Transjugular intrahepatic portosystemic stent-shunt in the management of portal hypertension.

These guidelines on transjugular intrahepatic portosystemic stent-shunt (TIPSS) in the management of portal hypertension have been commissioned by the Clinical Services and Standards Committee (CSSC) of the British Society of Gastroenterology (BSG) under the auspices of the Liver Section of the BSG. The guidelines are new and have been produced in collaboration with the British Society of Interventional Radiology (BSIR) and British Association of the Study of the Liver (BASL). The guidelines development group comprises elected members of the BSG Liver Section, representation from BASL, a nursing representative and two patient representatives. The quality of evidence and grading of recommendations was appraised using the GRADE system. These guidelines are aimed at healthcare professionals considering referring a patient for a TIPSS. They comprise the following subheadings: indications; patient selection; procedural details; complications; and research agenda. They are not designed to address: the management of the underlying liver disease; the role of TIPSS in children; or complex technical and procedural aspects of TIPSS. © Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

In patients who have gastro-oesophageal variceal bleeding refractory to endoscopic and drug therapy as defined by Baveno 6 critera,32 transjugular intrahepatic portosystemic stent-shunt (TIPSS) is recommended (strong recommendation, moderate-quality evidence). Salvage TIPSS is not recommended where the Child-Pugh score is >13 (strong recommendation, low quality of evidence).

In patients who have Child’s C disease (C10-13) or MELD ≥19, and bleeding from oesophageal varices or GOV1 and GOV2 gastric varices and are haemodynamically stable, early or pre-emptive TIPSS should be considered within 72 hours of a variceal bleed where local resources allow (weak recommendation, moderate quality of evidence). However, large multi-centre randomised controlled trials (RCTs) are necessary to determine whether patients with Child’s B disease and active bleeding or with MELD 12–18 benefit from early pre-emptive TIPSS.

In secondary prevention of oesophageal variceal bleeding, TIPSS can be considered where patients rebleed despite combination of VBL +NSBB taking into account the severity of rebleeding and other complications of portal hypertension, with careful patient selection to minimise hepatic encephalopathy (weak recommendation, moderate-quality evidence). Further large controlled trials are required to investigate the role of TIPSS as first-line therapy in secondary prevention (strong recommendation, low quality of evidence).

In secondary prevention of gastric variceal bleeding, TIPSS ±embolisation is recommended where patients rebleed despite endoscopic injection therapy (strong recommendation, moderate-quality evidence). TIPSS ±embolisation can also be considered in selected patients with large or multiple gastric varices as first-line therapy in secondary prevention (weak recommendation, moderate-quality evidence).

In patients with bleeding from ectopic varices refractory to local and pharmacological therapies, TIPSS usually with embolisation is suggested (weak recommendation, low-quality evidence).

In patients with bleeding from portal hypertensive gastropathy (PHG) refractory to NSBB and iron therapy, TIPSS may be considered (weak recommendation, low-quality evidence).

In patients who are eligible for liver transplantation, TIPSS for ascites should only be undertaken after discussion with the regional transplant centre (strong recommendation, very low quality evidence).

In selected patients with refractory or recurrent ascites, we recommend insertion of TIPSS provided there are no contraindications to the procedure (strong recommendation, high quality evidence).

In addition to the standard TIPSS contraindications, patients who may not benefit from TIPSS for ascites include those with bilirubin >50 µm/L and platelets<75×109, pre-existing encephalopathy, active infection, severe cardiac failure or severe pulmonary hypertension (strong recommendation, moderate quality evidence).

Selected patients with refractory hepatic hydrothorax may be considered for TIPSS insertion. (strong recommendation, moderate-quality evidence).

Although, renal function has been observed to improve following TIPSS, TIPSS for HRS (type 1 and type 2) remains experimental (weak recommendation, very low level of evidence).

It is recommended that all patients with Budd–Chiari syndrome (BCS) are managed in centres of high expertise which are either transplant centres or have formal links with a liver transplant centre (strong recommendation, very low-quality evidence).

TIPSS is recommended where patients fail to respond to medical therapy with anticoagulation or hepatic vein interventions (strong recommendation, moderate- quality evidence). TIPSS can be considered where hepatic vein interventions is not technically feasible (weak recommendation, low-quality evidence).

Patients with poor prognostic scores (see text), or those who do not respond to anticoagulation and radiological therapies, have a poor prognosis and should be considered for liver transplant assessment (strong recommendation, moderate-quality evidence).

There is insufficient data to recommend TIPSS prior to non-hepatic surgery, although in compensated cirrhotic patients undergoing curative surgery for cancer there may be a role (weak recommendation, low-quality evidence). Further research is recommended, with the focus on careful patient selection.

The indications for TIPSS in idiopathic non-cirrhotic portal hypertension (INCPH) should be similar to cirrhosis, and covered stents are preferred. The selection criteria should also be similar to cirrhosis with particular attention to risk factors for hepatic encephalopathy (weak recommendation, low-quality evidence).

Portal vein thrombosis (PVT) should not be considered an absolute contraindication to TIPSS placement, although the presence of cavernoma is associated with a significantly high failure rate (strong recommendation, high-quality evidence).

Patients with acute PVT should be discussed with experienced units (weak recommendation, very low-quality evidence).

Cirrhotic patients with PVT and variceal bleeding should be discussed with experienced units (weak recommendation, low-quality evidence).

TIPSS may worsen or precipitate encephalopathy. Patients undergoing elective TIPSS should be screened for covert and overt encephalopathy (strong recommendation, high-quality evidence).

Screening should ideally be at least two of the following: psychometric hepatic encephalopathy score (PHES) testing, Stroop testing, Critical Flicker Frequency and Spectral Enhanced or quantative EEG (strong recommendation, moderate-quality evidence).

The presence of covert hepatic encephalopathy is a relative contraindication to elective TIPSS (weak recommendation, low-quality evidence).

Although age >65 is not an absolute contraindication, it might increase the risk of encephalopathy and should be taken into account when deciding the eligibility for elective TIPSS (weak recommendation, low-quality evidence).

Patients who develop encephalopathy following a TIPSS should be managed according to standard guidelines, but if encephalopathy continues, consideration should be given to shunt reduction, embolisation or occlusion (weak recommendation, low level of evidence).

A cardiac history, examination, 12-lead ECG and N-Terminal pro-B-type natriuretic peptide (NT-proBNP) should be undertaken in all patients undergoing elective TIPSS insertion (strong recommendation, moderate-quality evidence). Further cardiac evaluation (echocardiogram +/-cardiology consultation) should be undertaken before elective TIPSS if any of these are abnormal (strong recommendation, moderate-quality evidence).

Elective TIPSS is not recommended in patients with severe left ventricular dysfunction or severe pulmonary hypertension (strong recommendation, moderate- quality evidence).

Echocardiogram in acute variceal haemorrhage may be inaccurate and should not delay an emergency, potential life-saving TIPSS insertion (strong recommendation, low-quality evidence).

Patients referred for elective TIPSS insertion should undergo a detailed nutritional and functional assessment (weak recommendation, low-level evidence).

In patients with significant intrinsic renal disease (stage 4/5), elective TIPSS is not recommended (strong recommendation, low-quality evidence).

TIPSS can be considered in patients presenting acutely with variceal bleeding and renal dysfunction (weak recommendation, very low-level evidence).

All patients considered for elective TIPSS should be discussed in a multidisciplinary team, and be reviewed by both hepatology and interventional radiology in the clinical setting as part of the work-up (strong recommendation, very low level of evidence).

Cross-sectional imaging is recommended prior to TIPSS where possible (strong recommendation, very low level of evidence).

Informed consent should follow established principles (strong recommendation, high level of evidence).

General anaesthetic or deep sedation using propofol is recommended for all procedures (strong recommendation, very low level of evidence).

Routine prophylactic antibiotics are not recommended with the exception of TIPSS for variceal bleeding, complex procedures or where there is previous biliary instrumentation (strong recommendation, very low level of evidence).

The decision to correct any coagulopathy should be based on thromboelastography since INR is often unreliable in liver disease (strong recommendation, moderate level of evidence). Platelet transfusion can be considered if platelet count <50×105/L (weak recommendation, very low level of evidence).

All TIPSS should be performed using PTFE-covered stents as they are associated with better patency rates than bare stents (strong recommendation, high level of evidence).

The portal pressure gradient should be measured as that between the portal pressure and IVC, and measured pre- and post-stent deployment (strong recommendation, moderate level of evidence)

The portal pressure gradient should be reduced to <12 mmHg or by>=20% of baseline in the case of variceal bleeding (strong recommendation, high level of evidence). For other indications, further reductions in the portal pressure gradient needs to balance efficacy with risk of hepatic encephalopathy, and should be individualised (weak recommendation, low level of evidence).

The role of embolisation with TIPSS is not clear and decisions should be individualised and based on cross-sectional imaging and portography showing large varices when portal pressure reduction alone may not be sufficient (weak recommendation, low level of evidence).

A Doppler ultrasound is recommended a week after TIPSS implantation in patients with prothrombotic conditions, and in other patients where TIPSS dysfunction is suspected (strong recommendation, low level of evidence). Doppler ultrasound is recommended at 6–12 monthly intervals or 6-monthly in patients undergoing HCC surveillance (weak recommendation, low level of evidence).

Patients with prothrombotic conditions such as BCS require follow-up with Doppler ultrasound with careful consideration for TIPSS venography as determined by the interventional radiologist. There is no indication for routine venography in other patients (strong recommendation, low level of evidence).

Units offering a TIPSS service should be performing a minimum of 10 cases per annum (strong recommendation, moderate quality of evidence).

