Prognostic implication of creatine kinase elevation following elective coronary artery interventions
T Q Kong1, C J Davidson, S N Meyers
1Department of Internal Medicine, Division of Cardiology, Northwestern University Medical School, Chicago, Ill, USA.
Insights
Creatine kinase (CK) elevation after percutaneous transluminal coronary angioplasty (PTCA) indicates higher late cardiac mortality risk. Even mild CK increases signal a significantly greater risk of cardiac death post-procedure.
Area of Science:
- Cardiology
- Biomarkers
- Interventional Cardiology
Background:
- Percutaneous transluminal coronary angioplasty (PTCA) is a common procedure for coronary artery disease.
- The prognostic significance of creatine kinase (CK) elevation post-PTCA requires further clarification.
Purpose of the Study:
- To investigate the prognostic value of creatine kinase (CK) elevation following elective percutaneous transluminal coronary angioplasty (PTCA).
Main Methods:
- Retrospective cohort study including 253 patients with CK elevation and 120 controls.
- Follow-up duration exceeded 3.5 years.
- Outcomes assessed included cardiac mortality and myocardial infarction.
Main Results:
- Patients with CK elevation post-PTCA had significantly greater cardiac mortality (P=.02).
- Cardiac mortality increased with higher peak CK levels (P=.007).
- Multivariate analysis identified higher peak CK and lower ejection fraction as key predictors of cardiac mortality.
Conclusions:
- Creatine kinase elevation after elective PTCA is an independent predictor of increased late cardiac mortality.
- Even minor CK elevations are associated with significantly increased risk for late cardiac death.
- This finding holds true irrespective of clinical factors, disease severity, or procedural characteristics.
Objective:
To determine the prognostic significance of creatine kinase (CK) elevation following elective percutaneous transluminal coronary angioplasty (PTCA).
Design:
Retrospective cohort study.
Setting:
Tertiary care referral center.
Subjects:
A total of 253 consecutive patients with total CK and CK-MB fraction (CK-MB) elevation (case patients) and 120 patients without CK elevation (controls). Control patients had undergone interventions during the same month and year using the same devices.
Main Outcome Measures:
In-hospital and late cardiac mortality, subsequent myocardial infarction, and the combined end point of cardiac mortality or myocardial infarction.
Results:
Patient groups were similar with respect to age, sex, extent of coronary artery disease, left ventricular function, number of lesions treated by PTCA, and mean duration of follow-up (>3.5 years). Cardiac mortality was significantly greater (P=.02) for patients with CK elevation after PTCA. When patients were categorized according to peak CK elevation, cardiac mortality differed significantly among patient groups (P=.007), with increased cardiac mortality observed for patients with high (>3.0 times normal) and intermediate (1.5 to 3.0 times normal) CK elevations. In multivariate analyses, higher peak CK and lower ejection fraction were the most important predictors of increased cardiac mortality (both, P<.001); the relative risk for cardiac mortality was 1.05 (95% confidence interval, 1.03-1.08) per 100-U/L increment increase in CK.
Conclusions:
Creatine kinase elevation following elective PTCA is associated with increased late cardiac mortality. This increase in cardiac mortality is independent of clinical variables, severity of heart disease, coronary artery lesion characteristics, interventional devices, and procedural outcomes. Even patients with lesser degrees of CK elevation are at significantly increased risk for late cardiac death.
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