Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 18 de 18
Filter
1.
Respir Care ; 46(8): 789-97, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11463369

ABSTRACT

INTRODUCTION: Mechanical ventilator failures expose patients to unacceptable risks and are expensive. By identifying factors that correlate with the amount of time between consecutive ventilator failures, we might reduce patient risk, save money, and shed light on a number of important questions concerning whether reliability changes as a function of time. OBJECTIVE: Investigate the correlation between several explanatory variables and the time between consecutive ventilator failures and address the following questions: (1) Are ventilators as safe and reliable following repairs as they were before failing? (2) Does reliability change significantly as a ventilator is used or ages? (3) Does a hospital's particular operating environment play a role in ventilator reliability? (4) Are ventilator service contracts worth the money? METHODS: A retrospective review was conducted using repair and maintenance records from 2 hospitals: a 570-bed teaching hospital and a 410-bed local community hospital. Records were examined from a total of 66 individual ventilators, of 5 different brands, used between July 1, 1991, and January 3, 2001. The ventilators included 13 Tyco-Mallinckrodt Infant Star, 10 Bird VIP, 11 Bird 6400ST, 16 Bird 8400STi, and 16 Tyco-Mallinckrodt 7200ae. The dependent variable was the operating time between or before unexpected mechanical failures; this was determined by the difference between hours logged on the ventilator hour meter at the time of failure and that recorded when the study began, or when the ventilator was new. Thereafter (when applicable), the time before failure was the difference in hours at consecutive failures. Seven independent explanatory covariates were selected and analyzed as potential correlates with time between failures. Another independent variable, the site of ventilator use (community or teaching hospital), was also tested for significance. Data were analyzed using the Cox proportional hazard model, the multiple-groups survival statistic, and the Cox-Mantel test. RESULTS: In 2,567,365 hours of ventilator operation, 290 observations were recorded (226 failures and 64 censored observations). Two of the 7 covariates were judged time-dependent, excluded from the Cox model, and evaluated using other techniques. Of the 5 remaining covariates, 2 were significantly related to reliability, both indirectly. There was no difference in reliability, regardless of how many times a ventilator had been previously repaired, but hospital environment did significantly affect reliability. CONCLUSIONS: Ventilator reliability depends on a number of factors. This study indicates that, on average, ventilator reliability improves the more a ventilator is used and the longer the brand has been commercially available. The number of previous ventilator repairs did not affect reliability, but the hospital environment did. These data, if validated, should help to enhance our understanding of ventilator reliability and could eventually have profound economic and safety implications as well.


Subject(s)
Ventilators, Mechanical/standards , Contract Services/standards , Critical Care/methods , Data Interpretation, Statistical , Equipment Failure Analysis/economics , Ventilators, Mechanical/economics
2.
Semin Respir Crit Care Med ; 21(3): 233-43, 2000.
Article in English | MEDLINE | ID: mdl-16088736

ABSTRACT

Tracheal pressure ventilator control (TPVC) is a ventilator mode that relies on tracheal pressure at the carinal end of the endotracheal tube for triggering the ventilator ;;on,'' controlling pressure, and cycling the ventilator ;;off.'' TPVC automatically nullifies imposed resistive work of the breathing apparatus (endotracheal tube plus ventilator) by providing automatic and variable levels of pressure assist. TPVC improves ventilator responsiveness for a spontaneously breathing patient by providing significantly higher peak inspiratory flow rates much closer to that demanded by a patient. TPVC also provides higher assist pressures and flow rates earlier in the breath and thus better-match ventilator-supplied flow to patient-demanded flow than an equivalent level of pressure support ventilation. Matching patient demand for flow to ventilator supply of flow, early in the breath, promotes patient-ventilator synchrony and minimizes work of breathing. We recommend moving the pressure-triggering and control site to the carinal end of the endotracheal tube to provide TPVC.

