Buscar en
Cirugía Española (English Edition)
Toda la web
Inicio Cirugía Española (English Edition) The Role of the Irreversible Electroporation in the Hepato-Pancreatico-Biliary S...
Journal Information
Vol. 95. Issue 6.
Pages 307-312 (June - July 2017)
Visits
2775
Vol. 95. Issue 6.
Pages 307-312 (June - July 2017)
Special article
Full text access
The Role of the Irreversible Electroporation in the Hepato-Pancreatico-Biliary Surgery
El rol de la electroporación irreversible en la cirugía hepato-bilio-pancreática
Visits
2775
Patricia Sánchez-Velázquez, Pierre-Alain Clavien
Corresponding author
clavien@access.uzh.ch

Corresponding author.
Departamento de cirugía y transplante, Hospital universitario de Zürich, Zürich, Switzerland
This item has received
Article information
Abstract
Full Text
Bibliography
Download PDF
Statistics
Figures (1)
Tables (1)
Table 1. Summary of the Series of Patients Treated With Hepatic Ablation Using IRE.
Abstract

Irreversible electroporation is a novel technique growing in popularity over the last years among the ablative modalities. Its unique action mechanism produces irreversible nanopores in the membrane of the cell leading to apoptosis; therefore irreversible electroporation can be used to ablate substantial volumes of tissue without the undesirable thermal effects as the “heat sink effect”. Moreover the extracellular matrix is left unperturbed, thus sparing the structural architecture of surrounding structures such as bile ducts and blood vessels. In the last years its use has been widespread in both liver and pancreatic ablation. Irreversible electroporation has shown its safety with however some caution, feasibility and favorable outcomes in clinical settings such as unresectable locally advanced disease in which the surgical and therapeutic options are very limited.

Keywords:
Irreversible electroporation
Hepatic ablation
IRE
Resumen

La electroporación irreversible es una entidad que ha ganado en popularidad entre las técnicas de ablación tumoral en los últimos años. Debido a su innovador mecanismo de acción, ya que induce poros en la membrana celular que conducen a la apoptosis celular, ha demostrado su capacidad para destruir el tejido sin presentar los efectos indeseables de la ablación térmica tales como el «heat sink effect». Asimismo mantiene la integridad de la matriz extracelular, por lo que estructuras como los vasos sanguíneos y los ductos biliares no son afectadas por la electroporación irreversible. Su utilización se ha ido extendiendo en los últimos años tanto en la ablación hepática como en la pancreática mostrando su seguridad y resultados prometedores en escenarios clínicos en los que la cirugía en el momento actual no puede ofrecer otras opciones terapéuticas.

Palabras clave:
Electroporación irreversible
Ablación hepática
IRE
Full Text
Introduction

Irreversible electroporation (IRE) is a new ablative technique that has gained popularity in the last decade. In contrast with the traditional paradigm of thermal issue ablation, IRE owes its growing popularity to its mechanism of action, which does not entail thermal damage.1 The application of thermal pulses on a specific frequency and voltage generates nanopores in the lipid structure of the cell plasma membrane that alter the electrical gradient between the intra- and extracellular medium, providing free diffusion of molecules.2,3 If this intense electrical field is maintained over a sufficient period of time, cell damage is irreversible, leading to cell death due to apoptosis.

Radiofrequency and microwave ablation base their mechanism of action on thermal tissue destruction by coagulative necrosis. After a certain temperature, protein denaturalization is triggered, and thus, irreversible structural damage that leads to cell death. Although the experience with these ablative techniques is very extensive, most authors agree that the size of the lesion and proximity to the large vessels are their limitations.4 The mechanism of cell death in IRE is very attractive compared to the spectrum of conventional ablative techniques, whose largest limitation lies in the heat sink effect that occurs in proximity to the blood vessels. The blood flow dissipates heat at this level, causing a refrigeration effect on the tissue treated and, consequently, incomplete tumor ablation.

Another advantage of IRE is its capability to preserve both the architecture of the extracellular matrix of the connective tissue as well as the integrity of the blood vessels,5,6 which, in the case of the liver, allows for ablations to be done close to the hepatic artery, portal vein and hepatic ducts without causing structural damage.

