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2.
J Pediatr ; 195: 182-189.e2, 2018 04.
Article in English | MEDLINE | ID: mdl-29397158

ABSTRACT

OBJECTIVES: To study whether the duration of breastfeeding and time for introduction of complementary foods was associated with the risk of childhood asthma. STUDY DESIGN: We used data from the Norwegian Mother and Child Study, a nationwide prospective cohort study that recruited pregnant women from across Norway between 1999 and 2008. Children with complete data of breastfeeding up to 18 months and current age >7 years were eligible (n = 41 020). Asthma as the primary outcome was defined based on ≥2 dispensed asthma medications at age 7 years registered in the Norwegian Prescription Database. We used log-binomial regression models to obtain crude relative risks (RRs) in the main analysis, and adjusted for selected confounders in multivariable analyses. RESULTS: For duration of any breastfeeding, 5.9% of infants breastfed <6 months (adjusted RR [aRR] 1.05, 0.93-1.19) and 4.6% breastfed 6-11 months (aRR 0.96, 0.87-1.07) had dispensed asthma medications at age 7 years compared with 4.6% of infants breastfed ≥12 months (Ptrend .62). Infants still breastfed at 6 months, but introduced to complementary foods <4 months and 4-6 months, had an aRR of 1.15 (0.98-1.36) and 1.09 (0.94-1.27) respectively, compared with infants fully breastfed for 6 months (Ptrend .09). Ages at introduction of solids or formula separately were not significant predictors (Ptrend .16 and .08, respectively). CONCLUSIONS: We found no association between duration of breastfeeding or age of introduction to complementary foods and asthma at age 7 years.


Subject(s)
Asthma/etiology , Breast Feeding , Asthma/prevention & control , Child , Child, Preschool , Female , Follow-Up Studies , Humans , Infant , Infant Nutritional Physiological Phenomena , Infant, Newborn , Male , Prospective Studies , Protective Factors , Regression Analysis , Risk Factors , Time Factors
3.
N Engl J Med ; 368(24): 2286-93, 2013 Jun 13.
Article in English | MEDLINE | ID: mdl-23758233

ABSTRACT

BACKGROUND: Acute bronchiolitis in infants frequently results in hospitalization, but there is no established consensus on inhalation therapy--either the type of medication or the frequency of administration--that may be of value. We aimed to assess the effectiveness of inhaled racemic adrenaline as compared with inhaled saline and the strategy for frequency of inhalation (on demand vs. fixed schedule) in infants hospitalized with acute bronchiolitis. METHODS: In this eight-center, randomized, double-blind trial with a 2-by-2 factorial design, we compared inhaled racemic adrenaline with inhaled saline and on-demand inhalation with fixed-schedule inhalation (up to every 2 hours) in infants (<12 months of age) with moderate-to-severe acute bronchiolitis. An overall clinical score of 4 or higher (on a scale of 0 to 10, with higher scores indicating more severe illness) was required for study inclusion. Any use of oxygen therapy, nasogastric-tube feeding, or ventilatory support was recorded. The primary outcome was the length of the hospital stay, with analyses conducted according to the intention-to-treat principle. RESULTS: The mean age of the 404 infants included in the study was 4.2 months, and 59.4% were boys. Length of stay, use of oxygen supplementation, nasogastric-tube feeding, ventilatory support, and relative improvement in the clinical score from baseline (preinhalation) were similar in the infants treated with inhaled racemic adrenaline and those treated with inhaled saline (P>0.1 for all comparisons). On-demand inhalation, as compared with fixed-schedule inhalation, was associated with a significantly shorter estimated mean length of stay--47.6 hours (95% confidence interval [CI], 30.6 to 64.6) versus 61.3 hours (95% CI, 45.4 to 77.2; P=0.01) - as well as less use of oxygen supplementation (in 38.3% of infants vs. 48.7%, P=0.04), less use of ventilatory support (in 4.0% vs. 10.8%, P=0.01), and fewer inhalation treatments (12.0 vs. 17.0, P<0.001). CONCLUSIONS: In the treatment of acute bronchiolitis in infants, inhaled racemic adrenaline is not more effective than inhaled saline. However, the strategy of inhalation on demand appears to be superior to that of inhalation on a fixed schedule. (Funded by Medicines for Children; ClinicalTrials.gov number, NCT00817466; EudraCT number, 2009-012667-34.).


