Early application of airway pressure release ventilation may reduce the duration of mechanical ventilation in acute respiratory distress syndrome

We performed this trial in the critical care medicine department of West China Hospital of Sichuan University, Sichuan province, China. This study was approved by the ethics committee of West China Hospital of Sichuan University in accordance with the Helsinki Declaration. Written informed consent was obtained from the patients’ authorized surrogates. The clinical trial registration number was NCT02639364.

Patients who met the inclusion criteria were enrolled in the study from May 2015 to October 2016: fulfilled the diagnostic criteria of ARDS, according to the Berlin definition [16]; had a ratio of partial pressure arterial oxygen and fraction of inspired oxygen (PaO₂: FiO₂) of ≤250 during invasive mechanical ventilation [17]; had received endotracheal intubation and mechanical ventilation for <48h prior to inclusion [17]. The exclusion criteria of the study were as follows: pregnancy; anticipated duration of invasive mechanical ventilation for <48 h; intracranial hypertension (suspected or confirmed); neuromuscular disorders that are known to prolong the need for mechanical ventilation; severe chronic obstructive pulmonary disease; preexisting conditions with an expected 6-month mortality exceeding 50%; presence of documented barotrauma; treatment with extracorporeal support (ECMO) at enrollment; refractory shock; lack of commitment to life support; age of <18 years or >85 years. Eligible patients were randomly assigned to the APRV group or to the LTV group by random selection of opaque sealed envelopes for consecutive patients from a box of 138 envelopes. Each envelope contained a number by a random allocation process using a computer-generated random block design.

Respiratory therapists performed ventilator management. All patients were initially ventilated with volume assisted-control ventilation (VCV) using a Puritan Bennett™ 840 Ventilator (Covidien, Medtronic Inc. Minneapolis, MN) prior to randomization to the APRV study arm or LTV study arm. In both groups, the mechanical ventilation goals were to maintain plateau airway pressure (P_plat) at no more than 30 cmH₂O, PaO₂ at between 55 and 100 mm Hg (or pulse oximeter between 88 and 98%), and arterial pH at ≥7.30. [4, 18].

In the LTV group, tidal volume target (V_T) was 6 mL/kg predicted body weight (PBW), with allowances for 4–8 mL/kg PBW to minimize asynchrony between the patient and ventilator; PEEP levels were adjusted, guided by the PEEP-FiO₂ table, and then V_T and the respiratory rate were regulated to achieve the above target pH and P_plat values according to the ARDSnet protocol [4, 19]. In the setting of hypotension (mean arterial pressure of <60 mm Hg) or pneumothorax occurrence, PEEP levels were allowed to be further modified, according to the individual patient’s needs; if the PaO₂:FiO₂ ratio was <150 with FiO₂ > 0.6, PEEP levels could be further titrated by the ways of optimum respiratory compliance or oxygenation, at the clinician’s discretion. If the patient presented severe respiratory acidosis (pH < 7.15), the respiratory rate was increased to 35 breaths per minute, with titrations made in V_T (P_plat target of 30 cmH₂0 may be exceeded), according to the ARDSnet protocol [4]. If severe respiratory acidosis persisted (pH < 7.15), NaHCO₃ could be given [Appendix in Electronic Supplementary Material (ESM)].

Patients were transitioned from their previous volume assist-controlled ventilation to APRV with the following initial settings: high airway pressure (P_high) was set at the P_plat measured at the previous VCV settings, not to exceed 30 cmH₂O; low airway pressure (P_low) was set at 5 cmH₂O (minimal pressure level was used to prevent atelectasis per standard practice); duration of release phase (T_low) was initially set at one- to 1.5-fold the expiratory time constant, and then adjusted to achieve a termination of peak expiratory flow rate (PEFR) of ≥50% of PEFR; release frequency was 10–14 frequency/min; duration of P_high (T_high) was indirectly calculated based on the T_low and release frequency [9, 20]; initially spontaneous respiratory level was targeted as spontaneous minute ventilation (MV_spont), approximately 30% total minute ventilation (MV_total) (for details on the APRV settings for titration, see ESM Appendix Tables 3–5).

In the both groups, analgesia and sedation were managed to achieve the desired level of analgesia and sedation. The analgesia target level was a Critical-Care Pain Observational Tool (CPOT) score of 0–2, and the sedation goal was a Richmond Agitation Sedation Scale (RASS) score of − 2 to 0. If patients exhibited anxiety, agitation, and/orrespiratory distress, or they fought the ventilator, they would receive deeper sedation at less than a RASS score of − 2. According to our local sedation procedure, RASS and CPOT scores were assessed and recorded every 4 h (or more frequently when indicated) by the nursing staff, who adjusted the dosages of analgesic and sedative drugs to maintain the analgesia and sedation target level. In the APRV group, respiratory therapists would further titrate APRV settings and dosages of analgesics and sedatives to achieve the target level of spontaneous breathing level [21] (for details, see ESM Appendix Tables 3–5).

