Total mesorectal excision (TME), often combined with neoadjuvant treatment is standard of care for curative rectal cancer treatment [1, 2]. The introduction of minimally invasive techniques reduced morbidity, infection rates and length of postoperative hospital stay [3, 4]. When possible, a sphincter-saving procedure is performed with an anastomosis to regain bowel continuity after resection.

Anastomotic leakage after a sphincter-saving procedure is a serious complication associated with severe morbidity [5]. It is a common complication, with an incidence up to 20% [5, 6]. Moreover, it predisposes rectal cancer patients to worse oncological outcomes [7]. Treatment of anastomotic leakage can result in anastomotic take-down with permanent stoma rates of 20%, associated with a significant impact on quality of life [8].

Construction of a temporary loop ileostomy during sphincter-saving TME surgery is a well-known procedure. A diverting stoma does not decrease the risk of anastomotic leakage. However, it might reduce clinical anastomotic leakage and reoperation rates [9, 10]. As a disadvantage a diverting ileostomy itself can induce significant discomfort, morbidity and impact on quality of life [8, 11, 12]. Stoma-related complications such as dermatitis, stoma dysfunction or high output stoma occur in more than half of the cases and result in more hospital admissions [11]. Moreover, patients have to go through a second surgery for stoma closure, which is associated with significant risks and morbidity as well [11]. All these stoma-related issues are associated with increased treatment costs [13].

Taking the above into account, routine diversion is increasingly debated. Already, there seems to be a large variation in the selection of patients who will receive a diverting stoma where surgeons’ preference and patient- and tumour related factors seem to play a role [14]. A temporary loop ileostomy is constructed in 76% of patients undergoing a TME, varying from 0 to 100% between centres [14]. Finally, a significant proportion of the diverting stomas are never closed [15]. Sometimes a secondary stoma is constructed after reversal and construction of a diverting ileostomy might even increase the risk of a permanent stoma [16, 17].

Most previous studies focussed on the impact of diversion on anastomotic leakage and several studies have assessed the efficacy of high selective diversion only, instead of routine diversion [18,19,20]. Unfortunately, only a few studies concentrated on the high numbers of stoma-related complications and the risk of a permanent stoma after loop ileostomy construction [8, 11, 12]. Therefore, the aim of this study is to gain in depth insight in the clinical consequences of a diverting ileostomy after TME with primary anastomosis for rectal cancer with respect to stoma rate at one year and stoma-related morbidity.

Materials and methods

Study design and patients

A retrospective multicentre cohort study was performed in eleven hospitals in the Netherlands. A study protocol was composed prior to initiation of the study and approved by the MEC-U medical ethics committee (AW 9.023/W18.100) and by the local boards of all participating hospitals.

All patients of 18 years old or older, diagnosed with histologically proven rectal cancer and operated between January 2015 and December 2017 were included. Excluded from analysis were patients without construction of a primary anastomosis, with sigmoidal tumours according to the sigmoidal take-off definition [21], with recurrent rectal cancer, with presence of multiple colonic tumours, that underwent transanal endoscopic microsurgery (TEM) or with construction of an end colostomy. Neoadjuvant treatment was administered, when deemed necessary according to the Dutch national guidelines [22]. No adjuvant therapy was administered, according to the Dutch guidelines. Each of the eleven participating hospitals performed at least 40 procedures per year, performing either laparoscopic, robot-assisted or transanal TME. Construction of a diverting ileostomy was based on the attending surgeon’s choice. All patients were treated according to local multidisciplinary enhanced recovery after surgery (ERAS) protocols, when possible. Stoma reversal was planned within a few months after primary surgery, based upon the hospitals’ local protocol. All patients had follow-up carried out according to the Dutch National Guidelines for Colorectal Cancer for a period of 5 years.

Data were derived from the Dutch Colo Rectal Audit (DCRA) [23]. Data not captured in this nationwide audit were completed using the local electronic medical record (EMR). Any missing variables were added to the database by one of the researchers using the EMR, including: location of the tumour on MRI, details on type of operation, anastomosis, intra-operative complications, postoperative complications, stoma-related complications and details on stoma reversal and reversal related complications. Patients were pseudo anonymised before consulting the EMR for data collection. All data were collected between January and April 2020 and stored in the data management system CASTOR.

