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Transjugular Intrahepatic Portosystemic Shunt (TIPSS)

Number: 0259



Policy

Aetna considers transjugular intrahepatic portosystemic shunt (TIPSS) medically necessary in members with bleeding gastric, esophageal or ectopic (including anorectal, intestinal, and stomal) varices, moderate Budd-Chiari syndrome and who have failed to respond to anticoagulation, portal hypertensive gastropathy with recurrent bleeding despite the use of beta-blockers, severe refractory ascites, and refractory hepatic hydrothorax (see background section for selection criteria).

Aetna considers polyflorotetraethylene (PTFE)-coated stents medically necessary for TIPSS.

Aetna considers TIPSS experimental and investigational for all other indications including any of the following conditions because the effectiveness of TIPSS for these conditions has not been proven:

  • Controlling bleeding from gastro antral vascular ectasia in persons with cirrhosis; or 
  • Correction of hypersplenism and thrombocytopenia; or
  • Hepatopulmonary syndrome; or
  • Hepatorenal syndrome; or
  • Initial therapy for acute variceal hemorrhage; or
  • Initial therapy to prevent first or recurrent variceal hemorrhage; or
  • Portal hypertension associated with polycystic liver disease or Caroli disease; or
  • Portal-mesenteric venous thrombosis; or
  • Pre-hepatic portal hypertension; or
  • Pre-operative reduction in portal hypertension before liver transplantation; or
  • Prophylaxis of variceal hemorrhage; or
  • Pulmonary hypertension; or
  • Sinusoidal obstruction syndrome (veno-occlusive disease).
Background

Transjugular intrahepatic portosystemic shunt (TIPSS) has been shown in a number of clinical studies to be an option in the treatment of acute variceal bleeding that can not be successfully controlled with sclerotherapy and for treatment of recurrent variceal bleeding that can not be successfully controlled with medical management or sclerotherapy.

Transjugular intrahepatic portosystemic shunt does not involve an incision; rather, a catheter is placed percutaneously into the jugular vein through which a permanent intrahepatic shunt is created between the hepatic and portal veins.  Blood flow is diverted around the diseased liver, thus easing portal hypertension.  It is usually performed in the angiography or interventional radiology laboratory under intravenous anesthesia.

The efficacy of TIPSS as the initial treatment of variceal bleeding or in the prevention of secondary variceal bleeding has not been established.

The American Association for the Study of Liver Diseases (AASLD) practice guidelines on the role of TIPSS creation in the management of portal hypertension has a number of recommendations, including the following (Boyer and Haskal, 2005):

  • The use of TIPSS to treat hepatopulmonary syndrome can not be recommended (grade II-3).
  • The use of TIPSS to treat sinusoidal obstruction syndrome can not be recommended (grade II-3).
  • TIPSS is effective in the control of hepatic hydrothorax, but it should be used only in patients whose effusion can not be controlled by diuretics and sodium restriction (grade II-3).
  • TIPSS is effective in the prevention of rebleeding from gastric and ectopic varices (including intestinal, stomal, and anorectal varices) and is the preferred approach for the prevention of rebleeding in this group of patients (grade II-3).

Grade II-3 refers to multiple time series, dramatic uncontrolled experiments.

Pan et al (2008) identified factors predictive of survival after TIPSS creation.  Log-rank tests were used to compare the cumulative survival functions among groups of patients who underwent TIPSS creation for various indications.  Thirty-day mortality after TIPSS creation was examined by logistic regression.  Cox proportional-hazards analyses were performed to analyze the cumulative 90-day and 1-year survival.  Selected variables such as creatinine, bilirubin, and International Normalized Ratio (INR) were assessed with respect to survival.  The study included 352 patients, of whom 229 (65.1 %) were male.  The mean age at the time of TIPSS creation was 53.6 years (range of 21 to 82).  A Model for End-stage Liver Disease (MELD) score greater than 15 was significantly associated with poor survival (p < 0.05) at 30 days, 90 days, and 1 year after TIPSS creation.  Independently, a serum total bilirubin level greater than 2.5 mg/dL, an INR greater than 1.4 (p < 0.05), and a serum creatinine level greater than 1.2 mg/dL were predictive of poor survival.  Finally, age greater than 70 years was associated with poor survival at 90 days and 1 year after TIPSS creation (p < 0.05).  The authors concluded that the choice to create a TIPSS in individuals whose MELD score is greater than 15 and/or whose age is greater than 70 years should involve a careful consideration of risk/benefit ratio, taking into account the finding that such patients have significantly poorer survival after TIPSS creation.

Garcia-Pagán et al (2008) reported the long-term results and prognostics factors in 124 patients with Budd-Chiari syndrome (BCS) who were treated with TIPSS.  Subjects were followed until death, orthotopic liver transplantation (OLT), or last clinical evaluation.  Prior to treatment with TIPSS, BCS patients had a high MELD and high Rotterdam BCS prognostic index (98 % of patients at intermediate-risk or high-risk) indicating severity of liver dysfunction.  However, 1- and 5-year OLT-free survival were 88 % and 78 %, respectively.  In the high-risk patients, 5-year OLT-free survival was much better than that estimated by the Rotterdam BCS index (71 % versus 42 %, respectively).  In the whole population, bilirubin, age, and INR for prothrombin time independently predicted 1-year OLT-free survival.  A prognostic score with a good discriminative capacity (area under the curve, 0.86) was developed from these variables.  Seven out of 8 patients with a score greater than 7 died or underwent transplantation versus 5 out of 114 patients with a score of less than 7.  The authors concluded that long-term outcome for patients with severe BCS treated with TIPSS is excellent even in high-risk patients, suggesting that TIPS may improve survival.  Furthermore, these researchers identified a small subgroup of BCS patients with poor prognosis despite TIPSS who might benefit from early OLT.

