Measure ID: MIPS 384|Ophthalmology|2026 Performance Year

2026 MIPS Measure #384: Adult Primary Rhegmatogenous Retinal Detachment Surgery: No Return to the Operating

Patients aged 18 years and older who had surgery for primary rhegmatogenous retinal detachment who did not require a return to the operating room within 90 days of surgery.

Outcome – High PriorityOphthalmologyPatient Safety
Measure ID:MIPS 384 (Quality ID 384)
Collection:MIPS CQM
Topped Out:Yes
View CMS Spec ↗

Measure Specification

Eligible Population
Patients aged ≥ 18 years on the date of the procedure
ANDPatient procedure during the performance period
Exclusions
G9756Surgical procedures that included the use of silicone oil
Numerator
Patients who did not return to the operating room within 90 days for complications within the operative eye. _NUMERATOR NOTE:_ For the purposes of meeting the numerator, complications are only those related to the following procedures: 67107, 67108, 67110
Reporting Codes

Performance Met:

G9515Patient did not require a return to the operating room within 90 days of surgery

Performance Not Met:

G9514Patient required a return to the operating room within 90 days of surgery
VBCA Insights

Why This Measure Matters

After retinal detachment surgery, did the patient need a second surgery within 90 days? A low rate of returns to OR means your surgical technique—cryotherapy or laser placement, retinopexy approach—is creating durable reattachment. Outcomes depend on careful preoperative planning, proper identification of all retinal breaks, and thorough treatment to the ora serrata. Low re-operation rates reflect technical excellence and patient satisfaction; high rates warrant review of case selection and operative technique.

VBCA is a CMS-approved Qualified Clinical Data Registry (QCDR) that submits MIPS Measure 384 to the Quality Payment Program (QPP). Practices can report this measure as a MIPS Clinical Quality Measure (CQM) or through qualified registry submission.

🧮MIPS Score Simulator

Estimate only — actual CMS scoring may vary based on reporting method, data completeness, and annual rule updates.

%Benchmarks vary by collection type
💡 Tip: Enter your performance rate to compare MIPS points across all collection types. The same rate can score differently depending on how you submit.

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 385: Adult Primary Rhegmatogenous Retinal Detachment Surgery: Visual Acuity ImprovementMIPS 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
MIPS 130: Documentation of Current Medications in the Medical RecordMIPS 145: Radiology: Exposure Dose Indices Reported for Procedures Using FluoroscopyMIPS 155: Falls: Plan of CareMIPS 164: Coronary Artery Bypass Graft (CABG): Prolonged IntubationMIPS 168: Coronary Artery Bypass Graft (CABG): Surgical Re-ExplorationMIPS 181: Elder Maltreatment Screen and Follow-Up PlanMIPS 259: Rate of Endovascular Aneurysm Repair (EVAR) of Small or Moderate Non-RupturedMIPS 275: Inflammatory Bowel Disease (IBD): Assessment of Hepatitis B Virus (HBV) Status BeforeMIPS 286: Dementia: Safety Concern Screening and Follow-Up for Patients with DementiaMIPS 351: Total Knee or Hip Replacement: Venous Thromboembolic and Cardiovascular RiskMIPS 354: Anastomotic Leak InterventionMIPS 355: Unplanned Reoperation within the 30-Day Postoperative PeriodMIPS 357: Surgical Site Infection (SSI)MIPS 374: Closing the Referral Loop: Receipt of Specialist ReportMIPS 385: Adult Primary Rhegmatogenous Retinal Detachment Surgery: Visual Acuity ImprovementMIPS 392: Cardiac Tamponade and/or Pericardiocentesis Following Atrial FibrillationMIPS 393: Infection within 180 Days of Cardiac Implantable Electronic Device (CIED) Implantation,MIPS 413: Door to Puncture Time for Endovascular Stroke TreatmentMIPS 422: Performing Cystoscopy at the Time of Hysterectomy for Pelvic Organ ProlapseMIPS 432: Proportion of Patients Sustaining a Bladder or Bowel Injury at the time of any PelvicMIPS 513: Patient Reported Falls and Plan of Care

Clinical Rationale

The goal of treatment for retinal breaks is to create a firm chorioretinal adhesion in the attached retina immediately adjacent to and surrounding the retinal tear using cryotherapy or laser photocoagulation to halt the progression of subretinal fluid from detaching the neurosensory retina. Treatment of peripheral horseshoe tears should be extended to the ora serrata if the tear cannot be surrounded using laser or cryotherapy.

The most common cause of failure in treating horseshoe tears is failure to adequately treat the tear, particularly the anterior border. Continued vitreous traction may extend the tear beyond the treated area and allow fluid to dissect through the subretinal space to cause a clinical retinal detachment. Treatment of dialyses must extend over the entire length of the dialysis, reaching the ora serrata beyond each horn or end of the dialysis.

Sufficient evidence exists for treating acute, symptomatic horseshoe tears. There is insufficient evidence for management of other vitreoretinal abnormalities. A Cochrane systematic review found that in making the decision to treat other vitreoretinal abnormalities, including lattice degeneration and asymptomatic retinal breaks, the risks that treatment will be unnecessary, ineffective, or harmful must be weighed against the possible benefit of reducing the rate of subsequent retinal detachment.

In a study published in 2011, Schall and colleagues studied the success rate with 4 surgical techniques. Initial success rate for retinal reattachment was 86% for scleral buckling only, 90% for vitrectomy only, 94% for the combination of scleral buckling and vitrectomy, and 63% for pneumatic retinopexy surgery. Patients undergoing pneumatic retinopexy had a lower initial success rate, however there was no statistically significant difference in initial reattachment rates between the other three groups.

In a 2002 study, Ling and colleagues reported an 85% success rate with a single procedure. Of the 15% that initially failed, 97% were successful with one additional surgery.

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 Merit-based Incentive Payment System (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 had to return to the operating room 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.

Report this measure through VBCA

Our QCDR handles measure selection, data validation, and submission—so you can focus on clinical performance.

Learn About Our QCDR →Talk to Us

© 2015-2025 American Academy of Ophthalmology. All Rights Reserved. Applicable FARS/DFARS Restrictions Apply to