Medical policy: Electromyography and Nerve Conduction Studies

Policy number: MP 2.063

Clinical benefit

  • Minimize safety risk or concern.
  • Minimize harmful or ineffective interventions.
  • Assure appropriate level of care.
  • Assure appropriate duration of service for interventions.
  • Assure that recommended medical prerequisites have been met.
  • Assure appropriate site of treatment or service.

Effective date: 9/1/2026

Policy

Electrodiagnostic assessment, consisting of electromyography (EMG), nerve conduction study (NCS), and related measures, may be considered medically necessary as an adjunct to history, physical exam (PE), and imaging studies when the following criteria are met:

  • Signs and symptoms of peripheral neuropathy and/or myopathy are present; and
  • Definitive diagnosis cannot be made by PE and imaging studies alone; and
  • Work-up for one or more of the following categories of disease is indicated (see Policy Guidelines section):
    • Compressive neuropathies
    • Nerve root compression
    • Traumatic nerve injuries
    • Generalized and focal neuropathies/myopathies
    • Plexopathies
    • Motor neuron diseases
    • Neuromuscular junction disorders.

A repeat electrodiagnostic assessment may be considered medically necessary when at least one of the following criteria have been met:

  • Development of new symptoms or signs suggesting a second diagnosis in an individual who has received an initial diagnosis; or
  • Interim progression of disease following an initial test that was inconclusive, such that a repeat test is likely to elicit additional findings; or
  • Unexpected change(s) in the course of disease or response to treatment, suggesting that the initial diagnosis may be incorrect, and that reexamination is indicated.

Electrodiagnostic assessment, consisting of EMG, NCS, and related measures, is investigational when the above criteria are not met, including but not limited to, the following situations:

  • Screening of asymptomatic individuals
  • Serial assessments to evaluate progression of disease in an individual with a previously diagnosed neuropathy or myopathy
  • Evaluation of treatment response in an individual with previously diagnosed neuropathy or myopathy
  • Evaluation of severity of disease in an individual with previously diagnosed neuropathy or myopathy

There is insufficient evidence to support a general conclusion concerning the health outcomes or benefits associated with testing for these indications.

Automatic nerve conduction tests are considered investigational as there is insufficient evidence to support a general conclusion concerning the health outcomes or benefits associated with this procedure.

Policy guidelines

The following list gives specific diagnoses, according to categories of testing listed in the policy statement, for which EMG/NCS generally provides useful information in confirming or excluding the diagnosis, above that provided by clinical examination and imaging alone. The list includes the most common diagnoses for testing, but is not exhaustive. There may also be other less common disorders for which EMG/NCS provides useful diagnostic information.

  • Compressive neuropathies
    • Carpal tunnel syndrome
    • Ulnar nerve entrapment
    • Thoracic outlet syndrome
    • Tarsal tunnel syndrome
    • Other peripheral nerve entrapments
  • Nerve root compression (when PE and magnetic resonance imaging [MRI] are inconclusive)
    • Cervical nerve root compression
    • Thoracic nerve root compression
    • Lumbosacral nerve root compression
  • Traumatic nerve injuries
  • Generalized and focal polyneuropathies
    • Diabetic neuropathy
    • Uremic neuropathy
    • Alcohol-related neuropathy
    • Hereditary neuropathies
      • Charcot-Marie-Tooth
      • Other hereditary neuropathies
    • Demyelinating polyneuropathies
      • Guillain-Barré syndrome (acute)
      • Chronic idiopathic demyelinating polyneuropathy
  • Generalized myopathies
    • Polymyositis
    • Dermatomyositis
    • Muscular dystrophies
  • Plexopathies
    • Cervical plexopathy
    • Brachial plexopathy
    • Lumbosacral plexopathy
  • Motor neuron diseases
    • Amyotrophic lateral sclerosis
    • Progressive muscular atrophy
    • Progressive bulbar palsy
    • Pseudobulbar palsy
    • Primary lateral sclerosis
  • Neuromuscular junction disorders
    • Myasthenia gravis
    • Myasthenic syndrome
    • Lambert-Eaton syndrome

The following recommendations on the number of repeat services are reproduced from the American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM) position statement (2023). These estimates do not represent absolute maximums for all individuals; they are defined by AANEM as being sufficient to make a diagnosis in at least 90% of individuals with that particular diagnosis. Therefore, there may be a small percentage of cases that require a greater number of tests than specified in table PG1.

Table PG1. Recommended Maximum Number of Electrodiagnostic Studies for Specific Diagnoses

Indication
Needle EMG
NCSs
Other studies
No. of tests
No. of tests
RNS testing

Carpal tunnel (unilateral)

1

7

0

Carpal tunnel (bilateral)

2

10

0

Radiculopathy

2

7

0

Mononeuropathy

1

8

0

Polyneuropathy or mononeuropathy multiplex

3

10

0

Myopathy

2

4

2

Motor neuropathy (e.g., amyotrophic lateral sclerosis)

4

6

2

Plexopathy

2

12

0

Neuromuscular junction

2

2

3

Tarsal tunnel syndrome (unilateral)

1

8

0

Tarsal tunnel syndrome (bilateral)

2

11

0

Weakness, fatigue, cramps, or twitching (focal)

2

7

2

Weakness, fatigue, cramps, or twitching (general)

4

8

2

Pain, numbness, or tingling (unilateral)

1

9

0

Pain, numbness, or tingling (bilateral)

2

12

0

Adapted from American Association of Electrodiagnostic Medicine (2023).

EMG: electromyography; NCS: nerve conduction study; RNS: repetitive nerve stimulation.

The American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) position statement (2023) also included minimum standards for a lab performing electrodiagnostic evaluation:

  • Tests should be medically indicated.
  • The tests should be performed using equipment that provides assessment of all parameters of the recorded signals. Equipment designed for screening purposes is not acceptable.
  • The number of tests performed should be the minimum needed to establish an accurate diagnosis.
  • The NCS should be performed by a physician or by a trained technician under the direct supervision of a physician.
  • A trained physician must perform the needle EMG exam.
  • One physician should perform and supervise all components of the electrodiagnostic testing and all testing should occur on the same date of service.
  • The NCS and needle EMG exam results should be integrated into a unifying report and diagnostic impression.

Cross-references:

  • MP 2.096 Electromyography (EMG) (Needle and Non-Needle) of the Anal or Urethral Sphincter
  • MP 2.097 Paraspinal Surface Electromyography to Evaluate and Monitor Back Pain

Product variations

This policy is only applicable to certain programs and products administered by Capital Blue Cross and subject to benefit variations. Please see additional information below.

FEP PPO - Refer to FEP Medical Policy Manual.

Description/Background

Electrodiagnostic Assessment

Electromyography (EMG) and nerve conduction study (NCS) are used as adjuncts to clinical evaluation of myopathy and peripheral neuropathy. These tests intend to evaluate the integrity and electrical function of muscles and peripheral nerves. They are performed when there is clinical suspicion for a myopathic or neuropathic process and when clinical examination and standard laboratory testing cannot make a definitive diagnosis.

Test results do not generally provide a specific diagnosis. Rather, they provide additional information that assists physicians in characterizing a clinical syndrome. EMG/NCS may be useful when there is no clear etiology when symptoms are severe or rapidly progressing, or when symptoms are atypical (e.g., asymmetrical, acute onset, or appearing to be autonomic).

According to the American Association of Neuromuscular and Electrodiagnostic Medicine (2023), electrodiagnostic assessment has the following goals:

  1. “Identify normal and abnormal nerve, muscle, motor or sensory neuron, and NMJ [neuromuscular junction] functioning.
  2. Localize region(s) of pathology.
  3. Characterize the pathology.
  4. Determine the distribution of abnormalities.
  5. Determine the severity of abnormalities.
  6. Estimate the chronology of the disease.
  7. Determine the progression and/or recovery from abnormal function.
  8. Aid in diagnosis and prognosis of disease.
  9. Aid in selecting treatment options.
  10. Aid in following response to treatment by providing objective evidence of change in NM [neuromuscular] function.
  11. Localize correct locations for injections of intramuscular agents….”

Components of the electrodiagnostic exam may include needle EMG, NCS, repetitive nerve stimulation study, somatosensory evoked potentials, and blink reflexes.

Electromyography

Needle EMG

An EMG needle electrode is inserted into selected muscles, chosen by the examining physician depending on the differential diagnosis and other information available during the exam. The response of the muscle to electrical stimulation is recorded. Three components are evaluated: observation at rest, action potential with minimal voluntary contraction, and action potential with maximum contraction.

Single Fiber EMG

In single fiber EMG, a needle electrode records the response of a single muscle fiber. This test can evaluate “jitter,” which is defined as the variability in time between activation of the nerve and generation of the muscle action potential. Single fiber EMG can also measure fiber density, which is defined as the mean number of muscle fibers for 1 motor unit.

Nerve Conduction Study

In NCS, both motor and sensory nerve conduction are assessed. For motor conduction, electrical stimuli are delivered along various points on the nerve, and the electrical response is recorded from the appropriate muscle. For sensory conduction, electrical stimuli are delivered to 1 point on the nerve and the response recorded at a distal point on the nerve. Parameters recorded include velocity, amplitude, latency, and configuration.

Late Wave Responses

Late waves are a complement to the basic NCS and evaluate the functioning of the proximal segment of peripheral nerves, such as the nerve root and the anterior horn cells. There are 2 types of late responses: the H-reflex and the F wave.

The H-reflex is elicited by stimulating the posterior tibial nerve and measuring the response in the gastrocnemius muscle. It is analogous to the ankle reflex and can be prolonged by radiculopathy at S1 or by peripheral neuropathy.

The F wave is assessed by supramaximal stimulation of the distal nerve and can help estimate the conduction velocity in the proximal portion of the nerve. This will provide information on the presence of proximal nerve abnormalities, such as radiculopathy or plexopathy.

