Pediatric Radiology

, Volume 42, Issue 10, pp 1223–1228

The impact of preparation and support procedures for children with sickle cell disease undergoing MRI

Authors

    • Child Life ProgramSt. Jude Children’s Research Hospital
  • Matthew P. Smeltzer
    • Department of BiostatisticsSt. Jude Children’s Research Hospital
  • Eileen N. Hansbury
    • Baylor International Hematology Center of Excellence and the Texas Children’s Center for Global Health
  • Mary Elizabeth McCarville
    • Department of Radiological SciencesSt. Jude Children’s Research Hospital
  • Kathleen J. Helton
    • Department of Radiological SciencesSt. Jude Children’s Research Hospital
  • Jane S. Hankins
    • Department of HematologySt. Jude Children’s Research Hospital
Original Article

DOI: 10.1007/s00247-012-2422-2

Cite this article as:
Cejda, K.R., Smeltzer, M.P., Hansbury, E.N. et al. Pediatr Radiol (2012) 42: 1223. doi:10.1007/s00247-012-2422-2

Abstract

Background

Children with sickle cell disease (SCD) often undergo MRI studies to assess brain injury or to quantify hepatic iron. MRI requires the child to lie motionless for 30–60 min, thus sedation/anesthesia might be used to facilitate successful completion of exams, but this poses additional risks for SCD patients. To improve children’s ability to cope with MRI examinations and avoid sedation, our institution established preparation and support procedures (PSP).

Objective

To investigate the impact of PSP in reducing the need for sedation during MRI exams among children with SCD.

Materials and methods

Data on successful completion of MRI testing were compared among 5- to 12-year-olds who underwent brain MRI or liver R2*MRI with or without receiving PSP.

Results

Seventy-one children with SCD (median age 9.85 years, range 5.57–12.99 years) underwent a brain MRI (n = 60) or liver R2*MRI (n = 11). Children who received PSP were more likely to complete an interpretable MRI exam than those who did not (30 of 33; 91% vs. 27 of 38; 71%, unadjusted OR = 4.1 (P = 0.04) and OR = 8.5 (P < 0.01) when adjusting for age.

Conclusion

PSP can help young children with SCD complete clinically interpretable, nonsedated MRI exams, avoiding the risks of sedation/anesthesia.

Keywords

Sickle cell anemiaSedationMRIMRAChild life specialistPreparation and support procedureChildren

Copyright information

© Springer-Verlag 2012