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Official Description

Electronic analysis of implanted neurostimulator pulse generator/transmitter (eg, contact group[s], interleaving, amplitude, pulse width, frequency [Hz], on/off cycling, burst, magnet mode, dose lockout, patient selectable parameters, responsive neurostimulation, detection algorithms, closed loop parameters, and passive parameters) by physician or other qualified health care professional; with complex cranial nerve neurostimulator pulse generator/transmitter programming by physician or other qualified health care professional

© Copyright 2025 American Medical Association. All rights reserved.

Common Language Description

The CPT® Code 95977 refers to the electronic analysis of an implanted neurostimulator pulse generator or transmitter, which is a device used to deliver electrical impulses to cranial nerves for therapeutic purposes. This procedure involves a comprehensive assessment of various parameters associated with the neurostimulator, including contact groups, interleaving, amplitude, pulse width, frequency (measured in Hertz), on/off cycling, burst mode, magnet mode, dose lockout, and patient-selectable parameters. Additionally, it encompasses the evaluation of responsive neurostimulation, detection algorithms, closed-loop parameters, and passive parameters. The analysis is conducted by a physician or another qualified healthcare professional to ensure the device is functioning optimally. The implanted neurostimulator system consists of a pulse generator that is surgically placed in a subcutaneous pocket, with leads that are tunneled from the nerve being stimulated to the generator. This setup allows for the delivery of electrical impulses to treat various conditions, such as chronic pain, epilepsy, and depression. Regular electronic analysis is crucial for monitoring the device's performance and making necessary adjustments to maintain its efficacy. During this analysis, the healthcare professional documents any logged events from the neurostimulator, assesses battery status, measures electrode impedance, and reviews the current programmed settings. For cranial nerve neurostimulator pulse generator programming, the healthcare provider adjusts specific parameters to achieve optimal therapeutic stimulation. This may involve modifying the frequency, pulse width, current, duration, magnetic mode, or sensing capabilities of the device. The programming process may include multiple trials where three or fewer parameters are adjusted for a simple cranial nerve neurostimulator pulse generator (CPT® Code 95976) and four or more parameters for a complex one (CPT® Code 95977), until the desired therapeutic effect is achieved.

© Copyright 2025 Coding Ahead. All rights reserved.

1. Indications

The electronic analysis and programming of an implanted neurostimulator pulse generator/transmitter, as described by CPT® Code 95977, is indicated for patients who require ongoing management of cranial nerve stimulation for various medical conditions. The specific indications include:

  • Chronic Pain Patients suffering from chronic pain conditions may benefit from neurostimulation to alleviate discomfort and improve quality of life.
  • Epilepsy Individuals with epilepsy may require neurostimulation to help control seizures and reduce their frequency.
  • Depression Neurostimulation can be utilized as a treatment option for patients with treatment-resistant depression, providing an alternative to traditional therapies.

2. Procedure

The procedure for electronic analysis and programming of the cranial nerve neurostimulator pulse generator/transmitter involves several detailed steps:

  • Step 1: Initial Assessment The healthcare professional begins by conducting an initial assessment of the patient’s condition and reviewing the history of the neurostimulator's performance. This includes checking for any reported issues or changes in the patient's symptoms since the last analysis.
  • Step 2: Electronic Analysis The physician or qualified healthcare professional performs an electronic analysis of the implanted neurostimulator. This involves evaluating various parameters such as contact groups, interleaving, amplitude, pulse width, frequency, on/off cycling, burst mode, magnet mode, dose lockout, and patient-selectable parameters. The analysis ensures that the device is functioning correctly and that all settings are optimal for the patient's needs.
  • Step 3: Documentation During the analysis, the healthcare provider documents critical information, including any logged events from the neurostimulator, battery status, electrode impedance, and the current programmed settings. This documentation is essential for tracking the device's performance over time and making informed decisions about adjustments.
  • Step 4: Programming Adjustments Following the analysis, the healthcare professional proceeds to program the neurostimulator. This step involves adjusting parameters such as frequency, pulse width, current, duration, magnetic mode, or sensing capabilities. For a complex cranial nerve neurostimulator, four or more parameters may be adjusted to achieve optimal therapeutic stimulation.
  • Step 5: Trial Stimulation The healthcare provider conducts multiple trials of nerve stimulation, adjusting three or fewer parameters for a simple cranial nerve neurostimulator (CPT® Code 95976) and four or more for a complex one (CPT® Code 95977). This iterative process continues until the desired therapeutic effect is achieved, ensuring that the patient receives the most effective stimulation possible.

