Clinical outcomes of over-the-scope-clip system for the treatment of acute upper non-variceal gastrointestinal bleeding: a systematic review and meta-analysis

Abstract

Background

Conventional endoscopic treatments can’t control bleeding in as many as 20% of patients with non-variceal gastrointestinal (GI) bleeding. Recent studies have shown that over-the-scope-clip (OTSC) system allowed for effective hemostasis for refractory GI bleeding lesions. So we aimed to conduct a systematic review to evaluate the effectiveness and safety of the OTSC system for management of acute non-variceal upper GI bleeding.

Method

A comprehensive literature search was conducted on PubMed, EMBASE, and Cochrane Library covering the period from January 2007 to May 2019. The search terms included “gastrointestinal bleeding” AND “OTSC OR over the scope clip”. The literature was selected independently by two reviewers according to the inclusion and exclusion criteria. The statistical analysis was carried out using Comprehensive Meta-Analysis software version 3.0.

Results

A total of 16 studies including 769 patients with 778 GI bleeding lesions were identified. Pooled technical success was achieved in 761 lesions [95.7%; 95% confidence interval (CI), 93.5%-97.2%], and the pooled clinical success was achieved in 666 lesions (84.2%; 95% CI, 77.4%-89.2%). The incidence of re-bleeding was reported in 81 patients and the post-procedure mortality was 10.9% (n=84). Only 2 (0.3%) patients occurred complications after OTSC system procedure.

Conclusions

Our study demonstrated that the OTSC system was a technically feasible modality and highly efficacious in achieving hemostasis in acute non-variceal upper gastrointestinal bleeding.

Introduction

Upper gastrointestinal bleeding is preponderantly non-variceal in origin and remains one of the commonest challenges faced by endoscopists in daily clinical practice. It is estimated that the incidence of annual acute upper non-variceal gastrointestinal bleeding (UNVGIB) ranges between 50 and 160 cases per 100,000 and commonly requires hospitalization [1]. Despite crucial advances in the treatment of UNVGIB over the past decade, including optimal use of endoscopic therapy and high-dose proton pump inhibition, UNVGIB still carried considerable morbidity, mortality and health economic burden [2]. The majority of UNVGIB could be managed by conventional endoscopic interventions. However, some studies have shown that conventional therapies such as epinephrine injections and hemoclips or coagulation could not achieve successful hemostasis in 4 to 20% of UNVGIB cases, and even caused severe complications.[3–8].

Hence, there was an urgent need for a safe and more effective endoscopic treatment modality for UNVGIB cases. Recently, a novel endoscopic device, called Over-the-scope clip (OTSC) (Ovesco Endoscopy AG, Tubingen, Germany) system has been developed. The OTSC system is a clipping device made of nitinol, and easily attached to the tip of the scope. By a procedure similar to ligation of esophageal varices, it can be readily released at the site of the bleeding site. Since the first report of the successful application of OTSC in GI bleeding by Kirschniak et al in 2007 [9], there have been many prospective or retrospective studies reported OTSC system to manage the UNVGIB. Thus, we aimed to perform a systematic review and structured meta-analysis of all eligible studies to evaluate the effectiveness and safety of OTSC system in patients with UNVGIB.

Materials and Methods

SEARCH STRATEGY

Studies published in PubMed, Embase and Cochrane library from January 2007 to May 2019 was searched systematically using the following search terms, "gastrointestinal bleeding” AND “OTSC OR over the scope clip”. The identified studies were subsequently screened for duplicates and relevance on the subject by their abstracts. Two reviewers independently searched literature and reviewed of the IDENTIFIED studies for eligibility. If there was any disagreement, it could be resolved through discussion between the two reviewers or judged with the assistance of a third party.

Criteria for inclusion and exclusion

Studies reporting primary data in which UNVGIB was managed with OTSC system were included. Essential results were defined as following: primary hemostasis defined as no re-bleeding immediately after OTSC placement. Primary failure defined as continuous bleeding after OTSC placement. Re-bleeding was diagnosed if a retreatment of the target lesion was required after initial successful endoscopic treatment. Technical success defined as successful placement of the OTSC on the target lesion. Clinical success defined as having no primary failure and no re-bleeding during follow-up. The above results must be reported in included studies. Only studies in English were included. And series with more than 5 cases described were included. Vivo trials were excluded. Chronic bleeding was excluded as well.

DATA EXTRACTION

The following data were extracted from each study: (a) characteristics of studies, including the author name, the publication country, publication year, type of study, sample size, age, gender, lengths of follow-up, and (b) clinical features of use OTSC system managing bleeding lesion, including indication, bleeding classification, number of patients receiving an antithrombotic, technical success, clinical success, re-bleeding, number of OTSC system deployments, number of blood units transfusion, number of patients requiring additional surgical procedures, complications and mortality.

