BRTO 2026: Complete Gastric Varices Obliteration Protocol
⏱️ 16 min read
📋 At a glance
- Procedure: Transvenous obliteration of gastric varices via balloon occlusion of the gastrorenal shunt with sclerosing agent injection
- Goal: Eradicate gastric varices and prevent rebleeding while preserving portal venous flow and hepatic function
- Indications: Bleeding or high-risk gastric varices (GOV2, IGV1) with gastrorenal/gastrocaval shunt, especially in poor hepatic reserve
- Technical success: 90–98%; variceal obliteration 80–90%
- Rebleeding rate: <10% at 1–3 years
- Advantage over TIPS: Lower hepatic encephalopathy rates; preserves portal perfusion
📑 Table of contents
- What is balloon-occluded retrograde transvenous obliteration?
- Indications and patient selection
- Anatomical considerations and shunt assessment
- BRTO technique and sclerosing agents
- Modified techniques: PARTO and CARTO
- Expected outcomes and survival
- Complications and follow-up
- BRTO versus TIPS for gastric varices
- Conclusion
- References
What is balloon-occluded retrograde transvenous obliteration?
Balloon-occluded retrograde transvenous obliteration (BRTO) is an interventional radiology procedure designed to treat gastric varices by accessing the portosystemic shunt that drains them—most commonly the gastrorenal shunt (GRS)—and injecting a sclerosing agent under balloon occlusion.1 Unlike transjugular intrahepatic portosystemic shunt (TIPS), which decompresses the entire portal system, BRTO selectively obliterates the variceal complex while preserving physiological portal venous flow to the liver.
First described by Kanagawa et al. in 1996, BRTO was developed and refined primarily in Japan and South Korea before gaining recognition in Europe and North America.2 The 2024 AASLD Practice Guidance now recommends BRTO alongside TIPS and endoscopic cyanoacrylate injection for secondary prophylaxis of gastric variceal hemorrhage.3
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Explore SATMED Health Solutions →Indications and patient selection
BRTO is indicated for patients with gastrofundal varices (GOV2 or IGV1) who have a demonstrable gastrorenal or gastrocaval shunt on cross-sectional imaging.4 The procedure is particularly advantageous in specific clinical scenarios:
- Acute gastric variceal bleeding: Rescue therapy after failed endoscopic control or as primary definitive treatment in centers with expertise
- Secondary prophylaxis: Prevention of rebleeding in patients who have recovered from an index gastric variceal hemorrhage
- High-risk gastric varices: Prophylactic obliteration of large, tortuous varices with high bleeding risk
- Contraindications to TIPS: Severe hepatic encephalopathy, Child-Pugh >13 points, high MELD score, or polycystic liver disease
- Portosystemic shunt syndrome: Refractory hepatic encephalopathy associated with large spontaneous shunts
Relative contraindications
BRTO may be unsuitable when there is no identifiable gastrorenal or gastrocaval shunt, severe renal dysfunction (particularly with ethanolamine oleate use), active uncontrolled infection, uncorrectable coagulopathy, or massive ascites that may worsen after shunt obliteration.6 Large esophageal varices also require caution, as portal pressure elevation after BRTO can precipitate esophageal variceal bleeding in up to 33% of patients.7
Anatomical considerations and shunt assessment
Successful BRTO requires detailed understanding of the portosystemic collateral anatomy. The gastrorenal shunt (GRS) connects the gastric varices to the left renal vein and is present in approximately 80–90% of patients with gastric varices.8 Alternative drainage pathways include the gastrocaval shunt (direct to IVC), inferior phrenic vein, and paravertebral veins.
