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Objectives Postoperative pulmonary complications increase mortality, length, and cost of hospitalization. A better diaphragmatic strength may help face an increased work of breathing postoperatively. We, therefore, sought to determine if a low preoperative diaphragm thickening fraction (TFdi) determined by ultrasonography helped predict the occurrence of postoperative pulmonary complications after cardiac surgery independently of indicators of frailty, sarcopenia, and pulmonary function. Design Prospective observational cohort study. Setting Montreal Heart Institute, an academic cardiac surgery center in Canada. Patients Adults undergoing nonemergency cardiac surgery. Interventions We measured the preoperative thickness of the right and left hemidiaphragms at their zone of apposition at end-expiration (Tdi,ee) and peak-inspiration (Tdi,ei) with ultrasonography. Maximal thickening fraction of the diaphragm during inspiration (TFdi,max) was calculated using the following formula: TFdi,max = (Tdi,ei-Tdi,ee)/Tdi,ee. We also evaluated other potential risk factors including demographic parameters, comorbidities, Clinical Frailty Scale, grip strength, 5-meter walk test, and pulmonary function tests. We repeated TFdi,max measurements within 24 hours of extubation. The primary composite outcome of this study was the occurrence of postoperative pulmonary complications, defined as pneumonia, clinically significant atelectasis, or prolonged mechanical ventilation (> 24 hr). Measurement and main results Of the 115 patients included, 34 (29.6%) developed postoperative pulmonary complications, including two with pneumonia, four with prolonged mechanical ventilation, and 32 with clinically significant atelectasis. Those with postoperative pulmonary complications had prolonged ICU and hospital length of stays. They had a lower TFdi,max (37% [interquartile range, 31-45%] vs 44% [interquartile range, 33-58%]; p = 0.03). In multiple logistic regression, a TFdi,max less than 38.1% was associated with postoperative pulmonary complications (odds ratio, 4.9; 95% CI, 1.81-13.50; p = 0.002). All patients who developed pneumonia or prolonged mechanical ventilation had a TFdi,max less than 38.1%. Respiratory rate and diabetes were also independently associated with postoperative pulmonary complications, while pulmonary function tests and the assessed indicators of frailty and sarcopenia were not. Conclusions A low preoperative TFdi,max can help to identify patients at increased risk of postoperative pulmonary complications after cardiac surgery.

OBJECTIVES: Inspiratory holds with measures of airway pressure to estimate driving pressure (elastic work) are often limited to patients without respiratory effort. We sought to evaluate if measures of airway pressure during inspiratory holds could be used for patients with spontaneous respiratory effort during mechanical ventilation to estimate the degree of spontaneous effort and elastic work. DESIGN: We compared the direction and degree of change in airway pressure during inspiratory holds versus esophageal pressure through secondary analysis of physiologic data. SETTING: ICUs at Children's Hospital Los Angeles. PATIENTS: Children with pediatric acute respiratory distress syndrome with evidence of spontaneous respiration while on pressure control or pressure support ventilation. INTERVENTIONS: Inspiratory hold maneuvers. MEASUREMENTS AND MAIN RESULTS: From airway pressure, we defined "plateau - peak pressure" as Pmusc, index, which was divided into three categories for analysis (< -1 ["negative"], between -1 and 1 ["neutral"], and > 1 cm H2O ["positive"]). A total of 30 children (age 36.8 mo [16.1-70.3 mo]) from 65 study days, comprising 118 inspiratory holds were included. Pmusc, index was "negative" in 29 cases, was "neutral" in 17 cases, and was "positive" in 72 cases. As Pmusc, index went from negative to neutral to positive, there was larger negative deflection in esophageal pressure -5.0 (-8.2 to 1.9), -5.9 (-7.6 to 4.3), and -10.7 (-18.1 to 7.9) cm H2O (p < 0.0001), respectively. There was a correlation between max negative esophageal pressure and Pmusc, index (r = -0.52), and when Pmusc, index was greater than or equal to 7 cm H2O, the max negative esophageal pressure was greater than 10 cm H2O. There was a stronger correlation between Pmusc, index and markers of elastic work from esophageal pressure (r = 0.84). CONCLUSIONS: The magnitude of plateau minus peak pressure during an inspiratory hold is correlated with the degree of inspiratory effort, particularly for those with high elastic work. It may be useful to identify patients with excessively high effort or high driving pressure.

High-flow nasal cannula is increasingly used in the management of respiratory failure. However, little is known about its impact on respiratory effort, which could explain part of the benefits in terms of comfort and efficiency. This study was designed to assess the effects of high-flow nasal cannula on indexes of respiratory effort (i.e., esophageal pressure variations, esophageal pressure-time product/min, and work of breathing/min) in adults.A randomized controlled crossover study was conducted in 12 patients with moderate respiratory distress (i.e., after partial recovery from an acute episode, allowing physiologic measurements).Institut Universitaire de Cardiologie et de Pneumologie de Québec, QC, Canada.Twelve adult patients with respiratory distress symptoms were enrolled in this study.Four experimental conditions were evaluated: baseline with conventional oxygen therapy and high-flow nasal cannula at 20, 40, and 60 L/min. The primary outcomes were the indexes of respiratory effort (i.e., esophageal pressure variations, esophageal pressure-time product/min, and work of breathing/min). Secondary outcomes included tidal volume, respiratory rate, minute volume, dynamic lung compliance, inspiratory resistance, and blood gases.Esophageal pressure variations decreased from 9.8 (5.8-14.6) cm H2O at baseline to 4.9 (2.1-9.1) cm H2O at 60 L/min (p = 0.035). Esophageal pressure-time product/min decreased from 165 (126-179) to 72 (54-137) cm H2O • s/min, respectively (p = 0.033). Work of breathing/min decreased from 4.3 (3.5-6.3) to 2.1 (1.5-5.0) J/min, respectively (p = 0.031). Respiratory pattern variables and capillary blood gases were not significantly modified between experimental conditions. Dynamic lung compliance increased from 38 (24-64) mL/cm H2O at baseline to 59 (43-175) mL/cm H2O at 60 L/min (p = 0.007), and inspiratory resistance decreased from 9.6 (5.5-13.4) to 5.0 (1.0-9.1) cm H2O/L/s, respectively (p = 0.07).High-flow nasal cannula, when set at 60 L/min, significantly reduces the indexes of respiratory effort in adult patients recovering from acute respiratory failure. This effect is associated with an improvement in respiratory mechanics.

INTRODUCTION: Although initially compared to ARDS, COVID-19 pneumonitis presents with unique features, suggesting tailored approaches may be required Gattinoni et al recently described two distinct phenotypes of COVID-19, L-type and H-type, with low or high elastance, V/Q ratio, lung weight, and recruitability, respectively METHODS: 76 F with lymphoma presented with worsening cough and fever and tested positive for COVID-19 She was saturating 93% on room air with no increased work of breathing (SpO2/FiO2 442), suggesting L-phenotype CT chest showed multifocal groundglass opacities On day 3, she developed worsening hypoxemia (SpO2/FiO2 158 3) Despite a significant drop in SpO2/FiO2 ratio, she denied subjective dyspnea and had no increased work of breathing, continuing to demonstrate L-phenotype The patient requested to avoid invasive mechanical ventilation and a timed trial of HFNC was agreed upon She received therapies as per institutional protocol, which included remdesivir, convalescent plasma, steroids, aspirin once daily, enoxaparin 40 mg twice daily, and three doses of tocilizumab Despite receiving all this, she continued to worsen, requiring 100% FiO2 HFNC A 7-day course of anakinra was started The patient continued to remain an L-phenotype with no increased work of breathing Following the first dose of anakinra, FiO2 requirements decreased significantly from 100 to 70%, and over the course of 2 weeks, she weaned to 2L NC, making a complete clinical recovery and was discharged to a long-term acute care facility for further rehabilitation RESULTS: The difference in pulmonary presentation and treatment of COVID-19 remains undetermined Our patient had severe hypoxemia with no increased work of breathing, consistent with L-phenotype Due to a high provider to patient ratio at our institution, we were able to provide a prolonged time limited trial of HFNC and avoid invasive mechanical ventilation We found the patient's respiratory status dramatically improved following anakinra The treatment of select COVID-19 patients with HFNC and anakinra may avoid invasive mechanical ventilation, preventing ventilator complications and conserving resources

