CC BY-NC-ND 4.0 · Endosc Int Open 2021; 09(09): E1342-E1349
DOI: 10.1055/a-1490-8783
Original article

Endo-sponge in management of anastomotic colorectal leaks: a systematic review and meta-analysis

Banreet S. Dhindsa
2   Division of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha Nebraska, United States
,
Yassin Naga
3   University of Nevada Las Vegas School of Medicine, Las Vegas, Nevada, United States
,
Syed M. Saghir
3   University of Nevada Las Vegas School of Medicine, Las Vegas, Nevada, United States
,
Sarav Gunjit Singh Daid
4   Metropolitan Hospital Center/New York Medical College, New York, New York, United States
,
Saurabh Chandan
5   Creighton University Medical Center, Omaha, Nebraska, United States
,
Harmeet Mashiana
2   Division of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha Nebraska, United States
,
Amaninder Dhaliwal
6   Division of Gastroenterology and Hepatology, Moffitt Cancer Center, Tampa, Florida, United States
,
Abhitej Sidhu
7   Bharati Vidyapeeth University Medical College, Pune, Maharashtra, India
,
Harlan Sayles
8   Department of Biostatistics, University of Nebraska Medical Center, Omaha, Nebraska, United States
,
Daryl Ramai
9   Department of Internal Medicine, The Brooklyn Hospital Center, Brooklyn, New York, United States
,
Ishfaq Bhat
2   Division of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha Nebraska, United States
,
Shailender Singh
2   Division of Gastroenterology and Hepatology, University of Nebraska Medical Center, Omaha Nebraska, United States
,
Stephanie McDonough
1   Division of Gastroenterology and Hepatology, University of Utah School of Medicine, Salt Lake City, Utah, United States
,
Douglas G. Adler
1   Division of Gastroenterology and Hepatology, University of Utah School of Medicine, Salt Lake City, Utah, United States
› Author Affiliations
 

Abstract

Background and study aims Following colorectal surgery, anastomotic dehiscence and leak formation has an incidence of 2 % to 7 %. Endo-SPONGE has been applied in the management of anastomatic leaks (ALs) after colorectal surgery. This is the first systematic review and meta analysis to evaluate the efficacy and safety of Endo-SPONGE in the management of colorectal ALs.

Patients and methods The primary outcomes assessed were the technical and clinical success of Endo-SPONGE placement in colorectal ALs. The secondary outcomes assessed were the overall adverse events (AEs) and the AE subtypes. Pooled estimates were calculated using random-effects models with 95 % confidence interval (C. I.). The statistical analysis was done using STATA v16.1 software (StataCorp, LLC College Station, Texas, United States).

Results The analysis included 17 independent cohort studies with a total of 384 patients. The rate of technical success was 99.86 % (95 % CI: 99.2 %, 100 %; P = 0.00; I2  = 70.69 %) and the calculated pooled rate of clinical success was 84.99 % (95 % CI: 77.4 %, 91.41 %; P = 0.00; I2  = 68.02 %). The calculated pooled rate of adverse events was 7.6 % (95 % CI: 3.99 %, 12.21 %; P = 0.03; I2  = 42.5 %) with recurrent abscess formation and bleeding being the most common AEs. Moderate to substantial heterogeneity was noted in our meta-analysis.

Conclusions Endoscopic vacuum therapy appears to be a minimally invasive, safe, and effective treatment modality for patients with a significant colorectal leak without any generalized peritonitis with high clinical and technical success rates and a low rate of adverse events. Further prospective or randomized controlled trials are needed to validate our findings.


#

Introduction

Following colorectal surgery, anastomotic dehiscence and subsequent leak formation has an incidence of 2 % to 7 % [1] [2] [3]. Depending upon the location of the leak, the rate may be as high as 10 % to 20 % (coloanal) or as low as 1 % to 3 % (ileocolic). Anastomotic leaks (ALs) in colorectal surgery have been associated with an increase in mortality from 1.6 % to 12 % [4]. A study by Alves et al showed that the risk of AL increased with the presence of risk factors such as leukocytosis, increased duration of the surgical procedure, recent steroid use, the location of procedure (ileorectal vs colocolic), and renal failure, among others [4]. The goal of treating anastomotic leakage is the prevention of sepsis and chronic fistula formation [5].

