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Corneal Hysteresis

Policy Number: MP-354

Latest Review Date:  July 2011

Category: Medicine                                                               

Policy Grade: Active Policy but no longer scheduled for regular literature reviews and updates.

Description of Procedure or Service:

Glaucoma is one of the leading causes of blindness.  The National Eye Institute reports that more than 2 million Americans have been diagnosed with glaucoma and another 2 million have the disease and are not diagnosed.  It is estimated that more than 3 million Americans will have glaucoma by 2020.  Glaucoma is a group of diseases that affects the optic nerve.  It is generally caused by ocular hypertension as in the most common type, primary open angle glaucoma (POAG) but not always.  Glaucoma can damage your vision gradually and may not be diagnosed until at an advanced state.  Another type of glaucoma is acute angle-closure glaucoma and presents with completely different symptoms such as severe eye pain and nausea and vomiting.  A third, much less common type of glaucoma, is low-tension glaucoma and is believed to be related to not enough blood reaching the optic nerve. 

Hysteresis is a property of physical systems that do not instantly follow the forces applied to them. The reaction is slow or does not return completely to the original state. Another defines it as the lagging of an effect behind its cause.  Corneal hysteresis (CH) is a measure of viscous damping in the corneal tissue.  It is the energy absorption capability of the cornea.  Corneal hysteresis is determined through inducing the cornea to move following an air pulse.  The difference in pressure values at the inward and outward applanation (flattening of the cornea by pressure) event times is defined as corneal hysteresis and the average provides a corrected intraocular pressure (IOP) measurement for an accurate IOP monitoring.  Corneal hysteresis is determined by the viscoelastic properties of the corneoscleral shell. 

The Goldman applanation tonometry is the most widely used method of measuring intraocular pressure and it is also known that corneal parameters affect the accuracy of this instrument.  This instrument is the gold standard in glaucoma measurement. 

The Reichert Ocular Response Analyzer (ORA) received 510(k) clearance from the U.S. Food and Drug Administration on January 20, 2004.  The approved indications are measurement of intraocular pressure and assessment of biomechanical response of the cornea as tools in the diagnosing and monitoring of patients with glaucoma.  There is no requirement by the 510(k) clearance process to submit evidence of extensive safety and efficacy.  The measurement of CH by the ORA device has also been proposed as a method to evaluate the potential for post-surgical complications in patients being considered for refractive surgery and for assessing the biomechanical properties of the cornea in keratoconus.

Keratoconus is a noninflammatory condition of unknown etiology affecting the central cornea characterized by thinning and bulging of the cornea.  It may significantly affect vision due to irregular astigmatism and corneal scarring.  Keratoconic eyes are known to be less rigid and more elastic than normal eyes and possibly may have a different hysteresis than normal eyes.  One possible measure of ocular rigidity in keratoconus is hysteresis. 

 

Policy:

Corneal hysteresis measurement is considered not medically necessary and investigational.

 

Key Points:

It has been known for over 30 years that central corneal thickness (CCT) affects IOP measurement.  Results from the Ocular Hypertension Treatment Study (OHTS) demonstrated that CCT is an important and independent risk factor for progression to initial glaucoma damage in persons with ocular hypertension.  The association between CCT and glaucoma include, thinner corneas give lower IOP levels and may be subjected to less aggressive IOP-lowering therapy.  Thinner corneas may be a risk factor due to an association with the response of the corneoscleral shell and the ocular vasculature to IOP-induced stress.  Patients with thick corneas as determined by corneal pachymetry and ocular hypertension are not as likely to be at risk for progression of glaucoma.  

Congdon et al (2006) reported on an observational study to measure the impact of CCT and corneal hysteresis as anatomic and physiologic parameters to the clinical features and history of progressive worsening among patients with glaucoma, ocular hypertension, or suspected glaucoma.  They concluded that the relationship between corneal features and glaucoma is more complex than simple anatomic thickness.  The authors also concluded that it is not clear what corneal hysteresis measures but that it does appear that this variable describes the response of the cornea to rapid deformation.  In this study, hysteresis was more closely associated with eyes that demonstrated progressive change than was the CCT.  They have also proposed that their results may give information about responsiveness of the eye to mean IOP or changes in IOP and should refocus interest to the behavior of the cornea rather than just the thickness of the cornea.  The authors did cite several limitations to their study.  This includes patient selection for the study as the participants were from an urban area serviced by a tertiary care facility.  The data or clinical information gathered for the study was based on retrospective chart review.  There was no standardized protocol for the measurement of some key outcomes.  This study was only to report associations among corneal thickness, corneal deformability, and glaucoma damage.  There was determination of how to direct patient care or to improve patient outcome.