Murad et al (2008) noted that the clinical outcome of a covered versus uncovered TIPSS for patients with BCS is as yet largely unknown.  These investigators compared patency rates of bare and polytetrafluoroethylene (PTFE)-covered stents, and examined clinical outcome using 4 prognostic indices (Child-Pugh score, Rotterdam BCS index, modified Clichy score and MELD).  A total of 23 TIPSS procedures were performed on 16 patients.  The primary patency rate at 2 years was 12 % using bare and 56 % using covered stents (p = 0.09).  These researchers found marked clinical improvement at 3 months post-TIPSS as determined by a drop in median Child-Pugh score (10 to 7, p = 0.04), Rotterdam BCS index (1.90 to 0.83, p = 0.02) and modified Clichy score (7.77 to 2.94, p = 0.003), but not in MELD (18.91 to 17.42, p = 0.9).  Survival at 1 and 3 years post-TIPSS was 80 % (95 % confidence interval [CI]: 59 to 100 %) and 72 % (95 % CI: 48 to 96 %).  Four patients (25 %) died and 1 required liver transplantation.  The authors concluded that a TIPSS using PTFE-covered stents shows better patency rates than bare stents in BCS.  Moreover, TIPSS leads to an improvement in important prognostic indicators for the survival of patients with BCS.

Corso et al (2008) evaluated the safety and effectiveness of TIPSS in the treatment of patients affected by BCS.  A total of 15 patients (7 male and 8 female subjects, age range of 7 to 52 years) with BCS uncontrolled by medical therapy were treated with TIPSS placement.  In 7 cases BCS was idiopathic, in 4 it was caused by myeloproliferative disorders and in 4 by other disorders.  One patient also had portal vein thrombosis.  In 5/15 cases TIPSS was created through a transcaval approach.  Eight patients (53.4 %) received a bare stent, and 7 (46.6 %) received a stent graft.  The follow-up lasted a median of 29.4 (range of 3.2 to 68) months.  Technical success was achieved in all patients without major complications.  Transjugular intrahepatic portosystemic shunt was very effective in decreasing the portosystemic pressure gradient from 26.2 +/- 5.8 to 10 +/- 6.2 mmHg.  All patients but 2 were alive at the time of writing.  Acute leukemia was the cause of the single early death and was unrelated to the procedure.  The patient with portal vein thrombosis underwent thrombolysis before TIPSS, but the vein occluded again after 3 weeks, and the patient died 6 months later.  The other patients showed significant improvements in liver function, ascites and symptoms related to portal hypertension.  Primary patency was 53.3 %, and primary assisted patency was 93.3 %.  No patient required or was scheduled for liver transplantation.  The authors concluded that TIPSS is an effective and safe treatment for BCS and may be considered a valuable alternative to traditional surgical portosystemic shunting or liver transplantation.

Amarapurkar and associates (2008) assessed patterns of obstruction, etiological spectrum and non-surgical treatment in patients with BCS.  A total of 49 consecutive cases were prospectively evaluated.  All patients with refractory ascites or deteriorating liver function were, depending on morphology of inferior vena cava (IVC) and/or hepatic vein (HV) obstruction, triaged for radiological intervention, in addition to anti-coagulation therapy.  Asymptomatic patients, patients with diuretic-responsive ascites and stable liver function, and patients unwilling for surgical intervention were treated symptomatically with anti-coagulation.  Mean duration of symptoms was 41.5 +/- 11.2 (range of 1 to 240) months.  Hepatic vein thrombosis (HVT) was present in 29 (59.1 %), IVC thrombosis in 8 (16.3 %), membranous obstruction of IVC in 2 (4 %) and both IVC-HV thrombosis in 10 (20.4 %) cases.  Of 35 cases tested for hyper-coagulability, 27 (77.1 %) were positive for 1 or more hyper-coagulable states.  Radiological intervention was technically successful in 37/38 (97.3 %): IVC stenting in 7 (18.9 %), IVC balloon angioplasty in 2 (5.4 %), combined IVC-HV stenting in 2 (5.4 %), HV stenting in 11 (29.7 %), TIPSS in 13 (35.1 %) and combined TIPSS-IVC stenting in 2 (5.4 %).  Complications encountered in follow-up: death in 5, re-stenosis of the stent in 5 (17.1 %), hepatic encephalopathy in 2 and hepatocellular carcinoma in 1 patient.  Of 9 patients treated medically, 2 showed complete resolution of HVT.  The authors concluded that in their series, HVT was the predominant cause of BCS.  In the last 5 years with the availability of sophisticated tests for hyper-coagulability, etiologies were defined in 85.7 % of cases.  Non-surgical management was successful in most cases.

Current guidelines from the AASLD on TIPSS (Boyer and Haskal, 2010) indicated that Teflon-coated stents are preferred over bare stents to lower the risk of shunt dysfunction. This position is supported by a number of studies of PTFE-covered stents in TIPSS.

Tripathi et al (2006) assessed the shunt function and clinical efficacy of PTFE-covered stents in a single center.  A total of 316 patients with uncovered stents before the introduction of covered stents (group 1) and 157 patients with the Viatorr Gore PTFE-covered stents at the time of TIPSS creation (group 2) were studied.  The mean follow-up was 22.8 +/- 25.4 and 13.1 +/- 12.5 months, respectively (p < 0.01).  Shunt insufficiency was greater in group 1 [54 % versus 8 % at 12 months; relative hazard (RH) 8.6; 95 % CI: 4.8 to 15.5; p < 0.001].  The incidence of variceal re-bleeding was greater in group 1 (11 % versus 6 % at 12 months; RH 2.4; 95 % CI: 1.1 to 5.1; p < 0.05). T he incidence of hepatic encephalopathy was greater in group 1 (32 % versus 22 % at 12 months; RH 1.5; 95 % CI: 1.1 to 2.3; p < 0.05).  Mortality was similar in the two groups.  The authors concluded that the Viatorr type of PTFE-covered stent results in vastly improved patency compared with uncovered stents, with reduced rates of variceal re-bleeding and hepatic encephalopathy.  This type of covered stent has the potential for superior clinical efficacy compared with uncovered stents.

