Local Coverage Determination (LCD)

Electroretinography (ERG)

L38992

Expand All | Collapse All
Proposed LCD
Proposed LCDs are works in progress that are available on the Medicare Coverage Database site for public review. Proposed LCDs are not necessarily a reflection of the current policies or practices of the contractor.

Document Note

Note History

Contractor Information

LCD Information

Document Information

Source LCD ID
N/A
LCD ID
L38992
Original ICD-9 LCD ID
Not Applicable
LCD Title
Electroretinography (ERG)
Proposed LCD in Comment Period
N/A
Source Proposed LCD
DL38992
Original Effective Date
For services performed on or after 01/30/2022
Revision Effective Date
For services performed on or after 01/12/2023
Revision Ending Date
N/A
Retirement Date
N/A
Notice Period Start Date
12/16/2021
Notice Period End Date
01/29/2022
AMA CPT / ADA CDT / AHA NUBC Copyright Statement

CPT codes, descriptions and other data only are copyright 2023 American Medical Association. All Rights Reserved. Applicable FARS/HHSARS apply.

Fee schedules, relative value units, conversion factors and/or related components are not assigned by the AMA, are not part of CPT, and the AMA is not recommending their use. The AMA does not directly or indirectly practice medicine or dispense medical services. The AMA assumes no liability for data contained or not contained herein.

Current Dental Terminology © 2023 American Dental Association. All rights reserved.

Copyright © 2023, the American Hospital Association, Chicago, Illinois. Reproduced with permission. No portion of the American Hospital Association (AHA) copyrighted materials contained within this publication may be copied without the express written consent of the AHA. AHA copyrighted materials including the UB‐04 codes and descriptions may not be removed, copied, or utilized within any software, product, service, solution or derivative work without the written consent of the AHA. If an entity wishes to utilize any AHA materials, please contact the AHA at 312‐893‐6816.

Making copies or utilizing the content of the UB‐04 Manual, including the codes and/or descriptions, for internal purposes, resale and/or to be used in any product or publication; creating any modified or derivative work of the UB‐04 Manual and/or codes and descriptions; and/or making any commercial use of UB‐04 Manual or any portion thereof, including the codes and/or descriptions, is only authorized with an express license from the American Hospital Association. The American Hospital Association (the "AHA") has not reviewed, and is not responsible for, the completeness or accuracy of any information contained in this material, nor was the AHA or any of its affiliates, involved in the preparation of this material, or the analysis of information provided in the material. The views and/or positions presented in the material do not necessarily represent the views of the AHA. CMS and its products and services are not endorsed by the AHA or any of its affiliates.

Issue

Issue Description

Updated links in bibliography

Issue - Explanation of Change Between Proposed LCD and Final LCD

CMS National Coverage Policy

Language quoted from Centers for Medicare and Medicaid Services (CMS), National Coverage Determinations (NCDs) and coverage provisions in interpretive manuals is italicized throughout the policy. NCDs and coverage provisions in interpretive manuals are not subject to the Local Coverage Determination (LCD) Review Process (42 CFR 405.860[b] and 42 CFR 426 [Subpart D]). In addition, an administrative law judge may not review an NCD. See §1869(f)(1)(A)(i) of the Social Security Act.

Unless otherwise specified, italicized text represents quotation from one or more of the following CMS sources:

Title XVIII of the Social Security Act (SSA):

Section 1862(a)(1)(A) excludes expenses incurred for items or services which are not reasonable and necessary for the diagnosis or treatment of illness or injury or to improve the functioning of a malformed body member.

Section 1833(e) prohibits Medicare payment for any claim which lacks the necessary information to process the claim.

Section 1862(a) (7) excludes routine physical examination unless otherwise covered by statute.

Code of Federal Regulations:

42 CFR Section 410.32 indicates that diagnostic tests may only be ordered by the treating physician (or other treating practitioner acting within the scope of his or her license and Medicare requirements) who furnishes a consultation or treats a beneficiary for a specific medical problem and who uses the results in the management of the beneficiary's specific medical problem. Tests not ordered by the physician (or other qualified non-physician provider) who is treating the beneficiary are not reasonable and necessary (see Sec. 411.15(k)(1) of this chapter).

CMS Publications:

CMS Publication 100-04, Medicare Claims Manual, chapter 12:

    40.1.A. Global surgery period

 

Coverage Guidance

Coverage Indications, Limitations, and/or Medical Necessity

Electroretinography (ERG) is considered reasonable and medically necessary for:

  1. Detection of loss of retinal function, OR
  2. To distinguish retinal from optic nerve lesions, OR
  3. Detecting chloroquine and hydroxychloroquine toxicity

ERG is investigational for all other indications, including glaucoma.

Background:

The full-field electroretinogram (ERG) is used to detect loss of retinal function or distinguish between retinal and optic nerve lesions. ERG measures the electrical activity generated by neural and non-neuronal cells in the retina in response to a light stimulus. ERGs are usually obtained using electrodes embedded in a corneal contact lens or a thin wire inside the lower eyelid, which measures a summation of retinal electrical activity at the corneal surface. The ERG provides information about the macula, composed mainly of cones and used for primary central and color vision, and the rest of the retina is mainly composed of rod photoreceptors, used in peripheral and night (scotopic) vision. By providing information about the rods and cones, ERG helps distinguish retinal degeneration and dystrophies.1 The International Society for Clinical Electrophysiology of Vision (ISCEV) introduced minimum ERG standards in 1989. The ERG helps to distinguish retinal degeneration and dystrophies.2 The widespread use of electrophysiological measurements has been hindered by limitations associated with its widespread clinical implication and large magnitude of measurement variability.3

Definitions:

Full-Field ERG (ffERG)- measures mass response for the retina in response to flashing lights and is valuable for conditions with widespread retinal dysfunction but not useful for small retinal lesions.4

Focal ERG (fERG)- also called foveal ERG, measures the functional integrity of the central macula.4

Multifocal ERG (mfERG)- higher resolution form of ERG, enabling assessment of ERG activity in small areas of the retina by measuring local ERG responses and providing spatial information. It measures the photoreceptors and aids in the detection of localized abnormalities within the macula.2,4

Pattern electroretinography (PERG) (also called reversal pattern ERG) uses pattern-reversal stimuli to elicit electrical activity in the retina and monitor retinal ganglion cell activity, and used to detect subtle optic neuropathies.2,5

Photopic Negative Response ERG (PhNR) is a slow ERG wave recorded under photopic conditions and accesses ganglion cells on cones and bipolar cells.6

Summary of Evidence

ERG for Retinal Dysfunction

ERG has played a role as a diagnostic tool for retinal disease since its inception in the 1940s. It has become a standard tool for the assessment of retinal function. It plays a role in the early detection of diabetic retinopathy, and there are treatments if detected early. ERG, in various forms, provides an objective assessment of retinal function and can aid in assessment and monitoring in treatment outcomes for acquired and hereditary retinal disorders. There is robust literature composed of hundreds of articles to support ERG and mfERG for retinal evaluation.7 Full-field ERG is limited as the recording is massed potential from the whole retina. Unless 20% or more of the retina is affected, the ffERG may be normal. Multi-focal ERG produces higher resolution images than ffERG, allowing assessment of a smaller area of the retina.8 The International Society for Clinical Electrophysiology of Vision (ISCEV) established a guideline for ERG testing.9-12 Literature for PERG is limited.

