Abstract
Background
Allergic rhinitis (AR) affects up to 40% of children in the United States and Europe. AR is often associated with asthma and has a negative impact on quality of life for the children and their families.
Objective
We investigated the AR burden in children with moderate to severe perennial AR in Canada, Denmark, and the United Kingdom, focusing on the role of concomitant asthma. We assessed the health impact on the children, their receipt of allergy medication and health care services, and the impact on their families.
Methods
An online survey was distributed to caregivers of children aged 5 to 17 with moderate to severe perennial AR (both with and without asthma) and to a control group of caregivers of children without allergies.
Results
In total, 877 and 855 caregivers of children with perennial AR and without allergies, respectively, completed the survey. Children with AR and asthma, compared with those without asthma, experienced more sleep disturbances (69% vs 58%), schoolwork limitations (33% vs 22%), daily activities restrictions (55% vs 41%), and missed school hours (7.2 vs 4.6 hours per month). Children with AR and asthma had a higher receipt of allergy medication compared with those without asthma, and they also visited their general practitioner more often (4.6 vs 3.5 times a year). Overall, 32% of all caregivers of children with AR expressed dissatisfaction with allergy medication.
Conclusion
Perennial AR, especially with concomitant asthma, imposes a substantial disease burden in children and their families, highlighting the need for long-term disease control.
Key words: Allergic rhinitis, perennial allergy, house dust mite allergy, burden of disease, caregiver burden, children, adolescents, health care resource use
Allergic rhinitis (AR) is a chronic inflammatory disorder affecting the nasal mucous membranes. The condition is mediated by IgE, which causes an inflammatory response in sensitized individuals.1, 2, 3 Epidemiologic studies have shown that AR affects approximately 20% to 30% of the population in both Europe and North America.4, 5, 6 Notably, children have a higher prevalence, with up to 40% of children and adolescents experiencing AR in the United States and Europe.2,7, 8, 9, 10, 11, 12
AR is associated with multiple comorbidities, including allergic conjunctivitis, atopic dermatitis, and allergic asthma.13, 14, 15 Particularly asthma is often linked to AR, and the co-occurrence of asthma can exacerbate symptoms in both disorders.16,17
Previous studies have established how poorly controlled AR among children hinders their daily activities and has a negative impact on their overall quality of life.18, 19, 20, 21 AR along with asthma in children can impair physical functioning and emotional well-being, and it can interfere with social interactions, learning abilities, and restorative sleep.22, 23, 24
When a child has severe AR, it negatively affects not only the child but also the entire family.19,25 A recent study has found that parents of children with allergic symptoms exhibited a significantly lower health-related quality of life compared with parents whose children did not experience such symptoms.26 Furthermore, AR has been associated with greater medication receipt and increased health care service utilization; studies indicate that individuals with AR may face double the medication costs and physician visits compared with individuals without AR.27, 28, 29 These facts highlight the widespread implications associated with this condition.
Little research exists on perennial AR in children, especially when concomitant asthma is present—despite the fact that they often coexist.30 Moreover, the majority of the existing literature on adults focuses either on perennial AR compared with seasonal AR or only on AR in general.30, 31, 32 This gap emphasizes the necessity of a more inclusive understanding of perennial AR’s and concomitant asthma’s impacts on children and their families in order to provide effective treatment strategies. Therefore, the aim of this cross-sectional study was to investigate the impact of moderate to severe perennial AR on children and their caregivers in Canada, Denmark, and the United Kingdom, with a specific focus on the impact of concomitant asthma.
Methods
We conducted an online cross-sectional survey in Canada, Denmark, and the United Kingdom to investigate the impact of moderate to severe perennial AR and concomitant asthma on the daily lives of children and their families.
Study and control population
Caregivers answered the survey about the relevant child, with inclusion criteria that required the child to be aged 5 to 17 years with caregiver-reported symptomatic, moderate to severe AR with at least one physician-diagnosed perennial allergy, no food allergy, and no previous or ongoing allergen immunotherapy (AIT) treatment. Severity and classification of AR were based on the Allergic Rhinitis and Its Impact on Asthma (ARIA) score. A matched control group of caregivers for children with no caregiver-reported allergies answered relevant sections of the survey. Caregivers in Canada and the United Kingdom with more than one child with perennial allergy were instructed to answer for the child whose allergy is worse.
Data collection
Data were collected during January through April 2023 to assess the impact of perennial AR during the winter months. The data collection process was conducted differently in Denmark compared with the United Kingdom and Canada. In Denmark, all relevant caregivers were identified through Statistics Denmark via the Danish registers. The caregivers were contacted and invited to participate in the survey if their child had filled at least 2 prescriptions for allergy medication (antihistamine or intranasal corticosteroids) in the winter season (from October through February) in 2 consecutive years. In Canada and the United Kingdom, recruitment was carried out via Norstat’s email panels, which distributed the survey to a representative population. Norstat specializes in data collection for research, including market and health studies.33 The process for recruiting control participants mirrored that of the cases in the 3 different countries. To ensure a valid comparison, controls were paired with cases by matching age and sex.
Because this study was not a clinical trial, did not include direct contact with patients, and did not gather biological and/or human samples or identifiable personal information, Danish legislation does not require ethical review board approval.34 Before answering the survey, all caregivers gave consent to participate and provide information about their child and his or her allergy. Written informed consent to participate was not directly obtained but was inferred by completion of the questionnaire and by confirming the participants had read, understood, and accepted the purpose of the survey.
Survey content and validation
The survey was developed through a multistage validation process. Initially, a focus group with individuals with long-term allergy was conducted to gain insights into living with AR. Furthermore, a comprehensive literature review and consultation with medical experts from Canada, Denmark, and the United Kingdom ensured the survey’s content was both relevant and applicable.
The study used the ARIA questionnaire, which has been validated in multiple studies for both AR and asthma.35 Before the final data collection, a pilot survey was conducted in order to make sure the respondents understood the questions and there were no technical errors, after which the survey was refined accordingly.
