HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

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

AbstractBACKGROUND:
Although hydroxyurea is the only effective agent for the treatment of sickle cell disease, published experience with this drug is limited to treatment of homozygous sickle cell anemia and HbS/β thalassemia. The role of hydroxyurea in the treatment of patients with HbSD-Punjab, a rare hemoglobinopathy with phenotypic expression similar to that of sickle cell anemia is unknown.
PROCEDURE:
Over a period of 10 years, we followed 42 patients with HbSD-Punjab, of which 20 presented with severe clinical manifestations (≥3 episodes of VOC and/or ≥2 units of blood transfusion in the previous 12 months). These 20 patients were enrolled for treatment with hydroxyurea at a dose of 10 mg/kg/day and followed prospectively for a period of 24 months.
RESULTS:
The frequency of VOC decreased significantly and none of them required blood transfusion while receiving hydroxyurea. The HbF, total hemoglobin, MCV, MCH, and MCHC levels increased significantly, whereas HbS, WBC, platelet count, total serum bilirubin, and LDH levels decreased significantly in all the patients. No short-term drug toxicity was observed.
CONCLUSION:
This study describes the use of hydroxyurea therapy in patients with HbSD-Punjab. Low dose hydroxyurea (10 mg/kg/day) was found to be effective in reducing the clinical severity in patients with HbSD-Punjab without any short-term toxicity. In view of easy affordability amongst poor patients, widespread acceptability by patients and doctors, the need of infrequent monitoring and its potential effectiveness, low dose hydroxyurea is suitable for treatment of patients with HbSD-Punjab.
AuthorsSiris Patel, Prasanta Purohit, Ranjeet Singh Mashon, Snehadhini Dehury, Satyabrata Meher, Sulia Sahoo, Subhransu Sekhar Dash, Kishalaya Das, Padmalaya Das, Dilip Kumar Patel
JournalPediatric blood & cancer (Pediatr Blood Cancer) Vol. 61 Issue 8 Pg. 1341-6 (Aug 2014) ISSN: 1545-5017 [Electronic] United States
PMID24616059 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Copyright© 2014 Wiley Periodicals, Inc.
Chemical References
  • Antisickling Agents
  • Hemoglobins, Abnormal
  • hemoglobin D Punjab
  • Hydroxyurea
Topics
  • Adult
  • Antisickling Agents (administration & dosage, adverse effects)
  • Child
  • Child, Preschool
  • Female
  • Follow-Up Studies
  • Hemoglobins, Abnormal
  • Heterozygote
  • Humans
  • Hydroxyurea (administration & dosage, adverse effects)
  • India
  • Infant
  • Male

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: