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Coronary artery dilation and left ventricular hypertrophy do not predict morbidity in children with sickle cell
Mark C Johnson1, Micean J Johnikin, Joshua C Euteneuer
1Division of Pediatric Cardiology, Department of Pediatrics, Washington University School of Medicine/St. Louis Children's Hospital, St. Louis, Missouri.
Insights
Coronary artery dilation (CAD) and left ventricular hypertrophy (LVH) are common in children with sickle cell disease (SCD). However, these findings do not predict future hospitalizations or intensive care unit admissions.
Area of Science:
- Cardiology
- Pediatrics
- Hematology
Background:
- The clinical significance of coronary artery dilation (CAD) and left ventricular hypertrophy (LVH) in pediatric sickle cell disease (SCD) is not well understood.
- Existing research has not established a clear link between these cardiac abnormalities and patient morbidity.
Purpose of the Study:
- To investigate the prevalence of CAD and LVH in children with SCD.
- To determine if CAD and LVH predict future hospitalizations or intensive care unit (ICU) admissions in this population.
Main Methods:
- A retrospective cohort study compared 101 children with SCD to 93 healthy African-American children.
- Echocardiography was used to assess CAD and LVH.
- Morbidity was measured by hospital days, number of admissions, and ICU admissions over a median follow-up of 6.1 years.
Main Results:
- Left ventricular hypertrophy (LVH) was present in 46% of children with SCD and inversely related to age.
- Prevalence of coronary artery dilation (CAD) was 49% for the left main coronary artery (LMCA), 29% for the left anterior descending (LAD), and 6% for the right coronary artery (RCA).
- Neither CAD nor LVH predicted subsequent ICU admission, hospital days, or number of hospital admissions. They were also not associated with vaso-occlusive pain, acute chest syndrome, or cerebrovascular accident.
Conclusions:
- LVH and CAD are frequent findings in children with SCD.
- These cardiac abnormalities do not appear to be associated with increased risk for future hospital or ICU admissions in pediatric SCD patients.
Background:
Little is known about the clinical significance of coronary artery dilation (CAD) and left ventricular hypertrophy (LVH) in patients with sickle cell disease (SCD).
Procedure:
In a retrospective cohort, we studied the prevalence of CAD and LVH in 101 children with SCD in comparison to 93 healthy African-American patients without SCD. Hospital days, number of admissions, and intensive care unit admission after the echocardiogram were assessed as measures of morbidity.
Results:
Multivariable analysis of echocardiographic measures of LVH and CAD did not predict subsequent intensive care unit admission, hospital days/year or number of hospital admissions/year during a median follow-up time of 6.1 years. LVH as measured by left ventricular mass index was present in 46% of children with SCD and was inversely related to age (P = 0.0004). Height-indexed dimensions in children with SCD demonstrated that the prevalence of dilation was 49% for the left main coronary artery (LMCA), 29% for the left anterior descending (LAD), and 6% for the right coronary artery (RCA). LMCA dilation was related to relative wall thickness (P = 0.006), inversely to age (P < 0.0006) and weakly to disease severity as determined by hemoglobin (P = 0.03). CAD and LVH were not related to a clinical history of vaso-occlusive pain episode, acute chest syndrome, or cerebrovascular accident.
Conclusion:
LVH and CAD are common findings in children with SCD; however, they are not associated with need for subsequent hospital or intensive care unit admission.
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