Key result
CHA2DS2-VASc score ≥4 linked to ~3.8-fold higher odds of post-PCI contrast-induced nephropathy.
Why the study?
Contrast-induced nephropathy after PCI increases morbidity and mortality, making early risk detection essential, and the simple CHA2DS2-VASc score may complement more advanced CIN risk score models in patients with chronic coronary syndromes.
Does a CHA2DS2-VASc score ≥ 4 predict the development of contrast-induced nephropathy within 24 to 48 hours in patients with chronic coronary syndromes undergoing percutaneous coronary intervention?
Cross-Sectional (n=100)
No
Does a CHA2DS2-VASc score ≥ 4 predict the development of contrast-induced nephropathy within 24 to 48 hours in patients with chronic coronary syndromes undergoing percutaneous coronary intervention?
A pre-procedural CHA2DS2-VASc score ≥ 4 is a simple, independent predictor of contrast-induced nephropathy in patients with chronic coronary syndromes undergoing PCI.
Answers are grounded in this paper and cite their sources.
May support CHA2DS2-VASc ≥4 for CIN risk stratification post-PCI; leaves open prospective validation before clinical adoption.
Background: Contrast-induced nephropathy (CIN) causes the third most hospital-related acute renal damage. Flexible percutaneous coronary intervention (PCI) is risky. CIN can occur in almost 50% of PCI patients. As this consequence increases patient morbidity and mortality beyond PCI. Thus, early CIN risk detection and prediction are essential to patient care. CHA2DS2-VASc, a simple risk assessment tool, can complement the more advanced CIN risk score model. Objective: To a find out the association between CHA2DS2-VASc score and contrast induced nephropathy after percutaneous coronary intervention in patients with chronic coronary syndromes. Methods: This cross-sectional observational study was conducted at the Department of Cardiology at National Institute of Cardiovascular Diseases (NICVD), Dhaka during the period from May, 2020 to April, 2021. A total 100 patients with chronic coronary syndromes undergoing PCI were enrolled in this study. CHA2DS2- VASc score was calculated for each patient. These patients were divided into two groups as Group I (score < 4) and Group II (score ≥ 4). After PCI was done, patients were followed up to see development of contrast induced nephropathy. CIN was defined as increase in serum creatinine level (≥ 0.5mg/dl) or relative increase (≥25%) increase from baseline within 24 to 48 hours after PCI. Results: The mean ±SD CHA2DS2-VASc score was 3.23 ± 1.14. Most of the subjects (41 out of 100) belonged to 51-60 years’ age group. Males were prevalent than females. No significant difference was noted regarding history of dyslipidaemia, smoking, family history of CAD between group I and group II except for DM, hypertension and lower ejection fraction. DM and hypertension were more frequent in group II than group I (28 % vs 56%, p=0.005) and (40 % vs 54%, p= 0.04) respectively. LVEF was lower in group II than group I (54.621% vs 48.06%, p = 0.001). Both pre and post catheterization serum creatinine were significantly higher in group II compared to group I. CIN was significantly higher in group I (16%) than group II (24%). In multivariate analysis demonstrated CHA2DS2- VASc score of ≥4 to be an independent predictor of contrast induced nephropathy (CIN). Conclusion: In patients with chronic coronary syndromes undergoing percutaneous coronary intervention CHA2DS2-VASc score may be used as a novel, simple, and a sensitive diagnostic tool for the prediction of contrast induced nephropathy (CIN).
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Islam et al. (2026) conducted a cross-sectional in Chronic coronary syndromes undergoing percutaneous coronary intervention (n=100). CHA2DS2-VASc score ≥ 4 vs. CHA2DS2-VASc score < 4 was evaluated on Contrast-induced nephropathy (increase in serum creatinine ≥ 0.5 mg/dl or relative increase ≥ 25% from baseline within 24 to 48 hours after PCI) (OR 3.81, p=0.029). A CHA2DS2-VASc score ≥4 was associated with a higher rate of contrast-induced nephropathy after PCI in chronic coronary syndrome patients compared to a score <4 (24.0% vs 8.0%, p=0.029; OR 3.81).
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