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Table 1 Clinical characteristics of the 30 CF children

From: Beneficial short-term effect of autogenic drainage on peripheral resistance in childhood cystic fibrosis disease

Characteristics

With bronchial congestion

N = 10

Without bronchial congestion

N = 20

Between 2 groups (with and without)

at baseline

Ethnicity C/B/A/M

9/0/1/0

16/2/0/2

0.253

Age, years

14.6 [9.7; 16.3]

11.8 [7.9; 14.5]

0.333

Sex, female/male

7/3

5/15

0.045

Weight, kg

40.5 [33.8; 48.0]

40.0 [23.0; 50.5]

0.552

Weight z-score

 − 0.60 [− 0.84; − 0.03]

 − 0.66 [− 1.13; 0.04]

0.391

Height, cm

150 [139; 160]

146 [122; 160]

0.843

Height z-score

 − 0.44 [− 1.03; 0.16]

 − 0.75 [− 1.04; 0.00]

0.644

BMI z-score

 − 0.48 [− 0.58; − 0.03]

 − 0.34 [− 0.89; 0.71]

0.509

Pancreatic insufficiency, n

10

17

0.519

Previous pseudomonas aeruginosa colonisation, n

10

13

0.093

Dornase alfa/azithromycin, n

9/3

17/5

ND

Inhaled β-agonist/corticosteroid, n

1/1

3/3

ND

CFTR modulator therapy, n

4

5

ND

Mutation

Homozygous /heterozygous/other*

4/4/2

7/6/7

0.689

Score (VAS) of congestion

6.5 [5.0; 7.0]

2.0 [1.0; 3.0]

ND

Sputum weight, g

7.9 [6.1; 12.1]

1.7 [0.9; 4.5]

 < 0.001

Congestion absent/present#

1/9

13/7

0.007

  1. Ethnicity Caucasian/Black/Asian/Mixed; BMI denotes Body Mass Index; VAS denotes Visual Analogical Score
  2. * homozygous and heterozygous ΔF508 mutations
  3. #based on child’s opinion, absent = absent (or almost absent), present = frank presence
  4. VAS denotes visual analog scale and ND denotes not done. Bold P values are those < 0.05