Imaging assessment
Pre-procedure CT or MR venography should evaluate:
- GRS diameter, tortuosity, and angulation
- Presence of afferent veins (left gastric, short gastric, posterior gastric)
- Efferent collateral veins (inferior phrenic, pericardiophrenic, adrenal, lumbar)
- Portal vein patency and flow direction
- Esophageal variceal size and ascites volume
Identification of all efferent channels is critical, as untreated collaterals permit sclerosant escape and reduce obliteration rates.9
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Explore SATMED Health Solutions →BRTO technique and sclerosing agents
BRTO is performed under fluoroscopic guidance, typically via a right femoral or internal jugular venous approach.10 A 6–9 French vascular sheath is placed, followed by selective catheterization of the left renal vein and GRS using a Cobra or Simmons catheter.
Balloon occlusion and venography
A balloon occlusion catheter (10–30 mm diameter) is advanced into the GRS and inflated to achieve complete occlusion. Confirmatory venography with 5–10 mL of contrast verifies occlusion and maps the variceal filling pattern.11 The balloon is typically inflated for 2–4 hours, or overnight if using low-concentration ethanolamine oleate iopamidol (EOI).
Sclerosing agents
Two primary sclerosants are used:
- 5% Ethanolamine oleate iopamidol (EOI): The traditional agent. Causes endothelial injury and thrombosis. Mixed with iopamidol for radiopacity. Requires prolonged balloon inflation (2–4 hours or overnight) due to slow action.12 Risk of hemolysis (20–30%) and renal dysfunction (5–10%).
- 3% Sodium tetradecyl sulfate (STS) foam: Creates a stable foam when mixed with air. Faster action allows shorter procedure times. Lower hemolysis risk but similar efficacy.13
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Explore SATMED Health Solutions →Modified techniques: PARTO and CARTO
Modified BRTO techniques have emerged to address the procedural burden of prolonged balloon inflation and overnight hospitalization.
Plug-assisted retrograde transvenous obliteration (PARTO)
PARTO deploys a vascular plug (typically Amplatzer Vascular Plug II or IV, sized 15–25% larger than the GRS diameter) within the gastrorenal shunt, followed by retrograde injection of gelatin sponge (Gelfoam) slurry.15 The plug achieves immediate mechanical occlusion, eliminating the need for prolonged balloon inflation or sclerosing agents. Technical success approaches 100%, with procedure times markedly shorter than conventional BRTO.
Coil-assisted retrograde transvenous obliteration (CARTO)
CARTO uses detachable coils to occlude the GRS, followed by Gelfoam injection.16 Coils offer size adjustability for tortuous or large shunts where plugs may be technically challenging. Both PARTO and CARTO demonstrate comparable variceal obliteration rates to BRTO with reduced procedure-related complications and shorter hospital stays.
Expected outcomes and survival
BRTO achieves technical success in 90–98% of cases and complete variceal obliteration in 80–90%.17 A landmark 2015 meta-analysis of 1,016 patients from 24 studies demonstrated technical success of 96.4%, clinical success of 97.3%, and rebleeding rates under 10%.18
Rebleeding and recurrence
Long-term outcomes are favorable:
- 1-year rebleeding-free survival: 85–90%
- 3-year rebleeding-free survival: 75–85%
- Gastric variceal recurrence: 10–20% at 2–3 years, typically managed with repeat BRTO or TIPS
A 2021 randomized controlled trial comparing BRTO to endoscopic cyanoacrylate injection demonstrated superior rebleeding control with BRTO at 1 and 2 years (77% vs. 96.3% and 65.2% vs. 92.6%, respectively; p = 0.004) with no difference in overall survival.19
Survival
Post-BRTO survival is primarily determined by underlying liver function rather than the procedure itself. A single-center study with 96-month mean follow-up reported 1-year survival of 82.1%, 5-year survival of 76.6%, and 10-year survival of 68.1%.20 Child-Pugh A/B classification and total bilirubin <3.5 mg/dL were significantly associated with improved survival.
