key: cord-0831883-m0zu8nvh
authors: Podda, Mauro; Coccolini, Federico; Gerardi, Chiara; Castellini, Greta; Wilson, Michael Samuel James; Sartelli, Massimo; Pacella, Daniela; Catena, Fausto; Peltrini, Roberto; Bracale, Umberto; Pisanu, Adolfo
title: Early versus delayed defunctioning ileostomy closure after low anterior resection for rectal cancer: a meta-analysis and trial sequential analysis of safety and functional outcomes
date: 2022-02-21
journal: Int J Colorectal Dis
DOI: 10.1007/s00384-022-04106-w
sha: 3cb72063c63f2cfe731ee217633aaa10aeeac86d
doc_id: 831883
cord_uid: m0zu8nvh

PURPOSE: We performed a systematic review and meta-analysis with trial sequential analysis (TSA) to answer whether early closure of defunctioning ileostomy may be suitable after low anterior resection. METHODS: MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials were searched, up to October 2021, for RCTs comparing early closure (EC ≤ 30 days) and delayed closure (DC ≥ 60 days) of defunctioning ileostomy. The risk ratio (RR) with 95% CI was calculated for dichotomous variables and the mean difference (MD) with 95% CI for continuous variables. The GRADE methodology was implemented for assessing Quality of Evidence (QoE). TSA was implemented to address the risk of random error associated with sparse data and/or multiple testing. RESULTS: Seven RCTs were included for quantitative synthesis. 599 patients were allocated to either EC (n = 306) or DC (n = 293). EC was associated with a higher rate of wound complications compared to DC (RR 2.56; 95% CI 1.33 to 4.93; P = 0.005; I(2) = 0%, QoE High), a lower incidence of postoperative small bowel obstruction (RR 0.46; 95% CI 0.24 to 0.89; P = 0.02; I(2) = 0%, QoE moderate), and a lower rate of stoma-related complications (RR 0.26; 95% CI 0.16 to 0.42; P < 0.00001; I(2) = 0%, QoE moderate). The rate of minor low anterior resection syndrome (LARS) (RR 1.13; 95% CI 0.55 to 2.33; P = 0.74; I(2) = 0%, QoE low) and major LARS (RR 0.80; 95% CI 0.59 to 1.09; P = 0.16; I(2) = 0%, QoE low) did not differ between the two groups. TSA demonstrated inconclusive evidence with insufficient sample sizes to detect the observed effects. CONCLUSION: EC may confer some advantages compared with a DC. However, TSA advocated a cautious interpretation of the results. PROSPERO REGISTER ID: CRD42021276557 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00384-022-04106-w.

Low anterior resection (LAR) with total mesorectal excision is considered the optimal surgical treatment for resectable primary rectal cancer [1, 2] . However, anastomotic leakage (AL) remains the most feared complication after LAR [3] , with an incidence of 3 to 25% [4] .

In order to protect the colorectal anastomosis and reduce the severity of pelvic sepsis associated with AL, a reversible faecal diversion through a temporary defunctioning ileostomy is usually fashioned during LAR [5] [6] [7] [8] [9] , especially for patients at increased risk for AL, such as those with locally advanced tumours, located in the low rectum, and treated with neoadjuvant radiotherapy [10] [11] [12] .

Defunctioning ileostomies are typically reversed after a time interval of 8-12 weeks, during which time 20 to 74% of patients will experience ileostomy-related complications [13] [14] [15] [16] .

As the incidence of stoma-related complications seems to increase with the time to ileostomy closure [17] , it has been suggested that early ileostomy closure could reduce the length of exposure to stoma-related morbidity, improve quality of life, and reduce stoma-related costs, with no detriment to the integrity of the colorectal anastomosis [18] [19] [20] .

Some recent meta-analyses have suggested that early ileostomy closure is effective and safe in selected patients [21] [22] [23] [24] . However, others reported that early closure increased the rate of post-operative complications [25] . Similarly, several randomised controlled trials (RCTs) have reported promising results [18, [26] [27] [28] [29] , whereas other RCTs had to be prematurely terminated due to safety concerns [30, 31] . Over the last year, a new RCT has been published that has provided further evidence concerning the safety and feasibility of early closure of defunctioning ileostomy, which has not been included in any of the systematic reviews published to date [30] .

Given the above, we decided to perform an updated systematic review and meta-analysis with trial sequential analysis (TSA) to answer whether early closure of temporary diverting ileostomy is suitable for selected patients without post-operative complications after LAR.

We performed a systematic review and meta-analysis with TSA of RCTs with the aim to systematically review the currently available evidence on early defunctioning ileostomy closure (≤ 30 days after index operation, EC) in patients who underwent LAR for rectal cancer in terms of safety, long-term functional outcomes and costs, and to compare the above with delayed timing of ileostomy closure (> 60 days after index operation, DC) using the meta-analytic method and The Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach [32] .

