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. 2021 Oct 12;11:744727. doi: 10.3389/fcimb.2021.744727

Table 1.

Epidemiological, microbiological, and clinical characteristics of the study groups.

Not exposed (n=27) Exposed (n=54) P-value a
Epidemiological characteristics
Age, months, median (IQR) 33 (19.0-49.5) 28.5 (18.5-48.5) 0.72
Gender, male (%) 12/27 (44.4) 35/54 (64.8) 0.13
Birth weight, grams, mean (sd) b 3260 (507) 3358 (444) 0.41
Gestational age, weeks, median (IQR) c 40 (38.2-40.4) 40.0 (39.0-40.0) 0.81
House surface per inhabitant, m2, median (IQR) d 20 (18.1-28.3) 22 (16.7-28.8) 0.87
Seasonality, samples collected during viral season (%)* 17/27 (63.0) 31/54 (57.4) 0.81
Ethnicity, Caucasian (%) 16/24 (66.7) 34/48 (70.8) 0.92
Delivery mode, C-section (%) 6/23 (26.1) 7/42 (16.7) 0.55
Breastfeeding (%) 23/26 (88.5) 41/52 (78.8) 0.36 k
Breastfeeding duration, months, median (IQR) e 6.5 (1.6-12.0) 6.0 (1.0-9.0) 0.41
Schooled (%) 21/26 (80.8) 44/51 (86.3) 0.52 k
Family members under 5 years (%) 9/25 (36.0) 12/46 (26.1) 0.55
Parental smoking (%) 8/26 (30.8) 18/49 (36.7) 0.79
Basic educational level (%) 3/19 (15.8) 9/43 (20.9) 0.74 k
≥1 dose of Pneumococcal Conjugate Vaccine (%) 15/27 (55.5) 36/52 (69.2) 0.34
Microbiological characteristics
 Viral study
DNA/RNA viral detection by multiplex PCR (%) 22/27 (81.5) 39/54 (72.2) 0.42 k
DNA/RNA viral detection >2 viruses by multiplex PCR (%) 9/27 (33.3) 15/54 (27.8) 0.79
Human rhinovirus/enterovirus (%) 16/27 (59.2) 31/53 (58.5) 1.00
Human respiratory syncitial virus (A and B) (%) 4/26 (15.4) 4/53 (7.5) 0.42 k
Human metapneumovirus (%) 1/27 (3.7) 2/53 (3.8) 1.00 k
Human coronaviruses (OC43/229E/NL63) (%) 2/27 (7.4) 2/54 (3.7) 0.60 k
Human parainfluenza viruses (1,2,3,4) (%) 1/27 (3.7) 6/53 (11.3) 0.41 k
Human influenza viruses (A and B) (%) 3/26 (11.5) 4/53 (7.5) 0.67 k
Human adenovirus (%) 3/27 (11.1) 8/53 (15.1) 0.74 k
Human bocavirus (%) 4/25 (16.0) 6/53 (11.3) 0.71 k
 Pneumococcal study in invasive samples #
Pneumococcal serotype with high invasive disease potential (%) 14/27 (51.8) 18/36 (50.0) 1.00
Pneumococcal serotype covered by PCV13 vaccination (%) 14/27 (51.8) 18/36 (50.0) 1.00
Clinical characteristics
Time of fever before NPA collection, hours, median (IQR) f 120 (78-144) 128 (33-192) 0.82
 Blood analytical parameters at admission
C -Reactive Protein, mg/L, median (IQR) g 300 (205-324) 268 (146-335) 0.83
Procalcitonin, ng/ml, median (IQR) h 11.3 (6.7-17.2) 4.3 (1.2 -15.1) 0.37
Hemoglobin, g/dl, median (IQR) i 10.7 (10.1-11.7) 10.8 (9.9-11.6) 0.97
Leukocytes, thousand/mm3, mean (SD) j 16.8 (8.3) 18.0 (8.9) 0.57
 Clinical syndromes
Complicated pneumonia (%) 16/27 (59.2) 29/54 (53.7) 0.81
Non-complicated pneumonia (%) 7/27 (25.9) 8/54 (14.8) 0.36
Meningitis (%) 3/27 (11.1) 5/54 (9.2) 1.00 k
Sepsis (%) 0/27 (0.0) 4/54 (7.4) 0.29 k
Bacteremia (%) 1/27 (3.7) 4/54 (7.4) 0.66 k
Arthritis (%) 0/27 (0.0) 4/54 (7.4) 0.29 k
 Hospital stay and complications
Length of Hospitalization stay, days, median (IQR) 11.0 (8.0-15.0) 10.0 (6.0-15.0) 0.69
ICU admission (%) 4/27 (14.8) 13/54 (24.1) 0.40 k
Respiratory support (noninvasive ventilation and/or mechanical ventilation) (%) 2/27 (7.4) 11/54 (20.4) 0.20 k
Thoracocentesis (%) 10/27 (37.0) 22/54 (40.7) 0.94
a

T-test and Wilcoxon test were used for parametric and nonparametric continuous variables, respectively. Chi-square test was used for categorical variables.

b

Comparisons performed on 25 not exposed cases and 53 exposed cases.

c

Comparisons performed on 26 not exposed cases and 53 exposed cases.

d

Comparisons performed on 23 not exposed and 47 exposed cases.

e

Comparisons performed on 26 not exposed cases and 50 exposed cases.

f

Comparisons performed on 26 not exposed cases and 52 exposed cases.

g

Comparisons performed on 26 not exposed cases and 53 exposed cases.

h

Comparisons performed on 12 not exposed cases and 25 exposed cases.

i

Comparisons performed on 25 not exposed cases and 51 exposed cases.

j

Comparisons performed on 25 not exposed cases and 52 exposed cases.

k

Fisher exact tests were performed for categorical variables instead of chi-square tests in case of ≥25% of cells presented expected frequencies <5.

*Viral season was defined as the period of time corresponding to Influenza A and VRS circulation over the basal levels according to the Surveillance Plan of ARIs in Catalonia (PIDIRAC) (https://canalsalut.gencat.cat/ca/professionals/vigilancia-epidemiologica/pla-dinformacio-de-les-infeccions-respiratories-agudes-a-catalunya-pidirac/) and reports from the Hospital Surveillance Network for VRS in Catalonia (Vall d’Hebrón Hospital) (https://hospital.vallhebron.com/ca/actualitat/publicacions/informe-xarxa-de-vigilancia-hospitalaria-de-vrs).

#A total of three pneumococci could not be serotyped due to low bacterial load.

SD, Standard Deviation; IQR, Interquartile Range; NPA, Nasopharyngeal aspirate.