Given the boom in IRE over the last 10 years, the aim of this article is to provide a global vision on the principles and indications of IRE in different clinical scenarios of HBP surgery, as well as to review the oncological results available to date.

Clinical Device for Applying Irreversible Electroporation

Currently, only one device has been approved by the FDA (510[k] Number: K080376) for the clinical use of IRE (Nanoknife® [AngioDynamics, Latham, NY, USA). The electrical pulses are applied by means of a varying number of bipolar or monopolar electrodes, depending on the lesions to treat. The device can generate a maximum energy of 70mA or 3000V. The application protocols are variable, but the majority of the studies execute 70–90 pulses with a duration of 70–100μs.7–10 The device admits up to a maximum of 6 electrodes of 19G, whose maximum distance should not surpass 2cm and whose alignment should be parallel to maintain the uniformity of the electrical field (Fig. 1). There is no standardized protocol for the number or placement of the electrodes, but the uniformity of the electrical field pays an essential role in the success of the ablation.11 Appelbaum et al.12 demonstrated that, by applying 4 electrodes in parallel, greater ablation volume is achieved with better oncological results, since in this manner the protocol can be personalized to each patient.

Fig. 1.

Images (A) and (B) show an example of the intraoperative placement of the electrodes for ablation of a hepatic lesion using the open approach. A closer look at the placement of the electrodes for the ablation of a lesion depending on its location in the neck/body of the pancreas (C) or the head (D). Images provided by Dr. ML de Oliveira.

(0.45MB).

A threshold for the electrical field has been reported at approximately 700V/cm, after which point the electroporation becomes irreversible.3 Nonetheless, it is important to note that this calculation is based on a theoretical mathematical model and that this threshold is probably not directly translatable to clinical practice since the extracellular matrix, blood vessels and other structures play a role in the homogeneity of the electrical field.13 Therefore, in general practice, an electrical field between 1000 and 1500V/cm is usually used.

For the application of the pulses, it is essential to synchronize them with the electrocardiogram in order to avoid arrhythmias. The electrical pulse should be applied exactly 50μs after the R wave to coincide with the absolute refractory period of the myocardium in the cardiac cycle.14 Likewise, it is necessary for patients to be under general anesthesia and under the effect of muscle relaxants, like rocuronium, to avoid muscle contractions triggered by the pulses. Most studies monitor patients with TOF-watch® type devices in order to ensure the maintenance of correct muscle relaxation, and defibrillator paddles are placed as a preventive measure.

Application of Irreversible Electroporation in Hepato-Bilio-Pancreatic TumorsHepatic Ablation

Ablation techniques are currently an essential part of the treatment of hepatic tumors. In primary tumors such as hepatocellular carcinoma (HCC), which is currently in the sixth position in worldwide prevalence,15 as well as metastatic gastrointestinal tumors, ablation is a reasonable alternative for patients who are not candidates for surgical resection.

The first experimental studies were aimed at hepatic ablation in HCC, since radiofrequency ablation has been internationally established as the treatment of choice in early stages (BCLC 0 or A).15 In a murine HCC model, Guo et al. described for the first time that ablation by means of IRE demonstrates a significant decrease in tumor size and a greater percentage of necrosis induced by the treatment in ablated tumors.16 In later use in clinical practice, the studies by Cheung et al.7 and Bhutiani et al.,8 directed specifically at the treatment of HCC in a limited series of 11 and 55 patients, reported the feasibility of the technique and very few adverse effects. Even in patients with Child B cirrhosis, good oncological results and very few complications have been demonstrated.8,17

In the same manner, IRE can be used in the ablation of colorectal metastases that are not surgically resectable due to their central or perivascular location. To date, greater effectiveness of IRE has not been demonstrated according to tumor type, although it has been indicated that the histologic subtype could play a role in the success of the ablation.18 In most series, the number of patients is limited and samples are very heterogeneous, which limits the interpretation of the oncological results. Only Scheffer et al.19 prospectively included 10 patients with exclusive diagnosis of hepatic metastasis of colorectal carcinoma, in which the lesion was ablated and then resected for histological analysis. The results showed extensive areas of non-viable tumor in 80% of patients confirmed by a positive marker for apoptosis, caspase-3. However, the study did not provide data on long-term follow-up or the recurrence rate.

