Ann Coloproctol Search

CLOSE


Chaouch, Kellil, Jeddi, Saidani, Chebbi, and Zouari: How to Prevent Anastomotic Leak in Colorectal Surgery? A Systematic Review

Abstract

Anastomosis leakage (AL) after colorectal surgery is an embarrassing problem. It is associated with poor consequence. This review aims to summarize published evidence on prevention of AL after colorectal surgery and provide recommendations according to the Oxford Centre for Evidence-Based Medicine. We conducted bibliographic research on January 15, 2020, of PubMed, Cochrane Library, Embase, Scopus, and Google Scholar. We retained meta-analysis, reviews, and randomized clinical trials. We concluded that mechanical bowel preparation did not reduce AL. It seems that oral antibiotic or oral antibiotic with mechanical bowel preparation could reduce the risk of AL. The surgical approach did not affect the AL rate. The low ligation of the inferior mesenteric artery could reduce the AL rate. The mechanical anastomosis is superior to handsewn anastomosis only in case of right colectomies, with similar results in rectal surgery between the 2 anastomosis techniques. In the case of right colectomies, this anastomosis could be performed intracorporeally or extracorporeally with similar outcomes. The air leak test did not reduce AL. There is no interest of external drainage in colonic surgery but drains reduced the rate of AL and rate of reoperation after low anterior resection. The transanal tube reduced the rate of AL.

INTRODUCTION

Acute peritonitis following colorectal surgery represents a serious complication with a high mortality incidence, between 6% and 22% [1, 2]. It is essentially secondary to anastomotic leak (AL) in 19% of cases [3]. Despite the effort in AL comprehension and prevention, its incidence remains stable. The septic complications and prolonged hospitalization induced could lead to a longer hospital stay, delayed adjuvant chemotherapy, or no chemotherapy at all. This could alter oncological outcomes such as cancer recurrence and disease-free survival. However, leakage rates differ from report to report. Such a difference is related to the heterogeneity in how surgeons define anastomotic dehiscence [4, 5]. Several studies have identified risk factors for this complication despite the lack of consensual definition. The identification of these risk factors, before surgery, constitutes an important step in management, allowing to act on modifiable factors and to adapt the surgical technique. Earlier diagnosis and management could reduce systemic complications but is hindered by current diagnostic methods that are nonspecific and often uninformative. This complication should be suspected in case of any postoperative abnormalities. The management is multidisciplinary and could be present some issues. For that, the best treatment remains prevention of AL.
This review aimed to evaluate the different means of prevention of AL in colorectal surgery, in light of the current literature.

METHODS

This systematic review was conducted according to PRISMA guidelines [6]. We conducted bibliographic research on January 15, 2020, in the following sources: The National Library of Medicine through PubMed, Cochrane Library, Embase, Scopus, and Google Scholar. The keywords used were “anastomotic leakage,” “rectal surgery,” “colic surgery,” “prevention,” “anastomosis,” “complications,” “meta-analysis,” “review,” and “randomized clinical trial.” As concern the inclusion criteria, we retained only meta-analysis, systematic reviews, and randomized clinical trials (RCTs) reporting different modalities of preoperative and intraoperative prevention of AL following colorectal surgery. We performed a restriction of articles published in the English language and including only humans. References of identified articles were searched for additional relevant articles. We excluded from this systematic review controlled clinical trials, case series, case reports, and editorial letters. Articles including AL after a noncolorectal surgery were also excluded from this study. The methodology of the studies that respond to the inclusion criteria was evaluated by 2 authors (TK and MAC), in case of discordance, a discussion was made with KZ. Risk of bias of RCTs was assessed using RobotReviewer [7]. We have excluded all the RCTs which were included in the meta-analysis to avoid redundancy. The strength of clinical data and subsequent recommendations for the prevention of AL in colorectal surgery were graded according to the Oxford Centre for Evidence-Based Medicine levels of evidence [8] by 2 authors independently, with discrepancies resolved after joint article review and discussion. Levels of evidence are as follows: level 1A, systematic reviews (with homogeneity of RCTs); level 1B, individual RCTs (with narrow confidence intervals); level 2A, systematic reviews (with homogeneity of cohort studies); and level 2B, individual cohort studies (including low-quality RCTs). Grades of recommendation are as follows: A, consistent level 1 studies; B, consistent level 2 or 3 studies or extrapolations from level 1 studies; C, level 4 studies or extrapolations from level 2 or 3 studies; and D, level 5 evidence or troublingly inconsistent or inconclusive studies of any level.

RESULTS

Literature research

After literature research, applying inclusion and exclusion criteria, we have retained 51 articles (Fig. 1) [3, 9-58] published between 2002 and 2020. These articles were distributed as follows: 44 reviews [3, 9-19, 21-28, 30-35, 40-44, 46-56] including 33 meta-analysis (Table 1) [10, 11, 16-19, 21, 23-28, 30, 31, 33-35, 40, 42-44, 46-52, 54-56] and 7 RCTs (Table 2) [20, 29, 36-39, 45]. Table 3 summarizes included studies’ findings and evidence levels.

Outcomes

Factors related to the patient

The predictive factors related to the patient were divided into 2 categories: nonmodifiable factors and modifiable factors. Several reviews [3, 9-15] were interested in identifying these essential factors: male sex [3, 9-14], ASA physical status classification > II [3, 9, 11, 14], alcohol and tobacco use [3, 12], associated comorbidities [3, 14, 15], obesity [3, 11-13], malnutrition [3, 9], hypoalbumin [9], steroid and nonsteroid anti-inflammatory use [3, 9, 14], neoadjuvant radiotherapy [3, 10], neoadjuvant chemotherapy [11-13], bevacizumab use [9, 12], advanced stage of the tumor [3, 11, 13] the distal localization of rectal tumor [3, 9-11], transfusion [9], and emergent surgery [3, 9].

