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Table 2 Treatment course and outcome in the fluoroquinolone and nonfluoroquinolone groups

From: Empirical use of fluoroquinolones improves the survival of critically ill patients with tuberculosis mimicking severe pneumonia

 

Fluoroquinolone (n= 43)

Nonfluoroquinolone (n= 34)

P value

ICU admission to TB study (days)

1.7 ± 5.9

5.6 ± 15.1

0.13

TB study in the ICU within 1 week

39 (91)

28 (82)

0.46

Died before ATT was begun

4 (9)

9 (27)

0.05

Initiation of ATT in the ICU within 2 weeks

11 (29)

7 (29)

>0.99

Length of ICU stay (days)

30.0 ± 20.5

17.5 ± 17.9

<0.01

   Nonsurvivors in the ICU

27.0 ± 18.0

22.0 ± 25.0

0.27

   Survivors in the ICU

31.0 ± 21.6

16.0 ± 14.0

0.03

Intubation period (days)

38.6 ± 61.5

19.5 ± 24.0

0.09

   Nonsurvivors in the ICU

28.0 ± 18.35

25.0 ± 29.2

0.13

   Survivors in the ICU

43.0 ± 71.5

16.9 ± 21.4

<0.01

Length of hospital stay(days)

71.2 ± 62.7

38.4 ± 25.5

<0.01

   Nonsurvivors in the hospital

42.0 ± 28.0

37.0 ± 26.41

0.83

   Survivors in the hospital

81.0 ± 63.3

40.0 ± 25.4

<0.01

100-day mortality rate

17 (40)

23 (68)

0.02

  1. Data presented as n (%) or mean ± standard deviation. ATT, anti-tuberculosis treatment; TB, tuberculosis.