OBJECTIVES: To calculate an index (termed Pmusc/Eadi index) relating the pressure generated by the respiratory muscles (Pmusc) to the electrical activity of the diaphragm (Eadi), during assisted mechanical ventilation and to assess if the Pmusc/Eadi index is affected by the type and level of ventilator assistance. The Pmusc/Eadi index was also used to measure the patient's inspiratory effort from Eadi without esophageal pressure. DESIGN: Crossover study. SETTING: One general ICU. PATIENTS: Ten patients undergoing assisted ventilation. INTERVENTION: Pressure support and neurally adjusted ventilator assist delivered, each, at three levels of ventilatory assistance. MEASUREMENT AND MAIN RESULTS: Airways flow and pressure, esophageal pressure, and Eadi were continuously recorded. Sixty tidal volumes for each ventilator settings were analyzed off-line, at three time points during inspiration. For each time point, Pmusc/Eadi index was calculated. Pmusc/Eadi index was also calculated from airway pressure drop during end-expiratory occlusions. Pmusc/Eadi index was very variable among patients, but within one patient it was not affected by type and level of ventilator assistance. Pmusc/Eadi index decreased during the inspiration. Pmusc/Eadi index obtained during an occlusion from airway pressure swing was tightly correlated with that derived from esophageal pressure during tidal ventilation and allowed to estimate pressure time product. CONCLUSIONS: Pmusc is tightly related to Eadi, by a proportionality coefficient that we termed Pmusc/Eadi index, stable within each patient under different conditions of ventilator assistance. The derivation of the Pmusc/Eadi index from Eadi and airway pressure during an expiratory occlusion enables a continuous estimate of patient's inspiratory effort.

Pressure-support ventilation is widely used during the weaning phase in patients with acute respiratory distress syndrome. The pressure-support level is adjusted to prevent ventilator-induced lung injury while limiting the patient's work of breathing. Neurally adjusted ventilatory assist is an assist mode that applies a positive pressure proportional to the integral of the electrical activity of the diaphragm. The objective was to assess the physiologic response to varying pressure-support ventilation and neurally adjusted ventilatory assist levels in selected acute respiratory distress syndrome patients and to evaluate the effect of neural triggering.We prospectively assessed 11 consecutive patients with acute respiratory distress syndrome attributable to pulmonary diseases. Pressure-support ventilation and neurally adjusted ventilatory assist were used in random order. Neurally adjusted ventilatory assist was used with a low electrical activity of the diaphragm trigger (neurally adjusted ventilatory assist-electrical activity of the diaphragm) and with a high electrical activity of the diaphragm trigger that led to rescue triggering by inspiratory flow (neurally adjusted ventilatory assist-inspiratory flow). With each ventilation modality, four levels of assistance (100%, 120%, 140%, and 160%) were used in random order. Statistical analysis was performed using analysis of variance for repeated measurements and mixed models.Contrary to pressure-support ventilation, neurally adjusted ventilatory assist-electrical activity of the diaphragm and neurally adjusted ventilatory assist-inspiratory flow were associated with stable tidal volume levels despite increasing assistance. For the asynchrony index, an interaction was present between ventilation mode and assist level (p = .0076) because asynchrony index increased significantly with the pressure-support ventilation level (p = .004), but not with the neurally adjusted ventilatory assist-electrical activity of the diaphragm or neurally adjusted ventilatory assist-inspiratory flow level. The lowest asynchrony index was obtained with neurally adjusted ventilatory assist-electrical activity of the diaphragm.Compared to pressure-support ventilation, neurally adjusted ventilatory assist in acute respiratory distress syndrome patients holds promise for limiting the risk of overassistance, preventing patient-ventilator asynchrony, and improving overall patient-ventilator interactions. Neural triggering (neurally adjusted ventilatory assist-electrical activity of the diaphragm) considerably decreased patient-ventilator asynchrony.

To evaluate the utility of serial measurements of plasma N-terminal pro-brain natriuretic peptide (NT-proBNP) to detect acute cardiac dysfunction during weaning failure in difficult to wean patients with chronic obstructive pulmonary disease.Prospective observational cohort study.A 14-bed general intensive care unit in a university hospital.Nineteen patients mechanically ventilated for chronic obstructive pulmonary disease exacerbation who were difficult to wean.None.Cardiac and hemodynamic variables, arterial and central venous blood gas, breathing pattern, respiratory mechanics, indexes of oxygen cost of breathing, and plasma levels of NT-proBNP were measured and analyzed immediately before (baseline) and at the end of a spontaneous breathing trial. Eight of 19 patients (42%) were identified with acute cardiac dysfunction at the end of the weaning trial. Baseline NT-proBNP levels were significantly higher (median 5000, interquartile range 4218 pg/mL) in these patients than in patients without evidence of acute cardiac dysfunction (median 1705, interquartile range 3491 pg/mL). Plasma levels of NT-proBNP increased significantly at the end of the spontaneous breathing trial only in patients with acute cardiac dysfunction (median 12,733, interquartile range 16,456 pg/mL, p.05). The elevation in NT-proBNP at the end of the weaning trial had a good diagnostic performance in detecting acute cardiac dysfunction, as estimated by area under the receiver operating characteristic curve analysis (area under the curve 0.909, se 0.077, 95% confidence interval 0.69-0.98; p.0001, cutoff = 184.7 pg/mL).Serial measurements of NT-proBNP plasma levels provided a noninvasive manner to detect acute cardiac dysfunction during an unsuccessful weaning trial in difficult to wean patients with chronic obstructive pulmonary disease. The utility of this test as a complement of the standard clinical monitoring of the weaning trial deserves further investigation.

We hypothesized that the additional use of automatic tube compensation (ATC) during a spontaneous breathing trial with continuous positive airway pressure (CPAP), by minimizing respiratory work, would result in more patients undergoing successful extubation.Prospective, randomized, controlled study.A ten-bed, general intensive care department at a tertiary-care hospital.Adult patients (n=99) who had undergone mechanical ventilation for24 hrs and met defined criteria for a weaning trial.Patients were randomized to undergo a 1-hr spontaneous breathing trial with either ATC with CPAP (ATC group, n=51) or CPAP alone (CPAP group, n=48). ATC was provided by commercially available mechanical ventilators. Patients tolerating the spontaneous breathing trial underwent immediate extubation. The primary outcome measure was successful extubation, defined as the ability to maintain spontaneous breathing for 48 hrs after discontinuation of mechanical ventilation and extubation.There were no significant differences in demographic, respiratory, or hemodynamic characteristics between the two groups at the start of the spontaneous breathing trial. There was a trend for more patients in the ATC group to tolerate the breathing trial and undergo extubation (96% vs. 85%; p=.08). The rate of reintubation was 14% in the ATC group and 24% in the CPAP group (p=.28). Significantly more patients in the ATC group thus met the criteria for successful extubation (82% vs. 65%; p=0.04).This is the largest single-center study to date assessing the use of commercially available ATC and suggests that this might be a useful mode for performing a spontaneous breathing trial preceding extubation in a general intensive care population.

