Примери за използване на Asthma exacerbations на Английски и техните преводи на Български
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Asthma exacerbations should receive treatment using an inhaler.
Omalizumab reduced the rate of asthma exacerbations by 19%(p= 0.153).
Asthma exacerbations in the past requiring medical intervention.
Xolair is not indicated for the treatment of acute asthma exacerbations, acute bronchospasm or status asthmaticus.
The rate of asthma exacerbations requiring treatment with bursts of systemic corticosteroids was the primary endpoint.
The primary efficacymeasure for both Studies I and II was the frequency of asthma exacerbations for each patient during the 52-week treatment period.
No treatment effect on asthma exacerbations was observed for this age group(asthma exacerbation rate ratio[reslizumab/placebo] of 2.09).
BiResp Spiromax contains formoterol and budesonide,which have different modes of action and show additive effects in terms of reduction of asthma exacerbations.
Efficacy with respect to severe asthma exacerbations and lung function was observed in both adolescents and adults.
Budesonide/Formoterol Teva Pharma B.V. contains formoterol and budesonide,which have different modes of action and show additive effects in terms of reduction of asthma exacerbations.
The rate of severe asthma exacerbations per patient per year was 0.19 in the FF 92 group(approximately 1 in every 5 years) and 0.14 in the fluticasone furoate/vilanterol.
Budesonide is a glucocorticosteroid which when inhaled has a dose-dependent anti-inflammatory action in the airways,resulting in reduced symptoms and fewer asthma exacerbations.
The primary endpoint was the annual rate of clinically significant asthma exacerbations in patients with baseline blood eosinophil counts≥300 cells/μL who were taking high-dose ICS and LABA.
In the overall population in DRI12544 and QUEST subjects receiving either dupilumab 200 mg or300 mg every other week had significant reductions in the rate of severe asthma exacerbations compared to placebo.
The aim of the MART approach is to reduce the rate of asthma exacerbations by“early intervention”, i.e. by giving additional doses of ICS plus FF in response to an increase in symptoms(2011 GINA Guidelines1).
The ability of these medications to reduce the production andsurvival of eosinophils improves the control of asthma exacerbations, increases FEV1, and improves patients' quality of life.
Eligible patients had experienced multiple asthma exacerbations requiring systemic corticosteroid treatment or had been hospitalised or attended an emergency room due to a severe asthma exacerbation in the past year despite continuous treatment with high-dose inhaled corticosteroids and a long-acting beta2-agonist.
Patients with severe refractory eosinophilic asthma Reslizumab produced significant reductions in asthma exacerbations relative to placebo in the refractory population(59%) and non-refractory population(49%).
In the specific subgroup of patients on high dose inhaled corticosteroids,the omalizumab group had a statistically significantly lower rate of clinically significant asthma exacerbations than the placebo group.
In the study of patients with severe allergic asthma, there was no difference in the number of asthma exacerbations between Xolair and placebo, but Xolair led to a similar reduction in the number of exacerbations as in previous studies.
Xolair is indicated as add-on therapy to improve asthma control in patients with severe persistent allergic asthma who have a positive skin test or in vitro reactivity to a perennial aeroallergen and frequent daytime symptoms ornight-time awakenings and who have had multiple documented severe asthma exacerbations despite daily high-dose inhaled corticosteroids, plus a long-acting inhaled beta2agonist.
In the study of patients with severe allergic asthma, although there was no difference in the rate of asthma exacerbations between Xolair- and placebo-treated patients, Xolair led to a reduction in the number of exacerbations that was consistent with previous studies.
Xolair is indicated as add-on therapy to improve asthma control in patients with severe persistent allergic asthma who have a positive skin test or in vitro reactivity to a perennial aeroallergen and who have reduced lung function(FEV1< 80%) as well as frequent daytime symptoms ornight-time awakenings and who have had multiple documented severe asthma exacerbations despite daily highdose inhaled corticosteroids, plus a long-acting inhaled beta2-agonist.
Comparable efficacy in controlling asthma was demonstrated by the two treatments at study end in terms of pulmonary function tests, asthma exacerbations, symptoms and the use of rescue salbutamol(Terzano et al., 2003).
Xolair is indicated as add-on therapy to improve asthma control in adult and adolescent patients( 12 years of age and above) with severe persistent allergic asthma who have a positive skin test or in vitro reactivity to a perennial aeroallergen and who have reduced lung function( FEV1< 80%) as well as frequent daytime symptoms ornight-time awakenings and who have had multiple documented severe asthma exacerbations despite daily high-dose inhaled corticosteroids, plus a long-acting inhaled beta2-agonist.
In the subset of patients requiring courses of OCS treatment for management of their asthma exacerbation, reslizumab was shown to reduce the frequency of asthma exacerbations by 56%(p< 0.0001) and 60%(p< 0.0001) in Study I and Study II, respectively.
In a study(D153-P515) of children 6 to 17 years of age with asthma(seasonal T/LAIV: n=1,114, seasonal injectable influenza vaccine: n=1,115),there were no significant differences between treatment groups in the incidence of asthma exacerbations, mean peak expiratory flow rate,asthma symptom scores, or night-time awakening scores.
Asthma exacerbation.
If this fact is ignored, asthma exacerbation may occur, which will provoke pneumonia.
Hospitalized, usually either children or people with asthma exacerbation.