There is no limit established on the size of the lesion to be treated, but better oncologic results are described in lesions smaller than 3cm,20 and an increased risk of local recurrence has been described when the tumor volume exceeds 5cm.3,18 The efficacy and viability of IRE in perivascular ablation is one of its greatest advantages,10,21 and ablations have been reported with a mean proximity to the large blood vessels of 0.5cm, with no observed thrombosis or stenosis at follow-up.22 In a comprehensive study, Dollinger et al.17 specifically reported that the risk of post-IRE thrombosis is greater in ablations done near the portal vein compared to the suprahepatic veins or hepatic artery. However, out of a total of 172 ablations near large vessels, only 9.9% of patients experienced vascular alterations, which became permanent in certain cases. In this context, it is important to highlight the potential role of IRE in the downstaging of tumors prior to surgery, a use that has already been described in the pancreas.23 In the era of ALPPS or 2-stage hepatectomy, IRE is a more-than-reasonable alternative to treat lesions that infiltrate the suprahepatic veins and to be able to complete the surgery in a deferred manner. Our group has experience in the use of IRE for the downstaging of liver metastases of colorectal carcinoma in the context of the ALPPS procedure, and even for the local control of tumors as a step prior to liver transplantation.

Oncologic outcomes vary greatly according to authors and series. Success rates range from 50% to 100%, depending on the diagnostic criteria applied and the length of follow-up (Table 1). Most authors have a maximum follow-up of 6 or 12 months post-ablation and in some cases the disease-free survival is not accurately reported since the objective is not so much to demonstrate the effectiveness of the treatment as it is to determine the tolerability of the treatment. It should also be taken into account that IRE is a technique that is in its early stages, so there are no established guidelines regarding the evaluation of the long-term radiological behavior of the lesion. In dynamic gadolinium-enhanced magnetic resonance studies, a hypointense area is usually observed in T1, corresponding with the treated area, surrounded by a halo of contrast uptake. This hypointense area decreases in diameter and the enhancement halo gradually disappears.24,25 However, the correlation of these radiological findings with the histology is challenging as no histological specimen is available to compare the results.

Table 1.

Summary of the Series of Patients Treated With Hepatic Ablation Using IRE.

Study  No. of patients  Tumor type  Disease-free survival (%)  Mean follow-up 
Thomson et al., 20112525HCC  83.3  3 months
CRLM  50 
Kingham et al., 201222  28  CCC, HCC; CRLM  92.4  6 months 
Cannon et al., 201310  44  CRLM, HCC, CCC  59.5  12 months 
Cheung et al., 20137  11 (18 lesions)  HCC  13/18 complete ablation (72) 100  22 months 
Scheffer et al., 201439  10  CRLM  –  No follow-up 
Bhutiani et al., 20168  55  HCC  97  6 months 
Niessen et al., 20169  34  CCC, HCC; CRLM  67.5  12 months 
Padia et al., 201624  20  HCC  90  1 month 

CCC, cholangiocarcinoma; CRLM, colorectal liver metastases; HCC, hepatocellular carcinoma; IRE, irreversible electroporation.

Pancreatic Ablation

Pancreatic adenocarcinoma is an entity with a grim prognosis, causing 266000 deaths/year worldwide.26 At the time of diagnosis, 80%–90% of patients present disseminated disease (stage IV) or regional lymphovascular infiltration (stage III), so the surgical results are not encouraging.27 Because of its complex anatomical location, conventional thermal ablation does not provide good palliation as it has a high rate of associated complications, such as hemorrhages, necrotizing pancreatitis or injury to the main biliary tract or the Wirsung duct.

