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Hydroxyurea for primary stroke prevention in children with sickle cell anaemia in Nigeria (SPRING): a double-blind, multicentre, randomised, phase 3 trial

Hydroxyurea for primary stroke prevention in children with sickle cell anaemia in Nigeria (SPRING): a double-blind, multicentre, randomised, phase 3 trial
Hydroxyurea for primary stroke prevention in children with sickle cell anaemia in Nigeria (SPRING): a double-blind, multicentre, randomised, phase 3 trial
Background: In high-income countries, standard care for primary stroke prevention in children with sickle cell anaemia and abnormal transcranial Doppler velocities results in a 92% relative risk reduction of strokes but mandates initial monthly blood transfusion. In Africa, where regular blood transfusion is not feasible for most children, we tested the hypothesis that initial moderate-dose compared with low-dose hydroxyurea decreases the incidence of strokes for children with abnormal transcranial Doppler velocities.
Methods: SPRING is a double-blind, parallel-group, randomised, controlled, phase 3 trial of children aged 5-12 years with sickle cell anaemia with abnormal transcranial Doppler velocities conducted at three teaching hospitals in Nigeria. For randomisation, we used a permuted block allocation scheme with block sizes of four, stratified by sex and site. Allocation was concealed from all but the pharmacists and statisticians. Participants were assigned in a 1:1 ratio to low-dose (10 mg/kg per day) or moderate-dose (20 mg/kg per day) oral hydroxyurea taken once daily with monthly clinical evaluation and laboratory monitoring. The primary outcome was initial stroke or transient ischaemic attack, centrally adjudicated. The secondary outcome was all-cause hospitalisation. We used the intention-to-treat population for data analysis. The trial was stopped early for futility after a planned minimum follow-up of 3·0 years to follow-up for participants. This trial was registered with ClinicalTrials.gov, number NCT02560935.FINDINGS: Between Aug 2, 2016, and June 14, 2018, 220 participants (median age 7·2 years [IQR 5·5-8·9]; 114 [52%] female) were randomly allocated and followed for a median of 2·4 years (IQR 2·0-2·8). All participants were Nigerian and were from the following ethnic groups: 179 (82%) people were Hausa, 25 (11%) were Fulani, and 16 (7%) identified as another ethnicity. In the low-dose hydroxyurea group, three (3%) of 109 participants had strokes, with an incidence rate of 1·19 per 100 person-years and in the moderate-dose hydroxyurea group five (5%) of 111 had strokes with an incidence rate of 1·92 per 100 person-years (incidence rate ratio 0·62 [95% CI 0·10-3·20], p=0·77). The incidence rate ratio of hospitalisation for any reason was 1·71 (95% CI 1·15-2·57, p=0·0071), with higher incidence rates per 100 person-years in the low-dose group versus the moderate-dose group (27·43 vs 16·08). No participant had hydroxyurea treatment stopped for myelosuppression.
Interpretation: Compared with low-dose hydroxyurea therapy, participants treated with moderate-dose hydroxyurea had no difference in the stroke incidence rate. However, secondary analyses suggest that the moderate-dose group could lower incidence rates for all-cause hospitalisations. These findings provide an evidence-based guideline for the use of low-dose hydroxyurea therapy for children with sickle cell anaemia at risk of stroke.
Funding: National Institute of Neurological Disorders and Stroke.
Anemia, Sickle Cell/complications, Antisickling Agents/therapeutic use, Child, Preschool, Double-Blind Method, Female, Humans, Hydroxyurea/therapeutic use, Nigeria, Stroke/etiology
2352-3026
e26-e37
Abdullahi, Shehu U
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Jibir, Binta W
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Bello-Manga, Halima
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Gambo, Safiya
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Inuwa, Hauwa
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Tijjani, Aliyu G
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Idris, Nura
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Galadanci, Aisha
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Hikima, Mustapha S
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Galadanci, Najibah
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Borodo, Awwal
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Tabari, Abdulkadir M
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Haliru, Lawal
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Suleiman, Aisha
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Ibrahim, Jamila
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Greene, Brittany C
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Ghafuri, Djamila L
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Rodeghier, Mark
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Slaughter, James C
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Kirkham, Fenella J
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Neville, Kathleen
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Kassim, Adetola
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Trevathan, Edwin
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Jordan, Lori C
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Aliyu, Muktar H
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et al.
Abdullahi, Shehu U
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Jibir, Binta W
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Bello-Manga, Halima
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Gambo, Safiya
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Inuwa, Hauwa
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Tijjani, Aliyu G
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Idris, Nura
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Galadanci, Aisha
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Hikima, Mustapha S
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Galadanci, Najibah
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Borodo, Awwal
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Tabari, Abdulkadir M
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Haliru, Lawal
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Suleiman, Aisha
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Ibrahim, Jamila
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Greene, Brittany C
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Ghafuri, Djamila L
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Rodeghier, Mark
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Slaughter, James C
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Kirkham, Fenella J
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Neville, Kathleen
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Kassim, Adetola
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Trevathan, Edwin
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Jordan, Lori C
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Aliyu, Muktar H
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DeBaun, Michael R
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Abdullahi, Shehu U, Jibir, Binta W, Bello-Manga, Halima, Gambo, Safiya and Kirkham, Fenella J , et al. (2022) Hydroxyurea for primary stroke prevention in children with sickle cell anaemia in Nigeria (SPRING): a double-blind, multicentre, randomised, phase 3 trial. The Lancet Haematology, 9 (1), e26-e37. (doi:10.1016/S2352-3026(21)00368-9).

