are not generalizable to all centers. High-quality prospective or randomised studies are needed to demonstrate benefits of acute laparoscopic sigmoidectomy compared to open sigmoidectomy for perforated diverticulitis.

  1. 21)

    Damage control surgery strategy may be suggested for clinically unstable patients with diverticular peritonitis (severe sepsis/septic shock) (Recommendation 1 B).

In an unstable patients with diverticular peritonitis ‘damage control surgery’ has become a valuable technique in the last years [79]. Damage control with lavage, limited bowel resection, laparostomy, and scheduled second-look operation represents a feasible strategy in patients with perforated diverticulitis (Hinchey III and IV) to enhance sepsis control and improve rate of anastomosis.

Generalized diverticular peritonitis is a life-threatening condition requiring prompt emergency operation. To improve outcome and reduce the rate of colostomy formation, a new algorithm with damage control operation, lavage, limited closure of perforation, and second look surgery to restore intestinal continuity was developed in recent years [80, 81]. Critically ill patients (patients with severe sepsis and septic shock) present with hypotension and myocardial depression, combined with coagulopathy. These patients, who are hemodynamically unstable, are not optimal candidates for immediate complex operative interventions. After initial surgery, which should be limited to source control e.g. primary closure of the perforation, the patient is taken to the ICU for physiologic optimization. This strategy may delay bowel anastomosis [81] and potentially avoid stoma formation.

In the setting of diverticulitis several reports (with low level of evidence) were published. In 2010 a prospective observational study was published by Kafka-Ritsch et al. [79]. A total of 51 patients (28 female, 55 %) with a median age of 69 (range) 28–87 years, with perforated diverticulitis Hinchey III (n = 40, 78 %) or Hinchey IV (n = 11, 22 %) were prospectively enrolled in the study. Patients were initially managed with limited resection, lavage and temporary abdominal closure followed by second, reconstructive operation 24–48 h later, which are supervised by a colorectal surgeon. Bowel continuity was restored in 38 (84 %) patients, of which four were protected by a loop ileostomy. Five anastomotic leaks (13 %) were encountered requiring loop ileostomy in two patients or Hartmann procedure in remaining three patients. The overall mortality rate was 9.8 % and 35/46 (76 %) of the surviving patients left the hospital with reconstructed colon continuity. Fascial closure was achieved in all patients.

Planning elective surgery

  1. 22)

    Patient-related factors and not number of previous episodes of diverticulitis, should be considered in planning elective sigmoid resection in patients with ALCD treated conservatively (Recommendation 1 C).

  2. 23)

    After a conservatively treated episode of ALCD an elective sigmoid resection should be planned in high-risk patients, such as immunocompromised patients (Recommendation 1 C).

Recurrence of acute diverticulitis is lower than previously thought. It has been frequently reported that about one third of all patients with acute diverticulitis will have a recurrent attack, often within one year [82, 83]. Recurrence after an uncomplicated episode of diverticulitis, however, has recently been shown to be much lower, with one prospective study reporting a recurrence of only 1.7 % over five years of follow up [84, 85].

In 2014, a systematic review of studies reviewing the diagnosis and management of chronic and recurrent diverticulitis (from studies published between January 2000 to March 2013) was published [86]. The 68 studies included were almost exclusively observational and had limited certainty of treatment effect. The authors found that complicated recurrence after recovery from an uncomplicated episode of diverticulitis was rare (<5 %) and that age at onset younger than 50 years and 2 or more recurrences did not increase the risk of complications.

The authors concluded that the indication for elective colectomy following 2 episodes of diverticulitis is no longer accepted. Indication to colectomy should be made based on consideration of the risks of recurrent diverticulitis, the morbidity of surgery, ongoing symptoms, the complexity of disease, and operative risk.

Clear indications for elective sigmoid resections are complaints of stenosis, fistulas, or recurrent diverticular bleeding. Furthermore, an elective sigmoid resection should be justified in high-risk patients such as immunocompromised patients, after a conservatively treated episode of diverticulitis [87].

Antimicrobial therapy

  1. 24)

    The empirically designed antimicrobial regimen depends on the underlying clinical condition of the patient, the pathogens presumed to be involved, and the risk factors indicative of major resistance patterns (Recommendation 1 C).

  2. 25)

    Although discontinuation of antimicrobial treatment should be based on clinical and laboratory criteria, a 4–6 days period of post-operative antimicrobial therapy in complicated ALCD is suggested if source control has been adequate (Recommendation 1 A).