Saad et al (2010) compared functional and anatomic outcomes of TIPSs created with the specialized Viatorr stent versus a Wallstent/Fluency stent combination.  Retrospective review of patients who underwent TIPS creation with stent-grafts was conducted over a 54-month period ending in June 2008.  Patients were divided into 3 groups: (i) Viatorr only, (ii) Fluency only, and )iii) combined Viatorr/Fluency, the latter of which was included in the overall evaluation but excluded from the comparative analysis between the Viatorr and Fluency groups.  Patient demographics, Child-Pugh scores, and PSG reduction were compared.  Patencies were calculated using the Kaplan-Meier method and compared.  A total of 126 TIPSs created with stent-grafts were found: 28 with Fluency stents, 93 with Viatorr devices, and 5 combined.  No significance in demographic factors or PSGs was found among groups (p > 0.05).  Major encephalopathy rates were 3.6 % and 4.3 % in the Fluency and Viatorr groups, respectively (p = 1.000).  Hemodynamic success rates were 93 % and 98 % in the Fluency and Viatorr groups, respectively (p = 0.099).  The primary unassisted patency rates at 6, 9, and 12 months were 87 %, 81 %, and 81 %, respectively, in the Fluency group and 95 %, 93 %, and 89 %, respectively, in the Viatorr group (p = 0.03).  Portal and hepatic end stenoses were the causes of TIPS narrowing in the Fluency and Viatorr groups, respectively.  The authors concluded that the Wallstent/Fluency stent combination is associated with a 1-year patency rate greater than 80 %, with no significant difference versus the Viatorr stent regarding technical and hemodynamic success and encephalopathy rate.  However, the Viatorr stent is associated with improved patency (89 %) versus this bare stent/stent-graft combination.

In a meta-analysis, Yang et al (2010) compared the patency and clinical outcomes of TIPS with PTFE-covered stent-grafts versus bare stents.  Pertinent studies were retrieved through PubMed (1950 to 2010), MEDLINE (1950 to 2010), and reference lists of key articles.  Outcome measures were primary patency, risk of encephalopathy and survival.  Time-to-event data analysis was used to calculate the overall hazard ratios (HR).  A total of 6 studies were identified including a total of 1,275 patients (346 TIPS with PTFE-covered stent-grafts and 929 TIPS with bare stents).  Pooled shunt patency data from 4 eligible studies suggested a significant improvement of primary patency in patients who were treated with PTFE-covered stent-grafts (HR = 0.28, 95 % CI: 0.20 to 0.35).  Pooled encephalopathy data from 3 eligible studies suggested a significant reduction of risk in the PTFE-covered group (HR = 0.65, 95 % CI: 0.45 to 0.86).  Pooled survival data from 4 eligible studies also suggested a significant decrease of mortality in the PTFE-covered group (HR = 0.76, 95 % CI: 0.58 to 0.94).  No statistical heterogeneity was observed between studies for either outcome.  The authors concluded that this meta-analysis showed that the use of PTFE-covered stent-grafts clearly improves shunt patency without increasing the risk of hepatic encephalopathy and with a trend towards better survival.

Wu et al (2010) examined the outcome of a modified TIPSS (MTIPSS) in the treatment of the BCS.  A total of 11 patients with severe BCS were selected for MTIPS treatment -- 3 patients had an acute history (less than 2 months) and 8 had a subacute or a chronic course of the disease.  All patients were associated with variceal bleeding and massive ascites.  The diagnosis of BCS was established by duplex sonography, computed tomography scan, magnetic resonance imaging, angiography of hepatic veins and inferior vena cava, and liver biopsy.  The shunt was established using conventional self-expandable stents with diameter of 10 cm in all patients.  The mean follow-up was 60.55 +/- 42.76 months.  The shunt reduced the portosystemic pressure gradient from 30.32 +/- 7.69 to 9.08 +/- 3.43 mmHg and improved the portal flow velocity from 11.24 +/- 2.75 to 52.16 +/- 13.68 cm/s.  Clinical symptoms as well as the biochemical test results improved significantly during 3 weeks after shunt treatment except for 1 death caused by hepatic failure.  Ten patients are alive without clinical symptoms.  Three revisions in 2 patients were needed during the follow-up.  The inflation of stenosised shunt was performed in 1 patient, and the inflation of stenosised shunt and the re-implantation of stent in another patient.  The other 8 patients had no revisions.  The authors concluded that MTIPSS provides an excellent outcome in patients with BCS.  It may be regarded as an option for the acute and long-term managements of these patients.

The AASLD's guideline on the role of TIPSS in the management of portal hypertension (Boyer and Haskal, 2005) stated that the decision to create a TIPSS in a patient with BCS should be based on the severity of disease, and only patients with moderate disease appear to be reasonable candidates for a TIPSS.  Patients with BCS and mild disease can be managed medically, whereas those with more severe disease or acute hepatic failure are best managed by liver transplantation.  Furthermore, the use of TIPSS to treat sinusoidal obstruction syndrome or hepatopulmonary syndrome can not be recommended.