The American Academy of Ophthalmology (AOA) Clinical Assessment of Patients with Inherited Retinal Degenerations13 includes ERG. The guidelines state: "The full-field electroretinogram (ERG) is important for diagnosis and staging of disease and is useful for many patients with diffuse photoreceptor disease to evaluate the retina-wide function of rods and cones. Multifocal ERG testing can be useful for detection and monitoring disease progression for diseases that primarily affect the macula. However, its accuracy can be limited in those patients with a notable loss of central vision who are unable to maintain steady foveal fixation." They also recommend following ISCEV standards so recordings can be compared between institutions and examiners.

The supporting literature includes support for the use of ERG for the following indications:4,7

Toxic retinopathies, including those caused by intraocular metallic foreign bodies, Vigabatrin, Chlorpromazine, and Amiodarone

  • Diabetic retinopathy
  • Retinal vascular disease [e.g., Central Retinal Artery Occlusion (CRAO), Central Retinal Vein

Occlusion (CRVO), Branch Vein Occlusion (BVO), and sickle cell retinopathy]

  • Autoimmune retinopathies [e.g., Cancer Associated Retinopathy (CAR), Melanoma Associated

Retinopathy (MAR), and Acute Zonal Occult Outer Retinopathy (AZOOR)]

  • Retinal detachment
  • Retinal transplantation
  • Assessment of retinal function after trauma [e.g., vitreous hemorrhage, dense cataracts, and other conditions where the fundus cannot be visualized]
  • Retinitis pigmentosa and related hereditary degenerations
  • Retinitis punctata albescens
  • Leber's congenital amaurosis
  • Choroideremia
  • Gyrate atrophy of the retina and choroid
  • Goldman-Favre syndrome
  • Congenital stationary night blindness
  • X-linked juvenile retinoschisis
  • Achromatopsia
  • Cone dystrophy
  • Disorders mimicking retinitis pigmentosa
  • Usher Syndrome
  • Retinal Dystrophies (e.g., Stargardt's disease, Fundus Flavimaculata, North Carolina macular dystrophy, Best's Vitelliform dystrophy, Sorsby's macular dystrophy)
  • Phototoxic Retinopathy

ERG for Glaucoma

Reports of using ERG for glaucoma management began to emerge in the 1950s, but clear normative values and standards have limited uptake of glaucoma technology. A 2011 report by the AAO summarized the literature through 2010. In this review, 185 papers were evaluated, and the quality of literature was rated with the Centre for Evidence-Based Medicine rating scale. The results of this analysis, "Assessment of Visual Function in Glaucoma," reported that while ERG, as objective measures of visual function, provided testing free of patient input, issues prevent their adoption for glaucoma management. It concluded that advances in technology have yet to produce definitive guidance on the diagnosis of glaucoma or its progression over time and that further research on an objective measure of visual function is needed.14 The 2011 APP report stated that while there was emerging evidence on the role of ERG in glaucoma, they concluded that the test was "not ready for widespread clinical use".14

Researchers have been interested in the early detection of glaucoma and the detection of potential converters to help reserve preventive treatment for those who need it. PERG has been explored as a potential modality to accomplish this. Bach et al. (2006) conducted a prospective study on 95 eyes of 54 patients with elevated intraocular pressure >25mg Hg. PERG was performed every six months over 8.2 years. This accumulated previous reported outcomes from the same cohort, so results were for findings over 12 years. They conclude that PERG can help predict the stability of progression to glaucoma at least one year ahead of conversion based on 8/95 eyes (5 patients) who converted to glaucoma.15 Limitations of the study include that treatment was allowed, and all converting eyes received treatment before conversion. They report a sensitivity of 80% and specificity of 71%, with only 1-2% of those with ocular hypertension at risk for conversion to glaucoma; this low specificity would not offer strong predictive value, and at best, would serve as an adjunct measurement. There were not clinical recommendations as to the benefit of early detection, and the treatment used at that time did not prevent the conversion to glaucoma. Finally, as refractive errors can interfere with PERG testing, they only included patients with good visual acuity, reducing the applicability of findings to the general population.

Between 2010-2013 additional longitudinal studies have shown the potential benefit of ERG, specifically PERG, in glaucoma management; still, these studies are challenged by longitudinal design, different methods used for the PERG test, and the actual analysis of the longitudinal studies. Bode et al. (2011) conducted a longitudinal study including 120 eyes (64 subjects) with elevated intraocular pressure >25mm HG over a mean period of 10.3 years. A PERG study was conducted at enrollment and every six months over the study period. 13/120 eyes converted to glaucoma according to visual field definition. The authors reported amplitude and PERG ratio predicted conversion to glaucoma four years ahead with sensitivity/specificity of 67%/64% and 75%/76%, respectively. They also compared the trends of converters and non-converters are and reported that while there were significant differences in the PERG ratio, the trends did not predict conversion as successfully as single-visit measures. They suggest a PERG ratio <1, based on 13/120 eyes converting over ten years, may have clinical value regarding when to initiate treatment. However, there is no analysis of how many non-converters would receive treatment using this threshold and if it resulted in clinical benefits.16 Ventura et al. (2013) enrolled 59 patients as glaucoma suspects and observed them untreated over an average of 5.7 years, during which PERG and Standard Automated Perimetry (SAP) was conducted twice per year. They reported that the PERG displayed clear longitudinal loss of signal, but the finding's pathophysiological significance was not determined. They conclude that additional investigation would be necessary to determine if PERG losses will have served as predictors of future visual field loss.17 Additional small studies reported similar findings, but these findings have yet to be confirmed in larger trials.18-20

A 2019 systematic review included thirty English language studies published after 2013. All studies were cohort or case-controlled, and there was no Level I studies included in the body of literature. The studies' quality score was based on the Newcastle-Ottawa Scale (NOS) for nonrandomized studies and case series graded using a modification of NOS and was listed as 6-10 in this series. Each study was assessed to determine if they used a standardized protocol, specifically the ISCEV protocol. The studies reviewed multiple types of electrophysiological tests, including ERG. They report nine papers on mfERG, largely comparing to optical coherence tomography (OCT). These reports showed relatively good spatial correlation with visual field defects and OCT scans, but most studies performed protocols modified from traditional mfERG. In evaluating mfPERG, they determined that results are not usually homogenous, and there was uncertainty in how it could contribute to the early diagnosis of glaucoma. PERG was described in seven studies and reported some accuracy in localized glaucomatous defects. PnHR was reported in three studies, and while it did have some promising preliminary findings, there is little research on its utility in glaucoma. Criticism for the electrophysiologic tests includes difficulties in performing a good exam, cost, some tests are invasive and require sensors in the patient's eye for up to 50 minutes, technical concerns, extensive data evaluation requiring experts for interpretation, and inconsistent protocols. The authors conclude a correlation between electrophysiological test and current standards in the visual field and optical coherence tomography testing and growing evidence the technology may play a role in glaucoma. However, they acknowledge that definitive indications of these tests are needed and have not been established for early detection or follow-up of glaucoma; there is a need for more straightforward protocols and better correspondence with current glaucoma tests for their routine use.6

