儿童哮喘恶化严重程度和治疗反应的病毒决定因素。

Nidhya Navanandan, Nathan D Jackson, Katharine L Hamlington, Jamie L Everman, Elmar Pruesse, Elizabeth A Secor, Zoe Stewart, Katrina Diener, Isabel Hardee, Alec Edid, Helio Sulbaran, Rakesh D Mistry, Todd A Florin, Angela C Yoder, Camille M Moore, Stanley J Szefler, Andrew H Liu, Max A Seibold
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引用次数: 0

摘要

背景:虽然呼吸道病毒是哮喘加重的常见诱因,但病毒感染特征对儿科急诊室(ED)哮喘加重表现和治疗反应的影响尚不清楚:评估急诊科哮喘加重儿童的病毒感染特征,并检验其与严重程度和治疗反应的关系:方法:对接受吸入支气管扩张剂和全身皮质类固醇标准急诊室哮喘加重治疗的 4-18 岁儿童进行前瞻性研究。采集鼻拭子进行病毒元基因组分析,确定病毒的存在、载量和种类。结果包括哮喘加重的严重程度(小儿哮喘严重程度(PAS)评分、临床医生的印象和生命体征)和治疗反应(出院回家后无需再接受哮喘治疗):结果:在107名儿童中,47%的儿童出现中度/重度哮喘,64%的儿童对治疗有反应。对 73 名儿童的鼻拭子进行病毒元基因组分析后发现,86% 的儿童感染了病毒,其中发现了 10 种不同的病毒,主要是鼻病毒 A(RV-A)、RV-C 和肠道病毒 D68。与非RV-A感染相比,涉及RV-A的病情加重较轻(几率比[OR]=0.25;95% CI=0.07-0.83),对治疗的反应也更强烈;而涉及肠道病毒D68的病情加重更严重(OR=8.3;95% CI=1.3-164.7),与治疗反应无关。病毒载量与治疗反应无关,但与心率(rpartial=0.48)、呼吸频率(rpartial=0.25)和血氧饱和度(rpartial=-0.25)呈强烈的线性关系,表明病情严重:结论:大多数急诊室哮喘加重是由呼吸道病毒引发的。病毒种类与严重程度和治疗反应相关,这表明早期病原体检测可为急诊室治疗决策提供依据。还需要进行更多的研究,以确定不同病毒种类引发的加重的病理生物学基础差异,以及如何有效治疗这些异质性加重。
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Viral Determinants of Childhood Asthma Exacerbation Severity and Treatment Response.

Background: Although respiratory viruses are common triggers of asthma exacerbations, the influence of viral infection characteristics on exacerbation presentation and treatment response in the pediatric emergency department (ED) is unclear.

Objective: To assess viral infection characteristics of children experiencing ED asthma exacerbations and to test their associations with severity and treatment response.

Methods: This is a prospective study of children, aged 4 to 18 years, who received standard ED asthma exacerbation treatment with inhaled bronchodilators and systemic corticosteroids. Nasal swabs collected for viral metagenomic analyses determined virus presence, load, and species. Outcomes included exacerbation severity (Pediatric Asthma Severity [PAS] score, clinician impression, and vital signs) and treatment response (discharge home without needing additional asthma therapies).

Results: Of 107 children, 47% had moderate/severe exacerbations by PAS and 64% demonstrated treatment response. Viral metagenomic analysis on nasal swabs from 73 children detected virus in 86%, with 10 different species identified, primarily rhinovirus A (RV-A), RV-C, and enterovirus D68. Exacerbations involving RV-A were milder (odds ratio [OR] = 0.25; 95% confidence interval [CI] = 0.07-0.83) and tended to be more responsive to treatment than non-RV-A infections, whereas exacerbations involving enterovirus D68 were more severe (OR = 8.3; 95% CI = 1.3-164.7) and had no treatment response association. Viral load was not associated with treatment response but exhibited a strong linear relationship with heart rate (rpartial = 0.48), respiratory rate (rpartial = 0.25), and oxygen saturation (rpartial = -0.25), indicative of severity.

Conclusions: The majority of ED asthma exacerbations are triggered by respiratory viruses. Viral species are associated with severity and treatment response, suggesting that early pathogen detection could inform ED treatment decisions. Additional studies are needed to identify differences in pathobiology underlying exacerbations triggered by different viral species, and how to effectively treat these heterogeneous exacerbations.

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来源期刊
CiteScore
11.10
自引率
9.60%
发文量
683
审稿时长
50 days
期刊介绍: JACI: In Practice is an official publication of the American Academy of Allergy, Asthma & Immunology (AAAAI). It is a companion title to The Journal of Allergy and Clinical Immunology, and it aims to provide timely clinical papers, case reports, and management recommendations to clinical allergists and other physicians dealing with allergic and immunologic diseases in their practice. The mission of JACI: In Practice is to offer valid and impactful information that supports evidence-based clinical decisions in the diagnosis and management of asthma, allergies, immunologic conditions, and related diseases. This journal publishes articles on various conditions treated by allergist-immunologists, including food allergy, respiratory disorders (such as asthma, rhinitis, nasal polyps, sinusitis, cough, ABPA, and hypersensitivity pneumonitis), drug allergy, insect sting allergy, anaphylaxis, dermatologic disorders (such as atopic dermatitis, contact dermatitis, urticaria, angioedema, and HAE), immunodeficiency, autoinflammatory syndromes, eosinophilic disorders, and mast cell disorders. The focus of the journal is on providing cutting-edge clinical information that practitioners can use in their everyday practice or to acquire new knowledge and skills for the benefit of their patients. However, mechanistic or translational studies without immediate or near future clinical relevance, as well as animal studies, are not within the scope of the journal.
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