A comparison was made between patients with or without diverting ileostomy construction during primary surgery. Subgroup analysis was performed for patients with anastomotic leakage. Univariate logistic regression followed by multivariate logistic regression with respect to patient and tumour related factors was performed for morbidity rates within 30 days, anastomotic leakage rates and stoma rate at one year postoperatively.

Outcomes and definitions

Baseline characteristics included were: age, sex, body mass index (BMI), ASA classification (American Society of Anesthesiologists), tumour height from the anorectal junction (ARJ) in centimetres based on pre-treatment MRI, tumour height based on pre-treatment MRI according to criteria from “The English National Low Rectal Cancer Development Programme”(LOREC) [24], clinical TNM staging based on MRI, mesorectal fascia (MRF) involvement on MRI, administration of pre-operative (chemo)radiation therapy, type of surgery, intra-operative details on stapled or hand sewn anastomosis, presence of intra-operative complications, conversion to laparotomy and operating time in minutes. Length of initial hospital stay was defined as the number of postoperative days during initial admission. Complications related to primary surgery were categorised according to Clavien-Dindo [25]. All reinterventions and readmissions within 30 days were scored. Stoma-related complications after 30 days were scored if they required any readmission.

Anastomotic leakage was defined as anastomotic dehiscence or intra-abdominal abscess adjacent to the anastomotic site, requiring radiological or surgical intervention during follow-up. Anastomotic leakage was graded according to the need for intervention, based on the definition of the International Study Group of Rectal Cancer (ISGRC) [26]. Grade A requires no change of management, grade B requires intervention other than relaparotomy and grade C requires relaparotomy. A secondary ileostomy was defined as a stoma constructed during a second procedure.

Primary endpoint was the overall stoma rate at one year, which included the presence of any type of stoma one year after primary surgery. Secondary endpoints were the overall morbidity rate within 30 days, the rate of anastomotic leakage and stoma reversal related morbidity.

Statistical analysis

Data of categorical variables were presented as numbers (%). Data of continuous variables were presented as mean (standard deviation) or median [interquartile range] depending on the type of distribution. Comparison of categorical data was done using a Chi-square test, or Fishers exact test. Comparison of continuous data between groups was done using a T-test in case of a normal distribution or Mann–Whitney-U test in case of a non-normal distribution. After univariate logistic regression, multivariate logistic regression was performed using backward selection. For anastomotic leakage grade C propensity score adjusted multivariate regression was performed because of low incidence of the primary outcome, and subsequent suspected problems with overfitting. For anastomotic leakage rate and complications within 30 days rate, univariate analysis was performed for sex, age, BMI, ASA, distance from ARJ on MRI, neoadjuvant treatment, conversion and intra-operative complications. For stoma rate at one-year follow-up, univariate analysis was performed for sex, age, BMI, ASA, distance from ARK on MRI, neoadjuvant treatment, conversion, intra-operative complications, cTNM stage and anastomotic leakage. All statistical analyses were carried out using SPSS Statistics version 24 (IBM, Chicago, IL, USA).

Results

A total of 1834 patients were registered in the DCRA between 2015 and 2017 in the participating hospitals. A total of 595 underwent sphincter-saving TME surgery for rectal cancer and met the inclusion criteria. In 353 patients (59.3%) a diverting ileostomy was constructed at primary surgery. An overview can be seen in the flow diagram (Fig. 1). The hospitals’ unadjusted proportion of diverting ileostomy construction varied from 7.1 to 83.0% (supplementary Fig. 1).

Fig. 1
figure 1

Flowchart

Characteristics

Comparing the ileostomy group to the non-ileostomy group, the ileostomy group had more male patients in the ileostomy group (68.3% vs 56.2%, p = 0.003), more MRI-defined low rectal cancers (43.9% vs 36.8%, p = 0.010), more cT3-4 tumours (p < 0.001), more neoadjuvant (chemo)radiation therapy administered (75.6% vs 38.4%, p < 0.001), and less cN0 stage (34.3% vs 61.6%, p < 0.001). Median length of follow-up was longer in the ileostomy group than in the non-ileostomy groups (38[46–48] vs 36[24–45] months, p = 0.019). Table 1 provides an overview of all characteristics of both groups.