Repetitive Nerve Stimulation

Repetitive nerve stimulation studies evaluate the integrity and function of the neuromuscular junction. The test involves stimulating a nerve repetitively at variable rates and recording the response of the corresponding muscle(s). Disorders of the neuromuscular junction will show a diminished muscular response to repetitive stimulation.

Somatosensory Evoked Potentials

Somatosensory evoked potentials evaluate nerve conduction in various sensory fibers of both the peripheral and central nervous system and test the integrity and function of these nerve pathways. They are typically used to assess nerve conduction in the spinal cord and other central pathways that cannot be assessed by standard NCS.

Blink Reflexes

The blink reflexes, which are analogs of the corneal reflex, are evaluated by stimulating the orbicularis orbis muscle at the lower eyelid. They are used to localize lesions in the fifth or seventh cranial nerves.

Differential Diagnosis

The specific components of an individual test are not standardized. Rather, a differential diagnosis is developed by the treating physician, and/or the clinician performing the test, and the specific components of the exam are determined by the disorders being considered in the differential. Also, the differential diagnosis may be modified during the exam to reflect initial findings, and this may also influence the specific components included in the final analysis.

Automated Point-of-Care Nerve Conduction Tests

Portable devices have been developed to provide point-of-care (POC) nerve conduction studies (NCSs). These devices have computational algorithms that can drive stimulus delivery, measure and analyze the response, and report study results. Automated nerve conduction could be used in various settings, including primary care, without the need for specialized training or equipment.

Electrodiagnostic Testing

Nerve conduction studies (NCSs) and needle electromyography (EMG), when properly performed by a trained practitioner, are considered the criterion standard of electrodiagnostic testing for the evaluation of focal and generalized disorders of peripheral nerves. However, the need for specialized equipment and personnel may limit the availability of electrodiagnostic testing for some patients.

Carpal Tunnel Syndrome

Carpal tunnel syndrome is a pressure-induced entrapment neuropathy of the median nerve as it passes through the carpal tunnel, resulting in sensorimotor disturbances. This syndrome is defined by its characteristic clinical symptoms, which may include pain, subjective feelings of swelling, and nocturnal paresthesia.

Diagnosis

A variety of simple diagnostic tools are available, and a positive response to conservative management (steroid injection, splints, modification of activity) can confirm the clinical diagnosis. Electrodiagnostic studies may also be used to confirm the presence or absence of median neuropathy at the wrist, assess the severity of the neuropathy, and assess associated diagnoses. Nerve conduction is typically assessed before the surgical release of the carpal tunnel, but the use of EMG in the diagnosis of carpal tunnel syndrome is controversial. One proposed use of automated nerve conduction devices is to assist in the diagnosis of carpal tunnel syndrome.

Lumbosacral Radiculopathy

Electrodiagnostic studies are useful in the evaluation of lumbosacral radiculopathy in the presence of disabling symptoms of radiculopathy or neuromuscular weakness. These tests are most commonly considered in patients with persistent disabling symptoms when neuroimaging findings are inconsistent with clinical presentation. Comparisons of automated point-of-care (POC) NCSs with EMGs and standardized NCSs have been evaluated as alternative electrodiagnostic tools.

Peripheral Neuropathy

Peripheral neuropathy is relatively common in patients with diabetes, and the diagnosis is often made clinically through physical examination. Diabetic peripheral neuropathy can lead to morbidity including pain, foot deformity, and foot ulceration.

Diagnosis

Clinical practice guidelines have recommended using simple sensory tools such as the 10-g Semmes-Weinstein monofilament or the 128-Hz vibration tuning fork for diagnosis. These simple tests predict the presence of neuropathy defined by electrophysiologic criteria with a high level of accuracy. Electrophysiologic testing may be used in research studies and may be required in cases with an atypical presentation. POC nerve conduction testing has been proposed as an alternative to standard electrodiagnostic methods for the diagnosis of peripheral neuropathy and, in particular, for detecting neuropathy in patients with diabetes.

Normative Values

NeuroMetrix (2009) published reference ranges for key nerve conduction parameters in healthy subjects. Data analyzed were pooled from 5 studies, including from 92 to 848 healthy subjects with data on the median, ulnar, peroneal, tibial, and sural nerves. Subject age and height were found to affect the parameters. In addition to providing reference ranges for clinicians to use (providing that NCS techniques are consistent with those described in the article), the authors stated that clinicians could use the same method to develop their own reference ranges. At this time, the proposed reference ranges have not been validated in a clinical patient population.

Due to the lack of uniform standards in nerve conduction testing in the United States, the American Association of Neuromuscular and Electrodiagnostic Medicine (AANEM) identified 7 criteria that would identify high-quality NCS articles that would be appropriate for using as referent standards (2016). AANEM identified normative criteria for nerve conduction velocity tests based on a review of high-quality published studies (see Table 1). In March 2017, the American Academy of Neurology affirmed AANEM’s recommendations.

Table 1. Criteria for Evaluating Published Sources for Normative Standards

Criteria
Description

Year published

Published during or after 1990, written in or translated from other languages into English

Sample size

>100 normal subjects

Subjects

Inclusion and exclusion criteria must be methodologically sound and reflect a true “normal” group of asymptomatic individuals

Testing factors

  • Use of digital electromyographic equipment
  • Methods of temperature control stated
  • Testing techniques with electrode placement and distances between stimulating and recording electrodes specified
  • Filter settings specified
  • Screen display parameters (milliseconds per division, microvolts/millivolts per division) specified

Age

Wide distribution of subject ages >18 years with adequate sampling of the elderly

Statistical analyses

  • Data distribution should be described, and appropriate statistical methods used to account for non-Gaussian distributions
  • Cutoff values expressed and derived as percentiles of the distribution (the preferred method)
  • Percentage of subjects who have an absent response should be reported

Data presentation

Reference values and cutoff points for NCS parameters clearly presented in a useful format

Adapted from Dillingham et al (2016).

Chen (2016) published reference values for upper and lower NCSs in adults, as a companion study to the Dillingham et al (2016) report (above), to address the need for greater standardization in the field of electrodiagnostic medicine. Using the consensus-based criteria developed by AANEM, a comprehensive literature search was conducted for 11 routinely performed sensory and motor NCS from 1990 to 2012. Over 7500 articles were found, but after review, a single acceptable study meeting all criteria was identified for the 11 nerves. Reviewers determined there were multifactorial reasons that so few studies met the criteria. Large-scale normative studies are time intensive, requiring significant resources and cost. Data from many studies did not address the non-Gaussian distribution of NCS parameters and often derived cutoff values using the mean and standard deviations rather than percentiles.

Regulatory status

EMG/NCS measure nerve and muscle function and may be indicated when evaluating limb pain, weakness related to possible spinal nerve compression, or other neurologic injury or disorder. A number of electromyographic devices have received marketing clearance by the U.S. Food and Drug Administration (FDA). Several devices are listed in Table 1.

Table 1. Electromyographic Devices Approved by FDA

Device
Manufacturer
FDA clearance
510(k) No.
FDA product code

NuVasive® NVM5 System

NuVasive

2011

K112718

ETN

CERSR® Electromyography System

SpineMatrix

2011

K110048

IKN

CareFusion Nicolet® EDX

CareFusion 209

2012

K120979

GWF

Physical Monitoring Registration Unit-S (PMRU-S)

Oktx

2013

K123902

IKN

MyoVision 3G Wirefree™ System

Precision Biometrics

2013

K123399

IKN

Neuro Omega™ System

Alpha Omega Engineering

2013

K123796

GZL

EPAD™

SafeOp Surgical

2014

K132616

GWF

Sierra Summit, Sierra Ascent

Cadwell Industries

2017

K162383

IKN, GWF

EPAD 2™

SafeOp Surgical

2019

K182542

GWF, IKN

Mediracer® NCS

Mediracer

2019

K190536

JXE, IKN

Mega-TMS™

Soterix Medical, Inc.

2021

K192823

GWF, JXE

SafeOp 3: Neural Informatix System

Alphatec Spine, Inc

2024

K234092

IKN, GWF, GXZ, GXY, ETN, PDQ

FDA: Food and Drug Administration

Multiple devices have been cleared for POC neural conduction testing. For example, in 1986, Neurometer® CPT/C® (Neurotron®) was cleared for marketing by the U.S. Food and Drug Administration (FDA) through the 510(k) process (K853608). The device evaluates and documents sensory nerve impairments at cutaneous or mucosal sites. The evaluation detects and quantifies hyperesthesia in early stages of progressive neuropathy and hypoesthesia in more advanced conditions.

In 1998 NC-stat® (NeuroMetrix) was cleared by FDA through the 510(k) process (K982359). NC-stat® is intended “to measure neuromuscular signals that are useful in diagnosing and evaluating systemic and entrapment neuropathies.” This version is no longer commercially available. It is the predicate device for the NC-stat DPNCheck® (K041320), cleared in 2004, and the NeuroMetrix Advance (K070109), cleared in 2008. The NC-stat DPNCheck device measures the sural nerve conduction velocity and sensory nerve action potential amplitude. It is a handheld device with an infrared thermometer, non-invasive electrical stimulation probes, and a single-use biosensor for each test. NC-stat DPNCheck is designed specifically for NCS of the sural nerve in the assessment of diabetic peripheral neuropathy. The NeuroMetrix ADVANCE is a POC test that can be used to perform needle EMG in addition to surface electrodes for the performance of NCSs. If the needle EMG module is used, then the device is also intended to measure signals useful in evaluating disorders of muscles.

On January 23, 2017, Cadwell Sierra Summit and Cadwell Sierra Ascent (Cadwell Industries) was cleared for marketing by FDA through the 510(k) process (K162383). There are portable laptop versions and a desktop application with a handheld device. The system is used for acquisition, display, storage, transmission, analysis, and reporting of electrophysiologic and environmental data including EMG, NCS, evoked potentials, and autonomic responses (RR interval variability). The Cadwell Sierra Summit is used to detect the physiologic function of the nervous system, and to support the diagnosis of neuromuscular diseases or conditions.