3.
J Clin Monit Comput ; 14(3): 157-64, 1998 Apr.
Article in English | MEDLINE | ID: mdl-9676862

ABSTRACT

OBJECTIVE: Infusing nitric oxide at a constant rate into a breathing circuit with intermittent mainstream flow causes formation of nitric oxide pools between successive breaths. We hypothesized that incomplete mixing of these pools can confound estimates of delivered nitric oxide concentrations. METHODS: Nitric oxide flowed at a constant rate into the upstream end of a standard adult breathing circuit connected to a lung model. One-milliliter gas samples were obtained from various sites within the breathing system and during various phases of the breathing cycle. These samples were aspirated periodically by a microprocessor controlled apparatus and analyzed using an electrochemical sensor. RESULTS: The pools of nitric oxide distorted into hollow parabolic cone shapes and remained unmixed during their propagation into the lungs. In our preparation, time-averaged nitric oxide concentrations were minimal 60 cm downstream of the infusion site (18 ppm) and maximal 15 cm upstream of the Y-piece (36 ppm). The concentrations were mid-range within the lung (23 ppm), yet were substantially less than predicted by assuming homogeneity of the gases (31 ppm). Generally, nitric oxide concentrations within the lung were different from all other sites tested. CONCLUSION: Incomplete mixing of nitric oxide confounds estimates of delivered nitric oxide concentrations. When nitric oxide is infused at a constant rate into a breathing circuit, we doubt that any sampling site outside the patient's lungs can reliably predict delivered nitric oxide concentrations. Strategies to ensure complete mixing and representative sampling of nitric oxide should be considered carefully when designing nitric oxide delivery systems.


Subject(s)
Nitric Oxide/administration & dosage , Respiration, Artificial/instrumentation , Adult , Humans , Lung/blood supply , Lung/physiology , Monitoring, Physiologic/methods , Nitric Oxide/analysis , Nitric Oxide/pharmacokinetics , Respiration, Artificial/methods , Vascular Capacitance
4.
Crit Care Med ; 25(8): 1410-6, 1997 Aug.
Article in English | MEDLINE | ID: mdl-9267958

ABSTRACT

OBJECTIVES: This study was designed to test the hypothesis that the practice of infusing nitric oxide at constant flow rates directly into breathing circuits with intermittent (pulsatile) flow can lead to streaming and tidal pooling of the nitric oxide. This study was also designed to show the extent to which streaming and tidal pooling of nitric oxide affect nitric oxide delivery. DESIGN: A series of five in vitro experiments was performed. For each experiment, either one or two features of the nitric oxide delivery/sampling system were varied, and the effects of these variations were evaluated with regard to measured nitric oxide concentration changes. The results from each experiment were analyzed using either one- or two-factor analysis of variance. SETTING: University research laboratory. SUBJECTS: Breaths were provided by a mechanical ventilator that was connected to a lung model. A standard, corrugated, adult breathing circuit was used. Gas samples were obtained from either the lung model's bellows or selected sites within the breathing circuit. Nitric oxide concentrations were measured, using an electrochemical gas analyzer. INTERVENTIONS: The system features that were varied included the cross-sectional position of the sampling site within the breathing circuit, the distance between the infusion port and the sampling site, the breathing frequency, the distance between the Y-piece and the infusion port, and the airway (deadspace) volume. MEASUREMENTS AND MAIN RESULTS: Streaming of nitric oxide within the breathing circuit was detected as far as 25 cm downstream of the infusion site (p < .0001). Pooling of nitric oxide was detected both near and downstream of the infusion site (p < .0001). Increasing the breathing frequency from 5 to 30 breaths/min increased mixing thoroughness (p < .005). Increasing the distance between the Y-piece and the infusion port from 15 to 180 cm decreased nitric oxide delivery to our lung model (p < .0001). Interestingly, increasing airway (deadspace) volume from 150 to 450 mL decreased nitric oxide delivery to our lung model (p < .0001). CONCLUSIONS: Estimates of nitric oxide delivery using a constant flow rate of nitric oxide infused directly into a breathing circuit during controlled mechanical ventilation can be confounded by streaming and tidal propagation of nitric oxide pools. Improved reproducibility of reported dose-response relationships is likely to be achieved through further study of nitric oxide behavior within the breathing circuits. Reduced toxicity associated with nitric oxide inhalation may also be achieved through a better understanding of this nitric oxide behavior.


