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Your Position: Home - Home & Garden - How do you treat TIPS thrombosis?

How do you treat TIPS thrombosis?

A TIPS relieves the high blood pressure in the portal vein (called portal hypertension) that often occurs in the setting of liver cirrhosis. A TIPS allows blood flowing into the liver from the portal vein to flow through the TIPS stent directly into the hepatic vein, the vein that drains blood out of the liver to the vena cava and then immediately into the heart.

Why would a person need a TIPS?

The two main reasons that a person might need a TIPS are:

  1. Ascites (fluid accumulation in the abdomen) that cannot be managed with dietary sodium restriction and diuretics (“water pills”). Sometimes ascites crosses the diaphragm muscle between one of the lungs and abdomen to fill the space around the lung, typically the right lung. This is called hepatic hydrothorax and TIPS can often help this as well. TIPS should not be considered if the fluid accumulation can be controlled by dietary sodium restriction and diuretics.
  2. Bleeding from varices (swollen veins, usually in the esophagus) that cannot be controlled with endoscopic treatment such as rubber band ligation. Bleeding varices in the stomach, rectum or elsewhere are more difficult to treat with rubber band ligation and a TIPS is often needed in these situations.

How is a TIPS inserted into the liver?

A radiologist with special training places the TIPS by going through a jugular vein in the neck and straight down into the liver. People are usually heavily sedated or asleep with general anesthesia for the procedure. After numbing up a spot in the skin over the jugular vein on the side of neck (typically the right side), a catheter like a large IV is temporarily placed through the skin into the jugular vein. A partially covered stent is inserted through the catheter, which is passed down through the superior vena cava, right atrium of the heart, inferior vena cava, into the hepatic vein and through the liver into the portal vein. The TIPS stent is very narrow when it is inserted, and it is passed into the liver over this device. It is expanded once it is in the liver with one end in a branch of the portal vein and the other end in a branch of the hepatic vein. Sometimes more than one stent is placed in a row to bridge that distance. At the end of the procedure, the catheter in the neck and the device used to place the shunt are removed. Just the TIPS stent is left in the liver and a small bandage is placed on the neck.

Can a TIPS be removed?

No, a TIPS cannot be removed. If the flow through the TIPS is greater than anticipated which reduces blood flow to the rest of the liver too much, its diameter can be reduced. This is called a TIPS revision.

What are the risks of having a TIPS?

One of the major functions of the liver is to remove toxins from the blood such ammonia and other toxins absorbed from the colon, so when a TIPS is placed, the blood going into the liver is not filtered as well. An increase in the blood levels of ammonia and other toxins can cause confusion, disorientation and even coma. This is called hepatic encephalopathy. Taking a medication called lactulose helps flush the toxins out of the colon and another medication called rifaximin reduces the amount of toxins produced in the colon. These are sometimes needed after a TIPS. If a person is already taking those medications, then a TIPS may not be a good option because there are no additional treatment options if hepatic encephalopathy occurs after a TIPS.

Other risks of having a TIPS include liver infarction which is when some of the liver dies because of a lack of blood flow, and also disruption of the bile ducts, bleeding from the liver into the abdomen, and infection. Fortunately, these are all rare events.

The decision to have a TIPS requires a careful consideration of the potential benefits and whether these benefits outweigh the risks.

What happens after a TIPS?

Immediately after a TIPS, people are typically kept in the hospital, sometimes in the ICU for a night, for close monitoring for signs of bleeding. People typically go home a day or two after a TIPS.

After going home, people with a TIPS should be monitored closely for signs of hepatic encephalopathy. This may not occur for a week or two after the TIPS was inserted and can cause confusion and disorientation. The hepatologist caring for the person should be notified immediately if this happens. People with evidence of hepatic encephalopathy should not drive or engage in activities that could be a danger to themselves or others (physically or financially).

Diuretic doses typically need to be reduced after a TIPS while monitoring for signs of re-accumulation of fluid or dehydration and impaired kidney function. Any dizziness or other signs of dehydration should be reported immediately to the hepatologist.

TIPS occlusion, or blockage, can occur within days, weeks or even years after a TIPS. This is caused by blood clotting in the TIPS or reduction in the TIPS diameter due to the excessive scar tissue in the liver. The TIPS is typically reevaluated periodically by ultrasound to confirm its adequate function. If it becomes narrowed or fully blocked, an interventional radiologist may need to reopen it.

What are the common reasons that a person cannot have a TIPS?