Antimicrobial therapy plays an important role in the management of complicated acute diverticulitis. It is typically empiric antibiotic treatment. The empirically designed antimicrobial regimen depends on the underlying severity of infection, the pathogens presumed to be involved, and the risk factors indicative of major resistance patterns [41]. Several recommendations have been recently published in literature [41, 88] in the setting of intra-abdominal infections. However consideration of local epidemiological data and regional resistance profiles is essential for antibiotic selection.

Considering intestinal microbiota of large bowel acute diverticulitis requires antimicrobial coverage for gram-positive and gram-negative bacteria, as well as for anaerobes. Most of the complicated acute diverticulitis is community acquired infection. The main resistance threat in intra-abdominal infections is posed by Extended-Spectrum Beta-Lactamase (ESBL)-producing Enterobacteriaceae, which are becoming increasingly common in community-acquired infections worldwide [41]. The most significant risk factors for ESBL producing infection include prior exposure to antibiotics and comorbidities requiring concurrent antibiotic therapy [41]. Anti-ESBL-producer coverage should be warranted for patients with these risk factors. Although discontinuation of antimicrobial treatment should be based on clinical and laboratory criteria such as fever and markers of inflammation, a period of 4–6 days for adult patients is generally sufficient to treat in patients with acute diverticulitis who have been treated with proper source control and prompt surgical intervention [41, 88].

The recent prospective trial by Sawyer et al. demonstrated that in patients with complicated intra-abdominal infections undergoing an adequate source-control procedure, the outcomes after approximately 4 days fixed-duration antibiotic therapy were similar to those after a longer course of antibiotics that extended until after the resolution of physiological abnormalities [89]. Patients who have signs of sepsis beyond 5 to 7 days of antibiotic treatment warrant aggressive diagnostic investigation to determine if an ongoing uncontrolled source of infection exists.

Conclusions

In appendix 1 WSES recommendations for the management of ALCD are illustrated.

Abbreviations

ALCD, acute left sided colonic diverticulitis; CT, computed tomography; US, ultrasound

References

  1. Weizman AV, Nguyen GC. Diverticular disease: epidemiology and management. Can J Gastroenterol. 2011;25:385–9.

    Article  PubMed  PubMed Central  Google Scholar 

  2. Schoetz DJ. Diverticular disease of the colon: a century-old problem. Dis Colon Rectum. 1999;42:703–9.

    Article  PubMed  Google Scholar 

  3. Collins D, Winter DC. Modern concepts in diverticular disease. J Clin Gastroenterol. 2015;49:358–69.

    Article  PubMed  Google Scholar 

  4. Warner E, Crighton EJ, Moineddin R, Mamdani M, Upshur R. Fourteen-year study of hospital admissions for diverticular disease in Ontario. Can J Gastroenterol. 2007;21:97–9.

    Article  PubMed  PubMed Central  Google Scholar 

  5. Jamal Talabani A, Lydersen S, Endreseth BH, Edna TH. Major increase in admission- and incidence rates of acute colonic diverticulitis. Int J Colorectal Dis. 2014;29:937–45.

    Article  PubMed  PubMed Central  Google Scholar 

  6. Shahedi K, Fuller G, Bolus R, Cohen E, Vu M, Shah R, et al. Long-term risk of acute diverticulitis among patients with incidental diverticulosis found during colonoscopy. Clin Gastroenterol Hepatol. 2013;11:1609–13.

    Article  PubMed  Google Scholar 

  7. Sartelli M, Moore FA, Ansaloni L, Di Saverio S, Coccolini F, Griffiths EA, et al. A proposal for a CT driven classification of left colon acute diverticulitis. World J Emerg Surg. 2015;10:3.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Guyatt G, Gutterman D, Baumann MH, Addrizzo-Harris D, Hylek EM, Phillips B, et al. Grading strength of recommendations and quality of evidence in clinical guidelines: Report from an American College of Chest Physicians task force. Chest. 2006;129:174–81.

    Article  PubMed  Google Scholar 

  9. Brozek JL, Akl EA, Jaeschke R, Lang DM, Bossuyt P, Glasziou P, et al. Grading quality of evidence and strength of recommendations in clinical practice guidelines: Part 2 of 3. The GRADE approach to grading quality of evidence about diagnostic tests and strategies. Allergy. 2009;64:1109–16.

    Article  CAS  PubMed  Google Scholar 

  10. Hinchey EJ, Schaal PH, Richards MB. Treatment of perforated diverticular disease of the colon. Adv Surg. 1978;12:85–109.

    CAS  PubMed  Google Scholar 

  11. Neff CC. vanSonnenberg E. CT of diverticulitis. Diagnosis and treatment. Radiol Clin North Am. 1989;27:743–52.

    CAS  PubMed  Google Scholar 

  12. Sher ME, Agachan F, Bortul M, Nogueras JJ, Weiss EG, Wexner SD. Laparoscopic surgery for diverticulitis. Surg Endosc. 1997;11:264–7.

