CardioVascular and Interventional Radiology

, Volume 33, Issue 3, pp 452–456 | Cite as

Quality Improvement for Portal Vein Embolization

  • Alban Denys
  • Pierre Bize
  • Nicolas Demartines
  • Frederic Deschamps
  • Thierry De Baere
Open Access
CIRSE Guidelines

Introduction

Major hepatectomy carries a significant risk of mortality. In patients with normal liver bearing metastases, mortality after major hepatectomy ranges from 0.5% to 4%, but in patients [1] with chronic liver disease, such as cholestatic or cirrhotic liver, mortality increases to 4% to 12% [2, 3]. The main cause of mortality as well as postoperative morbidity after major hepatic resection is liver insufficiency, often due to an insufficient liver remnant volume [4, 5]. It has been demonstrated from animal experiments and clinical data that redirection of the portal flow toward a part of the liver will induce hypertrophy of this part. This redirection of portal flow can be obtained by surgical ligation or by percutaneous embolization (PVE). Today, PVE is preferred to surgical ligation to avoid additional surgery. However, when surgery is performed, usually for resection of the primary tumor, and portal vein flow redistribution is required, no clear recommendations can be given regarding whether it is preferable to carry out percutaneous PVE in a second step or ligation at the time of surgery. Some studies have reported greater hypertrophy after PVE [6], whereas others have reported no differences in hypertrophy [7]. The aim of PVE is to (1) preoperatively increase the volume of the future liver remnant to enable surgery and (2) to decrease postoperative morbidity when the only contraindication to surgery is an initially insufficient remnant liver.

Definitions

Future liver remnant (FLR) is the liver that will be left in place after surgery and that was not targeted by embolization. The FLR must hypertrophy after portal vein embolization (PVE). Most teams wait 4 weeks before surgery. FLR hypertrophy must be measured by way of computed axial tomography (CAT) examination after injection of iodine with volumetric measurements of the FLR segments, with the results compared with the measurements performed before PVE using the same technique.

Hypertrophy can be quantified as FLR hypertrophy, which is defined as the difference between FLR after a waiting period from 3 to 6 weeks after PVE minus FLR before PVE divided by FLR before PVE. The waiting period must be long enough to allow hypertrophy and as short as possible to avoid tumor growth, which precludes surgery. Hypertrophy can also be quantified by increased FLR ratio. The FLR ratio is defined as (FLR volume—tumor in the FLR)/(total liver volume—total tumor volume) [8].

Technical success of PVE is defined by a complete occlusion of portal branches feeding the future resected liver segments. Branches of the FLR must be patent with hepatopetal flow. In the late phase of control portography, parenchymography must be visible only in the FLR.

Clinical success is considered to occur when the patient reaches the volumetric criteria for liver resection.

Major hepatic resection (or major hepatectomy) is defined as a resection of at least four of eight segments of the liver. Right hepatectomy is defined as a resection of segments V to VIII. Extended right hepatectomy additionally includes segment IV.

Resection rate is defined as the number of embolized patients that will ultimately be resected.

Materials and Methods

Patient Selection

Patients must be candidates for major hepatectomy or major hepatectomy associated with radiofrequency ablation on the FLR. This decision should be made in the context of a tumor board meeting that includes surgeons, hepatologists, oncologists, and interventional radiologists. The only contraindication to liver resection must be the initially insufficient volume of the FLR. PVE indication is determined by the liver volumetry obtained from liver CAT [9].

Liver volumetry is calculated manually from CAT slices after injection of contrast media, preferably in the portal or equilibrium phase to opacify all of the portal and hepatic veins. Slice thickness ≤5 mm is recommended. The FLR is determined according to the future resection plane in collaboration with the surgical team. If radiofrequency ablation (RFA) is planned on a tumor in the FLR, the expected volume of RFA must be taken into consideration and subtracted from the FLR volume. Tumor tissue must not be taken into consideration for volumetric evaluation because volumetry must evaluate liver tissue only.

Blood tests—including liver enzyme, bilirubin level, partial thromboplastin time, prothrombin time (PT), and platelet count must be obtained before PVE. Criteria to propose PVE are different according to the liver status and to the tumor involvement as follows:

Patients with Tumors that Developed in Normal Underlying Liver Parenchyma

PVE is recommended when the FRL-to-total liver ratio is <25 to 30 [7, 10, 11]. The indication of PVE can be extended to a 40% FLR ratio in patients having received chemotherapy or showing abnormal indocyanine green test results (or other abnormal liver function tests) [10, 12, 13].