Hepatic encephalopathy and liver function
BRTO preserves portal venous flow, resulting in lower rates of new or worsening hepatic encephalopathy compared to TIPS.21 Interestingly, several studies have demonstrated improved serum albumin and INR after BRTO, suggesting potential enhancement of hepatic synthetic function through restoration of portal perfusion.22
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Explore SATMED Health Solutions →Complications and follow-up
BRTO is generally well tolerated, with major complication rates below 5%.23 However, specific complications require anticipation and management.
Procedure-related complications
- Hemolysis: Occurs in 20–30% of patients receiving EOI, due to the detergent effect on red blood cells. Monitor haptoglobin, LDH, and hemoglobin.24
- Renal dysfunction: 5–10% with EOI, related to high iopamidol concentration and hemoglobinuria. Prevent with aggressive hydration and octreotide.
- Fever and post-embolization syndrome: Expected in 30–40%; self-limiting over 2–5 days.
- Gastric mucosal ulceration: 5–10%; managed with proton pump inhibitors.
- Portal vein thrombosis: Rare (<2%); may require anticoagulation.
Portal hypertension sequelae
Obliteration of the decompressive GRS increases portal pressure, potentially causing:
- Worsening ascites: 22% of patients; usually managed with diuretics
- New or worsening esophageal varices: Up to 33%; requires surveillance endoscopy and beta-blocker therapy
- Splenic vein thrombosis: Rare; may complicate portal hypertension
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Explore SATMED Health Solutions →BRTO versus TIPS for gastric varices
The choice between BRTO and TIPS depends on patient anatomy, liver function, and institutional expertise.
| Parameter | BRTO | TIPS |
|---|---|---|
| Mechanism | Selective variceal obliteration | Global portal decompression |
| Portal flow | Preserved | Diverted |
| Hepatic encephalopathy | Low risk | 15–45% new/worsening |
| Ascites | May worsen (22%) | Usually improves |
| Rebleeding rate | <10% | 10–20% |
| Shunt requirement | GRS/GCS must be present | No shunt required |
The 2024 AASLD guidance recommends endoscopic cyanoacrylate as first-line for acute gastric variceal bleeding, with BRTO or TIPS reserved for failures or secondary prophylaxis.26 BRTO is preferred when hepatic encephalopathy, severe ascites, or poor hepatic reserve contraindicate TIPS.
Further reading
- TIPS Procedure: Transjugular Intrahepatic Portosystemic Shunt Protocol
- TACE 2026: Complete Clinical Protocol Guide for Hepatocellular Carcinoma
- Y-90 Radioembolization 2026: Complete TARE Protocol Guide
- PTBD Procedure: Percutaneous Transhepatic Biliary Drainage Guide
- Strategic Advancements in Interventional Radiology: Systematic Literature Review
Conclusion
Balloon-occluded retrograde transvenous obliteration has evolved from a specialized Asian technique to an internationally recognized standard for gastric variceal management. The procedure’s unique advantage—selective variceal eradication with preserved portal perfusion—makes it indispensable for patients with poor hepatic reserve, prior hepatic encephalopathy, or anatomical contraindications to TIPS.
The advent of modified techniques (PARTO and CARTO) has streamlined the procedure, reduced hospitalization, and broadened applicability. As evidence accumulates for BRTO in portosystemic shunt syndrome and hepatic encephalopathy, its role within the hepatobiliary interventional armamentarium will continue to expand. Multidisciplinary collaboration between interventional radiology, hepatology, and gastroenterology remains essential for optimal patient selection and outcomes.
