Abstract
Assisted (interactive) breathing is generally preferred to controlled breaths in patients on mechanical ventilators. Assisted breaths allow the patient's respiratory muscles to be used, and ventilatory muscle atrophy can be prevented. Moreover, the respiratory drive of the patient does not have to be aggressively blunted. However, interactive breaths need to be synchronized with the patient's efforts during the trigger, the flow delivery, and the cycling phases. Asynchrony during any of these can put an intolerable load on the respiratory muscles, leading to fatigue and the need for a high level of sedation or even paralysis. Current ventilation modes have a number of features that can monitor and enhance synchrony, including adjustment of the trigger variable, the use of pressure-targeted versus fixed-flow-targeted breaths, and manipulations of the cycle variable. Clinicians need to know how to use these ventilation mode and monitor them properly, especially understanding the airway pressure and flow graphics. The clinical challenge is synchronizing ventilator gas delivery with patient effort.
Introduction
Breaths delivered by a mechanical ventilator can be considered as either controlled or assisted.1 A controlled breath means that the machine determines the rate, the inspiratory time, and the tidal volume (VT), so the patient does no work. With controlled breaths, sedation and paralysis may be needed to suppress patient activity that might interfere with breath delivery. There is also a risk of diaphragmatic muscle structural derangement and atrophy (ventilator-induced diaphragmatic dysfunction).2,3 In contrast, in an assisted breath the patient interacts in some way with the ventilator, so the work of breathing is shared between the ventilator and the patient.4–7 The level of patient work is minimal if all the patient does is trigger the breath, or the patient work can be considerable if the ventilator's flow delivery and/or pressure application is minimal.
With assisted breaths, sedation needs may be less and patient muscle function may recover more rapidly,5,6 but this requires that the ventilator's flow and pressure delivery are synchronized with the patient's effort during all 3 breath phases: initiation, delivery, and termination. Triggering delays, inadequate flow delivery, or mismatching of the end of inspiration and the beginning of expiration can place a considerable load on the patient5–7 and lead to muscle fatigue, discomfort, and an increasing need for sedation or even paralytics. The importance of patient-ventilator asynchrony has been shown in several studies.8–11 In one, substantial asynchrony was associated with much longer duration of mechanical ventilation and even a trend toward a worse mortality.8 The clinical challenge, then, is to provide ventilatory support that is in accordance with patient effort: this is the concept of synchronizing mechanical ventilation to the patient's respiratory drive.
Features Available on Conventional Modes That Enhance Synchrony
Breath and Mode Design Features
As noted above, ventilator breaths can be described by what initiates the breath, what governs gas flow during the breath, and what terminates the breath (the trigger, target, and cycle variables, respectively). Conventional ventilators today deliver 5 basic breath types (Table 1 and Fig. 1):
The volume-control breath is time-triggered, flow-targeted, and volume-cycled.
The volume-assist breath is effort-triggered, flow-targeted, and volume-cycled.
The pressure-control breath is time-triggered, pressure-targeted, and time-cycled.
The pressure-assist breath is effort-triggered, pressure-targeted, and time-cycled.
The pressure-support breath is effort-triggered, pressure-targeted, and flow-cycled.
Three of these breath types can be considered assisted or interactive breaths: volume-assist, pressure-assist, and pressure-support.
The mechanical ventilation modes are the ways in which these 5 basic breaths can be delivered to the patient (Table 2). The volume assist-control mode provides volume-control and volume-assisted breaths. If the machine breath rate is set very high, the mode becomes virtually only volume control; in contrast, if the mandatory breath rate is set very low and patient triggers most of these breaths, the mode essentially becomes a pure volume-assist mode. Similarly, the pressure assist-control mode has a combination of pressure-control and pressure-assisted breaths. Again, depending upon the set machine rate, the breaths can be predominantly pressure-control or predominantly pressure-assist. Synchronized intermittent mandatory ventilation (SIMV) modes mix either (1) volume-assist and volume-control breaths with pressure-support or spontaneous breaths, or (2) pressure-assist and pressure-control breaths interspersed with pressure-support and/or spontaneous breaths. Finally, pressure-support ventilation (PSV) can be a stand-alone mode in which only pressure-support breaths are given. As a side note, the novel mode airway pressure release ventilation (APRV) is really a form of SIMV in that APRV provides essentially a pressure-assist-control breath with a very long inspiratory time and allows spontaneous breathing during both the inflation and deflation phase.
