Biancosino C, Welker L, Krüger M, Bölükbas S, Bittmann I, Kirsten D
Department of Cardiac, Thoracic, Transplantation and Vascular Surgery, Hannover Medical School, Hannover, Germany.
Lung Clinic Grosshansdorf, Center for Pneumology and Thoracic Surgery, Grosshansdorf, Germany.
Pneumologie. 2016 Mar;70(3):205-10. doi: 10.1055/s-0042-100551. Epub 2016 Mar 15.
History, clinical presentation, lung function testing, radiographs including HRCT and nonsurgical biopsy techniques in most cases provide sufficient information for classification of interstitial lung disease (ILD). However, in a small percentage it is not possible to establish the diagnosis so that lung biopsy may be required. We analyzed under which circumstances a reduction of invasive procedures is reasonable.
Between January 1997 and December 2009 we examined 3399 specimens from 1299 patients with benign inflammatory and granulomatous diseases in whom ILD was clinically hypothesized. We compared the probability of disease according to Bayes before and after surgery which corresponds to the clinical diagnosis (a priori probability) and the final diagnosis (a posteriori probability). Additionally, procedures, operation related complications and the patients' smoking habits were documented.
In 111 patients (8.5 %) surgical evaluation was performed (14 mediastinoscopies, 97 thoracotomies/VATS biopsies). All mediastinoscopies substantiated a epitheloid cell granulomatosis. In 30 % of all VATS procedures a prolonged air leak of more than 4 days was observed. One patient died and one had to get a new chest tube after removal. Changes of a priori/a posteriori probabilities was shown for non-smokers in Wegner's granulomatosis (0.6 vs. 2.2 %) and IPF (16.7 vs. 34.8 %), for smokers in Langerhans' cell histiocytosis (1.4 vs. 7.8 %) and IPF (16.7 vs. 33.3 %). In the majority of cases even a reduction of probability was seen.
Considering complications and limited diagnostic gain, lung biopsies for diagnosis of ILD should be recommended only in selected patients.
病史、临床表现、肺功能测试、包括高分辨率计算机断层扫描(HRCT)在内的影像学检查以及大多数情况下的非手术活检技术,为间质性肺疾病(ILD)的分类提供了足够的信息。然而,在一小部分病例中无法确诊,因此可能需要进行肺活检。我们分析了在哪些情况下减少侵入性操作是合理的。
在1997年1月至2009年12月期间,我们检查了1299例临床疑似ILD的良性炎症和肉芽肿性疾病患者的3399份标本。我们比较了手术前后根据贝叶斯定理得出的疾病概率,这分别对应临床诊断(先验概率)和最终诊断(后验概率)。此外,还记录了操作过程、手术相关并发症以及患者的吸烟习惯。
111例患者(8.5%)接受了手术评估(14例纵隔镜检查,97例开胸手术/电视辅助胸腔镜手术活检)。所有纵隔镜检查均证实为上皮样细胞肉芽肿病。在所有电视辅助胸腔镜手术中,30%观察到持续漏气超过4天。1例患者死亡,1例在拔除胸管后需要重新置管。对于非吸烟者,韦格纳肉芽肿(0.6%对2.2%)和特发性肺纤维化(IPF,16.7%对34.8%),对于吸烟者,朗格汉斯细胞组织细胞增多症(1.4%对7.8%)和IPF(16.7%对33.3%),先验/后验概率发生了变化。在大多数情况下甚至出现了概率降低的情况。
考虑到并发症和有限的诊断收益,仅应在选定的患者中推荐进行肺活检以诊断ILD。