Other published peer-reviewed literature consisted of studies evaluating correlations and associations between CH and established measures of intraocular pressure and CCT (Kotecha, 2006; Medeiros, 2006; Shah, 2006, 2007).  These studies also do not demonstrate how CH measurement can be used to enhance patient management and improve patient health outcome.

Additional studies again do not reflect how the measurement of CH will enhance patient management and improve health outcomes (Hager, 2007, Herndon, 2006, Pepose 2007, Lam 2007, Bochman 2008, Kotecha 2006, 2007, Kirwan 2006).

Keratoconus is a noninflammatory condition of unknown etiology affecting the central cornea characterized by thinning and bulging of the cornea.  It may significantly affect vision due to irregular astigmatism and corneal scarring.  Keratoconic eyes are known to be less rigid and more elastic than normal eyes and possibly may have a different hysteresis than normal eyes.  One possible measure of ocular rigidity in keratoconus is hysteresis. 

The American Academy of Ophthalmology (AAO) does not mention measurement of CH in its Preferred Practice Pattern for the evaluation and management of Primary Open Angle Glaucoma.

2011 Update

Some of the recently published peer-reviewed literature consists of studies that evaluate correlations and associations between CH and established measures of intraocular pressure and CCT.  (Vanderwalle, 2009; Mangouritsas, 2009; Kopito, 2010; Renier, 2010; Carbonaro, 2010; Sullivan-Mee, 2009; Shah, 2008; Bayer, 2010; Schweitzer, 2010; Saad, 2009; Fontes, 2011; Bayoumi, 2010; Lau and Pye, 2011).  These studies do not demonstrate how CH measurement can be used to enhance patient management and improve health outcomes.  There is insufficient evidence available from the peer-reviewed literature to validate the clinical role for measurement of corneal hysteresis.

 

Key Words:

Glaucoma, corneal hysteresis, corneal, intraocular pressure, IOP, primary open angle glaucoma, POAG, keratoconus, Goldman tonometer, Reichert Ocular Response Analyzer, ORA, Ocular Response Analyzer

 

Approved by Governing Bodies:

Reichert Ocular Response Analyzer received 510(k) clearance from the FDA on January 20, 2004 for the intended use to measure intra-ocular pressure of the eye and the biomechanical response of the cornea for the purpose of aiding in the diagnosis and monitoring of glaucoma.  http://www.accessdata.fda.gov/cdrh_docs/pdf3/K032799.pdf.

 

Benefit Application:

Coverage is subject to member’s specific benefits.  Group specific policy will supersede this policy when applicable.

ITS: Home Policy provisions apply

FEP contracts: FEP does not consider investigational if FDA approved and will be reviewed for medical necessity. Special benefit consideration may apply.  Refer to member’s benefit plan.

 

Current Coding: 

CPT Codes:

92145              Corneal hysteresis determination, by air impulse stimulation, unilateral or bilateral,

                        with interpretation and report (Effective 01/01/15)

 

References:

  1. Bayer A, Sahin A, Hürmeric V, et al. Intraocular pressure values obtained by ocular response analyzer, dynamic contour tonometry, and Goldmann tonometry in keratokonic corneas.  J Glaucoma.  2010 Oct-Nov; 19(8):540-5.

  2. Bayoumi NH, Bessa AS, El Massry AA.  Ocular response analyzer and Goldmann applanation tonometry: a comparative study of findings.  J Glaucoma. 2010 Dec; 19(9):627-31.

  3. Bochmann F, Ang GS and Azuara-Blanco A.  Lower corneal hysteresis in glaucoma patients with acquired pit of the optic nerve (APON).  Graefes Arch Clin Exp Ophthalmol, May 2008; 246(5): 735-738.

  4. Carbonaro F, Andrew T, Mackey DA, et al.  Comparison of three methods of intraocular pressure measurement and their relation to central corneal thickness. Eye (Lond). 2010 Jul;24(7):1165-70.

  5. Congdon NG, Broman AT, et al.  Central corneal thickness and corneal hysteresis associated with glaucoma damage.  American Journal of Ophthalmology, May 2006, Vol. 141, Issue 5.

  6. ECRI Institute. Hotline Response. Central Corneal thickness measurement for the diagnosis of glaucoma and ocular hypertension.  April 2010.

  7. Elsheikh A, Wang D, Rama P, et al.  Experimental assessment of human corneal hysteresis.  Curr Eye Res, March 2008; 33(3): 205-213.

