Radiologic findings are strongly associated with a pathologic diagnosis of usual interstitial pneumonia.

PURPOSE To determine which clinical and radiologic findings are independently associated with a pathologic diagnosis of usual interstitial pneumonia (UIP). METHODS We recently reported, using a prospective, multicenter study of patients suspected of having idiopathic interstitial pneumonia (IIP), that a confident diagnosis of UIP made by experienced radiologists was correct in 95% of cases. In the current article, we further analyzed data from this study. Ninety-one patients were entered into the study. Clinical, physiologic, chest radiographic, and CT features were prospectively recorded, and analyzed using univariate and multivariate logistic regression analysis to compare the patients with a histologic diagnosis of UIP with those who received other pathologic diagnoses. RESULTS Fifty-four of 91 patients (59%) received a pathologic diagnosis of UIP. The following features recorded at the referring clinical centers were associated with a pathologic diagnosis of UIP on multivariate analysis: lower-lobe honeycombing on high-resolution CT (HRCT) [odds ratio, 11.45], radiographic findings consistent with UIP (odds ratio, 5.73), elevated ratio of FEV(1) to FVC (odds ratio, 4.8), and absence of smoking history (odds ratio, 0.19). On multivariate analysis of specific HRCT features recorded by four experienced chest radiologists, lower-lung honeycombing (odds ratio, 5.36) and upper-lung irregular lines (odds ratio, 6.28) were the only independent predictors of UIP. Using only these two factors, a diagnosis of UIP could be established with a sensitivity of 74%, a specificity of 81%, and a positive predictive value of 85%. CONCLUSION In patients presenting with a clinical syndrome suggestive of IIP, CT findings of lower-lung honeycombing and upper-lung irregular lines are most closely associated with a pathologic diagnosis of UIP.

[1]  C D Collins,et al.  Observer variation in pattern type and extent of disease in fibrosing alveolitis on thin section computed tomography and chest radiography. , 1994, Clinical radiology.

[2]  David A. Lynch,et al.  Idiopathic pulmonary fibrosis: Diagnosis and treatment: International Consensus Statement , 2000 .

[3]  A. Nicholson,et al.  The prognostic significance of the histologic pattern of interstitial pneumonia in patients presenting with the clinical entity of cryptogenic fibrosing alveolitis. , 2000, American journal of respiratory and critical care medicine.

[4]  M Ando,et al.  Idiopathic interstitial pneumonias: diagnostic accuracy of thin-section CT in 129 patients. , 1999, Radiology.

[5]  B. Burrows,et al.  Cryptogenic fibrosing alveolitis: clinical features and their influence on survival , 1980, Thorax.

[6]  N L Müller,et al.  Chronic diffuse infiltrative lung disease: comparison of diagnostic accuracy of CT and chest radiography. , 1989, Radiology.

[7]  J. Myers,et al.  Idiopathic pulmonary fibrosis: clinical relevance of pathologic classification. , 1998, American journal of respiratory and critical care medicine.

[8]  H. Itoh,et al.  The diagnostic accuracy of high-resolution computed tomography in diffuse infiltrative lung diseases. , 1993, Chest.

[9]  J. Im,et al.  Idiopathic pulmonary fibrosis vs. pulmonary involvement of collagen vascular disease: HRCT findings , 1993 .

[10]  K P Whittall,et al.  Quantification of idiopathic pulmonary fibrosis using computed tomography and histology. , 1997, American journal of respiratory and critical care medicine.

[11]  N L Müller,et al.  CT of interstitial lung disease: a diagnostic approach. , 1987, AJR. American journal of roentgenology.

[12]  D. Kleinbaum,et al.  Applied Regression Analysis and Other Multivariate Methods , 1978 .

[13]  J. Meier-Sydow,et al.  [Interstitial lung diseases of unknown etiology]. , 1978, Praxis und Klinik der Pneumologie.

[14]  D. Lynch,et al.  Utility of a lung biopsy for the diagnosis of idiopathic pulmonary fibrosis. , 2001, American journal of respiratory and critical care medicine.

[15]  N. Müller,et al.  Desquamative interstitial pneumonia: thin-section CT findings in 22 patients. , 1993, Radiology.

[16]  N. Müller,et al.  Fibrosing alveolitis: CT-pathologic correlation. , 1986, Radiology.

[17]  G. Raghu,et al.  The accuracy of the clinical diagnosis of new-onset idiopathic pulmonary fibrosis and other interstitial lung disease: A prospective study. , 1999, Chest.

[18]  K P Offord,et al.  Prognostic significance of histopathologic subsets in idiopathic pulmonary fibrosis. , 1998, American journal of respiratory and critical care medicine.

[19]  G. Hunninghake,et al.  Idiopathic pulmonary fibrosis. , 2001, The New England journal of medicine.

[20]  N. Müller,et al.  Disease activity in idiopathic pulmonary fibrosis: CT and pathologic correlation. , 1987, Radiology.

[21]  S. Swensen,et al.  Diffuse lung disease: diagnostic accuracy of CT in patients undergoing surgical biopsy of the lung. , 1997, Radiology.

[22]  T. Colby,et al.  Idiopathic nonspecific interstitial pneumonia/fibrosis: comparison with idiopathic pulmonary fibrosis and BOOP. , 1998, The European respiratory journal.

[23]  John F. Murray,et al.  Textbook of Respiratory Medicine , 1988 .

[24]  D. Hansell,et al.  Fibrosing alveolitis associated with systemic sclerosis has a better prognosis than lone cryptogenic fibrosing alveolitis. , 1994, American journal of respiratory and critical care medicine.

[25]  M. Suga,et al.  Chronic hypersensitivity pneumonitis in Japan: a nationwide epidemiologic survey. , 1999, The Journal of allergy and clinical immunology.

[26]  D. Hansell,et al.  Accuracy of the typical computed tomographic appearances of fibrosing alveolitis. , 1993, Thorax.