MEDICAL POLICY

POLICY
RELATED POLICIES
POLICY GUIDELINES
DESCRIPTION
SCOPE
BENEFIT APPLICATION
RATIONALE
REFERENCES
CODING
APPENDIX
HISTORY

Cochlear Implant

Number 7.01.05*

Effective Date August 12, 2013

Revision Date(s) 08/12/13; 08/14/12; 08/09/11; 04/13/10; 05/13/08; 04/10/07; 08/08/06; 08/09/05; 07/13/04; 05/11/04; 05/13/03; 03/11/03; 10/08/02; 10/09/01; 01/04/99; 11/03/98; 01/97

Replaces N/A

*Medicare has a policy

Policy

Unilateral or bilateral cochlear implantation of a U.S. Food and Drug Administration (FDA)-approved cochlear implant device may be considered medically necessary in patients age 12 months and older with bilateral severe to profound pre- or postlingual (sensorineural) hearing loss defined as a hearing threshold of pure-tone average of 70 dB (decibels) hearing loss or greater at 500 Hz (hertz), 1,000 Hz, and 2,000 Hz, and have shown limited or no benefit from hearing aids.

Cochlear implantation as a treatment for patients with unilateral hearing loss with or without tinnitus is considered investigational.

Upgrades of an existing, functioning external system to achieve aesthetic improvement, such as smaller profile components or a switch from a body-worn, external sound processor to a behind-the-ear (BTE) model, are considered not medically necessary.

Related Policies

7.01.84

Semi-Implantable and Fully Implantable Middle Ear Hearing Aids

7.01.547

Implantable Bone Conduction and Bone Anchored Hearing Aids

Policy Guidelines

Bilateral cochlear implantation should be considered only when it has been determined that the alternative of unilateral cochlear implant plus hearing aid in the contralateral ear will not result in a binaural benefit; i.e., in those patients with hearing loss of a magnitude where a hearing aid will not produce the required amplification.

In certain situations, implantation may be considered before 12 months of age. One scenario is post-meningitis when cochlear ossification may preclude implantation. Another is in cases with a strong family history, since establishing a precise diagnosis is less uncertain.

Hearing loss is rated on a scale based on the threshold of hearing. Severe hearing loss is defined as a bilateral hearing threshold of 7090 dB, and profound hearing loss is defined as a bilateral hearing threshold of 90 dB and above.

In adults, limited benefit from hearing aids is defined as scores 50% correct or less in the ear to be implanted on tape-recorded sets of open-set sentence recognition. In children, limited benefit is defined as failure to develop basic auditory skills, and in older children, 30% or less correct on openset tests.

A post-cochlear implant rehabilitation program is necessary to achieve benefit from the cochlear implant. The rehabilitation program consists of 6 to 10 sessions that last approximately 2.5 hours each. The rehabilitation program includes development of skills in understanding running speech, recognition of consonants and vowels, and tests of speech perception ability.

Contraindications to cochlear implantation may include deafness due to lesions of the eighth cranial (acoustic) nerve, central auditory pathway or brain stem, active or chronic infections of the external or middle ear and mastoid cavity or tympanic membrane perforation. Cochlear ossification may prevent electrode insertion, and the absence of cochlear development as demonstrated on computed tomography scans remains an absolute contraindication.

In 2003, CPT established a range of codes (9260192606) to define a variety of postoperative evaluative and therapeutic services related to cochlear implants. Codes 92601 and 92603 describe postoperative analysis and fitting of previously placed external devices, connection to cochlear implant, and programming of the stimulator. Codes 92602 and 92604 describe subsequent sessions for measurement and adjustment of the external transmitter and re-programming of the internal stimulator.

Description

Cochlear implant is a device for individuals with severe-to-profound hearing loss who only receive limited benefit from amplification with hearing aids. A cochlear implant provides direct electrical stimulation to the auditory nerve, bypassing the usual transducer cells that are absent or nonfunctional in deaf cochlea.

Background

The basic components of a cochlear implant include both external and internal components. The external components include a microphone, an external sound processor, and an external transmitter. The internal components are implanted surgically and include an internal receiver implanted within the temporal bone and an electrode array that extends from the receiver into the cochlea through a surgically created opening in the round window of the middle ear.

Sounds that are picked up by the microphone are carried to the external sound processor, which transforms sound into coded signals that are then transmitted transcutaneously to the implanted internal receiver. The receiver converts the incoming signals to electrical impulses that are then conveyed to the electrode array, ultimately resulting in stimulation of the auditory nerve.

Regulatory Status

Several cochlear implants are commercially available in the U.S. and are manufactured by Cochlear Corporation, Advanced Bionics, and the Med El Corporation. Over the years, subsequent generations of the various components of the devices have been approved by the U.S. Food and Drug Administration (FDA), focusing on improved electrode design and speech-processing capabilities. Furthermore, smaller devices and the accumulating experience in children have resulted in broadening of the selection criteria to include children as young as 12 months. The labeled indications from the FDA for currently marketed implant devices are summarized below.

FDA-Approved Cochlear Implant Systems*

Manufacturer and Currently Marketed Cochlear Implants

Advanced Bionics® HiResolution Bionic Ear System (HiRes 90K)

Cochlear®, Nucleus 5

Med El®, Maestro (Sonata or Pulsar)

Predecessor Cochlear Implants

Clarion Multi-Strategy or HiFocus CII Bionic Ear (P940022)

Nucleus 22, 24, Freedom with Contour (P840024)

Combi 40+ (P000025)

Indications

Adults:

• ≥ 18 years of age

• Post-lingual onset of severe-to-profound bilateral sensorineural hearing loss (≥70 decibels (dB))

• Limited benefit from appropriately fitted hearing aids, defined as scoring ≤ 50% on a test of open-set Hearing in Noise Test (HINT) sentence recognition

Children:

• 12 months to 17 years of age

• Profound bilateral sensorineural deafness (>90 dB)

• Use of appropriately fitted hearing aids for at least 6 months in children 2 to 17 years of age or at least 3 months in children 12 to 23 months of age

• Lack of benefit in children <4 years of age is defined as a failure to reach developmentally appropriate auditory milestones (e.g., spontaneous response to name in quiet or to environmental sounds) measured using the Infant-Toddler Meaningful Auditory Integration Scale or Meaningful Auditory Integration Scale or <20% correct on a simple open-set word recognition test (Multisyllabic Lexical Neighborhood Test) administered using monitored live voice (70 dB SPL [sound pressure level])

• Lack of hearing aid benefit in children >4 years of age is defined as scoring <12% on a difficult open-set word recognition test (Phonetically Balanced-Kindergarten Test) or <30% on an open-set sentence test (HINT for Children) administered using recorded materials in the soundfield (70 dB SPL)

Adults:

≥ 18 years old

Pre- or post-lingual onset of moderate -to -profound bilateral sensorineural hearing loss

≤50% sentence recognition in the ear to be implanted

≤60% sentence recognition in the opposite ear or binaurally

Children 25 months to 17 years 11 months:

Severe-to-profound bilateral sensorineural hearing loss

Multi-syllabic Lexical Neighborhood Test (MLNT) scores of ≤30% in best-aided condition in children 25 months to 4 years 11 months

Lexical Neighborhood Test (LNT) scores of ≤30% in best-aided condition in children 5 years to 17 years and 11 months

Lack of progress in the development of auditory skills

Children 12 months to 24 months:

Profound sensorineural hearing loss bilaterally

Limited benefit from appropriate binaural hearing aids

Lack of progress in the development of auditory skills

Adults:

≥ 18 -years -old

Severe-to-profound bilateral sensorineural hearing loss (≥70dB)

≤40% correct Hearing in Noise test (HINT) sentences with best-sided listening condition

Children:

12 months to 18 years with profound sensorineural hearing loss (≥90dB)

In younger children, little or no benefit is defined by lack of progress in the development of simple auditory skills with hearing aids over a 3-6 month period

In older children, lack of aided benefit is defined as <20% correct on the MLNT or LNT, depending upon the child’s cognitive ability and linguistic skills

A 3-6 month trial with hearing aids is required if not previously experienced

*Note: Cochlear, Ltd. voluntarily recalled the Nucleus CI500 range in September 2011 for device malfunction in the CI512 implant. The external Nucleus 5 sound processor is not a part of the recall. Advanced Bionics HiRes90K was voluntarily recalled in November 2010 and given FDA-approval for re-entry to market the device in September 2011.

While cochlear implants have typically been used unilaterally, in recent years, interest in bilateral cochlear implantation has arisen. The proposed benefits of bilateral cochlear implants are to improve understanding of speech in noise and localization of sounds. Improvements in speech intelligibility may occur with bilateral cochlear implants through binaural summation; i.e., signal processing of sound input from 2 sides may provide a better representation of sound and allow one to separate out noise from speech. Speech intelligibility and localization of sound or spatial hearing may also be improved with head shadow and squelch effects, i.e., the ear that is closest to the noise will be received at a different frequency and with different intensity, allowing one to sort out noise and identify the direction of sound. Bilateral cochlear implantation may be performed independently with separate implants and speech processors in each ear or with a single processor. However, no single processor for bilateral cochlear implantation has been approved by the FDA for use in the U.S. In addition, single processors do not provide binaural benefit and may impair sound localization and increase the signal-to-noise ratio received by the cochlear implant.

Scope

Medical policies are systematically developed guidelines that serve as a resource for Company staff when determining coverage for specific medical procedures, drugs or devices. Coverage for medical services is subject to the limits and conditions of the member benefit plan. Members and their providers should consult the member benefit booklet or contact a customer service representative to determine whether there are any benefit limitations applicable to this service or supply.

Benefit Application

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.

A cochlear implant is a surgically implanted device. The device and implantation surgery should be reimbursed under the medical benefit.

Rationale

This policy was originally created in 1995 and was updated regularly with searches of the MEDLINE database. The most recent literature search was performed for the period April 2012 through May 13, 2013. The following is a summary of the key literature to date.

Bilateral Hearing Loss

Cochlear Implantation in Adults: Unilateral Stimulation

Cochlear implants are recognized as an effective treatment of sensorineural deafness, as noted in a 1995 National Institutes of Health Consensus Development conference, which offered the following conclusions (1):

  • Cochlear implantation has a profound impact on hearing and speech reception in postlingually deafened adults with positive impacts on psychological and social functioning.
  • Prelingually deafened adults may also benefit, although to a lesser extent than postlingually deafened adults. These individuals achieve minimal improvement in speech recognition skills. However, other basic benefits, such as improved sound awareness, may meet safety needs.
  • Training and educational intervention are fundamental for optimal postimplant benefit.

In 2009, Bond et al. (2) authored a technology assessment in the United Kingdom to investigate the clinical and cost-effectiveness of unilateral cochlear implants (using or not using hearing aids) and bilateral cochlear implants compared to a single cochlear implant (unilateral or unilateral plus hearing aids) for severely to profoundly deaf children and adults. The clinical effectiveness review included 33 papers, 2 of which were randomized controlled trials (RCTs) [deaf children (n=1,513) and adults (n=1,379)]. They used 62 different outcome measures and overall evidence was of moderate to poor quality. All studies in children that compared one cochlear implant with non-technological support or an acoustic hearing aid reported gains on all outcome measures. Weak evidence shows greater gain from earlier implantation (prior to starting school). The strongest evidence for an advantage from bilateral over unilateral implantation was for understanding speech in noisy conditions. The comparison of bilateral with unilateral cochlear implants plus an acoustic hearing aid was limited by small sample sizes and poor reporting. The authors concluded, “Unilateral cochlear implantation is safe and effective for adults and children and likely to be cost-effective in profoundly deaf adults and profoundly and prelingually deaf children. There are likely to be overall additional benefits from bilateral implantation, enabling children and adults to hold conversations more easily in social situations.”

Bond and colleagues additionally published 2 systematic reviews on the clinical and cost-effectiveness of unilateral cochlear implants, first focusing on children in 2009 (3) and subsequently focusing on adults in 2010. (4) Both reviews were conducted with a literature search that identified 1,580 titles and abstracts on cochlear implants. In the 2010 review, the authors identified 9 studies that met their inclusion criteria addressing implantation in adults. (4) The authors found the studies available were methodologically weak and too heterogeneous to perform a meta-analysis. However, they concluded there is sufficient, consistent evidence demonstrating positive benefits with unilateral cochlear implants in severely to profoundly hearing impaired adults when compared to acoustic hearing aids or no hearing support.

In January 2009, the National Institute for Health and Care Excellence (NICE) released technology appraisal guidance 166, Cochlear Implants for children and adults with severe to profound deafness. (5)

This guidance was based on the above technology assessment report by Bond and colleagues. (2)

The NICE guidance includes the following recommendations:

  1. “Unilateral cochlear implantation is recommended as an option for people with severe to profound deafness who do not receive adequate benefit from acoustic hearing aids.
  2. For purposes of this guidance, severe to profound deafness is defined as hearing only sounds that are louder than 90 dB HL [hearing level] at frequencies of 2 and 4 k hertz (Hz) without acoustic hearing aids. For adults, adequate benefit from acoustic hearing aids is defined for this guidance as a score of 50% or greater on Bamford-Kowal-Bench (BKB) sentence testing at a sound intensity of 70 dB SPL [sound pressure level].
  3. Cochlear implantation should be considered for adults only after an assessment by a multidisciplinary team. As part of the assessment, implant candidates should also have had a valid trial of an acoustic hearing aid for at least 3 months (unless contraindicated or inappropriate).”