Colic mechanical preparation and oral antibiotic decontamination

The anastomotic contamination by the microbial digestive flora is considered as a major factor contributing to AL. Many means of colic preparation are routinely used to reduce bacterial translocation. Meanwhile, their contribution to the prevention of AL remains uncertain. The impact of the mechanical bowel preparation before the colorectal surgery has been evaluated by the first meta-analysis published by Slim et al. [16] including 7 RCTs (level 1A) which concluded that the mechanical bowel preparation before colorectal surgery significantly increases the AL rate. This study included only small sample trials of which some are not randomized. More recently, in a second meta-analysis [17] including 7 supplementary other randomized trials (level 1A) with 4,859 patients, the same author concluded that there is no significant difference between the group with mechanical bowel preparation and the group without mechanical bowel preparation concerning AL and intraabdominal abscess. These conclusions are confirmed by a Cochrane systematic review (level 1A) published in 2011 [18]. In 2019, in a meta-analysis including 36 studies of which 23 were randomized (level 2A), Rollins et al. [19] concluded also that mechanical bowel preparation before colorectal surgery does not reduce AL rate.
During the last decade, many studies have underlined the importance of oral antibiotics in the reduction of the AL rate. Until now, there are no randomized trials comparing preparation with oral antibiotics versus surgery without preparation. In 2014, in a trial (level 1B) including 310 patients randomized in 3 groups (antibiotic oral decontamination, probiotic use, and control group), Sadahiro et al. [20] demonstrated that oral antibiotic significantly reduced the AL rate in patients following elective surgery for colic cancer (1%, 12%, and 7.4%, respectively). Recently, Rollins et al. [21] concluded that the mechanical bowel preparation associated with oral antibiotic decontamination significantly reduced the AL rate in comparison with a group who had exclusively a mechanical bowel preparation in a meta-analysis including 40 studies of which 28 were randomized (level 2A) with 69,517 patients. Meanwhile, the comparison between mechanical bowel preparations associated with oral antibiotic decontamination versus oral antibiotic decontamination only does not reveal a difference between the 2 groups in terms of AL.
Based on current literature, sufficient evidence does not exist allowing the comparison between mechanical bowel preparation associated with oral antibiotic decontamination versus no preparation; oral antibiotic decontamination versus no preparation and oral antibiotic preparation versus mechanical bowel preparation.

Factors related to anesthesia

It is commonly admitted that cooperation between surgeons and anesthesiologist improves postoperative outcomes following colorectal surgery. Many intraoperative factors related to anesthesia were suspected to be risk factors of AL. In a systematic review published in 2015, Vasiliu et al. [9] concluded that intraoperative transfusion increases the risk of AL. In 2016, Van Rooijen et al. [22] have confirmed this finding. This author otherwise reported many other factors (multimodal analgesia, optimal intraoperative perfusion, use of vasoactive drogues, and oxygen therapy) that improve early postoperative outcomes, without any influence on the rate of AL.

Surgical approach: conventional versus mini-invasive approach

Since its first description in 1991, the mini-invasive approach has steadily progressed to currently become the gold standard for colectomies in case of benign and malignant diseases.
Two meta-analyses (level 2A) [23, 24] have compared the laparoscopic approach to conventional approach during right hemicolectomies for cancer. These meta-analyses have not demonstrated differences in terms of an AL between both approaches. Another meta-analysis (level 2A) [25] comparing the laparoscopic and the conventional approaches for transverse colectomies have not demonstrated any difference in terms of an AL between both approaches. Otherwise, neither meta-analysis nor RCTs are comparing both approaches for left colectomies in terms of AL. Concerning rectal surgery, the laparoscopic approach would be associated with a higher theoretical risk of AL, essentially in obese patients [57]. This is associated with the difficulty of the section using instruments with limited angulations and a confection of an anastomosis in a narrow space.
A meta-analysis of randomized trials (level 1A) published in 2019 [26] compared the different approaches in anterior resection for rectal cancer. Twenty-nine randomized trials were included. The authors concluded that the approach does not affect the AL rate.

High versus low inferior mesenteric artery ligation

Despite the multifactorial causes, the perfusion disorder and technical defects are considered as major factors of anastomotic dehiscence. The level of vascular ligation could, therefore, affect in some patients the blood flow at the level of the anastomosis and hinder its healing. This problem rises especially for tumors of the sigmoid colon and rectum, where the high ligation of the inferior mesenteric artery can impede vascularization of the proximal end of the anastomosis.
Si et al. [27] compared high versus low inferior mesenteric artery ligation in case of sigmoid or rectal cancer in a meta-analysis published in 2019 including 30 studies (level 2A), which 6 out of them were randomized. The conclusion was in favor of low ligation in terms of preventing anastomotic dehiscence. There was no difference in term of oncological outcomes (total number of lymph nodes retrieved, local recurrence, overall survival at 5 years, and survival without recurrence at 5 years). Since the appearance of the concept of image-guided surgery, several studies have evaluated the interest of fluorescence during colorectal surgery. Indocyanine green represents the most sophisticated technique and would allow an operative assessment of the quality of the vascular supply of the anastomosis. A meta-analysis published in 2018 by Shen et al. [28], including 4 controlled clinical trials (level 2A) with 1,177 patients, concluded that the use of Indocyanine green allows to significantly reduce the rate of AL. However, there was a heterogeneity observed between the different studies. In this report, the fluorescence contributed to the modification of the surgical technique in 4.7% to 16.4% of the cases [58, 59] and allowed to extend the resection margins in 19% of patients [60]. However, these results were not confirmed by a multicenter randomized study (level 1B) published by De Nardi et al. [29] in 2020. This study included 240 patients. The authors concluded fluorescence extended resection margin in 13 patients (11%) but did not significantly reduce the rate of AL.

