Performance Characteristics of Spirometry With Negative Bronchodilator Response and Methacholine Challenge Testing and Implications for Asthma Diagnosis

被引:23
作者
Selvanathan, Janannii [1 ,2 ]
Aaron, Shawn D. [3 ]
Sykes, Jenna R. [4 ]
Vandemheen, Katherine L. [3 ]
FitzGerald, J. Mark [5 ]
Ainslie, Martha [6 ]
Lemiere, Catherine [7 ]
Field, Stephen K. [8 ]
Mclvor, R. Andrew [9 ]
Hernandez, Paul [10 ]
Mayers, Irvin [11 ]
Mulpuru, Sunita [3 ]
Alvarez, Gonzalo G. [3 ]
Pakhale, Smita [3 ]
Mallick, Ranjeeta [3 ]
Boulet, Louis-Philippe [12 ]
Gupta, Samir [1 ,4 ]
机构
[1] Univ Toronto, St Michaels Hosp, Keenan Res Ctr, Li Ka Shing Knowledge Inst, Toronto, ON, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON, Canada
[3] Univ Ottawa, Ottawa Hosp Res Inst, Ottawa, ON, Canada
[4] St Michaels Hosp, Dept Med, Div Respirol, Toronto, ON, Canada
[5] Vancouver Coastal Hlth Res Inst, Ctr Heart & Lung Hlth, Vancouver, BC, Canada
[6] Univ Manitoba, Dept Med, Winnipeg, MB, Canada
[7] Univ Montreal, Dept Med, Montreal, PQ, Canada
[8] Univ Calgary, Dept Med, Cumming Sch Med, Calgary, AB, Canada
[9] McMaster Univ, Firestone Inst Resp Hlth, Hamilton, ON, Canada
[10] Dalhousie Univ, Dept Med, QEII Hlth Sci Ctr, Halifax, NS, Canada
[11] Univ Alberta, Dept Med, Edmonton, AB, Canada
[12] Univ Laval, Ctr Rech, Hop Laval, Quebec City, PQ, Canada
关键词
asthma; bronchial reactivity; bronchodilators; methacholine challenge testing; spirometry; INHALED FLUTICASONE PROPIONATE; AIRWAY HYPERRESPONSIVENESS; BRONCHIAL HYPERRESPONSIVENESS; RESPONSIVENESS; CHILDREN; MONTELUKAST; MANAGEMENT; HYPERREACTIVITY; CORTICOSTEROIDS; INDIVIDUALS;
D O I
10.1016/j.chest.2020.03.052
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
BACKGROUND: In patients with a history suggestive of asthma, diagnosis is usually confirmed by spirometry with bronchodilator response (BDR) or confirmatory methacholine challenge testing (MCT). RESEARCH QUESTION: We examined the proportion of participants with negative BDR testing who had a positive MCT (and its predictors) result and characteristics of MCT, including effects of controller medication tapering and temporal variability (and predictors of MCT result change), and concordance between MCT and pulmonologist asthma diagnosis. STUDY DESIGN AND METHODS: Adults with self-reported physician-diagnosed asthma were recruited by random-digit dialing across Canada. Subjects performed spirometry with BDR testing and returned for MCT if testing was nondiagnostic for asthma. Subjects on controllers underwent medication tapering with serial MCTs over 3 to 6 weeks. Subjects with a negative MCT (the provocative concentration of methacholine that results in a 20% drop in FEV1 [PC20] > 8 mg/mL) off medications were examined by a pulmonologist and had serial MCTs after 6 and 12 months. RESULTS: Of 500 subjects (50.5 +/- 16.6 years old, 68.0% female) with a negative BDR test for asthma, 215 (43.0%) had a positive MCT. Subjects with prebronchodilator airflow limitation were more likely to have a positive MCT (OR, 1.90; 95% CI, 1.17-3.04). MCT converted from negative to positive, with medication tapering in 18 of 94 (19.1%) participants, and spontaneously over time in 25 of 165 (15.2%) participants. Of 231 subjects with negative MCT, 28 (12.1%) subsequently received an asthma diagnosis from a pulmonologist. INTERPRETATION: In subjects with a self-reported physician diagnosis of asthma, absence of bronchodilator reversibility had a negative predictive value of only 57% to exclude asthma. A finding of spirometric airflow limitation significantly increased chances of asthma. MCT results varied with medication taper and over time, and pulmonologists were sometimes prepared to give a clinical diagnosis of asthma despite negative MCT. Correspondingly, in patients for whom a high clinical suspicion of asthma exists, repeat testing appears to be warranted.
引用
收藏
页码:479 / 490
页数:12
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