A small 2019 retrospective analysis of thirty-eight patients showed progressively decreased PERG amplitude overtime in a proportion of glaucoma suspects suggesting PERG progression can independently contribute to the prediction of visual field progression.21 In a 2020 comparative analysis between forty patients (eighty eyes) with open-angle glaucoma to 23 healthy patients (46 eyes) measured PERG, steady-state PERG (sspERG), computerized visual field screening, examination of retinal nerve fiber layer, and macular thickness on optical coherence tomography (OCT) were compared. They reported significantly lower amplitudes for both PERG and ssPERG in patients with the delay in patients with open-angle glaucoma than those with healthy eyes, with results of ssPERG being more pronounced. They conclude there may be a value of the addition of SSpERG to OCT parameters.22 This study distributed patients into the group to achieve a balanced demographic, but this introduced selection bias and was not sufficiently powered. A 2019 observational study was done with three groups: a control, primary open-angle glaucoma, and ocular hypertension with 30 eyes in each group measured visual fields, OCT and PERG. They concluded PERG can detect dysfunctional but still live retinal ganglion cells earlier than OCT in ocular hypertension cases, allowing an opportunity for earlier treatment and potential restoration of function before irreversible damage occurs.23 The study is limited by the small number of cases, observational design, and there was no evaluation of the potential impact on the disease but rather a hypothesis.

The International Society for Clinical Electrophysiology of Vision guidelines provides standards for electrodiagnostic procedures and common clinical indications. They state there may be a value in the evaluation of "glaucoma suspects." They state that there may be a reduction in components of transient recordings, but the emerging ssPERG are more affected. They also stated there is an increasing interest in photopic negative response (PHNR). They also report that standard mfERG may play a role in glaucoma, but standardization and clinical utility has not yet been established.24

In a 2017 review paper, the authors conclude that PERG may be altered at the earlier stages of glaucoma preceding losses of visual field and optic nerve tissue which, could be potentially reversible with lowering the intraocular pressure. Despite this potential, the paper also reviews several limitations of the PERG technique in early glaucoma, including the presence of cataracts and diabetes that may impair the PERG signal. Additional comorbidities that could potentially reduce the specificity of PERG alterations for early detection of glaucoma include high myopia, macular degeneration, and neurological conditions such as Parkinson's disease, Alzheimer's disease, and multiple sclerosis.25

Contractor Advisory Committee (CAC) Meeting

CGS Administrators hosted a CAC meeting to review the evidence for electroretinography with J15 CAC members for ophthalmology and optometry. The meeting was held on 11/18/2020, and transcription voting results are published on the CGS website at https://www.cgsmedicare.com/partb/medicalpolicy/lcd_discussion_recordings.html. The panel was in support of the use of ERG and the management of retinal disease and the important role that it plays in the treatment of these conditions. The one area of controversy was the role of the ERG in the diagnosis and management of glaucoma. The panel felt there was robust clinical evidence to support the use of PERG in the diagnosis and management of glaucoma with a voting score of 4/5. The discussion stated that there is value in equivocal cases where visual fields and OCT are not congruent or definitive. The panel had a consensus that it is used mainly as an adjunct test and not a standalone test and felt that it could help prevent patients' overtreatment with equivocal findings. The type of system used was discussed, and that the corneal electrodes are more sensitive than skin electrodes which can impact the interpretation of the test. There was no standardization for patient selection, frequency of test, and role in follow-up/management. The panel felt there was clinical evidence to support the role of other forms of ERG in glaucoma management with a score of 4/5, and the various types of ERG and applications were discussed. The panel did not feel there was evidence to support the role of PERG in retinal disease with a score of 1.6/5. Literature was submitted by the panel and included in the literature review conducted for this topic.26

Literature was submitted regarding the question of the sensitivity of skin electrodes compared to corneal electrodes. The placement of corneal or conjunctive electrodes typically used for recordings requires highly skilled technicians and compliant patients. The amplitude measured by the corneal electrodes is much lower and more accurate than skin electrodes. The 2013 ISCEV standards for PERG states, "Skin (surface) active electrodes should not routinely be used for recording the standard PERG, because skin electrodes positioned on the lower eyelid will record PERGs of lower amplitudes than those recorded from an electrode in contact with the eye.”9 Some literature has emerged documenting comparability between the skin and the conjunctive electrodes for PhNR. This literature seems to apply to PhNR rather than PERG recordings.3,27,28

Evidence Tables

The CAC panel voted for robust clinical evidence in support of ERG for glaucoma; however, our literature search could not identify any high-quality studies to support this use. Due to this discrepancy, a formal evidence analysis was conducted. A literature search was conducted using PubMed, EBSCO, and Medline. English language articles were identified that addressed the role of PERG, MFERG, and phNR for glaucoma evaluation. Articles already assessed in the 2019 SR were excluded. Retrospective studies and case series were excluded due to low quality. Studies with less than thirty eyes evaluated were excluded. All literature submitted by the CAC panel was reviewed. Individual studies were rated with the Scottish Intercollegiate Guideline Network (SIGN), which is used by AAO in their Preferred Practice Guidelines.

There were no high-quality randomized controlled trials. There were no trials with a direct comparison of ERG to the current standard test. No trials on clinical utility were identified.

Table 1. Pattern Electroretinography (PERG) for glaucoma

 

Study

Study Type

Protocol

Results

SIGN Rating

Bach (2006)15 Pattern ERG as an early glaucoma indicator in ocular hypertension: a long-term, prospective study

observational, long-term, prospective
study

95 eyes (54 patients) with intraocular pressure >25 mm Hg (or >23 mm Hg with additional risk factors), normal visual fields, normal optic disc cupping, and visual acuity >0.8 were evaluated to assess the pattern electroretinogram (PERG) as an early indicator of dysfunction preceding glaucoma.

Eight eyes developed glaucomatous visual field defects. Analysis of the receiver-operating characteristic (ROC) yielded steadily increasing ROC areas before conversion for the PERG to 0.8° checks and the PERG ratio. One year before conversion, the ROC area of the PERG ratio was 0.78, at a threshold of 1.06 with a sensitivity of 80% and a specificity of 71%.

