Retrospective Study Open Access
Copyright ©The Author(s) 2024. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastrointest Surg. May 27, 2024; 16(5): 1354-1362
Published online May 27, 2024. doi: 10.4240/wjgs.v16.i5.1354
Predictors of complications after prophylactic ileostomy reversal for rectal cancer: A retrospective study
Quan Lv, Xin-Peng Shu, Dong Peng, Si-Qi Li, Zheng Xiang, Department of Gastrointestinal Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
Zheng Xiang, Chongqing Key Laboratory of Department of General Surgery, The First Affiliated Hospital of Chongqing Medical University, Chongqing 400016, China
ORCID number: Quan Lv (0009-0005-8861-0181); Dong Peng (0000-0003-4050-4337); Zheng Xiang (0000-0002-6564-4806).
Co-first authors: Quan Lv and Xin-Peng Shu.
Author contributions: Peng D contributed to the data analysis; Lv Q and Xiang Z led the quality assessments; Lv Q and Shu XP wrote the original draft; Xiang Z and Shu XP revised the manuscript. All authors have agreed on the journal to which the manuscript will be submitted, gave final approval of the version to be published, and agree to be accountable for all aspects of the work. Both Lv Q and Shu XP have played important and indispensable roles in the experimental design, data interpretation and manuscript preparation as the co-first authors.
Supported by Science and Technology Planning Project of Yuzhong District of Chongqing City, No. 20210115.
Institutional review board statement: This study was reviewed and approved by the Ethics Committee of The First Affiliated Hospital of Chongqing Medical University.
Informed consent statement: The requirement for patients' informed consent for this study was waived due to its retrospective nature.
Conflict-of-interest statement: Academic Editor has no conflict of interest.
Data sharing statement: The datasets generated and/or analyzed during the current study are not publicly available due but are available from the corresponding author upon reasonable request.
Open-Access: This article is an open-access article that was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution NonCommercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: https://creativecommons.org/Licenses/by-nc/4.0/
Corresponding author: Zheng Xiang, Doctor, PhD, Chief Doctor, Professor, Department of Gastrointestinal Surgery, The First Affiliated Hospital of Chongqing Medical University, No. 1 Youyi Roud, Chongqing 400016, China. doctor13330209937@126.com
Received: January 31, 2024
Revised: April 7, 2024
Accepted: April 15, 2024
Published online: May 27, 2024
Processing time: 112 Days and 19.1 Hours

Abstract
BACKGROUND

Previous studies have analyzed the risk factors for complications after ileostomy reversal for rectal cancer (RC), but there were significant differences in the reported risk factors for complications after stoma reversal. No studies have analyzed the risk factors for stoma-related complications and overall postoperative complications separately.

AIM

To analyze the risk factors for overall complications and stoma-related complications after ileostomy reversal for patients with RC.

METHODS

This was a retrospective study of 439 patients who underwent ileostomy reversal at a clinical center and were followed up between September 2012 and September 2022. Continuous variables are expressed as the mean ± SD and were analyzed with independent-sample t tests, while frequency variables are expressed as n (%), and the χ2 test or Fisher’s exact test was used. Univariate and multivariate logistic regression analyses were used to identify predictors of overall complications and stoma-related complications.

RESULTS

The overall complication rate after ileostomy reversal was 11.4%. Patients with lower preoperative albumin concentration (P < 0.01), greater blood loss (P = 0.017), and longer operative times (P < 0.01) were more likely to experience postoperative complications. The incidence of stoma-related complications was 6.4%. Analysis of the study showed that a higher body mass index (BMI) (P < 0.01), preoperative comorbid hypertension (P = 0.049), time from primary surgery to ileostomy reversal (P < 0.01) and longer operation time (P = 0.010) were more likely to result in stoma-related complications postoperatively. Multivariate logistic regression analysis revealed that a lower preoperative albumin level (P < 0.01, OR = 0.888, 95%CI: 0.828-0.958) was an independent risk factor for overall complications. Moreover, multivariate analysis revealed that BMI (P < 0.01, OR = 1.176, 95%CI: 1.041-1.330) and time from primary surgery to ileostomy reversal (P < 0.01, OR = 1.140, 95%CI: 1.038-1.252) were independent risk factors for stoma-related complications after stoma reversal.

CONCLUSION

The preoperative albumin level was a predictor of overall complications. Preoperative BMI and the time from primary surgery to ileostomy reversal were predictors of stoma-related complications.