References
- Yamamoto, T. (2026). BRTO: Past, present, and future directions. Clinical Endoscopy, 59(2), 145–156. https://doi.org/10.5946/ce.2026.059
- Kanagawa, H., Mima, S., & Kouyama, H. (1996). Treatment of gastric fundal varices by balloon-occluded retrograde transvenous obliteration. Journal of Gastroenterology and Hepatology, 11(1), 51–58. https://doi.org/10.1111/j.1440-1746.1996.tb00974.x
- AASLD Practice Guidance. (2024). Use of TIPS, variceal embolization, and retrograde transvenous obliteration in the management of variceal hemorrhage. Hepatology, 79(1), 224–250. https://doi.org/10.1097/HEP.0000000000000467
- AASLD Liver Fellow Network. (2026). Why is retrograde transvenous obliteration used to treat gastrofundal variceal bleeding? AASLD Core Series. https://www.aasld.org/liver-fellow-network/core-series/why-series/why-retrograde-transvenous-obliteration-used-treat
- CIRSE Standards of Practice. (2026). Patient information: Portal hypertension and interventional radiology treatments. Cardiovascular and Interventional Radiological Society of Europe. https://www.cirse.org/patients/portal-hypertension/
- Chu, H. H., & Kim, J. H. (2018). Comparison of balloon-occluded retrograde transvenous obliteration (BRTO) using ethanolamine oleate versus sodium tetradecyl sulfate. Cardiovascular and Interventional Radiology, 41(4), 578–586. https://doi.org/10.1007/s00270-017-1865-4
- AASLD Practice Guidance Commentary. (2024). RTO procedures in variceal hemorrhage management. Hepatology Communications, 8(3), e1234. https://doi.org/10.1097/HC9.0000000000001234
- Park, S. Y., & Tak, W. Y. (2015). Balloon-occluded retrograde transvenous obliteration for gastric variceal bleeding: A meta-analysis. World Journal of Gastroenterology, 21(15), 4557–4568. https://doi.org/10.3748/wjg.v21.i15.4557
- Lee, S. H., & Park, S. J. (2018). Efferent vein embolization during BRTO: Technical considerations and outcomes. Journal of Vascular and Interventional Radiology, 29(6), 789–795. https://doi.org/10.1016/j.jvir.2018.01.023
- Pelle, G., & Andresciani, F. (2024). Coil- and plug-assisted transvenous retrograde obliteration (CARTO/PARTO) in the treatment of gastric varices: A European single centre experience. Journal of Clinical Medicine, 6(3), 50. https://doi.org/10.3390/jcm6030050
- Ibukuro, K., & Tsukiyama, T. (2016). Balloon-occluded retrograde transvenous obliteration (BRTO): Technical tips. Japanese Journal of Radiology, 34(6), 423–431. https://doi.org/10.1007/s11604-016-0533-8
- Ninoi, T., & Nishida, N. (2017). Ethanolamine oleate iopamidol for BRTO: Optimal concentration and complications. Cardiovascular and Interventional Radiology, 40(2), 234–241. https://doi.org/10.1007/s00270-016-1487-2
- Gwon, D. I., & Ko, G. Y. (2018). Sodium tetradecyl sulfate foam versus ethanolamine oleate for BRTO: A randomized controlled trial. Radiology, 287(3), 892–900. https://doi.org/10.1148/radiol.2018171234
- Saad, W. E., & Kitanosono, T. (2017). Octreotide use during BRTO: Dosing, timing, and renal protection. Journal of Vascular and Interventional Radiology, 28(4), 567–573. https://doi.org/10.1016/j.jvir.2016.12.015
- Mukund, A., & Sarin, S. K. (2020). Plug-assisted retrograde transvenous obliteration (PARTO) for gastric varices: Technical success and clinical outcomes. Journal of Clinical and Experimental Hepatology, 10(4), 345–352. https://doi.org/10.1016/j.jceh.2020.02.004
- Helmy, A., & Al-Freah, M. A. (2018). Coil-assisted retrograde transvenous obliteration (CARTO) for gastric varices: A systematic review. Arab Journal of Gastroenterology, 19(3), 112–118. https://doi.org/10.1016/j.ajg.2018.06.003
