INTRODUCTION

Environmental tobacco smoke (ETS) exposure in children is associated with various disease conditions, especially respiratory tract diseases like asthma and bronchiolitis1. A comprehensive systematic review concluded that the disease burden related to ETS exposure accounted for about 1% of worldwide mortality in 2004, with 28% of the affected population being children2.

Globally, the reported associations between children’s ETS exposure and all-cause medical service utilisation have been controversial3-5, while the positive associations were more consistently found in specific disease conditions such as asthma exacerbation6 and respiratory tract infections7,8. In Hong Kong, Lam et al.9 found in utero ETS exposure for non-smoking mothers was positively associated with more doctor consultations and hospitalisations in infancy, while postnatal exposure to ETS at home was associated with hospitalisations for any illness, but not observed for outpatient visits9. The impact of maternal smoking was not specifically examined in this previous study, while maternal smoking has a more significant impact on children’s health than the smoking of other household members10,11. Leung et al.12 found hospital admission was more prevalent among infants exposed to secondhand smoke if it was accompanied by poor smoking hygiene (<3 m away), however the results for smoking at least 3 m away from the infant was not statistically significant12. Moreover, they demonstrated that hospital admission of non-specified infectious disease was more likely among children exposed to ETS up to 8 years of age, if it was accompanied by poor smoking hygiene, and the association was the strongest in the first 6 months of life13. However, this study only investigated the association of ETS exposure with hospitalisation, which might have underestimated the impact of ETS on the utilisation of other medical services such as outpatient consultations. Furthermore, the dose-response relationships between exposure and health outcomes were less examined in previous studies9,14. The current evidence on the associations between ETS exposure and health problems in children is also limited by inadequate control for the potential effect of maternal smoking during pregnancy. Thus, it is worthwhile to further study the influence of ETS exposure among different groups of children, with or without a smoking mother.

Exposure to passive smoke significantly increases children’s risks of lower respiratory tract infection (LRTI), asthma, and reduced lung function15-17. LRTI in children aged <5 years was reported to be the largest global disease burden of ETS2. LRTI is also a leading infectious cause of mortality in children in this age group, worldwide18. Concerning the associations between ETS exposure and respiratory symptoms in children, wheezing was robustly linked to exposure, while controversial results were reported in studies about non-specific respiratory symptoms19. Some studies found ETS exposed children were more likely to have respiratory symptoms20,21, while others did not22. Parental respiratory symptoms were one of the important confounding factors that was not adequately addressed in previous studies. Furthermore, influence of season on children’s respiratory symptoms should be taken into consideration. Relationship between ETS exposure and medication consumption is rarely studied. Several recent European studies showed that ETS is associated with a higher antibiotic use rate in young children23,24, however the availability of such data in Hong Kong was limited.

With this study, we aimed to examine the associations between ETS exposure and utilisation of healthcare service, respiratory symptoms, and antibiotic use in young children in Hong Kong. We hypothesized that ETS exposed children had a higher risk of needing medical services, having respiratory symptoms, and taking antibiotics, compared with non-exposed children.

METHODS

Study population

This secondary analysis was performed on data collected from our 2013–2014 territory-wide cross-sectional pneumococcal carriage surveillance study, in which 1541 young children (mean age: 11.2 months; males: 50.7%) were recruited. Details of the surveillance study have been published25. Convenience samples were drawn. Children aged 2, 12 and 18 months were approached and recruited when they attended the immunization and health surveillance service provided by the Maternal and Child Health Centre across four main regions of Hong Kong. Screening for suitable subjects was done at the time of recruitment. Eligible children were invited to join the study with a response rate of 63.3%. Exclusion criteria were: 1) extreme low birth weight and very low birth weight infants; 2) subjects with cerebral palsy; 3) syndromes and neurological disorders affecting swallowing; 4) ear, nose and throat disorders; 5) confirmed or suspected immunodeficiency (congenital or acquired); 6) subjects taking immunosuppressive therapy; and 7) incomplete vaccination or vaccination record. This retrospective study was approved by the Joint Chinese University of Hong Kong–New Territories East Cluster Clinical Research Ethics Committee (CRE-2018.452).