II+

Bode (2011)16 Pattern electroretinogram in glaucoma suspects: new findings from a longitudinal study

longitudinal study

120 eyes (64 patients) with intraocular pressure greater than 25 mm Hg (or >23 mm Hg with additional risk factors), normal visual fields, normal optic disc appearance, and visual acuity >0.8 were included in the study to compare PERG measures from eyes that converted to glaucoma with eyes that did not convert.

13 eyes converted to glaucoma throughout the duration of the study according to a visual field definition. Amplitude to 0.8° check size, PERG ratio, and peak time was significantly lower in converters. Amplitude and PERG ratio predicted conversion 4 years ahead with a sensitivity and specificity of 67%/64% and 75%/76%, respectively. Converters and non converters trend comparisons revealed significant differences in the PERG ratio. However, trends did not predict conversion as successfully as single-visit measures. The PERG, especially the PERG ratio, detected glaucoma patients 4 years before visual field changes occurred, with a sensitivity of 75% and specificity of 76%. Slope analysis provided little information in detecting converters.

II+

Demir (2015)18 Comparison of Pattern Electroretinography and Optical Coherence Tomography Parameters in Patients with Primary Open-Angle Glaucoma and Ocular Hypertension

observational cohort study

72 eyes (37 patients) with early POAG, 76 eyes (38 patients) with OHT, and 60 eyes (30 controls) were enrolled to assess the correlation of visual field (VF), pattern electroretinography (PERG), and Fourier domain optical coherence tomography (FD-OCT) results in patients with ocular hypertension (OHT) and early primary open-angle glaucoma (POAG).

All GCC parameters and RNFL results were significantly lower in the POAG group compared to the OHT and control groups, except the nasal quadrant. There was no statistically significant difference between the OHT and control group. PERG amplitudes were lower in the POAG and OHT groups than in the control group. Reduction in N95 amplitude was greater than that of P50 amplitude. There was no difference detected in PERG latencies among groups. GCC was significantly correlated with VF and RNFL in the POAG groups.

II+

Ganekal (2013)29 Pattern Electroretinography Changes in Patients with Established or Suspected Primary Open Angle Glaucoma

observational cohort study

76 normal, 32 glaucomatous and 22 glaucoma suspect eyes were enrolled to assess pattern electroretinogram (PERG) changes in patients with established or suspected primary open-angle glaucoma (POAG).

The P50 and N95 amplitude of the POAG and glaucoma suspect groups were significantly reduced. Significant shortening in the P50 latency in the POAG and glaucoma suspect groups was observed. DFA using the P50 amplitude, N95 amplitude, and P50 latency waveform parameters yielded a sensitivity and specificity of 76.67% and 88.57%, respectively.

II+

Jeon (2019)30 Relationship Between Pattern Electroretinogram and Optic disc Morphology in Glaucoma 

cross-sectional study 

86 eyes (54 patients) glaucoma suspect and 145 eyes (84 patients) normal-tension glaucoma (NTG) 

 

PERG decrease earlier than perimetry according to scatter plots of changes of RNFL thickness. The linear and logarithmic R2 differences were largest for the scatter plot of SITA 24–2 (linear R2 = 0.415; logarithmic R2 = 0.443) and the smallest for P50 amplitude of PERG (linear R2 = 0.136, logarithmic R2 = 0.138). glaucoma suspect patients, HRT parameters such as cup shape measure (CSM) and linear cup-disc ratio (CDR) yielded significant correlations with PERG amplitudes (P= 0.016 for P50 and 0.049 for N95 in CSM, P= 0.012 for P50 in CDR). Mean RNFL thickness in glaucoma patients was associated with PERG amplitude (P= 0.011 for P50 and 0.002 for N95). Authors conclude that RNFL thickness change showed that purge started to decrease earlier than did perimetry and purge amplitudes were significantly correlated with dysmorphology in glaucoma suspects suggesting herb can detect ganglion cell dysfunction before cells die. Authors acknowledge the need for future studies to assess the effect of neuroprotective strategies for identifying RG C function restoration and dysfunctional but reversible ganglion cell with intact structure.

II+

Karaca (2020)22 Comparison of structural and functional tests in primary open-angle glaucoma

observational cohort study

80 eyes (40 patients) with primary open-angle glaucoma (POAG) and 46 eyes (23 healthy individuals) were enrolled to comparatively analyze the structural and functional tests used in the diagnosis and follow-up of glaucoma.

80 eyes (40 patients) with a diagnosis of POAG (18 mild 22 moderate POAG) and 46 eyes (23 healthy individuals) were enrolled. PERG P50 and N95 and ssPERG latency revealed a significant delay in the POAG group. Wave amplitudes were significantly lower in both PERG and sSPERG tests for the POAG group, with more pronounced results in ssPERG. The latency values of PERG and ssPERG tests were not significantly correlated with any of the parameters of the remaining tests. However, the amplitude values of these tests had a positive correlation with the mean deviation value and a negative correlation with the pattern standard deviation value of VF. All associated parameters were significant for the amplitude value of the ssPERG test.

II-

Mutolo (2016)31 Oral Administration of Forskolin, Homotaurine, Carnosine, and Folic Acid in Patients with Primary Open Angle Glaucoma: Changes in Intraocular Pressure, Pattern Electroretinogram Amplitude, and Foveal Sensitivity

short-term (12 months) randomized control clinical pilot study

44 eyes (22 patients) with POAG were enrolled and randomly assigned to the food supplement or control treatment group to evaluate the effects of a food supplement containing forskolin, homotaurine, carnosine, folic acid, vitamins B1, B2, B6, and magnesium in patients with primary open-angle glaucoma (POAG) already in treatment and compensated by intraocular pressure (IOP)-lowering drugs.

IOP response in the treated and the control: A decrease of IOP was observed in treated patients, starting at 6 months of treatment and becoming statistically significant at 9 (P< 0.05) and 12 months (P< 0.01). After 12 months, the average decrease for both eyes (on top of the topical treatment, which was not interrupted) was 1.9mmHg on the enrollment value. The control group resulted in no significant reductions of IOP values throughout the observation period. A significant improvement of PERG amplitude after 6 months (P< 0.05) was observed in treated patients. A trend of improvement was observed treated patients, which was significant after 12 months (P< 0.05). At this time, the average increase over enrollment values was 4.3 and 5.3 dB respectively for the right and the left eye. No adverse events were reported.

II-

Pfeiffer (1992)32 The pattern-electroretinogram in glaucoma and ocular hypertension. A cross-sectional and longitudinal study

cross-sectional, longitudinal study

65 eyes (44 patients) with normal eyes, 52 eyes (31 patients) in early stages of glaucoma, and 28 eyes (17 patients) with ocular hypertensive (OHT) eyes.