In applying these conventional ventilation modes, several design features can be used to improve patient-ventilator synchrony. For breath triggering the clinician can choose either a pressure trigger or a flow trigger, and can set the trigger as sensitive as possible. When breath triggering is impeded by intrinsic PEEP, the clinician can also add extrinsic or circuit PEEP to overcome that impedance. During flow delivery the clinician can choose either flow or pressure targeting. With flow targeting the flow is fixed. With pressure targeting the flow will adjust to maintain a target pressure. Pressure-targeted breaths also have additional features that control the rate of pressure rise, and algorithms that can adjust the pressure target to compensate for the endotracheal tube. For breath cycling, the clinician can set the volume (in volume-control and volume-assist breaths), the inspiratory time (in pressure-control and pressure-assist breaths), or the inspiratory flow cutoff (in pressure-support breaths) to optimize synchrony. Finally, the distribution of various breath types in various modes (ie, the number of controlled vs assisted breaths, and the number of assisted vs supported vs spontaneous unsupported breaths) can also be clinician-selected, based on various clinical goals. How these features can be used to optimize synchrony is described in more detail below.
Monitoring Techniques for Synchrony
There are a number of ways to monitor patient-ventilator interactions on current mechanical ventilator models.11–15 Importantly, clinical observation should always be at the forefront of monitoring. This includes not only monitoring vital signs, but also assessing the patient's comfort. While comfort may be difficult to define, discomfort is characterized by anxiety, diaphoresis, nasal flaring, and just “looking miserable.” A useful technique is to place one's hand on the chest to feel patient effort and then observe the ventilator's behavior, looking particularly for triggering delays, missed efforts, flow starvation, and mismatching of effort and breath cycling. Clinical monitoring also involves evaluating the patient's metabolic status (especially gas exchange and acid-base balance), and assuring that pain is adequately managed.
On the ventilator itself, understanding of the airway pressure and flow graphics is critical.11–13 Classical signs of asynchrony are airway pressure graphics that depict marked negative deflections during the triggering process, marked negative pressure during the flow delivery, and both positive and negative airway pressure graphics depict deflections during the cycling process.5,6,11–13 Indeed, when the area under the airway pressure graphic during an assisted breath is compared to a controlled breath, one can calculate the amount of patient work being done or patient load being borne during all 3 phases of interactive breaths.12 Esophageal and transdiaphragmatic pressure can also be used for the same purpose.
Flow graphics can also give clues to problems with patient-ventilator asynchrony.5,6,11–13 Spikes in flow or sluggish inspiratory flow often indicate that flow is not in synchrony with patient efforts. Expiratory flow is also important to evaluate. Reversals of flow during expiration may signify patient inspiratory efforts during expiration. Expiratory flow that does not return to the zero baseline before the next breath is delivered might reflect the development of intrinsic PEEP.11
Using These Conventional Features at the Bedside to Improve Patient-Ventilator Interaction
As noted above, the clinician has several tools to improve patient-ventilator synchrony. Importantly, as synchrony improves in one aspect of breath delivery (eg, triggering), patient dyspnea, and thus respiratory drive, may decrease, making other aspects of breath delivery easier to synchronize.16–18 Similarly, as asynchrony worsens in one aspect of breath delivery, dyspnea, and thus respiratory drive, may increase, making other aspects of breath delivery more difficult to synchronize. Another example is cycling asynchrony worsening air-trapping and thus triggering. Simply put: “synchrony begets synchrony, and asynchrony begets asynchrony.”
Optimizing Breath Triggering
The clinician should choose the trigger sensor (flow vs pressure) that is most sensitive and responsive to patient effort.19 Importantly, some ventilators have both types of effort sensors present and will respond to whichever signal is detected first. With either sensor, the clinician should adjust the triggering sensitivity to be as sensitive as possible without causing auto-triggering. Evaluation of the airway or esophageal pressure graphic before ventilator flow hits the target value allows quantification of the triggering load on the patient.19 The more insensitive and unresponsive the trigger is, the more negative will be the pressure-time profile. Indeed, the triggering load can be quantified either as work or pressure-time product via analysis of these tracings.
