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.

Pediatric Blood & Cancer
|February 14, 2025
PubMed

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.
Abstract

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