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Algorithms for monitoring home non-invasive ventilation (NIV) have been recently proposed.1–3 Following this strategy, we detected three cases of transient ineffective ventilation due to the use of a ‘ramp’ option on home pressure support (PS) ventilators. The ‘ramp’ option is a comfort setting initially made available on CPAP devices. This option exists in pressure-cycled ventilators, allowing a progressive increase of expiratory positive airway pressure (EPAP) only. A « ramp » option has also recently been made available for PS: to our knowledge, three home ventilators (Stellar, Resmed, Australia; Prisma, Weinmann, Germany; Dreamstar Duo, Sefam, France) now provide this feature, allowing a stepwise increase of PS from 2 cm H2O to the target PS within 5–45 min.
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Three patients previously treated for obstructive sleep apnoea (OSA) with CPAP devices, were switched to NIV because of uncontrolled hypoventilation due to obesity hypoventilation syndrome (OHS) (n=2) or diaphragmatic dysfunction (n=1) (table 1). NIV was introduced using a single circuit pressure-targeted ventilator (Stellar 100, Resmed, Australia) and a calibrated leak, in a ‘Spontaneous/Timed mode’ (assisted PS with a backup respiratory rate). Patients were monitored using a polygraph coupled to the ventilator (Reslink, Resmed, Australia)2 (table 1).
The three patients, who had previously used a ‘ramp’ option on their CPAP device, requested from their home care provider a similar setting on their home ventilator.
During ramp time, all three patients presented with dyspnoea and discomfort when launching NIV, probably due to insufficient PS, inducing deep desaturations in patient 1 and increase in respiratory rate and unrewarded inspiratory efforts in patients 2 and 3. Patients 1 and 2 removed transiently their device during the night, causing a recurrence of the reported respiratory abnormalities. Both patients were adequately ventilated when they reached the expected EPAP and PS settings (part B of the figure 1).
Patient 3 tolerated neither the ramp option on both EPAP and PS, nor the immediate exposure to high levels of PS (20 cm H2O). However, she tolerated perfectly well the same PS with a ramp only on EPAP (VPAP S9, Resmed, Australia)
This report shows that implementation of a ‘ramp’ on PS home ventilators may be a cause of transient ineffective ventilation and desaturation and/or patient discomfort.
For CPAP devices, the ‘ramp’ function is considered as a comfort setting and can be adjusted by the patient himself. Although use of a ‘ramp’ has been reported as a cause of treatment failure in OSA,4 clinicians usually tend to consider that a ‘ramp’ on CPAP is not dangerous and probably improves comfort.
The problem is not the same with PS. Only three ventilators, to our knowledge, have a ‘ramp’ function on PS. On these ventilators, the progressive increase in pressure applies to PS and PEP simultaneously.
There is a hypothetical indication for a ‘ramp’ option on PS devices for patients who do not tolerate immediate exposure to the preset level of PS when they put on their ventilator, and feel more comfortable with a progressive increase in PS. The pros and cons of this option would be difficult to determine in a clinical trial, because of the wide range of possible settings (duration and pressure span of ramp) and the subjective nature of the main end point (patient comfort). The three cases reported show that use of a ramp on PS may compromise the efficacy of NIV, especially in patients with orthopnoea requiring full PS immediately when reclining (as in case number 3). This option may be especially questionable in subjects who have multiple awakings during the night and thus could use this option repeatedly: patients would appear compliant but time under NIV would include multiple subtherapeutic episodes. Additionally, in patients with orthopnoea, that is, subjects with diaphragmatic dysfunction, this option may increase discomfort and delay relief from dyspnoea. Furthermore, in OHS, which is most often associated with OSAS, a prolonged ‘ramp time’ can delay appropriate pneumatic upper airway stenting and thus explain residual obstructive apnoeas during the ramp phase.
In summary, using a PS ramp option during NIV (1) can compromise NIV efficacy and may be poorly tolerated; (2) should not be an option that the patient can activate by himself as in CPAP devices; (3) should be set only by an experienced clinician aware of potential drawbacks; (4) its activation should appear explicitly on the screen of the device. If, in spite of the previously discussed drawbacks, a PS ‘ramp’ option is selected, initial PS level should be at least 5–6 cm H2O, and time to attain the preset PS should be as short as possible. All settings, including ramp function, should be not altered without detailed clinical assessment and consultation. Use of the ramp function should be to improve comfort and aid compliance and should be reviewed along with the rest of the ventilator prescription at each clinic assessment with the aim of always using the minimum time and pressure gap required to enhance sleep onset and NIV adherence.
Contributors JG-B: (1) Substantial contributions to the conception or design of the work, or the acquisition, analysis or interpretation of data. (2) Drafting the work or revising it critically for important intellectual content. (3) Final approval of the version published. (4) Contributor as being responsible for the overall content as guarantor(s). CR, CP, BL, JLP, DR and JPJ: (1) Substantial contributions to the conception or design of the work, or the acquisition, analysis or interpretation of data. (2) Drafting the work or revising it critically for important intellectual content. (3) Final approval of the version published.
Funding Investissement d'avenir ANR (10-AIHU 6).
Competing interests None declared.
Patient consent Obtained.
Ethics approval Institutional Review Board of the French learned society for respiratory medicine—Société de Pneumologie de Langue Française.
Provenance and peer review Not commissioned; externally peer reviewed.
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