Clinical Course of Enterovirus D68 in Hospitalized Children

被引:23
|
作者
Schuster, Jennifer E. [1 ]
Selvarangan, Rangaraj [1 ,2 ]
Hassan, Ferdaus [2 ]
Briggs, Kayla B. [3 ]
Hays, Lindsay [2 ]
Miller, Jenna O. [1 ]
Pahud, Barbara [1 ]
Puls, Henry T. [1 ]
Queen, Mary Ann [1 ]
Thompson, Marita T. [1 ]
Weddle, Gina [1 ]
Jackson, Mary Anne [1 ]
机构
[1] Childrens Mercy Hosp, Dept Pediat, Kansas City, MO 64108 USA
[2] Childrens Mercy Hosp, Dept Pathol & Lab Med, Kansas City, MO 64108 USA
[3] Univ Missouri, Sch Med, Kansas City, MO 64108 USA
关键词
acute respiratory illness; asthma; enterovirus D68; outbreak; wheeze; RESPIRATORY-TRACT INFECTIONS; YOUNG-CHILDREN; HUMAN METAPNEUMOVIRUS; ILLNESS; OUTBREAK; BURDEN; USA; SEVERITY; DISEASE;
D O I
10.1097/INF.0000000000001421
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Enterovirus D68 (EV-D68) has been sporadically reported as a cause of respiratory tract infections. In 2014, an international outbreak of EV-D68 occurred and caused severe respiratory disease in the pediatric population. Methods: A retrospective chart review was performed of children admitted to Children's Mercy Hospital from August 1, 2014, to September 15, 2014, with positive multiplex polymerase chain reaction testing for EV/rhinovirus (RV). Specimens were subsequently tested for EV-D68, and clinical data were obtained from the medical records. Patients with EV-D68 were compared with children presenting simultaneously with other EV/RV. Results: Of 542 eligible specimens, children with EV-D68 were significantly older than children with other EV/RV (4.6 vs. 2.2 years, P < 0.001). Children with EV-D68 were more likely to have a history of asthma (38.6% vs. 30.0%, P - 0.04) or recurrent wheezing (22.1% vs. 14.8%, P - 0.04). EV-D68-positive children more commonly received supplemental oxygen (86.7% vs. 65.0%, P < 0.001), albuterol (91.2% vs. 65.5%, P < 0.001) and corticosteroids (82.9% vs. 58.6%, P < 0.001). Age >= 5 years was an independent risk factor for intensive care unit management in EV-D68-infected children. Children with a history of asthma or recurrent wheezing and EV-D68 received supplemental oxygen (92.7% vs. 82.4%, P - 0.007) and magnesium (42.7% vs. 29.7%, P = 0.03) at higher rates and more continuous albuterol (3 vs. 2 hours, P - 0.03) than those with other EV/RV. Conclusions: EV-D68 causes severe disease in the pediatric population, particularly in children with a history of asthma or recurrent wheezing. EV-D68-positive children are more likely to require therapy for refractory bronchospasm and may need intensive care unit-level care.
引用
收藏
页码:290 / 295
页数:6
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