If intrinsic PEEP is producing a triggering load (a problem often seen in patients with substantial air-flow obstruction), clinical observation will reveal a marked delay between the initiation of patient effort and the beginning of flow delivery, and possibly missed efforts.20–22 Graphically there may be transient reductions in expiratory flow, due to efforts that did not trigger breaths. The airway pressure graphic, however, is often unremarkable because the patient's efforts are insufficient to overcome the intrinsic PEEP and thus are not detected in the ventilator circuit. In contrast, an esophageal pressure tracing will clearly show the elevated intrathoracic pressure from intrinsic PEEP and the ineffective patient efforts to overcome that pressure.
The first way to address this is to try reducing the intrinsic PEEP as much as possible by reducing minute ventilation (eg, reduce controlled ventilation, reduce the ventilation needs driving the patient efforts), lengthening the expiratory time, or improving the airway mechanics.23 In addition, the triggering load from intrinsic PEEP can be reduced by applying a judicious amount of circuit PEEP, which serves to narrow the difference between circuit and intrinsic PEEP.20–22,24,25 This could be guided by an esophageal pressure tracing, with the goal of providing around 70–80% of measured intrinsic PEEP as circuit PEEP.25 If an esophageal balloon is not available, an alternative approach is to empirically titrate PEEP and follow the patient's response. If the application of PEEP is benefiting the patient, the delay between effort and ventilator triggering will shorten and the patient will be observed to be more comfortable. Ironically, the breathing frequency may actually increase because more breaths that were previously missed are now being triggered. An important sign to look for is the amount of pressure required for the VT. As long as the applied PEEP is less than the intrinsic PEEP, this inspiratory pressure/VT relationship will not change. Excessive PEEP (above the intrinsic PEEP), however, will either drive up the end-inspiratory pressure (in volume-targeted ventilation) or reduce the VT (in pressure-targeted ventilation).
Optimizing Flow Delivery
Once the breath is triggered, the clinician can choose either a fixed gas flow or a variable gas flow delivery pattern, as described above. The fixed-flow breath allows the clinician control over the size of the VT, but because the flow is fixed, there is generally little opportunity for the patient to alter that flow. As a consequence, a number of studies over the last 20 years have suggested that flow asynchrony is common with volume-assisted breaths.26–28 The classic clinical sign of flow asynchrony is the airway pressure graphic literally being “sucked down” during the assisted breath, as compared to the controlled breath (Fig. 2).26,27,29 If an esophageal pressure tracing is available, marked negative deflections are prominent throughout gas delivery.
There are, however, things the clinician can do to improve synchrony with a fixed-flow breath. Because the size of the VT can impact synchrony, the VT itself can be adjusted30 Indeed in the ARDS Network trial that showed the superiority of a VT of 6 mL/kg versus 12 mL/kg, there was a provision to increase the VT to 8 mL/kg (provided the plateau pressure remained below 30 cm H2O) to improve synchrony.31 In addition to VT magnitude, the magnitude and shape (sinusoidal vs square vs decelerating) of the flow can be adjusted to enhance synchrony.16–18,32 Inspiratory-time adjustments can also be made with the application of an inspiratory pause (although this may cause air-trapping in patients with airway obstruction). These manipulations are usually applied with a trial-and-error approach while constantly monitoring the airway pressure graphic and patient comfort.
An alternative to flow-targeted breaths is the pressure-targeted breath. As noted above, the pressure-targeted breath has variable flow, and this may match up better with patient effort under many circumstances (Fig. 3). The pressure-targeted breath also has several features that can enhance synchrony. One is adjustment of the rate of pressure rise to the target.33–36 This setting goes by many names, including rise time, pressure slope, and inspiratory percent, and is essentially an adjustment of the initial flow characteristics of the pressure-targeted breath and how fast the ventilator attempts to get to the pressure target. In patients with very aggressive respiratory drive, a very rapid initial flow may synchronize easier; in contrast, in patients with very weak inspiratory drive a much slower pressure rise may be needed to enhance synchrony. A way to titrate this adjustment is simply to look at the airway pressure graphic and try to create a smooth square wave of pressure.35 Another approach is simply to look at the size of the VT as a marker of when the patient is synchronizing with the best pressure-slope setting: the larger the VT, the more the patient is probably working with the ventilator flow delivery (Fig. 4).35
Another feature of pressure-targeted breaths is the ability to compensate for the diameter of the endotracheal tube.37,38 Called by a number of proprietary names, this feature adjusts the pressure profile on the airway to create the target pressure profile at the end of the endotracheal tube. This results in a higher than set pressure target in the circuit but results in the desired square wave of pressure or more consistent CPAP application in the trachea (Fig. 5).