It is recommended that centres offering complex TIPSS (thrombosed hepatic or portal veins or in transplant recipients) should perform at least 20 cases per annum (strong recommendation, moderate quality of evidence).

Patients being referred for emergency TIPSS should be prioritised for transfer (strong recommendation, low quality of evidence).

The role of early or pre-emptive TIPSS in acute variceal bleeding in view of the conflicting evidence and uncertainly about patient selection. Large multi-centre RCTs would be the gold standard.

The role of TIPSS as first-line therapy in secondary prevention against variceal rebleeding.

A national registry or database to help inform us about the results in a variety of indications and evaluate current service provision.

Nutrition in patients undergoing TIPSS. Patients’ nutrition can significantly improve following TIPSS for ascites but cachexia may be associated with more encephalopathy.

TIPSS in the setting of chronic renal impairment and hepatorenal syndrome.

Cardiac evaluation prior to TIPSS due to the limitations of the present methods. The role of NT-proBNP is not clear.

Haemodynamic goals following TIPSS. Further study around the ideal reduction of portal pressure gradient both for variceal haemorrhage and the treatment of refractory ascites.

The role of TIPSS in hepatic hydrothorax, and further study comparing TIPSS with standard of care is recommended.

The role of prophylactic TIPSS prior to major non-hepatic surgery due to a lack of good-quality data on whether it improves outcome.

Role of TIPSS in patients with ectopic varices to allow access to the portal system as well as reducing portal pressure.

Patient summary

This guideline has been produced under the auspices of the British Society of Gastroenterology (BSG) with endorsements from the British Association for the Study of the Liver (BASL) and British Society of Interventional Radiology (BSIR). It is aimed at teams of health professionals who refer patients to specialists for a TIPSS. This patient summary aims to summarise the key recommendations.

TIPSS is a non-surgical treatment for patients with liver disease and higher than normal pressures in the liver and surrounding blood vessels (known as portal hypertension), in particular the portal vein and hepatic veins. It involves a specialist (doctor) known as an interventional radiologist or hepatologist placing a bespoke metal tube (stent) inside the liver by inserting a wire through the jugular vein in the neck, then threading and guiding it (using X-ray) through the liver. The procedure is normally done under general anaesthetic or deep sedation, and takes approximately 90–120 min in uncomplicated cases. In the UK there are more than 35 hospitals that offer this procedure.

The main reasons (“indications”) for performing a TIPSS are to treat bleeding from swollen veins in the gullet called varices (potentially an emergency) and excessive fluid build-up in the abdomen or stomach known as ascites. Other rarer indications involve diseases affecting the blood vessels leading out of (Budd Chiari syndrome) or into the liver (portal vein thrombosis).

The main complications of the procedure include bleeding, infection, heart failure, liver failure, kidney failure, fever, damage to blood vessels and bile ducts, and occur in less than 5% of patients. Long-term complications such as hepatic encephalopathy (HE) affects one-third of patients. HE is a condition where the liver is not able to get rid of unwanted toxic chemicals such as ammonia (produced in the gut). Patients can become confused, drowsy or may fall into a coma or worse. In most cases HE responds positively to simple measures and medical therapy, but in a few patients it may be necessary to block off the TIPSS. It is very important that the patient is made fully aware of all these complications where possible.

To minimise the risk of complications, the following preparation/preparatory work is recommended:

Specialised scans to look at the liver and surrounding vessels.

Liver and kidney function tests.

Tests of the blood’s ability to clot.

Heart function tests.

A nutrition/dietary assessment.

Tests to judge the risk of a patient developing HE after the TIPSS procedure.

It is also possible to modify the procedure to reduce the risks of developing HE following TIPSS by, for instance, reducing the diameter of stent.

We recommend TIPSS (where there is good evidence to support its use) is performed in the following clinical situations:

Acute variceal bleeding unresponsive to other treatments such as endoscopy (camera examination of the gullet) with banding of varices and drug therapy (so-called standard of care). Patients who have very severe liver disease are unlikely to benefit since they will not tolerate the physical insult of a TIPSS procedure.

In a non-emergency situation to prevent further re-bleeding from varices where patients have bled again despite standard of care endoscopic and medical therapies.

In selected patients to prevent the build-up of fluid in the stomach (ascites) or lung (hydrothorax) where there is recurrent fluid build-up despite other treatments which includes insertion of a drain or use of water tablets. Although TIPSS is effective in reducing fluid build-up, there is no clear evidence of better survival and impact on quality of life is not clear.

To treat selected patients with BCS in specialist hospitals which also offer liver transplantation.

To treat portal vein thrombosis in selected patients in specialist hospitals performing a large number of TIPSS.

The role of TIPSS in the following clinical situations is not clear:

To prevent variceal rebleeding in selected patients at the time of first presenting with an acute bleeding episode after satisfactory stabilisation with standard of care. This is also known as “early” or “pre-emptive” where TIPSS is performed within 72 hours of an acute variceal bleed in a stable patient who has stopped bleeding. There is conflicting data on whether it is effective, and which patients stand to benefit from this option.

In patients with long-standing kidney disease.

In a very rare condition called idiopathic non-cirrhotic portal hypertension where there is disease in the small blood vessels in the liver.

TIPSS as a preventative therapy in patients with portal hypertension being considered for surgery outside of the liver such as operations for bowel cancer.

Introduction

This document is the first such guideline produced by the BSG in collaboration with BASL and BSIR. There have been a number of recent advances, in the absence of an up-to-date UK-based guidance on TIPSS aimed at referring teams. The key aim of this guidance is to promote dialogue between referring teams and specialists at regional TIPSS centres. Along the referral pathway, members of the multidisciplinary team comprising gastroenterologists, hepatologists and interventional radiologists play equally important roles in decisions relating to clinical indications for TIPSS, patient selection and procedural aspects of TIPSS. The latest evidence would suggest that TIPSS has an increasing role in the management of acute variceal bleeding and ascites. However, recent publications report on major challenges with regards to available resources and knowledge of referring teams in implementing any changes in practice suggested by the evidence, particularly with regards to acute variceal bleeding.1 There is increasing importance of careful patient selection, and we believe that this requires particular attention in light of emerging data. We are also aware of rarer indications for TIPSS, which may have more of a place in routine practice.2–4 Unless stated otherwise, all sections are with reference to covered TIPSS.

Guideline development

These guidelines were drafted following discussions within the liver section of the BSG and acceptance by the proposal by the CSSC. The GDG comprised clinicians from hepatology, gastroenterology and interventional radiology with nursing and patient representation. There followed division of sections to be researched by designated authors as agreed by the GDG, and an exhaustive literature review. There was reference to previously published practice guidelines and positions statements, and guideline quality was assessed using the AGREE tool.

A preliminary guideline document was drafted by the authors following discussion and where necessary voting by members of the GDG. The draft guidelines were submitted for review by CSSC, then BSG council members. The guidelines were then reviewed by the BSIR and BASL. Finally, full peer review was undertaken by reviewers selected by the editorial board of Gut.

Assessing the quality of guidelines: the AGREE II instrument

The AGREE II instrument is an accepted method for appraising clinical guidelines.5 Six domains are listed:

Scope and purpose

The guidelines are intended for use by clinicians and other healthcare professionals managing patients with portal hypertensive complications of liver disease who are being considered for a TIPSS. The last international guidance on TIPSS was published by the American Association for the Study of Liver Diseases (AASLD) in 2009. Other guidelines exist incorporating some advice on the use of TIPSS,6 but a dedicated guideline focusing on referral pathways for TIPSS has not been published recently. Important developments are covered in depth due to the potential impact on clinical practice. The guidelines are primarily aimed at the management of adult patients

Guideline development group membership and stakeholder involvement

Membership of the group includes gastroenterologists, hepatologists and interventional radiologists with nursing and patient representation. The guideline has been reviewed and ratified by the BSIR and BASL.

Rigour of development

The published literature has been searched using Pubmed, Medline, Web of Knowledge and the Cochrane database between April 2018 and October 2019. The GDG met through a series of teleconferences and meetings in that time.

In accordance with the BSG advice on production of guidelines, the GDG applied the GRADE (Grading of Recommendations, Assessment, Development and Evaluations) system. Strength of recommendation was strong, or weak.7 Where the recommendation was unanimous a ‘strong’ recommendation was used, and where the decision was by majority and the recommendation was moderate or weak, ‘we suggest’ was used. Our grading of evidence was based on four level of evidence and the strength of our recommendation (strong, moderate or weak). (table 1)

Table 1

Levels of evidence

Certainty	Interpretation
Very low	The true effect is probably markedly different from the estimated effect
Low	The true effect might be markedly different from the estimated effect
Moderate	The authors believe that the true effect is probably close to the estimated effect
High	The authors have a lot of confidence that the true effect is similar to the estimated effect

Areas of disagreement about the recommendation grade were subjected to discussion and, if necessary, voting by members of the guidelines group. Where possible, the health benefits, side effects and risks of recommendations have been discussed. The guidelines will be subject to peer review after submission for consideration of publication in Gut.

Clarity and presentation

Recommendations are intended to be specific to particular situations and patient groups: where necessary, different options are listed. Key recommendations are linked to discussion threads on a discussion forum hosted on the BSG website.

Applicability

Where necessary, we have discussed organisational changes that may be needed in order to apply recommendations. We have attempted to identify key criteria for monitoring and audit purposes.

Editorial independence and conflict of interest

Guideline group members have declared any conflicts of interest.

