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Article

Endoscopic Vacuum Therapy in Patients with Transmural Defects of the Upper Gastrointestinal Tract: A Systematic Review with Meta-Analysis

1
Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Korea
2
Department of Internal Medicine, Yongin Severance Hospital, Yonsei University College of Medicine, Seoul 03722, Korea
3
Medical Library, Yonsei University College of Medicine, Seoul 03722, Korea
*
Author to whom correspondence should be addressed.
There are contributed equally to this work.
J. Clin. Med. 2021, 10(11), 2346; https://doi.org/10.3390/jcm10112346
Submission received: 16 April 2021 / Revised: 22 May 2021 / Accepted: 24 May 2021 / Published: 27 May 2021
(This article belongs to the Special Issue Gastrointestinal Tract Disorders)

Abstract

:
A transmural defect of the upper gastrointestinal (UGI) tract is a life-threatening condition associated with high morbidity and mortality. Recently, endoscopic vacuum therapy (EVT) was used for managing UGI defects and showed promising results. We conducted a systematic review and meta-analysis to synthesize evidence on the efficacy of EVT in patients with transmural defects of the UGI tract. We searched the PubMed, Cochrane Library, and Embase databases for publications on the effect of EVT on successful closure, mortality, complications, and post-EVT strictures. Methodological quality was assessed using the Newcastle–Ottawa quality assessment scale. This meta-analysis included 29 studies involving 498 participants. The pooled estimate rate of successful closure with EVT was 0.85 (95% confidence interval [CI]: 0.81–0.88). The pooled estimate rates for mortality, complications, and post-EVT strictures were 0.11, 0.10, and 0.14, respectively. According to the etiology of the transmural defect (perforation vs. leak and fistula), no significant difference was observed in successful closure (odds ratio [OR]: 1.45, 95% CI: 0.45–4.67, p = 0.53), mortality (OR: 0.77, 95% CI: 0.24–2.46, p = 0.66), complications (OR: 0.94, 95% CI: 0.17–5.15, p = 0.94), or post-EVT stricture rates (OR: 0.70, 95% CI: 0.12–4.24, p = 0.70). The successful closure rate was significantly higher with EVT than with self-expanding metal stent (SEMS) placement (OR: 3.14, 95% CI: 1.23–7.98, p = 0.02). EVT is an effective and safe treatment for leaks and fistulae, as well as for perforations in the UGI. Moreover, EVT seems to be a better treatment option than SEMS placement for UGI defects.

1. Introduction

Transmural defects of the upper gastrointestinal (UGI) tract are categorized as perforations, leaks, or fistulae. A perforation is defined as an acute rupture of the gastrointestinal wall that can occur after an endoscopic procedure or due to underlying pathology, such as massive vomiting (Boerhaave syndrome), foreign bodies, peptic ulcers [1,2]. A leak is a communication between the intraluminal and extraluminal spaces, which occurs because of postsurgical complications, most commonly at the anastomosis site. A fistula that develops owing to prolonged anastomotic leak is defined as an abnormal connection between the gastrointestinal tract and other organs or abscess cavities. Tracheoesophageal fistula is representative. Transmural defects of the UGI are life-threatening and associated with high morbidity and mortality rates [3,4]. The optimal management of UGI transmural defects remains controversial. Though surgery is an important treatment strategy, the associated mortality rate is about 12–50% [3,5,6]. Placement of a self-expanding metal stent (SEMS) was also proven to be an effective treatment strategy for UGI defects [7,8]. However, SEMS placement can also cause complications such as stent migration, stent ingrowth, perforation, bleeding, epidural abscess, and vascular fistula [9,10,11].
Recently, endoscopic vacuum therapy (EVT) was used with promising results for managing UGI defects [12,13,14]. This method involves the application of a continuous negative pressure to drain the infected fluid and accelerates wound healing [15]. EVT is suitable for localized defects for which stent placement is not feasible. Moreover, external drainage is not necessary in most cases [16]; however, the clinical success rate of EVT varies widely from 66.7–100% [17,18,19]. In addition, corroborating evidence is needed because most studies are limited to case series and retrospective cohort studies with small sample sizes.
We performed a meta-analysis of studies on the clinical outcomes of EVT in patients with transmural defects of the UGI tract. We aimed to assess the effect of EVT on successful closure, mortality, postprocedural complications, and stricture. In addition, we evaluated the efficacy of EVT according to the etiology of the transmural defect (perforation vs. leak and fistula) and treatment method (EVT vs. SEMS placement).

2. Material and Methods

2.1. Literature Search Strategy

We performed a systematic review and meta-analysis following the principles of the PRISMA (Preferred Reporting Items for Systematic reviews and Meta-Analyses) statement [20]. The PubMed, Cochrane Library, and Embase databases (from inception to April 2020) were independently searched by three authors (DHJ, HRY, and CWH). We used the following search string: anastomotic leak OR anastomotic leakage OR postoperative leak OR postoperative leakage OR esophageal leak OR esophageal leakage OR esophageal fistula OR leakage OR fistula OR leak OR perforation OR upper gastrointestinal tract OR esophagus OR esophageal OR gastric OR stomach OR esophagectomy OR anastomosis AND endoscopic vacuum therapy OR endoscopic vacuum-assisted closure OR endoluminal vacuum therapy OR vacuum therapy OR vacuum-assisted closure OR negative pressure wound therapy OR endoscopic negative pressure therapy OR negative pressure therapy OR endovac therapy OR endo sponge (as illustrated in supplementary Table S1). We manually and repetitively searched the cited references in published studies to identify other studies.