Table 1 Characteristics

Thirty-day morbidity

Table 2 shows an overview of the morbidity within 30 days postoperatively in both groups. Thirty-day morbidity rates were significantly higher in the ileostomy group than in the non-ileostomy group (56.1% vs 37.6%, p < 0.001). This was confirmed in a multivariate logistic regression analysis, after correction for sex and tumour distance from ARJ (OR 2.037(95%CI 1.434–2.892), p < 0.001), see Supplementary Table 1. Severe complications (Clavien-Dindo grade III or higher) were less frequently seen in the ileostomy group (39.7 vs 61.5%, p = 0.001) and median days of ICU admission was shorter in the ileostomy group (1[1, 2] vs 1[1], p = 0.046). The overall surgical complication rate was higher in the ileostomy group (42.8% vs 27.7%, p < 0.001), with the presence of ileus having the highest incidence in the ileostomy group (24.1% vs 8.3%, p < 0.001). Moreover, more readmissions within 30 days occurred in the ileostomy group (20.1% vs 11.2%, p = 0.003) and median length of hospital stay in days was longer (7[5–15] vs 5[4–7], p < 0.001).

Table 2 Morbidity

Stoma-related morbidity

Table 3 shows an overview of the stoma-related morbidity in both groups. In the non-ileostomy group 43 patients (17.8%) had secondary ileostomy construction. At four weeks postoperatively, 96.6% had a stoma in the ileostomy group and 15.3% of patients had a stoma in the non-ileostomy group (p < 0.001). The rate of stoma-related complications within 30 days was 45.5% in the ileostomy group and 6.6% in the non-ileostomy group (p < 0.001). Stoma-related complications during the remaining follow-up were 20.5% in the ileostomy group, 3.4% of them underwent stoma-related interventions. In the non-ileostomy group 17.8% had a secondary stoma at any time point during the first year.

Table 3 Stoma-related morbidity

Stoma rate at one year

At one year postoperatively, 18.7% of the patients in the ileostomy group and 9.9% of the patients in the non-ileostomy group had a stoma (p = 0.003). This difference in stoma rate at one year was maintained after a multivariate logistic regression analysis with correction for sex, age and anastomotic leakage (OR 2.563 (95%CI 1.424–4.611), p = 0.002), as can be seen in supplementary Table 1. Figure 2 shows the presence of stoma during one year follow-up in both groups.

Fig. 2
figure 2

Presence of a stoma during one-year follow-up Non-ileostomy group, Ileostomy group

Anastomotic leakage

The overall rate of anastomotic leakage did not differ between groups (17.3% in the ileostomy group and 17.8% in the non-ileostomy group, p = 0.913), see Table 2. Table 4 gives an overview of a subgroup analysis of the morbidity after anastomotic leakage in 104 patients. The rate of grade B leakage was higher in the ileostomy group than in the non-ileostomy group (49.2% vs 14%, p < 0.001). Grade C leakage rate was lower in the ileostomy group compared to the non-ileostomy group (29.5% and 76.7% of all leakages, respectively, p < 0.001). This was confirmed by a multivariate analysis after correction for sex, tumour distance from ARJ and neoadjuvant therapy [OR 0.263 (95%CI 0.138–0.505), p < 0.001], see supplementary Table 1. In all patient in the non-ileostomy group with a grade C leakage a stoma was constructed during reoperation. In 25 out of 33 (75.8%) of these patients an ileostomy was constructed. The others required direct take-down of the anastomosis.

Table 4 Subgroup analysis of anastomotic leakage

The median duration between primary surgery and diagnosis of anastomotic leakage was 5[3–11] days in the non-ileostomy group and 12[7–32] days in the ileostomy group (p < 0.001). More late leakages after four weeks were seen in the ileostomy group (24.6% vs 4.7%, p = 0.007). Leakage rate at four weeks was 13.0% in the ileostomy group and 16.9% in the non-ileostomy group (p = 0.185). Leakage rate at one year was 15.9% in the ileostomy group and 16.8% in the non-ileostomy group (p = 0.540). Univariate and multivariate analysis showed no impact of ileostomy on the anastomotic leakage rate (OR 0.737(95%CI 0.460–1.180), p = 0.204), see supplementary Table 1. At 1 year postoperatively, the rate and type of stoma did not differ between the two groups of patients with anastomotic leakage. At 1 year, 20.9% of the patients with an anastomotic leakage in the non-ileostomy group and 19.7% of the patients with an anastomotic leakage in the ileostomy group had an end-colostomy (p = 0.676).