History of TIPSS

The idea of TIPSS originated from animal studies exploring the transjugular route for imaging the biliary tree. The inadvertent portal vein puncture that occurred led Josef Rosch to consider this route as a potential way of decompressing the portal vein. In 1969 he discussed the potential of a radiological portacaval shunt.8 9 Early efforts at TIPSS were disappointing with poor primary patency of 2 weeks at most in animal models.10 Further developments in the late 1970s with balloon angioplasty improved secondary patency rates.11 The first clinical application of TIPSS in humans was in 1982 when Colapinto created a balloon dilated intrahepatic porto-sytemic shunt,11 in patients with cirrhosis and variceal bleeding. Clinical efficacy remained poor with high mortality from variceal rebleeding due to poor patency, until the introduction of the expandable 10 mm Palmaz stents later in the decade which offered much improved long-term patency in animal models.12 The first clinical application of TIPSS using expandable metal stents was in 1988 by Martin Rossle and Joerg Richter and colleagues from Freiburg who used Palmaz stents in a 9 mm channel.13 These early procedures lasted on average 8 hours and indeed the Freiberg programme was stopped briefly but recommenced in 1990 when Jean-Marc Perarnau introduced ultrasound guided portal vein puncture, dramatically reducing the procedure time. Seminal papers from the same group and from San Francisco heralded the clinical introduction of TIPSS.

Further clinical indications followed with TIPSS being used for ascites. However, the limitations of bare stents, namely shunt insufficiency became increasingly apparent. The introduction of bespoke PTFE-covered stents which featured a bile-resistant coating and covered the entire tract greatly improved shunt patency.14 with subsequent reduced need for shunt interventions. The indications for TIPSS thus became broarder with the use of TIPSS in Budd Chiari syndrome.4

Indications for TIPSS

TIPSS for variceal bleeding

The place of rescue TIPSS in the management of patients with active variceal bleeding refractory to endoscopic therapy is established despite the lack of RCTs.15–17 A recent large observational study of salvage TIPSS showed that pre-TIPSS intensive care unit stay was associated with poor outcomes.18 The authors commented on the futility of salvage TIPSS in patients with Child-Pugh score (CPS) >13. The role for TIPSS in the secondary prophylaxis of variceal bleeding is more debatable. When comparing bare TIPSS with endoscopic therapy, TIPSS results in reduced rebleeding, but increased hepatic encephalopathy and no difference in survival.19 Recent RCTs of TIPSS compared with endoscopic therapy in combination with drug therapy again show that variceal rebleeding is reduced with TIPSS.20–22 In a trial of TIPSS vs HVPG response guided drug therapy there was reduced rebleeding with TIPSS but this difference was not so marked in HVPG responders.20 This trial also showed that beyond 6 weeks there was no difference in rebleeding or mortality in the two arms. Hepatic encephalopathy was increased in two trials,20 21 although in one trial there was no difference in long-term hepatic encephalopathy when TIPSS was compared with VBL and NSBB.21 Another trial of TIPSS vs VBL plus NSBB in patients with cirrhotic portal vein thrombosis showed no difference in hepatic encephalopathy.22 This trial is notable for a high rate of recanalisation in the TIPSS arm (95% vs 70%) despite a significant number of patients having occlusion of the main portal vein and cavernoma. In all these trials there was no difference in survival, which may be related to the minimal impact of variceal rebleeding and TIPSS on survival after the acute bleeding episode, in contrast to early TIPSS as discussed below.20–24 TIPSS has been shown to be more effective than tissue adhesives in preventing variceal rebleeding in patients with gastric varices, with no differences in survival or complications in a RCT.25 The role of adjunctive variceal embolisation with TIPSS is not clear due to heterogeneity of studies with regards to the use of bare or covered stents and study methodology, and further controlled studies with covered stents are required.26

The concept that placement of a TIPSS early after endoscopic control of the index variceal bleed was first published by Monescillo et al using HVPG >20 mmHg to select patients for early TIPSS within 24 hours of index variceal bleed. The trial demonstrated better outcomes with improved survival in the early TIPSS arm compared with standard of care.27 However, only bare stents were used and standard of care did not reflect current practice. This was followed by the trial by Garcia-Pagan et al which reported better 12-month transplant-free survival in the early TIPSS group in Child's C patients or Child's B patients actively bleeding at the time of endoscopy ((86% vs 61%, P=0.001; ARR, 25%; 95% CI, 2 to 48; NNT, 4.0 patients; 95% CI, 2.1 to 50.0).28 The definition of ‘early’ was within 72 hours of endoscopically controlling the bleed. The standard of care was banding in combination with drug therapy. Patients with gastric varices gastro-oesophageal varices (GOV)1 and GOV2 were included. This was followed by a retrospective post-RCT surveillance study by the same group screening 659 patients of whom 584 were excluded.29 Again they found an 86% 12-month survival but only a trend to improvement in survival compared with endoscopy and drug therapy.29 A recent RCT from a single centre in China of early TIPSS (n=86, TIPSS within 72 hours of index endoscopy) vs standard of care (n=46) reported better transplant-free survival at 6 weeks and 1 year (HR 0·50, 95% CI 0·25 to 0·98; P=0·04) and improved control of bleeding or rebleeding with early TIPSS (HR 0·26 (95% CI 0·12 to 0·55; P<0·0001).30 There was no difference in the incidence of hepatic encephalopathy. The benefit was seen in all groups regardless of active bleeding or stage of liver disease. It is important to note that all patients with Child’s B and C disease were included irrespective of active bleeding, and that 75% of patients had chronic hepatitis B (HBV) infection (33% HBV-DNA negative). Therefore, antiviral therapy could have influenced outcomes in addition to TIPSS, and the difference in predominant aetiology would suggest the results may not be applicable to the developed world. Furthermore, endoscopic sclerotherapy was used in more than 5% of patients, which is not in keeping with current international guidelines where VBL is recommended.31 32 A RCT from the UK of early TIPSS in 58 patients with Child-Pugh score ≥8, published in abstract form, showed no difference in survival (HR 1.154 (95%CI 0.3289 to 3.422); P 0.79) nor rebleeding regardless of severity of liver disease or active bleeding.33 The 1-year transplant-free survival in the control arm was significantly better than in the 2010 study (76% vs 61%),28 suggesting improvements in overall care of patients with acute variceal bleeding in the past decade, and extrapolation of results from the 2010 study to the present time needs careful consideration. It is clear from these RCTs that rescue TIPSS, necessary in the 10%–31% of the control arm due to refractory rebleeding, was associated with very poor outcomes.

There have been a number of retrospective and prospective audits with variable results.1 34–37 The French study reported better outcomes with early TIPSS but only 6.7% of those eligible for early TIPSS had this undertaken and this group tended to have less severe liver disease and it was the liver disease severity which correlated with survival rather than early TIPSS.1 One of the major challenges with early TIPSS was found to be the logistical issue of arranging a procedure as an ‘emergency’ in a stable non-bleeding patient, even in centres with keen multidisciplinary teams. The study also showed that some clinicians were not convinced that early TIPSS would be beneficial for their patients. Recent data has led to some debate regarding the inclusion criteria for early TIPSS.1 36–39 While Child’s C disease has been shown consistently to correlate with improved survival following early TIPSS, this has not been the case for Child’s B patients with active bleeding.1 36–39 A recent large observational study from China showed that patients with Child’s B disease only obtain benefit from early TIPSS with regards to 1-year survival if they had active bleeding. However, the findings must be interpreted with caution in light of the intraobserver variability and heterogeneity of reporting active bleeding.39 Furthermore, patients with Child’s A disease were also included. Thus, the latter criteria is controversial and further controlled studies are necessary to confirm the utility of this criteria in selecting patients for early TIPSS. A recent observational study also showed that patients with a MELD score of ≥19 are likely to benefit from early TIPSS,38 a finding confirmed by Lv and colleagues.39

A systematic review of two RCTs and two observational studies comparing early TIPSS with standard of care showed reduced mortality with early TIPSS (OR=0.38, 95% CI=0.17 to 0.83, P=0.02) with moderate heterogeneity.36 There was a significant reduction in rebleeding with early TIPSS and no difference in hepatic encephalopathy. However, the authors concluded that further study was required to identify factors associated with poor prognosis after early TIPSS. Moreover, the recent RCTs by Lv et al and Dunne et al were not included.30 33

It is not clear from these studies if there is a maximal threshold of severity of liver disease beyond which there is no benefit from early TIPSS. In conclusion, the data to support universal adoption of early TIPSS in all high-risk groups currently is inadequate. A multi-centre trial collecting large numbers of patients is a research priority.

Ectopic variceal bleeding can be challenging to manage. The evidence for TIPSS in the management of bleeding ectopic varices is based on case series.40–45 Earlier reports showed excellent results for initial haemostasis, although rebleeding occurred in between 18%–42% of patients despite a patent shunt, leading the authors to recommend adjunctive measures such as coil embolisation or thrombin injections.40–44 The largest multicentre study of 53 patients found that TIPSS was a good option for those patients with stomal varices in particular.45 Covered stents were used in 85% of patients. Rebleeding occurred in up to 32% of patients and was related to MELD score, sites other than enterostomy and previous local therapy. Rebleeding was noted to be 50% in those with bleeding duodenal varices. An interesting observation was that neither post-TIPSS portal pressure gradient (PPG) at a threshold of 12 mm Hg nor coil emoblisation influenced rebleeding rates, although the numbers were small.

The evidence for TIPSS in the management of portal hypertensive gastropathy (PHG) is limited to case reports and small case series.46–48 The severity of liver disease, the presence of oesophageal varices and endoscopic therapy for oesophageal varices have been reported to influence the incidence of PHG.49 TIPSS has been found to be successful in improving the appearances of PHG and reducing transfusion requirements in patients refractory to conservative therapies with NSBB and iron replacement.46–48 It is important to differentiate PHG from gastric antral vascular ectasia (GAVE). GAVE has characteristic endoscopic appearances and can co-exist with PHG.50 51 The management of clinically significant bleeding from GAVE is challenging and options include medical therapies such as tranexamic acid, and endoscopic therapies such as argon plasma coagulation, band ligation and radiofrequency ablation.51–53 In refractory cases, surgical antrectomy can be considered in selected patients. TIPSS does not have a role in the management of bleeding solely from GAVE, although it could be considered where there is co-existing PHG.