Key Words: Ileostomy, Reversal, Risk factors, Complications, Rectal cancer

Core Tip: There were no studies that have analyzed the risk factors for stoma-related complications and overall postoperative complications after stoma reversal for rectal cancer (RC) separately. Our study showed that the preoperative serum albumin concentration was a predictor of overall complications. Preoperative body mass index and time between initial surgery and stoma reversal were predictors of stoma-related complications. Therefore, for RC patients undergoing ileostomy reversal, adequate albumin supplementation should be provided preoperatively to reduce the incidence of postoperative complications.



INTRODUCTION

Colorectal cancer (CRC) is a common malignancy that ranks as the third most common cancer and the second leading cause of cancer-related death worldwide[1]. Current treatments for CRC include endoscopic and surgical resection, radiotherapy, immunotherapy, palliative chemotherapy, targeted therapy, extensive surgery, and local ablation of metastases[2-4]. However, with the continuous improvement of surgical techniques, postoperative complications of rectal cancer (RC) are still inevitable, and anastomotic leakage (AL) is one of the most dangerous postoperative complications in RC patients[5-8]. In high-risk resettable RC surgery, temporary ileostomy is often used to reduce the incidence of AL after RC surgery[9-11].

Although protective ileostomy reduced the incidence of AL after RC, the construction of an ileostomy was associated with potential complications, and it reduced the quality of life of patients[12-15]. The overall complication rate of ileostomy is as high as 20%, including dehydration, electrolyte imbalance, parastomal hernia, and peristomal infections, with postoperative bowel obstruction and surgical site infections (SSI) being the most common[16-19]. The risk of complications after stoma reversal can easily reach 17%-20%[20,21], including surgical SSI, AL, intestinal obstruction, postoperative intestinal obstruction, wound dehiscence, extraintestinal leakage and other complications[22,23]. Protective ileostomy was often performed at the expense of the patient’s quality of life[24]. Therefore, correct identification of risk factors for postoperative complications after recovery of the peristomal stoma is necessary.

Previous studies have shown that age, operative time, preoperative comorbid diabetes mellitus and the time from primary surgery to ileostomy reversal are risk factors for complications after ileostomy reversal[25-27]. Li et al[28] reported that early reversal of the ileostomy before 3 months was both practical and safe, allowing sufficient time to recover from the initial resection and soften intra-abdominal adhesions. Ahmadi-Amoli H et al[29] concluded that early reversal of ileostomy was not better than late reversal, and there was no significant difference between the two groups in reducing the risk of stoma complications. There were significant differences in the reported risk factors for complications after stoma reversa and no studies have analyzed the risk factors for stoma-related complications and overall postoperative complications separately.

Based on the results of previous studies, we hypothesized that the time between initial surgery and ileostomy reversal was a risk factor for postoperative complications. The present study was aimed to analyze the risk factors for overall complications and stoma-related complications after ileostomy reversal for RC and to guide clinical practice.

MATERIALS AND METHODS
Patients

This was a retrospective study of 439 patients who underwent ileostomy reversal at a clinical center and were followed up between September 2012 and September 2022. The present study was performed according to the World Medical Association Declaration of Helsinki. Ethical approval from the institutional review board (K2024-002-01) was obtained. All patients signed the informed consent.

Inclusion and exclusion criteria

Patients with RC who underwent laparoscopic low anterior rectal resection with temporary ileostomy and concomitant ileostomy reversal were recruited for this study (n = 548). The exclusion criteria were as follows: (1) Incomplete perioperative medical information (n = 86); and (2) resection of the other organs (n = 23). Ultimately, a total of 439 patients were included in this study (Figure 1).

Figure 1
Figure 1 Flow chart of patient selection. RC: Rectal cancer.
Criteria for prophylactic ileostomy reversal

The criteria for prophylactic ileostomy reversal were as follows: (1) Regular postoperative follow-up, no new tumor recurrence, or metastasis; (2) satisfactory assessment of anal and rectal function; (3) no anastomotic stenosis, no AL, and no improvement in anastomotic stenosis symptoms; and (4) exclusion of intestinal obstruction and other contraindications to surgery.

Anesthesia management

All patients underwent general intravenous anesthesia in accordance with Chinese anesthesiology guidelines and expert consensus.

Data collection

All clinical information was collected from both inpatient health care systems and outpatient systems. These data included age, sex, body mass index (BMI), smoking status, drinking status, hypertension status, type 2 diabetes mellitus (T2DM) status, hemoglobin level, albumin level, time from primary surgery to ileostomy reversal, operation time, blood loss, length of hospital stay, overall complications, and stoma-related complications.

