Table 2.
Diagnosis | Total (N=271) | TBFB (n=151) | TBCB (n=120) | P valuec |
---|---|---|---|---|
Granulomatous, noninfectiousd | 133 (49) | 76 (50) | 57 (48) | .64 |
Non-IPF fibrotic ILDe | 66 (24) | 28 (19) | 38 (32) | .012 |
Infectionf | 60 (22) | 46 (31) | 14 (12) | <.001 |
Organizing pneumoniag | 53 (20) | 36 (24) | 17 (14) | .046 |
Indeterminate ILDh | 52 (19) | 31 (21) | 21 (18) | .53 |
IPF/UIPi | 33 (12) | 10 (7) | 23 (19) | .002 |
Eosinophilic pneumonia | 29 (11) | 23 (15) | 6 (5) | .007 |
Neoplasmj | 27 (10) | 14 (9) | 13 (11) | .67 |
Vasculitis | 21 (8) | 13 (9) | 8 (7) | .55 |
RB-ILD/DIP | 19 (7) | 10 (7) | 9 (8) | .78 |
Aspirationk | 17 (6) | 5 (3) | 12 (11) | .024 |
pLCH | 4 (2) | 3 (2) | 1 (0.8) | .43 |
DAH | 6 (2) | 4 (3) | 2 (2) | .59 |
Amyloid | 3 (1) | 1 (0.7) | 2 (2) | .43 |
CHFl | 3 (1) | 2 (1) | 1 (0.8) | .70 |
Bronchiolitis | 3 (1) | 2 (1) | 1 (0.8) | .70 |
PAP | 3 (1) | 2 (1) | 1 (0.8) | .70 |
LAM | 1 (0.4) | 1 (0.7) | 0 | .37 |
Pneumoconiosis | 1 (0.4) | 1 (0.7) | 0 | .37 |
CHF = congestive heart failure; DAH = diffuse alveolar hemorrhage; DIP = desquamative interstitial pneumonia; ILD = interstitial lung disease; IPF = idiopathic pulmonary fibrosis; LAM = lymphangioleiomyomatosis; NSIP = nonspecific interstitial pneumonia; PAP = pulmonary alveolar proteinosis; pLCH = pulmonary Langerhans cell histiocytosis; RB-ILD = respiratory bronchiolitis-interstitial lung disease; TBCB = transbronchial cryobiopsy; TBFB = transbronchial forceps biopsy; UIP = usual interstitial pneumonia.
Data are presented as No. (percentage).
Chi-square test.
Noninfectious granulomatous process, eg, sarcoidosis (well-formed noncaseating granulomas), hypersensitivity pneumonitis (poorly formed granulomas, lymphocytic interstitial infiltrates, and cellular bronchiolitis).
Non-IPF fibrotic ILD such as NSIP.
Infections presenting as ILD (eg, Cytomegalovirus pneumonia).
Organizing pneumonia, eg, cryptogenic organizing pneumonia, connective tissue disease–associated ILD, and drug-induced lung disease.
Indeterminate clinicoradiographic pattern.
Cases in which a radiographic pattern consistent with UIP and clinical diagnosis with IPF.
Neoplastic diseases presenting as ILD (eg, lymphangitis carcinomatosis and lymphoproliferative diseases).
Aspiration (eg, food or vegetable matter with pneumonia).
Congestive heart failure presenting as ILD.