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首页> 外文期刊>Expert opinion on drug delivery >An innovative corticosteroid/long-acting p2-agonist breath-triggered inhaler: facilitating lung delivery of fluticasone propionate/formoterol fumarate for the treatment of asthma
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An innovative corticosteroid/long-acting p2-agonist breath-triggered inhaler: facilitating lung delivery of fluticasone propionate/formoterol fumarate for the treatment of asthma

机译:一种创新的皮质类固醇/长效的P2激动剂呼吸触发吸入器:促进肺递送氟碳化丙酸盐/福莫特富马酸乳蛋白的治疗哮喘

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ABSTRACT Introduction: Incorrect inhaler technique is one reason why the efficacies of inhaled asthma treatments in clinical trials and effectiveness in the real world differ. Inhaler technique is critical for drug delivery to the lungs; incorrect technique negatively impacts asthma control and long-term outcomes. Breath-triggered inhalers (BTIs) can simplify drug administration and are suitable for most patients, including those with reduced inspiratory flow. Until recently, no inhaled corticosteroid/long-acting beta2-agonist combination BTI was available in Europe. The flutiform? (fluticasone propionate/formoterol fumarate [FP/FORM]) k-haler? is the first combination BTI now approved in Europe for asthma maintenance treatment. Areas covered: We review studies examining the challenges posed to patients by different inhaler types and explore evidence demonstrating the clinical efficacy of FP/FORM administered via a pressurized metered-dose inhaler. We also review the pharmacokinetic/pharmacodynamic studies supporting FP/ FORM k-haler use, and consider data showing high lung deposition with the device. Finally, we review patient experiences using the BTI, device characteristics, and health economic aspects. Expert opinion: Despite the availability of therapies, asthma control levels remain low, and there is a clear need for easy-to-use inhalers. Research to increase our understanding of critical errors with each inhaler and how to overcome them is important for improving care. Abbreviations: AUQ: area under the plasma concentration-time curve from the time of dosing to the last measurable concentration; BDP: beclometasone dipropionate; BTI: breath-triggered inhaler; BUD: budesonide; Cl: confidence interval; Cmax: maximum observed plasma concentration; DPI: dry powder inhaler; FDC: fixed-dose combination; FEV1: forced expiratory volume in 1 s; FORM: formoterol fumarate; FP: fluticasone propionate; HCP: health-care professional; ICS: inhaled corticosteroid; LABA: long-acting beta2-agonist; OR: odds ratio; PIL: patient information leaflet; pMDI: pressurized metered-dose inhaler; SAL: salmeterol xinafoate
机译:摘要介绍:吸入技术不正确是为什么吸入哮喘治疗在现实世界中的临床试验和有效性的疗效存在的一个原因。吸入器技术对于药物递送至肺部至关重要;技术不正确对哮喘控制和长期结果产生负面影响。呼吸触发的吸入器(BTIS)可以简化药物管理,适用于大多数患者,包括减少吸气流动的患者。直到最近,在欧洲可以使用吸入的皮质类固醇/长效β2-激动剂组合BTI。蓬蓬松? (氟丙酮丙酸酯/福莫特罗富马酸莫酸[FP / FORM])K-搅拌?是第一个组合BTI现在在欧洲批准的哮喘维护治疗。所涵盖的地区:我们审查了通过不同吸入器类型的挑战检查对患者提出的挑战,并探索证明通过加压计量吸入器给药的FP /形式的临床疗效的证据。我们还审查了支持FP / FORM K-HALER使用的药代动力学/药效学研究,并考虑与该装置显示高肺沉积的数据。最后,我们审查了使用BTI,设备特征和健康经济方面的患者体验。专家意见:尽管疗法可用,但哮喘控制水平仍然很低,易于使用易于使用的吸入器。研究增加我们对每个吸入器的关键错误的理解,以及如何克服它们对于改善护理是重要的。缩写:AUQ:等离子体浓度 - 时间曲线下的区域从给药到最后可测量的浓度; BDP:BECLOMERSONE Diproionate; BTI:呼吸触发吸入器;芽:布德尼斯; CL:置信区间; Cmax:最大观察到的等离子体浓度; DPI:干粉吸入器; FDC:固定剂量组合; FEV1:1 S强迫呼气量;形式:Formoterol Mumarate; FP:丙酸滴水; HCP:保健专业; ICS:吸入皮质类固醇; Laba:长效的Beta2激动剂;或:赔率比; PIL:患者信息传单; PMDI:加压计量吸入器; Sal:Salmeterol Xinafoate

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