The management of ALs is not standardized [6]. The patient’s clinical condition is the major determining factor for management. Patients with sepsis and signs of peritonitis generally undergo surgery while stable patients can be considered for endoscopic therapy [7]. Various endoscopic treatments have evolved for the management of AL in colorectal surgery and these include endoscopic self-expanding metal stents (SEMS), endoscopic clips, and endoscopic vacuum-assisted closure devices [8]. Smaller leaks are usually managed with stents or clips while endoscopic vacuum therapy (EVT) is preferred for larger leaks (> 2 cm) or for leaks with an associated abscess.

EVT was first described by Weidenhagen et al. in 2008 to treat patients with presacral abscesses [9]. Since then, it has been successfully applied in the management of ALs after colorectal surgery. In this technique, the cavity and the size of the leak are determined via direct endoscopic examination. A sponge is shaped to fit the size of the cavity/leak and inserted endoscopically through an overtube. This sponge is connected to a drainage tube which is in turn connected to vacuum suction device to continuously remove secretions. The sponge is exchanged every few days for a smaller replacement, to fit the diminishing cavity, until healing is complete. The applied negative pressure also improves microcirculation, and induces granulation formation in the area of the defect helping in the closure of the pelvic cavity [10]. The most commonly used commercially available EVT system is Endo-SPONGE System (B. Braun, Meslungen, Germany).

Our meta-analysis aims to evaluate the efficacy and safety of Endo-SPONGE System in the management of colorectal leaks.


#

Methods

Search strategy

We reviewed literature from several databases such as PubMed, EMBASE, CINAHL, Cochrane and Google Scholar (from inception to July 2020). We utilized several combinations of keywords in our literature search such as: ‘colorectal,’ ‘endoscopic,’ ‘leak,’ ‘anastomosis,’ ‘vacuum’ and ‘endosponge’. We had two authors (BD and SS) carry out the search and review the articles individually. If there were any discrepancies, then a third author (SD) would review for resolution. The references section of each selected article was reviewed for additional articles. Any article that did not meet the inclusion criteria was excluded. The preferred reporting items for systematic reviews and meta-analyses (PRISMA) guidelines were utilized to identify studies reporting outcomes on Endo-SPONGE for colorectal anastomotic leaks [11]. Refer to Supplementary Fig. 1.


#

Study selection

We reviewed studies evaluating the efficacy and safety of Endo-SPONGE for colorectal anastomotic leaks. Any study that met our inclusion criteria and had data to be extracted was included in our final analysis. The inclusion criteria was studies reporting technical success, clinical success and adverse events of endosponge in colorectal leaks. The following exclusion criteria were used: (1) studies utilizing other endoscopic methods to repair anastomotic leaks, (2) individuals age < 18, (3) sample size < 10 patients, and (4) studies not in English language. If overlapping cohorts were encountered, then the most appropriate study would be selected and the others were excluded.


#

Data abstraction and quality assessment

The selected articles were independently assessed for quality by two authors (BD and SS). The quality of the studies was ascertained by the Newcastle-Ottawa scale [12]. Refer to Supplementary Table 1.


#

Outcomes assessed

The primary outcomes assessed were the technical and clinical success of Endo-SPONGE placement in colorectal anastomotic leaks.

The secondary outcomes assessed were the overall adverse events and the adverse event subtypes.


#

Definitions

Technical success was defined as successful placement of the Endo-SPONGE in the cavity in 13 of 17 studies [5] [6] [10] [13] [14] [15] [16] [17] [18] [19] [20] [21] [22]. Clinical success was defined as closure of the anastomotic leak, confirmed via endoscopy or contrast enhanced computed tomography imaging [5] [6] [10] [13] [14] [17] [19] [21] [22] [23] [24]. Adverse events (AEs) were related directly to the procedure.


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Statistical analysis

A random effects model was used to calculate the pooled estimates for each outcome of interest as suggested by the meta-analysis techniques by DerSimonian and Laird [25]. A continuity correction of 0.5 would be added prior to statistical analysis if zero’s occurred in the incidence of an outcome of a study [26]. We utilized the Cochran Q statistical test and I2 statistics to assess heterogeneity [27] [28]. Low, moderate, substantial or considerable heterogeneity was classified by the values of < 30 %, 30 % to 60 %, 61 % to 75 %, and > 75 %, respectively [29]. To determine if publication bias was present, we qualitatively ascertained by direct visualization of the funnel plot [30]. All analyses were performed using STATA v16.1 software (StataCorp, LLC College Station, Texas, United States).