This meta-analysis was conducted according to the recommendations of the 2020 updated Preferred Reporting Items for Systematic reviews and Meta-analyses (PRISMA) guidelines [33] and the Cochrane Handbook for Systematic Reviews of Interventions [34] .

All stages of study identification, selection, quality assessment, and data extraction were performed independently by two reviewers (MP and AP). Inconsistencies were resolved through discussion between the two reviewers until a consensus was reached. This meta-analysis adheres to AMSTAR II criteria (A MeaSurement Tool to Assess Systematic Reviews) [35] .

The clinical question according to the PICOS framework was:

• (P) Population: patients with temporary defunctioning ileostomy after LAR for rectal cancer. • (I) Intervention: early ileostomy closure (EC); ≤ 30 days after ileostomy was performed. • (C) Comparison: delayed ileostomy closure (DC); ≥ 60 days after ileostomy was performed. • (O) Outcomes, as reported in the included studies:

intraoperative and post-operative outcomes of safety and feasibility; functional outcomes; quality of life. • (S) Studies: RCTs comparing the two approaches.

The following studies were excluded: emergency ileostomy in case of AL, ileostomy performed during other types of surgery other than LAR for cancer, studies that involved paediatric patients (< 18 years of age), studies that included other types of enteral stomas such as colostomy, proximal/mid small bowel stomas, or where the type of stoma was not specified, systematic or narrative reviews, meta-analyses, abstracts, case reports, study protocols, non-human studies, non-comparative studies. In addition, studies in which closure time was influenced by factors (i.e. chemotherapy, the occurrence of complications after LAR, delays due to operating theatre unavailability) other than patient's randomisation and allocation into a predefined study group were excluded.

MEDLINE (via PubMed), EMBASE, and the Cochrane Central Register of Controlled Trials were systematically searched for any relevant human clinical study comparing EC and DC of defunctioning ileostomy after LAR for rectal cancer. Grey literature searches were conducted on ClinicalTrials.gov, Google Scholar, CORE, Grey Literature Report, and Open Grey. Reference lists of relevant studies were searched manually, and the "related articles" function in PubMed was used. In addition, the reference list from the selected articles was also scrutinised. The search strategy combined medical subject headings (MeSH) and keywords, using the terms of "Ileostomy", "Defunctioning stoma", "Early", "Closure", "Reversal", "Proctectomy", "Low Anterior Resection", "Rectal Cancer", and "Colorectal Cancer". The detailed search strategy is accessible in the registered protocol (PROS-PERO: CRD42021276557). No restrictions were placed on publication status or language. Full-text articles in languages other than English with a title/abstract indicating fulfilment of the eligibility criteria were translated electronically. Literature was searched from inception to October 31, 2021.

The studies identified by the search strategy were subsequently selected based on title, abstract, and full-text review by two independent reviewers (MP and AP) in Rayyan web app for systematic reviews (https:// www. rayyan. ai/).

RCTs comparing EC (Intervention) and DC (Control) as the most appropriate timing for ileostomy reversal after LAR for rectal cancer were included in the meta-analysis. Whenever there was an overlap in patient cohorts of two or more studies, and no difference in the study period was reported, the most recent report was included in the pooled analysis. Secondary analyses from the included RCTs were also included if they focused on outcomes other than those analysed in the primary study.

A double-blinded procedure was performed to increase the accuracy of the data extracted, which resulted in high and satisfactory inter-observer agreement (Kappa = 0.92).

The following individual data were independently extracted using standardised extraction forms (Excel 2019, Microsoft Corporation®). Demographic and baseline characteristics collected for each report included the following predefined data: (1) study identifier (first author, nationality, year of publication, clinical trials centres, study period, inclusion criteria, exclusion criteria, index operation, intervention, comparator, analysed outcomes, follow-up times); (2) baseline characteristics of the enrolled patients (sex, Age, BMI, comorbidities, type of surgery and technique of primary anastomosis construction, indication for colorectal resection, neoadjuvant therapy); (3) clinical outcomes (post-operative morbidity, mortality, leak of rectal or ileal anastomosis, unplanned reoperations, operative time, post-operative length of hospital stay, time to start chemotherapy); (4) morbidity outcomes analysis (Clavien-Dindo complications ≥ 3, post-operative ileus/small bowel obstruction, wound complications, post-operative intra-abdominal abscess, post-operative enterocutaneous fistula, bleeding, stoma-related complications, anastomotic stenosis, other medical complications, hospital readmission); (5) quality of life, functional outcomes, and costs (Gastrointestinal Quality of Life Index (GQLI), EORTC QLQ-C30 Quality of Life, low anterior resection syndrome, Memorial Sloan Kettering Cancer Centre Bowel Function Instrument).

The following primary outcomes were analysed:

• Overall post-operative morbidity: defined as any complication occurring during the hospital stay, within 30 days, or 12 months after ileostomy closure.