Figure 1 is a summary of the recommendations.

Figure 1

Summary of recommendations for TIPSS in portal hypertensive bleeding. *Further research is required to determine whether patients with Child’s B disease and active bleeding or with MELD 12-18 benefit from pre-emptive TIPSS.

In patients who have gastro-oesophageal variceal bleeding refractory to endoscopic and drug therapy as defined by Baveno 6 critera,32 covered TIPSS is recommended (strong recommendation, moderate-quality evidence). Salvage TIPSS is not recommended where the Child-Pugh score is >13 (strong recommendation, low quality of evidence).

In patients who have Child’s C disease (C10-13) or MELD ≥19, and bleeding from oesophageal varices or GOV1 and GOV2 gastric varices and are haemodynamically stable, early or pre-emptive TIPSS should be considered within 72 hours of a variceal bleed where local resources allow (weak recommendation, moderate quality of evidence). However, large multi-centre RCTs are necessary to determine whether patients with Child’s B disease and active bleeding or with MELD 12–18 benefit from early pre-emptive TIPSS.

In secondary prevention of oesophageal variceal bleeding, TIPSS can be considered where patients rebleed despite the combination of VBL +NSBB taking into account the severity of rebleeding and other complications of portal hypertension, with careful patient selection to minimise hepatic encephalopathy (weak recommendation, moderate-quality evidence). Further large controlled trials are required to investigate the role of TIPSS as first-line therapy in secondary prevention (strong recommendation, low quality of evidence).

In secondary prevention of gastric variceal bleeding, TIPSS ±embolisation is recommended where patients rebleed despite endoscopic injection therapy (strong recommendation, moderate-quality evidence). TIPSS ±embolisation can also be considered in selected patients with large or multiple gastric varices as first-line therapy in secondary prevention (weak recommendation, moderate-quality evidence).

In patients with bleeding from ectopic varices refractory to local and pharmacological therapies, TIPSS usually with embolisation is suggested (weak recommendation, low-quality evidence).

In patients with bleeding from portal hypertensive gastropathy (PHG) refractory to NSBB and iron therapy, TIPSS may be considered (weak recommendation, low-quality evidence).

TIPSS for ascites, hepatic hydrothorax and hepatorenal syndrome

TIPSS for ascites

The initial randomised studies of TIPSS vs large-volume paracentesis (LVP) for patients with refractory and/or recurrent ascites published between 1996–2004 came to varying conclusions with regard to survival.54–58 However, these studies used relatively outmoded approaches including bare-metal stents and suboptimal approaches to patient selection. These studies generally excluded patients with more severe liver disease such as those with high bilirubin and INR, significant encephalopathy and renal failure. Two more recent randomised studies published in 2011 and 2017 both reported improved survival with TIPSS.59 60 It should be noted that the largest study recruited 109 patients,57 with the majority including fewer than 65 patients.

Several meta-analyses concluded that TIPSS led to better ascites control at the cost of increased encephalopathy.61–68 Importantly, some reported a higher transplant-free survival with TIPSS.

The most recent meta-analysis was published by the National Institute for Health and Care Excellence (NICE) in 2016 and concluded that TIPSS is better at ascites control and improves transplant-free survival, with less renal failure, but more encephalopathy.68 Spontaneous bacterial peritonitis and quality of life were similar. NICE also commented that all these patients should be considered for liver transplantation and noted that there was a wide variation in UK practice. They were concerned that many patients were not being offered TIPSS (see section on TIPSS service).

Covered stents appear to have better outcomes including survival, when used for treating refractory ascites. Two retrospective studies comparing bare vs covered stents reported improved survival +/-ascites control with covered stents.69 70 A further retrospective case-control study of 150 patients with propensity score analysis reported improved survival with covered TIPSS.71

In this context it is interesting that the most recent randomised study from France in 2017 compared TIPSS (using a covered stent) vs LVP in recurrent ascites, and reported improved transplant-free survival and similar encephalopathy with TIPSS.59 It should be noted that this study took the four centres 7 years to recruit 62 patients.

In contrast to the situation for variceal bleeding, the optimum target PPG when placing TIPSS for refractory ascites remains unclear. With regard to encephalopathy, the earlier TIPSS studies had described significant encephalopathy with bare-metal stents, however a much lower incidence of encephalopathy with 8 mm PTFE-covered TIPSS has been reported when used to treat variceal bleeding.20 72 Whether this can be extrapolated to the situation when TIPSS is used for refractory ascites is unclear. It should be noted that a randomised study comparing 8 mm vs 10 mm covered TIPSS for refractory ascites had to be stopped early after the results in the first 45 patients revealed worse ascites control with 8 mm stents.73 A recent retrospective study of 171 consecutive patients having 10 mm- or 8 mm-covered TIPSS for refractory ascites reported higher post-TIPSS PPG and greater need for long-term paracentesis with 8 mm stents, with similar encephalopathy.74 In addition, a recent report from the German TIPSS registry on 185 patients, most of whom had TIPSS for refractory ascites, described prolonged survival with 8 mm vs 10 mm stents.75 Therefore, the optimal diameter of covered TIPSS stents for this indication remains unclear.

The MELD score was initially developed to predict survival post-TIPSS for variceal rebleeding or refractory ascites, then extended to predict survival in various liver disease patient groups.76 77 Some studies and authors have suggested TIPSS should not be undertaken based on a high (eg ≥18) MELD score, however the role of MELD in patient selection remains unclear.78 Gaba et al compared various scores including MELD and CPS in the prediction of outcome after TIPSS and found that CPS had the best overall capability at predicting mortality when TIPSS is used for ascites.79 In addition, Bureau et al have proposed the use of simple laboratory parameters (bilirubin <50 umol/L and platelets>75×109) to predict 1-year survival following TIPSS for refractory ascites.80 Further studies on the use of these criteria are required.

Three recent guidelines recommend TIPSS in the management of refractory or recurrent ascites.6 49 68 The EASL guidelines also suggested useful parameters to identify higher-risk patients with more advanced liver disease who would not benefit from TIPSS.49 These include bilirubin >50µmol and platelets<75×109, current encephalopathy, active infection, progressive renal failure, severe systolic or diastolic dysfunction, or pulmonary hypertension. Many guidelines and studies have recommended that once a patient is being considered for TIPSS in the context of ascites, liver transplantation should also be considered at that stage for appropriate patients.

Figure 2 is a summary of the recommendations.

Figure 2

Summary of recommendations for TIPSS in recurrent or refractory ascites.

In patients who are eligible for liver transplantation, TIPSS for ascites should only be undertaken after discussion with the regional transplant centre (strong recommendation, very low-quality evidence).

In selected patients with refractory or recurrent ascites, we recommend insertion of TIPSS provided there are no contraindications to the procedure (strong recommendation, high-quality evidence).

In addition to the standard TIPSS contraindications, patients who may not benefit from TIPSS for ascites include those with bilirubin >50 µm/L and platelets<75×109, pre-existing encephalopathy, active infection, severe cardiac failure or severe pulmonary hypertension (strong recommendation, moderate- quality evidence).

TIPSS for hepatic hydrothorax

Hepatic hydrothorax is an uncommon complication of end-stage liver disease, affecting approximately 10% of individuals.81 Refractory hepatic hydrothorax is defined by a failure to control symptomatic fluid accumulation through optimisation of sodium intake and diuretic treatment. Management is challenging: thoracocentesis is recommended where there is respiratory compromise but where repeated intervention is required, TIPSS has been suggested. The published evidence supporting this approach is comprised of a number of case reports and six case series including 208 participants.82–87 These studies have been pooled in a meta-analysis.88 It is worth noting that the mortality estimates are different from those of the individual studies, and interpretation of the pooled estimates must take this into account. Good clinical responses are observed in a substantial proportion of patients treated with TIPSS and patient selection is critical to that. These studies indicate a probability of complete response of the hydrothorax of between 42% and 79%.82–87 However, there was appreciable early mortality reported in all but one of these series.85 There is clearly a risk of early mortality related to TIPSS for hepatic hydrothorax that appears related to progressive liver disease. The studies reported were done more than a decade ago and only one includes patients treated with PTFE covered TIPSS.82 Furthermore, since there are no studies comparing TIPSS with standard treatment, consequently, there is no available information on the impact of TIPSS on comparative survival in this population. Improvements in patient selection for TIPSS in general are likely to have reduced the reported early post-TIPSS mortality in patients with hydrothorax but there are no published data to support this.

Selected patients with refractory hepatic hydrothorax may be considered for TIPSS insertion. (strong recommendation, moderate-quality evidence).

TIPSS for hepatorenal syndrome

The severity of liver disease usually precludes TIPSS in patients with severe portal hypertension-related renal dysfunction (type 1 and type 2 HRS). The poor residual liver function does not cope with the reduced portal inflow, with an increased risk of hepatic encephalopathy, and a potential unmasking of cirrhotic cardiomyopathy. Although, renal function has been observed to improve following TIPSS, TIPSS for HRS remains experimental.56 89 90 A recent systematic review demonstrates the paucity of good-quality data, and heterogeneity with regards to patient selection and outcomes.91 Furthermore, in type 2 HRS patients with more severe renal dysfunction were excluded. The rate of hepatic encephalopathy approached 50% which is significantly higher than for other indications. Finally, most studies used bare stents. Liver transplantation should be considered.