Record type: Article

Abstract

Background: In high-income countries, standard care for primary stroke prevention in children with sickle cell anaemia and abnormal transcranial Doppler velocities results in a 92% relative risk reduction of strokes but mandates initial monthly blood transfusion. In Africa, where regular blood transfusion is not feasible for most children, we tested the hypothesis that initial moderate-dose compared with low-dose hydroxyurea decreases the incidence of strokes for children with abnormal transcranial Doppler velocities.
Methods: SPRING is a double-blind, parallel-group, randomised, controlled, phase 3 trial of children aged 5-12 years with sickle cell anaemia with abnormal transcranial Doppler velocities conducted at three teaching hospitals in Nigeria. For randomisation, we used a permuted block allocation scheme with block sizes of four, stratified by sex and site. Allocation was concealed from all but the pharmacists and statisticians. Participants were assigned in a 1:1 ratio to low-dose (10 mg/kg per day) or moderate-dose (20 mg/kg per day) oral hydroxyurea taken once daily with monthly clinical evaluation and laboratory monitoring. The primary outcome was initial stroke or transient ischaemic attack, centrally adjudicated. The secondary outcome was all-cause hospitalisation. We used the intention-to-treat population for data analysis. The trial was stopped early for futility after a planned minimum follow-up of 3·0 years to follow-up for participants. This trial was registered with ClinicalTrials.gov, number NCT02560935.FINDINGS: Between Aug 2, 2016, and June 14, 2018, 220 participants (median age 7·2 years [IQR 5·5-8·9]; 114 [52%] female) were randomly allocated and followed for a median of 2·4 years (IQR 2·0-2·8). All participants were Nigerian and were from the following ethnic groups: 179 (82%) people were Hausa, 25 (11%) were Fulani, and 16 (7%) identified as another ethnicity. In the low-dose hydroxyurea group, three (3%) of 109 participants had strokes, with an incidence rate of 1·19 per 100 person-years and in the moderate-dose hydroxyurea group five (5%) of 111 had strokes with an incidence rate of 1·92 per 100 person-years (incidence rate ratio 0·62 [95% CI 0·10-3·20], p=0·77). The incidence rate ratio of hospitalisation for any reason was 1·71 (95% CI 1·15-2·57, p=0·0071), with higher incidence rates per 100 person-years in the low-dose group versus the moderate-dose group (27·43 vs 16·08). No participant had hydroxyurea treatment stopped for myelosuppression.
Interpretation: Compared with low-dose hydroxyurea therapy, participants treated with moderate-dose hydroxyurea had no difference in the stroke incidence rate. However, secondary analyses suggest that the moderate-dose group could lower incidence rates for all-cause hospitalisations. These findings provide an evidence-based guideline for the use of low-dose hydroxyurea therapy for children with sickle cell anaemia at risk of stroke.
Funding: National Institute of Neurological Disorders and Stroke.

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More information

e-pub ahead of print date: 28 December 2021
Published date: 2 January 2022
Additional Information: Funding Information: Research reported in this publication was supported by the National Institutes of Health Grant #1R01NS094041, K24HL147017, NIH/NCATS UL1 TR000445, 1K43TW011583, and the generous donation of the Phillips family. The sponsors did not have any role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication. The findings and conclusions in this paper are those of the authors and do not necessarily represent the official position of the National Institute of Health. We are posthumously thankful to our certified radiologist Shehi Ali, who tirelessly worked to certify physicians and nurses to conduct the transcranial Doppler assessments in Nigeria. Without his effort, this trial would not have been completed. We are grateful to our research coordinators and study personnel who tirelessly coordinated the trial in Kano and Kaduna, Nigeria. We appreciate Bilya Sani Musa, Mustafa Nateqi, Khadijah Bulama, Murtala Umar, Charity Dooshima Agba-Dooyum, Fahad Usman, Abdulrasheed Sani, Awwal Gambo, Jamila Ibrahim, Gloria Bahago, Jamil Galadanci, Leshana Saint Jean, and Jennifer C Beck for facilitating administrative tasks required for the successful conduct of this study. Publisher Copyright: © 2022 Elsevier Ltd
Keywords: Anemia, Sickle Cell/complications, Antisickling Agents/therapeutic use, Child, Preschool, Double-Blind Method, Female, Humans, Hydroxyurea/therapeutic use, Nigeria, Stroke/etiology

Identifiers

Local EPrints ID: 474752
URI: http://eprints.soton.ac.uk/id/eprint/474752
ISSN: 2352-3026
PURE UUID: ec5e1c06-3810-4549-8afe-88d1ff4cb4a8
ORCID for Fenella J Kirkham: ORCID iD orcid.org/0000-0002-2443-7958

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Date deposited: 02 Mar 2023 17:41
Last modified: 17 Mar 2024 02:53

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Contributors

Author: Shehu U Abdullahi
Author: Binta W Jibir
Author: Halima Bello-Manga
Author: Safiya Gambo
Author: Hauwa Inuwa
Author: Aliyu G Tijjani
Author: Nura Idris
Author: Aisha Galadanci
Author: Mustapha S Hikima
Author: Najibah Galadanci
Author: Awwal Borodo
Author: Abdulkadir M Tabari
Author: Lawal Haliru
Author: Aisha Suleiman
Author: Jamila Ibrahim
Author: Brittany C Greene
Author: Djamila L Ghafuri
Author: Mark Rodeghier
Author: James C Slaughter
Author: Kathleen Neville
Author: Adetola Kassim
Author: Edwin Trevathan
Author: Lori C Jordan
Author: Muktar H Aliyu
Author: Michael R DeBaun
Corporate Author: et al.

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