Medical Policy
Policy Num: 02.001.015
Policy Name: Paraspinal Surface Electromyography to Evaluate and Monitor Back Pain
Policy ID: [02.001.015] [Ac / B / M- / P-] [2.01.35]
Last Review: July 15, 2024
Next Review: July 20, 2025
Related Policies: None
Population Reference No. | Populations | Interventions | Comparators | Outcomes |
1 | Individuals: · With back pain | Interventions of interest are: · Paraspinal surface electromyography for evaluation and monitoring | Comparators of interest are: · Clinical examination · Imaging technologies | Relevant outcomes include: · Test accuracy · Test validity · Symptoms · Functional outcomes · Quality of life · Resource utilization |
A noninvasive procedure that records the summation of muscle electrical activity, paraspinal surface electromyography (SEMG) has been investigated as a technique to evaluate the physiologic functioning of the back. Additionally, this procedure has been studied as a technique to evaluate abnormal patterns of electrical activity in the paraspinal muscles in patients with back pain symptoms, such as spasm, tenderness, limited range of motion, or postural disorders.
For individuals who have back pain who receive paraspinal surface electromyography (SEMG) for evaluation and monitoring, the evidence includes several nonrandomized studies on using findings to classify back pain. Relevant outcomes are test accuracy and validity, symptoms, functional outcomes, quality of life, and resource utilization. There have been no studies directly comparing SEMG with other noninvasive techniques for evaluating back pain, and standard criteria for normal and abnormal SEMG measurements have not been determined. Surface electromyography has been proposed as a noninvasive technique providing objective measurements that would inform treatment decisions in patients with back pain. While studies have shown that SEMG results have detected different pathologies in patients with back pain, none of the studies reported health outcomes. There are also no data on the impact of SEMG for managing patients. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
The objective of this evidence review is to determine whether the use of paraspinal surface electromyography improves the net health outcome in patients who have back pain.
Paraspinal surface electromyography is considered investigational as a technique to diagnose or monitor back pain.
Please see the Codes table for details.
BlueCard/National Account Issues
State or federal mandates (eg, Federal Employee Program) may dictate that certain U.S. Food and Drug Administration-approved devices, drugs, or biologics may not be considered investigational, and thus these devices may be assessed only by their medical necessity.
Some plans have reported that this technology has been billed using CPT code 95860-95872, which is an incorrect code range that addresses the use of the needle, not surface electromyography.
Some plans may perform spot audits of claims for needle electromyography to determine whether they represent surface electromyography.
Some plans may have notified their providers that use of surface electromyography would be considered part of the evaluation and management of the patient and thus not coded separately.
Benefits are determined by the group contract, member benefit booklet, and/or individual subscriber certificate in effect at the time services were rendered. Benefit products or negotiated coverages may have all or some of the services discussed in this medical policy excluded from their coverage.
Back Pain
Back pain is a common condition that affects most individuals at some point in their lives. Identifying the pathogenesis of back pain is challenging, in part due to the complex anatomy of the back, which includes vertebrae, intervertebral discs, facet joints, spinal nerve roots, and numerous muscles.Back pain may be related to osteoarthritis, disc disease, subluxation, or muscular pathologies, such as muscle strain or spasm. Moreover, due to referred pain patterns, the location of the pain may not be anatomically related to the pathogenesis of the pain. For example, buttock or leg pain may be related to pathology in the spine. In addition to the diagnostic challenges of back pain is the natural history of acute back pain.
Diagnosis
Aside from physical examination, diagnostic testing includes imaging technologies, such as magnetic resonance imaging, designed to identify pathology (eg, bulging discs), or tests such as discography to localize the abnormality by reproducing the pain syndrome. However, these tests lack specificity and must be carefully interpreted in the context of the clinical picture. For example, magnetic resonance imaging identifies 5% of asymptomatic patients as having bulging discs. However, the presence of a bulging disc may only be clinically significant if correlated with other symptoms. Assessment of the musculature may focus on a range of motion or strength exercises.
