Trends in Methicillin-Resistant Staphylococcus aureus Hospitalizations in the United States, 2010-2014

被引:87
作者
Klein, Eili Y. [1 ,2 ]
Mojica, Nestor [2 ]
Jiang, Wendi [2 ]
Cosgrove, Sara E. [3 ,4 ]
Septimus, Edward [5 ,6 ]
Morgan, Daniel J. [2 ,7 ]
Laxminarayan, Ramanan [2 ,8 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Emergency Med, 5801 Smith Ave,Davis Ste 3220, Baltimore, MD 21209 USA
[2] Ctr Dis Dynam Econ & Policy, Washington, DC USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Div Infect Dis, 5801 Smith Ave,Davis Ste 3220, Baltimore, MD 21209 USA
[4] Johns Hopkins Univ, Sch Med, Armstrong Inst Patient Safety & Qual, 5801 Smith Ave,Davis Ste 3220, Baltimore, MD 21209 USA
[5] Texas A&M Hlth Sci Ctr, Dept Internal Med, Houston, TX USA
[6] Hosp Corp Amer, Clin Serv Grp, Nashville, TN USA
[7] Univ Maryland, Sch Med, Dept Epidemiol & Publ Hlth, Baltimore, MD 21201 USA
[8] Princeton Univ, Princeton Environm Inst, Princeton, NJ 08544 USA
关键词
pediatrics; influenza; live attenuated influenza vaccine; influenza-like illness; developing country; EPIDEMIOLOGY; INFECTIONS;
D O I
10.1093/cid/cix640
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In a live attenuated influenza vaccine (LAIV) trial among young Bangladeshi children, we found no presenting combinations of clinical signs and/or symptoms that could distinguish influenza virus infection from other acute respiratory infections. LAIV was efficacious against moderate-to-severe influenza illness.Influenza causes substantial morbidity in children worldwide, although influenza vaccine is seldom used in low-resource settings. More information on the clinical presentation of influenza and the efficacy of vaccine is needed to inform policy. In 2013 we conducted a randomized, placebo-controlled clinical trial of live attenuated influenza vaccine (LAIV) in children aged 24-59 months in Bangladesh (N = 1761). If participants met prespecified specimen collection criteria, we collected nasopharyngeal washes for testing by singleplex reverse-transcription polymerase chain reaction (RT-PCR) for laboratory-confirmed influenza virus infection (LCI). A panel of RT-PCR assays was used to detect noninfluenza respiratory viruses. Primary efficacy results have been reported. In this analysis of prespecified and post hoc objectives from the trial, we compared signs and symptoms between LCI and non-LCI cases and estimated the efficacy of LAIV against moderate-to-severe LCI and other prespecified non-LCI clinical outcomes including all-cause pneumonia and acute otitis media. The most common signs and symptoms of LCI were fever, cough, and runny nose. The combination of subjective fever and cough had a 63% sensitivity for LCI. The combination of measured fever, cough, and runny nose was most specific (90%) but had low sensitivity (32%) for LCI. The efficacy of LAIV against vaccine-strain moderate-to-severe LCI was 56.7% (95% confidence interval, 9.5%-79.2%). No statistically significant vaccine efficacy was found against the non-laboratory-confirmed clinical outcomes. It was not possible to distinguish LCI from noninfluenza viral infections on clinical evaluations alone in this population of Bangladeshi children. LAIV was efficacious against moderate-to-severe LCI. NCT01797029.
引用
收藏
页码:1921 / 1923
页数:3
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