IRE has demonstrated good results in the palliative ablation of stage III tumors of the neck/body as well as in the head in a long series of 200 patients, with a mean survival of 24.9 months.28 Adverse effects include gastrointestinal/hematological complications and infections, although their spectrum of severity varies. There are reports of 36% of complications derived directly from the procedure, in spite of which groups with great experience in pancreatic ablation report no pancreatic fistulas or clinically relevant pancreatitis,29,30 as has already been shown in experimental studies.31

In its clinical application, staging by exploratory laparoscopy with cytology is required prior to ablation, as well as good local tumor control after induction chemotherapy for 3–4 months and a tumor diameter less than or equal to 3.5cm.32 In patients with metallic stents, their withdrawal is necessary prior to the application of pulses, as the presence of metal increases the risk for thermal damage in the surrounding tissue.33 In most cases, an open approach is necessary for the correct localization, placement of electrodes and tumor treatment (Fig. 1).

In a comparison with patients treated with standard therapy, Martin32 describes a clear benefit in the local recurrence-free survival in patients treated with IRE (14 vs 6 months, p=.01), disease-free survival (15 vs 9 months, p=.02), and overall survival (20 vs 13 months, p=.03).

Clinical Safety of Irreversible Electroporation

Since the introduction of the technique in humans, clinical safety has been the big question in IRE. The most common adverse effects are cardiovascular events since the application of the electric field as pulses entails, as previously reported, the frequent appearance of arrhythmias and even bursts of ventricular fibrillation.34 Since the introduction of standardized electrocardiogram synchronization, the appearance of these arrhythmias has decreased substantially.

Rhythm alterations vary depending on the area to be treated. Our group has recently shown in a series of 43 patients that cardiovascular events are significantly related to the location of the electrodes. Thus, ablations in the celiac trunk region were a risk factor in the multivariate analysis for developing a cardiovascular event.35 These arrhythmias do not usually involve hemodynamic compromise for the patient and only require medical treatment.36 Furthermore, IRE can cause a transient increase in the patient's blood pressure. Some 77% of the patients in our series had a mean increase in blood pressure of 15mmHg, a fact that correlates with the results of other authors.36 In some cases, extreme elevation of systolic blood pressure to 200mmHg has been reported, but these were tumors of the upper pole of the kidney or ablations related with the adrenal glands.34

Fluid and electrolyte imbalances have also been reported, such as hyperkalemia34,35 or metabolic acidosis. Taking into account the mechanism of action, the hypothesis is that the formation of nanopores in the plasma membrane of cells leads to the massive release of intracellular potassium into the blood flow, similar to what occurs in tumor lysis syndrome. This alteration has also been confirmed at the experimental level, since there are studies that indicate that very large ablations of tissue lead to severe fluid and electrolyte imbalance.37

Apart from those already mentioned, there are complications directly derived from the placement of the electrodes, such as pneumothorax (3.9%), pleural effusion or hematomas (11.8%), which are usually related to percutaneous procedures.36 Pain has also been reported after the procedure, triggered by muscle hyperstimulation.38

Future Perspectives

IRE is certainly a promising technique and a feasible alternative in cases of unresectable tumors in both the liver and the pancreas. Its characteristic mechanism of action gives it an essential role to play in perivascular ablation. However, it is a new technique, and the related evidence is based on case series and limited patient cohorts that do not provide conclusions that could be generalized or standardized for clinical use. Multicenter randomized clinical trials with extensive follow-up periods are necessary to determine long-term oncological outcomes.

Currently, there are more than 10 registered randomized studies underway. Among them is the COLFIRE-II study (NCT02082782), whose preliminary results (COLDFIRE I) have already been published,39 with 29 recruited patients with liver metastases of colorectal carcinoma. The primary objective is to assess disease-free survival with PET-MRI during a one-year follow-up.

In addition, it is also interesting to highlight the NCT02787954 study comparing with RECIST criteria the time until progression of the HCC depending on the TACE applied technique, radioembolization with Itrio90, MWA or IRE.

Beyond a doubt, IRE is a technique with great potential, whose future clinical uses have still yet to be seen. Until now, however, it has demonstrated its capacity for the treatment of certain tumors, for which there is currently no better therapeutic alternative.40

Conflict of Interest

The authors have no conflict of interest to declare.

