Abstract
Anastomotic leakage is a common yet one of the most feared complications following colorectal surgery. Dehiscence of the anastomosis can result in fatal complications such as peritonitis, abscess formation, and sepsis, thereby increasing morbidity and mortality, cost and length of hospital stay. Multiple factors contribute to the development of anastomotic dehiscence. Several studies have been published identifying various risk factors that may play a role in causing AL. Our study reviewed prospective and retrospective studies and summarized the risk factors into three categories: preoperative, intraoperative, and postoperative. Among these are various risk factors such as age, gender, comorbidities, American Society of Anesthesiologists (ASA) scores, operative time, smoking, alcohol use, obesity, nutritional status, mechanical bowel preparation, and steroid use. It is crucial for surgeons to have a thorough understanding of the risk factors associated with anastomotic leakage to identify patients at high risk preoperatively. It may also be relevant to intraoperative decision-making when establishing an anastomosis, such as considering proximal diversion or placing a drain if such high-risk features are present. Knowing high-risk features also helps to detect leaks as early as possible postoperatively.
Keywords: colorectal cancer, colorectal surgery, anastomotic dehiscence, anastomotic leak, anastomosis, risk factors
Introduction and background
Colorectal surgery is performed for various malignant and benign conditions such as colorectal cancer, inflammatory bowel disease, bowel obstruction, recurrent diverticulitis, trauma, and ischemia, often requiring bowel resection [1]. Following resection, the healthy sections of the intestine are reconnected by an anastomosis to ensure gastrointestinal continuity [2]. Bowel anastomosis has been practiced ever since the 19th century [2]. Over the last 200 years, the gastrointestinal anastomosis procedure has evolved from being a life-threatening surgery to a safe and commonly performed procedure [2].
One of the most significant surgical complications of gastrointestinal anastomosis is anastomotic leakage (AL), leading to an increase in the risk of morbidity and mortality [1]. The International Study Group of Rectal Cancer (ISREC) defined AL as "a communication between the intra- and extra-luminal compartments owing to a defect of the integrity of the intestinal wall at the anastomotic site" [3]. Anastomotic defects can lead to complications such as peritonitis, abscess formation, and sepsis, all of which can be fatal [4]. The incidence of anastomotic leak in colorectal surgery is up to 20% [5]. The mortality rates associated with AL range from 10% to 20% [6]. AL was found to have a detrimental influence on overall survival in a meta-analysis that included a total of 154,981 patients [7]. Furthermore, another systematic review and meta-analysis involving 78’434 colorectal cancer patients reported that AL was related to a higher likelihood of local recurrence [risk ratio (RR) 1.90] and a substantially lower overall survival (RR 1.36) [8]. The occurrence of AL following colorectal surgery is related to several factors (Table 1), such as preoperative, intra-operative, and postoperative factors [9].
Table 1. Factors associated with increased risk of anastomotic leakage (AL) after colorectal surgeries.
Preoperative | Intraoperative | Postoperative |
Age | Level of anastomosis | Intestinal microbes |
Gender | Vascularization of intestinal segments | Postoperative diet |
Obesity | Operative time | |
Preoperative nutritional status | Intraoperative blood loss | |
Smoking | Blood transfusion | |
Alcohol | Diverting stoma | |
American Society of Anesthesiologists (ASA) score | Prophylactic drains | |
Steroid use | ||
Neoadjuvant chemoradiotherapy | ||
Mechanical bowel preparation |
Our review article aims to provide an overview of the current literature on factors playing a role in causing AL in patients undergoing colorectal surgeries. Risk factors, when assessed, assist physicians in identifying patients at high risk, which has a great deal of clinical significance and ultimately improves patient outcomes.
Review
For this review article, electronic databases PubMed and Google Scholar were used. A literature search using the keywords colorectal surgery, anastomotic leak, dehiscence, and risk factors was carried out. All papers not in the English language were excluded. Prospective, retrospective, randomized studies, and meta-analyses were all included in this review. We categorized the factors that may potentially contribute to the leakage of anastomosis into three categories- preoperative, intraoperative, and postoperative factors.
Preoperative factors
Age
Very few studies have shown that age was significantly associated with AL [10-12]. A prospective study including patients undergoing rectal cancer surgery conducted by Lin et al. demonstrated age >70 years as an independent risk factor for AL with OR 2.17 (95% CI: 1.21-3.88) and p-value = 0.009 [12]. Also, a retrospective study published in 2008 by Jung et al., which included 1391 patients who underwent rectal cancer surgery, found that age >60 years was an independent risk factor for AL with a hazard ratio (HR) of 2.32 (95% CI: 1.12-7.83) [11]. But, in most of the studies reviewed, the patient's age did not have a statistically significant association with the AL rate [13-18]. In a meta-analysis conducted by Pommergaard et al. in Sweden, including 110,272 colorectal cancer patients, found a pooled OR of 0.99 (95% CI: 0.89-1.10), suggesting that age was not significantly associated with AL [19]. However, in a retrospective study conducted by Bakker et al. including 15667 colorectal cancer patients, it was found that increasing age was a significant risk factor for death after AL, with 30.1% deaths in patients aged>80 years compared to 18.3% deaths in age 65-80 years and 5.2% deaths in age < 65 years with a p-value of <0.001 [18].
Gender
Male gender has often been reported as an independent risk factor for leakage in colorectal [16,17,20-22]. A multivariate analysis performed by Lipska et al. in New Zealand revealed that among patients undergoing anastomoses involving the colon and rectum, male patients had a higher incidence of AL than female patients, with an OR of 3.5 [16]. Park et al., in their retrospective study of 1609 patients with rectal cancer, showed that the male sex was significantly associated with AL with an HR of 3.468 (95% CI: 1.646-7.305; p=0.001) [20]. A study by Hamabe et al. in Japan, including 296 patients undergoing Laparoscopic low anterior resection with anastomosis using the double stapling technique, demonstrated that men were at significantly higher risk of AL with OR=18.0 (95% CI: 2.4-138; p=0.0053) [21]. Anatomically, males have a narrower pelvis, leading to more difficult resections in both open and laparoscopic colorectal surgeries [22]. Low rectal procedures are likely to have this gender difference due to the more challenging dissection and anastomoses [17,20,21]. Also, androgen-related differences in intestinal microcirculation may contribute to anastomosis healing [23].
Obesity
Several studies have demonstrated that obesity measured by body mass index (BMI) is an independent indicator of an anastomotic leak [24-27]. In a study conducted by Biondo et al. including patients who underwent left colonic resection and primary anastomosis, it was found that obesity with BMI >30 is an independent risk factor associated with AL [27]. In another prospective study by Frasson et al. including 3193 colorectal cancer patients, it was demonstrated that patients with BMI >30 are at an increased risk of AL with an OR of 2.7 (95% CI: 1.4-5.1; p=0.003) [24]. In addition, a CT scan measurement of visceral fat provides a more sensitive indicator than the BMI of anastomotic dehiscence [28]. Yang et al. conducted a meta-analysis in which it was found that in patients undergoing colorectal surgery, visceral obesity is associated with complications including longer operative time, more conversion to open procedure, increased morbidity, more surgical site infections, and higher anastomotic leaks [29]. The association between obesity and AL has been explained by several hypotheses: obesity may indicate a problem with the tissue structure and healing, or a higher abdominal pressure may negatively affect anastomosis microcirculation. An additional assumption is that obese patients have a thicker mesocolon, making anastomosis more difficult [24].
