Literature DB >> 18293380

Resolution of chronic hypoxemia in pediatric sickle cell patients after treatment with hydroxyurea.

Sharon A Singh1, Anastassios C Koumbourlis, Banu Aygun.   

Abstract

Chronic hypoxemia is a common manifestation among patients with sickle cell anemia (SCA) who develop chronic lung disease. We report the beneficial effect of hydroxyurea on chronic hypoxemia in three pediatric patients with SCA and recurrent episodes of acute chest syndrome (ACS). All three patients improved rapidly after they were treated with hydroxyurea despite having additional risk factors for hypoxemia. A prospective trial is warranted to assess whether there is a therapeutic effect from the use of hydroxyurea in pediatric SCA patients with chronic hypoxemia. (c) 2007 Wiley-Liss, Inc.

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Year:  2008        PMID: 18293380     DOI: 10.1002/pbc.21480

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


  12 in total

Review 1.  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

2.  The association between hydroxyurea treatment and pain intensity, analgesic use, and utilization in ambulatory sickle cell anemia patients.

Authors:  Wally R Smith; Samir K Ballas; William F McCarthy; Robert L Bauserman; Paul S Swerdlow; Martin H Steinberg; Myron A Waclawiw
Journal:  Pain Med       Date:  2011-04-11       Impact factor: 3.750

Review 3.  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

Review 4.  Pharmacotherapy in sickle cell disease--state of the art and future prospects.

Authors:  Jane Hankins; Banu Aygun
Journal:  Br J Haematol       Date:  2009-02-17       Impact factor: 6.998

5.  Haemoglobin oxygen saturation is a determinant of cerebral artery blood flow velocity in children with sickle cell anaemia.

Authors:  Charles T Quinn; Jennifer Variste; Michael M Dowling
Journal:  Br J Haematol       Date:  2009-03-05       Impact factor: 6.998

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

Authors:  Courtney D Thornburg; Natalia Dixon; Shelly Burgett; Nicole A Mortier; William H Schultz; Sherri A Zimmerman; Melanie Bonner; Kristina K Hardy; Agustin Calatroni; Russell E Ware
Journal:  Pediatr Blood Cancer       Date:  2009-05       Impact factor: 3.167

7.  Hydroxyurea Improves Oxygen Saturation in Children With Sickle Cell Disease.

Authors:  Farzana D Pashankar; Deepa Manwani; Margaret T Lee; Nancy S Green
Journal:  J Pediatr Hematol Oncol       Date:  2015-04       Impact factor: 1.289

8.  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

9.  A 2-year-old girl with co-inherited cystic fibrosis and sickle cell-β+ thalassemia presenting with recurrent vaso-occlusive events during cystic fibrosis pulmonary exacerbations: a case report.

Authors:  Kurtis T Sobush; Courtney D Thornburg; Judith A Voynow; Stephanie D Davis; Stacey L Peterson-Carmichael
Journal:  J Med Case Rep       Date:  2013-07-26

Review 10.  Asthma management in sickle cell disease.

Authors:  Esteban Gomez; Claudia R Morris
Journal:  Biomed Res Int       Date:  2013-11-10       Impact factor: 3.411

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