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模拟婴儿中13种传染性致病微生物造成的不明死亡负担。

Modelling the unidentified mortality burden from thirteen infectious pathogenic microorganisms in infants.

作者信息

Markov P V, Crowcroft N S

机构信息

Immunisation Department, Health Protection Agency Communicable Disease Surveillance Centre, London, UK.

出版信息

Epidemiol Infect. 2007 Jan;135(1):17-26. doi: 10.1017/S0950268806006625. Epub 2006 Jun 2.

Abstract

Official statistics routinely underestimate mortality from specific microorganisms and deaths are assigned to non-specific syndromes. Here we estimate mortality attributed to specific pathogens by modelling non-specific infant deaths from laboratory reports and codes on death certificates for these pathogens, 1993-2000 in England and Wales using a generalized linear model. In total, 22.4-59.8% of non-specific deaths in infants (25-66 deaths a year) are attributable to specific pathogens. Yearly deaths from Bordetella pertussis in neonates are 6.8 [95% confidence interval (CI) 1.5-11.9]. In post-neonates 9.4 (95% CI 2.3-16.6) deaths a year are attributable to Neisseria meningitidis, 7.3 (95% CI 2.4-12.3) to Streptococcus pneumoniae, from 2.8 (95% CI 0.8-4.9) to 15.1 (95% CI 9.4-20.9) to respiratory syncytial virus (RSV) and 3 (95% CI 0.3-5.9) to parainfluenza type 2. Our results suggest there is substantial hidden mortality for a number of pathogens in infants. A considerable proportion of deaths classified to infectious syndromes are non-infectious, suggesting low specificity of death certification. Laboratory reports were the more reliable source, reinforcing the asset of strong surveillance systems.

摘要

官方统计数据通常会低估特定微生物导致的死亡率,死亡原因被归类为非特定综合征。在此,我们通过对1993 - 2000年英格兰和威尔士实验室报告及这些病原体死亡证明编码中的非特定婴儿死亡情况进行建模,使用广义线性模型来估计特定病原体导致的死亡率。总体而言,婴儿中非特定死亡的22.4% - 59.8%(每年25 - 66例死亡)可归因于特定病原体。新生儿中百日咳博德特氏菌每年导致的死亡为6.8例[95%置信区间(CI)1.5 - 11.9]。在新生儿期后的婴儿中,每年9.4例(95% CI 2.3 - 16.6)死亡可归因于脑膜炎奈瑟菌,7.3例(95% CI 2.4 - 12.3)可归因于肺炎链球菌,呼吸道合胞病毒(RSV)导致的死亡从2.8例(95% CI 0.8 - 4.9)到15.1例(95% CI 9.4 - 20.9),副流感2型导致3例(95% CI 0.3 - 5.9)死亡。我们的结果表明,婴儿中多种病原体存在大量隐性死亡。归类为感染性综合征的死亡中有相当一部分并非感染性原因,这表明死亡证明的特异性较低。实验室报告是更可靠的来源,这凸显了强大监测系统的价值。

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