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Poor Prognosis of Contrast-Induced Nephropathy during Long Term Follow Up
1Division of Cardiology, Department of Internal Medicine, Research Institute of Clinical Medicine, Jeonbuk National University Hospital, Jeonbuk National University Medical School, Jeonju, Korea.
Insights
Contrast-induced nephropathy (CIN) significantly increases long-term mortality and major adverse cardiovascular events (MACE) risk. Preventing CIN is crucial for improving patient outcomes after coronary angiography.
Area of Science:
- Cardiology
- Nephrology
- Clinical Research
Background:
- Contrast-induced nephropathy (CIN) is linked to adverse prognoses.
- Long-term follow-up studies on CIN prognosis are limited.
Purpose of the Study:
- To evaluate the 10-year prognosis of patients who developed contrast-induced nephropathy (CIN) after coronary angiography.
Main Methods:
- Retrospective analysis of 528 patients undergoing coronary angiography.
- Comparison of adverse events between patients with and without CIN.
- Exclusion of patients requiring regular dialysis.
- Propensity score matching for adjusted analysis.
Main Results:
- Patients with CIN showed significantly higher rates of all-cause death at 1, 5, and 10 years.
- CIN group experienced higher incidences of major adverse cardiovascular events (MACE) at 1, 5, and 10 years.
- CIN was identified as an independent predictor of 10-year MACE.
Conclusions:
- Contrast-induced nephropathy is associated with a persistently worse long-term prognosis.
- Preventing CIN is essential for improving long-term outcomes in patients undergoing coronary angiography.
Abstract:
Contrast-induced nephropathy (CIN) is known to associate with poor prognosis. However, there have been few studies for long-term follow up. The purpose of this study was to know the prognosis of CIN during a 10-year follow up. We retrospectively analyzed 528 patients who underwent coronary angiography in Jeonbuk National University Hospital (South Korea, Jeonju) between Jan 2005 to Dec 2006. We excluded the patients who required regular dialysis before study enrollment. We compared adverse events in the no CIN (group I, n=485, 61.9±11.4 years, male 64.1%) and CIN (group II, n=43, 65.7±11.1 years, male 62.8%). Baseline clinical characteristics and cardiovascular risk factors were not different between the two groups except the post-procedure creatinine level (1.04 mg/dL vs 1.84 mg/dL, p=0.0001). The higher rates of all-cause death were observed in group II at 1-year (3.7% vs 13.9%, log-rank, p=0.001), 5-years (17.9% vs 34.9%, log-rank, p=0.003), and 10-years (25.3% vs 48.8%, log-rank, p=0.000). MACE was higher in group II at 1-year (3.9% vs 11.6%, log-rank, p=0.013), 5-years (6.8% vs 20.9%, log-rank, p=0.000) and 10-years (13.4% vs 27.9%, log-rank, p=0.000). In addition, CIN was an independent predictor for 10-year MACE (adjusted HR 3.432, 95% CI 1.314-8.965, p=0.012) after propensity score matching. The worse prognosis of CIN was continuously observed after the 10-year follow-up. Our data suggests that it is worthwhile to prevent the appearance of CIN in order to improve longterm results.
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