The following secondary outcomes were analysed: Anastomotic leak was defined as any leak from the rectal anastomosis detected clinically and/or radiologically, including intra-abdominal abscess, enterocutaneous fistula, and anastomotic insufficiency [36] . Stoma-related complications were defined as the presence of any complications attributable to the presence of the ileostomy (i.e. dermatitis, parastomal infection, dehydration from high stoma output, renal insufficiency, stenosis, retraction, necrosis, prolapse, skin irritation, parastomal hernia) occurring between the index operation and stoma closure [37] .

Variables for meta-analysis were considered if they were reported by at least two RCTs. All statistical analyses were performed using Reviewer Manager software (Reviewer Manager -RevMan -version 5.4.1, Sept. 2020, The Nordic Cochrane Centre, Cochrane Collaboration, www. train ing. cochr ane. org) and RevMan Web 2020 [38]. The relative risk (RR) with 95% confidence interval (95% CI) was calculated for dichotomous variables and the mean difference (MD) with 95% CI for continuous variables. The point estimate of the RR value was considered statistically significant if the 95% CI did not cross the value at null hypothesis (RR = 1). The point estimate of the MD value was considered statistically significant if the 95% CI did not cross the value at null hypothesis (MD = 0). Statistical heterogeneity of the results across studies was assessed using the Higgins inconsistency index I 2 and Chi-square test. A Chi-square test P < 0.10 and an I 2 value of 50 to 90% were considered indicative of substantial heterogeneity. In addition to statistical heterogeneity, both clinical (variability in the baseline characteristics of the patients, interventions and outcomes studied) and methodological (variability in the study methods and risk of bias) heterogeneity were considered to inform the decision to use the fixed-or random-effects model. Fixed-effects model (Mantel-Haenszel) was used if substantial heterogeneity was absent, whereas a random-effects model was implemented for meta-analysis if substantial heterogeneity was found, according to the method of DerSimonian and Laird [39] . The analyses were performed using the Trial Sequential Analysis software version 0.9.5.10 Beta (The Copenhagen Trial Unit, Centre for Clinical Intervention Research, The Capital Region, Copenhagen University Hospital -Rigshospitalet, 2021).

The TSA was performed to address the risk of random error associated with sparse data and/or multiple testing which can affect cumulative meta-analysis analyses, and to assess whether further trials need to be conducted [40] . Indeed, the TSA can inform regarding how much more information is required to get a conclusive answer about the effect of the intervention versus its comparator and this is represented by the distance between the accrued information and the required information. We applied the TSA on the following patient-centred dichotomous outcomes, which are relevant for clinical practice due to their consequences for patient management, and are the most frequently reported in the literature: post-operative morbidity as the primary outcome, leak of rectal anastomosis, and unplanned reoperations as secondary outcomes.

We estimated the diversity-adjusted required information size (DARIS) based on the proportion of patients with an outcome in the control group, calculating the average control group event proportion, an alpha (type I error) of 5%, a beta (type II error) of 20%, and diversity modelbased. Both the naïve and TSA-adjusted confidence intervals were reported. We set the conservative trial monitoring boundaries by Lan-DeMets-O'Brien-Fleming as the α-spending function [41, 42] . We calculated the cumulative Z-curve (the series of Z-statistics after each consecutive trial) of each cumulative meta-analysis and plotted it against the above monitoring boundaries according to the random-effects models. The crossing of the cumulative Z-curve into the trial sequential monitoring boundary for benefit indicates that a sufficient level of evidence has been reached, and no further trials may be needed to demonstrate the superiority of the intervention. Otherwise, when the cumulative Z-curve does not cross any of the trial sequential monitoring boundaries, there is likely insufficient evidence to reach a conclusion, and additional trials may be required [43] .

We developed two scenarios according to two different risk ratio reduction (RRR) values. Scenario 1 was based on RRR values pragmatically chosen to represent a conservative intervention effect: 10% for post-operative morbidity outcome, 1% leak of rectal anastomosis, 5% unplanned reoperations [21] [22] [23] [24] [25] 44] . Scenario 2 represented a sensitivity analysis where an RRR of 25% was chosen to represent an optimistic intervention effect for all outcomes. The results are presented as the TSA figures with corresponding legends and interpretations.

Sensitivity analyses of post-operative morbidity and other clinically relevant outcomes were performed, depending on:

• The different primary bowel diseases (rectal cancer versus rectal cancer plus others); • Depending on some concerns of bias according to the ROB-2 evaluation.

Furthermore, given that substantial differences in clinical settings, especially regarding the timing of stoma closure within the EC group, the effect of the timing of EC for all outcomes was analysed by a subgroup analysis of very early closure (defined as closure ≤ 14 days), early closure (defined as closure between 15 and 30 days), in comparison with DC (defined as closure ≥ 60 days).

The risk of bias of the included RCTs was independently assessed by two authors (MP and AP) using the Cochrane Risk of Bias Tool version 2 (RoB 2) [45] . In addition, the Grading of Recommendations Assessment, Development and Evaluation (GRADE) methodology was implemented for assessing the quality of evidence (QoE) [46, 47] , which was reported in the results with Summary of Findings Tables.