2.2. Study Selection

In the first stage of the study selection, the titles and abstracts of the articles that our keyword search returned were scrutinised to rule out irrelevant articles. Thereafter, the full texts of all selected studies were screened according to our inclusion and exclusion criteria. The inclusion criteria were as follows: (1) a diagnosis of perforation, leak, or fistula of the UGI tract; (2) EVT as a primary or rescue treatment; and (3) investigations of adults aged ≥18 years. The exclusion criteria were as follows: (1) article types other than original articles; (2) case reports including fewer than two patients; (3) abstract-only publications; and (4) publications in a language other than English. Only the most recent study was selected if several publications covering the same study population existed.

2.3. Data Extraction

Three authors (DHJ, HRY, and CWH) of this review independently extracted data from the included studies using a predata extraction form. Further, we reviewed the titles and abstracts of all the included studies to exclude irrelevant publications. Any discrepancies in data interpretation were resolved through discussions, rereview of studies, and consultation with another author (SJL). We extracted the following information: year of publication, first author, study design, patient age and sex, sample size, study region, follow-up duration, transmural defect size, time to diagnosis, time to treatment, EVT type, successful closure rate, mortality rate, complication rate, post-EVT stricture rate, hospital length of stay, intensive care unit length of stay, treatment duration, and number of sponge or stent changes.

2.4. Primary and Secondary Outcomes

The primary outcome was the successful closure rate. Successful closure was defined as no evidence of leakage on direct endoscopic visualization and the absence of contrast extravasation on either a computed tomography scan with oral contrast, esophagography, or a UGI study. The secondary outcomes were mortality rate, complication rate (Clavien–Dindo score ≥ 3), and stricture rate after EVT.

2.5. Methodological Quality

The Newcastle–Ottawa quality assessment scale for cohort studies was used to evaluate the risk of bias. This scale rates studies on three sources of bias (selection, comparability, and outcome) based on eight criteria. Each criterion is rated with 1 star except comparability, which is rated a maximum of 2 stars. For this systematic review, the studies scoring 7–9 stars were defined be of low risk of bias, the studies scoring 4–6 stars were defined to be of moderate risk of bias, and the studies scoring 1–3 stars were defined to be of high risk of bias. Three authors (CWH, HRY, and DHJ) independently evaluated the methodological quality of the selected studies. Any disagreement between the three authors was resolved through discussions.

2.6. Statistical Analysis

A meta-analysis was performed using the statistical software R (version 3.3.3; R Foundation for Statistical Computing, Vienna, Austria). The Mantel–Haenszel random-effect model was applied to binary endpoints. The random-effects model was selected because it considers the possibility of heterogeneity. The median difference was used for continuous variables. Pooled medians were estimated using the quantile estimation method. In addition, we performed subgroup analyses according to the following criteria: closure rate, mortality rate, complication rate, post-EVT stricture rate according to the etiology of transmural defect (perforation vs. leak and fistula), closure rate, mortality, treatment duration, hospital stay, and number of sponge/stent changes of EVT and SEMS.
The I2 test developed by Higgins was used to determine heterogeneity [21]. This test measures the percentage of total variation across studies. In cases of significant heterogeneity (I2 > 25%), the methodological section of each publication was re-evaluated to determine whether any discrepancy could be checked. We used the Egger test to assess the extent of the publication bias. Statistical significance was set at p < 0.05.

3. Results

3.1. Study Selection

A total of 2585 studies were identified. Duplicate articles (n = 392) were excluded. Further, 2144 articles were rejected based on the title and abstracts. Forty-nine articles were reviewed. After assessing eligibility, 20 articles were excluded (as illustrated in Figure 1). Finally, a total of 29 articles were included involving 498 participants [13,14,18,22,23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47]