Morbidity after stoma reversal

A total of 347 patients (87.4%) had undergone stoma reversal. In the ileostomy group, 322 out of 353 patients (91.7%) had their bowel continuity restored. In the non-ileostomy group, 25 out of 46 patients (54.3%) who had a secondary ileostomy had undergone stoma reversal. After stoma reversal, 62 patients (17.9%) had postoperative complications of which ileus was the most common complication (7.8%). Wound infection rate was 1.4%. Median time to reversal in months was longer in patients who had a secondary ileostomy compared to those who received an ileostomy during primary surgery (6[4–11] vs 3[2–4], p < 0.001). Thirty-four patients (9.9%) developed an incisional hernia at the previous stoma site for which 41.2% underwent surgical treatment. A new stoma was constructed after reversal in 35 cases (10.1%). The most common type of new stoma after reversal was end colostomy in 21 patients (60%). The most common reason for new stoma after reversal was anastomotic leakage at the colorectal anastomosis in 11 patients (31.4%). Table 5 shows an overview of morbidity after stoma reversal.

Table 5 Stoma reversal related morbidity

Discussion

In this multicentre retrospective study, 353 patients with diverting ileostomy were compared to 242 without diverting ileostomy construction during primary TME. In the ileostomy group, 18.7% of the patients still had a stoma at one year postoperatively. In the non-ileostomy group a secondary stoma was created in 17.8% of the patients. Of these, the majority was reversed and only 9.9% of the total group had a stoma at one year postoperatively. Construction of an ileostomy at primary surgery was an independent predictor for presence of a stoma one year after surgery in a multivariate analysis. Significantly more postoperative and stoma-related morbidity was seen in the group with ileostomy construction during primary surgery. The overall rate and morbidity of anastomotic leakage was comparable between both groups, although more grade C leakages were seen in the group initially treated without ileostomy. In all the patients in the non-ileostomy group with a grade C leakage, a secondary stoma was constructed.

In most hospitals it is routine practice to construct a diverting ileostomy after a low anastomosis in rectal cancer surgery. However, a diverting ileostomy itself is related to substantial short- and long-term morbidity and therefore the advantages and disadvantages of a diverting ileostomy are debated [11, 12]. This debate results in a large variation in patient selection for diverting ileostomy construction [14]. The current data confirm that a more selective approach with proactive anastomotic leakage management might be beneficial for patients on the long-term, as was shown in previous studies [18, 19]. Routine diversion has been common practice for many years based on the idea that an ileostomy will improve the outcome of care in several ways. We would like to address several concerns that might rise at the suggestion of using a more selective approach.

First of all, critics of the selective approach suggest that the presence of an ileostomy decreases the severity of anastomotic leakage. We indeed found more severe complications (Clavien-Dindo grade 3 or higher) in the non-ileostomy group. However, the majority of these reinterventions were related to the selective diversion and active leakage management. More grade C leakage was seen in the non-ileostomy. In these cases, a secondary stoma was constructed. The more detailed subgroup analysis of patients with anastomotic leakage did not show increased severity of complications after anastomotic leakage in patients without ileostomy. Non-diverted patients do not seem to be in disadvantage in case of an anastomotic leakage. Comparable results were seen in previous studies [11, 12]. Results from a previously published Dutch cohort study showed that a high tendency towards stoma construction did not result in lower anastomotic leakage or mortality rates [14]. In accordance with the present results, Emmanuel et al. showed that although the number of reoperations after anastomotic leakage seems to be higher in patients without ileostomy, patients with an ileostomy generally require more reoperations, including planned stoma reversal [27]. With respect to the incidence of anastomotic leakage rates, the groups in the current study did not differ and anastomotic leakages rates matches those observed in previous studies [6, 28, 29]. In fact, more late leakages were seen in patients with a primary ileostomy. This is in agreement with Borstlap et al. who also showed that the diagnosis of leakage is delayed in presence of a diverting stoma [6]. Early detection and intervention for anastomotic leakage might improve the anastomotic healing rates [6, 18] and does not have an impact on oncological outcome [30]. This is more likely to succeed in absence of an ileostomy [30]. Instead of diminishing the consequences of an anastomotic leakage, delaying the diagnosis of an anastomotic leakage might actually be an important disadvantage of a diverting stoma.