Anastomosis technique

Hand sewn versus stapled anastomosis

A meta-analysis of RCTs (level 1A) [30] including 1,233 patients and comparing stapled and hand-sewn anastomosis for colorectal surgery concluded that there was no difference in terms of a radiological and clinical AL between the 2 techniques. However, this meta-analysis did not compare each colorectal segments separately which represent a judgment bias related to the difference in vascularization, the difference in the diameter of the intestinal lumen and the difference in the reconstruction technique between ilio-colic, colo-colic, colorectal anastomosis, and after colostomy closure. A meta-analysis published by Cochrane Library [31] including 7 trials (level 1A) compared 441 patients with stapled ilio-colic anastomosis with 684 patients with hand-sewn anastomosis. Although there was no difference reported by each of the studies in terms of an AL between the 2 techniques, the combined analysis was in favor of the mechanical anastomosis. These results were confirmed by a recent meta-analysis (level 2A) published in 2019 by Luglio and Corcione [32] the widespread of a circular stapler in recent years has meant that many patients who would have had amputation may currently benefit from anterior resection. A meta-analysis of randomized trials (level 1A) [33] published in 2002 did not show any difference in terms of AL, but stapled anastomosis shortened operating time and were useful in laparoscopic surgery. That is why most anastomosis is done by mechanical anastomosis nowadays.

Intracorporal versus extracorporal anastomosis

This comparison represents a subject of debate, especially after iliocolectomy. Two meta-analyses (level 2A) published in 2016 and 2017 [34, 35] compared the 2 techniques in terms of AL. The authors did not find a difference in favor of one of the 2 techniques. These results were consistent with 4 randomized trials published later (level 1B) [36-39].

Intraoperative tests to verify the anastomosis

The verification of the tightness of the anastomosis is crucial during the operation. There are 2 ways to isolate anastomosis with risk: air leak test and intraoperative endoscopy. Identifying these at-risk patients would allow for additional preventive measures such a repairing the anastomosis with stitches or making a diverting stoma.
A meta-analysis published by Wu et al. [40] in 2016 (including 20 studies, 2 of which are randomized [level 2A]) evaluated the effectiveness of the colorectal anastomosis air leak test at the end of the intervention. These authors concluded that this procedure did not decrease the risk of an AL but identified patients at high risk of a leak in whom prevention measures are necessary. The use of intraoperative endoscopy allows direct visualization of a defect or bleeding at the level of the anastomosis, iatrogenic lesion of the anastomotic rectal wall, the quality of the vascularization of the anastomosis and the detection of a possible lesion which was not detected in the preoperative assessment [41]. However, this procedure must be conducted by an endoscopic expert [41].

External drainage of the abdominal cavity

The use of intraabdominal drain in colorectal surgery has been widely debated in terms of early detection of complication and in terms of preventing anastomotic dehiscence. The current literature, according to 2 meta-analyses (level 1A and 2A), concluded with a high level of evidence that there is no longer any interest in a drainage after colon surgery [42, 43]. However, the external drainage of the abdominal cavity after anterior resection remains a subject of controversy.
After total mesorectal excision, the space left would promote the development of hematoma and seroma; factors favoring bacterial proliferation. The translocation of bacteria at the site of the anastomosis would cause an AL.
In 2014, Rondelli et al. [44] showed that pelvic drainage reduced the rate of anastomotic dehiscence and the rate reoperation in patients who had anterior resection with extraperitoneal anastomosis in a systematic review and meta-analysis including 3 randomized studies and 2,277 patients (level 2A). These conclusions were confirmed by a second meta-analysis (level 2A) in 2015 [11]. However, a recent randomized trial (level 1B) lead by Denost et al. [45] including 469 patients who had an anterior resection with an extraperitoneal anastomosis showed that there was no significant difference in terms of pelvic sepsis between the group of patients who had external abdominal drainage and the group of patients without drainage. Furthermore, there was no difference in terms of pelvic sepsis between early removal (less than 5 days) and late removal (more than 5 days).

Diverting stoma

Diverting stoma versus no stoma

Since its description by Heald [61], the total mesorectal excision increased the rate of sphincter preservation in the case of lower rectal cancer. However, this procedure presents Achilles heel which is the symptomatic AL.
Based on old literature, some factors related to the general condition of the patient, the low location of the tumor and the pelvic measurements are indications for performing diverting stoma. This procedure would reduce the risk of AL, and in case of occurrence the severity of septic complication related to this leak. This role has been confirmed by several meta-analyses (level 2A) [46-49] of which one (level 1A) published in 2019 [50] including 8 randomized trials and 892 patients. In this meta-analysis, Phan et al. [50] concluded that the diverting stoma significantly reduced the rate of AL and the rate of reoperation after anterior resection for low rectal cancer.
Regarding the choice of the type of ostomy (ileostomy or colostomy) opinions remain controversial. In a meta-analysis published in 2019 by including 10 studies (level 2A) and 1,534 patients, Gavriilidis et al. [51] compared ileostomy to transverse colostomy in colorectal surgery. This study found a higher rate of stoma prolapsed after a colostomy. Following the restoration of digestive continuity, there were more wound infections and incisional hernias in patients who had a colostomy. On the other hand, an ileostomy was correlated with a higher complication rate related to high stoma flow. Regarding the over mobility after the stoma was made or closed there was no superiority of 1 of the 2 procedures; however, the heterogeneity between the different studies included in this meta-analysis was high. Taking into account anterior resection only, a systematic review and meta-analysis (level 2A) [52] compared ileostomy and colostomy in terms of postoperative morbidity. Chudner et al. [52] included 2 randomized trials and 1,063 patients and concluded that the overall morbidity (after making and closing the stoma) was not different between these 2 techniques.

