过去10年(2013-2023年)住院的社区获得性肺炎成人肺炎球菌肺炎趋势和血清3型的作用

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM Thorax Pub Date : 2024-12-12 DOI:10.1136/thorax-2024-221976
Louise Lansbury, Tricia M McKeever, Hannah Lawrence, Harry Pick, Vadsala Baskaran, Rochelle Edwards-Pritchard, Laura Matthews, Helen Bailey, Deborah Ashton, Lesley Bendall, Chamira Rodrigo, Priya Daniel, David Litt, Seyi Eletu, Hanshi Parmar, Carmen Sheppard, Shamez N Ladhani, Caroline Trotter, Wei Shen Lim
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Methods We conducted a prospective cohort study of adults hospitalised with CAP between September 2013 and May 2023. Pneumococcal serotypes were identified using a serotype-specific 24-valent urinary-antigen assay. Trends in the proportion of CAP due to pneumococcus and causative serotypes were compared prepandemic and postpandemic. Risk factors and severity of serotype 3 pneumonia were compared with other serotypes using logistic regression. Results Of 5186 patients with CAP, 2193 (42.2%) had pneumococcal pneumonia. The proportion of CAP due to pneumococcus increased across all ages between 2013 and 2023 (36.4%–66.9%, p<0.001). The proportion due to serotype 3 increased significantly from 13.4% (2013) to 48.8% (2023). Serotype 3 pneumonia in adults was associated with older age (p<0.001), male sex (adjusted OR (aOR) 2.22, 95% CI 1.64 to 3.01) and chronic renal disease (aOR 1.81, 95% CI 1.09 to 3.02). 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引用次数: 0

摘要

背景:随着高价肺炎球菌疫苗的出现和新的成人免疫策略的讨论,我们旨在评估个体肺炎球菌血清型对肺炎球菌性社区获得性肺炎(CAP)负担的贡献。在过去的10年里,对CAP住院的成人肺炎球菌肺炎流行病学趋势进行了评估。检查与血清3型相关的危险因素和严重程度。方法:我们对2013年9月至2023年5月期间因CAP住院的成年人进行了一项前瞻性队列研究。采用血清型特异性24价尿抗原测定法鉴定肺炎球菌血清型。比较了大流行前和大流行后由肺炎球菌和致病血清型引起的CAP比例的趋势。采用logistic回归比较其他血清型肺炎的危险因素和严重程度。结果5186例CAP患者中,2193例(42.2%)为肺炎球菌性肺炎。2013 - 2023年间,肺炎球菌引起的CAP比例在所有年龄段均有所增加(36.4%-66.9%,p<0.001)。血清3型所占比例从2013年的13.4%显著上升至2023年的48.8%。成人血清3型肺炎与年龄较大(p<0.001)、男性(校正OR (aOR) 2.22, 95% CI 1.64 ~ 3.01)和慢性肾脏疾病(aOR 1.81, 95% CI 1.09 ~ 3.02)相关。血清3型肺炎未观察到与严重程度、重症监护要求、死亡率或再入院相关。血清型3是成人肺炎球菌CAP的主要血清型,尽管实施了成熟婴儿肺炎球菌免疫规划,但该血清型仍在增加,这与缺乏对该血清型的群体保护相一致。如有合理要求,可提供资料。
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Pneumococcal pneumonia trends in adults hospitalised with community-acquired pneumonia over 10 years (2013–2023) and the role of serotype 3
Background With higher valency pneumococcal vaccines on the horizon and new adult immunisation strategies under discussion, we aimed to evaluate the contribution of individual pneumococcal serotypes to the burden of pneumococcal community-acquired pneumonia (CAP). Over 10 years, trends in pneumococcal pneumonia epidemiology in adults hospitalised with CAP were assessed. The risk factors and severity associated with serotype 3 were examined. Methods We conducted a prospective cohort study of adults hospitalised with CAP between September 2013 and May 2023. Pneumococcal serotypes were identified using a serotype-specific 24-valent urinary-antigen assay. Trends in the proportion of CAP due to pneumococcus and causative serotypes were compared prepandemic and postpandemic. Risk factors and severity of serotype 3 pneumonia were compared with other serotypes using logistic regression. Results Of 5186 patients with CAP, 2193 (42.2%) had pneumococcal pneumonia. The proportion of CAP due to pneumococcus increased across all ages between 2013 and 2023 (36.4%–66.9%, p<0.001). The proportion due to serotype 3 increased significantly from 13.4% (2013) to 48.8% (2023). Serotype 3 pneumonia in adults was associated with older age (p<0.001), male sex (adjusted OR (aOR) 2.22, 95% CI 1.64 to 3.01) and chronic renal disease (aOR 1.81, 95% CI 1.09 to 3.02). Serotype 3 pneumonia was not observed to be associated with severity, critical care requirement, mortality or readmission. Interpretation Serotype 3 is the predominant serotype in adult pneumococcal CAP and has been increasing despite a mature infant pneumococcal immunisation programme, consistent with a lack of herd protection for this serotype. Data are available on reasonable request.
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来源期刊
Thorax
Thorax 医学-呼吸系统
CiteScore
16.10
自引率
2.00%
发文量
197
审稿时长
1 months
期刊介绍: Thorax stands as one of the premier respiratory medicine journals globally, featuring clinical and experimental research articles spanning respiratory medicine, pediatrics, immunology, pharmacology, pathology, and surgery. The journal's mission is to publish noteworthy advancements in scientific understanding that are poised to influence clinical practice significantly. This encompasses articles delving into basic and translational mechanisms applicable to clinical material, covering areas such as cell and molecular biology, genetics, epidemiology, and immunology.
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