The major reasons why a TIPS should usually not be placed are:

  1. The liver function is so poor that TIPS can cause further liver failure. Usually an INR above 2.0, or total bilirubin above 3 to 5 mg/dl predicts poor outcomes. Once the MELD score is above 15, a TIPS has a higher risk; it is generally not done if the MELD score is more than 18-20 unless it is needed in an emergency to control bleeding from varices and the person is on a liver transplant list.
  2. The right side of the heart, the side that pumps blood through the lungs, is not strong enough to handle the increased blood flow, or if there already is severe hypertension in the lung circulation because the increased flow from the TIPS can cause severe strain on the heart. This is commonly determined by an echocardiogram prior to TIPS placement
  3. The portal vein is blocked by a blood clot (portal vein thrombosis).
  4. The presence of liver cancer or other types of cancer within the liver.
  5. TIPS is generally not considered to treat large varices in esophagus or stomach if they have never bled.

What are the alternatives to having a TIPS?

For people who have a TIPS to control ascites (abdominal fluid) or hepatic hydrothorax (ascites that crosses the diaphragm muscle into the chest cavity and causes the lung to shrink), typically the only alternative is to continue to have fluid removed by paracentesis (from the abdomen) or thoracentesis (from the chest cavity). In end-of-life situations where palliative care is appropriate, a drain can sometimes be left in place and used to periodically withdraw fluid from the chest or abdomen. This is not done routinely because of the risk of infection and the continuous loss of protein in the fluid that is removed.

Information provided with the help of…

Brent A. Tetri, MD
Professor of Internal Medicine
Division of Gastroenterology & Hepatology
Saint Louis University

Kamran Qureshi, MD
Associate Professor of Internal Medicine
Division of Gastroenterology & Hepatology
Saint Louis University

Transjugular intrahepatic portosystemic shunt (TIPS) is increasingly used for the treatment of complications of portal hypertension, especially variceal bleeding and ascites refractory to conventional therapy (1,2). Development of thrombosis after TIPS placement is an uncommon complication, which was reported to occur in only 3% to 10% of patients when bare stents were used in several large series (3-6). Thrombosis usually develops acutely either at the time the stent is being deployed or within several days of TIPS placement (2,6). The cause of the thrombosis may be leakage of bile into the shunt, hypercoagulable syndromes, stent mispositioning, suboptimal stent sites, or inadequate coverage of the TIPS tract with sufficient stent (2,7-12). The direct result of thrombosis development is occlusion of the TIPS device, blocking flow in the portal vein and directly resulting in the recurrence of the complication of portal hypertension in addition to potentially causing bowel ischemia as a result of venous congestion in cases of thrombosis extending into the splenic and mesenteric veins (7). Thrombosis can be identified by Doppler ultrasound and patency can be re-established by repeat catheterization (2,7). The development of acute thrombosis also can be effectively prevented by prophylaxis anticoagulation or using e-PTFE-coated stents (13,14). One randomized controlled trial (RCT) showed that use of phenprocoumon (an anticoagulant) was associated with a lower rate of complete occlusion within the first three months following TIPS placement (13). In the RCT by Bureau (14), no early thrombosis was observed in the e-PTFE covered stent-graft group (n=39) as compared with three cases in the covered stent-graft group (n=41). A recent RCT also showed that early thromboses were less frequent in patients receiving covered stent TIPS compared with those receiving bare stents (10/67 in bare stent group vs. 3/63 in the covered stent group) (15).

In a recent issue of Clinical and Applied Thrombosis/Hemostasis, Yue-Meng et al. (16) reported their experience on thrombosis in a cohort of cirrhotic patients undergoing elective TIPS. In this study, the prevalence of thrombosis in cirrhotic patients undergoing elective TIPS was 26.7% (27/101), despite using prophylaxis anticoagulation (low-molecular-weight heparin then shifted to aspirin or clopidogrel) and ePTFE-covered stent. This value is unexpectedly higher than that reported in the literatures (3-6). Even though the authors declared this rate was similar to those without TIPS and compared their results with those without TIPS from beginning to end in their paper, it should be noted that development of portal vein thrombosis (PVT) in the presence or absence of TIPS was two distinct situations. In cirrhotic patients without TIPS, a prior decrease in portal blood flow velocity, in combination with a hypercoagulable state caused by cirrhosis and/or concomitant thrombophilic disorders, constitutes the main risk factors (17-19). Thus PVT is not an infrequent occurrence in patients with cirrhosis, with a prevalence ranging from 2% to 23% (20). However, the most determined risk factor has been overcome after TIPS by increasing the blood velocity. Indeed, the reported PVT recurrence rate after TIPS in the study by Luca et al. is only 5% (21). The common causes of thrombosis development after TIPS placement have been discussed above. Therefore, this high prevalence of thrombosis after TIPS in this study, if the report is true, questions the radiologist skills, which is related to stent mispositioning and incorrect release of the stent (7,11,12,14,15,22). Previous studies have shown that deployment of a stent with the cephalic end extending to the hepato-caval junction and the caudal end parallel to the vascular wall of the portal vein is favorable in a TIPS procedure to decrease the risk of thrombosis and shunt dysfunction (10,12). In contrast, an uncovered hepatic vein is more susceptible to shunt thrombosis caused by turbulence and the shear stress of high-velocity blood flow (10-12).

