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Pediatria Polska - Polish Journal of Paediatrics
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Original paper

The impact of selected behavioural and environmental factors on the incidence of upper respiratory tract infections in Polish children

Katarzyna Ślęzak
1
,
Łukasz Dembiński
2
,
Artur Konefał
3
,
Mikołaj Dąbrowski
4
,
Artur Mazur
5
,
Agnieszka Kruk
1
,
Dorota Konefał
3
,
Paweł Wawrykow
1
,
Teresa Jackowska
6
,
Tomasz Szczepański
7
,
Jarosław Peregud-Pogorzelski
1

  1. Department of Paediatrics, Paediatric Oncology and Immunology, Pomeranian Medical University, Szczecin, Poland
  2. Department of Paediatric Gastroenterology and Nutrition, Medical University of Warsaw, Warsaw, Poland
  3. Institute of Clinical Improvement, Warsaw, Poland
  4. Adult Spine Orthopaedics Department, Poznan University of Medical Sciences, Poznań, Poland
  5. Department of Paediatrics, Paediatric Endocrinology and Diabetes, Medical College of Rzeszow University, Rzeszów, Poland
  6. Department of Paediatrics, Medical Center of Postgraduate Education, Warsaw, Poland
  7. Department of Paediatric Haematology and Oncology, Medical University of Silesia in Katowice, Zabrze, Poland
Pediatr Pol 2022; 97 (3): 176-182
Online publish date: 2022/10/18
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INTRODUCTION

Upper respiratory tract infections (URTIs) are the most common reason for primary practice attendance among children and are therefore an important social and epidemiological problem [1–3]. Their increased incidence in children results from the immaturity of the immune system and the significantly shorter length of the airways, which are a mechanical and physiological barrier for pathogens. Frequent contact with peers in a nursery, kindergarten, or school may be an additional factor contributing to the incidence of infections in this group of patients [1]. Respiratory tract infections are classified as URTIs (including rhinitis and paranasal sinusitis, acute pharyngitis and tonsillitis, and laryngitis) and lower respiratory tract infections (including bronchitis, bronchiolitis, and pneumonia) [2].
Studies have shown that most URTIs have viral aetiology. Viral infections are the cause of about 70–85% of pharyngitis and more than 90% of bronchitis cases [1, 2, 4]. Bacterial infections are much less common and usually develop as a secondary infection (superinfection) following a viral infection. These infections are a common reason for parental absence from work [5, 6]. This is undoubtedly an important economic problem for employers of parents of young children [5]. The prevalence of URTIs prompted us to assess the influence of environmental factors and those responsible for the behaviour of parents of selected groups of patients, which could have a significant impact on the incidence of infections. This non-interventional, observational questionnaire study among the parents and guardians of 4389 children treated for URTIs identified behaviours and environmental factors that were found to be important predictors of disease.
To identify environmental and clinical factors and parental behaviours that are likely to affect the incidence of URTIs in the paediatric population.

MATERIAL AND METHODS

This study had a questionnaire-based, observational, non-interventional design. No additional, non-standard medical procedures were performed. The study was conducted in an outpatient setting (primary health-care clinics) by paediatricians. Before inclusion in the study, all physicians were obliged to provide the patient with written information about the assumptions and goals of the program, and to obtain oral consent for participation from the parent/guardian.
The inclusion criteria were being aged < 10 years and attending an appointment with a general practitioner (GP) due to a URTI. The following exclusion criteria were used: chronic cough of unknown cause for > 4 weeks; respiratory defects (e.g. tracheoesophageal fistula); gastroesophageal reflux disease; cystic fibrosis; chronic cardiovascular disease; asthma; immune deficiencies; immunosuppressant therapy; and fever > 39°C.
As part of the study, each patient attended a GP visit during which their parent/guardian was asked to complete a questionnaire to specify the following personal data for the child: current weight; birth weight; height/body length; place of residence; exposure to tobacco smoke; attendance at a nursery/kindergarten/school; and history of respiratory diseases including recurrent URTIs, recurrent tonsillopharyngitis, chronic (including obstructive) bronchitis, pneumonia within the past year, recurrent sinusitis, previous middle-ear infections, and bacterial superinfections. We also collected data on the factors increasing the risk of infection, including atopic diseases (e.g. asthma and allergy), malnutrition, obesity, having siblings, exposure to tobacco smoke, lack of vaccinations, breastfeeding, and the presence of gastroesophageal reflux and tonsillar hypertrophy. The questionnaire also inquired about the child’s immunity, including data on the number of infections, antibiotic treatments, hospital stays and missed days at a nursery/kindergarten/school due to infection, as well as the number of symptoms suggestive of primary immunodeficiency. We also asked about the symptoms of infection that were the reason for the visit to the interviewing doctor and the treatment used. A test of parental knowledge of antibiotic therapy was an important element of the questionnaire. In this study, we assessed data only on environmental factors and parental behaviours that could have an impact on the incidence of URTIs and hospitalization rates, absence from day-care/educational institutions, and parental absence from work. Statistical analysis was performed with the Statistica 13.3 PL version (StatSoft, Tulsa, USA). The Kolmogorov–Smirnov test was applied to verify a normal distribution. The mean values of certain parameters were compared using Student’s t-test or the Mann-Whitney U test for quantitative variables and the chi-squared (χ2) test for qualitative variables. The Kruskal-Wallis test was utilized for the analysis of variance. The correlation assessment was performed with the use of the Spearman’s rank correlation coefficient. Statistical significance was considered as p < 0.05. The data are presented as the mean value ± the standard deviation (SD) or as a percentage of the patients in the analysed groups. The odds ratio and 95% confidence interval are reported.

