Description:
An auditory brainstem implant (ABI) is designed to restore some hearing in people with neurofibromatosis type 2 (NF2) who are rendered deaf by bilateral removal of neurofibromas involving the auditory nerve. ABIs have also been studied to restore hearing for other non-neurofibromatosis indications.

For individuals who are deaf due to bilateral resection of neurofibromas of the auditory nerve who receive an ABI, the evidence includes a large prospective case series. Relevant outcomes are functional outcomes, quality of life, and treatment-related morbidity. The U.S. Food and Drug Administration (FDA) approval of the Nucleus 24 device in 2000 was based on a prospective case series of 90 patients 12 years of age or older, of whom 60 had the implant for at least 3 months. From this group, 95% had a significant improvement in lip reading or improvement on sound-alone tests. While use of an ABI is associated with a very modest improvement in hearing, this level of improvement is considered significant for those patients who have no other treatment options. Based on these results, ABIs are considered appropriate for the patient population included in the trial (i.e., age ≥ 12 years with NF2 and deafness following tumor removal). The evidence is sufficient to determine that the technology results in a meaningful improvement in the net health outcome.

For individuals who are deaf due to nontumor etiologies who receive an ABI, the evidence includes case series and systematic reviews of case series. Relevant outcomes are functional outcomes, quality of life, and treatment-related morbidity. In general, ABIs have not demonstrated hearing benefits over cochlear implants for many non-NF2 conditions. However, ABIs hold promise for select patients when the cochlea or cochlear nerve is absent. Many recent and ongoing ABI studies are being conducted in children. For children, hearing is critical for language development, and this device has potential to substantially improve health outcomes. The most common nontumor conditions in children are cochlear aplasia and cochlear nerve aplasia. There are questions about the durability of the now obsolete Nucleus 24 in active young children. Evaluation is currently ongoing with the recently available Nucleus ABI541to determine its efficacy and durability in children. In addition, ABI studies have shown inferior outcomes in children with other disabilities. Thus, further study is also needed to define populations that would benefit from these devices. The evidence is insufficient to determine the effects of the technology on health outcomes.

Background 
The auditory brainstem implant (ABI) is intended to restore some hearing in people with neurofibromatosis type 2 who are rendered deaf by bilateral removal of the characteristic neurofibromas involving the auditory nerve. The ABI consists of an externally worn speech processor that provides auditory information by electrical signal that is transferred to a receiver/stimulator implanted in the temporal bone. The receiver stimulator is, in turn, attached to an electrode array implanted on the surface of the cochlear nerve in the brainstem, thus bypassing the inner ear and auditory nerve. The electrode stimulates multiple sites on the cochlear nucleus, which is then processed normally by the brain. To place the electrode array on the surface of the cochlear nucleus, the surgeon must be able to visualize specific anatomic landmarks. Because large neurofibromas compress the brainstem and distort the underlying anatomy, it can be difficult or impossible for the surgeon to correctly place the electrode array. For this reason, patients with large, long-standing tumors may not benefit from the device.

ABIs are also being studied to determine whether they can restore hearing for other non-neurofibromatosis causes of hearing impairment in adults and children, including absence of or trauma to the cochlea or auditory nerve. It is estimated that 1.7 per 100,000 children are affected by bilateral cochlea or cochlear nerve aplasia and 2.6 per 100,000 children are affected by bilateral cochlea or cochlear nerve hypoplasia.¹  

Regulatory Status 
In 2000, the Nucleus^® 24 Auditory Brainstem Implant System (Cochlear Corp.) was approved by the U.S. Food and Drug Administration (FDA) through the premarket approval process. The speech processor and receiver are similar to the devices used in cochlear implants; the electrode array placed on the brainstem is the novel component of the device. The device is indicated for individuals 12 years of age or older who have been diagnosed with neurofibromatosis type 2. The Nucleus^® 24 Auditory Brainstem Implant System labeling states: "The efficacy of bilateral implantation with the ABI [auditory brainstem implant] has not been studied."² The Nucleus^® 24 is now obsolete.