3.2. Study Characteristics and Methodological Quality

The baseline characteristics of the included studies are presented in Table 1. Nineteen articles were retrospective cohort studies, and 10 were case series. Eight studies included only patients with postoperative leaks, [13,23,25,26,33,42,43,46] and two studies included only patients with perforations [24,27]. Eleven studies included patients with both postoperative leaks and perforations [14,18,29,31,32,34,35,38,40,41,44]. Four studies included patients with a fistula [36,37,45,47]. Four studies compared EVT with SEMS placement [22,28,30,39]. A total of 24 studies were conducted in Western countries (Germany 14, United States 4, Switzerland 2, United Kingdom 2, Portugal 1, and Australia 1), whereas five studies were conducted in Asia (Korea 4 and China 1).
Table 2 summarizes the clinical outcomes of the included studies. All studies except two [23,36] reported the successful closure rate. Mortality was reported in all studies except one [40]. The complications and post-EVT stricture rates were reported in 21 and 16 studies, respectively. Hospital stay, intensive care unit stay, duration of therapy, and the number of sponge changes were reported in 14, 5, 23, and 22 studies, respectively.
The definition of clinical success, detailed indications of treatment, and causes of mortality in the included studies are shown in supplementary Table S2. In addition, four studies that included fistula cases are summarized in supplementary Table S3.
The patient characteristics of studies comparing EVT and SEMS placement are summarized in supplementary Table S4. Brangewitz et al. [22] reported successful closure, mortality, duration of treatment, length of hospital stay, and stricture development in 71 patients with leaks or perforations after esophagectomies, fundoplications, esophageal diverticulotomies, Boerhaave syndrome, and iatrogenic perforations, and compared EVT (n = 32) with SEMS placement (n = 39). Schniewind et al. [23] assessed 47 patients diagnosed with postoperative leaks after esophagectomy. Mortality and length of hospital stay were compared between patients treated with EVT (n = 17) and SEMS placement (n = 12). Mennigen et al. [28] showed that successful closure, mortality, duration of treatment, length of hospital stay, and adverse events were analysed in 45 patients who were diagnosed with postoperative leak following esophagectomy in comparisons between EVT (n = 15) versus SEMS (n = 30). Hwang et al. [30] compared EVT (n = 7) and SEMS placement (n = 11) in South Korea. Although the number of enrolled patients was small, they also showed successful closure, duration of treatment, length of hospital stay, and adverse events. They included eighteen patients who were diagnosed with postoperative leak after esophagectomy or gastrectomy for cancer treatment. Lastly, Berlth et al. [39] reported successful closure, mortality, duration of treatment, length of hospital stay, and adverse events in comparisons between EVT (n = 34) and SEMS (n = 77). One hundred and eleven patients underwent curative surgery to treat malignancies and were diagnosed with postoperative leaks.
The methodological quality of the studies is presented in Supplementary Table S5. The quality was poor in 15 studies [24,25,27,29,32,34,36,37,38,41,42,43,44,45,47] and moderate in 14 studies [13,14,18,22,23,26,28,30,31,33,35,39,40,46].

3.3. Primary and Secondary Outcomes

3.3.1. Primary Outcome—Successful Closure Rate

Twenty-seven studies reported data on successful closure in 456 patients. The pooled estimate rate for successful closure was 0.85 (95% confidence interval [CI]: 0.81–0.88, Figure 2). No heterogeneity was found among the studies (I2 = 0%, p = 0.68). No publication bias was detected by the Egger test (p = 0.33).

3.3.2. Secondary Outcomes—Mortality, Complication, and Post-EVT Stricture Rates

Data on mortality were reported in 28 studies comprising a total of 412 patients. The pooled estimated mortality rate was 0.11 (95% CI: 0.09–0.15, as illustrated in Figure 3A). No heterogeneity was found among these studies (I2 = 0%, p = 0.96). No publication bias was detected by the Egger test (p = 0.38). Twenty-one studies reported data on complications in 304 patients. The pooled estimate rate for complications was 0.10 (95% CI: 0.06–0.15, as illustrated in Figure 3B). Low heterogeneity was found among the studies (I2 = 13.8%, p = 0.28). Publication bias was detected by the Egger test (p < 0.05). Sixteen studies reported data on post-EVT strictures in 240 patients. The pooled estimate rate for post-EVT stricture was 0.14 (95% CI: 0.10–0.20, as illustrated in Figure 3C). No heterogeneity was found among these studies (I2 = 0%, p = 0.45). The p-value of publication bias by the Egger test was 0.06.

3.4. Subgroup Analysis

3.4.1. Perforation vs. Leak and Fistula—Successful Closure, Mortality, Complications, and Post-EVT Stricture Rates

According to the etiology of the transmural defect, evaluation of the successful closure rate was performed in 11 studies. The pooled analysis showed that the successful closure rate was similar between the perforation and leak groups (odds ratio [OR]: 1.45, 95% CI: 0.45–4.67, p = 0.53; as illustrated in Figure 4A). We detected low heterogeneity among the studies (I2 = 24.1%, p = 0.24). Data on mortality according to the etiology of transmural defects were available for 10 studies. The analysis revealed no significant difference between the two groups in terms of mortality rate (OR: 0.77, 95% CI: 0.24–2.46, p = 0.66; as illustrated in Figure 4B), and there was no heterogeneity (I2 = 0%, p = 0.58). Eight studies reported data on complications according to the etiology of transmural defects. The pooled analysis showed that the complication rates were similar between the perforation and leak groups (OR: 0.94, 95% CI: 0.17–5.15, p = 0.94; as illustrated in Figure 4C). No heterogeneity was detected among the studies (I2 = 0%, p = 0.79). Data on post-EVT stricture rate according to the etiology of transmural defects were available for five studies. No significant difference was observed between the two groups in terms of post-EVT stricture rate (OR: 0.70, 95% CI: 0.12–4.24, p = 0.70; as illustrated in Figure 4D), and no heterogeneity was noted (I2 = 0%, p = 0.47).