RESULTS

In total, 4802 patients were enrolled in the study. Of these, 4386 were included in the statistical analysis. Overall, 413 patients (8.6% of those enrolled) were excluded due to incomplete data, failure to meet the inclusion criteria, or a lack of parental/guardian consent. The mean age of the children participating in the study was 4.9 years (with a median of 4.6 years), which fell between the lower quartile of 2.9 and the upper quartile of 6.6 years. The study group included 2108 (48.0%) girls and 2281 (52.0%) boys. There was no statistically significant difference between the genders in terms of age (p = 0.5). The girls had a statistically significantly lower birth weight (p < 0.001).
As reported by the parents/guardians, URTIs affected 3043 (69.3%) of the children: chronic (including obstructive) bronchitis had developed in 555 (12.6%) and pneumonia had occurred in 539 (12.3%) of the patients during the past year. The most common symptoms of infections in the patients included the following: rhinitis in 3262 (74.3%); cough in 2938 (66.9%); decreased appetite in 2869 (65.4%); deterioration of well-being in 2042 (46.5%); reduced physical activity in 1977 (45.0%); pharyngitis in 1894 (43.2%); hoarseness in 1471 (33.5%); and difficulty swallowing in 1171 (26.7%). The mean duration of symptoms in the children attending medical appointments was 3.7 days, with a median of 3 days, which fell within the lower quartile of 2 and the upper quartile of 5. The mean number of symptoms was 5, and this was significantly higher in the group of children who were exposed to tobacco smoke, attended educational institutions, had siblings, were treated with antibiotics, and presented with fever (p < 0.01) (Table 1).
Factors increasing the risk of infection were confirmed in 3160 (72.0%) of the respondents. Those most common included having siblings (43.0%), atopic diseases (30.0%), and exposure to tobacco smoke (21.8%). Nurseries, kindergartens, and schools were attended by 561 (12.8%), 1842 (42.0%), and 593 (13.5%) of the patients, respectively. In total, 337 (7.7%) children were home-schooled. The mean number of infections was significantly higher in children who had siblings, confirmed atopy, exposure to tobacco smoke, and a lack of vaccination (t-test for groups, p < 0.01), and those who attended nurseries compared to preschool and school children (t-test for groups, p < 0.001) (Table 2).
Large (> 100,000 inhabitants) municipalities, small and medium-sized municipalities (< 100,000 inhabitants), and rural regions were the places of residence for 796 (18.1%), 1893 (43.2%), and 1700 (38.7%) of the patients, respectively. The mean number of episodes of infection in medium-sized and large cities was significantly higher compared to those in small towns and villages (t-test for groups, p < 0.01) (Table 3).
The total number of hospitalizations was 713, which accounted for 16.2% of the children in the study group. Despite the infections, 1866 children (42.5%) did not miss a single day of attendance in educational institutions. The mean number of missed school days for children who stayed at home due to infection was 20 days, with a median of 15 days. The presence of cigarette smokers in a household significantly increased the number of missed days in nurseries/kindergartens/schools due to infection (p < 0.01). Children attending nurseries missed more days than those attending kindergartens and schools (Table 4).
There was a negative correlation between hospital admissions and age (Pearson’s test r = 0.09, p = 0.02). Having siblings, atopic diseases, exposure to tobacco smoke, lack of vaccination, attending nurseries, and living in small towns and villages predisposed children to more frequent hospitalization (t-test for groups, p < 0.01) (Table 5).