In June 2016, the Nucleus ABI541 Auditory Brainstem Implant (Cochlear Corp.) was approved by FDA through a supplement to the premarket approval for the Nucleus^® 24. The new implant is indicated for individuals 12 years of age or older who have been diagnosed with neurofibromatosis type 2.

FDA product code: MCM.

Policy: 
Unilateral use of an auditory brainstem implant (using surface electrodes on the cochlear nuclei) may be considered MEDICALLY NECESSARY in patients with neurofibromatosis type 2, who are 12 years of age or older, and who are rendered deaf due to bilateral resection of neurofibromas of the auditory nerve.

An auditory brainstem implant is investigational and /or unproven and therefore considered NOT MEDICALLY NECESSARY for all other conditions including non-neurofibromatosis-type 2 indications.

Bilateral use of an auditory brainstem implant is investigational and /or unproven and therefore considered NOT MEDICALLY NECESSARY.

Penetrating electrode auditory brainstem implant (PABI) is investigational and /or unproven and therefore considered NOT MEDICALLY NECESSARY . 

Policy Guidelines
Please see the Codes table for details.

Benefit Application
BlueCard^®/National Account Issues
Implantation of an auditory brainstem implant is a specialized procedure that may require out-of-network referral.

State or federal mandates (e.g., FEP) may dictate that all devices, drugs, or biologics approved by the U.S. Food and Drug Administration (FDA) may not be considered investigational, and thus these devices may be assessed only on the basis of their medical necessity.

Some facilities may negotiate a global fee for the implantation of the device and the associated aural rehabilitation. However, charges for rehabilitation may be subject to individual contractual limitations.

Rationale
Evidence reviews assess the clinical evidence to determine whether the use of a technology improves the net health outcome. Broadly defined, health outcomes are length of life, quality of life, and ability to function¾including benefits and harms. Every clinical condition has specific outcomes that are important to patients and to managing the course of that condition. Validated outcome measures are necessary to ascertain whether a condition improves or worsens; and whether the magnitude of that change is clinically significant. The net health outcome is a balance of benefits and harms.

To assess whether the evidence is sufficient to draw conclusions about the net health outcome of a technology, 2 domains are examined: the relevance and the quality and credibility. To be relevant, studies must represent one or more intended clinical use of the technology in the intended population and compare an effective and appropriate alternative at a comparable intensity. For some conditions, the alternative will be supportive care or surveillance. The quality and credibility of the evidence depend on study design and conduct, minimizing bias and confounding that can generate incorrect findings. The randomized controlled trial is preferred to assess efficacy; however, in some circumstances, nonrandomized studies may be adequate. Randomized controlled trials are rarely large enough or long enough to capture less common adverse events and long-term effects. Other types of studies can be used for these purposes and to assess generalizability to broader clinical populations and settings of clinical practice.

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.

In the case of the auditory brainstem implant (ABI), studies that compare outcomes before and after device implantation can provide useful information on health outcomes. Following is a summary of the key literature to date.

Auditory Brainstem Implant for Bilateral Resection of Neurofibromas of the Auditory Nerve
Clinical Context and Therapy Purpose
The purpose of an auditory brainstem implant in individuals who are deaf due to bilateral resection of neurofibromas of the auditory nerve is to provide a treatment option that is an alternative to observation alone.

The following PICO was used to select literature to inform this review.

Populations
The relevant population(s) of interest are individuals who are deaf and have undergone bilateral resection of neurofibromas of the auditory nerve.

Interventions
The therapy being considered is an auditory brainstem implant.

Comparators
The following practice is currently being used to make decisions about hearing restoration in individuals who are deaf due to bilateral resection of neurofibromas of the auditory nerve: observation alone.

Outcomes
The general outcomes of interest are functional outcomes, quality of life and treatment-related morbidity. Functional outcomes include change in hearing and hearing-related function (e.g., sound recognition and speech perception).

Study Selection Criteria
Methodologically credible studies were selected using the following principles:

• To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs.
• In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies.
• To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought.
• Consistent with a "best available evidence approach," within each category of study design, studies with larger sample sizes and longer durations were sought.
• Studies with duplicative or overlapping populations were excluded.

