- Department of Gastroenterology, Jiangxi Provincial Key Laboratory of Digestive Diseases, Jiangxi Clinical Research Center for Gastroenterology, Digestive Disease Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, China
Background: Vascular interventional therapy (TAE) is an effective treatment for most abdominal organ hemorrhages, especially for non-variceal gastrointestinal bleeding (NVGIB) unresponsive to endoscopy. While selective and super selective embolization are two key interventional hemostasis methods, research on their application in total gastrointestinal bleeding is limited. This study compares these two techniques to assess their safety in non-variceal gastrointestinal bleeding hemostasis.
Methods: We conducted a retrospective study on patients with NVGIB who received vascular interventional therapy from August 2014 to October 2024, comparing the clinical characteristics and outcomes of patients with selective or super-selective embolization. The primary outcome was clinical success, and secondary outcomes included technical success, rebleeding (overall and within 3 days), transfusion requirements, need for additional therapies, complications, and mortality.
Results: A total of 116 patients with NVGIB who received vascular interventional therapy were included. Among the 88 patients with non-variceal upper gastrointestinal bleeding (NVUGIB), 48 and 40 were treated with super-selective and selective embolization, respectively. Gastroduodenal artery was the most common embolized vessel in both groups. All cases achieved technical success. 85.42% of the super-selective embolization group achieved clinical success, and 70.00% of the selective embolization group achieved clinical success (p = 0.080). The rebleeding within 3 days rate of the super-selective embolization group was significantly lower than that in the selective embolization group (8.33% vs. 27.50%, p = 0.017). The bleeding related mortality was 6.25% in the super-selective embolization group and 7.50% in the selective embolization group. In the subgroup of 28 patients with lower gastrointestinal bleeding (LGIB), no significant differences in clinical outcomes were observed between the two embolization approaches. However, it is noteworthy that all 5 cases of post-procedural intestinal ischemia occurred in this LGIB subgroup. The embolic material used had a significant impact on early rebleeding and the subsequent need for additional therapy in LGIB (p < 0.05), but not in UGIB.
Conclusion: For refractory NVUGIB, super-selective TAE compared to selective TAE reduces early rebleeding. Decision-making should prioritize patient transfusion needs, which was the sole independent predictor of rebleeding. The embolization strategy for LGIB should carefully consider the choice of embolic material and the inherent risk of intestinal ischemia.
Introduction
Acute nonvariceal gastrointestinal bleeding (NVGIB) is a severe digestive system disease, characterized by rapid changes in condition, difficulty in accurately estimating blood loss, and a tendency to recur. Despite recent advances in endoscopy and pharmacological therapy, NVGIB mortality remains at 3–14% (1, 2). Lower gastrointestinal bleeding mortality is slightly lower, but severe lower gastrointestinal bleeding (LGIB) still has a 5—year mortality rate of up to 13% (3). Transcatheter arterial embolization (TAE) is typically used as a rescue treatment for NVGIB when endoscopic therapy fails (4). Compared with other treatments, TAE is less invasive, more accurate in localization, faster in hemostasis, and has wider applicability (5–7). Recent studies have confirmed the safety and effectiveness of TAE in gastrointestinal hemostasis. For non-variceal upper gastrointestinal bleeding (NVUGIB), TAE has a high technical success rate of 94.9% and a clinical success rate of 73.0% (4).
Selective and super-selective embolization are now the two main TAE methods for hemostasis. Selective embolization involves infusing embolic agents through a catheter into the main trunk or branches of target blood vessels to block local blood flow, offering a wide control range (8). Super-selective embolization, performed in finer vessels and targeting specific lesion areas or branches, is characterized by precise hemostasis (9). Numerous studies have compared these two embolization techniques in vascular interventional fields, especially in abdominal blood vessels such as the hepatic artery, renal artery, ureteral artery, and bladder artery (10–12). Concurrent with ongoing technological advances, both selective and super—selective embolization have demonstrated significant advancement in technical process, embolic agent selection, and indication criteria for NVGIB compared to previous non—selective embolization (6, 13). However, their comparative effectiveness in clinical use remains controversial. A retrospective study demonstrated that in hemodynamically unstable emergency patients, selective embolization has a higher technical success rate due to its low dependence on vascular conditions and equipment (14). Especially when DSA does not clearly identify bleeding sites, selective embolization can “blind—embolize” suspected blood vessels, effectively covering potential bleeding branches (15). Some studies indicate that super—selective embolization, which uses microcatheters (3 Fr) to deliver embolic materials to terminal arteries near bleeding sites, significantly reduces the risk of bowel ischemia compared to selective embolization (16).
