Medical policy: Electromyography (EMG) (Needle and Non-Needle) of the Anal or Urethral Sphincter

Policy number: MP 2.096

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

Needle and non-needle electromyography (EMG) of the anal or urethral sphincter may be considered medically necessary for the following indications:

  • For initial diagnostic evaluation of an individual with an evacuation or voiding dysfunction (e.g., fecal incontinence, urinary incontinence, bladder outlet obstruction, detrusor sphincter dyssynergia, neurogenic conditions) when the test is likely to affect the course of therapy (e.g., pelvic floor training, surgical intervention, pharmacologic intervention, biofeedback therapy or other clinically accepted interventions)
  • For the repeat assessment of an individual with neurogenic conditions of the anal or urethral sphincter resulting from disorders such as, but not limited to, multiple sclerosis, spinal cord injury, paralysis, or motor neuron disease. For these individuals, EMG testing of the anal or urethral sphincter may be required up to two times per year.

Policy guidelines

Note: Electromyography (EMG) performed as part of biofeedback therapy is inherent to the biofeedback service. EMG should not be reported in addition to biofeedback.

Cross-references:

  • MP 1.109 Periurethral Bulking Agents as a Treatment of Vesicoureteral Reflux
  • MP 2.030 Intraoperative Neurophysiologic Monitoring (Sensory Evoked Potentials, Motor Evoked Potentials, EEG Monitoring)
  • MP 2.063 Electromyography and Nerve Conduction Studies

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. The FEP medical policy manual can be found at: FEP Medical Policy Manual.

Description/Background

Electromyography (EMG) of the anal or urethral sphincter is a urodynamic study that quantitatively assesses the electrical activity from the striated muscles of the urethral or anal sphincter or from the perineal floor muscles. EMG provides objective data about the innervation to these muscles and the synchronization between the detrusor muscle of the bladder and the external sphincter; it is most useful to evaluate sphincter relaxation during voluntary detrusor contraction. EMG is used in the diagnosis and follow-up of known or suspected neurogenic (originating in nervous tissue) and non-neurogenic (originating in areas other than nervous tissue) conditions of the anal or urethral sphincters. An EMG of the anal or urethral sphincter can be performed using a needle electrode, a fine wire electrode, a surface electrode on the perianal skin, an anal plug, or an assembly of multiple-surface EMG electrodes placed in the anal canal.

Conditions commonly evaluated by EMG (needle and non-needle):

  • Fecal Incontinence.
  • Urinary incontinence.
  • Bladder outlet obstruction (a blockage at the base of the bladder that reduces or prevents the flow of urine into the urethra).
  • Detrusor sphincter dyssynergia (a neurogenic abnormality that involves an impaired coordination between bladder contraction and sphincter relaxation).
  • Neurogenic conditions of the anal or urethral sphincter resulting from disorders such as, but not limited to, multiple sclerosis, spinal cord injury, paralysis, or motor neuron disease.

An EMG alone gives useful information about sphincteric function. However, an EMG is more valuable when performed in conjunction with cystometry to determine whether the striated sphincter appropriately increases its activity during bladder filling and whether rest occurs normally before and during bladder contraction. EMG is useful in diagnosing detrusor sphincter dyssynergia, which can occur in individuals with neurogenic conditions such as multiple sclerosis, spinal cord injury, or other neurologic lesions. EMG is also valuable in conjunction with pressure-flow studies, which analyze detrusor pressure and flow rate during the voiding phase. EMG during pressure-flow studies is useful in diagnosing conditions such as detrusor sphincter dyssynergia, dysfunctional voiding (non-neurogenic), bladder outlet obstruction, or incontinence.

When injury to the sacral roots of the spinal cord is suspected, a separate study of the anal sphincter using needle EMG may be required, as this is the only muscle accessible to needle EMG examination that receives its innervation through these roots. Needle EMG of the anal sphincter may also be performed to assess the innervation and anatomic integrity of the sphincters. In addition, characteristics of neurogenic bladders can change with time and disease progression; therefore, re-evaluation may be needed when symptoms change despite medical intervention.

