Table 1

Data of the hospital treatment periods of the patients with acute exacerbation (AE) of idiopathic pulmonary fibrosis (IPF) and other fibrosing interstitial lung diseases (FILD)

VariableTotal no of patients (n=128)
Hospitalisations (n=142)
IPF (n=79)
Hospitalisations (n=84)
Other FILD (n=49)
Hospitalisations (n=58)
P value
LTOT preceding hospitalisation27 (19)16 (19)11 (19)0.990
Length of hospital treatment, days9 (6‒14)8 (5‒14)11 (7‒15)0.197
Admission in winter or spring*81 (57)49 (58)32 (55)0.708
Treatment unit in hospital
 Respiratory ward137 (97)79 (94)58 (100)0.079
 Respiratory ward only†79 (56)43 (51)36 (62)0.200
 Intermediate care unit61 (43)41 (49)20 (35)0.090
 Intensive care unit24 (17)16 (19)8 (14)0.411
Invasive mechanical ventilation16 (11)14 (17)2 (3.4)0.014
Trigger for AE-FILD
 No trigger122 (86)75 (89)47 (81)0.165
 Infection‡15 (11)7 (8.3)8 (14)0.298
 Drug4 (2.8)2 (2.4)2 (3.4)1.000
 Postoperative§1 (0.7)0 (0)1 (1.7)0.408
Histological confirmation of AE-FILD¶23 (16)15 (18)8 (14)0.518
  • Data are presented as numbers of patients (%) and median (IQR).

  • Each hospital admission is treated as unique event.

  • *Hospital admissions between December and May.

  • †Patients treated in respiratory ward throughout the whole treatment period (no transfers to intensive or intermediate care unit).

  • ‡Microbiologically or serologically confirmed respiratory infection.

  • §The patient had undergone minor surgery under larynx mask anaesthesia preceding the treatment period.

  • ¶Diffuse alveolar damage could be observed either in autopsy (15 IPF, 7 other FILD) or in thoracoscopic surgical lung biopsy (1 other FILD) samples.

  • LTOT, long-term oxygen treatment.