Although, renal function has been observed to improve following TIPSS, TIPSS for HRS (type 1 and type 2) remains experimental (weak recommendation, very low level of evidence).

TIPSS and Budd–Chiari syndrome

BCS is defined as obstruction of the hepatic venous outflow from the level of the sinusoids to the inferior vena cava. In most cases, BCS is primary, but secondary causes include tumour invasion or large hepatic cysts.92 In primary BCS, a procoagulant condition such as JAK2 positive myeloproliferative neoplasm is present in nearly 50% of patients.93 The stepwise management includes anticoagulation in all patients, and hepatic vein interventions in symptomatic BCS.92 The timing of TIPSS has been debated, but in the authors’ opinion it is indicated when hepatic vein interventions is unsuccessful or not possible. TIPSS may also be considered where there is an acute presentation and in small-vessel BCS. Where there is acute liver failure, patients may be eligible for super urgent liver transplantation. Due to the rarity of BCS no RCTs exist of TIPSS for BCS. It is important to note that BCS can present in a different way with more involvement of IVC in countries such as India and China.95, 96 Furthermore, the management strategies are more heterogeneous with regards to anticoagulation.

Numerous observational studies demonstrate very good long-term outcomes despite TIPSS being technically more challenging.4 93–104 The largest series demonstrate very good symptom resolution exceeding 70%, and excellent long-term outcomes with 5-year survival rates exceeding 70%. Primary patency rates are improved with the use of PTFE-covered stents. A direct intrahepatic porto-caval shunts (DIPS) procedure is also an alternative to the classic TIPSS where all hepatic veins are occluded. A tract is created by direct puncture from the IVC through the liver to the portal vein.105 The clinical outcomes following DIPS are similar to classical TIPSS.105 TIPSS is associated with the risk of hepatic encephalopathy which had been reported in up to 15% of patients.93 The risk of hepatic encephalopathy is considerably less with HV interventions which is more physiological. Recent data from a multicentre EU study102 suggests that Rotterdam Class III patients should also be considered for a TIPSS at an early stage, confirming previous data.106 This requires further validation. The BCS-TIPS score >7 has been consistently shown to predict poor outcomes in several studies, and such patients should be considered for liver transplantation.29 93 102 It is essential all patients with BCS are managed in specialised centres with an experienced multidisciplinary team comprising hepatology, interventional radiology and haematology, with access to liver transplantation which has a good outcome in selected cases.107 108

It is recommended that all patients with BCS are managed in centres of high expertise which are either transplant centres or have formal links with a liver transplant centre (strong recommendation, very low-quality evidence).

TIPSS is recommended where patients fail to respond to medical therapy with anticoagulation or hepatic vein interventions (strong recommendation, moderate-quality evidence). TIPSS can be considered where hepatic vein interventions is not technically feasible (weak recommendation, low-quality evidence).

Patients with poor prognostic scores (see text), or those who do not respond to anticoagulation and radiological therapies, have a poor prognosis and should be considered for liver transplant assessment (strong recommendation, moderate-quality evidence).

TIPSS prior to non-hepatic surgery in patients with portal hypertension (prophylactic TIPSS)

A rare indication for TIPSS is prior to elective non-hepatic surgery in patients with portal hypertension. This can reduce the potential deleterious effects of portal hypertension such as abdominal varices which can increase the risk of bleeding. There is a marked paucity of data. A recent systematic review studied all fully published studies.3 All publications are retrospective in nature. The largest series was with 18 patients with many case reports with just one patient. There is also a marked heterogeneity with regards to patient selection based on the severity of liver disease and criteria for successful TIPSS prior to surgery. However, in almost all cases, curative surgery was performed and there did not appear to be increased mortality above what would be expected. Possibly mortality was lower than in those patients with cirrhosis and portal hypertension without a TIPSS. However, there is a real risk of publication bias, and all data must be interpreted cautiously. Furthermore, a recent retrospective study comparing 66 patient with TIPSS prior to abdominal surgery (predominantly colorectal surgery) to 68 patients without a TIPSS pre-surgery showed no differences in post-operative complications and mortality.109 A retrospective study of patients with idiopathic non-cirrhotic portal hypertension (INCPH) undergoing non-hepatic surgery did not find that portal decompressive procedures prior to surgery affected outcomes, although the sample size was small.110 A prospective study showed the value of HVPG in predicting outcomes in cirrhotic patients undergoing non-hepatic surgery, with no patient having HVPG <10 mmHg developing decompensation.111 The American Gastroenterology Association does not recommend routine TIPSS prior to surgical procedures in patients with cirrhosis and portal hypertension.112 Therefore, in view of the lack of evidence, this indication for TIPSS has to be carefully balanced against that of the risk of TIPSS itself.

There is insufficient data to recommend TIPSS prior to non-hepatic surgery, although in compensated cirrhotic patients undergoing curative surgery for cancer there may be a role (weak recommendation, low-quality evidence). Further research is recommended, with the focus on careful patient selection.

TIPSS and idiopathic non-cirrhotic portal hypertension

INCPH or porto-sinusoidal vascular liver disease113 is a rare cause of intrahepatic portal hypertension. Its diagnostic criteria have been described previously, and rests on liver histology which shows an absence of cirrhosis and the presence of subtle lesions such as hepatoportal sclerosis or nodular regenerative hyperplasia.114 There are only six published observational studies on the utility of TIPSS in INCPH.2 115–119 The largest of these from China compared patients with INCPH (n=76) with a matched control group of cirrhotic patients (n=76) over a median follow-up of 34 months. The indication for TIPSS was variceal bleeding in all cases. Another study included a cohort of 41 patients from seven EU centres followed up over a mean of 27 months. In this study 80% of patients had a covered stent. The third study of 25 patients from a single centre in France extended over a mean follow-up of 39 months.118 The fourth study included 11 patients from two EU centres over a mean follow-up of 112 months.116 Two other studies have fewer than 10 patients.115 117

The main observations are of overall good clinical outcomes with good control of ascites and 5-year survival of 60%–89%. The rate of hepatic encephalopathy was high in most of these studies at more than 35%.2 114 116–118 The study by Lv et al showed lower mortality (12% vs 26%) and hepatic encephalopathy (32% vs 14%) in the INCPH group compared with cirrhotic patients.119 Ascites, malignancy, immunological disorders and female sex were associated with mortality. Bare stents had higher bleeding and shunt dysfunction. It should be noted that portal vein thrombosis was higher in the cirrhotic group, and 8 mm stents were used which could explain the low rates of encephalopathy. Having extra-hepatic co-morbidities, ascites as an indication and creatinine predicted worse survival, but no risk factor was identified after multivariate analysis in one of the largest of these studies.2 The risk of procedural bleeding seemed rather high in the study by Bissonnette et al, and authors suggested this may be due to increased arterialisation of the liver.2 The risk of associated splanchnic vein thrombosis was 39%, although this was not associated with mortality or rebleeding. Conversely, the presence of portal vein cavernoma led to increased morbidity in the study by Regnault et al.118

The indications for TIPSS in INCPH should be similar to cirrhosis, and covered stents are preferred. The selection criteria should also be similar to cirrhosis with particular attention to risk factors for hepatic encephalopathy (weak recommendation, low-quality evidence).

TIPSS in portal vein thrombosis

Portal vein thrombosis (PVT) has traditionally been seen as a contraindication to TIPSS placement. However, there have been a number of reports and small series where transjugular shunts have been successfully placed, from 1993 onwards.120 Indications have included patients with acute portal vein thrombosis and ischaemic bowel,121 cirrhotic patients with PVT and variceal bleeding,122 and patients with PVT where the degree of thrombosis is felt to compromise liver transplantation.123 These studies have been heterogeneous, including cirrhotic patients, patients with acute and chronic portal vein thrombosis,124 those with partial or complete thrombosis, and the presence or absence of cavernous transformation. Scoring systems that provide some objective analysis of the burden of thrombosis exist, but are not routinely used, further compounding the difficulty in assessing the role of TIPSS in portal vein thrombosis.125 126

A meta-analysis identified a 60%–99% technical success rate (pooled 86%), and likely reflects a significant reporting bias, with a 25% incidence of hepatic encephalopathy.127 Another systematic review reported similar findings, although heterogeneity was noted due to cavernous transformation.128 Thrombolysis was associated with more complications,

As mentioned earlier, there has been a single clinical randomised trial22 in a population of cirrhotic patients that had previous bleeding, that identified a lower re-bleeding rate in the TIPSS group compared with the group that received banding ligation plus propranolol ((15%vs 45% at 1 year, 25% vs 50% at 2 years). There was no significant difference in survival or encephalopathy. No published image scoring system was used.

Technical aspects which may facilitate success are reported and include: visibility of intra-hepatic PVT branches on US;124 transplenic/transhepatic “rendezvous” technique;129 local thrombolysis;130 and transjugular local thrombolysis and portal pressure guided stent placement.121

The publication bias skews the ability to make firm recommendation. Clearly at the advanced end of the technical spectrum of TIPSS placement, the absence of clear factors predicting success (apart from the visibility of intrahepatic portal vein radicles) limits referral criteria. At the same time, the therapeutic void between anticoagulation and major gut resection in patients with acute splanchnic vein thrombosis, and the ability to successfully convert patients into transplant candidates, means that units prepared to attempt these procedures should not be discouraged. Furthermore, the advance of digital image transfer platforms means that patients with PVT can be discussed with these centres without the patient automatically needing transfer.

PVT should not be considered an absolute contraindication to TIPSS placement, although the presence of cavernoma is associated with a significantly high failure rate (strong recommendation, high-quality evidence).

Patients with acute PVT should be discussed with experienced units (weak recommendation, very low-quality evidence).