3.4.2. EVT vs. SEMS—Successful Closure, Mortality, Treatment Duration, Length of Hospital Stay, and the Number of Endoscopic Stent/Sponge Changes

The length of hospital stay was mentioned in all included studies. Among the four studies that compared EVT and SEMS placement, successful closure rate, mortality rate, duration of treatment, and the number of endoscopic stent/sponge changes were demonstrated. The successful closure rate was significantly higher in the EVT group than in the SEMS group (OR: 3.14, 95% CI: 1.23–7.98, p = 0.02) (as illustrated in Figure 5A). The mortality rate was lower in the EVT group than in the SEMS group (OR: 0.39, 95% CI: 0.18–0.83, p = 0.01) (as illustrated in Figure 5B). Compared to SEMS placement, EVT showed a shorter treatment duration, with an estimated pooled median difference of 11.90 days (95% CI: −18.59–−5.21, p < 0.01), after excluding one study that reported a shorter duration of treatment with SEMS placement (as illustrated in Figure 5C). The length of hospital stay showed similar results between the EVT and SEMS groups with an estimated pooled median difference of 2.81 days (95% CI: 6.20–11.82, p = 0.27) (as illustrated in Figure 5D). In addition, the number of endoscopic stent/sponge changes were significantly higher in EVT than with SEMS placement, and an estimated pooled median difference of 3.09 was noted (95% CI 1.54–4.64, p = 0.03)) (as illustrated in Figure 5E).

4. Discussion

To date, many studies reported promising outcomes in patients with transmural defects of the UGI tract with EVT used as a definitive treatment. However, these previous studies included only a limited number of patients. Recently, several systematic reviews reported the usefulness of EVT in transmural defects of the UGI tract. [19,48,49,50]; however, these reviews were only descriptive and did not conduct statistical analysis with a summary estimate. Therefore, a meta-analysis is needed to compile and analyze the available data on the efficacy of EVT in transmural defects of the UGI tract. Our meta-analysis included case series in which a single group was assessed with no intrastudy comparisons. Nevertheless, this meta-analysis has an advantage over narrative reviews because it assessed effect sizes and integrated them into a single statistical analysis.
In this meta-analysis, the closure rate of transmural UGI defects with EVT was excellent (85%), and EVT was associated with low mortality (11%), complications (10%), and post-EVT stricture rates (14%) rates. Moreover, no significant difference was observed in successful closure (OR: 1.45, 95% CI: 0.45–4.67), mortality (OR: 0.77, 95% CI: 0.24–2.46), complications (OR: 0.94, 95% CI: 0.17–5.15, p = 0.94), and post-EVT stricture rates (OR: 0.70, 95% CI: 0.12–4.24, p = 0.70) according to the etiology of the transmural defect (perforation vs. leak and fistula). Although the etiology of transmural UGI defects was different, the efficacy of EVT was similar between the groups.
EVT had a significantly higher successful closure rate than with SEMS placement (OR: 3.14, 95% CI: 1.23–7.98). In addition, the mortality rate was lower (OR: 0.39, 95% CI: 0.18–0.83) and the treatment duration was shorter with EVT than with SEMS placement (−11.90, 95% CI: −18.59–−5.21). We believe that this was due to the difference in methodology between EVT and SEMS placement. Generally, SEMS removal or replacement is performed 4–6 weeks after SEMS insertion. Therefore, the successful closure rate with SEMS treatment was determined 4–6 weeks after the previous SEMS insertion. In contrast, because EVT is repeated every 3–5 days, clinicians can also check successful closure every 3–5 days. Therefore, successful closure could be detected sooner with EVT than with SEMS placement. In addition, EVT treatment could offer the possibility of performing endoscopic lavage and debridement with every change, which was shown to reduce pleural inflammation and leakage-associated mortality.
The principle of EVT is similar to the classical vacuum-assisted closure treatment, which is a well-established therapy for chronic superficial wounds [51]. In EVT, a polyurethane sponge is placed inside the defect to apply negative pressure. Defect healing is achieved through continuous abscess drainage, thus decreasing bacterial colonization, enhancing vascularity, and promoting tissue granulation [51,52]. An internal vacuum sponge (endo-SPONGE) device was first successfully used for treating a UGI anastomosis leak in 2008 [15]. Since then, EVT was used to manage UGI defects and showed good short- and long-term clinical outcomes. SEMS placement also showed effective outcomes for UGI defects [7,8]. However, stent therapy is usually accompanied by additional abscess drainage, local pressure necrosis of the mucosa, stent migration, stent ingrowth, bleeding, and perforation. Surgery is also one of the strategies for treating transmural defects of the UGI; however, it is associated with a high mortality rate [5,6]. To date, comparative studies assessing different treatment modalities for UGI defects are rare [53]. Therefore, clinical evidence of efficacy of EVT for treatment of UGI defects is still inadequate for directing treatment modalities. Our meta-analysis showed that EVT is an effective and safe treatment method for treating leaks, fistulae, and perforations.
Usually, transmural defects of the UGI tract are classified as perforations, leaks, or fistulae. Of these, fistulae are the most difficult to close because the epithelial tract is often fibrotic, and these arise in unhealthy tissues, which are inflamed, damaged, or ischemic. Although the included cases were too few (n = 8), this meta-analysis showed a successful closure rate of 50% in patients with a fistula. Given the inadequate response of fistulae to other treatments such as SEMS placement, EVT is a promising option for treating patients with fistula.
The major disadvantages of EVT are the need for repetitive endoscopic procedures, nasogastric tube-related discomfort, and sponge dislocation. The main and most dreadful event associated with EVT is massive bleeding [19,48]. It can occur from a fistula between the cavity and main vessels and from rupture of a pseudoaneurysm from circumjacent vessels or heart chambers. More frequent changes of the sponge may help prevent or reduce the risk of severe bleeding. Moreover, massive bleeding can occur in cases of intracavitary therapy in which direct contact with blood vessels is possible. Therefore, intraluminal EVT may be safer than intracavitary EVT. Additionally, computed tomography scans should be reviewed before initiating intracavitary EVT to exclude vascular complications. In our review, post-EVT strictures occurred in 14% of cases; however, all strictures were easily resolved through endoscopic dilatations (26 cases).
Although the results of this study are promising, it had several limitations. All included studies were retrospective in nature without randomisation. This could have resulted in a selection bias in this study. Typically, the choice of modalities (EVT, SEMS placement, operation, and nonoperative management) were chosen according to the severity of the patients. Patients managed conservatively tend not to be septic and have a contained leak versus those who have apparent mediastinal contamination and warrant endoscopic or surgical intervention. As EVT is a relatively new treatment method, it could be assumed that the first experience of the studies included in this meta-analysis was performed in cases in which a favorable outcome was expected, thus influencing the results. Although randomized controlled trials are considered the best method for evaluating treatment effects, performing such trials would be difficult owing to ethical concerns and methodological difficulties. Second, although the statistical heterogeneity was low, the clinical heterogeneity was high among the included studies. Patient heterogeneity and detailed indication were different among the included studies. Therefore, the complexity and comorbidities of each patient could affect the treatment success. In addition, SEMS placement is a more standard treatment compared to EVT, which may also affect treatment outcomes. To address this limitation, we have additionally summarized detailed information of the studies included in this meta-analysis (as illustrated in supplementary Tables S1–S4) Third, the included studies had a limited quality. Fourth, the sample size of each study was insufficient to reach definitive conclusions. Therefore, additional data are needed to define the role of EVT in patients with UGI defects. Finally, most of the included studies were from Western countries, especially Germany. Large-scale studies from other regions are required to validate the usefulness of EVT in treating UGI defects in patients of different ethnicities. Despite these limitations, to the best our knowledge, this meta-analysis contains the most comprehensive analysis of the effectiveness of EVT for treating UGI defects.

