Usefulness of the combined orthodontic rubber band and clip method for gastric endoscopic submucosal dissection
BMC Gastroenterology volume 22, Article number: 527 (2022)
Background and aims
Effective traction is an important prerequisite for successful endoscopic submucosal dissection (ESD). The combined orthodontic rubber band (ORB) and clip method was effective in colorectal cancer ESD. To date, the method was not reported in gastric ESD. This study aimed to investigate its efficacy and safety for gastric neoplasms ESD.
We retrospectively analyzed data of 118 patients with gastric neoplasms treated by ESD from November 2020 to April 2022, 43 by ORB-ESD and 75 by the conventional ESD. The primary outcome measure was the ESD procedure time. Clinical data on efficacy and safety were also collected and analyzed. Propensity score matching (PSM) matched the patients in both groups.
PSM successfully matched 31 pairs of patients. The ORB-ESD operation time was shorter (median [interquartile range], 35 [30–48] vs. 49 [40–70] min, P < 0.001) and dissection speed was higher (median [interquartile range], 22.6 [14.4–29.3] vs. 13.5 [9.6–17.9] mm2/min, P < 0.001) than in the conventional ESD. The groups were similar in muscular injury rate, frequency and time of use of thermal hemostatic forceps, postoperative adverse events, en bloc resection, and R0 resection rate (P > 0.05).
Compared to the conventional ESD, ORB-ESD significantly reduced the procedure time and increased the dissection speed, proving beneficial to gastric ESD.
Endoscopic submucosal dissection (ESD), developed from the endoscopic mucosal resection technique, has become an effective new method to treat early gastric cancer and precancerous lesions because it can completely resect the lesion and reduce the local recurrence rate . However, ESD is more difficult and time-consuming than endoscopic mucosal resection and has a higher rate of adverse events such as bleeding and perforation [2,3,4]. Therefore, endoscopists are presently highly concerned with finding ways to improve the efficiency of ESD and reduce its adverse events rate.
It has been reported that traction-assisted methods provide endoscopists with a better field of view of the submucosa, shortening the ESD duration and reducing its adverse events rate . Therefore, various ESD traction methods continued to emerge in recent years , all showing advantages and disadvantages. Our previous report showed that the combined orthodontic rubber band (ORB) and clip traction-assisted ESD achieved good results in colorectal tumors . ORBs are cheap, simple to operate, safe, and effective in the ESD procedure. No previous study reported this combined ORB and clip method in gastric ESD. Therefore, this study compared and analyzed patients with gastric neoplasms treated by ORB-ESD and the conventional ESD at our hospital, assessing the efficacy and safety of ORB-ESD for gastric neoplasms.
Materials and methods
This study included patients with superficial gastric neoplasms (early gastric cancer and precancerous lesions or gastric adenomas with a high risk of cancer) who underwent ESD at the 900th Hospital of the PLA from November 2020 to April 2022. All patients were scheduled to undergo ESD following the Chinese consensus on early gastric cancer treatment . ESD was recommended even if a submucosal invasion was suspected when the patient strongly preferred this procedure rather than surgery. Exclusion criteria were: (1) patients in whom other traction methods such as dental floss or endoscopic submucosal tunnel dissection (ESTD) were used; (2) patients who underwent gastrectomy (ESD is difficult in such patients) . If multiple gastric lesions underwent ESD, only lesion dissected first was included in this study. Patients taking anticoagulants were asked to stop taking them 5–7 days before the ESD procedure .
The ethics committee of the 900th Hospital of the PLA approved this retrospective study (institutional ID 2022-012). The ESD procedures were performed after the patients gave their informed consent.