Given the limited evidence on the comparative efficacy and safety of superselective and selective embolization in NVGIB patients with endoscopic treatment failure, we designed a retrospective study to evaluate the clinical outcomes of these two techniques in such patient populations.
Methods
Study design
Patients diagnosed with NVGIB and treated with abdominal angiography at our hospital from August 2014 to October 2024 were included, all cases were consecutive. All patients presented with clinical symptoms such as hematemesis, melena, or hematochezia, and underwent endoscopic examination or enhanced CT. The final diagnosis was made using digital subtraction angiography (DSA). Exclusion criteria were as follows: (1) Patients with negative angiography or no interventional embolization; (2) Patients with hemorrhage from the biliary tract, pancreas, or malignancy; (3) Patients with incomplete or missing data; the study was approved by our hospital’s ethics committee, and patients’ informed consent was exempted.
Variables
The baseline information incorporated gender, age, comorbidities (hypertension, diabetes, heart disease, liver cirrhosis, renal failure, abdominal surgical history), lifestyle factors (smoking, alcohol consumption), clinical data (pre-TAE blood pressure), time interval from bleeding to TAE (<6 h or not), Clip use, endoscopic and angiographic findings, blood transfusion details (including units transfused), and pre-TAE laboratory parameters [white blood cell count (WBC), hemoglobin (HB), platelet count (PLT), albumin, Blood urea nitrogen (BUN), creatinine (Cr), International Normalized Ratio (INR), Prothrombin Time (PT)]. The outcome measures comprised rebleeding rates (overall and﹤3 days), additional treatments required for rebleeding (endoscopy, re-embolization, surgery), Postoperative complications (fever, abdominal pain, nausea/vomiting, Intestinal ischemia), length of hospital stay, and mortality. Technical success is defined as the immediate termination of intravascular bleeding through TAE, that is, angiography shows no extravasation. Clinical success is defined as no recurrence of gastrointestinal bleeding within 30 days after TAE (17). Bleeding-related mortality was defined as deaths directly attributable to uncontrollable gastrointestinal bleeding.
Operating procedures
All TAE procedures were performed by experienced interventional radiologists. Patients were placed in the supine position, given local infiltration anesthesia, and percutaneous femoral puncture was performed using a 5 Fr catheter for angiography of the celiac axis, gastroduodenal artery, left gastric artery, superior and inferior mesenteric arteries. Selective angiography of branches was then done based on bleeding situation. The direct positive angiographic sign was considered as contrast agent extravasation, and aneurysms/pseudoaneurysms, vascular irregularities, vessel cutoffs, arteriovenous/arterioportal shunts, neovascularization, and increased small arterial vessels were regarded as indirect signs of bleeding, indicating embolization. If contrast agent extravasation or indirect bleeding signs were found, selective embolization was performed on the trunk or branch vessels. Otherwise, super—selective angiography was done as close to the bleeding site as possible using a 2.7 Fr microcatheter (Progreat, Terumo, Tokyo, Japan), and super—selective embolization was performed based on the vascular conditions. Some patients underwent prophylactic embolization according to endoscopic findings of the bleeding site and the operator’s experience. The embolization materials included spring coil and gelatin sponge. Post—TAE angiography was performed to confirm occlusion of the bleeding site. If bleeding remained uncontrolled, repeat angiography or surgical referral was done.
Statistical methods
Quantitative data distribution was determined using the Shapiro—Wilk normality test. Normally distributed variables were presented as mean ± standard deviation (SD), and skewness—distributed ones as median (interquartile range, IQR). Categorical data were presented as numbers and ratios. Student’s t—test or Mann–Whitney U test was used for quantitative data analysis, and χ2 test or Fisher’s exact test for categorical data. p-value < 0.05 was considered statistically significant. For univariate analysis, variables with p < 0.05 were selected; multivariate analysis was subsequently performed using logistic regression. All statistical analyses were conducted using R software (version 4.2.0, R Foundation for Statistical Computing, Vienna, Austria).