Review of Evidence
U.S. Food and Drug Administration (FDA) approval of the Nucleus 24 Auditory Brainstem Implant System was based on results in a case series of 90 patients with neurofibromatosis type 2 (neurofibromatosis type 2), ages 12 years and older.^1,4 Of the 90 subjects evaluated, 28 complications occurred in 26 patients; 26 of these complications resolved without surgical or extensive medical intervention. Two patients had infections of the postoperative flap requiring explantation of the device. Sixty patients had a minimum experience of 3 to 6 months with the device, and thus effectiveness outcomes were also evaluated. Overall device benefit was defined as a significant enhancement of lip reading or an above-chance improvement on sound-alone tests. Based on this definition, 95% (57/60) of patients derived benefit from the device. Among the 90 patients receiving the implant, 16 did not receive auditory stimulation from the device postoperatively, either due to migration of the implanted electrodes or surgical misplacement.

A single small (N = 10) trial from 2008 was identified on a penetrating ABI (PABI).⁵ This prospective clinical trial enrolled patients with neurofibromatosis type 2 who received a PABI after vestibular schwannoma removal. The PABI is an extension of the ABI technology that uses surface electrodes on cochlear nuclei. The PABI uses 8 or 10 penetrating microelectrodes in conjunction with a separate array of 10 to 13 surface electrodes. The PABI met the goals of lower threshold, increased pitch range, and high selectivity, but these properties did not improve speech recognition.

A systematic review conducted by Ontario (Canada) Health as part of a Health Technology Assessment included 16 observational studies (N = 491) comparing the effectiveness of ABI to no treatment in adults with neurofibromatosis type 2 (Table 1 and Table 2)⁶. Risk of bias among the included studies was assessed using the Risk of Bias in Non-randomized Studies — of Interventions (ROBINS-I) tool, and overall quality of evidence was assessed using the Grading of Recommendation, Assessment, Development and Evaluation (GRADE) Handbook. Results were reported qualitatively, and no meta-analyses were conducted due to heterogeneity in testing conditions and outcomes. The review found high quality of evidence of benefit of ABI on sound recognition (7 studies), speech perception with with lip reading (5 studies) and subjective hearing benefit (5 studies). Evidence favoring ABI was moderate for speech perception without lip reading (10 studies) and low for quality of life (1 study). The most commonly reported surgical complications, based on low quality evidence from 12 studies, were cerebrospinal fluid leak in 3% to 15% of participants and infection in 10% to 13% or participants.

Table 1. SR-MA Characteristics

Study	Dates	Trials	Participants	N (Range)	Design	Duration
Ontario Health6	1993 – 2016; literature searches conducted through June 2018	19 observational studies	Adults with neurofibromatosis type 2 who were not candidates for cochlear implantation	491 (8 – 61)	6 prospective cohort studies 11 retrospective cohort studies 2 cross-sectional studies	1 month to 18 years (mean, median not reported)

Table 2. SR-MA Results

Study	Sound Recognition	Speech Perception	Subjective Benefits of Hearing	Quality of Life	Surgical Complications
Ontario Health6	ABI vs. no treatment	ABI vs. no treatment	ABI vs. no treatment	ABI vs. no treatment	ABI vs. no treatment
Number of studies; N	7 observational studies; N = 169	15 observational studies; N = 348	5 observational studies; N = 141	1 observational study; N = 11	12 observational studies; N =
Qualitative assessment of ABI effectiveness	Allows any degree of improvement in sound recognition vs. no treatment	ABI only: Likely allows any degree of improvement in speech perception when used alone ABI + lip reading: Allows any degree of improvement in speech perception when used in conjunction with lip-reading	Provides subjective benefits of hearing	May improve quality of life	Most common complications were cerebrospinal fluid leak infection
Level of evidence (GRADE)	High	ABI only: Moderate ABI + lip reading: High	High	Low	Low

Section Summary: Auditory Brainstem Implant for Bilateral Resection of Neurofibromas of the Auditory Nerve
The evidence on ABI for bilateral resection of neurofibromas of the auditory nerve includes large case series, a clinical trial and a systematic review of small observational studies. A 2018 case series of 90 adults, 60 of which had the minimum experience of 3 to 6 months with the Nucleus 24 ABI system, suggested that adults may benefit from its usage. European studies followed 32 patients, 24 of which with an ABI activated experienced significant improvements on the Sound Effects Recognition Test and Monosyllable-Trochee-Polysyllable test. An Ontario (Canada) Health systematic review found ABI associated with better hearing function relative to no treatment, but evidence on other outcomes was limited.