A total of 455 records were identified through database searching. Seven more references were identified by searching lists of retrieved studies. After removing 163 duplicates and four study protocols of ongoing studies, 288 records had their titles and abstracts evaluated. This resulted in 39 articles suitable for full-text review, where ten were retrospective studies, four were prospective non-randomised studies, eight included colostomy closure procedures, five had no comparative cohort, and one did not focus on the selected outcomes of interest. Finally, 11 RCTs were included for quantitative synthesis, of which seven were primary studies [18, [26] [27] [28] [29] [30] [31] and four were secondary analyses of the primary RCTs [48] [49] [50] [51] (Table 1 ). In total, 599 patients were allocated to either Early ileostomy closure (EC) (n = 306) or Delayed ileostomy closure (DC) (n = 293). General patient characteristics of the patients as reported in the studies are shown in Supplementary Table 1. Supplementary Table 2 shows the evidence report of each included study. Figure 1 reports the flow diagram of the study selection phases and reported excluded reasons for full texts not being eligible.

Considerable variability was found among the included studies concerning the definition and the time frame of EC and DC. Some studies defined EC as the closure of the stoma within 8 days after LAR [18, 26] , whereas in others, patients allocated to EC had their ileostomy closed within 2 weeks of LAR [27, 28] . Delay until stoma closure in the EC group was 17 days in the study by Klek et al. [29] and 15 days in the study by Elsner et al. [30] . Finally, in the study by Bausys et al. patients in the EC group had undergone stoma closure 30 days after creation [31] . Significant heterogeneity also existed in terms of delay until ileostomy closure in the DC group, with timing for closure that varied between 57 [26] and 278 days [29] after stoma creation. Most studies included patients with rectal cancer as the sole indication for LAR. Two studies [18, 26] included benign, borderline, and inflammatory bowel diseases. Different follow-up times were reported, ranging from 30 days [31] to 12 months [18, 27] . Two RCTs were prematurely terminated for safety reasons [30, 31] .

No statistically significant difference was found between the two groups in terms of overall postoperative morbidity (7 studies, 599 patients; RR 0.99, 95% CI 0.78 to 1.78; P = 0.95; I 2 = 37%, fixed-effects; QoE low; test for subgroup differences: Chi 2 = 5.59, P = 0.02, I 2 = 82.1%) (Fig. 2 ) (Supplementary Table 3 ).

EC and DC showed equivalent results in terms of leak of the rectal anastomosis (7 studies, 599 patients; RR 1.04; 95% CI 0.46 to 2.36; P = 0.92; I 2 = 0%, Fixed-effects; QoE low; test for subgroup differences: Chi 2 = 2.63, P = 0.11, I 2 = 61.9%) (Fig. 3) EC was associated with a higher rate of wound complications compared to DC (6 studies, 534 patients; RR 2.56; 95% CI 1.33 to 4.93; P = 0.005; I 2 = 0%, fixed-effects; QoE high; test for subgroup differences: Chi 2 = 1.67, P = 0.20, I 2 = 40.2%) (Fig. 4) , a lower incidence of postoperative small bowel obstruction (7 studies, 599 patients; RR 0.46; 95% CI 0.24 to 0.89; P = 0.02; I 2 = 0%, fixed-effects; QoE moderate; test for subgroup differences: Chi 2 = 3.08, P = 0.08, I 2 = 67.6%) (Fig. 5) , and a lower rate of stoma-related complications (5 studies, 453 patients; RR 0.26; 95% CI 0.16 to 0.42; P < 0.00001; I 2 = 0%, fixed-effects; QoE moderate; test for subgroup differences: Chi 2 = 0.05, P = 0.82, I 2 = 0%) ( Table 4 ). Table 3 ). Quantitative synthesis was not performed for either operative time or length of hospital stay due to the lack of data reported as mean and standard deviation. The Hozo method to convert median and range into mean and standard deviation [52] was not used as the data distribution in the primary RCTs might be skewed, so the approach mentioned above may not be appropriate [34] .

Costs were evaluated by Lasithiotakis et al. [26] , Klek et al. [29] , and Park et al. [49] . However, quantitative synthesis was not performed due to the high methodological heterogeneity regarding outcome metrics and settings. Table 5 ).

Time to start chemoradiotherapy was analysed by Klek et al. [29] . Mean time to start adjuvant treatment was 38.7 ± 5.7 and 33.2 ± 5.8 days in the EC and DC groups, respectively (P < 0.001) (Supplementary Table 3 ).