The final survey, consisting of 53 questions, was divided into 5 sections. The first section focused on allergy type, severity, symptoms, treatment history, and comorbidities. Medication receipt was also assessed in terms of type, frequency, and caregiver satisfaction. Caregiver satisfaction was measured from a very low extent to a very high extent. The second section focused on the burden of AR, assessing the level of trouble experienced by the child in their everyday life (eg, sleep quality, school attendance, and impact on activities), with a scale ranging from not troubled at all to extremely troubled. The third section assessed the child’s general child health using the generic Child Health Questionnaire alongside questions on health care service utilization. The fourth section consisted of the family impact of AR, including caregivers’ stress levels, family limitations, work absence, and household chores. Last, the fifth section consisted of questions related to socioeconomic factors.
Statistical analysis
Survey responses were checked for errors and consistency before inclusion in the statistical analysis. The survey data underwent analysis through univariate descriptive statistics, including means (reported as results of the descriptive analyses), medians, frequencies, and standard deviation. Chi-square tests (for categorial variables) and t tests (for continuous variables) were performed to examine significant differences between groups. These tests, selected for their suitability in analyzing the types of data collected, are effective and intuitive for identifying significant patterns within subgroups. Significance was assessed at a level of P < .05. All analyses were conducted on complete case data, as the survey design required all relevant questions to be answered before submission, thus ensuring that no data were missing from the analyzed sample.
Data are presented for the full population, with additional subgroup analyses for the children with AR as well as for those with and without asthma. Because the allergy questions were not asked for the control population, differences were primarily assessed between children with and without asthma.
Results
A total of 877 caregivers (315 in Canada, 251 in Denmark, and 311 in the United Kingdom) for a child with perennial AR, plus 855 caregivers (353 in Canada, 132 in Denmark, and 370 in the United Kingdom) for a child without any allergies, were included, with all caregivers answering on behalf of only one child. Table I provides the baseline characteristics of the 877 children with AR, and Table E1 (available in this article’s Online Repository at www.jaci-global.org) provides the baseline characteristics for the caregivers of children with AR. Table E2, also in the Online Repository, presents the demographics for the control population (both children and caregivers). Results are presented for all 3 countries combined.
Table I.
Baseline demographics and characteristics of children with AR
| All (n = 877) | Asthma (n = 356) | No asthma (n = 521) | P values (asthma vs no asthma group) | |
|---|---|---|---|---|
| Biological sex, n (%) | .600 | |||
| Female | 364 (42%) | 144 (40%) | 220 (42%) | |
| Male | 513 (58%) | 212 (60%) | 301 (58%) | |
| Age, years | ||||
| Mean | 11.6 | 11.5 | 11.7 | .622 |
| Types of allergies, n (%) | ||||
| Dust mites | 797 (91%) | 322 (90%) | 475 (91%) | .716 |
| Pollen | 686 (78%) | 298 (84%) | 388 (74%) | .001 |
| Animals | 419 (48%) | 214 (60%) | 205 (39%) | <.001 |
| Other year-round allergies | 283 (32%) | 133 (37%) | 150 (29%) | .008 |
| Oral allergy syndrome | 101 (12%) | 43 (12%) | 58 (11%) | .666 |
| No. of allergies, n (%) | <.001 | |||
| 1 | 82 (9%) | 17 (5%) | 65 (13%) | |
| 2 | 330 (38%) | 109 (31%) | 221 (42%) | |
| 3 | 327 (37%) | 150 (42%) | 177 (34%) | |
| ≥4 | 138 (16%) | 80 (22%) | 58 (11%) | |
| Comorbidities, n (%) | ||||
| Asthma | 356 (41%) | 356 (100%) | 0 (0%) | - |
| Eczema/atopic dermatitis | 335 (38%) | 149 (42%) | 186 (36%) | .066 |
| Wheezing | 244 (28%) | 162 (46%) | 82 (16%) | <.001 |
| Recurrent respiratory infection | 211 (24%) | 137 (38%) | 74 (14%) | <.001 |
| Dental malocclusion | 187 (21%) | 80 (22%) | 107 (20%) | .492 |
| ADHD or other mental illness | 142 (16%) | 66 (19%) | 76 (15%) | .119 |
| Nasal polyps | 86 (10%) | 37 (10%) | 49 (9%) | .629 |
| ASD | 82 (9%) | 41 (12%) | 41 (8%) | .068 |
| No. of comorbidities, n (%) | <.001 | |||
| 0 | 177 (20%) | 0 (0%) | 177 (34%) | |
| 1 | 232 (26%) | 61 (17%) | 171 (33%) | |
| 2 | 204 (23%) | 100 (28%) | 104 (20%) | |
| 3 | 133 (15%) | 86 (24%) | 47 (9%) | |
| ≥4 | 131 (15%) | 109 (31%) | 22 (4%) | |
| Symptoms related to AR, n (%) | ||||
| Stuffy nose, runny nose, sneezing, itchy nose, or postnasal drip | 792 (90%) | 316 (89%) | 476 (91%) | .201 |
| Itchy, red, swollen, sore, or watery eyes | 600 (68%) | 233 (65%) | 367 (70%) | .118 |
| Shortness of breath, chest tightness or pain, coughing, or wheezing | 361 (41%) | 238 (67%) | 123 (24%) | <.001 |
| Itchy skin reactions, skin pain, or redness of skin | 386 (44%) | 157 (44%) | 229 (44%) | .966 |
| No. of weeks during a month the child is affected by their AR, n (%) | .001 | |||
| 1-3 weeks | 587 (67%) | 215 (60%) | 372 (71%) | |
| More than 3 weeks | 290 (33%) | 141 (40%) | 149 (29%) | |
| ARIA items, n (%) | ||||
| The allergy is troublesome to the child | 716 (82%) | 287 (81%) | 429 (82%) | .517 |
| The allergy disturbs the child’s sleep | 545 (62%) | 244 (69%) | 301 (58%) | .001 |
| The allergy restricts the child’s daily activities (social life, sports, leisure) | 407 (46%) | 195 (55%) | 212 (41%) | <.001 |
| The allergy restricts the child’s participation in school or work | 232 (26%) | 116 (33%) | 116 (22%) | .001 |
| Hours missed from class or school due to AR, mean | ||||
| Mean number of hours | 5.6 | 7.2 | 4.6 | .001 |
Data are presented as nos. (%) unless otherwise indicated. Information was caregiver reported.