5. Conclusions

In summary, this meta-analysis revealed that EVT could be an effective and safe treatment method for leaks and fistulae as well as perforations in the UGI. In addition, EVT may be a better treatment option than SEMS placement for UGI defects. However, a definite recommendation cannot be made for the treatment of UGI defects due to the limitations of the included studies mentioned above. We believe that prospective large-scale studies from various regions worldwide are needed to validate the effectiveness of EVT for treating UGI defects.

Supplementary Materials

The following are available online at https://www.mdpi.com/article/10.3390/jcm10112346/s1: Table S1, search terms in PubMed, Embase and Cochrane Library; Table S2, definition of clinical success, detail indication, and cause of mortality in the 29 studies included; Table S3, detailed information of the 4 studies included patients with fistula; Table S4, patients’ characteristics of studies comparing endoscopic vacuum therapy and self-expanding metal stent, and Table S5, methodological quality.

Author Contributions

Conceptualization, D.H.J., H.-R.Y., C.W.H.; data curation, N.W.K., C.W.H.; formal analysis, D.H.J., H.-R.Y., C.W.H.; investigation, D.H.J., H.-R.Y., S.J.L., N.W.K., C.W.H.; methodology, D.H.J., H.-R.Y., S.J.L., N.W.K., C.W.H.; project administration, C.W.H.; resources, C.W.H.; software, D.H.J., H.-R.Y., S.J.L., N.W.K., C.W.H.; supervision, S.J.L., C.W.H.; validation, C.W.H.; visualization, H.-R.Y.; writing—original draft, D.H.J., H.-R.Y.; writing—review & editing, C.W.H. All authors read and agreed to the published version of the manuscript, including authorship list.