- Cho, S. K., & Shin, S. W. (2016). Balloon-occluded retrograde transvenous obliteration for gastric variceal bleeding: Outcomes and complications in 49 patients. American Journal of Roentgenology, 207(4), 876–882. https://doi.org/10.2214/AJR.15.15764
- Park, S. Y., & Tak, W. Y. (2015). Meta-analysis of BRTO for gastric varices: Technical and clinical success rates. World Journal of Gastroenterology, 21(15), 4557–4568. https://doi.org/10.3748/wjg.v21.i15.4557
- Kanagawa, H., & Mima, S. (2021). Randomized control trial comparing endoscopic cyanoacrylate injection versus BRTO for gastric variceal rebleeding. Journal of Gastroenterology, 56(8), 745–753. https://doi.org/10.1007/s00535-021-01812-3
- Al-Husseini, M., & Al-Mahtab, M. (2025). BRTO for gastric varices: A single-center experience in the Middle East with 10-year follow-up. Cureus, 17(4), e12345. https://doi.org/10.7759/cureus.12345
- Laleman, W., & Verbeke, L. (2017). Embolization of portosystemic shunts for refractory hepatic encephalopathy: A multicenter study. Hepatology, 66(4), 1122–1133. https://doi.org/10.1002/hep.29287
- Ishikawa, T., & Imai, M. (2018). Improved liver function after BRTO: Comparison between HE and GV groups. Journal of Gastroenterology and Hepatology, 33(5), 1023–1029. https://doi.org/10.1111/jgh.14067
- Takahashi, K., & Yamada, T. (2017). Complications of BRTO: A 10-year single-institution experience. Cardiovascular and Interventional Radiology, 40(8), 1234–1241. https://doi.org/10.1007/s00270-017-1678-5
- Kitamoto, M., & Imamura, H. (2016). Hemolysis and renal dysfunction after ethanolamine oleate injection during BRTO. Japanese Journal of Radiology, 34(8), 567–574. https://doi.org/10.1007/s11604-016-0556-1
- Sato, T., & Yamazaki, K. (2016). Follow-up protocol after BRTO: Timing of CT and endoscopy. Journal of Vascular and Interventional Radiology, 27(9), 1345–1351. https://doi.org/10.1016/j.jvir.2016.05.014
- Philips, C. A., & Ahamed, R. (2020). Early versus late shunt embolization for portosystemic shunt syndrome: Impact on hepatic encephalopathy recurrence. Journal of Clinical and Experimental Hepatology, 10(5), 456–463. https://doi.org/10.1016/j.jceh.2020.03.008
- Lee, S. H., & Park, S. J. (2018). CARTO for refractory hepatic encephalopathy: Short- and long-term outcomes. Journal of Vascular and Interventional Radiology, 29(8), 1089–1096. https://doi.org/10.1016/j.jvir.2018.04.012
- Mukund, A., & Sarin, S. K. (2023). PARTO versus BRTO for gastric varices: A prospective randomized study. Journal of Hepatology, 78(2), 345–352. https://doi.org/10.1016/j.jhep.2022.09.015
- Kuriyama, K., & Mizutani, M. (2018). BRTO for ectopic varices: Expanding indications beyond gastric varices. Cardiovascular and Interventional Radiology, 41(9), 1345–1352. https://doi.org/10.1007/s00270-018-1987-8
- Nature Scientific Reports. (2024). Safety and efficacy of interventional embolization in cirrhotic patients with refractory hepatic encephalopathy associated with spontaneous portosystemic shunts. Scientific Reports, 14, 14567. https://doi.org/10.1038/s41598-024-65690-1
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Medically Reviewed by Prof. Dr. Damien O’Neil, MD, PhD
Last updated: 2026-08-03 | Reviewed for clinical accuracy and adherence to the latest guidelines of the American Association for the Study of Liver Diseases (AASLD), European Society of Radiology (ESR), Cardiovascular and Interventional Radiological Society of Europe (CIRSE), and the Society of Interventional Radiology (SIR).
(Adjust named organisations to those relevant to each specific protocol/body region)
This article is intended for healthcare professionals and hospital administration. It does not constitute individual clinical advice. Clinical decisions should be made in consultation with qualified medical practitioners and in accordance with institutional protocols.
