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首页> 外文期刊>Journal of tropical pediatrics. >Change in Pneumococcus Serotypes but not Mortality or Morbidity in Pre- and Post-13-Valent Polysaccharide Conjugate Vaccine Era: Epidemiology in a Pediatric Intensive Care Unit over 10 Years
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Change in Pneumococcus Serotypes but not Mortality or Morbidity in Pre- and Post-13-Valent Polysaccharide Conjugate Vaccine Era: Epidemiology in a Pediatric Intensive Care Unit over 10 Years

机译:在13例和后13岁的多糖缀合物疫苗时代和13例多糖的死亡率或发病率的变化:10年超过10年的儿科重症监护单元的流行病学

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摘要

Aim: Pneumococcus is a common commensal and an important pathogen among children for which immunization is available. Some serotypes occasionally cause severe pneumococcal disease with high mortality and morbidity. We reviewed all pneumococcal serotypes and mortality/morbid-ity in a pediatric intensive care unit (PICU) following universal pneumococcal conjugate vaccine (PCV) immunization. Methods: A 13-valent PCV was introduced in the universal immunization program in late 2011 in Hong Kong. We retrospectively reviewed all pneumococcal serotypes in the pre-(2007-11) and post-(2012-16) 13-valent PCV era. Results: There were 29 (1.9%) PICU patients with pneumococcal isolation, of which 6 died (20% motality). Serogroups 6 and 19 predominated before and Serogroup 3 after 2012. In the post-13-valent PCV era, the prevalence of pneumococcus isolation in PICU was increased from 1 to 2% (p = 0.04);Serogroup 3 was the major serotype of morbidity, despite supposedly under vaccine coverage. The majority of pneumococcus were penicillin-sensitive (94%) in the post 13-valent PCV era. All pneumococcus specimens were sensitive to cefotaxime and vancomycin. Binary logistic regression showed that there were reductions in Serogroup 6 (odds ratio [OR], 0.050;95% confidence interval [CI], 0.004-0.574;p = 0.016) and Serogroup 19 (odds ratio [OR], 0.105;95% confidence interval [CI], 0.014-0.786;p = 0.028) but not mortality or morbidity for patients admitted after 2012. Conclusions: SPD is associated with significant morbidity and mortality, despite treatment with systemic antibiotics and ICU support. The expanded coverage of 13-valent PCV results in the reduction of Serotypes 6 and 19 but not mortality/morbidity associated with SPD in the setting of a PICU.
机译:目的:肺炎球菌是一种常见的共生和免疫接种的儿童之间的重要病原体。一些血清型偶尔会导致严重的肺炎球菌病,具有高死亡率和发病率。在通用肺炎球菌缀合物疫苗(PCV)免疫之后,我们在儿科重症监护室(PICU)中审查了所有肺炎球菌血清型和死亡率/病态。方法:2011年底,在香港普遍免疫计划中引入了13年的PCV。我们回顾性地在第(2007-11)前的所有肺炎球菌血清型和(2012-16)的13 VentCCV时代。结果:39例(1.9%)PICU患者肺炎球菌患者,其中6例死亡(20%的动力)。血清小组6和19以前占主导地位和血清组3。在13年后的PCV时代,PICU中肺炎球菌分离的患病率从1%增加到2%(P = 0.04);血清组3是发病率的主要血清型尽管在疫苗覆盖范围内。大多数肺炎球菌在第13 Vent PCV时代术后青霉素敏感(94%)。所有肺炎球菌标本对头孢噻肟和万古霉素敏感。二元逻辑回归表明,血清组6的减少(差距[或],0.050; 95%; 95%置信区间[CI],0.004-0.574; P = 0.016)和血清组19(差距率[或],0.105; 95%置信区间[CI],0.014-0.786; p = 0.028),但在2012年后患者的死亡率或发病率不是死亡率或发病率。结论:尽管用全身抗生素和ICU支持治疗,SPD与大量发病率和死亡率有关。 13价PCV的扩大覆盖率导致血清型6和19的减少,但不会在PICU的设置中与SPD相关的死亡率/发病率。

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