CLINICAL RESEARCH: ACUTE MYOCARDIAL INFARCTION
Prognostic Implications of Creatine Kinase Elevation After Primary Percutaneous Coronary Intervention for Acute Myocardial Infarction
Amir Halkin, MD*,
Gregg W. Stone, MD, FACC ,*,
Cindy L. Grines, MD, FACC ,
David A. Cox, MD, FACC ,
Barry D. Rutherford, MD, FACC||,
Paolo Esente, MD, FACC¶,
Carol M. Meils, MD, FACC#,
Per Albertsson, MD, FACC**,
Anthony Farah, MD, FACC ,
James E. Tcheng, MD, FACC ,
Alexandra J. Lansky, MD, FACC*, and
Roxana Mehran, MD, FACC*,
* Cardiovascular Research Foundation, New York, New York
Columbia University Medical Center, New York, New York
William Beaumont Hospital, Royal Oak, Michigan
Mid Carolina Cardiology, Charlotte, North Carolina
|| St. Lukes Hospital, Kansas City, Missouri
¶ St. Josephs Hospital, Syracuse, New York
# St. Joseph Regional Medical Center, Milwaukee, Wisconsin
** Sahlgrenska University Hospital, Göteborg, Sweden
 Allegheny General Hospital, Pittsburgh, Pennsylvania
 Duke Clinical Research Institute, Durham, North Carolina
Manuscript received June 15, 2005;
revised manuscript received July 25, 2005,
accepted August 20, 2005.
* Reprint requests and correspondence: Dr. Gregg W. Stone, The Cardiovascular Research Foundation, 55 East 59th Street, 6th Floor, New York, New York 10022 (Email: gstone{at}crf.org).
OBJECTIVES: We examined the prognostic implications of the absolute level and rate of increase of creatine kinase (CK) elevation after primary percutaneous coronary intervention (PCI).
BACKGROUND: Peak creatine kinase (CKpeak) and the rate of CK increase are related to reperfusion success and clinical outcomes after thrombolytic therapy for acute myocardial infarction (AMI). The utility of routine serial CK monitoring after primary PCI, in which normal antegrade blood flow is restored in most patients, is unknown.
METHODS: In the Controlled Abciximab and Device Investigation to Lower Late Angioplasty Complications (CADILLAC) trial, 1,529 patients with AMI randomized to either stenting or balloon angioplasty, each with or without abciximab, had CK levels determined at baseline and at 8 ± 1 h, 16 ± 1 h, and 24 ± 1 h after PCI.
RESULTS: The CKpeak occurred at baseline in 3.9% of patients, at 8 ± 1 h in 69.6%, at 16 ± 1 h in 20.0%, and at 24 ± 1 h in 6.5%. The CK levels at all post-procedural time points were significantly higher in patients who died compared with the one-year survivors, as was CKpeak (mean, 2,865 U/l vs. 1,885 U/l, respectively, p 0.001). By multivariate analysis, CKpeak was a significant predictor of one-year mortality (hazard ratio = 2.15, p = 0.0002), independent from post-PCI Thrombolysis In Myocardial Infarction (TIMI) flow. Both the improvement in left ventricular ejection fraction from baseline to seven months and its absolute level were inversely correlated with CKpeak (p < 0.001 for both). In contrast, the time to CKpeak was not an independent predictor of mortality or myocardial recovery.
CONCLUSIONS: The CKpeak after primary PCI is a powerful predictor of one-year mortality independent of other clinical and angiographic measures.
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Abbreviations and Acronyms
| | AMI = acute myocardial infarction | | CADILLAC = Controlled Abciximab and Device Investigation to Lower Late Angioplasty Complications | | CK = creatine kinase | | CKpeak = peak creatine kinase | | LVEF = left ventricular ejection fraction | | PCI = percutaneous coronary intervention | | TIMI = Thrombolysis In Myocardial Infarction |
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