Literature DB >> 26557561

Clinical and Haematological Effects of Hydroxyurea in β-Thalassemia Intermedia Patients.

Bijan Keikhaei1, Homayon Yousefi2, Mohammad Bahadoram3.   

Abstract

INTRODUCTION: It is well known that hydroxyurea (HU) impacts on clinical and haematologic indices in thalassemia. We aimed to evaluate the effect of hydroxyurea on clinical and haematological improvement in children with thalassemia intermedia.
MATERIALS AND METHODS: After the patients' enrollment in the study their data such as transfusion, hospitalization, spleen size, visit, total Hb, HbF levels, MCV and MCH were compared before and after treatment with HU 10 mg/kg/day/for one year.
RESULTS: In patients with thalassemia intermedia, HU significantly diminished the rate of transfusion, hospitalization, spleen size and significantly increased Hb MCH, HbF and MCV. Moreover HU was well tolerated in our patients and we got no remarkable adverse effect.
CONCLUSION: We divulged hydroxyurea 10 mg/kg/day during one year. This significantly increased HbF, total haemoglobin, MCV, MCH, without any remarkable adverse events.

Entities:  

Keywords:  Adverse effects; Fetal hemoglobin; Hematologic tests; Hospitalization; Spleen; Treatment outcome

Year:  2015        PMID: 26557561      PMCID: PMC4625280          DOI: 10.7860/JCDR/2015/14807.6660

Source DB:  PubMed          Journal:  J Clin Diagn Res        ISSN: 0973-709X


  13 in total

1.  Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India.

Authors:  Khushnooma Y Italia; Farah J Jijina; Rashid Merchant; Sangeeta Panjwani; Anita H Nadkarni; Pratibha M Sawant; Sona B Nair; Kanjaksha Ghosh; Roshan B Colah
Journal:  Clin Chim Acta       Date:  2009-06-21       Impact factor: 3.786

2.  The effect of hydroxyurea on compound heterozygotes for sickle cell-hemoglobin D-Punjab--a single centre experience in eastern India.

Authors:  Siris Patel; Prasanta Purohit; Ranjeet Singh Mashon; Snehadhini Dehury; Satyabrata Meher; Sulia Sahoo; Subhransu Sekhar Dash; Kishalaya Das; Padmalaya Das; Dilip Kumar Patel
Journal:  Pediatr Blood Cancer       Date:  2014-02-24       Impact factor: 3.167

3.  Hematologic and clinical responses of thalassemia intermedia patients to hydroxyurea during 6 years of therapy in Iran.

Authors:  Mehran Karimi; Hadi Darzi; Majid Yavarian
Journal:  J Pediatr Hematol Oncol       Date:  2005-07       Impact factor: 1.289

4.  Hydroxyurea therapy requires HbF induction for clinical benefit in a sickle cell mouse model.

Authors:  Jeffrey D Lebensburger; Tamara I Pestina; Russell E Ware; Kelli L Boyd; Derek A Persons
Journal:  Haematologica       Date:  2010-04-07       Impact factor: 9.941

Review 5.  Hydroxyurea for the treatment of sickle cell disease.

Authors:  Jodi B Segal; John J Strouse; Mary Catherine Beach; Carlton Haywood; Catherine Witkop; Haeseong Park; Renee F Wilson; Eric B Bass; Sophie Lanzkron
Journal:  Evid Rep Technol Assess (Full Rep)       Date:  2008-03

Review 6.  Hydroxyurea-induced hematological response in transfusion-independent beta-thalassemia intermedia: case series and review of literature.

Authors:  Mohammad Ali Ehsani; Amir Abbas Hedayati-Asl; Alireza Bagheri; Syrus Zeinali; Armin Rashidi
Journal:  Pediatr Hematol Oncol       Date:  2009-11       Impact factor: 1.969

Review 7.  Clinical experience with fetal hemoglobin induction therapy in patients with β-thalassemia.

Authors:  Khaled M Musallam; Ali T Taher; Maria Domenica Cappellini; Vijay G Sankaran
Journal:  Blood       Date:  2013-01-11       Impact factor: 22.113

8.  Low dose hydroxyurea is effective in reducing the incidence of painful crisis and frequency of blood transfusion in sickle cell anemia patients from eastern India.

Authors:  Dilip K Patel; Ranjeet S Mashon; Siris Patel; Bhabani S Das; Prasanta Purohit; Subasa C Bishwal
Journal:  Hemoglobin       Date:  2012       Impact factor: 0.849

9.  Hydroxyurea therapy in 49 patients with major beta-thalassemia.

Authors:  Farhad Zamani; Ramin Shakeri; Seyyedeh-Masoomeh Eslami; Seyyed-Mohsen Razavi; Ali Basi
Journal:  Arch Iran Med       Date:  2009-05       Impact factor: 1.354

10.  Side effects of hydroxyurea in patients with Thalassemia major and thalassemia intermedia and sickle cell anemia.

Authors:  A Ghasemi; B Keikhaei; R Ghodsi
Journal:  Iran J Ped Hematol Oncol       Date:  2014-07-20
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  5 in total

1.  Long-term safety and efficacy of hydroxyurea in patients with non-transfusion-dependent β-thalassemia: a comprehensive single-center experience.

Authors:  Mehran Karimi; Tahereh Zarei; Ardeshir Bahmanimehr; Azam Aramesh; Saeed Daryanoush; Sezaneh Haghpanah
Journal:  Ann Hematol       Date:  2021-08-12       Impact factor: 3.673

Review 2.  A comprehensive review of hydroxyurea for β-haemoglobinopathies: the role revisited during COVID-19 pandemic.

Authors:  Nirmani Yasara; Anuja Premawardhena; Sachith Mettananda
Journal:  Orphanet J Rare Dis       Date:  2021-03-01       Impact factor: 4.123

3.  Trends in 5-, 10-, 20-, and 30-year survival rates of beta-thalassemia patients in Southern Iran, 1995-2016: A retrospective cohort study.

Authors:  Jafar Hassanzadeh; Alireza Mirahmadizadeh; Mehran Karimi; Yousef Veisani; Shahab Rezaeian
Journal:  J Public Health Res       Date:  2017-12-13

Review 4.  Pharmacological Induction of Fetal Hemoglobin in β-Thalassemia and Sickle Cell Disease: An Updated Perspective.

Authors:  Rayan Bou-Fakhredin; Lucia De Franceschi; Irene Motta; Maria Domenica Cappellini; Ali T Taher
Journal:  Pharmaceuticals (Basel)       Date:  2022-06-16

Review 5.  Epigenetic Insights and Potential Modifiers as Therapeutic Targets in β-Thalassemia.

Authors:  Nur Atikah Zakaria; Md Asiful Islam; Wan Zaidah Abdullah; Rosnah Bahar; Abdul Aziz Mohamed Yusoff; Ridhwan Abdul Wahab; Shaharum Shamsuddin; Muhammad Farid Johan
Journal:  Biomolecules       Date:  2021-05-18
  5 in total

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