Mannitol Challenge to Assess Therapy Response in Asthmatic Children: An Interventional Cohort Study

Bronchial provocation tests, such as the mannitol challenge, can be performed to identify and quantify the severity of bronchial hyperresponsiveness in asthmatic patients. Studies of the mannitol challenge as a monitoring tool in asthmatic children are limited. Our primary aim was to compare the bro...

Full description

Saved in:
Bibliographic Details
Main Authors: Nikolaos Karantaglis (Author), Fotios Kirvassilis (Author), Elpis Hatziagorou (Author), Antonios Gkantaras (Author), Kalliopi Kontouli (Author), John Tsanakas (Author), Maria Emporiadou (Author)
Format: Book
Published: MDPI AG, 2023-04-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

MARC

LEADER 00000 am a22000003u 4500
001 doaj_81fa043c9fcc49d0a2dda0d517e7b5d5
042 |a dc 
100 1 0 |a Nikolaos Karantaglis  |e author 
700 1 0 |a Fotios Kirvassilis  |e author 
700 1 0 |a Elpis Hatziagorou  |e author 
700 1 0 |a Antonios Gkantaras  |e author 
700 1 0 |a Kalliopi Kontouli  |e author 
700 1 0 |a John Tsanakas  |e author 
700 1 0 |a Maria Emporiadou  |e author 
245 0 0 |a Mannitol Challenge to Assess Therapy Response in Asthmatic Children: An Interventional Cohort Study 
260 |b MDPI AG,   |c 2023-04-01T00:00:00Z. 
500 |a 10.3390/children10050802 
500 |a 2227-9067 
520 |a Bronchial provocation tests, such as the mannitol challenge, can be performed to identify and quantify the severity of bronchial hyperresponsiveness in asthmatic patients. Studies of the mannitol challenge as a monitoring tool in asthmatic children are limited. Our primary aim was to compare the bronchial hyperresponsiveness to mannitol in treatment-naive asthmatic children between baseline and three months after receiving the indicated asthma prophylaxis. Twenty-three asthmatic patients aged 4-16 years were analyzed in this prospective cohort study. All subjects underwent the mannitol challenge at baseline and after three months of treatment with budesonide ± formoterol. The difference in the provocative dose of mannitol to induce a 15% drop in FEV<sub>1</sub> (PD<sub>15</sub>) between baseline and follow-up, as well as its association with the presence of exercise-induced or nocturnal asthma symptoms, were evaluated. The PD<sub>15</sub> value increased significantly post-treatment (228.5 mg [4.50-458.15]; <i>p</i> = 0.04). Independently of the evaluation time point, the PD<sub>15</sub> values were significantly lower in the presence of nocturnal asthma symptoms (490 mg [122-635] vs. 635 mg [635-635]; <i>p</i> = 0.03), whereas there was no association between the PD<sub>15</sub> value and the presence of exercise-induced asthma (<i>p</i> = 0.73). These results suggest that bronchial hyperresponsiveness to mannitol may be a potential monitoring tool in the pediatric asthmatic population, reflecting therapy response in children receiving prophylactic treatment. 
546 |a EN 
690 |a pediatric asthma 
690 |a mannitol challenge 
690 |a bronchial hyperresponsiveness 
690 |a bronchial provocation tests 
690 |a asthma prophylaxis 
690 |a Pediatrics 
690 |a RJ1-570 
655 7 |a article  |2 local 
786 0 |n Children, Vol 10, Iss 5, p 802 (2023) 
787 0 |n https://www.mdpi.com/2227-9067/10/5/802 
787 0 |n https://doaj.org/toc/2227-9067 
856 4 1 |u https://doaj.org/article/81fa043c9fcc49d0a2dda0d517e7b5d5  |z Connect to this object online.