For patients with severe hypoxemia (with no response to the assigned protocol and a PaO₂:FiO₂ ratio of <100 during invasive mechanical ventilation for at least 12 h), clinicians could apply other supportive therapies for hypoxemia (e.g., recruitment maneuvers, prone positioning, neuromuscular blockade, or inhalation nitric oxide) in both groups (see ESM Appendix for details). Patients could receive rescue measures (including high frequency oscillatory ventilation or ECMO) at the clinician’s discretion, in case of any one of the following life-threatening events: refractory hypoxemia (PaO₂ < 55 mm Hg with an FiO₂ of 1.0), refractory barotrauma (chest tube with active air leak, persistent pneumothorax, and/or subcutaneous emphysema despite pleural space drainage), refractory respiratory acidosis (pH of ≤7.15), or refractory shock (even if sufficient fluid resuscitation and usage of vasoactive drugs).

Additionally, physicians applied usual care interventions for the general management of critically ill patients, according to the current guideline standards. Starting the first day following enrollment, in the LTV group if patients received deeper sedation (RASS score of <−2), the physicians would once daily interrupt the sedation, and the respiratory therapists would manage patients with the Spontaneous Breathing Trials (SBT) safety screen every morning. Those patients who passed the SBT safety screen underwent a 30-min SBT with a pressure support ventilation of 5–7 cmH₂O, PEEP of 5 cmH₂O, and FiO₂ of ≤40% [21]. In the APRV group, in the first stage, as published previously [15, 20], P_high was gradually reduced by 2 cmH₂O, simultaneously with a reduction in release rate by two frequencies/min, twice daily unless the patient’s cardiopulmonary function deteriorated. In the second stage, when patients achieved the criteria with a P_high of 20 cmH₂O on 40% FiO₂, the respiratory therapist immediately started to perform the same weaning protocol with SBT trial as in the LTV group [17]. When the SBT was successful, physicians and respiratory therapists decided to extubate the patients (for details see ESM Appendix).

The primary endpoint was the number of ventilator-free days at day 28 (if patients died during the 28-day period after enrollment, the number of ventilator-free days was zero). The secondary endpoints included oxygenation and respiratory mechanics, such as P_plat, mean airway pressure, respiratory system compliance at baseline and on days 1, 2, 3, and 7, as well as clinical outcomes [the length of stay in the intensive care unit (ICU) and hospital, ICU mortality and hospital mortality, and the occurrence of adverse events]. (P_plat and respiratory system compliance measurements during the APRV are detailed in ESM Appendix. Fig. S1).

The primary outcome was the number of ventilator-free days at day 28. The mean (± standard deviation) number of ventilator-free days from day 1 to day 28 is 14.5 ± 10.4 days in the low tidal volume and lower PEEP group according to Brower and colleagues, the ARDS network [22]. Putensen reported that APRV could shorted the duration of ventilator support by 6 days in patients at risk of ARDS compared with those pressure-controlled ventilation [11]. We conservatively estimated that a sample size of 110 patients would be required to detect an increment of 5 days in the number ventilator-free days at day 28 in the APRV group with 80% power and a two-sided significance level of 0.05. In total, 138 patients were enrolled in the study in order to manage the drop-outs.

Data are expressed as the mean ± standard deviation, and as the median and interquartile ranges (IQR), or percentages. Continuous variables with a normal distribution were analyzed with the Student’s t test, Continuous variables with non-normal distribution were compared with the use of the Kruskal–Wallis analysis of variance. Dichotomous or nominal categorical variables were analyzed by either the Pearson Chi-square or Fisher’s exact test. The trend was assessed over time in oxygenation and respiratory mechanics repeated measurements by comparing the LTV group and APRV group at baseline and on days 1, 2, 3, and 7, with the use of the repeated-measures analysis. A two-sided P value of <0.05 was considered to indicate statistical significance.

