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Table 2 Pathogen Identification

From: Efficacy and safety of aerosol inhalation of recombinant human interferon α1b (IFNα1b) injection for noninfluenza viral pneumonia, a multicenter, randomized, double-blind, placebo-controlled trial

Item

Total

IFNα1b Group

Control Group

Influenza virusa

16 (9.94%)

9 (11.84%)

7 (8.24%)

Parainfluenza virus

4 (2.48%)

3 (3.95%)

1 (1.18%)

Respiratory syncytial virus

7 (4.35%)

2 (2.63%)

5 (5.88%)

Rhinovirus

7 (4.35%)

3 (3.95%)

4 (4.71%)

Adenovirus

7 (4.35%)

5 (6.58%)

2 (2.35%)

EB virus

16 (9.94%)

7 (9.21%)

9 (10.59%)

Herpes virus

14 (8.64%)

8 (10.53%)

6 (7.06%)

Coronavirus

2 (1.24%)

1 (1.32%)

1 (1.18%)

Human metapneumovirus

1 (0.62%)

0 (0.00%)

1 (1.18%)

Streptococcus pneumoniae

2 (1.24%)

2 (2.63%)

0 (0.00%)

Mycoplasma

10 (6.21%)

4 (5.26%)

6 (7.06%)

Chlamydia

2 (1.24%)

1 (1.32%)

1 (1.18%)

Moraxella catarrhalis

2 (1.24%)

0 (0.00%)

2 (2.35%)

Simple virus infection

49 (30.43%)

21 (27.63%)

28 (32.94%)

Single virus infection

30 (18.63%)

9 (11.84%)

21 (24.71%)

Two-virus infection

9 (5.59%)

7 (9.21%)

2 (2.35%)

Multivirus infection

10 (6.21%)

5 (6.58%)

5 (5.88%)

Mycoplasma + virus

5 (3.11%)

2 (2.63%)

3 (3.53%)

Chlamydia + virus

2 (1.24%)

1 (1.32%)

1 (1.18%)

  1. arepresents negative results from a rapid influenza antigen test during screening and positive results from an influenza virus nucleic acid test at the central laboratory. No anti-influenza drugs were given during clinical treatment.