Literature DB >> 29056404

Changes in Transcranial Doppler Flow Velocities in Children with Sickle Cell Disease: The Impact of Hydroxyurea Therapy.

Samuel Ademola Adegoke1, Rejane de Souza Macedo-Campos2, Josefina Aparecida Pellegrini Braga3, Maria Stella Figueiredo4, Gisele Sampaio Silva5.   

Abstract

BACKGROUND AND OBJECTIVES: Hydroxyurea (HU) was recently described as a substitute for chronic transfusion for children with sickle cell disease (SCD) and abnormal transcranial Doppler (TCD) velocities who have received at least 1 year of transfusions. However, the role of HU in reverting elevated TCD velocities in patients not treated with transfusion is still debatable. The objective of the study was to examine whether HU influences the progression of TCD velocities in children with SCD. PATIENTS AND METHODS: Children with SCD with at least 2 TCDs not less than 6 months apart were evaluated over 51 months. Time-averaged maximum mean (TAMM) velocities for the initial and the last transcranial Doppler examinations were noted and differences compared between HU and HU-naive groups.
RESULTS: Overall, 68.8% of the HU-group with elevated TCD velocities compared with 40.0% of the HU-naive experienced TCD reversal (P = .047). A higher proportion of the HU-naive group, 7 (14.3%) versus 9.8% of the HU group experienced TCD conversion. Those with initial conditional velocities in the HU-group experienced a significant reduction in TAMM velocities (from 176.8 ± 5.3 to 162.7 ± 13.9 cm/s, difference of 14.1 cm/s; P = .001) unlike those in the HU-naive group (176.3 ± 5.3 to 170.0 ± 18.6 cm/s, difference of 6.3 cm/s; P = .148). The change in the TAMM velocities was also significantly higher among the HU-group (14.1 ± 12.4 cm/s versus 6.3 ± 18.5 cm/s, P = .015).
CONCLUSION: Our data suggest a beneficial role of HU in TCD velocity reduction in patients not treated with chronic transfusions, particularly among those with initial conditional TCD velocities.
Copyright © 2018 National Stroke Association. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Children; chronic blood transfusions; hydroxyurea; sickle cell disease; transcranial Doppler

Mesh:

Substances:

Year:  2017        PMID: 29056404     DOI: 10.1016/j.jstrokecerebrovasdis.2017.09.020

Source DB:  PubMed          Journal:  J Stroke Cerebrovasc Dis        ISSN: 1052-3057            Impact factor:   2.136


  12 in total

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3.  Low Stroke Risk in Children With Sickle Cell Disease in French Guiana: A Retrospective Cohort Study.

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4.  Primary prevention of stroke in children with sickle cell anemia in sub-Saharan Africa: rationale and design of phase III randomized clinical trial.

Authors:  Shehu U Abdullahi; Binta J Wudil; Halima Bello-Manga; Aisha B Musa; Safiya Gambo; Najibah A Galadanci; Hauwa Aminu; Aliyu Tijjani Gaya; Surayya Sanusi; Musa A Tabari; Aisha Galadanci; Awwal Borodo; Muhammed S Abba; Abdu H Dambatta; Lawal Haliru; Awwal Gambo; Holly Cassell; Mark Rodeghier; Djamila L Ghafuri; Brittany V Covert Greene; Kathleen Neville; Adetola A Kassim; Fenella Kirkham; Edwin Trevathan; Lori C Jordan; Muktar H Aliyu; Michael R DeBaun
Journal:  Pediatr Hematol Oncol       Date:  2020-11-25       Impact factor: 1.969

5.  Hydroyxurea improves cerebral oxygen saturation in children with sickle cell anemia.

Authors:  Kristine Karkoska; Charles T Quinn; Omar Niss; Amanda Pfeiffer; Min Dong; Alexander A Vinks; Patrick T McGann
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Journal:  Health Qual Life Outcomes       Date:  2019-10-16       Impact factor: 3.186

7.  Evidence-based interventions implemented in low-and middle-income countries for sickle cell disease management: A systematic review of randomized controlled trials.

Authors:  Joyce Gyamfi; Temitope Ojo; Sabrina Epou; Amy Diawara; Lotanna Dike; Deborah Adenikinju; Scholastica Enechukwu; Dorice Vieira; Obiageli Nnodu; Gbenga Ogedegbe; Emmanuel Peprah
Journal:  PLoS One       Date:  2021-02-17       Impact factor: 3.240

8.  Hydroxyurea reduces cerebral metabolic stress in patients with sickle cell anemia.

Authors:  Melanie E Fields; Kristin P Guilliams; Dustin Ragan; Michael M Binkley; Amy Mirro; Slim Fellah; Monica L Hulbert; Morey Blinder; Cihat Eldeniz; Katie Vo; Joshua S Shimony; Yasheng Chen; Robert C McKinstry; Hongyu An; Jin-Moo Lee; Andria L Ford
Journal:  Blood       Date:  2019-03-11       Impact factor: 22.113

9.  American Society of Hematology 2020 guidelines for sickle cell disease: prevention, diagnosis, and treatment of cerebrovascular disease in children and adults.

Authors:  M R DeBaun; L C Jordan; A A King; J Schatz; E Vichinsky; C K Fox; R C McKinstry; P Telfer; M A Kraut; L Daraz; F J Kirkham; M H Murad
Journal:  Blood Adv       Date:  2020-04-28

10.  Hydroxyurea treatment and neurocognitive functioning in sickle cell disease from school age to young adulthood.

Authors:  Andrew M Heitzer; Jennifer Longoria; Victoria Okhomina; Winfred C Wang; Darcy Raches; Brian Potter; Lisa M Jacola; Jerlym Porter; Jane E Schreiber; Allison A King; Guolian Kang; Jane S Hankins
Journal:  Br J Haematol       Date:  2021-07-16       Impact factor: 8.615

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