Subject(s)
Bronchiolitis/drug therapy , Epinephrine/administration & dosage , Racepinephrine , Sodium Chloride/administration & dosage , Acute Disease , Administration, Inhalation , Age Factors , Bronchiolitis/therapy , Combined Modality Therapy , Double-Blind Method , Drug Administration Schedule , Female , Humans , Hypersensitivity/complications , Infant , Isomerism , Kaplan-Meier Estimate , Length of Stay , Male , Oxygen Inhalation Therapy , Respiration, Artificial , Sex Factors
4.
Pediatr Allergy Immunol ; 21(6): 945-53, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20718926

ABSTRACT

Assessment of childhood asthma severity and asthma control encompasses heterogeneous clinical presentations. The relationship between patterns of asthma symptoms and objective measurements is poorly defined in paediatric asthma. This study includes 115 asthmatic schoolchildren, of which 31 were at inclusion defined as Problematic severe asthma because of inadequate asthma control in the presence of high-dose inhaled corticosteroid (HD-ICS) treatment and at least one other asthma controller drug. Two partially overlapping clinical outcomes were defined irrespective of severity classification (Exacerbations and Chronic persistent asthma) in patients with uncontrolled asthma. The same symptom criteria were used as for Problematic severe asthma, but disregarding current medication. Lung function, exhaled nitric oxide (FE(NO)), bronchial hyperresponsiveness, allergic sensitization and Quality of life (QoL) in the symptom subgroups were compared to children with well-controlled asthma. Multifactor analysis was performed to assess the relative explanatory power of clinical asthma presentations and of HD-ICS treatment on objective measurements. Whereas children included in the Exacerbations subgroup had objective features similar to patients with well-controlled asthma, the Chronic persistent asthma subgroup demonstrated significantly reduced lung function, increased immunoglobin E, allergic poly-sensitization and impaired QoL, similar to that in patients pre-defined as Problematic severe asthma. The presence of chronic asthma symptoms was a significant explanatory factor for reduced lung function, QoL and increased FE(NO) in multifactor analysis. Differences in objective measurements suggest that children with Chronic persistent asthma and those who are symptomatic predominantly during exacerbations may represent distinct phenotypes of childhood asthma with different clinical prognoses.


Subject(s)
Asthma/diagnosis , Asthma/physiopathology , Adolescent , Bronchial Hyperreactivity , Child , Chronic Disease , Disease Progression , Female , Humans , Male , Prognosis , Severity of Illness Index , Spirometry
5.
Tidsskr Nor Laegeforen ; 127(21): 2806-9, 2007 Nov 01.
Article in Norwegian | MEDLINE | ID: mdl-17987071

ABSTRACT

BACKGROUND: A growing number of extremely preterm neonates survive; a high percentage develop chronic lung disease/bronchopulmonal dysplasia. The short-term effect of glucocorticoids in prevention or treatment is beneficial, but short- and long-term side effects are of concern. METHODS: Based on non-systematic searches in the Medline and Cochrane databases, this article provides an overview of beneficial and detrimental effects (emphasis on long-term side effects) of glucocorticoids in the neonatal period. RESULTS AND INTERPRETATION: Steroids have a beneficial short-term effect on bronchopulmonal dysplasia, with reduced duration of ventilator treatment and decreased needs for oxygen supplementation at 36 weeks gestational age (odds ratio 0.62-0.76). However, survival at 40 weeks is not improved due to severe side effects. Long-term effects on neurodevelopmental outcome show a significant increase in the risk for cerebral palsy (odds ratio 1.69) and a significant increase in the risk for abnormal neurological development and cognitive impairment of equal size. No significant effects on lung function, growth and metabolic outcome later in childhood have been proven so far. Given that glucocorticoids do not increase survival of neonates, their serious side effects indicate that they should only be considered with severe ventilator-dependent lung disease after 2-3 weeks.


Subject(s)
Bronchopulmonary Dysplasia/drug therapy , Glucocorticoids/administration & dosage , Bronchopulmonary Dysplasia/prevention & control , Child Development/drug effects , Glucocorticoids/adverse effects , Humans , Infant Mortality , Infant, Newborn , Infant, Premature , Prognosis , Risk Factors
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