To assess the effects of step-changes in tidal volume on work of breathing during lung-protective ventilation in patients with acute lung injury (ALI) or the acute respiratory distress syndrome (ARDS).Prospective, nonconsecutive patients with ALI/ARDS.Adult surgical, trauma, and medical intensive care units at a major inner-city, university-affiliated hospital.Ten patients with ALI/ARDS managed clinically with lung-protective ventilation.Five patients were ventilated at a progressively smaller tidal volume in 1 mL/kg steps between 8 and 5 mL/kg; five other patients were ventilated at a progressively larger tidal volume from 5 to 8 mL/kg. The volume mode was used with a flow rate of 75 L/min. Minute ventilation was maintained constant at each tidal volume setting. Afterward, patients were placed on continuous positive airway pressure for 1-2 mins to measure their spontaneous tidal volume.Work of breathing and other variables were measured with a pulmonary mechanics monitor (Bicore CP-100). Work of breathing progressively increased (0.86 +/- 0.32, 1.05 +/- 0.40, 1.22 +/- 0.36, and 1.57 +/- 0.43 J/L) at a tidal volume of 8, 7, 6, and 5 mL/kg, respectively. In nine of ten patients there was a strong negative correlation between work of breathing and the ventilator-to-patient tidal volume difference (R = -.75 to -.998).: The ventilator-delivered tidal volume exerts an independent influence on work of breathing during lung-protective ventilation in patients with ALI/ARDS. Patient work of breathing is inversely related to the difference between the ventilator-delivered tidal volume and patient-generated tidal volume during a brief trial of unassisted breathing.

To test the hypothesis that in response to increased ventilatory demand, dynamic inspiratory pressure assistance better compensates for increased workload compared with static pressure support ventilation (PSV).Randomized clinical crossover study.General intensive care u nits of a university hospital.Twelve patients with acute respiratory failure.Patients received PSV, proportional assist ventilation (PAV), and PAV+ automatic tube compensation (ATC) in random order while maintaining mean inspiratory airway pressure constant. During each setting, ventilatory demand was increased by adding deadspace without ventilator readjustment.Cardiorespiratory, ventilatory, and work of breathing variables were assessed by routine monitoring plus pneumotachography; airway, esophageal, and abdominal pressure measurements; and nitrogen washout. After deadspace addition, tidal volume and end-expiratory lung volume increased similarly in all ventilatory modalities. Ventilator work, peak inspiratory flow, and maximum airway pressure increased significantly during PAV+ATC when compared with PSV after deadspace addition. However, increase in ventilator work did not result in a smaller increase in patients' work of breathing with elevated ventilatory demand during PAV+ATC (PSV 807 +/- 204 mJ/L, PAV 802 +/- 193 mJ/L, and PAV+ATC 715 +/- 202 mJ/L, p = .11). Increase in patients' work of breathing was mainly caused by a significantly higher resistive workload during PAV and PAV+ATC.In patients with acute respiratory failure, dynamic inspiratory pressure assistance modalities are not superior to PSV with respect to cardiorespiratory function and inspiratory muscles unloading after increasing ventilatory demand. The latter might be explained by higher peak flows resulting in nonlinearly increased resistive workload that was incompletely compensated by PAV+ATC.

OBJECTIVE: To study whether noninvasive pressure support ventilation (NIPSV) with helium/oxygen (He/oxygen), which can reduce dyspnea, PaCO2, and work of breathing more than NIPSV with air/oxygen in decompensated chronic obstructive pulmonary disease, could have beneficial consequences on outcome and hospitalization costs. DESIGN: Prospective, randomized, multicenter study. SETTING: Intensive care units of three tertiary care university hospitals. PATIENTS: All patients with chronic obstructive pulmonary disease admitted to the intensive care units for NIPSV during a 24-month period. INTERVENTIONS: Patients were randomized to NIPSV with air/oxygen or He/oxygen. NIPSV settings, number of daily trials, decision to intubate, and intensive care unit and hospital discharge criteria followed standard practice guidelines. RESULTS: A total of 123 patients (male/female ratio, 71:52; age, 71 +/- 10 yrs, Acute Physiology and Chronic Health Evaluation II, 17 +/- 4) were included. Intubation rate (air/oxygen 20% vs. He/oxygen 13%) and length of stay in the intensive care unit (air/oxygen 6.2 +/- 5.6 vs. He/oxygen 5.1 +/- 4 days) were comparable. The post-intensive care unit hospital stay was lower with He/oxygen (air/oxygen 19 +/- 12 vs. He/oxygen 13 +/- 6 days, p < .002). Cost of NIPSV gases was higher with He/oxygen, but total hospitalization costs were lower by $3,348 per patient with He/oxygen. No complications were associated with the use of He/oxygen. CONCLUSION: He/oxygen did not significantly reduce intubation rate or intensive care unit stay, but hospital stay was shorter and total costs were lower. He/oxygen NIPSV can be safely administered and could prove to be a cost-effective strategy.

OBJECTIVE To evaluate patients without prior pulmonary disease after cardiac surgery and to determine whether resistive unloading by automatic tube compensation, pressure support ventilation, and continuous positive airway pressure has different effects on oxygen consumption, breathing pattern, gas exchange, and hemodynamics. DESIGN Prospective, randomized, controlled study. SETTING Tertiary care, postoperative intensive care unit. PATIENTS Twenty-one patients scheduled for open heart coronary artery bypass graft surgery. INTERVENTIONS Each patient was ventilated with all three modes in random order. MEASUREMENTS AND MAIN RESULTS Patients were ventilated in three modes, each applied for 30 mins according to computer-generated randomization: pressure support ventilation with 5 cm H2O, continuous positive airway pressure, and automatic tube compensation. Oxygen consumption was calculated by means of indirect calorimetry. The hypnotic state of the patients was monitored by Bispectral Index. For hemodynamic measurements, a fiberoptic pulmonary artery catheter was inserted. The main finding of our study was that oxygen consumption and breathing pattern (tidal volume and respiratory rate) did not differ significantly during automatic tube compensation and pressure support ventilation compared with continuous positive airway pressure (oxygen consumption, 170 +/- 29 vs. 170 +/- 26 vs. 174 +/- 29 mL.min.m, respectively; tidal volume, 466 +/- 132 vs. 484 +/- 125 vs. 470 +/- 119 mL, respectively; respiratory rate, 16 +/- 4 vs. 15 +/- 4 vs. 16 +/- 4 breaths/min, respectively). Automatic tube compensation and pressure support ventilation had no clinical effects on gas exchange and hemodynamic variables compared with continuous positive airway pressure. None of the variables differed significantly during the three ventilatory settings. CONCLUSION In postoperative tracheally intubated patients with normal ventilatory demand, automatic tube compensation and pressure support ventilation with 5 cm H2O lead to identical oxygen consumption, breathing patterns, gas exchange, and hemodynamics. We, therefore, suggest that this group of patients does not need any additional positive pressure support from the ventilator to overcome the additional work of breathing imposed by the endotracheal tube during the weaning phase from mechanical ventilation.

To evaluate the operation of a continuous positive airway pressure system by using tracheal airway pressure (PT) as the control signal for system operation (i.e., tracheal pressure control).Repeated measures.University research laboratory.Twelve anesthetized, spontaneously breathing swine.Subjects were intubated and connected to a tracheal pressure control system (5 cm H2O continuous positive airway pressure). Varying inspiratory flow demands and degrees of partial endotracheal tube occlusion (25%, 50%, and 75%) were studied. Tracheal pressure control was compared with a conventionally controlled system (pressure from breathing circuit Y-piece [PY] used as control signal) during endotracheal tube occlusion.Imposed resistive work of breathing (work to spontaneously inhale through endotracheal tube and ventilator circuit), work by ventilation system assisting inhalation, PT, PY, tidal volume, and inspiratory flow demands were measured. As inspiratory flow demands increased (range, 0.2-2.3 L/sec), pressure assist increased automatically (range, 5-40 cm H2O) as well as work of breathing by ventilation system assisting inhalation (range, 0.2-2.5 J/L). Imposed resistive work of breathing was nullified at the lower and was negligible at the higher flow demands. During endotracheal tube occlusion with a conventionally controlled system, PY was unchanged, whereas PT decreased (up to -15 cm H2O) and imposed resistive work of breathing increased (up to 1.05 J/L). With tracheal pressure control, PY increased automatically (range, 8-52 cm H2O), whereas PT varied slightly (range, 2 to -4.6 cm H2O). Imposed resistive work of breathing was negligible (range, 0-0.2 J/L). Breathing circuit pressure (PY), not pulmonary airway pressure (PT), increased significantly during tracheal pressure control.Tracheal pressure control results in automatic and variable levels of pressure assist to decrease imposed resistive work of breathing under conditions of varying spontaneous inspiratory flow demands and endotracheal tube occlusion. Conventional systems are potentially flawed when PY is used as the control signal because they do not function in this manner and do not accurately assess pulmonary airway pressure.