References
[1]
R.V. Davalos, B. Rubinsky, L.M. Mir.
Theoretical analysis of the thermal effects during in vivo tissue electroporation.
Bioelectrochemistry, 61 (2003), pp. 99-107
PMID: 14642915
[2]
L. Miller, J. Leor, B. Rubinsky.
Cancer cells ablation with irreversible electroporation.
Technol Cancer Res Treat, 4 (2005), pp. 699-705
PMID: 16292891
[3]
R.V. Davalos, I.L.M. Mir, B. Rubinsky.
Tissue ablation with irreversible electroporation.
Ann Biomed Eng, 33 (2005), pp. 223-231
PMID: 15771276
[4]
S. Mulier, Y. Ni, J. Jamart, T. Ruers, G. Marchal, L. Michel.
Local recurrence after hepatic radiofrequency coagulation: multivariate meta-analysis and review of contributing factors.
Ann Surg, 242 (2005), pp. 158-171
PMID: 16041205
[5]
K.P. Charpentier, F. Wolf, L. Noble, B. Winn, M. Resnick, D.E. Dupuy.
Irreversible electroporation of the liver and liver hilum in swine.
HPB (Oxford), 13 (2011), pp. 168-173
PMID: 21309933
[6]
J.F. Edd, L. Horowitz, R.V. Davalos, L.M. Mir, B. Rubinsky.
In vivo results of a new focal tissue ablation technique: irreversible electroporation.
IEEE Trans Biomed Eng, 53 (2006), pp. 1409-1415
PMID: 16830945
[7]
W. Cheung, H. Kavnoudias, S. Roberts, B. Szkandera, W. Kemp, K.R. Thomson.
Irreversible electroporation for unresectable hepatocellular carcinoma: initial experience and review of safety and outcomes.
Technol Cancer Res Treat, 12 (2013), pp. 233-241
PMID: 23369152
[8]
N. Bhutiani, P. Philips, C.R. Scoggins, K.M. McMasters, M.H. Potts, R.C. Martin.
Evaluation of tolerability and efficacy of irreversible electroporation (IRE) in treatment of Child-Pugh B (7/8) hepatocellular carcinoma (HCC).
HPB (Oxford), 18 (2016), pp. 593-599
[9]
C. Niessen, L.P. Beyer, B. Pregler, M. Dollinger, B. Trabold, H.J. Schlitt, et al.
Percutaneous ablation of hepatic tumors using irreversible electroporation: a prospective safety and midterm efficacy study in 34 patients.
J Vasc Interv Radiol, 27 (2016), pp. 480-486
PMID: 26922979
[10]
R. Cannon, S. Ellis, D. Hayes, G. Narayanan, R.C.G. Martin.
Safety and early efficacy of irreversible electroporation for hepatic tumors in proximity to vital structures.
J Surg Oncol, 107 (2013), pp. 544-549
PMID: 23090720
[11]
D. Miklavcic, K. Beravs, D. Semrov, M. Cemazar, F. Demsar, G. Sera.
The importance of electric field distribution for effective in vivo electroporation of tissues.
Biophys J, 74 (1998), pp. 2152-2158
PMID: 9591642
[12]
L. Applaud, E. Ben-David, M. Farina, Y. Nissenbaum, J. Sosa, S.N. Goldberg, et al.
Irreversible electroporation ablation: creation of large-volume ablation zones in in vivo porcine liver with four-electrode arrays.
Radiology, 270 (2014), pp. 416-424
PMID: 24126371
[13]
A. Goldberg, B.G. Bruins, B.E. Outgun, M.L. Yarmouth.
Tissue heterogeneity in structure and conductivity contribute to cell survival during irreversible electroporation ablation by “electric field sinks”.
Sci Rep, 5 (2015), pp. 8485
PMID: 25684630
[14]
A. Deodar, T. Decked, G.W. Single, W.C. Hamilton, R.H. Thornton, C.T. Sofocleous, et al.
Irreversible electroporation near the heart: ventricular arrhythmias can be prevented with ECG synchronization.
AJR Am J Roentgenol, 196 (2011), pp. W330-W335