Importantly, the level of assistance supplied by pressure targeting will also affect synchrony in several ways. First, in the presence of air-trapping, ventilatory support reduction can reduce the air-trapping and thereby improve triggering. On the other hand, in patients without air-trapping, as the level of assistance is reduced (ie, the inspiratory pressure settings are reduced), patient respiratory drive may increase and the potential for flow asynchrony may increase.39 Reducing the inspiratory pressure is often done as part of the weaning effort as the patient recovers from respiratory failure. It is important to point out, however, that evidence-based reviews of the weaning process, done over the last 20 years, have never shown an advantage from gradual reduction in support, versus simply providing stable support and doing daily spontaneous breathing trials.40 Thus, the notion of protocolized or automated reduction in inspiratory pressure in between spontaneous breathing trials must be challenged as a desirable strategy. It may be that, if one does daily spontaneous breathing trials, the level of support in between the trials is irrelevant, so aggressive pressure-reduction strategies may only increase the need for sedation from asynchrony.
A critical question is whether clinical studies support the notion that pressure targeting provides better synchrony than flow targeting. The weight of evidence suggests that indeed this is true, as most studies have shown benefit or at least comparability.29,41–44 There are times, however, when the pressure-targeting strategy may not be better. For example, at a very low pressure setting, patient assistance is minimal, so patient work may be higher than during flow-targeted breaths.45 However, this is often an intentional pressure reduction for the purpose of weaning.
There also is the risk that excessive pressure could cause central apneas during sleep.46,47 Another concern with pressure support is in obstructive-lung-disease patients, in whom the low initial flow caused by high airway resistance and a low flow-cycle criteria with pressure support results in excessively long inspiratory time and consequent air-trapping.48 Some studies have also pointed out that the benefit of pressure targeting seems to be less when the flow-targeted strategy uses a very high inspiratory flow.32,49
One concern about pressure targeting is that VT control is lost.50 One way to address this is to use a feedback mode that allows the clinician to set the target VT and then automatically adjusts the ventilator's pressure-targeting algorithm. While this has theoretical appeal, it is possible that a patient with a high anxiety or pain drive to breathe may create a large VT that then results in inappropriate lowering of the inspiratory pressure.51 This is more common with a pressure-regulated volume-control mode and volume support than it is with adaptive support ventilation, in which the feedback control mechanism also includes an optimal VT and inspiratory-expiratory ratio.52
Optimizing Breath Cycling
There are several tools to improve cycling synchrony. As noted above, the size of the VT in volume-cycled ventilation can affect synchrony, often with larger VT satisfying the patient's respiratory drive.30 With pressure targeting the clinician has the option of using a set inspiratory time with pressure-assisted breaths, or, on most modern ventilators, of adjusting the flow-cycling criteria in pressure support.33 These features, as noted above, may be particularly important in the patient with obstructive lung disease receiving a pressure-targeted mode.
The Distribution of Ventilator Breaths May Affect Synchrony
The pattern of support may also be important in enhancing synchrony. Specifically, when more than one breath type is being delivered, the patient's respiratory controller in the brainstem is unable to predict what the next breath will be, and the potential for asynchrony may go up. In essence, the load sensed by the brainstem during one type of breath will probably alter the effort pattern response for the next breath. This has been well documented in volume-targeted SIMV,53 in which, as more and more spontaneous breaths without ventilator assistance are allowed, respiratory drive goes up, which then translates to less synchrony during the flow-targeted volume-assisted breaths. Using pressure support during these spontaneous breaths may reduce some of this effect. However, it would seem that the best clinical strategy is to provide as consistent a breath pattern as possible (ie, avoiding SIMV and supplying the fewest possible controlled backup breaths with assist-control modes). This is the most direct approach to stabilizing respiratory drive, which, conceptually, makes it easier to synchronize the ventilator and the patient.