Preoperative Nutrition
Malnutrition negatively impacts anastomotic healing by impairing collagen synthesis or fibroblast proliferation [30]. A retrospective study conducted by Kang et al. involving 72,055 patients who underwent elective anterior resection showed that preoperative weight loss and malnutrition (OR= 2.81; 95% CI: 2.32-3.40), fluid and electrolyte disorders (OR= 1.79; 95% CI: 1.58-2.03) were significantly associated with AL [31]. Zhu et al. conducted a study in which preoperative nutritious status was mainly evaluated by hemoglobin and albumin and found that anemia (hemoglobin < 100 g/L) or hypoproteinemia (albumin ≤ 32 g/L) was found to be significantly associated with AL [32]. Similarly, in a case-control study conducted by Telem et al. which included patients undergoing colorectal resection, it was demonstrated that preoperative albumin level <3.5 mg/dL increased the risk of AL with OR of 2.8 (95% CI: 1.3-5.1; P = 0.03) [14].
Smoking and Alcohol
Smoking and alcohol abuse are significant factors contributing to AL [17,33-35]. Researchers have found that smoking impairs tissue healing and increases AL [34]. Sørensen et al. conducted a retrospective study including patients who underwent colonic or rectal resection with anastomosis that showed an increased risk of AL in smokers compared to non-smokers with a RR of 3.18 and alcohol abusers compared to non-alcoholics with a RR of 7.18 [33]. Another prospective study in Germany demonstrated smoking and alcohol use as independent risk factors for AL [17]. An excessive amount of alcohol consumption may reflect poor nutritional status. In smokers, vascular ischemia from nicotine-induced vasoconstriction and microthromboses, in combination with carbon monoxide-induced cellular hypoxia, inhibits anastomotic circulation [35].
American Society of Anesthesiologists (ASA) Score
The American Society of Anesthesiologists (ASA) Classification is a tool used by anesthesiologists to evaluate the preoperative health condition of a patient before surgery to predict the operative risks [36]. The ASA score is classified on a scale ranging from I to VI [36]. A high ASA grade(≥3) has been shown to be an important risk factor for AL [15,18,37]. Bakker et al. conducted a study that demonstrated higher rates of AL in colorectal cancer patients with ASA scores III and IV (9.2%) compared with ASA scores I and II (7.1%) with a significant p-value of < 0.001 [18]. In a retrospective study by Choi et al. including 1417 colorectal cancer patients, it was found that a high ASA score (III to V) is a significant risk factor for leakage of the anastomosis with OR 5.6 (95%CI: 1.6-15.3; p=0.04) [37]. In a prospective study including all colorectal procedures conducted over 40 months by Buchs et al. in Switzerland, it was observed that the risk of leakage increased 2.5 times for each unit increase of ASA score [15].
Steroid Use
Chronic steroid use refers to the use of long-term, systemic steroids, which require the administration of additional stress-dose steroids during surgery [13]. In a randomized control trial study in a rat model conducted by Mantzoros et al., it was demonstrated that colonic anastomotic healing was affected in the steroid treatment group with statistically significant higher leakage rates in the treatment group than in the control group (p<0.001) [38]. It was postulated that steroid use causes a significant decrease in inflammatory cell infiltration and collagen deposition affecting anastomotic healing [38]. Slieker et al. conducted a prospective study including 259 patients undergoing left-sided colorectal anastomoses that showed that the incidence of AL was 50% in patients on long-term steroid use (p=0.002) and 19% in patients taking corticosteroids perioperatively (p=0.001) [39]. In a prospective study conducted over four years in Japan, it was found that long-term steroid use was a significant risk factor for AL in colorectal cancer surgery, with a leakage rate of 11.8% vs. 2.4% in patients with and without steroid use, respectively [13]. Chronic use of corticosteroids can increase the risk of AL, especially when combined with other immunosuppressive drugs [13].
Neoadjuvant Chemoradiotherapy
Neoadjuvant chemoradiotherapy is a part of multimodality treatment for patients with locally advanced primary and recurrent rectal cancers [40]. Preoperative chemotherapy is known to increase the risk of AL [41]. There are also many harmful effects of radiotherapy on intestinal tissue and wound healing, and it has long been known to contribute as a risk factor for AL [42]. However, various studies reviewed have found conflicting results. In a retrospective study conducted in Korea by Park et al., including 1609 patients with rectal cancer, it was found that preoperative chemoradiation was not associated with an increased risk of AL on univariate analysis. However, in a subgroup of patients without a protective stoma, it was demonstrated that preoperative chemoradiation increased the risk of AL with an HR of 6.284 (95%CI: 2.829-13.961; p<0.001) [20]. In contrast, a retrospective study conducted by Chang et al. using propensity score matching analysis showed that preoperative chemoradiotherapy did not increase the risk of AL after rectal cancer resection [43]. A meta-analysis conducted by Qu et al. indicated that preoperative chemotherapy was associated with the development of AL (OR 1.67, 95 % CI 1.10-2.55, P = 0.02) [41]. However, a randomized trial conducted by Marijnen et al. found that there was no significant difference in AL rates with or without preoperative radiotherapy [44]. Due to inconsistent results, there should certainly be more studies designed to determine the effect of preoperative chemoradiation in AL.
Mechanical Bowel Preparation
Mechanical bowel preparation aims to reduce bowel contents before colorectal surgery, which are sources of infectious bacteria that increase the risk of surgical site infections and AL [45]. According to a meta-analysis conducted by Rollins et al., it was concluded that the use of mechanical bowel preparation in elective colorectal surgery did not impact the incidence of postoperative complications when compared with those who did not undergo preparation (OR = 0.90, 95%CI: 0.74 to 1.10, P = 0.32) [46]. Scarborough et al. conducted a study including 4999 patients which showed that compared to no preoperative bowel preparation, combination of mechanical bowel preparation and oral antibiotics significantly reduced the postoperative complications such as surgical site infections (3.2% vs 9.0%, P < 0.001), AL (2.8% vs 5.7%, P = 0.001), and hospital readmission (5.5% vs 8.0%, P = 0.03) [45]. In a retrospective study performed by Garfinkle et al., that included 40,446 patients undergoing elective colectomy, it was reported that compared with oral antibiotics alone, a combined regimen of oral antibiotics and mechanical bowel preparation offered no superiority in postoperative outcomes [47]. Further studies are needed to give a clearer picture of the effects of mechanical bowel preparation on AL.
