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Preliminary data in a randomly selected pediatric cohort study in 8-year-olds suggested a rate of positivity to a methacholine challenge test that was unexpectedly high, roughly 30%. The current recommendation for a negative methacholine test is a 20% decrease in the forced expiratory volume in one second at a dose greater than 400 μg. This was derived from studies in adults using the obsolete English Wright nebulizer. One explanation for the high incidence of positivity in the study in 8-year-olds could be that children deposit more methacholine on a μg/kg basis than adults, due to differences in their breathing patterns. The purpose of this study was to determine if pediatric breathing patterns could result in a higher dose of methacholine depositing in the lungs of children based on μg/kg body weight compared with adults. An AeroEclipse Breath Actuated nebulizer delivered methacholine aerosol, generated from a 16 mg/mL solution, for one minute, using age-appropriate breathing patterns for a 70 kg adult and a 30 and 50 kg child produced by a breathing simulator. Predicted lung deposition was calculated from the collected dose of methacholine on a filter placed at the nebulizer outport, multiplied by the fraction of the aerosol mass contained in particles ≤5 μm. The dose of methacholine on the inspiratory filter was assayed by high performance liquid chromatography (HPLC). Particle size was measured using laser diffraction technology. The mean (95% confidence intervals) predicted pulmonary dose of methacholine was 46.1 (45.4, 46.8), 48.6 (45.3, 51.9), and 36.1 (34.2, 37.9) μg/kg body weight for the 30 kg child, 50 kg child, and 70 kg adult, respectively. On a μg/kg body weight, the predicted pulmonary dose of methacholine was greater with the pediatric breathing patterns than with the adult pattern.
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http://dx.doi.org/10.1089/jamp.2024.0012 | DOI Listing |
Eur Clin Respir J
August 2025
Department of Clinical Physiology and Nuclear Medicine, Copenhagen University Hospital, Rigshospitalet, Copenhagen, Denmark.
Unlabelled: Methacholine bronchial provocation (BMP) is a valuable tool in supporting the diagnosis of asthma, but the BMP must be validated regarding dosing, since the BMP basically is a dose response study. Historically, the dose delivered by a nebulizer has been calibrated gravimetrically, by weighing the nebulizer before and after dosing. However, this method is no longer recommended, since it has been recognized that a large fraction of the weight loss was due to evaporation.
View Article and Find Full Text PDFLung
July 2025
Division of Immunology, Immunity to infection and Respiratory Medicine, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester and Manchester University NHS Foundation Trust, Manchester, UK.
Background: The methacholine challenge requires a 20% fall in forced expiratory volume in one second (FEV). The fall is measured as litre (L) change from the pre-challenge (baseline) value. A higher baseline FEV requires a greater volume change to reach a 20% fall.
View Article and Find Full Text PDFEur Radiol
June 2025
PhyMedExp, INSERM U1046, CNRS, University of Montpellier, Montpellier, France.
Objectives: Severe airway hyper-responsiveness is associated with poor outcomes in asthma. Spatial heterogeneities in airway closures and subsequent air trapping (AT) during bronchoconstriction have been poorly assessed in asthma.
Materials And Methods: We assessed the spatial distribution of AT by acquiring expiratory lung CT at each dose of a methacholine challenge in 31 women with asthma.
PLoS One
June 2025
Sydney School of Veterinary Science, Faculty of Science, University of Sydney, Sydney, Australia.
Camel milk has demonstrated robust immunomodulatory and anti-inflammatory properties in various clinical and experimental studies. However, no previous studies have characterized the cellular immunological effects of camel milk in the context of allergic asthma. Therefore, the present work aimed to evaluate the protective effects of camel milk in house dust mite induced asthma in mice, which emulate human pulmonary inflammation.
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