Summary
Conventional ventilation modes have features that can monitor and enhance synchrony, including adjustment of the trigger variable, the choice of pressure-targeted versus flow-targeted breaths, and manipulation of the cycle variable. Clinicians need to know how to use these modes and monitor them properly, especially understanding airway pressure and flow graphics. Newer ventilation modes and strategies, discussed in other contributions to this Journal Conference, which involve more sophisticated flow interactive strategies and novel sensing mechanisms such as neuromuscular signals, hold promise for improving synchrony in the future, in patients with very active respiratory drive.
Discussion
Epstein:
Neil, you showed data from the study by Jubran1 that found that pressure support led to cycling problems in patients with COPD, but wasn't that only at fairly high levels of pressure support, above 15 cm H2O?
MacIntyre:
It requires a fair amount of pressure support to really magnify this issue. But you know, Scott, I still think it's important to assess any time you have someone with an obstructive disease in pressure support, just to make sure you don't run into trouble. When it happens, you get long inspiratory times and clear air-trapping, and it's just a question of being aware of it. You're right that it certainly becomes more obvious and more manifest if you're using a perhaps excessive level of pressure support.
Epstein:
I'm not an advocate of it, but the cycle criteria of just 5 L/min may not be an ideal setting.
MacIntyre:
My conclusion is not to abandon pressure support in those patients, but to recognize this possibility and to recognize that you have a lot of tools that you can use to fix it. Maybe a lower pressure support: certainly adjusting the cycle criterion. What I do is put the patient on pressure assist and set the inspiratory time.
Epstein:
I have no particular opinion about automated weaning or the SmartCare system, but I think it is important to note that the Australian study1 came from a very different setting; I think those units had 24-hour-a-day attending coverage, and a much higher caregiver-to-patient ratio than in the Brochard study.2 So maybe they were not studying quite the same patient population.
MacIntyre:
I think it's absolutely critical in looking at any clinical study (and I'm preaching to the choir here) to recognize the potential for 3 fatal flaws:
Picking the wrong population that either would not benefit from or would be harmed by the intervention. I think large studies that take all comers are guilty of that.
Picking an end point that doesn't make any sense, or trying to use a physiologic end point that may have no relationship whatsoever to outcome.
Failing to make sure your control group is a fair control group.
With those thoughts in mind, I'd like to address a few recently published automated weaning studies. We've had the weaning guidelines for 9 years now, and I get asked to update them from time to time, but I really have no interest in updating them because I don't think anything that new has come out. Clearly, the guidelines state that the daily SBT [spontaneous breathing trial] is the way to manage these patients, and to be aggressive about doing those. If you're going to sell me on SmartCare or another automated system, it's got to be compared to a control group that gets a daily SBT. I'm not sure you need one-to-one nursing to do that, what you need is a team who understands the daily SBT requirement and does it.
Kacmarek:
I agree with everything you said, Neil. But that SmartCare trial demonstrated at least equivalence to SBTs. It showed that in the average ICU throughout theworld the SmartCare was a better approach because a daily SBT is not normally done in the average ICU. In my own institution, where we have harped and harped on doing daily SBTs, they are not always done every day. If a ventilation mode ensures that the patient gets weaned as quickly as with a therapist-driven protocolized SBT, that mode is pretty good to me. The study does present evidence in support of SmartCare.
MacIntyre:
But the notion is that SmartCare tells you to do a daily SBT. A cheaper, simpler way to do it would be to put up a sign that reads “Do a Daily SBT.”
Kacmarek:
But SmartCare will do the SBT for you, so you don't have to do anything. The closed-loop controlled approach is currently available in Europe; it's not yet approved in the United States. SmartCare will decrease pressure support to the level that meets criteria for the SBT and does the SBT automatically, then puts them back on pressure support, and then tells you if the patient is ready to be discontinued from ventilatory support.
MacIntyre:
I like the part about telling you and doing an automatic SBT for you. My problem is that it first must reduce (wean) the pressure support to a minimal level before it proceeds to an SBT. Remember that the 2 large weaning trials1,2 in the 1990s showed that weaning often delayed conducting an SBT. My point is that I think that you may end up wasting a day or more weaning the pressure support when you could've just done an SBT that day. One of the assumptions of SmartCare is that you've got to wean the pressure support to a certain level before you can do an SBT, and I would challenge that assumption.
