González Martínez F, Navarro Gómez M L, Saavedra Lozano J, Santos Sebastián M M, Rodríguez Fernández R, González Sanchéz M, Cercenado Mansilla E, Hernández-Sampelayo Matos T
Departamento de Pediatría, Sección de Infectología Pediátrica, Hospital Infantil Universitario Gregorio Marañón, Madrid, España.
Departamento de Pediatría, Sección de Infectología Pediátrica, Hospital Infantil Universitario Gregorio Marañón, Madrid, España.
An Pediatr (Barc). 2014 Mar;80(3):173-80. doi: 10.1016/j.anpedi.2013.05.003. Epub 2013 Jun 21.
There has been an increased incidence in invasive pneumococcal disease (IPD) produced by non-vaccine serotype (NVS) of Streptococcus pneumoniae after the introduction of PCV7. Our objective was to describe the epidemiological, clinical and microbiological characteristics of IPD caused by NVS in a tertiary hospital in Madrid.
Retrospective (1998-2004) and prospective (2005-2009) study evaluating IPD caused by NVS in children. The study was divided into three periods: P1 (1998-2001) when PCV7 was not commercialized; P2 (2002-2005) with 40% vaccine coverage among children; and P3 (2006-2009) when the vaccine was added to the Childhood Immunization Schedule in Madrid.
We analyzed 155 cases of IPD. One hundred and fifty of these isolates were serotyped (100 were NVS). There was an increase in the prevalence of IPD from P1 (31%) to P2 (54%) and P3 (91%). The most relevant emerging serotypes were 19A, 7F, 1, 5, 3 and 15C. The most significant clinical syndromes produced by some specific serotypes were as follows: lower respiratory tract infection (LRTI) by serotypes 1, 3, 5 and 15C; LRTI, primary bacteremia and meningitis by serotype 19A; and primary bacteremia by serotype 7F (66%). The large majority (83.8%) of NVS were sensitive to penicillin.
There has been an increased prevalence of IPD caused by NVS since the introduction of PCV7. These changes should prompt the introduction of new pneumococcal vaccines, which include most of the NVS, in the childhood immunization calendar to prevent IPD in children.
在引入PCV7后,由肺炎链球菌非疫苗血清型(NVS)引起的侵袭性肺炎球菌疾病(IPD)发病率有所上升。我们的目的是描述马德里一家三级医院中由NVS引起的IPD的流行病学、临床和微生物学特征。
对儿童中由NVS引起的IPD进行回顾性(1998 - 2004年)和前瞻性(2005 - 2009年)研究。该研究分为三个时期:P1(1998 - 2001年),此时PCV7未商业化;P2(2002 - 2005年),儿童疫苗接种覆盖率为40%;P3(2006 - 2009年),此时该疫苗被纳入马德里儿童免疫规划。
我们分析了155例IPD病例。其中150株分离株进行了血清分型(100株为NVS)。IPD的患病率从P1(31%)到P2(54%)再到P3(91%)呈上升趋势。最相关的新兴血清型为19A、7F、1、5、3和15C。一些特定血清型引起的最显著临床综合征如下:血清型1、3、5和15C引起下呼吸道感染(LRTI);血清型19A引起LRTI、原发性菌血症和脑膜炎;血清型7F引起原发性菌血症(66%)。绝大多数(83.8%)的NVS对青霉素敏感。
自引入PCV7以来,由NVS引起的IPD患病率有所上升。这些变化应促使在儿童免疫规划中引入包含大多数NVS的新型肺炎球菌疫苗,以预防儿童IPD。