    Article  CAS  PubMed  Google Scholar 

  13. Ambrosetti P, Becker C, Terrier F. Colonic diverticulitis: impact of imaging on surgical management - a prospective study of 542 patients. Eur Radiol. 2002;12:1145–9.

    Article  CAS  PubMed  Google Scholar 

  14. Kaiser AM, Jiang JK, Lake JP, Ault G, Artinyan A, Gonzalez-Ruiz C, et al. The management of complicated diverticulitis and the role of computed tomography. Am J Gastroenterol. 2005;100:910–7.

    Article  PubMed  Google Scholar 

  15. Mora Lopez L, Serra Pla S, Serra-Aracil X, Ballesteros E, Navarro S. Application of a modified Neff classification to patients with uncomplicated diverticulitis. Colorectal Dis. 2013;15:1442–7.

    Article  CAS  PubMed  Google Scholar 

  16. Sallinen VJ, Leppäniemi AK, Mentula PJ. Staging of acute diverticulitis based on clinical, radiologic, and physiologic parameters. J Trauma Acute Care Surg. 2015;78:543–51.

    Article  PubMed  Google Scholar 

  17. Toorenvliet BR1. Colonic diverticulitis: a prospective analysis of diagnostic accuracy and clinical decision-making. Colorectal Dis. 2010;12:179–86.

    Article  CAS  PubMed  Google Scholar 

  18. Laméris W, van Randen A, van Gulik TM, Busch OR, Winkelhagen J, Bossuyt PM, et al. A clinical decision rule to establish the diagnosis of acute diverticulitis at the emergency department. Dis Colon Rectum. 2010;53:896–904.

    Article  PubMed  Google Scholar 

  19. Andeweg CS, Knobben L, Hendriks JC, Bleichrodt RP, van Goor H. How to diagnose acute left-sided colonic diverticulitis: proposal for a clinical scoring system. Ann Surg. 2011;253:940–6.

    Article  PubMed  Google Scholar 

  20. Kechagias A, Rautio T, Kechagias G, Mäkelä J. The role of C-reactive protein in the prediction of the clinical severity of acute diverticulitis. Am Surg. 2014;80:391–5.

    PubMed  Google Scholar 

  21. Van de Wall BJ, Draaisma WA, van der Kaaij RT, Consten EC, Wiezer MJ, Broeders IA. The value of inflammation markers and body temperature in acute diverticulitis. Colorectal Dis. 2013;15:621–6.

    Article  PubMed  Google Scholar 

  22. Mäkelä JT, Klintrup K, Takala H, Rautio T. The role of C-reactive protein in prediction of the severity of acute diverticulitis in an emergency unit. Scand J Gastroenterol. 2015;50:536–41.

    Article  PubMed  Google Scholar 

  23. Laméris W, van Randen A, Bipat S, Bossuyt PM, Boermeester MA, Stoker J. Graded compression ultrasonography and computed tomography in acute colonic diverticulitis: meta- analysis of test accuracy. Eur Radiol. 2008;18:2498–511.

    Article  PubMed  Google Scholar 

  24. Liljegren G, Chabok A, Wickbom M, Smedh K, Nilsson K. Acute colonic diverticulitis: a systematic review of diagnostic accuracy. Colorectal Dis. 2007;9:480–8.

    Article  CAS  PubMed  Google Scholar 

  25. Ambrosetti P, Jenny A, Becker C, Terrier TF, Morel P. Acute left colonic diverticulitis–compared performance of computed tomography and water-soluble contrast enema: prospective evaluation of 420 patients. Dis Colon Rectum. 2000;43:1363–7.

    Article  CAS  PubMed  Google Scholar 

  26. Mazzei MA, Cioffi Squitieri N, Guerrini S, Stabile Ianora AA, Cagini L, Macarini L, et al. Sigmoid diverticulitis: US findings. Crit Ultrasound J. 2013;5:5.

    Article  Google Scholar 

  27. Puylaert JB. Ultrasound of colon diverticulitis. Dig Dis. 2012;30:56–9.

    Article  PubMed  Google Scholar 

  28. Andeweg CS, Wegdam JA, Groenewoud J, van der Wilt GJ, van Goor H, Bleichrodt RP. Toward an evidence-based step-up approach in diagnosing diverticulitis. Scand J Gastroenterol. 2014;49:775–84.

