Caring for Africa's sickle cell children: will we rise to the challenge?

Assaf P Oron1, Dennis L Chao1, Echezona E Ezeanolue2,3

  • 1Maternal, Newborn and Child Health, Institute for Disease Modeling, Bellevue, WA, USA.

BMC Medicine
|April 29, 2020
PubMed

Insights

Sickle cell disease (SCD) in Africa requires immediate, scalable interventions like early screening and proven treatments. While cures are developing, focusing on existing, affordable care is crucial for saving children

Area of Science:

  • Global Health
  • Pediatrics
  • Genetics

Background:

  • Sickle Cell Disease (SCD) disproportionately affects African children, contributing significantly to child mortality.
  • Insufficient resource allocation and lagging public health efforts hinder SCD management in Africa.
  • While curative therapies are promising long-term, immediate, cost-effective interventions are needed for current SCD burden in Africa.

Purpose of the Study:

  • To highlight the critical need for scalable, early-life screening for Sickle Cell Disease (SCD) in Africa.
  • To emphasize the potential of newly available, inexpensive point-of-care SCD tests for universal screening.
  • To advocate for the scaled implementation of proven, cost-effective SCD healthcare strategies in Africa.

Main Methods:

  • Review of recent advancements in SCD diagnostics, including point-of-care test kits.
  • Assessment of existing public health infrastructure and healthcare strategies applicable to SCD in Africa.
  • Analysis of logistical, cultural, and awareness barriers to widespread SCD care implementation.

Main Results:

  • Inexpensive SCD point-of-care tests are available and effective in African field settings, enabling early diagnosis.
  • Expansion of the pneumococcal conjugate vaccine and increased availability of hydroxyurea support comprehensive SCD care.
  • Existing SCD care guidelines and research networks in Africa provide a foundation for scaling up public health systems.

Conclusions:

  • Several African nations possess the political will and infrastructure to rapidly implement comprehensive SCD childcare.
  • A globally funded initiative, starting with high-burden countries, can transform outcomes for children with SCD worldwide.
  • Ongoing research tailored to the specific needs of children with SCD in high-prevalence regions is essential.
Abstract

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