Cirrhotic patients with PVT and variceal bleeding should be discussed with experienced units (weak recommendation, low-quality evidence).

Patient selection

Figure 3 is a summary of the key aspects of patient selection.

Figure 3

Summary of recommendations for patient selection prior to TIPSS.

Hepatic encephalopathy

Pre-TIPSS assessment of encephalopathy

As with all portosystemic shunts, the major complication post-TIPSS is HE. This is particularly heartbreaking for the relatives/carers, who will be the first to notice changes in cognition. Phrases such as “I no longer recognise my husband/wife” reflect a poor outcome, especially when the TIPSS has been a palliative procedure in someone with recurrent ascites. The incidence of encephalopathy has been quoted as high as 55% and is dependent on patient and attainment factors: assiduous searching for encephalopathy will identify a higher incidence.

Every effort needs to be made to identify those at risk of post-TIPSS HE, especially in the elective setting. This is harder to do when the TIPSS is being considered in an emergency, and under these circumstances, a history may be all that is available, for example, a history of debilitating encephalopathy in someone with an acute variceal bleed is a contraindication to a TIPSS unless there is a major competing portosystemic shunt that can be embolised.

Patient-related factors perhaps predictably include: age, severity of liver disease, history of preceding encephalopathy131 and size of shunt. A Child-Pugh score equal or greater than 10 was a proposed cut-off point. The recently recognised additional risk factor of diabetes may well reflect altered renal handling of ammonia.132 This latter consideration is increasingly important, as many of the referrals for TIPSS for diuretic resistant ascites are in patients who have non-alcoholic steatohepatitis (NASH) and who are diabetic.

While these simple clinical markers are easy to obtain, most elective patients will have well-preserved liver function. The major advance has been the recognition of the clinical disorder “covert” or subclinical encephalopathy. This is a disorder in which patients with chronic liver disease exhibit specific, reversible, quantifiable, neuropsychological or electroencephalographic abnormalities in the absence of clinically obvious mental or neurologic defects.133 The critical next step is the identification that covert hepatic encephalopathy predicts the development of overt hepatic encephalopathty.134 This has driven the search for accurate techniques that identify covert encephalopathy, and parameters which predict the development of overt encephalopathy post-TIPSS.

EEG has been one of the most utilised investigations prior to patients undergoing TIPSS procedure but it has limitations. Visual EEG alone will underevaluate the risk of encephalopathy135 and the use of spectral analysis using the P3-4 lead has been shown to be superior to visual assessment alone.136 A value of less than 8 hz is abnormal.

The Stroop test is a downloadable application that has shown sensitivity in diagnosis covert encephalopathy.137 It is cheap and easily reproducible. It is underused in clinical practice.

Critical flicker frequency (CFF) involves the patient observing a flickering image. The frequency at which the image “fuses” from flickering to a constant is defined as the CFF, and patients with encephalopathy will have a lower value compared with a normal individual. The absence of a pre-TIPSS history of overt hepatic encephalopathy and a CCF value of >39 Hz had a 100% negative predictive value for post-TIPSS overt encephalopathy.138

Psychometric hepatic encephalopathy score (PHES) psychometric testing is a well validated tool for establishing the presence of encephalopathy, both covert and overt.139 This technique has been studied prospectively, is readily available and utility confirmed.140 A patient with refractory ascites with a normal PHES score has a 90% probability of remaining free of HE post-procedure.138

Diagnostic guidelines have recommended that a diagnosis of covert encephalopathy requires at least two abnormal psychometric tests or an abnormal PHES, and, wherever possible a quantitative EEG.141 Patients who have evidence of covert encephalopathy should not undergo a TIPSS unless additional techniques are employed.

Post-TIPSS encephalopathy management

Despite attempts to carefully select patients for TIPSS, HE remains the most common complication following TIPSS, affecting almost one-third of patients. The management of post-TIPSS HE is challenging and is medical or radiological or a combination of both.

Basic encephalopathy management should be followed. Biochemical abnormalities should be corrected, night sedation ceased and lactulose prescribed in order to achieve two bowel movements per day. Proton-pump inhibitors should be stopped. If HE continues, rifaxamin should be started. If HE continues then options in escalating order are competing shunt embolisation, TIPSS stent reduction and TIPSS occlusion. The latter is necessary in approximately 5% of patients with post-TIPSS HE.142

TIPSS may worsen or precipitate encephalopathy. Patients undergoing elective TIPSS should be screened for covert and overt encephalopathy (strong recommendation, high-quality evidence).

Screening should ideally be at least two of the following: PHES testing, Stroop testing, CFF and Spectral Enhanced or quantative EEG (strong recommendation, moderate-quality evidence).

The presence of covert hepatic encephalopathy is a relative contraindication to elective TIPSS (weak recommendation, low-quality evidence).

Although age >65 is not an absolute contraindication, it might increase the risk of encephalopathy and should be taken into account when deciding the eligibility for elective TIPSS (weak recommendation, low-quality evidence).

Patients who develop encephalopathy following a TIPSS should be managed according to standard guidelines, but if encephalopathy continues, consideration should be given to shunt reduction, embolisation or occlusion (weak recommendation, low level of evidence).

Cardiac assessment

There is a growing awareness that the presence of cirrhosis is associated with significant cardiovascular abnormalities.143 This is commonly termed cirrhotic cardiomyopathy and comprises a constellation of cardiac abnormalities, which include myocardial hypertrophy, electrophysiological abnormalities (ie, prolonged QT), decreased ventricular compliance and normal systolic function at rest, but incompetence when under physical or pharmacological stress.144 145 The assessment of cardiovascular risk pre-TIPSS is therefore important, as shunting a significant volume of the portal to the central circulation, the cardiac output and right atrial pressures increase by 50% and 100%, respectively. Despite these physiological changes, the clinical importance of underlying cardiac cardiomyopathy in patients undergoing TIPSS remains a subject of considerable debate. While some argue that cardiac (in particular diastolic) dysfunction predicts worse outcomes after TIPSS,146–149 others are more sceptical, as overt cardiac failure is very rarely reported.150–153

Of particular interest in the field is diastolic dysfunction, as the incidence approaches 40% in patients awaiting a TIPSS.146 154 Three prospective studies (n=33–101) reported that diastolic dysfunction is related to post-TIPSS mortality within 1 year.146–148 It must be noted that these studies solely utilised E/A (early maximal ventricular filling velocity/atrial maximal ventricular filling velocity) ratio <1.0 to define diastolic dysfunction (limited by its dependence on cardiac loading conditions and age), lacked an independent echocardiographer and also that only 3/144 reported deaths were attributed to cardiac failure. In contrast, despite pre-TIPSS rates of diastolic dysfunction ranging from 30%–45%, five more recent studies (two retrospective studies, n=27–117; three prospective studies, n=15–883) found no relationship between diastolic dysfunction and post-TIPSS survival or cardiac failure.150–153 155 Although retrospective in design, Modha et al reported that post-TIPSS symptomatic heart disease is rare (8/883; 0.9%) and even when present there was no difference in mortality compared with controls (6.3 vs 12.0% at 30 days, respectively).153 In contrast, a recent prospective French study of 100 patients undergoing TIPSS and a detailed cardiac assessment, highlighted that 20% were diagnosed with cardiac failure (requiring hospitalisation) within 1 year of TIPSS of who 5/20 died.149 It is noteworthy that 55% had a preceding established diagnosis of heart disease (including moderate-severe aortic stenosis).149 There is a large degree of heterogeneity in these studies, and with the exception of the recent French study,149 the majority excluded patients with a history of IHD and CVS risk factors, thereby limiting the applicability to the findings to higher-risk individuals.

Serum N-Terminal pro-B-type natriuretic peptide (NT-proBNP) has been shown to predict heart failure in patients with cirrhosis156 157 and peri-operative cardiac events in non-cardiac surgery.158 NT-proBNP has also been shown to correlate with severity of liver disease and QTc interval in cirrhosis.159 160 However, there is conflicting data in the setting of TIPSS of whether NT-proBNP is predictive of cardiac events following TIPSS.149 152 In the largest afore-mentioned prospective study of 100 patients, NT-proBNP was found to be predictive of cardiac decompensation after TIPSS, but not mortality.149 The authors recommended that a NT-proBNP level of less than 125 pg/mL enabled identification pre-TIPSS of those patients not at risk of cardiac decompensation.149

The decision to perform a TIPSS in a high-risk patient, should be reached by a team of a gastroenterologist/hepatologist, interventional radiologist, anaesthetists/intensivists and where appropriate a transplant physician. However, there remains limited data to support the utility of echocardiogram in the absence of a positive cardiac history, examination or ECG (prolonged QT interval) and NT-proBNP) prior to TIPSS. The utility of alternative echocardiographic methods of assessing cardiac function such as left ventricular global longitudinal strain remains a research area.161

A cardiac history, examination, 12-lead ECG and N-Terminal pro-B-type natriuretic peptide (NT-proBNP) should be undertaken in all patients undergoing elective TIPSS insertion (strong recommendation, moderate-quality evidence). Further cardiac evaluation (echocardiogram +/-cardiology consultation) should be undertaken before elective TIPSS if any of these are abnormal (strong recommendation, moderate-quality evidence).

Elective TIPSS is not recommended in patients with severe left ventricular dysfunction or severe pulmonary hypertension (strong recommendation, moderate- quality evidence).

Echocardiogram in acute variceal haemorrhage may be inaccurate and should not delay an emergency, potential life-saving TIPSS insertion (strong recommendation, low-quality evidence).