    Article  PubMed  Google Scholar 

  29. Laméris W, van Randen A, van Es HW, van Heesewijk JP, van Ramshorst B, Bouma WH, et al. OPTIMA study group: Imaging strategies for detection of urgent conditions in patients with acute abdominal pain: diagnostic accuracy study. BMJ. 2009;338:b2431.

    Article  PubMed  PubMed Central  Google Scholar 

  30. Heverhagen JT, Sitter H, Zielke A, Klose KJ. Prospective evaluation of the value of magnetic resonance imaging in suspected acute sigmoid diverticulitis. Dis Colon Rectum. 2008;51:1810–5.

    Article  PubMed  Google Scholar 

  31. Halpenny DF, McNeil G, Snow A, Geoghegan T, Torreggiani WC. Prospective evaluation of the value of magnetic resonance imaging in suspected acute sigmoid diverticulitis. Dis Colon Rectum. 2009;52:1030–1.

    Article  PubMed  Google Scholar 

  32. Hwang SS, Cannom RR, Abbas MA, Etzioni D. Diverticulitis in transplant patients and patients on chronic corticosteroid therapy: a systematic review. Dis Colon Rectum. 2010;53:1699–707.

    Article  PubMed  Google Scholar 

  33. Dalla Valle R, Capocasale E, Mazzoni MP, Busi N, Benozzi L, Sivelli R, et al. Acute diverticulitis with colon perforation in renal transplantation. Transplant Proc. 2005;37:2507–10.

    Article  CAS  PubMed  Google Scholar 

  34. Qasabian RA, Meagher AP, Lee R, Dore GJ, Keogh A. Severe diverticulitis after heart, lung, and heart-lung transplantation. J Heart Lung Transplant. 2004;23:845–9.

    Article  PubMed  Google Scholar 

  35. Lederman ED, Conti DJ, Lempert N, Singh TP, Lee EC. Complicated diverticulitis following renal transplantation. Dis Colon Rectum. 1998;41:613–8.

    Article  CAS  PubMed  Google Scholar 

  36. Bordeianou L, Hodin R. Controversies in the surgical management of sigmoid diverticulitis. J Gastrointest Surg. 2007;11:542–8.

    Article  PubMed  PubMed Central  Google Scholar 

  37. Biondo S, Trenti L, Elvira J, Golda T, Kreisler E. Outcomes of colonic diverticulitis according to the reason of immunosuppression. Am J Surg. 2016. doi: 10.1016/j.amjsurg.2016.01.038

  38. Shabanzadeh DM, Wille-Jørgensen P. Antibiotics for uncomplicated diverticulitis. Cochrane Database Syst Rev. 2012;11:CD009092.

    PubMed  Google Scholar 

  39. Chabok A, Påhlman 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.

    Article  CAS  PubMed  Google Scholar 

  40. Mali JP, Mentula PJ, Leppäniemi AK, Sallinen VJ. Symptomatic Treatment for Uncomplicated Acute Diverticulitis: A Prospective Cohort Study. Dis Colon Rectum. 2016;59(6):529–34.

    Article  PubMed  Google Scholar 

  41. Sartelli M, Viale P, Catena F, Ansaloni L, Moore E, Malangoni M, et al. 2013 WSES guidelines for management of intra-abdominal infections. World J Emerg Surg. 2013;8:3.

    Article  PubMed  PubMed Central  Google Scholar 

  42. Ridgway PF, Latif A, Shabbir J, Ofriokuma F, Hurley MJ, Evoy D, et al. Randomized controlled trial of oral vs intravenous therapy for the clinically diagnosed acute uncomplicated diverticulitis. Colorectal Dis. 2009;11:941–6.

    Article  CAS  PubMed  Google Scholar 

  43. Fozard JB, Armitage NC, Schofield JB, Jones OM. Association of Coloproctology of Great Britain and Ireland. ACPGBI position statement on elective resection for diverticulitis. Colorectal Dis. 2011;13:1–11.

    Article  PubMed  Google Scholar 

  44. Etzioni DA, Chiu VY, Cannom RR, Burchette RJ, Haigh PI, Abbas MA. Outpatient treatment of acute diverticulitis: rates and predictors of failure. Dis Colon Rectum. 2010;53:861–5.

    Article  PubMed  Google Scholar 

  45. Jackson JD, Hammond T. Systematic review: outpatient management of acute uncomplicated diverticulitis. Int J Colorectal Dis. 2014;29:775–81.

    Article  CAS  PubMed  Google Scholar 

  46. Rodrìguez-Cerrillo M, Poza-Montoro A, Fernandez-Diaz E, Matesanz-David M, Inurrieta RA. Treatment of elderly patients with uncomplicated diverticulitis, even with comorbidity, at home. Eur J Intern Med. 2013;24:430–2.