The AASLD's 2009 updated guidelines on the role of TIPS in the management of portal hypertension (Boyer and Haskal, 2010) has the following recommendations:

  • The use of TIPS in the management of portal hypertensive gastropathy should be limited to those who have recurrent bleeding despite the use of betablockers.  Evidence-II-3.
  • TIPS is ineffective in controlling bleeding from gastro antral vascular ectasia in patients with cirrhosis and should not be used in this situation.  Evidence-II-3.
  • TIPS will decrease the need for repeated large volume paracentesis in patients with refractory cirrhotic ascites.  However, given the uncertainty as to the effect of TIPS creation on survival and the increased risk of encephalopathy, TIPS should be used in those patients who are intolerant of repeated large volume paracentesis.  Evidence-I.
  • TIPS is effective in the control of hepatic hydrothorax, but it only should be used in patients whose effusion can not be controlled by diuretics and sodium restriction.  Evidence-II-3.
  • TIPS is of investigatory use for the treatment of HRS, especially type 1, pending the publication of controlled trials.  Evidence-II-3.
  • The decision to create a TIPS in a patient with Budd-Chiari syndrome should be based on the severity of their disease and only those with moderate disease and who have failed to respond to anticoagulation appear to be reasonable candidates for a TIPS.  Evidence-II-3.
  • Patients with Budd-Chiari syndrome and mild disease can be managed medically whereas those with more severe disease or acute hepatic failure are best managed by liver transplantation.  Evidence-II-3.
  • The use of TIPS to treat sinusoidal obstruction syndrome (veno-occlusive disease) can not be recommended.  Evidence-II-3.
  • The use of TIPS to treat hepatopulmonary syndrome is not recommended.  Evidence-II-3.

García-Pagán et al (2010) stated that patients with cirrhosis in Child-Pugh class C or those in class B who have persistent bleeding at endoscopy are at high-risk for treatment failure and a poor prognosis, even if they have undergone rescue treatment with a TIPSS.  These researchers evaluated the earlier use of TIPSS in such patients; they randomly assigned, within 24 hours after admission, 63 patients with cirrhosis and acute variceal bleeding who had been treated with vasoactive drugs plus endoscopic therapy to treatment with a PTFE-covered stent within 72 hours after randomization (early-TIPSS group, n = 32) or continuation of vasoactive-drug therapy, followed after 3 to 5 days by treatment with propranolol or nadolol and long-term endoscopic band ligation (EBL), with insertion of a TIPSS if needed as rescue therapy (pharmacotherapy-EBL group, n = 31).  During a median follow-up of 16 months, re-bleeding or failure to control bleeding occurred in 14 patients in the pharmacotherapy-EBL group as compared with 1 patient in the early-TIPSS group (p = 0.001).  The 1-year actuarial probability of remaining free of this composite end point was 50 % in the pharmacotherapy-EBL group versus 97 % in the early-TIPSS group (p < 0.001).  Sixteen patients died (12 in the pharmacotherapy-EBL group and 4 in the early-TIPSS group, p = 0.01).  The 1-year actuarial survival was 61 % in the pharmacotherapy-EBL group versus 86 % in the early-TIPSS group (p < 0.001).  Seven patients in the pharmacotherapy-EBL group received TIPSS as rescue therapy, but 4 died.  The number of days in the intensive care unit and the percentage of time in the hospital during follow-up were significantly higher in the pharmacotherapy-EBL group than in the early-TIPSS group.  No significant differences were observed between the 2 treatment groups with respect to serious adverse events.  The authors concluded that in these patients with cirrhosis who were hospitalized for acute variceal bleeding and at high-risk for treatment failure, the early use of TIPSS was associated with significant reductions in treatment failure and in mortality.

In an editorial that accompanied the afore-mentioned study, Afdhal and Curry (2010) state that additional clinical trials of adequate size should be carried out to confirm these findings and to examine the effect of a rapid reduction in portal pressure on disease progression in patients with cirrhosis of other causes.

In a retrospective analysis, Goykhman et al (2010) reviewed their experience with TIPSS and analyzed the results with emphasis on patient selection and indication (conventional versus atypical).  All cases were managed by a single-center multi-disciplinary team comprising liver surgery and transplantation, hepatology, imaging, interventional radiology and intensive care).  Between August 2003 and December 2009, a total of 34 patients (mean age of 51, range of 27 to 76 years) were treated with TIPSS.  The cause of portal hypertension was cirrhosis (n = 23), hyper-coagulability complicated by BCS (n = 6), and acute portal vein thrombosis (n = 5).  Clinical indications for TIPSS included treatment or secondary prevention of variceal bleeding (n = 10), refractory ascites (n = 18), mesenteric ischemia due to acute portal vein thrombosis (n = 5), and acute liver failure (n = 1).  Transjugular intrahepatic portosystemic shunt was urgent in 18 cases (53 %) and elective in 16.  Three deaths occurred following urgent TIPSS.  The overall related complication rate was 32 %: trasient encephalopathy (n = 6), ischemic hepatitis (n = 2), acute renal failure (n = 2) and bleeding (n = 1).  Long-term results of TIPSS were defined as good in 25 cases (73 %), fair in 4 (12 %) and failure in 5 (15 %).  In 3 of 5 patients with mesenteric ischemia following acute portal vein thrombosis, surgery was obviated.  Revision of TIPSS due to stenosis or thrombosis was needed in 7 cases (20 %).  The authors concluded that TIPSS is safe and effective.  Furthermore, they noted that while its benefit for patients with portal hypertension is clear, the role of TIPSS in treatment of portal-mesenteric venous thrombosis needs further evaluation.