Statistical analysis

According to the previous literature[20,21], the complication rate of ileostomy reversal is 20%. The significance level was 0.05, the data distribution was 0.10, the permissible error was 0.10, and a two-sided test was performed, which showed that at least 168 patients who underwent ileostomy reversal needed to be included in this study. A total of 439 ileostomy-returned patients were selected for this study, which meant adequate. PASS (version 11) software was used for sample size calculations. Continuous variables are expressed as the means ± SD, and independent-sample t tests were used to analyze the data. Moreover, frequency variables are expressed as n (%), and the χ2 test or Fisher’s exact test was used. A logistic regression model with a backward selection approach was constructed to predict overall complications and stoma-related complications predictors. P < 0.05 was considered to indicate significance. All the data analyses were performed with SPSS (version 22.0).

RESULTS
Clinical characteristics

Overall, 439 RC patients were included in the study (292 males and 147 females). The mean age of the participants was 61.6 ± 11.4 years, and the mean BMI was 22.3 ± 3.0 kg/m2. There were 164 (37.4%) patients with a history of smoking, 144 (32.8%) with a history of drinking, 105 (23.9%) with a history of hypertension, and 42 (9.6%) with a history of T2DM. The mean hemoglobin concentration was 124.7 ± 17.3 g/L, and the mean albumin concentration was 40.5 ± 4.3 g/L. The time from primary surgery to ileostomy reversal was 4.6 ± 2.9 months, the mean operation time was 94.2 ± 41.7 min, the mean blood loss was 29.7 ± 34.5 mL, and the mean hospital stay was 5.7 ± 3.1 days. There was no 30-d mortality. Postoperative complications occurred in 50 (11.4%) patients, and stoma-related complications occurred in 28 (6.4%) patients. The clinical characteristics of the patients in the study groups are summarized in Table 1.

Table 1 Clinical characteristics of the whole cohort, n (%).
Characteristics
No. 439
Age (yr)61.6 ± 11.4
Sex
    Male292 (66.5)
    Female147 (33.5)
BMI (kg/m2)22.3 ± 3.0
Smoking164 (37.4)
Drinking144 (32.8)
Hypertension105 (23.9)
T2DM42 (9.6)
Hemoglobin (g/L)124.7 ± 17.3
Albumin (g/L)40.5 ± 4.3
The time from primary surgery to ileostomy reversal (months)4.6 ± 2.9
Operation time (min)94.2 ± 41.7
Blood loss (mL)29.7 ± 34.5
Hospital stay (d)5.7 ± 3.1
Overall complications50 (11.4)
Stoma-related complications28 (6.4)
Statistical analysis of overall complications and stoma-related complications

The overall complication rate after ileostomy reversal was 11.4%. Patients with lower preoperative albumin concentration (P < 0.01), greater blood loss (P = 0.017), and longer operative times (P < 0.01) were more likely to experience postoperative complications (Table 2). The incidence of stoma-related complications was 6.4%. Analysis of the study showed that a higher BMI (P < 0.01), preoperative comorbid hypertension (P = 0.049), time from initial surgery to ileostomy reversal (P < 0.01) and longer operative time (P = 0.010) were more likely to result in stoma-related complications postoperativel (Table 3).

