Evidence map›Paper›PMID 36322937›Full record

Trial reportBlood2023

Hydroxyurea for secondary stroke prevention in children with sickle cell anemia in Nigeria: a randomized controlled trial.

Shehu U Abdullahi, Surayya Sunusi, Mohammed Sani Abba, Saifuddeen Sani, Hauwau Aminu Inuwa, Safiya Gambo, Awwal Gambo, Bilya Musa, Brittany V Covert Greene, Adetola A Kassim and 6 more

Open access · hybridAbstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in Blood, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
5.4field-weighted citation impact, top 3% of its field
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

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 39 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Article
  9. Optimizing the "right" patient selection for treatment for sickle cell disease.Hematology. American Society of Hematology. Education Program · 2025
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. A Novel Newborn Screening Program for Sickle Cell Disease in Nigeria.International journal of neonatal screening · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

Shehu U AbdullahiDepartment of Pediatrics, Bayero University and Aminu Kano Teaching Hospital, Kano, Nigeria.
Surayya SunusiDepartment of Community Medicine, Aminu Kano Teaching Hospital, Kano, Nigeria.ORCID 0000-0002-9985-1635
Mohammed Sani AbbaDepartment of Pharmacy, Aminu Kano Teaching Hospital, Kano, Nigeria.
Saifuddeen SaniDepartment of Administration, Aminu Kano Teaching Hospital, Kano, Nigeria.
Hauwau Aminu InuwaDepartment of Internal Medicine, Aminu Kano Teaching Hospital, Kano, Nigeria.
Safiya GamboDepartment of Pediatrics, Murtala Mohammed Specialist Hospital, Kano, Nigeria.
Awwal GamboDepartment of Pediatrics, Murtala Mohammed Specialist Hospital, Kano, Nigeria.
Bilya MusaDepartment of Administration, Aminu Kano Teaching Hospital, Kano, Nigeria.
Brittany V Covert GreeneDepartment of Pediatrics, Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN.
Adetola A KassimDepartment of Hematology and Oncology, Vanderbilt School of Medicine, Vanderbilt University, Nashville, TN.
Mark RodeghierRodeghier Consultants, Chicago, IL.ORCID 0000-0001-7258-0073
Nafiu HussainiDepartment of Mathematical Sciences, Bayero University, Kano, Nigeria.ORCID 0000-0002-9922-0454
Mariana CiobanuPediatric Neurology, Vanderbilt University Medical Center, Nashville, TN.
Muktar H AliyuVanderbilt Institute for Global Health, Vanderbilt University and Vanderbilt University Medical Center, Nashville, TN.
Lori C JordanPediatric Neurology, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0001-7240-0415
Michael R DeBaunDepartment of Pediatrics, Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease, Vanderbilt University Medical Center, Nashville, TN.ORCID 0000-0002-0574-1604
Aminu Kano Teaching Hospital · NGVanderbilt University Medical Center · USUniversity of Abuja Teaching Hospital · NGBayero University Kano · NGVanderbilt University · US

Funding

The Vanderbilt Institute for Clinical and Translational Research (VICTR)UL1TR000445 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BERNARD, GORDON RAPHAEL · 2012 to 2016
$41.4M
Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lea K Davis · 2020 to 2026
$10.3M
Mentoring in Patient-Oriented Research focused on Neurological Complications of Sickle Cell DiseaseK24HL147017 · NHLBI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI JORDAN, LORI CHAFFIN · 2019 to 2023
$547k
NCATS NIH HHS UL1 TR000445NHLBI NIH HHS K24 HL147017NICHD NIH HHS P50 HD103537
6 · The paper itself

Abstract

We tested the hypothesis that fixed oral moderate-dose hydroxyurea (20 mg/kg per day) for initial treatment of secondary stroke prevention results in an 80% relative risk reduction of stroke or death when compared with fixed oral low-dose hydroxyurea (10 mg/kg per day) in a phase 3 double-blind, parallel-group, randomized controlled trial in children with sickle cell anemia (SCA) living in Nigeria. A total of 101 participants were randomly allocated to low-dose (n = 49) and moderate-dose (n = 52) hydroxyurea treatment groups. The median participant follow-up was 1.6 years (interquartile range, 1.0-2.3), with a planned minimum follow-up of 3.0 years. A total of 6 recurrent strokes and 2 deaths vs 5 recurrent strokes and 3 deaths occurred in the low- and moderate-dose groups, respectively. The incidence rate ratio (IRR) of the primary outcome measure of stroke or death in the low- and moderate-dose hydroxyurea treatment groups was 0.98 (95% confidence interval [CI], 0.32-3.00; P = .97). The trial was stopped early owing to no clinical difference in the incidence rates of the primary outcome measure. The incidence rates of recurrent strokes were 7.1 and 6.0 per 100 person-years in the low- and moderate-dose groups, respectively, (IRR, 1.18; 95% CI, 0.30-4.88; P = .74). As a measure of adherence to the oral hydroxyurea therapy, the median percent of returned pills was 3.0% and 2.6% in the low- and moderate-dose groups, respectively. No participant had hydroxyurea therapy stopped for myelosuppression. For children with SCA in low-income settings without access to regular blood transfusion therapy, initial low-dose hydroxyurea is a minimum known efficacious dose for secondary stroke prevention.

Indexed as

Anemia, Sickle CellStrokeAntisickling AgentsChildHumansHydroxyureaNigeriaSecondary PreventionAntisickling AgentsHydroxyurea

Identifiers

PMID36322937
PMCPMC10023719
OpenAlexW4308055702

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.