Funding

This research received no external funding.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Flowchart of studies included in meta-analysis.
Figure 1. Flowchart of studies included in meta-analysis.
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Figure 2. Pooled estimate rate for successful closure in patients with transmural defects of upper gastrointestinal tract.
Figure 2. Pooled estimate rate for successful closure in patients with transmural defects of upper gastrointestinal tract.
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Figure 3. (A) Pooled estimate rate for mortality in patients with transmural defects of upper gastrointestinal tract. (B) Pooled estimate rate for complications in patients with transmural defects of the upper gastrointestinal tract. (C) Pooled estimate rate for postendoscopic vacuum therapy stricture in patients with transmural defects of upper gastrointestinal tract. Abbreviations: No, number; OR, odds ratio; CI, confidence interval.
Figure 3. (A) Pooled estimate rate for mortality in patients with transmural defects of upper gastrointestinal tract. (B) Pooled estimate rate for complications in patients with transmural defects of the upper gastrointestinal tract. (C) Pooled estimate rate for postendoscopic vacuum therapy stricture in patients with transmural defects of upper gastrointestinal tract. Abbreviations: No, number; OR, odds ratio; CI, confidence interval.
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Figure 4. (A) Forrest plot of successful closure rate for comparison between the perforation and leak group. (B) Forrest plot of mortality rate for comparison between perforation and leak groups. (C) Forrest plot of complication rate for comparison between perforation and leak groups. (D) Forrest plot of postendoscopic vacuum therapy stricture rate for comparison between perforation and leak groups. Abbreviations: No, number; OR, odds ratio; CI, confidence interval.
Figure 4. (A) Forrest plot of successful closure rate for comparison between the perforation and leak group. (B) Forrest plot of mortality rate for comparison between perforation and leak groups. (C) Forrest plot of complication rate for comparison between perforation and leak groups. (D) Forrest plot of postendoscopic vacuum therapy stricture rate for comparison between perforation and leak groups. Abbreviations: No, number; OR, odds ratio; CI, confidence interval.
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Figure 5. (A) Successful closure rate between endoscopic vacuum therapy and self-expanding metal stent groups, (B) Mortality rate between endoscopic vacuum therapy and self-expanding metal stent groups, (C) Treatment duration between endoscopic vacuum therapy and self-expanding metal stent groups, (D) Hospitalization duration between endoscopic vacuum therapy and self-expanding metal stent groups, (E) Number of stent/sponge changes between endoscopic vacuum therapy and self-expanding metal stent groups. Abbreviations: EVT, endoscopic vacuum therapy; SEMS self-expanding metal stent; No, number; OR, odds ratio; CI, confidence interval; QE, quantitative estimation.
Figure 5. (A) Successful closure rate between endoscopic vacuum therapy and self-expanding metal stent groups, (B) Mortality rate between endoscopic vacuum therapy and self-expanding metal stent groups, (C) Treatment duration between endoscopic vacuum therapy and self-expanding metal stent groups, (D) Hospitalization duration between endoscopic vacuum therapy and self-expanding metal stent groups, (E) Number of stent/sponge changes between endoscopic vacuum therapy and self-expanding metal stent groups. Abbreviations: EVT, endoscopic vacuum therapy; SEMS self-expanding metal stent; No, number; OR, odds ratio; CI, confidence interval; QE, quantitative estimation.