Table 2 Comparison between the complication group and the no complication group, n (%).
Characteristics
Complication (50)
No complication (389)
P value
Age (yr)63.2 ± 10.061.4 ± 11.50.300
Sex0.579
    Male35 (53.2)257 (64.0)
    Female15 (46.8)132 (36.0)
BMI (kg/m2)22.5 ± 2.722.3 ± 3.10.710
Smoking20 (35.3)144 (39.2)0.682
Drinking16 (28.5)128 (32.6)0.898
Hypertension10 (26.4)95 (24.1)0.490
T2DM7 (12.8)35 (10.2)0.258
Hemoglobin (g/L)122.6 ± 18.6125.0 ± 17.10.366
Albumin (g/L)38.8 ± 4.040.8 ± 4.2< 0.01a
The time from primary surgery to ileostomy reversal (months)5.0 ± 3.34.6 ± 2.80.369
Operation time (min)103.6 ± 43.493.0 ± 41.40.090
Blood loss (mL)40.7 ± 49.628.3 ± 31.80.017a
Hospital stay (d)9.1 ± 6.05.3 ± 2.1< 0.01a
Table 3 Comparison between the stoma-related group and the no stoma-related complication group.
Characteristics
Stoma-related Complication (28)
No stoma-related complication (411)
P value
Age, (yr)64.8 ± 10.761.4 ± 11.40.133
Sex0.277
    Male16 (53.2)276 (64.0)
    Female12 (46.8)135 (36.0)
BMI (kg/m2)23.8 ± 2.922.2 ± 3.0< 0.01a
Smoking10 (35.3)154 (39.2)0.853
Drinking8 (28.5)136 (32.6)0.622
Hypertension11 (26.4)94 (24.1)0.049a
T2DM4 (12.8)38 (10.2)0.329
Hemoglobin123.9 ± 21.9124.8 ± 17.00.793
Albumin (g/L)39.7 ± 4.040.6 ± 4.30.287
The time from primary surgery to ileostomy reversal (months)6.3 ± 3.84.5 ± 2.8< 0.01a
Operation time (min)113.7 ± 60.392.9 ± 39.50.010a
Blood loss (mL)39.6 ± 36.929.1 ± 34.30.116
Hospital stay (d)5.3 ± 1.75.7 ± 3.10.452
Univariate and multivariate logistic regression analyses of overall complications

Univariate analysis suggested that patients with a lower preoperative albumin concentration (P < 0.01, OR = 0.887, 95%CI: 0.822-0.957) had a greater risk of ileostomy reversal complications, and multivariate analysis suggested that a lower preoperative albumin concentration (P < 0.01, OR = 0.888, 95%CI: 0.828-0.958) was an independent risk factor for overall complications. Other factors, including age, sex, BMI, T2DM status, smoking status, drinking status, hypertension status, hemoglobin, and the time from primary surgery to ileostomy reversal, had no predictive value for overall complications (P > 0.01) (Table 4).

Table 4 Univariate and multivariate logistic regression analysis of overall complications.
Risk factors
Univariate analysis
Multivariate analysis
OR (95%CI)
P value
OR (95%CI)
P value
Age (yr)1.014 (0.988-1.041)0.300
Sex (female/male)0.834 (0.440-1.583)0.579
BMI (kg/m2)1.019 (0.924-1.122)0.710
T2DM (yes/no)1.647 (0.689-3.934)0.262
Smoking (yes/no)1.134 (0.621-2.071)0.682
Drinking (yes/no)0.960 (0.511-1.803)0.898
Hypertension (yes/no)0.774 (0.373-1.606)0.491
Hemoglobin (g/L)0.992 (0.976-1.009)0.365
Albumin (g/L)0.887 (0.822-0.957)< 0.01a0.888 (0.828-0.958)< 0.01a
The time from primary surgery to ileostomy reversal (months)1.042 (0.952-1.141)0.3711.030 (0.939-1.130)0.534
Univariate and multivariate logistic regression analyses of stoma-related complications

Univariate analysis revealed that patients with a higher BMI (P < 0.01, OR = 1.175, 95%CI: 1.044-1.324) and a longer time from primary surgery to ileostomy reversal (P < 0.01, OR = 1.142, 95%CI: 1.041-1.253) had a greater risk of postoperative stoma-related complications. Multivariate analysis revealed that BMI (P < 0.01, OR = 1.176, 95%CI: 1.041-1.330) and the time from primary surgery to ileostomy reversal (P < 0.01, OR = 1.140, 95%CI: 1.038-1.252) were independent risk factors for stoma-related complications after stoma reversal. There was no association between age, sex, T2DM status, smoking status, drinking status, hypertension status, hemoglobin, or albumin concentration (Table 5).

Table 5 Univariate and multivariate logistic regression analysis of stoma-related complications.
Risk factors
Univariate analysis
Multivariate analysis
OR (95%CI)
P value
OR (95%CI)
P value
Age (yr)1.027 (0.992-1.064)0.134
Sex (female/male)1.533 (0.706-3.332)0.280
BMI (kg/m2)1.175 (1.044-1.324)< 0.01a1.176 (1.041-1.330)< 0.01a
T2DM (yes/no)1.636 (0.539-4.963)0.385
Smoking (yes/no)0.927 (0.417-2.060)0.853
Drinking (yes/no)0.809 (0.347-1.883)0.623
Hypertension (yes/no)2.182 (0.988-4.820)0.054
Hemoglobin (g/L)0.997 (0.975-1.019)0.792
Albumin (g/L)0.951 (0.867-1.043)0.287
The time from primary surgery to ileostomy reversal (months)1.142 (1.041-1.253)< 0.01a1.140 (1.038-1.252)< 0.01a
DISCUSSION

In the present study, we found that a lower preoperative albumin, intraoperative hemorrhage, and length of postoperative hospital stay were associated with overall complications after ileostomy. A higher preoperative BMI, preoperative combined hypertension, time from primary surgery to ileostomy reversal, and operative time were associated with stoma-related complications after ileostomy reversal. Pre-operative albumin level was a predictor of overall complications. Preoperative BMI and the time from primary surgery to ileostomy reversal were predictors of stoma-related complications.

