What is the effect of Micardis (Telmisartan) on Chronic Kidney Disease (CKD)?

Medical Advisory BoardAll articles are reviewed for accuracy by our Medical Advisory Board
Educational purpose only • Exercise caution as content is pending human review
Article Review Status
Submitted
Under Review
Approved

Last updated: April 1, 2025View editorial policy

Personalize

Help us tailor your experience

Which best describes you? Your choice helps us use language that's most understandable for you.

From the Guidelines

Micardis (telmisartan) is a recommended treatment for patients with chronic kidney disease (CKD) as it provides renoprotective effects beyond blood pressure control, as evidenced by the KDIGO 2020 clinical practice guideline for diabetes management in CKD 1. The use of angiotensin receptor blockers (ARBs) like telmisartan has been shown to reduce the risk of progression of CKD, with a dose-dependent reduction in the risk of progression, as seen in the IRMA-2 study 1. Key benefits of Micardis for CKD patients include:

  • Reduced risk of progression to severely increased albuminuria
  • Delayed progression to overt nephropathy
  • Reduced incidence of doubling of serum creatinine and end-stage kidney disease (ESKD)
  • Renoprotective effects independent of blood pressure control The typical dosage of Micardis for CKD patients ranges from 20-80 mg once daily, with 40 mg being a common starting dose. It is essential to monitor kidney function and potassium levels regularly while taking Micardis, especially when starting treatment or adjusting doses, as it can cause elevated potassium levels as a side effect 1. Overall, Micardis is a valuable treatment option for CKD patients, particularly those with hypertension or diabetes, as it provides kidney protection beyond just blood pressure control, as supported by the KDIGO 2020 guideline 1.

From the FDA Drug Label

5.5 Impaired Renal Function As a consequence of inhibiting the renin-angiotensin-aldosterone system, anticipate changes in renal function in susceptible individuals. In patients whose renal function may depend on the activity of the renin-angiotensin-aldosterone system (e.g., patients with severe congestive heart failure or renal dysfunction), treatment with angiotensin-converting enzyme (ACE) inhibitors and angiotensin receptor antagonists has been associated with oliguria and/or progressive azotemia and (rarely) with acute renal failure and/or death. Similar results have been reported with telmisartan [see Clinical Pharmacology (12.3)].

Telmilo (Telmisartan) and CKD: In patients with Chronic Kidney Disease (CKD), telmisartan may cause changes in renal function.

  • Key considerations:
    • Patients with severe congestive heart failure or renal dysfunction may be at higher risk.
    • Treatment with telmisartan may be associated with oliguria, progressive azotemia, and rarely, acute renal failure or death.
    • Monitoring of renal function and electrolytes is recommended, particularly in patients at risk.
    • The use of telmisartan in patients with unilateral or bilateral renal artery stenosis has not been extensively studied, but similar effects to ACE inhibitors can be anticipated. 2

From the Research

Micardis and CKD

  • Micardis, also known as telmisartan, is an angiotensin receptor blocker (ARB) that has been shown to be effective in reducing proteinuria and slowing the progression of chronic kidney disease (CKD) 3, 4, 5.
  • The use of ARBs, such as telmisartan, has been recommended as a first-line treatment for patients with CKD, particularly those with hypertension and/or diabetes, due to their ability to provide renoprotection and reduce the risk of cardiovascular disease 4, 6.
  • Studies have demonstrated that telmisartan can effectively reduce blood pressure and proteinuria in patients with CKD, even in those with advanced disease 3, 5.
  • The optimal blood pressure target for patients with CKD is less than 130/80 mmHg, or 125/75 mmHg if the amount of urinary protein is more than 1 g/day 7, 6.
  • Telmisartan has been shown to be well-tolerated and safe in patients with CKD, although monitoring for hyperkalemia is recommended 3, 5.

Related Questions

Can Angiotensin Receptor Blockers (ARBs), such as telmisartan, slow down the progression of Chronic Kidney Disease (CKD)?
What is the appropriate assessment and plan for a 54‑year‑old male with hypertension, diabetes mellitus, chronic kidney disease on atorvastatin, atenolol, glicazide, and telmisartan who presented at 9 pm with acute rotatory vertigo, bilateral lower‑extremity weakness, chills, and mild headache, without vomiting, speech changes, visual loss, facial weakness, or gait instability, and who now has a completely normal neurological examination?
Is a kidney biopsy necessary for a 51-year-old patient with chronic kidney disease (CKD) and proteinuria, with stable impaired renal function, currently taking olmesartan (Olmesartan medoxomil) 10mg daily, and well-controlled blood pressure?
What are the guidelines for blood pressure management in Chronic Kidney Disease (CKD)?
What is Chronic Kidney Disease (CKD)?
What is recommended for a patient with post-Roux-en-Y gastric bypass surgery experiencing dumping syndrome: octreotide, loperamide, or soluble fiber?
What is the use of quetiapine (Seroquel)?
What is the efficacy of quetiapine (quetiapine) for sleep disturbances in patients with dementia?
What are the tests for Hepatitis B (HBV) infection?
Should a 30-year-old woman with a history of hypoglycemic (low blood sugar) seizures and nocturnal (night-time) diaphoresis (excessive sweating) with normal glucose levels on four times daily self-monitoring of blood glucose (SMBG) checks undergo continuous glucose monitoring (CGM) or add an additional check at 3:00 AM?
What are the benefits of Magnetic Resonance Imaging (MRI) versus Non-Contrast Computed Tomography (CT) scan for evaluating renal (kidney) function?

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

Have a follow-up question?

Our Medical A.I. is used by practicing medical doctors at top research institutions around the world. Ask any follow up question and get world-class guideline-backed answers instantly.