# Is it Always Safe to Administer RAS Inhibitors to Patients Who Underwent Unilateral Radical Nephrectomy?

**Authors:** Giulio Romano, Alessandro Crestani, Giuseppe Como, Erika Cucchiaro, Nicholas Fiorini, Gianluca Colussi

PMC · DOI: 10.1155/crin/5481521 · Case Reports in Nephrology · 2026-02-23

## TL;DR

A patient's kidney function after surgery did not improve as expected while on certain medications, suggesting these drugs might interfere with recovery in some cases.

## Contribution

This case suggests combined ACE and SGLT2 inhibition may hinder early kidney compensation after nephrectomy.

## Key findings

- GFR did not improve as expected while on ramipril and dapagliflozin.
- Discontinuing the drugs led to GFR recovery above the expected threshold.
- The effect may be due to hemodynamic mechanisms in atherosclerotic nephropathy.

## Abstract

Compensatory increases in single‐kidney glomerular filtration rate (GFR) are usually observed after unilateral radical nephrectomy. However, the influence of hemodynamically active therapies on early functional compensation remains uncertain. We describe a 65‐year‐old man with latent autoimmune diabetes of adulthood, nonproteinuric chronic kidney disease consistent with atherosclerotic nephropathy, and mildly reduced baseline renal function who underwent right radical nephrectomy with caval thrombus removal for clear cell renal cell carcinoma. Based on preoperative split renal function, a postnephrectomy GFR above 45 mL/min was anticipated. Despite continued treatment with ramipril and dapagliflozin, GFR at 3 months remained close to the immediate postoperative value. After discontinuation of both agents, GFR increased above the expected threshold and remained stable, without albuminuria. This observation is hypothesis‐generating and suggests that combined ACE and SGLT2 inhibition may transiently attenuate early functional compensation through hemodynamic mechanisms, particularly in patients with atherosclerotic nephropathy, supporting individualized perioperative management and close renal function monitoring.

## Linked entities

- **Chemicals:** ramipril (PubChem CID 5362129), dapagliflozin (PubChem CID 9887712)
- **Diseases:** chronic kidney disease (MONDO:0005300), clear cell renal cell carcinoma (MONDO:0005005)

## Full-text entities

- **Genes:** INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, AP2B1 (adaptor related protein complex 2 subunit beta 1) [NCBI Gene 163] {aka ADTB2, AP105B, AP2-BETA, CLAPB1}
- **Diseases:** Tumor (MESH:D009369), diabetes (MESH:D003920), vascular disease (MESH:D014652), blood loss (MESH:D016063), chronic kidney disease (MESH:D051436), acute kidney injury (MESH:D058186), hypotension (MESH:D007022), nephron mass loss (MESH:C536030), caval thrombus (MESH:D013927), albuminuria (MESH:D000419), hypertension (MESH:D006973), atherosclerotic nephropathy (MESH:D050197), renal artery stenosis (MESH:D012078), diabetic retinopathy (MESH:D003930), CH (MESH:D006984), Nonproteinuric kidney disease (MESH:D007674), LADA (MESH:D000071698), autoimmune diabetes (MESH:D003922), Kimmelstiel-Wilson's glomerulonephritis (MESH:D003928), clear cell renal cell carcinoma (MESH:D002292)
- **Chemicals:** aldosterone (MESH:D000450), ACEi (-), sodium (MESH:D012964), Ramipril (MESH:D017257), dapagliflozin (MESH:C529054), creatinine (MESH:D003404)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12927968/full.md

## References

18 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927968/full.md

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Source: https://tomesphere.com/paper/PMC12927968