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Tiotropium as an add‑on treatment to inhaled corticosteroids in children with severe and mild symptomatic asthma: Multi‑center observational study for efficacy and safety analysis

Children aged 6-11 years with uncontrolled asthma are treated with low-dose inhaled corticosteroid (ICS) with stepwise increase in ICS dosage and/or add-on maintenance treatment, as necessary. The objective of the present study was to evaluate the efficacy and safety of tiotropium add-on treatment i...

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Published in:Experimental and therapeutic medicine 2022-09, Vol.24 (3), Article 577
Main Authors: Aierken, Aibibai, Fu, Bu Wei Mai Erye Mu Yu Su, Xu, Peiru
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description Children aged 6-11 years with uncontrolled asthma are treated with low-dose inhaled corticosteroid (ICS) with stepwise increase in ICS dosage and/or add-on maintenance treatment, as necessary. The objective of the present study was to evaluate the efficacy and safety of tiotropium add-on treatment in children with severe and mild symptomatic asthma. The present prospective cohort study included 144 children with severe and mild asthma (age, 6-11 years) who received ICS (budesonide) with [greater than or equal to] 1 controller treatment combination therapies for [greater than or equal to] 1 month and score [greater than or equal to] 1.5 based on Asthma Control Questionnaire-Interviewer-Administered. In addition to ICS with [greater than or equal to] 1 controller treatment, children received 5 [micro]g once-daily tiotropium (treatment group; n=72) or did not receive tiotropium (control group; n=72). The peak forced expiratory volume in 1-sec change from the baseline 3 h post-administration of tiotropium was significantly improved in the treatment group compared with the control group (384 [+ or -] 31 vs. 248 [+ or -] 28 ml; P
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The objective of the present study was to evaluate the efficacy and safety of tiotropium add-on treatment in children with severe and mild symptomatic asthma. The present prospective cohort study included 144 children with severe and mild asthma (age, 6-11 years) who received ICS (budesonide) with [greater than or equal to] 1 controller treatment combination therapies for [greater than or equal to] 1 month and score [greater than or equal to] 1.5 based on Asthma Control Questionnaire-Interviewer-Administered. In addition to ICS with [greater than or equal to] 1 controller treatment, children received 5 [micro]g once-daily tiotropium (treatment group; n=72) or did not receive tiotropium (control group; n=72). The peak forced expiratory volume in 1-sec change from the baseline 3 h post-administration of tiotropium was significantly improved in the treatment group compared with the control group (384 [+ or -] 31 vs. 248 [+ or -] 28 ml; P<0.0001). The trough forced expiratory volume in 1-sec (224 [+ or -] 28 vs. 140 [+ or -] 31 ml; P<0.0001) and forced expiratory flow at 25-75% of forced vital capacity (389 [+ or -] 36 vs. 116 [+ or -] 27 ml/sec; P<0.0001) showed significant improvement following treatment with tiotropium. Significant differences were noted for trough forced vital capacity (153 [+ or -] 29 vs. 139 [+ or -] 30 ml/sec; P<0.0001), mean weekly rescue treatment usage (0.29 [+ or -] 0.08 vs. 0.36 [+ or -] 0.09; P<0.0001), mean weekly peak expiratory flow measurement (4.12 [+ or -] 3.56 vs. 7.46 [+ or -] 3.29 l/min; P<0.0001) and mean weekly symptom-free time (0.19 [+ or -] 0.04 vs. 0.16 [+ or -] 0.04 days; P<0.0001) between both cohorts. Children of both groups tolerated any adverse effects. Tiotropium 5 [micro]g administered once/day as an add-on treatment to ICS with [greater than or equal to] 1 controller treatments in children (6-11 years of age) with severe and mild symptomatic