Subject(s)
Lung/drug effects , Nitric Oxide/administration & dosage , Nitric Oxide/pharmacology , Respiration, Artificial/methods , Administration, Inhalation , Adult , Analysis of Variance , Breath Tests , Confounding Factors, Epidemiologic , Dose-Response Relationship, Drug , Factor Analysis, Statistical , Humans , Models, Biological , Pulsatile Flow
6.
Chest ; 108(5): 1338-44, 1995 Nov.
Article in English | MEDLINE | ID: mdl-7587438

ABSTRACT

OBJECTIVE: To evaluate the relationships between directly measured work of breathing (WOB) and variables of the breathing pattern commonly used at the bedside to infer WOB for intubated, spontaneously breathing patients treated with pressure support ventilation (PSV). DESIGN: In vivo measurements of the WOB were obtained on a consecutive series of adults. Breathing frequency (f), tidal volume (VT), the index of rapid, shallow breathing (f/V T), the duration of respiratory muscle contraction expressed as the ratio of inspiratory time over total respiratory cycle time (TI/TTOT), and a breathing pattern score (applied to approximately 50% of the patients) which ranks f, VT, sternocleidomastoid muscle activity, substernal retraction, and abdominal paradox on a scale were variables of the breathing pattern were also measured. The greater the breathing pattern score, the lower the WOB and vice versa. SETTING: Surgical ICUs in two university teaching hospitals. PATIENTS: Sixty-seven adults (42 men and 25 women, aged 20 to 78 years) who had acute respiratory failure from various etiologies were studied. All patients were breathing spontaneously receiving continuous positive airway pressure and PSV. INTERVENTIONS: Intraesophageal pressure (indirect measurement of intrapleural pressure) was measured with an esophageal balloon integrated into a nasogastric tube. VT was obtained by positioning a flow sensor between the "Y" piece of breathing circuit and the endotracheal tube. Data from these measurements were directed to a bedside respiratory monitor (Bicore; Allied Healthcare Products; Riverside, Calif) that calculates WOB using the Campbell diagram. Patients received PSV at levels deemed reasonable to unload the respiratory muscles. All measurements were obtained after 15 to 20 min at each level of PSV, averaged over 1 min, and then variables of the breathing pattern were regressed with directly measured values for WOB. RESULTS: All breathing pattern variables poorly predicted WOB as evidenced by the low values for the coefficients of determination (r2). Breathing frequency correlated positively with WOB (r = 0.47, p < 0.001) and predicted or explained only 22% (r2 = .22) of the variance in WOB. VT correlated negatively and f/VT and TI/TTOT each correlated positively with WOB. However, these variables predicted only 20 to 27% of the variance in WOB. The breathing pattern score correlated negatively with WOB and predicted only 43% of the variance in WOB. A prediction model taking all variables into consideration using multiple regression analysis predicted only 50% of the variance in WOB; thus, it too was a poor to moderate predictor of WOB. CONCLUSION: Our data reveal that WOB should be measured directly because variables of the breathing pattern commonly used at the bedside appear to be inaccurate and misleading inferences of the WOB. The clinical implication of these findings involves the traditional and empirical practice of titrating PSV based on the breathing pattern. We do not imply that the patient's breathing pattern should be ignored, nor undermine its importance, for it provides useful diagnostic information. It appears, however, that relying primarily on the breathing pattern alone does not provide enough information to accurately assess the respiratory muscle workload. Using the breathing pattern as the primary guideline for selecting a level of PSV may result in inappropriate respiratory muscle workloads. A more comprehensive strategy is to employ WOB measurements and the breathing pattern in a complementary manner when titrating PSV in critically ill patients.


Subject(s)
Positive-Pressure Respiration , Respiration , Respiratory Insufficiency/physiopathology , Work of Breathing , Adult , Aged , Female , Humans , Male , Middle Aged , Predictive Value of Tests , Respiratory Insufficiency/therapy , Respiratory Muscles/physiopathology
7.
Chest ; 108(4): 1065-72, 1995 Oct.
Article in English | MEDLINE | ID: mdl-7555121