Virtual (ghost) stoma

Based on current literature, the role of diverting stoma in patients at high risk of AL does not need to be demonstrated. However, this procedure exposes patients to local and general complications prompting some authors to propose virtual stoma.
The interest of virtual stoma was recently evaluated by Baloyiannis et al. [53] (level 2A) who concluded that this procedure presents a safe and feasible alternative that can replace the diverting stoma. Meanwhile, it does not reduce the risk of anastomotic dehiscence; the rate of AL and conversion to ostomy was 11.9% and 10.46%, respectively.

Transanal tube

The use of transanastomotic tube has been suggested as a means to reduce the risk of anastomotic fistulas in patients who have had an anterior resection with a low level of anastomosis. On the other hand, this procedure would avoid complications related to diverting stoma.
Wang et al. [54] in a meta-analysis (level 2A) including 909 patients who had an anterior resection showed that the placement of a transanal tube reduces the risk of AL and reoperation related to this complication. Similar results have been reported by another more recent meta-analysis (level 2A) [55] including 1,772 patients, there was no difference reported in terms of anastomotic bleeding and mortality between the 2 groups with and without a transanal tube.
Another meta-analysis (level 2A) published by Chen et al. [56], including patients who had anterior resection with or without diverting stoma, concluded that transanal tube placement significantly reduced the risk of anastomotic dehiscence even in patients with an ostomy.
In conclusion, decompression through transanal tube could be a means of preventing AL in high-risk patients. It could replace the diverting stoma, avoiding complications related to this procedure. However, randomized studies comparing the 2 techniques are necessary.

CONCLUSION

Despite the advances in surgical procedures, the rate of AL following colorectal surgery remains high. Prevention of this complication represents a huge challenge. We have tried to identify with a high level of evidence, mainly coming from reviews and RCTs, the risk factors and measures to reduce this complication and subsequent effects. Several modifiable and nonmodifiable factors have been extensively investigated. There was unanimity in the involvement of some of these factors in the genesis of anastomotic fistulas. However, others are still a subject of controversy. This underlines that the pathogenesis of AL is multifactorial and other potential factors remain unexplored.

Notes

CONFLICT OF INTEREST

No potential conflict of interest relevant to this article was reported.

Fig. 1.
Flow diagram of the included studies.
ac-2020-05-14-2f1.jpg
Table 1.
Characteristics of the included meta-analysis
First author Year No. of studies RCT in the meta-analysis No. of patients Population Intervention Comparison
Pommergaard [10] 2014 11 0 110,272 Colorectal cancer Age, sex, BMI, low anastomosis, ASA PS classification, preoperative radiotherapy, tumor stage
Qu [11] 2015 14 0 4,580 Laparoscopic anterior resection Age, sex, BMI, previous abdominal surgery, ASA PS classification, albumin, anemia, diabetes, tumor size, TNM stage, preoperative chemotherapy, operative time, level of inferior artery ligation, diverting stoma, intraoperative transfusion, length of first cartridge, diameter of circular stapler, anastomosis level, pelvic drain, rectal tube
Slim [16] 2004 7 7 1,454 Elective colorectal surgery Mechanical bowel preparation No preparation
Slim [17] 2009 14 14 1,859 Elective colorectal surgery Mechanical bowel preparation No preparation
Güenaga [18] 2011 13 13 4,533 Elective colorectal surgery Mechanical bowel preparation No preparation
Rollins [19] 2018 36 23 21,568 Elective colorectal surgery Mechanical bowel preparation No preparation
Rollins [21] 2019 40 28 69,517 Elective colorectal surgery Mechanical bowel preparation + oral antibiotic decontamination Mechanical bowel preparation
Ding [23] 2013 12 1 1,057 Right hemicolectomy for colon cancer Laparoscopic surgery Open surgery
Chaouch [24] 2019 10 0 2,778 Right hemicolectomy for colon cancer with complete mesocolon excision Laparoscopic complete mesocolon excision Open complete mesocolon excision
Gavriilidis [25] 2018 8 0 947 Transverse colon cancer Laparoscopic surgery Open surgery
Simillis [26] 2019 37 29 6,237 Rectal cancer Laparoscopic surgery Open surgery
Si [27] 2019 30 6 11,014 Colorectal cancer High inferior mesenteric artery ligation Low inferior mesenteric artery ligation
Shen [28] 2018 4 4 1,177 Colorectal cancer Indocyanine green No Indocyanine green
Neutzling [30] 2012 9 1,233 Colorectal anastomosis Stapled anastomosis Hand-sewn anastomosis
Choy [31] 2011 7 7 1,125 Ileocolic anastomosis Stapled anastomosis Hand-sewn anastomosis
Lustosa [33] 2002 9 9 1,233 Colorectal anastomosis Stapled anastomosis Hand-sewn anastomosis
van Oostendorp [34] 2017 12 1 1,492 Right hemicolectomy Intracorporeal anastomosis Extracorporeal anastomosis
Wu [35] 2017 19 1 1,957 Right hemicolectomy Intracorporeal anastomosis Extracorporeal anastomosis
Wu [40] 2016 12 2 5,283 Colorectal surgery Air leak test No air leak test
Karliczek [42] 2006 6 6 1,140 Colorectal surgery Drain No drain
Rolph [43] 2004 3 3 908 Colorectal surgery Drain Placebo (blind ended drain) or no drain
Rondelli [44] 2014 8 3 2,277 Anterior resection Drain No drain
Hüser [46] 2008 27 4 15,180 Low rectal cancer Diverting stoma No diverting stoma
Montedori [47] 2010 6 6 648 Anterior resection Diverting stoma No diverting stoma
Wu [48] 2014 11 3 5,612 Low anterior resection Diverting stoma No diverting stoma
Gu [49] 2015 13 4 8,002 Low anterior resection Diverting stoma No diverting stoma
Phan [50] 2019 8 8 892 Low anterior resection Diverting stoma No diverting stoma
Gavriilidis [51] 2019 10 6 1,534 Colorectal surgery Loop ileostomy Loop colostomy
Chudner [52] 2019 6 2 1,063 Anterior resection Loop ileostomy Loop colostomy
Wang [54] 2016 4 1 909 Anterior resection Transanal tube No transanal tube
Yang [55] 2017 7 2 1,772 Low anterior resection Transanal tube No transanal tube
Chen [56] 2018 11 1 2,432 Anterior resection Transanal tube No transanal tube