Prophylactic ileostomy after low anterior resection is the preferred surgical procedure for patients with resettable and survivable RC, which could reduce the incidence of AL after RC[9-11]. However, the overall complication rate of stoma reversal is as high as 20%, including dehydration, electrolyte imbalance, parastomal hernia, and peristomal infections, with postoperative bowel obstruction and SSI being the most common[16-18]. In our study, postoperative complications occurred in 50 (11.4%) patients, and stoma-related complications occurred in 28 (6.4%) patients; these rates are slightly lower than those previously reported in the literature[30,31].

Studies have shown that hypoalbuminemia negatively affects wound healing and disease severity[32]. In RC surgery, low preoperative protein levels significantly increase the incidence of postoperative complications[33,34]. Similarly, low albumin levels have been associated with postoperative complications in RC patients[35-37]. Our results were similar to those of a previous study showing that low preoperative albumin levels were an independent risk factor for overall complications after ileostomy reversal[30]. Moreover, preoperative albumin levels were not significantly associated with stoma-related complications. This might be related to the fact that the included patients all had normal preoperative albumin values.

Multivariate risk factor analysis revealed that obesity was a risk factor for stoma-related complications. Previous studies have shown that obesity is also a risk factor for AL after resection of RC resection[38], and obese patients are at increased risk of incisional hernia[39]. The postoperative healing process might also be impaired in obese patients due to the impaired visual field in overweight patients and the more complex release of adhesions during ileostomy reversal. Currently, there is no definitive conclusion on the optimal timing of stoma reversal. We found that prolonged time from initial surgery to stoma reversal was an independent risk factor for stoma-related complications, which was similar to the findings of previous studies[15,27].

In this study, we investigated for the first time the risk factors for overall complications and stoma-related complications after stoma reversal for RC. However, our study has several limitations. First, there was a lack of analysis of the long-term prognosis of the patients. Second, there was no categorical analysis of postoperative complications. Third, there was a lack of adequate preoperative baseline information on patients and tumor staging studies. In the future, we hope to collect more clinical information and evaluate more variables through multicenter collaborations.

CONCLUSION

In summary, the preoperative serum albumin concentration was a predictor of overall complications. Preoperative BMI and time between initial surgery and stoma reversal were predictors of stoma-related complications. Therefore, for RC patients undergoing ileostomy reversal, adequate albumin supplementation should be provided preoperatively to reduce the incidence of postoperative complications.

ACKNOWLEDGEMENTS

We acknowledge all the authors whose publications are referred in our article.

Footnotes

Provenance and peer review: Unsolicited article; Externally peer reviewed.

