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Remote Ischemic Preconditioning To Reduce Contrast-Induced Nephropathy: A Randomized Controlled Trial.
T P Menting1, T B Sterenborg1, Y de Waal2
1Department of Surgery, Division of Vascular and Transplant Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.
Remote ischemic preconditioning (RIPC) did not prevent contrast induced nephropathy (CIN) in at-risk patients. However, RIPC showed potential benefits for those with a high risk score (Mehran score ≥11).
Area of Science:
- Nephrology
- Cardiology
- Intensive Care Medicine
Background:
- Contrast-induced nephropathy (CIN) remains a significant concern despite current preventive strategies.
- Contrast media can induce renal medulla ischemia-reperfusion injury.
- Remote ischemic preconditioning (RIPC) is a safe, non-invasive method to mitigate ischemia-reperfusion injury.
Purpose of the Study:
- To evaluate the efficacy of RIPC as an adjunct to standard preventive measures for CIN.
- To determine if RIPC reduces the incidence or severity of contrast-induced acute kidney injury in at-risk patients.
Main Methods:
- A multicenter, single-blinded, randomized controlled trial (RIPCIN study) involving 76 at-risk patients.
- Intervention group received standard hydration plus RIPC (4 cycles of 5-min ischemia/5-min reperfusion).
- Control group received standard hydration with sham preconditioning.
- Primary outcome: change in serum creatinine from baseline to 48-72 hours post-contrast.
Main Results:
- No significant difference in serum creatinine change was observed between RIPC and sham groups for the overall study population.
- CIN occurred in 4 patients (2 in each group).
- Subgroup analysis of patients with a Mehran risk score ≥11 revealed a significantly reduced serum creatinine increase in the RIPC group compared to the sham group.
Conclusions:
- RIPC, when added to standard care, did not significantly improve serum creatinine levels in patients at risk of CIN based on Dutch guidelines.
- RIPC may offer a protective benefit for patients identified as having a high or very high risk of CIN (Mehran score ≥11).
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