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Thorax 2005;60:1019-1024; doi:10.1136/thx.2004.037424
Copyright © 2005 BMJ Publishing Group Ltd & British Thoracic Society

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MECHANICAL VENTILATION

Randomised controlled trial of non-invasive ventilation (NIV) for nocturnal hypoventilation in neuromuscular and chest wall disease patients with daytime normocapnia

S Ward, M Chatwin, S Heather, A K Simonds

Clinical and Academic Department of Sleep and Breathing, Royal Brompton & Harefield NHS Trust, London SW3 6NP, UK

Correspondence to:
Correspondence to:
Dr A K Simonds
Clinical and Academic Department of Sleep and Breathing, Royal Brompton & Harefield NHS Trust, Sydney Street, London SW3 6NP, UK; A.Simonds{at}rbht.nhs.uk

Background: Long term non-invasive ventilation (NIV) reduces morbidity and mortality in patients with neuromuscular and chest wall disease with hypercapnic ventilatory failure, but preventive use has not produced benefit in normocapnic patients with Duchenne muscular dystrophy. Individuals with nocturnal hypercapnia but daytime normocapnia were randomised to a control group or nocturnal NIV to examine whether nocturnal hypoventilation is a valid indication for NIV.

Methods: Forty eight patients with congenital neuromuscular or chest wall disease aged 7–51 years and vital capacity <50% predicted underwent overnight respiratory monitoring. Twenty six with daytime normocapnia and nocturnal hypercapnia were randomised to either nocturnal NIV or to a control group without ventilatory support. NIV was started in the control group if patients fulfilled preset safety criteria.

Results: Peak nocturnal transcutaneous carbon dioxide tension (TcCO2) did not differ between the groups, but the mean (SD) percentage of the night during which TcCO2 was >6.5 kPa decreased in the NIV group (–57.7 (26.1)%) but not in controls (–11.75 (46.1)%; p = 0.049, 95% CI –91.5 to –0.35). Mean (SD) arterial oxygen saturation increased in the NIV group (+2.97 (2.57)%) but not in controls (–1.12 (2.02)%; p = 0.024, 95% CI 0.69 to 7.5). Nine of the 10 controls failed non-intervention by fulfilling criteria to initiate NIV after a mean (SD) of 8.3 (7.3) months.

Conclusion: Patients with neuromuscular disease with nocturnal hypoventilation are likely to deteriorate with the development of daytime hypercapnia and/or progressive symptoms within 2 years and may benefit from the introduction of nocturnal NIV before daytime hypercapnia ensues.


Abbreviations: CPF, cough peak flow; FRC, functional residual capacity; NIV, non-invasive ventilation; PaO2, arterial oxygen tension; PaCO2, arterial carbon dioxide tension; PImax, maximum inspiratory mouth pressure; PEmax, maximum expiratory mouth pressure; SNIP, sniff inspiratory pressure; TcCO2, transcutaneous carbon dioxide tension

Keywords: non-invasive ventilation; neuromuscular disease; chest wall disease; nocturnal hypoventilation




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