  8. Fontes BM, Ambrósio R Jr, Velarde GC, et al. Ocular response analyzer measurements in keratoconus with normal central corneal thickness compared with matched normal control eyes.  J Refract Surg, 2011 Mar;27(3):209-15.

  9. Gatinel D, Chaabouni S, Adam PA, Munck J, et al.  Corneal hysteresis, resistance factor, topography, and pachymetry after corneal lamellar flap.  J Refract Surg, January 2007; 23(1): 76-84.

  10. Hager A, Loge K, Kutschan A and Wiegand W.  [The effect of cataract and vitreoretinal surgery on central corneal thickness and corneal hysteresis].  Klin Monatsbl Augenheilkd, March 2008; 225(3): 207-211.

  11. Jorge JM, Gonzalez-Meijome JM, et al.  Correlations between corneal biomechanical properties measured with the ocular response analyzer and ICare rebound tonometry.  J Glaucoma, Sept 2008; 17(6): 442-448.

  12. Kirwan Caitriona, O’keefe Michael and Lanigan Bernadette.  Corneal hysteresis and intraocular pressure measurement in children using the Reichert Ocular Response Analyzer.  American Journal of Ophthalmology, December 2006, Vol. 142, Issue 6.

  13. Kopito R, Gaujoux T, Montard R, et al.  Reproducibility of viscoelastic property and intraocular pressure measurements obtained with the Ocular Response Analyzer.  Acta Ophthalmol. 2010 Aug 25.

  14. Kotecha A, Elsheikh A, Roberts CR, et al.  Corneal thickness- and age-related biomechanical properties of the cornea measured with the ocular response analyzer.  IOVS, December 2006, Vol. 47, No. 12.

  15. Kotecha A.  What biomechanical properties of the cornea are relevant for the clinician?  Surv Ophthalmol, November 2007; 52 Suppl 2: S109-114.

  16. Lam A, Chen D, Chiu R and Chui WS.  Comparison of IOP measurements between ORA and GAT in normal Chinese.  Optom Vis Sci, September 2007; 84(9): 909-914.

  17. Lau W, Pye D.  Changes in corneal biomechanics and applanation tonometry with induced corneal swelling.  Invest Ophthalmol Vis Sci. 2011 Feb 23.

  18. Lu F, Xu S, Qu J, Shen M, Wang X, et al.  Central corneal thickness and corneal hysteresis during corneal swelling induced by contact lens wear with eye closure.  Am J Ophthalmol, April 2007; 143(4): 616-622.

  19. Mangouritsas G, Morphis G, Mourtzoukos S, et al.  Association between corneal hysteresis and central corneal thickness in glaucomatous and non-glaucomatous eyes.  Acta Ophthalmol.  2009 Nov;87(8):901-5.

  20. Martinez-de-la-Casa J, Garcia-Feijoo J, et al.  Ocular response analyzer versus Goldmann applanation tonometry for intraocular pressure measurements.  IOVS, October 2006, Vol. 47, No. 10.

  21. Medeiros FA and Weinreb RN.  Evaluation of the influence of corneal biomechanical properties on intraocular pressure measurements using the ocular response analyzer.  J Glaucoma 2006; 15(5): 364-370.

  22. Ortiz D, Shabayek MH, et al.  Corneal biomechanical properties in normal, post-laser in situ keratomileusis, and keratoconic eyes.  Cataract Refract Surg, August 2007; 33(8): 1371-1375.

  23. Pepose JS, Feigenbaum SK, Qazi MA, et al.  Changes in corneal biomechanics and intraocular pressure following LASIK using static, dynamic, and noncontact tonometry.  American Journal of Ophthalmology, January 2007, Vol. 143, Issue 1.

  24. Renier C, Zeyen T, Fieuws S, et al.  Comparison of ocular response analyzer, dynamic contour tonometer and Goldmann applanation tonometer Int Ophthalmol. 2010 Dec; 30(6):651-9.

  25. Saad A, Lteif Y, Azan E, et al.  Biomechanical properties of keratoconus suspect eyes.  Invest Ophthalmos Vis Sci. 2009 Dec 30.

  26. Schweitzer C, Roberts CJ, Mahmoud AM, et al.  Screening of forme gruste keratoconus wth the ocular response analyzer. Invest Ophthalmol Vis Sci.  2010 May;51(5):2403-10.

  27. Shah S, Laiquzzaman M, Cunliffe I and Mantry S.  The use of the Reichert ocular response analyser to establish the relationship between ocular hysteresis, corneal resistance factor and central corneal thickness in normal eyes.  Cont Lens Anterior Eye, December 2006; 29(5): 257-262.

