Literature DB >> 19061213

A pilot study of hydroxyurea to prevent chronic organ damage in young children with sickle cell anemia.

Courtney D Thornburg1, Natalia Dixon, Shelly Burgett, Nicole A Mortier, William H Schultz, Sherri A Zimmerman, Melanie Bonner, Kristina K Hardy, Agustin Calatroni, Russell E Ware.   

Abstract

BACKGROUND: Hydroxyurea improves laboratory parameters and prevents acute clinical complications of sickle cell anemia (SCA) in children and adults, but its effects on organ function remain incompletely defined.
METHODS: To assess the safety and efficacy of hydroxyurea in young children with SCA and to prospectively assess kidney and brain function, 14 young children (mean age 35 months) received hydroxyurea at a mean maximum tolerated dose (MTD) of 28 mg/kg/day.
RESULTS: After a mean of 25 months, expected laboratory effects included significant increases in hemoglobin, MCV and %HbF along with significant decreases in reticulocytes, absolute neutrophil count, and bilirubin. There was no significant increase in glomerular filtration rate by DTPA clearance or Schwartz estimate. Mean transcranial Doppler (TCD) velocity changes were -25.6 cm/sec (P < 0.01) and -26.8 cm/sec (P < 0.05) in the right and left MCA vessels, respectively. At study exit, no child had conditional or abnormal TCD values, and none developed brain ischemic lesions or vasculopathy progression by MRI/MRA. Growth and neurocognitive scores were preserved and Impact-on-Family scores improved.
CONCLUSIONS: These pilot data indicate hydroxyurea at MTD is well-tolerated by both children and families, and may prevent chronic organ damage in young children with SCA. (c) 2008 Wiley-Liss, Inc.

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Year:  2009        PMID: 19061213      PMCID: PMC5600482          DOI: 10.1002/pbc.21738

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


  38 in total

1.  Neurocognitive development of young children with sickle cell disease through three years of age.

Authors:  Robert J Thompson; Kathryn E Gustafson; Melanie J Bonner; Russell E Ware
Journal:  J Pediatr Psychol       Date:  2002 Apr-May

2.  Long-term hydroxyurea therapy for infants with sickle cell anemia: the HUSOFT extension study.

Authors:  Jane S Hankins; Russell E Ware; Zora R Rogers; Lynn W Wynn; Peter A Lane; J Paul Scott; Winfred C Wang
Journal:  Blood       Date:  2005-10-01       Impact factor: 22.113

3.  Neuropsychologic impairment in children with sickle cell anemia.

Authors:  A V Swift; M J Cohen; G W Hynd; J M Wisenbaker; K M McKie; G Makari; V C McKie
Journal:  Pediatrics       Date:  1989-12       Impact factor: 7.124

4.  Safety of hydroxyurea in children with sickle cell anemia: results of the HUG-KIDS study, a phase I/II trial. Pediatric Hydroxyurea Group.

Authors:  T R Kinney; R W Helms; E E O'Branski; K Ohene-Frempong; W Wang; C Daeschner; E Vichinsky; R Redding-Lallinger; B Gee; O S Platt; R E Ware
Journal:  Blood       Date:  1999-09-01       Impact factor: 22.113

5.  Subtle neuropsychological deficits in children with sickle cell disease.

Authors:  A L Wasserman; J A Wilimas; D L Fairclough; R K Mulhern; W Wang
Journal:  Am J Pediatr Hematol Oncol       Date:  1991

6.  Hydroxyurea for treatment of severe sickle cell anemia: a pediatric clinical trial.

Authors:  A Ferster; C Vermylen; G Cornu; M Buyse; F Corazza; C Devalck; P Fondu; M Toppet; E Sariban
Journal:  Blood       Date:  1996-09-15       Impact factor: 22.113

7.  A simple estimate of glomerular filtration rate in full-term infants during the first year of life.

Authors:  G J Schwartz; L G Feld; D J Langford
Journal:  J Pediatr       Date:  1984-06       Impact factor: 4.406

8.  Chemical and functional analysis of hydroxyurea oral solutions.

Authors:  Matthew M Heeney; Matthew R Whorton; Thad A Howard; Christina A Johnson; Russell E Ware
Journal:  J Pediatr Hematol Oncol       Date:  2004-03       Impact factor: 1.289

Review 9.  Clinical events in the first decade in a cohort of infants with sickle cell disease. Cooperative Study of Sickle Cell Disease.

