A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD: the DuoSleep study

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Standard

A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD : the DuoSleep study. / Lehmann, Sverre; Ringbæk, Thomas; Løkke, Anders; Grote, Ludger; Hedner, Jan; Lindberg, Eva.

I: International Journal of Chronic Obstructive Pulmonary Disease, Bind 14, 23.01.2019, s. 199-210.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Lehmann, S, Ringbæk, T, Løkke, A, Grote, L, Hedner, J & Lindberg, E 2019, 'A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD: the DuoSleep study', International Journal of Chronic Obstructive Pulmonary Disease, bind 14, s. 199-210. https://doi.org/10.2147/COPD.S184127

APA

Lehmann, S., Ringbæk, T., Løkke, A., Grote, L., Hedner, J., & Lindberg, E. (2019). A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD: the DuoSleep study. International Journal of Chronic Obstructive Pulmonary Disease, 14, 199-210. https://doi.org/10.2147/COPD.S184127

Vancouver

Lehmann S, Ringbæk T, Løkke A, Grote L, Hedner J, Lindberg E. A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD: the DuoSleep study. International Journal of Chronic Obstructive Pulmonary Disease. 2019 jan. 23;14:199-210. https://doi.org/10.2147/COPD.S184127

Author

Lehmann, Sverre ; Ringbæk, Thomas ; Løkke, Anders ; Grote, Ludger ; Hedner, Jan ; Lindberg, Eva. / A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD : the DuoSleep study. I: International Journal of Chronic Obstructive Pulmonary Disease. 2019 ; Bind 14. s. 199-210.

Bibtex

@article{e200e8cea175464d8a8087a44e9a3131,
title = "A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD: the DuoSleep study",
abstract = "Purpose: This study investigated the effect of dual bronchodilation with the long-acting β-receptor agonist/long-acting muscarinic antagonist combination, indacaterol/glycopyrronium (IND/GLY), on nighttime oxygenation, lung function, sleep quality, and symptoms in patients with moderate-to-severe COPD.Patients and methods: This was a 4-week, double-blind, multicenter, placebo-controlled, two-period crossover study. Patients were randomized in a 1:1 ratio to receive IND/GLY 110/50 µg once daily or matching placebo. The primary objective was to evaluate the effect of treatment with IND/GLY on mean nighttime oxygenation, compared with placebo. The secondary objective was to determine the time spent <90% in blood oxygen saturation (SpO2) compared with placebo. Exploratory objectives were to assess the effect of IND/GLY, compared with placebo, on sleep quality measured by the Medical Outcomes Study (MOS) Sleep Scale and the COPD and Asthma Sleep Impact Scale (CASIS) questionnaires and on symptoms assessed by COPD Assessment Test (CAT) questionnaire.Results: In total, 38 patients were randomized (n=22, IND/GLY; n=16, placebo). The change in nighttime oxygenation (SpO2) was similar, and there was a comparable difference in time spent <90% SpO2 between IND/GLY and placebo. Increases from baseline for the difference between IND/GLY and placebo for trough FEV1, FVC, and inspiratory capacity (P<0.05) were seen, with a corresponding reduction in residual volume and functional residual capacity (P<0.05). IND/GLY treatment showed an improvement in scores for CAT (P=0.0208), CASIS, and the MOS Sleep Scale measures, Sleep Problems Index I, Sleep Problems Index II (P=0.0315), Sleep Adequacy, Sleep Disturbance Scale, Somnolence Scale, and Short of Breath Scale (P=0.0031).Conclusion: In this study, IND/GLY 110/50 µg once daily improved symptoms, sleep quality, and lung function, but showed no effect on nighttime oxygenation in patients with moderate-to-severe COPD.",
keywords = "Adrenergic beta-2 Receptor Agonists/administration & dosage, Adult, Aged, Biomarkers/blood, Bronchodilator Agents/administration & dosage, Cross-Over Studies, Double-Blind Method, Female, Forced Expiratory Volume, Glycopyrrolate/administration & dosage, Health Status, Humans, Indans/administration & dosage, Lung/drug effects, Male, Middle Aged, Muscarinic Antagonists/administration & dosage, Norway, Oxygen/blood, Pulmonary Disease, Chronic Obstructive/blood, Quality of Life, Quinolones/administration & dosage, Severity of Illness Index, Sleep, Surveys and Questionnaires, Time Factors, Treatment Outcome, Vital Capacity",
author = "Sverre Lehmann and Thomas Ringb{\ae}k and Anders L{\o}kke and Ludger Grote and Jan Hedner and Eva Lindberg",
year = "2019",
month = jan,
day = "23",
doi = "10.2147/COPD.S184127",
language = "English",
volume = "14",
pages = "199--210",
journal = "International Journal of COPD",
issn = "1176-9106",
publisher = "Dove Medical Press Ltd",

}

RIS

TY - JOUR

T1 - A randomized trial to determine the impact of indacaterol/glycopyrronium on nighttime oxygenation and symptoms in patients with moderate-to-severe COPD

