Measure ID: MIPS 489|Nephrology|2026 Performance Year

Adult Kidney Disease: Angiotensin Converting Enzyme (ACE) Inhibitor or

Percentage of patients aged 18 years and older with a diagnosis of chronic kidney disease (CKD) (Stages 1-5, not receiving Renal Replacement Therapy (RRT)) and proteinuria who were prescribed ACE inhibitor or ARB therapy within a 12-month period.

ProcessNephrologyMedication Management

Last updated: January 15, 2026

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Measure Specification

Denominator (Eligible Population)

All patients aged 18 years and older on the date of the encounter
ANDDiagnosis of CKD (Stages 1-5)
ANDDiagnosis of Proteinuria
ANDPatient encounter during the performance period

Denominator Exclusions1

M1199Patients receiving RRT: M1199

Numerator

Patients who were prescribed ACE inhibitor or ARB therapy within a 12-month period.

Submission Codes (QDCs)

✓ Performance Met
M1200ACE Inhibitor (ACE-I) or ARB therapy prescribed during the measurement period
✗ Performance Not Met
M1203ACE inhibitor or ARB therapy not prescribed during the measurement period, reason not given

Denominator Exceptions

M1201Documentation of medical reason(s) for not prescribing ACE inhibitor (ACE-I) or ARB therapy during the measurement period (e.g., pregnancy, history of angioedema to ACE-I, other allergy to ACE-I and ARB, hyperkalemia or history of hyperkalemia while on ACE-I or ARB therapy, acute kidney injury due to ACE-I or ARB therapy, other medical reasons.)
M1202Documentation of patient reason(s) for not prescribing ACE inhibitor or ARB therapy during the measurement period (e.g., patient declined, other patient reasons)

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VBCA Insights

💡Why This Measure Matters

Patients with chronic kidney disease and protein in their urine benefit dramatically from ACE inhibitors or ARBs, which slow kidney disease progression, lower blood pressure, and reduce heart attack and stroke risk. These drugs work for both diabetic and non-diabetic kidney disease. Make sure your CKD patients with proteinuria are on an ACE-I or ARB unless they have a documented contraindication or intolerance. Check dosing regularly and titrate up to target doses for maximum kidney protection.

📖Clinical Rationale

This measure is aimed at increasing the number of patients with CKD and proteinuria who are prescribed ACE inhibitor or ARB therapy. ACE inhibitors and ARBs are preferred agents for diabetic kidney disease and nondiabetic kidney diseases with proteinuria (albuminuria), even in the absence of hypertension. In these diseases, ACE inhibitors and ARBs lower blood pressure, reduce proteinuria (albuminuria), slow the progression of kidney disease, and likely reduce cardiovascular disease risk by mechanisms in addition to lowering blood pressure.

These benefits have been shown across high quality, multi-center, randomized controlled trials such as RENAAL (Reduction of Endpoints in NIDDM with the Angiotensin II Antagonist Losartan). A meta-analysis of randomized trials showed that ACEi/ARB therapy lowered the odds of kidney failure (also known as end-stage renal disease [ESRD]) by 30-39 percent and of cardiovascular disease events by 18 percent-24 percent.

In a meta-analysis including primarily diabetic patients with proteinuria, use of ACEi/ARB therapy had a 0.36 to 0.78 odds of incident kidney failure. Similarly, in a Cochrane meta-analysis, patients with early (stage 1 to 3) non-diabetic CKD who were treated versus not treated with ACEi/ARB had 31 percent lower risk of kidney failure. Based upon this robust evidence, ACE inhibitors and ARBs are recommended for patients with CKD and proteinuria by the Kidney Disease: Improving Global Outcomes (KDIGO) international guidelines and the Kidney Disease Outcomes Quality Initiative.

CKD is a major public health problem; a total of 37 million Americans have CKD. There is a clear performance gap in ACE inhibitor and ARB usage among patients with CKD, with only 40 percent of CKD patients receiving an ACEi/ARB in NHANES data. Population health efforts to increase the use of ACEi/ARB in American Indians and Alaska Natives have been associated with a decrease in incident kidney failure related to diabetic kidney disease.

In summary, this measure is a central component of high-quality nephrology care, as ACE inhibitors and ARBs decrease the rate of kidney failure, cardiovascular outcomes, and mortality in patients with CKD and proteinuria.

📝Clinical Recommendations

Clinical practice guidelines support the use of ACE and ARB in CKD patients not on RRT. The Kidney Disease Improving Global Outcomes (KDIGO) 2012 guidelines for the evaluation and management of CKD recommend that “an ARB or ACE-I be used in both diabetic and non-diabetic adults with CKD and urine albumin excretion > 300 mg/24 hours (or equivalent)” (Recommendation 3.

1.7, 1B). Guideline available at https://kdigo.org/wp- content/uploads/2017/02/KDIGO_2012_CKD_GL.pdf. The KDIGO 2021 Clinical Practice Guideline on the Management of Blood Pressure (BP) in CKD recommends “starting renin-angiotensin-system inhibitors (RASi) (ACEi or ARB) for people with high BP, CKD, and severely increased albuminuria (G1–G4, A3) without diabetes” and “for people with high BP, CKD, and moderately-to-severely increased albuminuria (G1–G4, A2 and A3) with diabetes” (Recommendations 3.

2.1 and 3.2.3, 1B). Guideline available at https://kdigo.org/wp-content/uploads/2016/10/KDIGO-2021-BP-GL.pdf. This measure was rated as HIGH for Overall Measure Validity in Mendu ML, Tummalapalli SL, Lentine KL, Erickson KF, Lew SQ, Liu F, Gould E, Somers M, Garimella PS, O'Neil T, White DL, Meyer R, Bieber SD, Weiner DE. Measuring Quality in Kidney Care: An Evaluation of Existing Quality Metrics and Approach to Facilitating Improvements in Care Delivery.

J Am Soc Nephrol. 2020 Mar;31(3):602-614. doi: 10.1681/ASN.2019090869. Epub 2020 Feb 13. PMID: 32054692; PMCID: PMC7062216.

📋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 patient-process measure is submitted a minimum of once per patient for the performance period. The most advantageous quality data code (QDC) will be used if the measure is submitted more than once.

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