3. Post-Procedure

After the electronic analysis and programming of the neurostimulator pulse generator/transmitter, the patient may be monitored for any immediate reactions to the adjustments made. It is essential to provide the patient with information regarding potential side effects and the importance of reporting any changes in their symptoms or device performance. Follow-up appointments may be scheduled to reassess the device's effectiveness and make further adjustments as necessary. The healthcare provider will also review the patient's overall treatment plan to ensure that the neurostimulation continues to meet their therapeutic needs.

Short Descr ALYS CPLX CN NPGT PRGRMG
Medium Descr ELEC ALYS IMPLT CPLX CN NPGT PRGRMG
Long Descr Electronic analysis of implanted neurostimulator pulse generator/transmitter (eg, contact group[s], interleaving, amplitude, pulse width, frequency [Hz], on/off cycling, burst, magnet mode, dose lockout, patient selectable parameters, responsive neurostimulation, detection algorithms, closed loop parameters, and passive parameters) by physician or other qualified health care professional; with complex cranial nerve neurostimulator pulse generator/transmitter programming by physician or other qualified health care professional
Status Code Active Code
Global Days XXX - Global Concept Does Not Apply
PC/TC Indicator (26, TC) 0 - Physician Service Code
Multiple Procedures (51) 0 - No payment adjustment rules for multiple procedures apply.
Bilateral Surgery (50) 0 - 150% payment adjustment for bilateral procedures does NOT apply.
Physician Supervisions 09 - Concept does not apply.
Assistant Surgeon (80, 82) 0 - Payment restriction for assistants at surgery applies to this procedure...
Co-Surgeons (62) 0 - Co-surgeons not permitted for this procedure.
Team Surgery (66) 0 - Team surgeons not permitted for this procedure.
Diagnostic Imaging Family 99 - Concept Does Not Apply
APC Status Indicator Procedure or Service, Not Discounted when Multiple
Berenson-Eggers TOS (BETOS) none
MUE 1
GZ Item or service expected to be denied as not reasonable and necessary
59 Distinct procedural service: under certain circumstances, it may be necessary to indicate that a procedure or service was distinct or independent from other non-e/m services performed on the same day. modifier 59 is used to identify procedures/services, other than e/m services, that are not normally reported together, but are appropriate under the circumstances. documentation must support a different session, different procedure or surgery, different site or organ system, separate incision/excision, separate lesion, or separate injury (or area of injury in extensive injuries) not ordinarily encountered or performed on the same day by the same individual. however, when another already established modifier is appropriate it should be used rather than modifier 59. only if no more descriptive modifier is available, and the use of modifier 59 best explains the circumstances, should modifier 59 be used. note: modifier 59 should not be appended to an e/m service. to report a separate and distinct e/m service with a non-e/m service performed on the same date, see modifier 25.
79 Unrelated procedure or service by the same physician or other qualified health care professional during the postoperative period: the individual may need to indicate that the performance of a procedure or service during the postoperative period was unrelated to the original procedure. this circumstance may be reported by using modifier 79. (for repeat procedures on the same day, see modifier 76.)
GC This service has been performed in part by a resident under the direction of a teaching physician
GA Waiver of liability statement issued as required by payer policy, individual case
52 Reduced services: under certain circumstances a service or procedure is partially reduced or eliminated at the discretion of the physician or other qualified health care professional. under these circumstances the service provided can be identified by its usual procedure number and the addition of modifier 52, signifying that the service is reduced. this provides a means of reporting reduced services without disturbing the identification of the basic service. note: for hospital outpatient reporting of a previously scheduled procedure/service that is partially reduced or cancelled as a result of extenuating circumstances or those that threaten the well-being of the patient prior to or after administration of anesthesia, see modifiers 73 and 74 (see modifiers approved for asc hospital outpatient use).
22 Increased procedural services: when the work required to provide a service is substantially greater than typically required, it may be identified by adding modifier 22 to the usual procedure code. documentation must support the substantial additional work and the reason for the additional work (ie, increased intensity, time, technical difficulty of procedure, severity of patient's condition, physical and mental effort required). note: this modifier should not be appended to an e/m service.
24 Unrelated evaluation and management service by the same physician or other qualified health care professional during a postoperative period: the physician or other qualified health care professional may need to indicate that an evaluation and management service was performed during a postoperative period for a reason(s) unrelated to the original procedure. this circumstance may be reported by adding modifier 24 to the appropriate level of e/m service.
