Literature DB >> 28035747

Secondary benefit of maintaining normal transcranial Doppler velocities when using hydroxyurea for prevention of severe sickle cell anemia.

Djamila Labib Ghafuri1, Shruti Chaturvedi2, Mark Rodeghier3, Sarah-Jo Stimpson4, Brandi McClain4, Jeannie Byrd4, Michael R DeBaun4.   

Abstract

In a retrospective cohort study, we tested the hypothesis that when prescribing hydroxyurea (HU) to children with sickle cell anemia (SCA) to prevent vaso-occlusive events, there will be a secondary benefit of maintaining low transcranial Doppler (TCD) velocity, measured by imaging technique (TCDi). HU was prescribed for 90.9% (110 of 120) of children with SCA ≥5 years of age and followed for a median of 4.4 years, with 70% (n = 77) receiving at least one TCDi evaluation after starting HU. No child prescribed HU had a conditional or abnormal TCDi measurement. HU initiation for disease severity prevention decreases the prevalence of abnormal TCDi velocities.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  hydroxyurea therapy; red cells; sickle cell disease; transcranial Doppler velocity

Mesh:

Substances:

Year:  2016        PMID: 28035747     DOI: 10.1002/pbc.26401

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  7 in total

1.  Associations of transcranial doppler velocity, age, and gender with cognitive function in children with sickle cell anemia in Nigeria.

Authors:  Kemar V Prussien; Auwal Salihu; Shehu U Abdullahi; Najibah A Galadanci; Khadija Bulama; Raymond O Belonwu; Fenella J Kirkham; Janet Yarboi; Heather Bemis; Michael R DeBaun; Bruce E Compas
Journal:  Child Neuropsychol       Date:  2018-10-01       Impact factor: 2.500

2.  Correlates of Cognitive Function in Sickle Cell Disease: A Meta-Analysis.

Authors:  Kemar V Prussien; Rachel E Siciliano; Abagail E Ciriegio; Allegra S Anderson; Radha Sathanayagam; Michael R DeBaun; Lori C Jordan; Bruce E Compas
Journal:  J Pediatr Psychol       Date:  2020-03-01

3.  Targeted Hydroxyurea Education after an Emergency Department Visit Increases Hydroxyurea Use in Children with Sickle Cell Anemia.

Authors:  Lydia H Pecker; Sarah Kappa; Adam Greenfest; Deepika S Darbari; Robert Sheppard Nickel
Journal:  J Pediatr       Date:  2018-06-29       Impact factor: 4.406

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.  Transcranial Doppler Screening in a Current Cohort of Children With Sickle Cell Anemia: Results From the DISPLACE Study.

Authors:  Julie Kanter; Shannon Phillips; Alyssa M Schlenz; Martina Mueller; Mary Dooley; Logan Sirline; Robert Nickel; Robert Clark Brown; Lee Hilliard; Cathy L Melvin; Robert J Adams
Journal:  J Pediatr Hematol Oncol       Date:  2021-11-01       Impact factor: 1.289

6.  Combination dose-escalated hydroxyurea and transfusion: an approach to conserve blood during the COVID-19 pandemic.

Authors:  Robert Sheppard Nickel; Stefanie Margulies; Brittany Frazer; Naomi L C Luban; Jennifer Webb
Journal:  Blood       Date:  2020-06-18       Impact factor: 22.113

7.  Initiating adjunct low-dose hydroxyurea therapy for stroke prevention in children with SCA during the COVID-19 pandemic.

Authors:  Michael R DeBaun
Journal:  Blood       Date:  2020-05-28       Impact factor: 22.113

  7 in total

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