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Table 1. Characteristics of 29 studies included.
Table 1. Characteristics of 29 studies included.
AuthorsStudy DesignNMale (n)Age (Median, Years)BMI (Median)Region of StudyFollow-Up (Median, Months)Method of DiagnosisDefect Size (Median, mm)Time to Diagnosis (Median, Days)Time to Treatment (Median, Days)Intracavitary/Intraluminary
Palmes 2020Case seriesFistula: 4NANANAWestern (Germany)MAEndoscopy
CT
Esophagogram
NANANANA
Jung 2019RetrospectiveLeak: 23
Perforation: 7
2065.1 NAWestern (Germany)11.8 NANALeak: 8.5
Perforation: <1
NAIC: 6, IL: 24
Jeon 2019RetrospectiveLeak: 221768NAEastern (Korea)29.8Endoscopy
CT
Esophagogram
NA11NAIC: 10, IL: 12
Watson 2019Case seriesLeak: 2
Fistula: 1
269.6 NAWestern (USA)2.7EndoscopyNANANANA
Pinto 2019Case seriesLeak: 2144.0 NAWestern (Portugal)NAEndoscopy
CT
NANANAIC: 2, IL: 1
Morell 2019Case seriesLeak: 6249.0 44.2Western (Switzerland)NAEndoscopy
CT
204.5 3.3 NA
Min 2019RetrospectiveLeak: 202066.5NAEastern (Korea)7.1Endoscopy
Esophagogram
17.512.53IC: 20
Loske 2019Case seriesLeak: 1
Perforation: 10
465.7 NAWestern (Germany)NAEndoscopy
CT
NANANAIC: 1 IL: 10
Leeds 2019RetrospectiveLeak: 54
Perforation: 20
NANANAWestern (USA)NANANANANANA
Walsh 2019Case seriesLeak: 1
Perforation: 1
169.5NAWestern (USA)NANA2021NANA
Alakkari 2019Case seriesLeak: 1
Perforation: 1
067 NAWestern (UK)NANANANA19 IC: 2
Berlth 2018RetrospectiveLeak: 111
EVT: 34
SEMS 77
92EVT: 65
SEMS: 64
EVT: 26
SEMS: 26
Western (Germany)NAEndoscopy
CT
Esophagogram
NAEVT: 8
SEMS: 8
EVT: 0
SEMS: 0
NA
Valli 2018RetrospectiveLeak: 11
Fistula: 1
9Leak: 57.5
Fistula: 80
NAWestern (Switzerland)NAEndoscopy
CT
Esophagogram
NANALeak: 18.4
Fistula: 52
IC: 7, IL: 5
Still 2018RetrospectiveLeak: 2
Perforation: 9
Fistula: 2
66323Western (USA)NAEndoscopy
CT
Esophagogram
NANANAIC: 3, IL: 7
Pournaras 2018RetrospectiveLeak: 14
Perforation: 7
NANANAWestern (UK)NANANANANANA
Ooi 2018RetrospectiveLeak: 6
Perforation: 4
NA56.7 NAWestern (Australia)NANA18.3NA33.6NA
Noh 2018RetrospectiveLeak: 121257.0NAEastern (Korea) 12.9CT
Esophagogram
1313.511IC: 3, IL: 9
Loske 2018Case seriesLeak: 3
Perforation: 1
NANANAWestern (Germany)NANANANANANA
Laukoetter 2017RetrospectiveLeak: 39
Perforation: 13
3165NAWestern (Germany)5.4Endoscopy
CT
Esophagogram
NANA8NA
Kuehn 2016RetrospectiveLeak: 11
Perforation: 10
1572NAWestern (Germany)17Endoscopy
CT
Esophagogram
NANANAIC: 10, IL: 11
Hwang 2016RetrospectiveLeak: 18
EVT: 7
SEMS 11
14EVT: 71.1
SEMS: 67.3
NAEastern (Korea) NANAEVT: 8.1
SEMS: 6.6
NANANA
Möschler 2015RetrospectiveLeak: 5
Perforation: 5
573.9 NAWestern (Germany)4NANANANAIC: 6, IL: 4
Mennigen 2015RetrospectiveLeak: 45
EVT: 15
SEMS 30
35EVT: 56
SEMS: 65.5
NAWestern (Germany)EVT: 8.3
SEMS: 16.8
Endoscopy
CT
Esophagogram
NAEVT: 7
SEMS: 7
NAIC: 22
Loske 2015Case seriesPerforation: 10NANANAWestern (Germany)2.8Endoscopy19<1NAIC: 1, IL: 9
Heits 2014RetrospectivePerforation: 10566 NAWestern (Germany)9Endoscopy
CT
Esophagogram
4.2NANANA
Liu 2014Case seriesLeak: 5NA61.8 NAEastern (China)NAEndoscopy
CT
Esophagogram
NA9.2NANA
Schorsch 2013RetrospectiveLeak: 17NANANAWestern (Germany)NANA14.710NAIC: 8, IL: 9
Schniewind 2013RetrospectiveLeak: 47NANANAWestern (Germany)NANANANANANA
Brangewitz 2013RetrospectiveEVT:32
SEMS: 39
58EVT:63
SEMS: 62
EVT: 25.2
SEMS: 26.4
Western (Germany)NANANANANANA
EVT, endoscopic vacuum therapy; CT, computed tomography; IC, intracavitary; IL, intraluminary; NA, not available; SEMS, self-expanding metal stent Data expressed as mean.
Table 2. Clinical outcomes of 29 studies included.
Table 2. Clinical outcomes of 29 studies included.
AuthorsNSuccessful Closure Rate (n, %)Mortality Rate (n, %)Complication Rate (n, %)Stricture Rate (n, %)Hospital Stay (Median, Days)ICU Stay (Median, Days)Duration of Therapy (Median, Days)Sponge Changes
