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Stockert generator

Manufactured by Johnson & Johnson
Sourced in United States

The Stockert generator is a piece of laboratory equipment used to generate and regulate electrical currents or voltages. It is a versatile device that can be utilized in various scientific and research applications that require a controlled electrical output.

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6 protocols using stockert generator

1

Catheter-based Ablation of Atrial Fibrillation

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Catheter-based ablation of AF was performed using a three-dimensional mapping (NavX, St Jude Medical Inc.) in all 84 patients. An intracardiac electrogram was recorded using a Prucka CardioLab™ Electrophysiology system (General Electric Medical Systems Inc.). For the electric isolation of arrhythmogenic substrates, radiofrequency energy was delivered through a Stockert generator (Biosense Webster Inc.) in a temperature-controlled mode and limited to 50℃ using a maximal power of 35 W and duration of 30–40 seconds. In the routine catheter ablation of AF, the procedure endpoint was the complete electric isolation of the arrhythmogenic substrates such as the left atrium, LAA, and pulmonary veins.
Following sinus rhythm, LAA activation was evaluated using a catheter-based intracardiac electrogram. LAA activation was defined as the local “a” wave of LAA with or after the onset of the left ventricular QRS complex on the intracardiac electrogram (Fig. 2). Depending on the intracardiac electrogram results, all patients were divided into two groups: 1) LAA isolation (with the delay or absence of LAA activation) and 2) LAA normal activation (without the delay or absence of LAA activation).
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2

Catheter Ablation for Persistent Atrial Fibrillation

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An open‐irrigation 3.5‐mm‐tip deflectable catheter (Celsius, Johnson & Johnson Inc, Diamond Bar, CA; Coolflex, St. Jude Medical Inc, Minnetonka, MN; 30 to 35 W; 47°C) was used for the RFCA (Stockert generator; Biosense Webster Inc, Diamond Bar, CA). All patients initially underwent circumferential PV isolation and the creation of cavo‐tricuspid isthmus block. For the patients with persistent AF, we added a roof line, posterior inferior line, and anterior line15 (link) as a standard lesion set. Depending on the operator's decision, additional ablation of the superior vena cava, non‐PV foci, or complex fractionated electrograms was conducted. The procedure ended when there was no immediate recurrence of AF after cardioversion with an isoproterenol infusion (5 to 10 μg/min). If there were non‐PV foci under the isoproterenol infusion, we ablated them all.
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3

Comprehensive Ablation Protocol for Persistent Atrial Fibrillation

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Intracardiac electrograms were recorded using the Prucka Cardio Lab™ electrophysiology system (General Electric Health Care System Inc., Milwaukee, WI, USA), and catheter ablation was performed in all patients using 3D electroanatomical mapping (St. Jude Medical Inc., Minnetonka, MN, USA) merged with 3D spiral CT. We used an open irrigated-tip catheter (Celsius, Johnson & Johnson Inc., Diamond Bar, CA, USA; Coolflex, St. Jude Medical Inc., Minnetonka, MN, USA; 30-35 W; 47℃) to deliver RF energy for ablation (Stockert generator, Biosense Webster Inc.; Diamond Bar, CA, USA). All patients initially underwent circumferential PV isolation and bi-directional block of the cavo-tricuspid isthmus. For patients with PeAF, we added the roof line, posterior inferior line, and anterior line10 (link) as a standard lesion set. All procedures were conducted by two operators with over 10 years of experience.
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4

Ablation Strategies for Atrial Fibrillation

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We used an open irrigated-tip catheter (Celsius, Johnson & Johnson Inc., Diamond Bar, CA, USA; irrigation flow rate 20 to 30 mL/min; 30 W; 47℃) to deliver RF energy for ablation (Stockert generator, Biosense Webster Inc., Diamond Bar, CA, USA). Patients with both PAF and PeAF initially underwent circumferential pulmonary vein isolation (CPVI) and cavotricuspid isthmus block. Following CPVI in PeAF patients, we generated an LA roof line, a posterior inferior line, and an LA anterior line, and confirmed bidirectional blocks by differential pacing.12 (link) Depending on the operator's decision, additional ablations for superior vena cava, non-PV foci or complex fractionated electrogram were conducted. If AF persisted beyond the aforementioned ablation protocols for PAF or PeAF, we stopped the procedure after internal cardioversion. The end point of our procedure was the point of no immediate recurrence of AF after cardioversion with isoproterenol infusion (5 µg/min). If there were non-PV foci under isoproterenol infusion, we ablated them all.
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5

Catheter Ablation for Persistent Atrial Fibrillation

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During the procedure, intracardiac electrograms were recorded using a Prucka CardioLab electrophysiology system (General Electric Health Care System Inc). Ablation was guided by 3-dimensional electroanatomical mapping (NavX system; St. Jude Medical Inc). An open irrigation 3.5-mm-tip deflectable catheter (Celsius, Johnson & Johnson Inc; Cool Flex, St. Jude Medical Inc; 30 to 35 W; 47°C) was used for RFCA (Stockert generator; Biosense Webster Inc). All patients initially underwent circumferential pulmonary vein (PV) isolation and cavotricuspid isthmus ablation. For patients with persistent AF, we added a roof line, posterior inferior line, and anterior line19 (link) as a standard lesion set. At the operator’s discretion, additional ablations were delivered to the superior vena cava, non-PV foci, or regions of complex fractionated electrograms. We confirmed the PV isolation by both entrance and exit block and rechecked it under an isoproterenol infusion before finishing the procedure. In addition, we attempted to reinduce AF by isoproterenol infusion with rapid atrial pacing before finishing the procedure. The end point of our procedure was defined as no immediate recurrence of AF after cardioversion while receiving an isoproterenol infusion (5 to 10 μg/min). If there was immediate recurrence of AF after cardioversion, we then ablated these non-PV foci.
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6

Comprehensive Ablation Approach for Atrial Fibrillation

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Details regarding electrophysiological mapping and RFCA technique and strategy were described in previous studies.17 (link)18 (link) In brief, an open irrigation 3.5-mm-tip deflectable catheter (Celsius, Johnson & Johnson Inc.; Diamond Bar, CA, USA; Coolflex, St. Jude Medical Inc., Minnetonka, MN, USA; 30–35 W; 47℃) was used for RFCA (Stockert generator, Biosense Webster Inc., Diamond Bar, CA, USA). Circumferential pulmonary vein isolation and bi-directional block of the cavotricuspid isthmus ablation were performed in all patients. For patients with persistent AF, we added a roof line, posterior inferior line, and anterior line as a standard lesion set. Additional ablation of the superior vena cava or non-pulmonary vein foci or after complex fractionated electrography was determined by the operator.
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