STUDY QUALITY

Downs and Black checklist were used to evaluate the quality of the included studies [10]. We scored each study in accordance with the evaluation scale, high methodological quality articles were defined as scoring higher than 19, moderate quality articles as scoring 15 to 19, moderate to low-quality articles as scoring 10 to 14, and low quality articles as scoring lower than 10.

Statistical analysis

Continuous data were presented as mean ± standard deviation (SD) or variation range. The statistical analysis was carried out using Comprehensive Meta-Analysis software version 3.0. The overall success rate of clinical trials was expressed by the pooled proportion with 95 % confidence intervals (CI), which was presented as forest plots. Statistical heterogeneity of included studies was evaluated using Cochran Q test and I² statistic, I² value of greater than 50% or a P value of less than 0.05 for the Q statistic was considered to indicating significant heterogeneity. Then, the pooled proportion used a random-effects model or fixed-effects model. Publication bias was assessed via visual inspection of the funnel plot and Egger’s test, the P value of greater than 0.05 WAS CONSIDERED TO NO PUBLICATION BIAS [11].

Results

INCLUDED STUDIES

THE INITIAL SEARCH TERMS IDENTIFIED 218 STUDIES AFTER DUPLICATES REMOVED. OF THESE, 169 STUDIES WERE EXCLUDED ACCORDING TO THE PREDEFINED CRITERIA AND 49 STUDIES WERE REVIEWED THE FULL-TEXT. FINAL LITERATURE SEARCH AND SELECTION ACCORDING TO THE INCLUSION AND EXCLUSION CRITERIA YIELDED 16 STUDIES ABOUT OTSC SYSTEM TREATMENT FOR UNVGIB [12–27]. FIGURE 1 SHOWED THE SEARCH AND SELECTION PROCESS.

STUDIES CHARACTERISTICS

STUDIES CHARACTERISTICS ARE SUMMARIZED IN TABLE 1. ALL THE STUDIES WERE PUBLISHED BETWEEN 2011 AND 2019, AND MOST STUDIES PUBLISHED IN GERMANY (N = 7). ONLY ONE PROSPECTIVE RANDOMIZED TRIAL WAS INCLUDED [24], AND THE REMAINING STUDIES WERE RETROSPECTIVE STUDIES (N = 13) OR PROSPECTIVE STUDIES (N = 2).

A TOTAL OF 769 patients with 778 GI bleeding lesions was managed by OTSC system. Among them, OTSC system was used as the primary treatment modality in 507 lesions, while 190 lesions as rescue treatment modality after previous endoscopic treatment failure. Only 10 studies included 501 patients reported the patients’ gender and age. Of them, 303 (60.5%) patients were male, and the mean age ranged from 59 to 77 years. Follow-up time was reported in 8 studies, with at least 1 month.

CLINICAL OUTCOMES

THE ETIOLOGY OF ACUTE UPPER NON-VARICEAL GASTROINTESTINAL BLEEDING WAS AVAILABLE IN 14 STUDIES. AS SHOWN IN FIGURE 2, THE MAJOR CAUSE WAS PEPTIC ULCER (N = 446, 75.59%), THE REMAIN CAUSES WERE MALLORY-WEISS LESION (N = 38, 6.44%), POST-ENDOSCOPIC PROCEDURES (N = 33, 5.59%), ANASTOMOSIS (N = 29, 5.92%), DIEULAFOY LESION (N = 31, 5.25%), TUMOR (N = 11, 1.86%) AND OTHERS (N = 2, 0.34%). THERE WERE 7 STUDIES REPORTING PATIENTS WHO WERE UNDER THE ANTITHROMBOTIC THERAPY, THE PROPORTION OF WHICH RANG FROM 16.7% TO 75.6%. THE AVERAGE LENGTH OF HOSPITAL STAYS REPORTED IN 4 STUDIES, WHICH RANGE FROM 4 TO 19.8 DAYS. ADDITIONALLY, 13 STUDIES REPORTED 81 PATIENTS OCCURRED RE-BLEEDING, AND THE RATE VARIED FROM 0 TO 35.3%. THE NUMBER OF OTSC system deployment per lesion was reported in 8 studies, varying from 1 to 2. SIX STUDIES REPORTED THE PATIENTS RECEIVED TRANSFUSION RED BLOOD CELLS, THE MEAN NUMBER OF BLOOD UNITS TRANSFUSED RANGED FROM 0 TO 5.1 UNITS (TABLE 2).