Two subgroup meta-analyses (very early closure, defined as closure 8 − 14 days, and early closure, defined as closure between 15 and 30 days) showed that the rate of postoperative morbidity was slightly higher in the early closure group compared to the DC group (RR 1.60; 95% CI 0.99 to 2.58; P = 0.05; I 2 = 35%, fixed-effects), although without statistical significance. Similarly, the unplanned reoperation rate showed an increased rate in the early closure group compared to the DC (RR 4.19; 95% CI 0.91 to 19.30; P = 0.07; I 2 = 0% fixed-effects). The rate of Clavien-Dindo ≥ 3 complications was lower in the very early closure group compared to the DC group (RR 0.57; 95% CI 0.34 to 0.97; P = 0.04; I 2 = 0%, fixed-effects), whereas the rate of wound complication was comparable between the early closure group and the DC group (RR 1.45; 95% CI 0.51 to 4.15; P = 0.48; I 2 = 0%, Fixed-effects).

Sensitivity analyses excluding the RCTs by Lasithiotakis et al. [26] and Alves et al. [18] that also included patients with benign disease in the study population found an equivalent rate of post-operative small bowel obstruction comparing the very early closure (8 − 14 days) and the DC groups (RR 0.64; 95% CI 0.09 to 4.76; P = 0.66; I 2 = 0%, fixed-effects). Sensitivity analyses excluding studies with some concerns of bias according to the ROB-2 evaluation found similar outcomes between the EC and DC groups in terms of overall post-operative morbidity, although in the subgroup comparison between the early closure group (15 − 30 days) and the DC group a statistically significant difference was found in favour of DC (RR 1.82; 95% CI 1.08 to 3.04; P = 0.02; I 2 = 53%, random-effects). Equivalent outcomes were also found regarding the leak of rectal anastomosis and unplanned reoperation. Wound complication rate was higher in the EC 

For post-operative morbidity, scenario 1, using an RRR of 10% and a control event rate of 29.7%, we obtained a DARIS (Diversity Adjusted Required Information Size) of 16,330 patients. The cumulative Z-curve did not surpass either the traditional monitoring boundary or the trial sequential monitoring boundaries. TSA graph was not available due to insufficient information use (3.67%). Using an RRR of 25%, scenario 2, we obtained a DARIS of 2478 patients: the cumulative Z-curve did not surpass either the traditional monitoring boundary or the trial sequential monitoring boundaries with an alpha-spending adjusted CI of 0.61-1.63.

For leak of rectal anastomosis, scenario 1, using an RRR of 1% and a control event rate of 3%, we obtained a DARIS of 10,102,024 patients. The cumulative Z-curve did not surpass either the traditional or the trial sequential monitoring boundaries. Using an RRR of 25% and a control event rate of 3%, scenario 2, we obtained a DARIS of 14,267 patients: the cumulative Z-curve did not surpass either the traditional or the trial sequential monitoring boundaries. TSA graphs were unavailable for both scenarios due to insufficient information use (< 4%).

For unplanned reoperations, scenario 1, using an RRR of 5% and a control event rate of 4%, we obtained a DARIS of 294,169 patients. The cumulative Z-curve did not surpass either the traditional or the trial sequential monitoring boundaries. TSA graph was not available due to little information use (0.19%). Using an RRR of 25% and a control event rate of 4%, scenario 2, we obtained a DARIS of 10,604 patients: the cumulative Z-curve did not surpass either the traditional or the trial sequential monitoring boundaries with an alpha-spending adjusted CI of 0.11-22.54 (Fig. 7) (Supplementary Table 6 ). 

The quality of the seven included primary RCTs was evaluated according to the Cochrane Risk of Bias Tool (RoB) version 2 (Fig. 8) . Four RCTs were considered at low risk of bias [18, 27, 30, 31] , whereas three RCTs contained some concerns [26, 28, 29] (Supplementary Table 1 ). According to the GRADE criteria, the overall QoE was high only for wound complications. It was moderate for post-operative ileus/small bowel obstruction and stoma-related complication but low for post-operative morbidity, leak of rectal anastomosis, unplanned reoperation, and Clavien-Dindo complication ≥ 3 (Fig. 9) . Potential publication bias was present for Clavien-Dindo complication ≥ 3. Funnel plots have been provided as supplemental digital content (Supp. Digit. Content Fig. 1 ).

In keeping with previous studies, the current meta-analysis with TSA of RCTs, including data of 599 patients, indicates that patients who had undergone early ileostomy closure within 30 days from LAR for rectal cancer experienced lower occurrence of small bowel obstruction and stoma-related complication but, at the same time, incur a higher rate of ileostomy closure-related wound complications [21] [22] [23] [24] [25] . Wound complications after ileostomy closure can be decreased by the implementation of evidence-based recommendations on closure techniques. As reported in the Italian guidelines for the surgical management of enteral stomas in adults, purse-string closure in stoma reversal should be the preferred skin closure technique because it is associated with lower surgical site infection rates compared to other techniques [53] . All patients undergoing enterostomy closure should receive antibiotic prophylaxis. Although various regimens have been described, oral preoperative antibiotics appear to be associated with less morbidity than parenteral antibiotics, similar to findings already reported for colon surgery [54] .