RCT, randomized clinical trial; BMI, body mass index; ASA, American Society of Anesthesiologists; PS, physical status.

Table 2.
Characteristics of the included randomized clinical trials
First author Year Country No. of patients Population Intervention/comparison Random sequence generation Allocation concealment Blinding of participants and personnel Blinding of outcome assessment
Sadahiro [20] 2014 Japan 310 Colon cancer Three groups: (1) probiotics, bifidobacteria-treated group (group A); (2) oral antibiotics-treated group (group B); and (3) control group (to which neither probiotics nor oral antibiotics were administered) (group C) Low Low High/unclear Low
De Nardi [29] 2020 Italy 240 Laparoscopic left sided colon and rectal resection Indocyanie green angiography Low Low High/unclear High/unclear
Bollo [36] 2020 Spain 140 Laparoscopic right colectomy Intracorporeal/extracorporeal anastomosis Low Low High/unclear High/unclear
Vignali [37] 2016 Italy 60 Laparoscopic right colectomy Intracorporeal/extracorporeal anastomosis Low Low High/unclear High/unclear
Mari [38] 2018 Italy 60 Laparoscopic right colectomy Intracorporeal/extracorporeal anastomosis Low Low High/unclear Low
Allaix [39] 2019 Italy 140 Laparoscopic right colectomy Intracorporeal/extracorporeal anastomosis Low Low High/unclear Low
Denost [45] 2017 France 494 Low anterior resection Drain/no drain Low Low High/unclear High/unclear
Table 3.
Recommendations according to the literature findings
Feature No. of studies by evidence level Findingsa Grade of recommendationb
Evidence for use of mechanical bowel preparation 3 level 1A studies No difference A
1 level 2A study
Evidence for use of oral antibiotic decontamination 1 level 1B study Oral antibiotic reduced leak rate -
1 level 2A study Oral antibiotic with mechanical bowel preparation reduced anastomotic leak in comparison with mechanical bowel preparation alone
No difference between oral antibiotic + mechanical preparation versus oral antibiotic alone
Evidence of the surgical approach: conventional versus mini-invasive approach 1 level 1A study No difference between surgical approach in anterior resection for rectal cancer -
2 level 2A studies No difference between surgical approach in right colectomies for cancer B
1 level 2A study No difference between surgical approach in transverse colectomies -
Evidence of the level of inferior mesenteric artery ligation 1 level 2A study Low ligation reduce the rate of anastomotic leak compared to high ligation with no difference in terms of oncological outcomes -
Evidence of the anastomosis technique: hand sewn versus stapled anastomosis
Colorectal surgery 1 level 1A study No difference -
Right colectomies 1 level 1A study Mechanical anastomosis reduces the rate of anastomosis leak B
1 level 2A study
Rectal surgery 1 level 1A study No difference -
Evidence of the anastomosis technique: intracorporeal versus extracorporeal ileocolic anastomosis 4 level 1B studies No difference A
2 level 2A studies
Evidence for use of air leak test 1 level 2A study No difference -
Evidence for use of external drainage of the abdominal cavity after colon surgery 1 level 1A study There is no interest in drainage B
1 level 2A study
Evidence for use of external drainage of the abdominal cavity after rectal surgery 1 level 1B study No difference -
2 level 2A studies Pelvic drainage reduced the rate of anastomotic leak and the rate of reoperation B
Evidence for use of diverting stoma after low anterior resection 1 level 1A study Diverting stoma reduced the rate of anastomotic leak and the rate of reoperation B
4 level 2A studies
Evidence for use of transanal tube 2 level 2A studies Transanal tube reduced the rate of anastomotic leak and the rate of reoperation B
1 level 2A study Transanal tube reduced the rate of anastomotic leak even in patients with ostomy

a Levels of evidence are as follows: level 1A, systematic reviews (with homogeneity of randomized clinical trials [RCTs]); level 1B, individual RCTs (with narrow confidence intervals); level 2A, systematic reviews (with homogeneity of cohort studies); and level 2B, individual cohort studies (including low-quality RCTs).

b Grades of recommendation are as follows: A, consistent level 1 studies; B, consistent level 2 or 3 studies or extrapolations from level 1 studies; C, level 4 studies or extrapolations from level 2 or 3 studies; and D, level 5 evidence or troublingly inconsistent or inconclusive studies of any level.