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#

Results

Search results and population characteristics

From an initial group of 655 studies, 17 studies reported data regarding the use of Endo-SPONGE in 384 patients with colorectal leaks. Studies with overlapping cohorts were identified and the most appropriate ones were included in final analysis. The majority of the patients were males (68.22 % reported in 16 studies) and the mean age was 61.62 (range 37–71) years. Four cases were secondary to traumatic perforation and the remainder were anastomotic leaks.

Average time to detection of leaks was 28.08 (range 7.1–85) days from surgery (reported in 9/17 studies) and average length of therapy was 33.1 (range 15–108) days. The average number of procedures was 8.23 (range 2.2–16.2) and the average follow-up was 18.2 (range 2–48) months. [Table 1] describes the characteristics of the included studies. The schematic diagram of study selection is shown in Supplementary Fig. 1.

Table 1

Characteristics of the included studies.

Study

Year

Country

Type of study

Single/multicenter

Manuscript/abstract

No. of patients

No. of procedures

Mean age

Males

Females

Wasmann [22]

2019

Austria

Retrospective

Single

Manuscript

18

 57

40.56

12

 6

Van Koperen [21]

2008

France

Retrospective

Multicenter

Manuscript

16

208

64

 9

 7

Keskin [17]

2015

Netherlands

Retrospective

Single

Manuscript

15

 33

55

 8

 7

Jimenez-Rodriguez [16]

2018

Netherlands

Retrospective

Single

Manuscript

22

 69

64.8

18

 4

Grande [34]

2020

Netherlands

Retrospective

Single

Abstract

40

320

31

 9

Glitsch [14]

2008

Spain

Retrospective

Single

manuscript

17

161

61.1

14

 3

Gardenbroek [5]

2014

Spain/USA

Retrospective

Single

Manuscript

15

 45

37

12

 3

Arezzo [13]

2015

Turkey

Retrospective

Single

Manuscript

14

228

68

 7

 7

Abdalla [6]

2020

France

Retrospective

Multicenter

Manuscript

47

310

64.7

36

11

Strangio [10]

2015

Germany

Prospective

Single

Manuscript

25

225

67

18

 7

Riss [36]

2010

Austria

Retrospective

Multicenter

Manuscript

20

66.3

13

 7

Nerup [20]

2013

Denmark

Retrospective

Multicenter

Manuscript

13

104

64

11

 2

Mussetto [19]

2017

Italy

Retrospective

Single

Manuscript

11

176

71

 6

 5

Mansilla-Vivar [6]

2020

Spain

Prospective

Multicenter

Abstract

20

70

17

 3

Lisi [24]

2017

Italy

Prospective

Single

Abstract

14

Kuhn + Zimmerman [18]

2020

Germany

Retrospective

Single

Manuscript

56

448

66

34

22

Kuhn + Janisch [23]

2020

Germany

Retrospective

Single

Manuscript

21

64.9

16

 5


#

Characteristics and quality of included studies

The analysis included 17 independent cohort studies with a total of 384 patients. There were five multicenter studies, no population-based and 12 single-center studies included in our final analysis. Three studies had more than 30 patients, five studies had more than 20 patients, and nine studies had more than 10 patients. Fourteen studies were published in manuscript form and three studies were published in abstract form. [Table 1] describes the characteristics of the included studies.

Quality assessment was performed with the help of the NOS scale. Nine studies were of good quality and eleven study were of fair quality. No poor quality studies were found. Details of quality assessment can be seen in Supplementary Table 1.


#

Meta-analysis outcomes

Primary outcomes

The rate of technical success was 99.86 % (95 % CI: 99.20 %, 100.00 %; I2 = 70.69 %) and the calculated pooled rate of clinical success was 84.99 % (95 % CI: 77.40 %, 91.41 %; I2 = 68.02 %). [Fig. 1] and [Fig. 2] shows the Forest Plots for technical and clinical successes of Endo-SPONGE in colorectal leaks.

Zoom Image
Fig. 1 Forest plot showing technical success with Endo-SPONGE for colorectal leaks.
Zoom Image
Fig. 2 Forest plot showing clinical success with Endo-SPONGE for colorectal leaks.

#

Secondary outcomes

The calculated pooled rate of AEs was 7.69 % (95 % CI: 3.99 %, 12.21 %; I2 = 42.5 %) with recurrent abscess formation and bleeding being the most common AEs. [Fig. 3] shows the Forest Plots for total adverse events of Endo-SPONGE in colorectal leaks. As per American Society of Gastrointestinal Endoscopy criteria, 60.06 % of the AEs were mild and 36.36 % were moderate [31]. [Table 2] describes the AEs in different studies.