Qi and colleagues (2014) conducted a meta-analysis to compare the incidence of shunt dysfunction, variceal re-bleeding, encephalopathy, and death between patients treated with TIPS alone and those treated with TIPS combined with variceal embolization.  All relevant studies were searched via PubMed, EMBASE, and Cochrane Library databases.  Odds ratios (ORs) with 95 % CIs were pooled.  Heterogeneity among studies and publication bias were assessed.  A total of 6 articles were included in this study.  Type of stents was covered (n = 2), bare (n = 2), mixed (n = 1), and unknown (n = 1).  Varices were angiographically embolized by coils in 6 studies.  Additional liquids agents were employed in 3 studies.  Compared with TIPS alone group, TIPS combined with variceal embolization group had a significantly lower incidence of variceal re-bleeding (OR = 2.02, 95 % CI: 1.29 to 3.17, p = 0.002), but a similar incidence of shunt dysfunction (OR = 1.26, 95 % CI: 0.76 to 2.08, p = 0.38), encephalopathy (OR = 0.81, 95 % CI: 0.46 to 1.43, p = 0.47), and death (OR = 0.90, 95 % CI: 0.55 to 1.47, p = 0.68).  Neither any significant heterogeneity nor proof of publication bias among studies was found in all meta-analyses.  The authors concluded that adjunctive variceal embolization during TIPS procedures might be beneficial in the prevention of variceal re-bleeding.  However, they stated that given the heterogeneity of type of stents, embolic agents, type of varices, and indications of variceal embolization among studies, additional well-designed randomized controlled trials with larger sample size and use of covered stents should be warranted to confirm these findings.

Qi et al (2015) performed a meta-analysis to compare the outcomes of TIPS to those of medical/endoscopic therapy for acute variceal bleeding in cirrhotic patients.  The PubMed, EMBASE, and Cochrane Library databases were searched for all relevant comparative studies.  Odds ratios and HR with 95 % CIwere pooled for dichotomous and time-dependent variables, respectively.  Subgroup analyses were performed according to the type of study design (randomized or non-randomized studies), source of bleeding (esophageal or gastric varices), type of stent (covered or bare stent), and patient selection (high risk or unselected patients).  A total of 6 papers were eligible.  Transjugular intrahepatic portosystemic shunt was superior to medical/endoscopic therapy in decreasing the incidence of treatment failure (OR = 0.22; 95 % CI: 0.11 to 0.44), improving overall survival (HR = 0.55; 95 % CI: 0.38 to 0.812), and decreasing the incidence of bleeding-related death (OR = 0.19; 95 % CI: 0.06 to 0.59).  Although TIPS did not significantly decrease the incidence of re-bleeding (OR = 0.27; 95 % CI: 0.06 to 1.29), it became significantly greater in the subgroup meta-analyses of randomized studies (OR = 0.09; 95 % CI: 0.03 to 0.32) than in those of non-randomized studies (OR = 0.76; 95 % CI: 0.40 to 1.45; subgroup difference, p = 0.003), and in the subgroup meta-analyses of studies including high-risk patients (OR = 0.06; 95 % CI: 0.01 to 0.23) than in those including low-risk patients (OR = 0.83; 95 % CI: 0.44 to 1.56; subgroup difference, p = 0.0007).  In addition, TIPS did not significantly increase the incidence of post-treatment hepatic encephalopathy (OR = 1.37; 95 % CI: 0.63 to 2.99).  The authors concluded that with the exception of the benefit of prevention from treatment failure, TIPS with covered stents might improve the overall survival of high-risk patients with acute variceal bleeding.

Deltenre and colleagues (2015) stated that there is conflicting evidence on the benefit of early TIPSS on the survival of patients with acute variceal bleeding (AVB).  These researchers evaluated the effect of early TIPSS on patient prognosis.  They performed a meta-analysis of studies evaluating early TIPSS in cirrhotic patients with AVB.  A total of 4 studies were included.  Early TIPSS was associated with fewer deaths [OR = 0.38, 95 % CI: 0.17 to 0.83, p =0.02], with moderate heterogeneity between studies (p = 0.15, I = 44 %).  Early TIPSS was not significantly associated with fewer deaths among Child-Pugh B patients (OR = 0.35, 95 CI: 0.10 to 1.17, p = 0.087) nor among Child-Pugh C patients (OR = 0.34, 95 % CI: 0.10 to 1.11, p = 0.074).  There was no heterogeneity between studies in the Child-Pugh B analysis (p = 0.6, I = 0 %), but there was a high heterogeneity in the Child-Pugh C analysis (p = 0.06, I = 60 %).  Early TIPSS was associated with lower rates of bleeding within 1 year (OR = 0.08, 95 % CI: 0.04 to 0.17, p < 0.001) both among Child-Pugh B patients, (OR = 0.15, 95 % CI: 0.05 to 0.47, p = 0.001) and among Child-Pugh C patients (OR = 0.05, 95 % CI: 0.02 to 0.15, p < 0.001), with no heterogeneity between studies.  Early TIPSS was not associated with higher rates of encephalopathy (OR = 0.84, 95 % CI: 0.50 to 1.42, p = 0.5).  The authors concluded that cirrhotic patients with AVB treated with early TIPSS had lower death rates and lower rates of clinically significant bleeding within 1 year compared with patients treated without early TIPSS.  Moreover, they stated that additional studies are needed to identify the potential risk factors leading to a poor prognosis after early TIPSS in patients with AVB and to determine the impact of the degree of liver failure on the patient's prognosis.

