Minimal adverse effects profile following implantation of periauricular percutaneous electrical nerve field stimulators: a retrospective cohort study

Arthur Roberts,1–3 Alec Sithole,4 Marcos Sedghi,5 Charles A Walker,6,7 Theresa M Quinn,8 1Indiana Craniofacial Center, 2Department of Oral Pathology, Medicine and Radiology, Indiana University School of Dentistry, Indianapolis, IN, USA; 3Department of Anesthesia, Critical Care, and Pain Ma...

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Bibliographic Details
Main Authors:	Roberts A, Sithole A, Sedghi M, Walker CA, Quinn TM
Format:	article
Language:	EN
Published:	Dove Medical Press 2016
Subjects:	The peri-auricular percutaneous implantation of the Neuro-Stim System (NSS©) family of devices EAD© MFS© BRIDGE© (Innovative Health Solutions Versailles IN) is a non-opiate neuromodulation analgesic used for acute and chronic pain conditions. It is cleared as a minimal risk procedure by multiple governmental and institutional facilities. This retrospective report of findings will help quantify the incidence of clinically observed bleeding localized dermatitis and infections at the implantation sites of the electrode/needle arrays dermatitis at the site of the generator and patient syncope. A total of 1 207 devices each producing up to 16 percutaneous punctures for a total of 19 312 punctures were monitored for adverse effects based on retrospective chart audits conducted at 6 clinical facilities over a one-year period. Medical technology R855-855.5
Online Access:	https://doaj.org/article/3a767777e98a4c1a9c6046983d71db8f
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Minimal adverse effects profile following implantation of periauricular percutaneous electrical nerve field stimulators: a retrospective cohort study

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