asthma was found to be efficacious and safe (level of evidence 2; technical efficacy stage 4). Abbreviations: ICS, inhaled corticosteroid; LABA, long-acting [beta]-agonist; LTRA, leukotriene receptor antagonist; ACQ-IA, Asthma Control Questionnaire-Interviewer-Administered; FEV, forced expiratory volume; FVC, forced vital capacity; PEF, peak expiratory flow; FEF, forced expiratory flow; df, degree of freedom Key words: add-on treatment, anticholinergic drug, inhaled corticosteroid, lung function, pediatric asthma, tiotropium]]></description><identifier>ISSN: 1792-0981</identifier><identifier>EISSN: 1792-1015</identifier><identifier>DOI: 10.3892/etm.2022.11514</identifier><identifier>PMID: 35949336</identifier><language>eng</language><publisher>Athens: Spandidos Publications</publisher><subject>Asthma ; Asthma in children ; Chronic illnesses ; Corticosteroids ; Dosage and administration ; Drug therapy ; Drug therapy, Combination ; Immunomodulators ; Observational studies ; Pediatric research ; Pediatrics ; Respiratory system ; Statistical analysis ; Steroids ; Testing ; Tiotropium</subject><ispartof>Experimental and therapeutic medicine, 2022-09, Vol.24 (3), Article 577</ispartof><rights>COPYRIGHT 2022 Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2022</rights><rights>Copyright © 2020, Spandidos Publications 2020</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c392t-5bcd522674624a5d20ad048237b1f0a3a95772f1182884e0c0840eb0732b84a13</citedby><cites>FETCH-LOGICAL-c392t-5bcd522674624a5d20ad048237b1f0a3a95772f1182884e0c0840eb0732b84a13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353548/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353548/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids></links><search><creatorcontrib>Aierken, Aibibai</creatorcontrib><creatorcontrib>Fu, Bu Wei Mai Erye Mu Yu Su</creatorcontrib><creatorcontrib>Xu, Peiru</creatorcontrib><title>Tiotropium as an add‑on treatment to inhaled corticosteroids in children with severe and mild symptomatic asthma: Multi‑center observational study for efficacy and safety analysis</title><title>Experimental and therapeutic medicine</title><description><![CDATA[Children aged 6-11 years with uncontrolled asthma are treated with low-dose inhaled corticosteroid (ICS) with stepwise increase in ICS dosage and/or add-on maintenance treatment, as necessary. The objective of the present study was to evaluate the efficacy and safety of tiotropium add-on treatment in children with severe and mild symptomatic asthma. The present prospective cohort study included 144 children with severe and mild asthma (age, 6-11 years) who received ICS (budesonide) with [greater than or equal to] 1 controller treatment combination therapies for [greater than or equal to] 1 month and score [greater than or equal to] 1.5 based on Asthma Control Questionnaire-Interviewer-Administered. In addition to ICS with [greater than or equal to] 1 controller treatment, children received 5 [micro]g once-daily tiotropium (treatment group; n=72) or did not receive tiotropium (control group; n=72). The peak forced expiratory volume in 1-sec change from the baseline 3 h post-administration of tiotropium was significantly improved in the treatment group compared with the control group (384 [+ or -] 31 vs. 248 [+ or -] 28 ml; P<0.0001). The trough forced expiratory volume in 1-sec (224 [+ or -] 28 vs. 140 [+ or -] 31 ml; P<0.0001) and forced expiratory flow at 25-75% of forced vital capacity (389 [+ or -] 36 vs. 116 [+ or -] 27 ml/sec; P<0.0001) showed significant improvement following treatment with tiotropium. Significant differences were noted for trough forced vital capacity (153 [+ or -] 29 vs. 139 [+ or -] 30 ml/sec; P<0.0001), mean weekly rescue treatment usage (0.29 [+ or -] 0.08 vs. 0.36 [+ or -] 0.09; P<0.0001), mean weekly peak expiratory flow measurement (4.12 [+ or -] 3.56 vs. 7.46 [+ or -] 3.29 l/min; P<0.0001) and mean weekly symptom-free time (0.19 [+ or -] 0.04 vs. 0.16 [+ or -] 0.04 days; P<0.0001) between both cohorts. Children of both groups tolerated any adverse effects. Tiotropium 5 [micro]g administered once/day as an add-on treatment to ICS with [greater than or equal to] 1 controller treatments in children (6-11 years of age) with severe and mild symptomatic asthma was found to be efficacious and safe (level of evidence 2; technical efficacy stage 4). 