Literature DB >> 10771862

Hematological responses to hydroxyurea therapy in multitransfused thalassemic children.

V P Choudhry1, A Lal, H P Pati, L S Arya.   

Abstract

Fifteen multi-transfused thalassemic children between 3-6 years of age (seven boys and eight girls) were administered hydroxyurea for 5 days and three such cycles were repeated at 15 days interval. Rise in hemoglobin levels was observed in 13, 8 and 7 cases, while rise in mean hemoglobin F was seen in 8, 11 and 10 cases following 1st, 2nd and 3rd course of hydroxyurea therapy respectively. Rise in hemoglobin level was associated with transient rise in fetal hemoglobin level. Though the changes in mean hemoglobin levels and hemoglobin F levels were statistically insignificant, a definite trend of rise in hemoglobin and hemoglobin F was observed.

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Year:  1997        PMID: 10771862     DOI: 10.1007/bf02845212

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN: 0019-5456            Impact factor:   1.967


  11 in total

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Journal:  Br J Haematol       Date:  1979-02       Impact factor: 6.998

6.  Hematologic responses of patients with sickle cell disease to treatment with hydroxyurea.

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Journal:  N Engl J Med       Date:  1990-04-12       Impact factor: 91.245

7.  5-azacytidine selectively increases gamma-globin synthesis in a patient with beta+ thalassemia.

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Journal:  N Engl J Med       Date:  1982-12-09       Impact factor: 91.245

8.  Hydroxyurea-induced augmentation of fetal hemoglobin production in patients with sickle cell anemia.

Authors:  S Charache; G J Dover; M A Moyer; J W Moore
Journal:  Blood       Date:  1987-01       Impact factor: 22.113

9.  Hydroxyurea enhances fetal hemoglobin production in sickle cell anemia.

Authors:  O S Platt; S H Orkin; G Dover; G P Beardsley; B Miller; D G Nathan
Journal:  J Clin Invest       Date:  1984-08       Impact factor: 14.808

10.  Bone marrow transplantation for thalassemia.

Authors:  G Lucarelli; E Angelucci; C Giardini; D Baronciani; M Galimberti; P Polchi; B Erer
Journal:  Indian J Pediatr       Date:  1993 Jul-Aug       Impact factor: 1.967

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  3 in total

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Review 2.  Past, present & future scenario of thalassaemic care & control in India.

Authors:  Ishwar C Verma; Renu Saxena; Sudha Kohli
Journal:  Indian J Med Res       Date:  2011-10       Impact factor: 2.375

3.  Hydroxyurea Treatment in Transfusion-Dependent β-Thalassemia Patients.

Authors:  Mohammad Reza Bordbar; Samir Silavizadeh; Sezaneh Haghpanah; Roza Kamfiroozi; Marzieh Bardestani; Mehran Karimi
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  3 in total

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