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Neurophysiologic Testing and Monitoring
UnitedHealthcare® Commercial Medical Policy Neurophysiologic Testing and Monitoring Policy Number: 2021T0493Z Effective Date: January 1, 2021 Instructions for Use Table of Contents Page Community Plan Policy Coverage Rationale ........................................................................... 1 • Neurophysiologic Testing and Monitoring Applicable Codes .............................................................................. 2 Description of Services ..................................................................... 4 Medicare Advantage Coverage Summary Clinical Evidence ............................................................................... 6 • Neurophysiological Studies U.S. Food and Drug Administration ..............................................16 References .......................................................................................18 Policy History/Revision Information..............................................21 Instructions for Use .........................................................................22 Coverage Rationale Nerve Conduction Studies The following are proven and medically necessary: • Nerve conduction studies with or without late responses (e.g., F-wave and H-reflex tests) and neuromuscular junction testing when performed in conjunction with needle electromyography for any of the following known or suspected disorders: o Peripheral neuropathy/polyneuropathy (e.g., inherited, metabolic, traumatic, entrapment syndromes) o Plexopathy o Neuromuscular junction disorders (e.g., -
ANMC Specialty Clinic Services
Cardiology Dermatology Diabetes Endocrinology Ear, Nose and Throat (ENT) Gastroenterology General Medicine General Surgery HIV/Early Intervention Services Infectious Disease Liver Clinic Neurology Neurosurgery/Comprehensive Pain Management Oncology Ophthalmology Orthopedics Orthopedics – Back and Spine Podiatry Pulmonology Rheumatology Urology Cardiology • Cardiology • Adult transthoracic echocardiography • Ambulatory electrocardiology monitor interpretation • Cardioversion, electrical, elective • Central line placement and venous angiography • ECG interpretation, including signal average ECG • Infusion and management of Gp IIb/IIIa agents and thrombolytic agents and antithrombotic agents • Insertion and management of central venous catheters, pulmonary artery catheters, and arterial lines • Insertion and management of automatic implantable cardiac defibrillators • Insertion of permanent pacemaker, including single/dual chamber and biventricular • Interpretation of results of noninvasive testing relevant to arrhythmia diagnoses and treatment • Hemodynamic monitoring with balloon flotation devices • Non-invasive hemodynamic monitoring • Perform history and physical exam • Pericardiocentesis • Placement of temporary transvenous pacemaker • Pacemaker programming/reprogramming and interrogation • Stress echocardiography (exercise and pharmacologic stress) • Tilt table testing • Transcutaneous external pacemaker placement • Transthoracic 2D echocardiography, Doppler, and color flow Dermatology • Chemical face peels • Cryosurgery • Diagnosis -
What Is the Autonomic Nervous System?
J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.74.suppl_3.iii31 on 21 August 2003. Downloaded from AUTONOMIC DISEASES: CLINICAL FEATURES AND LABORATORY EVALUATION *iii31 Christopher J Mathias J Neurol Neurosurg Psychiatry 2003;74(Suppl III):iii31–iii41 he autonomic nervous system has a craniosacral parasympathetic and a thoracolumbar sym- pathetic pathway (fig 1) and supplies every organ in the body. It influences localised organ Tfunction and also integrated processes that control vital functions such as arterial blood pres- sure and body temperature. There are specific neurotransmitters in each system that influence ganglionic and post-ganglionic function (fig 2). The symptoms and signs of autonomic disease cover a wide spectrum (table 1) that vary depending upon the aetiology (tables 2 and 3). In some they are localised (table 4). Autonomic dis- ease can result in underactivity or overactivity. Sympathetic adrenergic failure causes orthostatic (postural) hypotension and in the male ejaculatory failure, while sympathetic cholinergic failure results in anhidrosis; parasympathetic failure causes dilated pupils, a fixed heart rate, a sluggish urinary bladder, an atonic large bowel and, in the male, erectile failure. With autonomic hyperac- tivity, the reverse occurs. In some disorders, particularly in neurally mediated syncope, there may be a combination of effects, with bradycardia caused by parasympathetic activity and hypotension resulting from withdrawal of sympathetic activity. The history is of particular importance in the consideration and recognition of autonomic disease, and in separating dysfunction that may result from non-autonomic disorders. CLINICAL FEATURES c copyright. General aspects Autonomic disease may present at any age group; at birth in familial dysautonomia (Riley-Day syndrome), in teenage years in vasovagal syncope, and between the ages of 30–50 years in familial amyloid polyneuropathy (FAP). -
New Insights in Lumbosacral Plexopathy
New Insights in Lumbosacral Plexopathy Kerry H. Levin, MD Gérard Said, MD, FRCP P. James B. Dyck, MD Suraj A. Muley, MD Kurt A. Jaeckle, MD 2006 COURSE C AANEM 53rd Annual Meeting Washington, DC Copyright © October 2006 American Association of Neuromuscular & Electrodiagnostic Medicine 2621 Superior Drive NW Rochester, MN 55901 PRINTED BY JOHNSON PRINTING COMPANY, INC. C-ii New Insights in Lumbosacral Plexopathy Faculty Kerry H. Levin, MD P. James. B. Dyck, MD Vice-Chairman Associate Professor Department of Neurology Department of Neurology Head Mayo Clinic Section of Neuromuscular Disease/Electromyography Rochester, Minnesota Cleveland Clinic Dr. Dyck received his medical degree from the University of Minnesota Cleveland, Ohio School of Medicine, performed an internship at Virginia Mason Hospital Dr. Levin received his bachelor of arts degree and his medical degree from in Seattle, Washington, and a residency at Barnes Hospital and Washington Johns Hopkins University in Baltimore, Maryland. He then performed University in Saint Louis, Missouri. He then performed fellowships at a residency in internal medicine at the University of Chicago Hospitals, the Mayo Clinic in peripheral nerve and electromyography. He is cur- where he later became the chief resident in neurology. He is currently Vice- rently Associate Professor of Neurology at the Mayo Clinic. Dr. Dyck is chairman of the Department of Neurology and Head of the Section of a member of several professional societies, including the AANEM, the Neuromuscular Disease/Electromyography at Cleveland Clinic. Dr. Levin American Academy of Neurology, the Peripheral Nerve Society, and the is also a professor of medicine at the Cleveland Clinic College of Medicine American Neurological Association. -
A Clinical Study on the Utility of Nerve Biopsy in Peripheral Neuropathy
A CLINICAL STUDY ON THE UTILITY OF NERVE BIOPSY IN PERIPHERAL NEUROPATHY Thesis submitted for the partial fulfilment for the requirement of the degree of DM Neurology DR. JITESH GOEL DM NEUROLOGY RESIDENT 2014–2016 DEPARTMENT OF NEUROLOGY SREE CHITRA TIRUNAL INSTITUTE FOR MEDICAL SCIENCES AND TECHNOLOGY, TRIVANDRUM, KERALA 695011 i DECLARATION I, Dr Jitesh hereby declare that the thesis “A CLINICAL STUDY ON THE UTILITY OF NERVE BIOPSY IN PERIPHERAL NEUROPATHY” was undertaken by me under the guidance and supervision of Dr MD Nair, Senior Professor and Head of Department, Department of Neurology at the Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram. Dr.Jitesh Goel Thiruvananthapuram Senior Resident Date: Dept. of Neurology SCTIMST Thiruvananthapuram ii CERTIFICATE This is to certify that the thesis titled “A CLINICAL STUDY ON THE UTILITY OF NERVE BIOPSY IN PERIPHERAL NEUROPATHY”, is the bonafide work of Dr Jitesh Goel, Senior Resident, DM Neurology and has been done under my direct guidance and supervision at the Sree Chitra Tirunal Institute for Medical Sciences and Technology, Thiruvananthapuram. He has shown keen interest in the research project and actively participated in all its phases. Thiruvananthapuram Dr MD Nair (Guide) Date: Senior Professor and Head of Department Department of Neurology, SCTIMST. Thiruvananthapuram iii CONTENTS Sl. No. Title Page No. 1 Introduction 1 2 Review of Literature 3 3 Aim of The Study 32 4 Materials And Methods 32 5 Results 34 6 Discussion 62 7 Conclusion 72 8 References 75 9 Annexures 84 IEC Approval Proforma iv INTRODUCTION Peripheral neuropathy is among the common disorders in patients attending neuromuscular clinic. -