In April 2011, a technology assessment was completed by the Tufts Evidence-based Practice Center for the Agency for Health Care Research and Quality (AHRQ) on the effectiveness of cochlear implants in adults. (6) This assessment examined 22 studies with 30 or more patients and concluded that while the studies reviewed were rated as poor to fair quality, unilateral cochlear implants are effective in adults with sensorineural hearing loss. Pre- and post-cochlear implant scores on multi-syllable tests and open-set sentence tests demonstrated significant gains in speech perception regardless of whether a contralateral hearing aid was used along with the cochlear implant. Additionally, the assessment found generic and disease-specific health-related quality of life (QOL) improved with unilateral cochlear implants. However, the available evidence was insufficient to draw conclusions on improvements in open-set sentence test scores (i.e., >40% and ≤50% or >50% and ≤60%), and any relationship between pre-implantation patient characteristics and outcomes (e.g., age, duration of hearing impairment, Hearing in Noise Test [HINT] scores and pre- or post-linguistic deafness).

In 2013, Gaylor and colleagues published an update to the AHRQ technology assessment. (7) Sixteen (of 42) studies published through May 2012 were of unilateral cochlear implants. Most unilateral implant studies showed a statistically significant improvement in mean speech scores, as measured by open-set sentence or multisyllable word tests; meta-analysis of 4 studies revealed a significant improvement in cochlear-implant relevant QOL after unilateral implantation (standard mean difference: 1.71; 95% confidence interval [CI]: 1.15-2.27). However, these studies varied in design and there was considerable heterogeneity observed across studies. (7) Similarly, A 2012 systematic review of 11 studies by Bittencourt et al. also concluded cochlear implants improved hearing outcomes over conventional hearing aids in patients with severe to profound postlingual deafness. (8)

In October 2011, Berrettini and colleagues published results of a systematic review of cochlear implant effectiveness in adults. (9) Included in the review, were 8 articles on unilateral cochlear implants in advanced age patients. All of the studies reported benefits with cochlear implantation despite advanced age at time of implant (age 70 years or older). In 6 studies, results were not significantly different between younger and older patients. However, 2 studies reported statistically significant inferior perceptive results (e.g., hearing in noise test and consonant nucleus consonant test) in older patients. This systematic review also examined 3 studies totaling 56 adults with pre-lingual deafness who received unilateral cochlear implants. The authors concluded unilateral cochlear implants provided hearing and quality-of-life benefits in prelingually deaf patients, but results were variable.

Cochlear Implantation in Adults: Bilateral Stimulation

While use of unilateral cochlear implants in patients with severe to profound hearing loss has become a well-established intervention, (6) bilateral cochlear implantation is becoming more common. Many publications have reported slight to modest improvements in sound localization and speech intelligibility with bilateral cochlear implants, especially with noisy backgrounds but not necessarily in quiet environments. When reported, the combined use of binaural stimulation improved hearing by a few decibels or percentage points.

In January 2009, the NICE technology appraisal guidance noted above (5) indicates:

  1. Simultaneous bilateral cochlear implantation in adults is recommended as an option in people with severe to profound deafness who do not receive adequate benefit from acoustic hearing aids and are blind or have other disabilities that increase their reliance on auditory stimuli as a primary sensory mechanism for spatial awareness.
  2. Sequential bilateral cochlear implantation is not recommended as an option for people with severe to profound deafness.
  3. For purposes of this guidance, severe to profound deafness is defined as hearing only sounds that are louder than 90 dB HL at frequencies of 2 and 4 k hertz (Hz) without acoustic hearing aids. Adequate benefit from acoustic hearing aids for adults is defined for this guidance as a score of 50% or greater on Bamford-Kowal-Bench (BKB) sentence testing at a sound intensity of 70 dB SPL [sound pressure level].
  4. Cochlear implantation should be considered for adults only after an assessment by a multidisciplinary team. As part of the assessment, implant candidates should also have had a valid trial of an acoustic hearing aid for at least 3 months (unless contraindicated or inappropriate).”

Crathorne and colleagues published an update of the NICE systematic review in 2012. (10) The objective was to conduct a systematic review of the clinical and cost-effectiveness of bilateral multichannel cochlear implants compared with unilateral cochlear implantation alone or in conjunction with an acoustic hearing aid, in adults with severe-to-profound hearing loss. A literature search was updated in July 2011 and January 2012. Nineteen studies were included in this update; 6 of these studies were included in the original NICE review. Two studies were RCTs with waiting list controls, 10 were prospective pre-⁄post repeated measure or cohort designs, 6 were cross-sectional in design, and one was an economic evaluation. The studies were conducted in the U.S. and Europe; all compared bilateral with unilateral implantation, and 2 compared bilateral implants with a unilateral implant plus acoustic hearing aid. (10)

The included studies in the Crathorne review were of moderate-to-poor quality, including 2 RCTs. (10) Meta-analyses could not be performed due to heterogeneity between studies in outcome measures and study design. However, all studies reported that bilateral cochlear implants improved hearing and speech perception. One RCT found a significant binaural benefit over the first ear alone for speech and noise from the front (12.6 + 5.4%, p<0.001) and when noise was ipsilateral to the first ear (21 + 6%, p<0.001), and another RCT found a significant benefit for spatial hearing at 3 months post-implantation compared with preimplantation (mean difference [standard deviation] scores: 1.46 [0.83–2.09], p<0.01). QOL results varied, showing bilateral implantation may improve QOL in the absence of worsening tinnitus. (10)

van Schoonhoven and colleagues independently published a systematic review in 2013 as an update to the original NICE review. (11) As with the Crathorne review, all studies (n=19, published through March 2011) showed a significant bilateral benefit in localization over unilateral cochlear implantation. Similarly, meta-analyses could not be performed due to the heterogeneity of the studies and the level of evidence of the included studies, which was of moderate-to-poor quality. (11)

The April 2011 AHRQ technology assessment, noted above, completed by the Tufts Evidence-based Practice Center on the effectiveness of cochlear implants in adults examined 16 studies on bilateral cochlear implantation of fair -to -moderate quality published since 2004. (6) The assessment concluded bilateral cochlear implants provide greater benefits in speech perception test scores, especially in noise, when compared to unilateral cochlear implants (with or without contralateral hearing aids). Significant binaural head shadow benefits were noted along with some benefit in binaural summation, binaural squelch effects, and sound localization with bilateral cochlear implants. However, it was unclear if these benefits were experienced under quiet conditions, although benefits increased with longer bilateral cochlear implant usage indicating a need for longer term studies. Hearing-specific quality of life could not be assessed because only one study evaluated this outcome. Additionally, the evidence available on simultaneous bilateral implantation was found to be insufficient, although gains were experienced in speech perception using open-set sentences or multi-syllable tests compared to unilateral cochlear implants or unilateral listening conditions. The assessment noted longer term studies are needed to further understand the benefits with bilateral cochlear implantation and identify candidacy criteria given the risks of a second surgery and the destruction of the cochlea preventing future medical intervention.