Peer-review model: Single blind

Specialty type: Gastroenterology and hepatology

Country of origin: China

Peer-review report’s classification

Scientific Quality: Grade C

Novelty: Grade C

Creativity or Innovation: Grade C

Scientific Significance: Grade C

P-Reviewer: Glumac S, Croatia S-Editor: Qu XL L-Editor: A P-Editor: Zheng XM

References
1.  Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, Bray F. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin. 2021;71:209-249.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 50630]  [Cited by in F6Publishing: 46713]  [Article Influence: 15571.0]  [Reference Citation Analysis (47)]
2.  Dekker E, Tanis PJ, Vleugels JLA, Kasi PM, Wallace MB. Colorectal cancer. Lancet. 2019;394:1467-1480.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1570]  [Cited by in F6Publishing: 2200]  [Article Influence: 440.0]  [Reference Citation Analysis (2)]
3.  Guren MG. The global challenge of colorectal cancer. Lancet Gastroenterol Hepatol. 2019;4:894-895.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 28]  [Cited by in F6Publishing: 22]  [Article Influence: 4.4]  [Reference Citation Analysis (0)]
4.  Peng D, Yu DL, Liu XY, Tao W, Kang B, Zhang H, Wei ZQ, Ji GY. Does temporary ileostomy via specimen extraction site affect the short outcomes and complications after laparoscopic low anterior resection in rectal cancer patients? A propensity score matching analysis. BMC Surg. 2022;22:263.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
5.  Chiarello MM, Fransvea P, Cariati M, Adams NJ, Bianchi V, Brisinda G. Anastomotic leakage in colorectal cancer surgery. Surg Oncol. 2022;40:101708.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 16]  [Cited by in F6Publishing: 32]  [Article Influence: 16.0]  [Reference Citation Analysis (0)]
6.  McDermott FD, Heeney A, Kelly ME, Steele RJ, Carlson GL, Winter DC. Systematic review of preoperative, intraoperative and postoperative risk factors for colorectal anastomotic leaks. Br J Surg. 2015;102:462-479.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 427]  [Cited by in F6Publishing: 514]  [Article Influence: 57.1]  [Reference Citation Analysis (0)]
7.  Shiga M, Maeda H, Oba K, Okamoto K, Namikawa T, Fujisawa K, Yokota K, Kobayashi M, Hanazaki K. Safety of laparoscopic surgery for colorectal cancer in patients over 80 years old: a propensity score matching study. Surg Today. 2017;47:951-958.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 18]  [Cited by in F6Publishing: 17]  [Article Influence: 2.4]  [Reference Citation Analysis (0)]
8.  Hain E, Maggiori L, Manceau G, Mongin C, Prost À la Denise J, Panis Y. Oncological impact of anastomotic leakage after laparoscopic mesorectal excision. Br J Surg. 2017;104:288-295.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 45]  [Cited by in F6Publishing: 58]  [Article Influence: 7.3]  [Reference Citation Analysis (0)]
9.  Phan K, Oh L, Ctercteko G, Pathma-Nathan N, El Khoury T, Azam H, Wright D, Toh JWT. Does a stoma reduce the risk of anastomotic leak and need for re-operation following low anterior resection for rectal cancer: systematic review and meta-analysis of randomized controlled trials. J Gastrointest Oncol. 2019;10:179-187.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 34]  [Article Influence: 6.8]  [Reference Citation Analysis (0)]
10.  Garg PK, Goel A, Sharma S, Chishi N, Gaur MK. Protective Diversion Stoma in Low Anterior Resection for Rectal Cancer: A Meta-Analysis of Randomized Controlled Trials. Visc Med. 2019;35:156-160.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 20]  [Cited by in F6Publishing: 27]  [Article Influence: 5.4]  [Reference Citation Analysis (0)]
11.  Gu WL, Wu SW. Meta-analysis of defunctioning stoma in low anterior resection with total mesorectal excision for rectal cancer: evidence based on thirteen studies. World J Surg Oncol. 2015;13:9.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 73]  [Cited by in F6Publishing: 72]  [Article Influence: 8.0]  [Reference Citation Analysis (0)]
12.  Dulskas A, Petrauskas V, Kuliavas J, Bickaite K, Kairys M, Pauza K, Kilius A, Sangaila E, Bausys R, Stratilatovas E. Quality of Life and Bowel Function Following Early Closure of a Temporary Ileostomy in Patients with Rectal Cancer: A Report from a Single-Center Randomized Controlled Trial. J Clin Med. 2021;10.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 6]  [Article Influence: 2.0]  [Reference Citation Analysis (0)]
