Acessibilidade / Reportar erro

Liver venous deprivation prior to hepatectomy: an interventional radiology procedure

Deprivação hepática venosa previamente a hepatectomia: um procedimento de radiologia intervencionista

INTRODUCTION

In many cases, hepatectomy is the only option for long-term survival in patients with primary or secondary liver malignancies. When a tumor proves unresectable because the resection will result in insufficient remnant liver volume, portal vein embolization (PVE) can be performed to stimulate future liver growth, the objective being to avoid post-hepatectomy liver failure(11 van Lienden KP, van den Esschert JW, de Graaf W, et al. Portal vein embolization before liver resection: a systematic review. Cardiovasc Intervent Radiol. 2013;36:25-34.). Although PVE is safe and effective, it does not always induce sufficient hypertrophy of the future remnant liver, even after a significant time. Consequently, several other approaches have been proposed as alternatives to PVE(22 Guiu B, Chevallier P, Denys A, et al. Simultaneous trans-hepatic portal and hepatic vein embolization before major hepatectomy: the liver venous deprivation technique. Eur Radiol. 2016;26:4259-67.). The most recently developed of such approaches is liver venous deprivation (LVD), a technique that combines hepatic vein embolization of the right hepatic vein (RHV) and accessory RHV, if present and PVE. Among the various interventional procedures that could be used for this purpose, LVD has been shown to promote the fastest and greatest increase in the future remnant liver volume, the reported growth at 14 days being 62.5% after LVD, compared with 8-27% after PVE(22 Guiu B, Chevallier P, Denys A, et al. Simultaneous trans-hepatic portal and hepatic vein embolization before major hepatectomy: the liver venous deprivation technique. Eur Radiol. 2016;26:4259-67.

3 Guiu B, Quenet F, Escal L, et al. Extended liver venous deprivation before major hepatectomy induces marked and very rapid increase in future liver remnant function. Eur Radiol. 2017;27:3343-52.
-44 Deshayes E, Schadde E, Piron L, et al. Extended liver venous deprivation leads to a higher increase in liver function that ALPPS in early assessment. J Gastrointest Surg. 2017;21:1754-5.).

Here, we describe the case of a 70-year-old patient diagnosed with Bismuth type IIIa cholangiocarcinoma. The patient was treated successfully with LVD prior to hepatectomy.

LVD TECHNIQUE

The patient underwent computed tomography (CT) with angiography and volumetric analysis of the liver, processed with specific software (IntelliSpace Portal 9.0; Philips Health Care, Eindhoven, The Netherlands), 30 days before the procedure in order to determine the remnant liver volume, which was found to be insufficient. Hepatectomy was also contraindicated because the patient showed an elevated bilirubin level, and an internal-external biliary catheter was therefore inserted for. The patient received antibiotic prophylaxis with a single dose (3 g) of ampicillin/sulbactam. Because of the long duration of the procedure and need for cooperation, as well as the possible benefit of apnea to facilitate punctures, general anesthesia was administered.

The intervention begins with embolization of the right portal vein (RPV). A decision must be made as to whether access should be gained through the RPV, with the disadvantage of requiring a countercurrent catheter to deliver the embolization materials, or through the left portal vein (LPV), our preferred method, which, despite the manipulation of the future remnant liver, grants direct access to the RPV. The LPV was accessed under ultrasound guidance with a percutaneous access set, containing a 15-cm 22-gauge Chiba needle, a 0.018-in. nitinol guidewire, and a 0.038-in. introducer. The distal part of the LPV was punctured with the Chiba needle and opacified. The nitinol guidewire was then introduced through the needle to gain initial access. The Chiba needle was then removed, and the access set introducer was advanced over the wire, after which a stiff 0.035-in. hydrophilic guidewire was advanced over the introducer. A 5 Fr angiographic catheter was then advanced over the introducer and the stiff guidewire into the portal trunk, where portography was performed. We then performed selective catheterization of the segmental RPV and posterior embolization of the portal branches of segments V, VI, VII, and VIII, one by one with n-butyl-2-cyanoacrylate (Glubran 2; GEM SRL, Viareggio, Italy) and iodized oil (Lipiodol; Guerbet, Villepinte, France), at a ratio of 1:2 or 1:3 when injected via a 4 Fr or 5 Fr catheter and 1:4 or 1:5 when injected via a microcatheter. That was followed by selective microcatheterization of the portal branches of segment IVa, distal embolization with microspheres, and proximal embolization with a metal coil (Figure 1).