Based on the primary pooled analysis, the incidence of post-operative morbidity was similar for patients who underwent early and delayed ileostomy closure ≥ 60 days from LAR. However, the sensitivity analysis that excluded the study by Alves et al. suggested that the higher rate of wound complications in the early closure group was mainly attributable to a closure strategy within 8 days of the primary resection [18] .

The subgroup meta-analyses on very early closure (closure 8-14 days) and early closure (closure between 15 and 30 days) showed that the rate of post-operative morbidity was lower if stoma closure was performed between the 8 th and the 14 th post-operative day after the primary LAR. In contrast, patients who underwent stoma closure between the 15 th and the 30 th day were exposed to 60% increased risk of post-operative complications compared to the delayed closure. Furthermore, patients in the early ileostomy closure group had 4.2 times increased risk of a second, unplanned reoperation and a 4.6 times increased risk of a Clavien-Dindo ≥ 3 complication compared to the delayed closure group.

In synthesis, our findings suggest that the ideal timing for ileostomy closure should be approximately between days 8 and 14 after construction, provided that a satisfactory CT scan-assessed gastrografin enema or a flexible endoscopy, or both, demonstrates no signs of anastomotic insufficiency. This is based on two primary considerations: the first is that the tensile strength of an anastomosis has been shown to rapidly increase at day 5 and to exceed its initial strength at day 7, and by this time, the vast majority of anastomotic leaks will have occurred [19, 55] . The second is that severe dense adhesions around the ileostomy site tend to form after 2 weeks and up to 6 weeks post-operation [56] .

LARS is pragmatically defined as disordered bowel function leading to a detriment in quality of life after rectal resection, which encompasses the vital aspects of the patient experience [57] . The risk of developing major LARS seems higher with a defunctioning ileostomy, and a prolonged time to ileostomy closure seems to reinforce the negative effect on bowel function, suggesting that early reversal should be an essential part of the patient pathway [58] . Similarly, a subanalysis of the EASY trial showed that patients undergoing early ileostomy closure had fewer problems with soiling and fewer had a permanent stoma [50] . Regarding the analysis of functional outcomes, our meta-analysis did not show any advantages for the early ileostomy closure group in terms of quality of life and incidence of LARS. However, our findings may be hampered by small sample sizes and a high risk of imprecision.

Two years of COVID-19 pandemic have dramatically modified the usual clinical practice. Some scientific surgical societies have recommended a prudent approach towards colorectal anastomosis [59, 60] . The majority of surgical procedures have been performed for emergent or oncological reasons to the detriment of the remaining elective procedures for benign conditions. The pandemic may have caused a delay in enterostomy closure, especially in cases of patients who are candidates for adjuvant chemotherapy, with a prolonged deterioration in quality of life, an increase in number of enterostomies that will never be closed, and increased associated health care costs for the management of this new patient cohort. In this regard, a same-admission ileostomy closure strategy in selected patients [18, 26] can contribute on the one hand to reducing the burden on hospitals caused by new hospitalizations due to the presence of ileostomy-related complications, and on the other hand to guarantee a better quality of life for the patient. Also, ghost ileostomy may be a safe and cost-effective method in patients who underwent LAR with low or medium risk factors for AL [61] .

A recent meta-analysis with TSA provided "firm evidence the early closure of ileostomy reduced the incidence of small bowel obstruction and post-operative ileus and required less total operative time, but increased the incidence of surgical site infections compared with late closure of ileostomy" [22] . Though in keeping with the results of the meta-analysis by Cheng et al., our TSA was not able to reach any firm conclusion on either of the two scenarios according to different RRR: the one that represented a conservative and more realistic intervention effect and the one that represented a sensitivity analysis where an RRR of 25% was chosen to represent an optimistic intervention effect for all outcomes.

The current literature has substantial limitations, especially concerning multiple studies with small sample sizes, as highlighted in our TSA. In contrast to other systematic reviews and meta-analyses that provided more optimistic conclusions about the feasibility, efficacy, and safety of early closure of defunctioning ileostomies in selected patients without taking into account the high risk of imprecision and all the risks of drawing firm evidence based on small sample sizes [23] , we are more conservative with our conclusions. Even though our results do affirm the view that early ileostomy closure is a valid option, they should be interpreted with caution. In fact, according to the GRADE criteria, the overall quality of evidence was moderate to low for outcomes classified as "critical" in the preplanned analysis.

Further limitations of the present meta-analysis relate to relatively high inter-study heterogeneity for some of the analysed outcomes that required exploration of potential sources. The timing of intervention differed substantially in the study by Bausys et al. [31] , where the median time to early ileostomy closure after LAR was 34 days and [18, 26] . In the study by Bausys et al. which was prematurely terminated due to a high rate of post-operative morbidity in the early closure group, the authors argue that the high complication rate could be due to a greater technical difficulty of ileostomy closure at day 30, when adhesions have formed, and the inflammatory phase of cicatrisation is still active.

