Is electrocardiogram-gated irreversible electroporation still effective in liver ablation? A validation study in swine liver irreversible electroporation model
1
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
Background: To evaluate and compare the efficacy of tissue ablation in electrocardiogram (ECG)-synchronized and non-synchronized irreversible electroporation (IRE) ablation using radiological and histological analyses. Methods: Five Yorkshire swine underwent 2,250 or 3,000 volt IRE ablation of multiple liver zones with high-rate, non-synchronized irreversible electroporation (nsIRE) pulses delivered at 240 pulses per minute (PPM) (n = 12) and ECG-synchronized irreversible electroporation (esIRE) pulses at either medium rate delivered at 50 PPM (n = 12) or low rate at 20 PPM (n = 6). We evaluated and compared the volume of ablation zones and IREinduced cell death between esIRE and nsIRE groups using radiological and histological analyses. Results: In ultrasound examination, no significant difference was observed between the size of esIRE and nsIRE treated areas in all three dimensions (P = 0.93, 240 PPM vs. 50 PPM and P = 0.89, 240 PPM vs. 20 PPM). The ablation areas were also well-correlated in gross pathological analysis, with no significant difference between esIRE and nsIRE groups (P = 0.55, 240 PPM vs. 50 PPM and P = 0.56, 240 PPM vs. 20 PPM). Gross and microscopic examinations demonstrated complete cell death in both esIRE and nsIRE cohorts with preservation of large blood vessels and bile ducts in both groups. No cardiac dysrhythmia was noted in esIRE group. Conclusion: In our study, no histological or radiological differences were observed between esIRE and nsIRE ablated areas. The esIRE ablation maintained its ability to create complete focal cell death.
Abstract
Background: To evaluate and compare the efficacy of tissue ablation in electrocardiogram (ECG)-synchronized and non-synchronized irreversible electroporation (IRE) ablation using radiological and histological analyses. Methods: Five Yorkshire swine underwent 2,250 or 3,000 volt IRE ablation of multiple liver zones with high-rate, non-synchronized irreversible electroporation (nsIRE) pulses delivered at 240 pulses per minute (PPM) (n = 12) and ECG-synchronized irreversible electroporation (esIRE) pulses at either medium rate delivered at 50 PPM (n = 12) or low rate at 20 PPM (n = 6). We evaluated and compared the volume of ablation zones and IREinduced cell death between esIRE and nsIRE groups using radiological and histological analyses. Results: In ultrasound examination, no significant difference was observed between the size of esIRE and nsIRE treated areas in all three dimensions (P = 0.93, 240 PPM vs. 50 PPM and P = 0.89, 240 PPM vs. 20 PPM). The ablation areas were also well-correlated in gross pathological analysis, with no significant difference between esIRE and nsIRE groups (P = 0.55, 240 PPM vs. 50 PPM and P = 0.56, 240 PPM vs. 20 PPM). Gross and microscopic examinations demonstrated complete cell death in both esIRE and nsIRE cohorts with preservation of large blood vessels and bile ducts in both groups. No cardiac dysrhythmia was noted in esIRE group. Conclusion: In our study, no histological or radiological differences were observed between esIRE and nsIRE ablated areas. The esIRE ablation maintained its ability to create complete focal cell death.
