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Home mechanical ventilation (HMV) is a well-established treatment option for patients with chronic hypercapnic respiratory failure, whereby non-invasive positive pressure ventilation (NPPV) serves as the predominant means of HMV delivery.1 2 In general, there are two physiologically-different modes of NPPV deliveries, volume-preset NPPV and pressure-preset NPPV. During volume-preset NPPV a fixed inspiratory volume (Vinsp) is set at the ventilator, while the inspiratory positive airway pressure (IPAP) varies depending on airway resistance. Conversely, Vinsp varies during pressure-preset NPPV, while IPAP remains fixed. The advantage of volume-preset NPPV is that Vinsp, and hence tidal volume, are relatively stable; however, this can lead to a breath-by-breath variation in IPAP levels that can become a burden for the patient, and the leakages that regularly occur during NPPV are not compensated for. In contrast, the Vinsp that is delivered during pressure-preset NPPV may be unstable due to increased airway resistance; however, given that the variation in IPAP is lower, this is often better tolerated by the patient. In addition, leak compensation is provided by pressure-preset NPPV, as shown by in vitro3 and in vivo4 studies. In addition, ventilators providing pressure-preset NPPV are cheaper. Thus, pressure-preset NPPV has become the predominant means of delivering HMV. Nevertheless, randomised controlled trials have shown that volume- and pressure-preset NPPV generally have comparable effects on improvements in blood gases, sleep quality and health-related quality of life (HRQL),5 6 although pressure-preset NPPV is reportedly better tolerated due to fewer gastrointestinal side effects.5 However, clinicians should always weigh the advantages and disadvantages of the two different approaches on an individual patient basis.
Recently, the so-called hybrid modes have been developed to overcome the disadvantages of volume- and pressure-preset NPPV, respectively. These modes seek to combine the advantages of the two classical modes, that is, the stability of Vinsp and the avoidance of cumbersome variations in breath-by-breath IPAP levels. This is achieved by setting a so-called ‘target volume’. Here, pressure-preset NPPV is primarily used, but instead of a fixed IPAP, a pressure range with minimal and maximal IPAP values is set at the ventilator. In response to the automatic calculations and adjustments made by the ventilator, IPAP can undergo a smooth transition within a preset range in order to reach the target volume.
The most extensively studied hybrid mode is the Average Volume Assured Pressure Support (AVAPS) mode. An initial randomised-controlled cross-over trial suggested that the addition of AVAPS to pressure-preset NPPV resulted in better control of nocturnal ventilation compared with pure pressure-preset NPPV in patients with obesity hypoventilation syndrome (OHS).7 However, both HRQL, as assessed by the Severe Respiratory Insufficiency (SRI) questionnaire,8 9 and sleep quality, as measured by polysomnography, showed similar improvements under each of the two modes. Subsequent trials that primarily included OHS and chronic obstructive pulmonary disease (COPD) patients showed an overall comparable outcome, although nocturnal hypoventilation was better controlled in some trials (table 1). However, in one study polysomnographic sleep quality was shown to be reduced during AVAPS compared with pure pressure-preset NPPV,10 probably as a result of considerably high target volume settings (table 1). However, observational periods were rather short in the previous trials, and in some cases patients were already familiar with pressure-preset NPPV prior to randomisation, thus indicating a selection bias. Therefore, the evidence for target volume setting remains inconclusive, and it is yet to be established whether these hybrid modes of ventilation have benefits that are clear and consistent enough to warrant official recommendations.
Murphy and colleagues randomly allocated 50 NPPV-naive patients with severe OHS (body mass index 50±7 kg/m2) either to pure pressure-preset NPPV using pressure support ventilation or to AVAPS mode, with 46 patients completing the trial.14 After 3 months of treatment, daytime arterial partial pressure of carbon dioxide (primary outcome) improved comparably in both groups by a mean 0.6 kPa. In addition, improvements in HRQL—again measured with the highly specific SRI8 9—also showed a similar improvement in both groups, while both treatment strategies resulted in equivalent degrees of weight loss (table 1); therefore, AVAPS was not advantageous. This study significantly adds to the current body of knowledge about target volume setting used for HMV for the following reasons.