FDA product code: JXE.

Table 2. Select FDA-Cleared Devices for Neural Conduction Testing

Device
Manufacturer
Date cleared
510(k)
Indications

Axon II™

PainDX

1998

K980866

Part of a routine neurologic exam or screening procedure to detect peripheral neuropathy, which may be caused by various pathologic conditions or exposures to toxic substances

Brevio®

Neurotron Medical

2001

K012069

To measure nerve response latency and amplitude in the diagnosis and monitoring of peripheral neuropathies

NC-stat®, NC-stat DPNCheck

NeuroMetrix

2004

K041320

To stimulate and measure neuromuscular signals in diagnosing and evaluating systemic and entrapment neuropathies. Added the sural biosensor for use in diagnosing neuropathies affecting the sural nerve.

NC-stat®

NeuroMetrix

2006

K060584

Addition of the modified median motor-sensory biosensor to stimulate and measure neuromuscular signals useful in diagnosing and evaluating systemic and entrapment neuropathies

NeuroMetrix Advance™

NeuroMetrix

2008

K070109

To measure neuromuscular signals useful as an aid in diagnosing and evaluating patients suspected of having focal or systemic neuropathies. If the elective needle EMG module is used, then the device is also intended to measure signals useful as an aid in evaluating disorders of muscles.

XLTEK NEUROPATH

Excel Tech

2006

K053058

To stimulate and measure neuromuscular signals useful in diagnosing and evaluating systemic and entrapment neuropathies

Rationale

Summary of evidence

For individuals with suspected peripheral neuropathy or myopathy who receive electrodiagnostic assessment including EMG and NCS, the evidence includes small observational studies on a few diagnoses, such as carpal tunnel syndrome, radiculopathy, and myopathy. Relevant outcomes are test accuracy, symptoms, functional outcomes, and quality of life. Because electrodiagnostic assessment is considered the criterion standard for evaluating the electrical function of peripheral nerves and muscles, there is no true alternative reference standard against which the sensitivity and specificity of particular EMG/NCS abnormalities for particular clinical disorders can be calculated. Different studies have used different reference standards, such as EMG/NCS measures of healthy individuals or clinical examination results. In general, these tests are considered more specific than sensitive, and normal results do not rule out disease. The limited evidence has shown a wide range of sensitivities, which are often less than 50%. The specificity is expected to be considerably higher, but the data are insufficient to provide precise estimates of either sensitivity or specificity. The evidence is insufficient to determine the effects of the technology on health outcomes.

For individuals who have entrapment carpal tunnel syndrome who received automated POC NCSs, the evidence includes studies on the diagnostic accuracy and clinical outcomes from industry-sponsored trials, nonrandomized trials, and registry data. Relevant outcomes are test accuracy and validity, symptoms, and functional outcomes. Four RCTs have reported on the diagnostic accuracy of automated POC nerve conduction testing for carpal tunnel syndrome. Sensitivity testing has suggested there could be diagnostic value in detecting carpal tunnel syndrome; specificity testing was inconsistent across trials. No reference ranges were validated, and normative values were not defined in these studies. No validation testing by trained medical assistants vs trained specialist was reported in the studies. The evidence on clinical outcomes is limited to a single nonrandomized clinical trial and NeuroMetrix registry data. Neither reported health outcomes assessing patient symptoms or changes in functional status. The evidence is insufficient to determine the effects of the technology on health outcomes.

For individuals with lumbosacral radiculopathy who received automated POC NCSs, the evidence includes industry-sponsored trials and a nonrandomized study of diagnostic accuracy. Relevant outcomes are test accuracy and validity, symptoms, and functional outcomes. The evidence on the diagnostic accuracy of POC NCS in this population has shown variable test results across reported trials. No normative values were defined. Weaknesses of the studies included lack of applicable or valid reference ranges for testing, and variable test results validating or confirming pathology. The results of the 2 studies on diagnostic performance were inconclusive, with high false-positive results in a single trial. No trials on health outcomes assessing patient symptoms or changes in functional status were identified. The evidence is insufficient to determine the effects of the technology on health outcomes.

For individuals with diabetic peripheral neuropathy who received automated POC NCSs, the evidence includes industry-sponsored observational trials and nonrandomized studies on the diagnostic accuracy. Relevant outcomes are test accuracy and validity, symptoms, and functional outcomes. Of 3 studies reporting evidence on diagnostic accuracy, 2 used NC-stat DPNCheck. Sensitivity testing has suggested there could be diagnostic value in detecting diabetic peripheral neuropathy in symptomatic patients; the evidence to detect patients who are suspected of disease but who have mild symptoms was inconsistent. No reference ranges were validated, and normative values were not defined in 2 of the 3 studies. No validation testing by trained medical assistants vs trained specialist was reported in the studies. No trials on health outcomes assessing patient symptoms or changes in functional status were identified. The evidence is insufficient to determine the effects of the technology on health outcomes.

Definitions

510(k) is a premarketing submission made to FDA to demonstrate that the device to be marketed is as safe and effective, that is, substantially equivalent (SE), to a legally marketed device that is not subject to premarket approval (PMA). Applicants must compare their 510(k) device to one or more similar devices currently on the U.S. market and make and support their substantial equivalency claims.

Neuropathy refers to any disease of the nerves.

Peripheral refers to something that occurs away from the center.

Disclaimer

Capital Blue Cross’ medical policies are used to determine coverage for specific medical technologies, procedures, equipment, and services. These medical policies do not constitute medical advice and are subject to change as permitted by law or applicable clinical evidence from independent treatment guidelines. Treating providers are solely responsible for medical advice and treatment of members. These policies are not a guarantee of coverage or payment. Payment of claims is subject to a determination regarding the member’s benefit program and eligibility on the date of service, and a determination that the services are medically necessary and appropriate. Final processing of a claim is based upon the terms of contract that applies to the members’ benefit program, including benefit limitations and exclusions. If a provider or a member has a question concerning this medical policy, please contact Capital Blue Cross’ Provider Services or Member Services.

Coding information

Note: This list of codes may not be all-inclusive, and codes are subject to change at any time. The identification of a code in this section does not denote coverage as coverage is determined by the terms of member benefit information. In addition, not all covered services are eligible for separate reimbursement.

Investigational; therefore, not covered:

Procedure codes

95905

95999

G0255

 

 

Covered when medically necessary:

Procedure codes

92265

95860

95861

95863

95864

95865

95866

95867

95868

95869

95870

95872

95874

95885

95886

95887

95907

95908

95909

95910

95911

95912

95913

95937

 

ICD-10-CM diagnosis code
Description

A14.139A

Anterior cord syndrome at unspecified level of cervical spinal cord, initial encounter

A52.15

Late syphilitic neuropathy

E08.41

Diabetes mellitus due to underlying condition with diabetic mononeuropathy

E08.42

Diabetes mellitus due to underlying condition with diabetic polyneuropathy

E08.43

Diabetes mellitus due to underlying condition with diabetic autonomic (poly)neuropathy

E08.44

Diabetes mellitus due to underlying condition with diabetic amyotrophy

E08.49

Diabetes mellitus due to underlying condition with other diabetic neurological complication

E08.610

Diabetes mellitus due to underlying condition with diabetic neuropathic arthropathy

E09.41

Drug or chemical induced diabetes mellitus with neurological complications with diabetic mononeuropathy

E09.42

Drug or chemical induced diabetes mellitus with neurological complications with diabetic polyneuropathy

E09.43

Drug or chemical induced diabetes mellitus with neurological complications with diabetic autonomic (poly)neuropathy

E09.44

Drug or chemical induced diabetes mellitus with neurological complications with diabetic amyotrophy

E09.49

Drug or chemical induced diabetes mellitus with neurological complications with other diabetic neurological complication

E09.610

Drug or chemical induced diabetes mellitus with diabetic neuropathic arthropathy

E10.40

Type 1 diabetes mellitus with diabetic neuropathy, unspecified

E10.41

Type 1 diabetes mellitus with diabetic mononeuropathy

E10.42

Type 1 diabetes mellitus with diabetic polyneuropathy

E10.43

Type 1 diabetes mellitus with diabetic autonomic (poly)neuropathy

E10.44

Type 1 diabetes mellitus with diabetic amyotrophy

E10.49

Type 1 diabetes mellitus with other diabetic neurological complication

E10.610

Type 1 diabetes mellitus with diabetic neuropathic arthropathy

E11.40

Type 2 diabetes mellitus with diabetic neuropathy, unspecified

E11.41

Type 2 diabetes mellitus with diabetic mononeuropathy

E11.42

Type 2 diabetes mellitus with diabetic polyneuropathy

E11.43

Type 2 diabetes mellitus with diabetic autonomic (poly)neuropathy

E11.44

Type 2 diabetes mellitus with diabetic amyotrophy

E11.49

Type 2 diabetes mellitus with other diabetic neurological complication

E11.610

Type 2 diabetes mellitus with diabetic neuropathic arthropathy

E13.41

Other specified diabetes mellitus with diabetic mononeuropathy

E13.42

Other specified diabetes mellitus with diabetic polyneuropathy

E13.43

Other specified diabetes mellitus with diabetic autonomic (poly)neuropathy

E13.44

Other specified diabetes mellitus with diabetic amyotrophy

E13.49

Other specified diabetes mellitus with other diabetic neurological complication

E13.610

Other specified diabetes mellitus with diabetic neuropathic arthropathy

G12.20

Motor neuron disease, unspecified

G12.21

Amyotrophic lateral sclerosis

G12.22

Progressive bulbar palsy

G12.23

Primary lateral sclerosis

G12.24

Familial motor neuron disease

G12.25

Progressive spinal muscle atrophy

G12.29

Other motor neuron disease

G12.8

Other spinal muscular atrophies and related syndromes

G12.9

Spinal muscular atrophy, unspecified

G13.0

Paraneoplastic neuromyopathy and neuropathy

G13.1

Other systemic atrophy primarily affecting central nervous system in neoplastic disease

