Evidence map›Paper›PMID 42577886›Full record

ArticleEJHaem2026

Evaluation of The Use of Hydroxyurea in Treating Children With Sickle Cell Anemia in Central Africa's Rural Area.

Gloire Mbayabo, Paul Lumbala Kabuyi, Mamy Ngole, Aimé Lumaka, Valerie Race, Gert Matthijs, Tite Mikobi Minga, Koenraad Devriendt, Chris Van Geet, Prosper Tshilobo Lukusa

Abstract read
In one paragraph

Article in EJHaem, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

1 citing paper in PubMed.

  1. Article
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

10 authors.

Gloire MbayaboDepartment of Pediatrics University of Kinshasa Kinshasa Democratic Republic of the Congo.
Paul Lumbala KabuyiDepartment of Pediatrics University of Kinshasa Kinshasa Democratic Republic of the Congo.
Mamy NgoleCentre for Human Genetics KU Leuven and University Hospitals Leuven Leuven Belgium.
Aimé LumakaDepartment of Pediatrics University of Kinshasa Kinshasa Democratic Republic of the Congo.
Valerie RaceCentre for Human Genetics KU Leuven and University Hospitals Leuven Leuven Belgium.
Gert MatthijsCentre for Human Genetics KU Leuven and University Hospitals Leuven Leuven Belgium.
Tite Mikobi MingaCentre for Human Genetics Faculty of Medicine University of Kinshasa Kinshasa Democratic Republic of the Congo.
Koenraad DevriendtCentre for Human Genetics KU Leuven and University Hospitals Leuven Leuven Belgium.
Chris Van GeetDepartment of Cardiovascular Sciences and Pediatrics (Hemato-oncology) KU Leuven and University Hospitals Leuven Leuven Belgium.
Prosper Tshilobo LukusaDepartment of Pediatrics University of Kinshasa Kinshasa Democratic Republic of the Congo.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sickle cell anemia (SCA) is highly prevalent in Central Africa. This disease causes severe manifestations in children, requiring treatment. Hydroxyurea (HU) is currently the most effective treatment for SCA. We evaluated the use of HU in children living in rural Central Africa. Methods: We conducted a clinical trial using HU in the Kisantu Saint Luc Hospital (KSLH) in the DR Congo (DRC) from November 2017 to February 2020. SCA patients aged 6 months to 18 years, with a moderate to severe form of SCA (Adegoke score), were treated with an entry HU dose of 15 mg/kg per day, followed with gradual dose escalation of 5 mg/kg per day increments every 6 months, up to a maximally tolerated dose of 30 mg/Kg/day. To determine the clinical and biological response to the treatment (efficacy of HU), we compared the clinical and biological data collected during the first and second year of treatment to the baseline values. Results: Sixty-nine patients (37 boys and 32 girls; sex-ratio M/F 1.15) were eligible for the clinical trial using HU. Only 39 patients remained at the end of the clinical trial (56.5%). On average, the HbF increased to 3-fold at 12 months and 3.3-fold at 24 months, which was significantly different to the baseline. Thirty-seven (80.4%) patients presented a good clinical response, whereas 9 (19.6%) did not. Conclusion: This clinical demonstrated the clinical and biological effectiveness of HU treatment in a cohort of young Congolese patients. In addition to tremendous logistical challenges, low adherence is the major threat to HU treatment in a rural area. There is a need to implement appropriate strategies to increase the adherence to the HU treatment in these rural settings.

Indexed as

Central Africahydroxyurearural areasickle cell anemia

Identifiers

PMID42577886
PMCPMC13455541

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.