DISCUSSION

To our knowledge, this is the first Polish non-interventional questionnaire study conducted in the developmental age population (represented by 4389 patients) to assess the impact of selected environmental factors and parental behaviours on the incidence of URTIs in children. The study showed that environmental factors may have an impact on both the incidence of URTIs and the treatment approach in children, particularly including the length and type of antibiotic therapy. This was confirmed by our results and the findings presented by other authors [7]. In our study, the number of episodes of infections was significantly higher in children from large municipalities, those with atopy, and those chronically exposed to tobacco smoke (p < 0.01) (Table 1). Similar observations were presented by Forssell et al. for a group of 190 children [8]. Our findings were also consistent with those of a 2015 meta-analysis of respiratory syncytial virus infections and a meta-analysis on the risk factors for community-acquired pneumonia in New Zealand [9].
We also showed that having siblings was an important risk factor for respiratory infections (p < 0.01). This has been confirmed by other researchers [10–15]. However, studies have shown that having siblings has no influence on the severity of the disease, as confirmed in our research. Antibiotic therapy was used significantly less often in this group (p < 0.01). This was probably due to parental experience in dealing with mild respiratory infections and additional knowledge acquired through previous medical appointments with children. Therefore, it seems necessary to educate parents attending medical appointments due to respiratory tract infections in their children to reduce the frequency of antibiotic use [16–18]. Our observations showed that the type of educational institution attended by children significantly influenced the number of episodes of infection. Many studies have confirmed that attending a day-care facility is an important predictor of respiratory tract infections [10–12, 14, 15, 17, 19–23]. In a study in 2017, Schuez-Havupalo et al. showed significantly increased rates of infections in children after 2 months of attending a nursery, which persisted throughout the attendance period without dropping to the baseline. This is undoubtedly a significant economic problem for the employers of parents with young children [5]. We showed that young children attending nurseries were more likely to develop URTIs compared to preschool and school children (p < 0.001). This was also confirmed in other research that analysed large groups of patients [10, 11, 23, 24]. Forastiere et al. and von Mutius et al. showed that having siblings reduced the risk of atopy, which is an important risk factor for infection [12, 13]. Unfortunately, we could not confirm these observations because we did not analyse similar correlations in our study. However, we did show that the mean number of infections was significantly higher in children with confirmed atopy who had siblings (p < 0.01). Compulsory vaccinations for children had a significant impact on both the mean number of URTIs and the hospital admissions (p < 0.01). This is a particularly important argument confirming the appropriateness and necessity of vaccinating children, as confirmed by Jackson et al. in their 2013 meta-analysis of risk factors for respiratory tract infections [7].
Although the percentage of smokers has significantly decreased in recent years, exposure to tobacco smoke remains a major health problem [25]. Many studies in large groups of patients have confirmed that the risk of respiratory tract infections (and their severity), asthma, and respiratory symptoms (such as cough, bronchial hyperreactivity, and recurrent infections) is also increased in passive smokers [26–30]. In our study, the number of episodes of URTIs and antibiotic therapy were significantly higher in the group of children exposed to tobacco smoke (p < 0.01). The proportion of patients receiving antibiotics increased from 23.8% in children not exposed to tobacco smoke to 31.5% in those with chronic exposure. This clearly indicates an urgent need for intensive education of parents on the impact of tobacco smoke on the health of children.
The significant increase in the number of infections in urban vs. rural children (p < 0.01) may also be associated with air pollution, which is a major health and environmental problem. This was already known in 2005, when the World Health Organization published a European report on the relationship between poor air quality and the rates of respiratory tract infections [31, 32]. A study conducted in California in 2001 showed that air pollution and the associated increase in the rates of respiratory infections caused a 67% drop in school attendance [33]. Our study also showed that infections significantly reduced attendance rates at nurseries, kindergartens, and schools (p < 0.01). The increased rates of respiratory tract infections among urban children are attributable to poor air quality in Poland, which should prompt us to take rapid measures to reduce emissions. The increased incidence of infections in urban children may also result from the fact that they are more likely to attend day-care and thus are exposed to pathogens to a larger extent [34].

CONCLUSIONS

The environmental factors identified in this study had a significant impact on the behaviours of the parents/guardians of children with URTIs. They clearly indicated the involvement of social factors, including place of residence, attending day-care, having siblings, and parental knowledge concerning breastfeeding, vaccinations, and the harmful effects of tobacco smoke on their children. These factors had indirect negative economic effects on employers and the Polish economy because they significantly increased hospitalization rates and the number of days missed at work by the parents/legal guardians of children with URTIs. Therefore, ongoing parental education about the role of vaccinations and the harmful effects of tobacco smoke on children is necessary.

DISCLOSURE

The authors declare no conflict of interest.

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