Intraoperative factors
Level of Anastomosis
Among the most important factors predicting leakage is the distance of the anastomosis from the anal verge [48]. An anastomosis of 5 cm or less from the anal verge is defined as a low rectal anastomosis [48]. In a case-control study by Jestin et al. including rectal cancer patients, it was shown that anastomosis level ≤ 6cm was an independent risk factor significantly associated with AL both on univariate (OR=1.38; 95%CI: 1.08-1.77) and multivariate analysis (OR=1.39; 95%CI: 1.01-1.90) [49]. In a retrospective study conducted by Choi et al. including patients undergoing rectal resection, it was demonstrated that the AL rate was 10 times higher (20.6% vs. 2.3%) when the anastomotic region was located within 5 cm of the anal verge [48]. Also, in a meta-analysis conducted by Pommergaard et al., including 110,272 colorectal cancer patients, it was found that a low rectal anastomosis was associated with a high risk of leakage with an OR of 3.26 (95% CI: 2.31-4.62) [19]. There is a hypothesis that low anastomosis is associated with technical difficulties that result in tissue trauma, tension, or poor blood supply [9]. The collateral arteries in the rectal region are few and highly variable; therefore, unrecognized damage to small arteries during resection may adversely affect perfusion, resulting in AL [50].
Vascularization of Intestinal Segments
It is vital that blood flow to the intestinal segments is adequate during the healing process of the sutures [51]. Therefore, surgeons usually assess intestinal perfusion during surgery according to their experience by assessing the color of the intestinal segment, pulsations, and the presence of bleeding. These observations are subjective and may lead to misinterpretations [52]. Doppler ultrasound was routinely used intraoperatively because of its low cost and simple technique and was considered more reliable than doing clinical assessment alone [53]. However, in a study conducted by Dyess et al., doppler ultrasonography had a high rate of false-positive and false-negative results. It was found to be an unreliable tool for assessing intestinal perfusion [54]. Recently, it was suggested that a real-time assessment of intestinal perfusion could be obtained utilizing near-infrared (NIR) fluorescence technology with indocyanine green (ICG) [55]. In a study conducted by Kudszus et al. in patients undergoing colorectal cancer resections, it was reported that intraoperative fluorescence imaging resulted in the reduction of AL by 4% in the study group compared with the control group [55]. Similarly, a multi-institutional prospective study conducted by Jafari et al. demonstrated that fluorescence imaging changed surgical plans in 8% of patients, and there were no anastomotic leaks in those patients [56].
Operative Time
Many factors play a role in influencing the duration of operation, such as obesity, type of surgery (open vs. laparoscopic), surgeon's experience, presence of adhesions due to prior abdominal surgery, and other intraoperative complications [57]. Prolonged operative time increases the risk of bacterial exposure and tissue damage causing inflammation and resulting in complications such as ischemia, sepsis, and AL [9]. In a retrospective analysis conducted by Midura et al., which included 13,684 patients who underwent segmental colectomy, it was reported that operative time > 3 hours was associated with increased AL (OR=1.50; 95% CI: 1.19-1.90; p= 0.001) [58]. In another prospective study by Konishi et al., it was found that ≥ 4 hours of surgery duration was associated with AL with OR 9.9 (95% CI: 1.7-186.2; p=0.034) [13]. Studies have shown that prolonged operative time significantly increases the risk of developing AL, with the threshold varying from 180 to 240 minutes [13-15,48].
Intraoperative Blood loss and Blood Transfusion
Intraoperative blood loss is an important risk factor in predicting AL [20]. Loss of blood during surgery may predispose to hypovolemia, resulting in tissue ischemia and impending anastomotic healing, which increases the risk of leakage [59]. In a meta-analysis conducted by Qu et al. involving 4580 rectal cancer patients, it was demonstrated that intraoperative blood loss >100 ml increased the risk of AL with OR 3.79 (95% CI: 2.48-5.49; P < 0.001) [41]. Leichtle et al. conducted a study including all cases of colectomy with primary anastomosis, which reported that intraoperative blood loss of more than 100 mL (OR 1.62; 95% CI: 1.10 to 2.40; p = 0.02) and 300 mL (OR 2.22; 95% CI: 1.32 to 3.76; p = 0.003) were associated with risk of developing AL [60]. Bleeding resulting in the need for blood transfusion is another risk factor [41]. Blood transfusion can lead to impairment of cell-mediated immune response, which increases the risk of infection around anastomoses and also impairs their healing [61]. In a retrospective study conducted by Park et al. including 1609 rectal cancer patients, it was shown that ≥2 units of perioperative blood transfusions were significantly associated with AL both on univariate (HR=6.030; p<0.001) and multivariate analysis (HR = 8.432; 95% CI: 4.715-15.185; P < 0.001) [20]. In another prospective multicenter study including 17,867 patients, Jannasch et al. found a 1.5-fold increased risk of anastomotic leak in patients undergoing blood transfusions, regardless of the number of blood units [17].
Diverting Stoma
After an anastomosis is constructed, diverting stoma is created to redirect the fecal flow away from the anastomotic site to help in anastomotic healing and protect from anastomotic failure [62]. However, there are controversial views regarding the link between a diversion stoma and anastomotic leakage. Matthiessen et al. conducted a randomized multicenter trial including 234 rectal cancer patients, in which it was demonstrated that the construction of a protective stoma had a significant association with decreased rates of AL. The leakage rate in patients with diverting stoma was 10.3% compared to 28.0% in patients without a stoma (OR = 3.4; 95% CI: 1.6-6.9; P < 0.001) [63]. In another meta-analysis study conducted by Huser et al., it was found that after surgery for low rectal cancers, there was a significant difference in the overall leakage and reoperation rates among patients with and without protective stomas with OR = 0.32 (95% CI 0.17-0.59) and OR = 0.27 (95% CI 0.14-0.51) respectively [64]. It is most beneficial when used selectively in high-risk patients with low pelvic anastomoses that are at an increased risk for AL. Contrary to the above studies, in a study done by Gastinger et al. including patients undergoing low anterior resection for rectal cancer, there was no difference in AL rates in patients with or without a stoma (14·5% vs. 14·2%, respectively; p=0.806) [65]. Similarly, Akiyoshi et al. conducted a study in Japan, including 363 rectal cancer patients who reported no significant association in AL rates in patients with (4.8%) and without stoma (3.3%) with a p-value of 0.4718 [66]. While this topic remains controversial, it is generally agreed that diverting stoma reduces the adverse effects of AL, such as fecal peritonitis, septic complications, and the need for repeat surgery if AL is to occur [67-69].
