Suppr超能文献

五价轮状病毒疫苗在美国大城市人群中的有效性。

Effectiveness of pentavalent rotavirus vaccine in a large urban population in the United States.

机构信息

Baylor College of Medicine, Center for Vaccine Awareness and Research, Texas Children's Hospital, 6701 Fannin St, CC1540, Houston, TX 77030, USA.

出版信息

Pediatrics. 2010 Feb;125(2):e199-207. doi: 10.1542/peds.2009-1021. Epub 2010 Jan 18.

Abstract

OBJECTIVE

The goal was to assess the effectiveness of complete (3-dose) or partial (1- or 2-dose) immunization with pentavalent rotavirus vaccine (RV5) against rotavirus acute gastroenteritis (AGE) in US clinical practice.

METHODS

A case-control evaluation was conducted in February through June 2008 at an emergency department in Houston, Texas. Case patients with rotavirus AGE (N = 90) were identified through testing for rotavirus in fecal specimens obtained from 205 children 15 days through 23 months of age presenting with AGE. Control groups included rotavirus-negative AGE patients (N = 115), concurrently enrolled patients with acute respiratory infection (ARI) (N = 228), and up to 10 age- and zip code-matched children sampled from the Houston-Harris County Immunization Registry (HHCIR) for each case patient >8 months of age. Immunization data were obtained from parent records, health care providers, and/or the HHCIR. Vaccine effectiveness was calculated as 1 minus odds of RV5 vaccination for case patients versus control patients, after adjustment for age at presentation and birth date.

RESULTS

The vaccine effectiveness of a complete RV5 series was 89% (95% confidence interval [CI]: 70%-96%) and 85% (95% CI: 55%-95%) with rotavirus-negative AGE and ARI control patients, respectively. Immunization data were available for 44% of case patients (n = 40) from the HHCIR; the estimated 3-dose vaccine effectiveness with these HHCIR control patients was 82% (95% CI: 19%-96%). A complete RV5 series conferred 100% protection (95% CI: 71%-100%) against severe rotavirus disease requiring hospitalization and 96% protection (95% CI: 72%-99%) against disease requiring intravenous hydration. Vaccine effectiveness of 1 and 2 doses against hospitalization and emergency department visits was 69% (95% CI: 13%-89%) and 81% (95% CI: 13%-96%), respectively, using rotavirus-negative AGE and ARI control groups combined.

CONCLUSIONS

In this setting, a complete series of RV5 was highly effective against severe rotavirus AGE. Partial immunization also conferred substantial protection.

摘要

目的

评估五价轮状病毒疫苗(RV5)完全免疫(3 剂)或部分免疫(1 剂或 2 剂)对美国临床实践中轮状病毒急性胃肠炎(AGE)的效果。

方法

2008 年 2 月至 6 月在德克萨斯州休斯顿的一家急诊室进行了病例对照评估。通过对 205 名 15 天至 23 个月龄出现 AGE 的儿童粪便样本中轮状病毒的检测,确定轮状病毒 AGE 病例患者(N=90)。对照组包括轮状病毒阴性 AGE 患者(N=115)、同期急性呼吸道感染(ARI)患者(N=228),以及每个大于 8 个月龄的病例患者从休斯顿-哈里斯县免疫登记处(HHCIR)中匹配年龄和邮政编码的最多 10 名儿童。免疫接种数据来自父母记录、医疗保健提供者和/或 HHCIR。疫苗效力的计算方法为病例患者与对照患者 RV5 疫苗接种率的差值,调整了就诊时的年龄和出生日期。

结果

完全 RV5 系列疫苗的效力分别为 89%(95%置信区间[CI]:70%-96%)和 85%(95% CI:55%-95%),针对轮状病毒阴性 AGE 和 ARI 对照患者。HHCIR 中有 44%的病例患者(n=40)可获得免疫接种数据;使用这些 HHCIR 对照患者的 3 剂疫苗效力估计为 82%(95% CI:19%-96%)。完全 RV5 系列疫苗对需要住院治疗的严重轮状病毒疾病提供 100%的保护(95% CI:71%-100%),对需要静脉补液治疗的疾病提供 96%的保护(95% CI:72%-99%)。1 剂和 2 剂疫苗对住院和急诊就诊的效力分别为 69%(95% CI:13%-89%)和 81%(95% CI:13%-96%),使用轮状病毒阴性 AGE 和 ARI 对照组合并。

结论

在这种情况下,RV5 的完全系列对严重轮状病毒 AGE 非常有效。部分免疫也提供了实质性的保护。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验