In contrast to anatomic imaging, surface electromyography (SEMG), which records the summation of muscle activity from groups of muscles, has been investigated as a technique to evaluate the physiologic functioning of the back 2, . A noninvasive procedure, SEMG differs from needle electromyography, an invasive procedure in which the electrical activity of individual muscles is recorded. Paraspinal SEMG has been explored to evaluate abnormal patterns of electrical activity in the paraspinal muscles in patients with back pain symptoms such as spasm, tenderness, limited range of motion, or postural disorders. The technique is performed using a single or an array of electrodes placed on the skin surface, with recordings made at rest, in various positions, or after a series of exercises. Recordings can also be made by using a handheld device, which is applied to the skin at different sites. Electrical activity is assessed by computer analysis of the frequency spectrum (ie, spectral analysis), amplitude, or root mean square of the electrical action potentials. In particular, a spectral analysis that focuses on the median frequency has been used to assess paraspinal muscle fatigue during isometric endurance exercises. Paraspinal SEMG has been researched as a technique to establish the etiology of back pain and has been used to monitor the response to therapy and establish physical activity limits, such as assessing capacity to lift heavy objects or ability to return to work.
Paraspinal SEMG is an office-based procedure that may be most commonly used by physiatrists or chiropractors. The following clinical applications of the paraspinal SEMG have been proposed:
Treatment
Most cases of acute low back pain resolve with conservative therapy (eg, physical therapy) while continuing normal activities within limits permitted by the pain. Therefore, initial imaging or other diagnostic testing is generally not recommended unless "red flag" warning signs are present or the pain persists for more than four to six weeks. Red flag findings include significant trauma, history of cancer, unrelenting night pain, fevers or chills, and progressive motor or sensory deficits.
SEMG devices approved by the U.S. Food and Drug Administration include those that use a single electrode or a fixed array of multiple surface electrodes. Examples include the CMAP Pro (Medical Technologies) and Model 9200 EMG System (Myotronics-Noromed).
Several U.S. Food and Drug Administration-approved devices combine SEMG along the spine with other types of monitors. For example, in 2007, the Insight Discovery (Fasstech) was cleared for marketing through the 510(k) process. The device contains six sensor types, one of which is for SEMG. The indications include measuring bilateral differences in SEMG along the spine and measuring SEMG along the spine during functional tasks. (Earlier Insight models had fewer sensors.) U.S. Food and Drug Administration product code: IKN.
This evidence review was created in August 2000 and has been updated regularly with searches of the PubMed database. The most recent literature update was performed through April 10, 2024.
Evidence reviews assess whether a medical test is clinically useful. A useful test provides information to make a clinical management decision that improves the net health outcome. That is, the balance of benefits and harms is better when the test is used to manage the condition than when another test or no test is used to manage the condition.
The first step in assessing a medical test is to formulate the clinical context and purpose of the test. The test must be technically reliable, clinically valid, and clinically useful for that purpose. Evidence reviews assess the evidence on whether a test is clinically valid and clinically useful. Technical reliability is outside the scope of these reviews, and credible information on technical reliability is available from other sources.
Promotion of greater diversity and inclusion in clinical research of historically marginalized groups (e.g., People of Color [African-American, Asian, Black, Latino and Native American]; LGBTQIA (Lesbian, Gay, Bisexual, Transgender, Queer, Intersex, Asexual); Women; and People with Disabilities [Physical and Invisible]) allows policy populations to be more reflective of and findings more applicable to our diverse members. While we also strive to use inclusive language related to these groups in our policies, use of gender-specific nouns (e.g., women, men, sisters, etc.) will continue when reflective of language used in publications describing study populations.
Surface Electromyography
Paraspinal surface electomyography (SEMG) has been used as a research tool to evaluate the performance of paraspinal muscles in patients with back pain and to further understand the etiology of low back pain (LBP).3,4,5,6, Preliminary research has also been performed to determine which SEMG parameters best differentiate patients with and without back pain.7,8,
Clinical Context and Test Purpose
The purpose of paraspinal SEMG in patients who have back pain is to identify the pathogenesis of the pain (ie, muscle, joint, or disc disease) to inform a decision on a treatment plan.
The following PICO was used to select literature to inform this review.
The relevant population of interest is individuals with back pain.
Paraspinal SEMG is a noninvasive technique that aggregates data on muscle activity from groups of muscles. One or more electrodes are placed on the skin surface, and recordings are taken at rest, in various positions, or during a series of exercises.
Other noninvasive techniques to assess back pain include clinical examination and imaging technologies.
The general outcomes of interest are a reduction in back pain and improvement in activities of daily living.
Both false-positive test results and false-negative results can lead to an incorrect recommendation for the type of treatment or no treatment at all. Some treatments are long-term programs, and if individuals are incorrectly referred to the program, more appropriate therapy will be delayed.
For the evaluation of clinical validity of the paraspinal SEMG test, studies that meet the following eligibility criteria were considered:
Reported on the accuracy of the marketed version of the technology (including any algorithms used to calculate scores);
Included a suitable reference standard;
Patient/sample clinical characteristics were described;
Patient/sample selection criteria were described.