Results
Baseline characteristics
Figure 1 shows the flowchart of this study. From August 2014 to October 2024, a total of 116 patients with NVGIB who received vascular interventional therapy were included. As shown in Table 1, Of the 88 patients with NVUGIB, 48 underwent super-selective embolization and 40 received selective embolization. The median (IQR) age of patients in the super-selective embolization group and the selective embolization group was 65.50 (53.75, 73.25) and 59.00 (43.75, 72.50) years, respectively. The proportion of patients with positive results under endoscopy in the super-selective embolization group was 72.92% (35/48), while that in the selective embolization group was 85.00% (34/40). There was no significant difference in the proportion of patients receiving blood transfusion between the two groups. However, the mean blood transfusion units in the selective embolization group were 4.55 ± 5.20, which was significantly higher than that in the super-selective embolization group (p = 0.017). There were no significant differences between super-selective embolization group and selective embolization group in terms of gender, alcohol, smoking, laboratory index, time to treatment ≤6 h and etc. (p > 0.05). Similarly, Supplementary Table 1 summarizes the baseline characteristics of the 28 patients with lower gastrointestinal bleeding, of whom 19 underwent super-selective embolization and 9 received selective embolization. No statistically significant differences were observed in any variables between the selective and super-selective embolization groups (p > 0.05).
Comparison of the embolized artery between super-selective embolization group and selective embolization group
As detailed in Table 2, the most frequently embolized vessels in the super-selective embolization group among patients with NVUGIB and LGIB included the gastroduodenal artery (20/67, 29.9%), left gastric artery (10/67, 14.9%), superior mesenteric artery (10/67, 14.9%), and ileocolic artery (9/67, 13.4%). In the selective embolization group, gastroduodenal artery (40.8%, 20/49), left gastric artery (18.4%, 9/49) and right gastric artery (12.2%, 6/49) were the common embolization vessels. In addition, two or more vessels were embolized in eight patients in the super-selective embolization group and five patients in the selective embolization group.
Comparison of clinical outcomes between the two groups
All patients with NVUGIB were treated with super-selective or selective embolization. All cases achieved technical success. 85.42% of the super-selective embolization group achieved clinical success, and 70.00% of the selective embolization group achieved clinical success. The rebleeding rate of super-selective embolization group was 14.58% (7/48), which was slightly lower than that of selective embolization group (30.00%, 12/40), but the difference was not statistically significant (p = 0.080). the rebleeding within 3 days rate of the super-selective embolization group was statistically lower than that in the selective embolization group (8.33 vs. 27.50, p = 0.017). The super-selective embolization group showed a non-significant reduction in the need for additional therapy after rebleeding (p = 0.082). In the super-selective embolization group, 3 patients with rebleeding underwent endoscopic treatment. Rebleeding patients in the selective embolization group were treated endoscopically in 2 patients, embolization in 3 patients, surgery in 2 patients. There were no significant differences in postoperative adverse events between the two groups (p > 0.05). The median length of hospital stay was 10 (8.00–14.00) days in the super-selective embolization group and 11 (7.75–13.25) days in the selective embolization group. The mortality was 16.67% in the super-selective embolization group and 15.00% in the selective embolization group, and the difference was not statistically significant. In terms of bleeding-related mortality, superselective embolization shows a slightly lower rate than selective embolization. However, there was no statistically significant difference between the two (6.25% vs. 7.50%, p = 1.000) (Table 3). A multivariable analysis was performed to determine whether super-selective embolization was an independent risk factor for rebleeding after TAE (Table 4). The analysis revealed no significant association between superselective embolization and rebleeding (odds ratio: 0.40, 95% confidence interval: 0.14–1.14, p = 0.085), whereas the units of blood transfused showed a significant association with rebleeding (odds ratio: 1.35, 95% confidence interval:1.10–1.67, p = 0.005). Additionally, Supplementary Table 2 compares the outcomes between superselective and selective embolization in patients with LGIB. No significant differences were observed in clinical success, adverse events, rebleeding, or mortality between the two groups. Notably, all 5 cases of intestinal ischemia following TAE occurred in this patient subset, with 3 in the super-selective and 2 in the selective embolization group. Among these, 4 patients underwent surgical intervention and 1was managed conservatively.
