Evidence map›Paper›PMID 40330631›Full record

ArticleEJHaem2025

Sickle Cell Disease in Africa: SickleInAfrica Registry in Ghana, Nigeria and Tanzania.

Jack Morrice, Wilson Mupfururirwa, Reuben I Chianumba, Evans Xorse Amuzu, Daniel Kandonga, Victoria Nembaware, Mario Jonas, Jade Hotchkiss, Upendo Masamu, Arthemon Nguweneza and 14 more

Abstract read
In one paragraph

Article in EJHaem, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. 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

24 authors.

Jack MorriceDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Wilson MupfururirwaDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Reuben I ChianumbaCentre of Excellence for Sickle Cell Disease Research & Training University of Abuja (CESRTA) Abuja Federal Capital Territory Nigeria.
Evans Xorse AmuzuDirectorate of Child Health-Komfo Anokye Teaching Hospital Kumasi Ghana.
Daniel KandongaSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Victoria NembawareDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Mario JonasDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Jade HotchkissDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Upendo MasamuSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Arthemon NguwenezaDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Bruno P MmbandoSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Irene MinjaSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Agnes JonathanSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Nicola MulderDepartment of Integrative Biomedical Sciences Computational Biology Division IDM, CIDRI-Africa WT Centre, University of Cape Town, Health Sciences Campus Observatory South Africa.
Emmanuel BalandyaDepartment of Physiology Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.ORCID https://orcid.org/0000-0002-3707-9985
Alex Osei-AkotoChild Health Directorate, Komfo Anokye Teaching Hospital Kumasi Ghana.
Vivian PaintsilChild Health Directorate, Komfo Anokye Teaching Hospital Kumasi Ghana.
Julie MakaniSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Obiageli NnoduCentre of Excellence for Sickle Cell Disease Research & Training University of Abuja (CESRTA) Abuja Federal Capital Territory Nigeria.
Members of SPARCO Nigeria
Raphael Z SangedaSickle Cell Programme Muhimbili University of Health and Allied Sciences Dar es Salaam Tanzania.
Andre Pascal KengneDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Gaston KuzamunuDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.
Ambroise WonkamDivision of Human Genetics Department of Pathology University of Cape Town, Health Sciences Campus Observatory South Africa.ORCID https://orcid.org/0000-0003-1420-9051

Funding

The Sickle Pan-African Research Consortium (SPARCO)U24HL135881 · NHLBI · MUHIMBILI UNIVERSITY/ ALLIED HLTH SCIS · PI MAKANI, JULIE · 2017 to 2025
$5.3M
Sickle Pan-African Research Consortium (SPARCO)- TanzaniaU01HL156853 · NHLBI · MUHIMBILI UNIVERSITY/ ALLIED HLTH SCIS · PI BALANDYA, EMMANUEL · 2021 to 2025
$1.5M
NHLBI NIH HHS U01 HL156853NHLBI NIH HHS U24 HL135881
6 · The paper itself

Abstract

Introduction: Sickle cell disease (SCD) is most prevalent in Sub-Saharan Africa (SSA), where incomplete patient profiles and limited management strategies hinder research and healthcare standards. Methods: We describe the first large-scale and multinational assessment of 13,403 SCD patients enrolled from 2017-2021 across 31 facilities in Ghana, Nigeria, and Tanzania into the SickleInAfrica consortium registry. We used hierarchical regression models to estimate and analyze the demographics, adoption levels of SCD diagnosis and therapies. Results: The average age at diagnosis was 3 months, 19 months and 3 years in Ghana, Nigeria and Tanzania respectively, reflecting differences in country-specific newborn screening programs and policies. Hydroxyurea (HU) use was highest in Ghana (21%), followed by Nigeria (12%) and Tanzania (6%), with significant variability across facilities. Sex differences in SCD management were observed, with males more likely to receive HU and blood transfusions. At the consortium level, HU initiation correlated with enrolment age rather than age at diagnosis, highlighting the need for earlier intervention. Conclusions: Our findings highlight the potential of the SickleInAfrica registry toward enhancing understanding of regional disparities in SCD care and potential gender inequalities, emphasizing the need for enabling policies toward strengthened SCD research and improved quality of life and care of patients in Africa.

Indexed as

disease managementmeta‐analysisregistryregression modelssickle cell diseaseSickleInAfrica

Identifiers

PMID40330631
PMCPMC12053511

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.