    Article  PubMed  Google Scholar 

  47. Biondo S, Golda T, Kreisler E, Espin E, Vallribera F, Oteiza F, et al. Outpatient versus hospitalization management for uncomplicated diverticulitis: a prospective, multicenter randomized clinical trial (DIVER Trial). Ann Surg. 2014;259:38–44.

    Article  PubMed  Google Scholar 

  48. Andersen JC, Bundgaard L, Elbrønd H, Laurberg S, Walker LR, Støvring J. Danish Surgical Society. Danish national guidelines for treatment of diverticular disease. Dan Med J. 2012;59:C4453.

    PubMed  Google Scholar 

  49. Ambrosetti P, Chautems R, Soravia C, Peiris-Waser N, Terrier F. Long-term outcome of mesocolic and pelvic diverticular abscesses of the left colon: a prospective study of 73 cases. Dis Colon Rectum. 2005;48:787–91.

    Article  PubMed  Google Scholar 

  50. Brandt D, Gervaz P, Durmishi Y, Platon A, Morel P, Poletti PA. Percutaneous CT scan guided drainage versus antibiotherapy alone for Hinchey II diverticulitis: a case–control study. Dis Colon Rectum. 2006;49:1533–8.

    Article  CAS  PubMed  Google Scholar 

  51. Siewert B, Tye G, Kruskal J, Sosna J, Opelka F, Raptopoulos V, Goldberg SN. Impact of CT-guided drainage in the treatment of diverticular abscesses: size matters. AJR Am J Roentgenol. 2006;186:680–6.

    Article  PubMed  Google Scholar 

  52. Singh B, May K, Coltart I, Moore NR, Cunningham C. The long-term results of percutaneous drainage of diverticular abscess. Ann R Coll Surg Engl. 2008;90:297–301.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  53. Kumar RR, Kim JT, Haukoos JS, Macias LH, Dixon MR, Stamos MJ, Konyalian VR. Factors affecting the successful management of intra-abdominal abscesses with antibiotics and the need for percutaneous drainage. Dis Colon Rectum. 2006;49:183–9.

    Article  PubMed  Google Scholar 

  54. Elagili F, Stocchi L, Ozuner G, Kiran RP. Antibiotics alone instead of percutaneous drainage as initial treatment of large diverticular abscess. Tech Coloproctol. 2015;19(2):97–103.

    Article  CAS  PubMed  Google Scholar 

  55. Tsai HL, Hsieh JS, Yu FJ, Wu DC, Chen FM, Huang CJ, et al. Perforated colonic cancer presenting as intra-abdominal abscess. Int J Colorectal Dis. 2007;22:15–9.

    Article  PubMed  Google Scholar 

  56. Yeo ES, Ng KH, Eu KW. Perforated colorectal cancer: an important differential diagnosis in all presumed diverticular abscesses. Ann Acad Med Singapore. 2011;40:375.

    PubMed  Google Scholar 

  57. de Vries HS, Boerma D, Timmer R, van Ramshorst B, Dieleman LA, van Westreenen HL. Routine colonoscopy is not required in uncomplicated diverticulitis: a systematic review. Surg Endosc. 2014;28(7):2039–47.

    Article  PubMed  Google Scholar 

  58. Sharma PV, Eglinton T, Hider P, Frizelle F. Systematic review and meta-analysis of the role of routine colonic evaluation after radiologically confirmed acute diverticulitis. Ann Surg. 2014;259:263–72.

    Article  PubMed  Google Scholar 

  59. Sallinen V, Mentula P, Leppäniemi A. Risk of colon cancer after computed tomography-diagnosed acute diverticulitis: is routine colonoscopy necessary? Surg Endosc. 2014;28:961.

    Article  PubMed  Google Scholar 

  60. Feingold D, Steele SR, Lee S, Kaiser A, Boushey R, Buie WD, Rafferty JF. Practice parameters for the treatment of sigmoid diverticulitis. Dis Colon Rectum. 2014;57:284–94.

    Article  PubMed  Google Scholar 

  61. Dharmarajan S, Hunt SR, Birnbaum EH, Fleshman JW, Mutch MG. The efficacy of nonoperative management of acute complicated diverticulitis. Dis Colon Rectum. 2011;54:663–71.

    Article  PubMed  Google Scholar 

  62. Sallinen VJ, Mentula PJ, Leppäniemi AK. Nonoperative management of perforated diverticulitis with extraluminal air is safe and effective in selected patients. Dis Colon Rectum. 2014;57:875–81.