Auditory Brainstem Implant for Nontumor Etiologies
Clinical Context and Therapy Purpose
The purpose of an auditory brainstem implant in individuals who are deaf due to nontumor etiologies is to provide a treatment option that is an alternative to observation alone.

The following PICO was used to select literature to inform this review.

Populations
The relevant population(s) of interest are individuals who are deaf due to nontumor etiologies.

Interventions
The therapy being considered is an auditory brainstem implant.

Comparators
The following practice is currently being used to make decisions about hearing restoration in individuals who are deaf due to nontumor etiologies: observation alone.

Outcomes
The general outcomes of interest are functional outcomes, quality of life and treatment-related morbidity. Functional outcomes include change in hearing and hearing-related function (e.g., sound recognition and speech perception).

Study Selection Criteria
Methodologically credible studies were selected using the following principles:

• To assess efficacy outcomes, comparative controlled prospective trials were sought, with a preference for RCTs.
• In the absence of such trials, comparative observational studies were sought, with a preference for prospective studies.
• To assess long-term outcomes and adverse events, single-arm studies that capture longer periods of follow-up and/or larger populations were sought.
• Consistent with a 'best available evidence approach,' within each category of study design, studies with larger sample sizes and longer durations were sought.
• Studies with duplicative or overlapping populations were excluded.

Review of Evidence
Adults
Merkus et al. (2014) conducted a systematic review of ABIs for non-neurofibromatosis type 2 indications.⁷ Included in the review were 144 non-neurofibromatosis type 2 ABI cases from 31 articles. Non-neurofibromatosis type 2 indications for which ABIs have been evaluated include cochlear otosclerosis, temporal bone fractures, bilateral traumatic cochlear nerve disruption, autoimmune inner ear disease, auditory neuropathy, cochlear nerve aplasia, and vestibular schwannoma in the only hearing ear. Cochlear implants have generally provided better hearing than ABIs when the cochlea and cochlear nerve are intact. Complete bilateral disruption of the cochlear nerve from trauma did not exist in the literature and cochlear malformation did not preclude cochlear implant. While the evidence is limited, it appears as if cochlear implants demonstrate greater hearing benefits than ABIs in patients with non-neurofibromatosis type 2 indications.

In a literature review by Medina et al. (2014) assessing ABI for traumatic deafness, cochlear implant performed better than ABI.⁸ However, there was limited evidence on which to draw conclusions, because only 3 articles (total N = 7 patients) were identified in the review on ABI for traumatic deafness.

Children
Systematic Reviews
A systematic review of nontumor pediatric ABI outcomes was reported by Noij et al. (2015).⁹ It included 21 studies with 162 children, at a mean age of 4.3 years (range, 11 months to 17 years). Nine reports were from a single group from Italy (described below) and it could not be determined if there was patient overlap across these studies. Nearly all studies were retrospective series or cohorts; 1 was a case-control. Most children (63.6%) had cochlear nerve aplasia. Other conditions were cochlear aplasia, cochlear nerve hypoplasia, cochlear malformations, ossified cochlea, auditory neuropathy, trauma, and cochlear hypoplasia. Twenty-five percent of the patients had previously received a cochlear implant. Forty major and minor implant-related complications were reported, the most common being cerebrospinal fluid leak (8.5% of patients).The most common side effects associated with ABI use were discomfort of the body and/or limb, dizziness/vertigo/nystagmus, pain in the head and/or neck, and stimulation of the facial nerve or involuntary swallowing, gagging, or coughing. A variety of auditory tests were used; the most common (6 studies) was the Categories of Auditory Performance (CAP) index (range, 0 – 7; high score indicates better hearing). There was an improvement in CAP scores over time. After 5 years, almost 50% of patients had CAP scores greater than 4 (5 [understanding of common phrases without lip reading] to 7 [use of telephone with known speaker]). Children who also had nonauditory disabilities never attained a CAP score greater than 4. There was no significant effect of the age of implantation.

