![]() | Clinical UM Guideline |
| Subject: | Electrical Nerve Stimulation, Transcutaneous, Percutaneous | ||
| Guideline #: | CG-DME-04 | Current Effective Date: | 10/12/2011 |
| Status: | Reviewed | Last Review Date: | 08/18/2011 |
| Description |
Electrical stimulation is a method used to treat pain through electrodes placed on or just beneath the skin that send small electrical impulses to underlying sensory nerve fibers to modify pain perception. It is theorized that electrical stimulation of the nerve fibers close to a segment of the spinal cord blocks the pain signals from reaching the brain or that electrical stimulation reduces inflammation, swelling and relaxes muscle fibers by releasing endorphins in the brain which act like analgesics. Transcutaneous electrical nerve stimulation (TENS) and percutaneous electrical nerve stimulation (PENS) are considered in this document.
Note: Please see the following related document(s) for additional information:
CG-ANC-03 Acupuncture
| Clinical Indications |
Medically Necessary:
FDA approved TENS and PENS units are considered medically necessary when prescribed as a treatment for pain for those who have not responded to other modalities, in the following situations:
An FDA approved TENS garment, when prescribed, is considered medically necessary when:
| Coding |
The following codes for treatments and procedures applicable to this document are included below for informational purposes. Inclusion or exclusion of a procedure, diagnosis or device code(s) does not constitute or imply member coverage or provider reimbursement policy. Please refer to the member's contract benefits in effect at the time of service to determine coverage or non-coverage of these services as it applies to an individual member.
| HCPCS | |
| A4595 | Electrical stimulator supplies, 2 lead, per month (e.g., TENS, NMES) |
| A4630 | Replacement batteries, medically necessary, transcutaneous electrical stimulator, owned by patient |
| E0720 | Transcutaneous electrical nerve stimulation (TENS) device, two lead, localized stimulation |
| E0730 | Transcutaneous electrical nerve stimulation (TENS) device, four or more leads, for multiple nerve stimulation |
| E0731 | Form-fitting conductive garment for delivery of TENS or NMES (with conductive fibers separated from the patient's skin by layers of fabric) |
| ICD-9 Diagnosis | |
| All diagnoses | |
| Discussion/General Information |
Transcutaneous electrical nerve stimulation (TENS) uses a battery operated device that applies electrical stimulation at the site of the pain by wired electrodes that are taped to the surface of the skin. TENS can also be delivered by a form-fitting conductive garment (e.g., a garment with conductive fibers which are separated from the individuals' skin by layers of fabric) and is used when a condition exists that precludes conventional TENS electrode placement. TENS has been used to relieve pain related to musculoskeletal conditions, or pain associated with active or post trauma injury.
Percutaneous electrical nerve stimulation (PENS) is similar in concept to TENS, but differs in that needle electrodes are implanted just beneath the skin instead of being taped to the surface of the skin. It is important to distinguish PENS from acupuncture with electrical stimulation. In electrical acupuncture, needle electrodes are also inserted just below the skin, but they are not necessarily inserted at the site of pain, but placed according to acupuncture meridians.
There are many published reports regarding the use of TENS and PENS for various types of conditions such as low back pain (LBP), myofascial and arthritic pain, sympathetically mediated pain, neurogenic pain, visceral pain, diabetic neuropathy and postsurgical pain. While randomized trials have focused on both TENS and PENS, all of the studies have methodologic flaws limiting interpretation, including adequate blinding, drop outs, stimulation variables and outcome measures. However, it is recognized that both TENS and PENS are widely accepted in the physician community as a treatment of a variety of etiologies of pain.
The American Society of Anesthesiologists (ASA) and American Society of Regional Anesthesia and Pain Medicine (ASRA) support the use of TENS in their revised guideline recommending that "TENS should be used as a multimodal approach to pain management for patients with chronic back pain and may be used for other pain conditions (e.g. neck and phantom limb pain)" (ASA/ASRA, 2010).
| References |
Peer Reviewed Publications:
Government Agency, Medical Society and Other Authoritative Publications:
| Index |
Electrical Nerve Stimulation, Transcutaneous and Percutaneous
PENS (Percutaneous Electrical Nerve Stimulation)
Percutaneous Electrical Nerve Stimulation (PENS)
TENS (Transcutaneous Electrical Nerve Stimulation)
Transcutaneous Electrical Nerve Stimulation (TENS)
| History |
| Status | Date | Action |
| Reviewed | 08/18/2011 | Medical Policy & Technology Assessment (MPTAC) review. No change to criteria. Coding and References updated. |
| Reviewed | 08/19/2010 | MPTAC review. No change to criteria. Discussion and References updated. |
| Reviewed | 08/27/2009 | MPTAC review. References updated. |
| Reviewed | 08/28/2008 | MPTAC review. References updated. |
| Reviewed | 08/23/2007 | MPTAC review. References updated. |
| 01/01/2007 | Updated coding section with 01/01/2007 CPT/HCPCS changes. | |
| Revised | 09/14/2006 | MPTAC review. Revision included addressing TENS garment. References updated. |
| 11/22/2005 | Added reference for Centers for Medicare and Medicaid Services (CMS) – National Coverage Determination (NCD). | |
| Revised | 09/22/2005 | MPTAC review. Revisions based on Pre-merger Anthem and Pre-merger WellPoint Harmonization. |
| Pre-Merger Organizations | Last Review Date | Document Number | Title |
| Anthem, Inc. | None | ||
| Anthem BCBS | None | ||
| WellPoint Health Networks, Inc. | 04/28/2005 | 5.10.01 | Electrical Nerve Stimulation, Transcutaneous, Percutaneous |