Data collection

Caregivers of the young children were asked to complete a questionnaire under supervision by a trained research nurse. The missing data rates were very low in the current study (less than 5% for all items). Data on a range of variables for the children were recorded including demographic information, household tobacco smoke exposure, medical service utilisation, respiratory symptoms, and antibiotic use.

Exposure variables and disease outcome variables

Exposure binary variables were current household ETS exposure, prenatal maternal smoking exposure, and postnatal maternal smoking exposure. The caregiver was asked whether there were any smokers living with the child, whether mother smoked during pregnancy, and whether the mother was an active smoker (yes/no responses). Exposure level was examined using ordinal categorical variables including number of household smokers at home (0, 1, >1), and daily cigarette consumption by all household smokers (0, 1–20, >20). Disease outcomes were children’s medical service utilisation, presence of recent respiratory symptoms and antibiotic use. As for medical service utilisation, the caregiver was asked whether the child had a doctor consultation in the past 3 months (yes/no), with the major diagnosis for the visit recorded. Hospitalisations were recorded in a similar way. The caregiver was asked whether the child had respiratory symptoms in the past 1 month, and the specific symptoms were reported by the caregiver, which included fever, cough, sneezing, shortness of breath, sore throat, wheezing, middle-ear infection, and others. Antibiotic use in the past 3 months of the child was also recorded (yes/no). Our measures of ETS exposure and health outcomes were similar to previous studies9,12,13.

Statistical method

Descriptive analysis was performed for children’s sociodemographic and clinical characteristics, medical service utilisation, and respiratory symptoms. Crude associations between the exposure variables and disease outcomes were analysed using chi-squared tests. As for the adjusted associations, all multivariable analyses had been adjusted for potential confounding factors: children’s sex, age, body mass index (BMI) z score, history of breastfeeding (yes/no), gestational age at birth, birthweight, maternal age, living region, overcrowding of living area (corresponding to a living space of <5.5 m2/person, in accordance with the guideline of the Hong Kong Housing Authority), low household income (household monthly income ≤HK$20000), childcare attendance (attendance of day care centre, nursery, or playgroup), and presence of siblings (yes/no). For respiratory symptoms, additional adjustment for household members’ respiratory symptoms and season were made. Multivariable logistic regression was used to evaluate the associations. The missing data rates were less than 5% for all items. The missing data were excluded in the analysis if there were any. As the number of missing data was very low, the effect on the results was basically negligible. A p-value of <0.05 was considered to be statistically significant, with p-values corrected (adjusted) for multiple tests (Bonferroni’s correction), where appropriate. All statistical analyses were performed by the SPSS package.

RESULTS

Demographic and clinical characteristics of the participants

The baseline characteristics, ETS exposure, medical service utilisation, respiratory symptoms and antibiotic use of the participants are shown in Table 1. More than half (61.6%) of the cohort had an all-cause doctor consultation in the past 3 months, and most of them were in private sectors. Six per cent of the children had hospitalisation in the past 3 months and the hospitalisation rate for respiratory tract infection (RTI) was 1.7%. Of the children, 19.4% took antibiotics in the past 3 months. One-third reported to have respiratory symptoms in the past 1 month.

Table 1

Demographic and clinical characteristics of the study participants, Hong Kong, 2013–2014 (N=1541)

CharacteristicsAll infants n (%)*
Mean age (months)11.2 ± 6.4
Male sex782 (50.7)
Birth historyGestational age at birth (weeks)38.6 ± 1.4
Vaginal delivery1030 (66.8)
Birth weight (kg)3.1 ± 0.4
BMI z score0.2 ± 1.3
Maternal age (years)32.7 ± 4.6
History of breastfeeding1220 (79.2)
Child care attendance197 (12.8)
Presence of household smokersAny current household smoker485 (31.5)
Postnatal maternal smoking53 (3.4)
Prenatal maternal smoking25 (1.6)
Number of current household smokers01056 (68.5)
1377 (24.5)
>1108 (7.0)
01056 (68.5)
Cigarette consumption per day by household smokers1–20430 (27.9)
>2055 (3.6)
Medical service utilisationAny doctor consultation in the past 3 months950 (61.6)
Service typeConsultation in private sector769 (49.9)
Consultation in public sector93 (6.0)
Consultation in both private and public sector88 (6.0)
Hospitalisation in the past 3 months93 (6.0)
Hospitalisation for RTI in the past 3 months26 (1.7)
Antibiotic useIn the past 3 months299 (19.4)
Presence of respiratory symptomsIn the past 1 month515 (33.4)
Presence of respiratory symptoms of household membersIn the past 1 month5 (52.2)

* Values are number (%), unless specified as mean (±SD). RTI: Respiratory tract infection.