Case Series
Many of the larger series on ABI in nontumor patients are from a group that includes Colletti and Colletti. In 2013, this group reported on ABIs in 21 children, ranging in age from 1.7 to 5 years, with deafness unrelated to neurofibromatosis, who had a poor response to cochlear implants.¹⁰ At surgery, the cochlear nerve was absent in each patient. Significant improvements in CAP index scores were seen after ABI (p < 0.001).

Sennaroglu et al. (2016) reported on follow-up of at least 1 year for 35 children who had received ABI.¹¹ This followed a 2009 preliminary report of 11 prelingually deaf children ages 30 to 56 months who received an ABI.¹² Sixty children had received an ABI from this center in Turkey. The children who had received the ABI in the previous year were excluded from the 2016 analysis. Over half (n = 19) of the cases were due to cochlear hypoplasia. ABI models implanted were Cochlear, Med El, and Neurelec. At regular follow-up, children were evaluated with the CAP, Speech Intelligibility Rate, Functional Auditory Performance of Cochlea Implantation, and Manchester scores. About half the children were in the CAP category 5 and could understand common phrases without lip reading. In the subgroup with better hearing thresholds (25 – 40 decibels), some (17.6%) were able to understand conversation without lip reading, use the telephone with known speaker (11.8%), and follow group conversation in a noisy room (5.9%). For children with higher hearing thresholds (> 50 decibels), none exceeded CAP category 5. Speech Intelligibility Rate and Manchester scores were also better with greater hearing thresholds. Auditory performance measured with the Functional Auditory Performance of Cochlea Implantation was in the 10th percentile for all groups and was worse compared with cochlear implantation. As was also found in the Noij systematic review (discussed above), children with additional nonauditory disabilities had worse outcomes.

Mixed Populations
Other reports from the group of Colletti and Colletti include a 2005 report on ABIs in 16 children and adults who had nontumor diseases of the cochlear nerve or cochlea and 13 patients with NF2.¹³ Ages ranged from 14 months to 70 years; the nontumor group included patients with head trauma, complete cochlear ossification, auditory neuropathy, and bilateral cochlear nerve aplasia. Following implantation, the adult nontumor group scored substantially higher than the patients with NF2 in open set speech perception tests. Some children showed dramatic improvements in word and sentence recognition over a 1-year follow-up. Short-term adverse events included dizziness or tingling sensations in the leg, arm, and throat (20/29 patients). Additional studies from this group have reported improvements in hearing with ABIs in “nontumor” patients, including a 2006 report on 54 nontumor patients¹⁴ and a 2007 report on 22 non-neurofibromatosis patients.¹⁵

In a retrospective review, Colletti et al. (2010) reported on complications from ABI surgery in 83 adults and 31 children, 78 of whom had nontumor cochlear or cochlear nerve disorders.¹⁶ Authors found that ABI complication rates were similar to those for cochlear implant surgery. Additionally, there were significantly fewer major and minor complications in nontumor patients than in NF2 patients.

Section Summary: Auditory Brainstem Implant in Nontumor Etiologies
The evidence on ABI in nontumor patients includes case series and systematic reviews. A 2014 systematic review suggested that ABI might improve outcomes in bilateral complete cochlear and inner ear aplasia. Recent research includes studies of children who are deaf but would not benefit from a cochlear implant. The most common conditions in these studies are cochlear aplasia and cochlear nerve aplasia. Hearing in this age group is critical for language development, and the ABI has potential to substantially improve health outcomes for this age group. However, studies of early (now obsolete) ABI devices found a high rate of failure in children and high rates of adverse events in adults. Evidence from ongoing studies assessing newer ABI models is needed to evaluate efficacy and durability in patients with nontumor ABI indications.

The purpose of the following information is to provide reference material. Inclusion does not imply endorsement or alignment with the evidence review conclusions.

