Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial

<p>Abstract</p> <p>Background</p> <p>The use of noninvasive intermittent positive pressure ventilation (NIPPV) in chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure remains controversial as long-term data are almost lackin...

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Main Authors: Zijlstra Jan G, Vonk Judith M, Bladder Gerrie, Wempe Johan B, Duiverman Marieke L, Kerstjens Huib AM, Wijkstra Peter J
Format: Article
Language:English
Published: BMC 2011-08-01
Series:Respiratory Research
Online Access:http://respiratory-research.com/content/12/1/112
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spelling doaj-e7ab855f24af4cb8ba298b585068042d2020-11-24T22:16:23ZengBMCRespiratory Research1465-99212011-08-0112111210.1186/1465-9921-12-112Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trialZijlstra Jan GVonk Judith MBladder GerrieWempe Johan BDuiverman Marieke LKerstjens Huib AMWijkstra Peter J<p>Abstract</p> <p>Background</p> <p>The use of noninvasive intermittent positive pressure ventilation (NIPPV) in chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure remains controversial as long-term data are almost lacking.</p> <p>The aim was to compare the outcome of 2-year home-based nocturnal NIPPV in addition to rehabilitation (NIPPV + PR) with rehabilitation alone (PR) in COPD patients with chronic hypercapnic respiratory failure.</p> <p>Methods</p> <p>Sixty-six patients could be analyzed for the two-year home-based follow-up period. Differences in change between the NIPPV + PR and PR group were assessed by a linear mixed effects model with a random effect on the intercept, and adjustment for baseline values. The primary outcome was health-related quality of life (HRQoL); secondary outcomes were mood state, dyspnea, gas exchange, functional status, pulmonary function, and exacerbation frequency.</p> <p>Results</p> <p>Although the addition of NIPPV did not significantly improve the Chronic Respiratory Questionnaire compared to rehabilitation alone (mean difference in change between groups -1.3 points (95% CI: -9.7 to 7.4)), the addition of NIPPV did improve HRQoL assessed with the Maugeri Respiratory Failure questionnaire (-13.4% (-22.7 to -4.2; p = 0.005)), mood state (Hospital Anxiety and Depression scale -4.0 points (-7.8 to 0.0; p = 0.05)), dyspnea (Medical Research Council -0.4 points (-0.8 to -0.0; p = 0.05)), daytime arterial blood gases (PaCO<sub>2 </sub>-0.4 kPa (-0.8 to -0.2; p = 0.01); PaO<sub>2 </sub>0.8 kPa (0.0 to 1.5; p = 0.03)), 6-minute walking distance (77.3 m (46.4 to 108.0; p < 0.001)), Groningen Activity and Restriction scale (-3.8 points (-7.4 to -0.4; p = 0.03)), and forced expiratory volume in 1 second (115 ml (19 to 211; p = 0.019)). Exacerbation frequency was not changed.</p> <p>Conclusions</p> <p>The addition of NIPPV to pulmonary rehabilitation for 2 years in severe COPD patients with chronic hypercapnic respiratory failure improves HRQoL, mood, dyspnea, gas exchange, exercise tolerance and lung function decline. The benefits increase further with time.</p> <p>Trial registration</p> <p>ClinicalTrials.Gov (ID <a href="http://www.clinicaltrials.gov/ct2/show/NCT00135538">NCT00135538</a>).</p> http://respiratory-research.com/content/12/1/112
collection DOAJ
language English
format Article
sources DOAJ
author Zijlstra Jan G
Vonk Judith M
Bladder Gerrie
Wempe Johan B
Duiverman Marieke L
Kerstjens Huib AM
Wijkstra Peter J
spellingShingle Zijlstra Jan G
Vonk Judith M
Bladder Gerrie
Wempe Johan B
Duiverman Marieke L
Kerstjens Huib AM
Wijkstra Peter J
Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial
Respiratory Research
author_facet Zijlstra Jan G
Vonk Judith M
Bladder Gerrie
Wempe Johan B
Duiverman Marieke L
Kerstjens Huib AM
Wijkstra Peter J
author_sort Zijlstra Jan G
title Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial
title_short Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial
title_full Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial
title_fullStr Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial
title_full_unstemmed Two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: A randomized controlled trial
title_sort two-year home-based nocturnal noninvasive ventilation added to rehabilitation in chronic obstructive pulmonary disease patients: a randomized controlled trial
publisher BMC
series Respiratory Research
issn 1465-9921
publishDate 2011-08-01
description <p>Abstract</p> <p>Background</p> <p>The use of noninvasive intermittent positive pressure ventilation (NIPPV) in chronic obstructive pulmonary disease (COPD) patients with chronic hypercapnic respiratory failure remains controversial as long-term data are almost lacking.</p> <p>The aim was to compare the outcome of 2-year home-based nocturnal NIPPV in addition to rehabilitation (NIPPV + PR) with rehabilitation alone (PR) in COPD patients with chronic hypercapnic respiratory failure.</p> <p>Methods</p> <p>Sixty-six patients could be analyzed for the two-year home-based follow-up period. Differences in change between the NIPPV + PR and PR group were assessed by a linear mixed effects model with a random effect on the intercept, and adjustment for baseline values. The primary outcome was health-related quality of life (HRQoL); secondary outcomes were mood state, dyspnea, gas exchange, functional status, pulmonary function, and exacerbation frequency.</p> <p>Results</p> <p>Although the addition of NIPPV did not significantly improve the Chronic Respiratory Questionnaire compared to rehabilitation alone (mean difference in change between groups -1.3 points (95% CI: -9.7 to 7.4)), the addition of NIPPV did improve HRQoL assessed with the Maugeri Respiratory Failure questionnaire (-13.4% (-22.7 to -4.2; p = 0.005)), mood state (Hospital Anxiety and Depression scale -4.0 points (-7.8 to 0.0; p = 0.05)), dyspnea (Medical Research Council -0.4 points (-0.8 to -0.0; p = 0.05)), daytime arterial blood gases (PaCO<sub>2 </sub>-0.4 kPa (-0.8 to -0.2; p = 0.01); PaO<sub>2 </sub>0.8 kPa (0.0 to 1.5; p = 0.03)), 6-minute walking distance (77.3 m (46.4 to 108.0; p < 0.001)), Groningen Activity and Restriction scale (-3.8 points (-7.4 to -0.4; p = 0.03)), and forced expiratory volume in 1 second (115 ml (19 to 211; p = 0.019)). Exacerbation frequency was not changed.</p> <p>Conclusions</p> <p>The addition of NIPPV to pulmonary rehabilitation for 2 years in severe COPD patients with chronic hypercapnic respiratory failure improves HRQoL, mood, dyspnea, gas exchange, exercise tolerance and lung function decline. The benefits increase further with time.</p> <p>Trial registration</p> <p>ClinicalTrials.Gov (ID <a href="http://www.clinicaltrials.gov/ct2/show/NCT00135538">NCT00135538</a>).</p>
url http://respiratory-research.com/content/12/1/112
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