Table 4. Univariable and multivariable analyses examining rebleeding as the primary outcome in patients with NVUGIB.
Comparison of clinical outcomes among patients receiving different embolic materials during TAE
As summarized in Table 5, clinical outcomes were compared among patients receiving spring coils, gelatin sponge, or a combination of both during TAE for NVUGIB. No significant differences were observed across any outcome measure, including technical success (100% in all groups), clinical success (78.41% overall), rebleeding, complication rates, or mortality (all p > 0.05). In contrast, among patients with LGIB (Supplementary Table 3), the embolic material showed a significant impact on early rebleeding (p = 0.041), with the highest rate observed in the combination therapy group (45.45%). Consequently, the need for additional therapy for rebleeding also differed significantly among the groups (p = 0.027).
Discussion
NVGIB is one of the common acute and critical conditions in clinical practice, and it’s incidence rate has gradually decreased in recent years (18). Endoscopic hemostasis is a common and effective hemostasis method, but its rebleeding rate is still very high, approximately 5–15% of patients cannot stop bleeding through endoscopy and require TAE or surgery (18, 19). TAE is a very effective intervention measure for managing NVGIB. Compared with surgical operations, it provides a more minimally invasive alternative for bleeding failed hemostasis under endoscopy. Although the rebleeding rate of TAE is higher compared with surgery, the risk of complications of TAE is significantly lower and the length of hospital stay is shorter (4). In a British national audit, the mortality rate of salvage surgery after NVGIB endoscopic hemostasis failure remained as high as 23%, while that of TAE was 10% (20). Therefore, TAE is the preferred salvage therapy for patients who have failed endoscopic treatment.
Due to concerns that the embolized intestinal segment may be infarcted, there has always been a debate on the most suitable embolizing agent, location and device for TAE, among which the selectivity of the embolizing location is very important (21, 22). It is crucial to select the most selective embolization location as much as possible to minimize the risk of ischemia. The safety and efficacy of super-selective embolization in the treatment of acute lower gastrointestinal bleeding have been reported by several studies, while there are still relatively few studies on acute upper gastrointestinal bleeding (21, 23–27).
This study focuses on the outcomes of TAE in patients with NVGIB. We found that super-selective embolization of NVUGIB resulted in a significantly lower rate of early rebleeding (within 3 days) than selective embolization, which was similar to the result of a previous study (24). Importantly, the average blood transfusion unit was identified as an independent predictor of rebleeding, consistent with previous literature showing that higher transfusion volume was associated with clinical failure in TAE. Previous studies have shown that the use of higher units of red blood cell concentrate is associated with clinical failure of TAE (28). Although the overall clinical success rate was higher in the super-selective group, this difference did not reach statistical significance, possibly due to the sample size. However, no outcome difference was observed between the two groups in LGIB.
In the choice of embolic agent, we usually use gelatin sponge for prophylactic embolization in patients with unclear bleeding site, and spring coil or spring coil combined with gelatin sponge for patients with clear bleeding site. This selection bias might lead to an overestimation of the clinical efficacy of gelatin sponge when used alone. In UGIB subgroup, the type of embolic agent did not significantly influence clinical success, rebleeding, or complication rates. In contrast, within the LGIB subgroup, the choice of embolic material significantly affected the rate of early rebleeding and the subsequent need for additional therapy. As in previous studies, we found that the combination of spring coil and gelatin sponge was superior to spring coil alone (15).
Due to the insufficient collateral blood supply of the lower gastrointestinal blood vessels, the ischemia rate after embolization of lower gastrointestinal bleeding is higher than that after embolization of the upper gastrointestinal tract (29). In this study, intestinal ischemia occurred after embolization treatment in patients with lower gastrointestinal bleeding. In a study on the treatment of acute small intestinal bleeding, it was found that super-selective embolism was an important prognostic factor associated with fewer major complications (30). In a study of TAE in the treatment of acute lower gastrointestinal bleeding, it was found that super-selective embolization is an important prognostic factor associated with reduced recurrent bleeding and fewer major complications (24). However, in this study, it was not observed that the postoperative intestinal ischemia rate in the super-selective embolization group was significantly lower than that in the selective embolization group. This might be because more cases of lower gastrointestinal bleeding in this study chose super-selective embolization. There were no significant differences in the incidence of postoperative adverse events, hospital stay and mortality between the two groups of patients.
