Literature DB >> 17984691

Efficacy of hydroxyurea (HU) in reduction of pack red cell (PRC) transfusion requirement among children having beta-thalassemia major: Karachi HU trial (KHUT).

Saqib H Ansari1, Tahir S Shamsi, Fahad J Siddiqui, Muhammad Irfan, Kausar Perveen, Tasneem Farzana, Vinodh K Panjwani, Ayesha Yousuf, Tabassum Mehboob.   

Abstract

BACKGROUND: Packed red blood cell (PRC) transfusion with iron chelation is the mainstay of treatment for patients with beta-thalassemia major. Hemoglobin F augmentation is another approach to treat this hemoglobinopathy. This study evaluates the efficacy and safety of hydroxyurea (HU) in minimizing PRC transfusions in patients with beta-thalassemia major.
METHOD: Twenty-three patients with beta-thalassemia major received HU at a mean dose of 16 mg/kg/d. The results were analyzed at the end of 24 months. Transfusion requirement during the 6 months preceding the study was considered as the control. RESULT: Twenty patients were evaluable after 24 months. The mean volume of PRC transfused was reduced from 2126.45 mL to 1489.59 mL (P<0.001). The interval between transfusions was increased by 68.7%. Grade I myelosuppression was observed in 4 patients and diarrhea in 2 patients.
CONCLUSIONS: HU was found to be safe in patients with beta-thalassemia major, and resulted in reduction in the transfusion requirements and in increase of the intervals between transfusions.

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Year:  2007        PMID: 17984691     DOI: 10.1097/MPH.0b013e318157fd75

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN: 1077-4114            Impact factor:   1.289


  3 in total

1.  Managing thalassemia in the developing world: an evidence-based approach for prevention, transfusion independency, and curative treatment with hematopoietic stem cell transplantation.

Authors:  Saqib Hussain Ansari; Sadia Parveen; Saima Siddiqui; Kousar Perveen; Ghazala Ahmed; Bushra Kaleem; Shariq Ahmed; Muhammad Zohaib; Tasneem Farzana; Tahir Shamsi
Journal:  Blood Adv       Date:  2018-11-30

2.  Hydroxyurea (hydroxycarbamide) for transfusion-dependent β-thalassaemia.

Authors:  Saqib H Ansari; Zohra S Lassi; Salima M Khowaja; Syed Omair Adil; Tahir S Shamsi
Journal:  Cochrane Database Syst Rev       Date:  2019-03-16

3.  Hydroxyurea Treated β-Thalassemia Children Demonstrate a Shift in Metabolism Towards Healthy Pattern.

Authors:  Ayesha Iqbal; Saqib Hussain Ansari; Sadia Parveen; Ishtiaq Ahmad Khan; Amna Jabbar Siddiqui; Syed Ghulam Musharraf
Journal:  Sci Rep       Date:  2018-10-11       Impact factor: 4.379

  3 in total

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