ADHD, Attention-deficit/hyperactivity disorder; ASD, autism spectrum disorder.
The most common perennial allergy was house dust mite (HDM) at 91%, and 41% of the children had concomitant asthma (Table I). The children with concomitant asthma had a higher number of both allergies and comorbidities compared with the children without asthma, whereas 55% and 13% of the children with and without asthma had 3 or more comorbidities, respectively, and 64% and 45% of the children with and without asthma had 3 or more allergies.
Caregivers for children both with and without asthma equally reported AR as troublesome for the child (81% and 82%). Compared with children without asthma, however, more children with concomitant asthma experienced sleep disturbance and were restricted in school participation and daily activities. They also missed more hours from class or school because of allergy-related problems: 7.2 hours on average during the previous month, compared with 4.6 hours on average for the children without asthma.
Receipt of allergy medication and health care services
As Table II shows, about two thirds of the children with AR were prescribed 2 or 3 different types of allergy medication, with 76%, 74%, and 51% prescribed tablets or capsules, nasal sprays, and eye drops, respectively. The children with concomitant asthma were prescribed tablets or capsules and nasal sprays more frequently than the children without asthma. Receipt of allergy medication among the children with AR persisted for several months each year—an average of 7.1 months for tablets or capsules, 6.8 months for nasal sprays, and 5.2 months for eye drops—and all such time periods were longer for the children with concomitant asthma. In addition, the children aged 12 to 17 years received all 3 types of medication for longer periods compared with the children aged 5 to 11 years (see Table E3 in the Online Repository available at www.jaci-global.org).
Table II.
Receipt of allergy medication
| All (n = 877) | Asthma (n = 356) | No asthma (n = 521) | P values (asthma vs no asthma group) | |
|---|---|---|---|---|
| No. of medications, n (%) | .707 | |||
| 0 | 48 (5%) | 17 (5%) | 31 (6%) | |
| 1 | 217 (25%) | 88 (25%) | 129 (25%) | |
| 2 | 284 (32%) | 111 (31%) | 173 (33%) | |
| 3 | 328 (37%) | 140 (39%) | 188 (36%) | |
| Types of allergy medication, n (%) | ||||
| Tablets or capsules | 668 (76%) | 270 (76%) | 398 (76%) | .851 |
| Nasal sprays | 651 (74%) | 282 (79%) | 369 (71%) | .005 |
| Eye drops | 450 (51%) | 178 (50%) | 272 (52%) | .521 |
| Frequency of medication use, n (%) | ||||
| Tablets or capsules | NA | |||
| Every day | 267 (40%) | 129 (48%) | 138 (35%) | |
| 2-6 times a week | 162 (24%) | 69 (26%) | 93 (23%) | |
| Once a week | 90 (13%) | 34 (13%) | 56 (14%) | |
| 1-3 times a month | 85 (13%) | 18 (7%) | 67 (17%) | |
| Less than once a month | 52 (8%) | 15 (6%) | 37 (9%) | |
| I do not know | 12 (2%) | 5 (2%) | 7 (2%) | |
| Nasal sprays | .043 | |||
| Every day | 238 (36%) | 116 (41%) | 122 (33%) | |
| 2-6 times a week | 171 (26%) | 79 (28%) | 92 (25%) | |
| Once a week | 84 (13%) | 25 (9%) | 59 (16%) | |
| 1-3 times a month | 96 (15%) | 36 (13%) | 60 (16%) | |
| Less than once a month | 50 (8%) | 20 (7%) | 30 (8%) | |
| I do not know | 12 (2%) | 6 (2%) | 6 (2%) | |
| Eye drops | .257 | |||
| Every day | 73 (16%) | 25 (14%) | 48 (18%) | |
| 2-6 times a week | 123 (27%) | 58 (33%) | 65 (24%) | |
| Once a week | 95 (21%) | 38 (21%) | 57 (21%) | |
| 1-3 times a month | 81 (18%) | 30 (17%) | 51 (19%) | |
| Less than once a month | 64 (14%) | 20 (11%) | 44 (16%) | |
| I do not know | 14 (3%) | 7 (4%) | 7 (3%) | |
| Months per year when the child takes medication, mean | ||||
| Tablets or capsules | 7.1 | 8.0 | 6.6 | <.001 |
| Nasal sprays | 6.8 | 7.4 | 6.4 | .002 |
| Eye drops | 5.2 | 5.4 | 5.1 | .507 |
| Days after AR flare-up when the child was affected, mean | ||||
| Mean number of days | 3.3 | 3.6 | 3.1 | .408 |
| Did the child use more medication in the days following the AR flare-up? | <.001 | |||
| Yes | 434 (49%) | 216 (61%) | 218 (42%) | |
| No | 370 (42%) | 113 (32%) | 257 (49%) | |
| Don’t know | 73 (8%) | 27 (8%) | 46 (9%) | |
| Days after AR flare-up when the child used more medication than usual, mean | ||||
| Mean number of days | 3.6 | 4.1 | 3.2 | .003 |
Data are presented as nos. (%) unless otherwise indicated. NA, Not applicable.