G54.0

Brachial plexus disorders

G54.1

Lumbosacral plexus disorders

G54.2

Cervical root disorders, not elsewhere classified

G54.3

Thoracic root disorders, not elsewhere classified

G54.4

Lumbosacral root disorders, not elsewhere classified

G54.5

Neuralgic amyotrophy

G54.6

Phantom limb syndrome with pain

G54.7

Phantom limb syndrome without pain

G54.8

Other nerve root and plexus disorders

G54.9

Nerve root and plexus disorder, unspecified

G55

Nerve root and plexus compressions in diseases classified elsewhere

G56.00

Carpal tunnel syndrome, unspecified upper limb

G56.01

Carpal tunnel syndrome, right upper limb

G56.02

Carpal tunnel syndrome, left upper limb

G56.03

Carpal tunnel syndrome, bilateral upper limbs

G56.10

Other lesions of median nerve, unspecified upper limb

G56.11

Other lesions of median nerve, right upper limb

G56.12

Other lesions of median nerve, left upper limb

G56.13

Other lesions of median nerve, bilateral upper limbs

G56.20

Lesion of ulnar nerve, unspecified upper limb

G56.21

Lesion of ulnar nerve, right upper limb

G56.22

Lesion of ulnar nerve, left upper limb

G56.23

Lesion of ulnar nerve, bilateral upper limbs

G56.31

Lesion of radial nerve, right upper limb

G56.32

Lesion of radial nerve, left upper limb

G56.33

Lesion of radial nerve, bilateral upper limbs

G56.41

Causalgia of right upper limb

G56.42

Causalgia of left upper limb

G56.43

Causalgia of bilateral upper limbs

G56.81

Other specified mononeuropathies of right upper limb

G56.82

Other specified mononeuropathies of left upper limb

G56.83

Other specified mononeuropathies of bilateral upper limbs

G56.91

Unspecified mononeuropathy of right upper limb

G56.92

Unspecified mononeuropathy of left upper limb

G56.93

Unspecified mononeuropathy of bilateral upper limbs

G57.00

Lesion of sciatic nerve, unspecified lower limb

G57.01

Lesion of sciatic nerve, right lower limb

G57.02

Lesion of sciatic nerve, left lower limb

G57.03

Lesion of sciatic nerve, bilateral lower limbs

G57.10

Meralgia paresthetica, unspecified lower limb

G57.11

Meralgia paresthetica, right lower limb

G57.12

Meralgia paresthetica, left lower limb

G57.13

Meralgia paresthetica, bilateral lower limbs

G57.20

Lesion of femoral nerve, unspecified lower limb

G57.21

Lesion of femoral nerve, right lower limb

G57.22

Lesion of femoral nerve, left lower limb

G57.23

Lesion of femoral nerve, bilateral lower limbs

G57.30

Lesion of lateral popliteal nerve, unspecified lower limb

G57.31

Lesion of lateral popliteal nerve, right lower limb

G57.32

Lesion of lateral popliteal nerve, left lower limb

G57.33

Lesion of lateral popliteal nerve, bilateral lower limbs

G57.40

Lesion of medial popliteal nerve, unspecified lower limb

G57.41

Lesion of medial popliteal nerve, right lower limb

G57.42

Lesion of medial popliteal nerve, left lower limb

G57.43

Lesion of medial popliteal nerve, bilateral lower limbs

G57.50

Tarsal tunnel syndrome, unspecified lower limb

G57.51

Tarsal tunnel syndrome, right lower limb

G57.52

Tarsal tunnel syndrome, left lower limb

G57.53

Tarsal tunnel syndrome, bilateral lower limbs

G57.60

Lesion of plantar nerve, unspecified lower limb

G57.61

Lesion of plantar nerve, right lower limb

G57.62

Lesion of plantar nerve, left lower limb

G57.63

Lesion of plantar nerve, bilateral lower limbs

G57.70

Causalgia of unspecified lower limb

G57.71

Causalgia of right lower limb

G57.72

Causalgia of left lower limb

G57.73

Causalgia of bilateral lower limbs

G57.80

Other specified mononeuropathies of unspecified lower limb

G57.81

Other specified mononeuropathies of right lower limb

G57.82

Other specified mononeuropathies of left lower limb

G57.83

Other specified mononeuropathies of bilateral lower limbs

G57.90

Unspecified mononeuropathy of unspecified lower limb

G57.91

Unspecified mononeuropathy of right lower limb

G57.92

Unspecified mononeuropathy of left lower limb

G57.93

Unspecified mononeuropathy of bilateral lower limbs

G58.0

Intercostal neuropathy

G58.7

Mononeuritis multiplex

G58.9

Mononeuropathy, unspecified

G59

Mononeuropathy in diseases classified elsewhere

G60.0

Hereditary motor and sensory neuropathy

G60.1

Refsum's disease

G60.2

Neuropathy in association with hereditary ataxia

G60.3

Idiopathic progressive neuropathy

G60.8

Other hereditary and idiopathic neuropathies

G60.9

Hereditary and idiopathic neuropathy, unspecified

G61.0

Guillain-Barre syndrome

G61.1

Serum neuropathy

G61.81

Chronic inflammatory demyelinating polyneuritis

G61.82

Multifocal motor neuropathy

G61.89

Other inflammatory polyneuropathies

G61.9

Inflammatory polyneuropathy, unspecified

G62.0

Drug-induced polyneuropathy

G62.1

Alcoholic polyneuropathy

G62.2

Polyneuropathy due to other toxic agents

G62.81

Critical illness polyneuropathy

G62.82

Radiation-induced polyneuropathy

G62.89

Other specified polyneuropathies

G62.9

Polyneuropathy, unspecified

G63

Polyneuropathy in diseases classified elsewhere

G64

Other disorders of peripheral nervous system

G70.00

Myasthenia gravis without (acute) exacerbation

G70.01

Myasthenia gravis with (acute) exacerbation

G70.1

Toxic myoneural disorders

G70.2

Congenital and developmental myasthenia

G70.80

Lambert-Eaton syndrome, unspecified

G70.81

Lambert-Eaton syndrome in disease classified elsewhere

G70.89

Other specified myoneural disorders

G70.9

Myoneural disorder, unspecified

G71.00

Muscular dystrophy, unspecified

G71.01

Duchenne or Becker muscular dystrophy

G71.02

Facioscapulohumeral muscular dystrophy

G71.036

Limb girdle muscular dystrophy due to fukutin related protein dysfunction

G71.09

Other specified muscular dystrophies

G71.11

Myotonic muscular dystrophy

G71.12

Myotonia congenita

G71.13

Myotonic chondrodystrophy

G71.14

Drug induced myotonia

G71.19

Other specified myotonic disorders

G71.20

Congenital myopathies, unspecified

G71.21

Nemaline myopathy

G71.220

X-Linked myotubular myopathy

G71.228

Other centronuclear myopathy

G71.29

Other congenital myopathy

G71.3

Mitochondrial myopathy, not elsewhere classified

G71.8

Other primary disorders of muscles

G71.9

Primary disorder of muscle, unspecified

G72.0

Drug-induced myopathy

G72.1

Alcoholic myopathy

G72.2

Myopathy due to other toxic agents

G72.3

Periodic paralysis

G72.41

Inclusion body myositis [IBM]

