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1 June 2007

Volume 44, Number 11
Clinical Infectious Diseases 2007;44:1428–1433
1058-4838/2007/4411-0005$15.00
DOI: 10.1086/516781
MAJOR ARTICLE

Incidence of Invasive Pneumococcal Disease among Individuals with Sickle Cell Disease before and after the Introduction of the Pneumococcal Conjugate Vaccine

Natasha B. Halasa,1

Sadhna M. Shankar,1

Thomas R. Talbot,2,3

Patrick G. Arbogast,4,5

Ed F. Mitchel,3

Winfred C. Wang,8

William Schaffner,2,3

Allen S. Craig,3,6 and

Marie R. Griffin2,3,5,7

Departments of 1Pediatrics, 2Medicine, 3Preventive Medicine, and 4Biostatistics, and 5Center for Education and Research on Therapeutics, Vanderbilt University School of Medicine, 6Tennessee Department of Health, and 7Geriatric Research Education and Clinical Center and Clinical Research Center of Excellence, Veterans Affairs, Tennessee Valley Healthcare System, Nashville, and 8Department of Hematology, St. Jude Children’s Research Hospital, Memphis, Tennessee

Background.We sought to determine the incidence of invasive pneumococcal disease (IPD) among individuals with sickle cell disease (SCD) before and after the introduction of the pneumococcal conjugate vaccine (PCV).

Methods.Individuals with SCD who were enrolled in Tennessee Medicaid from January 1995 through December 2004 were identified using SCD‐specific International Classification of Diseases, Ninth Revision, Clinical Modification codes. Population‐based surveillance data were used to identify individuals with IPD and were linked to patients with SCD in the Tennessee Medicaid database to determine incidence rates of IPD. Clinical data were collected on all subjects with IPD, and antibiotic susceptibility testing and serotyping were performed on all available pneumococcal isolates.

Results.We identified 2026 individuals with SCD, who constituted 13,687 person‐years of follow‐up. During the study period, 37 individuals with SCD developed IPD, and 21 of these patients were aged <5 years. In a comparison of the pre‐PCV period (1995–1999) with the post‐PCV period (2001–2004), the rate of IPD decreased by 90.8% in children aged <2 years (from 3630 to 335 cases per 100,000 person‐years; ) and by 93.4% in children aged <5 years (from 2044 to 134 cases per 100,000 person‐years; ). Rates of IPD for patients with SCD who were aged 5 years decreased from 161 cases per 100,000 person‐years during the pre‐PCV period to 99 cases per 100,000 person‐years during the post‐PCV period ( ).

Conclusion.The rate of IPD among children with SCD who are aged <5 years has decreased markedly since the introduction of routine administration of PCV to young children.

Received 24 October 2006; accepted 26 January 2007; electronically published 18 April 2007.

  • (See the editorial commentary by Steinberg on pages 1434–5)

Reprints or correspondence: Dr. Natasha Halasa, Dept. of Pediatric Infectious Diseases, D7232 MCN, 1161 21st Ave. S., Nashville, TN 37232 ().

Cited by

Timothy L. McCavit, Steve Grube, Paula Revell, Charles T. Quinn. (2009) Bordetella holmesii bacteremia in sickle cell disease. Pediatric Blood & Cancer 51:6, 814-816
Online publication date: 1-Jan-2009.
CrossRef
Stephen I. Pelton. (2008) Editorial Commentary: Replacement Pneumococcal Disease in Perspective. Clinical Infectious Diseases 46:9, 1353-1355
Online publication date: 1-May-2008.
Carlos G Grijalva, Marie R Griffin. (2008) Population-based impact of routine infant immunization with pneumococcal conjugate vaccine in the USA. Expert Review of Vaccines 7:1, 83-95
Online publication date: 1-Mar-2008.
CrossRef
Martin H. Steinberg. (2007) Editorial Commentary: Pneumococcus and Sickle Cell Disease: The Beginning of the End?. Clinical Infectious Diseases 44:11, 1434-1435
Online publication date: 1-Jun-2007.
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