PERG was recorded using steady-state high contrast (98%) counterphasing checkerboard patterns at check sizes of 0.8 degrees and 15 degrees at 16 reversals/s and 98% contrast. Stimulation area was 27 degrees x 30 degrees. Compared to normals, in glaucoma eyes PERG amplitudes are reduced to 56 +/- 3.6%, (P < 0.0001) for 0.8 degrees and to 79 +/- 4.0% (P < 0.001) for 15 degrees check sizes. Preferential reduction for the small check size allows classification of patients on an individually. Discriminant analysis revealed normal, and glaucoma eyes were classified with a sensitivity of 82.7% and a specificity of 90.8%. Nineteen of 28 OHT eyes were classified as pathological. Eyes with OHT were tested to determine whether the PERG can be used to predict visual field damage. At the repeat visit 5 to 35 months later (mean follow-up 20.2 +/- 8.2 months), in eyes with normal PERGs the average loss in mean sensitivity was -0.61 +/- 0.5 dB, while in eyes with pathological PERGs it was -2.6 +/- 0.7 dB (P = 0.05).

II+

Sehi (2011)33 The impact of intraocular pressure reduction on retinal ganglion cell function measured using pattern electroretinogram in eyes receiving latanoprost 0.005% versus placebo

prospective, placebo-controlled, double masked, cross-over

68 eyes (68 patients) 35 glaucoma, and 33 glaucoma suspect were enrolled to assess the impact of intraocular (IOP) reduction on retinal ganglion cell (RGC) function measured using pattern electroretinogram optimized for glaucoma (PERGLA) in glaucoma suspect and glaucomatous eyes receiving latanoprost 0.005% versus placebo.

68 eyes (68 patients) were included in the analysis. 35 eyes with perimetric glaucoma (PG) and 33 glaucoma suspect (GS) eyes, comprised of nine pre-perimetric glaucoma (glaucomatous optic neuropathy and normal SAP) and 24 ocular hypertensive (OHT, no optic neuropathy, normal SAP) eyes. 46 patients (23 glaucoma, 18 OHT, five preperimetric glaucoma) were using topical anti-glaucomatous treatment prior to the initiation of this study. The mean IOP (mm Hg) after latanoprost 0.005% therapy (14.9 ± 3.8) was significantly lower than baseline (18.8 ± 4.7, p < 0.001) or placebo (18.0 ± 4.3), with a mean reduction of -20 ± 13%. Mean PERGLA amplitude (lV) and phase (p-radian) using latanoprost (0.49 ± 0.22 and 1.71 ± 0.22, respectively) were similar (p > 0.05) to baseline (0.49 ± 0.24 and 1.69 ± 0.19) and placebo (0.50 ± 0.24 and 1.72 ± 0.23). No significant (p > 0.05) diurnal variation in PERGLA amplitude was observed at baseline, or using latanoprost or placebo. Treatment with latanoprost, time of day, and IOP were not significantly (p > 0.05) associated with PERGLA amplitude or phase.

II-

Ventura (2013)17 Pattern electroretinogram progression in glaucoma suspects

observational, longitudinal cohort study

Fifty-nine (59) glaucoma suspects (GS) patients were enrolled to prospectively monitor progressive changes of retinal ganglion cell (RGC) function in early glaucoma using the pattern electroretinogram (PERG).

"On average, progression slopes of PERG amplitude/phase were skewed toward negative values, and mean being significantly (P<0.01) different from zero. Mean slopes of SAP-MD and PSD were not significantly different from zero. SNRs were higher for PERG than SAP (P<0.01). A substantial number of eyes resulted in a significant (P < 0.05) progression of PERG amplitude (15–20%) or PERG phase (16–25%). Fewer eyes resulted in a significant progression of SAP-MD (0–2%) or SAP-PSD (4–8%)."

II+

Table 2. Photopic Negative Response (PhNR) and glaucoma

 

Study

Study Type

Protocol

Results

SIGN Rating

Turno-Krecicka (1998)34 Flash electroretinography and pattern-type visual evoked potentials in early glaucoma

prospective observational study

416 eyes - primary open-angle glaucoma (120 eyes), normal tension glaucoma (137), ocular hypertension (74), glaucoma-like discs (86)

No statistically significant difference between parameters of flash-erg and pVEP of examined population and control group. There was a significant reduction in OPs amplitude in NTG patients.

II+ *

     

*Based on abstract only. Full-Text article not available.

         

Table 3. Multifocal Electroretinography (mfERG) and glaucoma

 

Study

Study Type

Protocol

Results

SIGN Rating

Golemez (2016)35 Is multifocal electroretinography an early predictor of glaucoma?

observational, cohort study

126 patients were included. There were 30 healthy (Group 1), 28 glaucoma suspect (Group 2), 48 early glaucoma (Group 3), and 20 advanced glaucoma cases (Group 4) patients enrolled to investigate the potential use of mfERG as an objective functional test that can express inner and outer retinal changes during the early stages of glaucoma. Subjects were divided into four groups according to their disease state (healthy control, glaucoma suspect, early glaucoma, and advanced glaucoma).

A one-way ANOVA revealed no statistically significant differences in patient age between groups (p = 0.126). Statistically significant differences were detected for the mean implicit time (latency) of the N1, P1, and N2 components between the advanced glaucoma and control subjects and between the advanced glaucoma and glaucoma suspects for all rings. Compared to control subjects, the N2 amplitudes were significantly decreased in all rings in the advanced glaucoma patients. The N2 amplitude was significantly different when compared to healthy subjects (Group 1) and early glaucoma subjects (Group 3) in the central 2° and 2°–5° rings. MedClac ROC curve analysis was utilized to identify parameters for discriminating between control subjects (Group 1) and early glaucoma patients (Group 3). The N2 implicit time for the central 2° ring (p\0.0001), N2 amplitude for the central 2° ring (p = 0.0001), P1 implicit time for the 2°–5° ring (p = 0.0001), N2 implicit time for the 2°– 5° ring (p = 0.0003), and N2 amplitude for the 2°–5° ring (p = 0.001) had C0.7 AUC values and were the best parameters in the ROC curve analyses that included the VFA parameters.

II+

         

To rate individual studies, a scale based on SIGN is used. The definitions and levels of evidence to rate individual studies are as follows:

 

I++

High-quality meta-analyses, systematic reviews of randomized controlled trials (RCTs), or RCTs with a very low risk of bias

I+

Well-conducted meta-analyses, systematic reviews of RCTs, or RCTs with a low risk of bias Meta-analyses, systematic reviews of RCTs, or RCTs with a high risk of bias

I-

Meta-analyses, systematic reviews of RCTs, or RCTs with a high risk of bias

 

II++

High-quality systematic reviews of case-control or cohort studies High-quality case-control or cohort studies with a very low risk of confounding or bias and a high probability that the relationship is causal

II+

Well-conducted case-control or cohort studies with a low risk of confounding or bias and a moderate probability that the relationship is causal

II-

Case-control or cohort studies with a high risk of confounding or bias and a significant risk that the relationship is not causal

III

Nonanalytic studies (e.g., case reports, case series)

 

The highest quality of literature identified was II+ per SIGN scale which is a well-conducted case control or cohort studies with low risk of bias and moderate probability that  the relationship is causal. This body of literature contributed further knowledge to defining abnormalities found with ERG in glaucoma but collectively do not define the objective measure of visual function with ERG for glaucoma or clinical utility of the test.36-40

These findings are consistent with a recent technical assessment.

