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Table 1 Demographics and baseline characteristics

From: Effectiveness of montelukast administered as monotherapy or in combination with inhaled corticosteroid in pediatric patients with uncontrolled asthma: a prospective cohort study

Characteristics

Montelukast monotherapy

Montelukast + ICS

Total

Preschool age

School age

All

Preschool age

School age

All

N

34

42

76

112

140

252

328

Age (years), mean (SD)

4.01 (1.12)

9.19 (2.26)

6.87 (3.19)

3.86 (1.13)

9.54 (2.35)

7.02 (3.41)

6.92 (3.35)

Gender, n (%)

       

   Male

18 (52.9)

25 (59.5)

43 (56.6)

60 (53.6)

89 (63.6)

149 (59.1)

192 (58.5)

   Female

16 (47.1)

17 (40.5)

33 (43.4)

52 (46.4)

51 (36.4)

103 (40.9)

136 (41.5)

Race, n (%)

       

   Caucasian

25 (73.5)

32 (76.2)

57 (75.0)

66 (58.9)

86 (61.4)

152 (60.3)

209 (63.7)

   Black

0 (0.0)

1 (2.4)

1 (1.3)

8 (7.1)

13 (9.3)

21 (8.3)

22 (6.7)

   Asian

4 (11.8)

8 (19.0)

12 (15.8)

32 (28.6)

32 (22.9)

64 (25.4)

76 (23.2)

   Hispanic

0 (0.0)

1 (2.4)

1 (1.3)

3 (2.7)

3 (2.1)

6 (2.4)

7 (2.1)

   Other

3 (8.8)

0 (0.0)

3 (3.9)

2 (1.8)

6 (4.3)

8 (3.2)

11 (3.4)

   Missing

2 (5.9)

0 (0.0)

2 (2.6)

1 (0.9)

0 (0.0)

1 (0.4)

3 (0.9)

Duration of asthma since diagnosis (years), mean (SD)

2.06 (1.11)

4.32 (3.25)

3.31 (2.76)

2.11 (1.27)

5.46 (3.08)

3.97 (2.96)

3.82 (2.92)

Smoking history, n (%)

       

   Patient is a smoker

0 (0.0)

0 (0.0)

0 (0.0)

0 (0.0)

0 (0.0)

0 (0.0)

0 (0.0)

   Patient quit smoking

0 (0.0)

0 (0.0)

0 (0.0)

0 (0.0)

1 (0.7)

1 (0.4)

1 (0.3)

   Patient never smoked

34 (100.0)

41 (97.6)

75 (98.7)

104 (92.9)

133 (95.0)

237 (94.0)

312 (95.1)

   Member of household is a smoker

8 (23.5)

14 (33.3)

22 (28.9)

20 (17.9)

40 (28.6)

60 (23.8)

82 (25.0)

   Member of household quit smoking

5 (14.7)

11 (26.2)

16 (21.1)

8 (7.1)

7 (5.0)

15 (6.0)

31 (9.5)

Use of ICS at baseline, n (%)

       

   Low dose*

-

-

-

58 (51.8)

39 (27.9)

97 (38.5)

97 (29.6)

   Moderate dose

-

-

-

53 (47.3)

90 (64.3)

143 (56.7)

143 (43.6)

   High dose

-

-

-

1 (0.9)

11 (7.9)

12 (4.8)

12 (3.7)

Profile of asthma symptoms, n (%)

       

1. Daytime symptoms ≥ 4 days/week

24 (70.6)

26 (61.9)

50 (65.8)

91 (81.3)

106 (75.7)

197 (78.2)

247 (75.3)

2. Night-time symptoms ≥ 1 night/week

29 (85.3)

30 (71.4)

59 (77.6)

99 (88.4)

111 (79.3)

210 (83.3)

269 (82.0)

3. Absenteeism from school due to asthma in the last week

7 (20.6)

16 (38.1)

23 (30.3)

33 (29.5)

66 (47.1)

99 (39.3)

122 (37.2)

4. SABA ≥ 4 doses in the last week§

13 (38.2)

13 (31.0)

26 (34.2)

76 (67.9)

92 (65.7)

168 (66.7)

194 (59.1)

5. FEV in one second or PEF ≥90% of their personal best in the last week

2 (5.9)

9 (21.4)

11 (14.5)

11 (9.8)

41 (29.3)

52 (20.6)

63 (19.2)

6. Diurnal variability in peak expiratory flow >10% to 15% in the last week

2 (5.9)

2 (4.8)

4 (5.3)

8 (7.1)

22 (15.7)

30 (11.9)

34 (10.4)

  1. *Low dose was defined as ≤ 200 μg/day for fluticasone propionate or equivalent (≤200 μg/day for beclomethasone dipropionate and ≤200 μg/day for budesonide).
  2. Moderate dose was defined as >200 to 500 μg/day for fluticasone propionate or equivalent (>200 to 400 μg/day for beclomethasone dipropionate and >200 to 400 μg/day for budesonide) [18].
  3. High dose was defined as > 500 μg/day for fluticasone propionate or equivalent (>400 μg/day for beclomethasone dipropionate and >400 μg/day for budesonide).
  4. §Excluding one dose/day before exercise.