Pelton Stephen I, Shea Kimberly M, Farkouh Raymond A, Strutton David R, Braun Sebastian, Jacob Christian, Klok Rogier, Gruen Elana S, Weycker Derek
Boston University School of Public Health, Boston, MA, USA.
Boston Medical Center, Boston, MA, USA.
BMC Infect Dis. 2015 Oct 30;15:470. doi: 10.1186/s12879-015-1162-y.
The objective of this study is to evaluate rates of all-cause pneumonia among "at-risk" and "high-risk" children and adults in Germany-in comparison with age-stratified healthy counterparts-during the period following the 2006 recommendation for universal immunization of infants with pneumococcal conjugate vaccine.
Retrospective cohort design and healthcare claims information for 3.4 M persons in Germany (2009-2012) were employed. Study population was stratified by age and risk profile (healthy, "at-risk" [with chronic medical conditions], and "high-risk" [immunocompromised]). At-risk and high-risk conditions, as well as episodes of all-cause pneumonia, were identified via diagnosis, procedure, and drug codes.
Rates of all-cause pneumonia were 1.7 (95 % CI 1.7-1.8) to 2.5 (2.4-2.5) times higher among children and adults with at-risk conditions versus healthy counterparts, and 1.8 (1.8-1.9) to 4.1 (4.0-4.2) times higher among children and adults with high-risk conditions. Rates of all-cause pneumonia among at-risk persons increased in a graded and monotonic fashion with increasing numbers of conditions (i.e., risk stacking).
An increased risk for all-cause pneumonia in German children and adults with a spectrum of medical conditions persists in the era of widespread pneumococcal vaccination, and pneumonia risk in persons with ≥2 at-risk conditions is comparable or higher than those with high-risk conditions.
本研究的目的是评估在2006年推荐对婴儿普遍接种肺炎球菌结合疫苗之后的时期内,德国“高危”和“极高危”儿童及成人中全因性肺炎的发生率,并与按年龄分层的健康对照者进行比较。
采用回顾性队列设计,并利用德国340万人(2009 - 2012年)的医疗保健索赔信息。研究人群按年龄和风险状况(健康、“高危”[患有慢性疾病]和“极高危”[免疫功能低下])进行分层。通过诊断、操作和药物代码确定高危和极高危状况以及全因性肺炎发作情况。
患有高危状况的儿童和成人中全因性肺炎的发生率比健康对照者高1.7(95%可信区间1.7 - 1.8)至2.5(2.4 - 2.5)倍,而患有极高危状况的儿童和成人中则高1.8(1.8 - 1.9)至4.1(4.0 - 4.2)倍。高危人群中全因性肺炎的发生率随着疾病数量的增加(即风险叠加)呈分级和单调上升趋势。
在肺炎球菌广泛接种的时代,患有一系列疾病的德国儿童和成人中全因性肺炎的风险仍然增加,且患有≥2种高危状况的人群的肺炎风险与极高危人群相当或更高。