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The coronary sinus side branch stenting

4. Results

4.8. The coronary sinus side branch stenting

Coronary sinus side branch stenting was successfully performed in 312 of 317 patients (98.4%). In five cases it was not possible to introduce the stent into the side branch due to tortuosity of the proximal part or the small diameter of the vessel. In four cases the electrode was left in the side branch without stenting add, in one patient we changed to transseptal endocardial implantation because of intraoperative dislocation. No implantation related death occurred in our patient group. Mechanical injury caused by CS stenting was not experienced. During implantation coronary sinus dissection with pericardial tamponade was detected in one patient. Since contrast dye extravasation was seen in the pericardial space of the first CS venogram prior to stent deployment, the effusion was presumably caused by CS dissection during positioning of the CS guide.

Following percutaneous aspiration from a subxyphoideal puncture, pericardial effusion did not recur.

Early lead dislocation with loss of LV capture was detected in two patients (0.6%).

Potential causes of the dislocation might be in both cases proximal lead position in a lateral side branch, underestimation of the diameter of the stent and the localization of

the stent in a curvature of the vessel. Re-operation was performed; in one patient left ventricular pacing was carried out via the anterolateral branch. Phrenic nerve stimulation was found in the in-hospital period in seven patients (2.2%). Changing of the pacing parameters finally or transiently solved the problem. During follow-up 54 patients died, an average 13.4 months after implantation (n=11 in the first 1-3 months, n=17 in the 3 month-1 year period, n=16 in the 1-2 year period, n=10 after 2 years).

Compared with the values measured after the implantation, the LV pacing threshold did not change significantly either after 6 months (1.0 [0.6-1.6] V vs. 0.8 [0.6-1.3] V, p=0.052; Figure 23, panel A) or after 24 months follow-up (0.8 1.6] V vs. 0.8 [0.6-1.5] V, p=0.419; Figure 23, panel C). A clinically remarkable rise in pacing threshold was observed in two cases (0.6%). In one patient the threshold increased after two years (2.2 vs 5.6 V). In the other case the lowest threshold value was 5.8 V @ 0.5 ms during implantation which increased to 7.2 V @ 0.5 ms. In two other cases the threshold increased more than 2 V, but did not exceed 4 V @ 0.5 ms. Macroscopic dislocation was not detected on X-ray in these four patients. Although a slight decrease of the LV pacing impedance was found both at 6 months (600 [522-720] Ω vs. 550 [475-639] Ω, p=0.0007; Figure 23, panel B) and 24 months visits (608 [535-780] Ω vs. 575 [508-656]

Ω, p=0.0181; Figure 23, panel D), results of impedance measurements did not suggest insulation failure or fracture of the left ventricular electrode in any cases during follow-up. In patients with three (n=47, Figure 23, panel E-F) or four years’ (n=13) follow-up, pacing threshold remained stable (median 0.9 [0.6-1.65] V vs. 0.9 [0.6-1.3] V and 0.9 [0.7-2] V vs. 1.25 [0.85-2.1] V @0.5 respectively), no signs of lead injury were detected (608 [522-810] Ω vs. 563 [511-676] Ω and 600 [529-688] Ω vs. 636 [553-709]

Ω).

Figure 23. Changes in LV pacing and impedance values at 6, 24, and 36 months after implantation. LV pacing threshold did not change at 6, 24, and 36 months of follow-up, while a slight decrease in the LV pacing impedance values was found without any signs of injury of the lead insulation. (n = 293 at 6 months, n = 153 at 24 months, n = 47 at 36 months). Medians and interquartile ranges are presented. P-values were calculated with the Wilcoxon signed rank test.

Phrenic nerve stimulation was observed in 18 patients (5.7%). In 11 cases reprogramming of pacing parameters was successful to terminate PNS. In 7 cases (2.2%) repositioning of the lead was necessary. The stented LV leads were retracted with an ablation catheter introduced via the femoral vein in all patients 1-28 months after implantation. In 5 cases suitable pacing threshold was reached, while in one patient the threshold increased to 5.0 V@1 ms. In another patient the CS lead dislocated into the right atrium, it was explanted and a new lead was implanted. PNS was not detected after repositioning.

4.8.2. The extraction of the stented lead

Explantation of the stented LV lead was needed in three patients because of pocket infection (n=2) and endocarditis (n=1) after 3, 49 and 18 months. Leads were extracted without any complication while the stent remained in the CS side branch. Neither signs of insulation failure nor other macroscopic damage was seen on the extracted electrodes. Four patients underwent heart transplantation (7-27 months after implantation). During the operation, leads were cut in the superior vena cava and after explantation of the heart (Figure 24.) the surgeon was able to extract easily the stented leads from the CS side branch. Between the stent and the lead, macroscopically identifiable layer of tissue was observed. Macroscopic injuries could not be seen.

Figure 24. Epicardial view of the explanted heart: Arterial (left) and venous (right) coronary stents in an explantated heart. An endothelial sheath separates the stent from the lead. The left arterial stent was implantated percutaneously when a nSTEMI was experienced and PCI performed during follow-up.

Microscopic evaluation was performed on five CS electrodes. (Figure 25.) The examination of the stented area revealed surface damages as a result of the continuous friction between the stent and the electrode with a depth of 3-7 µm. This depth involved 1.7 – 4 % of the total insulation wall thickness, therefore the integrity and safety of insulation was not threatened. In one lead a deeper injury (27% of the insulation thickness) was also found, but the sharp edges and long, narrow shape of the deepest injury suggest, that it was produced during the extraction of the lead.

Figure 25. CS lead extracted during heart transplantation. Metal-microscopic imaging about the surface covered by the stent: no remarkable injury was observed.

5. Discussion