All ESD procedures were performed with a single-channel endoscope with a water jet system (GIF-Q260J; Olympus Co., Tokyo, Japan), a transparent cap, and an electrosurgical generator (VIO200S; Elektromedizin Gmbh, Tubingen, Germany). We used 1:100,000 sodium adrenaline hyaluronate and an injection needle (nm-4U; Olympus Co.) for submucosal injection. A Dual knife (KD-650L, Olympus Co.) or golden knife (MK-T-2-195, Micro-tech (Nanjing) Co., Nanjing, China) was used for marking, incision, and submucosal dissection. Carbon dioxide was used for gas injection. Other equipment included opening-and-closing clip (Micro-tech (Nanjing) Co., Nanjing, China), ORB (inner diameter, 6.5 mm, (1/4”), 3.5 OZ.) (Fig. 1), and hemostatic forceps (Coagrasper, Olympus Co.).
The ESD procedure
The conventional ESD process was as follows: a Dual knife or golden knife was used to open a 5-mm line mark next to the lesion. Subsequently, we performed submucosal injection and lifting, followed by an incision around the lesion and dissection using the Dual knife or golden knife. ORB traction was selected according to the specific conditions of gastric lesions. In the ORB-ESD group (Fig. 2), a clip holding the ORB was inserted into the gastric cavity through the endoscope working channel and clamped to the lesion mucosa after performing an incision around it. Subsequently, another clip was passed through the working channel into the stomach and attached the ORB to the contralateral normal mucosa. The lesion was then dissected. After complete resection of the lesion, the ORB traction device fixed on gastric mucosa and the specimen were removed with a snare. If we need to the retroflexed endoscopic position for submucosal dissection, set the direction of traction in advance, and try to turn the endoscope over from the greater curvature in the retroflexed process, so that the operation is relatively not easy to encounter the traction device (Fig. 3).
The primary outcome measure was the ESD procedure duration. The secondary outcome measures included the dissection speed, muscular injury rate, frequency and time of thermal hemostatic forceps use, and the rates of en bloc resection, R0 resection, bleeding, and perforation. In the ORB-ESD group, we also counted the times the ORB was attached to the lesion and whether the ORB traction device affected the specimen integrity.
The procedure time was defined as the time from submucosal injection to complete lesion resection. This interval included the time for inserting and attaching the ORB system. Time was recorded in minutes. The dissection speed was defined as the specimen resected area divided by the procedure duration (mm2/min). The specimen area was measured by multiplying half the length by half the width by 3.14 .
Muscular injury was defined as the damage caused to the muscle layer during electrosurgery. The frequency of hemostatic forceps use refers to the number of active bleeding requiring the use of the hemostatic forceps. Hemostasis time was defined as the time interval from the appearance of the hemostatic forceps on the monitor to the completion of hemostasis. The total time dedicated to hemostasis during the procedure was calculated . En bloc resection means that the lesion was removed by endoscopy, and an entire sample was obtained. R0 resection means that negative margins were achieved in the horizontal and vertical directions. Bleeding included immediate and delayed bleeding. Immediate bleeding was defined as bleeding that occurred during the ESD procedure and required endoscopic hemostasis. Delayed bleeding was defined as hematochezia within 30 days after surgery and a decrease in hemoglobin by 20 g/L, requiring blood transfusion or endoscopic or surgical intervention. Perforation was defined as the discovery of abdominal fat or intraperitoneal space during the ESD procedure or the presence of free gas in the abdominal cavity viewed on postsurgical radiographs or CT scans.
Propensity score matching (PSM)
Previous studies reported that lesions in the greater curvature and upper 2/3 of the stomach , tumor size , ulcer scarring presence , and the operator level  (trainee with fewer than 40 cases or an expert with over 40 cases of gastric ESD) affected the gastric ESD procedure. Therefore, we used PSM to adjust sampling bias and reduce potential confounding factors. We set the caliper value to 0.2 (nearest neighbor matching ties no replacement) for a 1:1 match to select patients.
Analysis was performed using IBM SPSS Statistics for Windows, Version 22.0 (IBM Corp., Armonk, NY, USA). Categorical variables were compared using the chi-squared or Fisher's exact test (e.g., R0 resection rate and surgical adverse events). Continuous variables were compared using the Student’s t test or Mann–Whitney U test (e.g., procedure time, dissection speed, and lesion size). Continuous variables are expressed as mean (standard deviation; SD) or median (interquartile range), while categorical variables are expressed as counts and percentages. Differences with P < 0.05 were considered statistically significant.