ABSTRACT

Nitric oxide (NO) gas is known as both a vasodilator and a toxin. It can react with oxygen to form compounds more toxic than itself, such as nitrogen dioxide (NO2). The reactions are time dependent; thus, infusing NO into breathing circuits as close to ventilated subjects as possible may help minimize toxic byproduct exposure. Unfortunately, flow rates commonly used with mechanical ventilation favor laminar gas flow (streaming) within the breathing circuits. Streaming could delay mixing of NO with other inhaled gases. This mixing delay may interfere with accurate monitoring and/or delivery of NO. We tested the hypothesis that streaming of NO infused by constant flow into the inspiratory limb of a constant-flow mechanical ventilation system can lead to NO concentration delivery estimate errors. We then compared the NO2 concentrations at the ventilator Y-piece with three different NO mixing methods: blending the gases before they reach the breathing circuit inspiratory limb, infusing NO directly into the breathing circuit inspiratory limb far enough from the Y-piece to ensure thorough mixing, and infusing NO directly into the breathing circuit inspiratory limb immediately before the gases reach an in-line mixing device placed close to the Y-piece. Our results indicate that streaming can lead to NO concentration delivery estimate errors and that these errors can be characterized by measuring NO concentration variations across the inspiratory tubing's luminal diameter. NO2 concentration measured at the ventilator Y-piece were dependent on NO concentrations (p < 0.0001), NO delivery methods (p < 0.0001), and interactions between NO concentrations and NO delivery methods (p < 0.0001). We conclude that gas streaming and toxic byproduct exposure should be considered together when choosing an NO delivery method.


Subject(s)
Nitric Oxide/administration & dosage , Respiration, Artificial/methods , Vasodilator Agents/administration & dosage , Dose-Response Relationship, Drug , Equipment Design , Evaluation Studies as Topic , Humans , Intubation, Intratracheal/instrumentation , Nitric Oxide/adverse effects , Nitrogen Dioxide/analysis , Respiration, Artificial/instrumentation , Respiration, Artificial/statistics & numerical data , Vasodilator Agents/adverse effects , Ventilators, Mechanical
8.
Chest ; 108(2): 509-14, 1995 Aug.
Article in English | MEDLINE | ID: mdl-7634891

ABSTRACT

STUDY OBJECTIVE: We evaluated the difference in work of breathing (WOB) during spontaneous ventilation with continuous positive airway pressure (CPAP) among three methods of triggering the ventilator: conventional pressure triggering, tracheal pressure triggering, and flow-by triggering. METHODS: In an in vitro model of the respiratory system consisting of a bellows (lungs) in a plastic canister (chest wall), spontaneous ventilation was simulated with a piston-driven pump (respiratory muscles). Data were recorded during CPAP of 5 cm H2O (model 7200ae ventilator, Puritan-Bennett, Overland Park, Kan) at peak sinusoidal inspiratory flow rate demands of 60 and 80 L/min and airway resistances of 5 and 20 cm H2O/L/s, with the demand flow system triggered by conventional pressure, tracheal pressure, or flow. Under each condition, tidal volume, pressure-time product (PTP), WOB, and changes in intrapleural pressure (Ppl) and airway pressure were recorded in real time by means of a computerized portable respiratory monitor (model CP-100, Bicore, Irvine, Calif). The Ppl was measured from within the canister, tidal volume by positioning a flow sensor between the Y-piece of the breathing circuit and the endotracheal tube (ETT), and airway pressure from a catheter attached to the flow sensor. The WOB was calculated by the monitor in real time. RESULTS: Changes in Ppl were greatest with conventional pressure triggering, less with flow-by triggering, and least with tracheal pressure triggering. The WOB was significantly lower (approximately 50%) with tracheal pressure triggering than with the other two methods. With tracheal pressure triggering only, an effect similar to that of pressure support ventilation (PSV) occurred, which accounted in part for the significant decrease in WOB. The PTP/breath ratio correlated strongly and was a good predictor of WOB (r2 = 0.95). CONCLUSIONS: Compared with conventional pressure and flow-by methods, triggering with tracheal pressure decreased WOB significantly. This method of triggering may improve patient-ventilator interaction.