13.  Vogel I, Reeves N, Tanis PJ, Bemelman WA, Torkington J, Hompes R, Cornish JA. Impact of a defunctioning ileostomy and time to stoma closure on bowel function after low anterior resection for rectal cancer: a systematic review and meta-analysis. Tech Coloproctol. 2021;25:751-760.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 43]  [Cited by in F6Publishing: 41]  [Article Influence: 13.7]  [Reference Citation Analysis (0)]
14.  Rhemouga A, Buettner S, Bechstein WO, Woeste G, Schreckenbach T. The association of age with decline in renal function after low anterior resection and loop ileostomy for rectal cancer: a retrospective cohort prognostic factor study. BMC Geriatr. 2021;21:65.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Cited by in F6Publishing: 1]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
15.  Ourô S, Ferreira MP, Albergaria D, Maio R. Loop ileostomy in rectal cancer surgery: factors predicting reversal and stoma related morbidity. Langenbecks Arch Surg. 2021;406:843-853.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 7]  [Article Influence: 2.3]  [Reference Citation Analysis (0)]
16.  Garfinkle R, Filion KB, Bhatnagar S, Sigler G, Banks A, Letarte F, Liberman S, Brown CJ, Boutros M. Prediction model and web-based risk calculator for postoperative ileus after loop ileostomy closure. Br J Surg. 2019;106:1676-1684.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 1.0]  [Reference Citation Analysis (0)]
17.  Prassas D, Vossos V, Rehders A, Knoefel WT, Krieg A. Loop ileostomy versus loop colostomy as temporary deviation after anterior resection for rectal cancer. Langenbecks Arch Surg. 2020;405:1147-1153.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 1]  [Article Influence: 0.3]  [Reference Citation Analysis (0)]
18.  Fielding A, Woods R, Moosvi SR, Wharton RQ, Speakman CTM, Kapur S, Shaikh I, Hernon JM, Lines SW, Stearns AT. Renal impairment after ileostomy formation: a frequent event with long-term consequences. Colorectal Dis. 2020;22:269-278.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 31]  [Cited by in F6Publishing: 41]  [Article Influence: 10.3]  [Reference Citation Analysis (0)]
19.  Liu F, Wang LL, Liu XR, Li ZW, Peng D. Risk Factors for Radical Rectal Cancer Surgery with a Temporary Stoma Becoming a Permanent Stoma: A Pooling Up Analysis. J Laparoendosc Adv Surg Tech A. 2023;33:743-749.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
20.  Chow A, Tilney HS, Paraskeva P, Jeyarajah S, Zacharakis E, Purkayastha S. The morbidity surrounding reversal of defunctioning ileostomies: a systematic review of 48 studies including 6,107 cases. Int J Colorectal Dis. 2009;24:711-723.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 259]  [Cited by in F6Publishing: 276]  [Article Influence: 18.4]  [Reference Citation Analysis (0)]
21.  Musters GD, Atema JJ, van Westreenen HL, Buskens CJ, Bemelman WA, Tanis PJ. Ileostomy closure by colorectal surgeons results in less major morbidity: results from an institutional change in practice and awareness. Int J Colorectal Dis. 2016;31:661-667.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 13]  [Cited by in F6Publishing: 12]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
22.  Hsieh MC, Kuo LT, Chi CC, Huang WS, Chin CC. Pursestring Closure versus Conventional Primary Closure Following Stoma Reversal to Reduce Surgical Site Infection Rate: A Meta-analysis of Randomized Controlled Trials. Dis Colon Rectum. 2015;58:808-815.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 33]  [Cited by in F6Publishing: 36]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
23.  Mennigen R, Sewald W, Senninger N, Rijcken E. Morbidity of loop ileostomy closure after restorative proctocolectomy for ulcerative colitis and familial adenomatous polyposis: a systematic review. J Gastrointest Surg. 2014;18:2192-2200.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 29]  [Cited by in F6Publishing: 29]  [Article Influence: 2.9]  [Reference Citation Analysis (0)]
24.  Silva MA, Ratnayake G, Deen KI. Quality of life of stoma patients: temporary ileostomy versus colostomy. World J Surg. 2003;27:421-424.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 80]  [Cited by in F6Publishing: 84]  [Article Influence: 4.0]  [Reference Citation Analysis (0)]
25.  Nakamura T, Sato T, Naito M, Yamanashi T, Miura H, Tsutsui A, Watanabe M. Risk factors for complications after diverting ileostomy closure in patients who have undergone rectal cancer surgery. Surg Today. 2017;47:1238-1242.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 10]  [Cited by in F6Publishing: 10]  [Article Influence: 1.4]  [Reference Citation Analysis (0)]