Prophylactic Drains
In colorectal surgery, there has been a lot of controversy surrounding the use of prophylactic drains. It was expected that the purpose of prophylactic drains was to eliminate perianastomotic fluid collections, thereby preventing abscess formation and reducing contamination that may otherwise extend to the anastomosis and cause AL [70]. A pelvic drain may also reduce the severity of leaks if they do occur, resulting in a less severe clinical outcome [41]. Prophylactic drains were also viewed as a potential early warning tool for anastomotic dehiscence [71]. In a retrospective study conducted by Peeters et al., it was concluded that the lack of pelvic drain after total mesorectal resection of rectal cancer was associated with an increased AL rate with a relative risk of 2.53 (95% CI: 1.57 -4.09; p <0.001) [72]. Also, a meta-analysis conducted by Rondelli et al., including 2277 patients, found a decreased AL rate with the use of pelvic drainage (OR = 0·51; 95% CI: 0·36 to 0·73) in patients undergoing anterior rectal resection with extraperitoneal colorectal anastomosis [73]. However, in contrast to the above assumptions, many studies claimed that using prophylactic drains was not associated with reducing AL rates [16,24,74,75]. A randomized trial conducted by Denost et al. reported that the use of pelvic drainage did not reduce AL rates [75]. In a meta-analysis conducted by Karliczek et al., it was concluded that after elective colorectal surgery the use of drains after colorectal anastomoses did not significantly improve outcomes in terms of wound infections, anastomotic dehiscence, reintervention, or mortality [74]. Despite the controversial conclusions, most surgeons use a drain in the abdominal or pelvic cavity following colorectal anastomotic surgery according to their personal preferences and own experiences [70].
Postoperative factors
Intestinal Microbes
The human gastrointestinal tract is inhabited by around 1014 bacteria [76]. Some studies on animal models have suggested that alteration in intestinal flora appears to affect bowel anastomosis [77,78]. Cohn et al. demonstrated that intraluminal administration of antibiotics at an anastomotic site was capable of protecting a devascularized segment of the colon in their animal experiment [77]. In another study conducted by Shogan et al., it was found that cues released by surgically injured tissue can induce phenotypic changes in intraluminal microbes, thus making them pathogenic. It has been suggested that these may act as causative factors in the development of AL by increasing collagenase levels and activating host metalloproteinases [79]. Radiation is another powerful modality exerting a significant effect on gastrointestinal microflora by altering composition and virulence. It has been suggested that differential colonization could be linked to susceptibility to RT-induced diarrhea [80]. There is, nonetheless, a lack of evidence regarding the influence of gut microbiota on postoperative anastomotic complications.
Postoperative diet
Early initiation of enteral nutrition is critical in postoperative recovery [57]. Early administration of oral feeding has several benefits: it increases regular bowel movements, which improves microcirculation and perfusion at the anastomosis site, enhances anastomotic healing, and also prevents intestinal bacterial overgrowth [81]. In a retrospective study conducted by Jasarovic et al., including 153 colorectal cancer patients, it was reported that patients who started their oral intake in the immediate postoperative period had reduced AL than those who began later [81]. Studies have shown that an early postoperative diet helps in the early recovery of bowel function and reduces the length of hospital stay [82,83] (Table 2).
Table 2. Risk factors of Anastomotic leakage (AL) - Overview of studies.
Author | Year | Country | Type of Study | No. of anastomoses | Anastomotic Leakage % | Conclusion |
Jasarovic et al. [75] | 2020 | Serbia | Retrospective study | 153 | 9.80% | Early initiation of oral feeding during the postoperative period reduces the AL rates |
Hamabe et al. [21] | 2018 | Japan | Retrospective study | 296 | 8.10% | Men undergoing LAR were at high risk of AL |
Jannasch et al. [17] | 2015 | Germany | Prospective study | 17 867 | 11.90% | Smoking and alcohol use increase the risk of AL |
Midura et al. [58] | 2015 | United States | Retrospective study | 13 684 | 3.80% | A prolonged operation duration of > 3 hours increases the risk of AL |
Qu et al. [41] | 2015 | China | Meta-analysis | 4589 | 6.30% | Preoperative chemotherapy increases the risk of AL; Intraoperative blood loss > 100ml increases the risk of AL |
Frasson et al. [24] | 2015 | Spain | Prospective study | 3193 | 8.70% | BMI > 30 increases AL rates |
Pommergaard et al. [19] | 2014 | Sweden | Meta-analysis | 110 272 | 7.20% | The patient's age did not correlate with AL risk; Low rectal anastomosis increases AL rates |
Bakker et al. [18] | 2014 | Netherlands | Retrospective Study | 15 667 | 7.50% | Increasing patient age is associated with an increased risk of death after AL; Patients with ASA scores III and IV are at risk of AL |
Chang et al. [43] | 2014 | Korea | Retrospective study | 1437 | 6.30% | Preoperative chemoradiotherapy is not associated with an increased risk of AL |
Kang et al. [31] | 2013 | United States | Retrospective study | 72 055 | 13.68% | Preoperative weight loss and malnutrition increase AL |
Park et al. [20] | 2013 | Korea | Retrospective study | 1699 | 6.30% | Male sex is significantly associated with the risk of AL; Perioperative transfusion of ≥ 2 units of blood increases the risk of AL |
Leichtle et al. [60] | 2012 | United States | Retrospective study | 4340 | 3.10% | Intraoperative blood loss > 100ml is associated with an increased risk of AL |
Slieker et al. [39] | 2012 | Netherlands | Prospective study | 259 | 7.30% | Steroid use increases the risk of AL |
Lin et al. [12] | 2011 | Taiwan | Retrospective study | 999 | 5.30% | Age > 70 years the significant risk of AL |
Akiyoshi et al. [66] | 2011 | Japan | Retrospective study | 363 | 3.60% | No statistical difference in AL between patients with and without diverting stoma |
Telem et al. [14] | 2010 | United States | Case-Control study | 3501 | 2.60% | Preoperative albumin < 3.5 mg/dl increases the risk of AL |
Choi et al. [48] | 2010 | Korea | Retrospective study | 156 | 10.30% | The level of anastomosis < 5cm from the anal verge is associated with an increased risk of AL |
Zhu et al. [32] | 2010 | China | Retrospective study | 132 | 9.10% | Preoperative anemia and hypoproteinemia increase the risk of AL |
Jung et al. [11] | 2008 | Korea | Retrospective study | 1391 | 2.50% | Age > 60 years the significant risk of AL |
Jestin et al. [49] | 2008 | Sweden | Case-Control study | 1381 | 9.70% | The level of anastomosis ≤ 6cm from the anal verge increases the risk of AL |
Buchs et al. [15] | 2007 | Switzerland | Prospective study | 811 | 3.80% | The risk of AL increases 2.5 times for every unit increase in ASA score |
Matthiessen et al. [63] | 2007 | Sweden | Randomized control trial | 234 | 19.20% | Diverting stoma is associated with reduced AL rates |
Choi et al. [37] | 2006 | China | Retrospective study | 1417 | 1.80% | ASA scores III and IV increase AL |
Lipska et al. [16] | 2006 | New Zealand | Retrospective study | 541 | 6.50% | Men are at increased risk of AL. |
Konishi et al. [13] | 2006 | Japan | Prospective study | 391 | 2.80% | Long-term steroid use is associated with an increased risk of AL; Operative time > 4 hours increases AL rates |
Peeters et al. [72] | 2005 | Netherlands | Retrospective study | 924 | 11.6% | Pelvic drain is associated with lower AL rates |
Biondo et al. [27] | 2005 | Spain | Retrospective study | 208 | 5.70% | Patients with BMI > 30 were at high risk of AL |
Sørensen et al. [33] | 1999 | Denmark | Retrospective study | 333 | 15.90% | Smoking and alcohol use increase the risk of AL |
Limitations
This study has some limitations. Our review article used only PubMed and Google Scholar databases. While the study included all procedures under colorectal surgery, most of the data were related to colorectal cancer.
