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. 2021 Jul 29;8(1):e000889. doi: 10.1136/bmjresp-2021-000889

Table 1.

Patient characteristics in this study*

Parameters AE-IIPs (n=28) AE-IPF (n=8) AE-non-IPF (n=20) P value
Stable state
 Sex, male/female 21/7 8/0 13/7 0.0749
 Smoking, yes/no 19/9 7/1 12/8 0.2144
 mMRC, ≤1/≥2 10/18 3/5 7/13 1.0000
 Stage, I–III/IV 17/11 4/4 13/7 0.6715
 LTOT before AE, yes/no 11/17 4/4 7/13 0.6175
 Prednisolone before AE, yes/no 9/19 2/6 7/13 1.0000
 Antifibrotic drugs, yes/no 5†/23 2‡/6 3§/17 0.6056
At the time of diagnosis of AE
 Age, years 74.5 (69.75–79.0) 74.5 (69.5–78.25) 74.5 (69.75–84.0) 0.7405
 HRCT pattern, diffuse/non-diffuse 12/16 4/4 8/12 0.6908
 PaO2/FiO2 ratio, ≤200/>200 17/11 6/2 11/9 0.4188
 WCC, /μL 10 150 (9050–12 950) 10 300 (9000–14 400) 10 150 (9250–12 950) 0.9594
 LDH, U/L 317.0 (245.5–404.5) 296.5 (246.5–414.25) 341.0 (245.5–403.75) 0.9797
 KL-6, U/mL 1196 (889–2,142) 1024.5 (889.5–1394) 1346 (849.75–2359) 0.3091
 CRP, mg/dL 12.38 (5.07–14.28) 5.455 (0.38–12.56) 2.982 (0.871–9.815) 0.8787
 FDP, 10</≥10 mg/L 21/7 4/4 17/3 0.1423
 90-day survival, yes/no 19/9 6/2 13/7 1.0000

*Each parameter was compared between the AE-IPF and AE-non-IPF groups using Fisher’s exact test or the Wilcoxon rank-sum test.

†Pirfenidone (n=4) and nintedanib (n=1).

‡Pirfenidone (n=1) and nintedanib (n=1).

§Pirfenidone (n=3) and nintedanib (n=0).

AE, acute exacerbation; CRP, C reactive protein; FDP, fibrin degradation product; FiO2, fraction of inspired oxygen; HRCT, high-resolution CT; IIPs, idiopathic interstitial pneumonias; IPF, idiopathic pulmonary fibrosis; KL-6, Krebs von den Lungen-6; LDH, lactate dehydrogenase; LTOT, long-term oxygen therapy; mMRC, modified medical research council score; PaO2, arterial oxygen tension; WCC, white blood cell count.