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《复合哮喘严重程度指数的制定与验证——一种适用于儿童和青少年的结局指标》。

Development and validation of the Composite Asthma Severity Index--an outcome measure for use in children and adolescents.

机构信息

Rho Federal Systems Division, Inc, Chapel Hill, NC 27517, USA.

出版信息

J Allergy Clin Immunol. 2012 Mar;129(3):694-701. doi: 10.1016/j.jaci.2011.12.962. Epub 2012 Jan 12.

Abstract

BACKGROUND

Asthma severity is reflected in many aspects of the disease, including impairment and future risks, particularly for exacerbations. According to the Expert Panel Report 3: Guidelines for the Diagnosis and Management of Asthma, however, to assess more comprehensively the severity of asthma the level of current treatment needed to maintain a level of control should be included.

OBJECTIVE

Development and validation of a new instrument, the Composite Asthma Severity Index (CASI), which can quantify disease severity by taking into account impairment, risk, and the amount of medication needed to maintain control. At present, there is no instrument available to measure and assess the multidimensional nature of asthma.

METHODS

Twenty-six established asthma investigators, who are part of the National Institutes of Health-supported Inner City Asthma Consortium, participated in a modified Delphi consensus process to identify and weight the dimensions of asthma. Factor analysis was performed to identify independent domains of asthma by using the Asthma Control Evaluation trial. CASI was validated by using the Inner City Anti-IgE Therapy for Asthma trial.

RESULTS

CASI scores include 5 domains: day symptoms and albuterol use, night symptoms and albuterol use, controller treatment, lung function measures, and exacerbations. At Asthma Control Evaluation trial enrollment, CASI ranged from 0 to 17, with a mean of 6.2. CASI was stable, with minimal change in variance after 1 year of treatment. In external validation, CASI detected a 32% larger improvement than did symptoms alone.

CONCLUSION

CASI retained its discriminatory ability even with low levels of symptoms reported after months of guidelines-directed care. Thus, CASI has the ability to determine the level of asthma severity and provide a composite clinical characterization of asthma.

摘要

背景

哮喘的严重程度反映在疾病的多个方面,包括受损程度和未来风险,尤其是哮喘恶化的风险。然而,根据《哮喘诊治指南》(Expert Panel Report 3),为了更全面地评估哮喘的严重程度,需要纳入当前治疗以维持控制水平的程度。

目的

开发和验证一种新的工具,即综合哮喘严重程度指数(Composite Asthma Severity Index,CASI),该指数可以通过考虑受损程度、风险以及维持控制所需的药物剂量来量化疾病的严重程度。目前,尚无测量和评估哮喘多维性质的工具。

方法

26 位已确立的哮喘研究人员参与了一项经过改良的 Delphi 共识过程,以确定和加权哮喘的各个维度。通过使用哮喘控制评估试验(Asthma Control Evaluation trial)进行因子分析,以确定哮喘的独立领域。通过城市内部抗 IgE 治疗哮喘试验(Inner City Anti-IgE Therapy for Asthma trial)对 CASI 进行验证。

结果

CASI 评分包括 5 个领域:日间症状和沙丁胺醇使用、夜间症状和沙丁胺醇使用、控制器治疗、肺功能测量和恶化。在哮喘控制评估试验登记时,CASI 范围从 0 到 17,平均为 6.2。CASI 稳定,治疗 1 年后方差变化最小。在外部验证中,CASI 检测到的改善比仅症状改善大 32%。

结论

即使在接受了数月指南指导的治疗后报告的症状水平较低的情况下,CASI 仍保留其区分能力。因此,CASI 有能力确定哮喘严重程度水平,并提供哮喘的综合临床特征描述。

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