Secondly, surgeons in favour of routine diversion might also claim that patients who develop anastomotic leakage might be at risk of losing the anastomosis in case of anastomotic leakage [8]. The present study however, did not show a higher anastomotic takedown rate after anastomotic leakage in the group without ileostomy. The one-year stoma rate after anastomotic leakage was comparable. In both groups about 30% end up with a loop ileostomy after anastomotic leakage, suggesting the ileostomy is not reversed after anastomotic leakage. This is in line with previous studies [10]. Interestingly, current data suggest the rate of patients with a stoma at one year was higher in the ileostomy group. Although a diverting stoma is intended to be restored, up to 20% of all patients end up with a permanent stoma. These results match those of previous studies, showing that the construction of a diverting ileostomy itself is an independent risk factor for a permanent stoma [16, 17, 31]. A logical explanation for this might be that the presence of an ileostomy is a confounder, as this group might have more advanced tumor stage and received more neoadjuvant therapy. There was a higher rate of neoadjuvant therapy administration in the ileostomy group. Indeed, neoadjuvant therapy is an independent risk factor for non-reversal of a secondary stoma [6, 15, 17]. However, in our study construction of a stoma during primary surgery was an independent risk factor for presence of a stoma at one year, even after correction for sex, age, anastomotic leakage and neoadjuvant therapy in a multivariate analysis. The increased risk of a permanent stoma after ileostomy construction during primary surgery is a clinically important problem as it exposes patients to long-term stoma related morbidity and the associated impact on quality of life [8].

Finally, other effects of a diverting ileostomy should also be considered, such as the substantial stoma-related morbidity and high readmission rates [11,12,13]. Postoperative morbidity rates within 30 days postoperatively were significantly higher in patients with a diverting ileostomy and stoma-related complications were present in almost half of all patients with a diverting ileostomy. Comparable results were seen in previous studies, confirming that the diverting ileostomy itself is associated with substantial morbidity, occurring in half of the patients [11, 27]. Although the grade of severity of the morbidity seemed lower in patients with an ileostomy, the overall morbidity rates were higher in this group. Stoma-related complications are known to be distressing and embarrassing for patients and cause a major burden [32]. Moreover, the general reoperation rate is higher in patients with an ileostomy, including planned stoma reversal. Stoma reversal related morbidity was 17.9%. These results match those observed in earlier studies stating that stoma reversal comes at a high risk [11, 33]. All of above can lead to increased treatment cost beyond the initial cancer treatment [13].

The current study is unique in its size and comprehensive overview of stoma-related morbidity. All diverting stomas were ileostomies to create a more homogeneous cohort. However, the study has several limitations that should be mentioned. First of all, this is a retrospective cohort study and multiple hospitals participated in this study. Therefore, different treatment protocols for anastomotic leakage were used. Moreover, like in many non-randomized studies selection bias might be apparent. There was a tendency to construct a diverting ileostomy in patients with an estimated higher risk of postoperative complications. This is reflected by a higher rate of MRI-defined low rectal cancers, cT3-4 tumours and neoadjuvant therapy in the ileostomy group. The patient- and tumour-related case-mix factors may also be responsible for a large part of the hospital variation. However, this was corrected for in a multivariate analysis, taking known confounders into account, such as: sex, comorbidity, tumour height and the administration of neoadjuvant therapy [17]. However, other confounders like individual consideration of the surgeon cannot be accounted for in this study design. Finally, some relevant data were not studied. For example, minor stoma-related morbidity such as skin irritation and plaque leakage were not registered. These complications can be distressing, are often underestimated and might require unplanned readmissions [32]. Also, data on the total length of hospital stay for the entire treatment would be interesting [34]. However, it seems very unlikely that these extra data will strengthen the conclusion of the study even more.

In conclusion, faecal diversion through diverting ileostomy after rectal cancer surgery with primary anastomosis does not reduce the anastomotic leakage rate or the morbidity caused by anastomotic leakage. On the contrary, the morbidity related to the presence and reversal of a diverting ileostomy is substantial. Furthermore, the stoma rate at one year was higher in patients who received a diverting ileostomy during primary surgery. A secondary ileostomy does not seem to hamper clinical outcomes. Future research should focus on early detection of anastomotic leakage and possible treatment options. A more selective approach to diversion could result in reduced stoma-related morbidity and stoma reversal related morbidity [18, 19]. In theory, this could lead to better quality of life and lower treatment costs [34]. Selective diversion might be safe and feasible [18, 19] and should be evaluated further, taking cost-effectivity into account.