Subject(s)
Air Pressure , Positive-Pressure Respiration/methods , Trachea/physiology , Ventilators, Mechanical , Work of Breathing/physiology , Humans , In Vitro Techniques , Lung/physiology , Models, Structural , Positive-Pressure Respiration/instrumentation
9.
J Clin Monit ; 11(1): 14-7, 1995 Jan.
Article in English | MEDLINE | ID: mdl-7745447

ABSTRACT

OBJECTIVE: A new, microprocessor-controlled respiratory monitor (model CP-100 Pediatric, Bicore Monitoring Systems, Irvine, CA) that measures imposed work of breathing and a variety of respiratory parameters for pediatric patients receiving ventilatory support has recently been developed. To validate its accuracy, measurements obtained using this monitor were compared with those obtained using conventional laboratory equipment. METHODS: An in vitro lung model was used to simulate spontaneously breathing pediatric patients ranging from infancy to 10 years of age. Tidal volume, respiratory rate, and peak inspiratory flow rates were simulated in a stepwise manner. Values for imposed work, tidal volume, peak inspiratory flow rate, and change in airway pressure for both methods were compared using regression analysis. RESULTS: The coefficients of determination (r2) describing the relationships of both methods of measuring imposed work, tidal volume, peak inspiratory flow rate, and the change in airway pressure ranged from 0.99 to 1.00, and were highly significant (p < 0.001). For all measurements, bias was minimal and precision was calculated. CONCLUSIONS: Our data reveal that this pediatric respiratory monitor accurately measures imposed work of breathing, as well as tidal volume, flow rate, and airway pressure. Imposed work of breathing measurements obtained from the monitor may be used to adjust pressure support ventilation, so that the imposed work of the breathing apparatus is reduced to zero and the patient's total work of breathing is thus decreased.


Subject(s)
Monitoring, Physiologic/instrumentation , Work of Breathing/physiology , Child , Humans , Lung/physiology , Models, Structural , Reproducibility of Results , Respiration, Artificial
10.
Chest ; 106(6): 1835-42, 1994 Dec.
Article in English | MEDLINE | ID: mdl-7988210

ABSTRACT

OBJECTIVE: To evaluate the clinical feasibility of using real-time measurements of work of breathing obtained at the bedside with a portable, commercially available respiratory monitor as an objective and quantifiable guideline for appropriately setting pressure support ventilation (PSV) to partially and totally unload the respiratory muscles in patients with respiratory failure. DESIGN: In vivo measurements of work of breathing were performed on a consecutive series of patients after applying incremental levels of PSV. SETTING: University teaching hospital in a surgical ICU. PATIENTS: Thirty adults (18 men and 12 women, ages 20 to 77 years) who had acute respiratory failure were studied. All patients had an endotracheal or a tracheostomy tube in place and were breathing spontaneously, receiving continuous positive airway pressure and PSV. INTERVENTIONS: Intraesophageal pressure (indirect measurement of intrapleural pressure) was measured with an esophageal balloon catheter positioned in the mid- to lower-third of the esophagus. Tidal volume was obtained by positioning a flow sensor between the "Y" piece of the breathing circuit and the endotracheal or tracheostomy tube. Airway pressure was measured from a catheter attached to the flow sensor. Data from these measurements were directed to the respiratory monitor (CP-100, Bicore Monitoring Systems) which calculates work of breathing performed by the patient using the Campbell diagram. Work of breathing performed by the ventilator to inflate the respiratory system was calculated by the monitor by integrating the change in airway pressure and tidal volume. Initially, the level of PSV was set to 0 cm H2O and work measurements were obtained. Pressure support ventilation was then increased until the work performed by the patient decreased to a range of 0.3 to 0.6 J/L, which corresponds to a normal range for physiologic work of breathing (ie, partial respiratory muscle unloading), and then until the work decreased to 0 J/L (ie, total respiratory muscle unloading). RESULTS: Work performed by the patient varied inversely (r = -0.83; p < 0.001) and work performed by the ventilator varied directly with the level of PSV (r = 0.94; p < 0.001). Work performed by the patient was 1.5 +/- 0.3 J/L at zero pressure support ventilation and decreased significantly to 0.50 +/- 0.1 J/L (p < 0.05) as the level of PSV was increased to 18 +/- 7 cm H2O. The respiratory muscles were partially unloaded under these conditions. Patient work decreased to 0 J/L and ventilator work increased when the muscles were totally unloaded at a PSV level of 31 +/- 8 cm H2O. CONCLUSION: We propose an objective and goal-oriented clinical approach for using PSV by directly measuring the work of breathing performed by the patient with an easy to operate, bedside respiratory monitor and then applying pressure support ventilation to decrease the work to appropriate levels. Partially or totally shifting the workload from the respiratory muscles to the ventilator is appropriate under specific clinical conditions.