Peripheral Nerve Endoscopy: a Cadaveric Study
THE UNIVERSITY OF NEW SOUTH WALES Thesis/Dissertation Sheet Surname or Family name: MOBBS First name: RALPH Other name/s: JASPER Abbreviation for degree: MASTER OF SURGERY School: ANATOMY Faculty: SURGERY Title: Peripheral Nerve Endoscopy: a cadaveric study. Peripheral nerve problems are common and encompass a wide ~pectrum of diseases, traumatic injuries and mass lesions. There have been few major technical advances in peripheral nerve surgery over the last three decades with exception of endoscopic carpal tunnel release, intraoperative nerve action potential recording and nerve grafting. Certain nerves in the upper and lower extremities are vulnerable to entrapment at specific anatomic locations by virtue of th ere being superficial, fixed in position, or coursing across a joint. Peripheral nerve surgeons often encounter patients who suffer fr :>m these entrapment syndromes, the most common being carpal tunnel syndrome, for which endoscopic techniques have been d;scussed in the Iiterature since the early 1980' s. Otherwise there have been few reports in the literature that discuss the utility of endoscopic surgery for the treatment of peripheral nerve problems. Endoscopy has however been alluded to as a possible future less invasive technique for the exploration and treatment of nerve pathologies. The aim of this cadaveric study is to illustrate that using standard equipment available in most hospitals, and using principles of subcutaneous fascial dissection and expansion, that a select range of peripheral nerve problems can be dealt with using endoscopy. A study using both embalmed cadaveric specimens and fresh cadavers v.as used to evaluate potential endoscopic techniques. A set of rules was developed to decide if a nerve exposure was possible. -
Peripheral Neurectomies: a Treatment Option for Trigeminal Neuralgia in Rural Practice
Published online: 2019-11-13 Original Article Peripheral neurectomies: A treatment option for trigeminal neuralgia in rural practice Fareedi Mukram Ali, Prasant MC, Deepak Pai1, Vinit A Aher, Sanjay Kar2, Safiya T Department of Oral and Maxillofacial Surgery, SMBT Dental College and Hospital, Amrutnagar, Sangamner, 1Consultant Oral & Maxillofacial Surgeon,Sangamner; 2KIMSU, Karad, Maharashtra, India ABSTRACT Background: Trigeminal neuralgia is a commonly diagnosed neurosensory disease of head, neck and face region, involving 5th cranial nerve. Carbamazepine is the first line drug if there is decrease in efficacy or tolerability of medication, surgery needs to be considered. Factors such as pain relief, recurrence rates, morbidity and mortality rates should be taken in to account while considering which technique to use. Peripheral neurectomy is a safe and effective procedure for elderly patients and in rural and remote centers where neurosurgical facilities are not available. It is also effective in those patients who are reluctant for major neurosurgical procedures. Although loss of sensation along the branches of trigeminal nerve and recurrence rate are associated with peripheral neurectomy, we consider it as the safe and effective procedure in rural practice, which can be done under local anesthesia.Aims: The aim of this prospective study is to evaluate the long term efficacy of peripheral neurectomy with and without the placement of stainless steel screws in the foramina and to calculate the mean remission period after peripheral neurectomies for different branches of trigeminal nerve. Setting and Design: The sample was divided into 2 groups by selecting randomly the patients, satisfying inclusion criteria. Both groups were operated under local anesthesia by regional nerve blocks. -