Caregivers were also asked to assess the impact of the allergy medication using a scale of 0 (representing the poorest health) to 100 (representing optimal health) to indicate the child’s health when using the medication and when the medication is not available. The results were similar among the children with and without concomitant asthma, with caregivers rating the child’s health better while receiving the medication compared with when the child did not have access (74 vs 44). Furthermore, regarding satisfaction with the medication, the results in Fig 1 show that 69% of all caregivers of a child with AR were satisfied to a very high or high extent with the medication’s ability to relieve the child’s allergy symptoms. However, the data also show that one-third of caregivers were satisfied only to a low or very low extent with the allergy medication.
Fig 1.
To what extent are you satisfied with the medication’s ability to relieve your child’s allergy symptoms?
In terms of number of medications prescribed, no differences existed between the group that was satisfied to a high or very high extent and the group that was satisfied to a low or very low extent. However, the children in the group with low satisfaction were more affected by AR: 35% were affected 4 days a week or more and 40% more than 3 weeks a month, versus 17% and 30%, respectively, for the group with high satisfaction. The low satisfaction group also scored the child’s health lower on the 1-100 scale with access to medication compared with the high satisfaction group (64 vs 78).
Caregivers for a child with AR also rated statements about the child’s allergy medication (see Fig E1 in the Online Repository available at www.jaci-global.org), and more than half agreed or strongly agreed that the child’s health depends on the medication, that they sometimes worry about long-term effects of the medication, and that the medication prevents the child’s health from getting worse.
Caregivers both for the children with AR and for those without were asked about the child’s use of health care resources. Fig 2, A, shows that caregivers for the children with AR sought medical care for the child more often than did caregivers for the children without allergy. This difference was significant (P < .001) for visits to general practitioners, allergy specialists, dermatologists, and ear, nose, and throat specialists. These results are highly driven by the children with AR and concomitant asthma, who sought medical care from a general practitioner, an allergy specialist, or a pediatrician significantly more often than the AR children without asthma and the children without allergy (P < .005) (Fig 2, B and C).
Fig 2.
How many times per year do you normally seek medical care for your child? ∗P < .05, ∗∗P < .01, ∗∗∗P < .001.
Impact on caregivers and family
Table III shows that caregivers for a child with AR experienced feelings of stress and concern because of the child’s condition, with almost half reporting that the child’s AR has caused some, quite a bit, or a lot of stress. In addition, more than half (56-58%) expressed varying degrees of concern regarding the allergy’s impact on the child’s future education, work life, and social/family life (Table IV). A larger proportion of caregivers for a child with concomitant asthma reported feelings of stress and concern regarding their child’s future. However, caregivers for children aged 5 to 11 years were more concerned about the child’s future regarding education, work life, and social/family life compared with caregivers for children aged 12 to 17 years (Table E3).
Table III.
Stress in caregivers and families due to AR
| All (n = 877) | Asthma (n = 356) | No asthma (n = 521) | P values (asthma vs no asthma group) | |
|---|---|---|---|---|
| Level of stress that AR causes in the caregiver, n (%) | .007 | |||
| A lot | 75 (9%) | 39 (11%) | 36 (7%) | |
| Quite a bit | 132 (15%) | 69 (19%) | 63 (12%) | |
| Some | 158 (18%) | 63 (18%) | 95 (18%) | |
| A little bit | 284 (32%) | 105 (29%) | 179 (34%) | |
| None at all | 180 (21%) | 64 (18%) | 116 (22%) | |
| Not relevant | 48 (5%) | 16 (4%) | 32 (6%) | |
| Level of stress that AR causes in the caregiver’s partner, n (%) | .023 | |||
| A lot | 32 (4%) | 16 (4%) | 16 (3%) | |
| Quite a bit | 106 (12%) | 54 (15%) | 52 (10%) | |
| Some | 154 (18%) | 71 (20%) | 83 (16%) | |
| A little bit | 212 (24%) | 85 (24%) | 127 (24%) | |
| None at all | 231 (26%) | 79 (22%) | 152 (29%) | |
| Not relevant | 142 (16%) | 51 (14%) | 91 (17%) | |
| Level of stress that AR causes in the family, n (%) | .001 | |||
| A lot | 23 (3%) | 14 (4%) | 9 (2%) | |
| Quite a bit | 82 (9%) | 47 (13%) | 35 (7%) | |
| Some | 164 (19%) | 76 (21%) | 88 (17%) | |
| A little bit | 242 (28%) | 86 (24%) | 156 (30%) | |
| None at all | 266 (30%) | 98 (28%) | 168 (32%) | |
| Not relevant | 100 (11%) | 35 (10%) | 65 (12%) | |
Data are presented as nos. (%).
Table IV.
Burden of AR among caregivers and families
| All (n = 877) | Asthma (n = 356) | No asthma (n = 521) | P values (asthma vs no asthma group) | |
|---|---|---|---|---|
| Caregiver’s concerns about the future, n (%) | ||||
| Future work life | <.001 | |||
| A lot | 51 (6%) | 28 (8%) | 23 (4%) | |
| Quite a bit | 98 (11%) | 52 (15%) | 46 (9%) | |
| Some | 141 (16%) | 63 (18%) | 78 (15%) | |
| A little bit | 220 (25%) | 98 (28%) | 122 (23%) | |
| None at all | 367 (42%) | 115 (32%) | 252 (48%) | |
| Future social/family life | <.001 | |||
| A lot | 46 (5%) | 20 (6%) | 26 (5%) | |
| Quite a bit | 106 (12%) | 60 (17%) | 46 (9%) | |
| Some | 140 (16%) | 63 (18%) | 77 (15%) | |
| A little bit | 219 (25%) | 91 (26%) | 128 (25%) | |
| None at all | 366 (42%) | 122 (34%) | 244 (47%) | |
| Future education | <.001 | |||
| A lot | 73 (8%) | 33 (9%) | 40 (8%) | |
| Quite a bit | 89 (10%) | 52 (15%) | 37 (7%) | |
| Some | 122 (14%) | 59 (17%) | 63 (12%) | |
| A little bit | 211 (24%) | 92 (26%) | 119 (23%) | |
| None at all | 382 (44%) | 120 (34%) | 262 (50%) | |
| How much AR has limited family activities, n (%) | <.001 | |||
| A lot | 67 (8%) | 34 (10%) | 33 (6%) | |
| Quite a bit | 87 (10%) | 42 (12%) | 45 (9%) | |
| Some | 146 (17%) | 70 (20%) | 76 (15%) | |
| A little bit | 239 (27%) | 107 (30%) | 132 (25%) | |
| None at all | 338 (39%) | 103 (29%) | 235 (45%) | |
| No. of caregivers who took time off from work due to AR in the past year, n (%) | <.001 | |||
| Yes | 290 (33%) | 164 (46%) | 126 (24%) | |
| No | 543 (62%) | 168 (47%) | 375 (72%) | |
| Don’t know | 44 (5%) | 24 (7%) | 20 (4%) | |
| Days absent from work in the past year due to AR, mean | ||||
| Mean number of days | 6.8 | 6.6 | 7.1 | .704 |
Data are presented as nos. (%) unless otherwise indicated.
