TY - JOUR
T1 - Stellate ganglion instrumentation for pharmacological blockade, nerve recording, and stimulation in patients with ventricular arrhythmias
T2 - Preliminary experience
AU - Lador, Adi
AU - Wang, Sufen
AU - Schurmann, Paul A.
AU - Chihara, Ray
AU - Dave, Amish S.
AU - Valderrábano, Miguel
N1 - Funding Information:
Funding Sources: This work was supported by the Charles Burnett III and Lois and Carl Davis Centennial Chair endowments (MV) (Houston, TX).
Publisher Copyright:
© 2023 Heart Rhythm Society
PY - 2023
Y1 - 2023
N2 - Background: Stellate ganglion blockade (SGB) can control ventricular arrhythmias (VAs), but outcomes are unclear. Percutaneous stellate ganglion (SG) recording and stimulation in humans has not been reported. Objective: The purpose of this study was to assess the outcomes of SGB and the feasibility of SG stimulation and recording in humans with VAs. Methods: Two patient cohorts were included—group 1: patients undergoing SGB for drug-refractory VAs. SGB was performed by injection of liposomal bupivacaine. Incidence of VAs at 24 and 72 hours and clinical outcomes were collected; group 2: patients undergoing SG stimulation and recording during VA ablation; a 2-F octapolar catheter was placed at the SG at the C7 level. Recording (30 kHz sampling, 0.5–2 kHz filter) and stimulation (up to 80 mA output, 50 Hz, 2 ms pulse width for 20–30 seconds) was performed. Results: Group 1 included 25 patients [age 59.2 ± 12.8 years; 19 (76%) men] who underwent SGB for VAs. Nineteen patients (76.0%) were free of VA up to 72 hours postprocedure. However, 15 (60.0%) had VAs recurrence for a mean of 5.47 ± 4.52 days. Group 2 included 11 patients (mean age 63 ± 12.7 years; 82.7% men). SG stimulation caused consistent increases in systolic blood pressure. We recorded unequivocal signals with temporal association with arrhythmias in 4 of 11 patients. Conclusion: SGB provides short-term VA control, but has no benefit in the absence of definitive VA therapies. SG recording and stimulation is feasible and may have value to elicit VA and understand neural mechanisms of VA in the electrophysiology laboratory.
AB - Background: Stellate ganglion blockade (SGB) can control ventricular arrhythmias (VAs), but outcomes are unclear. Percutaneous stellate ganglion (SG) recording and stimulation in humans has not been reported. Objective: The purpose of this study was to assess the outcomes of SGB and the feasibility of SG stimulation and recording in humans with VAs. Methods: Two patient cohorts were included—group 1: patients undergoing SGB for drug-refractory VAs. SGB was performed by injection of liposomal bupivacaine. Incidence of VAs at 24 and 72 hours and clinical outcomes were collected; group 2: patients undergoing SG stimulation and recording during VA ablation; a 2-F octapolar catheter was placed at the SG at the C7 level. Recording (30 kHz sampling, 0.5–2 kHz filter) and stimulation (up to 80 mA output, 50 Hz, 2 ms pulse width for 20–30 seconds) was performed. Results: Group 1 included 25 patients [age 59.2 ± 12.8 years; 19 (76%) men] who underwent SGB for VAs. Nineteen patients (76.0%) were free of VA up to 72 hours postprocedure. However, 15 (60.0%) had VAs recurrence for a mean of 5.47 ± 4.52 days. Group 2 included 11 patients (mean age 63 ± 12.7 years; 82.7% men). SG stimulation caused consistent increases in systolic blood pressure. We recorded unequivocal signals with temporal association with arrhythmias in 4 of 11 patients. Conclusion: SGB provides short-term VA control, but has no benefit in the absence of definitive VA therapies. SG recording and stimulation is feasible and may have value to elicit VA and understand neural mechanisms of VA in the electrophysiology laboratory.
KW - Neuromodulation
KW - Stellate ganglion blockade
KW - Stellate ganglion recording
KW - Stellate ganglion stimulation
KW - Ventricular tachycardia
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U2 - 10.1016/j.hrthm.2023.02.024
DO - 10.1016/j.hrthm.2023.02.024
M3 - Article
C2 - 36863635
AN - SCOPUS:85151418333
VL - 20
SP - 797
EP - 805
JO - Heart Rhythm
JF - Heart Rhythm
SN - 1547-5271
IS - 6
ER -