Practice Guidelines and Position Statements
Guidelines or position statements will be considered for inclusion in "Supplemental Information" if they were issued by, or jointly by, a U.S. professional society, an international society with U.S. 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.

National Institute for Health and Care Excellence
In 2005, the National Institute for Health and Care Excellence issued guidance on interventional procedures for auditory brainstem implants.¹⁷ The guidance stated: “ …evidence on safety and efficacy of auditory brain stem implants appears adequate to support the use of this procedure by surgical teams experienced in this technique.”

U.S. Preventive Services Task Force Recommendations
Not applicable.

Ongoing and Unpublished Clinical Trials
Some currently unpublished trials that might influence this review are listed in Table 3.

Table 3. Summary of Key Trials

Trial Name		Planned Enrollment	Completion Date
Ongoing
NCT02310399	Auditory Brainstem Implant (ABI) in Children With No Cochlear or Auditory Nerves	20	May 2022
NCT02630589	Implantation of an Auditory Brainstem Implant for the Treatment of Incapacitating Unilateral Tinnitus	10	Jan 2026
Unpublished
NCT01904448	An Early Feasibility Study of the Safety and Efficacy of the Nucleus 24 Auditory Brainstem Implant in Children With Cochlear or Cochlear Nerve Disorders Not Resulting From Neurofibromatosis Type II	5	Oct 2017

IRB: Institutional Review Board; NCT: national clinical trial.

References:

1. Food and Drug Administration. Nucleus 24 Auditory Brainstem Implant System. FDA Summary of Safety and Effectiveness. 2000; https://www.accessdata.fda.gov/cdrh_docs/pdf/P000015B.pdf; Accessed January 20, 2023.
2. Kaplan AB, Kozin ED, Puram SV, et al. Auditory brainstem implant candidacy in the United States in children 0-17 years old. Int J Pediatr Otorhinolaryngol. Mar 2015; 79(3): 310-315. PMID 25577282
3. Food and Drug Administration. Premarket Approval (PMA). Nucleus ABI541 Auditory Brainstem Implant. 2016. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpma/pma.cfm?id=P000015S012. Accessed January 19, 2023.
4. Ebinger K, Otto S, Arcaroli J, et al. Multichannel auditory brainstem implant: US clinical trial results. J Laryngol Otol Suppl. 2000; (27): 50-3. PMID 11211440
5. Otto SR, Shannon RV, Wilkinson EP, et al. Audiologic outcomes with the penetrating electrode auditory brainstem implant. Otol Neurotol. Dec 2008; 29(8): 1147-54. PMID 18931643
6. Ontario Health (Quality). Auditory brainstem implantation for adults with neurofibromatosis 2 or severe inner ear abnormalities: a health technology assessment. Ont Health Technol Assess Ser [Internet]. 2020 Mar;20(4): 185. https://www.hqontario.ca/evidence-to-improve-care/health-technology- assessment/reviews-and-recommendations/auditory-brainstem-implantation-for-adults-with- neurofibromatosis-2-or-severe-inner-ear-abnormalities; Accessed February 2, 2023.
7. Merkus P, Di Lella F, Di Trapani G, et al. Indications and contraindications of auditory brainstem implants: systematic review and illustrative cases. Eur Arch Otorhinolaryngol. Jan 2014; 271(1): 3-13. PMID 23404468
8. Medina M, Di Lella F, Di Trapani G, et al. Cochlear implantation versus auditory brainstem implantation in bilateral total deafness after head trauma: personal experience and review of the literature. Otol Neurotol. Feb 2014; 35(2): 260-70. PMID 24448286
9. Noij KS, Kozin ED, Sethi R, et al. Systematic Review of Nontumor Pediatric Auditory Brainstem Implant Outcomes. Otolaryngol Head Neck Surg. Nov 2015; 153(5): 739-50. PMID 26227469
10. Colletti L, Wilkinson EP, Colletti V. Auditory brainstem implantation after unsuccessful cochlear implantation of children with clinical diagnosis of cochlear nerve deficiency. Ann Otol Rhinol Laryngol. Oct 2013; 122(10): 605-12. PMID 24294682
11. Sennaroglu L, Sennaroglu G, Yucel E, et al. Long-term Results of ABI in Children With Severe Inner Ear Malformations. Otol Neurotol. Aug 2016; 37(7): 865-72. PMID 27273392
12. Sennaroglu L, Ziyal I, Atas A, et al. Preliminary results of auditory brainstem implantation in prelingually deaf children with inner ear malformations including severe stenosis of the cochlear aperture and aplasia of the cochlear nerve. Otol Neurotol. Sep 2009; 30(6): 708-15. PMID 19704357
13. Colletti V, Carner M, Miorelli V, et al. Auditory brainstem implant (ABI): new frontiers in adults and children. Otolaryngol Head Neck Surg. Jul 2005; 133(1): 126-38. PMID 16025066
14. Colletti V. Auditory outcomes in tumor vs. nontumor patients fitted with auditory brainstem implants. Adv Otorhinolaryngol. 2006; 64: 167-185. PMID 16891842
15. Colletti L. Beneficial auditory and cognitive effects of auditory brainstem implantation in children. Acta Otolaryngol. Sep 2007; 127(9): 943-6. PMID 17712673
16. Colletti V, Shannon RV, Carner M, et al. Complications in auditory brainstem implant surgery in adults and children. Otol Neurotol. Jun 2010; 31(4): 558-64. PMID 20393378
17. National Institute Health and Care Excellence (NICE). Auditory brain stem implants [IPG108]. 2005 https://www.nice.org.uk/guidance/ipg108. Accessed February 2, 2023.