26.  Rubinkiewicz M, Witowski J, Wysocki M, Pisarska M, Kłęk S, Budzyński A, Pędziwiatr M. Investigating Risk Factors for Complications after Ileostomy Reversal in Low Anterior Rectal Resection Patients: An Observational Study. J Clin Med. 2019;8.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 6]  [Cited by in F6Publishing: 6]  [Article Influence: 1.2]  [Reference Citation Analysis (0)]
27.  Climent M, Frago R, Cornellà N, Serrano M, Kreisler E, Biondo S. Prognostic factors for complications after loop ileostomy reversal. Tech Coloproctol. 2022;26:45-52.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 1]  [Reference Citation Analysis (0)]
28.  Li W, Ozuner G. Does the timing of loop ileostomy closure affect outcome: A case-matched study. Int J Surg. 2017;43:52-55.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 9]  [Cited by in F6Publishing: 15]  [Article Influence: 2.1]  [Reference Citation Analysis (0)]
29.  Ahmadi-Amoli H, Rahimi M, Abedi-Kichi R, Ebrahimian N, Hosseiniasl SM, Hajebi R, Rahimpour E. Early closure compared to late closure of temporary ileostomy in rectal cancer: a randomized controlled trial study. Langenbecks Arch Surg. 2023;408:234.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
30.  Baik H, Bae KB. Low albumin level and longer interval to closure increase the early complications after ileostomy closure. Asian J Surg. 2021;44:352-357.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 5]  [Cited by in F6Publishing: 5]  [Article Influence: 1.7]  [Reference Citation Analysis (0)]
31.  Kilinc G, Ustun M, Tuncer K, Sert I. Risk Factors for the Morbidity and Mortality of Stoma Closure. J Coll Physicians Surg Pak. 2021;31:1085-1088.  [PubMed]  [DOI]  [Cited in This Article: ]  [Reference Citation Analysis (0)]
32.  Issangya CE, Msuya D, Chilonga K, Herman A, Shao E, Shirima F, Naman E, Mkumbi H, Pyuza J, Mtui E, Sanga LA, Abdul S, Leyaro BJ, Chugulu S. Perioperative serum albumin as a predictor of adverse outcomes in abdominal surgery: prospective cohort hospital based study in Northern Tanzania. BMC Surg. 2020;20:155.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 4]  [Cited by in F6Publishing: 5]  [Article Influence: 1.3]  [Reference Citation Analysis (0)]
33.  Lohsiriwat V, Chinswangwatanakul V, Lohsiriwat S, Akaraviputh T, Boonnuch W, Methasade A, Lohsiriwat D. Hypoalbuminemia is a predictor of delayed postoperative bowel function and poor surgical outcomes in right-sided colon cancer patients. Asia Pac J Clin Nutr. 2007;16:213-217.  [PubMed]  [DOI]  [Cited in This Article: ]
34.  Liu ZJ, Ge XL, Ai SC, Wang HK, Sun F, Chen L, Guan WX. Postoperative decrease of serum albumin predicts short-term complications in patients undergoing gastric cancer resection. World J Gastroenterol. 2017;23:4978-4985.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in CrossRef: 23]  [Cited by in F6Publishing: 23]  [Article Influence: 3.3]  [Reference Citation Analysis (0)]
35.  Shimura T, Toiyama Y, Hiro J, Imaoka H, Fujikawa H, Kobayashi M, Ohi M, Inoue Y, Mohri Y, Kusunoki M. Monitoring perioperative serum albumin can identify anastomotic leakage in colorectal cancer patients with curative intent. Asian J Surg. 2018;41:30-38.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 19]  [Cited by in F6Publishing: 22]  [Article Influence: 2.8]  [Reference Citation Analysis (0)]
36.  Liu XY, Zhang B, Kang B, Cheng YX, Yuan C, Tao W, Wei ZQ, Peng D. The Effect of Complications on Oncological Outcomes of Colorectal Cancer Patients After Primary Surgery: A Propensity Score Matching Analysis. Front Oncol. 2022;12:857062.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in F6Publishing: 2]  [Reference Citation Analysis (0)]
37.  Hardt J, Pilz L, Magdeburg J, Kienle P, Post S, Magdeburg R. Preoperative hypoalbuminemia is an independent risk factor for increased high-grade morbidity after elective rectal cancer resection. Int J Colorectal Dis. 2017;32:1439-1446.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 23]  [Cited by in F6Publishing: 34]  [Article Influence: 4.9]  [Reference Citation Analysis (0)]
38.  Schneider V, Lee LD, Stroux A, Buhr HJ, Ritz JP, Kreis ME, Lauscher JC. Risk factors for reoperation after ileostomy reversal - Results from a prospective cohort study. Int J Surg. 2016;36:233-239.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 11]  [Cited by in F6Publishing: 12]  [Article Influence: 1.5]  [Reference Citation Analysis (0)]
39.  Kelly-Schuette K, Wilkes A, Kyriakakis R, Ogilvie J. Predictors of hernia after loop ileostomy closure: a single-center retrospective review. Int J Colorectal Dis. 2020;35:1695-1702.  [PubMed]  [DOI]  [Cited in This Article: ]  [Cited by in Crossref: 2]  [Cited by in F6Publishing: 2]  [Article Influence: 0.5]  [Reference Citation Analysis (0)]