Kacmarek:
Neil, I agree with you 100%. Daily SBTs is the way everybody should be doing it, but it is not being done. So whether or not we believe it's the best approach, if this automated mode is equivalent to the best approach, then it's pretty good. That's what you said, and that is what the data indicate.
MacIntyre:
If I could design the system, it would ask 4 basic questions:
Is the respiratory status stable or improving?
Is gas exchange at a reasonable level? And you can define whatever reasonable level you want.
Are the hemodynamics stable? An easy way to do that is to ask if they're on pressors.
Will they take a spontaneous breath?
If they meet those 4 criteria, I think they should have an SBT. If they have a machine that will do that for me, I'll get one.
Chatburn:
Wouldn't you make an exception for patients who have failed multiple SBTs and are ventilator-dependent? In those patients doesn't it look like you have to more gradually reduce the support?
MacIntyre:
Rob, you're exactly right. The population you just mentioned used to be very uncommon, but it's certainly becoming more common. I had the privilege of being involved with a prolonged-mechanical-ventilation consensus group, and that group agreed with you and said that if the patient has had multiple SBT failures and you're looking at 2 or 3 weeks on the ventilator, maybe daily SBT “flogs” are not in that patient's best interest. The consensus from that group is interesting: they said that what you need to do is to find out what level of support they're on, get it to at least below 50% of that level, and then restart the SBT attempts. I agree with you: the prolonged ventilator-dependent patient is a more challenging one.
Kallet:
Neil, I want to touch on something you said earlier that I think is extremely important to this conference. You talked about mixing breath types and how that might confuse the patient, and this is something that we discovered in one of our work-of-breathing studies.1 My impression is that with dual modes such as AutoFlow and APRV [airway pressure release ventilation], if the breathing environment is constantly changing (either directly trying to adapt to the patient's demand or irrespective of it), that it can increase the work of breathing and increase central respiratory drive.
I thought back to the times when I've gotten the wind knocked out of me playing sports. You're lying on the ground gasping for air and your brain is throbbing with an incredible drive to breathe! But in that situation, you only have only one external signal to deal with: an airway opening pressure that is ambient and constant. If you're getting support from a ventilator, if that signal's constantly changing, trying to adapt to you, you may get into this feedback loop that just spins off.
What I didn't expect to find in our study was that volume control with a high flow would be better, and next best was pressure control. That's when I started to think that maybe if you hit the patient in distress with a constant volume or constant airway pressure, and a constant inspiratory time, that it gives them something to lock into. It may not apply to weaning, but when the patient is in distress, we might be getting too smart for ourselves trying to find modes that constantly adapt to the patient, when, ironically, the patient is trying to find something to adapt to!
MacIntyre:
Rich, that makes a lot of sense to me. I would point out one thing, though, about respiratory drive. I've been intrigued over the last several years by a number of papers that have pointed out that none of us has a homogenous constant tidal volume. It's natural to have some variability, and that volume variability has benefits in terms of gas distribution. Having said that, I think having a somewhat reliable delivery pattern with every breath from the ventilator does make some sense.
Branson:
I agree with Bob that the promise of closed-loop weaning is consistency and preventing people going off in their different directions. I'm with you. There were limitations to that study, but I think that's really where the advantage is. And if we were sitting here with the marketing managers of a company, the next question would be, “So, what would you be willing to pay for that?” I think it's $5,000 to $6,000 to add SmartCare to your Dräger ventilator. The question is, depending on how many ventilators you have, what's the total cost/potential benefit of that in your particular ICU?
Kacmarek:
Two days in the ICU over a year and you'd save the money. Just 2 days, not 2 patients.
MacIntyre:
At our place, our education coordinator Bob Campbell routinely monitors the things that I think are important: how often do we exceed plateau pressure limits, how often do we exceed the 6-mL/kg tidal volume limit, and how often do we do the daily SBTs when they're indicated? I'm the first to admit that we're not 100% on any of those parameters, but we're working on it.
