Robinson K A, Baughman W, Rothrock G, Barrett N L, Pass M, Lexau C, Damaske B, Stefonek K, Barnes B, Patterson J, Zell E R, Schuchat A, Whitney C G
Respiratory Diseases Branch, Division of Bacterial and Mycotic Diseases, National Center for Infectious Diseases, Centers for Disease Control and Prevention, MS D-65, 1600 Clifton Rd NE, Atlanta, GA 30333, USA.
JAMA. 2001 Apr 4;285(13):1729-35. doi: 10.1001/jama.285.13.1729.
Pneumococcal polysaccharide vaccine is recommended for elderly persons and adults with certain chronic illnesses. Additionally, a recently licensed pneumococcal 7-valent conjugate vaccine has been recommended for use in young children and could dramatically change the epidemiology of pneumococcal disease.
To assess pneumococcal disease burden in the United States, estimate the potential impact of new vaccines, and identify gaps in vaccine recommendations.
Analysis of data from the Active Bacterial Core Surveillance (ABCs)/Emerging Infections Program Network, an active, population-based system in 9 states.
A total of 15 860 cases of invasive pneumococcal disease occurring between January 1, 1995, and December 31, 1998.
Age- and race-specific pneumoccocal disease incidence rates per 100 000 persons, case-fatality rates, and vaccine preventability.
In 1998, overall incidence was 23.2 cases per 100 000, corresponding to an estimated 62 840 cases in the United States. Incidence was highest among children younger than 2 years (166.9) and adults aged 65 years or older (59.7). Incidence among blacks was 2.6 times higher than among whites (95% confidence interval [CI], 2.4-2.8). Overall, 28.6% of case-patients were at least 65 years old and 85.9% of cases in this age group were due to serotypes included in the 23-valent polysaccharide vaccine; 19.3% of case-patients were younger than 2 years and 82.2% of cases in this age group were due to serotypes included in the 7-valent conjugate vaccine. Among patients aged 2 to 64 years, 50.6% had a vaccine indication as defined by the Advisory Committee on Immunization Practices (ACIP). The case-fatality rate among patients aged 18 to 64 years with an ACIP indication was 12.1% compared with 5.4% for those without an indication (relative risk, 2.2; 95% CI, 1.7-2.9).
Young children, elderly persons, and black persons of all ages are disproportionately affected by invasive pneumococcal disease. Current ACIP recommendations do not address a subset of persons aged 18 to 64 years but do include those at highest risk for death from invasive pneumococcal disease.
肺炎球菌多糖疫苗推荐用于老年人及患有某些慢性病的成年人。此外,一种最近获得许可的7价肺炎球菌结合疫苗已被推荐用于幼儿,这可能会极大地改变肺炎球菌疾病的流行病学状况。
评估美国肺炎球菌疾病负担,估计新疫苗的潜在影响,并确定疫苗推荐方面的差距。
对来自9个州基于人群的主动监测系统——主动细菌核心监测(ABCs)/新发感染项目网络的数据进行分析。
1995年1月1日至1998年12月31日期间共15860例侵袭性肺炎球菌疾病病例。
每10万人中按年龄和种族划分的肺炎球菌疾病发病率、病死率及疫苗可预防率。
1998年,总体发病率为每10万人23.2例,在美国估计有62840例。2岁以下儿童(166.9例)和65岁及以上成年人(59.7例)的发病率最高。黑人的发病率比白人高2.6倍(95%置信区间[CI],2.4 - 2.8)。总体而言,28.6%的病例患者年龄至少65岁,该年龄组85.9%的病例由23价多糖疫苗包含的血清型引起;19.3%的病例患者年龄小于2岁,该年龄组82.2%的病例由7价结合疫苗包含的血清型引起。在2至64岁的患者中,50.6%有免疫实践咨询委员会(ACIP)定义的疫苗接种指征。有ACIP指征的18至64岁患者的病死率为12.1%,无指征患者的病死率为5.4%(相对风险,2.2;95%CI,1.7 - 2.9)。
幼儿、老年人及各年龄段黑人受侵袭性肺炎球菌疾病的影响尤为严重。当前ACIP的推荐未涉及18至64岁的一部分人群,但确实涵盖了侵袭性肺炎球菌疾病死亡风险最高的人群。