Evidence map›Paper›PMID 32340612›Full record

ArticleBMC medicine2020

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

Assaf P Oron, Dennis L Chao, Echezona E Ezeanolue, Loveth N Ezenwa, Frédéric B Piel, Osifo Telison Ojogun, Sophie Uyoga, Thomas N Williams, Obiageli E Nnodu

Abstract read
In one paragraph

Article in BMC medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 2 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Assaf P OronMaternal, Newborn and Child Health, Institute for Disease Modeling, Bellevue, WA, USA.
Dennis L ChaoMaternal, Newborn and Child Health, Institute for Disease Modeling, Bellevue, WA, USA.
Echezona E EzeanolueHealthy Sunrise Foundation, Las Vegas, NV, USA.
Loveth N EzenwaNational Population Commission, Abuja, Nigeria.
Frédéric B PielDepartment of Epidemiology & Biostatistics, School of Public Health, Faculty of Medicine, Imperial College London, London, UK.
Osifo Telison OjogunNational Population Commission, Abuja, Nigeria.
Sophie UyogaKEMRI-Wellcome Trust Research Programme, PO Box 230, Kilifi, Kenya.
Thomas N WilliamsKEMRI-Wellcome Trust Research Programme, PO Box 230, Kilifi, Kenya. tom.williams@imperial.ac.com.
Obiageli E NnoduCentre of Excellence for Sickle Cell Disease Research & Training, University of Abuja, Abuja, Nigeria.

Funding

The Sickle Pan-African Research Consortium (SPARCO)U24HL135881 · NHLBI · MUHIMBILI UNIVERSITY/ ALLIED HLTH SCIS · PI MAKANI, JULIE · 2017 to 2025
$5.3M
NHLBI NIH HHS 1 U24 HL135881-01NHLBI NIH HHS U24 HL135881Wellcome Trust 202800Wellcome Trust 202800/Z/16/Z
6 · The paper itself

Abstract

backgroundMost of the world's sickle cell disease (SCD) burden is in Africa, where it is a major contributor to child morbidity and mortality. Despite the low cost of many preventive SCD interventions, insufficient resources have been allocated, and progress in alleviating the SCD burden has lagged behind other public-health efforts in Africa. The recent announcement of massive new funding for research into curative SCD therapies is encouraging in the long term, but over the next few decades, it is unlikely to help Africa's SCD children substantially. MAIN DISCUSSION: A major barrier to progress has been the absence of large-scale early-life screening. Most SCD deaths in Africa probably occur before cases are even diagnosed. In the last few years, novel inexpensive SCD point-of-care test kits have become widely available and have been deployed successfully in African field settings. These kits could potentially enable universal early SCD screening. Other recent developments are the expansion of the pneumococcal conjugate vaccine towards near-universal coverage, and the demonstrated safety, efficacy, and increasing availability and affordability of hydroxyurea across the continent. Most elements of standard healthcare for SCD children that are already proven to work in the West, could and should now be implemented at scale in Africa. National and continental SCD research and care networks in Africa have also made substantial progress, assembling care guidelines and enabling the deployment and scale-up of SCD public-health systems. Substantial logistical, cultural, and awareness barriers remain, but with sufficient financial and political will, similar barriers have already been overcome in efforts to control other diseases in Africa. CONCLUSION AND RECOMMENDATIONS: Despite remaining challenges, several high-SCD-burden African countries have the political will and infrastructure for the rapid implementation and scale-up of comprehensive SCD childcare programs. A globally funded effort starting with these countries and expanding elsewhere in Africa and to other high-burden countries, including India, could transform the lives of SCD children worldwide and help countries to attain their Sustainable Development Goals. This endeavor would also require ongoing research focused on the unique needs and challenges of SCD patients, and children in particular, in regions of high prevalence.

Indexed as

AfricaAnemia, Sickle CellChild, PreschoolFemaleHumansInfantMaleChild mortalityMaternal newborn and child health (MNCH)Newborn screeningSickle cell anemia (SCA)Sickle cell disease (SCD)Sustainable Development Goals (SDGs)

Identifiers

PMID32340612
PMCPMC7187492

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.