Caregivers also experienced the impact in more practical aspects of their everyday lives. In the past year, 33% of caregivers took time off from work, for a mean of 6.8 days, because of the child’s AR. Caregivers of a child with concomitant asthma took time off from work more often compared with caregivers of a child without asthma (46% vs 24%). Furthermore, caregivers of a child with AR spent more time each week on household chores such as cleaning compared with caregivers of a child without allergies (Fig 3, A). Caregivers of a child with AR and concomitant asthma spent more time washing clothes and bedsheets compared with caregivers of a child with AR and without concomitant asthma (Fig 3, B). Caregivers of a child with AR and no concomitant asthma spent significantly more time cleaning the house and driving the child, compared with caregivers of a child without any allergies (Fig 3, C).
Fig 3.
How many hours in total last week did you, your partner, or others spend on household chores? ∗P < .05, ∗∗P < .01, ∗∗∗P < .001.
Discussion
Our study of caregivers showed that moderate to severe perennial AR in children is associated with a considerable burden of disease—and an even bigger burden when concomitant asthma is present. In our multinational study population, the children were affected by both physical symptoms and restrictions in their leisure, school, and home activities. Children with perennial AR frequently required medication, often daily or multiple times a week, and children with concomitant asthma experienced even higher medication receipt throughout the year.
Our survey aimed to assess the overall satisfaction with current treatment standards for AR, not compare the effectiveness of different specific medication groups. Caregivers’ responses indicate that reported measures of children’s health were improved by taking the allergy medication. However, one third of the caregivers were satisfied with their current medication only to a very low or low extent. When comparing the low satisfaction group with the high satisfaction group, there was no difference in the number of different allergy medications prescribed. However, the group with low satisfaction was affected more days per week, as well as more weeks per month, compared with the group with high satisfaction. Additionally, caregivers in the group expressing low satisfaction with the current medication scored the child’s health lower, which indicates that the children in this group are treated with medication to the same extent as children in the high satisfaction group but may not experience the same effect of symptom relief.
Observational studies have reported inconsistent levels of satisfaction with allergy medications, contrasting with clinical research that demonstrates high efficacy. In a French study, 33% of children and adults perceived their symptomatic AR medication as unhelpful in the past month, and an Italian study indicated that more than half of patients were not satisfied with their treatment.36,37 In contrast, high satisfaction rates were reported in Finland, where 93% of patients undergoing HDM AIT were satisfied with their treatment, and a different French study indicated that 85% of children with AR and concomitant asthma were satisfied with AIT medication.38,39
Despite effective treatments and their frequent administration, dissatisfaction and a considerable disease burden remain. It is crucial for future research to delve into the reasons for this dissatisfaction by considering factors such as medication type, symptom specificity, and age differences. Additionally, studies often rely on physician-perceived patient satisfaction, which may not accurately reflect true patient sentiment, as health care providers tend to overestimate patient satisfaction.29,38 This underscores the need for general practitioners to recognize this matter and to implement regular follow-ups and personalized treatment adjustments.
Previous research has consistently indicated that AR in general is associated with increased utilization of health care services, encompassing both medication costs and visits to physicians.27, 28, 29 Our study confirmed that children with perennial AR sought medical care more often compared with children without AR, and that perennial AR impacts not only the child but also the entire family in terms of stress, worrying, and limitation in family activities. Thus, perennial AR in children has negative consequences for both the affected children and their families and regarding health care costs.
The co-occurrence of asthma intensified the challenges associated with AR, leading to multiple restrictions in the everyday life for children with AR, increased medication receipt, and an increase in caregiver anxiety. Our findings underscore the critical importance of adopting proactive measures to manage AR and minimize the risk of asthma persistence.40 In addition, our study showed a higher occurrence of recurrent respiratory infection among the children with perennial AR and concomitant asthma, which could be the reason for the increased medication receipt, health care resource use, and absence from school in this population.
From a policy perspective, our findings highlight a crucial need for treatments providing long-term symptom control in children with perennial AR and concomitant asthma. Effective allergy medication has the potential not only to improve the health and well-being of the affected children but also to alleviate the broader negative societal and familial impacts associated with the conditions. According to the caregivers participating in this study, the children are dependent of their allergy medication, which indicates that allergy medication serves an important role in managing AR. However, the results also indicate an unmet need in the field of children’s allergy medication. AIT is advised for the treatment of AR in individuals with disease that does not respond to corticosteroids or antihistamines, and clinical studies have shown that symptoms of both perennial AR and asthma can be reduced by AIT.41, 42, 43, 44, 45, 46 In both clinical trials and real-world studies, sublingual immunotherapy tablets have shown to be a safe and effective treatment in adolescents and children with HDM AR, indicating a promising long-term treatment solution for these age groups.38,47, 48, 49 For a deeper understanding, however, a more comprehensive evaluation of caregiver satisfaction with AIT is necessary.