From November 2020 to April 2022, 171 patients with 178 gastric epithelial neoplasms underwent ESD. After excluding 51 patients (51 lesions) who underwent ESD with dental floss traction or ESTD, two lesions (two patients) in remnant stomachs, and seven patients with multiple lesions, the study included 118 lesions in 118 patients, 43 ORB-ESD and 75 conventional ESD (Fig. 4). The median specimen size in the ORB-ESD group was larger than in the conventional ESD group [40.0 (33.5–48.0) vs. 30.0 (23.0–38.0) mm, P < 0.001], while the groups were similar in other baseline characteristics (Table 1). Table 2 shows the results for the two groups before PSM. The median operation time in the ORB-ESD group was insignificantly shorter than in the conventional ESD group [40 (30, 57.5) vs. 44 (35, 61) min, P = 0.15], while its median dissection speed was significantly faster [22.6 (16.4, 30.4), vs. 12.6 (7.8, 17.1) mm2/min, P < 0.001].
The average time for ORB placement and completion of traction was 2.39 ± 1.67 min. Two patients in the ORB-ESD group lost the clip during the procedure; clips were re-inserted to complete traction. All clips were successfully removed in this group, and no bleeding event due to the removal of the ORB clips or damage to the specimens caused by the ORB device was noted (Table 2).
Table 3 shows the patient characteristics and results after PSM. The groups were similar in specimen size, lesion location, lesion position, macroscopic type, ulceration positive, and operator experiences. The matched groups were similar in muscular injury rate, frequency and time of hemostasis, complete resection, R0 resection rate, postoperative adverse events, and postoperative pathology (P > 0.05 for all). However, compared to the conventional ESD group, the ORB-ESD group had a significantly shorter median operation time (35 [30–48] vs. 49 [40–70] min, P < 0.001) and faster dissection speed (22.6 [14.4–29.3] vs. 13.5 [9.6–17.9] mm2/min, P < 0.001).
Table 4 shows subgroup analysis results. When the lesion was ≤ 2 cm, in the middle or upper stomach, or anywhere other than the greater curvature, the median surgical time was shorter, and the median dissection speed was faster in the ORB-ESD group than in the conventional ESD group.
As with any other surgery, the surgical field of view is critical in ESD . Poor submucosal exposure can greatly increase the operation difficulty. Uncertain dissection could lead to adverse events such as bleeding and perforation. By performing traction, the submucosa can be well exposed, achieving a better visual field and improved dissection efficiency. Furthermore, blood vessel branches can be detected, and electrocoagulation be timely applied to reduce the occurrence of bleeding and perforation. Therefore, traction technologies for gastric ESD are constantly emerging. These include double-endoscope endoscopic submucosal dissection [18, 19], ESTD, [17, 20] spring‑and‑loop with clip (S–O clip) traction [21, 22], and dental floss clip traction [12, 23]. Each of these traction technologies has its limitations. For example, two endoscopists should participate in the double-endoscope endoscopic submucosal dissection procedure. ESTD is difficult for trainees to master. The S–O traction technique requires an S–O clip, which is relatively expensive and available only in some endoscopy centers. Therefore, besides dental floss clip traction, these traction methods were not widely used in gastric ESD.
To place the dental floss traction, one needs to exit the endoscope and install the traction device. The traction is in a single direction, and the friction between dental floss and the endoscope might sometimes tear the dental floss or interfere with the ESD procedure. The ORB is commonly used in orthodontics. It comes in various diameters, has good elasticity, is cheap, and can be passed through the endoscope working channel. We showed in our previous study that the ESD procedure could be shortened by using ORB with a clip to assist ESD of colorectal tumors . Therefore, we hypothesized that the use of ORB to assist gastric ESD could improve its efficiency.
