Dysanapsis and the Spirometric Response to Inhaled Bronchodilators.
Dysanapsis and the Spirometric Response to Inhaled Bronchodilators.
复制标题
呼吸衰竭和吸入支气管扩张剂的肺活量反应。
DOI:
10.1164/rccm.202107-1574le
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发表时间:
2021
影响因子:
24.7
通讯作者:
CanCOLDInvestigators
中科院分区:
文献类型:
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作者:
Vameghestahbanati,Motahareh;Kirby,Miranda;Maltais,François;Jensen,Dennis;Doiron,Dany;Tan,WanC;Bourbeau,Jean;Smith,BenjaminM;CanCOLDInvestigators
MethodsParticipants. The COLD (Canadian Obstructive Lung Disease) prevalence study used census data to recruit a random sample of noninstitutionalized adults> 40 years old from nine communities (2005-2009). In 2010-2014, the ongoing CanCOLD (Canadian Cohort Obstructive Lung Disease) study enrolled COLD participants with COPD, and representative random subsets of COLD nonsmoking and smoking participants without COPD matched on age and sex (6). Data from the baseline CanCOLD visit were included in this analysis. Institutional review board approval was obtained, and all participants provided written informed consent. CT assessment of dysanapsis. Full-inspiration CT was performed on helical scanners according to a standardized protocol. Airway lumen diameters at 19 standard anatomic locations (tracheato-subsegments) and total lung volume were measured from CT images using Apollo Software (VIDA Diagnostics) by trained readers unaware of other participant information. Trained readers achieved a minimum training set interrater intraclass correlation of 0.9 (3). Dysanapsis was quantified as the mean of airway lumen diameters in centimeters divided by the cube root of total lung volume in cubic centimeters (airway-to-lung ratio). Lower values of airway-to-lung ratio indicate smaller airway tree-to-lung size, and higher values indicate larger airway tree-to-lung size. Secondary dysanapsis measures were percent-predicted airway tree caliber calculated from reference equations that account for age, sex, height, and lung volume (3), and the mean of airway lumen diameters in centimeters.Lung function. Spirometry was performed before and 15 minutes after inhalation of 200 mg of salbutamol (albuterol) that was administered from a metered-dose inhaler with spacer device (100 mg/actuation)(7). Participants were instructed to not use regular inhaled medications 6-24 hours before spirometry depending on medication class. Spirometric COPD was defined by post-bronchodilator FEV1/FVC, 0.7 (1). Bronchodilator-associated change in FEV1 (DFEV1) and FEV1/FVC (DFEV1/FVC) were calculated as post-bronchodilator minus prebronchodilator values. Other variables. Age, sex, cigarette smoking status, and regular inhaled medication use were self-reported. Clinical diagnoses of asthma and COPD corresponded to an affirmative response to