Zoom Image
Fig. 3 Forest plot showing total adverse events with Endo-SPONGE for colorectal leaks.
Table 2

Adverse events with the Endo-SPONGE.

Study

Year

Total adverse events

Bleeding

Perforation

Pain

Stent migration

Abscess

Restenosis

Others

Wasmann [22]

2019

2

0

0

0

0

1

0

1

Van Koperen [21]

2008

5

1

0

1

0

2

0

1

Keskin [17]

2015

3

1

0

0

0

0

0

2

Jimenez- Rodriguez [16]

2018

1

0

0

0

0

0

1

0

Grande [34]

2020

2

1

0

0

0

0

0

1

Glitsch [14]

2008

2

0

0

0

0

0

0

2

Gardenbroek [5]

2014

1

0

0

0

0

0

0

1

Arezzo [13]

2015

1

0

0

0

0

1

0

0

Abdalla [6]

2020

2

0

0

0

0

2

0

0

Strangio [10]

2015

3

0

0

0

0

1

0

2

Riss [36]

2010

1

0

0

0

0

0

1

0

Nerup [20]

2013

1

0

0

0

0

0

1

0

Mussetto [19]

2017

2

0

0

0

0

0

2

0

Mansilla-Vivar [6]

2020

0

0

0

0

0

0

0

0

Lisi [24]

2017

5

0

0

5

0

0

0

0

Kuhn + Zimmerman [18]

2020

2

2

0

0

0

0

0

0

Kuhn + Janisch [23]

2020

0

0

0

0

0

0

0

0


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#

Validation of meta-analysis results

Sensitivity analysis

To assess whether any one study had a dominant effect on the meta-analysis, we excluded one study at a time and analyzed its effect on the main summary estimate. Based on this analysis, no single study significantly affected the outcome or the heterogeneity.


#

Heterogeneity

Based on Q statistics, and I2 analysis for heterogeneity, substantial heterogeneity was noted in the analysis of technical and clinical success of Endo-SPONGE and moderate heterogeneity was seen for total AEs.


#

Publication bias

Assessment of publication bias was difficult due to the small size of the majority of studies. These studies are one-arm with dichotomous outcomes.


#
#
#

Discussion

Our study is the first meta-analysis that demonstrates that EVT is a minimally invasive treatment option for management of colorectal ALs. This meta-analysis shows that EVT has a high technical and clinical success rate with a low rate of AEs.

The technical success of EVT in our meta-analysis was 99.86 % while the clinical success rate was also high at 84.99 %. The overall success of EVT is increased when it is used as an early intervention [6] [13] [16] [17] [21]. In the study by Abdalla et al, early endoluminal therapy (within 15 days) showed a higher clinical success rate when compared to late endoluminal therapy performed after 15 days (72.4 % vs 27.8 %) [6]. The poor outcomes seen with delayed intervention were largely attributed to the development of fibrosis of the neorectum, which impairs healing and closure [6]. Abdalla et al also reported that the use of EVT as the primary treatment for colorectal ALs had a significantly higher success rate than salvage EVT in patients who underwent prior surgical procedures. (73 % vs 33 %) [6]. In the study by Kuhn et al, the use of EVT in the treatment of rectal stump leakage following Hartmann’s procedure also demonstrated a high clinical success rate (84 %) [18]. EVT was directly compared to conventional therapy including drainage, stoma diversion, or surgical revision in the study by Kuhn et al, which showed that patients who underwent EVT had significantly higher success rates compared to those who underwent conventional therapy and demonstrated significantly higher rates of stoma reversal [23].

Preoperative neoadjuvant chemoradiotherapy affected EVT treatment duration and success. In a study by Bernstorff et al, chemoradiation therapy was associated with larger cavity sizes, longer treatment durations, and a higher number of sponge exchanges [32]. However, most patients were ultimately successfully treated and avoided additional surgery [32]. Conversely, in the study by Kuhn et al, preoperative chemoradiation therapy was a significant predictor of EVT treatment failure [18]. This can be potentially attributed tissue atrophy, fibrosis, and vascular damage associated with chemoradiation therapy [33]. Patient comorbidities and patient counselling should be taken into consideration in the decision making to undergo EVT in the setting of preoperative radiochemotherapy [33]. In one study, EVT was shown to preserve bowel continuity through ileostomy reversal in 86.7 % of patients as compared to 37.5 % among patients undergoing conservative treatment [23].

