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. 2017 Dec 29;177(2):181–192. doi: 10.1007/s00431-017-3044-3

Table 1.

Demographic and clinical characteristics of the study participants

Evaluable participants (N = 191)
Age (mean ± SD), months 39.84 ± 17.76
Female, n (%) 92 (48.2)
Weight (mean ± SD), kg 14.67 ± 3.83
Height (mean ± SD), cm 96.04 ± 13.10
Age distribution, n (%)
 6–11 months 14 (7.3)
 12–23 months 29 (15.2)
 24–35 months 32 (16.8)
 36–47 months 38 (19.9)
 48–59 months 52 (27.2)
 60–71 months 26 (13.6)
Indications observed, n (%)
 Cough 151 (79.1)
 Wheezing 86 (45.0)
 Pathologic auscultation 74 (38.7)
 Infiltrates/atelectasis (diagnosed by X-ray) 131 (68.6)
Any pre-existing respiratory conditions, n (%)
 Asthma 72 (37.7)
 Pneumonia 114 (59.7)
 Bronchiolitis 85 (44.5)
 Bronchiectasis 15 (7.9)
 Bronchitis 143 (74.9)
 Rhinitis 15 (7.9)
Pre-existing otitis media conditions, n (%)
 Acute otitis media 53 (27.8)
 Otitis media with effusion or “glue ear” 6 (3.1)
 Otitis media with perforation and discharge 8 (4.2)
Relevant vaccination history, n (%)
 Any PCVa 168 (88.0)
 ≥ 2 doses of PCV7 13 (6.8)
 ≥ 2 doses of PCV13 or PHiD-CV 120 (62.8)
 Hib vaccine, ≥ 2 doses 186 (97.4)
 Influenza vaccine, ≥ 1 dose 58 (30.4)
 Antibiotic takenb, n (%) 153 (80.1)
 Penicillin 83 (43.5)
 Amoxicillin/ clavulanate 76 (39.8)
 Azithromycin 57 (29.8)
 Cephalosporins 24 (12.6)
 Clarithromycin 8 (4.2)
 Otherc 6 (3.0)

N, number of children included in the analyses; SD, standard deviation; n (%), number (percentage) of children in each category; PCV, pneumococcal conjugate vaccine; PCV7/13, 7/13-valent PCV; PHiD-CV, pneumococcal polysaccharide non-typeable Haemophilus influenzae protein D-conjugate vaccine; Hib, Haemophilus influenzae type b

aTwo children received one dose of a polysaccharide pneumococcal vaccine and four doses of PCV13 at subsequent vaccinations

bIn the period ≥ 2 weeks and < 6 months prior to enrollment in the study

cOther antibiotics were ciprofloxacin (taken by two children) and erythromycin, clindamycin, linezolid, and meropenem (each taken by one child)