Use of Magnetic Resonance Neurography for Evaluating The
Original Article | Neuroimaging and Head & Neck eISSN 2005-8330 https://doi.org/10.3348/kjr.2019.0739 Korean J Radiol 2020;21(4):483-493 Use of Magnetic Resonance Neurography for Evaluating the Distribution and Patterns of Chronic Inflammatory Demyelinating Polyneuropathy Xiaoyun Su, PhD1, 2, Xiangquan Kong, PhD1, 2, Zuneng Lu, PhD3, Min Zhou, PhD1, 2, Jing Wang, PhD1, 2, Xiaoming Liu, MD1, 2, Xiangchuang Kong, MD1, 2, Huiting Zhang, PhD4, Chuansheng Zheng, PhD1, 2 1Department of Radiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China; 2Hubei Province Key Laboratory of Molecular Imaging, Wuhan, China; 3Department of Neurology, Renming Hospital of Wuhan University, Wuhan, China; 4MR Scientific Marketing, Siemens Healthineers, Shanghai, China Objective: To evaluate the distribution and characteristics of peripheral nerve abnormalities in chronic inflammatory demyelinating polyneuropathy (CIDP) using magnetic resonance neurography (MRN) and to examine the diagnostic efficiency. Materials and Methods: Thirty-one CIDP patients and 21 controls underwent MR scans. Three-dimensional sampling perfections with application-optimized contrasts using different flip-angle evolutions and T1-/T2- weighted turbo spin- echo sequences were performed for neurography of the brachial and lumbosacral (LS) plexus and cauda equina, respectively. Clinical data and scores of the inflammatory Rasch-built overall disability scale (I-RODS) in CIDP were obtained. Results: The bilateral extracranial vagus (n = 11), trigeminal (n = 12), and intercostal nerves (n = 10) were hypertrophic. Plexus hypertrophies were observed in the brachial plexus of 19 patients (61.3%) and in the LS plexus of 25 patients (80.6%). Patterns of hypertrophy included uniform hypertrophy (17 [54.8%] brachial plexuses and 21 [67.7%] LS plexuses), and multifocal fusiform hypertrophy (2 [6.5%] brachial plexuses and 4 [12.9%] LS plexuses) was present. -
Assessment and Treatment of Dizziness
J Neurol Neurosurg Psychiatry 2000;68:129–136 129 J Neurol Neurosurg Psychiatry: first published as 10.1136/jnnp.68.2.129 on 1 February 2000. Downloaded from EDITORIAL Assessment and treatment of dizziness “There can be few physicians so dedicated to their art that they do not experience a slight decline in spirits when they learn that their patient’s complaint is giddiness. This frequently means that after exhaustive enquiry it will still not be entirely clear what it is that the patient feels wrong and even less so why he feels it.” From W B Matthews. Practical Neurology. Oxford, Blackwell, 1963. These words are not quite as true today as when Bryan Convinced? One can be reasonably sure then that the Matthews wrote them nearly 40 years ago. There is now patient who is happy to move around while dizzy does not cause for cautious optimism. Recent clinical and scientific have vertigo, and that the patient who is dizzy all the time developments in the study of the vestibular system have and whose dizziness is not made better by keeping still, made the clinician’s task a little easier. We now know more either hasn’t got vertigo or hasn’t got the story right. Now about the diagnosis and even the treatment of conditions that we are sure that our patient has vertigo the next ques- such as benign paroxysmal positioning vertigo, Menière’s tion to answer is whether the vertigo attacks are spontane- disease, acute vestibular neuritis, migrainous vertigo, and ous or positional. But before we go on to answer that let us bilateral vestibulopathy than we did in 1963 and our consider briefly the diagnosis of other common paroxysmal purpose here is to introduce the clinician to facts worth disorders such as syncope, seizure, hypoglycaemia, and knowing. -
Neurolymphomatosis Presenting As Brachial Plexopathy with Involvement of Cranial Nerves