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The objective of the present study was to evaluate the efficacy and safety of tiotropium add-on treatment in children with severe and mild symptomatic asthma. The present prospective cohort study included 144 children with severe and mild asthma (age, 6-11 years) who received ICS (budesonide) with [greater than or equal to] 1 controller treatment combination therapies for [greater than or equal to] 1 month and score [greater than or equal to] 1.5 based on Asthma Control Questionnaire-Interviewer-Administered. In addition to ICS with [greater than or equal to] 1 controller treatment, children received 5 [micro]g once-daily tiotropium (treatment group; n=72) or did not receive tiotropium (control group; n=72). The peak forced expiratory volume in 1-sec change from the baseline 3 h post-administration of tiotropium was significantly improved in the treatment group compared with the control group (384 [+ or -] 31 vs. 248 [+ or -] 28 ml; P<0.0001). The trough forced expiratory volume in 1-sec (224 [+ or -] 28 vs. 140 [+ or -] 31 ml; P<0.0001) and forced expiratory flow at 25-75% of forced vital capacity (389 [+ or -] 36 vs. 116 [+ or -] 27 ml/sec; P<0.0001) showed significant improvement following treatment with tiotropium. Significant differences were noted for trough forced vital capacity (153 [+ or -] 29 vs. 139 [+ or -] 30 ml/sec; P<0.0001), mean weekly rescue treatment usage (0.29 [+ or -] 0.08 vs. 0.36 [+ or -] 0.09; P<0.0001), mean weekly peak expiratory flow measurement (4.12 [+ or -] 3.56 vs. 7.46 [+ or -] 3.29 l/min; P<0.0001) and mean weekly symptom-free time (0.19 [+ or -] 0.04 vs. 0.16 [+ or -] 0.04 days; P<0.0001) between both cohorts. Children of both groups tolerated any adverse effects. Tiotropium 5 [micro]g administered once/day as an add-on treatment to ICS with [greater than or equal to] 1 controller treatments in children (6-11 years of age) with severe and mild symptomatic asthma was found to be efficacious and safe (level of evidence 2; technical efficacy stage 4). Abbreviations: ICS, inhaled corticosteroid; LABA, long-acting [beta]-agonist; LTRA, leukotriene receptor antagonist; ACQ-IA, Asthma Control Questionnaire-Interviewer-Administered; FEV, forced expiratory volume; FVC, forced vital capacity; PEF, peak expiratory flow; FEF, forced expiratory flow; df, degree of freedom Key words: add-on treatment, anticholinergic drug, inhaled corticosteroid, lung function, pediatric asthma, tiotropium]]></abstract><cop>Athens</cop><pub>Spandidos Publications</pub><pmid>35949336</pmid><doi>10.3892/etm.2022.11514</doi><oa>free_for_read</oa></addata></record>
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ispartof Experimental and therapeutic medicine, 2022-09, Vol.24 (3), Article 577
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1792-1015
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9353548
source PubMed Central
subjects Asthma
Asthma in children
Chronic illnesses
Corticosteroids
Dosage and administration
Drug therapy
Drug therapy, Combination
Immunomodulators
Observational studies
Pediatric research
Pediatrics
Respiratory system
Statistical analysis
Steroids
Testing
Tiotropium
title Tiotropium as an add‑on treatment to inhaled corticosteroids in children with severe and mild symptomatic asthma: Multi‑center observational study for efficacy and safety analysis
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