  • A 2020 ECRI report concludes that the evidence is "inconclusive" for PERG for detecting central retinal damage from glaucoma. This report included one systematic review and five case-controlled studies (not included in the systematic review) that suggested changes in PERG waveform may indicate retinal ganglion cell damage in individuals with glaucoma. However, no evidence was found to determine if these findings correlated with earlier interventions or improved patient outcomes.5
  • UpToDate does not include any electroretinography in the newer technology section for glaucoma diagnosis.41

Societal Guidance and Recommendations

  • The 2015 AAO Primary Open-Angle Glaucoma Preferred Practice Pattern Guideline recommends comprehensive eye examinations for patients with risk factors for glaucoma and screening but does not address ERG as a diagnostic tool.42
  • The 2015 AAO Preferred Practice Guidelines, "Primary Open-Angle Glaucoma Suspect also omits ERG as a diagnostic tool.43
  • The 2016 AAO Comprehensive Adult Medical Eye Evaluation Guideline states, "electrophysiologic testing" is not part of a routine comprehensive medical eye evaluation but does acknowledge it as an "additional option for diagnostic testing." Furthermore, the guideline does not explicitly address ERG or offer any grade of evidence specific to electrophysiologic testing.44
  • The 2016 AAO POAG Preferred Practice Pattern Guidelines42, the 2017 AAO for Diabetic Retinopathy45, and the 2018 AAO summary benchmarks for preferred practice pattern guidelines46 do not specifically mention PERG as a diagnostic tool.
  • The American Optometric Association Care of the Patient with Open Angle Glaucoma omits ERG.47
  • The 2019 Canadian Agency for Drugs and Technologies in Health: Automated Perimetry or Electroretinography for Visual Field Testing in Eye Examinations: Guideline did not include PERG.48
  • The 2019 Royal Australian College of General Practitioners, Ophthalmology Clinical Committee. Medicare Benefits Schedule Review Taskforce: Ophthalmology Report states Electroretinography helps diagnose disease of the retina, including retinitis and hereditary conditions as well as diabetic retinopathy. They state that it requires specialized training and equipment to conduct and interpret the test. It does not include a role in glaucoma management or evaluation.49
  • International Society for Clinical Electrophysiology of Vision (ISCEV). ISCEV Standard for Clinical Pattern Electroretinography (PERG): updated 2013 report States the role of PERG for both neurological and ophthalmological practice, including glaucoma, optic neuropathy, and primary ganglion cell disease.9

Other indications

Childhood Brain Tumors

ERG has been investigated as a tool for clinical evaluation in childhood brain tumor survivors. A small cross-sectional study did not show the value of EMG for this population.50

Chloroquine and Hydroxychloroquine Toxicity

Multiple studies have shown the benefit of ERG in evaluation for Chloroquine and Hydroxychloroquine toxicity. A 2015 systematic review reported mfERG for retinal toxicity has a high sensitivity of 90% (95% confidence interval [CI], 0.62-0.98) and 52% (CI, 0.29-0.74), respectively, with automated visual fields (AVF) testing as a reference standard (13 studies), but specificity was variable when compared to other testing modalities.41 In 2016 AAO revised recommendations for screening of Chloroquine and Hydroxychloroquine Toxicity retinopathy, stating the preliminary screening tests are automated visual fields plus spectral-domain optical coherence tomography (SD-OCT).42 The multifocal electroretinogram (mfERG) can provide objective corroboration for visual fields, and fundus autofluorescence (FAF) can show damage topographically. The guidance stated that mfERG is similar in sensitivity to visual field testing and can provide objective information about suspected visual field loss52. Using the definition of toxicity from AAO Guidelines, a 2019 study of 120 eyes reported a sensitivity of 1.00 (95% CI 0.79-1.00) and a specificity of 0.78 (95% CI 0.69-0.85) of MFErG for detection of toxicity.53

Evaluation of autism spectrum disorder

A 2016 paper explored a relationship between reduced scotopic ERG b-wave amplitudes and early findings of autism. ERG was performed on 11 patients with autism spectrum disorder (ASD) and 15 typically developing controls. They noted that some ASD patients showed subnormal dark adaptive ERG b-wave amplitudes. They conclude that the exploratory findings suggest there is altered cone-ON bipolar signaling in ASD.54

 

Analysis of Evidence (Rationale for Determination)

ERG and Glaucoma

The current literature on the use of ERG for the early detection of glaucoma is limited. There were no studies that compare ERG to a diagnostic gold standard test for retinal ganglion cell damage. The current body of literature is limited to case-controlled studies, which are at risk of inflating estimates of sensitivity and specificity of the test.5 Most studies did not have an adequate sample size, protocols were not standardized, and normal and abnormal values were unclear. While glaucoma is included in the ISCEV guidelines, but the clinical application is still not clearly defined.

While we appreciate that there may be an emerging role for the use of ERG in glaucoma, there are many challenges. There is a lack of standardized protocols, including the best form of ERG (PERG, ssPERG, phRG), type, and placement of electrodes, and standardized reference range. The appropriate patient selection is uncertain, and the impact of co-morbidities such as cataracts, diabetes and other underlying conditions which may impact PERG specificity is not clear. Timing and frequency of the test, and how to use the results are still under investigation. There is a lack of evidence on how to use ERG for clinical glaucoma management or improve outcomes. There is a lack of support for this technology as part of the routine evaluation of glaucoma by AAO. Therefore, CGS Administrators considers the use of ERG for glaucoma diagnosis or management investigational.

Other indications

There is strong evidence in support of ERG (ffERG and MFERG) as part of the evaluation and for treatment monitoring of retinal function and distinguishing retinal from optic nerve lesions. There is also sufficient evidence of the role of mfERG in the assessment of the detection of chloroquine and hydroxychloroquine toxicity. There is not sufficient evidence for other indications since there is little supporting data in other populations.