Palmes 2020Fistula: 42/4 (50)2/4 (50)NANANANA88.5NA
Jung 2019Leak: 2320/23 (87.0)1/23 (4.3)0/23 (0)3/13 (23.1)54.4NA15.73.4
Perforation: 75/7 (71.4)1/7 (14.3)0/7 (0)1/2 (50.0)33.727.06.4
Jeon 2019Leak: 2219/22 (86.4)0/22 (0)0/22 (0)3/15 (20.0)24NA133
Watson 2019Leak: 22/2 (100.0)0/2 (0)0/2 (0)0/2 (0)NANA163
Fistula: 11/1 (100.0)0/1 (0)0/1 (0)0/1 (0)409
Pinto 2019Leak: 21/2 (50.0)0/2 (0)0/2 (0)NANANA223
Morell 2019Leak: 66/6 (100.0)0/6 (0)0/6 (0)0/6 (0)39.8 10.2 32.3 4
Min 2019Leak: 2019/20 1/20 NA6/19 49NA14.55
Loske 2019Leak: 11/1 (100.0)0/1 (0)NANANANA111.8
Perforation: 1010/10 (100.0)2/10 (20.0)
Leeds 2019Leak: 5444/54 (81.5)NANANANANANANA
Perforation: 2019/20 (95.0)
Walsh 2019Leak: 12/2 (100.0)1/1 (100.0)0/1 (0)NANANA5510
Perforation: 10/1 (0)0/1 (0)423
Alakkari 2019Leak: 11/1 (100.0)0/1 (0)0/1 (0)0/1 (0)NANA286
Perforation: 11/1 (100.0)0/1 (0)0/1 (0)0/1 (0)5613
Berlth 2018Leak: 111
EVT: 34
SEMS 77
24/34 (70.6)3/34 (0.9)0/27 (0)1/27 (3.7)378123
49/77 (63.6)11/77 (14.3)13/69 (18.8)5/69 (7.2)387271
Valli 2018Leak: 119/11 (81.8)0/11 (0)0/11 (0)2/11 (18.1)NANA20.85
Fistula: 10/1 (0)1/1 (100.0)0/1 (0)0/1 (0)164
Still 2018Leak: 2NA1/13 1/13 NANANANANA
Perforation: 9
Fistula: 2
Pournaras 2018Leak: 1414/14 (100.0)0/14 (0)1/14 (7.1)NA35NANA7
Perforation: 76/7 (85.7)1/7 (14.3)1/7 (14.3)
Ooi 2018Leak: 64/6 (66.7)1/6 (16.7)2/6 (33.3)NA621225.5 8.3
Perforation: 42/4 (50.0)1/4 (25.0)1/4 (25.0)
Noh 2018Leak: 1210/12 (83.3)1/12 (8.3)1/12 (8.3)1/12 (8.3)NANA252.7
Loske 2018Leak: 33/3 (100.0)0/3 (0)0/3 (0)0/3 (0)NANANANA
Perforation: 11/1 (100.0)0/1 (0)0/1 (0)0/1 (0)
Laukoetter 2017Leak: 3936/39 (92.3)5/39 (12.8)2/39 (5.1) §4/39 (10.2)60NA206
Perforation: 1313/13 (100.0)0/13 (0)0/13 (0)0/13 (0)46246
Kuehn 2016Leak: 119/11 (81.8)1/11 (18.2)NA1/11 (18.2)NANA124
Perforation: 1010/10 (100.0)0/10 (0)0/10 (0)155
Hwang 2016Leak: 18
EVT: 7
SEMS 11
7/7 (100.0)NA0/7 (0)NA37.1NA274.3
7/11 (63.6)6/11 (54.5) 87.319.21.6
Möschler 2015Leak: 52/5 (40.0)2/5 (40.0)0/5 (0)1/10 (10.0) §38NA34.28.4
Perforation: 55/5 (100.0)0/5 (0)0/5 (0)132
Mennigen 2015Leak: 45
EVT: 15
SEMS 30
14/15 (93.3)1/15 (6.6)0/15 (0)NA58NA26.56.5
19/30 (63.3)8/30 (26.6)0/30 (0)53361
Loske 2015Perforation: 1010/10 (100.0)0/10 (0)0/10 (0)0/10 (0)NANA52
Heits 2014Perforation: 109/10 (90.0)1/10 (10.0)NANA48 22 NA5.4
Liu 2014Leak: 55/5 (100.0)0/5 (0)0/5 (0)NANANA34.2NA
Schorsch 2013Leak: 1716/17 (94.1)1/17 (5.9)NA1/17 (5.9)NANA12NA
Schniewind 2013Leak: 29
EVT: 17
SEMS 12
NA2/17 (11.8)NANA57 26 NANA
5/12 (41.7)62 38
Brangewitz 2013EVT:3227/32 (84.4)5/32 (15.6)9/32 (28.1)3/32 (9.4)48.5NA237
SEMS: 3921/39 (53.8)11/39 (28.2)3/39 (76.9)11/39 (28.2)41333
EVT, endoscopic vacuum therapy; ICU, intensive care unit; NA, not available; SEMS, self-expanding metal stent Data expressed as mean. Only total rate was available. § Two patients died because of fatal hemorrhage during EVT.
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Jung, D.H.; Yun, H.-R.; Lee, S.J.; Kim, N.W.; Huh, C.W. Endoscopic Vacuum Therapy in Patients with Transmural Defects of the Upper Gastrointestinal Tract: A Systematic Review with Meta-Analysis. J. Clin. Med. 2021, 10, 2346. https://doi.org/10.3390/jcm10112346

AMA Style

Jung DH, Yun H-R, Lee SJ, Kim NW, Huh CW. Endoscopic Vacuum Therapy in Patients with Transmural Defects of the Upper Gastrointestinal Tract: A Systematic Review with Meta-Analysis. Journal of Clinical Medicine. 2021; 10(11):2346. https://doi.org/10.3390/jcm10112346

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Jung, Da Hyun, Hae-Ryong Yun, Se Joon Lee, Na Won Kim, and Cheal Wung Huh. 2021. "Endoscopic Vacuum Therapy in Patients with Transmural Defects of the Upper Gastrointestinal Tract: A Systematic Review with Meta-Analysis" Journal of Clinical Medicine 10, no. 11: 2346. https://doi.org/10.3390/jcm10112346

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