G72.49

Other inflammatory and immune myopathies, not elsewhere classified

G72.81

Critical illness myopathy

G72.89

Other specified myopathies

G72.9

Myopathy, unspecified

G73.1

Lambert-Eaton syndrome in neoplastic disease

G73.3

Myasthenic syndromes in other diseases classified elsewhere

G73.7

Myopathy in diseases classified elsewhere

G90.01

Carotid sinus syncope

G90.09

Other idiopathic peripheral autonomic neuropathy

G90.2

Horner's syndrome

G90.4

Autonomic dysreflexia

G90.511

Complex regional pain syndrome I of right upper limb

G90.512

Complex regional pain syndrome I of left upper limb

G90.513

Complex regional pain syndrome I of upper limb, bilateral

G90.521

Complex regional pain syndrome I of right lower limb

G90.522

Complex regional pain syndrome I of left lower limb

G90.523

Complex regional pain syndrome I of lower limb, bilateral

G90.59

Complex regional pain syndrome I of other specified site

G90.8

Other disorders of autonomic nervous system

G90.9

Disorder of the autonomic nervous system, unspecified

G99.0

Autonomic neuropathy in diseases classified elsewhere

M05.411

Rheumatoid myopathy with rheumatoid arthritis of right shoulder

M05.412

Rheumatoid myopathy with rheumatoid arthritis of left shoulder

M05.421

Rheumatoid myopathy with rheumatoid arthritis of right elbow

M05.422

Rheumatoid myopathy with rheumatoid arthritis of left elbow

M05.431

Rheumatoid myopathy with rheumatoid arthritis of right wrist

M05.432

Rheumatoid myopathy with rheumatoid arthritis of left wrist

M05.441

Rheumatoid myopathy with rheumatoid arthritis of right hand

M05.442

Rheumatoid myopathy with rheumatoid arthritis of left hand

M05.451

Rheumatoid myopathy with rheumatoid arthritis of right hip

M05.452

Rheumatoid myopathy with rheumatoid arthritis of left hip

M05.461

Rheumatoid myopathy with rheumatoid arthritis of right knee

M05.462

Rheumatoid myopathy with rheumatoid arthritis of left knee

M05.471

Rheumatoid myopathy with rheumatoid arthritis of right ankle and foot

M05.472

Rheumatoid myopathy with rheumatoid arthritis of left ankle and foot

M05.49

Rheumatoid myopathy with rheumatoid arthritis of multiple sites

M05.511

Rheumatoid polyneuropathy with rheumatoid arthritis of right shoulder

M05.512

Rheumatoid polyneuropathy with rheumatoid arthritis of left shoulder

M05.521

Rheumatoid polyneuropathy with rheumatoid arthritis of right elbow

M05.522

Rheumatoid polyneuropathy with rheumatoid arthritis of left elbow

M05.531

Rheumatoid polyneuropathy with rheumatoid arthritis of right wrist

M05.532

Rheumatoid polyneuropathy with rheumatoid arthritis of left wrist

M05.541

Rheumatoid polyneuropathy with rheumatoid arthritis of right hand

M05.542

Rheumatoid polyneuropathy with rheumatoid arthritis of left hand

M05.551

Rheumatoid polyneuropathy with rheumatoid arthritis of right hip

M05.552

Rheumatoid polyneuropathy with rheumatoid arthritis of left hip

M05.561

Rheumatoid polyneuropathy with rheumatoid arthritis of right knee

M05.562

Rheumatoid polyneuropathy with rheumatoid arthritis of left knee

M05.571

Rheumatoid polyneuropathy with rheumatoid arthritis of right ankle and foot

M05.572

Rheumatoid polyneuropathy with rheumatoid arthritis of left ankle and foot

M05.59

Rheumatoid polyneuropathy with rheumatoid arthritis of multiple sites

M33.00

Juvenile dermatomyositis, organ involvement unspecified

M33.01

Juvenile dermatomyositis with respiratory involvement

M33.02

Juvenile dermatomyositis with myopathy

M33.03

Juvenile dermatomyositis without myopathy

M33.09

Juvenile dermatomyositis with other organ involvement

M33.10

Other dermatomyositis, organ involvement unspecified

M33.11

Other dermatomyositis with respiratory involvement

M33.12

Other dermatomyositis with myopathy

M33.13

Other dermatomyositis without myopathy

M33.19

Other dermatomyositis with other organ involvement

M33.20

Polymyositis, organ involvement unspecified

M33.21

Polymyositis with respiratory involvement

M33.22

Polymyositis with myopathy

M33.29

Polymyositis with other organ involvement

M33.90

Dermatopolymyositis, unspecified, organ involvement unspecified

M33.91

Dermatopolymyositis, unspecified with respiratory involvement

M33.92

Dermatopolymyositis, unspecified with myopathy

M33.93

Dermatopolymyositis, unspecified without myopathy

M33.99

Dermatopolymyositis, unspecified with other organ involvement

M34.82

Systemic sclerosis with myopathy

M34.83

Systemic sclerosis with polyneuropathy

M35.03

Sicca syndrome with myopathy

M36.0

Dermato(poly)myositis in neoplastic disease

M51.14

Intervertebral disc disorders with radiculopathy, thoracic region

M51.15

Intervertebral disc disorders with radiculopathy, thoracolumbar region

M51.16

Intervertebral disc disorders with radiculopathy, lumbar region

M51.17

Intervertebral disc disorders with radiculopathy, lumbosacral region

M54.10

Radiculopathy, site unspecified

M54.11

Radiculopathy, occipito-atlanto-axial region

M54.12

Radiculopathy, cervical region

M54.13

Radiculopathy, cervicothoracic region

M54.14

Radiculopathy, thoracic region

M54.15

Radiculopathy, thoracolumbar region

M54.16

Radiculopathy, lumbar region

M54.17

Radiculopathy, lumbosacral region

M54.18

Radiculopathy, sacral and sacrococcygeal region

S04.10XA

Injury of oculomotor nerve, unspecified side, initial encounter

S04.11XA

Injury of oculomotor nerve, right side, initial encounter

S04.12XA

Injury of oculomotor nerve, left side, initial encounter

S04.21XA

Injury of trochlear nerve, right side, initial encounter

S04.22XA

Injury of trochlear nerve, left side, initial encounter

S04.31XA

Injury of trigeminal nerve, right side, initial encounter

S04.32XA

Injury of trigeminal nerve, left side, initial encounter

S04.41XA

Injury of abducent nerve, right side, initial encounter

S04.42XA

Injury of abducent nerve, left side, initial encounter

S04.51XA

Injury of facial nerve, right side, initial encounter

S04.52XA

Injury of facial nerve, left side, initial encounter

S04.61XA

Injury of acoustic nerve, right side, initial encounter

S04.62XA

Injury of acoustic nerve, left side, initial encounter

S04.71XA

Injury of accessory nerve, right side, initial encounter

S04.72XA

Injury of accessory nerve, left side, initial encounter

S04.811A

Injury of olfactory [1st] nerve, right side, initial encounter

S04.812A

Injury of olfactory [1st] nerve, left side, initial encounter

S04.891A

Injury of other cranial nerves, right side, initial encounter

S04.892A

Injury of other cranial nerves, left side, initial encounter

S04.9XXA

Injury of unspecified cranial nerve, initial encounter

S12.000A

Unspecified displaced fracture of first cervical vertebra, initial encounter for closed fracture

S12.000B

Unspecified displaced fracture of first cervical vertebra, initial encounter for open fracture

S12.001A

Unspecified nondisplaced fracture of first cervical vertebra, initial encounter for closed fracture

S12.001B

Unspecified nondisplaced fracture of first cervical vertebra, initial encounter for open fracture

S12.100A

Unspecified displaced fracture of second cervical vertebra, initial encounter for closed fracture

S12.100B

Unspecified displaced fracture of second cervical vertebra, initial encounter for open fracture

S12.101A

Unspecified nondisplaced fracture of second cervical vertebra, initial encounter for closed fracture

S12.101B

Unspecified nondisplaced fracture of second cervical vertebra, initial encounter for open fracture

S12.200A

Unspecified displaced fracture of third cervical vertebra, initial encounter for closed fracture

S12.200B

Unspecified displaced fracture of third cervical vertebra, initial encounter for open fracture

S12.201A

Unspecified nondisplaced fracture of third cervical vertebra, initial encounter for closed fracture

S12.201B

Unspecified nondisplaced fracture of third cervical vertebra, initial encounter for open fracture

S12.300A

Unspecified displaced fracture of fourth cervical vertebra, initial encounter for closed fracture

S12.300B

Unspecified displaced fracture of fourth cervical vertebra, initial encounter for open fracture

S12.301A

Unspecified nondisplaced fracture of fourth cervical vertebra, initial encounter for closed fracture

S12.301B

Unspecified nondisplaced fracture of fourth cervical vertebra, initial encounter for open fracture

S12.400A

Unspecified displaced fracture of fifth cervical vertebra, initial encounter for closed fracture

S12.400B

Unspecified displaced fracture of fifth cervical vertebra, initial encounter for open fracture

S12.401A

Unspecified nondisplaced fracture of fifth cervical vertebra, initial encounter for closed fracture

S12.401B

Unspecified nondisplaced fracture of fifth cervical vertebra, initial encounter for open fracture

S12.500A

Unspecified displaced fracture of sixth cervical vertebra, initial encounter for closed fracture

S12.500B

Unspecified displaced fracture of sixth cervical vertebra, initial encounter for open fracture

S12.501A

Unspecified nondisplaced fracture of sixth cervical vertebra, initial encounter for closed fracture

S12.501B

Unspecified nondisplaced fracture of sixth cervical vertebra, initial encounter for open fracture

S12.600A

Unspecified displaced fracture of seventh cervical vertebra, initial encounter for closed fracture

S12.600B

Unspecified displaced fracture of seventh cervical vertebra, initial encounter for open fracture

S12.601A

Unspecified nondisplaced fracture of seventh cervical vertebra, initial encounter for closed fracture

S12.601B

Unspecified nondisplaced fracture of seventh cervical vertebra, initial encounter for open fracture

S12.9XXA

Fracture of neck, unspecified, initial encounter

S14.0XXA

Concussion and edema of cervical spinal cord, initial encounter

S14.101A

Unspecified injury at C1 level of cervical spinal cord, initial encounter

S14.102A

Unspecified injury at C2 level of cervical spinal cord, initial encounter

S14.103A

Unspecified injury at C3 level of cervical spinal cord, initial encounter

S14.104A

Unspecified injury at C4 level of cervical spinal cord, initial encounter

S14.105A

Unspecified injury at C5 level of cervical spinal cord, initial encounter

S14.106A

Unspecified injury at C6 level of cervical spinal cord, initial encounter

S14.107A

Unspecified injury at C7 level of cervical spinal cord, initial encounter

S14.108A

Unspecified injury at C8 level of cervical spinal cord, initial encounter

S14.111A

Complete lesion at C1 level of cervical spinal cord, initial encounter

S14.112A

Complete lesion at C2 level of cervical spinal cord, initial encounter

S14.113A

Complete lesion at C3 level of cervical spinal cord, initial encounter

S14.114A

Complete lesion at C4 level of cervical spinal cord, initial encounter

S14.115A

Complete lesion at C5 level of cervical spinal cord, initial encounter

S14.116A

Complete lesion at C6 level of cervical spinal cord, initial encounter

S14.117A

Complete lesion at C7 level of cervical spinal cord, initial encounter

S14.118A

Complete lesion at C8 level of cervical spinal cord, initial encounter

S14.121A

Central cord syndrome at C1 level of cervical spinal cord, initial encounter

S14.122A

Central cord syndrome at C2 level of cervical spinal cord, initial encounter

S14.123A

Central cord syndrome at C3 level of cervical spinal cord, initial encounter

S14.124A

Central cord syndrome at C4 level of cervical spinal cord, initial encounter

S14.125A

Central cord syndrome at C5 level of cervical spinal cord, initial encounter

S14.126A

Central cord syndrome at C6 level of cervical spinal cord, initial encounter

S14.127A

Central cord syndrome at C7 level of cervical spinal cord, initial encounter

S14.128A

Central cord syndrome at C8 level of cervical spinal cord, initial encounter

S14.129A

Central cord syndrome at unspecified level of cervical spinal cord, initial encounter