Strengths and limitations
This study has several strengths, including the large sample size of caregivers across 3 countries, which provides a comprehensive understanding of the impact of perennial AR and enhances the robustness of the findings. Using the Danish registers to identify the Danish population of children with AR (and the control group) ensures that these findings are based on a representative sample. The use of a control group is also a strength of this study, as it establishes a benchmark for the results and enriches understanding of the excess burden associated with perennial AR.
Limitations of our study include unavailable population registries for identifying the Canadian and United Kingdom populations, resulting in 2 different processes of recruitment. Selection bias is also a potential limitation as a result of the unknown characteristics of nonrespondents, which might affect the estimation of disease burden. However, the recruitment via the Danish registers and the email panels in Canada and the United Kingdom aimed to minimize this challenge, enhancing the reliability of the findings.
The multicenter approach of this study, while contributing to a larger and more diverse sample size, did not extend to a detailed analysis at each center level. This may have resulted in potential confounding factors specific to each local setting, such as allergen exposure, treatment approaches, health care access, and demographic factors. Another potential challenge is the timing of data collection in early 2023, which may coincide with coronavirus disease 2019 postlockdown infection, potentially amplifying the perceived burden of both AR and asthma. However, the alignment of our findings with existing research indicates that the reported burden in our study is unlikely to be solely a consequence of a postlockdown context.
Furthermore, the study’s cross-sectional and descriptive design captures data at a single point in time, which restricts the ability to establish causation. Another limitation of the study arises from the reliance on caregiver self-reports for perennial AR diagnoses. Furthermore, while caregiver reports can provide valuable insight into the experiences of children with AR, this approach also introduces potential biases in accurately representing the child’s experience.21,50
Conclusion
Our study showed that the AR burden is high in children living with perennial AR, affecting several aspects of a child’s life, with implications for caregivers and immediate family. This impact is especially distinct for children with concomitant asthma. Increased medication receipt and increased health care resource use among these children, combined with the third of caregivers who express low satisfaction with the child’s current medication, emphasize a need for more effective long-term, disease-modifying treatment options.
Disclosure statement
Supported by ALK-Abelló A/S, Hørsholm.
Disclosure of potential conflict of interest: E. Lavine and J. A. d. G. d. Maia e Costa received fees from ALK-Abelló A/S for advisory services. S. V. Vahlkvist and T. H. Petersen received fees from ALK as coauthors of this study. M. R. Rodriguez and M. Aagren are employees of ALK-Abelló A/S. A. S. L. Loftager and M. Bøgelund are employees of EY Parthenon P/S, a paid vendor of ALK-Abelló A/S.
Supplementary data
References
- 1.Seidman M.D., Gurgel R.K., Lin S.Y., Schwartz S.R., Baroody F.M., Bonner J.R., et al. Clinical practice guideline: allergic rhinitis. Otolaryngol Neck Surg. 2015;152:197–206. doi: 10.1177/0194599814561600. [DOI] [PubMed] [Google Scholar]
- 2.Skoner D.P. Allergic rhinitis: definition, epidemiology, pathophysiology, detection, and diagnosis. J Allergy Clin Immunol. 2001;108:S2–S8. doi: 10.1067/mai.2001.115569. [DOI] [PubMed] [Google Scholar]
- 3.Nur Husna S.M., Tan H.T.T., Md Shukri N., Mohd Ashari N.S., Wong K.K. Allergic rhinitis: a clinical and pathophysiological overview. Front Med. 2022;9 doi: 10.3389/fmed.2022.874114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Keith P.K., Desrosiers M., Laister T., Schellenberg R.R., Waserman S. The burden of allergic rhinitis (AR) in Canada: perspectives of physicians and patients. Allergy Asthma Clin Immunol. 2012;8:7. doi: 10.1186/1710-1492-8-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Bauchau V., Durham S.R. Prevalence and rate of diagnosis of allergic rhinitis in Europe. Eur Respir J. 2004;24:758–764. doi: 10.1183/09031936.04.00013904. [DOI] [PubMed] [Google Scholar]
- 6.Meltzer E.O. Allergic rhinitis: burden of illness, quality of life, comorbidities, and control. Immunol Allergy Clin North Am. 2016;36:235–248. doi: 10.1016/j.iac.2015.12.002. [DOI] [PubMed] [Google Scholar]
- 7.Wright A.L., Holberg C.J., Martinez F.D., Halonen M., Morgan W., Taussig L.M. Epidemiology of physician-diagnosed allergic rhinitis in childhood. Pediatrics. 1994;94:895–901. doi: 10.1542/peds.94.6.895. [DOI] [PubMed] [Google Scholar]
- 8.McCrory D.C., Williams J.W., Dolor R.J., Kolimaga J.T., Reed S., Sundy J., et al. US Agency for Healthcare Research and Quality; Rockville (Md): March 2003. Management of allergic rhinitis in the working-age population. Report No. 03-E015. [PMC free article] [PubMed] [Google Scholar]
- 9.Berger W.E. Allergic rhinitis in children. Pediatr Drugs. 2004;6:233–250. doi: 10.2165/00148581-200406040-00003. [DOI] [PubMed] [Google Scholar]