Conclusions
Anastomotic leak in colorectal surgery is a multifactorial complication associated with an increased morbidity and mortality rate. It has remained the most feared complication over the past several years, despite numerous studies and technological advances like robotic surgery, staplers, and other anastomotic techniques. The clinical significance of reviewing and summarizing the risk factors of AL is to identify high-risk patients. Awareness and understanding of these factors will provide an opportunity to offer more comprehensive preoperative patient counseling. They will also facilitate early detection of leaks allowing appropriate treatment to be tailored accordingly, resulting in better patient outcomes. Among preoperative factors, gender played a more important role than a patient's age. Obesity, smoking, and alcohol abuse were all found to be significantly associated with the risk of AL. Among obese patients, visceral fat was a more significant indicator than BMI. The risk of AL increased with each unit increase in ASA score. Preoperative albumin level was the most critical factor in evaluating the preoperative nutritional status, influencing AL. Patients with chronic steroid use were at a higher risk than those on short-term steroids. The effect of neoadjuvant chemoradiation on AL had conflicting results in the literature review. Mechanical bowel preparation did not show any significant impact on postoperative complications. Intraoperative factors play a crucial role in predicting AL. The level of anastomosis was the most important of all factors. Anastomosis ≤ 5cm from the anal verge was at higher risk of leakage. Assessment of intestinal perfusion using intraoperative fluorescence imaging was beneficial in reducing the rate of AL. Operative time >3 hours increased the risk of AL. Intraoperative blood loss requiring blood transfusion also played a significant role in AL. Even though the use of diverting stoma was controversial, it was beneficial in the anastomotic healing of low pelvic anastomosis. Prophylactic drains remain controversial despite their widespread use among surgeons. The intestinal microbes appear to play a role in AL, but there was a lack of solid evidence in the literature reviewed. Early initiation of enteral feeding has shown to be beneficial in anastomotic healing and early postoperative recovery. It is beneficial to conduct future studies to focus on controversial risk factors that have not been adequately explored. The effect of neoadjuvant chemoradiation on AL needs to be further analyzed and interpreted in the context of overall survival. The role of intestinal microbes and the impact of intraluminal administration of antibiotics need further investigation.
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Footnotes
The authors have declared that no competing interests exist.
References
- 1.A collaborative review of the current concepts and challenges of anastomotic leaks in colorectal surgery. Vallance A, Wexner S, Berho M, et al. Colorectal Dis. 2017;19:0. doi: 10.1111/codi.13534. [DOI] [PubMed] [Google Scholar]
- 2.The art of bowel anastomosis. Chen C. Scand J Surg. 2012;101:238–240. doi: 10.1177/145749691210100403. [DOI] [PubMed] [Google Scholar]
- 3.Definition and grading of anastomotic leakage following anterior resection of the rectum: a proposal by the International Study Group of Rectal Cancer. Rahbari NN, Weitz J, Hohenberger W, et al. Surgery. 2010;147:339–351. doi: 10.1016/j.surg.2009.10.012. [DOI] [PubMed] [Google Scholar]
- 4.Colorectal anastomosis leak: rate, risk factors and outcome in a tertiary teaching hospital, Addis Ababa Ethiopia, a five year retrospective study. Wako G, Teshome H, Abebe E. Ethiop J Health Sci. 2019;29:767–774. doi: 10.4314/ejhs.v29i6.14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Anastomotic leaks after intestinal anastomosis: it's later than you think. Hyman N, Manchester TL, Osler T, Burns B, Cataldo PA. Ann Surg. 2007;245:254–258. doi: 10.1097/01.sla.0000225083.27182.85. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Prognosis after anastomotic leakage in colorectal surgery. Branagan G, Finnis D. Dis Colon Rectum. 2005;48:1021–1026. doi: 10.1007/s10350-004-0869-4. [DOI] [PubMed] [Google Scholar]
- 7.Meta-analysis of the impact of postoperative infective complications on oncological outcomes in colorectal cancer surgery. Lawler J, Choynowski M, Bailey K, Bucholc M, Johnston A, Sugrue M. BJS Open. 2020;4:737–747. doi: 10.1002/bjs5.50302. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Oncologic impact of anastomotic leakage following colorectal cancer surgery: a systematic review and meta-analysis. Ha GW, Kim JH, Lee MR. Ann Surg Oncol. 2017;24:3289–3299. doi: 10.1245/s10434-017-5881-8. [DOI] [PubMed] [Google Scholar]
- 9.Preoperative, intraoperative and postoperative risk factors for anastomotic leakage after laparoscopic low anterior resection with double stapling technique anastomosis. Kawada K, Sakai Y. World J Gastroenterol. 2016;22:5718–5727. doi: 10.3748/wjg.v22.i25.5718. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.A nationwide study on anastomotic leakage after colonic cancer surgery. Krarup PM, Jorgensen LN, Andreasen AH, Harling H. Colorectal Dis. 2012;14:0–7. doi: 10.1111/j.1463-1318.2012.03079.x. [DOI] [PubMed] [Google Scholar]
- 11.Risk factors and oncologic impact of anastomotic leakage after rectal cancer surgery. Jung SH, Yu CS, Choi PW, Kim DD, Park IJ, Kim HC, Kim JC. Dis Colon Rectum. 2008;51:902–908. doi: 10.1007/s10350-008-9272-x. [DOI] [PubMed] [Google Scholar]
- 12.The influence of fecal diversion and anastomotic leakage on survival after resection of rectal cancer. Lin JK, Yueh TC, Chang SC, et al. J Gastrointest Surg. 2011;15:2251–2261. doi: 10.1007/s11605-011-1721-5. [DOI] [PubMed] [Google Scholar]
- 13.Risk factors for anastomotic leakage after surgery for colorectal cancer: results of prospective surveillance. Konishi T, Watanabe T, Kishimoto J, Nagawa H. J Am Coll Surg. 2006;202:439–444. doi: 10.1016/j.jamcollsurg.2005.10.019. [DOI] [PubMed] [Google Scholar]