An UpToDate review on “Transjugular intrahepatic portosystemic shunts: Indications and contraindications” (Sanyal and Bajaj, 2016) states that TIPS should not be used for:

  • Correction of hypersplenism and thrombocytopenia
  • Portal hypertension associated with polycystic liver disease or Caroli disease
  • Pre-hepatic portal hypertension
  • Primary prophylaxis of variceal hemorrhage
  • Pulmonary hypertension and hepatopulmonary syndrome

Appendix

Selection Criteria of TIPSS for the Treatment of Varices and Ascites:

Aetna considers transjugular intrahepatic portosystemic shunt (TIPSS) medically necessary in members who meet any of the following criteria:

  • Surgery is contraindicated and the member requires bleeding control from varices; or
  • The member has failed sclerotherapy and has acute bleeding from varices; or
  • The member has failed sclerotherapy and has had 2 or more episodes of re-bleeding requiring a transfusion during a 2-week period; or
  • The member has severe debilitating ascites or hepatic hydrothorax refractory to medical management (e.g., oral diuretics and sodium restriction; and repeated large-volume paracentesis); or
  • The member is a liver transplant candidate who requires bleeding control from varices.
CPT Codes / HCPCS Codes / ICD-10 Codes
Information in the [brackets] below has been added for clarification purposes.   Codes requiring a 7th character are represented by "+":
CPT codes covered if selection criteria are met:
37182 Insertion of transvenous intrahepatic portosystemic shunt(s) (TIPS) (includes venous access, hepatic and portal vein catheterization, portography with hemodynamic evaluation, intrahepatic tract formation/dilatation, stent placement and all associated imaging guidance and documentation)
37183 Revision of transvenous intrahepatic portosystemic shunt(s) (TIPS) (includes venous access, hepatic and portal vein catheterization, portography with hemodynamic evaluation, intrahepatic tract recanulization/dilatation, stent placement and all associated imaging guidance and documentation)
HCPCS codes covered if selection criteria are met:
C1874 Stent, coated/covered, with delivery system [PTFE coated]
C1875 Stent, coated/covered, without delivery system [PTFE coated]
ICD-10 codes covered if selection criteria are met:
I82.0 Budd-Chiari syndrome [moderate with failed response to anticoagulation] [not covered for sinusoidal obstruction syndrome or veno-occlusive disease]
I85.00 Esophageal varices without bleeding
I85.01 Esophageal varices with bleeding [not covered for prophylaxis of variceal hemorrhage]
I85.10 Secondary esophageal varices without bleeding
I85.11 Secondary esophageal varices with bleeding [not covered for prophylaxis of variceal hemorrhage]
I86.4 Gastric varices
I86.8 Varicose veins of other specified sites
J90 Pleural effusion, not elsewhere classified [hepatic hydrothorax]
K31.89 Other diseases of stomach and duodenum [portal hypertensive gastropathy with recurrent bleeding despite the use of beta-blockers]
K64.0 - K64.9 Hemorrhoids and perianal venous thrombosis
K74.0 Hepatic fibrosis
K74.60 - K74.69 Other and unspecified cirrhosis of liver
K76.6 Portal hypertension
K92.0 Hematemesis
K92.1 Melena
K92.2 Gastrointestinal hemorrhage, unspecified
R18.0 - R18.8 Ascites
ICD-10 codes not covered for indications listed in the CPB (not all-inclusive):
D69.3 - D69.6 Thrombocytopenia
D73.1 Hypersplenism
I27.0 Primary pulmonary hypertension
I27.2 Other secondary pulmonary hypertension
I81 Portal vein thrombosis [portal-mesenteric venous thrombosis]
K31.811 Angiodysplasia of stomach and duodenum with bleeding [with cirrhosis]
K55.0 - K55.1 Acute and chronic vascular disorders of intestine [portal-mesenteric venous thrombosis]
K76.5 Hepatic veno-occlusive disease [Sinusoidal obstruction syndrome]
K76.6 Portal hypertension
K76.7 Hepatorenal syndrome
K76.81 Hepatopulmonary syndrome
Q44.6 Cystic disease of liver [Caroli disease]
Z76.82 Awaiting organ transplant status [preoperative reduction in portal hypertension before liver transplantation]


