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J Am Coll Cardiol, 2007; 50:584-590, doi:10.1016/j.jacc.2007.03.058 (Published online 29 July 2007).
© 2007 by the American College of Cardiology Foundation
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CLINICAL RESEARCH: INTERVENTIONAL CARDIOLOGY

Volume-to-Creatinine Clearance Ratio

A Pharmacokinetically Based Risk Factor for Prediction of Early Creatinine Increase After Percutaneous Coronary Intervention

Warren K. Laskey, MD, FACC*,*, Charles Jenkins, MD*, Faith Selzer, PhD{dagger}, Oscar C. Marroquin, MD, FACC{dagger}, Robert L. Wilensky, MD, FACC{ddagger}, Ruchira Glaser, MD, FACC{ddagger}, Howard A. Cohen, MD, FACC§, David R. Holmes, Jr, MD, FACC|| for the NHLBI Dynamic Registry Investigators

* University of New Mexico School of Medicine, Albuquerque, New Mexico
{dagger} University of Pittsburgh, Pittsburgh, Pennsylvania
{ddagger} University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania
§ Lenox Hill Heart and Vascular Institute, New York, New York
|| Mayo Clinic, Rochester, Minnesota.

Manuscript received January 29, 2007; revised manuscript received March 1, 2007, accepted March 28, 2007.

* Reprint requests and correspondence: Dr. Warren K. Laskey, Division of Cardiology, Department of Internal Medicine, University of New Mexico School of Medicine, MSC10-5550 1, University of New Mexico, Albuquerque, New Mexico 87131-0001. (Email: wlaskey{at}salud.unm.edu).

Objectives: This study sought to validate a pharmacokinetically derived measure of the risk of an early increase in serum creatinine after percutaneous coronary intervention (PCI).

Background: The ratio of the volume of contrast media to the creatinine clearance (V/CrCl) has been shown to correlate with the area under the curve of contrast media concentration over time.

Methods: We calculated V/CrCl in 3,179 consecutive patients undergoing PCI. An increase in serum creatinine of >0.5 mg/dl by 24 to 48 h was considered abnormal. Receiver-operator characteristic methods were used to identify the optimal sensitivity and specificity for the observed range of V/CrCl. The predictive value of V/CrCl for the risk of an early increase in creatinine was assessed using multivariable logistic regression.

Results: The overall incidence of an abnormal, early increase in creatinine was 1.5%. The mean and median values of V/CrCl for patients with (mean 5.2 ± 4.4, median 4.3, interquartile range 2.7 to 6.0) and without (mean 3.0 ± 2.0, median 2.5, interquartile range 1.7 to 3.8) an early creatinine increase were each significantly (p < 0.001) different between groups. Furthermore, there was a significant association between V/CrCl and an early increase in creatinine (overall and trend, p < 0.001). The receiver-operator characteristic curve analysis indicated that a V/CrCl ratio of 3.7 was a fair discriminator for the early creatinine increase (C-statistic 0.69). After adjusting for other known predictors of post-PCI creatinine increase, V/CrCl ≥3.7 remained significantly associated with an early abnormal increase in serum creatinine (odds ratio 3.84; 95% confidence interval 2.0 to 7.3, p < 0.001).

Conclusions: A V/CrCl ratio >3.7 was a significant and independent predictor of an early abnormal increase in serum creatinine after PCI in this unselected patient population.

Abbreviations and Acronyms
  CAN = contrast media-associated nephrotoxicity
  CrCl = creatinine clearance
  PCI = percutaneous coronary intervention




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