- 10.Roberts G., Xatzipsalti M., Borrego L.M., Custovic A., Halken S., Hellings P.W., et al. Paediatric rhinitis: position paper of the European Academy of Allergy and Clinical Immunology. Allergy. 2013;68:1102–1116. doi: 10.1111/all.12235. [DOI] [PubMed] [Google Scholar]
- 11.Sultész M., Horváth A., Molnár D., Katona G., Mezei G., Hirschberg A., et al. Prevalence of allergic rhinitis, related comorbidities and risk factors in schoolchildren. Allergy Asthma Clin Immunol. 2020;16:98. doi: 10.1186/s13223-020-00495-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Asher M.I., Montefort S., Björkstén B., Lai C.K., Strachan D.P., Weiland S.K., et al. Worldwide time trends in the prevalence of symptoms of asthma, allergic rhinoconjunctivitis, and eczema in childhood: ISAAC Phases One and Three repeat multicountry cross-sectional surveys. Lancet. 2006;368:733–743. doi: 10.1016/S0140-6736(06)69283-0. [DOI] [PubMed] [Google Scholar]
- 13.Licari A., Magri P., Silvestri A.D., Giannetti A., Indolfi C., Mori F., et al. Epidemiology of allergic rhinitis in children: a systematic review and meta-analysis. J Allergy Clin Immunol Pract. 2023;11:2547–2556. doi: 10.1016/j.jaip.2023.05.016. [DOI] [PubMed] [Google Scholar]
- 14.Scadding G.K., Kariyawasam H.H., Scadding G., Mirakian R., Buckley R.J., Dixon T., et al. BSACI guideline for the diagnosis and management of allergic and non-allergic rhinitis (revised edition 2017; first edition 2007) Clin Exp Allergy. 2017;47:856–889. doi: 10.1111/cea.12953. [DOI] [PubMed] [Google Scholar]
- 15.Cingi C., Gevaert P., Mösges R., Rondon C., Hox V., Rudenko M., et al. Multi-morbidities of allergic rhinitis in adults: European Academy of Allergy and Clinical Immunology Task Force Report. Clin Transl Allergy. 2017;7:17. doi: 10.1186/s13601-017-0153-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Sukhan V.S. Allergic rhinitis and asthma co-morbidity. Wiadomosci Lek Wars Pol. 2019;72:622–626. doi: 10.36740/WLek201904122. [DOI] [PubMed] [Google Scholar]
- 17.Deliu M., Belgrave D., Simpson A., Murray C.S., Kerry G., Custovic A. Impact of rhinitis on asthma severity in school-age children. Allergy. 2014;69:1515–1521. doi: 10.1111/all.12467. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.Blaiss M.S., Hammerby E., Robinson S., Kennedy-Martin T., Buchs S. The burden of allergic rhinitis and allergic rhinoconjunctivitis on adolescents. Ann Allergy Asthma Immunol. 2018;121:43–52.e3. doi: 10.1016/j.anai.2018.03.028. [DOI] [PubMed] [Google Scholar]
- 19.Silva C.H., Silva T.E., Morales N.M., Fernandes K.P., Pinto R.M. Quality of life in children and adolescents with allergic rhinitis. Braz J Otorhinolaryngol. 2009;75:642–649. doi: 10.1016/S1808-8694(15)30511-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Meltzer E.O. Quality of life in adults and children with allergic rhinitis. J Allergy Clin Immunol. 2001;108:S45–S53. doi: 10.1067/mai.2001.115566. [DOI] [PubMed] [Google Scholar]
- 21.Bosnic-Anticevich S., Smith P., Abramson M., Hespe C.M., Johnson M., Stosic R., et al. Impact of allergic rhinitis on the day-to-day lives of children: insights from an Australian cross-sectional study. BMJ Open. 2020;10 doi: 10.1136/bmjopen-2020-038870. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Mir E., Panjabi C., Shah A. Impact of allergic rhinitis in school going children. Asia Pac Allergy. 2012;2:93–100. doi: 10.5415/apallergy.2012.2.2.93. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 23.Schuler C.F., IV, Montejo J.M. Allergic rhinitis in children and adolescents. Pediatr Clin North Am. 2019;66:981–993. doi: 10.1016/j.pcl.2019.06.004. [DOI] [PubMed] [Google Scholar]
- 24.Walker S., Khan-Wasti S., Fletcher M., Cullinan P., Harris J., Sheikh A. Seasonal allergic rhinitis is associated with a detrimental effect on examination performance in United Kingdom teenagers: case–control study. J Allergy Clin Immunol. 2007;120:381–387. doi: 10.1016/j.jaci.2007.03.034. [DOI] [PubMed] [Google Scholar]
- 25.Del Giudice M.M., Marseglia A., Leonardi S., La Rosa M., Salpietro C., Brunese F., et al. Allergic rhinitis and quality of life in children. Int J Immunopathol Pharmacol. 2011;24:25–28. doi: 10.1177/03946320110240S406. [DOI] [PubMed] [Google Scholar]
- 26.Hwang T.Y., Kim S.K., Kim S.H., Kim M. A cross sectional survey on health-related quality of life among parents of children with allergic symptoms using the EQ-5D-5L. J Asthma. 2019;56:1239–1245. doi: 10.1080/02770903.2019.1571086. [DOI] [PubMed] [Google Scholar]
- 27.Price D., Scadding G., Ryan D., Bachert C., Canonica G.W., Mullol J., et al. The hidden burden of adult allergic rhinitis: UK healthcare resource utilisation survey. Clin Transl Allergy. 2015;5:39. doi: 10.1186/s13601-015-0083-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Bhattacharyya N. Incremental healthcare utilization and expenditures for allergic rhinitis in the United States: healthcare expenditures in allergic rhinitis. Laryngoscope. 2011;121:1830–1833. doi: 10.1002/lary.22034. [DOI] [PubMed] [Google Scholar]
- 29.Nathan R.A. The burden of allergic rhinitis. Allergy Asthma Proc. 2007;28:3–9. doi: 10.2500/aap.2007.28.2934. [DOI] [PubMed] [Google Scholar]
- 30.Ozdoganoglu T., Songu M. The burden of allergic rhinitis and asthma. Ther Adv Respir Dis. 2012;6:11–23. doi: 10.1177/1753465811431975. [DOI] [PubMed] [Google Scholar]