In order to address heterogeneity, we performed several subgroup analyses for very early ileostomy closure and two different sensitivity analyses. Sensitivity analyses excluding studies with some bias concerns according to the ROB-2 evaluation found similar outcomes between the two groups in terms of post-operative morbidity, leak of rectal anastomosis, and unplanned reoperation. Finally, although the concept of late anastomotic leak is still a matter of debate [5, 62] , delayed leak of the colorectal anastomosis may occur after the eighth post-operative day despite a negative contrast enema examination or endoscopy. For this reason, we have investigated this specific outcome by excluding the studies by Alves et al. [18] and Lasithiotakis et al. [26] in which the ileostomy was closed between the 7 th and the 8 th post-operative days in the early closure group, with the result that no difference was found between the two groups in terms of colorectal anastomotic leak.

Several large randomised trials have assessed the outcomes of laparoscopic colectomy compared to conventional open surgery [63] [64] [65] [66] . The widespread implementation of laparoscopic surgery in colorectal cancer has been associated with improved postoperative clinical outcomes, including lower blood loss and less postoperative pain, as well as fewer abdominal wall complications, without negatively affecting the oncological outcomes. Conversely, robust evidence on minimally invasive LAR remains lacking [67] [68] [69] . Appropriately in light of this, another potential limitation of our study is the lack of information on the type of surgical approach used for the rectal resection. This might have an impact on the results because, after minimal access surgery, it can be expected that adhesions around the ileostomy are less even in the early period after surgery.

This meta-analysis also has significant strengths. It only included RCTs, increasing the likelihood that estimated effects favouring early ileostomy closure for selected patients with an uneventful recovery from the rectal resection may be investigated safely in the future.

Besides the high risk of imprecision, our results should be interpreted with caution, as the patients randomized to early ileostomy closure were selected based on a set of strict criteria where the patients have a low prevalence of coexisting morbidity and have an uneventful post-operative course after rectal resection. Unfortunately, despite the completeness of the analysis, numerous doubts remain, which will be clarified by future studies with a high level of evidence. Should it be decided to transfer our results into daily clinical practice, maximum attention should be paid to carefully select patients, both regarding the general clinical status and the effective healing of the colorectal anastomosis.

Findings of this meta-analysis with TSA indicate that a narrow window of chance for early closure might exist between the 8 th and the 14 th post-operative days following LAR.

Preliminary results suggest that very early closure in selected patients is feasible in the absence of radiological or endoscopic signs of anastomotic insufficiency, and may confer some advantages compared with delayed closure after 2 months. The results of our TSA should be interpreted with caution, especially in terms of leak of the colorectal anastomosis, post-operative morbidity, and unplanned reoperations. Therefore, future research should be conducted in the context of randomized controlled trials to determine the effectiveness of early ileostomy closure definitively.

The online version contains supplementary material available at https:// doi. org/ 10. 1007/ s00384-022-04106-w.

Authors' contribution MP: study conception and design, literature search, acquisition, interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. FC: study conception and design, literature search, acquisition, interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. CG: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. GC: interpretation and analysis of data (trial sequential analysis); drafting and critically revising the article for important intellectual content; and final approval of the version to be published. MSJW: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; editing and revising the English for the final version to be published; and final approval of the version to be published. MS: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. DP: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. FC: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. RP: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. UB: interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published. AP: study conception and design, literature search, acquisition, interpretation and analysis of data; drafting and critically revising the article for important intellectual content; and final approval of the version to be published.

Data availability Template data collection forms, data extracted from included studies, data used for all meta-analyses and trial sequential analysis, and any other materials used in the present research are available on request from the corresponding author (MP).

Ethical approval No ethical approval was required for this article.

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/.

Functional outcome following rectal surgery-predisposing factors for low anterior resection syndrome

Total mesorectal excision is optimal surgery for rectal cancer: a Scandinavian consensus

Prophylactic intra-abdominal drainage following colorectal anastomoses. A systematic review and meta-analysis of randomised controlled trials

Meta-analysis of the risk for anastomotic leakage, the postoperative mortality caused by leakage in relation to the overall postoperative mortality

Different risk factors for early and late colorectal anastomotic leakage in a nationwide audit

Value of a protective stoma in low anterior resections for rectal cancer

Meta-analysis of defunctioning stomas in low anterior resection for rectal cancer

Covering ileo-or colostomy in anterior resection for rectal carcinoma

Anastomotic leaks after restorative resections for rectal cancer compromise cancer outcomes and survival

Multicenter analysis of risk factors for anastomotic leakage after laparoscopic rectal cancer excision: the Korean laparoscopic colorectal surgery study group

Risk factors for anastomotic leakage after resection of rectal cancer

Risk factors for anastomotic leakage after left-sided colorectal resection with rectal anastomosis

A temporary loop ileostomy affects renal function

Prevention of incisional hernia at the site of stoma closure with different reinforcing mesh types: a systematic review and meta-analysis

Renal impairment caused by temporary loop ileostomy

Prospective analysis of stoma-related complications

Randomized clinical trial of early versus delayed temporary stoma closure after proctectomy

Feasibility of early closure of loop ileostomies: a pilot study

Closure of small bowel stomas on postoperative day 10

Safety of early ileostomy closure: a systematic review and metaanalysis of randomised controlled trials

Early versus late preventive ileostomy closure following colorectal surgery: systematic review and meta-analysis with trial sequential analysis of randomized controlled trials

Early closure of defunctioning loop ileostomy: is it beneficial for the patient? A meta-analysis

The feasibility and safety of early ileostomy reversal: a systematic review and meta-analysis

Early versus late closure of temporary ileostomy after rectal cancer surgery: a meta-analysis

Is early reversal of defunctioning ileostomy a shorter, easier and less expensive operation?