Rationale

The 2012 American Urological Association/Society of Urodynamics, Female Pelvic Medicine and Urogenital Reconstruction (AUA/SUFU) Guideline on Adult Urodynamics recommends EMG testing in patients with relevant neurologic disease at risk for neurogenic bladder, or in patients with other neurologic disease and elevated post void residual (PVR) volume or urinary symptoms (Evidence Strength - Grade C).

The signal source for measurement of EMG activity is the activity of the external urethral sphincter, the external anal sphincter, and the pelvic floor musculature. The two most commonly used sources of measurement are surface electrodes and concentric needle electrodes. Needle placement may be a significant source of discomfort for patients, and reproducibility may be an issue without significant operator experience. The surface electrode has the advantage of ease (reproducibility) of placement and patient comfort. Although the signal source is less specific, surface electrodes can provide a good quality signal if properly used. The practical application of EMG involves determination of whether the perineal muscles are relaxed or contracting. The most important information provided by the EMG is the determination of whether perineal contractions are coordinated or uncoordinated with detrusor contractions.

The major limitation of EMG testing is that it is technically challenging and often non-specific within urodynamic studies. Artifacts are common, and accurate interpretation requires close interaction between the clinician and the patient. The clinician must have a solid understanding of the patient’s history and relevant physical findings. EMG by itself rarely establishes a diagnosis of an uncoordinated sphincter; instead, the findings must be interpreted alongside fluoroscopy, cystometry, and flow rate to achieve the most accurate diagnosis.

Definitions

N/A

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 member’s 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.

Covered when medically necessary:

Procedure codes

51784

51785

 

 

 

ICD-10-CM diagnosis code
Description

G04.1

Tropical spastic paraplegia

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

G35

Multiple sclerosis

G35.A

Relapsing-remitting multiple sclerosis

G35.B

Primary progressive multiple sclerosis

G35.B0

Primary progressive multiple sclerosis, unspecified

G35.B1

Active primary progressive multiple sclerosis

G35.B2

Non-active primary progressive multiple sclerosis

G35.C

Secondary progressive multiple sclerosis

G35.C0

Secondary progressive multiple sclerosis, unspecified

G35.C1

Active secondary progressive multiple sclerosis

G35.C2

Non-active secondary progressive multiple sclerosis

G35.D

Multiple sclerosis, unspecified

G81.01

Flaccid hemiplegia affecting right dominant side

G81.02

Flaccid hemiplegia affecting left dominant side

G81.03

Flaccid hemiplegia affecting right nondominant side

G81.04

Flaccid hemiplegia affecting left nondominant side

G81.11

Spastic hemiplegia affecting right dominant side

G81.12

Spastic hemiplegia affecting left dominant side

G81.13

Spastic hemiplegia affecting right nondominant side

G81.14

Spastic hemiplegia affecting left nondominant side

G82.21

Paraplegia, complete

G82.22

Paraplegia, incomplete

G82.51

Quadriplegia, C1-C4 complete

G82.52

Quadriplegia, C1-C4 incomplete

G82.53

Quadriplegia, C5-C7 complete

G82.54

Quadriplegia, C5-C7 incomplete

G83.11

Monoplegia of lower limb affecting right dominant side

G83.12

Monoplegia of lower limb affecting left dominant side

G83.13

Monoplegia of lower limb affecting right nondominant side

G83.14

Monoplegia of lower limb affecting left nondominant side

G83.4

Cauda equina syndrome

G83.9

Paralytic syndrome, unspecified

K59.01

Slow transit constipation

K59.02

Outlet dysfunction constipation

K59.09

Other constipation

K59.4

Anal spasm

N31.0

Uninhibited neuropathic bladder, not elsewhere classified

N31.1

Reflex neuropathic bladder, not elsewhere classified

N31.2

Flaccid neuropathic bladder, not elsewhere classified

N31.8

Other neuromuscular dysfunction of bladder

N31.9

Neuromuscular dysfunction of bladder, unspecified

N32.0

Bladder-neck obstruction

N32.81

Overactive bladder

N32.89

Other specified disorders of bladder

N35.016

Post-traumatic urethral stricture, male, overlapping sites

N35.116

Post-infective urethral stricture, not elsewhere classified, male, overlapping sites

