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血清型 19A 是导致儿童侵袭性肺炎球菌感染最常见的血清型。

Serotype 19A Is the most common serotype causing invasive pneumococcal infections in children.

机构信息

Texas Children's Hospital, 6621 Fannin MC 3-2371, Houston, TX 77030, USA.

出版信息

Pediatrics. 2010 Mar;125(3):429-36. doi: 10.1542/peds.2008-1702. Epub 2010 Feb 22.

DOI:10.1542/peds.2008-1702
PMID:20176669
Abstract

OBJECTIVE

The purpose of this study was to monitor the clinical and microbiologic features of invasive infections caused by Streptococcus pneumoniae among children before and after the introduction of the 7-valent pneumococcal conjugate vaccine (PCV7).

DESIGN

We conducted a 15-year prospective surveillance study of all invasive pneumococcal infections in children. The sample included infants and children at 8 children's hospitals in the United States with culture-proven invasive S pneumoniae infections.

RESULTS

Since the implementation of routine PCV7 immunization in 2000, invasive infections have decreased yearly from 2001 through 2004, to a nadir of 151 infections; the rate then increased from 2005 through 2008. Compared with the pre-PCV7 era, a greater proportion of children with invasive pneumococcal infection had an underlying condition in the post-PCV7 period. Compared with the total number of annual admissions, the number of 19A isolates increased significantly from 2001 to 2008 (P < .00001). In 2007 and 2008, only 16 isolates (4%) were vaccine serotypes; 19A accounted for 46% (168 of 369) of the non-PCV7 serotypes. Thirty percent of the 19A isolates were multidrug resistant. Serotypes 1, 3, and 7F accounted for 22% of the non-PCV7 serotypes. Among children with invasive pneumococcal infections, the likelihood of a 19A serotype increased with the number of preceding PCV7 doses.

CONCLUSIONS

Since 2005, the number of invasive pneumococcal infections in children has increased at 8 children's hospitals, primarily as a result of serotype 19A isolates, one third of which were resistant to multiple antibiotics in 2007 and 2008. Continued surveillance is necessary to detect emerging serotypes after the planned introduction of 13-valent or other pneumococcal vaccines.

摘要

目的

本研究旨在监测 7 价肺炎球菌结合疫苗(PCV7)引入前后儿童侵袭性肺炎球菌感染的临床和微生物学特征。

设计

我们对美国 8 家儿童医院所有经培养证实的侵袭性肺炎链球菌感染的儿童进行了为期 15 年的前瞻性监测研究。

结果

自 2000 年常规接种 PCV7 以来,侵袭性感染在 2001 年至 2004 年期间每年减少,至 2005 年至 2008 年达到最低点 151 例;此后感染率有所增加。与 PCV7 前时期相比,PCV7 后时期患有侵袭性肺炎球菌感染的儿童中,有基础疾病的比例更高。与每年住院总人数相比,2001 年至 2008 年 19A 分离株的数量显著增加(P<0.00001)。2007 年和 2008 年,只有 16 株(4%)为疫苗血清型;19A 占非 PCV7 血清型的 46%(369 株中的 168 株)。19A 分离株中有 30%为多药耐药株。19A 血清型占非 PCV7 血清型的 22%。在患有侵袭性肺炎球菌感染的儿童中,19A 血清型的可能性随着 PCV7 剂量的增加而增加。

结论

自 2005 年以来,8 家儿童医院儿童侵袭性肺炎球菌感染的数量有所增加,主要是由于 19A 血清型的分离株所致,其中三分之一在 2007 年和 2008 年对多种抗生素耐药。在计划引入 13 价或其他肺炎球菌疫苗后,需要继续监测以发现新出现的血清型。

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