- 31.Romano M.R., James S., Farrington E., Perry R., Elliott L. The impact of perennial allergic rhinitis with/without allergic asthma on sleep, work and activity level. Allergy Asthma Clin Immunol. 2019;15:81. doi: 10.1186/s13223-019-0391-9. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Canonica G.W., Mullol J., Pradalier A., Didier A. Patient perceptions of allergic rhinitis and quality of Life. World Allergy Organ J. 2008;1:138–144. doi: 10.1097/WOX.0b013e3181865faf. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 33.Norstat About Norstatpanel and online surveys. https://www.norstatpanel.com/en/about-norstatpanel-and-online-surveys Available at:
- 34.Danish National Center for Ethics; Danish Research Ethics Committees Overview of mandatory reporting. https://researchethics.dk/information-for-researchers/overview-of-mandatory-reporting Available at:
- 35.Demoly P., Allaert F.A., Lecasble M., Bousquet J., Pragma Validation of the classification of ARIA (allergic rhinitis and its impact on asthma) Allergy. 2003;58:672–675. doi: 10.1034/j.1398-9995.2003.t01-1-00202.x. [DOI] [PubMed] [Google Scholar]
- 36.Demoly P., Broué-Chabbert A., Wessel F., Chartier A. Severity and disease control before house dust mite immunotherapy initiation: ANTARES, a French observational survey. Allergy Asthma Clin Immunol. 2016;12:13. doi: 10.1186/s13223-016-0119-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Frati F., Scurati S., Dell’Albani I., Puccinelli P., Incorvaia C., Passalacqua G. Evaluation of house dust mite allergy in real life: patients’ characteristics and satisfaction with treatment. Eur Ann Allergy Clin Immunol. 2014;46:17–21. [PubMed] [Google Scholar]
- 38.Trebuchon F., Lhéritier-Barrand M., David M., Demoly P. Characteristics and management of sublingual allergen immunotherapy in children with allergic rhinitis and asthma induced by house dust mite allergens. Clin Transl Allergy. 2014;4:15. doi: 10.1186/2045-7022-4-15. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Ünal D. Effects of perennial allergen immunotherapy in allergic rhinitis in patients with/without asthma: a randomized controlled real-life study. Int Arch Allergy Immunol. 2020;181:141–148. doi: 10.1159/000504916. [DOI] [PubMed] [Google Scholar]
- 40.Kaya Akca Ü., Maslak İ.C., Uygun D., Bingöl A. The asthma risk is increased in children with severe allergic rhinitis. Turk Arch Pediatr. 2022;57:391–397. doi: 10.5152/TurkArchPediatr.2022.21269. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Bousquet J., Khaltaev N., Cruz A.A., Denburg J., Fokkens W.J., Togias A., et al. Allergic rhinitis and its impact on asthma (ARIA) 2008. Allergy. 2008;63:8–160. doi: 10.1111/j.1398-9995.2007.01620.x. [DOI] [PubMed] [Google Scholar]
- 42.Cox L., Nelson H., Lockey R., Calabria C., Chacko T., Finegold I., et al. Allergen immunotherapy: a practice parameter third update. J Allergy Clin Immunol. 2011;127:S1–S55. doi: 10.1016/j.jaci.2010.09.034. [DOI] [PubMed] [Google Scholar]
- 43.Canonica W., Durham S.R. World Allergy Organization; Milwaukee (Wis): 2016. Allergen immunotherapy for allergic rhinitis and asthma: a synopsis. [Google Scholar]
- 44.Virchow J.C., Backer V., Kuna P., Prieto L., Nolte H., Villesen H.H., et al. Efficacy of a house dust mite sublingual allergen immunotherapy tablet in adults with allergic asthma: a randomized clinical trial. JAMA. 2016;315:1715–1725. doi: 10.1001/jama.2016.3964. [DOI] [PubMed] [Google Scholar]
- 45.Mosbech H., Deckelmann R., de Blay F., Pastorello E.A., Trebas-Pietras E., Andres L.P., et al. Standardized quality (SQ) house dust mite sublingual immunotherapy tablet (ALK) reduces inhaled corticosteroid use while maintaining asthma control: a randomized, double-blind, placebo-controlled trial. J Allergy Clin Immunol. 2014;134:568–575.e7. doi: 10.1016/j.jaci.2014.03.019. [DOI] [PubMed] [Google Scholar]
- 46.Bernstein D.I., Kleine-Tebbe J., Nelson H.S., Bardelas J.A., Sussman G.L., Lu S., et al. SQ house dust mite sublingual immunotherapy tablet subgroup efficacy and local application site reaction duration. Ann Allergy Asthma Immunol. 2018;121:105–110. doi: 10.1016/j.anai.2018.04.007. [DOI] [PubMed] [Google Scholar]
- 47.De Filippo M., Votto M., Caminiti L., Panasiti I., Carella F., De Castro G., et al. Safety of allergen-specific immunotherapy in children. Pediatr Allergy Immunol. 2022;33:27–30. doi: 10.1111/pai.13622. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Horn A., Bernstein D.I., Okubo K., Dalgaard T., Hels O., Sørensen H.F., et al. House dust mite sublingual immunotherapy tablet safety in adolescents with allergic rhinoconjunctivitis: worldwide clinical trial results. Ann Allergy Asthma Immunol. 2023;130:797–804.e2. doi: 10.1016/j.anai.2023.03.006. [DOI] [PubMed] [Google Scholar]
- 49.EU Clinical Trials Register House dust mite allergy trial in children (MATIC) https://www.clinicaltrialsregister.eu/ctr-search/trial/2019-000560-22/SK
- 50.Varni J.W., Limbers C.A., Burwinkle T.M. Parent proxy-report of their children’s health-related quality of life: an analysis of 13,878 parents’ reliability and validity across age subgroups using the PedsQLTM 4.0 Generic Core Scales. Health Qual Life Outcomes. 2007;5:2. doi: 10.1186/1477-7525-5-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.