N35.811

Other urethral stricture, male, meatal

N35.812

Other bulbous urethral stricture, male

N35.813

Other membranous urethral stricture, male

N35.814

Other anterior urethral stricture, male, anterior

N35.816

Other urethral stricture, male, overlapping sites

N35.819

Other urethral stricture, male, unspecified site

N35.82

Other urethral stricture, female

N35.911

Unspecified urethral stricture, male, meatal

N35.912

Unspecified bulbous urethral stricture, male

N35.913

Unspecified membranous urethral stricture, male

N35.914

Unspecified anterior urethral stricture, male

N35.916

Unspecified urethral stricture, male, overlapping sites

N35.919

Unspecified urethral stricture, male, unspecified site

N35.92

Unspecified urethral stricture, female

N36.41

Hypermobility of urethra

N36.42

Intrinsic sphincter deficiency (ISD)

N36.43

Combined hypermobility of urethra and intrinsic sphincter deficiency

N36.44

Muscular disorders of urethra

N36.8

Other specified disorders of urethra

N39.3

Stress incontinence (female) (male)

N39.41

Urge incontinence

N39.42

Incontinence without sensory awareness

N39.43

Post-void dribbling

N39.44

Nocturnal enuresis

N39.45

Continuous leakage

N39.46

Mixed incontinence

N39.490

Overflow incontinence

N39.491

Coital incontinence

N39.492

Postural (urinary) incontinence

N39.498

Other specified urinary incontinence

N40.1

Benign prostatic hyperplasia with lower urinary tract symptoms

N40.3

Nodular prostate with lower urinary tract symptoms

N81.0

Urethrocele

N81.10

Cystocele, unspecified

N81.11

Cystocele, midline

N81.12

Cystocele, lateral

N81.89

Other female genital prolapse

N81.9

Female genital prolapse, unspecified

N99.116

Postprocedural urethral stricture, male, overlapping sites

Q64.31

Congenital bladder neck obstruction

Q64.32

Congenital stricture of urethra

Q64.33

Congenital stricture of urinary meatus

Q64.39

Other atresia and stenosis of urethra and bladder neck

R15.0

Incomplete defecation

R15.1

Fecal smearing

R15.2

Fecal urgency

R15.9

Full incontinence of feces

R30.0

Dysuria

R32

Unspecified urinary incontinence

R33.8

Other retention of urine

R33.9

Retention of urine, unspecified

R35.0

Frequency of micturition

R35.1

Nocturia

R35.8

Other polyuria

R35.81

Nocturnal polyuria

R35.89

Other polyuria

R39.11

Hesitancy of micturition

R39.12

Poor urinary stream

R39.13

Splitting of urinary stream

R39.14

Feeling of incomplete bladder emptying

R39.15

Urgency of urination

R39.16

Straining to void

R39.191

Need to immediately re-void

R39.192

Position dependent micturition

R39.198

Other difficulties with micturition

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

S14.131A

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

S14.151A

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

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

S24.131A

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

S24.141A

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

S24.151A

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

S34.01XA

Concussion and edema of lumbar spinal cord, initial encounter

S34.02XA

Concussion and edema of sacral 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

