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Articles

Percutaneous radiofrequency ablation near large vessels in beagle livers: the impact of time and distance on the ablation zone

, , ORCID Icon, , , , & show all
Pages 1263-1270 | Received 08 May 2021, Accepted 05 Aug 2021, Published online: 18 Aug 2021

Figures & data

Figure 1. Evaluation of the distance between the radiofrequency ablation (RFA) electrode tip and large vessel, ablation time and specimens/images of different groups. Tissue specimens obtained after euthanizing beagles at 24 h after RFA (first column), conventional ultrasound before RFA (second column), color Doppler ultrasound before RFA (third column) and post-RFA ultrasound (fourth column) are shown. The first row represents a distance of 0.5 cm from the tip of the RFA electrode to a large vessel with the ablation time set at 3 min (3 min 0.5 cm). The second row shows the electrode tip near the large vessel with the ablation time set at 3 min (3 min 0 cm). The third row represents a distance of 0.5 cm from the tip of the RFA electrode to a large vessel with the ablation time set at 5 min (5 min 0.5 cm). The fourth row represents that the electrode tip was near the large vessel with the ablation time set at 5 min (5 min 0 cm).

Figure 1. Evaluation of the distance between the radiofrequency ablation (RFA) electrode tip and large vessel, ablation time and specimens/images of different groups. Tissue specimens obtained after euthanizing beagles at 24 h after RFA (first column), conventional ultrasound before RFA (second column), color Doppler ultrasound before RFA (third column) and post-RFA ultrasound (fourth column) are shown. The first row represents a distance of 0.5 cm from the tip of the RFA electrode to a large vessel with the ablation time set at 3 min (3 min 0.5 cm). The second row shows the electrode tip near the large vessel with the ablation time set at 3 min (3 min 0 cm). The third row represents a distance of 0.5 cm from the tip of the RFA electrode to a large vessel with the ablation time set at 5 min (5 min 0.5 cm). The fourth row represents that the electrode tip was near the large vessel with the ablation time set at 5 min (5 min 0 cm).

Table 1. Comparison of the ablation zones among different groups.

Figure 2. Comparison of protocols with a fixed time. The graph depicts the mean (± standard deviation) distance and area of the two groups. (A) With the time fixed at 3 min, the ablation length, width, depth and area created using a distance of 0.5 cm were significantly larger than those created using a distance of 0 cm (length: p = .001; width: p < .001; depth: p = .019; area: p < .001). (B) With the time fixed at 5 min, there was no significant difference when the distances were 0 cm and 0.5 cm (length: p = .140; depth: p = .611). The ablation width and area when the distance was 0 cm were significantly smaller than when the distance was 0.5 cm (width: p = .007; area: p = .001). ***p < .001. **p < .01. *p < .05.

Figure 2. Comparison of protocols with a fixed time. The graph depicts the mean (± standard deviation) distance and area of the two groups. (A) With the time fixed at 3 min, the ablation length, width, depth and area created using a distance of 0.5 cm were significantly larger than those created using a distance of 0 cm (length: p = .001; width: p < .001; depth: p = .019; area: p < .001). (B) With the time fixed at 5 min, there was no significant difference when the distances were 0 cm and 0.5 cm (length: p = .140; depth: p = .611). The ablation width and area when the distance was 0 cm were significantly smaller than when the distance was 0.5 cm (width: p = .007; area: p = .001). ***p < .001. **p < .01. *p < .05.

Figure 3. Comparison of protocols with a fixed distance. The graph depicts the mean (± standard deviation) distance and area of the two groups. (A) At a fixed distance of 0 cm, the statistically significant differences were observed when the ablation times were 3 min and 5 min (length: p < .001; width: p < .001; depth: p < .001; area: p < .001). (B) At a fixed distance of 0.5 cm, the ablation length created with an ablation time of 3 min was not statistically different from that created with an ablation time of 5 min (length: p = .112). The ablation width and ablation zone created with an ablation time of 5 min were significantly larger than those created with an ablation time of 3 min (width: p = .001; depth: p = .002; area: p = .001). ***p < .001. **p < .01. *p < .05.

Figure 3. Comparison of protocols with a fixed distance. The graph depicts the mean (± standard deviation) distance and area of the two groups. (A) At a fixed distance of 0 cm, the statistically significant differences were observed when the ablation times were 3 min and 5 min (length: p < .001; width: p < .001; depth: p < .001; area: p < .001). (B) At a fixed distance of 0.5 cm, the ablation length created with an ablation time of 3 min was not statistically different from that created with an ablation time of 5 min (length: p = .112). The ablation width and ablation zone created with an ablation time of 5 min were significantly larger than those created with an ablation time of 3 min (width: p = .001; depth: p = .002; area: p = .001). ***p < .001. **p < .01. *p < .05.

Figure 4. Comparison of the ablation zones in the specimens and hematoxylin and eosin tissue taken from different areas using a light microscope (×200). (A) Normal liver. (B) Vascular wall. (C) Central ablation zone. (D) Peripheral ablation zone. All specimens were obtained 24 h after ablation.

Figure 4. Comparison of the ablation zones in the specimens and hematoxylin and eosin tissue taken from different areas using a light microscope (×200). (A) Normal liver. (B) Vascular wall. (C) Central ablation zone. (D) Peripheral ablation zone. All specimens were obtained 24 h after ablation.

Figure 5. Pathological staining and TUNEL immunofluorescence staining results of beagle liver vessels. Results of pathological staining with hematoxylin and eosin (HE), staining with DAPI (blue), co-stained with TUNEL (green representing apoptosis) and merging (blue and green) (from the first column to the fourth column) (×50). The vascular wall cells are still well-formed in (A–D). The vascular wall is damaged in (E–H). The thrombus is observed in (I–L).

Figure 5. Pathological staining and TUNEL immunofluorescence staining results of beagle liver vessels. Results of pathological staining with hematoxylin and eosin (HE), staining with DAPI (blue), co-stained with TUNEL (green representing apoptosis) and merging (blue and green) (from the first column to the fourth column) (×50). The vascular wall cells are still well-formed in (A–D). The vascular wall is damaged in (E–H). The thrombus is observed in (I–L).

Table 2. Pathological evaluation of the vessels.

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Supplemental Material

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