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Makale detayı · 2016 · article

Bronchodilator efficacy of 18 microg once-daily tiotropium inhalation via Discairsupreg/sup versus HandiHalersupreg/sup in adults with chronic obstructive pulmonary disease: randomized, active-controlled, parallel-group, open-label, Phase IV trial

Dergi International Journal of Chronic Obstructive Pulmonary Disease ISSN kaydı başka bir dergiye işaret ediyor; ad YÖKSİS kaydından.
ISSN1178-2005
YÖKSİS OpenAlex Açık erişim · gold
Yıl2016
Atıf2OpenAlex
Yüzdelik%71,0
FWCI0,471,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q2

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıInternational Journal of Chronic Obstructive Pulmonary Disease
  • Katalog eşleşmesi (ISSN)International Journal of COPD
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Purpose: To compare the bronchodilator efficacy of 18 µg once-daily tiotropium inhalation administered via Discair ® versus HandiHaler ® in adults with moderate-to-severe chronic obstructive pulmonary disease (COPD). Patients and methods: Fifty-eight patients with moderate-to-severe COPD were enrolled in this randomized, active-controlled, parallel-group, open-label, Phase IV non-inferiority trial. Patients were randomly assigned to a test group (n=29, inhalation with Discair) or a reference group (n=29, inhalation with HandiHaler). The primary efficacy parameter was the average maximum change in forced expiratory volume in 1 second (FEV 1 , in L). Change in forced vital capacity (FVC, in L), %FEV 1 and %FVC, the standardized area under the response–time curve (AUC) for the absolute change in FEV 1 and FVC, time to onset and peak of response, and safety data were also evaluated. Results: The test inhaler was non-inferior to the reference inhaler in terms of maximum change in FEV 1 at 24 h (unadjusted change: 0.0017 L [95% confidence interval [CI]: –0.0777, 0.0812]; change adjusted for time to reach maximum change in FEV 1 and smoking in pack-years: 0.0116 L [95% CI: –0.0699, 0.0931]), based on a non-inferiority margin of 0.100 L. There were also no significant differences between the two groups in maximum change in FVC value from baseline (0.3417 L vs 0.4438 L, P =0.113), percent change from baseline (22.235 vs 20.783 for FEV 1 , P =0.662; 16.719 vs 20.337 for FVC, P =0.257), and AUC 0–24 h (2.949 vs 2.833 L for FEV 1 , P =0.891; 2.897 vs 4.729 L for FVC, P =0.178). There were no adverse events, serious adverse events, or deaths. Conclusion: Our findings show that the Discair was non-inferior to the HandiHaler. More specifically, these devices had similar clinical efficacy in terms of time-dependent response over 24 h for patients with moderate-to-severe COPD. Keywords: non-inferiority, tiotropium, Discair ® , HandiHaler ® , bronchodilator efficacy, spirometry

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

2atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 4 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2019 Bronchodilator efficacy of tiotropium/formoterol (18/12 µg once daily via a Discair inhaler), tiotropium alone (18 µg by Handihaler) or combined with formoterol (12 µg twice daily by Aerolizer) in adults with moderate-to-severe stable COPDAtıf 4 · OpenAlex
  2. 2019 Bronchodilator efficacy of tiotropium/formoterol (18/12 µg once daily via a Discair inhaler), tiotropium alone (18 µg by Handihaler) or combined with formoterol (12 µg twice daily by Aerolizer) in adults with moderate-to-severe stable COPDAtıf 4 · OpenAlex
  3. 2019 Bronchodilator Efficacy of a Single-Dose 12/400-µg Formoterol/Budesonide Combination as a Dry Powder for Inhalation Delivered by Discair® in Adult Patients with Moderate-to-Severe Stable COPD: Open-Label, Single-Arm, Phase IV TrialAtıf 0 · OpenAlex
  4. 2019 Bronchodilator Efficacy of a Single-Dose 12/400-µg Formoterol/Budesonide Combination as a Dry Powder for Inhalation Delivered by Discair® in Adult Patients with Moderate-to-Severe Stable COPD: Open-Label, Single-Arm, Phase IV Trial.Atıf 0 · OpenAlex

Yazarlar

4
  1. BİRSEN PINAR YILDIZ SAĞLIK BİLİMLERİ ÜNİVERSİTESİ 1
  2. Mesut Bayraktaroglu 2
  3. Didem Görgün 3
  4. Funda Secik 4