Our results showed that the procedure time in the ORB-ESD group was insignificantly shorter than in the conventional ESD group. This could be due to the larger specimen size in the ORB-ESD group than in the conventional ESD group. After matching the groups to reduce the influence of the specimen size, lesion location, ulceration, and operator experience, the procedure time in the ORB-ESD group was significantly shorter than in the conventional ESD group (35 vs. 49 min, P < 0.001). Furthermore, the dissection speed in the ORB-ESD group was faster than in the conventional ESD group both before and after PSM (P < 0.001). The possible reason for the higher speed could be the tension maintained throughout the ORB-assisted ESD procedure, exposing sufficient submucosa, reducing the operation difficulty, and speeding dissection.
Goto et al. reported that a tumor size greater than 20 mm was a predictor of an ESD surgery longer than 120 min . Our subgroup analysis showed that when the tumor size exceeded 20 mm, the ESD procedure duration and dissection speed were insignificantly better in the ORB-ESD group than in the conventional ESD group. This difference could be because the traction force gradually decreases when dissecting large-area lesions during the ESD process, resulting in a decreased exposure of the submucosa. We have encountered similar situations in the colorectal ORB-ESD. Our experience suggests that placing a clip to clamp the rubber band to the opposite side of the lesion can reestablish effective traction . Therefore, the ESD procedure may be shortened by re-inserting a new ORB for traction when dissecting lesions larger than 20 mm.
It was reported that tumors in the middle and upper stomach were more difficult to manage with ESD, a factor affecting gastric ESD [14, 25]. Our subgroup analysis showed that, compared to the conventional ESD group, the ORB-ESD group had a shorter procedure time (35.0 vs. 52.0 min, P = 0.003) and faster dissection speed (24.4 vs. 10.9 mm2/min, P < 0.001) when the lesion was in the middle or upper stomach. Therefore, we suggest using ORB-assisted ESD to improve the ESD efficiency when lesions are in the upper 2/3 of the stomach. However, when the lesion is in the lower 1/3 of the stomach, especially in the antrum, the submucosa is well exposed even without traction, the endoscope can be well manipulated, and the operation is technically easy. For this reason, our data suggest that the ORB-ESD and conventional ESD groups had similar procedure times and dissection speeds when the lesion was in the lower 1/3 of the stomach (P > 0.05), consistent with the report by Nagata . Furthermore, our subgroup analysis suggested that the procedure time and dissection speed were similar in both groups when the lesion was in the greater curvature of the stomach, possibly reflecting the small sample size.
The reported primary adverse events during gastric ESD included bleeding and perforation. The incidence of delayed bleeding was 4.1–8.5% [26,27,28,29] and that of perforation was 0.0–2.7% [30, 31]. In our study, the incidences of delayed bleeding in the ORB-ESD and conventional ESD groups were 2.3 and 4.0%, respectively. No perforation occurred in either group, consistent with previous reports [26,27,28,29,30,31]. Yoshida et al. reported a clip slip-off rate of 13.2% when using dental floss and clip traction . Nagata reported that slip-off rate of 3.9% during S–O clip-assisted gastric ESD . In our study, ORB clips slipped off due to over-inflation in two patients, with an incidence of 5%. Both cases occurred when a trainee performed the procedure. Therefore, it is suggested that trainees performing ORB-ESD should pay attention to avoid clip slip-off caused by excessive insufflation.
This study had some limitations. First, it was a single-center retrospective study. However, we maintain a prospective, continuous database since we started using ORB-assisted ESD, and PSM was used to reduce the influence of confounding factors. Second, while five ORB inner diameters were available (3.16, 4.70, 6.35, 7.90, and 9.50 mm), we used only the 6.35-mm ORB. Further research is needed to determine whether larger-diameter ORB can produce a better traction effect for large neoplasms. Thirdly, for lesions that develop in anatomically narrow areas, such as those near the gastroesophageal junction or pyloric ring, ORB traction may not work well at times. Finally, the sample size in this study was relatively small. The effectiveness of the ORB-assisted ESD procedure could be reconfirmed through future multi-center prospective large-sample studies.