S14.131A

Anterior cord syndrome at C1 level of cervical spinal cord, initial encounter

S14.132A

Anterior cord syndrome at C2 level of cervical spinal cord, initial encounter

S14.133A

Anterior cord syndrome at C3 level of cervical spinal cord, initial encounter

S14.134A

Anterior cord syndrome at C4 level of cervical spinal cord, initial encounter

S14.135A

Anterior cord syndrome at C5 level of cervical spinal cord, initial encounter

S14.136A

Anterior cord syndrome at C6 level of cervical spinal cord, initial encounter

S14.137A

Anterior cord syndrome at C7 level of cervical spinal cord, initial encounter

S14.138A

Anterior cord syndrome at C8 level of cervical spinal cord, initial encounter

S14.141A

Brown-Sequard syndrome at C1 level of cervical spinal cord, initial encounter

S14.142A

Brown-Sequard syndrome at C2 level of cervical spinal cord, initial encounter

S14.143A

Brown-Sequard syndrome at C3 level of cervical spinal cord, initial encounter

S14.144A

Brown-Sequard syndrome at C4 level of cervical spinal cord, initial encounter

S14.145A

Brown-Sequard syndrome at C5 level of cervical spinal cord, initial encounter

S14.146A

Brown-Sequard syndrome at C6 level of cervical spinal cord, initial encounter

S14.147A

Brown-Sequard syndrome at C7 level of cervical spinal cord, initial encounter

S14.148A

Brown-Sequard syndrome at C8 level of cervical spinal cord, initial encounter

S14.149A

Brown-Sequard syndrome at unspecified level of cervical spinal cord, initial encounter

S14.151A

Other incomplete lesion at C1 level of cervical spinal cord, initial encounter

S14.152A

Other incomplete lesion at C2 level of cervical spinal cord, initial encounter

S14.153A

Other incomplete lesion at C3 level of cervical spinal cord, initial encounter

S14.154A

Other incomplete lesion at C4 level of cervical spinal cord, initial encounter

S14.155A

Other incomplete lesion at C5 level of cervical spinal cord, initial encounter

S14.156A

Other incomplete lesion at C6 level of cervical spinal cord, initial encounter

S14.157A

Other incomplete lesion at C7 level of cervical spinal cord, initial encounter

S14.158A

Other incomplete lesion at C8 level of cervical spinal cord, initial encounter

S14.159A

Other incomplete lesion at unspecified level of cervical spinal cord, initial encounter

S14.2XXA

Injury of nerve root of cervical spine, initial encounter

S14.4XXA

Injury of peripheral nerves of neck, initial encounter

S14.5XXA

Injury of cervical sympathetic nerves, initial encounter

S14.8XXA

Injury of other specified nerves of neck, initial encounter

S14.9XXA

Injury of unspecified nerves of neck, initial encounter

S14.3XXA

Injury of brachial plexus, initial encounter

S22.019A

Unspecified fracture of first thoracic vertebra, initial encounter for closed fracture

S22.019B

Unspecified fracture of first thoracic vertebra, initial encounter for open fracture

S22.029A

Unspecified fracture of second thoracic vertebra, initial encounter for closed fracture

S22.029B

Unspecified fracture of second thoracic vertebra, initial encounter for open fracture

S22.039A

Unspecified fracture of third thoracic vertebra, initial encounter for closed fracture

S22.039B

Unspecified fracture of third thoracic vertebra, initial encounter for open fracture

S22.049A

Unspecified fracture of fourth thoracic vertebra, initial encounter for closed fracture

S22.049B

Unspecified fracture of fourth thoracic vertebra, initial encounter for open fracture

S22.059A

Unspecified fracture of T5-T6 vertebra, initial encounter for closed fracture

S22.059B

Unspecified fracture of T5-T6 vertebra, initial encounter for open fracture

S22.069A

Unspecified fracture of T7-T8 vertebra, initial encounter for closed fracture

S22.069B

Unspecified fracture of T7-T8 vertebra, initial encounter for open fracture

S22.079A

Unspecified fracture of T9-T10 vertebra, initial encounter for closed fracture

S22.079B

Unspecified fracture of T9-T10 vertebra, initial encounter for open fracture

S22.089A

Unspecified fracture of T11-T12 vertebra, initial encounter for closed fracture

S22.089B

Unspecified fracture of T11-T12 vertebra, initial encounter for open fracture

S24.0XXA

Concussion and edema of thoracic spinal cord, initial encounter

S24.101A

Unspecified injury at T1 level of thoracic spinal cord, initial encounter

S24.102A

Unspecified injury at T2-T6 level of thoracic spinal cord, initial encounter

S24.103A

Unspecified injury at T7-T10 level of thoracic spinal cord, initial encounter

S24.104A

Unspecified injury at T11-T12 level of thoracic spinal cord, initial encounter

S24.109A

Unspecified injury at unspecified level of thoracic spinal cord, initial encounter

S24.111A

Complete lesion at T1 level of thoracic spinal cord, initial encounter

S24.112A

Complete lesion at T2-T6 level of thoracic spinal cord, initial encounter

S24.113A

Complete lesion at T7-T10 level of thoracic spinal cord, initial encounter

S24.114A

Complete lesion at T11-T12 level of thoracic spinal cord, initial encounter

S24.119A

Complete lesion at unspecified level of thoracic spinal cord, initial encounter

S24.131A

Anterior cord syndrome at T1 level of thoracic spinal cord, initial encounter

S24.132A

Anterior cord syndrome at T2-T6 level of thoracic spinal cord, initial encounter

S24.133A

Anterior cord syndrome at T7-T10 level of thoracic spinal cord, initial encounter

S24.134A

Anterior cord syndrome at T11-T12 level of thoracic spinal cord, initial encounter

S24.139A

Anterior cord syndrome at unspecified level of thoracic spinal cord, initial encounter

S24.141A

Brown-Sequard syndrome at T1 level of thoracic spinal cord, initial encounter

S24.142A

Brown-Sequard syndrome at T2-T6 level of thoracic spinal cord, initial encounter

S24.143A

Brown-Sequard syndrome at T7-T10 level of thoracic spinal cord, initial encounter

S24.144A

Brown-Sequard syndrome at T11-T12 level of thoracic spinal cord, initial encounter

S24.149A

Brown-Sequard syndrome at unspecified level of thoracic spinal cord, initial encounter

S24.151A

Other incomplete lesion at T1 level of thoracic spinal cord, initial encounter

S24.152A

Other incomplete lesion at T2-T6 level of thoracic spinal cord, initial encounter

S24.153A

Other incomplete lesion at T7-T10 level of thoracic spinal cord, initial encounter

S24.154A

Other incomplete lesion at T11-T12 level of thoracic spinal cord, initial encounter

S24.159A

Other incomplete lesion at unspecified level of thoracic spinal cord, initial encounter

S24.2XXA

Injury of nerve root of thoracic spine, initial encounter

S24.3XXA

Injury of peripheral nerves of thorax, initial encounter

S24.4XXA

Injury of thoracic sympathetic nervous system, initial encounter

S24.8XXA

Injury of other specified nerves of thorax, initial encounter

S24.9XXA

Injury of unspecified nerve of thorax, initial encounter

S32.019A

Unspecified fracture of first lumbar vertebra, initial encounter for closed fracture

S32.019B

Unspecified fracture of first lumbar vertebra, initial encounter for open fracture

S32.029A

Unspecified fracture of second lumbar vertebra, initial encounter for closed fracture

S32.029B

Unspecified fracture of second lumbar vertebra, initial encounter for open fracture

S32.039A

Unspecified fracture of third lumbar vertebra, initial encounter for closed fracture

S32.039B

Unspecified fracture of third lumbar vertebra, initial encounter for open fracture

S32.049A

Unspecified fracture of fourth lumbar vertebra, initial encounter for closed fracture

S32.049B

Unspecified fracture of fourth lumbar vertebra, initial encounter for open fracture

S32.059A

Unspecified fracture of fifth lumbar vertebra, initial encounter for closed fracture

S32.059B

Unspecified fracture of fifth lumbar vertebra, initial encounter for open fracture

S32.2XXA

Fracture of coccyx, initial encounter for closed fracture

S32.2XXB

Fracture of coccyx, initial encounter for open fracture

S34.01XA

Concussion and edema of lumbar spinal cord, initial encounter

S34.02XA

Concussion and edema of sacral spinal cord, initial encounter

S34.101A

Unspecified injury to L1 level of lumbar spinal cord, initial encounter

S34.102A

Unspecified injury to L2 level of lumbar spinal cord, initial encounter

S34.103A

Unspecified injury to L3 level of lumbar spinal cord, initial encounter

S34.104A

Unspecified injury to L4 level of lumbar spinal cord, initial encounter

S34.105A

Unspecified injury to L5 level of lumbar spinal cord, initial encounter

S34.111A

Complete lesion of L1 level of lumbar spinal cord, initial encounter

S34.112A

Complete lesion of L2 level of lumbar spinal cord, initial encounter

S34.113A

Complete lesion of L3 level of lumbar spinal cord, initial encounter

S34.114A

Complete lesion of L4 level of lumbar spinal cord, initial encounter

S34.115A

Complete lesion of L5 level of lumbar spinal cord, initial encounter

S34.121A

Incomplete lesion of L1 level of lumbar spinal cord, initial encounter

S34.122A

Incomplete lesion of L2 level of lumbar spinal cord, initial encounter

S34.123A

Incomplete lesion of L3 level of lumbar spinal cord, initial encounter

S34.124A

Incomplete lesion of L4 level of lumbar spinal cord, initial encounter

S34.125A

Incomplete lesion of L5 level of lumbar spinal cord, initial encounter

S34.131A

Complete lesion of sacral spinal cord, initial encounter

S34.132A

Incomplete lesion of sacral spinal cord, initial encounter

S34.139A

Unspecified injury to sacral spinal cord, initial encounter

S34.21XA

Injury of nerve root of lumbar spine, initial encounter

S34.22XA

Injury of nerve root of sacral spine, initial encounter

S34.3XXA

Injury of cauda equina, initial encounter

S34.4XXA

Injury of lumbosacral plexus, initial encounter

S34.5XXA

Injury of lumbar, sacral and pelvic sympathetic nerves, initial encounter

S34.6XXA

Injury of peripheral nerve(s) at abdomen, lower back and pelvis level, initial encounter

