Skip to main content

Advertisement

Log in

Beneficial Effect of Low Fixed Dose of Hydroxyurea in Vaso-occlusive Crisis and Transfusion Requirements in Adult HbSS Patients: A Prospective Study in a Tertiary Care Center

  • Original Article
  • Published:
Indian Journal of Hematology and Blood Transfusion Aims and scope Submit manuscript

Abstract

Significant reduction in morbidity and mortality have been documented in patients with sickle cell disease (HbSS) by most of the studies using hydroxyurea at a dose of 25–35 mg/kg/day or maximum tolerated dose. But toxicities, need for frequent monitoring, compliance and cost are important hurdles particularly in Indian set up. We undertook this study to find out the efficacy, safety compliance rate of low fixed dose of hydroxyurea (10 mg/kg/day) in patients presenting to our hospital and its impact on clinical profile and laboratory parameters. A cohort of 128 (82 males, 46 females) confirmed HbSS cases (each >18 years age, vaso-occlusive crisis >2/years and/ or rate of transfusion 1–2 units/month) with no disease related end organ damage were assessed prospectively between 2013 and 2016. They were started on 10 mg/kg/day hydroxyurea along with other supportive care and followed up monthly for 1 year. Clinical and laboratory parameters before and after therapy were reviewed and compared. In 92% of cases presenting with repeated vaso-occlusive crisis, VOC disappeared completely during follow up and in 8% we found significant reduction in severity as well as frequency of attacks (p < 0.01). Again in 87%, no further transfusion was required during follow up and in 13%, it further reduced the rate of transfusion (p < 0.01). The median time of response for VOC was 3 months and in transfusion requirement was 5 months. There was also significant reduction in S.Billirubin, S.LDH, disease related complications and rate of hospitalisation with significant improvement in Hb, MCV, and MCH. There is insignificant increase in HbF with median (1.5–2.4)% and in 5 cases >5%. We did not find any remarkable adverse effect of the drug during the study period. Low fixed dose hydroxyurea (10 mg/kg/day) is beneficial in reducing the vaso-occlusive crisis and transfusion requirement in adult HbSS Patients (Arab-Indian Haplotype). It is safe, suitable and is a effective mode of treatment in resource poor setting like India.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2

Similar content being viewed by others

References

  1. Charache S, Terrin ML, Moore RD et al (1995) Investigators of the multicenter study of hydroxyurea in sickle cell anemia. Effect of hydroxyurea on the frequency of painful crises in sickle cell anemia. N Engl J Med 332(20):1317–1322

    Article  CAS  PubMed  Google Scholar 

  2. Gilmore A, Cho G, Howard J et al (2011) North West London Haemoglobinopathy Registry Group. Feasibility and benefit of hydroxycarbamide as a long-term treatment for sickle cell disease patients: results from the North West London Sickle Cell Disease Registry. Am J Hematol 86(11):958–961

    Article  CAS  PubMed  Google Scholar 

  3. Lobo CL, Pinto JF, Nascimento EM, Moura PG, Cardoso GP, Hankins JS (2013) The effect of hydroxcarbamide therapy on survival of children with sickle cell disease. Br J Haematol 161(6):852–860

    Article  CAS  PubMed  Google Scholar 

  4. Ware RE, Helms RW, SWiTCH Investigators (2012) Stroke with transfusions changing to hydroxyurea (SWiTCH). Blood 119(17):3925–3932

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  5. Patel DK, Mashon RS, Patel S, Das BS, Purohit P, Bishwal SC (2012) 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. Hemoglobin 36:409–420

    Article  CAS  PubMed  Google Scholar 

  6. Jain DL, Apte M, Colah R, Sarathi V, Desai S, Gokhale A et al (2013) Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: a single centre experience. Indian Pediatr 50(10):929–933

    Article  PubMed  Google Scholar 

  7. Zimmerman SA, Schultz WH, Davis JS, PickensCV MortierNA, Howard TA et al (2004) Sustained long-term hematologic efficacy of hydroxyurea at maximum tolerated dose in children with sickle cell disease. Blood 103:2039–2045

    Article  CAS  PubMed  Google Scholar 

  8. Svarch E, Machín S, Nieves RM, Mancia de Reyes AG, Navarrete M, Rodríguez H (2006) Hydroxyurea treatment in children with sickle cell anemia in Central America and the Caribbean countries. Pediatr Blood Cancer 47:111–112

    Article  PubMed  Google Scholar 

  9. Al-Nood HA, Al-Khawlani MM, Al-Akwa A (2011) Fetalhemoglobin response to hydroxyurea in Yemeni sicklecell disease patients. Hemoglobin 35:13–21

    Article  CAS  PubMed  Google Scholar 

  10. Flanagan JM, Steward S, Howard TA, Mortier NA, Kimble AC, Aygun B et al (2012) Hydroxycarbamide alters erythroid gene expression in children with sickle cell anaemia. Br J Haematol 157(2):240–248

    Article  CAS  PubMed  Google Scholar 

  11. Goldberg MA, Brugnara C, Dover GJ, Schapira L, Charache S, Bunn HF (1990) Treatment of sickle cell anemia with hydroxyurea and erythropoietin. N Engl J Med 323:366–372

    Article  CAS  PubMed  Google Scholar 

  12. Adragna NC, Fonseca P, Lauf PK (1994) Hydroxyurea affects cell morphology, cation transport, and red blood cell adhesion in cultured vascular endothelial cells. Blood 83:553–560

    CAS  PubMed  Google Scholar 

  13. Orringer EP, Blythe DSB, Johnson AE, Phillips G Jr, Dover GJ, Parker JC (1991) Effects of hydroxyurea on hemoglobin F and water content in the red blood cells of dogs and of patients with sickle cell anemia. Blood 78:212–216

    CAS  PubMed  Google Scholar 

  14. Ballas SK, Dover GJ, Charache S (1989) The effect of hydroxyurea on the rheological properties of sickle erythrocytes in vivo. Am J Hematol 32:104–111

    Article  CAS  PubMed  Google Scholar 

  15. Ware RE (2010) How I use hydroxyurea to treat young patients with sickle cell anemia. Blood 115:5300–5311

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. King SB (2004) Nitric oxide production from Hydroxyurea. Free Radic Biol Med 37(6):737–744

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

We would like to thank all the patients and the family members, the data collectors and the laboratory technicians who participated in the study.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Tribikram Panda.

Ethics declarations

Conflict of Interest

All the authors have equal contribution for this study.

Informed Consent

Informed consent was obtained from all the participants included under the study.

Ethical Standard

Institutional Ethical Clearance has been done for this study as per the protocol. All the procedures perform in this study were in accordance with the Ethical Standard of the Institutional Ethical Committee and with the 1964 Helsinki declaration and its later amendments or comparable Ethical standard.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Sethy, S., Panda, T. & Jena, R.K. Beneficial Effect of Low Fixed Dose of Hydroxyurea in Vaso-occlusive Crisis and Transfusion Requirements in Adult HbSS Patients: A Prospective Study in a Tertiary Care Center. Indian J Hematol Blood Transfus 34, 294–298 (2018). https://doi.org/10.1007/s12288-017-0869-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12288-017-0869-x

Keywords

Navigation