In conclusion, this study showed that using ORB to assist gastric ESD can shorten the procedure time and improve the dissection speed. ORBs are easy to obtain and operate. This technique has the potential to become a simple, safe, and reliable gastric ESD traction method widely used in clinical practice.
Availability of data and materials
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
Suzuki H, Oda I, Abe S, et al. High rate of 5-year survival among patients with early gastric cancer undergoing curative endoscopic submucosal dissection. Gastric Cancer. 2016;19(1):198–205.
Shimura T, Sasaki M, Kataoka H, et al. Advantages of endoscopic submucosal dissection over conventional endoscopic mucosal resection. J Gastroenterol Hepatol. 2007;22(6):821–6.
Yamamoto S, Uedo N, Ishihara R, et al. Endoscopic submucosal dissection for early gastric cancer performed by supervised residents: assessment of feasibility and learning curve. Endoscopy. 2009;41(11):923–8.
Zhao Y, Wang C. Long-term clinical efficacy and perioperative safety of endoscopic submucosal dissection versus endoscopic mucosal resection for early gastric cancer: an updated meta-analysis. Biomed Res Int. 2018;2018:3152346.
Nagata M. Advances in traction methods for endoscopic submucosal dissection: what is the best traction method and traction direction. World J Gastroenterol. 2022;28(1):1–22.
Su YF, Cheng SW, Chang CC, Kang YN. Efficacy and safety of traction-assisted endoscopic submucosal dissection: a meta-regression of randomized clinical trials. Endoscopy. 2020;52(5):338–48.
Zheng L, Wang W, Li D, et al. Orthodontic rubber band-assisted endoscopic submucosal dissection: an efficient method for treating superficial colorectal tumors. Gastroenterol Res Pract. 2022;2022:2835258.
Beijing Science and Technology Commission Major Project. “Early gastric cancer treatment standard research" expert group. Chin J Digest Endosc. 2019. 36(6): 381–392.
Ojima T, Takifuji K, Nakamura M, et al. Endoscopic submucosal dissection for gastric tumors in various types of remnant stomach. Endoscopy. 2014;46(8):645–9.
Veitch AM, Baglin TP, Gershlick AH, Harnden SM, Tighe R, Cairns S. Guidelines for the management of anticoagulant and antiplatelet therapy in patients undergoing endoscopic procedures. Gut. 2008;57(9):1322–9.
Ye L, Yuan X, Pang M, et al. Magnetic bead-assisted endoscopic submucosal dissection: a gravity-based traction method for treating large superficial colorectal tumors. Surg Endosc. 2019;33(6):2034–41.
Yoshida M, Takizawa K, Suzuki S, et al. Conventional versus traction-assisted endoscopic submucosal dissection for gastric neoplasms: a multicenter, randomized controlled trial (with video). Gastrointest Endosc. 2018;87(5):1231–40.
Ahn JY, Choi KD, Choi JY, et al. Procedure time of endoscopic submucosal dissection according to the size and location of early gastric cancers: analysis of 916 dissections performed by 4 experts. Gastrointest Endosc. 2011;73(5):911–6.
Nagata S, Jin YF, Tomoeda M, et al. Influential factors in procedure time of endoscopic submucosal dissection for gastric cancer with fibrotic change. Dig Endosc. 2011;23(4):296–301.
Ono S, Kato M, Nakagawa M, Imai A, Yamamoto K, Shimizu Y. Outcomes and predictive factors of “not self-completion” in gastric endoscopic submucosal dissection for novice operators. Surg Endosc. 2013;27(10):3577–83.
Gotoda T, Friedland S, Hamanaka H, Soetikno R. A learning curve for advanced endoscopic resection. Gastrointest Endosc. 2005;62(6):866–7.
Zhang X, Shi D, Yu Z, et al. A multicenter retrospective study of endoscopic submucosal tunnel dissection for large lesser gastric curvature superficial neoplasms. Surg Endosc. 2019;33(6):1910–9.
Higuchi K, Tanabe S, Azuma M, et al. Double-endoscope endoscopic submucosal dissection for the treatment of early gastric cancer accompanied by an ulcer scar (with video). Gastrointest Endosc. 2013;78(2):266–73.
Ogata K, Yanai M, Kuriyama K, et al. Double endoscopic intraluminal operation (DEILO) for early gastric cancer: outcome of novel procedure for endoscopic submucosal dissection. Anticancer Res. 2017;37(1):343–7.
Ojima T, Takifuji K, Nakamura M, et al. Endoscopic submucosal tunnel dissection versus conventional endoscopic submucosal dissection for early gastric cancers: outcomes of 799 consecutive cases in a single institution. Surg Endosc. 2020;34(12):5625–31.
Hashimoto R, Hirasawa D, Iwaki T, et al. Usefulness of the S–O clip for gastric endoscopic submucosal dissection (with video). Surg Endosc. 2018;32(2):908–14.
Nagata M. Internal traction method using a spring-and-loop with clip (S–O clip) allows countertraction in gastric endoscopic submucosal dissection. Surg Endosc. 2020;34(8):3722–33.
Suzuki S, Gotoda T, Kobayashi Y, et al. Usefulness of a traction method using dental floss and a hemoclip for gastric endoscopic submucosal dissection: a propensity score matching analysis (with videos). Gastrointest Endosc. 2016;83(2):337–46.
Goto O, Fujishiro M, Kodashima S, Ono S, Omata M. Is it possible to predict the procedural time of endoscopic submucosal dissection for early gastric cancer. J Gastroenterol Hepatol. 2009;24(3):379–83.
Yano T, Hasuike N, Ono H, et al. Factors associated with technical difficulty of endoscopic submucosal dissection for early gastric cancer that met the expanded indication criteria: post hoc analysis of a multi-institutional prospective confirmatory trial (JCOG0607). Gastric Cancer. 2020;23(1):168–74.
Yano T, Tanabe S, Ishido K, et al. Different clinical characteristics associated with acute bleeding and delayed bleeding after endoscopic submucosal dissection in patients with early gastric cancer. Surg Endosc. 2017;31(11):4542–50.
Sato C, Hirasawa K, Koh R, et al. Postoperative bleeding in patients on antithrombotic therapy after gastric endoscopic submucosal dissection. World J Gastroenterol. 2017;23(30):5557–66.
Nam HS, Choi CW, Kim SJ, et al. Risk factors for delayed bleeding by onset time after endoscopic submucosal dissection for gastric neoplasm. Sci Rep. 2019;9(1):2674.
Hasatani K, Yoshida N, Aoyagi H, et al. Usefulness of the clip-and-snare method using the pre-looping technique for endoscopic submucosal dissection of gastric neoplasia: a randomized controlled trial. Ann Gastroenterol. 2022;35(1):48–55.
Akintoye E, Obaitan I, Muthusamy A, Akanbi O, Olusunmade M, Levine D. Endoscopic submucosal dissection of gastric tumors: a systematic review and meta-analysis. World J Gastrointest Endosc. 2016;8(15):517–32.
Suzuki H, Takizawa K, Hirasawa T, et al. Short-term outcomes of multicenter prospective cohort study of gastric endoscopic resection: “Real-world evidence” in Japan. Dig Endosc. 2019;31(1):30–9.
This project was supported by the Fujian Science and Technology Innovation Joint Fund Project (research funder: Wen Wang, grant number: 2018Y9116) and Foreign cooperation Project of Fujian Province (research funder: Dazhou Li, grant number: 2022I0033).
Ethics approval and consent to participate
This study was approved by the Ethics Committee of 900TH Hospital of PLA (2022-012). All methods of this study were performed in accordance with the Declaration of Helsinki. Written informed consent was obtained from all participating patients.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Li, D., Zheng, L., Zhang, Z. et al. Usefulness of the combined orthodontic rubber band and clip method for gastric endoscopic submucosal dissection. BMC Gastroenterol 22, 527 (2022). https://doi.org/10.1186/s12876-022-02606-1