Nocturnal mechanical ventilation for chronic hypoventilation in patients with neuromuscular and chest wall disorders
- PMID: 25503955
- PMCID: PMC7068159
- DOI: 10.1002/14651858.CD001941.pub3
Nocturnal mechanical ventilation for chronic hypoventilation in patients with neuromuscular and chest wall disorders
Abstract
Background: Chronic alveolar hypoventilation is a common complication of many neuromuscular and chest wall disorders. Long-term nocturnal mechanical ventilation is commonly used to treat it. This is a 2014 update of a review first published in 2000 and previously updated in 2007.
Objectives: To examine the effects on mortality of nocturnal mechanical ventilation in people with neuromuscular or chest wall disorders. Subsidiary endpoints were to examine the effects of respiratory assistance on improvement of chronic hypoventilation, sleep quality, hospital admissions and quality of life.
Search methods: We searched the Cochrane Neuromuscular Disease Group Specialized Register, CENTRAL, MEDLINE and EMBASE on 10 June 2014. We contacted authors of identified trials and other experts in the field.
Selection criteria: We searched for quasi-randomised or randomised controlled trials of participants of all ages with neuromuscular or chest wall disorder-related stable chronic hypoventilation of all degrees of severity, receiving any type and any mode of long-term nocturnal mechanical ventilation. The primary outcome measure was one-year mortality and secondary outcomes were unplanned hospital admission, short-term and long-term reversal of hypoventilation-related clinical symptoms and daytime hypercapnia, improvement of lung function and sleep breathing disorders.
Data collection and analysis: We used standard Cochrane methodology to select studies, extract data and assess the risk of bias in included studies.
Main results: The 10 eligible trials included a total of 173 participants. Roughly half of the trials were at low risk of selection, attrition or reporting bias, and almost all were at high risk of performance and detection bias. Four trials reported mortality data in the long term. The pooled risk ratio (RR) of dying was 0.62 (95% confidence interval (CI) 0.42 to 0.91, P value = 0.01) in favour of nocturnal mechanical ventilation compared to spontaneous breathing. There was considerable and significant heterogeneity between the trials, possibly related to differences between the study populations. Information on unplanned hospitalisation was available from two studies. The corresponding pooled RR was 0.25 (95% CI 0.08 to 0.82, P value = 0.02) in favour of nocturnal mechanical ventilation. For most of the outcome measures there was no significant long-term difference between nocturnal mechanical ventilation and no ventilation. Most of the secondary outcomes were not assessed in the eligible trials. Three out of the 10 trials, accounting for 39 participants, two with a cross-over design and one with two parallel groups, compared volume- and pressure-cycled non-invasive mechanical ventilation in the short term. From the only trial (16 participants) on parallel groups, there was no difference in mortality (one death in each arm) between volume- and pressure-cycled mechanical ventilation. Data from the two cross-over trials suggested that compared with pressure-cycled ventilation, volume-cycled ventilation was associated with less sleep time spent with an arterial oxygen saturation below 90% (mean difference (MD) 6.83 minutes, 95% CI 4.68 to 8.98, P value = 0.00001) and a lower apnoea-hypopnoea (per sleep hour) index (MD -0.65, 95% CI -0.84 to -0.46, P value = 0.00001). We found no study that compared invasive and non-invasive mechanical ventilation or intermittent positive pressure versus negative pressure ventilation.
Authors' conclusions: Current evidence about the therapeutic benefit of mechanical ventilation is of very low quality, but is consistent, suggesting alleviation of the symptoms of chronic hypoventilation in the short term. In four small studies, survival was prolonged and unplanned hospitalisation was reduced, mainly in participants with motor neuron diseases. With the exception of motor neuron disease and Duchenne muscular dystrophy, for which the natural history supports the survival benefit of mechanical ventilation against no ventilation, further larger randomised trials should assess the long-term benefit of different types and modes of nocturnal mechanical ventilation on quality of life, morbidity and mortality, and its cost-benefit ratio in neuromuscular and chest wall diseases.
Conflict of interest statement
D Annane: my group was the co‐ordinating centre of a publicly funded multicentre trial of non‐invasive ventilation in DMD that has been included in this review (Raphaël 1994), and we are co‐ordinating an ongoing, publicly funded, multicentre trial of non‐invasive ventilation in adults with myotonic dystrophy type 1.
S Chevret: none known.
D Orlikowski declares the following:
grants from AFM for a randomised study of non‐invasive ventilation in myotonic dystrophy type 1 and from Phillips for a study of Average Volume Assured Pressure Support (AVAPS) in myotonic dystrophy type 1;
fees from IP Santé à domicile;
he has acted as a medical referee for Foyer ADEP Evry.
All the activities mentioned are in the field of care and research conducted in neuromuscular diseases and home ventilation.
Outside this work, he received funding from Covidien and from Genzyme to attend the AAN conference 2012.
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Update of
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Nocturnal mechanical ventilation for chronic hypoventilation in patients with neuromuscular and chest wall disorders.Cochrane Database Syst Rev. 2007 Oct 17;(4):CD001941. doi: 10.1002/14651858.CD001941.pub2. Cochrane Database Syst Rev. 2007. Update in: Cochrane Database Syst Rev. 2014 Dec 13;(12):CD001941. doi: 10.1002/14651858.CD001941.pub3. PMID: 17943762 Updated.
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