Parthasarathy:
If there's that variability or that issue in ivory tower universities, then it is certainly going to be an issue in community-based hospitals. This is where I think we need to move from evidence-based medicine (derived from randomized controlled trials) to translating such knowledge to the patient's bedside. There is this whole field of implementation science or cost-effectiveness medicine. These are not physiology researchers or critical care researchers: they are health-services researchers. So if someone were to do a study wherein they study implementation science in that they study the effect of SmartCare on bedside implementation of such principles in a community rather than tertiary-care hospital, then the odds are extremely good that they will show improvement and the cost-effectiveness of such a system. I think that because we have the equivalence in one particular setting that doesn't mean that the SmartCare should never see the light of day again.
MacIntyre:
I agree to a certain extent. I think machines that can remind us to do things like that are important. Does it have to be something that incorporates pressure-support weaning and then automatically does it, or could there be a simpler $500 addition such as a decision-support tool on your ventilator that lights up a section of the display in fancy colors and indicates that this needs to be done, that your tidal volume's too high, that your PEEP is off the table, or that you haven't done your SBT.
Sassoon:
In the graph that you showed us of volume control and pressure control, there's a concavity toward the Y axis on the airway-pressure waveform with volume control. In that case, if you just raise the flow rate, wouldn't that just take care of it, similar to pressure control?
MacIntyre:
It does sometimes. We frequently put patients on volume assist and many of them do just fine; I don't want to make it sound like it's a public health hazard, that volume control is harming people.
Branson:
SIMV [synchronized intermittent mandatory ventilation] is a public health hazard.
Sassoon:
Have you used pressure-control volume-assured ventilation? In my experience that seems to be a better mode than just plain pressure control.
MacIntyre:
We kind of like the pressure-regulated volume control. I'm very anxious to hear Rich's presentation tomorrow, because he's collected some interesting data on that. It does have some logic to it; it tries to stay more or less on the ARDS [acute respiratory distress syndrome] Network algorithm. There's some logic, if you want to use pressure-targeted modes, that putting that feedback mode feature into it might help you stay within your target ranges a little better. I know Rich has some data that suggest that's not always the case, and I think we'll have some fun talking about that.
Kallet:
Actually, I'm speaking on APRV tomorrow.
MacIntyre:
Well, I'm going to make you talk about it, and PRVC [pressure-regulated volume control] as well.
Kallet:
OK.
MacIntyre:
Rich has shown some interesting data, and we actually see this too in the ARDS Network data. When we looked at when and where we were violating 6 mL/kg (and all 12 sites do violate 6 mL/kg), it's almost always happening at very low levels of support in the so-called weaning phase, when they often are on pressure support and their respiratory drive has recovered, and they should probably be extubated a lot faster than we're doing it. At least in our institution, most of our tidal-volume violations are at very low levels of pressure support or pressure assist, and perhaps we need that reminder to get the tube out a little faster.
Kallet:
I think the problem with dual modes like APRV is just that. The problem happens when the patient wants a higher tidal volume than the target; it'll give it to them but it thinks the compliance is improving, so it brings down the pressure.
We've all but outlawed it at San Francisco General Hospital. We had a lot of problems when we used dual-mode AutoFlow as our default mode. In a 6-month period alone, I found 4 patients in overt shock on AutoFlow with a peak pressure of 12 cm H2O and a pH of around 7.15. Two of these patients were in cardiogenic shock, so it didn't exactly help their after-load!
The rule of thumb is basically that if your peak pressure on someone who's very sick is less than 20 cm H2O, you need to take a closer look. If your peak pressures on a dual mode are in the mid-20s to mid-30s, I don't have a problem with it at all. It's a clinician problem, the same way that asynchrony is primarily a clinician problem, in that a lot of times the clinician is not recognizing that there's a problem going on.
MacIntyre:
My last comment is that we have not outlawed PRVC at Duke.
Footnotes
- Correspondence: Neil R MacIntyre MD FAARC, Division of Pulmonary and Critical Care Medicine, Duke University Hospital, Box 3911, Durham NC 27710. E-mail: neil.macintyre{at}duke.edu.
Dr MacIntyre presented a version of this paper at the 46th Respiratory Care Journal Conference, “Patient-Ventilator Interaction,” held March 19-21, 2010, in Cancún, Quintana Roo, Mexico.
Dr MacIntyre has disclosed a relationship with CareFusion.
- Copyright © 2011 by Daedalus Enterprises Inc.