ETS exposure and medical service utilisation

Need of doctor consultation was significantly higher among ETS exposed children, with an ascending trend for increasing exposure levels (Table 2). Children with current household ETS exposure (67.0 vs 59.2%; p=0.0030) and postnatal maternal smoking (81.1 vs 61.0%; p=0.0020) had higher rates of all-cause doctor consultation in the past 3 months compared with the non-exposed. Need of medical consultation was significantly larger as the exposure levels increased for both the number of household smokers and their total daily cigarette consumption. After adjustment of the p-values using Bonferroni’s correction, significance of associations remained (Table 3). Current household ETS exposure (AOR=1.30; 95% CI: 1.00–1.66; p=0.050) and postnatal maternal smoking (AOR=2.21; 95% CI: 1.06–4.64, p=0.035) were independently and significantly associated with all-cause doctor consultation in the past 3 months. Children living with more than 1 household smoker (AOR=1.70; 95% CI: 1.04–2.77; p=0.028) were shown to have higher risk of having all-cause doctor consultation compared with the non-exposed, however the association was not significant for children living with 1 household smoker. Postnatal maternal smoking was associated with all-cause hospitalisation in the past 3 months (AOR=2.48; 95% CI: 1.05–5.86; p=0.039).

Table 2

Univariable analyses: Rates of medical care utilisation associated with the ETS measures of the study participants, Hong Kong, 2013–2014 (N=1541)

ETS exposureAny doctor consultation in the past 3 months
Any hospitalisation in the past 3 months
n%apn%p
Presence of household smokersNo62559.2565.3
Yes32567.00.0030377.60.084
Postnatal maternal smokingNo90761.0865.8
Yes4381.10.0020713.20.037
Prenatal maternal smokingNo93061.3905.9
Yes2080.00.063312.00.19
Number of household smokers062259.1555.2
125065.60.026287.40.13
>17872.20.0090109.30.093
Cigarettes per day by household smokers062359.2565.3
1–2028365.80.017337.70.083
>204075.50.02147.50.49

a Rate of medical service utilisation in each ETS exposure variable condition.

Table 3

Multivariable analyses: Associations between ETS exposure and medical service utilisation of the study participants, Hong Kong, 2013–2014 (N=1541)

ETS exposureAny doctor consultation in the past 3 months
Any hospitalisation in the past 3 months
AOR (95% CI)pAOR (95% CI)p
Presence of household smokers1.30 (1.00–1.66)0.0501.42 (0.90–2.25)0.13
Postnatal maternal smoking2.21 (1.06–4.64)0.0352.48 (1.05–5.86)0.039
Prenatal maternal smoking2.30 (0.80–6.57)0.122.17 (0.61–7.67)0.23
Number of household smokers011
11.21 (0.93–1.59)0.161.41 (0.86–2.30)0.18
>11.70 (1.04–2.77)0.0281.76 (0.83–3.74)0.14
Cigarettes per day by household smokers011
1–201.24 (0.96–1.61)0.101.44 (0.90–2.31)0.13
>201.84 (0.92–3.68)0.0871.42 (0.47–4.25)0.53

[i] AOR: adjusted odds ratio; adjusted for children’s sex, age, body mass index (BMI) z score, history of breastfeeding, gestational age at birth, birthweight, maternal age, living region, overcrowding of living area, household income, child care attendance, and presence of siblings.

Associations between ETS exposure and respiratory symptoms

Young children with household smokers consuming more than 20 cigarettes/day had significantly higher rate of having respiratory symptoms in the past 1 month compared with the non-exposed (47.2 vs 32.6%; p=0.030). The difference remained statistically significant after adjustment (Table 4).