Figure 1.
Direct portography after RPV embolization, showing where the RPV was embolized with Histoacryl (blue arrow) and coils (black arrow). Note the interrupted portal flow to the right lobe.

After RPV embolization, the hepatic vein embolization was initiated. The hepatic veins can be accessed via a transparietal approach or a transjugular approach. At our institution, the transjugular approach is preferred. An ultrasound-guided right internal jugular vein puncture was performed with a micropuncture access set kit. After the introducer was in place, a 5 Fr diagnostic catheter and hydrophilic 0.035-in. guidewire were passed through, RHV was catheterized, and pre-embolization venography was performed. A stiff Teflon guidewire was then introduced, and 7 Fr Multiport guide catheter was introduced up to the RHV. Through that guide catheter, an 18 mm × 22 mm vascular plug was deployed with its distal part 10 mm before the junction with the lower superior vena cava, to facilitate subsequent surgical ligature of the hepatic vein, and the RHV was embolized (Figures 2 and 3). It is of note that the plug chosen is oversized by at least 50%, which substantially reduces the risk of migration(22 Guiu B, Chevallier P, Denys A, et al. Simultaneous trans-hepatic portal and hepatic vein embolization before major hepatectomy: the liver venous deprivation technique. Eur Radiol. 2016;26:4259-67.). A control CT with volumetric analysis of the liver (Figures 3 and 4) was performed 31 days after the intervention, and the patient underwent hepatectomy 10 days after the control CT. Therefore, the total time from embolization to surgery was 41 days.

Figure 2
Hepatic venography showing the vascular plug (arrow) in the RHV and the interrupted venous flow in the vessel.

Figure 3
Reconstruction of contrast-enhanced oblique coronal venous phase CT scan, acquired after LVD, showing the RHV embolized with the vascular plug (red arrow) and some portal branches embolized with Histoacryl and Lipiodol (blue arrow).

Figure 4
Volumetric analysis of the liver, performed 30 days after LVD, demonstrating that the total liver volume was 1146 cc and that 532.1 cc (46.4%) of that volume was embolized.

REFERENCES

  • 1
    van Lienden KP, van den Esschert JW, de Graaf W, et al. Portal vein embolization before liver resection: a systematic review. Cardiovasc Intervent Radiol. 2013;36:25-34.
  • 2
    Guiu B, Chevallier P, Denys A, et al. Simultaneous trans-hepatic portal and hepatic vein embolization before major hepatectomy: the liver venous deprivation technique. Eur Radiol. 2016;26:4259-67.
  • 3
    Guiu B, Quenet F, Escal L, et al. Extended liver venous deprivation before major hepatectomy induces marked and very rapid increase in future liver remnant function. Eur Radiol. 2017;27:3343-52.
  • 4
    Deshayes E, Schadde E, Piron L, et al. Extended liver venous deprivation leads to a higher increase in liver function that ALPPS in early assessment. J Gastrointest Surg. 2017;21:1754-5.

Publication Dates

  • Publication in this collection
    03 Feb 2021
  • Date of issue
    Jan-Feb 2021

History

  • Received
    21 Oct 2019
  • Accepted
    17 Dec 2019
Publicação do Colégio Brasileiro de Radiologia e Diagnóstico por Imagem Av. Paulista, 37 - 7º andar - conjunto 71, 01311-902 - São Paulo - SP, Tel.: +55 11 3372-4541, Fax: 3285-1690, Fax: +55 11 3285-1690 - São Paulo - SP - Brazil
E-mail: radiologiabrasileira@cbr.org.br