This study has several limitations. Firstly, its retrospective nature introduces potential selection bias. Secondly, the sample size was small, particularly in the LGIB subgroup, may have been underpowered to detect significant differences in some outcomes, such as the rate of intestinal ischemia. Thirdly, embolic materials were not randomized, and their influence, especially in LGIB, warrants further investigation. Finally, the diagnosis of intestinal ischemia was only confirmed in clinically suspected cases via CT or surgery, potentially underestimating its true incidence.
Conclusion
In conclusion, for the management of refractory NVUGIB, super-selective TAE is associated with a significant reduction in early rebleeding compared to selective TAE, without increasing the risk of mortality. The embolization technique itself was not an independent predictor of rebleeding, whereas a higher transfusion requirement was. When embolizing for LGIB, clinicians must remain vigilant about the risk of intestinal ischemia. The choice of embolic agent appears to have a more pronounced effect on outcomes in LGIB than in UGIB.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by Ethics Committee of the First Affiliated Hospital of Nanchang University. The studies were conducted in accordance with the local legislation and institutional requirements. The participants provided their written informed consent to participate in this study.
Author contributions
JZ: Formal analysis, Data curation, Writing – review & editing, Conceptualization. KL: Writing – review & editing, Writing – original draft, Formal analysis, Methodology. TC: Formal analysis, Writing – review & editing, Methodology, Writing – original draft. FL: Formal analysis, Supervision, Methodology, Conceptualization, Writing – review & editing. XS: Writing – review & editing, Supervision, Conceptualization, Methodology, Formal analysis.
Funding
The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the National Natural Science Foundation of China (82360119) and the Double-Thousand Plan of Jiangxi Province (jxsq2023201044).
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Generative AI statement
The author(s) declare that no Gen AI was used in the creation of this manuscript.
Any alternative text (alt text) provided alongside figures in this article has been generated by Frontiers with the support of artificial intelligence and reasonable efforts have been made to ensure accuracy, including review by the authors wherever possible. If you identify any issues, please contact us.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fmed.2025.1697511/full#supplementary-material
Abbreviations
NVGIB, non-variceal gastrointestinal bleeding; NVUGIB, non-variceal upper gastrointestinal bleeding; LGIB, lower gastrointestinal bleeding; TAE, transcatheter arterial embolization; WBC, white blood cell count; HB, Hemoglobin; PLT, Platelet count; BUN, blood urea nitrogen; Cr, creatinine; INR, international normalized ratio; PT, prothrombin time; SD, standard deviation; IQR, interquartile range.
References
1. Hearnshaw, SA, Logan, RFA, Lowe, D, Travis, SPL, Murphy, MF, and Palmer, KR. Acute upper gastrointestinal bleeding in the UK: patient characteristics, diagnoses and outcomes in the 2007 UK audit. Gut. (2011) 60:1327–35. doi: 10.1136/gut.2010.228437
2. van Leerdam, ME. Epidemiology of acute upper gastrointestinal bleeding. Best Pract Res Clin Gastroenterol. (2008) 22:209–24. doi: 10.1016/j.bpg.2007.10.011
3. Aoki, T, Nagata, N, Niikura, R, Shimbo, T, Tanaka, S, Sekine, K, et al. Recurrence and mortality among patients hospitalized for acute lower gastrointestinal bleeding. Clin Gastroenterol Hepatol. (2015) 13:488–494.e1. doi: 10.1016/j.cgh.2014.06.023