EVT appears to be a safe procedure with a low rate of AEs. The overall AE rate observed in our meta-analysis was 7.6 % with only a few cases of bleeding (0.35 %) and no cases of perforation. The rate of recurrent abscess formation was also very low (0.52 %). No procedure-related deaths were observed. The rate of anastomotic stenosis was very low (0.14 %) and these strictures can be treated in some cases with balloon dilation, avoiding surgical intervention [16].

This meta-analysis has several limitations. The retrospective study design in most studies, small sample sizes, and the lack of any randomized controlled studies is a major limitation. There was moderate to substantial heterogeneity noted in our analysis. There were also no direct comparisons to other treatment modalities in colorectal ALs in most studies. In addition, there are no standardized criteria for treatment success in EVT, so data presented must be viewed with caution [6].


#

Conclusions

EVT appears to be a minimally invasive, safe, and effective treatment for patients with significant colorectal ALs with no generalized peritonitis. EVT has been shown to have high clinical and technical success rates with a low rate of AEs. Early intervention is the most important predictor of overall success. EVT also appears to increase the ability to maintain bowel continuity with increased rates of ileostomy reversal. Long-term randomized controlled trials and direct comparison studies are needed to further evaluate success of this procedure.


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Competing interests

The authors declare that they have no conflicts of interest.

Supplementary material

  • References

  • 1 Hyman N, Manchester TL, Osler T. et al. Anastomotic leaks after intestinal anastomosis: it's later than you think. Annals of surgery 2007; 245: 254-258
  • 2 Kingham TP, Pachter HL. Colonic anastomotic leak: risk factors, diagnosis, and treatment. J Am Coll Surg 2009; 208: 269-278
  • 3 Slieker JC, Komen N, Mannaerts GH. et al. Long-term and perioperative corticosteroids in anastomotic leakage: a prospective study of 259 left-sided colorectal anastomoses. Arch Surg 2012; 147: 447-452
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Corresponding author

Douglas G. Adler, MD, FACG, AGAF, FASGE, Professor of Medicine, Director of Therapeutic endoscopy, Director, GI fellowship program
Gastroenterology and Hepatology
University of Utah School of Medicine
Huntsman Cancer Center
30 N 1900 E, Room 4R118
Salt Lake City, Utah 84132
United States   
Fax: +1-801-581-8007   

Publication History

Received: 05 January 2021

Accepted: 29 March 2021

Article published online:
16 August 2021

© 2021. The Author(s). This is an open access article published by Thieme under the terms of the Creative Commons Attribution-NonDerivative-NonCommercial License, permitting copying and reproduction so long as the original work is given appropriate credit. Contents may not be used for commercial purposes, or adapted, remixed, transformed or built upon. (https://creativecommons.org/licenses/by-nc-nd/4.0/)

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Rüdigerstraße 14, 70469 Stuttgart, Germany

  • References

  • 1 Hyman N, Manchester TL, Osler T. et al. Anastomotic leaks after intestinal anastomosis: it's later than you think. Annals of surgery 2007; 245: 254-258
  • 2 Kingham TP, Pachter HL. Colonic anastomotic leak: risk factors, diagnosis, and treatment. J Am Coll Surg 2009; 208: 269-278
  • 3 Slieker JC, Komen N, Mannaerts GH. et al. Long-term and perioperative corticosteroids in anastomotic leakage: a prospective study of 259 left-sided colorectal anastomoses. Arch Surg 2012; 147: 447-452
  • 4 Alves A, Panis Y, Trancart D. et al. Factors associated with clinically significant anastomotic leakage after large bowel resection: multivariate analysis of 707 patients. World J Surg 2002; 26: 499-502
  • 5 Gardenbroek TJ, Musters GD, Buskens CJ. et al. Early reconstruction of the leaking ileal pouch-anal anastomosis: a novel solution to an old problem. Colorectal Dis 2015; 17: 426-432
  • 6 Abdalla S, Cotte E, Epin A. et al. Short-term and long-term outcome of endoluminal vacuum therapy for colorectal or coloanal anastomotic leakage: results of a nationwide multicenter cohort study from the French GRECCAR Group. Dis Colon Rectum 2020; 63: 371-380
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Fig. 1 Forest plot showing technical success with Endo-SPONGE for colorectal leaks.
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Fig. 2 Forest plot showing clinical success with Endo-SPONGE for colorectal leaks.
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Fig. 3 Forest plot showing total adverse events with Endo-SPONGE for colorectal leaks.