Characteristics and Outcomes of Coronavirus Infection in Children: The Role of Viral Factors and an Immunocompromised State

被引:110
|
作者
Ogimi, Chikara [1 ,3 ,6 ]
Englund, Janet A. [3 ,6 ]
Bradford, Miranda C. [8 ]
Qin, Xuan [5 ,7 ]
Boeckh, Michael [1 ,2 ,4 ]
Waghmare, Alpana [1 ,3 ,6 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, 1124 Columbia St, Seattle, WA 98104 USA
[2] Fred Hutchinson Canc Res Ctr, Clin Res Div, 1124 Columbia St, Seattle, WA 98104 USA
[3] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[4] Univ Washington, Dept Med, Seattle, WA USA
[5] Univ Washington, Dept Lab Med, Seattle, WA 98195 USA
[6] Seattle Childrens Hosp, Pediat Infect Dis Div, Washington, DC USA
[7] Seattle Childrens Hosp, Microbiol Lab, Washington, DC USA
[8] Seattle Childrens Res Inst, Ctr Clin & Translat Res, Childrens Core Biomed Stat, Washington, DC USA
基金
美国国家卫生研究院;
关键词
human coronavirus; immunocompromised host; lower respiratory tract disease; respiratory copathogen; respiratory polymerase chain reaction (PCR); RESPIRATORY-TRACT INFECTIONS; CELL TRANSPLANT RECIPIENTS; HEMATOPOIETIC STEM-CELL; CLINICAL-OUTCOMES; HUMAN RHINOVIRUS; NL63; INFECTIONS; MULTIPLEX PCR; EPIDEMIOLOGY; DISEASE; VIRUSES;
D O I
10.1093/jpids/pix093
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background. Immunocompromised children might be predisposed to serious infections from human coronaviruses (HCoVs), including strains OC43, NL63, HKU1, and 229E; however, the virologic and clinical features of HCoV infection in immunocompromised children have not been compared to those in nonimmunocompromised children. Methods. We retrospectively analyzed a cohort of children who presented to Seattle Children's Hospital and in whom HCoV was detected by a multiplex respiratory polymerase chain reaction assay of a nasal sample between October 2012 and March 2016. Lower respiratory tract disease (LRTD) was defined as possible or definite infiltrate seen in chest imaging, need for oxygen, or abnormal lung examination in conjunction with a physician diagnosis of LRTD. We used logistic regression modeling to evaluate risk factors for LRTD and LRTD that necessitated oxygen use (severe LRTD), including an immunocompromised state, in children with HCoV infection. Results. The median ages of 85 immunocompromised and 1152 nonimmunocompromised children with HCoV infection were 6.3 and 1.6 years, respectively. The prevalence of LRTD and of severe LRTD did not differ greatly between the immunocompromised and nonimmunocompromised patients (22% vs 26% [LRTD] and 15% vs 11% [severe LRTD], respectively); however, in a multivariable model, an immunocompromised state was associated with an increased likelihood of severe LRTD (adjusted odds ratio, 2.5 [95% confidence interval, 1.2-4.9]; P=.01). Younger age, having an underlying pulmonary disorder, and the presence of respiratory syncytial virus were also associated with LRTD or severe LRTD in multivariable models. The risks of LRTD or severe LRTD did not differ among the children with different HCoV strains. Conclusions. The presence of a copathogen and host factors, including an immunocompromised state, were associated with increased risk for severe LRTD. Recognizing risk factors for severe respiratory illness might assist in risk stratification.
引用
收藏
页码:21 / 28
页数:8
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