FIGURE 3 SHOWED THE POOLED TECHNICAL SUCCESS of OTSC system which WAS ACHIEVED IN 761 LESIONS (95.7%; 95%CI, 93.5%–97.2%). Heterogeneity was not significant among the studies (I² = 24.5%, P = 0.177). FIGURE 4 SHOWED THE POOLED CLINICAL SUCCESS WAS ACHIEved in 666 lesions (84.2%; 95% CI, 77.4%–89.2%). Heterogeneity was significant among the studies (I² = 69.5%, P = 0.000). However, a total of 63 patient required additional endoscopic therapy, surgery or vascular embolization.

ADVERSE EVENTS

Most of the involved studies reported no complication occurred related to OTSC system. Complications just occurred on 2 (0.3%) patients after application OTSC system. One case occurred on a duodenal ulcer bleeding patient who experienced a tiny GI leak which was suspected to be caused by the clip. Another adverse event was lumen obstruction after a duodenal OTSC application. None of these studies reported severe and fatal complication. Twelve studies reported the mortality rate was 10.9% (n = 84), which related to re-bleeding or continued bleeding was 3.9% (n = 30) and due to other causes were 7.0% (n = 54).

QUALITY OF INCLUDED STUDIES

TABLE 3 SHOWED THE QUALITY SCORES OF EACH STUDY ACCORDING TO THE Downs and Black checklist. Five studies scored low methodological quality (score range 8 to 9), 8 studies scored low to moderate quality (score range 10 to 14), two study scored moderate-quality (score range 15 to 17), and one study which was RANDOMIZED TRIAL SCORED 20 CONSIDERED AS high-quality.

PUBLICATION BIAS

FUNNEL PLOT OF TECHNICAL SUCCESS AND CLINICAL SUCCESS WAS DEMONSTRATED IN FIGURE 5 AND FIGURE 6. THROUGH visual inspection of the funnel plot, no publication bias can be generally considered. BY Egger’s test, TECHNICAL success rate (P = 0.123) and clinical success rate (P = 0.346) had no significant publication bias.

Tables

Table 1 Characteristics of included studies

M:F male to female, P primary treatment, R rescue treatment

Table 2 Clinical outcomes of OTSC

OTSC Over-the-Scope Clip, E endoscopic, S surgery, V vascular embolization, EMR endoscopic mucosal resection, Post-endoscopic procedures, after gastric biopsy, gastric polypectomy, endoscopic ultrasonography guided fine needle aspiration of peri-gastricmass, endoscopic mucosal resection and endoscopic submucosal dissection

Table 3 Quality assessment of included studies

Discussion

UNVGIB is a common and potentially life-threatening emergency. Currently, endoscopic hemostatic treatment has been a gold standard therapy for UNVGIB, which included endoscopic hemoclips, thermal therapy and injection therapy, alone or in combination with each other [18]. However, the total re-bleeding rate after endoscopic treatment was reported to 5%–20% [28–30]. So it is urgent to develop a more effective endoscopic device or technique for UNVGIB. Recently, the OTSC system, as novel management for GI bleeding, has drawn great attention in clinical practice. The OTSC system is a full-thickness suturing device designed for flexible endoscopy. It can be used to close the wound surface of target diseases, such as non-variceal GI bleeding, perforation, fistula, and anastomotic dehiscence [31]. At present, a number of studies reported the usefulness of OTSC system for UNVGIB. In this study, we combined the data from these reports, which allowed us to provide the best evidence on the effectiveness and safety of OTSC system for UNVGIB.

Our study demonstrated that the OTSC system was a technically feasible and effective (95.7% technical success rate and 84.2% clinical success rate) modality in achieving hemostasis of UNVGIB. The OTSC system was relatively safe with a tiny minority adverse events. The high clinical success rate and minimal complication profile indicated that the OTSC system was a viable method for patients with UNVGIB.

There was just one comparative study in our systematic review, which aimed to compare standard endoscopic treatment versus OTSC system [24]. It was demonstrated that OTSC system was associated with greater efficacy and lower re-bleeding rate when compared to standard therapy with through-the-scope clips in patients with recurrent peptic ulcer bleeding after successful initial hemostasis. So the authors favored the use of OTSC system for patients with recurrent bleeding of peptic ulcers. But we still can not reach the conclusion that OTSC system was superior to other endoscopic treatments for recurrent bleeding because of the limited data in our study.