REFERENCES

1. Rullier E, Laurent C, Garrelon JL, Michel P, Saric J, Parneix M. Risk factors for anastomotic leakage after resection of rectal cancer. Br J Surg 1998;85:355–8.
crossref pmid
2. Hyman N, Manchester TL, Osler T, Burns B, Cataldo PA. Anastomotic leaks after intestinal anastomosis: it’s later than you think. Ann Surg 2007;245:254–8.
crossref pmid pmc
3. McDermott FD, Heeney A, Kelly ME, Steele RJ, Carlson GL, Winter DC. Systematic review of preoperative, intraoperative and postoperative risk factors for colorectal anastomotic leaks. Br J Surg 2015;102:462–79.
crossref pmid
4. Daniel VT, Alavi K, Davids JS, Sturrock PR, Harnsberger CR, Steele SR, et al. The utility of the Delphi method in defining anastomotic leak following colorectal surgery. Am J Surg 2020;219:75–9.
crossref pmid
5. Guyton KL, Hyman NH, Alverdy JC. Prevention of perioperative anastomotic healing complications: anastomotic stricture and anastomotic leak. Adv Surg 2016;50:129–41.
crossref pmid pmc
6. Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg 2010;8:336–41.
crossref pmid
7. Marshall IJ, Kuiper J, Wallace BC. RobotReviewer: evaluation of a system for automatically assessing bias in clinical trials. J Am Med Inform Assoc 2016;23:193–201.
crossref pmid pdf
8. Centre for Evidence-Based Medicine. Oxford Centre for Evidence-based Medicine - levels of evidence (March 2009) [Internet]. Oxford (UK), Centre for Evidence-Based Medicine; 2009 [cited 2019 Feb 3]. Available from: https://www.cebm.net/2009/06/oxford-centre-evidence-based-medicine-levels-evidence-march-2009/

