Literature DB >> 21744485

Massive accidental overdose of hydroxyurea in a young child with sickle cell anemia.

Scott T Miller1, Kathy Rey, Jin He, Jonathan Flanagan, Billie J Fish, Zora R Rogers, Winfred C Wang, Russell E Ware.   

Abstract

The Pediatric Hydroxyurea Phase III Clinical Trial (BABY HUG) confirmed safety and efficacy of hydroxyurea therapy for infants with sickle cell anemia. Treatment was associated with reduction in rates of pain, acute chest syndrome, hospitalizations, and blood transfusions; improved hematologic values; and, perhaps, preservation of organ function. During the study, a 2-year-old ingested at one time an entire 35-day supply of hydroxyurea (612 mg/kg body weight). Despite a serum level of 7,756 µM 4 hours post-ingestion, the only toxicity was transient mild myelosuppression. With wider usage of hydroxyurea anticipated, conservative management of future overdoses seems reasonable (ClinicalTrials.gov NCT00006400).
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 21744485      PMCID: PMC3193862          DOI: 10.1002/pbc.23244

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


  20 in total

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Authors: 
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2.  A bioavailability and pharmacokinetic study of oral and intravenous hydroxyurea.

Authors:  G I Rodriguez; J G Kuhn; G R Weiss; S G Hilsenbeck; J R Eckardt; A Thurman; D A Rinaldi; S Hodges; D D Von Hoff; E K Rowinsky
Journal:  Blood       Date:  1998-03-01       Impact factor: 22.113

3.  Effect of hydroxyurea on mortality and morbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment.

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Journal:  JAMA       Date:  2003-04-02       Impact factor: 56.272

4.  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

5.  A two-year pilot trial of hydroxyurea in very young children with sickle-cell anemia.

Authors:  W C Wang; L W Wynn; Z R Rogers; J P Scott; P A Lane; R E Ware
Journal:  J Pediatr       Date:  2001-12       Impact factor: 4.406

Review 6.  How I use hydroxyurea to treat young patients with sickle cell anemia.

Authors:  Russell E Ware
Journal:  Blood       Date:  2010-03-11       Impact factor: 22.113

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8.  Hydroxyurea: effects on hemoglobin F production in patients with sickle cell anemia.

Authors:  S Charache; G J Dover; R D Moore; S Eckert; S K Ballas; M Koshy; P F Milner; E P Orringer; G Phillips; O S Platt
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Authors:  Matthew M Heeney; Matthew R Whorton; Thad A Howard; Christina A Johnson; Russell E Ware
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10.  Studies of hydroxyurea administered by continuous infusion: toxicity, pharmacokinetics, and cell synchronization.

Authors:  R J Belt; C D Haas; J Kennedy; S Taylor
Journal:  Cancer       Date:  1980-08-01       Impact factor: 6.860

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  4 in total

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Authors:  Noemi Ba Roy; Patricia M Fortin; Katherine R Bull; Carolyn Doree; Marialena Trivella; Sally Hopewell; Lise J Estcourt
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Review 2.  Hydroxyurea (hydroxycarbamide) for sickle cell disease.

Authors:  Angela E Rankine-Mullings; Sarah J Nevitt
Journal:  Cochrane Database Syst Rev       Date:  2022-09-01

Review 3.  Hydroxyurea (hydroxycarbamide) for sickle cell disease.

Authors:  Sarah J Nevitt; Ashley P Jones; Jo Howard
Journal:  Cochrane Database Syst Rev       Date:  2017-04-20

4.  Safety and efficacy of plerixafor dose escalation for the mobilization of CD34+ hematopoietic progenitor cells in patients with sickle cell disease: interim results.

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Journal:  Haematologica       Date:  2018-02-01       Impact factor: 9.941

  4 in total

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