The update by Gaylor and colleagues to this assessment reported above showed improvement across 13 studies in communication-related outcomes with bilateral implantation compared with unilateral implantation and additional improvements in sound localization compared with unilateral device use or implantation only. (7) The risk of bias varied from medium to high across studies. Based on results from at least 2 studies, the QOL outcomes varied across tests after bilateral implantation; meta-analysis was not performed because of heterogeneity in design between the studies. (7)

In the 2011 Berrettini et al. review of cochlear implant effectiveness in adults (noted above), 13 articles on bilateral cochlear implants were reviewed. (9) Sound localization improved with bilateral cochlear implants compared to monaural hearing in 6 studies. Significant improvements in hearing in noise and in quiet environments with bilateral implants compared to unilateral implants were reported in 10 studies and 7 studies, respectively. Five of the studies reviewed addressed simultaneous implantation, 5 studies reviewed sequential implantation, and 3 studies included a mix of simultaneous and sequential implantation. However, no studies compared simultaneous to sequential bilateral implantation results, and no conclusions could be made on the timing of bilateral cochlear implantation. Smulders et al. also examined the timing of cochlear implantation in a systematic review of 11 studies; 5 studies addressed postlingually deafened adults and 7 studies addressed prelingually deafened children (discussed below). (12) One study on adults showed a delay in the timing of the second implantation resulted in poorer outcomes in quiet environments. Nevertheless, all studies reported benefits with bilateral implants, but all studies were considered to be of poor quality and with a high risk of bias.

In May 2008, the British Cochlear Implant Group (BCIG) released a position paper on bilateral cochlear implants. (13) The position paper includes the following regarding indications for use of bilateral implantation:

  • “For all profoundly deaf children in order to stimulate both auditory pathways and optimize speech, language and auditory development and maximize potential academic achievement.
  • For all profoundly deaf adults, unable to benefit from bimodal hearing;
  • For patients following meningitis or other risk of ossification, where failure to implant may result in obliteration or the cochlea, preventing future stimulation;
  • For patients with additional sensory handicap, where there is greater reliance on binaural hearing;
  • For patients who experience a loss of performance in the first implanted ear or loss of device function in the first ear but re-implantation in the same ear is contra-indicated;
  • For patients who agree to participate in research studies into bilateral implantation.”

Based on literature available, it was felt that several issues needed to be resolved through additional studies before bilateral cochlear implantation might be routinely used in patients with severe -to -profound hearing loss. Patient selection criteria need to be identified to determine in which patients the brain will be able to integrate bilateral electrical stimulation and when benefit with bilateral cochlear implants can be expected, e.g., pre- or post-lingual patients, age, duration of hearing loss, the etiology and physiology of the hearing loss, and number of auditory nerve fibers surviving. In addition, bilateral implantation poses twice the risk of unilateral implantation including surgical risk, infection, and facial nerve damage. While the potential to restore cochlear function is not foreseeable in the near future, destruction of the cochlea eliminates this possibility.

Cochlear Implantation in Pediatrics

While there is current research investigating the ability to restore hearing by stimulating cochlear hair cell regrowth, cochlear implantation damages the cochlea and eliminates this possibility. However, the potential to restore cochlear function is not foreseeable in the near future. If cochlear implantation is believed to be most beneficial at a younger age, when the nervous system is “plastic,” the potential for cochlear hair cell regrowth seems too far in the future to benefit young children and should not be a deterrent to current candidates for a cochlear implant.

As reported by Sharma and Dorman, central auditory pathways are “maximally plastic” for a period of about 3.5 years, making a case for earlier cochlear implantation of children with hearing impairment. (14) Stimulation delivered prior to about 3.5 years of age results in auditory evoked potentials that reach normal values in 3 to 6 months. However, when stimulation occurs after 7 years of age, changes occur within 1 month, but then have little to no subsequent change. Sharma et al. observed this result when they reported on auditory development in 23 children with unilateral or bilateral implants. (15) In one child who received a bilateral device with implantation of the second ear after age 7 years, the auditory responses in the second ear were similar to that seen in “late-implanted” children.

In 2011, Forli and colleagues conducted a systematic review of 49 studies on cochlear implant effectiveness in children. (16) Heterogeneity of studies precluded performance of a meta-analysis. Early implantation was examined in 22 studies, but few studies compared outcomes of implantations performed prior to one year of age to implantations performed after one year of age. Studies suggest improvements in hearing and communicative outcomes in children receiving implants prior to one year of age; although, it is not certain whether these improvements are related to duration of cochlear implant usage rather than age of implantation. However, the reviewers noted hearing outcomes have been shown to be significantly inferior in patients implanted after 24-36 months. Bilateral cochlear implants improved verbal perception in noise and sound localization compared to unilateral implants in 19 of 20 studies reviewed, but none of the studies compared learning development and language in bilateral versus unilateral cochlear implant recipients. Simultaneous versus sequential bilateral cochlear implantation results were not examined in any of the studies reviewed. Finally, 7 studies were reviewed that examined cochlear implant outcomes in children with associated disabilities. In this population, cochlear implant outcomes were inferior and occurred more slowly but were considered to be beneficial.

As noted above, the 1995 National Institutes of Health Consensus Development conference concluded cochlear implants are recognized as an effective treatment of sensorineural deafness. (1) This conference offered the following conclusions regarding cochlear implantation in children:

  • Cochlear implantation has variable results in children. Benefits are not realized immediately but rather are manifested over time, with some children continuing to show improvement over several years.
  • Cochlear implants in children under 2 -years-old are complicated by the inability to perform detailed assessment of hearing and functional communication. However, a younger age of implantation may limit the negative consequences of auditory deprivation and may allow more efficient acquisition of speech and language. Some children with postmeningitis hearing loss under the age of 2 years have received an implant due to the risk of new bone formation associated with meningitis, which may preclude a cochlear implant at a later date.

The 2008 British Cochlear Implant Group (BCIG) position paper on Bilateral Cochlear Implants, (13) as noted above, includes the following regarding indications for use of bilateral implantation in children:

  • “For all profoundly deaf children in order to stimulate both auditory pathways and optimize speech, language and auditory development and maximize potential academic achievement.
  • For patients following meningitis or other risk of ossification, where failure to implant may result in obliteration of the cochlea, preventing future stimulation;
  • For patients with additional sensory handicap, where there is greater reliance on binaural hearing;
  • For patients who experience a loss of performance in the first implanted ear or loss of device function in the first ear but re-implantation in the same ear is contra-indicated;
  • For patients who agree to participate in research studies into bilateral implantation.”

As also noted above, Bond and colleagues published 2 systematic reviews on the clinical and cost-effectiveness of unilateral cochlear implants, first focusing on children in 2009 (3) and subsequently focusing on adults in 2010. (4) Both reviews were conducted with a literature search that identified 1,580 titles and abstracts on cochlear implants. In the 2009 review, the authors identified 15 studies that met their inclusion criteria addressing cochlear implantation in children. (3) The authors found the studies available were methodologically weak and too heterogeneous to perform a meta-analysis. However, they concluded there is sufficient, consistent evidence demonstrating positive benefits with unilateral cochlear implants in severely to profoundly hearing impaired children when compared to acoustic hearing aids or no hearing support.

