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Is Splenic Dysfunction Correlated with Sickle Cell Anemia in Kids?

By Landon Jones, MD, and Richard M. Cantor, MD, FAAP, FACEP | on September 13, 2023 | 0 Comment
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As might reasonably be expected with splenic dysfunction, the prevalence of bacteremia in children with SCA appears to be higher. Occult bacteremia in healthy children aged 3 to 36 months in the ED setting was found to be 0.25 percent in the post-pneumococcal-conjugate-vaccine era.6 A retrospective study of all pediatric patients less than 18 years old with SCA at a single institution (outpatient, emergency, and inpatient) who had blood cultures drawn yielded a true bacteremia rate of 1 percent which is significantly higher.7 Clinically, a febrile patient with SCA should be evaluated for bacteremia via blood culture, and according to the 2014 National Heart, Lung, and Blood Institute treatment guidelines, pediatric patients with sickle cell anemia presenting with fever should receive empiric parenteral antibiotics.8

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ACEP Now: Vol 42 – No 09 – September 2023

Summary

Splenic dysfunction appears to develop within 6 to 12 months of age in pediatric patients with sickle cell anemia and functional asplenia should be assumed in all SCA patients. In febrile children with SCA, physicians should evaluate for bacteremia via blood culture and consider empiric antibiotics.


Dr. JonesDr. Jones is assistant professor of pediatric emergency medicine at the University of Kentucky in Lexington.

Dr. CantorDr. Cantor is professor of emergency medicine and pediatrics, director of the pediatric emergency department, and medical director of the Central New York Regional Poison Control Center at Upstate Medical University in Syracuse, New York.

References

  1. Cober MP, Phelps SJ. Penicillin prophylaxis in children with sickle cell disease. J Pediatr Pharmacol Ther. 2010;15(3):152-9.
  2. Pearson HA, Gallagher D, Chilcote R, et al. Developmental pattern of splenic dysfunction in sickle cell disorders. Pediatr. 1985;76(3):392-7.
  3. Brown AK, Sleeper LA, Miller ST, et al. Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative study of Sickle cell disease. Arch Pediatr Adolesc Med. 1994;148:(8):796-804.
  4. McCarville MB, Luo Z, Huang X, et al. Abdominal ultrasound with scintigraphic and clinical correlates in infants with sickle cell anemia: baseline data from the BABY HUG trial. Am J Roentgenol. 2011;196(6):1399-404.
  5. Nardo-Marino A, Glenthoj A, Brewin JN, et al. The significance of spleen size in children with sickle cell anemia. Am J Hematol. 2022;97(12):1520-1528.
  6. Wilkinson M, Bulloch B, Smith M. Prevalence of occult bacteremia in children aged 3 to 36 months presenting to the emergency department with fever in the post-pneumococcal conjugate vaccine era. Acad Emerg Med. 2009;16(3):220-5.
  7. Yee ME, Lai KW, Bakshi N, et al. Bloodstream infections in children with sickle cell disease: 2010-2019. Pediatr. 2022;149(1):e2021051892.
  8. US Department of Health and Human Services. Appropriate emergency department fever management for children with sickle cell disease (AHRQ Publication No. 14). Agency for Healthcare Research and Quality website. Published February 2018. Accessed August 10,

    Pages: 1 2 3 | Single Page

Topics: asplenicClinicalinfectionPediatricsSickle Cell Diseasespleensplenic dysfunction

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