Children hospitalized for varicella: A prevaccine review

被引:81
作者
Peterson, CL
Mascola, L
Chao, SM
Lieberman, JM
Arcinue, EL
Blumberg, DA
Kim, KS
Kovacs, A
Wong, VK
Brunell, PA
机构
[1] UNIV CALIF LOS ANGELES, HARBOR MED CTR, DIV PEDIAT INFECT DIS, TORRANCE, CA 90509 USA
[2] MEM MILLER CHILDRENS HOSP, LONG BEACH, CA USA
[3] HUNTINGTON MEM HOSP, DEPT PEDIAT, PASADENA, CA USA
[4] UNIV CALIF LOS ANGELES, DEPT PEDIAT INFECT DIS, LOS ANGELES, CA USA
[5] CHILDRENS HOSP LOS ANGELES, DIV INFECT DIS, LOS ANGELES, CA 90027 USA
[6] UNIV SO CALIF, LOS ANGELES CTY MED CTR, MATERNAL CHILD AIDS DIV, LOS ANGELES, CA 90033 USA
[7] BELLFLOWER KAISER FDN HOSP, DEPT PEDIAT, BELLFLOWER, CA USA
[8] CEDARS SINAI MED CTR, DEPT PEDIAT INFECT DIS, LOS ANGELES, CA 90048 USA
关键词
D O I
10.1016/S0022-3476(96)70117-8
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Objectives: To describe varicella complications in healthy and previously ill children hospitalized for varicella and to explore trends In group A beta-hemolytic streptococcus complications of varicella. Methods: A retrospective record review of children hospitalized for varicella between January 1, 1990, and March 31, 1994, was conducted in nine large acute care hospitals in Los Angeles County, California. Results: We identified 574 children hospitalized for varicella in study hospitals during the 4.25-year study period (estimated risk of hospitalization, approximately 1 in 550 cases of varicella); 53% of the children were healthy before the onset of varicella and 47% were previously ill with underlying cancers or other chronic illnesses, Children were hospitalized for treatment of complications (n = 427, 74%) or for prophylactic antiviral therapy or observation (n = 147, 26%). Systems involved in complications included skin/soft tissue (45%), neurologic (18%), respiratory (14%), gastrointestinal (10%), and hematologic, renal, or hepatic (8% or less). The mean age of children with skin/soft tissue infections was 2.7 years (range <1 to 16 years) compared with 4.7 years (<1 to 18 years) for other complications. Children with skin/soft tissue and neurologic complications were more often previously healthy (p < 0.05), whereas those with respiratory complications were more often previously ill (p < 0.001). Hospitalizations for skin/soft tissue infections increased during the study period. The proportion of complications as a result of group A beta-hemolytic streptococcus infection increased from 4.7% before 1993 to 12.2% for the remainder of the study period (p = 0.02). Conclusions: Prior health status was predictive of the type of complications experienced by children with varicella requiring hospitalization. Our data suggest a recent increase in skin/soft tissue complications of varicella requiring hospitalization and an increase in the proportion of complications related to group A beta-hemolytic streptococcus. Wide-scale vaccine use should reverse this trend and reduce the overall impact of varicella on both healthy and previously ill children.
引用
收藏
页码:529 / 536
页数:8
相关论文
共 31 条
[21]  
PETERSON C, 1996, PEDIATR INFECT DIS J, V15, P161
[22]  
PITEL PA, 1980, PEDIATRICS, V65, P631
[23]  
Plotkin SA, 1996, PEDIATRICS, V97, P251
[24]  
PREBLUD SR, 1981, PEDIATRICS, V68, P14
[25]  
PREBLUD SR, 1986, PEDIATRICS, V78, P728
[26]   CHANGING EPIDEMIOLOGY OF GROUP-A STREPTOCOCCAL INFECTION IN THE USA [J].
SCHWARTZ, B ;
FACKLAM, RR ;
BREIMAN, RF .
LANCET, 1990, 336 (8724) :1167-1171
[27]   INVASIVE AND TOXIN-RELATED DISEASES CAUSED BY GROUP-A STREPTOCOCCI [J].
SHULMAN, ST .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1991, 10 (10) :S28-S31
[28]   INVASIVE GROUP-A STREPTOCOCCAL INFECTIONS - THE PAST, PRESENT AND FUTURE [J].
STEVENS, DL .
PEDIATRIC INFECTIOUS DISEASE JOURNAL, 1994, 13 (06) :561-566
[29]   SEVERE GROUP-A STREPTOCOCCAL INFECTIONS ASSOCIATED WITH A TOXIC SHOCK LIKE SYNDROME AND SCARLET FEVER TOXIN-A [J].
STEVENS, DL ;
TANNER, MH ;
WINSHIP, J ;
SWARTS, R ;
RIES, KM ;
SCHLIEVERT, PM ;
KAPLAN, E .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 321 (01) :1-7
[30]   INVASIVE GROUP A STREPTOCOCCUS INFECTIONS [J].
STEVENS, DL .
CLINICAL INFECTIOUS DISEASES, 1992, 14 (01) :2-13