T2 - the DuoSleep study

AU - Lehmann, Sverre

AU - Ringbæk, Thomas

AU - Løkke, Anders

AU - Grote, Ludger

AU - Hedner, Jan

AU - Lindberg, Eva

PY - 2019/1/23

Y1 - 2019/1/23

N2 - Purpose: This study investigated the effect of dual bronchodilation with the long-acting β-receptor agonist/long-acting muscarinic antagonist combination, indacaterol/glycopyrronium (IND/GLY), on nighttime oxygenation, lung function, sleep quality, and symptoms in patients with moderate-to-severe COPD.Patients and methods: This was a 4-week, double-blind, multicenter, placebo-controlled, two-period crossover study. Patients were randomized in a 1:1 ratio to receive IND/GLY 110/50 µg once daily or matching placebo. The primary objective was to evaluate the effect of treatment with IND/GLY on mean nighttime oxygenation, compared with placebo. The secondary objective was to determine the time spent <90% in blood oxygen saturation (SpO2) compared with placebo. Exploratory objectives were to assess the effect of IND/GLY, compared with placebo, on sleep quality measured by the Medical Outcomes Study (MOS) Sleep Scale and the COPD and Asthma Sleep Impact Scale (CASIS) questionnaires and on symptoms assessed by COPD Assessment Test (CAT) questionnaire.Results: In total, 38 patients were randomized (n=22, IND/GLY; n=16, placebo). The change in nighttime oxygenation (SpO2) was similar, and there was a comparable difference in time spent <90% SpO2 between IND/GLY and placebo. Increases from baseline for the difference between IND/GLY and placebo for trough FEV1, FVC, and inspiratory capacity (P<0.05) were seen, with a corresponding reduction in residual volume and functional residual capacity (P<0.05). IND/GLY treatment showed an improvement in scores for CAT (P=0.0208), CASIS, and the MOS Sleep Scale measures, Sleep Problems Index I, Sleep Problems Index II (P=0.0315), Sleep Adequacy, Sleep Disturbance Scale, Somnolence Scale, and Short of Breath Scale (P=0.0031).Conclusion: In this study, IND/GLY 110/50 µg once daily improved symptoms, sleep quality, and lung function, but showed no effect on nighttime oxygenation in patients with moderate-to-severe COPD.

AB - Purpose: This study investigated the effect of dual bronchodilation with the long-acting β-receptor agonist/long-acting muscarinic antagonist combination, indacaterol/glycopyrronium (IND/GLY), on nighttime oxygenation, lung function, sleep quality, and symptoms in patients with moderate-to-severe COPD.Patients and methods: This was a 4-week, double-blind, multicenter, placebo-controlled, two-period crossover study. Patients were randomized in a 1:1 ratio to receive IND/GLY 110/50 µg once daily or matching placebo. The primary objective was to evaluate the effect of treatment with IND/GLY on mean nighttime oxygenation, compared with placebo. The secondary objective was to determine the time spent <90% in blood oxygen saturation (SpO2) compared with placebo. Exploratory objectives were to assess the effect of IND/GLY, compared with placebo, on sleep quality measured by the Medical Outcomes Study (MOS) Sleep Scale and the COPD and Asthma Sleep Impact Scale (CASIS) questionnaires and on symptoms assessed by COPD Assessment Test (CAT) questionnaire.Results: In total, 38 patients were randomized (n=22, IND/GLY; n=16, placebo). The change in nighttime oxygenation (SpO2) was similar, and there was a comparable difference in time spent <90% SpO2 between IND/GLY and placebo. Increases from baseline for the difference between IND/GLY and placebo for trough FEV1, FVC, and inspiratory capacity (P<0.05) were seen, with a corresponding reduction in residual volume and functional residual capacity (P<0.05). IND/GLY treatment showed an improvement in scores for CAT (P=0.0208), CASIS, and the MOS Sleep Scale measures, Sleep Problems Index I, Sleep Problems Index II (P=0.0315), Sleep Adequacy, Sleep Disturbance Scale, Somnolence Scale, and Short of Breath Scale (P=0.0031).Conclusion: In this study, IND/GLY 110/50 µg once daily improved symptoms, sleep quality, and lung function, but showed no effect on nighttime oxygenation in patients with moderate-to-severe COPD.

KW - Adrenergic beta-2 Receptor Agonists/administration & dosage

KW - Adult

KW - Aged

KW - Biomarkers/blood

KW - Bronchodilator Agents/administration & dosage

KW - Cross-Over Studies

KW - Double-Blind Method

KW - Female

KW - Forced Expiratory Volume

KW - Glycopyrrolate/administration & dosage

KW - Health Status

KW - Humans

KW - Indans/administration & dosage

KW - Lung/drug effects

KW - Male

KW - Middle Aged

KW - Muscarinic Antagonists/administration & dosage

KW - Norway

KW - Oxygen/blood

KW - Pulmonary Disease, Chronic Obstructive/blood

KW - Quality of Life

KW - Quinolones/administration & dosage

KW - Severity of Illness Index

KW - Sleep

KW - Surveys and Questionnaires

KW - Time Factors

KW - Treatment Outcome

KW - Vital Capacity

U2 - 10.2147/COPD.S184127

DO - 10.2147/COPD.S184127

M3 - Journal article

C2 - 30666100

VL - 14

SP - 199

EP - 210

JO - International Journal of COPD

JF - International Journal of COPD

SN - 1176-9106

ER -

ID: 235001085