Subject(s)
Respiratory Muscles/physiopathology , Work of Breathing , Acute Disease , Adult , Aged , Female , Humans , Male , Middle Aged , Respiration, Artificial , Respiratory Insufficiency/physiopathology , Respiratory Insufficiency/therapy , Tidal Volume
11.
Respir Care ; 39(9): 897-905, 1994 Sep.
Article in English | MEDLINE | ID: mdl-10146116

ABSTRACT

BACKGROUND: Computerized, yet portable, bedside pulmonary monitors that can measure work of breathing (WOB) are now commercially available; however, none accurately measures WOB. The purpose of this study was to evaluate new software designed to measure WOB by means of the Campbell diagram and to test the agreement between a monitor (Model CP-100, Bicore, Irvine CA) programmed with the new software and the conventional method of measuring WOB. MATERIALS & METHODS: Using a lung model of our own devising, we compared WOB measurements between the monitor and conventional laboratory equipment. Inspiratory flow-rate, tidal volume (VT), and resistance of the model were adjusted to produce WOB ranging from 0.80 to 3.25 J/L. Regression analysis and calculation of bias and precision were performed for these data. RESULTS: For total, elastic, and resistive WOB, the two methods of measurement correlated strongly and positively. For all values of WOB, the correlation coefficients (r) and coefficients of determination (r2) were close to 0.99 (p < 0.0001); bias was minimal (-0.05 J/L) and precision acceptable (0.06 J/L). CONCLUSION: Data from a lung model reveal that a respiratory monitor programmed with appropriate software can accurately measure total, elastic, and resistive WOB. The monitor may eventually prove useful for clinically assessing WOB, which then can be used to adjust the ventilator to optimize respiratory muscle loads.


Subject(s)
Monitoring, Physiologic/instrumentation , Respiratory Therapy/instrumentation , Software/standards , Work of Breathing/physiology , Equipment Design , Evaluation Studies as Topic , Humans , Models, Theoretical
13.
Crit Care Med ; 21(9): 1333-8, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8370298

ABSTRACT

OBJECTIVES: To apply pressure-support ventilation with the goal of decreasing the imposed work of the breathing apparatus (endotracheal tube, breathing circuit tubing, and the ventilator's demand-flow system) to zero and to evaluate a clinical method of measuring the imposed work of breathing. DESIGN: A prospective evaluation of adult and pediatric patients receiving mechanical ventilatory support. SETTING: A surgical and a pediatric intensive care unit in a university hospital. PATIENTS: Fifteen patients (11 adult and four pediatric), who were diagnosed with acute respiratory failure from various etiologies, and who were intubated and spontaneously breathing, received continuous positive airway pressure and pressure-support ventilation. MEASUREMENTS AND MAIN RESULTS: Imposed work of the breathing apparatus was calculated by integrating pressure measured at the tracheal end of the endotracheal tube from a narrow air-filled catheter and the change in volume from a miniature pneumotachograph (flow sensor) positioned between the "Y" piece of the breathing circuit and the endotracheal tube. Pressure and volume signals were directed to a computerized, portable respiratory monitor (Bicore Monitoring Systems) that provides real-time display of the pressure-volume (work) loops and calculation of the imposed work. Imposed work was measured at 0 cm H2O pressure-support ventilation, and then incremental levels of pressure-support ventilation were applied until the imposed work decreased to zero. Imposed work decreased in a quadratic fashion after incremental levels of pressure-support ventilation (r = -.83 [r2 = .69]; p < .001). At pressure-support ventilation level of 0 cm H2O, the imposed work was 0.60 +/- 0.17 joule/L. At mean pressure-support ventilation levels of 13.5 +/- 4.8 cm H2O, imposed work decreased to 0 joule/L. CONCLUSIONS: Ideally, the imposed work of the breathing apparatus should be zero to decrease the afterload on the ventilatory muscles and, thus, the patient's work of breathing. Eliminating the imposed work is achieved using appropriate levels of pressure-support ventilation. We describe an easily applied, practical method of measuring imposed work using a commercially available, portable, bedside respiratory monitor. We recommend that all patients diagnosed with respiratory failure and compromised pulmonary mechanics and who are intubated and breathing spontaneously, receive at least a minimal level of pressure-support ventilation that results in zero breathing apparatus-imposed work of breathing.