Authors:  F M Gill; L A Sleeper; S J Weiner; A K Brown; R Bellevue; R Grover; C H Pegelow; E Vichinsky
Journal:  Blood       Date:  1995-07-15       Impact factor: 22.113

10.  Hydroxyurea therapy lowers TCD velocities in children with sickle cell disease.

Authors:  Tonya Kratovil; Dorothy Bulas; M Catherine Driscoll; Barbara Speller-Brown; Robert McCarter; Caterina P Minniti
Journal:  Pediatr Blood Cancer       Date:  2006-12       Impact factor: 3.167

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  38 in total

1.  Differences in health-related quality of life in children with sickle cell disease receiving hydroxyurea.

Authors:  Courtney D Thornburg; Agustin Calatroni; Julie A Panepinto
Journal:  J Pediatr Hematol Oncol       Date:  2011-05       Impact factor: 1.289

Review 2.  Hydroxyurea for children with sickle cell disease.

Authors:  Matthew M Heeney; Russell E Ware
Journal:  Hematol Oncol Clin North Am       Date:  2010-02       Impact factor: 3.722

3.  Hydroxyurea for Children with Sickle Cell Anemia in Sub-Saharan Africa.

Authors:  Léon Tshilolo; George Tomlinson; Thomas N Williams; Brígida Santos; Peter Olupot-Olupot; Adam Lane; Banu Aygun; Susan E Stuber; Teresa S Latham; Patrick T McGann; Russell E Ware
Journal:  N Engl J Med       Date:  2018-12-01       Impact factor: 91.245

4.  Robust clinical and laboratory response to hydroxyurea using pharmacokinetically guided dosing for young children with sickle cell anemia.

Authors:  Patrick T McGann; Omar Niss; Min Dong; Anu Marahatta; Thad A Howard; Tomoyuki Mizuno; Adam Lane; Theodosia A Kalfa; Punam Malik; Charles T Quinn; Russell E Ware; Alexander A Vinks
Journal:  Am J Hematol       Date:  2019-06-12       Impact factor: 10.047

5.  Adherence to hydroxyurea therapy in children with sickle cell anemia.

Authors:  Courtney D Thornburg; Agustin Calatroni; Marilyn Telen; Alex R Kemper
Journal:  J Pediatr       Date:  2009-11-01       Impact factor: 4.406

Review 6.  Hydroxyurea in sickle cell disease: drug review.

Authors:  Rohit Kumar Agrawal; Rakesh Kantilal Patel; Varsha Shah; Lalit Nainiwal; Bhadra Trivedi
Journal:  Indian J Hematol Blood Transfus       Date:  2013-05-24       Impact factor: 0.900

7.  Hydroxycarbamide in very young children with sickle-cell anaemia: a multicentre, randomised, controlled trial (BABY HUG).

Authors:  Winfred C Wang; Russell E Ware; Scott T Miller; Rathi V Iyer; James F Casella; Caterina P Minniti; Sohail Rana; Courtney D Thornburg; Zora R Rogers; Ram V Kalpatthi; Julio C Barredo; R Clark Brown; Sharada A Sarnaik; Thomas H Howard; Lynn W Wynn; Abdullah Kutlar; F Daniel Armstrong; Beatrice A Files; Jonathan C Goldsmith; Myron A Waclawiw; Xiangke Huang; Bruce W Thompson
Journal:  Lancet       Date:  2011-05-14       Impact factor: 79.321

8.  Hydroxyurea treatment decreases glomerular hyperfiltration in children with sickle cell anemia.

Authors:  Banu Aygun; Nicole A Mortier; Matthew P Smeltzer; Barry L Shulkin; Jane S Hankins; Russell E Ware
Journal:  Am J Hematol       Date:  2012-12-17       Impact factor: 10.047

9.  Hemoglobin F as a predictor of health-related quality of life in children with sickle cell anemia.

Authors:  Mohamed-Rachid Boulassel; Amira Al-Badi; Mohamed Elshinawy; Juhaina Al-Hinai; Muna Al-Saadoon; Zahra Al-Qarni; Hammad Khan; Rizwan Nabi Qureshi; Yasser Wali
Journal:  Qual Life Res       Date:  2018-10-22       Impact factor: 4.147

10.  Role of hydroxycarbamide in prevention of complications in patients with sickle cell disease.

Authors:  Nm Wiles; J Howard
Journal:  Ther Clin Risk Manag       Date:  2009-09-24       Impact factor: 2.423

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