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. 2024 Sep 26;13(19):5733. doi: 10.3390/jcm13195733

Table 1.

Patient characteristics.

Number of Patients (n = 93)
Age 80.0 (74.0–86.0)
Sex (Male) 64.5% (n = 60)
Smoking
  Ex or Current 66.7% (n = 62)
IIPs
  IPF 44.1% (n = 42)
  non-IPF (iNSIP) 40.9% (n = 37)
CTD-ILD (N = 14)
  RA 7.5% (n = 7)
  DM 4.3% (n = 4)
  SLE 1.1% (n = 1)
  SSc 2.2% (n = 2)
Stage I or II 14.0% (n = 13)
Duration of illness (years) 4.0 (2.0–5.0)
Comorbidities
  Asthma 0% (n = 0)
  COPD 14.0% (n = 13)
  Cardiac diseases 23.7% (n = 22)
  NIDDM type 2 14.0% (n = 13)
  Maintenance hemodialysis 1.1% (n = 1)
  Malignant diseases 19.3% (n = 18)
Respiratory viruses *
  SARS-CoV-2 2.5% (n = 2)
Bacteria
  MRSA 1.1% (n = 1)
  Pseudomonas aeruginosa 1.1% (n = 1)
Vital signs
  BT (°C) 37.0 ± 0.76
  RR (breaths/min) 24.0 (18.0–28.0)
  ΔHR/ΔBT 27.8 (15.2–56.0)
  SpO2 (%) 82.1 (78.6–85.3)
  BMI 21.5 (18.7–24.1)
Symptoms
  nasal discharge 5.4% (n = 5)
  sore throat 1.1% (n = 1)
  dyspnea 73.1% (n = 68)
Antifibrotic agents 9.7% (n = 9)
Previous episodes of AEs 14.0% (n = 13)

* The FilmArray® Respiratory Panel 2.1 was applied for 79 admitted patients from Jan 2020 to 2023. Data are expressed as percentages (numbers) or medians (interquartile ranges). The stage classification was based on the Japanese Respiratory Society guideline 2022. AE, acute exacerbation; BMI, body mass index; BT, body temperature; COPD, chronic obstructive pulmonary disease; CTD-ILD, connective tissue disease–interstitial lung disease; IIPs, idiopathic interstitial pneumonias; IPF, idiopathic pulmonary fibrosis; non-IPF (iNSIP), idiopathic nonspecific interstitial pneumonia; MRSA, methicillin-resistant Staphylococcus aureus; NIDDM, non-insulin-dependent diabetes mellitus; RA, rheumatoid arthritis; RR, respiratory rate; SARS-CoV-2, severe acute respiratory syndrome coronavirus 2; SLE, systemic lupus erythematosus; SSc, systemic scleroderma.