The 2009 National Institute for Health and Clinical Excellence (NICE) technology appraisal guidance 166, Cochlear Implants for children and adults with severe to profound deafness, (5) noted above includes the following recommendations for children:

  1. “Unilateral cochlear implantation is recommended as an option for people with severe to profound deafness who do not receive adequate benefit from acoustic hearing aids.
  2. Simultaneous bilateral cochlear implantation is recommended as an option for children with severe to profound deafness who do not receive adequate benefit from acoustic hearing aids:
  3. Sequential bilateral cochlear implantation is not recommended as an option for people with severe to profound deafness.
  4. For purposes of this guidance, severe to profound deafness is defined as hearing only sounds that are louder than 90 dB HL at frequencies of 2 and 4 k hertz (Hz) without acoustic hearing aids. For children, adequate benefit from acoustic hearing aids is defined for this guidance as, speech, language and listening skills appropriate to age, developmental stage and cognitive ability.
  5. Cochlear implantation should be considered for children only after an assessment by a multidisciplinary team. As part of the assessment, children should also have had a valid trial of an acoustic hearing aid for at least 3 months (unless contraindicated or inappropriate).”

In 2010, Sparreboom and colleagues conducted a systematic review of bilateral cochlear implants in children with severe-to-profound deafness. (17) Due to the heterogeneity of the studies identified, the authors were unable to perform a meta-analysis. A qualitative review of the studies found binaural ability takes time to develop; bilateral cochlear implants seem to provide better speech perception over unilateral implants; and delays in implanting the second cochlear implant seem to decrease speech perception in quiet and decrease or eliminate the potential for binaural summation. The authors concluded while bilateral cochlear implants provide benefits of bilateral hearing in children, further research is needed,

Johr et al. (18) highlighted the surgical and anesthesiological considerations when performing cochlear implant surgery in very young infants (younger than one year of age). This is an observational and literature review by pediatricians at a tertiary children’s hospital in Switzerland. Patients younger than 1 year of age undergoing cochlear implant surgeries were analyzed concerning surgical techniques and anesthesiological aspects of elective surgeries in small infants. The results demonstrated that the age of the patient and the pediatric experience of the anesthesiologist, but not the duration of the surgery, are relevant risk factors. The authors concluded, “Further research is needed to provide more conclusive evidence that the performance outcome for children implanted before 12 months of age does not converge with the results of children implanted between 12 and 18 months.” Currently, there is no conclusive published evidence to support performing cochlear implant surgery on an infant younger than 12 months of age.

A number of small studies from outside the U.S. have reported results on cochlear implantation in infants younger than 12 months, which would be an off-label indication. For example, in a study from Australia, Ching and colleagues (19) published an interim report on early language outcomes of children with cochlear implants. This study evaluated 16 children who had implants before 12 months of age compared to 23 who had implants after 12 months (specific time of implantation was not provided). The preliminary results demonstrated that children who received an implant before 12 months of age developed normal language skills at a rate comparable to normal-hearing children, while those with later implants performed at two standard deviations below normal. The authors noted that these results are preliminary, as there is a need to examine the effect of multiple factors on language outcomes and the rate of language development. Similarly, in a study from Italy, Colletti (20) reported on findings from 13 infants who had implants placed before 12 months. The procedures were performed between 1998 and 2004. In this small study, the rate of receptive language growth for these earlyimplant infants overlapped scores of normal-hearing children. This overlap was not detected for those implanted at 1223 or 2436 months. Data from these small studies are viewed as preliminary and not conclusive. Subsequently, Colletti et al. reported on the 10-year results comparing 19 children with cochlear implants received between the ages of 2-11 months to 21 children implanted between 12-23 months and 33 children implanted between 24-35 months. (21) Within the first 6 months post-implantation, there was no significant difference among groups in Category of Auditory Performance testing, but differences became significantly better in the infant group (early implantation) at the 12- and 36 -month testing.

In 2010, Vlastarakos, et al, conducted a systematic review of studies on bilateral cochlear implants in a total of 125 children implanted before age 1. (22) The authors noted follow-up times ranged from a median duration of 6 to 12 months and, while results seemed to indicate accelerated rates of improvement in implanted infants, the evidence available is limited and of lower quality. Additionally, the lack of reliable outcome measures for infants demonstrates the need for further research before wide-spread cochlear implantation before 1 year of age.

Litovsky et al. reported that 9 of 13 (70%) children with bilateral cochlear implants discriminated source separations of equal to or less than 20 degrees and 7 of 9 performed better when using bilateral (vs. unilateral) devices. (23) Kuhn-Inacker et al. reported on a group of 39 European children who had bilateral cochlear implants. (24) From qualitative and quantitative data, they concluded that bilateral implants improve the children’s communicative behavior, especially in complex listening situations.

As noted above, Smulders et al. examined the timing of cochlear implantation in a systematic review of 11 studies; 5 studies addressed postlingually deafened adults (discussed above), and 7 studies addressed prelingually deafened children. (12) Sound localization was not affected by second implantation delay in any study of the studies on children, but delays in second implantation resulted in poorer outcomes in quiet environments in one study and poorer outcomes in noise in 2 studies. However, all studies were considered to be of poor quality and with a high risk of bias.

In a 2011 systematic review of 38 studies, Black and colleagues sought to identify prognostic factors for cochlear implantation in pediatric patients. (25) A quantitative meta-analysis was not able to be performed due to study heterogeneity. However, 4 prognostic factors: age at implantation, inner ear malformations, meningitis, and Connexin 26 (a genetic cause of hearing loss), consistently influenced hearing outcomes.

Pakdaman et al. conducted a systematic review of cochlear implants in children with cochleovestibular anomalies in 2011. (26) Anomalies included inner ear dysplasia such as large vestibular aqueduct and anomalous facial nerve anatomy. Twenty-two studies were reviewed totaling 311 patients. The authors found implantation surgery was more difficult and speech perception was lower in patients with severe inner ear dysplasia. However, heterogeneity in the studies limited interpretation of these findings.

In another 2011 systematic review, Roush and colleagues examined the audiologic management of children with auditory neuropathy spectrum disorder. (27) The review included 15 studies that addressed cochlear implantation in these patients. All of the studies reported auditory benefit with cochlear implantation in children with auditory neuropathy spectrum disorder. However, the studies were noted to be limited methodologically and further research is needed in this population.

Unilateral Hearing Loss

A number of small observational studies from outside the U.S. have reported results on cochlear implantation primarily for adult patients with unilateral deafness, which would be an off-label indication. (28, 29) At least 3 narrative literature reviews on this indication have also been published. (30-32)

Arndt and colleagues, for example, published a German pilot study in 2010 of 11 adult patients with unilateral hearing loss of various causes. (28) The aim was to evaluate the use of unilateral electrical stimulation with normal hearing on the contralateral side and after a period of 6 months compared with the preoperative unaided situation, conventional contralateral routing of signal or bone-anchored hearing aid hearing aids. Ten (of 11) patients also suffered from tinnitus. Two tests were used to assess speech comprehension, localization was assessed using an array of multiple speakers, and QOL was evaluated using 3 questionnaires. The study results were presented as p values without adjustment for multiple testing. The authors reported that cochlear implantation improved hearing abilities in these study patients and was superior to the above alternative treatment options. The use of the cochlear implant did not interfere with speech understanding in the normal-hearing ear.