Recently, a systematic review by Ofosu et al. reported a total of 16 studies which involved 475 non-variceal gastrointestinal bleeding patients treated with OTSC. In their report, the hemostasis rate achieved with primary application of OTSC was 93% (95% CI, 89%–96%). Similarly, the hemostasis rate achieved with rescue OTSC therapy was 91% (95% CI, 84%–95%). Re-bleeding rates after primary OTSC therapy were 21% (95% CI, 8%–43%) and 25% (95% CI, 17%–34%) with rescue OTSC therapy [32]. Our results were quite close to their report. We found the OTSC system applied as the primary treatment modality in 507 lesions, while 190 lesions as rescue treatment modality after previous endoscopic treatment failure. And most of those patients we included were at high risk of re-bleeding. Five of 15 studies emphasized the OTSC system could reduce significantly re-bleeding rates and mortality in high-risk cohort and could be a first-line treatment for UNVGIB [18, 20, 23, 25–26]. Conversely, some authors concluded that OTSC system might be considered as a secondary option for high-risk patients after conventional endoscopic hemostasis failed [16–17, 20–21]. Therefore, OTSC may be considered as first-line treatment for UNVGIB in high risk patients and rescue treatment for initial failed hemostasis with conventional endoscopic methods.

Seven of 16 studies in our systematic review reported the reasons for OTSC treatment failure: 1) delayed closure of OTSC occurring in lesions with large caliber artery and those with deep fibrotic base; 2) shallow placement of OTSC resulting from inadequate suction or premature clip deployment; and 3) misplacement of OTSC because of poor visualization, difficult anatomy, and unstable endoscope position [14, 16–17, 20–21, 25, 27]. These failure causes of OTSC above may enlighten its further application in future.

The safety of OTSC system for management of UNVGIB should be carefully assessed. Our study revealed that adverse events were rare. Just 2 of 16 studies reported 2 patients experienced the complications. Albert et al. reported one patient with duodenal oozing ulcer experienced a tiny GI leak which was suspected to be caused by the OTSC system, then the patients were converted to the surgical department [13]. Richter-Schrag et al. reported lumen obstruction after a duodenal OTSC application. Then, the obstruction released with 3 balloon-dilatations [20]. In addition, there were other OTSC-related complications reported in some studies when OTSC was applied for closure GI perforation or fistula, such as esophageal perforation, acute cholangitis, inadvertent tongue piercing and jejunal stenosis [33–36]. Our study showed 10.9% of patients died during the follow-up time. Although this data was surprising, only 3.9% patient died related to OTSC system application failure and most of these patients died due to fatal comorbidity. Gölder S. et al deemed that in case of severe recurrent bleeding, the bleeding source could be controlled by endoscopic treatment, but the patient refused any further therapy and died, which was one of the reasons for the high mortality [27].

While our study suggested a promising role of OTSC system for UNVGIB, further consideration is warranted regarding cost. In addition, clinical expertise and unfamiliarity among endoscopists in the small center may factor into variable technical and clinical success results. The expense of this modality for UNVGIB as well as availability remains unclear in our included studies. Future studies are needed to truly assess the cost-effectiveness of OTSC system placement for the management of UNVGIB.

Certainly, we recognized that some limitations in our study. First, our systematic review and meta-analysis were based completely and only on the published literature. We could not get the data of the individual patient, which would allow us to perform more detailed analysis, especially on whether application of the OTSC system as the primary therapy or the rescue therapy. Second, some included studies were missing data for our review variables of interest, such as bleeding classification, lengths of hospital stay and additional therapy modality. Finally, just one literature was high methodological quality study, and our review was lack of comparing OTSC system to other therapy modality.

Conclusion

Our study demonstrated that the OTSC system was a technically feasible modality and highly efficacious in achieving hemostasis in acute UNVGIB. It is a promising endoscopic technique with high success rate and the rare adverse event. In the future, more randomized controlled trials are needed to compare OTSC to other therapy modality.

Abbreviations

GI: gastrointestinal; OTSC: over-the-scope-clip; CI confidence interval; UNVGIB: upper non-variceal gastrointestinal bleeding; SD: standard deviation

Declarations

Acknowledgments

None.

Authors’ contributions

Study conception and design: Xiaowei Tang. Drafting of manuscript: Chunyu Zhong and Shali Tan. Acquisition of data and critical revision: Chunyu Zhong and Yutang Ren. Revision of manuscript, and final approval of manuscript: Muhan Lü, Yan Peng, Xiangsheng Fu, Xiaowei Tang.

Funding

This study is independent research funded by the following grants: Medical science and technology plan projects of Zhejiang Province (No. 2017196257), Youth Foundation of Southwest Medical University (No. 0903–00031099), Doctoral research start-up funding project of Affiliated Hospital of Southwest Medical University (No. 16229).

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

Author details

¹Department of Gastroenterology, Affiliated Hospital of Southwest Medical University, Luzhou, China

²Departmemt of Gastroenterology, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua University, Beijing, China

³Department of Gastroenterology, Affiliated Hospital of North Sichuan Medical College, Nanchong, China

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