Wiese Andrew D, Griffin Marie R, Zhu Yuwei, Mitchel Edward F, Grijalva Carlos G
Department of Health Policy, Vanderbilt University, Nashville, USA.
Department of Health Policy, Vanderbilt University, Nashville, USA; Department of Medicine, Vanderbilt University, Nashville, USA; VA TN Valley Health Care System, Nashville, USA.
Vaccine. 2016 Dec 7;34(50):6243-6249. doi: 10.1016/j.vaccine.2016.10.062. Epub 2016 Nov 7.
Parapneumonic empyema, a serious complication of pneumonia, started increasing among U.S. children before the introduction of the 7-valent pneumococcal conjugate vaccine (PCV7) in 2000, and continued afterwards. This increase was due in part to pneumococcal serotypes not included in PCV7 that were included in the new 13-valent (PCV13) vaccine introduced in 2010. We assessed changes in the incidence of empyema hospitalizations among U.S. children after PCV13 introduction.
We calculated annualized empyema hospitalization rates among U.S. children <18years using Nationwide Inpatient Sample and Census data (1997-2013) for four periods based on PCV7 and PCV13 introductions. Relative rates (RR) and 95% confidence intervals (CI) were calculated by age group and sex, comparing PCV7 [early-PCV7 (2001-2005) and late-PCV7 (2006-2009)] and PCV13 (2011-2013) periods with the pre-PCV7 period (1997-1999). Secondary analyses examined changes in pneumococcal, streptococcal, staphylococcal and unspecified empyema.
Among children <18years of age, annualized empyema hospitalization rates peaked at 3.6 per 100,000 in the late-PCV7 period compared with 2.1 per 100,000 in the pre-PCV7 period [RR: 1.70 (95% CI: 1.11-2.60)]. However, annualized rates in the post-PCV13 period declined to 2.0 per 100,000, similar to rates in the pre-PCV7 period. Empyema rates among children <2years were lower in the post-PCV13 period compared to the pre-PCV7 period [RR: 0.77 (95% CI: 0.61-0.96)], but rates in the two periods among children 2-4 and 5-17years were similar. Most empyema were of unspecified etiology. Pneumococcal and unspecified empyema declined after PCV13 introduction.
Although empyema hospitalization rates among U.S. children peaked after PCV7 introduction, rates decreased substantially following the introduction of PCV13.
肺炎旁胸腔积液是肺炎的一种严重并发症,在2000年7价肺炎球菌结合疫苗(PCV7)引入美国儿童之前开始增加,并在之后持续上升。这种增加部分归因于PCV7中未包含但在2010年引入的新型13价(PCV13)疫苗中包含的肺炎球菌血清型。我们评估了PCV13引入后美国儿童胸腔积液住院率的变化。
我们使用全国住院患者样本和人口普查数据(1997 - 2013年),根据PCV7和PCV13的引入情况,计算了四个时期内18岁以下美国儿童的年度胸腔积液住院率。通过年龄组和性别计算相对率(RR)和95%置信区间(CI),将PCV7时期[早期PCV7(2001 - 2005年)和晚期PCV7(2006 - 2009年)]和PCV13时期(2011 - 2013年)与PCV7引入前时期(1997 - 1999年)进行比较。二次分析检查了肺炎球菌、链球菌、葡萄球菌和未明确病因的胸腔积液的变化。
在18岁以下儿童中,晚期PCV7时期年度胸腔积液住院率峰值为每10万人3.6例,而PCV7引入前时期为每10万人2.1例[RR:1.70(95%CI:1.11 - 2.60)]。然而,PCV13引入后时期的年度住院率降至每10万人2.0例,与PCV7引入前时期相似。PCV13引入后时期2岁以下儿童的胸腔积液率低于PCV7引入前时期[RR:0.77(95%CI:0.61 - 0.96)],但2 - 4岁和5 - 17岁儿童在这两个时期的胸腔积液率相似。大多数胸腔积液病因未明确。PCV13引入后,肺炎球菌性和未明确病因的胸腔积液有所下降。
尽管美国儿童胸腔积液住院率在PCV7引入后达到峰值,但在PCV13引入后大幅下降。