  28. Shah S, Laiquzzaman M, Bhojwani R, Mantry S and Cunliffe I.  Assessment of the biomechanical properties of the cornea with the ocular response analyzer in normal and keratoconic eyes.  Investigative Ophthalmology & Visual Science, July 2007; 48(7): 3026-3031.

  29. Shah S, Laiquzzaman M, Mantry S and Cunliffe I.  Ocular response analyser to assess hysteresis and corneal resistance factor in low tension, open angle glaucoma and ocular hypertension.  Clin Experiment Ophthalmol, August 2008; 36(6): 508-513.

  30. Sullivan-Mee M, Gerhardt G, Halverson KD, et al.  Repeatability and reproducibility for intraocular pressure measurement by dynamic contour, ocular response analyzer and Goldmann applanation tonometry. J Glaucoma.  2009 Dec:18(9):666-73.

  31. Sullivan-Mee M, Billingsley SC, Patel AD, Halverson KD, et al.  Ocular Response Analyzer in subjects with and without glaucoma.  Optom Vis Sci, June 2008; 85(6): 463-470.

  32. Sun L, Shen M, Wang J et al.  Recovery of corneal hysteresis after reduction of intraocular pressure in chronic primary angle-closure glaucoma.  Am J Ophthalmol.  2009 Jun:147(6):1061-6., 1066.e1-2.

  33. Touboul D, Roberts C, Kerautret J, Garra C, et al.  Correlations between corneal hysteresis, intraocular pressure, and corneal central pachymetry.  J Cataract Refract Surgery 2008; 34(4): 616-622.

  34. Vandewalle E, Vandenbroeck S, Stalmans I, et al. Comparison of ICare, dynamic contour tonometer, and ocular response analyzer with Goldmann applanation tonometer in patients with glaucoma,  Eur J Ophthalmol. 2009 Sep-Oct;19(5):783-9.

 

Policy History:

Medical Policy Group, April 2009 (1)

Medical Policy Administration Committee, May 2009

Available for comment May 12-June 24, 2009

Medical Policy Group, July 2011; Updated Key Points and References

Medical Policy Group, September 2012: Effective September 14, 2012 this policy is no longer scheduled for regular literature reviews and updates.

Medical Policy Group, November 2014: 2015 Annual Coding update. Added code 92145 to current coding and added Previous Coding section to include deleted code 0181T.


This medical policy is not an authorization, certification, explanation of benefits, or a contract. Eligibility and benefits are determined on a case-by-case basis according to the terms of the member’s plan in effect as of the date services are rendered. All medical policies are based on (i) research of current medical literature and (ii) review of common medical practices in the treatment and diagnosis of disease as of the date hereof. Physicians and other providers are solely responsible for all aspects of medical care and treatment, including the type, quality, and levels of care and treatment.

This policy is intended to be used for adjudication of claims (including pre-admission certification, pre-determinations, and pre-procedure review) in Blue Cross and Blue Shield’s administration of plan contracts.

The plan does not approve or deny procedures, services, testing, or equipment for our members. Our decisions concern coverage only. The decision of whether or not to have a certain test, treatment or procedure is one made between the physician and his/her patient. The plan administers benefits based on the member’s contract and corporate medical policies. Physicians should always exercise their best medical judgment in providing the care they feel is most appropriate for their patients. Needed care should not be delayed or refused because of a coverage determination.

As a general rule, benefits are payable under health plans only in cases of medical necessity and only if services or supplies are not investigational, provided the customer group contracts have such coverage.

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1. The technology must have final approval from the appropriate government regulatory bodies;

2. The scientific evidence must permit conclusions concerning the effect of the technology on health outcomes;

3. The technology must improve the net health outcome;

4. The technology must be as beneficial as any established alternatives;

5. The improvement must be attainable outside the investigational setting.

Medical Necessity means that health care services (e.g., procedures, treatments, supplies, devices, equipment, facilities or drugs) that a physician, exercising prudent clinical judgment, would provide to a patient for the purpose of preventing, evaluating, diagnosing or treating an illness, injury or disease or its symptoms, and that are:

1. In accordance with generally accepted standards of medical practice; and

2. Clinically appropriate in terms of type, frequency, extent, site and duration and considered effective for the patient’s illness, injury or disease; and

3. Not primarily for the convenience of the patient, physician or other health care provider; and

4. Not more costly than an alternative service or sequence of services at least as likely to produce equivalent therapeutic or diagnostic results as to the diagnosis or treatment of that patient’s illness, injury or disease.