To compare the effects of adaptive support ventilation (ASV) and synchronized intermittent mandatory ventilation plus pressure support (SIMV-PS) on patient-ventilator interactions in patients undergoing partial ventilatory support.Prospective, crossover interventional study.Medical intensive care unit, university tertiary care center.Ten patients, intubated and mechanically ventilated for acute respiratory failure of diverse causes, in the early weaning period, ventilated with SIMV-PS and clinically detectable sternocleidomastoid activity suggesting increased inspiratory load and patient-ventilator dyssynchrony.Measurement of respiratory mechanics, P0.1, sternocleidomastoid electromyographic activity, arterial blood gases, and systemic hemodynamics in three conditions: 1) after 45 mins with SIMV-PS (SIMV-PS 1); 2) after 45 mins with ASV, set to deliver the same minute-ventilation as during SIMV-PS; 3) 45 mins after return to SIMV-PS (SIMV-PS 2), with settings identical to those of the first SIMV-PS period.The same minute ventilation was observed during ASV (11.4 +/- 3.1 l/min [mean +/- sd]) as during SIMV-PS 1 (11.6 +/- 3.5 L/min) and SIMV-PS 2 (10.8 +/- 3.4 L/min). No parameter was significantly different between SIMV-PS 1 and 2, hence subsequent results refer to ASV vs. SIMV-PS 1. During ASV, tidal volume increased (538 +/- 91 vs. 671 +/- 100 mL, p.05) and total respiratory rate decreased (22 +/- 7 vs. 17 +/- 3 breaths/min, p.05) vs. SIMV-PS. However, spontaneous respiratory rate increased in six patients, decreased in four, and remained unchanged in one. P0.1 decreased during ASV in all patients except three in whom no change was noted (1.8 +/- 0.9 vs. 1.1 +/- 1 cm H2O, p.05). During ASV, sternocleidomastoid electromyogram activity was markedly reduced (electromyogram index, where SIMV-PS 1 = 100, ASV 34 +/- 41, SIMV-PS 2 89 +/- 36, p.02) as was palpable muscle activity. No changes were noted in arterial blood gases, pH, or mean systemic pressure during the trial.In patients undergoing partial ventilatory support, with clinical and electromyographic signs of increased respiratory muscle loading, ASV provided levels of minute ventilation comparable to those of SIMV-PS. However, with ASV, central respiratory drive and sternocleidomastoid activity were markedly reduced, suggesting decreased inspiratory load and improved patient-ventilator interactions. These preliminary results warrant further testing of ASV for partial ventilatory support.

To compare short-term administration of noninvasive proportional assist ventilation (NIV-PAV) and pressure support ventilation (NIV-PSV).Prospective, crossover, randomized study.Medicosurgical intensive care unit in a nonteaching hospital.Twelve chronic obstructive pulmonary disease patients admitted for hypercapnic acute respiratory failure.NIV-PSV and NIV-PAV given in a randomized order after baseline evaluation in continuous positive airway pressure. Using a flow-triggering ventilator, NIV-PAV was adjusted using the runaway method and compared with NIV-PSV at similar peak inspiratory airway pressure.Flow, airway pressure, and changes in esophageal pressure were measured and the tidal volume, the patient's inspiratory work of breathing, and the esophageal pressure--time product were calculated. Arterial pH and PaCO(2) were measured and breathing comfort was assessed using a visual analogic scale. Peak inspiratory airway pressure (17 +/- 3 cm H(2)O) and tidal volume were similarly increased with the two modalities with no change in respiratory rate. The change in esophageal pressure was similarly decreased (from 20 +/- 8 cm H(2)O in continuous positive airway pressure to 12 +/- 7 in NIV-PSV and 10 +/- 5 cm H(2)O in NIV-PAV) as well as inspiratory muscle effort indexes. Arterial pH and PaCO(2) were similarly improved. Breathing comfort was significantly improved in NIV-PAV (+38 +/- 38%) but not in NIV-PSV (+11 +/- 23%). The tidal volume was more variable in NIV-PAV (89 +/- 18%) than in NIV-PSV (15 +/- 8%) and changes in tidal volume variability were significantly correlated (p =.02) with changes in breathing comfort.In chronic obstructive pulmonary disease patients with hypercapnic acute respiratory failure, NIV-PAV was able to unload inspiratory muscles similarly to NIV-PSV but may be more comfortable than NIV-PSV.

Objective: To investigate whether transtracheal open ventilation (TOV), pressure control ventilation (PCV) through a minitracheotomy tube (internal diameter 4 mm), is an effective method of inspiratory assistance under high upper airway resistance in postextubation patients; to compare, in a lung model study, TOV with other methods. Design: Clinical study: A prospective, controlled, crossover study. Lung model study: A prospective laboratory trial. Setting: Clinical study: A six-bed general intensive care unit in a teaching hospital. Lung model study: Animal research laboratory. Patients: Clinical study: Eleven postextubation patients, who had undergone minitracheotomy for sputum retention between January 1997 and December 1997. Subject: Lung model study: Two-bellows-in-a-box lung model, which included ordinary and high levels of upper airway resistance. Interventions: Clinical study: Ventilatory settings were: assist/control (A/C) mode, 2 breaths/min of AIC back-up rate, 35-40 cm H 2 O of PCV, 0.6-0.8 secs of inspiratory time, and 0 cm H 2 O of positive end-expiratory pressure. The ventilatory parameters of TOV were compared with those of spontaneous breathing (SB). Lung model study: Effect of TOV on inspiratory assistance was compared with those of SB, open minitracheotomy, 5 Umin of transtracheal gas insufflation, and 5 and 10 cm H 2 O of pressure support ventilation (PSV), which simulated noninvasive positive ventilation. TOV ventilatory settings were: A/C mode; 30, 40, and 50 cm H 2 O of PCV, 0.9 secs of inspiratory time, and 0 cm H 2 O of positive end-expiratory pressure. At each ventilatory setting, we adjusted the inspiratory effort of the model to give a tidal volume of 0.5 L. Measurements and Main Results: Clinical study: TOV was performed for 76.6 ± 38.6 hrs (mean ± SD) over 5.6 ± 2.6 days without major complication. Peak tracheal pressure, which was measured distal to the minitracheotomy tube in six patients by a catheter pressure transducer, was 4.33 ± 0.59 cm H 2 O. Inspiratory tidal volume delivered by the ventilator was 0.51 ± 0.06 L. Respiratory rate during TOV was lower than during SB. According to esophageal pressure and respiratory inductive plethysmography, TOV reduced the patient's inspiratory work and improved the breathing pattern. Lung model study: Mean tracheal pressure during TOV and 10 cm H 2 O of PSV were positive values and they had larger inspiratory assistance according to the pressure-time product of pleural pressure. Although high upper airway resistance reduced the inspiratory assistance of PSV, it did not change the effects of TOV. Conclusions: TOV effectively reduced patient's inspiratory work and was more useful than open minitracheotomy and transtracheal gas insufflation. TOV also improved the breathing pattern. TOV may be useful for resolving some postextubation respiratory problems and avoiding the need for reintubation.

