Measure ID: MIPS 385|Ophthalmology|2026 Performance Year

2026 MIPS Measure #385: Adult Primary Rhegmatogenous Retinal Detachment Surgery: Visual Acuity Improvement

Patients aged 18 years and older who had surgery for primary rhegmatogenous retinal detachment and achieved an improvement in their visual acuity, from their preoperative level, within 90 days of surgery in the operative eye.

Outcome – High PriorityOphthalmologyPatient Safety
Measure ID:MIPS 385 (Quality ID 385)
Collection:MIPS CQM
Topped Out:No
View CMS Spec ↗

Measure Specification

Eligible Population
Patients aged ≥ 18 years on the date of the procedure
ANDPatient procedure during the performance period
Exclusions
M1453Patients with a pre-operative visual acuity better than 20/40
G9757Surgical procedures that included the use of silicone oil
Numerator
Patients who achieved an improvement in their visual acuity, from their preoperative level, within 90 days of surgery in the operative eye.
Reporting Codes

Performance Met:

G9516Patient achieved an improvement in visual acuity, from their preoperative level, within 90 days of surgery

Performance Not Met:

G9517Patient did not achieve an improvement in visual acuity, from their preoperative level, within 90 days of surgery, reason not given
VBCA Insights

Why This Measure Matters

Did the patient's vision improve after retinal detachment surgery? This measures whether your surgical outcomes actually restored function—not just reattached the retina, but improved visual acuity within 90 days. Improvement happens when you use modern surgical techniques, achieve solid reattachment, and manage postoperative inflammation well. Visual improvement is the outcome that matters to patients; it justifies the surgery and reduces the psychological burden of vision loss.

VBCA is a CMS-approved Qualified Clinical Data Registry (QCDR) that submits MIPS Measure 385 to the Quality Payment Program (QPP). Practices can report this measure as a MIPS Clinical Quality Measure (CQM) or through qualified registry submission.

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Specialty Measure Sets

Related Measures

Ophthalmology
MIPS 117: Diabetes: Eye ExamMIPS 141: Primary Open-Angle Glaucoma (POAG): Reduction of Intraocular Pressure (IOP) by 20% ORMIPS 191: Cataracts: 20/40 or Better Visual Acuity within 90 Days Following Cataract SurgeryMIPS 303: Cataracts: Improvement in Patient’s Visual Function within 90 Days Following CataractMIPS 304: Cataracts: Patient Satisfaction within 90 Days Following Cataract SurgeryMIPS 384: Adult Primary Rhegmatogenous Retinal Detachment Surgery: No Return to the OperatingMIPS 389: Cataract Surgery: Difference Between Planned and Final RefractionMIPS 499: Appropriate Screening and Plan of Care for Elevated Intraocular Pressure FollowingMIPS 500: Acute Posterior Vitreous Detachment Appropriate Examination and Follow-upMIPS 501: Acute Posterior Vitreous Detachment and Acute Vitreous Hemorrhage Appropriate
Patient Safety
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Clinical Rationale

For management and treatment for PVD and RRD, the following apply (for goals of treatment): • Prevention of visual loss and functional impairment • Maintenance of quality of life All patients with risk factors should be instructed to notify their ophthalmologist as soon as possible if they have a substantial change in symptoms, such as an increase in floaters, loss of visual field, or decrease in visual acuity develop.

Studies demonstrate that the success rate increases with the recognition of risk factors and the practice of retina subspecialization. International studies report primary rhegmatogenous retinal surgery success rates ranging from 64 to 91%.

Clinical Recommendations

This is an outcome measure. As such, no clinical recommendations are included.

Implementation Notes

This measure contains one strata defined by a single submission criteria. This measure produces a single performance rate. For the purposes of MIPS implementation, this procedure measure is submitted each time a procedure is performed. This is an outcome measure and will be calculated solely using MIPS eligible clinician, group, or third-party intermediary submitted data.

• For patients who receive the surgical procedures specified in the denominator coding, it should be submitted whether or not the patient achieved an improvement of their visual acuity within 90 days of surgery. • Include only procedures performed between January 1st and September 30th of the performance period. This will allow the post-operative period to occur before third-party intermediaries must submit data to CMS.

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