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Impact of White Blood Cell Count After Percutaneous Coronary Intervention on Long-Term Prognosis in Patients with
Zhiyuan Zhang1,2,3, Heyan Wang4, Ruiyu Wang5
1Department of Cardiology, the Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang Province, People's Republic of China.
Insights
Post-PCI leukocytosis in unstable angina patients predicts increased major adverse cardiovascular events (MACE) risk over 5 years. White blood cell and neutrophil counts rise, while lymphocyte counts decrease after percutaneous coronary intervention.
Area of Science:
- Cardiology
- Clinical Medicine
- Biomarkers
Background:
- Elevated white blood cell count (WBC-C) pre-PCI correlates with prognosis in patients undergoing percutaneous coronary intervention (PCI).
- The impact of post-PCI WBC-C on long-term outcomes for unstable angina pectoris (UA) patients remains unclear.
Purpose of the Study:
- To investigate the association between white blood cell count (WBC-C) after percutaneous coronary intervention (PCI) and the long-term prognosis in patients with unstable angina pectoris (UA).
Main Methods:
- Retrospective cohort study of 1811 UA patients.
- Analysis of WBC and subgroup counts pre- and post-PCI using paired Wilcoxon signed-rank test.
- Kaplan-Meier method and COX regression to assess 5-year endpoint events and post-PCI leukocytosis.
Main Results:
- Post-PCI leukocytosis and neutrocytosis were common; lymphocyte counts decreased.
- No significant difference in 5-year all-cause mortality or MACCE between groups.
- Significantly increased 5-year MACE incidence in the post-PCI leukocytosis group (p=0.017).
- Post-PCI leukocytosis independently associated with MACE (HR 1.36, 95% CI 1.06-1.75, p=0.015).
Conclusions:
- PCI increases peripheral WBC and neutrophil counts while decreasing lymphocyte counts in UA patients.
- Post-PCI leukocytosis is a significant predictor of increased MACE risk up to 5 years in UA patients.
Objective:
An association between white blood cell count (WBC-C) before percutaneous coronary intervention (PCI) and prognosis has been established in patients undergoing PCI. However, the effect of WBC-C after PCI on the long-term prognosis of patients with unstable angina pectoris (UA) is unclear.
Methods:
A retrospective cohort study was conducted in 1811 consecutive patients with UA. The changes of WBC and subgroup counts before and in the early postoperative stages after PCI were observed by paired Wilcoxon signed-rank test. The Kaplan-Meier method and COX proportional regression model were used to evaluate the association between the incidence of 5-year endpoint events and post-PCI leukocytosis.
Results:
Leukocytosis and neutrocytosis within 24 hours after PCI were observed in majority of patients with UA, while lymphocyte count significantly decreased after PCI in those patients. There were no significant differences in 5-year all-cause mortality and major adverse cardiovascular and cerebrovascular events (MACCE) between patients in the post-PCI leukocytosis and the control group. However, the 5-year incidence of major adverse cardiovascular events (MACE) was significantly increased in the post-PCI leukocytosis group (p = 0.017, Log rank test). Leukocytosis after PCI was independently associated with the occurrence of MACE (hazard ratio: 1.36; 95% confidence interval: 1.06-1.75; p = 0.015).
Conclusion:
Peripheral WBC and neutrophil counts within 24 hours after PCI significantly increased in response to PCI in patients with UA, while lymphocyte count significantly decreased after PCI in those patients. The post-PCI leukocytosis offered predictive value for an increased risk of MACE for up to 5 years in patients with UA.
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