PMID: 21343484
[15]
A. Former, J.M. Loved, J. Bruit.
Hepatocellular carcinoma.
Lancet, 379 (2012), pp. 1245-1255
PMID: 22353262
[16]
Y. Go, Y. Zhang, R. Klein, G.M. Nigh, A.V. Samarian, R.A. Omar, et al.
Irreversible electroporation therapy in the liver: longitudinal efficacy studies in a rat model of hepatocellular carcinoma.
Cancer Res, 70 (2010), pp. 1555-1563
PMID: 20124486
[17]
M. Dollinger, R. Müller-Wille, F. Semen, M. Hammer, C. Niessen, L.P. Beyer, et al.
Irreversible electroporation of malignant hepatic tumors – alterations in venous structures at subacute follow-up and evolution at mid-term follow-up.
PLOS ONE, 10 (2015), pp. e0135773
PMID: 26270651
[18]
C. Niessen, J. Gill, B. Pregler, L. Beyer, E. Nova, M. Dollinger, et al.
Factors associated with short-term local recurrence of liver cancer after percutaneous ablation using irreversible electroporation: a prospective single-center study.
J Vasc Interv Radiol, 26 (2015), pp. 694-702
PMID: 25812712
[19]
H.J. Schaffer, K. Nielsen, A.A.J.M. van Tilbury, J.M. Vivien, R.A. Bowman, G. Kashmir, et al.
Ablation of colorectal liver metastases by irreversible electroporation: results of the COLDFIRE-I ablate-and-resect study.
Eur Radiol, 24 (2014), pp. 2467-2475
PMID: 24939670
[20]
H.J. Schaffer, K. Nielsen, M.C. de Jung, A.A.J.M. van Tilbury, J.M. Vivien, A.R.A. Bowman, et al.
Irreversible electroporation for nonthermal tumor ablation in the clinical setting: a systematic review of safety and efficacy.
J Vasc Interv Radiol, 25 (2014), pp. 997-1011
PMID: 24656178
[21]
X. Chen, Z. Ran, T. Zhu, X. Zhang, Z. Pang, H. Die, et al.
Electric ablation with irreversible electroporation (IRE) in vital hepatic structures and follow-up investigation.
Sci Rep, 9 (2015), pp. 16233
PMID: 26549662
[22]
T.P. King ham, A.M. Kara, M.I. D’Angelica, P.J. Allen, R.P. Demotte, G.I. Getrajdman, et al.
Ablation of perivascular hepatic malignant tumors with irreversible electroporation.
J Am Coll Surg, 215 (2012), pp. 379-387
PMID: 22704820
[23]
G. Narayanan, P.J. Hussein, G. Aurora, K.J. Barberry, T. Fraud, A.S. Livingston, et al.
Percutaneous irreversible electroporation for downstaging and control of unresectable pancreatic adenocarcinoma.
J Vasc Interv Radiol, 23 (2012), pp. 1613-1621
PMID: 23177107
[24]
S.A. Paid, G.E. Johnson, R.S. Young, J.O. Park, D.S. Hipper, M.J. Knout.
Irreversible electroporation in patients with hepatocellular carcinoma: immediate versus delayed findings at MR imaging.
Radiology, 278 (2016), pp. 285-294
PMID: 26523493
[25]
K.R. Thomson, W. Cheung, S.J. Ellis, D. Federman, H. Kavnoudias, D. Loader-Oliver, et al.
Investigation of the safety of irreversible electroporation in humans.
J Vasc Interv Radiol, 22 (2011), pp. 611-621
PMID: 21439847
[26]
A. Jamul, F. Bray, M.M. Centre, J. Farley, E. Ward, D. Forman.
Global cancer statistics.
CA Cancer J Clin, 61 (2011), pp. 69-90
PMID: 10200776
[27]
R. Siegel, D.J.A. Naishadham.
Cancer statistics, 2013.
Am Cancer Soc, 8 (2010), pp. 1-34
PMID: 23335087
[28]
R.C.G. Martin.
Irreversible electroporation of locally advanced pancreatic neck/body adenocarcinoma.
J Gastrointest Oncol, 6 (2015), pp. 329-335
