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Invasive pneumococcal infections in children with asplenia

SCHUTZE, GORDON E. MD; MASON, EDWARD O. JR. PhD; BARSON, WILLIAM J. MD; KIM, KWANG SIK MD; WALD, ELLEN R. MD; GIVNER, LAURENCE B. MD; TAN, TINA Q. MD; BRADLEY, JOHN S. MD; YOGEV, RAM MD; KAPLAN, SHELDON L. MD

Pediatric Infectious Disease Journal: April 2002 - Volume 21 - Issue 4 - pp 278-282
Original Studies

Background. Asplenia is associated with an increased risk of infections caused by Streptococcus pneumoniae. Overwhelming infection can be fulminate and lead to a fatal outcome.

Objective. To review the epidemiology and clinical course of invasive S. pneumoniae infections in children with asplenia before the release of the conjugate pneumococcal vaccine.

Methods. Children with S. pneumoniae infections from eight children’s hospitals in the US were identified prospectively from September, 1993, to August, 1999. Further demographic, medical and microbiologic information was gathered retrospectively from the charts of patients with asplenia.

Results. Twenty-two asplenic patients with 26 episodes of invasive S. pneumoniae were identified. This represents 1% of the 2581 episodes of invasive S. pneumoniae infections identified in our study. Twelve had congenital asplenia (CA), and 10 had undergone surgical splenectomy. Nine of the patients with CA had associated complex congenital heart disease. The median age at first infection was 12.5 months for CA patients as compared with 69 months in children with surgical splenectomy (P < 0.001). Seventy-five percent of those eligible had received the polysaccharide pneumococcal vaccine. The most common serotypes isolated were 6B (8), 23F (7), 18C (2) and 19A (2). Antimicrobial prophylaxis had been prescribed for 82% of the study cohort. Clinical presentations of the 26 episodes included fever (22), shock (7), petechiae or purpura (7), disseminated intravascular coagulation (5) and respiratory distress (5). Clinical illness included bacteremia alone (12), meningitis alone (8), bacteremia with otitis media-sinusitis (3), bacteremia with pneumonia (2) and meningitis with osteomyelitis (1). Five of the 6 patients who died had meningitis. Three of the survivors (19%) had significant morbidity, and all of them had meningitis. Two patients had 2 episodes each, and 1 patient had 3 episodes. All but 1 of the multiple episodes was with a different serotype. Forty-six percent of isolates were nonsusceptible to penicillin, and 19% were nonsusceptible to ceftriaxone. There was no association between antimicrobial resistance and mortality.

Conclusions. Invasive pneumococcal disease in patients with asplenia has a high mortality, especially in those with meningitis. Even though the new conjugate vaccine might increase protection, 19% of patients had disease caused by serotypes not included in the current heptavalent vaccine. Clinicians should continue to be aggressive in evaluating asplenic patients with unexplained fevers.

From the Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, AR (GES); the Department of Pediatrics, Baylor College of Medicine, Houston, TX (EOM, SLK); the Department of Pediatrics, Ohio State University College of Medicine, Columbus, OH (WJB); the Department of Pediatrics, University of Southern California School of Medicine, Los Angeles, CA (KSK); the Department of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, PA (ERW); the Department of Pediatrics, Wake Forest University School of Medicine, Winston-Salem, NC (LBG); the Department of Pediatrics, Northwestern University Medical School, Chicago, IL (TQT, RY); and the Department of Pediatrics, Children’s Hospital-San Diego, San Diego, CA (JSB).

Accepted for publication Oct. 12, 2001.

Address for reprints: Gordon E. Schutze, M.D., Arkansas Children’s Hospital, 800 Marshall Street, Little Rock, AR 72202-3591. Fax 501-320-3196; E-mail schutzegordone@uams.edu.

© 2002 Lippincott Williams & Wilkins, Inc.