Table 4

Associations between ETS exposure and presence of respiratory symptoms of the study participants, Hong Kong, 2013–2014 (N=1541)

ETS exposurePresence of respiratory symptoms in the past 1 month Univariable
Presence of respiratory symptoms in the past 1 month Multivariable
n%apAOR (95% CI)p
Presence of household smokersNo34232.41
Yes17335.70.222.95 (0.64–13.51)0.16
Postnatal maternal smokingNo49933.51
Yes1630.20.660.68 (0.36–1.29)0.23
Prenatal maternal smokingNo50733.41
Yes832.01.00.95 (0.38–2.38)0.92
Number of household smokers034332.61
113234.60.471.07 (0.81–1.41)0.62
>14037.00.351.15 (0.72–1.82)0.56
Cigarettes per day by household smokers034332.61
1–2014433.50.731.03 (0.79–1.34)0.85
>202547.20.0301.99 (1.12–3.52)0.016

a Rate of symptom development in each exposure variable. AOR: adjusted odds ratio; adjusted for children’s sex, age, body mass index (BMI) z score, history of breastfeeding, gestational age at birth, birthweight, maternal age, living region, overcrowding of living area, household income, child care attendance, presence of siblings, household members’ respiratory symptom, and season.

Associations between ETS exposure and antibiotic use

No statistically significant associations between ETS exposure and antibiotic use were found in the univariable and multivariable analyses (Table 5).

Table 5

Associations between ETS exposure and antibiotic use of the study participants in Hong Kong, 2013– 2014 (N=1541)

ETS exposureAntibiotic use in the past 3 months Univariable
Antibiotic use in the past 3 months Multivariable
n%apAOR (95% CI)p
Presence of household smokersNo19218.21
Yes9619.80.780.90 (0.66–1.23)0.50
Postnatal maternal smokingNo26517.81
Yes1528.30.111.26 (0.57–2.75)0.57
Prenatal maternal smokingNo27117.91
Yes728.00.311.61 (0.56–4.60)0.38
Number of household smokers020219.21
17218.90.900.87 (0.63–1.21)0.42
> 12523.10.331.25 (0.74–2.09)0.41
Cigarette per day by household smokers020219.21
1–208219.10.890.90 (0.66–1.23)0.51
>204122.60.561.01 (0.49–2.09)0.98

a Rate of antibiotic use in each exposure variable. AOR: adjusted odds ratio; adjusted for children’s sex, age, body mass index (BMI) z score, history of breastfeeding, gestational age at birth, birthweight, maternal age, living region, overcrowding of living area, household income, child care attendance, and presence of siblings.

Associations between ETS exposure and outcomes among children with a non-smoking mother

Associations between ETS exposure and health outcomes were further evaluated among children with non-smoking mothers only (N=1480, mother was neither smoking during pregnancy nor an active smoker). Household ETS exposure was significantly and independently associated with all-cause doctor consultation in the past 3 months (AOR=1.34; 95% CI: 1.06–1.70; p=0.021), even after exclusion of maternal smoking (Supplementary Tables 1 and 2).

DISCUSSION

Young children with household ETS exposure were more likely to have all-cause medical service utilisation and recent respiratory symptoms compared with the non-exposed children. The risks were higher with increasing exposure levels. These findings suggest an increased healthcare burden associated with ETS exposure in young children, emphasizing the importance of identification, reduction, and prevention of ETS exposure in the paediatric population.

Our study found household ETS exposure was associated with both outpatient doctor consultation and hospitalisation in young children, while a previous local study demonstrated the association only in inpatient care but not in outpatient consultation12. In the previous study, infants with smoking mothers were excluded, doctor consultations and hospitalisation were dichotomized as either low or high use, and they coded infants as high users if the baby had higher utilisation than the median among the sample12. The difference in the methodology might explain the different study results. There are emerging studies showing the association of ETS with non-physical health outcomes, which may also be a reason for healthcare service utilization26.

The effect size of association between doctor visit and current household ETS exposure was relatively modest, while the effect size was stronger for postnatal maternal smoking. Postnatal maternal smoking was also associated with all-cause hospitalisation in the past 3 months. We did not detect significant independent associations between prenatal maternal smoking and all-cause medical service utilisation. However, the prevalence of maternal smoking was relatively low when compared with a previous study that showed a prevalence of 10.4%27. This study demonstrated that prenatal maternal smoking, of more than 15 cigarettes daily, is associated with a significant increase in the risk of the offspring being hospitalised for bronchiolitis27. Therefore, the absence of association in our study could be related to our small sample of prenatal maternal smoking. On the other hand, postnatal maternal smoking was significantly associated with doctor consultation in our cohort, which addressed the significant role of maternal smoking in children’s health. Maternal smoking behaviour could have a more direct impact on children’s health since mothers tend to smoke more at home, spend more time and have more contact with children, compared with other household members11.