PMID: 26029461
[29]
R.C.G. Martin, K. McFarland, S. Ellis, V. Velanovich.
Irreversible electroporation therapy in the management of locally advanced pancreatic adenocarcinoma.
J Am Coll Surg, 215 (2012), pp. 361-369
PMID: 22726894
[30]
R.C.G. Martin, D. Kwon, S. Chaliced, M. Sellers, E. Katz, C. Scoggins, et al.
Treatment of 200 locally advanced (stage III) pancreatic adenocarcinoma patients with irreversible electroporation safety and efficacy.
Ann Surg, 262 (2015), pp. 486-494
[31]
S. Fritz, C.M. Summer, D. Vollherbst, M.F. Watcher, T. Long Erich, M. Sachsenmeier, et al.
Irreversible electroporation of the pancreas is feasible and safe in a porcine survival model.
Pancreas, 44 (2015), pp. 791-798
PMID: 25931252
[32]
R.C.G. Martin.
Irreversible electroporation of locally advanced pancreatic head adenocarcinoma.
J Gastrointest Surg, 17 (2013), pp. 1850-1856
PMID: 23929188
[33]
E.M. Dunk-Jacobs, P. Philips, R.C.G. Martin.
Evaluation of thermal injury to liver, pancreas and kidney during irreversible electroporation in an in vivo experimental model.
Br J Surg, 101 (2014), pp. 1113-1121
PMID: 24961953
[34]
C. Ball, K.R. Thomson, H. Kavnoudias.
Irreversible electroporation: a new challenge in “out of operating theater” anesthesia.
Anesth Analg, 110 (2010), pp. 1305-1309
PMID: 20142349
[35]
P. Kambakamba, J.M. Bovine, M. Glance, L. Castrezana Lopez, T. Paymaster, P.-A. Clavier, et al.
Intraoperative adverse events during irreversible electroporation – a call for caution.
Am J Surg, 212 (2016), pp. 715-721
[36]
K. Nielsen, H.J. Schaffer, J.M. Vivien, A.A.J.M. van Tilbury, S. Meier, C. van Kink, et al.
Anaesthetic management during open and percutaneous irreversible electroporation.
Br J Anaesth, 113 (2014), pp. 985-992
PMID: 25173767
[37]
P. Sánchez-Velázquez, Q. Castellví, A. Villanueva, R. Quesada, C. Paella, M. Cancers, et al.
Irreversible electroporation of the liver: is there a safe limit to the ablation volume?.
Sci Rep, 6 (2016), pp. 23781
PMID: 27032535
[38]
G. Narayanan, T. Fraud, K. Lo, K.J. Barberry, E. Pérez-Rojas, J. Rosary.
Pain analysis in patients with hepatocellular carcinoma: irreversible electroporation versus radiofrequency ablation-initial observations.
Cardiovasc Intervent Radiol, 36 (2013), pp. 176-182
PMID: 22752100
[39]
H.J. Schaffer, K. Nielsen, A.A. van Tilbury, J.M. Vivien, R.A. Bowman, G. Kashmir, et al.
Ablation of colorectal liver metastases by irreversible electroporation: results of the COLDFIRE-I ablate-and-resect study.
Eur Radiol, 24 (2014), pp. 2467-2475
PMID: 24939670
[40]
M. Lancer, T. Paymaster, P. Kambakamba, M.L. Deliver.
Ablation strategies for locally advanced pancreatic cancer.
Dig Surg, 33 (2016), pp. 351-359
PMID: 27216160

Please cite this article as: Sánchez-Velázquez P, Clavien P-A. El rol de la electroporación irreversible en la cirugía hepato-bilio-pancreática. Cir Esp. 2017;95:307–312.

Copyright © 2017. AEC
Article options
Tools
es en pt

¿Es usted profesional sanitario apto para prescribir o dispensar medicamentos?

Are you a health professional able to prescribe or dispense drugs?

Você é um profissional de saúde habilitado a prescrever ou dispensar medicamentos