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Chapter  • Ablation Therapy of Liver Tumors
Laparoscopic approach
Step1
Positioning of the patient and access
Depending on the location of the tumor or tumors, the patient is placed in the supine or le lateral decubitus position. A minimum of two laparoscopic trocars are placed: a 12-mm periumbilical camera port and a 12-mm laparoscopic ultrasound port in the right ank. e RFA or MWA probe can be placed percutaneously, through a sheath, or through a 5-mm right subcostal port. More ports may be required if additional procedures are to be performed (e. g., liver mobilization, partial resection) (. Fig. 53.4).


. Fig.53.4
Section III • Liver: Nontransplant Procedures
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Step2
Assessment of tumors and ablation
Laparoscopic intra-abdominal ultrasound is performed by either rigid or exible IOUS probes to identify/conrm the location and the size of the lesions.
e abdomen is explored for the presence of extrahepatic disease. As described for the open technique, the probe is oriented parallel with the IOUS crystal to facilitate probe guidance (
. Fig. 53.5a and 53.5b). Limited mobility can make this more dicult than with the open tech-
nique. e ablation process and monitoring are otherwise performed as described for the open approach.
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. Fig.53.5
Chapter  • Ablation Therapy of Liver Tumors
Postoperative Evaluation
Follow-up post-ablation imaging (CT or MRI) is performed 3 to 30days aer the procedure to assess the completeness of ablation.
Postoperative Complications
z Short-term
Pleural eusion
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Regional hemorrhage into needle track or into RFA lesion
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Fever
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Hepatic abscess (more common with enterobiliary anastomosis)
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Biliary stricture secondary to ablation near major bile duct
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Grounding pad burns
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z Long-term
Biloma
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Biliary stula
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Ascites
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Hepatic insuciency
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Arteriovenous stula
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

Indications
Non-thermal Ablation: Irreversible Electroporation (IRE)
is novel technology oers the possibility for non-thermal ablation procedure for unresectable tumors in the liver, hilum, and pancreas. It uses an electric eld to change the electrochemical potential of the membrane, forming nanopores leading to cell membrane instability followed by cell death. It is applied using short pulses of high energy (1,500–3,000 V), applying electrical eld to tissue between the probes. Access is either laparotomic or percutaneous.
Indications and Contraindications
IRE is indicated for unresectable malignant tumors located on surrounding hepatic veins or peri­hilar area (. Fig. 53.6).
IRE seems not to damage connective tissue, preserving vascular structures and bile ducts. is is the most relevant advantage of IRE compared to other ablative techniques. Of note, lesions located in areas other than the hilum and hepatic veins should be treated by thermal ablation (MWA or RFA).
. Fig.53.6
Section III • Liver: Nontransplant Procedures
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Contraindications
Step1
z Access
Open: under intraoperative ultrasound (IOUS) guidance
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Laparoscopic: multiple needle insertion under IOUS guidance may be demanding, as
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needles usually bend and must be re-inserted
Percutaneous: under CT guidance
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Similar to RFA and MWA: coagulopathy, ascites, and tumor progression under chemotherapy.
(atrial brillation), recent myocardial infarction, and presence of any metal in the proximity of the ablation area.
Preoperative Investigation and Preparation for the Procedure
MRI, MDCT, and PET-CT: same preoperative image as used for thermal ablation.
Procedures
General anesthesia
is is mandatory for all IRE cases (either via laparotomy or percutaneous access). Neuromuscular blockade with level0 paralysis is paramount to avoid patient movement while pulses are delivered. Before starting, place the external synchronization device lids for ECG synchronization. e leads should be placed before draping and debrillator pads.
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Step2
Step3
Ablation planning
Treatment plan is based on preoperative tumor dimensions, which should be further conrmed by IOUS. is information of tumor width, length and depth, as well as the tumor free desirable margin goes into the Ablation Zone estimator soware. e IRE generator will calculate the number and spacing probes to ablate the tumor.
Probe selection
Monopolar electrode probe is a 19-gauge needle with a depth-map echogenic surface. e active length ranges from 0.5 cm to 4.0 cm and should be adjusted for tissue type. Usually in the liver, 2 cm can be used (
. Fig.53.7
. Fig. 53.7).
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Chapter  • Ablation Therapy of Liver Tumors
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Step4
Needle placement
Needle placement is guided by US or CT direct visualization e number of monopolar probes depends on tumor size, adequate margin, and area of ablation. . ablation area using four needles.
Figure 53.8
demonstrates an
. Fig. 53.8
One important fact for needle placement to achieve irreversible electroporation is the position of needles. ey must be parallel, avoiding convergent or divergent-needled tips.
Section III • Liver: Nontransplant Procedures
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Step4 (continued)
Procedure summary
General anesthesia with full muscle relaxation is required for all cases
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Image guide of the liver to assess 3D tumor size
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Plan needle placement (. Fig. 53.8). Needle insertion is around the tumor. When overlap-
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ping is requiring for lesions larger than 4 cm, active needle can be placed centrally. For lesions larger than 3 cm, pullbacks are required.
Guidance imaging by IOUS or CT around the tumor (percutaneous ablation)
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IRE delivery: using deep paralytic upstart with 10pulses test all needle pairs to assess tissue
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resistance, followed by 80pulses for ecacy
Check amperage graphic to verify IRE ecacy
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Aer ablation therapy, US Doppler or CT (percutaneous ablation) should conrm patency
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of vascular structures (
CT/MRI should be performed before discharge to exclude complications
. Fig. 53.9)
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. Fig.53.9
Postoperative Testing
MDCT or MRI at the time of discharge to exclude complications
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Every 3months for assessing ablation completeness using PET-CT (CT with contrast) or
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MRI or MDCT
Postoperative Complications
z Short term
Cardiac arrhythmia
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Cardiac arrest
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Bleeding
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Fever
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Portal vein thrombosis
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Fistula/stenosis when probe placed in contact with metal stents
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z Long term
Tumor recurrence
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z Summary
IRE (NanoKnife system) is more expensive than RFA and MWA
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Uses electric pulse energy
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Can be applied on bile ducts and large vessels
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Promising novel technology, however ecacy still under investigation
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Chapter  • Ablation Therapy of Liver Tumors

