Utility of routine screening for alpha-1 antitrypsin deficiency in patients with bronchiectasis

被引:19
|
作者
Carreto, Luis [1 ]
Morrison, Meghan [2 ]
Donovan, Jackie [3 ]
Finch, Simon [4 ]
Tan, Gan Liang [5 ]
Fardon, Tom [6 ,7 ]
Wilson, Robert [8 ]
Furrie, Elisabeth [9 ]
Loebinger, Michael [8 ]
Chalmers, James D. [4 ]
机构
[1] Hosp Prof Fernando Fonseca HFF, Resp Med, Lisbon, Portugal
[2] Univ Dundee, Sch Med, Dundee, Scotland
[3] Royal Brompton & Harefield NHS Fdn Trust, Biochem, London, England
[4] Univ Dundee, Div Mol & Clin Med, Dundee, Scotland
[5] Singapore Gen Hosp, Resp & Crit Care Med, Singapore, Singapore
[6] Univ Dundee, Resp Med, Dundee, Scotland
[7] NHS Tayside, Resp Med, Dundee, Scotland
[8] Royal Brompton Hosp, Div Resp Med, Host Def Unit, London, England
[9] Ninewells Hosp, Dept Immunol, Dept Med, Dundee, Scotland
关键词
bronchiectasis; alpha1 antitrypsin deficiency; clinical epidemiology;
D O I
10.1136/thoraxjnl-2019-214195
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Alpha-1 antitrypsin deficiency (AATD) is a cause of bronchiectasis. Guidelines for bronchiectasis from the British Thoracic Society do not recommend to routinely test patients for AATD. In contrast, guidelines for AATD recommend routine screening. This contradiction, in part, results from the lack of data from large studies performing comprehensive screening. We screened 1600 patients with bronchiectasis at two centres in the UK from 2012 to 2016. In total, only eight individuals with AATD were identified representing 0.5% of the overall population. We conclude that routine screening for AATD in bronchiectasis in the UK has a low rate of detection. Further studies are required in different geographical regions, which may have a higher prevalence of AATD.
引用
收藏
页码:592 / 593
页数:2
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