Objective: To test the hypothesis that nitric oxide inhalation facilitates CO 2 elimination by decreasing alveolar deadspace in an ovine model of acute lung injury. Design: Prospective, placebo-controlled, randomized, crossover model. Setting: University research laboratory. Subjects: Eleven mixed-breed adult sheep. Interventions: To induce acute lung injury, hydrochloric acid was instilled into the tracheas of paralyzed sheep receiving controlled mechanical ventilation. Each sheep breathed 0 ppm, 5 ppm, and 20 ppm nitric oxide in random order. Measurements and Main Results: Estimates of alveolar deadspace volumes and arterial-to-end tidal CO 2 partial pressure differences were used as indicators of CO 2 elimination efficiency. At a constant minute ventilation, nitric oxide inhalation caused dose-independent decreases in Paco 2 (p

OBJECTIVE To investigate, in restrictive patients, the influence of pressure ramp slope values on the efficacy of pressure support ventilation. DESIGN Prospective study. SETTING A university hospital medical intensive care unit. PATIENTS Twelve intubated restrictive patients. INTERVENTIONS Patients were randomly assigned to four sequences in which the values of the slope of the pressure ramp increase were modulated so that the plateau pressure was reached within a predetermined time: 0.1, 0.50, 1, or 1.50 secs. The more rapidly the pressure plateau was achieved, the higher was the initial flow rate. For convenience, these four different ventilatory settings were termed T 0.1, T 0.5, T 1, and T 1.5. MEASUREMENTS AND MAIN RESULTS We measured the following parameters 10 mins after application of each pressure ramp slope: inspiratory work of breathing, breathing pattern, and intrinsic PEEP (PEEPi). Work of breathing was evaluated using Campbell's diagram, and expressed as a percentage of the values observed under spontaneous ventilation. A marked interindividual variation of the values for work of breathing was observed under spontaneous ventilation; the mean value for work of breathing was 1.97 +/- 0.82 joule/L, with a range of 1.22 to 4.10 joule/L. Comparison between the means for each sequence and each variable measured was performed by two-way analysis of variance with internal comparisons between sequences by Duncan's test. Between the first (T 0.1) and the last (T 1.5) sequence, the reduction of values of the pressure ramp slope induced a progressive increase in the values for work of breathing, regardless of the mode of expression (in joule, joule/L, or joule/min). The values for work of breathing (joule/ L), expressed as a percentage of the values observed under spontaneous ventilation, increased from 44.2 +/- 14.4% to 78.3 +/- 17.8% (p < .001). In contrast, the reduction of the pressure ramp slope values and initial flow rate did not induce any significant change in tidal volume, respiratory frequency, and PEEPi. CONCLUSION Among the four tested slope values, the steepest was that which induced the lowest possible work of breathing in restrictive patients ventilated by pressure support ventilation. In this type of patient, we therefore suggest that the programmed pressure value should be reached by using a steep pressure ramp slope.

To compare the effects of pressure- and flow-triggered pressure-support ventilation on weaning parameters during recovery from acute respiratory failure.Prospective, randomized, clinical trial.Intensive care unit in a university hospital.Sixteen orotracheally intubated adult patients recovering from acute respiratory failure of various etiologies, without chronic obstructive pulmonary disease.Randomized application of pressure- and flow-triggered pressure-support ventilation at 100% and 75% ventilatory support levels in each triggering system. A total of four conditions were applied for 30 mins each in all patients.Ventilatory, respiratory, and hemodynamic data were measured. For the measurement of weaning parameters, pressure and volume signals were directed to a computerized respiratory monitor by means of an esophageal probe and a flow sensor between the "Y" piece of the ventilatory circuit and the endotracheal tube. During both pressure-triggered (trigger sensitivity of -1 cm H2O) and flow-triggered (trigger sensitivity of 0.7 to 2.0 L/min) pressure-support ventilation with a ventilator, peak airway pressures were applied so as to decrease the work of breathing performed by the patient to zero (full ventilatory support). Partial ventilatory support was applied at 75% of the peak airway pressures achieved during full ventilatory support with each triggering system. A total of four experimental conditions were evaluated at identical FiO2 and positive and-expiratory pressure levels during pressure-support ventilation in each patient. Total ventilation volumes, arterial blood gas data, and hemodynamics did not differ among the four experimental conditions. During partial ventilatory support, the work of breathing, rapid shallow breathing index, and esophageal pressure increased significantly with both triggering systems when compared with data obtained at full ventilatory support. The mean data for the weaning parameters during the condition of partial ventilatory support were comparable between pressure- and flow-triggered pressure-support ventilation (i.e., 0.38 +/- 0.24 vs. 0.42 +/- 0.26 joule/L for work of breathing, 2.6 +/- 1.6 vs. 3.3 +/- 1.7 cm H2O for tracheal occlusion pressure, and 40.2 +/- 12.9 vs. 50.4 +/- 18.3 breaths/min/L for rapid shallow breathing index, respectively).The application of either a pressure- or flow-triggered system during pressure-support ventilation with the ventilator did not significantly affect short-term changes in gas exchange, respiratory mechanics, and inspiratory workload in patients recovering from acute respiratory failure of various etiologies without chronic obstructive pulmonary disease.

Objectives Triggering a ventilator "ON" at the carinal end of the endotracheal tube decreases imposed work of breathing by bypassing the resistance imposed by the breathing circuit and the endotracheal tube. We compared work of breathing during spontaneous ventilation between three methods of triggering the ventilator "ON": a) conventional pressure triggering from inside the ventilator; b) flow-by triggering; or c) tracheal pressure triggering at the carinal end of the endotracheal tube. We hypothesized that the work of breathing would be substantially decreased with tracheal pressure triggering compared with conventional pressure and flow-by methods in patients receiving continuous positive airway pressure. Design Clinical, prospective study. Setting University teaching hospital. Patients Fourteen adults diagnosed with acute respiratory failure. Interventions All patients were breathing spontaneously at an FIO2 of 0.30 to 0.40 and received 5 cm H2O of continuous positive airway pressure. Three different methods of triggering the ventilator while set in the continuous positive airway pressure mode were administered in random order. Measurements and main results Real-time measurements of esophageal pressure and tidal volume were integrated with a respiratory monitor (CP-100, Bicore, Riverside, CA) that uses the Campbell diagram to calculate total work of breathing. Imposed work of breathing was calculated by integrating tidal volume with the pressure at the carinal end of the endotracheal tube. Physiologic work of breathing was calculated by subtracting imposed work of breathing from the total work of breathing. Breathing frequency, the index of rapid shallow breathing (breathing frequency/tidal volume), peak inspiratory flow rate demand, exhaled minute ventilation, and the duration of respiratory muscle contraction assessed by the ratio of inspiratory time to total cycle time were also measured. Data were analyzed by Friedman's repeated-measures analysis of variance on ranks. Alpha was set at .05 for statistical significance. Imposed work of breathing decreased to approximately zero during tracheal pressure triggering. As a result, total work of breathing decreased by approximately 40% compared with the flow-by and conventional methods. During tracheal pressure triggering only, airway pressure increased above baseline pressure to approximately 11 cm H2O, which resembled pressure-support ventilation. Also, during tracheal pressure triggering, tidal volume and peak inspiratory flow rate were significantly increased, while the pressure-time product and the index of rapid shallow breathing were significantly decreased. Hemodynamic status and oxygen saturation were not clinically affected. Conclusions The tracheal pressure triggering of a demand-flow continuous positive airway pressure system creates an effect similar to pressure-support ventilation that significantly decreases imposed work of breathing and, thus, total work of breathing. We recommend moving the triggering site of the ventilator to the carinal end of the endotracheal tube.

