| Literature DB >> 34935084 |
Catalina Gómez1, Judit Barrena2, Vanesa García-Paz3, Ana M Plaza4, Paula Crespo5, José A Bejarano5, Ana B Rodríguez5, Laia Ferré1, Lidia Farrarons1, Marta Viñas2, Carla Torán-Barona6, Andrea Pereiro7, José L Justicia7, Santiago Nevot1.
Abstract
Evidence regarding asthma's impact on children's daily lives is limited. This prospective and cross-sectional, observational, multicenter study assessed school/work and activity impairment in children and adolescents with allergic asthma and their caregivers and allergen immunotherapy (AIT) effects. Included patients were schooled children and adolescents (5 to 17 years) with allergic asthma due to house dust mites (HDM). Impairment of school/work (i.e., absenteeism and presenteeism) and activity was measured in patients and their caregivers using the Work Productivity Impairment Questionnaire plus Classroom Impairment Questions: Allergy Specific (WPAI + CIQ:AS). HDM allergic patients with school impairment received subcutaneous AIT with a MicroCrystalline Tyrosine-associated allergoid. WPAI + CIQ:AS and effectiveness variables were compared between baseline and 1-year post-AIT. Of the 113 patients included, 59 (52.2%) and 51 (45.1%) showed school and activity impairment, respectively, missing a mean (SD) of 37.6 (24.4) % and 42.6 (25.6) % of school and activity time, respectively. Twenty-six (23%) caregivers reported activity impairment and, of the 79 (69.9%) employed, 30 (38%) reported work impairment. Of the 65 patients with school/activities impairment, 41 (63.1%) received AIT, of which 21 (51.2%) completed 1 year of treatment. Effectiveness variables and WPAI + CIQ:AS significantly improved: Mean (SD) school impairment decreased from 39.7 (26.7) to 2.1 (7.1) % (p < 0.001) and activity impairment from 46.2 (34.6) to 1.4 (3.6) % (p < 0.001).Entities:
Keywords: Absenteeism; Allergic asthma; Microcrystalline tyrosine; School impairment; Subcutaneous allergen immunotherapy; Work impairment
Mesh:
Year: 2021 PMID: 34935084 PMCID: PMC8691866 DOI: 10.1007/s00431-021-04346-y
Source DB: PubMed Journal: Eur J Pediatr ISSN: 0340-6199 Impact factor: 3.183
Demographic, clinical, and treatment characteristics of study patients, n (%) N = 113
| Age, years | |
| Children (5–11) | 76 (67.3) |
| Adolescents (12–17) | 37 (32.7) |
| Sex | |
| Male | 75 (66.4) |
| Female | 37 (33.6) |
| Studies | |
| Primary school | 77 (68.1) |
| Secondary school | 36 (31.9) |
| Asthma severity (GEMA) | |
| Intermittent | 50 (44.2) |
| Mild persistent | 28 (24.8) |
| Moderate persistent | 32 (28.3) |
| Unknown | 3 (2.7) |
| Asthma control | |
| Complete | 32 (28.3) |
| Good | 51 (45.1) |
| Partial | 26 (23.0) |
| Bad | 1 (0.9) |
| Unknown | 3 (2.7) |
| Allergic comorbidities | |
| Rhinitis | 98 (87.6) |
| Conjunctivitis | 27 (23.9) |
| Atopic dermatitis | 34 (30.1) |
| Food allergy | 9 (8.0) |
| Sensitizations to aeroallergens | |
| 113 (100) | |
| Other mites | 43 (38.1) |
| Pollens | 33 (29.2) |
| 4 (3.5) | |
| Asthma medication | |
| Short-acting beta-agonists | 62 (54.9) |
| Inhaled corticosteroids | 45 (39.8) |
| Long-acting beta-agonists | 20 (17.7) |
| Leukotriene receptor antagonists | 17 (15) |
| Oral corticosteroids | 2 (1.8) |
Abbreviations: GEMA, Guía Española del Manejo del Asthma (Spanish guideline on the management of asthma)
Demographic characteristics of caregivers, n (%) N = 113
| Sex | |
|---|---|
| Male | 24 (21.2) |
| Female | 86 (76.1) |
| Unknown | 3 (2.7) |
| Relationship | |
| Parent | 105 (92.9) |
| Legal tutor | 1 (0.9) |
| Grandparent | 1 (0.9) |
| Other | 4 (3.5) |
| Unknown | 2 (1.8) |
| Employment status | |
| Employed | 79 (69.9) |
| Unemployed | 27 (23.9) |
| Retired | 2 (1.8) |
| Other | 2 (1.8) |
| Unknown | 3 (2.7) |
Patients’ school impairment, caregivers’ work impairment, and patients’ and caregivers’ routine activities impairment due to allergic disease
| With time missed (absenteeism), | 30 (26.5) |
| With classroom impairment (presenteeism), | 54 (47.8) |
| Overall impairment (absenteeism plus presenteeism), | 59 (52.2) |
| With activity impairment, | 51 (45.1) |
| % of impairment, | |
| % of classroom time missed (absenteeism), | 16.1 (12.8) |
| % of classroom impairment (presenteeism), | 36.5 (22.7) |
| % of overall impairment (absenteeism plus presenteeism), | 37.6 (24.4) |
| % of activity impairment, | 42.6 (25.6) |
| With time missed (absenteeism), | 24 (30.4) |
| With while working impairment (presenteeism), | 25 (31.6) |
| Overall impairment (absenteeism plus presenteeism), | 30 (38.0) |
| Caregivers with activity impairment, | 26 (23.0) |
| % of impairment, | |
| % of work time missed (absenteeism), | 11.4 (9.4) |
| % of while working impairment (presenteeism), | 40.8 (27.4) |
| % of overall impairment (absenteeism plus presenteeism), | 38.9 (29.4) |
| % of activity impairment, | 32.7 (23.2) |
SD, standard deviation
aNumber of employed caregivers
bPatients/caregivers with the corresponding impairments
Fig. 1School time missed, classroom impairment, overall impairment, and activity impairment in patients who received allergen immunotherapy with a MicroCrystalline Tyrosine-associated house dust mite allergoid and attended the final visit at the indicated timepoints. Columns and error bars represent mean percentages and standard deviation, respectively. p-values were calculated using the Wilcoxon test
Fig. 2Asthma severity (A) and control (B) at visit 1 and after 1 year (final visit) of treatment with allergen immunotherapy with a microcrystalline tyrosine-adsorbed house dust mite allergoid. McNemar test, p = 0.021 (A) and p = 0.001 (B)
Fig. 3Use of medication to treat asthma before and after 1 year of treatment with allergen immunotherapy with a MicroCrystalline Tyrosine-associated house dust mite allergoid. LABAs, long-acting beta-2 agonists; LTRAs, leukotriene receptor antagonists; ns, not significant; SABAs, short-acting beta-2 agonists. p-values were calculated using the McNemar test