Respiratory parameters and arterial blood gas measurements at baseline in the APRV group were similar to those in the LTV group, with the exception of respiratory rate which was higher in the APRV group (P = 0.039) (Table 2). On the third therapeutic day (Table 2), respiratory system compliance and the PaO₂:FiO₂ ratio were significantly improved in the APRV group compared to the LTV group (P < 0.001, respectively). The ventilation setting frequency was lower in the APRV group (P = 0.002), but the monitoring of respiratory rates was similar in both groups. The values of P_peak, PEEP, and P_plat were significantly lower in the APRV group (P < 0.01), the mean airway pressure was 5.8 cmH₂O higher in the APRV group than in the LTV group (P < 0.001), but the driving pressure was similar in both groups. The mean spontaneous minute ventilation was 1.78 ± 1.37 L/min in the APRV group. The total minute ventilation was lower in the APRV group than in the LTV group (P = 0.001); however, the values of PaCO₂ and pH were similar in both groups. Heart rate and arterial blood pressure were slightly improved (P < 0.05, respectively).

On days 1, 2, 3, and 7, compared to the LTV group, the mean airway pressure was higher in the APRV group (P < 0.001, by repeated-measures analysis of variance) (Fig. 2b) and respiratory system compliance and PaO₂:FiO₂ were significantly better in the APRV group (P = 0.003 by repeated-measures analysis of variance) (Fig. 2c, d). On day 1, the PaO₂:FiO₂ value was 66.3 mmHg higher in the APRV group than in the LTV group (P < 0.001). Heart rates were lower and mean arterial pressures were a little higher in the APRV group than in the LTV group on days 2, 3, and 7 (P < 0.05 by repeated-measures analysis of variance) (Fig. 2e, f). The average doses of norepinephrine were similar (P = 0.612) (Fig. 2g). Compared with the LTV group, the sedation depth in the APRV group was lighter (P < 0.001) (Fig. 2h), and the average doses of fentanyl and midazolam were significantly lower (P < 0.01) (Fig. 2i, j), and the average doses of propofol were similar (P = 0.112) (Fig. 2k).

Study outcomes are presented in Table 3. The APRV protocol was associated with an increased number of ventilator-free days on day 28 than the LTV protocol [median 19 days (IQR 8–22) vs. 2 days (IQR 0–15), respectively; P < 0.001] (Table 3 and Fig. 3); this result was supported by the per-protocol analysis results which also showed a similar difference [median 19 days (IQR 11–22) vs. 8 days (IQR 0–16), respectively; P < 0.001] (ESM Appendix Table S5). Although there were more patients with coexisting chronic diseases and lower sedation depth in the APRV group than in the LTV group (P < 0.05), only lighter sedation increased ventilator-free days at day 28, and APRV still significantly increased ventilator-free days at day 28 (P < 0.001) according to the multiple linear regression analysis for correction of the coexisting chronic diseases and sedation depth differences (ESM Appendix Table S4). There was a higher rate of successful extubation in the APRV group than in the LTV group (66.2 vs. 38.8%; P = 0.001), and fewer patients underwent tracheostomy in the APRV group (P = 0.013). The APRV protocol significantly decreased the length of ICU stay (P = 0.015). The ICU and hospital mortality rates and length of hospital stay were similar for both groups. During the course of the study, more patients in the LTV group received neuromuscular blockers, recruitment maneuvers, and prone ventilation than in the APRV group (P < 0.05).

The data of the present study are in agreement with previously reported clinical and experimental findings [8‐11, 21, 23], namely, that the early use of this APRV protocol in patients with ARDS significantly decreased plateau airway pressure, elevated mean airway pressure, and improved oxygenation and respiratory system compliance, in comparison with LTV ventilation. Furthermore, there was no difference in PaCO₂ and pH between the groups, despite APRV with lower minute ventilation, which indirectly indicated APRV decreasing dead space ventilation.

However, at present, data are only available from a limited number of small randomized prospective human studies with different APRV settings, with some studies showing benefits of APRV on pulmonary function and others showing similarities, as compared with CPPV or LTV [8, 11, 12, 15]. For example, one small randomized prospective trial [15] showed that adult trauma patients with acute respiratory failure on APRV or LTV had similar physiological parameters. However, the APRV methodology used in that study was outdated: the upper limit of P_high was 40 cmH₂O, while current evidence suggests that inspiratory-end pressure should be limited to 30 cmH₂O [4]; the T_low was set at 25–75% of the PEFR, while T_low of <50% of PEFR could result in dynamic heterogeneity between inspiration and expiration [10]. According to recent experimental findings, we set the P_high not to exceed 30 cmH₂O and the T_low to be at ≥50% of PEFR; these settings were combined with APRV settings and sedation titration to achieve the spontaneous breath target level.