25 Significant, separately identifiable evaluation and management service by the same physician or other qualified health care professional on the same day of the procedure or other service: it may be necessary to indicate that on the day a procedure or service identified by a cpt code was performed, the patient's condition required a significant, separately identifiable e/m service above and beyond the other service provided or beyond the usual preoperative and postoperative care associated with the procedure that was performed. a significant, separately identifiable e/m service is defined or substantiated by documentation that satisfies the relevant criteria for the respective e/m service to be reported (see evaluation and management services guidelines for instructions on determining level of e/m service). the e/m service may be prompted by the symptom or condition for which the procedure and/or service was provided. as such, different diagnoses are not required for reporting of the e/m services on the same date. this circumstance may be reported by adding modifier 25 to the appropriate level of e/m service. note: this modifier is not used to report an e/m service that resulted in a decision to perform surgery. see modifier 57 for significant, separately identifiable non-e/m services, see modifier 59.
51 Multiple procedures: when multiple procedures, other than e/m services, physical medicine and rehabilitation services or provision of supplies (eg, vaccines), are performed at the same session by the same individual, the primary procedure or service may be reported as listed. the additional procedure(s) or service(s) may be identified by appending modifier 51 to the additional procedure or service code(s). note: this modifier should not be appended to designated "add-on" codes (see appendix d).
58 Staged or related procedure or service by the same physician or other qualified health care professional during the postoperative period: it may be necessary to indicate that the performance of a procedure or service during the postoperative period was: (a) planned or anticipated (staged); (b) more extensive than the original procedure; or (c) for therapy following a surgical procedure. this circumstance may be reported by adding modifier 58 to the staged or related procedure. note: for treatment of a problem that requires a return to the operating/procedure room (eg, unanticipated clinical condition), see modifier 78.
80 Assistant surgeon: surgical assistant services may be identified by adding modifier 80 to the usual procedure number(s).
95 Synchronous telemedicine service rendered via a real-time interactive audio and video telecommunications system: synchronous telemedicine service is defined as a real-time interaction between a physician or other qualified health care professional and a patient who is located at a distant site from the physician or other qualified health care professional. the totality of the communication of information exchanged between the physician or other qualified health care professional and the patient during the course of the synchronous telemedicine service must be of an amount and nature that would be sufficient to meet the key components and/or requirements of the same service when rendered via a face-to-face interaction. modifier 95 may only be appended to the services listed in appendix p. appendix p is the list of cpt codes for services that are typically performed face-to-face, but may be rendered via a real-time (synchronous) interactive audio and video telecommunications system.
CC Procedure code change (use 'cc' when the procedure code submitted was changed either for administrative reasons or because an incorrect code was filed)
CR Catastrophe/disaster related
FS Split (or shared) evaluation and management visit
GW Service not related to the hospice patient's terminal condition
GY Item or service statutorily excluded, does not meet the definition of any medicare benefit or, for non-medicare insurers, is not a contract benefit
LT Left side (used to identify procedures performed on the left side of the body)
PD Diagnostic or related non diagnostic item or service provided in a wholly owned or operated entity to a patient who is admitted as an inpatient within 3 days
Q0 Investigational clinical service provided in a clinical research study that is in an approved clinical research study
SA Nurse practitioner rendering service in collaboration with a physician
X4 Episodic/focused services: for reporting services by clinicians who provide focused care on particular types of treatment limited to a defined period and circumstance; the patient has a problem, acute or chronic, that will be treated with surgery, radiation, or some other type of generally time-limited intervention; reporting clinician service examples include but are not limited to, the orthopedic surgeon performing a knee replacement and seeing the patient through the postoperative period
XU Unusual non-overlapping service, the use of a service that is distinct because it does not overlap usual components of the main service
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2019-01-01 Added Added
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