Spanish Reference Laboratory for Pneumococci, Centro Nacional de Microbiología, Madrid, Spain.
Microbiology Department, Hospital Universitari de Bellvitge-IDIBELL, Barcelona, Spain; CIBER de Enfermedades Respiratorias (CIBERES), Madrid, Spain.
Vaccine. 2018 Dec 18;36(52):7993-8000. doi: 10.1016/j.vaccine.2018.10.098. Epub 2018 Nov 16.
Serotypes/genotypes causing invasive pneumococcal disease (IPD) in adults are determined by vaccination strategies. The aim of this study was to assess the epidemiology of IPD in adults (≥18 years) after PCV13 introduction for children: serotypes, clonal complexes, antibiotic non-susceptibility and clinical presentations. We performed a prospective, clinical surveillance of hospitalized culture-confirmed IPDs in adults in nine Spanish hospitals (August 2010-June 2015). A total of 1087 culture-confirmed IPD episodes were included, of which 772 (71.0%) had bacteremic pneumonia (401 complicated/371 uncomplicated pneumonia), 122 (11.2%) meningitis, 102 (9.4%) non-focal bacteremia, 34 (3.1%) peritonitis and 57 (5.3%) others. The most common serotypes were: 3 (12.7%), 19A (8.5%), 8 (7.7%), 7F (6.3%), 1 (4.2%), 6C (4.2%), 11A (4.2%), 22F (4.2%) and 14 (4.0%). Vaccine types (PCV13 + 6C) caused 49.8% of IPD episodes, with a significant decrease over the 5-year period, and significant decreases in serotypes 6C and 7F. The most common genotypes were: CC180 (8.4%), CC191 (6.0%), and CC53 (5.0%). Vaccine types caused 53.9% (414/768) pneumonia episodes and 58.9% (235/399) complicated pneumonia, 53.4% IPD in adults <50 years (143/268), and 54.7% IPD in immunocompetent patients (337/616). Overall non-susceptibility was 25.9% to penicillin (1.1% for parenteral criteria), 24.9% to erythromycin and 2.7% to levofloxacin. CONCLUSIONS: Although the percentage of vaccine-types causing IPDs in adults significantly decreased, it remained high. Associations of vaccine types with pneumonia (with complicated pneumonia for specific serotypes), and immunocompetent patients point to the burden of IPD caused by PCV13 serotypes.
导致成人侵袭性肺炎球菌病(IPD)的血清型/基因型由疫苗接种策略决定。本研究旨在评估 PCV13 用于儿童后成人 IPD(≥18 岁)的流行病学:血清型、克隆复合体、抗生素耐药性和临床表现。我们对 9 家西班牙医院(2010 年 8 月至 2015 年 6 月)住院确诊为 IPD 的成人进行了前瞻性临床监测。共纳入 1087 例培养确诊的 IPD 病例,其中 772 例(71.0%)为菌血症性肺炎(401 例为复杂性/371 例为单纯性肺炎),122 例(11.2%)为脑膜炎,102 例(9.4%)为非局灶性菌血症,34 例(3.1%)为腹膜炎,57 例(5.3%)为其他类型。最常见的血清型为:3 型(12.7%)、19A 型(8.5%)、8 型(7.7%)、7F 型(6.3%)、1 型(4.2%)、6C 型(4.2%)、11A 型(4.2%)、22F 型(4.2%)和 14 型(4.0%)。疫苗类型(PCV13+6C)引起 49.8%的 IPD 发作,在 5 年期间显著下降,血清型 6C 和 7F 显著下降。最常见的基因型为:CC180(8.4%)、CC191(6.0%)和 CC53(5.0%)。疫苗类型引起 53.9%(414/768)肺炎发作和 58.9%(235/399)复杂性肺炎,53.4%的 IPD 发生在<50 岁的成年人(143/268),54.7%的 IPD 发生在免疫功能正常的患者(337/616)。青霉素总体不敏感率为 25.9%(根据静脉注射标准为 1.1%),红霉素不敏感率为 24.9%,左氧氟沙星不敏感率为 2.7%。结论:尽管导致成人 IPD 的疫苗类型百分比显著下降,但仍居高不下。疫苗类型与肺炎(特定血清型与复杂性肺炎相关)以及免疫功能正常患者之间的关联表明 PCV13 血清型引起的 IPD 负担很重。