Coding Section

Codes	Number	Description
CPT	61863	Twist drill, burr hole, craniotomy, or craniectomy with stereotactic implantation of neurostimulator electrode array in subcortical site (e.g., thalamus, globus pallidus, subthalamic nucleus, periventricular, periaqueductal gray), without use of intraoperative microelectrode recording; first array
	61864	Twist drill, burr hole, craniotomy, or craniectomy with stereotactic implantation of neurostimulator electrode array in subcortical site (e.g., thalamus, globus pallidus, subthalamic nucleus, periventricular, periaqueductal gray), without use of intraoperative microelectrode recording; each additional array (List separately in addition to primary procedure)
	61867	Twist drill, burr hole, craniotomy, or craniectomy with stereotactic implantation of neurostimulator electrode array in subcortical site (e.g., thalamus, globus pallidus, subthalamic nucleus, periventricular, periaqueductal gray), with use of intraoperative microelectrode recording; first array
	61868	Twist drill, burr hole, craniotomy, or craniectomy with stereotactic implantation of neurostimulator electrode array in subcortical site (e.g., thalamus, globus pallidus, subthalamic nucleus, periventricular, periaqueductal gray), with use of intraoperative microelectrode recording; each additional array (List separately in addition to primary procedure)
	92640	Diagnosis analysis with programming of auditory brainstem implant, per hour
HCPCS	S2235	Implantation of auditory brainstem implant
ICD-10-CM	Q85.02	Neurofibromatosis, type 2
ICD-10-PCS		ICD-10-PCS codes are only used for inpatient services. There is no specific ICD-10-PCS code for this procedure.
	00H00MZ, 00H03MZ, 00H04MZ	Insertion of neurostimulator electrode, brain, code by approach (open, percutaneous, percutaneous endoscopic)
Type of Service
Place of Service

Procedure and diagnosis codes on Medical Policy documents are included only as a general reference tool for each policy. They may not be all-inclusive.  

This medical policy was developed through consideration of peer-reviewed medical literature generally recognized by the relevant medical community, U.S. FDA approval status, nationally accepted standards of medical practice and accepted standards of medical practice in this community, Blue Cross Blue Shield Association technology assessment program (TEC) and other nonaffiliated technology evaluation centers, reference to federal regulations, other plan medical policies, and accredited national guidelines.

"Current Procedural Terminology © American Medical Association. All Rights Reserved" 

History From 2024 Forward     

07/11/2024 Annual review, no change to policy intent

01012024  NEW POLICY