Nutritional assessment

Over the past 5 years, our understanding of the impact of sarcopenia and malnutrition on survival in patients with cirrhosis has exponentially grown. As many as 20% and 50% of patients with compensated or decompensated cirrhosis, respectively, have sarcopenia. This, in turn, accelerates progression to liver failure and increases the rates of infections, ascites and encephalopathy. Recent international guidelines recommend that all patients with cirrhosis should undergo a rapid nutritional screen and in those deemed at risk of malnutrition, a more detailed expert dietetic assessment (ie, anthropometry, sarcopenia measures) should be undertaken.162 However, very few studies have focused on the impact of sarcopenia and malnutrition on the clinical outcomes of TIPSS. To date, a prospective study of 46 patients with cirrhosis from Italy has shown that sarcopenia (on CT) is independently associated with the development of hepatic encephalopathy post-TIPSS.163 The authors hypothesised that this maybe be attributed to reduced processing of ammonia.163 In addition, a European study of 116 patients with radiological measures of sarcopenia pre and post-TIPSS, highlighted that persistence of sarcopenia post-TIPSS was associated with reduced effectiveness of TIPSS (especially with ascites) and a higher risk of liver failure and mortality.163 However, the study included patients where the indication for TIPSS was both variceal bleeding and ascites. Another study published in abstract form of patients undergoing TIPSS for ascites reported that the presence of sarcopenia pre-TIPSS did not impact on outcomes post-TIPSS.164 Even though very few studies exist, these data suggest the need for prospective studies on the role of nutritional assessment both pre- and post-TIPSS.

Patients referred for elective TIPSS insertion should undergo a detailed nutritional and functional assessment (weak recommendation, low-level evidence).

Renal function

Differentiating portal hypertension-related renal dysfunction from intrinsic kidney disease, and acute kidney injury from stable chronic renal disease, is probably important. However, there is limited supporting evidence at present: the RCTs of TIPSS largely excluded patients with intrinsic kidney disease or significant renal dysfunction, with a mean baseline creatinine of 70–124 µmol/l.27 28 39 54–60 165–169

In portal hypertension-related renal dysfunction, reflecting more advanced disease, a higher serum creatinine is predictive of post-TIPSS mortality.77 170 In portal hypertension-related renal dysfunction and intrinsic kidney disease, a higher baseline serum creatinine may be associated with a lesser natriuretic effect of TIPSS171 172 and an increased frequency of the development of hepatic encephalopathy.173 The presence of severe intrinsic kidney disease (stage 4/5) may lead to an unacceptably high rate of severe encephalopathy.174

The indication for TIPSS may also be relevant. In rescue TIPSS, renal dysfunction is often acute and the key determinant of the risk benefit ratio is multiorgan dysfunction. However, in elective TIPSS for refractory ascites, suitability for a life-prolonging liver transplant and quality of life should be the focus.

In patients with significant intrinsic renal disease (stage 4/5), elective TIPSS is not recommended (strong recommendation, low-quality evidence).

TIPSS can be considered in patients presenting acutely with variceal bleeding and renal dysfunction (weak recommendation, very low-level evidence).

Procedural details

The indications and pre-implantation work-up of a patient prior to TIPSS is discussed elsewhere. Elective patients should be discussed in a multidisciplinary forum. Implantation of a TIPSS is one of the most technically challenging interventional radiological procedures, and early dialogue with an interventional radiologist is essential. The interventional radiologist should ideally review elective patients in a clinical setting and be intimately involved with the decisions relating to suitability of a TIPSS. Emergency TIPSS (eg, uncontrolled variceal bleeding) will still naturally involve a discussion, which may also include issues of futility. TIPSS in patients with advanced liver disease, encephalopathy and multi-organ failure (especially aspiration) does not usually alter patient outcomes. All risk should be measured against clinical need and anticipated survival benefit.

Significant pulmonary hypertension

Heart failure or severe cardiac valvular insufficiency

Rapidly progressive liver failure

Severe or uncontrolled hepatic encephalopathy

Uncontrolled systemic infection or sepsis

Unrelieved biliary obstruction

Polycystic liver disease (though successful cases reports exist)

Extensive primary or metastatic hepatic malignancy

Preparation for TIPSS

Imaging

Contrast-enhanced CT of liver (portal venous phase) or contrast-enhanced MRI of liver is recommended for assessing suitability and planning the TIPSS procedure. In certain circumstances such as significant renal impairment, ultrasound can be used for this purpose, particularly if performed by the TIPSS operator. In the emergency situation, if the patient is well enough to be transferred to the interventional radiology suite, then they are well enough to undergo CT.

Consent

Consent should follow established principles and local procedures observed to ensure the WHO checklist completed. The PARQ mnemonic (Procedure, Alternatives, Risks, Questions) provides a useful framework. The procedure itself is quoted as having a 5% major complication rate including a 2% incidence of procedure-related death, although these figures included data from early series and reflected the emergency situation in which TIPSS was first deployed. Patients should be informed explicitly of the risk of encephalopathy, and intra-abdominal bleeding related to capsular puncture. The American Society of Interventional Radiology Standards of Practice Committee provides an evidence base for these discussions.175 Consent should also be obtained if paracentesis or transjugular biopsy is also planned during the same procedure.

Sedation

It is the authors’ opinion that the TIPSS procedure should be performed either under general anaesthetic or with propofol-based deep sedation. The procedure itself may be painful, particularly during the time of intrahepatic balloon dilatation. General anaesthetic, allows controlled breath holds which facilitate portal vein cannulation, and in the emergency situation the airway is protected should variceal bleeding occur. While some high-volume units have successfully used conscious sedation for many years, there was general agreement that this was not an ideal environment to be performing this procedure

Therefore, all patients should be prepared for general anaesthetic as per local policy. All patients should have up-to-date biochemistry (renal and liver function), haematology (full blood count and INR) and an ECG. Patients should be hydrated to facilitate central venous puncture, and to minimise the risk of contrast nephropathy. There is no role for pre-procedure N-acetyl cysteine or bicarbonate.176

In patients with tense ascites, large-volume paracentesis should be considered either pre- or peri-procedure in order to facilitate extubation.

Antibiotics

Routine prophylactic antibiotics are not recommended. If a long/complex procedure is anticipated (when inadvertent biliary puncture may occur) or previous biliary surgery, then prophylactic antibiotics can be given according to local antibiotic policy to cover gram negative bacteria. for example, piperacillin/tazobactam or ceftriaxone IV for 48 hours.177

Blood products

As INR is often inaccurate, thromboelastography (TEG) can inform whether FFP is required. Consider platelet transfusion if platelet count <50×105.

All patients considered for elective TIPSS should be discussed in a multidisciplinary team, and be reviewed by both hepatology and interventional radiology in the clinical setting as part of the work-up (strong recommendation, very low level of evidence).

Cross-sectional imaging is recommended prior to TIPSS where possible (strong recommendation, very low level of evidence).

Informed consent should follow established principles (strong recommendation, high level of evidence).

General anaesthetic or deep sedation using propofol is recommended for all procedures (strong recommendation, very low level of evidence).

Routine prophylactic antibiotics are not recommended with the exception of TIPSS for variceal bleeding, complex procedures or where there is previous biliary instrumentation (strong recommendation, very low level of evidence).

The decision to correct any coagulopathy should be based on thromboelastography since INR is often unreliable in liver disease (strong recommendation, moderate level of evidence). Platelet transfusion can be considered if platelet count <50×105/L (weak recommendation, very low level of evidence).

The TIPSS procedure

Equipment requirements

Access to high-resolution, large field-of-view, flat panel detector with digital subtraction angiography.

CO2 angiography and C-arm CT can be useful. A large angiography suite suitable for general anaesthesia and equipment for invasive pressure monitoring is required. Box 1 lists the standard equipment

C-arm (preferably ceiling-mounted and capable of rotational cone-beam CT)

Large room suitable for general anaesthesia with piped anaesthetic gases and suction

Vital sign monitoring and display (ECG, pulse oximetry, invasive pressure monitoring)

U/S (preferable integrated with the fluoroscopic unit)

TIPSS access sets

Range of appropriate stent grafts (covered stents should be used 8–10 mm diameter)

Angioplasty balloons 5–10 mm diameters (high-pressure balloons desirable)

Embolisation equipment (vascular coils, plugs and liquid embolics such as cyanoacrylate glue)

Drainage catheters (for ascites and pleural effusions)

Range of angiographic catheters for pressure measurements, vessel access and subtraction angiography

Staff capable of invasive pressure monitoring and familiar with the equipment

CO2 angiography is not essential but would be desirable

TIPSS technique

A detailed description of the technique is beyond the scope of this guideline and can be found elsewhere. The key technical element of the procedure is the portal vein puncture. This may be facilitated by ultrasound guidance, which has been shown to reduce screen time.178 Stent placement should not compromise future options for transplantation, and should therefore not extend towards splenic/superior mesenteric vein confluence, as this disrupts surgical portal vein anastomosis. Stents placed near or in the right atrium will likewise seriously compromise the caval anastomosis. PTFE-covered stents have been shown to reduce the stenosis rate compared with bare stents, and are cost effective.179 TIPSS provides access to the splanchnic circulation, and allows variceal embolisation. The portal pressure gradient (PPG) is that between the portal pressure and IVC pressure, that is, porto-caval gradient. The porto-atrial gradient can give a false higher PPG and is affected by intra-abdominal pressures.180

Mitigation of encephalopathy during the TIPSS procedure

Large-diameter portosystemic shunts are associated with a greater risk of HE, so logically a smaller diameter TIPSS stent will reduce that risk. Unfortunately, this also runs the risk of not achieving adequate portal pressure reduction. The concept was investigated in a RCT which compared 8 mm stents and 10 mm stents and was stopped early as the smaller stent diameter was associated with less control of complications of the portal hypertension.73 The introduction of controlled expansion stents (with a “dial-able" diameter of 8 or 10 mm) may allow the operator to modulate the encephalopathy rate, but this is not evidence-based.