First, it is the largest randomised controlled trial investigating HMV with target volume settings, and second, the observational period is the longest implemented to date (table 1). Third, and most importantly, ventilator settings were individually adjusted according to a predefined protocol that included a nocturnal assessment period aimed at achieving optimal control of nocturnal ventilation. This protocol was a unique aspect of the study and held true for both modes, rather than just for the AVAPS settings. Therefore, patients could be discharged after optimal treatment had been established, with or without AVAPS. As a consequence, target volume settings did not provide any additional benefits compared with pressure-preset NPPV.
In reality, clinicians are regularly confronted with new technical developments for HMV, whereby new modes and features are increasingly provided without any evidence of benefits or even without clear recommendations on how to adjust the settings. Target volume serves as an excellent example: despite the lack of evidence for any actual benefits, many new-generation ventilators provide target volume modes. Confusingly, the nomenclature and algorithms used for IPAP adaptation vary considerably among different types of ventilators and manufacturers. In addition, real target volume settings also show considerable variation among different studies (table 1); this is most likely due to the lack in the availability of recommendations for its use. Indeed, the inappropriate use of these settings can even be harmful. Of note, Murphy and colleagues established that a target volume of 10 ml/kg ideal body weight was the most appropriate for AVAPS in their cohort.
New modes and features like target volume might provide an impression of improved alveolar ventilation control; however, it is important to note that HMV has already been successfully applied for nearly 20 years.15 16 Indeed, it is obviously the details of the settings rather than the mode of ventilation which seems to matter the most. The new study by Murphy and colleagues teaches us that thoughtful adjustment of ventilator settings according to nocturnal monitoring is essential for proper control of nocturnal hypoventilation, thus relegating the ventilation mode to secondary importance. Clearly, patients may benefit on an individual basis when they are switched from one NPPV mode to another,6 and this idea might also be valid for target volume. Therefore, while target volume should not be entirely disregarded, the results of the present and previous trials suggest that target volume setting is generally not recommendable.
Finally, the study by Murphy and colleagues provides another clinically important detail: The authors convincingly showed that patients who received more than 50% of breaths without triggering (controlled ventilation) had a substantially better outcome compared with patients who received more than 50% of breaths with triggering (supported ventilation), irrespective of whether AVAPS or pure pressure-preset NPPV was used. Thereby, both daytime and nocturnal gas exchange was improved clearly favoured by controlled NPPV. This resulted in an impressive mean difference of 1.9 kg/m2 body mass index (reduction) and led to a score difference of 10 points (= improvement) as assessed by the SRI; there was also an improvement in subjective sleepiness. These findings also highlight the importance of measuring HRQL as specifically as possible when assessing specific treatment interventions. The SRI is specifically tailored to patients receiving HMV,8 9 and the present study shows that this tool is capable of differentiating between different ventilatory approaches. In contrast, there was no difference detected in HRQL (SRI) between AVAPS and pure pressure-preset NPPV, not because an insensitive assessment tool was used, but simply because there was no difference present.
Controlled NPPV with high inspiratory pressures has recently been developed for COPD patients and is referred to as high-intensity NPPV.17 18 This approach was shown to be superior to assisted NPPV with lower pressures (low-intensity NPPV) in terms of controlling nocturnal hypoventilation in chronic hypercapnic COPD patients; moreover, high-intensity NPPV promoted better lung function, and improved both dyspnoea and HRQL (again assessed by the SRI).19 20 The study by Murphy and colleagues also supports the idea that a controlled form of ventilation is the primary determinant for successful NPPV in OHS patients. However, as this was not the primary aim of the study, further work on this issue is definitely warranted. Nevertheless, we anticipate a paradigm shift towards the use of controlled NPPV being used in favour of assisted or supported NPPV modes for nocturnal HMV. Controlled ventilation, however, can be achieved by all classical modes. In this regard, target volume appears to be more of a gadget than a great progressive tool.
Competing interests None.
Provenance and peer review Commissioned; internally peer reviewed.
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