To predict extubation success and failure in mechanically ventilated infants and children using bedside measures of respiratory function.Prospective collection of data.A university-affiliated children's hospital with a 51-bed critical care unit.All infants and children who were mechanically ventilated for at least 24 hrs, except neonatesor = 37 wks gestation and patients with neuromuscular disease.Bedside measurements of cardiorespiratory function were obtained immediately before extubation.Extubation failure was defined as reintubation within 48 hrs of extubation in the absence of upper airway obstruction. Failure rates were calculated for different ranges (selected a priori) of preextubation measures of breathing effort, ventilatory support, respiratory mechanics, central inspiratory drive, and integrated indices useful in adults. Effort of spontaneous breathing was assessed by the respiratory rate standardized to age, the presence of retractions and paradoxical breathing, inspiratory pressure, maximal negative inspiratory pressure (maximal negative inspiratory pressure), inspiratory pressure/maximal negative inspiratory pressure ratio, and tidal volume indexed to body weight of a spontaneous breath. Ventilatory support was measured by the fraction of inspired oxygen (F10(2)), mean airway pressure, oxygenation index, and the fraction of total minute ventilation provided by the ventilator. Respiratory mechanics were assessed by determination of peak ventilatory inspiratory pressure and dynamic compliance. Central inspiratory drive was assessed by mean inspiratory flow. Frequency to tidal volume ratio and the compliance, rate, oxygenation, and pressure indexed to body weight, the integrated indices useful in predicting extubation failure in adults, were also calculated. Thirty-four of the 208 patients who were studied were reintubated for an overall failure rate of 16.3% (95% confidence interval 11.3% to 21.4%). The reasons for reintubation were poor effort (n = 8), excessive effort (n = 14), altered mental status or absent airway reflexes (n = 2), cardiovascular instability (n = 3), inadequate oxygenation (n = 3), respiratory acidosis (n = 3), and undocumented (n = 1). Extubation failure increased significantly with decreasing tidal volume indexed to body weight of a spontaneous breath, increasing F10(2), increasing mean airway pressure, increasing oxygenation index, increasing fraction of total minute ventilation provided by the ventilator, increasing peak ventilatory inspiratory pressure, or decreasing mean inspiratory flow (p.05). Dynamic compliance showed a trend of increasing failure rate with decreasing dynamic compliance but did not reach statistical significance (p = .116). Respiratory rate standardized to age, inspiratory pressure, maximal negative inspiratory pressure, inspiratory pressure/maximal negative inspiratory pressure ratio, frequency to tidal volume ratio, and compliance, rate, oxygenation, and pressure did not show any trend in failure rate with increasing or decreasing values. Threshold values that defined a low risk (or = 10%) and a high risk (or = 25%) of extubation failure could be determined for tidal volume indexed to body weight of a spontaneous breath, F10(2), mean airway pressure, oxygenation index, fraction of total minute ventilation provided by the ventilator, peak ventilatory inspiratory pressure, dynamic compliance, and mean inspiratory flow. Neither a low nor a high risk of failure could be defined for frequency to tidal volume ratio or the compliance, rate, oxygenation, and pressure (CROP) index.Bedside measurements of respiratory function can predict extubation success and failure in infants and children. Both a low risk and a high risk of failure can be determined using these measures. Integrated indices useful in adults do not reliably predict extubation success or failure in

Objective To evaluate the effect of two commonly used heat and moisture exchangers on respiratory function and gas exchange in patients with acute respiratory failure during pressure-support ventilation. Design Prospective, randomized trial. Setting Intensive care unit of a university hospital. Patients Fourteen patients with moderate acute respiratory failure, receiving pressure-support ventilation. Interventions Patients were assigned randomly to two treatment groups, in which two different heat and moisture exchangers were used: Hygroster Registered Trademark (DAR S.p.A., Mirandola, Italy) with higher deadspace and lower resistance (group 1, n equals 7), and Hygrobac-S Registered Trademark (DAR S.p.A.) with lower deadspace and higher resistance (group 2, n equals 7). Patients were assessed at three pressure-support levels: a) baseline (10.3 plus minus 2.4 cm H2 O for group 1, 9.3 plus minus 1.3 cm H2 O for group 2); b) 5 cm H2 O above baseline; and c) 5 cm H2 O below baseline. Measurements obtained with the heat and moisture exchangers were compared with those values obtained using the standard heated hot water humidifier. Measurements and Main Results At baseline pressure-support ventilation, the insertion of both heat and moisture exchangers induced in all patients a significant increase in the following parameters: minute ventilation (12.4 plus minus 3.2 to 15.0 plus minus 2.6 L/min for group 1, and 11.8 plus minus 3.6 to 14.2 plus minus 3.5 L/min for group 2); static intrinsic positive end-expiratory pressure (2.9 plus minus 2.0 to 5.1 plus minus 3.2 cm H2 O for group 1, and 2.9 plus minus 1.7 to 5.5 plus minus 3.0 cm H2 O for group 2); ventilatory drive, expressed as P0.1 (2.7 plus minus 2.0 to 5.2 plus minus 4.0 cm H2 O for group 1, and 3.3 plus minus 2.0 to 5.3 plus minus 3.0 cm H2 O for group 2); and work of breathing, expressed as either power (8.8 plus minus 9.4 to 14.5 plus minus 10.3 joule/min for group 1, and 10.5 plus minus 7.4 to 16.8 plus minus 11.0 joule/min for group 2) or work per liter of ventilation (0.6 plus minus 0.6 to 1.0 plus minus 0.7 joule/L for group 1, and 0.8 plus minus 0.4 to 1.1 plus minus 0.5 joule/L for group 2). These increases also occurred when pressure-support ventilation was both above and below the baseline level, although at high pressure support the increase in work of breathing with heat and moisture exchangers was less evident. Gas exchange was unaffected by heat and moisture exchangers, as minute ventilation increased to compensate for the higher deadspace produced in the circuit by the insertion of heat and moisture exchangers. Conclusions The tested heat and moisture exchangers should be used carefully in patients with acute respiratory failure during pressure-support ventilation, since these devices substantially increase minute ventilation, ventilatory drive, and work of breathing. However, an increase in pressure-support ventilation (5 to 10 cm H sub 2 O) may compensate for the increased work of breathing.

Objectives:a) To investigate whether the patient work of breathing needed to trigger inspiration is affected by the type of ventilator delivering pressure-support ventilation for mechanically ventilated pediatric patients. b) To determine whether changes in oxygen consumption (Vo2) trend with chang

OBJECTIVE To determine which of a series of disposable or interchangeable positive end-expiratory pressure (PEEP) devices functions with the least imposition of inspiratory and expiratory work during continuous positive airway pressure. DESIGN Prospective laboratory evaluation performed on a lung model. SETTING Research laboratory at a university medical center. INTERVENTIONS A spontaneously breathing lung model, created from a training test lung and a volume ventilator, were used to simulate a patient spontaneously breathing at a tidal volume of 0.4 L, peak inspiratory flow of 40 L/min, an inspiration/expiration ratio of 1:2, and a respiratory rate of 20 breaths/min. Ten PEEP valves attached to a continuous high-flow system were evaluated. MEASUREMENTS AND MAIN RESULTS All of the PEEP valves studied imposed high levels of both inspiratory and expiratory work of breathing. The BE-171 and BE-142 valves (Instrumentation Industries) imposed the least amount of inspiratory work. In general, imposed inspiratory work accounted for approximately 70% to 80% of total imposed work of breathing. CONCLUSIONS All of the disposable/interchangeable PEEP valves that were studied imposed a considerable amount of both inspiratory and expiratory work, even when the continuous flow provided exceeded the peak inspiratory flow demands of the lung model. The primary reason for the high imposed work levels is the high gas-flow resistance of all of the valves studied.