9. Vasiliu EC, Zarnescu NO, Costea R, Neagu S. Review of risk factors for anastomotic leakage in colorectal surgery. Chirurgia (Bucur) 2015;110:319–26.
pmid
10. Pommergaard HC, Gessler B, Burcharth J, Angenete E, Haglind E, Rosenberg J. Preoperative risk factors for anastomotic leakage after resection for colorectal cancer: a systematic review and meta-analysis. Colorectal Dis 2014;16:662–71.
crossref pmid
11. Qu H, Liu Y, Bi DS. Clinical risk factors for anastomotic leakage after laparoscopic anterior resection for rectal cancer: a systematic review and meta-analysis. Surg Endosc 2015;29:3608–17.
crossref pmid pdf
12. Kawada K, Sakai Y. Preoperative, intraoperative and postoperative risk factors for anastomotic leakage after laparoscopic low anterior resection with double stapling technique anastomosis. World J Gastroenterol 2016;22:5718–27.
crossref pmid pmc
13. Sciuto A, Merola G, De Palma GD, Sodo M, Pirozzi F, Bracale UM, et al. Predictive factors for anastomotic leakage after laparoscopic colorectal surgery. World J Gastroenterol 2018;24:2247–60.
crossref pmid pmc
14. Fujita F, Torashima Y, Kuroki T, Eguchi S. Risk factors and predictive factors for anastomotic leakage after resection for colorectal cancer: reappraisal of the literature. Surg Today 2014;44:1595–602.
crossref pmid pdf
15. Stergios K, Kontzoglou K, Pergialiotis V, Korou LM, Frountzas M, Lalude O, et al. The potential effect of biological sealants on colorectal anastomosis healing in experimental research involving severe diabetes. Ann R Coll Surg Engl 2017;99:189–92.
crossref pmid
16. Slim K, Vicaut E, Panis Y, Chipponi J. Meta-analysis of randomized clinical trials of colorectal surgery with or without mechanical bowel preparation. Br J Surg 2004;91:1125–30.
crossref pmid
17. Slim K, Vicaut E, Launay-Savary MV, Contant C, Chipponi J. Updated systematic review and meta-analysis of randomized clinical trials on the role of mechanical bowel preparation before colorectal surgery. Ann Surg 2009;249:203–9.
crossref pmid
18. Güenaga KF, Matos D, Wille-Jørgensen P. Mechanical bowel preparation for elective colorectal surgery. Cochrane Database Syst Rev 2011;2011:CD001544.
crossref pmid pmc
19. Rollins KE, Javanmard-Emamghissi H, Lobo DN. Impact of mechanical bowel preparation in elective colorectal surgery: a meta-analysis. World J Gastroenterol 2018;24:519–36.
crossref pmid pmc
20. Sadahiro S, Suzuki T, Tanaka A, Okada K, Kamata H, Ozaki T, et al. Comparison between oral antibiotics and probiotics as bowel preparation for elective colon cancer surgery to prevent infection: prospective randomized trial. Surgery 2014;155:493–503.
crossref pmid
21. Rollins KE, Javanmard-Emamghissi H, Acheson AG, Lobo DN. The role of oral antibiotic preparation in elective colorectal surgery: a meta-analysis. Ann Surg 2019;270:43–58.
crossref pmid pmc
22. Van Rooijen SJ, Huisman D, Stuijvenberg M, Stens J, Roumen RMH, Daams F, et al. Intraoperative modifiable risk factors of colorectal anastomotic leakage: why surgeons and anesthesiologists should act together. Int J Surg 2016;36(Pt A):183–200.
crossref
23. Ding J, Liao GQ, Xia Y, Zhang ZM, Liu S, Yan ZS. Laparoscopic versus open right hemicolectomy for colon cancer: a meta-analysis. J Laparoendosc Adv Surg Tech A 2013;23:8–16.
crossref pmid
24. Chaouch MA, Dougaz MW, Bouasker I, Jerraya H, Ghariani W, Khalfallah M, et al. Laparoscopic versus open complete mesocolon excision in right colon cancer: a systematic review and meta-analysis. World J Surg 2019;43:3179–90.
crossref pmid pdf
25. Gavriilidis P, Katsanos K. Laparoscopic versus open transverse colectomy: a systematic review and meta-analysis. World J Surg 2018;42:3008–14.
crossref pmid pdf
26. Simillis C, Lal N, Thoukididou SN, Kontovounisios C, Smith JJ, Hompes R, et al. Open versus laparoscopic versus robotic versus transanal mesorectal excision for rectal cancer: a systematic review and network meta-analysis. Ann Surg 2019;270:59–68.
crossref pmid
27. Si MB, Yan PJ, Du ZY, Li LY, Tian HW, Jiang WJ, et al. Lymph node yield, survival benefit, and safety of high and low ligation of the inferior mesenteric artery in colorectal cancer surgery: a systematic review and meta-analysis. Int J Colorectal Dis 2019;34:947–62.
crossref pmid pdf
28. Shen R, Zhang Y, Wang T. Indocyanine green fluorescence angiography and the incidence of anastomotic leak after colorectal resection for colorectal cancer: a meta-analysis. Dis Colon Rectum 2018;61:1228–34.
crossref pmid
29. De Nardi P, Elmore U, Maggi G, Maggiore R, Boni L, Cassinotti E, et al. Intraoperative angiography with indocyanine green to assess anastomosis perfusion in patients undergoing laparoscopic colorectal resection: results of a multicenter randomized controlled trial. Surg Endosc 2020;34:53–60.
crossref pmid pdf
30. Neutzling CB, Lustosa SA, Proenca IM, da Silva EM, Matos D. Stapled versus handsewn methods for colorectal anastomosis surgery. Cochrane Database Syst Rev 2012;(2):CD003144.
crossref
31. Choy PY, Bissett IP, Docherty JG, Parry BR, Merrie A, Fitzgerald A. Stapled versus handsewn methods for ileocolic anastomoses. Cochrane Database Syst Rev 2011;(9):CD004320.
crossref
32. Luglio G, Corcione F. Stapled versus handsewn methods for ileocolic anastomoses. Tech Coloproctol 2019;23:1093–5.
crossref pmid pdf
33. Lustosa SA, Matos D, Atallah AN, Castro AA. Stapled versus handsewn methods for colorectal anastomosis surgery: a systematic review of randomized controlled trials. Sao Paulo Med J 2002;120:132–6.
crossref pmid pdf
34. van Oostendorp S, Elfrink A, Borstlap W, Schoonmade L, Sietses C, Meijerink J, et al. Intracorporeal versus extracorporeal anastomosis in right hemicolectomy: a systematic review and metaanalysis. Surg Endosc 2017;31:64–77.
crossref pmid pdf
35. Wu Q, Jin C, Hu T, Wei M, Wang Z. Intracorporeal versus extracorporeal anastomosis in laparoscopic right colectomy: a systematic review and meta-analysis. J Laparoendosc Adv Surg Tech A 2017;27:348–57.
crossref pmid
36. Bollo J, Turrado V, Rabal A, Carrillo E, Gich I, Martinez MC, et al. Randomized clinical trial of intracorporeal versus extracorporeal anastomosis in laparoscopic right colectomy (IEA trial). Br J Surg 2020;107:364–72.
