Incidence of occult bacteremia among highly febrile young children in the era of the pneumococcal conjugate vaccine - A study from a children's hospital emergency department and urgent care center

被引:103
作者
Stoll, ML
Rubin, LG
机构
[1] Albert Einstein Coll Med, N Shore Long Isl Jewish Hlth Syst, Schneider Childrens Hosp, Div Infect Dis, New Hyde Pk, NY 11040 USA
[2] Albert Einstein Coll Med, N Shore Long Isl Jewish Hlth Syst, Schneider Childrens Hosp, Dept Pediat, New Hyde Pk, NY 11040 USA
来源
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE | 2004年 / 158卷 / 07期
关键词
D O I
10.1001/archpedi.158.7.671
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: The optimal diagnostic approach to and management of well-appearing, highly febrile young children has been a matter of debate owing to the possibility of clinically inapparent, or occult, bacteremia (OB). The most common causative organism of OB is Streptococcus pneumoniae. Universal immunization with a heptavalent pneumococcal conjugate vaccine (PCV7) has recently been implemented, but there are limited data on the impact of this vaccine on the incidence of OB. Objective: To evaluate the incidence of OB in the era of routine use of PCV7. Methods: We conducted a retrospective cohort study of highly febrile (temperature, 39degreesC) children between the ages of 2 months and 36 months who had blood cultures performed in the emergency department or urgent care center between December 11, 2001, and March 5, 2003, and were discharged to home at the time of the initial Visit. Results: Of 329 blood cultures obtained from children who met inclusion criteria and did not meet exclusion criteria, 3 (0.91%; 95% confidence interval, 0%-1.9%) yielded a pathogenic bacterium; all were S. pneumoniae. Neither an elevated total white blood cell count, an elevated absolute neutrophil count, nor an increased percentage of bands was highly predictive of OB. Blood cultures positive for organisms were more commonly due to contaminants (4; 95% confidence interval, 0%-2.4%) than pathogens. Conclusions: In the PCV7 era, OB is uncommon in highly febrile children 2 to 36 months of age. With continued use of PCV7, the routine practice of obtaining blood cultures and complete blood cell counts may no longer be indicated in previously healthy, well-appearing, highly febrile children 2 to 36 months of age, particularly those who have received at least 1 dose of PCV7.
引用
收藏
页码:671 / 675
页数:5
相关论文
共 33 条
[1]  
Abramson JS, 2000, PEDIATRICS, V106, P362
[2]   Occult bacteremia from a pediatric emergency department: Current prevalence, time to detection, and outcome [J].
Alpern, ER ;
Alessandrini, EA ;
Bell, LM ;
Shaw, KN ;
McGowan, KL .
PEDIATRICS, 2000, 106 (03) :505-511
[3]  
[Anonymous], 2000, MMWR Recomm Rep, V49, P1
[4]   Risk of serious bacterial infection in children with fever without a source in the post-Haemophilus influenzae era when antibiotics are reserved for culture-proven bacteremia [J].
Bandyopadhyay, S ;
Bergholte, J ;
Blackwell, CD ;
Friedlander, JR ;
Hennes, H .
ARCHIVES OF PEDIATRICS & ADOLESCENT MEDICINE, 2002, 156 (05) :512-517
[5]   PRACTICE GUIDELINE FOR THE MANAGEMENT OF INFANTS AND CHILDREN 0 TO 36 MONTHS OF AGE WITH FEVER WITHOUT SOURCE [J].
BARAFF, LJ ;
BASS, JW ;
FLEISHER, GR ;
KLEIN, JO ;
MCCRACKEN, GH ;
POWELL, KR ;
SCHRIGER, DL .
ANNALS OF EMERGENCY MEDICINE, 1993, 22 (07) :1198-1210
[6]   Efficacy, safety and immunogenicity of heptavalent pneumococcal conjugate vaccine in children [J].
Black, S ;
Shinefield, H ;
Fireman, B ;
Lewis, E ;
Ray, P ;
Hansen, JR ;
Elvin, L ;
Ensor, KM ;
Hackell, J ;
Siber, G ;
Malinoski, F ;
Madore, D ;
Chang, I ;
Kohberger, R ;
Watson, W ;
Austrian, R ;
Edwards, K .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2000, 19 (03) :187-195
[7]   Postlicensure evaluation of the effectiveness of seven valent pneumococcal conjugate vaccine [J].
Black, SB ;
Shinefield, HR ;
Hansen, J ;
Elvin, L ;
Laufer, D ;
Malinoski, F .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2001, 20 (12) :1105-1107
[8]   OUTCOME OF UNSUSPECTED PNEUMOCOCCEMIA IN CHILDREN NOT INITIALLY ADMITTED TO HOSPITAL [J].
BRATTON, L ;
TEELE, DW ;
KLEIN, JO .
JOURNAL OF PEDIATRICS, 1977, 90 (05) :703-706
[9]  
CARROLL WL, 1983, PEDIATRICS, V72, P608
[10]  
Centers for Disease Control and Prevention (CDC), 1996, MMWR Morb Mortal Wkly Rep, V45, P901