The application of cochlear implants for tinnitus relief in patients with unilateral deafness has also been described in previous studies. van de Heyning and colleagues, for example, published a study in 2008 of 21 patients with unilateral hearing loss accompanied by severe tinnitus for at least 2 years who underwent cochlear implants at a university center in Belgium. (29) Three (of 21) patients showed complete tinnitus relief, whereas the majority demonstrated a significant reduction in tinnitus loudness based on a visual analogue scale (2 years after implantation, 2.5 +/- 1.9; before implantation, 8.5 +/- 1.3). Based on the above data and narrative reviews, the evidence-base to date on unilateral hearing loss is based on a few observational studies with a small number of patients (n ≤30), with a tendency toward reporting bias across these studies. (30)

Ongoing Clinical Trials

A May 24, 2013 search of clinical trials at online site: ClinicalTrials.gov identified 2 interventional trials on cochlear implant outcomes.

  • In a prospective, controlled, multicenter study in Finland, auditory performance skills will be assessed in 40 children with bilateral or unilateral cochlear implants for up to 5 years of hearing age (NCT00960102). In this study, speech perception ability, language acquisition, and speech production and speech recognition will be evaluated in addition to QOL and parent assessment of functional communication performance. This study is currently recruiting participants with the estimated completion date of December 2017.
  • In another prospective, randomized trial in the United States, auditory, linguistic and cognitive development, along with QOL outcomes will be evaluated in 252 children up to age 5 years with developmental delay and deafness (NCT01256229). Children with cochlear implants or hearing aids and developmental delays will be compared to children with cochlear implants and without developmental delay. This study is currently recruiting participants with the estimated completion date of August 2014.

Clinical Input Received through Physician Specialty Societies and Academic Medical Centers

In response to requests, input was received through 2 physician specialty societies and 4 academic medical centers while this policy was under review for February 2010. In addition, unsolicited input was received from a specialty society. While the various physician specialty societies and academic medical centers may collaborate with and make recommendations during this process, through the provision of appropriate reviewers, input received does not represent an endorsement or position statement by the physician specialty societies or academic medical centers, unless otherwise noted. A majority of those providing input supported use of cochlear implants in infants younger than 12 months of age; many of those supporting this use noted that there are major issues determining hearing level in infants of this age group, and others commented that use could be considered in these young infants in certain situations only. Those providing input were divided in their comments regarding the medical necessity of upgrading functioning external systems; some agreed with this and others did not.

Summary

Cochlear implant is a device for individuals with severe-to-profound hearing loss who only receive limited benefit from amplification with hearing aids. A cochlear implant provides direct electrical stimulation to the auditory nerve, bypassing the usual transducer cells that are absent or nonfunctional in deaf cochlea.

Studies show consistent improvement in speech reception (especially in noise) and in sound localization with bilateral devices. Studies also suggest that earlier implantation may be preferred. Based on these studies, and several systematic reviews that have provided additional evidence in support of unilateral and bilateral cochlear implantation, cochlear implants have been shown to provide benefits sufficient to improve net health outcomes in patients with bilateral hearing loss. Therefore, the policy statement for their use as medically necessary for bilateral hearing loss in those ages 12 months and older remains unchanged.

The evidence is insufficient to permit conclusions concerning the effect of cochlear implantation for the treatment of unilateral hearing loss. Future controlled studies with appropriate patient selection comparing cochlear implants to alternative treatment options are needed to yield stronger evidence. Therefore, cochlear implantation as a treatment for patients with unilateral hearing loss is considered to be investigational.

Practice Guidelines and Position Statements

In 2006, the American Academy of Otolaryngology-Head and Neck Surgery Foundation (33) released criteria for cochlear implants for adults and pediatric patients.

Adult Criteria

  • Be 18 years or older, with bilateral, severe to profound sensorineural hearing loss, i.e., 70dB or greater PTA (pure-tone air-conduction average) at 500, 1000, and 2000 Hz;
  • Have tried but have limited benefit from adequately fitted binaural hearing aid; or
  • Have sentence recognition score of 50 percent or less in the ear to be implanted and 60 percent or less in the contralateral ear in best aided conditions using Hearing in Noise Test (HINT) or City University of New York (CUNY) tests.

Pediatric Criteria

  • Be 12 months to 17 years of age.
  • Infants age 12-24 months should have bilateral, profound hearing loss with thresholds of 90dB or greater at 1000 Hz.
  • Children 24 months to 17 years should have bilateral severe to profound (greater than 70dB) hearing loss.
  • Infants and older children should demonstrate lack of progress in simple auditory skills in conjunction with appropriate auditory amplification and participation in intensive aural habilitation for three to six months. Less than 0.14520 percent correct on the Multi-syllabic Lexical Neighborhood Test (MLNT) or Lexical Neighborhood Test (LNT), depending on the child’s cognitive and linguistic abilities.
  • A three-to six-month trial of appropriate hearing aids is required. If meningitis is the cause of hearing loss or if there is radiologic evidence of cochlear ossification a shorter hearing aid trial and earlier implantation may be reasonable.”

In May 2008, The British Cochlear Implant Group (BCIG) released a position paper on “Bilateral Cochlear Implants. (13) The position paper includes indications for use of bilateral implantation as noted above.

In January 2009, NICE released technology appraisal guidance 166, (5)Cochlear Implants for children and adults with severe to profound deafness,” which includes recommendations for use of unilateral and bilateral cochlear implants in children and adults as noted above.

In April 2011, a technology assessment was completed by the Tufts Evidence-based Practice Center for the AHRQ on the effectiveness of cochlear implants in adults. (6) The assessment conclusions are noted above.

Medicare National Coverage

Existing national coverage states (34), “…cochlear implantation may be covered for treatment of bilateral pre- or-post-linguistic, sensorineural, moderate-to-profound hearing loss in individuals who demonstrate limited benefit from amplification” which “is defined by test scores of less than or equal to 40% correct in the best-aided listening condition on tape-recorded tests of open-set sentence cognition.” Coverage for cochlear implants may also be provided when the patient has “hearing test scores of greater than 40% and less than or equal to 60% only when the provider is participating in, and patients are enrolled in, either an FDA-approved category B investigational device exemption clinical trial as defined at 42 CFR 405.201, a trial under the Centers for Medicare & Medicaid (CMS) Clinical Trial Policy as defined at section 310.1 of the National Coverage Determinations Manual, or a prospective, controlled comparative trial approved by CMS as consistent with the evidentiary requirements for National Coverage Analyses and meeting specific quality standards.”

