Related Experiment Video
Updated: Dec 29, 2025

Continuous Manual Exchange Transfusion for Patients with Sickle Cell Disease: An Efficient Method to Avoid Iron Overload
Published on: March 14, 2017
[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.
Abstract:
The objective of this study is to reduce the morbidity of children with homozygous sickle cell disease presenting severe forms. We have conducted a longitudinal study between November 2015 and September 2017 at the Brazzaville University Hospital. Children with sickle cell disease requiring treatment with hydroxyurea were included. The variables studied were therapeutic compliance, evolutive profile of nutritional status, indications of hydroxyurea, electrophoresis of hemoglobin, blood count, and toxicity. The statistical test used was Student test with a significance threshold of less than 0.05. One thousand twenty-four children were monitored for sickle cell disease, 107 of which had received hydroxyurea (10.4%). The indications for hydroxyurea were recurrent anemic attacks (≥ 4) in 62 cases (57.9%), neurological crises 19 cases (17.8%), recurrent hyperalgesic crises in 17 cases (15.9%), priapism in 4 cases (3.7), and acute thoracic syndrome in 2 cases (1.9%). Therapeutic compliance was good in 89.5% of them. A rapid and lasting clinical improvement was noted in the majority of patients with hyperalgesic attacks (88.2%) and anemic attacks (88.7%), two recurrences for the cerebrovascular accidents, and an absence of recurrence of priapism and of the acute thoracic syndrome. From the biological point of view, there was a significant increase in fetal hemoglobin (1.2 to 16.2%; P < 0.05), hemoglobin (7 to 8.3 g/dl; P < 0.05), mean cell volume (80.8 to 96 fl; P < 0.05) and a significant decrease in mean white blood cell count (15,633 to 9,872/mm3; P < 0.05) and platelets (387,002 to 324,400/mm3; P < 0.05). The signs of toxicity observed were mainly vomiting and thrombocytopenia in two cases each, one case with headache and the other with neutropenia. Indications for use of hydroxyurea therapy in children with sickle cell disease in Brazzaville are common. These are dominated by recurrent anemic seizures, strokes, and hyperalgesic seizures. The excellent evolution of these complications under hydroxyurea represents an interesting alternative in our countries with limited resources.
More Related Videos
Related Concept Videos
Treatment for Pulmonary Arterial Hypertension: Oxygen Therapy for Respiratory Failure
Oxygen therapy is vital in increasing and maintaining blood oxygen levels in PAH patients. As a result, it aids in reducing fatigue,...
Cystic Fibrosis: Management
Sinus disease and chronic...
Bone Marrow Sampling and Transplants
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy...
Treatment Resistant Cancers
Pulmonary Tuberculosis IV
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
Continuous Renal Replacement Therapy