Clinically Valid
A test must detect the presence or absence of a condition, the risk of developing a condition in the future, or treatment response (beneficial or adverse).
No articles that directly compare the results of SEMG (which tests groups of muscles) with needle electromyography (which tests individual muscles) for diagnosing any specific muscle pathology were identified in literature searches. However, the pathology of individual muscles (ie, radiculopathy, neuropathy) may represent a different process than the pathology of muscle groups (ie, muscle strain, spasm), and thus SEMG may be considered by its advocates as a unique test for which there is currently no criterion standard. Nevertheless, even if one accepts this premise, there are inadequate data to evaluate the diagnostic performance of SEMG. In some instances, the asymmetrical electrical activity may have been used to define abnormality; results may be compared with normative data. However, no published literature was identified defining what degree of asymmetry would constitute abnormality.
A study by du Rose and Breen (2016) looked into the relationship between lumbar intervertebral range of motion and paraspinal muscle activity in healthy adults, as measured by SEMG and quantitative fluoroscopy, to establish "normal" measurements. .9, Fluoroscopic images and SEMG measurements were taken for 20 men with no history of low back pain (LBP). What would be considered normal intervertebral ranges of motion were related to a diverse set of muscle activation patterns as measured by SEMG. The authors concluded that larger sample sizes and measurements from patients with LB Pwould be needed to established standard criterion.
Absent a criterion standard diagnostic test, correlation with the clinical symptoms and physical exam is critical. De Luca (1993) published a series of studies investigating a type of SEMG called the Back Analysis System, consisting of surface electrodes and other components to measure the electrical activity of muscles during isometric exercises designed to produce muscle fatigue 4, . Using physical exam and clinical history as a criterion standard, De Luca (1993) found that the Back Analysis System accurately identified control and back pain patients 84% and 91% of the time, respectively, with the values increasing to 100% in some populations. (Accuracy was defined as the sum of true-positive and true-negative results.) However, these studies were not designed as a clinical diagnostic tool per se but were intended to investigate the etiology of back pain and to investigate muscular fatigue patterns in patients with and without back pain.
Hu et al (2010, 2014) published 2 articles on dynamic topography, an approach to analyzing SEMG findings.10,11, Both studies included patients with LBP and healthy controls. All participants underwent SEMG at study enrollment and then back pain patients participated in a rehabilitation program. The first study found different dynamic topography at baseline between the healthy people and back pain samples (a more symmetric pattern in healthy controls).10, After physical therapy, the dynamic topography images of back pain patients were more similar to the healthy controls on some of the parameters assessed. In the second study, following rehabilitation, back pain patients were classified as responders or nonresponders based on changes in back pain severity.11, Some associations were found between baseline SEMG parameters and response to rehabilitation. Surface electromyography was not repeated after the rehabilitation program, and thus it is unclear whether there are any significant associations between continued symptoms and SEMG abnormalities. Moreover, it is unclear how SEMG analysis would affect treatment decisions for patients with LBP.
Clinically Useful
A test is clinically useful if the use of the results informs management decisions that improve the net health outcome of care. The net health outcome can be improved if patients receive correct therapy, or more effective therapy, or avoid unnecessary therapy, or avoid unnecessary testing.
Direct Evidence
Direct evidence of clinical utility is provided by studies that have compared health outcomes for patients managed with and without the test. Because these are intervention studies, the preferred evidence would be from randomized controlled trials.
A number of studies have described SEMG as an aid in classifying LBP .12,13,14,15,16, .Most of this research has focused on the use of SEMG to assess muscle fatigability rather than on how information from test findings could enhance patient management. While SEMG may be used to document muscle spasm or other muscular abnormalities objectively, it is unclear how such objective documentation would supplant or enhance clinical evaluation, or how this information would be used to alter the treatment plan. In part, the difficulty in clinical interpretation is understanding the extent to which the SEMG abnormalities are primary or secondary. Additionally, as noted in the Background section, no specific workup is recommended for acute LBP without warning signs.
The following studies have proposed using SEMG results to inform treatment decisions; however, none provided data to validate whether treatment based on SEMG results in improved outcomes.
In a study of patients with chronic LBP (N=216) by Kienbacher et al (2016), SEMG showed potential to discriminate between impaired and unimpaired neuromuscular regulation of back extensors, which would provide useful information for designing individualized exercise programs.17,
In a study of patients with LBP (n=27) and pain-free controls (n=23) by Schabrun et al (2017), SEMG detected a loss of discrete motor cortical organization of the paraspinal muscles among those with LBP.18, The invasive technique of needle electromyography is usually performed to detect this pathology. Patients with cortical reorganization may benefit from motor skill training.