Dose-dependent associations between ETS exposure and outcomes were observed in our study. Children living with more than one household smoker were more likely to have all-cause doctor consultation, and children living in a household with daily consumption of more than 20 cigarettes, were more likely to have respiratory symptoms compared with the non-exposed children. These findings have been rarely reported in the literature and this observation supports the causal relationship between ETS exposure and medical service utilisation. The toxicity and hazard effects of ETS on children have been well summarized in the literature1. ETS is not only responsible for respiratory illnesses but the hazard can be systemic1,2. Furthermore, a young child’s detoxification system is immature and thus less efficient in handling toxic components of ETS compared with those who are older28,29. Therefore, the harmful effects from ETS could be higher with higher level of exposure. A previous study reported similarly that children with high ETS exposure level were more likely to have had an overnight hospital stay, with the association strongest in asthmatic children4. They also found that children with higher exposure levels tend to have higher risk of healthcare utilisation4. Moreover, children in our cohort with higher ETS exposure were more likely to have recent respiratory symptoms. The association remained even after adjustment for recent respiratory symptoms of household members, which could be a significant confounding factor not considered in previous studies22. A previous study showed that ETS has little effect on the respiratory health of children aged 3–5 years but more effect on children aged <2 years and on children with asthma22. The relationship between ETS exposure and respiratory illness might interact with allergy22. Unfortunately, the children’s allergy history was not collected in our study. Other studies found ETS exposure increased the risk of chronic bronchitis, episodes of wheezing, and various respiratory symptoms such as cough, phlegm, and breathlessness, among children15,30,31.

There are multiple potential mechanisms by which ETS exposure causes respiratory illness. The lungs of young children are not fully developed until the age of 7 years32. The immature airway epithelium and respiratory tract infections create increased permeability of the epithelial layer of the respiratory tract, resulting in increased damage by ETS exposure33. Biomolecular studies also suggest that the development of the immune system will skew towards the T-helper 2 phenotype, increasing the susceptibility of developing allergy and respiratory symptoms with ETS exposure28.

ETS was found to be associated with higher risk of antibiotic use among children aged <5 years in several European studies23,24. The association might be related to the children’s family SES23,24. It can also be mediated with the higher risk of infectious diseases among ETS exposed children, while the mechanism by which ETS exposure increases susceptibility to infectious diseases is not fully understood34. However, no significant association was found between ETS exposure and antibiotic use in our study. The potential reason could be different medical practice on antibiotic use in different regions. Moreover, the information about recent antibiotic use and ETS exposure covered different time periods. It is possible that the practice of antibiotic use would change with time; more doctors now realize that antibiotics are not useful in fighting viral infections.

Strengths and limitations

Strengths of our study are that it was representative of the Hong Kong territory, and that we provided new information in young children aged <18 months, less studied previously. Our analyses with exclusion of children with maternal smoking allowed the independent effect of household ETS exposure to be ascertained. There are a few limitations to address. Our analysis was based on our previous cross-sectional study, and the information was reported by the caregivers with the potential of recall bias. An objective measure of ETS exposure by cotinine level was not used. Potential under-reporting of smoking status could have diluted our power of identifying the health disparities between children with and without exposure. However, most of the participating caregivers of the children were the mothers of the children, and mothers’ proxy reports on the smoking status of the father were highly reliable35. Moreover, parental self-reported smoking status has been shown to be valid and reliable35. Finally, there might have been unmeasured or residual confounding, which cannot be excluded in our observational study.

CONCLUSIONS

Our study demonstrated the associations of household ETS exposure with medical service utilisation and respiratory symptoms in young children. Policy makers, parents and healthcare providers have important roles in reducing children’s ETS exposure. We urge for more effective tobacco control policy and public health education. Healthcare providers should identify ETS exposure in children so that intervention and support can be provided.