crossref pmid
37. Vignali A, Bissolati M, De Nardi P, Di Palo S, Staudacher C. Extracorporeal vs. intracorporeal ileocolic stapled anastomoses in laparoscopic right colectomy: an interim analysis of a randomized clinical trial. J Laparoendosc Adv Surg Tech A 2016;26:343–8.
crossref pmid
38. Mari GM, Crippa J, Costanzi AT, Pellegrino R, Siracusa C, Berardi V, et al. Intracorporeal anastomosis reduces surgical stress response in laparoscopic right hemicolectomy: a prospective randomized trial. Surg Laparosc Endosc Percutan Tech 2018;28:77–81.
crossref pmid
39. Allaix ME, Degiuli M, Bonino MA, Arezzo A, Mistrangelo M, Passera R, et al. Intracorporeal or extracorporeal ileocolic anastomosis after laparoscopic right colectomy: a double-blinded randomized controlled trial. Ann Surg 2019;270:762–7.
crossref pmid
40. Wu Z, van de Haar RC, Sparreboom CL, Boersema GS, Li Z, Ji J, et al. Is the intraoperative air leak test effective in the prevention of colorectal anastomotic leakage?: a systematic review and meta-analysis. Int J Colorectal Dis 2016;31:1409–17.
crossref pmid pmc pdf
41. Liu ZH, Liu JW, Chan FS, Li MK, Fan JK. Intraoperative colonoscopy in laparoscopic colorectal surgery: a review of recent publications. Asian J Endosc Surg 2020;13:19–24.
crossref pmid
42. Karliczek A, Jesus EC, Matos D, Castro AA, Atallah AN, Wiggers T. Drainage or nondrainage in elective colorectal anastomosis: a systematic review and meta-analysis. Colorectal Dis 2006;8:259–65.
crossref pmid
43. Rolph R, Duffy JM, Alagaratnam S, Ng P, Novell R. Intra‐-abdominal drains for the prophylaxis of anastomotic leak in elective colorectal surgery. Cochrane Database Syst Rev 2004;(4):CD002100.
crossref
44. Rondelli F, Bugiantella W, Vedovati MC, Balzarotti R, Avenia N, Mariani E, et al. To drain or not to drain extraperitoneal colorectal anastomosis?: a systematic review and meta-analysis. Colorectal Dis 2014;16:O35–42.
crossref pmid
45. Denost Q, Rouanet P, Faucheron JL, Panis Y, Meunier B, Cotte E, et al. To drain or not to drain infraperitoneal anastomosis after rectal excision for cancer: the GRECCAR 5 randomized trial. Ann Surg 2017;265:474–80.
crossref pmid
46. Hüser N, Michalski CW, Erkan M, Schuster T, Rosenberg R, Kleeff J, et al. Systematic review and meta-analysis of the role of defunctioning stoma in low rectal cancer surgery. Ann Surg 2008;248:52–60.
crossref pmid
47. Montedori A, Cirocchi R, Farinella E, Sciannameo F, Abraha I. Covering ileo- or colostomy in anterior resection for rectal carcinoma. Cochrane Database Syst Rev 2010;(5):CD006878.
crossref
48. Wu SW, Ma CC, Yang Y. Role of protective stoma in low anterior resection for rectal cancer: a meta-analysis. World J Gastroenterol 2014;20:18031–7.
crossref pmid pmc
49. Gu WL, Wu SW. Meta-analysis of defunctioning stoma in low anterior resection with total mesorectal excision for rectal cancer: evidence based on thirteen studies. World J Surg Oncol 2015;13:9.
crossref pmid pmc pdf
50. Phan K, Oh L, Ctercteko G, Pathma-Nathan N, El Khoury T, Azam H, et al. Does a stoma reduce the risk of anastomotic leak and need for re-operation following low anterior resection for rectal cancer: systematic review and meta-analysis of randomized controlled trials. J Gastrointest Oncol 2019;10:179–87.
crossref pmid pmc
51. Gavriilidis P, Azoulay D, Taflampas P. Loop transverse colostomy versus loop ileostomy for defunctioning of colorectal anastomosis: a systematic review, updated conventional meta-analysis, and cumulative meta-analysis. Surg Today 2019;49:108–17.
crossref pmid pdf
52. Chudner A, Gachabayov M, Dyatlov A, Lee H, Essani R, Bergamaschi R. The influence of diverting loop ileostomy vs. colostomy on postoperative morbidity in restorative anterior resection for rectal cancer: a systematic review and meta-analysis. Langenbecks Arch Surg 2019;404:129–39.
crossref pmid pdf
53. Baloyiannis I, Perivoliotis K, Diamantis A, Tzovaras G. Virtual ileostomy in elective colorectal surgery: a systematic review of the literature. Tech Coloproctol 2020;24:23–31.
crossref pmid pdf
54. Wang S, Zhang Z, Liu M, Li S, Jiang C. Efficacy of transanal tube placement after anterior resection for rectal cancer: a systematic review and meta-analysis. World J Surg Oncol 2016;14:92.
crossref pmid pmc
55. Yang Y, Shu Y, Su F, Xia L, Duan B, Wu X. Prophylactic transanal decompression tube versus non-prophylactic transanal decompression tube for anastomotic leakage prevention in low anterior resection for rectal cancer: a meta-analysis. Surg Endosc 2017;31:1513–23.
crossref pmid pdf
56. Chen H, Cai HK, Tang YH. An updated meta-analysis of transanal drainage tube for prevention of anastomotic leak in anterior resection for rectal cancer. Surg Oncol 2018;27:333–40.
crossref pmid
57. Scheidbach H, Benedix F, Hugel O, Kose D, Kockerling F, Lippert H. Laparoscopic approach to colorectal procedures in the obese patient: risk factor or benefit? Obes Surg 2008;18:66–70.
crossref pmid pdf
58. Kudszus S, Roesel C, Schachtrupp A, Hoer JJ. Intraoperative laser fluorescence angiography in colorectal surgery: a noninvasive analysis to reduce the rate of anastomotic leakage. Langenbecks Arch Surg 2010;395:1025–30.
crossref pmid pdf
59. Boni L, Fingerhut A, Marzorati A, Rausei S, Dionigi G, Cassinotti E. Indocyanine green fluorescence angiography during laparoscopic low anterior resection: results of a case-matched study. Surg Endosc 2017;31:1836–40.
crossref pmid pdf
60. Jafari MD, Lee KH, Halabi WJ, Mills SD, Carmichael JC, Stamos MJ, et al. The use of indocyanine green fluorescence to assess anastomotic perfusion during robotic assisted laparoscopic rectal surgery. Surg Endosc 2013;27:3003–8.
crossref pmid pdf
61. Heald RJ. A new approach to rectal cancer. Br J Hosp Med 1979;22:277–81.
pmid


ABOUT
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
AUTHOR INFORMATION
Editorial Office
Room 1519, Suseo Hyundai Venture-vill, 10 Bamgogae-ro 1-gil, Gangnam-gu, Seoul 06349, Korea
Tel: +82-2-2040-7737    Fax: +82-2-2040-7735    E-mail: editor@coloproctol.org                

Copyright © 2024 by Korean Society of Coloproctology.

Developed in M2PI

Close layer