OBJECTIVES Flow-triggered continuous positive airway pressure decreases the inspiratory work of breathing in adults when compared with pressure-triggered continuous positive airway pressure. However, the effect of flow-triggered continuous positive airway pressure on work of breathing in neonates is not known. Our objective was to determine if flow-triggering was superior to pressure triggering in the presence of narrow endotracheal tubes, such as those tubes used in neonates. DESIGN Prospective evaluation using within-animal comparison of flow-triggering and pressure-triggering demand flow systems. SETTING The animal laboratory in a university hospital. SUBJECTS Six spontaneously breathing white rabbits, tracheostomized and intubated with 3- and 4-mm inner diameter endotracheal tubes. INTERVENTIONS The animals were connected to a ventilator through a standard respiratory circuit. The ventilator was randomly operated in the following modes: flow-triggered continuous positive airway pressure, pressure-triggered continuous positive airway pressure, flow-triggered with 5 cm H2O pressure support ventilation, and pressure-triggered with 5 cm H2O pressure support ventilation. MEASUREMENTS AND MAIN RESULTS Esophageal pressure, airway pressure, and flow signals were monitored. Control data were obtained while the rabbits were breathing room air through the endotracheal tube. With 3-mm inner diameter endotracheal tubes, the negative deflection of esophageal pressure during flow-triggered continuous positive airway pressure was significantly less than control; however, negative deflection of esophageal pressure during pressure-triggered continuous positive airway pressure did not significantly differ from control. The application of 5 cm H2O pressure support ventilation with flow-triggering decreased negative deflection of esophageal pressure significantly compared with flow-triggered continuous positive airway pressure, pressure-triggered continuous positive airway pressure, and control. With endotracheal tube inner diameter of 4 mm, flow-triggered continuous positive airway pressure and pressure-triggered continuous positive airway pressure did not show any differences compared to control. Negative deflection of esophageal pressure differed under all conditions except control when results with the 3-mm inner diameter endotracheal tube were compared with the 4-mm inner diameter endotracheal tube. CONCLUSIONS Flow-triggering is superior to pressure-triggering in the presence of a 3-mm inner diameter endotracheal tube. This difference was not clear with a 4-mm inner diameter endotracheal tube. The size of the endotracheal tube may be the most important variable in evaluating the approach used to ventilate small neonates.

OBJECTIVES To combine the patient synchrony effects of pressure-limited breath delivery strategies with the volume guarantee of volume-cycled breath delivery strategies, we designed a positive-pressure breath that incorporates both features. This breath is patient triggered and can be pressure limited. Breath termination (i.e., cycling) can either be flow- or volume-cycled, depending on whether a target volume has been attained. The pressure-limiting features are further enhanced by the capability to adjust demand-valve responsiveness at breath initiation. DESIGN Prospective, mechanical simulation studies. SETTING Engineering laboratory. INTERVENTIONS A mechanical lung model that could simulate patient ventilatory efforts was used. Vigorous and weak patient efforts were studied in conjunction with use of volume assist, pressure support, and a combination pressure-limited and volume-cycled breath. MEASUREMENTS AND MAIN RESULTS Two clinical situations were simulated by the model: a) a patient requiring total mechanical ventilatory support who had a very active ventilatory drive; and b) a patient receiving only partial ventilatory support who had an unstable ventilatory drive. A range of pressure-limiting and volume-cycling settings were given. Volume, pressure, and flow delivery were measured. Synchrony with patient effort was assessed by visual inspection of airway pressure graphics as well as by calculations of patient work during these support strategies. CONCLUSIONS Flow dyssynchrony during fixed-flow, volume-cycled assisted breaths in patients with active ventilatory drives can be improved with this breath design while a guaranteed tidal volume is maintained. In addition, this combination breath can provide a volume "safety net" for patients in whom partial support with pressure-support ventilation is desired.

OBJECTIVE Recent observations suggest that central hypoventilation with slowing of respiratory frequency contributes to hypoventilation during severe inspiratory resistive loads. We carried out a study to further characterize this bradypneic response. DESIGN Prospective, controlled laboratory study. SETTING Basic science laboratory of a university hospital. SUBJECTS Anesthetized adult cats (loading experiment n = 7, nonloaded hypercapnic controls n = 11). INTERVENTIONS Experimental inspiratory loads increased transdiaphragmatic pressure to 75% of the maximum for each animal. Respiratory responses were observed at midrun or moderate conditions of respiratory insufficiency (defined as PaCO2 > or = 60 torr [> or = 8.0 kPa]) and failure (PaCO2 > or = 80 torr [> or = 10.6 kPa]). Nonloaded hypercapnic controls were studied with similar durations of exposure to CO2 in the same CO2 range. MEASUREMENTS Inspiratory airflow, tidal volume, respiratory frequency, airway pressure, transdiaphragmatic pressure, transdiaphragmatic pressure response to phrenic nerve electrical stimulation, blood gas analysis. Severe inspiratory loads were applied to anesthetized adult cats to determine whether bradypnea could be observed in an anesthesized model that eliminated conscious responses. Experiments were performed in hyperoxic conditions to determine whether bradypnea develops in the absence of hypoxia. An additional control group was studied under hypercapnic conditions without loading to determine whether comparable hypercapnia is a sufficient stimulus to elicit bradypnea. RESULTS From midrun until failure, minute ventilation decreased by 16% in loaded animals. Hypoventilation was associated with a decrease in respiratory frequency from 40.1 to 29.9 breaths/min, whereas tidal volume, spontaneous transdiaphragmatic pressure, and transdiaphragmatic pressure response to phrenic nerve electrical stimulation remained unchanged. Control animals had no significant reduction in ventilation or respiratory frequency over similar levels and durations of hypercapnia. CONCLUSIONS Centrally mediated bradypnea contributed to hypoventilation in respiratory failure associated with inspiratory loading. Bradypnea preceded evidence of muscle fatigue. This change in respiratory cycle timing occurred under anesthesia, and thus, did not depend on conscious perception of dyspnea. Bradypnea does not depend on either hypercapnia or hypoxia.

To compare the inspiratory imposed work of breathing during spontaneous ventilation with continuous positive airway pressure using three methods of triggering "ON" the demand-flow system of a ventilator: a) conventional pressure triggering with the pressure measuring/triggering site inside the ventilator on the exhalation limb of the breathing circuit; b) tracheal pressure triggering from the tracheal or carinal end of the endotracheal tube; and c) flow-by (flow triggered) triggering.Multitrial tests under simulated clinical conditions using a mechanical lung model.A research laboratory at a university medical center.Spontaneous breathing with continuous positive airway pressure, at peak sinusoidal inspiratory flow rate demands of 30, 60, and 90 L/min with sizes 6, 7, 8, and 9 mm internal diameter endotracheal tubes at each flow rate during conventional pressure triggering, tracheal pressure triggering, and flow-by.Pressures were measured at the tracheal end of the endotracheal tube, "Y" piece of the breathing circuit, and inside the ventilator on the exhalation limb of the breathing circuit. Volume measured between the endotracheal tube and lung model and pressure measured at the tracheal end of the endotracheal tube were integrated to generate pressure-volume (work) loops to calculate the inspiratory imposed work of the total breathing apparatus (i.e., endotracheal tube, breathing circuit, and ventilator). Significantly (p.05) greater decreases in pressure during spontaneous inhalation were measured for all methods of triggering at the tracheal end of the endotracheal tube than at the Y piece or inside the ventilator. Inspiratory-imposed work was significantly lower during tracheal pressure triggering compared with conventional pressure triggering and flow-by under most conditions. For example, with a 7-mm internal diameter endotracheal tube at a peak inspiratory flow rate demand of 60 L/min, imposed work was 382% and 315% lower, respectively, during tracheal pressure triggering compared with the conventional pressure triggering and flow-by triggering methods. Under all conditions, inspiratory imposed work was lower during flow-by triggering compared with conventional pressure triggering. The smaller the internal diameter of the endotracheal tube and the greater the peak inspiratory flow rate demand, the greater the inspiratory imposed work of breathing for all methods of triggering. Under all conditions, inspiratory-imposed work was significantly greater at a peak inspiratory flow rate demand of 90 L/min than at 60 L/min, and at a peak inspiratory flow rate demand of 60 L/min than at 30 L/min.An endotracheal tube is a resistor in the breathing apparatus over which a pressure decrease must be developed by the patient in order to inhale spontaneously. An endotracheal tube, therefore, imposes substantial resistance and work. The results indicate that the pressure measuring/triggering site for a ventilator's demand-flow system should be at the tracheal or carinal end of an endotracheal tube so as to effectively decrease the resistance of the endotracheal tube, thus, decreasing the patient's work of breathing.

