To study the effect of hydroxyurea on transcranial doppler in patients with sickle cell anemia

  • Dr. Sharja Phuljhele Professor and Head of Department, Department of Pediatrics, Pt. Jawaharlal Nehru Memorial Medical College, and Dr. B.R. A. M. H, Raipur, Chhattisgarh, India
  • Dr. Prankur Pandey Assistant Professor, Department of Pediatrics, Pt. Jawaharlal Nehru Memorial Medical College, and Dr. B.R. A. M. H, Raipur, Chhattisgarh, India
  • Dr. Rajesh Banjare Post-Graduate, Department of Pediatrics, Pt. Jawaharlal Nehru Memorial Medical College, and Dr. B.R. A. M. H, Raipur, Chhattisgarh, India
Keywords: Stroke in SSD, Transcranial doppler, Risk for stroke, HU-hydroxyurea

Abstract

Background: The estimated rate of prevalence of SCD in the population of Chhattisgarh is about 10 to 15% of which about 1 to 1.27% are likely to be sufferers and the rest carriers.The frequency of stroke in SCD is estimated at 0.61 per 100 patients per year. TCD is a valuable screening test in many clinical conditions such as SCD, to identify the patients at risk of stroke. An abnormally high blood speed is an indicator of a narrowed cerebral blood vessel and/or increased blood volume and a warning marker of high risk for stroke.

Methods: This was a prospective comparative cross-sectional observational hospital based study, conducted over a period of 17 months (July 2016 to November 2017) in the Department Of Pediatrics and Radiodiagnosis, Dr. B.R.A.M.H, Raipur (C.G.).Children between 2 to 14 years diagnosed as SCD SS who were receiving long term (>6months) HU(hydroxyurea) treatment (cases) – HU group, and those who had never received this treatment (control) – HU naïve group, were enrolled.

Results: The total number of children enrolled in the present study was 120, out of which 40 were cases and 80 were controls. The mean blood flow velocity of cases was significantly lower than controls. Among cases and controls maximum mean blood flow velocity was found in Left MCA followed by Right MCA. In addition to this, it was also found that there was no significant interhemispheric difference in both group. (p-value more than 0.05).There were significant associations between blood flow of Right andLeft Side of MCA, ACA and ophthalmic arteries among cases.

Conclusion: The mean blood flow velocity in the HU group and HU naïve group was within the normal range (<170cm/sec), as per STOP criteria. The mean blood flow velocity in patients who were on the HU group was found to be significantly lower than the HU naïve group.

Downloads

Download data is not yet available.

References

Lehmann H, Cutbush M, Sickle-cell trait in southern India. Br Med J. 1952 Feb 23;1(4755):404-405.doi: https://dx.doi.org/10.1136%2Fbmj.1.4755.404.

Negi RS., Sickle cell trait in India. A review of known distribution. Bull AnthropolSurv India. 1972; 17:439-449.

Balgir RS, Genetic epidemiology of the three predominant abnormal haemoglobins in India. J Assoc Physicians India. 1996 Jan;44(1):25-28.

Ambekar SS, Phadke MA, Mokashi GD. Bankar MP, Khedkar VA, Venkat V, et al.Basutkar DG Pattern of haemoglobinopathies in western Maharashtra, Indian Pediatr. 2001 May;38(5):530-534. Available at https://www.indianpediatrics.net/may2001/may-530-534.htm

Patra PK, Chauhan VS, Khodiar PK, Dalla AR, Serjeant GR. Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem. J Community Genet. 2011;2(3):147-151Pradeep K. Patra Virander S. Chauhan, Prafulla K. Khodiar, Abdul R. Dalla, and Graham R. Serjeant et al Screening for the sickle cell gene in Chhattisgarh state, India: an approach to a major public health problem J Community Genet. 2011 September,2(3):147-151. doi: https://dx.doi.org/10.1007%2Fs12687-011-0050-4.

Chhattisgarh Apip 2012-13 Department Of Women And ChildDevelopment.Project Implementation Plan 2012-13, Chhattisgarh Available at https://icds-wcd.nic.in/apip/Final%20APIP%202012-13%20%28Chhattisgarh%29-27June12.pdf cg.nic.in/health/programonitoring/PIPHealthFinancing/PIP201213.

Shah V, Muley P, Choraria C, Rana P, Kanara D, Markana A. Clinical and hematological profile of sickle cell disease affected children in rural tertiary level hospital. Pediatric Rev: Int JPediatrRes. 2017;4(3):202-206. Available from: https://pediatrics.medresearch.in/index.php/ijpr/article/view/256Ohene-Frempong K, Weiner SJ, Sleeper LA, Miller ST, Embury S, Moohr JW, et al. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. 1998 Jan 1; 91(1):288-94.

M. Kamble M, and P. Chaturvedi P. Epidemiology of sickle cell disease in a rural hospital of central India. Indian Pediatrics. 2000:37(4):391-396.

Adams R. McKie V, Nichols F, Carl E, Zhang DL, McKie K, Figueroa R, et al. The Use of Transcranial Ultrasonography to Predict Stroke in Sickle Cell Disease. N Engl J Med. 1992;326(9):605-610. doi: https://doi.org/10.1056/nejm199202273260905.

Lowe L, Bulas D. Transcranial Doppler imaging in children: sickle cell screening and beyond.PediatrRadiol. 2005 Jan;35(1):54-65.doi: https://doi.org/10.1007/s00247-004-1257-x.

Adams RJ, McKie VC, Carl EM, Nichols FT, Perry R, Brock K, et al. Long-term stroke risk in children with sickle cell disease screened with transcranial doppler.Ann Neurol. 1997;42(5):699-704.doi: https://doi.org/10.1002/ana.410420505.