4. Tarasconi, A, Baiocchi, GL, Pattonieri, V, Perrone, G, Abongwa, HK, Molfino, S, et al. Transcatheter arterial embolization versus surgery for refractory non-variceal upper gastrointestinal bleeding: a meta-analysis. World J Emerg Surg. (2019) 14:3. doi: 10.1186/s13017-019-0223-8
5. Beggs, AD, Dilworth, MP, Powell, SL, Atherton, H, and Griffiths, EA. A systematic review of transarterial embolization versus emergency surgery in treatment of major nonvariceal upper gastrointestinal bleeding. Clin Exp Gastroenterol. (2014) 7:93–104. doi: 10.2147/CEG.S56725
6. Ramaswamy, RS, Choi, HW, Mouser, HC, Narsinh, KH, McCammack, KC, Treesit, T, et al. Role of interventional radiology in the management of acute gastrointestinal bleeding. World J Radiol. (2014) 6:82–92. doi: 10.4329/wjr.v6.i4.82
7. Kojima, Y, Katano, T, Shimura, T, Shimohira, M, Sugiyama, T, Ebi, M, et al. Efficacy of transcatheter arterial embolization for first-line treatment of colonic diverticular bleeding with extravasation on contrast-enhanced computed tomography. Medicine (Baltimore). (2022) 101:e31442. doi: 10.1097/MD.0000000000031442
8. Loffroy, R, Pottecher, P, Cherblanc, V, Favelier, S, Estivalet, L, Koutlidis, N, et al. Current role of transcatheter arterial embolization for bladder and prostate hemorrhage. Diagn Interv Imaging. (2014) 95:1027–34. doi: 10.1016/j.diii.2014.03.008
9. Delgal, A, Cercueil, J-P, Koutlidis, N, Michel, F, Kermarrec, I, Mourey, E, et al. Outcome of transcatheter arterial embolization for bladder and prostate hemorrhage. J Urol. (2010) 183:1947–53. doi: 10.1016/j.juro.2010.01.003
10. Tashi, S, Tan, Z, and Gogna, A. Use of the triple coaxial (triaxial) microcatheter system in superselective arterial embolisation for complex interventional cases: an initial experience with the system. CVIR Endovasc. (2022) 5:67. doi: 10.1186/s42155-022-00340-z
11. Tayal, M, Nandolia, KK, Sharma, P, Mittal, A, and Chauhan, U. N-butyl 2-cyanoacrylate (NBCA) in nephron sparing Superselective embolization of iatrogenic Renovascular injuries: a single Centre experience. Cureus. (2022) 14:e33166. doi: 10.7759/cureus.33166
12. Saadi, A, Bouzouita, A, Rebai, MH, Cherif, M, Kerkeni, W, Ayed, H, et al. Superselective embolisation of bilateral superior vesical arteries for management of intractable hematuria in context of metastatic bladder cancer. Asian J Urol. (2017) 4:131–4. doi: 10.1016/j.ajur.2016.03.003
13. Walker, TG, Salazar, GM, and Waltman, AC. Angiographic evaluation and management of acute gastrointestinal hemorrhage. World J Gastroenterol. (2012) 18:1191–201. doi: 10.3748/wjg.v18.i11.1191
14. Ali, M, Ul Haq, T, Salam, B, Beg, M, Sayani, R, and Azeemuddin, M. Treatment of nonvariceal gastrointestinal hemorrhage by transcatheter embolization. Radiol Res Pract. (2013) 2013:604328. doi: 10.1155/2013/604328
15. Loffroy, R, Rao, P, Ota, S, De Lin, M, Kwak, B-K, and Geschwind, J-F. Embolization of acute nonvariceal upper gastrointestinal hemorrhage resistant to endoscopic treatment: results and predictors of recurrent bleeding. Cardiovasc Intervent Radiol. (2010) 33:1088–100. doi: 10.1007/s00270-010-9829-7
16. Kuo, WT, Lee, DE, Saad, WEA, Patel, N, Sahler, LG, and Waldman, DL. Superselective microcoil embolization for the treatment of lower gastrointestinal hemorrhage. J Vasc Interv Radiol. (2003) 14:1503–9. doi: 10.1097/01.rvi.0000099780.23569.e6
17. Dariushnia, SR, Redstone, EA, Heran, MKS, Cramer, HR, Ganguli, S, Gomes, AS, et al. Society of Interventional Radiology quality improvement standards for percutaneous transcatheter embolization. J Vasc Interv Radiol. (2021) 32:476.e1–476.e33. doi: 10.1016/j.jvir.2020.10.022
18. Wuerth, BA, and Rockey, DC. Changing epidemiology of upper gastrointestinal Hemorrhage in the last decade: a Nationwide analysis. Dig Dis Sci. (2018) 63:1286–93. doi: 10.1007/s10620-017-4882-6
19. Mullady, DK, Wang, AY, and Waschke, KA. AGA clinical practice update on endoscopic therapies for non-Variceal upper gastrointestinal bleeding: expert review. Gastroenterology. (2020) 159:1120–8. doi: 10.1053/j.gastro.2020.05.095
20. Jairath, V, Kahan, BC, Logan, RFA, Hearnshaw, SA, Dore, CJ, Travis, SPL, et al. National audit of the use of surgery and radiological embolization after failed endoscopic haemostasis for non-variceal upper gastrointestinal bleeding. Br J Surg. (2012) 99:1672–80. doi: 10.1002/bjs.8932
21. Hosse, C, Moos, M, Becker, LS, Sieren, M, Müller, L, Stoehr, F, et al. Trans-arterial embolization for treatment of acute lower gastrointestinal bleeding-a multicenter analysis. Eur Radiol. (2025) 35:2746–54. doi: 10.1007/s00330-024-11102-x
22. Ini’, C, Distefano, G, Sanfilippo, F, Castiglione, DG, Falsaperla, D, Giurazza, F, et al. Embolization for acute nonvariceal bleeding of upper and lower gastrointestinal tract: a systematic review. CVIR Endovasc. (2023) 6:18. doi: 10.1186/s42155-023-00360-3
23. Tiralongo, F, Perini, D, Crimi, L, Taninokuchi Tomassoni, M, Braccischi, L, Castiglione, DG, et al. Transarterial embolization for acute lower gastrointestinal bleeding: a retrospective bicentric study. Radiol Med. (2025) 130:1050–7. doi: 10.1007/s11547-025-02012-z
24. Kwon, JH, Kim, M-D, Han, K, Choi, W, Kim, YS, Lee, J, et al. Transcatheter arterial embolisation for acute lower gastrointestinal haemorrhage: a single-Centre study. Eur Radiol. (2019) 29:57–67. doi: 10.1007/s00330-018-5587-8
25. Nykänen, T, Peltola, E, Kylänpää, L, and Udd, M. Transcatheter arterial embolization in lower gastrointestinal bleeding: ischemia remains a concern even with a Superselective approach. J Gastrointest Surg. (2018) 22:1394–403. doi: 10.1007/s11605-018-3728-7
26. McGraw, JR, Kiefer, RM, Shah, A, Clark, TWI, Shlansky-Goldberg, RD, Nadolski, GJ, et al. Outcomes of transarterial embolization for acute nonvariceal upper gastrointestinal bleeding: correlation with periprocedural endoscopy. J Vasc Interv Radiol. (2023) 34:1062–9. doi: 10.1016/j.jvir.2023.01.026
27. Gong, T, Tsauo, J, Ding, M, Jin, L, Duan, F, Yu, Y, et al. Transcatheter arterial embolization for cancer-related non-variceal upper gastrointestinal bleeding: a multicenter retrospective study of 107 patients. Diagn Interv Imaging. (2023) 104:60–6. doi: 10.1016/j.diii.2022.07.006
28. Pech, M, Serafin, Z, Fischbach, F, Damm, R, Jargiełło, T, Seidensticker, M, et al. Transarterial embolization of acute iatrogenic hemorrhages: predictive factors for mortality and outcome. Br J Radiol. (2020) 93:20190413. doi: 10.1259/bjr.20190413
29. Yu, Q, Funaki, B, and Ahmed, O. Twenty years of embolization for acute lower gastrointestinal bleeding: a meta-analysis of rebleeding and ischaemia rates. Br J Radiol. (2024) 97:920–32. doi: 10.1093/bjr/tqae037
Keywords: acute nonvariceal gastrointestinal bleeding, selective embolization, super-selective embolization, clinical success, rebleeding
Citation: Zhong J, Li K, Chen T, Liao F and Shu X (2025) Comparison of the efficacy and safety of super-selective and selective transcatheter arterial embolization in non-variceal gastrointestinal bleeding. Front. Med. 12:1697511. doi: 10.3389/fmed.2025.1697511
Edited by:
Francesco Tiralongo, U.O.C. Radiologia I, A.O.U. Policlinico San Marco, P.O. "G.Rodolico", ItalyReviewed by:
Makoto Taninokuchi Tomassoni, University of Bologna, ItalyNodar Sulashvili, National Teaching University SEU, Georgia
Copyright © 2025 Zhong, Li, Chen, Liao and Shu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Xu Shu, bmR5ZnkwMjAxNkBuY3UuZWR1LmNu
†These authors share first authorship