2017 MIPS Measure #389: Cataract Surgery: Difference Between Planned and Final Refraction

Valid Data Submission Method(s) Measure Type High Priority Measure? NQS Domain Specialty Measure Sets
Registry Outcome Yes Effective Clinical Care Ophthalmology

Measure Description

Percentage of patients aged 18 years and older who had cataract surgery performed and who achieved a final refraction within +/- 0.5 diopters of their planned (target) refraction

Instruction

This measure is to be calculated each time a cataract procedure is performed during the performance period. This measure is intended to reflect the quality of services provided for the patient receiving cataract surgery.

Note: This is an outcome measure and will be calculated solely using registry data.

  • For patients who receive the surgical procedures specified in the denominator coding, it should be reportedwhether or not the patient had a difference between planned and final refraction.
  • Include only procedures performed through September 30 of the performance period. This will allow thepost- operative period to occur before registries must submit data to CMS.

Denominator

All patients aged 18 years and older who had cataract surgery

Denominator Criteria (Eligible Cases):
Patients aged ≥ 18 years on date of encounter
AND
Patient encounter during the performance period (CPT): 66840, 66850, 66852, 66920, 66930, 66940, 66982, 66983, 66984
WITHOUT
Modifier: 56 or 55

Numerator

Patients who achieved a final refraction (spherical equivalent) of +/- 1.0 diopters of their planned (target) refraction (spherical equivalent) within 90 days following cataract surgery. The refraction planned and final refraction values should correspond to the eye that underwent the cataract procedure

Numerator Options:
Performance Met: Patient achieves final refraction (spherical equivalent) +/- 1.0 Diopters of their planned refraction within 90 days of surgery (G9519)
OR
Performance Not Met: Patient does not achieve final refraction (spherical equivalent) +/- 1.0 Diopters of their planned refraction within 90 days of surgery (G9520)

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