References

  1. Cochlear Implants in Adults and Children. NIH Consens Statement Online 1995 May 15-17; 13(2):1-30. Available online at: http://consensus.nih.gov/1995/1995CochlearImplants100html.htm. Last accessed July 15, 2013.
  2. Bond M, Mealing S, Anderson R et al. The effectiveness and cost-effectiveness of cochlear implants for severe to profound deafness in children and adults: a systematic review and economic model. Health Technol Assess 2009; 13(44):1-330.
  3. Bond M, Elston J, Mealing S et al. Effectiveness of multi-channel unilateral cochlear implants for profoundly deaf children: a systematic review. Clin Otolaryngol 2009; 34(3):199-211.
  4. Bond M, Elston J, Mealing S et al. Systematic reviews of the effectiveness and cost-effectiveness of multi-channel unilateral cochlear implants for adults. Clin Otolaryngol 2010; 35(2):87-96.
  5. Barentsz MW, van den Bosch MA, Veldhuis WB et al. Radioactive seed localization for non-palpable breast cancer. Br J Surg 2013; 100(5):582-8.
  6. Gobardhan PD, de Wall LL, van der Laan L et al. The role of radioactive iodine-125 seed localization in breast-conserving therapy following neoadjuvant chemotherapy. Ann Oncol 2013; 24(3):668-73.
  7. Gaylor JM, Raman G, Chung M et al. Cochlear implantation in adults: a systematic review and meta-analysis. JAMA Otolaryngol Head Neck Surg 2013; 139(3):265-72.
  8. Bittencourt AG, Ikari LS, Della Torre AA et al. Post-lingual deafness: benefits of cochlear implants vs. conventional hearing aids. Braz J Otorhinolaryngol 2012; 78(2):124-7.
  9. Berrettini S, Baggiani A, Bruschini L et al. Systematic review of the literature on the clinical effectiveness of the cochlear implant procedure in adult patients. Acta Otorhinolaryngol Ital 2011; 31(5):299-310.
  10. Crathorne L, Bond M, Cooper C et al. A systematic review of the effectiveness and cost-effectiveness of bilateral multichannel cochlear implants in adults with severe-to-profound hearing loss. Clin Otolaryngol 2012; 37(5):342-54.
  11. van Schoonhoven J, Sparreboom M, van Zanten BG et al. The effectiveness of bilateral cochlear implants for severe-to-profound deafness in adults: a systematic review. Otol Neurotol 2013; 34(2):190-8.
  12. Smulders YE, Rinia AB, Rovers MM et al. What is the effect of time between sequential cochlear implantations on hearing in adults and children? A systematic review of the literature. Laryngoscope 2011; 121(9):1942-9.
  13. British Cochlear Implant Group (BCIG). Position Statement - Bilateral Cochlear Implantation. May 2007. Revised May 2008. Available online at: http://www.bcig.org.uk/downloads/pdfs/BCIG%20position%20statement%20-%20Bilateral%20Cochlear%20Implantation%20May%2007.pdf. Last accessed July 15, 2013.
  14. Sharma A, Dorman MF. Central auditory development in children with cochlear implants: clinical implications. Adv Otorhinolaryngol 2006; 64:66-88.
  15. Sharma A, Dorman MF, Kral A. The influence of a sensitive period on central auditory development in children with unilateral and bilateral cochlear implants. Hear Res 2005; 203(1-2):134-43.
  16. Forli F, Arslan E, Bellelli S et al. Systematic review of the literature on the clinical effectiveness of the cochlear implant procedure in paediatric patients. Acta Otorhinolaryngol Ital 2011; 31(5):281-98.
  17. Sparreboom M, van Schoonhoven J, van Zanten BG et al. The effectiveness of bilateral cochlear implants for severe-to-profound deafness in children: a systematic review. Otol Neurotol 2010; 31(7):1062-71.
  18. Johr M, Ho A, Wagner CS et al. Ear surgery in infants under one year of age: its risks and implications for cochlear implant surgery. Otol Neurotol 2008; 29(3):310-3.
  19. Ching TY, Dillon H, Day J et al. Early language outcomes of children with cochlear implants: interim findings of the NAL study on longitudinal outcomes of children with hearing impairment. Cochlear Implants Int 2009; 10 Suppl 1:28-32.
  20. Colletti L. Long-term follow-up of infants (4-11 months) fitted with cochlear implants. Acta Otolaryngol 2009; 129(4):361-6.
  21. Colletti L, Mandala M, Zoccante L et al. Infants versus older children fitted with cochlear implants: performance over 10 years. Int J Pediatr Otorhinolaryngol 2011; 75(4):504-9.
  22. Vlastarakos PV, Proikas K, Papacharalampous G et al. Cochlear implantation under the first year of age--the outcomes. A critical systematic review and meta-analysis. Int J Pediatr Otorhinolaryngol 2010; 74(2):119-26.
  23. Litovsky RY, Johnstone PM, Godar S et al. Bilateral cochlear implants in children: localization acuity measured with minimum audible angle. Ear Hear 2006; 27(1):43-59.
  24. Kuhn-Inacker H, Shehata-Dieler W, Muller J et al. Bilateral cochlear implants: a way to optimize auditory perception abilities in deaf children? Int J Pediatr Otorhinolaryngol 2004; 68(10):1257-66.
  25. Black J, Hickson L, Black B et al. Prognostic indicators in paediatric cochlear implant surgery: a systematic literature review. Cochlear Implants Int 2011; 12(2):67-93.
  26. Pakdaman MN, Herrmann BS, Curtin HD et al. Cochlear Implantation in Children with Anomalous Cochleovestibular Anatomy: A Systematic Review. Otolaryngol Head Neck Surg 2011 [Epub ahead of print].
  27. Roush P, Frymark T, Venediktov R et al. Audiologic management of auditory neuropathy spectrum disorder in children: a systematic review of the literature. Am J Audiol 2011; 20(2):159-70.
  28. Arndt S, Aschendorff A, Laszig R et al. Comparison of pseudobinaural hearing to real binaural hearing rehabilitation after cochlear implantation in patients with unilateral deafness and tinnitus. Otol Neurotol 2011; 32(1):39-47.
  29. Van de Heyning P, Vermeire K, Diebl M et al. Incapacitating unilateral tinnitus in single-sided deafness treated by cochlear implantation. Ann Otol Rhinol Laryngol 2008; 117(9):645-52.
  30. Arts RA, George EL, Stokroos RJ et al. Review: cochlear implants as a treatment of tinnitus in single-sided deafness. Curr Opin Otolaryngol Head Neck Surg 2012; 20(5):398-403.
  31. Kamal SM, Robinson AD, Diaz RC. Cochlear implantation in single-sided deafness for enhancement of sound localization and speech perception. Curr Opin Otolaryngol Head Neck Surg 2012; 20(5):393-7.
  32. Sampaio AL, Araujo MF, Oliveira CA. New criteria of indication and selection of patients to cochlear implant. Int J Otolaryngol 2011; 2011:573968.
  33. Blakely B. Hearing: when surgery is appropriate for age-related hearing loss. In Geriatric Care Otolaryngology. American Academy of Otolaryngology-Head and Neck Surgery Foundation, 2006. Pages 11- 14. Available online at: http://www.entnet.org/EducationAndResearch/upload/Chapter-1.pdf. Last accessed July 15, 2013.
  34. Centers for Medicare and Medicaid (CMS). National Coverage Determination (NCD) Pub. 100.3, section 50.3 Cochlear Implantation. Available online at: http://www.cms.gov/Regulations-and-Guidance/Guidance/Transmittals/downloads/R42NCD.pdf. Last accessed July 15, 2013.

