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Table 4 Pre-specified study clinical endpoints

From: Continuous versus intermittent short-acting β2-agonists nebulization as first-line therapy in hospitalized children with severe asthma exacerbation: a propensity score matching analysis

Clinical endpoints

Continuous nebulization

(n = 56)

Intermittent nebulization

(n = 56)

Treatment effect (continuous vs. intermittent nebulization)

n

%

n

%

Clinical parameters

Unadjusted analysis

Adjusted analysisa

Effect

95%CI

P-value

Effect

95%CI

P-value

Success

49

87.5

32

57.1

Risk difference (%)

30.4

14.6, 46.1

< 0.001

39.5

22.7, 56.3

< 0.001

     

SHR

2.03

1.30, 3.17

0.002

2.70

1.72, 4.22

< 0.001

Failure

7

12.5

24

42.9

Risk difference (%)

−30.4

−46.1, −14.6

< 0.001

−39.5

−56.3, −22.7

< 0.001

     

SHR

0.25

0.11, 0.58

0.001

0.12

0.05, 0.31

< 0.001

LOS (hour), mean ± SD

52.8

±28.2

59.1

±66.4

RMST difference (mean)

−2.92

−14.54, 8.70

0.623

−9.88

−24.18, 4.42

0.176

  1. Abbreviation: LOS Length of stay; RMST Restricted mean survival time; SHR Sub-distributional hazard ratio (under competing risk time-to-event analysis).amultivariable analysis adjusted for potential confounders (prognostic factors, treatment at emergency room, and co-medications during admission)