Proposed Process Information

Synopsis of Changes
Changes Fields Changed
N/A
Associated Information
Sources of Information
Bibliography
Open Meetings
Meeting Date Meeting States Meeting Information
N/A
Contractor Advisory Committee (CAC) Meetings
Meeting Date Meeting States Meeting Information
N/A
MAC Meeting Information URLs
N/A
Proposed LCD Posting Date
Comment Period Start Date
Comment Period End Date
Reason for Proposed LCD
Requestor Information
This request was MAC initiated.
Requestor Name Requestor Letter
N/A
Contact for Comments on Proposed LCD

Coding Information

Bill Type Codes

Code Description
N/A

Revenue Codes

Code Description
N/A

CPT/HCPCS Codes

Group 1

Group 1 Paragraph

N/A

Group 1 Codes

N/A

N/A

ICD-10-CM Codes that Support Medical Necessity

Group 1

Group 1 Paragraph:

N/A

Group 1 Codes:

N/A

N/A

ICD-10-CM Codes that DO NOT Support Medical Necessity

Group 1

Group 1 Paragraph:

N/A

Group 1 Codes:

N/A

N/A

Additional ICD-10 Information

General Information

Associated Information
N/A
Sources of Information
N/A
Bibliography
  1. Aetna. Electroretinography Clinical Policy Bulletins. http://www.aetna.com/cpb/medical/data/800_899/0854.html. Accessed 8/20/2020.
  2. CMS. Novitas Solutions I. Electroretinogrpahy (ERG) L37371. http://www.cms.hhs.gov. Accessed 08/20/2020.
  3. Wu Z, Hadoux X, Gaskin JCF, Sarossy MG, Crowston JG. Measuring the photopic negative response: viability of skin electrodes and variability across disease severities in glaucoma. Transl Vis Sci Technol. 2016;5(2):13-13.
  4. Ramkumar H, Lim J, Epley K, et al. Electroretinogram. https://eyewiki.org/Electroretinogram. Accessed 8/20/2020.
  5. ECRI. Pattern Electroretinography for Detecting Central Retinal Damage from Glaucoma. 2019.
  6. Senger C, Moreto R, Watanabe SE, Matos AG, Paula JS. Electrophysiology in Glaucoma. J Glaucoma. 2020;29(2):147-153.
  7. Lai T, Chan W, Lai R, Ngai J, Li H, Lam D. The clinical applications of multifocal electroretinography: a systematic review. Surv Ophthalmol. 2007;52(1):61-96.
  8. Florida BCBS. Electroretinography. 2015; http://mcgs.bcbsfl.com/MCG?activity=openSearchedDocMcg&imgId=75RXX2AOC77BLXC4IHL. Accessed 9/10/2020.
  9. Bach M, Brigell MG, Hawlina M, et al. ISCEV standard for clinical pattern electroretinography (PERG): 2012 update. Doc Ophthalmol. 2013;126(1):1-7.
  10. Hood DC, Bach M, Brigell M, et al. ISCEV standard for clinical multifocal electroretinography (mfERG) (2011 edition). Doc Ophthalmol. 2012;124(1):1-13.
  11. McCulloch DL, Marmor MF, Brigell MG, et al. ISCEV Standard for full-field clinical electroretinography (2015 update). Doc Ophthalmol. 2015;130(1):1-12.
  12. Marmor M. An updated standard for clinical electroretinography. Arch Ophthalmol. 1995;113(11):1375-1376.
  13. American Academy of Ophthalmology. Recommendations on Clinical Assessment of Patients with Inherited Retinal Degenerations. 2016; https://www.aao.org/. Accessed 01/03/2023.
  14. Jampel H, Singh K, Lin S, et al. Assessment of visual function in glaucoma: a report by the American Academy of Ophthalmology. Ophthalmology. 2011;118(5):986-1002.
  15. Bach M, Unsoeld AS, Philippin H. Pattern ERG as an early glaucoma indicator in ocular hypertension: a long-term, prospective study. Invest Ophthalmol Vis Sci. 2006;47(11):4881–4887.
  16. Bode S, Jehle T, Bach M. Pattern electroretinogram in glaucoma suspects: new findings from a longitudinal study. Invest Ophthalmol Vis Sci. 2011;52(7):4300-4306.
  17. Ventura L, Golubev L, Feuer W, Porciatti V. Pattern electroretinogram progression in glaucoma suspects. J Glaucoma. 2013;22(3):219-225.
  18. Demir S, Oba M, Erdogan E, et al. Comparison of Pattern Electroretinography and Optical Coherence Tomography Parameters in Patients with Primary Open-Angle Glaucoma and Ocular Hypertension. Turk J Ophthalmol. 2015;45(6):229-234.
  19. Wilsey L, Gowrisankaran S, Cull G, Hardin C, Burgoyne C, Fortune B. Comparing three different modes of electroretinography in experimental glaucoma: diagnostic performance and correlation to structure. Doc Ophthalmol. 2017;134(2):111-128.
  20. Jafarzadehpour E, Radinmehr F, Pakravan M, Mirzajani A, Yazdani S. Pattern electroretinography in glaucoma suspects and early primary open angle glaucoma. J Ophthalmic Vis Res. 2013;8(3):199-206.
  21. Gordon P, Kostic M, Monsalve P, et al. Long-term PERG monitoring of untreated and treated glaucoma suspects. Documenta Ophthalmologica. 2020;141(2):1-8.
  22. Karaca U, Dagli O, Ozge G, Mumcuoglu T, Bayer A. Comparison of structural and functional tests in primary open angle glaucoma. Indian Journal of Ophthalmology. 2020;68(5):805.
  23. Turkey E, Elsanabary Z, Elshazly L, Osman M. Role of pattern electroretinogram in ocular hypertension and early glaucoma. J Glaucoma. 2019;28(10):871-877.
  24. Robson A, Nilsson J, Li S, et al. ISCEV guide to visual electrodiagnostic procedures. Documenta Ophthalmologica. 2018;136(1):1-26.
  25. Porciatti V, Ventura LM. The PERG as a tool for early detection and monitoring of glaucoma. J Current Ophthalmology Reports. 2017;5(1):7-13.
  26. Resende A, Sanvicente C, Eshraghi H, et al. Test–retest repeatability of the pattern electroretinogram and flicker electroretinogram. Documenta Ophthalmologica 2019;139(3):185-195.
  27. Tang J, Edwards T, Crowston J, Sarossy M. The test–retest reliability of the photopic negative response (PhNR). Transl Vis Sci Technol. 2014;3(6):1-1.
  28. Mortlock K, Binns A, Aldebasi Y, North R. Inter-subject, inter-ocular and inter-session repeatability of the photopic negative response of the electroretinogram recorded using DTL and skin electrodes. Documenta Ophthalmologica. 2010;121(2):123-134.
  29. Ganekal S, Dorairaj S, Jhanji V. Pattern Electroretinography Changes in Patients with Established or Suspected Primary Open Angle Glaucoma. J Curr Glaucoma Pract. 2013;7(2):39-42.
  30. Jeon SJ, Park H-YL, Jung KI, Park CK. Relationship between pattern electroretinogram and optic disc morphology in glaucoma. J PloS one. 2019;14(11):e0220992.