    Article  PubMed  Google Scholar 

  63. Rossi GL, Mentz R, Bertone S, Ojea Quintana G, Bilbao S, et al. Laparoscopic Peritoneal Lavage for Hinchey III Diverticulitis: is it as effective as it is applicable? Dis Colon Rectum. 2014;57:1384–90.

    Article  PubMed  Google Scholar 

  64. Swank HA, Mulder IM, Hoofwijk AG, Nienhuijs SW, Lange JF, Bemelman WA. Dutch Diverticular disease collaborative study G. Early experience with laparoscopic lavage for perforated diverticulitis. Br J Surg. 2013;100:704–10.

    Article  CAS  PubMed  Google Scholar 

  65. Angenete E, Thornell A, Burcharth J, Pommergaard HC, Skullman S, Bisgaard T, et al. Laparoscopic lavage is feasible and safe for the treatment of perforated diverticulitis with purulent peritonitis: the first results from the randomized controlled trial DILALA. Ann Surg. 2016;263:117–22.

    Article  PubMed  Google Scholar 

  66. Schultz JK, Yaqub S, Wallon C, Blecic L, Forsmo HM, Folkesson J, et al. Laparoscopic Lavage vs Primary Resection for Acute Perforated Diverticulitis: The SCANDIV Randomized Clinical Trial. JAMA. 2015;314:1364–75.

    Article  CAS  PubMed  Google Scholar 

  67. Vennix S, Musters GD, Mulder IM, Swank HA, Consten EC, Belgers EH, et al. Laparoscopic peritoneal lavage or sigmoidectomy for perforated diverticulitis with purulent peritonitis: a multicentre, parallel-group, randomised, open-label trial. Lancet. 2015;386(10000):1269–77.

    Article  PubMed  Google Scholar 

  68. McCafferty MH, Roth L, Jorden J. Current management of diverticulitis. Am Surg. 2008;74:1041–9.

    PubMed  Google Scholar 

  69. Fleming FJ, Gillen P. Reversal of Hartmann's procedure following acute diverticulitis: is timing everything? Int J Colorectal Dis. 2009;24:1219–25.

    Article  PubMed  Google Scholar 

  70. Hong MK, Tomlin AM, Hayes IP, Skandarajah AR. Operative intervention rates for acute diverticulitis: a multicentre state-wide study. ANZ J Surg. 2015;85:734–8.

    Article  PubMed  Google Scholar 

  71. Li D, Baxter NN, McLeod RS, Moineddin R, Wilton AS, Nathens AB. Evolving practice patterns in the management of acute colonic diverticulitis: a population-based analysis. Dis Colon Rectum. 2014;57:1397–405.

    Article  PubMed  Google Scholar 

  72. Chandra V, Nelson H, Larson DR, Harrington JR. Impact of primary resection on the outcome of patients with perforated diverticulitis. Arch Surg. 2004;139:1221–4.

    Article  PubMed  Google Scholar 

  73. Salem L, Flum DR. Primary anastomosis or Hartmann's procedure for patients with diverticular peritonitis? A systematic review. Dis Colon Rectum. 2004;47:1953–64.

    Article  PubMed  Google Scholar 

  74. Abbas S. Resection and primary anastomosis in acute complicated diverticulitis, a systematic review of the literature. Int J Colorectal Dis. 2007;22:351–7.

    Article  PubMed  Google Scholar 

  75. Cirocchi R, Trastulli S, Desiderio J, Listorti C, Boselli C, Parisi A, et al. Treatment of Hinchey stage III-IV diverticulitis: a systematic review and meta-analysis. Int J Colorectal Dis. 2013;28:447–57.

    Article  PubMed  Google Scholar 

  76. Constantinides VA, Heriot A, Remzi F, Darzi A, Senapati A, Fazio VW, Tekkis PP. Operative strategies for diverticular peritonitis: a decision analysis between primary resection and anastomosis versus Hartmann’s procedures. Ann Surg. 2007;245:94–103.

    Article  PubMed  PubMed Central  Google Scholar 

  77. Oberkofler CE, Rickenbacher A, Raptis DA, Lehmann K, Villiger P, Buchli C, et al. A multicenter randomized clinical trial of primary anastomosis or Hartmann’s procedure for perforated left colonic diverticulitis with purulent or fecal peritonitis. Ann Surg. 2012;256:819–26.

    Article  PubMed  Google Scholar 

  78. Vennix S, Boersema GS, Buskens CJ, Menon AG, Tanis PJ, Lange JF, Bemelman WA. Emergency Laparoscopic Sigmoidectomy for Perforated Diverticulitis with Generalised Peritonitis: A Systematic Review. Dig Surg. 2016;33:1–7.

