[Homozygous Sickle Cell Children Treated with Hydroxyurea in Brazzaville (Congo)]

J R Mabiala-Babela1,2, E R Nika2, L C Ollandzobo Ikobo1,2

  • 1Faculté des sciences de la santé, université Marien-Ngouabi, Brazzaville, Congo.

Insights

Hydroxyurea treatment significantly improved severe sickle cell disease symptoms in children, including anemia and pain crises. This therapy showed good compliance and reduced complications, offering a valuable option in resource-limited settings.

Area of Science:

  • Hematology
  • Pediatrics
  • Pharmacology

Background:

  • Sickle cell disease (SCD) is a severe inherited blood disorder.
  • Children with severe SCD experience significant morbidity.
  • Hydroxyurea is a treatment option for SCD, but its use in resource-limited settings requires evaluation.

Purpose of the Study:

  • To assess the efficacy and safety of hydroxyurea in children with severe homozygous sickle cell disease.
  • To evaluate therapeutic compliance and clinical outcomes.
  • To analyze biological changes and toxicity associated with hydroxyurea treatment.

Main Methods:

  • A longitudinal study was conducted from November 2015 to September 2017 at Brazzaville University Hospital.
  • 107 children with SCD receiving hydroxyurea were monitored.
  • Data collected included therapeutic compliance, nutritional status, hemoglobin electrophoresis, blood count, and toxicity. Statistical analysis used the Student test (P < 0.05).

Main Results:

  • Hydroxyurea indications included recurrent anemic (57.9%), neurological (17.8%), and hyperalgesic crises (15.9%).
  • Therapeutic compliance was high (89.5%), with significant clinical improvement in anemic (88.7%) and hyperalgesic crises (88.2%).
  • Biological improvements included increased fetal hemoglobin and hemoglobin levels, and decreased white blood cell counts and platelets. Toxicity was minimal (vomiting, thrombocytopenia, headache, neutropenia).

Conclusions:

  • Hydroxyurea is indicated for severe SCD complications in children in Brazzaville, primarily anemic, neurological, and hyperalgesic crises.
  • The treatment demonstrates excellent clinical evolution and is a viable therapeutic alternative in resource-limited areas.
  • High compliance and manageable toxicity support hydroxyurea's role in improving SCD outcomes.

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