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Factors Associated With Electrocardiographic Abnormalities in Patients With Sickle Cell Disease: A Systematic Review
Parisa Zare1, Alireza Ahmadkhani2, Ehsan Taherifard1,3
1Student Research Committee, Shiraz University of Medical Sciences, Shiraz, Iran.
Insights
Sickle cell disease (SCD) is linked to ECG abnormalities, especially during crises. Moderate SCD severity and lower hemoglobin levels increase the risk of cardiac issues, necessitating monitoring.
Area of Science:
- Cardiology
- Hematology
- Medical Research
Background:
- Sickle cell disease (SCD) frequently leads to cardiovascular complications.
- Electrocardiogram (ECG) changes are common indicators of cardiac involvement in SCD patients.
Purpose of the Study:
- To systematically review and analyze factors associated with ECG abnormalities in patients with sickle cell disease.
Main Methods:
- A comprehensive literature search was conducted across five major databases.
- Meta-analysis of 23 studies involving 2943 SCD patients was performed using Comprehensive Meta-Analysis software.
- Effect sizes, including odds ratios and mean differences, were pooled using a random effects model.
Main Results:
- Increased odds of prolonged QTc interval, ST segment elevation, and ST segment depression were observed during SCD crises.
- Moderate SCD severity was associated with higher odds of any ECG abnormality compared to mild severity.
- Lower mean hemoglobin levels were noted in patients with prolonged QTc intervals.
Conclusions:
- SCD status, severity, and hemoglobin levels are significantly associated with ECG abnormalities.
- Routine ECG assessments and cardiac monitoring are crucial for SCD patients.
- Caution is advised with QTc-prolonging medications in this high-risk population.
Introduction:
Sickle cell disease (SCD) is frequently associated with cardiovascular complications, with cardiac involvement being evident in the electrocardiogram (ECG). This study aimed to systematically research the literature to investigate factors associated with ECG abnormalities in SCD patients.
Method:
Five online databases of PubMed, Scopus, Web of Science, Embase, and Google Scholar were reviewed using a broad search strategy to identify original studies reporting factors associated with abnormal ECG findings among patients with SCD. Using Comprehensive Meta-Analysis software, various effect sizes-odds ratios (ORs), mean differences, and correlation coefficients-were analyzed, pooled with a random effects model, and visualized through forest plots.
Results:
Data analysis from 23 studies covering 2943 SCD patients revealed increased odds of prolonged QTc interval (2.54, 95% CI = 1.34-4.83), ST segment elevation (9.23, 95% CI = 3.15-27.07), and ST segment depression (3.82, 95% CI = 1.99-7.33) during crises. Patients with moderate SCD severity had higher odds of having any ECG abnormalities compared to those with mild severity (2.80, 95% CI = 1.47-5.33). No significant associations were observed between moderate and mild severity for left ventricular hypertrophy, sinus arrhythmia, and sinus tachycardia, or between male and female for having any ECG abnormalities, left ventricular hypertrophy, and prolonged QTc interval. Additionally, mean hemoglobin level was 0.60 mg/dL lower (95% CI = -0.91 to 0.28) in those with prolonged QTc interval.
Conclusion:
This study highlights the link between SCD status and severity, and hemoglobin, and ECG abnormalities. It emphasizes the need for cardiac monitoring, caution with QTc-prolonging medications, and routine ECG assessments to prevent cardiovascular complications in these high-risk patients.
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