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Transcranial Doppler in 150 Congolese children with sickle cell disease

Article scientifique 2024 Anglais

Résumé

Introduction: Sickle Cell Disease (SCD) ranks among the most prevalent genetic disorders globally. The incidence in sub-Saharan African countries has been estimated to be 230.000/y with a high prevalence (1%) in the Democratic Republic of Congo (DRC). Stroke is a significant complication of Sickle Cell Disease (SCD), and carries a high risk of disability and mortality. Transcranial Doppler (TCD) is currently the non-invasive exploration recommended for the prevention of stroke in young SCD patients. Objective: To determine the prevalence of pathological TCD in a population of young Congolese SCA patients and to assess its association with hematological parameters. Population and methods: This cross sectional study was carried out on 150 Congolese SS homozygous children between the ages 2-16 years old (mean age: 8.5 ± 4.0 years) in stable condition, and followed from January 1 to December 31, 2013. TCD was performed using the STOP I method in the main cerebral arteries. The risk of stroke was absent when the average maximum speed during a cycle (TAMMV) in middle cerebral artery (MCA) was < 170 cm/s, but present when TAMMV was borderline or conditional for values between 170 and 199 cm/s and pathological for values ≥ 200 cm/s. Results: = 0.005) parameters when comparing normal and at risk TCD (conditional and abnormal). However, no significant association was found for the categorical corresponding parameters. Conclusion: Globally, 14% of patients were at risk of stroke, hence the interest in integrating TCD in the routine monitoring of children with SCD in order to prevent overt stroke by implementing a chronic blood transfusion program or the use of hydroxycarbamide.

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Kazadi, G., Didier, M., Kitenge, R., Mpaka, S., Gini, J., Ngiyulu, R., Tshilolo, L. (2024). Transcranial Doppler in 150 Congolese children with sickle cell disease. https://doi.org/10.3389/fstro.2024.1384767

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