Purposes To discuss the theoretical relationship of mean alveolar pressure to its most easily measured analog, the mean airway pressure, and to describe the key determinants, measurement considerations, and clinical implications of this index. Data sources Relevant articles from the medical and physiologic literature, as well as mathematical arguments developed in this article from first principles. Study selection Theoretical, experimental, and clinical information that elucidates the physiologic importance, measurement, or adverse consequences of mean airway pressure. Data extraction Mathematical models were used in conjunction with data from the published literature to develop a unified description of the physiological and clinical relevance of mean airway pressure. Synthesis Geometrical and mathematical analyses demonstrate that shared elements comprise mean airway pressure and mean alveolar pressure, two variables that are related by the formula: mean alveolar pressure = mean airway pressure + (VE/60) x (RE-RI), where VE, RE, and RI are minute ventilation and expiratory and inspiratory resistances, respectively. Clear guidelines can be developed for selecting the site of mean airway pressure determination, for specifying technical requirements for mean airway pressure measurement, and for delineating clinical options to adjust the level of mean airway pressure. Problems in viewing mean airway pressure as a reflection of mean alveolar pressure can be interpreted against the theoretical basis of their interrelationship. In certain settings, mean airway pressure closely relates to levels of ventilation, arterial oxygenation, cardiovascular function, and barotrauma. Because mean airway pressure is associated with both beneficial and adverse effects, a thorough understanding of its theoretical and practical basis is integral to formulating an effective pressure-targeted strategy of ventilatory support. Conclusions Mean airway pressure closely reflects mean alveolar pressure, except when flow-resistive pressure losses differ greatly for the inspiratory and expiratory phases of the ventilatory cycle. Under conditions of passive inflation, mean airway pressure correlates with alveolar ventilation, arterial oxygenation, hemodynamic performance, and barotrauma. We encourage wider use of this index, appropriately measured and interpreted, as well as its incorporation into rational strategies for the ventilatory management of critical illness.

OBJECTIVE To describe the importance of measuring pressure at the tracheal end of the endotracheal tube during spontaneous breathing with continuous positive airway pressure in order to correctly assess: a) the changes in airway pressure and b) the work imposed by the breathing apparatus. DESIGN Multitrial tests under simulated clinical conditions using a mechanical lung model. SETTING A research laboratory at a university medical center. INTERVENTIONS Spontaneous breathing with continuous positive airway pressure, at peak sinusoidal inspiratory flow-rate demands of 30 and then 60 L/min with sizes 6, 7, 8, and 9 mm internal diameter endotracheal tubes at each flow rate. MEASUREMENTS AND MAIN RESULTS Pressure, flow rate, and inhaled and exhaled volumes, during simulated spontaneous ventilation with continuous positive airway pressure were measured. Pressure was measured alternately at the "Y" piece of the breathing tubing of the continuous positive airway pressure system and at the tracheal end of the endotracheal tube to calculate the work imposed by the breathing circuit, endotracheal tube, and the total breathing apparatus. Greater changes in pressure and work were measured at the tracheal end of the endotracheal tube than at the "Y" piece of the breathing tubing for all test conditions. For example, at a peak inspiratory flow-rate demand of 30 L/min when pressures measured at the tracheal end of endotracheal tubes were compared with pressures measured at the "Y"piece, the total work imposed by the breathing apparatus increased by approximately 145% with a 6-mm tube, 95% with a 7-mm tube, 50% with an 8-mm tube, and 40% with a 9-mm tube (p less than .05). Measuring pressure at the "Y" piece of the tubing results in significant underestimations of the changes in pressure and the work imposed, especially when the endotracheal tube has a small internal diameter and/or when the peak inspiratory flow-rate demand is high. CONCLUSIONS The results indicate that pressure should be measured as close to the patient's airway as possible, i.e., at the tracheal end of the endotracheal tube, rather than using the traditional approach of measuring pressure and assessing work at the inspiratory or expiratory limbs, or "Y" piece of the breathing tubing.

Objective To determine pulmonary mechanical characteristics in neonates after cardiac surgery. Design A prospective study. Setting A 23-bed, pediatric ICU in a 280-bed children's hospital. Patients Twenty-six infants on the first post-operative day after cardiac surgery. Methods Pulmonary mechanics measurements were made during spontaneous breathing, using the esophageal balloon technique and a pneumotachometer. The least mean square method of analysis was used to calculate mechanics. Infants who tolerated withdrawal of mechanical ventilation (group 1) were compared with those infants with respiratory failure (group 2). Results Spontaneous respiratory rate, tidal volume, and minute ventilation were similar in groups 1 and 2. Lung compliance was decreased, with no difference between groups. Total lung resistance (34.3 +/- 21.6 cm H2O/L.sec in group 1 vs. 136.8 +/- 105.8 cm H2O/L.sec in group 2, p = .002) and resistive work of breathing (33.4 +/- 29.9 g.cm/kg in group 1 vs. 212.9 +/- 173.8 g.cm/kg in group 2, p = .001) were significantly higher in group 2. All infants with a total lung resistance greater than 75 cm H2O/L.sec exhibited respiratory failure (resistance greater than 75 cm H2O/L.sec correlated with respiratory failure, r2 = .73, odds ratio of 70 [confidence interval, 4.4 to 3240], p less than .001). Conclusions Increased lung resistance identifies neonates with respiratory failure after cardiac surgery. Pulmonary mechanics testing may be useful in timing withdrawal of mechanical ventilation.

Objective: Maintenance breathing is advocated in mechanical ventilation, which is difficult for the high-frequency oscillatory (HFO) ventilation. To facilitate spontaneous breathing during HFO ventilation, a demand flow system (DFS) was designed. The aim of the present study was to evaluate the system. Design: Animal experiment. Setting: University animal laboratory. Subjects: Eight pigs (47-64 kg). Interventions: Lung injury was induced by lung lavage with normal saline. After spontaneous breathing was restored HFO ventilation was applied, in runs of 30 minutes, with continuous fresh gas flow (CF) or the DFS operated in two different setups. Pressure to regulate the DFS was sampled directly at the Y-piece of the ventilator circuit (DFS) or between the endotracheal tube and measurement equipment at the proximal end of the endotracheal tube. In the end, animals were paralyzed. Breathing pattern, work of breathing, and gas exchange were evaluated. Measurements and Main Results: HFO ventilation with demand flow decreased breathing frequency and increased tidal volume compared with CF. Comparing HFO modes CF, DFS, and DFSPROX, total pressure-time product (PTP) was 66 cm H 2 O·sec·min -1 (interquartile range 59-74), 64 cm H 2 O·sec·min -1 (50-72), and 51 cm H 2 O·see·min -1 (41-63). Ventilator PTP was 36 cm H 2 O·sec·min -1 (32-42), 8.6 cm H 2 O·sec·min -1 (7.4-10), and 1 cm H 2 O·sec·min -1 (-1.0 to 2.8). Oxygenation, evaluated by Pao 2 , was preserved when spontaneous breathing was maintained and deteriorated when pigs were paralyzed. Ventilation, evaluated by Paco 2 , improved with demand flow. Paco 2 increased when using continuous flow and during muscular paralysis. Conclusions: In moderately lung-injured anesthetized pigs during HFO ventilation, demand flow facilitated spontaneous breathing and augmented gas exchange. Demand flow decreased total breathing effort as quantified by PTP. Imposed work caused by the HFO ventilator appeared totally reduced by demand flow.