  31. Mutolo MG, Albanese G, Rusciano D, Pescosolido N. Oral Administration of Forskolin, Homotaurine, Carnosine, and Folic Acid in Patients with Primary Open Angle Glaucoma: Changes in Intraocular Pressure, Pattern Electroretinogram Amplitude, and Foveal Sensitivity. J Ocul Pharmacol Ther. 2016;32(3):178-183.
  32. Pfeiffer N, Bach M. The pattern-electroretinogram in glaucoma and ocular hypertension. A cross-sectional and longitudinal study. Ger J Ophthalmol. 1992;1(1):35-40.
  33. Sehi M, Grewal DS, Feuer WJ, Greenfield DS. The impact of intraocular pressure reduction on retinal ganglion cell function measured using pattern electroretinogram in eyes receiving latanoprost 0.005% versus placebo. Vision Res. 2011;51(2):235-242.
  34. Turno-Krecicka A, Nizankowska MH, Zajac-Pytrus H, Koziorowska M, Pelczar E, Robaczynska M. [Flash electroretinography and pattern-type visual evoked potentials in early glaucoma]. Klin Oczna. 1998;100(5):285-288.
  35. Golemez H, Yildirim N, Ozer A. Is multifocal electroretinography an early predictor of glaucoma? Doc Ophthalmol. 2016;132(1):27-37.
  36. Jung K, Jeon S, Kim Y, Park C. Comparison of pattern electroretinograms of glaucoma patients with parafoveal scotoma versus peripheral nasal step. Sci Rep. 2019;1(1):3547.
  37. Mavilio A, Sisto D, Ferreri P, Dammacco R, Alessio G. RE-PERG, a new paradigm for glaucoma diagnosis, in myopic eyes. Clin Ophthalmol. 2019;13:1315-1132.
  38. Elgohary A, Elbedewy H, Saad H, Eid T. Pattern electroretinogram changes in patients with primary open-angle glaucoma in correlation with visual field and optical coherence tomography changes. Eur J Ophthalmol. 2019;30(6):1362-1369.
  39. Strakhov V, Yartsev A, Alekseev V, Klimova O, Kazanova S, Voronin N. Structural and functional changes in the retinal layers in patients with primary glaucoma and possible means of retinoprotection. Vestn Oftalmol. 2019;135(2):70-82.
  40. Kurysheva N, Maslova E, Zolnikova I, Fomin A, Lagutin M. A comparative study of structural, functional and circulatory parameters in glaucoma diagnostics. PLoS One. 2018;13(8):e0201599.
  41. Jacobs D. Open-angle glaucoma: Epidemiology, clinical presentation, and diagnosis. https://www.uptodate.com/contents/open-angle-glaucoma-epidemiology-clinical-presentation-and-diagnosis?search=glacoma&source=search_result&selectedTitle=1~150&usage_type=default&display_rank=1. Accessed 2/16/2021.
  42. Prum Jr. B, Rosenberg L, Gedde S, et al. American Acedemy of Ophthalmology. Primary Open-Angle Glaucoma Preferred Practice Pattern Guidelines. Ophthalmology. 2015;123(1):PP41-111.
  43. Prum Jr. B, Rosenberg L, Gedde S. American Acedemy of Ophthalmology. Primary Open-Angle Glaucoma Suspect Preferred Practice Patterns. Ophthalmology 2015; Primary Open-Angle Glaucoma Suspect Preferred Practice Pattern(®) Guidelines - PubMed (nih.gov) Accessed 04/28/2022.
  44. Feder R, Olsen T, Prum J, BE, et al. American Academy of Ophthalmology Comprehensive Adult Medical Eye Evaluation Preferred Practice Pattern Guidelines. 2016; http://www.aao.org>. Accessed 8/21/2020.
  45. Flaxel C, Bailey S, Fawzi A, et al. American Academy of Ophthalmology Diabetic Retinopathy Preferred Practice Pattern Guidelines. Ophthalmology 2019; http://www.aao.org. Accessed 8/21/2020.
  46. American Academy of Ophthalmology. Summary benchmarks for preferred practice pattern guidelines. 2019; PPP Summary Benchmarks.21.full set.pdf Accessed 04/28/2022.
  47. American Optometric Association (AOA) Optometric Clinical Practice Guideline: Care of the Patient with Open Angle Glaucoma. 2010 (revised); Microsoft Word - CPG 9 Open Angle Glaucoma Guideline-MWedit-FINAL REVISION.doc (aoa.org). Accessed04/28/2022.
  48. Canadian Agency for Drugs and Technologies in Health. Automated Perimetry or Electroretinography for Visual Field Testing in Eye Examinations: Guideline. 2019; https://www.cadth.ca/automated-perimetry-or-electroretinography-visual-field-testing-eye-examinations-guideline. Accessed Oct. 27, 2021.
  49. Royal Australian College of General Practitioners, Ophthalmology Clinical Committee. Medicare Benefits Schedule Review Taskforce: Ophthalmology Report 2020; https://www.health.gov.au/sites/default/files/documents/2021/06/final-clinical-committee-report-for-ophthalmology.pdf. Accessed Oct. 27, 2021.
  50. Pietilä S, Lenko H, Oja S, Koivisto A, Pietilä T, Makipernaa A. Electroretinography and Visual Evoked Potentials in Childhood Brain Tumor Survivors. J Child Neurol. 2016;31(8):998-1004.
  51. Tsang A, Pirshahid S, Virgili G, Gottlieb C, Hamilton J, Coupland S. Hydroxychloroquine and chloroquine retinopathy: a systematic review evaluating the multifocal electroretinogram as a screening test. Ophthalmology. 2015;122(6):1239-1251 e1234.
  52. Marmor M, Kellner U, Lai T, Lyons J, Mieler W. American Academy of Ophthalmology revised recommendations on screening for chloroquine and hydroxychloroquine retinopathy. Ophthalmology. 2017;2:415-422.
  53. Tsang AC, Ahmadi S, Hamilton J, et al. The Diagnostic Utility of Multifocal Electroretinography in Detecting Chloroquine and Hydroxychloroquine Retinal Toxicity. Am J Ophthalmol. 2019;206:132-139.
  54. Constable PA GS, Bowler DM, et al. Full-field electroretinogram in autism spectrum disorder. Doc Ophthalmol. 2016;132(2):82-99.

Revision History Information

Revision History Date Revision History Number Revision History Explanation Reasons for Change
01/12/2023 R4

Revision Effective: 01/12/2023

Revision Explanation: Updated link for #13 in the bibliography section.

  • Provider Education/Guidance
12/15/2022 R3

Revision Effective: 12/15/2022

Revision Explanation: Updated link for #13 in the bibliography section.

  • Provider Education/Guidance
07/21/2022 R2

Revision Effective: 07/21/2022

Revision Explanation: Updated link in bibliography for # 46.

  • Typographical Error
07/07/2022 R1

Revision Effective: 05/05/2022

Revision Explanation: Updated links in bibliography for #'s 43, 46, and 47.

  • Provider Education/Guidance
N/A

Associated Documents

Attachments
N/A
Related National Coverage Documents
N/A
Public Versions
Updated On Effective Dates Status
01/04/2023 01/12/2023 - N/A Currently in Effect You are here
Some older versions have been archived. Please visit the MCD Archive Site to retrieve them.

Keywords

N/A

Read the LCD Disclaimer