S34.8XXA

Injury of other nerves at abdomen, lower back and pelvis level, initial encounter

S34.9XXA

Injury of unspecified nerves at abdomen, lower back and pelvis level, initial encounter

S44.00XA

Injury of ulnar nerve at upper arm level, unspecified arm, initial encounter

S44.01XA

Injury of ulnar nerve at upper arm level, right arm, initial encounter

S44.02XA

Injury of ulnar nerve at upper arm level, left arm, initial encounter

S44.10XA

Injury of median nerve at upper arm level, unspecified arm, initial encounter

S44.11XA

Injury of median nerve at upper arm level, right arm, initial encounter

S44.12XA

Injury of median nerve at upper arm level, left arm, initial encounter

S44.20XA

Injury of radial nerve at upper arm level, unspecified arm, initial encounter

S44.21XA

Injury of radial nerve at upper arm level, right arm, initial encounter

S44.22XA

Injury of radial nerve at upper arm level, left arm, initial encounter

S44.30XA

Injury of axillary nerve, unspecified arm, initial encounter

S44.31XA

Injury of axillary nerve, right arm, initial encounter

S44.32XA

Injury of axillary nerve, left arm, initial encounter

S44.40XA

Injury of musculocutaneous nerve, unspecified arm, initial encounter

S44.41XA

Injury of musculocutaneous nerve, right arm, initial encounter

S44.42XA

Injury of musculocutaneous nerve, left arm, initial encounter

S44.50XA

Injury of cutaneous sensory nerve at shoulder and upper arm level, unspecified arm, initial encounter

S44.51XA

Injury of cutaneous sensory nerve at shoulder and upper arm level, right arm, initial encounter

S44.52XA

Injury of cutaneous sensory nerve at shoulder and upper arm level, left arm, initial encounter

S44.8X1A

Injury of other nerves at shoulder and upper arm level, right arm, initial encounter

S44.8X2A

Injury of other nerves at shoulder and upper arm level, left arm, initial encounter

S44.8X9A

Injury of other nerves at shoulder and upper arm level, unspecified arm, initial encounter

S54.00XA

Injury of ulnar nerve at forearm level, unspecified arm, initial encounter

S54.01XA

Injury of ulnar nerve at forearm level, right arm, initial encounter

S54.02XA

Injury of ulnar nerve at forearm level, left arm, initial encounter

S54.10XA

Injury of median nerve at forearm level, unspecified arm, initial encounter

S54.11XA

Injury of median nerve at forearm level, right arm, initial encounter

S54.12XA

Injury of median nerve at forearm level, left arm, initial encounter

S54.20XA

Injury of radial nerve at forearm level, unspecified arm, initial encounter

S54.21XA

Injury of radial nerve at forearm level, right arm, initial encounter

S54.22XA

Injury of radial nerve at forearm level, left arm, initial encounter

S54.31XA

Injury of cutaneous sensory nerve at forearm level, right arm, initial encounter

S54.32XA

Injury of cutaneous sensory nerve at forearm level, left arm, initial encounter

S54.8X1A

Injury of other nerves at forearm level, right arm, initial encounter

S54.8X2A

Injury of other nerves at forearm level, left arm, initial encounter

S54.8X9A

Injury of other nerves at forearm level, unspecified arm, initial encounter

S54.90XA

Injury of unspecified nerve at forearm level, unspecified arm, initial encounter

S54.91XA

Injury of unspecified nerve at forearm level, right arm, initial encounter

S54.92XA

Injury of unspecified nerve at forearm level, left arm, initial encounter

S64.00XA

Injury of ulnar nerve at wrist and hand level of unspecified arm, initial encounter

S64.01XA

Injury of ulnar nerve at wrist and hand level of right arm, initial encounter

S64.02XA

Injury of ulnar nerve at wrist and hand level of left arm, initial encounter

S64.10XA

Injury of median nerve at wrist and hand level of unspecified arm, initial encounter

S64.11XA

Injury of median nerve at wrist and hand level of right arm, initial encounter

S64.12XA

Injury of median nerve at wrist and hand level of left arm, initial encounter

S64.20XA

Injury of radial nerve at wrist and hand level of unspecified arm, initial encounter

S64.21XA

Injury of radial nerve at wrist and hand level of right arm, initial encounter

S64.22XA

Injury of radial nerve at wrist and hand level of left arm, initial encounter

S64.30XA

Injury of digital nerve of unspecified thumb, initial encounter

S64.31XA

Injury of digital nerve of right thumb, initial encounter

S64.32XA

Injury of digital nerve of left thumb, initial encounter

S64.40XA

Injury of digital nerve of unspecified finger, initial encounter

S64.490A

Injury of digital nerve of right index finger, initial encounter

S64.491A

Injury of digital nerve of left index finger, initial encounter

S64.492A

Injury of digital nerve of right middle finger, initial encounter

S64.493A

Injury of digital nerve of left middle finger, initial encounter

S64.494A

Injury of digital nerve of right ring finger, initial encounter

S64.495A

Injury of digital nerve of left ring finger, initial encounter

S64.496A

Injury of digital nerve of right little finger, initial encounter

S64.497A

Injury of digital nerve of left little finger, initial encounter

S64.498A

Injury of digital nerve of other finger, initial encounter

S64.8X1A

Injury of other nerves at wrist and hand level of right arm, initial encounter

S64.8X2A

Injury of other nerves at wrist and hand level of left arm, initial encounter

S64.91XA

Injury of unspecified nerve at wrist and hand level of right arm, initial encounter

S64.92XA

Injury of unspecified nerve at wrist and hand level of left arm, initial encounter

S74.00XA

Injury of sciatic nerve at hip and thigh level, unspecified leg, initial encounter

S74.01XA

Injury of sciatic nerve at hip and thigh level, right leg, initial encounter

S74.02XA

Injury of sciatic nerve at hip and thigh level, left leg, initial encounter

S74.10XA

Injury of femoral nerve at hip and thigh level, unspecified leg, initial encounter

S74.11XA

Injury of femoral nerve at hip and thigh level, right leg, initial encounter

S74.12XA

Injury of femoral nerve at hip and thigh level, left leg, initial encounter

S74.20XA

Injury of cutaneous sensory nerve at hip and thigh level, unspecified leg, initial encounter

S74.21XA

Injury of cutaneous sensory nerve at hip and thigh level, right leg, initial encounter

S74.22XA

Injury of cutaneous sensory nerve at hip and thigh level, left leg, initial encounter

S74.8X1A

Injury of other nerves at hip and thigh level, right leg, initial encounter

S74.8X2A

Injury of other nerves at hip and thigh level, left leg, initial encounter

S74.8X9A

Injury of other nerves at hip and thigh level, unspecified leg, initial encounter

S74.91XA

Injury of unspecified nerve at hip and thigh level, right leg, initial encounter

S74.92XA

Injury of unspecified nerve at hip and thigh level, left leg, initial encounter

S84.00XA

Injury of tibial nerve at lower leg level, unspecified leg, initial encounter

S84.01XA

Injury of tibial nerve at lower leg level, right leg, initial encounter

S84.10XA

Injury of peroneal nerve at lower leg level, unspecified leg, initial encounter

S84.11XA

Injury of peroneal nerve at lower leg level, right leg, initial encounter

S84.12XA

Injury of peroneal nerve at lower leg level, left leg, initial encounter

S84.20XA

Injury of cutaneous sensory nerve at lower leg level, unspecified leg, initial encounter

S84.21XA

Injury of cutaneous sensory nerve at lower leg level, right leg, initial encounter

S84.22XA

Injury of cutaneous sensory nerve at lower leg level, left leg, initial encounter

S84.8X1A

Injury of other nerves at lower leg level, right leg, initial encounter

S84.8X2A

Injury of other nerves at lower leg level, left leg, initial encounter

S84.8X9A

Injury of other nerves at lower leg level, unspecified leg, initial encounter

S84.90XA

Injury of unspecified nerve at lower leg level, unspecified leg, initial encounter

S84.91XA

Injury of unspecified nerve at lower leg level, right leg, initial encounter

S84.92XA

Injury of unspecified nerve at lower leg level, left leg, initial encounter

S94.00XA

Injury of lateral plantar nerve, unspecified leg, initial encounter

S94.01XA

Injury of lateral plantar nerve, right leg, initial encounter

S94.02XA

Injury of lateral plantar nerve, left leg, initial encounter

S94.10XA

Injury of medial plantar nerve, unspecified leg, initial encounter

S94.11XA

Injury of medial plantar nerve, right leg, initial encounter

S94.12XA

Injury of medial plantar nerve, left leg, initial encounter

S94.20XA

Injury of deep peroneal nerve at ankle and foot level, unspecified leg, initial encounter

S94.21XA

Injury of deep peroneal nerve at ankle and foot level, right leg, initial encounter

S94.22XA

Injury of deep peroneal nerve at ankle and foot level, left leg, initial encounter

S94.30XA

Injury of cutaneous sensory nerve at ankle and foot level, unspecified leg, initial encounter

S94.31XA

Injury of cutaneous sensory nerve at ankle and foot level, right leg, initial encounter

S94.32XA

Injury of cutaneous sensory nerve at ankle and foot level, left leg, initial encounter

S94.8X1A

Injury of other nerves at ankle and foot level, right leg, initial encounter

S94.8X2A

Injury of other nerves at ankle and foot level, left leg, initial encounter

S94.90XA

Injury of unspecified nerve at ankle and foot level, unspecified leg, initial encounter

S94.91XA

Injury of unspecified nerve at ankle and foot level, right leg, initial encounter