- 14.Risk factors for anastomotic leak following colorectal surgery: a case-control study. Telem DA, Chin EH, Nguyen SQ, Divino CM. Arch Surg. 2010;145:371–376. doi: 10.1001/archsurg.2010.40. [DOI] [PubMed] [Google Scholar]
- 15.Incidence, consequences, and risk factors for anastomotic dehiscence after colorectal surgery: a prospective monocentric study. Buchs NC, Gervaz P, Secic M, Bucher P, Mugnier-Konrad B, Morel P. Int J Colorectal Dis. 2008;23:265–270. doi: 10.1007/s00384-007-0399-3. [DOI] [PubMed] [Google Scholar]
- 16.Anastomotic leakage after lower gastrointestinal anastomosis: men are at a higher risk. Lipska MA, Bissett IP, Parry BR, Merrie AE. ANZ J Surg. 2006;76:579–585. doi: 10.1111/j.1445-2197.2006.03780.x. [DOI] [PubMed] [Google Scholar]
- 17.Risk factors, short and long term outcome of anastomotic leaks in rectal cancer. Jannasch O, Klinge T, Otto R, et al. Oncotarget. 2015;6:36884–36893. doi: 10.18632/oncotarget.5170. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Risk factors for anastomotic leakage and leak-related mortality after colonic cancer surgery in a nationwide audit. Bakker IS, Grossmann I, Henneman D, Havenga K, Wiggers T. Br J Surg. 2014;101:424–432. doi: 10.1002/bjs.9395. [DOI] [PubMed] [Google Scholar]
- 19.Preoperative risk factors for anastomotic leakage after resection for colorectal cancer: a systematic review and meta-analysis. Pommergaard HC, Gessler B, Burcharth J, Angenete E, Haglind E, Rosenberg J. Colorectal Dis. 2014;16:662–671. doi: 10.1111/codi.12618. [DOI] [PubMed] [Google Scholar]
- 20.Multicenter analysis of risk factors for anastomotic leakage after laparoscopic rectal cancer excision: the Korean laparoscopic colorectal surgery study group. Park JS, Choi GS, Kim SH, et al. Ann Surg. 2013;257:665–671. doi: 10.1097/SLA.0b013e31827b8ed9. [DOI] [PubMed] [Google Scholar]
- 21.Preventive effect of diverting stoma on anastomotic leakage after laparoscopic low anterior resection with double stapling technique reconstruction applied based on risk stratification. Hamabe A, Ito M, Nishigori H, Nishizawa Y, Sasaki T. Asian J Endosc Surg. 2018;11:220–226. doi: 10.1111/ases.12439. [DOI] [PubMed] [Google Scholar]
- 22.Trends in risk factors of anastomotic leakage after colorectal cancer surgery (2011-2019): A Dutch population-based study. Arron MN, Greijdanus NG, Ten Broek RP, et al. Colorectal Dis. 2021;23:3251–3261. doi: 10.1111/codi.15911. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Gender differences in small intestinal endothelial function: inhibitory role of androgens. Ba ZF, Yokoyama Y, Toth B, Rue LW 3rd, Bland KI, Chaudry IH. Am J Physiol Gastrointest Liver Physiol. 2004;286:0–7. doi: 10.1152/ajpgi.00357.2003. [DOI] [PubMed] [Google Scholar]
- 24.Risk factors for anastomotic leak after colon resection for cancer: multivariate analysis and nomogram from a multicentric, prospective, national study with 3193 patients. Frasson M, Flor-Lorente B, Rodríguez JL, et al. Ann Surg. 2015;262:321–330. doi: 10.1097/SLA.0000000000000973. [DOI] [PubMed] [Google Scholar]
- 25.Risk factors for anastomotic leakage after resection of rectal cancer. Rullier E, Laurent C, Garrelon JL, Michel P, Saric J, Parneix M. Br J Surg. 1998;85:355–358. doi: 10.1046/j.1365-2168.1998.00615.x. [DOI] [PubMed] [Google Scholar]
- 26.Laparoscopic colectomy in obese and nonobese patients. Senagore AJ, Delaney CP, Madboulay K, Brady KM, Fazio VW. J Gastrointest Surg. 2003;7:558–561. doi: 10.1016/s1091-255x(02)00124-5. [DOI] [PubMed] [Google Scholar]
- 27.Anastomotic dehiscence after resection and primary anastomosis in left-sided colonic emergencies. Biondo S, Parés D, Kreisler E, Ragué JM, Fraccalvieri D, Ruiz AG, Jaurrieta E. Dis Colon Rectum. 2005;48:2272–2280. doi: 10.1007/s10350-005-0159-9. [DOI] [PubMed] [Google Scholar]
- 28.The impact of visceral obesity on surgical outcomes of laparoscopic surgery for colon cancer. Watanabe J, Tatsumi K, Ota M, et al. Int J Colorectal Dis. 2014;29:343–351. doi: 10.1007/s00384-013-1803-9. [DOI] [PubMed] [Google Scholar]
- 29.Impact of visceral obesity on outcomes of laparoscopic colorectal surgery: a meta-analysis. Yang T, Wei M, He Y, Deng X, Wang Z. ANZ J Surg. 2015;85:507–513. doi: 10.1111/ans.13132. [DOI] [PubMed] [Google Scholar]
- 30.Risk factors for anastomotic leakage after left-sided colorectal resection with rectal anastomosis. Mäkelä JT, Kiviniemi H, Laitinen S. Dis Colon Rectum. 2003;46:653–660. doi: 10.1007/s10350-004-6627-9. [DOI] [PubMed] [Google Scholar]
- 31.Risk factors for anastomotic leakage after anterior resection for rectal cancer. Kang CY, Halabi WJ, Chaudhry OO, et al. JAMA Surg. 2013;148:65–71. doi: 10.1001/2013.jamasurg.2. [DOI] [PubMed] [Google Scholar]
- 32.Laparoscopic low anterior resection for rectal carcinoma: complications and management in 132 consecutive patients. Zhu QL, Feng B, Lu AG, et al. World J Gastroenterol. 2010;16:4605–4610. doi: 10.3748/wjg.v16.i36.4605. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Smoking and alcohol abuse are major risk factors for anastomotic leakage in colorectal surgery. Sørensen LT, Jørgensen T, Kirkeby LT, Skovdal J, Vennits B, Wille-Jørgensen P. Br J Surg. 1999;86:927–931. doi: 10.1046/j.1365-2168.1999.01165.x. [DOI] [PubMed] [Google Scholar]
- 34.Risk factors for tissue and wound complications in gastrointestinal surgery. Sørensen LT, Hemmingsen U, Kallehave F, Wille-Jørgensen P, Kjaergaard J, Møller LN, Jørgensen T. Ann Surg. 2005;241:654–658. doi: 10.1097/01.sla.0000157131.84130.12. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Risk factors and oncologic outcomes of anastomosis leakage after laparoscopic right colectomy. Kwak HD, Kim SH, Kang DW, Baek SJ, Kwak JM, Kim J. Surg Laparosc Endosc Percutan Tech. 2017;27:440–444. doi: 10.1097/SLE.0000000000000471. [DOI] [PubMed] [Google Scholar]
- 36.Doyle DJ, Goyal A, Garmon EH. Treasure Island, FL: StatPearls; 2022. American Society of Anesthesiologists Classification. [PubMed] [Google Scholar]
