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Symplicity flex catheter

Manufactured by Medtronic
Sourced in United States

The Symplicity Flex catheter is a medical device designed for use in diagnostic procedures. It is intended to facilitate the measurement and assessment of various physiological parameters. The core function of the Symplicity Flex catheter is to collect data, without interpretation or extrapolation on its intended use.

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2 protocols using symplicity flex catheter

1

Standardized Renal Denervation Procedure

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RDN was performed according to a standardized protocol, as described previously.10, 11 In brief, repeated ablation runs were delivered to each renal artery. The ablation points were placed circumferentially to the renal artery wall from distal to proximal. All patients received intravenous remifentanil to control visceral pain. Overall, 83 patients underwent ablation with a Symplicity Flex catheter, 21 patients were treated with Spyral catheters (both from Medtronic), and 27 patients underwent ablation with an ultrasound‐based denervation system (Paradise; ReCor Medical).
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2

Renal Denervation Procedure Protocol

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Patients received peri-procedural analgesia and conscious sedation with propofol/midazolam and remifentanil intravenous perfusion. Anti-thrombotic treatment included aspirin and a bolus of weight-adjusted unfractioned heparin (70–100 U/Kg). Femoral arterial access was obtained with 6F or 8F sheaths. Radiofrequency energy was delivered using the single-tip radiofrequency Symplicity Flex catheter (Medtronic Inc., Santa Rosa, CA, USA), the EnligHTN system (St. Jude Medical, MN, USA), or the Symplicity Spyral catheter (Medtronic Inc., Santa Rosa, CA, USA) in 9.5%, 38.1%, and 52.4% of the patients, respectively. Energy was applied to the main artery and branches, when feasible and according to the characteristics of each device with the goal of achieving a maximum number of circumferential ablation points. Radiofrequency energy was delivered according to a programmed algorithm specific to each device. Administration of intra-renal nitrates and a final renal angiogram was performed. All procedures were conducted by one interventional cardiologist dedicated to the field. Hemostasis was accomplished with a vascular closure device. All patients were monitored for 24 h before discharge.
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