A study of patients with isolated mediastinal and hilar lymphadenopathy undergoing EBUS-TBNA

被引:33
作者
Evison, Matthew [1 ,2 ]
Crosbie, Philip A. J. [1 ,2 ]
Morris, Julie [3 ]
Martin, Julie [1 ]
Barber, Philip V. [1 ]
Booton, Richard [1 ,2 ]
机构
[1] Univ South Manchester Hosp, North West Lung Ctr, Manchester, Lancs, England
[2] Univ Manchester, Inst Inflammat & Repair, Manchester, Lancs, England
[3] Univ South Manchester Hosp, Dept Med, Manchester, Lancs, England
来源
BMJ OPEN RESPIRATORY RESEARCH | 2013年 / 1卷 / 01期
关键词
D O I
10.1136/bmjresp-2014-000040
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Isolated mediastinal and/or hilar lymphadenopathy (IMHL) may be caused by benign and malignant disorders or be 'reactive'. Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) has a reported low negative predictive value (NPV) in IMHL, necessitating mediastinoscopy in selected patients. The aim of this study was to examine the NPV of EBUS-TBNA in an IMHL population and determine whether clinical variables differentiate between pathological and reactive IMHL. Methods: Analysis of a prospectively maintained database of consecutive patients with IMHL referred to a single UK centre for EBUS-TBNA. Results: 100 patients with IMHL had EBUS-TBNA during the study (March 2010-February 2013), mean age 58.6 +/- 15.7 years, 63% men, 70% white British and mean follow-up 16.8 +/- 8.6 months. Pathological cause of IMHL established in 52 patients (sarcoidosis n=20, tuberculosis n=18, carcinoma n=7, lymphoma n=6, benign cyst n=1), 43 from EBUS-TBNA. 48/57 negative EBUS-TBNA samples were true negatives reflecting reactive lymphadenopathy in 48%. The diagnostic accuracy of EBUS-TBNA was 91% and NPV was 84.2% (95% CI 72.6% to 91.5%). Multivariate analysis of clinical covariates showed age (odds ratio (OR) 1.07, 95% CI 1.01 to 1.13; p=0.033), the presence of a relevant comorbidity (OR 9.49, 95% CI 2.20 to 41.04; p=0.003) and maximum lymph node size (OR 0.70, 95% CI 0.59 to 0.83; p=0.00004) to differentiate between reactive and pathological IMHL. Stratification of the study population according to comorbidity and maximum lymph node size (<20 mm) identified a lowrisk cohort (n=32) where the NPV of EBUS-TBNA was 93.8% (95% CI 79.9% to 98.3%). Conclusions: Reactive lymphadenopathy accounts for a significant proportion of patients with IMHL. In carefully selected patients with IMHL and a negative EBUS-TBNA, surveillance rather than further invasive sampling may be an appropriate strategy.
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