Key result
Hydroxyurea improves TCD velocity in sickle cell anemia but leaves residual stroke risk at ~0.6%/year.
Why the study?
Does hydroxyurea prevent incident stroke in pediatric sickle cell anemia patients in Uganda?
Does hydroxyurea prevent incident stroke in pediatric sickle cell anemia patients in Uganda?
In Ugandan children with sickle cell anemia, incident strokes occurred despite hydroxyurea therapy and overall improved TCD velocities, suggesting TCD alone may not fully identify highest stroke risk in this region.
INTRODUCTION: Transcranial Doppler ultrasound (TCD) screening for primary stroke prevention in children with sickle cell anemia (SCA) was established in higher-resource regions, targeting interventions for highest velocity ("abnormal"). We sought to identify additional stroke risk factors in Uganda. METHODS: We conducted a 30-month open-label single-arm Ugandan hydroxyurea trial, dose-escalated to maximum-tolerated dose, aimed to test brain protection for children aged 3-9 years with SCA. Study procedures included history, clinical stroke examination, and prospective TCD and laboratory assessments. RESULTS: Overall, 264 children received study HU, mean age 5.6 ± 1.7, hemoglobin 7.8 ± 1.2 g/dL, fetal hemoglobin (HbF) 11.9% ± 8.1%, enrolment TCD mean TAMV 148.4 ± 29.3 cm/sec; 15 (5.7%) had abnormal TCD. The mean TAMV at trial completion was 131.9 ± SD 25.7 cm/sec. Four participants without abnormal enrolment TCD developed acute stroke within the initial 16 months (incidence 0.62 per 100 person-years): two had enrolment HbF ≤3.1%, two had low oxygen saturation (90%), and one had recurring severe anemia necessitating multiple transfusions. Apparent stroke precipitants were severe malaria, acute chest syndrome, recent pain crisis, or uncertain cause. At trial completion, eight additional participants had a higher risk TCD category than at enrolment. CONCLUSION: The effectiveness of TCD screening for stroke prevention may vary by region, as no participant with an incident stroke was at the highest risk. Antecedent and/or ongoing SCA-related risks of anemia, low HbF, hypoxemia, infections, and/or disease complications likely contributed to stroke despite trial HU. Results suggest that TCD alone may not fully identify the highest stroke risk in the region, and there is a need for primary stroke prevention from early childhood and continuous hydroxyurea therapy.
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Wambaka et al. (2025) studied sickle cell anemia (n=264). Hydroxyurea was evaluated on Acute stroke. Hydroxyurea therapy in children with sickle cell anemia resulted in 4 incident strokes (0.62 per 100 person-years) despite improved TCD velocity, suggesting TCD alone may not identify highest risk.
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