References

  1. American Association of Neuromuscular & Electrodiagnostic Medicine (AANEM). Recommended policy for electrodiagnostic medicine. November 2021
  2. American Urological Association. Adult Urodynamics: AUA/SUFU Guideline (2012).
  3. Bauer SB. Neurogenic bladder: etiology and assessment. Pediatr Nephrol. 2008; 23(4):541-551
  4. Bharucha AE. Update of tests of colon and rectal structure and function. J Clin Gastroenterol. 2006; 40(2):96-103
  5. Gill, B. Neurogenic bladder. [eMedicine Web site]. 05/15/14. Updated December 24, 2020.
  6. Dorflinger A, Monga A. Voiding dysfunction. Curr Opin Obstet Gynecol. 2001; 13(5):507-512
  7. Elneil S. Urinary retention in women and sacral neuromodulation. Int Urogynecol J Pelvic Floor Dysfunct. 2010; 21 Suppl 2:475-483
  8. Griffiths D, Kondo A, Bauer S, et al. Dynamic testing. In: Abrams P, Cardozo L, Khoury S, Wein A, eds. Incontinence. Volume I: Basics & Evaluation. Paris, France: Health Publication Ltd; 2005: 587-674
  9. Heesakkers JP, Gerresten RR. Urinary incontinence sphincter functioning from a urological perspective. Digestion. 2004; 69(2):93-101
  10. Lefaucheur JP. Neurophysiological testing in anorectal disorders. Muscle & Nerve. 2006; 33(3):324-333
  11. Novitas Solutions, Inc. Local Coverage Determination (LCD). L35081: Nerve Conduction Studies and Electromyography. Effective 10/1/17
  12. Novitas Solutions, Inc. Local Coverage Determination (LCD). L34977: Anorectal Manometry, Anal Electromyography, and Biofeedback Training for Perineal Muscles and Anorectal or Urethral Sphincters. Effective 10/1/16.
  13. Peterson AC, Webster GD. Urodynamic and videourodynamic evaluation of voiding dysfunction. Campbell-Walsh's Urology, 9th edition. Philadelphia: WB Saunders, Chapter 28, 2007
  14. Podnar S. Neurophysiology of the neurogenic lower urinary tract disorders. Clinical Neurophysiol. 2007; 118(7):1423-1437
  15. Robson, K. Lembo A. Fecal Incontinence in Adults: Etiology and Evaluation. In: UpToDate Online Journal [serial online]. Waltham, MA: UpToDate; updated February 27, 2025
  16. Sakakibara R, Uchiyama T, Yamanishi T, et al. Sphincter EMG as a diagnostic tool in autonomic disorders. Clin Auton Res. 2009; 19(1):20-31
  17. Scott SM, Gladman MA. Manometric, sensorimotor, and neurophysiologic evaluation of anorectal function. Gastroenterol Clin North Am. 2008; 37(3):511-538
  18. Ginsberg DA, Boone TB, Cameron AP et al: The AUA/SUFU Guideline on Adult Neurogenic Lower Urinary Tract Dysfunction: Diagnosis and Evaluation. J Urol 2021; 206: 1097
  19. Wald, Arnold MD, MACG; Bharucha, Adil E. MBBS, MD²; Limketkai, Berkeley MD, PhD, FACG³; Malcolm, Allison MBBS, FRACP⁴; Remes-Troche, Jose M. MD, MSc⁵; Whitehead, William E. PhD⁶; Zutshi, Massarat MD⁷,⁸. ACG Clinical Guidelines: Management of Benign Anorectal Disorders. The American Journal of Gastroenterology 116(10): p 1987-2008, October 2021. DOI: 10.14309/ajg.0000000000001507
  20. Ginsberg DA, Boone TB, Cameron AP, Gousse A, Kaufman MR, Keays E, et al. The AUA/SUFU Guideline on Adult Neurogenic Lower Urinary Tract Dysfunction: Treatment and Follow-up. Journal of Urology [Internet]. 2021 Nov 1 [cited 2024 Sep 20];206(5):1106-13
  21. Ginsberg DA, Boone TB, Cameron AP, Gousse A, Kaufman MR, Keays E, et al. The AUA/SUFU Guideline on Adult Neurogenic Lower Urinary Tract Dysfunction: Diagnosis and Evaluation. Journal of Urology [Internet]. 2021 Nov 1 [cited 2024 Sep 20];206(5):1097-105

Policy history

MP 2.096

06/19/2020 Consensus Review. Policy statement unchanged. Product variation, benefit variation, and disclaimer updated. Coding and references reviewed.

02/11/2021 Consensus Review. Policy statement unchanged. References updated.

09/07/2021 Administrative Update. New ICD-10 codes added to policy, effective 10/01/2021.

02/23/2022 Consensus Review. Policy statement unchanged. Product Variation and FEP language revised. Background and references updated.

04/24/2023 Consensus Review. Policy statement unchanged. Updated references. No coding changes.

09/08/2023 Administrative Update. Revised ICD 10 codes, eff 10/01/2023.

09/20/2024 Consensus Review. Policy statement unchanged. References updated. No coding changes.

07/18/2025 Consensus Review. No change to policy statement. References updated.

09/02/2025 Administrative Update. New ICD 10 codes, eff 10/01/2025 added.

09/23/2025 Administrative Update. Removed Benefit Variations Section and updated Disclaimer.

05/29/2026 Consensus Review. No change to policy statement. Rationale updated.