The above policy is based on the following references:
    1. Ring EJ, Lake JR, Roberts JP, et al. Using transjugular intra-hepatic portosystemic shunts to control variceal bleeding before liver transplantation. Ann Int Med. 1992;116(4):304-309.
    2. Rossle M, Haag K, Ochs A, et al. The transjugular intrahepatic portosystemic stent-shunt procedure for variceal bleeding. N Eng J Med. 1994;330(3):165-171.
    3. LaBerge JM, Ring EJ, Gordon RL, et al. Creation of transjugular intrahepatic portosystemic shunts with the Wallstent endoprosthesis: Results in 100 patients. Radiol. 1993;187(2):413-420.
    4. Jalan R, Redhead DN, Hayes PC. Transjugular intrahepatic portasystemic stent-shunt in the treatment of variceal haemorrhage. Br J Surg. 1995;82(9):1158-1164.
    5. Brown RS Jr, Lake JR. Transjugular intrahepatic portosystemic shunt as a form of treatment for portal hypertension: Indications and contraindications. Adv Intern Med. 1997;42:485-504.
    6. Stanley AJ, Redhead DN, Hayes PC. Review article: Update on the role of transjugular intrahepatic portosystemic stent-shunt (TIPSS) in the management of complications of portal hypertension. Aliment Pharmacol Ther. 1997;11(2):261-272.
    7. Svoboda P, Kantorova I, Brhelova H, et al. Recent position of transjugular intrahepatic portosystemic shunt in the treatment of portal hypertension. Hepatogastroenterology. 1997;44(15):647-655.
    8. Kamath PS, McKusick MA. Transjugular intrahepatic portosystemic shunts (TIPS). Baillieres Clin Gastroenterol. 1997;11(2):327-349.
    9. Carr-Locke DL, Branch SM, Byrne WJ, et al. Technology assessment status evaluation: Transvenous intrahepatic portosystemic shunt (TIPS). Gastrointestinal Endoscopy. 1998;47(6):584-587.
    10. National Institutes of Health (NIH). Consensus Development Conference Statement: Transjugular Intrahepatic Portosystemic Shunt. Bethesda, MD: NIH; 1996.
    11. Miller-Catchpole R. Transjugular intrahepatic portosystemic shunt (TIPS). Diagnostic and Therapeutic Technology Assessment. JAMA. 1995;273(23):1824-1830.
    12. Burroughs AK, Patch D. Transjugular intrahepatic portosystemic shunt. Semin Liver Dis. 1999;19(4):457-473.
    13. Rosch J, Keller FS. Transjugular intrahepatic portosystemic shunt: Present status, comparison with endoscopic therapy and shunt surgery, and future prospectives. World J Surg. 2001;25(3):337-456.
    14. Bizollon T, Dumortier J, Jouisse C, et al. Transjugular intra-hepatic portosystemic shunt for refractory variceal bleeding. Eur J Gastroenterol Hepatol. 2001;13(4):369-375.
    15. Ong JP, Sands M, Younossi ZM. Transjugular intrahepatic portosystemic shunts (TIPS): A decade later. J Clin Gastroenterol. 2000;30(1):14-28.
    16. Gow PJ, Chapman RW. Modern management of oesophageal varices. Postgrad Med J. 2001;77(904):75-81.
    17. Rossle M. Prevention of rebleeding from oesophageal-gastric varices. Eur J Gastroenterol Hepatol. 2001;13(4):343-348.
    18. Seewald S, Seitz U, Yang AM, et al. Variceal bleeding and portal hypertension: Still a therapeutic challenge? Endoscopy. 2001;33(2):126-139.
    19. Dagher L, Burroughs A. Variceal bleeding and portal hypertensive gastropathy. Eur J Gastroenterol Hepatol. 2001;13(1):81-88.
    20. Suzuki H, Stanley AJ. Current management and novel therapeutic strategies for refractory ascites and hepatorenal syndrome. QJM. 2001;94(6):293-300.
    21. Yu AS, Hu KQ. Management of ascites. Clin Liver Dis. 2001;5(2):541-568, viii.
    22. Chutaputti A. Management of refractory ascites and hepatorenal syndrome. J Gastroenterol Hepatol. 2002;17(4):456-461.
    23. Russo MW, Sood A, Jacobson IM, Brown RS Jr. Transjugular intrahepatic portosystemic shunt for refractory ascites: An analysis of the literature on efficacy, morbidity, and mortality. Am J Gastroenterol. 2003;98(11):2521-2527.
    24. Salerno F, Merli M, Riggio O, et al. Randomized controlled study of TIPS versus paracentesis plus albumin in cirrhosis with severe ascites. Hepatology. 2004;40(3):629-635.
    25. Riggio O, Masini A, Efrati C, et al. Pharmacological prophylaxis of hepatic encephalopathy after transjugular intrahepatic portosystemic shunt: A randomized controlled study. J Hepatol. 2005;42(5):674-679.
    26. D'Amico G, Luca A, Morabito A, et al. Uncovered transjugular intrahepatic portosystemic shunt for refractory ascites: A meta-analysis. Gastroenterology. 2005;129(4):1282-1293.
    27. Boyer TD, Haskal ZJ. American Association for the Study of Liver Diseases Practice Guidelines: The role of transjugular intrahepatic portosystemic shunt creation in the management of portal hypertension. J Vasc Interv Radiol. 2005;16(5):615-629.
    28. LaBerge JM. Transjugular intrahepatic portosystemic shunt--role in treating intractable variceal bleeding, ascites, and hepatic hydrothorax. Clin Liver Dis. 2006;10(3):583-598, ix.
    29. Lo GH. Prevention of esophageal variceal rebleeding. J Chin Med Assoc. 2006;69(12):553-560.
    30. Cardenas A, Gines P. Therapy insight: Management of hepatorenal syndrome. Nat Clin Pract Gastroenterol Hepatol. 2006;3(6):338-348.
    31. Khan S, Tudur Smith C, Williamson P, Sutton R. Portosystemic shunts versus endoscopic therapy for variceal rebleeding in patients with cirrhosis. Cochrane Database Syst Rev. 2006;(4):CD000553.
    32. Saab S, Nieto JM, Lewis SK, Runyon BA. TIPS versus paracentesis for cirrhotic patients with refractory ascites. Cochrane Database Syst Rev. 2006;(4):CD004889.  
    33. Kravetz D. Prevention of recurrent esophageal variceal hemorrhage: Review and current recommendations. J Clin Gastroenterol. 2007;41(10 Suppl 3):S318-S322.
    34. Colombato L. The role of transjugular intrahepatic portosystemic shunt (TIPS) in the management of portal hypertension. Clin Gastroenterol. 2007;41(10 Suppl 3):S344-S351.
    35. Lo GH, Liang HL, Chen WC, et al. A prospective, randomized controlled trial of transjugular intrahepatic portosystemic shunt versus cyanoacrylate injection in the prevention of gastric variceal rebleeding. Endoscopy. 2007;39(8):679-685.
    36. Boyer TD, Haskal ZJ. The role of transjugular intrahepatic portosystemic shunt in the management of portal hypertension. Hepatology. 2005;41(2):386-400.