Ohene-Frempong K, Weiner SJ, Sleeper LA, Miller ST, Embury S, Moohr JW, et al. Sickle Cell Disease TC. Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood. J Am Soc Hematol. 1998;91(1):288-294Ohene-Frempong K, Weiner S, Sleeper L etal. Cerebrovascular accidents in sickle cell disease; rates and risk factors, Blood 1998; 91:288-94.

Lanzkowsky P.:Hemolytic Anaemias. Manual of pediatric haematology oncology. 4th ed,n Elsevier academic press, 2005;136-198.

Adams R, McKie V, Nichols F, Carl E, Zhang DL, McKie K, et al. The use of transcranial ultrasonography to predict stroke in sickle cell disease. New Engl J Med. 1992;326(9):605-610. doi: https://doi.org/10.1056/nejm199202273260905.

Neish AS, Blews DE, Simms CA, Merritt RK, Spinks AJ. Screening for stroke in sickle cell anemia: comparison of transcranial Doppler imaging and nonimaging US techniques. Radiol. 2002;222(3):709-714. doi: https://doi.org/10.1148/radiol.2223010524.

Zimmerman SA, Schultz WH, Burgett S, Mortier NA, Ware REZimmerman SA, et al. Hydroxyurea therapy lowers transcranial Doppler flow velocities in children with sickle cell anaemia. Blood. 2007 Aug 1;110(3):1043-1047. doi: https://doi.org/10.1182/blood-2006-11-057893.Epub 2007 Apr 11

Bay-Hansen J, Ravn T, Knudsen GM. Application of interhemispheric index for transcranial Doppler sonography velocity measurements and evaluation of recording time. Stroke. 1997;28(5):1009-1014. doi: https://doi.org/10.1161/01.str.28.5.1009.Jesper Bay Hansen, BM: Thomas Ravn, BM: Gitte Moos Knudsen, MDSc et al Application of Interhemispheric Index for Transcranial Doppler Sonography Velocity Measurements and Evaluation of Recording Time Stroke. 1997:28:1009 1014

Pawlak MA, Krejza J, Rudzinski W, Kwiatkowski JL, Ichord R, Jawad AF, et al. Sickle cell disease: ratio of blood flow velocity of intracranial to extracranial cerebral arteries—initial experience. Radiol. 2009;251(2):525-534Mikolaj A. Pawlak, MD, PhD JaroslawKreiza, MD, PhD Wojciech Rudzinski, MD, PhD Janet L. Kwiatkowski, MD Rebecca Ichord, MD Abbas F. Jawad, DSc Maciej Tomaszewski, MD, PhD Elias R. Melhem, MD, PhD et al Sickle Cell Disease: Ratio of BloodFlow Velocity of Intracranial to Extracranial Cerebral Arteries—Initial Experience ,Radiology: Volume 251: Number 2—May 2009. doi: https://dx.doi.org/10.1148%2Fradiol.2512071180.

Molavi M, Alizade M, Negahi A, Hamedi Y, Nazemi A, Molavi K.MohammadAliMolavi, MohammadRezaAlizade, Ahmad Negahi, YaghoobHamedi, AbdolmajidNazemi, KamyarMolavi et al Study of Transcranial Doppler in Children with Sickle-Cell Anaemia in Bandar Abbas Children's Hospital in Period of 2010-2011.Asian Journal of Medical and Pharmaceutical Researches AJMPR Asian J. Med. Pharm. Res. 2012;. 2(1):16-20, 2012. Available at http://ajmpr.science-line.com/attachments/article/14/Asian%20J.%20Med.%20Pharm.%20Res.%202(1)%2016-20,%202012-.pdf.

HyderAragão de Melo, José Augusto S. Barreto-Filho2, Roberto César P. do Prado, Rosana Cipolotti et al Transcranial Doppler in Sickle Cell AnaemiaEvaluation of brain blood flow parameters in children of Aracaju. Northeast Brazil ArqNeuropsiquiatr 2008;66(2-B):360-364,360.doi: https://doi.org/10.1590/S0004-282X2008000300015.

Park MVF, Pádua SS, Passos RA, et al. Avaliação do Doppler transcranianoempacientes com doençafalciforme. Rev Bras HematolHemoter. 2006;28(2):14

Valadi N, Silva GS, Bowman LS, Ramsingh D, Vicari P, Massaro AR, Kutlar A, Nichols FT, Adams RJ. Transcranial Doppler ultrasonography in adults with sickle cell disease. Neurol. 2006;67(4):572-574. doi: https://doi.org/10.1212/01.wnl.0000230150.39429.8e.

Lee MT, Piomelli S, Granger S, Miller ST, Harkness S, Brambilla DJ, Adams RJ. Study Investigators. Stroke Prevention Trial in Sickle Cell Anemia (STOP): extended follow-up and final results. Blood. 2006;108(3):847-852Margaret T. Lee, Sergio Piomelli, Suzanne Granger, Scott T. Miller, Shannon Harkness, Donald J. Brambilla, and Robert J. Adams et al Stroke Prevention Trial in Sickle Cell Anaemia (STOP):extended follow-up and final results Blood. 2006; 108:847-852. doi: https://doi.org/10.1182/blood-2005-10-009506

CITATION
DOI: 10.17511/ijpr.2020.i03.04
Published: 2020-03-31
How to Cite
Phuljhele, S., Pandey, P., & Banjare, R. (2020). To study the effect of hydroxyurea on transcranial doppler in patients with sickle cell anemia. Pediatric Review: International Journal of Pediatric Research, 7(3), 136-141. https://doi.org/10.17511/ijpr.2020.i03.04
Section
Original Article