González Martínez F, Saavedra Lozano J, Navarro Gómez M L, Santos Sebastián M M, Rodríguez Fernández R, González Sánchez M, Hernández-Sampelayo Matos T
Departamento de Pediatría, Sección de Infectología Pediátrica, Hospital Infantil Universitario Gregorio Marañón, Madrid, España.
An Pediatr (Barc). 2013 Nov;79(5):288-92. doi: 10.1016/j.anpedi.2013.02.005. Epub 2013 Apr 13.
To describe the epidemiology, clinical syndromes and microbiological characteristics of serotype 19A as the main cause of invasive pneumococcal disease (IPD) in children admitted to a tertiary hospital in Spain.
A retrospective (1998-2004) and prospective (2005-2009) study was conducted on children with IPD produced by serotype 19A. The study was divided into three periods (P): P1 (1998-2001) when PCV7 had not been 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.
A total of 155 isolates of Streptococcus pneumoniae (SP) producing IPD were analysed, with 21 of them being serotype 19A (14%). An increased prevalence of serotype 19A was found: 2/45 cases (4.4%) in P1, 3/41 cases (7.3%) in P2 and 16/69 cases (23.2%) in P3. It occurred mostly in children younger than 2 years (16/21; 76%). This serotype was the main cause of meningitis (5/20; 25%), pleural empyema (3/22; 14%) and bacteraemic mastoiditis (2/4; 50%). Thirteen isolates (61.5%) had an MIC ≥ 0.12μ/ml for penicillin in extra-meningeal infections, and 3 of the 5 isolates causing meningitis (60%) had an MIC ≥ 1μ/ml for cefotaxime.
Serotype 19A was the main causal agent of IPD in the PCV7 era (P3), with high antibiotic resistance rates. This serotype was responsible for all types of IPD, being the main cause of meningitis.
描述西班牙一家三级医院收治的儿童侵袭性肺炎球菌病(IPD)主要病因19A血清型的流行病学、临床综合征及微生物学特征。
对19A血清型引起的IPD患儿进行回顾性(1998 - 2004年)和前瞻性(2005 - 2009年)研究。该研究分为三个时期(P):P1(1998 - 2001年),此时PCV7尚未商业化;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。
共分析了155株引起IPD的肺炎链球菌(SP)分离株,其中21株为19A血清型(14%)。发现19A血清型患病率增加:P1期45例中有2例(4.4%),P2期41例中有3例(7.3%),P3期69例中有16例(23.2%)。其主要发生在2岁以下儿童(21例中的16例;76%)。该血清型是脑膜炎(20例中的5例;25%)、胸膜脓胸(22例中的3例;14%)和菌血症性乳突炎(4例中的2例;50%)的主要病因。在脑膜外感染中,13株分离株(61.5%)对青霉素的最低抑菌浓度(MIC)≥0.12μg/ml,5株引起脑膜炎的分离株中有3株(60%)对头孢噻肟的MIC≥1μg/ml。
在PCV7时代(P3),19A血清型是IPD的主要病原体,抗生素耐药率高。该血清型可导致所有类型的IPD,是脑膜炎的主要病因。