Key result
Intracoronary ST-segment shift ≥1 mm after PCI predicts periprocedural myocardial damage in ~93% of patients.
Why the study?
Does intracoronary ST-segment shift after elective PCI predict periprocedural myocardial injury in stable patients?
Cohort (n=108)
Does intracoronary ST-segment shift after elective PCI predict periprocedural myocardial injury in stable patients?
Odds Ratio: 54.1 (95% CI 12.1–240)
Absolute Event Rate: 93% vs 19%
p-value: p=<0.0001
Intracoronary ST-segment shift recorded via guidewire immediately after successful elective PCI accurately predicts periprocedural myocardial injury and worse long-term event-free survival.
May support post-PCI ST monitoring for risk stratification; hypothesis-generating and requires prospective validation before practice change.
BACKGROUND: Elevation of cardiac biomarkers after coronary angioplasty (percutaneous coronary intervention [PCI]) reflects periprocedural myocardial damage and is associated with adverse cardiac events. We assessed whether periprocedural myocardial damage that occurs despite successful PCI could be rapidly and easily identified by intracoronary ST-segment recording with the use of a catheter guidewire. METHODS AND RESULTS: In 108 consecutive stable patients undergoing elective single-vessel PCI, we recorded unipolar ECG from the intracoronary guidewire in the distal coronary before PCI and 2 minutes after the last balloon inflation. After PCI, intracoronary ST-segment shift > or = 1 mm from baseline was considered significant. Troponin I levels were measured at baseline and at 8 and 24 hours after intervention, and myocardial damage was defined as troponin I increase above the upper normal value after intervention. All patients had normal cardiac marker values before PCI, and PCI was successful in all (residual stenosis < 20%, Thrombolysis in Myocardial Infarction grade 3 flow). After PCI, long-term follow-up data were collected; myocardial damage was detected in 50 patients (46%), although abnormal creatine kinase-MB values were documented in only 11 (10%). Significant intracoronary ST-segment shift after PCI was present in 40 patients (37%; group A) and absent in the remaining 68 (63%; group B). Procedural myocardial damage was documented in 37 group A patients (93%) and in 13 group B patients (19%; P<0.001); significant ECG changes were found on standard ECG after intervention in only 5 patients (13%) and 1 patient (1%) (P<0.05). Sensitivity of intracoronary ST-segment shift for predicting myocardial damage was 74%, and specificity was 95%, with positive and negative predictive values of 93% and 81%, respectively. On multivariate analysis, intracoronary ST-segment shift was the sole independent predictor of myocardial damage (odds ratio, 54.1; 95% confidence interval, 12.1 to 240; P<0.0001). At a median follow-up of 12+/-5 months, major coronary event-free survival was significantly worse in group A patients (log-rank test chi2=4.0; P<0.05). CONCLUSIONS: After successful single-vessel PCI, intracoronary ST-segment shift allows the prompt and inexpensive identification of patients developing myocardial injury, who may require adjunctive therapy and longer in-hospital stay.
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Balian et al. (2006) conducted a cohort in Stable patients undergoing elective single-vessel PCI (n=108). Intracoronary ST-segment shift ≥ 1 mm from baseline vs. Absence of significant intracoronary ST-segment shift was evaluated on Periprocedural myocardial damage (troponin I increase above upper normal value) (OR 54.1, 95% CI 12.1 to 240, p=<0.0001). Intracoronary ST-segment shift ≥1 mm after elective PCI strongly predicted periprocedural myocardial damage compared to no shift (93% vs 19%; OR 54.1; 95% CI 12.1-240; P<0.0001).
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