Iloprost prevents contrast-induced nephropathy in patients with renal dysfunction undergoing coronary angiography or

Konstantinos Spargias1, Elias Adreanides, Eftihia Demerouti

  • 1Department of Cardiology, Onassis Cardiac Surgery Centre, Athens, Greece. spargias@ocsc.gr

Circulation
|October 21, 2009
PubMed

Insights

Iloprost significantly reduced contrast-induced nephropathy in high-risk patients undergoing coronary procedures. This prostacyclin analog offers a potential protective strategy against kidney damage from contrast agents.

Area of Science:

  • Nephrology
  • Cardiology
  • Pharmacology

Background:

  • Contrast-induced nephropathy (CIN) is a significant cause of morbidity and mortality.
  • Renal vasoconstriction is a key factor in CIN development.
  • Effective prevention strategies for CIN are urgently needed, especially in patients with renal dysfunction.

Purpose of the Study:

  • To evaluate the efficacy of iloprost, a prostacyclin analog, in preventing CIN.
  • To assess iloprost's protective effects in patients with pre-existing renal dysfunction undergoing coronary procedures.

Main Methods:

  • A randomized, double-blind, placebo-controlled trial was conducted.
  • 208 patients with serum creatinine >= 1.4 mg/dL undergoing coronary angiography/intervention were enrolled.
  • Iloprost (1 ng/kg/min) or placebo was administered intravenously before and after the procedure.

Main Results:

  • CIN incidence was 22% in the placebo group versus 8% in the iloprost group (OR, 0.29; P=0.005).
  • The estimated glomerular filtration rate (eGFR) declined in the control group but showed a marginal increase in the iloprost group.
  • Iloprost administration was associated with a significantly smaller decline in eGFR compared to placebo.

Conclusions:

  • Prophylactic iloprost administration demonstrates potential protective effects against CIN.
  • Iloprost may be a valuable therapeutic option for high-risk patients undergoing coronary procedures.
  • Further research may confirm iloprost's role in CIN prevention.
Abstract

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