Publications by authors named "B Toure"

Background: Sickle cell disease (SCD) is a prevalent inherited blood disorder. Globally, approximately 515 000 babies are born with SCD annually, with 75% of these births occurring in Africa. Integrating newborn screening (NBS) for SCD into primary healthcare structures, such as immunisation programmes, holds significant promise, with dried blood spots (DBS)-point-of-care technologies (POCT) like HaemoTypeSC offering cost-effective screening solutions.

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Aim: This study aimed to evaluate the antibiotic-prescribing attitudes of dental students during the management of endodontic infections.

Materials And Methods: This study was conducted in the five faculties of dental medicine in Morocco. A self-administered questionnaire was used and completed online.

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Introduction: Many aspects of tooth development have been documented, particularly in Caucasian populations. However, dental development has not been extensively studied in West Africa.

Objective: The present study was designed to provide information on the sequences of tooth calcification in West African black Senegalese children and to compare the results with those of other populations, notably the London Atlas.

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Article Synopsis
  • Pregnancy in women with sickle cell disease (SCD) poses significant risks, particularly due to red blood cell (RBC) alloimmunisation, which complicates transfusion options.
  • A study conducted in Bamako between August 2022 and January 2023 involved 95 pregnant women with SCD, revealing that 62% had prior blood transfusions and a 14% prevalence of RBC alloantibodies, with anti-E and pan-agglutinins being the most common.
  • The findings indicate that history of miscarriage, blood transfusions, and the number of pregnancies are key risk factors, highlighting the need for improved screening and collaboration among healthcare providers to better manage care for SCD patients during pregnancy.
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