Early closure of a temporary ileostomy in patients with rectal cancer: a multicenter randomized controlled trial

Early ileostomy closure in patients with rectal cancer. Primary results of the randomised controlled multicenter trial

Early closure of the protective ileostomy after rectal resection should become part of the Enhanced Recovery After Surgery (ERAS) protocol: a randomized, prospective, two-center clinical trial

Closure of temporary ileostomy 2 versus 12 weeks after rectal resection for cancer: a word of caution from a prospective, randomized controlled multicenter trial

Early versus standard closure of temporary ileostomy in patients with rectal cancer: a randomised controlled trial

The PRISMA 2020 statement: an updated guideline for reporting systematic reviews

2021) Cochrane handbook for systematic reviews of interventions version 6

AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both

Definition and grading of anastomotic leakage following anterior resection of the rectum: a proposal by the International Study Group of Rectal Cancer

Review Manager Web (RevMan Web). Version (1.22.0). The Cochrane Collaboration

Meta-analysis in clinical trials revisited

Trial sequential analysis may establish when firm evidence is reached in cumulative meta-analysis

A multiple testing procedure for clinical trials

Can trial sequential monitoring boundaries reduce spurious inferences from meta-analyses?

Apparently conclusive meta-analyses may be inconclusive-trial sequential analysis adjustment of random error risk due to repetitive testing of accumulating data in apparently conclusive neonatal meta-analyses

Early vs delayed closure of loop defunctioning ileostomy in patients undergoing distal colorectal resections: an integrated systematic review and meta-analysis of published randomised controlled trials

RoB 2: a revised tool for assessing risk of bias in randomised trials

GRADEpro Guideline Development Tool

2020 (developed by Evidence Prime

2013) GRADE handbook for grading quality of evidence and strength of recommendations

Quality of life in a randomised trial of early closure of temporary ileostomy after rectal resection for cancer (EASY trial)

Cost analysis in a randomised trial of early closure of a temporary ileostomy after rectal resection for cancer (EASY trial)

Functional outcomes from a randomised trial of early closure of temporary ileostomy after rectal excision for cancer

Quality of life and bowel function following early closure of a temporary ileostomy in patients with rectal cancer: a report from a singlecenter randomized controlled trial

Estimating the mean and variance from the median, range, and the size of a sample

Multidisciplinary Italian Study group for STOmas (MISSTO) (2019) Italian guidelines for the surgical management of enteral stomas in adults

Preoperative oral antibiotics and surgical-site infections in colon surgery (ORALEV): a multicentre, single-blind, pragmatic, randomised controlled trial

Anastomotic leak after colorectal surgery: does timing affect failure to rescue?

Bioresorbable adhesion barrier facilitates early closure of the defunctioning ileostomy after rectal excision: a prospective, randomised trial

International Consensus Definition of Low Anterior Resection Syndrome

Impact of a defunctioning ileostomy and time to stoma closure on bowel function after low anterior resection for rectal cancer: a systematic review and metaanalysis

European Society of Trauma and Emergency Surgery (ESTES) recommendations for trauma and emergency surgery preparation during times of COVID-19 infection

SAGES and EAES recommendations for minimally invasive surgery during COVID-19 pandemic

Comparative study between ghost ileostomy and defunctioning ileostomy in terms of morbidity and cost-effectiveness in low anterior resection for rectal cancer

Late anastomotic leakage in colorectal surgery: a significant problem

A comparison of laparoscopically assisted and open colectomy for colon cancer

The long-term results of a randomised clinical trial of laparoscopy-assisted versus open surgery for colon cancer

Survival after laparoscopic surgery versus open surgery for colon cancer: long-term outcome of a randomised clinical trial

Shortterm endpoints of conventional versus laparoscopic-assisted surgery in patients with colorectal cancer (MRC CLASICC trial): multicentre, randomised controlled trial

Effect of laparoscopic-assisted resection vs open resection of stage II or III rectal cancer on pathologic outcomes: the ACOSOG Z6051 randomized clinical trial

Laparoscopic versus open total mesorectal excision with anal sphincter preservation for low rectal cancer

Effect of roboticassisted vs conventional laparoscopic surgery on risk of conversion to open laparotomy among patients undergoing resection for rectal cancer: the ROLARR randomized clinical trial