    Article  PubMed  Google Scholar 

  79. Kafka-Ritsch R, Birkfellner F, Perathoner A, Raab H, Nehoda H, Pratschke J, Zitt M. Damage control surgery with abdominal vacuum and delayed bowel reconstruction in patients with perforated diverticulitis Hinchey III/IV. J Gastrointest Surg. 2012;16:1915–22.

    Article  PubMed  Google Scholar 

  80. Perathoner A, Klaus A, Mühlmann G, Oberwalder M, Margreiter R, Kafka-Ritsch R. Damage control with abdominal vacuum therapy (VAC) to manage perforated diverticulitis with advanced generalized peritonitis--a proof of concept. Int J Colorectal Dis. 2010;25:767–74.

    Article  PubMed  Google Scholar 

  81. Ordóñez CA, Sánchez AI, Pineda JA, Badiel M, Mesa R, Cardona U, et al. Deferred primary anastomosis versus diversion in patients with severe secondary peritonitis managed with staged laparotomies. World J Surg. 2010;34:169–76.

    Article  PubMed  PubMed Central  Google Scholar 

  82. Rafferty J, Shellito P, Hyman NH, Buie WD. Standards committee of the american society of colon and rectal surgeons. Practice parameters for sigmoid diverticulitis. Dis Colon Rectum. 2006;49:939–44.

    Article  PubMed  Google Scholar 

  83. Hall JF, Roberts PL, Ricciardi R, Read T, Scheirey C, Wald C, et al. Long-term follow-up after an initial episode of diverticulitis: what are the predictors of recurrence? Dis Colon Rectum. 2011;54:283–8.

    Article  PubMed  Google Scholar 

  84. Humes DJ, West J. Role of acute diverticulitis in the development of complicated colonic diverticular disease and 1-year mortality after diagnosis in the UK: population-based cohort. Gut. 2012;61:95–100.

    Article  PubMed  Google Scholar 

  85. Salem TA, Molloy RG, O’Dwyer PJ. Prospective, five-year follow up study of patients with symptomatic uncomplicated diverticular disease. Dis Colon Rectum. 2007;50:1–5.

    Article  Google Scholar 

  86. Regenbogen SE, Hardiman KM, Hendren S, Morris AM. Surgery for diverticulitis in the 21st Century: a systematic review. JAMA Surg. 2014;149:292–303.

    Article  PubMed  Google Scholar 

  87. Klarenbeek BR, Samuels M, van der Wal MA, van der Peet DL, Meijerink WJ, Cuesta MA. Indications for elective sigmoid resection in diverticular disease. Ann Surg. 2010;251:670–4.

    Article  PubMed  Google Scholar 

  88. Solomkin JS, Mazuski JE, Bradley JS, Rodvold KA, Goldstein EJ, Baron EJ, et al. Diagnosis and management of complicated intra-abdominal infection in adults and children: guidelines by the surgical infection society and the infectious diseases society of America. Surg Infect (Larchmt). 2010;11:79–109.

    Article  Google Scholar 

  89. Sawyer RG, Claridge JA, Nathens AB, Rotstein OD, Duane TM, Evans HL, et al. Trial of short-course antimicrobial therapy for intraabdominal infection. N Engl J Med. 2015;372:1996–2005.

    Article  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

Not applicable.

Funding

No funding sources to disclose.

Availability of data and materials

Not applicable.

Authors’ contributions

MS wrote the first draft of the manuscript. All authors reviewed and approved the manuscript.

Competing interest

The authors declare that they have no competing interests.

Consent for publication

Not applicable.

Ethics approval and consent to participate

Not applicable.

Disclosure statement

The authors have nothing to disclose.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Massimo Sartelli.

Appendix 1

Appendix 1

  1. 1)

    An accurate assessment of the patients using clinical signs, laboratory inflammation markers and radiological findings is recommended to identify the best treatment for each patient with ALCD (Recommendation 1 C).

  2. 2)

    The clinical diagnosis of ALCD alone is not sufficiently accurate for patients with suspected diverticulitis (Recommendation 1 C).

  3. 3)

    Pain in the lower left abdomen on physical examination and C-reactive protein (CRP) 50 mg/l or more suggests a diagnosis of ALCD (Recommendation 1 C).

  4. 4)

    Computed tomography (CT) scan of the abdomen and pelvis is indicated for all patients with suspected ALCD. It has high sensitivity and specificity and can assess the severity of diverticulitis guiding clinicians in planning treatment (Recommendation 1 C).

