Abstract

ObjectiveOur purpose was to assess the effect of ligustrazine in the prevention of contrast-induced nephropathy (CIN) in patients with unstable angina (UA).Methods148 patients with UA undergoing coronary angiography and/or percutaneous coronary intervention (PCI) were selected for observation; the patients were divided into a control group (group A, n=74) and a ligustrazine group (group B, n=74). Group A was given routine treatment, while group B was given routine treatment combined with ligustrazine. Serum creatinine (Scr), cystatin C and glomerular filtration rate (eGFR) concentrations were measured before and 1 day, 2 days and 3 days after treatment, and the incidence of contrast-induced nephropathy (CIN) and major cardiovascular events (MACE) were observed in both groups.ResultsThe Scr, Cystatin C and eGRF levels in group B were better than in group A after 1 day (OR: 2.64, 95% CI: 2.47-4.98; OR: 2.66, 95% CI: 2.62-5.77; OR: 4.02, 95% CI: 3.02-5.53, respectively), 2 days (OR: 3.58, 95% CI: 2.41-4.92; OR: 2.92, 95% CI: 2.83-5.02; OR: 3.28, 95% CI: 3.24-5.14, respectively) and 3 days of treatment (OR: 3.26, 95% CI: 2.17-4.35; OR: 2.85, 95% CI: 2.26-4.02; OR: 3.19, 95% CI: 2.53-4.34, respectively). The incidence of CIN (9.26% vs 16.67%) and MACE (7.41% vs 18.51%) of group B were significantly lower than in group A (P<0.05).ConclusionsOur study suggests that ligustrazine can reduce CIN and MACE in patients with UA when undergoing coronary angiography and/or PCI.

Highlights

  • Contrast-induced nephropathy (CIN) [1, 2, 3] is an acute renal function injury that occurs within 3 days after using contrast agent when excluding other factors that may damage renal function

  • Our study suggests that ligustrazine can reduce CIN and major cardiovascular events (MACE) in patients with unstable angina (UA) when undergoing coronary angiography and/or percutaneous coronary intervention (PCI)

  • After adjusting for smoking, previous myocardial infarction (MI), albumin, HDL-C, iodixanol dosage, ACEIs/ARBs, beta-blockers and GPIIb/IIIa inhibitors, the Serum creatinine (Scr), Cystatin C and eGRF levels in group B were better than in group A after 1 day of treatment (OR: 2.64, 95% CI: 2.47-4.98; OR: 2.66, 95% CI: 2.62-5.77; OR: 4.02, 95% CI: 3.02-5.53, respectively)

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Summary

Introduction

Contrast-induced nephropathy (CIN) [1, 2, 3] is an acute renal function injury that occurs within 3 days after using contrast agent when excluding other factors that may damage renal function. In hospital-acquired acute kidney injury, CIN has become the third major cause of renal perfusion decrease and renal drug toxicity [4, 5]. Previous research results have shown that in patients who receive contrast agents, the incidence of CIN is approximately 1%-6% [8]. Once CIN has occurred, hospitalization time is longer, and the cost of health care increases, presenting a considerable economic burden to society. Because no effective measure for the treatment of CIN has been developed, research for CIN is primarily focused on prevention

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