Coding

Codes

Number

Description

CPT

69930

Cochlear device implantation, with or without mastoidectomy

 

92507

Treatment of speech, language, voice, communication, and/or auditory processing disorder; individual

 

92601

Diagnostic analysis of cochlear implant, patient under 7 years of age; with programming

 

92602

;subsequent programming

 

92603

Diagnostic analysis of cochlear implant, age 7 years or older; with programming

 

92604

;subsequent reprogramming

 

92605

Evaluation for prescription of non-speech-generating augmentative and alternative communication device

 

92606

Therapeutic service(s) for the use of non-speech-generating device, including programming and modification

 

92607

Evaluation for prescription for speech generating augmentative and alternative communication device, face-to-face with the patient; first hour

 

92608

; each additional 30 minutes

 

92609

Therapeutic services for the use of speech generating device, including programming and modification

 

92626

Evaluation of auditory rehabilitation status; first hour

 

92627

;each additional 15 minutes (list separately in addition to code for primary procedure)

 

92630

Auditory rehabilitation; pre-lingual hearing loss

 

92633

;post-lingual hearing loss

ICD-9 Diagnosis

389.10

Sensorineural hearing loss, unspecified

 

389.11

Sensory hearing loss, bilateral

 

389.12

Neural hearing loss, bilateral

 

389.14

Central hearing loss

 

389.15

Sensorineural hearing loss, unilateral

 

389.16

Sensorineural hearing loss, asymmetrical

 

389.18

Sensorineural hearing loss, bilateral

ICD-10-CM (effective 10/01/14)

H90.3 – H90.8

Sensorineural hearing loss code range

ICD-10-PCS (effective 10/01/14)

09HD0SY, 09HE0SY, 09HD0S2, 09HE0S2, 09HD0S3, 09HE0S3

Surgical, ear, nose, sinus, insertion, inner ear, open, hearing device, code by ear (left or right) and type of hearing device

HCPCS

L8614

Cochlear device, includes all internal and external components

 

L8615

Headset/headpiece for use with cochlear implant device, replacement

 

L8616

Microphone for use with cochlear implant device, replacement

 

L8617

Transmitting coil for use with cochlear implant device, replacement

 

L8618

Transmitter cable for use with cochlear implant device, replacement

 

L8619

Cochlear implant external speech processor and controller, integrated system, replacement

 

L8621

Zinc air battery for use with cochlear implant device, replacement, each

 

L8622

Alkaline battery for use with cochlear implant device, any size, replacement, each

 

L8623

Lithium ion battery for use with cochlear implant device speech processor, other than ear level, replacement, each

 

L8624

Lithium ion battery for use with cochlear implant device speech processor, ear level, replacement, each

 

L8627

Cochlear implant, external speech processor, component, replacement

 

L8328

Cochlear implant, external controller component, replacement

 

L8629

Transmitting coil and cable, integrated, for use with cochlear implant device, replacement

Type of Service

Surgery

 

Place of Service

Inpatient

 

Appendix

N/A

History

Date

Reason

01/97

Add to Surgery Section - New Policy

11/03/98

Replace Policy - Revised Description and Policy Guidelines

01/04/99

Replace Policy - Policy reviewed; new devices added.

10/09/01

Replace Policy - Policy reviewed; new devices and FDA approval status added.

10/08/02

Replace Policy - Policy reviewed; new FDA-approved device added (Med E1 Combi 40+).

03/11/03

Replace Policy - Policy Benefit Application section added. No change to Policy Statement.

05/13/03

Replace Policy - Update CPT code only.

05/11/04

Replace Policy - Policy reviewed without literature review; no change to policy statement.

07/13/04

Replace Policy - Policy reviewed; discussion of bilateral cochlear implants and its investigational status added.

08/09/05

Replace Policy - Policy reviewed with literature search; policy statement unchanged.

02/06/06

Codes updated - No other changes.

06/09/06

Disclaimer and Scope update - No other changes.

08/08/06

Replace Policy - Policy updated with literature review; no change in policy statement.

04/10/07

Replace Policy - Policy updated with literature review. Policy statement changed to indicate bilateral cochlear implants are medically necessary. Reference numbers added.

05/13/08

Replace Policy - Policy updated with literature search; no change to the policy statement. References and codes added.

04/13/10

Replace Policy - Policy updated with literature search. Policy statements modified for clarity, intent unchanged. References and codes added.

08/09/11

Replace Policy – Policy updated with literature review; Rationale section and references reorganized. No changes in policy statements. Reference numbers 3-4, 6, 12, 16-17 added; numerous references to early, small studies removed. ICD-10 codes added to policy.

08/24/11

Benefit Application updated.

02/09/12

The CPT codes 92605 and 92606 were removed from the policy.

06/26/12

Related Policies update; title for 7.01.84 has been changed.

08/20/12

Replace policy. Clarification statement added to the policy guidelines second paragraph: In addition, unique clinical circumstance may justify individual consideration for implantation before 12 months of age, based on review of applicable medical records to verify the other pediatric criteria noted in this policy are met. Rationale section revised based on literature review through April 2012. Reference numbers 7-9, 13 and 22-24 added. Other references renumbered. CPT codes 92605 and 92606 added. Policy statements unchanged.

09/25/12

Update Coding Section – ICD-10 codes are now effective 10/01/2014.

10/18/12

Update Related Policies – 7.01.03 renumbered to 7.01.547.

08/12/13

Replace policy. Policy statement added: cochlear implantation as a treatment for patients with unilateral hearing loss with or without tinnitus is considered investigational. Rationale updated based on literature review through May 2013. References 7, 10, 11, 28-32 added; others renumbered/removed. Policy statement changed as noted.

03/11/14

Coding Update. Remove codes 20.96, 20.97, and 20.98 per ICD-10 mapping project; these codes are not utilized for adjudication of policy.


Disclaimer: This medical policy is a guide in evaluating the medical necessity of a particular service or treatment. The Company adopts policies after careful review of published peer-reviewed scientific literature, national guidelines and local standards of practice. Since medical technology is constantly changing, the Company reserves the right to review and update policies as appropriate. Member contracts differ in their benefits. Always consult the member benefit booklet or contact a member service representative to determine coverage for a specific medical service or supply. CPT codes, descriptions and materials are copyrighted by the American Medical Association (AMA).
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