There are collateral channels of ventilation, such as pores of Kohn, which might be additional pathways to facilitate recruitment and redistribute alveolar volume (pressure) throughout the lung over time [24]. The results of previous studies indicate that the process of recruitment and decruitment of lung units should be determined not only by pressure but also by time [25]. For heterogeneous lung injury, during APRV ventilation, the proper elevated baseline airway pressure (P_high) and prolonged duration of P_high would optimize the recruitment of alveoli gradually over time, while prevention of overinflation, and brief release phase (T_low) could permit only partial lung volume loss at the release phase, avoid cyclic alveoli collapse, and provide dynamic homogeneity [10]. Recent animal experiments [8‐10, 21, 23] have also documented that the updated APRV methodologies attenuate lung injury, preserve surfactant protein and lung architecture, and improve oxygenation, resulting in dynamic alveolar homogeneity without any increase in lung stress and strain.

Additionally, during APRV, allowing moderate spontaneous breath level at the P_high phase (providing sufficient PEEP) favored lung recruitment and improved ventilation/perfusion matching and lung homogeneous aeration, while minimizing pendelluft and its associated injury [20, 26‐28].

The hemodynamic performance and sedation requirement of the patients on APRV in this study are in accordance with previous study findings [11, 29, 30]. APRV favored hemodynamic improvement and reduced sedative and paralysis use, despite the higher mean airway pressure. Ventilation with APRV permitting spontaneous breaths decreased the intrathoracic pressure, thus improving systematic venous return and cardiovascular performance and reducing sedation requirement and the need for paralysis, which may decrease the cardiovascular depression caused by elevated airway pressures [10, 20, 30].

This study showed that the APRV group was associated with more days without mechanical ventilation at day 28 and a shorter ICU stay than the LTV group. This finding is consistent with previously published results [11], and possible explanations for this finding are as follows. Firstly, early use of APRV improved pulmonary function, such as gas exchange and respiratory compliance. Recent experiments have also documented that early preventative use of APRV can more effectively block ARDS development than LTV [9, 21]. Putensen et al. reported that the use of APRV in patients with ARDS after 72 h on pressure-control ventilation improved but did not restore gas exchange and lung mechanics, and prolonged the mechanical ventilation and ICU stay [11]. Secondly, APRV allows moderate spontaneous breathing, reduces sedation and paralysis requirements, and decreases the duration of mechanical ventilation [11, 20, 30, 31]. In the present study, respiratory therapists titrated the APRV settings and dosages of analgesics and sedatives to achieve a moderate spontaneous breath level at the P_high phase. Our results also show that APRV was associated with lighter sedation, which could increase the number of ventilator-free days at day 28. Thirdly, in our study there was respiratory therapist-guided weaning protocol with the SBT trial in the LTV group. In the APRV group, in the first stage, to avoid aggressive weaning, the weaning process consisted of simultaneously decreasing both P_high by 2 cmH₂O and the release rate by two frequencies/min, twice daily unless the patient’s cardiopulmonary function deteriorated. In the second stage, when patients achieved the criteria with a P_high of 20 cmH₂O on 40% FiO₂, respiratory therapists also performed the weaning protocol with the SBT trial as in the LTV group. Two trauma population studies have shown that APRV may increase the number of ventilator days; however, the APRV settings were outdated, and no formal weaning protocol was used [13, 15]. The current primary APRV weaning process is based on gradual withdrawal, using an alternate decrease in P_high by 2 cmH₂O, followed by an increase in T_high of 0.5–1.0 s [15], and extubation is assessed until the criteria of a P_high of 12 cmH₂O on 40% FiO₂ is achieved [10, 13, 15, 20]. However, evidence suggests that daily SBT can expedite weaning and reduce the duration of mechanical ventilation as compared with gradually reducing ventilator support [32].

There are several limitations to our study. First, the study was not blinded, as the ventilator settings were obviously different. Secondly, the sample size was small. APRV has evolved into a highly sophisticated, physiology-driven, dynamic mechanical breath profile with precise settings [13], thus a possibility of knowledge bias by the staff was another limitation. However, prior to conducting our study, we first conducted a single-center randomized controlled study and found that all of the respiratory therapists were well trained and skillfully used this study protocol. Thirdly, there were more patients with coexisting chronic diseases in the LTV group than in the APRV group (P = 0.029). Using a multivariable analysis for the correction of the coexisting chronic diseases difference, APRV was independent of increasing ventilator-free days at day 28. Finally, in accordance with our APRV protocol, in addition to nursing staff, respiratory therapists were able to further titrate APRV settings and dosages of analgesics and sedatives to achieve the target level of spontaneous breathing. The results of our study show that APRV was associated with lighter sedation, which could increase the number of ventilator-free days at day 28. However, APRV still significantly increased ventilator-free days at day 28 after correcting the sedation difference. Additionally, this study did not measure the patient–ventilator interaction. The questions of whether APRV permitting spontaneous breathing could promote the patient–ventilator synchrony and how the patient–ventilator dyssynchrony could affect the outcome require further study.