S94.92XA

Injury of unspecified nerve at ankle and foot level, left leg, initial encounter

SS84.02XA

Injury of tibial nerve at lower leg level, left leg, initial encounter

References

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  2. American Association of Neuromuscular & Electrodiagnostic Medicine. Recommended policy for electrodiagnostic medicine. 2023.
  3. Lee DH, Claussen GC, Oh S. Clinical nerve conduction and needle electromyography studies. J Am Acad Orthop Surg. 2004; 12(4): 276-87. PMID 15473679
  4. American Academy of Orthopaedic Surgeons. Management of Carpal Tunnel Syndrome Evidence-Based Clinical Practice Guideline. February 29, 2016;
  5. Fowler JR, Munsch M, Tosti R, et al. Comparison of ultrasound and electrodiagnostic testing for diagnosis of carpal tunnel syndrome: study using a validated clinical tool as the reference standard. J Bone Joint Surg Am. Sep 03 2014; 96(17): e148. PMID 25187592
  6. Chang MH, Liu LH, Lee YC, et al. Comparison of sensitivity of transcarpal median motor conduction velocity and conventional conduction techniques in electrodiagnosis of carpal tunnel syndrome. Clin Neurophysiol. May 2006; 117(5): 984-91. PMID 16551510
  7. Homan MM, Franzblau A, Werner RA, et al. Agreement between symptom surveys, physical examination procedures and electrodiagnostic findings for the carpal tunnel syndrome. Scand J Work Environ Health. Apr 1999; 25(2): 115-24. PMID 10360466
  8. Tulipan JE, Lutsky KF, Maltenfort MG, et al. Patient-Reported Disability Measures Do Not Correlate with Electrodiagnostic Severity in Carpal Tunnel Syndrome. Plast Reconstr Surg Glob Open. Aug 2017; 5(8): e1440. PMID 28894661
  9. North American Spine Society (NASS) Evidence-Based Clinical Guidelines Committee. Evidence-Based Clinical Guidelines for Multidisciplinary Spine Care. 2012;
  10. Mondelli M, Aretini A, Arrigucci U, et al. Clinical findings and electrodiagnostic testing in 108 consecutive cases of lumbosacral radiculopathy due to herniated disc. Neurophysiol Clin. Oct 2013; 43(4): 205-15. PMID 24094906
  11. Marciniak C, Armon C, Wilson J, et al. Practice parameter: utility of electrodiagnostic techniques in evaluating patients with suspected peroneal neuropathy: an evidence-based review. Muscle Nerve. Apr 2005; 31(4): 520-7. PMID 15768387
  12. Rabie M, Jossiphov J, Nevo Y. Electromyography (EMG) accuracy compared to muscle biopsy in childhood. J Child Neurol. Jul 2007; 22(7): 803-8. PMID 17715269
  13. Ghosh PS, Sorenson EJ. Diagnostic yield of electromyography in children with myopathic disorders. Pediatr Neurol. Aug 2014; 51(2): 215-9. PMID 24950662
  14. American Academy of Neurology (AAN). Position Statement: diagnostic electromyography in the practice of medicine. 2004;
  15. American Association of Neuromuscular & Electrodiagnostic Medicine. Model Policy for Needle Electromyography and Nerve Conduction Studies. 2022;
  16. Olney RK, Lewis RA, Putnam TD, et al. Consensus criteria for the diagnosis of multifocal motor neuropathy. Muscle Nerve. Jan 2003; 27(1): 117-21. PMID 12508306
  17. AANEM policy statement on electrodiagnosis for distal symmetric polyneuropathy. Muscle Nerve. Feb 2018; 57(2): 337-339. PMID 29178499
  18. Kang PB, McMillan HJ, Kuntz NL, et al. Utility and practice of electrodiagnostic testing in the pediatric population: An AANEM consensus statement. Muscle Nerve. Feb 2020; 61(2): 143-155. PMID 31724199
  19. Centers for Medicare & Medicaid Services. National Coverage Determination (NCD) for Sensory Nerve Conduction Threshold Tests (sNCTs) (160.23). 2004;
  20. MacDermid JC, Doherty T. Clinical and electrodiagnostic testing of carpal tunnel syndrome: a narrative review. J Orthop Sports Phys Ther. Oct 2004; 34(10): 565-88. PMID 15552704
  21. Boulton AJ, Vinik AI, Arezzo JC, et al. Diabetic neuropathies: a statement by the American Diabetes Association. Diabetes Care. Apr 2005; 28(4): 956-62. PMID 15793206
  22. Kong X, Lesser EA, Gozani SN. Repeatability of nerve conduction measurements derived entirely by computer methods. Biomed Eng Online. Nov 06 2009; 8: 33. PMID 19895683
  23. American Academy of Neurology (AAN). Policy & Guidelines: Endorsed or Affirmed Guidelines. n.d.;
  24. Dillingham T, Chen S, Andary M, et al. Establishing high-quality reference values for nerve conduction studies: A report from the normative data task force of the American Association Of Neuromuscular Electrodiagnostic Medicine. Muscle Nerve. Sep 2016; 54(3): 366-70. PMID 27238858
  25. Chen S, Andary M, Buschbacher R, et al. Electrodiagnostic reference values for upper and lower limb nerve conduction studies in adult populations. Muscle Nerve. Sep 2016; 54(3): 371-7. PMID 27238640
  26. Leffler CT, Gozani SN, Cros D. Median neuropathy at the wrist: diagnostic utility of clinical findings and an automated electrodiagnostic device. J Occup Environ Med. Apr 2000; 42(4): 398-409. PMID 10774509
  27. Rotman MB, Enkvetchakul BV, Megerian JT, et al. Time course and predictors of median nerve conduction after carpal tunnel release. J Hand Surg Am. May 2004; 29(3): 367-72. PMID 15140473
  28. Katz RT. NC-stat as a screening tool for carpal tunnel syndrome in industrial workers. J Occup Environ Med. Apr 2006; 48(4): 414-8. PMID 16607197
  29. Armstrong TN, Dale AM, Al-Lozi MT, et al. Median and ulnar nerve conduction studies at the wrist: criterion validity of the NC-stat automated device. J Occup Environ Med. Jul 2008; 50(7): 758-64. PMID 18617831
  30. Bourke HE, Read J, Kampa R, et al. Clinic-based nerve conduction studies reduce time to surgery and are cost effective: a comparison with formal electrophysiological testing. Ann R Coll Surg Engl. Apr 2011; 93(3): 236-40. PMID 21477439
  31. Megerian JT, Kong X, Gozani SN. Utility of nerve conduction for carpal tunnel syndrome by family medicine, primary care, and internal medicine physicians. J Am Board Fam Med. Jan-Feb 2007; 20(1): 60-4. PMID 17204736
  32. Fisher MA, Bajwa R, Somashekar KN. Routine electrodiagnosis and a multiparameter technique in lumbosacral radiculopathies. Acta Neurol Scand. Aug 2008; 118(2): 99-105. PMID 18355396
  33. Schmidt K, Chinea NM, Sorenson EJ, et al. Accuracy of diagnoses delivered by an automated hand-held nerve conduction device in comparison to standard electrodiagnostic testing in patients with unilateral leg symptoms. Muscle Nerve. Jan 2011; 43(1): 9-13. PMID 21108323
  34. England JD, Franklin GM. Automated hand-held nerve conduction devices: raw data, raw interpretations. Muscle Nerve. Jun 2011; 43(1): 6-8. PMID 21171092
  35. Perkins BA, Grewal J, Ng E, et al. Validation of a novel point-of-care nerve conduction device for the detection of diabetic sensorimotor polyneuropathy. Diabetes Care. Sep 2006; 29(9): 2023-7. PMID 16936147
  36. Sharma S, Vas PR, Rayman G. Assessment of diabetic neuropathy using a point-of-care nerve conduction device shows significant associations with the LDIFLARE method and clinical neuropathy scoring. J Diabetes Sci Technol. Jan 2015; 9(1): 123-31. PMID 25231114
  37. Chatzikosma D, Patili K, Demetriou M, et al. Evaluation of sural nerve automated nerve conduction study in the diagnosis of peripheral neuropathy in patients with type 2 diabetes mellitus. Arch Med Sci. Apr 01 2016; 12(2): 390-3. PMID 27186185
  38. Young MJ, Boulton AJ, MacLeod AF, et al. A multicentre study of the prevalence of diabetic peripheral neuropathy in the United Kingdom hospital clinic population. Diabetologia. Feb 1993; 36(2): 150-4. PMID 8458529
  39. American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM). Proper Performance and Interpretation of Electrodiagnostic Studies. 2025

Other Sources:

  • Mosby's Medical, Nursing and Allied Health Dictionary, 6th edition.

Policy history

MP 2.063

02/20/2020 Consensus Review. Policy statement unchanged. References updated.

09/02/2020 Administrative Update. ICD codes added, G71.20, G71.21, G71.22, G71.220, G71.228, G71.29

01/14/2021 Consensus Review. Background updated. Coding reviewed and references updated.

07/19/2022 Consensus Review. No change to policy statement. References reviewed and updated. FEP language updated.

12/18/2023 Consensus Review. No change to policy statement. Policy guidelines, background, and cross-references updated. Coding reviewed, no changes.

08/27/2024 Minor Review. Added automated nerve conduction tests as INV with codes 95905, 95999, and G0255. Updated background, rationale, references.

05/15/2025 Consensus Review. No change to policy statement. Coding reviewed, no changes.

07/18/2025 Administrative Update. Removed Benefit Variations Section and updated Disclaimer.

09/02/2025 Administrative Update. Added ICD10 code G71.036 as part of the new code update for 10/02/2025

05/14/2026 Consensus Review. Editorial updates to policy statements by changing ‘patient’ to ‘individual’, no change to intent. Updated policy guidelines, background, definition, rationale, and references. Coding reviewed, updated ICD-10 coding table.