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Table 4 Subgroup analyses for the secondary endpoint recurrence

From: Adjunct prednisone in community-acquired pneumonia: 180-day outcome of a multicentre, double-blind, randomized, placebo-controlled trial

Subgroup variables

Placebo (n = 366)

Prednisone (n = 361)

Logistic regression, OR (95%CI)

p for heterogeneity (interaction)b

Median age

0.498

 Age ≤ 73 years

8/192 (4.2%)

15/177 (8.5%)

2.21 (0.91–5.39)

 

 Age > 73 years

4/174 (2.3%)

14/184 (7.6%)

3.49 (1.12–10.84)

 

Initial median CRP

0.251

 CRP ≤ 158 mg/L

3/181 (1.7%)

13/180 (7.2%)

4.54 (1.27–16.23)

 

 CRP > 158 mg/L

9/182 (4.9%)

16/179 (8.9%)

1.89 (0.81–4.40)

 

History of Chronic Obstructive Pulmonary Disease

0.991

 no

9/312 (2.9%)

20/291 (6.9%)

2.49 (1.11–5.55)

 

 yes

3/54 (6%)

9/70 (13%)

2.58 (0.64–10.41)

 

Pneumonia severity indexa

0.869

 PSI class I-III

6/193 (3.1%)

14/174 (8.0%)

2.75 (1.03–7.32)

 

 PSI class IV-V

6/173 (3.5%)

15/187 (8.0%)

2.54 (0.96–6.74)

 

Blood culture positivity

0.014

 Blood culture negative

7/321 (2.2%)

28/324 (8.6%)

4.23 (1.82–9.84)

 

 Blood culture positive

5/45 (11%)

1/37 (3%)

0.14 (0.01–1.75)

 

Sex

0.730

 Male

8/231 (3.5%)

17/219 (7.8%)

2.33 (0.98–5.53)

 

 Female

4/135 (3.0%)

12/142 (8.5%)

3.03 (0.95–9.66)

 

Microbiological etiology

 Bacterial proof

0.013

  Yes

7/87 (8%)

5/81 (6%)

0.71 (0.21–2.37)

 

  No

4/245 (1.6%)

22/254 (8.7%)

5.69 (1.93–16.77)

 

 Viral prof

0.200

  Yes

3/38 (8%)

4/38 (11%)

1.57 (0.32–7.79)

 

  No

3/181 (1.7%)

14/176 (8.0%)

5.15 (1.45–18.29)

 
  1. Data are number (%) unless otherwise stated. OR odds ratio. CI confidence interval.
  2. aThe PSI is a clinical prediction rule to calculate the probability of morbidity and mortality in patients with community-acquired pneumonia; PSI risk class I corresponds to age ≤ 50 years, and no risk factors (≤50 points), risk class II to < 70 points, risk class III to 71–90 points, risk class IV to 91–130 points, and risk class V to > 130 points [20].
  3. bLogistic regression including an interaction term of the respective subgroup variable with treatment group