Tricks of the Senior Surgeon
Thermal ablation
When the lesion lies near a major blood vessel, thermal energy from the probe may be drawn
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away from the ablation zone, limiting ablation ecacy. This is known as the “heat sink” eect. This eect can be limited using in-ow occlusion techniques (e. g., Pringle maneuver) or repositioning the array closer to the vascular structure. The heat sink eect appears to aect RFA more than MWA.
In case of a deployable probe, stabilization of the ablation probe at the skin or liver surface
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should be done during deployment to avoid “push back”.
Depending on the device, monitoring of the impedance pattern and tine deployment shape
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by ultrasound can conrm success of the ablation in real time.
With some devices, temperature proles can also be helpful in conrming successful abla-
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tion, including consistent tine temperatures and adequately slow cool-down temperatures.
Non-thermal ablation: irreversible electroporation
Probes too far apart may result in low current and cause an inecient ablation treatment.
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The optimal probe distance is from 1.5–1.8 cm.
If the generator does not recognize the ECG signal, change the lead pair; check if the cable is
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properly connected.
In case of troubleshooting, re-image needle placement and inter-probe distance.
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

Selective Hepatic Intra-arterial Chemotherapy

Diane Goéré, Dominique Elias
Placement of a hepatic intra-arterial infusion pump (HAIP) provides liver-specic, continuous infusion of chemotherapeutic agents. e chemotherapeutic agents selected for use with the HAIP should exhibit a high degree of rst-pass kinetics, to minimize systemic toxicity. Agents used include uorodeoxyuridine (FUDR), oxaliplatin, cisplatin, 5-uorouracil, mitomycin C, and Adriamycin.
Indications and Contraindications
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Indications
Contraindications
Unresectable hepatic metastatic colorectal carcinoma (to make lesions resectable)
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Liver-specic adjuvant chemotherapy following resection of colorectal metastases, in
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patients at high risk of hepatic recurrence (≥ 4 liver metastases or disappeared and missing
metastases)
Hepatocellular carcinoma and other metastatic carcinomas, under certain circumstances
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Portal hypertension (portal pressure > 12 mm Hg)
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Known extrahepatic malignancy
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Poor liver reserve (e. g., Child class B or C cirrhosis)
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Severe coagulopathy (e. g., platelets < 30,000/mL)
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Active hepatitis
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Preoperative Studies
History: Specic for hepatic function (e. g., alcohol use, hepatitis)
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Clinical evaluation: To rule out obvious extrahepatic malignancy (lymph node exam) and
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underlying liver dysfunction (ascites, nutrition status, signs of portal hypertension)
Imaging:
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Triple-phase CT scan: For denition of tumor and arterial anatomy
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CT angiogram or MRI of abdomen
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Chest CT scan: To rule out pulmonary metastases, except for colorectal carcinoma
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FDG-PET: In cases of metastatic colorectal carcinoma
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Hepatic arteriogram: Mandatory if HAIP will be placed laparoscopically and CT or MR
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angiograms have not been performed. Not mandatory if HAIP is to be placed via lapa­rotomy (but it may decrease operative time)
P.-A. Clavien, M. G. Sarr, Y. Fong, M. Miyazaki (Eds.), Atlas of Upper Gastrointestinal and Hepato-Pancreato-Biliary Surger y, DOI 10.1007/978-3-662-46546-2_54, © Springer-Verlag Berlin Heidelberg 2016
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Step1
Section III • Liver: Nontransplant Procedures
Procedure
Incision and exposure
A right subcostal approach or a midline incision can be used. e falciform ligament is divided and the porta hepatis is exposed further by gentle superior retraction of the liver. Usually, a cho­lecystectomy is performed to eliminate the postoperative complication of chemical cholecystitis induced by infusional chemotherapy. (Cholecystectomy is not performed when the catheter is ra­diologically inserted.) e gastrohepatic ligament is divided with care to avoid injury to a replaced le hepatic artery (if present). All duodenal and antral vessels must be ligated to eliminate the possibility of reux of chemotherapy into these regions, which may lead to chemical duodenitis or gastritis. e common hepatic, gastroduodenal, and proper hepatic arteries are identied by dissection of the hepatoduodenal ligament and marked with vessel loops (
. Fig. 54.1).
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. Fig.54.1
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Chapter  • Selective Hepatic Intra-arterial Chemotherapy
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
Step2
Determination of arterial anatomy
At this point it is imperative to accurately determine the hepatic arterial anatomy if no preop­erative arteriogram was performed. e more common variants in hepatic arterial anatomy are shown in the gures:
e common hepatic artery may originate from the celiac trunk (typical) (. Fig. 54.2a).
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A replaced right hepatic artery may arise directly from the superior mesenteric artery
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(
. Fig. 54.2b).
A replaced le hepatic artery may arise directly from the le gastric artery (. Fig. 54.2c).
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Common origin of the right hepatic artery, le hepatic artery, and gastroduodenal artery
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(
. Fig. 54.2d), commonly referred to as “trifurcation anatomy.”
. Fig.54.2