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Table 4 Final clinical outcome (FCO) and times to onset of symptom relief (OSR) and achievement of FCO

From: Review of icatibant use in the Winnipeg Regional Health Authority

Category

n

Stratification

Hours (95% CI)

Reference value

p-value (*< 0.05)

FCO available

21

Any outcome

NA

NA

NA

18

Fully resolved

3

Discharged without complete resolution

Median time to OSR

21

All

1.34 (1.00–5.63)

0.8b

0.04*

10

HAE vs natural history

1.13 (0.75–NE)

0.8b

3.5b

0.34

0.10

9a

ACEI-induced (n = 9) vs. natural history

4.86 (2.17–NE)

0.8b

1.6c

0.01*

0.29

14

Face/oropharolarynx symptoms present

2.17 (0.83–NE)

0.7b

0.09

7

Face/oropharolarynx symptoms not present

1.00 (0.75–NE)

0.8b

0.45

Median time to FCO

21

All groups

7.75 (2.5–43.41)

8.0b

1.00

10

HAE vs natural history

3.50 (1.83–NE)

8.0b

36.0b

0.11

0.02*

9a

ACEI-induced vs. natural history

19.53 (8.13–NE)

4.5b

4.0c

0.18

0.18

14

Face/oropharolarynx symptoms present

8.93 (4.67–73.28)

6.0b

0.42

7

Face/oropharolarynx symptoms not present

2.18 (1.83–NE)

8.0b

0.45

Median time from attack onset to icatibant dose

10

HAE

9.58 (8.20–NE)

Pairwise

0.80

9

ACEI-induced

16.53 (4.25–NE)

  1. FCO  Final clinical outcome, OSR onset of symptom relief, NE not estimable, NA not applicable
  2. aTwo presentations were for neither HAE or ACEIIAE
  3. bFrom Lumry et al. [5]
  4. cFrom Sinert et al. [4]