참고문헌 (28)
- Adam R, "A comparison of percutaneous cryosurgery and percutaneous radiofrequency for unresectable hepatic malignancies", Arch Surg, 137, pp.1332~1339 (2002)
- Davalos RV, "Tissue ablation with irreversible electroporation", Ann Biomed Eng, 33, pp.223~231 (2005)
- Edd JF, "In vivo results of a new focal tissue ablation technique : irreversible electroporation", IEEE Trans Biomed Eng, 53, pp.1409~1415 (2006)
- Goldberg SN, "Percutaneous radiofrequency tissue ablation : does perfusion-mediated tissue cooling limit coagulation necrosis?", J Vasc Interv Radiol, 9(1 Pt 1), pp.101~111 (1998)
- Miller L, "Cancer cells ablation with irreversible electroporation", Technol Cancer Res Treat, 4, pp.699~705 (2005)
- Lee EW, "Advanced hepatic ablation technique for creating complete cell death : irreversible electroporation", Radiology, 255, pp.426~433 (2010)
- Lee EW, "Imaging guided percutaneous irreversible electroporation : ultrasound and immunohistological correlation", Technol Cancer Res Treat, 6, pp.287~294 (2007)
- Maor E, "The effect of irreversible electroporation on blood vessels", Technol Cancer Res Treat, 6, pp.307~312 (2007)
- Onik G, "Irreversible electroporation : implications for prostate ablation", Technol Cancer Res Treat, 6, pp.295~300 (2007)
- Al-Sakere B, "Tumor ablation with irreversible electroporation", PLoS One, 2, pp.e1135~ (2007)
- Månsson C, "Percutaneous irreversible electroporation as first-line treatment of locally advanced pancreatic cancer", Anticancer Res, 39, pp.2509~2512 (2019)
- Buijs M, "Feasibility and safety of irreversible electroporation(IRE)in patients with small renal masses : results of a prospective study", Urol Oncol, 37, pp.183.e1~183.e8 (2019)
- Blazevski A, "Oncological and quality-of-life outcomes following focal irreversible electroporation as primary treatment for localised prostate cancer : a biopsy-monitored prospective cohort", Eur Urol Oncol, 3, pp.283~290 (2020)
- Bertacchini C, "Design of an irreversible electroporation system for clinical use", Technol Cancer Res Treat, 6, pp.313~320 (2007)
- Mali B, "An algorithm for synchronization of in vivo electroporation with ECG", J Med Eng Technol, 29, pp.288~296 (2005)
- Deodhar A, "Irreversible electroporation near the heart : ventricular arrhythmias can be prevented with ECG synchronization", AJR Am J Roentgenol, 196, pp.W330~W335 (2011)
- Mali B, "The effect of electroporation pulses on functioning of the heart", Med Biol Eng Comput, 46, pp.745~757 (2008)
- Ball C, "Irreversible electroporation : a new challenge in"out of operating theater"anesthesia", Anesth Analg, 110, pp.1305~1309 (2010)
- Pech M, "Irreversible electroporation of renal cell carcinoma : a first-in-man phase I clinical study", Cardiovasc Intervent Radiol, 34, pp.132~138 (2011)
- Thomson KR, "Investigation of the safety of irreversible electroporation in humans", J Vasc Interv Radiol, 22, pp.611~621 (2011)
- Onik G, "Irreversible electroporation", pp.235~247 (2010), Springer
- Shen J, "Safety and efficacy of irreversible electroporation in locally advanced pancreatic cancer : an evaluation from a surgeon's perspective", Cancers(Basel), 14, pp.5677~ (2022)
- Scheltema MJ, "Median 5-year outcomes of primary focal irreversible electroporation for localised prostate cancer", BJU Int, 131(Suppl 4), pp.6~13 (2023)
- Shahrouki P, "Irreversible electroporation : a novel treatment modality in locally advanced and unresectable pancreatic adenocarcinoma", Pancreas, 50, pp.e79~e80 (2021)
- Lee EW, "Safety of irreversible electroporation ablation of the pancreas", Pancreas, 50, pp.1281~1286 (2021)
- Pucihar G, "A time-dependent numerical model of transmembrane voltage inducement and electroporation of irregularly shaped cells", IEEE Trans Biomed Eng, 56, pp.1491~1501 (2009)
- Mercadal B, "Dynamics of cell death after conventional IRE and H-FIRE treatments", Ann Biomed Eng, 48, pp.1451~1462 (2020)
- Siddiqui IA, "Induction of rapid, reproducible hepatic ablations using next-generation, high frequency irreversible electroporation(H-FIRE)in vivo", HPB(Oxford), 18, pp.726~734 (2016)