Subject(s)
Positive-Pressure Respiration , Respiratory Insufficiency/physiopathology , Respiratory Insufficiency/therapy , Therapy, Computer-Assisted/methods , Work of Breathing , Acute Disease , Adolescent , Adult , Airway Resistance , Child , Elasticity , Evaluation Studies as Topic , Humans , Lung Compliance , Lung Volume Measurements , Middle Aged , Monitoring, Physiologic , Pressure , Prospective Studies , Reproducibility of Results , Therapy, Computer-Assisted/instrumentation
15.
Crit Care Med ; 21(2): 183-90, 1993 Feb.
Article in English | MEDLINE | ID: mdl-8428467

ABSTRACT

OBJECTIVES: 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. 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, 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. MEASUREMENTS AND MAIN RESULTS: 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. CONCLUSIONS: 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.


Subject(s)
Positive-Pressure Respiration/instrumentation , Work of Breathing , Airway Resistance , Equipment Design , Humans , Intubation, Intratracheal , Models, Biological , Pressure , Tidal Volume , Ventilators, Mechanical
16.
Crit Care Med ; 20(4): 528-33, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1559368

ABSTRACT

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.


Subject(s)
Intubation, Intratracheal , Positive-Pressure Respiration , Pressure , Work of Breathing/physiology , Humans , Mathematics
17.
J Clin Anesth ; 4(2): 147-52, 1992.
Article in English | MEDLINE | ID: mdl-1562339

ABSTRACT

Tracheal injury resulting from tracheal intubation is common. Injuries vary in type and severity, from mucosal sloughing to tracheal stenosis and fistula formation. We report a patient with poor lung compliance and massive tracheal dilatation as a result of prolonged mechanical ventilation with high inflation pressure despite the use of a high-volume, low-pressure cuff. To reduce the tracheal dilatation but maintain adequate ventilation and continuous positive airway pressure, we substituted a longer double-cuff tracheotomy appliance and used an automatic intermittent cuff inflator. The problems related to the design of modern tracheal tube cuffs are discussed.


Subject(s)
Cesarean Section , Lung Compliance/physiology , Pneumonia, Viral/physiopathology , Pregnancy Complications, Infectious/physiopathology , Respiration, Artificial/methods , Trachea , Adult , Chickenpox/physiopathology , Dilatation, Pathologic , Female , Humans , Postoperative Period , Pregnancy , Respiration, Artificial/instrumentation
18.
Chest ; 97(6): 1426-30, 1990 Jun.
Article in English | MEDLINE | ID: mdl-2347229

ABSTRACT

Controlling a massively leaking bronchopleural fistula (BPF) can prove difficult. In combination with acute respiratory failure (ARF), BPF results in a mortality of 81 percent. Intermittent inspiratory chest tube occlusion (IICTO) is recognized as effective in controlling even the largest BPF; however, IICTO, as previously described, is difficult to use for a variety of reasons. We report two cases of BPF in association with ARF managed with a simple new device that allows the application of IICTO with virtually any mechanical ventilator. The effectiveness of the device and associated technique in controlling BPF leaks is clearly demonstrated and may have played a role in the eventual recovery of a patient with BPF. Further study of the technique is warranted.


Subject(s)
Bronchial Fistula/therapy , Chest Tubes , Fistula/therapy , Pleural Diseases/therapy , Respiration, Artificial , Ventilators, Mechanical , Adult , Bronchial Fistula/complications , Equipment Design , Fistula/complications , Humans , Male , Pleural Diseases/complications , Respiratory Insufficiency/complications
SELECTION OF CITATIONS
SEARCH DETAIL
...