  5. 5)

    Ultrasound (US) may be a useful alternative in the initial evaluation of patients with suspected ALCD. It has wide availability and easy accessibility. It may have satisfactory sensitivity and specificity when performed by an expert operator. A step-up approach with CT performed after an inconclusive or negative US may be a safe approach for patients suspected of acute diverticulitis (Recommendation 1 C).

  6. 6)

    Immunosuppression can increase the complication rate in patients with ALCD. Elective sigmoid resection after an episode of ALCD should be recommended in immunocompromised patients (Recommendation 1 C).

  7. 7)

    Antimicrobial therapy can be avoided in immunocompetent patients with uncomplicated diverticulitis without systemic manifestations of infection (Recommendation 1 A).

  8. 8)

    If patients need antimicrobial therapy, oral administration may be acceptable (Recommendation 1 B).

  9. 9)

    Outpatient management is suggested for patients with uncomplicated acute diverticulitis, with no comorbidities. These patients should be clinically monitored as outpatients and re-evaluated within 7 days to assess for resolution of the inflammatory processes. Earlier revaluation is necessary if the clinical condition deteriorates (Recommendation 1 B).

  10. 10)

    Patients with CT findings of pericolic air or small fluid collection should be managed by antimicrobial therapy. (Recommendation 1 C).

  11. 11)

    Patients with small diverticular abscesses (<4-5 cm) may be treated by antibiotics alone (Recommendation 1 C).

  12. 12)

    Patients with large abscesses (>4–5 cm) can best be treated by percutaneous drainage combined with antibiotic treatment (Recommendation 1 C).

  13. 13)

    Whenever percutaneous drainage of the abscess is not feasible or not available, based on the clinical conditions patients with large abscesses can be initially treated by antibiotic therapy alone. However careful clinical monitoring is mandatory. (Recommendation 1 C).

  14. 14)

    In patients with diverticular abscesses treated conservatively early colonic evaluation (4–6 weeks) should be planned (Recommendation 1 C).

  15. 15)

    In patients with CT-proven uncomplicated diverticulitis treated conservatively (without other risk factors) early follow-up colonoscopy is not required. Patients aged 50 years or older should participate in colorectal cancer screening programs (Recommendation 1 C).

  16. 16)

    Patients with CT findings of distant air without diffuse fluid may be treated by conservative treatment in selected cases. However, there is a risk of treatment failure and emergency surgery may be required. Careful monitoring is mandatory. A CT scan should be repeated early on the basis of the clinical and laboratory evaluation (Recommendation 1 C).

  17. 17)

    If the conservative treatment fails in patients with distant air without diffuse fluid, surgical resection and anastomosis with or without stoma or Hartmann resection is suggested according to the patient clinical conditions and comorbidities (Recommendation 1 B).

  18. 18)

    Laparoscopic peritoneal lavage and drainage should not be considered the treatment of choice in patients with generalized peritonitis. (Recommendation 1 A).

  19. 19)

    Hartmann resection is still advised for managing diffuse peritonitis in critically ill patients and in patients with multiple comorbidities. However in clinically stable patients with no co-morbidities primary resection with anastomosis with or without a diverting stoma may be performed (Recommendation 1 B).

  20. 20)

    Emergency laparoscopic sigmoidectomy for the treatment of perforated diverticulitis with generalised peritonitis is feasible in selected patients provided they are handled by experienced hands (Recommendation 2 C).

  21. 21)

    Damage control surgery strategy may be suggested for clinically unstable patients with diverticular peritonitis (severe sepsis/septic shock) (Recommendation 1 B).

  22. 22)

    Patient-related factors and not number of previous episodes of diverticulitis, should be considered in planning elective sigmoid resection in patients with ALCD treated conservatively (Recommendation 1 C).

  23. 23)

    After a conservatively treated episode of ALCD an elective sigmoid resection should be planned in high-risk patients, such as immunocompromised patients (Recommendation 1 C).

  24. 24)

    The empirically designed antimicrobial regimen depends on the underlying clinical condition of the patient, the pathogens presumed to be involved, and the risk factors indicative of major resistance patterns (Recommendation 1 C).

  25. 25)

    Although discontinuation of antimicrobial treatment should be based on clinical and laboratory criteria, a 4–6 days period of post-operative antimicrobial therapy in complicated ALCD is suggested if source control has been adequate (Recommendation 1 A).

Rights and permissions

Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sartelli, M., Catena, F., Ansaloni, L. et al. WSES Guidelines for the management of acute left sided colonic diverticulitis in the emergency setting. World J Emerg Surg 11, 37 (2016). https://doi.org/10.1186/s13017-016-0095-0

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13017-016-0095-0

Keywords