- 37.Leakage after resection and intraperitoneal anastomosis for colorectal malignancy: analysis of risk factors. Choi HK, Law WL, Ho JW. Dis Colon Rectum. 2006;49:1719–1725. doi: 10.1007/s10350-006-0703-2. [DOI] [PubMed] [Google Scholar]
- 38.Effects of steroid on the healing of colonic anastomoses in the rat. Mantzoros I, Kanellos I, Demetriades H, et al. Tech Coloproctol. 2004;8 Suppl 1:0–3. doi: 10.1007/s10151-004-0150-9. [DOI] [PubMed] [Google Scholar]
- 39.Long-term and perioperative corticosteroids in anastomotic leakage: a prospective study of 259 left-sided colorectal anastomoses. Slieker JC, Komen N, Mannaerts GH, et al. Arch Surg. 2012;147:447–452. doi: 10.1001/archsurg.2011.1690. [DOI] [PubMed] [Google Scholar]
- 40.Management of locally advanced primary and recurrent rectal cancer. de Wilt JH, Vermaas M, Ferenschild FT, Verhoef C. Clin Colon Rectal Surg. 2007;20:255–263. doi: 10.1055/s-2007-984870. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Clinical risk factors for anastomotic leakage after laparoscopic anterior resection for rectal cancer: a systematic review and meta-analysis. Qu H, Liu Y, Bi DS. Surg Endosc. 2015;29:3608–3617. doi: 10.1007/s00464-015-4117-x. [DOI] [PubMed] [Google Scholar]
- 42.Risk factors for anastomotic leakage after anterior resection of the rectum. Matthiessen P, Hallböök O, Andersson M, Rutegård J, Sjödahl R. Colorectal Dis. 2004;6:462–469. doi: 10.1111/j.1463-1318.2004.00657.x. [DOI] [PubMed] [Google Scholar]
- 43.Preoperative chemoradiotherapy effects on anastomotic leakage after rectal cancer resection: a propensity score matching analysis. Chang JS, Keum KC, Kim NK, et al. Ann Surg. 2014;259:516–521. doi: 10.1097/SLA.0b013e31829068c5. [DOI] [PubMed] [Google Scholar]
- 44.Acute side effects and complications after short-term preoperative radiotherapy combined with total mesorectal excision in primary rectal cancer: report of a multicenter randomized trial. Marijnen CA, Kapiteijn E, van de Velde CJ, et al. J Clin Oncol. 2002;20:817–825. doi: 10.1200/JCO.2002.20.3.817. [DOI] [PubMed] [Google Scholar]
- 45.Combined mechanical and oral antibiotic bowel preparation reduces incisional surgical site infection and anastomotic leak rates after elective colorectal resection: an analysis of colectomy-targeted ACS NSQIP. Scarborough JE, Mantyh CR, Sun Z, Migaly J. Ann Surg. 2015;262:331–337. doi: 10.1097/SLA.0000000000001041. [DOI] [PubMed] [Google Scholar]
- 46.Impact of mechanical bowel preparation in elective colorectal surgery: A meta-analysis. Rollins KE, Javanmard-Emamghissi H, Lobo DN. World J Gastroenterol. 2018;24:519–536. doi: 10.3748/wjg.v24.i4.519. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Is there a role for oral antibiotic preparation alone before colorectal surgery? ACS-NSQIP analysis by coarsened exact matching. Garfinkle R, Abou-Khalil J, Morin N, et al. Dis Colon Rectum. 2017;60:729–737. doi: 10.1097/DCR.0000000000000851. [DOI] [PubMed] [Google Scholar]
- 48.Risk factors for anastomotic leakage after laparoscopic rectal resection. Choi DH, Hwang JK, Ko YT, et al. J Korean Soc Coloproctol. 2010;26:265–273. doi: 10.3393/jksc.2010.26.4.265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Risk factors for anastomotic leakage after rectal cancer surgery: a case-control study. Jestin P, Påhlman L, Gunnarsson U. Colorectal Dis. 2008;10:715–721. doi: 10.1111/j.1463-1318.2007.01466.x. [DOI] [PubMed] [Google Scholar]
- 50.The angiographic anatomy of the small arteries and their collaterals in colorectal resections: some insights into anastomotic perfusion. Allison AS, Bloor C, Faux W, Arumugam P, Widdison A, Lloyd-Davies E, Maskell G. Ann Surg. 2010;251:1092–1097. doi: 10.1097/SLA.0b013e3181deb649. [DOI] [PubMed] [Google Scholar]
- 51.Colonic anastomotic leak: risk factors, diagnosis, and treatment. Kingham TP, Pachter HL. J Am Coll Surg. 2009;208:269–278. doi: 10.1016/j.jamcollsurg.2008.10.015. [DOI] [PubMed] [Google Scholar]
- 52.Surgeons lack predictive accuracy for anastomotic leakage in gastrointestinal surgery. Karliczek A, Harlaar NJ, Zeebregts CJ, Wiggers T, Baas PC, van Dam GM. Int J Colorectal Dis. 2009;24:569–576. doi: 10.1007/s00384-009-0658-6. [DOI] [PubMed] [Google Scholar]
- 53.Evaluation of ischemic intestine by Doppler ultrasound. Cooperman M, Martin EW Jr, Carey LC. Am J Surg. 1980;139:73–77. doi: 10.1016/0002-9610(80)90232-9. [DOI] [PubMed] [Google Scholar]
- 54.Intraoperative evaluation of intestinal ischemia: a comparison of methods. Dyess DL, Bruner BW, Donnell CA, Ferrara JJ, Powell RW. South Med J. 1991;84:966-9, 974. doi: 10.1097/00007611-199108000-00008. [DOI] [PubMed] [Google Scholar]
- 55.Intraoperative laser fluorescence angiography in colorectal surgery: a noninvasive analysis to reduce the rate of anastomotic leakage. Kudszus S, Roesel C, Schachtrupp A, Höer JJ. Langenbecks Arch Surg. 2010;395:1025–1030. doi: 10.1007/s00423-010-0699-x. [DOI] [PubMed] [Google Scholar]
- 56.Perfusion assessment in laparoscopic left-sided/anterior resection (PILLAR II): a multi-institutional study. Jafari MD, Wexner SD, Martz JE, et al. J Am Coll Surg. 2015;220:82–92. doi: 10.1016/j.jamcollsurg.2014.09.015. [DOI] [PubMed] [Google Scholar]
- 57.Complications in colorectal surgery: risk factors and preventive strategies. Kirchhoff P, Clavien PA, Hahnloser D. Patient Saf Surg. 2010;4:5. doi: 10.1186/1754-9493-4-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 58.Risk factors and consequences of anastomotic leak after colectomy: a national analysis. Midura EF, Hanseman D, Davis BR, Atkinson SJ, Abbott DE, Shah SA, Paquette IM. Dis Colon Rectum. 2015;58:333–338. doi: 10.1097/DCR.0000000000000249. [DOI] [PubMed] [Google Scholar]
- 59.Hypovolaemia and healing in colonic anastomoses. Foster ME, Laycock JR, Silver IA, Leaper DJ. Br J Surg. 1985;72:831–834. doi: 10.1002/bjs.1800721019. [DOI] [PubMed] [Google Scholar]
- 60.Risk factors for anastomotic leakage after colectomy. Leichtle SW, Mouawad NJ, Welch KB, Lampman RM, Cleary RK. Dis Colon Rectum. 2012;55:569–575. doi: 10.1097/DCR.0b013e3182423c0d. [DOI] [PubMed] [Google Scholar]