Allied to the shunt diameter as a determinant of encephalopathy, targeting post-TIPSS portosystemic gradient values of <12 mmHg,181 may result in the formation of very large shunts in patients with high portal pressure, and percentage reductions may be more practical (eg, 20%). Indeed a proposed PSG of between 6 and 8 mmHg in patients undergoing TIPSS for diuretic resistant ascites182 may be too low, especially in a group who exhibit more advanced liver disease, and who have a higher risk of encephalopathy.

Adjunctive variceal/shunt embolisation

Conceptually, placement of a TIPSS associated with competing shunt embolisation should preserve portal blood flow, and hence reduce HE. This can be as simple as embolising a bleeding varix to the placement of multiple occlusion devices in umbilical veins and splenorenal shunts. The evidence supporting this approach ab initio is conflicting26 183 184 however, pre-TIPSS cross-sectional imaging review should allow procedural planning and encephalopathy mitigation if there is thought to be a significant risk.

Post-operative care

Post-operative right upper quadrant discomfort is common, and usually responds to parenteral paracetamol or opiate-based analgesia. Persistent severe pain, particularly when associated with haemodynamic compromise, warrants urgent investigation and contrast-enhanced CT is recommended.

Early Doppler US (within 7 days of implantation) is unreliable,185 but confirmation of TIPSS flow prior to discharge is recommended in pro-thrombotic patients (eg, BCS and splanchnic vein thrombosis)

Long-term follow up

The majority of patients who undergo TIPSS will have cirrhosis, and Doppler studies may be performed at the time of routine 6-monthly HCC screening where offered. Routine transjugular venography is not required unless stent dysfunction is seen on Doppler studies, or clinically suspected (eg, recurrent ascites).

Patients with BCS form a unique group due to their prothrombotic tendency and should have careful follow-up including routine TIPSS venography as determined by the interventional radiologist.

Procedural complications

Complications will partially depend on the case mix and the data in table 2 is related to uncomplicated TIPSS as above.175 It is established that complication rates and survival are related to the number of cases performed by the centre and operators independently. It is clear from published data and case series that gathering enough data locally to reach any kind of statistical significance over a short period of time is challenging (<5 years). The complication rates only act as a guide to help inform local or ideally networked outcomes. However, if a programme is failing to meet expected outcomes then a review of the service should take place.

Table 2

Complication	Classification	Definition	Expected rate
Minor	Fever, haemobilia	No additional therapy and no prolonged in- patient care	<10%
Major	Haemoperitoneum, biliary peritonitis, hepatic infarction, trauma to hepatic artery or branches, renal failure, liver failure, heart failure, TIPSS infection (TIPSSitis)	Requiring additional therapy and/or prolonged hospital admission	<5%
Death			<2%

All TIPSS should be performed using PTFE-covered stents as they are associated with better patency rates than bare stents (strong recommendation, high level of evidence).

The portal pressure gradient should be measured as that between the portal pressure and IVC, and measured pre- and post-stent deployment (strong recommendation, moderate level of evidence).

The portal pressure gradient should be reduced to <12 mmHg or by>=20% of baseline in the case of variceal bleeding (strong recommendation, high level of evidence). For other indications, further reductions in the portal pressure gradient needs to balance efficacy with the risk of hepatic encephalopathy, and should be individualised (weak recommendation, low level of evidence).

The role of embolisation with TIPSS is not clear and decisions should be individualised and based on cross-sectional imaging and portography showing large varices when portal pressure reduction alone may not be sufficient (weak recommendation, low level of evidence).

A Doppler ultrasound is recommended a week after TIPSS implantation in patients with prothrombotic conditions, and in other patients where TIPSS dysfunction is suspected (strong recommendation, low level of evidence). Doppler ultrasound is recommended at 6–12 monthly intervals or 6-monthly in patients undergoing HCC surveillance (weak recommendation, low level of evidence).

Patients with prothrombotic conditions such as BCS require follow-up with Doppler ultrasound with careful consideration for TIPSS venography as determined by the interventional radiologist. There is no indication for routine venography in other patients (strong recommendation, low level of evidence).

Service delivery and development

Service provision in the UK

A detailed national audit using data from NHS England and utilising the metric of Finished Consultant Episodes (FCEs) and Finished Admission Episodes (FAEs) provides some important information in terms of service provision, and service planning. The definition of service provision is clearly vital and interpretation may vary from a 24/7 service, a 7/7 service, a 5/7 service or a 1/7 service.

The majority of units that indicated they provided a TIPSS service performed 11–20 emergency procedures per year. Four units reported doing more than 30 emergency procedures per year. Additionally, there were units reporting a total number of procedures performed (elective and emergency) in a year of eight, raising the challenging question of numbers required for competency. A recent Canadian publication indicated that outcomes improved with units performing a minimum of 10 procedures per year.186 Furthermore, between 2006–2017, there was no clear evidence of an increase in emergency procedures, despite published evidence and recommendations. This may reflect a failure of clinical uptake, but may also reflect lack of capacity, ie, there is demand but not the ability to transfer patients in an emergency to a unit that has the available beds. Logically, each hospital should know who its TIPSS provider is, and each TIPSS provider should be equipped to deliver on that expectation.

Personnel

Each centre will need to staff according to the level of urgency they are prepared to undertake. TIPSS may be performed in emergency (uncontrolled variceal haemorrhage), urgent (eg, controlled but refractory variceal haemorrhage) and elective (eg, refractory ascites). table 3 lists the key personnel and their roles.

Table 3

Personnel	Description
Interventional radiologists	At least two fully trained interventional radiologists or similarly-trained physicians able to carry out TIPSS independently and other related procedures such as variceal embolisation. Forming viable networks would be advised. Please see section on Networks (https://www.england.nhs.uk/wp-content/uploads/2012/11/scn-sof.pdf)
Hepatology	Hepatology team used to caring for patients with portal hypertension and its major complications (variceal haemorrhage, ascites and encephalopathy etc)
Intensive care	Intensivists used to care for patients with portal hypertension and variceal haemorrhage.
Anaesthesia	Anaesthetists who are used to working in Interventional radiology suites and are used to dealing with patients who may have the complications of portal hypertension (pleural effusions, heart failure, encephalopathy, variceal haemorrhage etc).
Key support staff	Fully trained interventional support staff including nurses (capable of invasive pressure measurements) and radiographers
Other disciplines as necessary	Nephrology with access to renal replacement therapy.Microbiology.Cardiology assessment.Liver transplant services (These will not always be locally available but networked communication channels should be clearly defined)Addiction services with pathways clearly defined.

Pathways and protocols

All centres should have locally agreed guidelines and protocols in place and coordinated between the major stake holders. These should be reviewed on a regular basis in light of new and emerging data.

M&M and audit

All participants in a TIPSS service should have arrangements, either locally or as part of a network, to submit data and outcomes to formal morbidity and mortality review and audit. These data should be measured against national data if available and be open to scrutiny.

Benchmarking

This should form an essential part of M&M and audit. Agreed standards of practice are hard to judge given the small number of cases performed in most UK centres, and therefore submission of data to a national registry to help inform future planning and benchmarking would be ideal (as yet none exist). The figures quoted in table 4 are a guide and consideration has to be given to the case mix and severity of liver disease being treated.175

Suggested outcomes for uncomplicated TIPSS (ie, no portal vein thrombosis and patent hepatic veins) is given in table 4.

Table 4

	Measure	Outcome
Technical success	Creation of a connection between the IVC and portal vein with a stent graft	>90%
Haemodynamic	Target reduction of porto-systemic gradient	>90%
Clinical success	No further variceal bleedingResolution of ascites	90%55%

For complex TIPSS (thrombosed portal or hepatic veins, or previous transplant) it is recommended that these are performed in centres with >20 cases per annum and given the small numbers of outcome data and benchmarking, is difficult.187 Further evidence supports the need to ensure that centres wishing to start a TIPSS perform at least 10 procedures a year, regardless of whether the centre is a teaching hospital or not.186

Units offering a TIPSS service should be performing a minimum of 10 cases per annum (strong recommendation, moderate quality of evidence).

It is recommended that centres offering complex TIPSS (thrombosed hepatic or portal veins or in transplant recipients) should perform at least 20 cases per annum (strong recommendation, moderate quality of evidence).

Patients being referred for emergency TIPSS should be prioritised for transfer (strong recommendation, low quality of evidence).

The role of early or pre-emptive TIPSS in acute variceal bleeding in view of the conflicting evidence and uncertainly about patient selection. Large multi-centre RCTs would be the gold standard.

The role of TIPSS as first-line therapy in secondary prevention against variceal rebleeding.

A national registry or database to help inform us about the results in a variety of indications and evaluate current service provision.

Nutrition in patients undergoing TIPSS. Patients’ nutrition can significantly improve following TIPSS for ascites but sarcopenia may be associated with more encephalopathy.

TIPSS in the setting of chronic renal impairment and hepatorenal syndrome.

Cardiac evaluation prior to TIPSS due to the limitations of the present methods. The role of NT-proBNP is not clear.

Haemodynamic goals following TIPSS. Further study around the ideal reduction of portal pressure gradient both for variceal haemorrhage and the treatment of refractory ascites.

The role of TIPSS in hepatic hydrothorax, and further study comparing TIPSS with standard of care is recommended.

The role of prophylactic TIPSS prior to major non-hepatic surgery due to a lack of good quality data on whether it improves outcome.

Role of TIPSS in patients with ectopic varices to allow access to the portal system as well as reducing portal pressure.