CASE REPORT Ann Clin Neurophysiol 2018;20(1):44-48 https://doi.org/10.14253/acn.2018.20.1.44 ANNALS OF CLINICAL NEUROPHYSIOLOGY Neurolymphomatosis presenting as brachial plexopathy with involvement of cranial nerves Hye Jung Lee1, Keun Soo Kim1, Pamela Song1, Jae-Jung Lee1, Jung-Joon Sung2, Kyomin Choi3, Bohyun Kim4, and Joong-Yang Cho1 1Department of Neurology, Ilsan Paik Hospital, Inje University College of Medicine, Goyang, Korea 2Department of Neurology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea 3Department of Neurology, Konkuk University Medical Center, Seoul, Korea 4Department of Pathology, Seoul National University Hospital, Seoul National University College of Medicine, Received: June 23, 2017 Seoul, Korea Revised: September 5, 2017 Accepted: September 25, 2017 Neurolymphomatosis (NL) is a rare disease characterized by lymphomatous invasion of the cranial or peripheral nerves by lymphoma. A high suspicion is important due to the various presenting symptoms mandating consideration of many differential diagnoses. We report a case of NL of the cranial nerves and plexus presenting as diplopia, facial palsy, and weakness of the upper and lower limbs in sequence. Key words: Neurolymphomatosis; Cranial nerves; Plexus Correspondence to Joong-Yang Cho Department of Neurology, Ilsan Paik Hospital, Inje University College of Medicine, 170 Juhwa-ro, Ilsanseo-gu, Neurolymphomatosis (NL) is defined as the infiltration of the peripheral nervous system Goyang 10380, Korea including cranial -
Peripheral Nerve Destruction for Pain Conditions (0525)
Medical Coverage Policy Effective Date ............................................. 3/15/2021 Next Review Date ....................................... 2/15/2022 Coverage Policy Number .................................. 0525 Peripheral Nerve Destruction for Pain Conditions Table of Contents Related Coverage Resources Overview .............................................................. 1 Headache and Occipital Neuralgia Treatment Coverage Policy ................................................... 1 Minimally Invasive Intradiscal/ Annular Procedures General Background ............................................ 2 and Trigger Point Injections Medicare Coverage Determinations .................. 17 Plantar Fasciitis Treatments Coding/Billing Information .................................. 17 Radiofrequency Joint Ablation/Denervation References ........................................................ 29 INSTRUCTIONS FOR USE The following Coverage Policy applies to health benefit plans administered by Cigna Companies. Certain Cigna Companies and/or lines of business only provide utilization review services to clients and do not make coverage determinations. References to standard benefit plan language and coverage determinations do not apply to those clients. Coverage Policies are intended to provide guidance in interpreting certain standard benefit plans administered by Cigna Companies. Please note, the terms of a customer’s particular benefit plan document [Group Service Agreement, Evidence of Coverage, Certificate of Coverage, Summary Plan -
Form 8-K AXOGEN, INC
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 Form 8-K Current Report Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934 Date of Report (Date of earliest event reported): February 22, 2021 AXOGEN, INC. (Exact Name of Registrant as Specified in Charter) Minnesota 001-36046 41-1301878 (State or Other Jurisdiction of (Commission File Number) (I.R.S. Employer Identification No.) Incorporation or Organization) 13631 Progress Boulevard, Suite 400 Alachua, Florida 32615 (Address of principal executive offices) (Zip Code) (386) 462-6800 (Registrant's telephone number, including area code) N/A (Former Name or Former Address, if Changed Since Last Report) Check the appropriate box if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below): Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e- 4(c)) Securities registered pursuant to Section 12(b) of the Act: Title of each class Trading Symbol(s) Name of exchange on which registered Common Stock, $0.01 par value AXGN The Nasdaq Stock Market Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).