Patients with Tumors that Develop in Chronic Liver Disease and Cirrhosis States

In such cases, the decision is based either on liver volume or on liver volume plus estimation of overall liver function by indocyanin green retention rate at 15 min (ICCG 15). An FRLR of 40% is recommended when the ICCG 15 is between 10% and 20%. When the ICCG 15 is >20%, an FRLR of 50% is recommended [12, 13, 14].

Patients with Tumors Invading the Biliary Tree Associated with Cholestasis

Because biliary obstruction has impaired liver regeneration and hypertrophy, the biliary tree of the FRL must be drained first, and PVE can be performed secondarily. The indication is an FRLR <40% [15].

Contraindication for PVE [11]

PVE is contraindicated in the following types of patients:
  1. 1.
    Tumors invading the portal vein
    1. (a)

      Portal hypertension (blocked to free hepatic vein pressure gradient >12 mmHg)

       
     
  2. 2.
    Coagulation disorders (PT < 60%, platelet count <50 G/l)
    1. (a)

      Even if previous transarterial chemoembolization (TACE) may improve PVE results [16], a minimum of 3-week delay between TACE and PVE is recommended.

       
     

Patient Information to be Given Before Treatment

Patients should be informed that this procedure is not an antitumoral treatment but a treatment made to increase safety or to enable a surgical procedure. Minor complications are encountered in 20% to 25% of cases and are mainly associated with slight fever and abdominal discomfort and pain. Major complications are infrequent and mainly include infection and subcapsular hematoma, hemobilia, and portal vein thrombosis (<2% of cases). Mortality due to PVE has not been reported.

When tumors (usually small nodules) are present in the nonembolized lobe, it must be explained to the patient that those lesions might increase in size more quickly due to PVE [17]. Patients must also be told that the efficacy of the procedure can be estimated approximately 4 weeks after PVE by way of CAT with injection of contrast media and liver volumetry.

Embolization Method

Access to the portal system should be done under ultrasound guidance to puncture a peripheral branch [8]. Access can be obtained by way of controlateral approach (i.e., puncture of the left portal branch and embolization of the right portal branches) or ispsilateral approach (puncture of the right portal branch to embolize right portal branches. The advantage of the controlateral approach is easier catheterization, but there is a risk of damage to the FLR.

Five-French materials (catheter or introductory sheath) are usually recommended. The catheter should be placed at the splenomesenteric confluence to perform a portography to visualize portal anatomy, including its variations, and to localize segment IV branches. Measurement of portal pressure is not routinely performed in patients with normal liver. In cirrhotic patients, measuring the portal and central venous pressures is useful to determine whether the patient has a portostemic gradient >12 mmHg in, which case the patient is at major risk of perisurgical complications [18, 19]. These patients are not eligible for PVE.

The aim of embolization is complete obstruction of the targeted branches and redistribution of flow to the FLR branches only. Final portography is mandatory to verify this objective. A final pressure measurement should be obtained at the end of the procedure in patients with chronic liver disease to document portal pressure increase, which is usually approximately 3 mmHg. Embolization of segment IV branches is recommended in patients with tumors who are undergoing extended right hepatectomy. However, if embolization of that segment causes risk of reflux into the portal branch of the FRL, such embolization must not be performed because any major reflux into FRL portal branches might preclude surgery.

Various embolic materials have been used. Some products are not recommended due to reported recanalization or lower induced hypertrophy as follows:

Gelfoam

Gelfoam is associated with a high rate of portal vein recanalization and seems less efficient than other products [8].

Nonspherical Polyvinyl Alcohol Particles

Polyvinyl alcohol particles (PVA) have been used but are less efficient than spherical particles [20].

Alcohol

Direct intraportal injection has been described. Although efficient, it is hard to control and has been associated with significant morbidity (liver necrosis, portal vein thrombosis) [21].

Drug-Loadable Embols

These have not been reported in PVE and cannot be recommended.

Recommended products [14, 20, 22] include the following:

Mixture of n-Butyl-cyanoacrylate and Iodized Oil

This has been described extensively as showing good results and low morbidity. Usually a mixture of one part n-butyl-cyanoacrylate (NBCA) to one or to parts lipiodol is used. Injections of small aliquots in between abundant flushing with nonionic liquid, such as dextran or glucose 5%, is the most commonly reported technique.