    37. Pan JJ, Chen C, Caridi JG, et al. Factors predicting survival after transjugular intrahepatic portosystemic shunt creation: 15 years' experience from a single tertiary medical center. J Vasc Interv Radiol. 2008;19(11):1576-1581.
    38. Garcia-Pagán JC, Heydtmann M, Raffa S, et al; Budd-Chiari Syndrome-Transjugular Intrahepatic Portosystemic Shunt Group. TIPS for Budd-Chiari syndrome: Long-term results and prognostics factors in 124 patients. Gastroenterology. 2008;135(3):808-815.
    39. Murad SD, Luong TK, Pattynama PM, et al. Long-term outcome of a covered vs. uncovered transjugular intrahepatic portosystemic shunt in Budd-Chiari syndrome. Liver Int. 2008;28(2):249-256.
    40. Corso R, Intotero M, Solcia M, et al. Treatment of Budd-Chiari syndrome with transjugular intrahepatic portosystemic shunt (TIPS). Radiol Med. 2008;113(5):727-738.
    41. Amarapurkar DN, Punamiya SJ, Patel ND. Changing spectrum of Budd-Chiari syndrome in India with special reference to non-surgical treatment. World J Gastroenterol. 2008;14(2):278-285.
    42. Zheng M, Chen Y, Bai J, et al. Transjugular intrahepatic portosystemic shunt versus endoscopic therapy in the secondary prophylaxis of variceal rebleeding in cirrhotic patients: Meta-analysis update. J Clin Gastroenterol. 2008;42(5):507-516.
    43. Wu X, Ding W, Cao J, et al. Modified transjugular intrahepatic portosystemic shunt in the treatment of Budd-Chiari syndrome. Int J Clin Pract. 2010;64(4):460-464.
    44. Boyer TD, Haskal ZJ; American Association for the Study of Liver Diseases. The role of transjugular intrahepatic portosystemic shunt (TIPS) in the management of portal hypertension: Update 2009. Alexandria, VA: AASLD; 2009. Available at: http://www.aasld.org/practiceguidelines/Documents/Bookmarked%20Practice%20Guidelines/TIPS%20Update%20Nov%202009.pdf. Accessed February 26, 2010.
    45. Clark W, Hernandez J, McKeon B., et al. Surgical shunting versus transjugular intrahepatic portasystemic shunting for bleeding varices resulting from portal hypertension and cirrhosis: A meta-analysis. Am Surg. 2010;76(8):857-864.
    46. García-Pagán JC, Caca K, Bureau C, et al; Early TIPS (Transjugular Intrahepatic Portosystemic Shunt) Cooperative Study Group. Early use of TIPS in patients with cirrhosis and variceal bleeding. N Engl J Med. 2010;362(25):2370-2379.
    47. Afdhal NH, Curry MP. Early TIPS to improve survival in acute variceal bleeding. N Engl J Med. 2010;362(25):2421-2422.
    48. Goykhman Y, Ben-Haim M, Rosen G, et al. Transjugular intrahepatic portosystemic shunt: Current indications, patient selection and results. Isr Med Assoc J. 2010;12(11):687-691.
    49. Tripathi D, Ferguson J, Barkell H, et al. Improved clinical outcome with transjugular intrahepatic portosystemic stent-shunt utilizing polytetrafluoroethylene-covered stents. Eur J Gastroenterol Hepatol. 2006;18(3):225-232.
    50. Saad WE, Darwish WM, Davies MG, Waldman DL. Stent-grafts for transjugular intrahepatic portosystemic shunt creation: Specialized TIPS stent-graft versus generic stent-graft/bare stent combination. J Vasc Interv Radiol. 2010;21(10):1512-1520.
    51. Yang Z, Han G, Wu Q, et al. Patency and clinical outcomes of transjugular intrahepatic portosystemic shunt with polytetrafluoroethylene-covered stents versus bare stents: A meta-analysis. J Gastroenterol Hepatol. 2010;25(11):1718-1725.
    52. Boyer T, Haskal Z; American Association for the Study of Liver Disease (AASLD). AASLD practice guidelines: The role of transjugular intrahepatic portosystemic shunt (TIPS) in the management of portal hypertension. Hepatology 2010;51(1):1-16.
    53. Saugel B, Phillip V, Gaa J, Berger H, et al. Advanced hemodynamic monitoring before and after transjugular intrahepatic portosystemic shunt: Implications for selection of patients -- a prospective study. Radiology. 2012 Jan;262(1):343-352.
    54. National Clinical Guideline Centre (NCGC). Acute upper gastrointestinal bleeding: Management. Clinical Guideline. London, UK: National Institute for Health and Clinical Excellence (NICE); June 2012. (Reaffirmed 2014)
    55. Pennick MO, Artioukh DY. Management of parastomal varices: Who re-bleeds and who does not? A systematic review of the literature. Tech Coloproctol. 2013;17(2):163-170.
    56. Qi X, Yang M, Fan D, Han G. Transjugular intrahepatic portosystemic shunt in the treatment of Budd-Chiari syndrome: A critical review of literatures. Scand J Gastroenterol. 2013;48(7):771-784.
    57. Chen RP, Zhu Ge XJ, Huang ZM, et al. Prophylactic use of transjugular intrahepatic portosystemic shunt aids in the treatment of refractory ascites: Metaregression and trial sequential meta-analysis. J Clin Gastroenterol. 2014;48(3):290-299.
    58. Qi X, Liu L, Bai M, et al. Transjugular intrahepatic portosystemic shunt in combination with or without variceal embolization for the prevention of variceal rebleeding: A meta-analysis. J Gastroenterol Hepatol. 2014;29(4):688-696.
    59. Tripathi D, Macnicholas R, Kothari C, et al. Good clinical outcomes following transjugular intrahepatic portosystemic stent-shunts in Budd-Chiari syndrome. Aliment Pharmacol Ther. 2014;39(8):864-872.
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    62. Deltenre P, Trepo E, Rudler M, et al. Early transjugular intrahepatic portosystemic shunt in cirrhotic patients with acute variceal bleeding: A systematic review and meta-analysis of controlled trials. Eur J Gastroenterol Hepatol. 2015;27(9):e1-e9.
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Copyright Aetna Inc. All rights reserved. Clinical Policy Bulletins are developed by Aetna to assist in administering plan benefits and constitute neither offers of coverage nor medical advice. This Clinical Policy Bulletin contains only a partial, general description of plan or program benefits and does not constitute a contract. Aetna does not provide health care services and, therefore, cannot guarantee any results or outcomes. Participating providers are independent contractors in private practice and are neither employees nor agents of Aetna or its affiliates. Treating providers are solely responsible for medical advice and treatment of members. This Clinical Policy Bulletin may be updated and therefore is subject to change.
 
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