Another interesting finding in this study is that thrombosis after TIPS seem to seldom cause shunt dysfunction as the portion of patients who developed thrombosis (27/101, 27%) was higher than that developed shunt dysfunction (21/101, 21%) and most shunt dysfunction was revealed to be shunt stenosis which seems caused by pseudointimal hyperplasia (16/21, 76%) (16). This low rate shunt dysfunction resulted from thrombosis questions the adverse impact of the thrombosis. In addition, it has been shown that shunting branch of portal vein and stent position is associated with shunt dysfunction, hepatic encephalopathy and survival after TIPS (12). Thus, whether the poorer clinical outcomes in TIPS-treated patients who developed thrombosis are due to their suboptimal stent sites or thrombosis is hard to say.

Furthermore, several aspects in the misuse of statistical methods in this study should be considered. Firstly, the authors compared the results in patients with and without thrombosis; however, other potential confounders were not adjusted. Second, as the development of thrombosis change over time, they should be included in a Cox model treating as time-dependent covariates after adjusting other potential confounders (23).

Collectively, considering the unexpected high incidence of thrombosis after TIPS and inappropriate statistical methods, the results of this study should be interpreted with some caution.

Acknowledgements

Funding: None.

Provenance and Peer Review: This article was commissioned by the editorial office, AME Medical Journal. The article did not undergo external peer review.

Conflicts of Interest: The authors have completed the ICMJE uniform disclosure form (available at http://dx.doi.org/10.21037/amj.2017.03.07). The authors have no conflicts of interest to declare.

Ethical Statement: The authors are accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.

References

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  10. Clark TW, Agarwal R, Haskal ZJ, et al. The effect of initial shunt outflow position on patency of transjugular intrahepatic portosystemic shunts. J Vasc Interv Radiol 2004;15:147-52. [Crossref] [PubMed]
  11. Angeloni S, Merli M, Salvatori FM, et al. Polytetrafluoroethylene-covered stent grafts for TIPS procedure: 1-year patency and clinical results. Am J Gastroenterol 2004;99:280-5. [Crossref] [PubMed]
  12. Bai M, He CY, Qi XS, et al. Shunting branch of portal vein and stent position predict survival after transjugular intrahepatic portosystemic shunt. World J Gastroenterol 2014;20:774-85. [Crossref] [PubMed]
  13. Sauer P, Theilmann L, Herrmann S, et al. Phenprocoumon for prevention of shunt occlusion after transjugular intrahepatic portosystemic stent shunt: a randomized trial. Hepatology 1996;24:1433-6. [PubMed]
  14. Bureau C, Garcia-Pagan JC, Otal P, et al. Improved clinical outcome using polytetrafluoroethylene-coated stents for TIPS: results of a randomized study. Gastroenterology 2004;126:469-75. [Crossref] [PubMed]
  15. Perarnau JM, Le Gouge A, Nicolas C, et al. Covered vs. uncovered stents for transjugular intrahepatic portosystemic shunt: a randomized controlled trial. J Hepatol 2014;60:962-8. [Crossref] [PubMed]
  16. Yue-Meng W, Li YH, Wu HM, et al. Portal Vein Thrombosis in Patients With Cirrhosis Undergoing Elective Transjugular Intrahepatic Portosystemic Shunt. Clin Appl Thromb Hemost 2017; [Epub ahead of print]. [Crossref] [PubMed]
  17. Tripodi A, Primignani M, Chantarangkul V, et al. An imbalance of pro- vs anti-coagulation factors in plasma from patients with cirrhosis. Gastroenterology 2009;137:2105-11. [Crossref] [PubMed]
  18. Zocco MA, Di Stasio E, De Cristofaro R, et al. Thrombotic risk factors in patients with liver cirrhosis: correlation with MELD scoring system and portal vein thrombosis development. J Hepatol 2009;51:682-9. [Crossref] [PubMed]
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  22. Shah RP, Sze DY. Complications During Transjugular Intrahepatic Portosystemic Shunt Creation. Tech Vasc Interv Radiol 2016;19:61-73. [Crossref] [PubMed]
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doi: 10.21037/amj.2017.03.07
Cite this article as: Lv Y, Han G, Fan D. Thrombosis after transjugular intrahepatic portosystemic shunt: an ominous sign? AME Med J 2017;2:40.

How do you treat TIPS thrombosis?

Thrombosis after transjugular intrahepatic portosystemic shunt

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