Spherical Microparticles

These are associated with coil embolization, which is mostly described in North American reports, and have been reported to be superior to nonspherical PVA. It seems as efficient as NBCA, although it has never been compared in randomized trials. Most teams start with 300- to 500-μm particles and finish with 700- to 900-μm particles. Coils are used at the end of the procedure to allow for complete occlusion of the proximal trunk. It is advisable to avoid all too proximal occlusions and rather leave 1 cm unembolized segment of the right portal branch to facilitate surgical ligation at the time of liver resection.

Association of Fibrin Glue with Iodized Oil

This has mostly been described in Japan and has the drawback of requiring special catheters that are only available in Asia.

Medication and Periprocedural Cure

PVE can be carried out as an outpatient procedure when conscious sedation is used. A 1- or 2-day hospital stay is recommended, as reported by most teams using either conscious sedation associated with local anesthesia or general anesthesia.

There is no consensus on the use of antibiotics, and the type of antibiotics and the length of treatment vary from one report to another [11], except in patients with an associated biliary procedure. Because little to no liver tissue necrosis is found after PVE if an antibiotic is given, it must be administered for a very short period of time, from a single dose to 48 h. Mild to moderate abdominal pain after PVE has been reported in 20% to 30% of patients and is usually easily controlled by oral analgesia. Use of pure alcohol as embolic material is associated with more severe abdominal pain.

Biologic tests are not mandatory after the procedure. Slightly increased aspartate aminotransferase and alanine aminotransferase levels with a peak at day 3 after the procedure have been reported, but these are without clinical significance.

Results [14]

The technical success rate should be close to 100%. Few cases of failures or repeated procedures have been reported in the literature. The resection rate should be approximately 85%. This rate may decrease to 70% in the case of cirrhotic patients. Reasons for nonresection are tumor progression, peritoneal metastases, or unsuspected metastases discovered at laparotomy. Absence of hypertrophy is rare, <10% in metastatic liver, but it can reach 20% in cirrhotic patients.

In patients with normal liver and liver metastases, the increase of the FLR ratio is between 8% and 25%, and regeneration is always observed after PVE. In cirrhotic patients, PVE fails to induce left-lobe hypertrophy in 20% of cases. Increased rate of FLR ratio in this population is slightly lower, between 6% and 20%.

Recent studies have demonstrated that hypertrophy is inversely proportional to the FRL ratio before PVE, meaning that the smaller FRL before PVE will have the larger hypertrophy. Consequently there is no lower limit for the FRL ratio to perform PVE.

Complications [14, 23]

In terms of complications (Table 1), a rate of minor complications (20% to 25%) is considered acceptable. With major complications, this rate should be <5% and should not preclude further liver resection. Except for inadvertent embolization, most complications will occur in the punctured lobe, which is an argument in favour of a homolateral approach. However, complication rates for homolateral and controlateral approaches are the same. Reported in the literature as the only factor increasing complications is puncture of the posterior segment versus puncture of the anterior segment [24], thus advocating puncture of the anterior segment when compatible with the location of the PVE to be performed.
Table 1

PVE procedure

 

Mean reported rate (%)

Suggested procedure threshold (%)

Minor complications

 Abdominal pain

20

40

 Fever

25

50

 Nausea

2.5

5

 Embolic material displaced in FRL without portal thrombosis

0.2

0.4

Major complications

 Liver abscess

0.3

0.6

 Cholangitis

0.2

0.4

 Main or left portal vein thrombosis

0.2

0.4

 Subcapsular hematoma

0.2

0.4

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Copyright information

© Springer Science+Business Media, LLC and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE) 2010

Authors and Affiliations

  • Alban Denys
    • 1
  • Pierre Bize
    • 1
  • Nicolas Demartines
    • 2
  • Frederic Deschamps
    • 3
  • Thierry De Baere
    • 3
  1. 1.Department of Radiology and Interventional Radiology, Centre Hospitalier Universitaire VaudoisUniversity of LausanneLausanneSwitzerland
  2. 2.Department of Visceral Surgery, Centre Hospitalier Universitaire VaudoisUniversity of LausanneLausanneSwitzerland
  3. 3.Department of Interventional RadiologyInstitut Gustave RoussyVillejuifFrance

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