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Clinical Features and Outcomes of Pneumococcal Bacteremia in Children with Sickle Cell Disease in the Pneumococcal Conjugate Vaccine Era
  • +8
  • Marianne Yee,
  • Lindsey Abel,
  • Grace Kalmus,
  • Ashwin Patel,
  • Mohnd Elmontser,
  • Nitya Bakshi,
  • Yun Wang,
  • Mark D. Gonzalez,
  • Thomas Adamkiewicz,
  • Inci Yildirim,
  • Peter Lane
Marianne Yee
Children's Healthcare of Atlanta Inc Aflac Cancer and Blood Disorders Center

Corresponding Author:memcphe@emory.edu

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Lindsey Abel
Children's Healthcare of Atlanta Inc Aflac Cancer and Blood Disorders Center
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Grace Kalmus
Children's Healthcare of Atlanta Inc Aflac Cancer and Blood Disorders Center
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Ashwin Patel
Emory University Department of Pediatrics
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Mohnd Elmontser
Emory University Department of Pediatrics
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Nitya Bakshi
Children's Healthcare of Atlanta Inc Aflac Cancer and Blood Disorders Center
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Yun Wang
Emory University Department of Pathology and Laboratory Medicine
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Mark D. Gonzalez
Emory University Department of Pathology and Laboratory Medicine
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Thomas Adamkiewicz
Emory University Department of Pediatrics
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Inci Yildirim
Emory University Department of Pediatrics
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Peter Lane
Children's Healthcare of Atlanta Inc Aflac Cancer and Blood Disorders Center
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Abstract

Introduction: Children with sickle cell disease (SCD) remain at higher risk for invasive infection with Streptococcus pneumoniae compared to the general pediatric population. Penicillin prophylaxis, pneumococcal conjugate (PCV), and polysaccharide vaccines (PPSV) have reduced the incidence of pneumococcal disease. Methods: A single institution cohort of children with SCD aged <19 years was reviewed over the 14-year period after PCV13 licensure (January 2010 – December 2023) to identify and characterize the clinical features and outcomes of S. pneumoniae bacteremia, including serotypes and antibiotic susceptibility. Results: The cohort included 4,356 children with SCD (24,076 person-years). Thirty-eight pneumococcal bacteremia cases were identified (32 HbSS, 5 HbSC, 1 HbSβ +-thalassemia), 21 (55%) in children age ≥5 years. The median time to culture positivity was 10.6 hours (range 3.4–20.2) from collection. Meningitis occurred in 4 (11%) and acute chest syndrome in 13 (34%). Serotype information was available for 36 (95%) isolates, which included 16 (44%) PPSV23 serotypes and 1 (2.6%) PCV13 serotype (serotype 3). Penicillin nonsusceptibility occurred in 12/31 (39%) at meningitis and 1/31 (3%) at non-meningitis breakpoints. Three (8%) deaths occurred (serotypes 12F, 23B, and 15B), all in children age ≥5 years, who had discontinued prophylactic penicillin. Long-term sequelae occurred in 5 (14%) surviving children, including hearing loss, limb amputation, motor and neurocognitive defects. Conclusion: Pneumococcal bacteremia continues to occur in children with SCD, with a risk of rapid progression to severe disease. Pneumococcal prevention strategies and urgent empiric treatment for fever remain important for children and adolescents of all ages with SCD.
13 Dec 2024Submitted to Pediatric Blood & Cancer
13 Dec 2024Submission Checks Completed
13 Dec 2024Assigned to Editor
14 Dec 2024Review(s) Completed, Editorial Evaluation Pending
15 Dec 2024Reviewer(s) Assigned