In 2 older studies (1988, 1992), SEMG was shown to differentiate muscle spasm from muscle contracture.19,20, Muscle spasm would be treated with relaxation therapy, and contracture would be treated with stretching exercises.
Chain of Evidence
Indirect evidence on clinical utility rests on clinical validity. If the evidence is insufficient to demonstrate test performance, no inferences can be made about clinical utility. Current evidence on clinical validity does not permit construction of a chain of evidence to support the use of SEMG as a diagnostic tool for evaluating and monitoring back pain.
For individuals who have back pain who receive paraspinal SEMG for evaluation and monitoring, the evidence includes several nonrandomized studies on using findings to classify back pain. Relevant outcomes are test accuracy and validity, symptoms, functional outcomes, quality of life, and resource utilization. There have been no studies directly comparing SEMG with other noninvasive techniques for evaluating back pain, and standard criteria for normal and abnormal SEMG measurements have not been determined. Surface electromyography has been proposed as a noninvasive technique providing objective measurements that would inform treatment decisions in patients with back pain. While studies have shown that SEMG results have detected different pathologies in patients with back pain, none of the studies reported health outcomes. There are also no data on the impact of SEMG for managing patients. The evidence is insufficient to determine that the technology results in an improvement in the net health outcome.
[ ] MedicallyNecessary | [X] Investigational |
The purpose of the following information is to provide reference material. Inclusion does not imply endorsement or alignment with the evidence review conclusions.
Guidelines or position statements will be considered for inclusion in ‘Supplemental Information' if they were issued by, or jointly by, a US professional society, an international society with US representation, or National Institute for Health and Care Excellence (NICE). Priority will be given to guidelines that are informed by a systematic review, include strength of evidence ratings, and include a description of management of conflict of interest.
In 2019, the guideline from the American College of Occupational and Environmental Medicine on diagnostic tests for low back disorders does not recommend surface electromyography as a technique for diagnosing low back disorders, based on insufficient evidence of efficacy. 2,
In 2020, the North American Spine Society with input from the American Academy of Pain Medicine issued a guideline on the diagnosis and treatment of low back pain. 21, When discussing the diagnostic accuracy of nonimaging tests, the guideline lacks any statement on surface electromyography.
Not applicable.
Medicare National Coverage
There is no national coverage determination. In the absence of a national coverage determination, coverage decisions are left to the discretion of local Medicare carriers.
Ongoing and Unpublished Clinical Trials
A search of ClinicalTrials.gov in April 2024 did not identify any ongoing or unpublished trials that would likely influence this review.
Codes | Number | Description |
---|---|---|
CPT | 96002 | Dynamic surface electromyography, during walking or other functional activities, 1-12 muscles |
95999 | Unlisted neurological or neuromuscular diagnostic procedure | |
97799 | Unlisted physical medicine/rehabilitation service or procedure | |
HCPCS | S3900 | Surface electromyography (EMG) |
ICD-10-CM | Investigational for all applicable diagnosis codes | |
M54.00-M54.9 | Dorsalgia code range | |
ICD-10-PCS | ICD-10-PCS codes are only used for inpatient services | |
4A0FX3Z | Measuring and monitoring, physiological systems, measurement, musculoskeletal, external, contractility | |
Type of Service | Medicine | |
Place of Service | Outpatient/Inpatient |
As per correct coding guidelines
Date | Action | Description |
07/15/2024 | Annual Review | Policy updated with literature review through April 10, 2024; no references added. Policy statement unchanged. |
07/06/2023 | Annual Review | Policy updated with literature review through April 13, 2023; references added. Policy statement unchanged. A paragraph for promotion of greater diversity and inclusion in clinical research of historically marginalized groups was added. |
07/08/2022 | Annual Review | Policy updated with literature review through April 14, 2022; no references added. Policy statement unchanged. |
07/20/2021 | Annual Review | Policy updated with literature review through April 30, 2021; no references added. Policy statement unchanged. |
11/16/2020 | Review | Policy updated with literature review through August 12, 2020; references added. Policy statement unchanged. |
07/06/2020 | Annual Review | No changes |
07/26/2019 | Annual Review | Policy updated with literature review through April 1, 2019, no references added. Policy statement unchanged. |
08/22/2017 | | |
09/10/2015 | | |
09/10/2014 | | |
02/10/2012 | ICD-10 added | |
03/25/2009 | (iCES) | |
04/09/2007 | | |