- 61.Blood transfusion impairs the healing of experimental intestinal anastomoses. Tadros T, Wobbes T, Hendriks T. Ann Surg. 1992;215:276–281. doi: 10.1097/00000658-199203000-00013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Risk factors and predictive factors for anastomotic leakage after resection for colorectal cancer: reappraisal of the literature. Fujita F, Torashima Y, Kuroki T, Eguchi S. Surg Today. 2014;44:1595–1602. doi: 10.1007/s00595-013-0685-3. [DOI] [PubMed] [Google Scholar]
- 63.Defunctioning stoma reduces symptomatic anastomotic leakage after low anterior resection of the rectum for cancer: a randomized multicenter trial. Matthiessen P, Hallböök O, Rutegård J, Simert G, Sjödahl R. Ann Surg. 2007;246:207–214. doi: 10.1097/SLA.0b013e3180603024. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Systematic review and meta-analysis of the role of defunctioning stoma in low rectal cancer surgery. Hüser N, Michalski CW, Erkan M, Schuster T, Rosenberg R, Kleeff J, Friess H. Ann Surg. 2008;248:52–60. doi: 10.1097/SLA.0b013e318176bf65. [DOI] [PubMed] [Google Scholar]
- 65.Protective defunctioning stoma in low anterior resection for rectal carcinoma. Gastinger I, Marusch F, Steinert R, Wolff S, Koeckerling F, Lippert H. Br J Surg. 2005;92:1137–1142. doi: 10.1002/bjs.5045. [DOI] [PubMed] [Google Scholar]
- 66.Incidence of and risk factors for anastomotic leakage after laparoscopic anterior resection with intracorporeal rectal transection and double-stapling technique anastomosis for rectal cancer. Akiyoshi T, Ueno M, Fukunaga Y, et al. Am J Surg. 2011;202:259–264. doi: 10.1016/j.amjsurg.2010.11.014. [DOI] [PubMed] [Google Scholar]
- 67.Anastomotic leakage after anterior resection for rectal cancer with mesorectal excision: incidence, risk factors, and management. Tortorelli AP, Alfieri S, Sanchez AM, et al. https://pubmed.ncbi.nlm.nih.gov/25569064/ Am Surg. 2015;81:41–47. [PubMed] [Google Scholar]
- 68.Defunctioning stoma- a prognosticator for leaks in low rectal restorative cancer resection: A retrospective analysis of stoma database. Abudeeb H, Hammad A, Ugwu A, et al. Ann Med Surg (Lond) 2017;21:114–117. doi: 10.1016/j.amsu.2017.07.044. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Effects of a diverting stoma on symptomatic anastomotic leakage after low anterior resection for rectal cancer: a propensity score matching analysis of 1,014 consecutive patients. Shiomi A, Ito M, Maeda K, et al. J Am Coll Surg. 2015;220:186–194. doi: 10.1016/j.jamcollsurg.2014.10.017. [DOI] [PubMed] [Google Scholar]
- 70.To drain or not to drain in colorectal anastomosis: a meta-analysis. Zhang HY, Zhao CL, Xie J, et al. Int J Colorectal Dis. 2016;31:951–960. doi: 10.1007/s00384-016-2509-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 71.Pelvic drainage for anterior resection revisited: use of drains in anastomotic leaks. Tsujinaka S, Kawamura YJ, Konishi F, Maeda T, Mizokami K. ANZ J Surg. 2008;78:461–465. doi: 10.1111/j.1445-2197.2008.04535.x. [DOI] [PubMed] [Google Scholar]
- 72.Risk factors for anastomotic failure after total mesorectal excision of rectal cancer. Peeters KC, Tollenaar RA, Marijnen CA, et al. Br J Surg. 2005;92:211–216. doi: 10.1002/bjs.4806. [DOI] [PubMed] [Google Scholar]
- 73.To drain or not to drain extraperitoneal colorectal anastomosis? A systematic review and meta-analysis. Rondelli F, Bugiantella W, Vedovati MC, et al. Colorectal Dis. 2014;16:0–42. doi: 10.1111/codi.12491. [DOI] [PubMed] [Google Scholar]
- 74.Drainage or nondrainage in elective colorectal anastomosis: a systematic review and meta-analysis. Karliczek A, Jesus EC, Matos D, Castro AA, Atallah AN, Wiggers T. Colorectal Dis. 2006;8:259–265. doi: 10.1111/j.1463-1318.2006.00999.x. [DOI] [PubMed] [Google Scholar]
- 75.To drain or not to drain infraperitoneal anastomosis after rectal excision for cancer: the GRECCAR 5 randomized trial. Denost Q, Rouanet P, Faucheron JL, et al. Ann Surg. 2017;265:474–480. doi: 10.1097/SLA.0000000000001991. [DOI] [PubMed] [Google Scholar]
- 76.Do we really know why colorectal anastomoses leak? Shogan BD, Carlisle EM, Alverdy JC, Umanskiy K. J Gastrointest Surg. 2013;17:1698–1707. doi: 10.1007/s11605-013-2227-0. [DOI] [PubMed] [Google Scholar]
- 77.Antibiotic protection of colon anastomoses. Cohn IJ, Rives JD. Ann Surg. 1955;141:707–717. doi: 10.1097/00000658-195505000-00016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 78.Healing of ischemic colonic anastomoses in the rat: role of antibiotic preparation. Cohen SR, Cornell CN, Collins MH, Sell JE, Blanc WA, Altman RP. https://pubmed.ncbi.nlm.nih.gov/3983820/ Surgery. 1985;97:443–446. [PubMed] [Google Scholar]
- 79.Collagen degradation and MMP9 activation by Enterococcus faecalis contribute to intestinal anastomotic leak. Shogan BD, Belogortseva N, Luong PM, et al. Sci Transl Med. 2015;7:286. doi: 10.1126/scitranslmed.3010658. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 80.Proceedings of the first international summit on intestinal anastomotic leak, Chicago, Illinois, October 4-5, 2012. Shogan BD, An GC, Schardey HM, et al. Surg Infect (Larchmt) 2014;15:479–489. doi: 10.1089/sur.2013.114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 81.Anastomotic leak after colorectal cancer surgery - risk factors in 21th century. Jasarovic D, Stojanovic D, Mitrovic N, Stevanovic D. https://www.jbuon.com/archive/25-5-2199.pdf. J BUON. 2020;25:2199–2204. [PubMed] [Google Scholar]
- 82.The effect of diets delivered into the gastrointestinal tract on gut motility after colorectal surgery-a systematic review and meta-analysis of randomised controlled trials. Hogan S, Steffens D, Rangan A, Solomon M, Carey S. Eur J Clin Nutr. 2019;73:1331–1342. doi: 10.1038/s41430-019-0474-1. [DOI] [PubMed] [Google Scholar]
- 83.A randomized controlled trial evaluating early versus traditional oral feeding after colorectal surgery. Dag A, Colak T, Turkmenoglu O, Gundogdu R, Aydin S. Clinics (Sao Paulo) 2011;66:2001–2005. doi: 10.1590/S1807-59322011001200001. [DOI] [PMC free article] [PubMed] [Google Scholar]