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ABSTRACT |
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Tracheotomy is widely performed on ventilator-dependent patients, but its effects on respiratory mechanics have not been studied. We measured the work of breathing (WOB) in eight patients before and after tracheotomy during breathing at three identical levels of pressure support (PS): baseline
level (PS-B), PS + 5 cm H2O (PS+5), and PS
5 cm H2O (PS
5). After the procedure, we also compared the resistive work induced by the patients' endotracheal tubes (ETTs) and by a new tracheotomy cannula in an in vitro bench study. A significant reduction in the WOB was observed after tracheotomy for PS-B (from 0.9 ± 0.4 to 0.4 ± 0.2 J/L, p < 0.05), and for PS
5 (1.4 ± 0.6 to 0.6 ± 0.3 J/L,
p < 0.05), with a near-significant reduction for PS+5 (0.5 ± 0.5 to 0.2 ± 0.1 J/L, p = 0.05). A significant reduction was also observed in the pressure-time index of the respiratory muscles (181 ± 92 to
80 ± 56 cm H2O · s/min for PS-B, p < 0.05). Resistive and elastic work computed from transpulmonary pressure measurements decreased significantly at PS-B and PS
5. A significant reduction in occlusion pressure and intrinsic positive end-expiratory pressure (PEEP) was also observed for all conditions, with no significant change in breathing pattern. Three patients had ineffective breathing
efforts before tracheotomy, and all had improved synchrony with the ventilator after the procedure. In vitro measurements made with ETTs removed from the patients, with new ETTs, and with the tracheotomy cannula showed that the cannula reduced the resistive work induced by the artificial airway. Part of these results was explained by a slight, subtle reduction of the inner diameter of used
ETTs. We conclude that tracheotomy can substantially reduce the mechanical workload of ventilator-dependent patients.
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INTRODUCTION |
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Tracheotomy is commonly performed on mechanically ventilated patients with prolonged difficulties in weaning from the ventilator. Many reasons are often mentioned for the decision to perform tracheotomy on these patients, very few of which are supported by convincing evidence (1). Conversely, tracheotomy carries a risk of immediate and long-term complications (4, 5).
Failure of weaning from the ventilator often results from an imbalance between respiratory muscle capacity and the loads imposed on the respiratory system (6). Information about the effect of tracheotomy on the work of breathing (WOB) may explain a possible influence of tracheotomy on the weaning process, and may therefore help in making individual decisions to perform this invasive procedure. Indeed, both the resistance of the tracheotomy cannula and its internal dead space (volume) may be smaller than those of an endotracheal tube (ETT), and tracheotomy may therefore ease the respiratory workload. On the other hand, the relative influence of the artificial airway in difficult-to-wean patients may be relatively small, and the total effort of breathing may be essentially dictated by the respiratory mechanics of the patient.
The purpose of the prospective study described here was to evaluate the effects of tracheotomy on breathing pattern and patients' efforts to breathe by examining these two parameters before and shortly after the procedure (7). In order to correlate the results observed in patients with the resistive properties of the prosthesis, a bench study was also performed, using the patients' ETTs after their removal.
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METHODS |
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Patients
Eight consecutive adult patients hospitalized in the medical intensive care unit of our hospital, requiring prolonged mechanical ventilation and who were candidates for tracheotomy according to current recommendations, were included in the study (3, 16). The patient group was quite representative of medical patients converted to tracheotomy, with indications for the procedure that were neurological (coma), respiratory (chronic obstructive pulmonary disease [COPD]), or neuromuscular (diaphragmatic dysfunction). All patients were studied while spontaneously breathing in the pressure-support (PS) ventilation mode. The study was performed between November 1993 and June 1994. All patients had given their informed consent to participate in the study, which was approved by the ethics committee for research of our institution.
Clinical Measurements
Measurements were made on the day before and 6 h after the end of the tracheotomy procedure. Airflow was recorded with a Fleisch No. 2 pneumotachograph (Fleisch, Lausanne, Switzerland) connected to a differential pressure transducer (MP 45, ± 2 cm H2O; Validyne Corp., Northridge, CA). The flow signal was integrated to yield tidal volume (VT). The pneumotachograph was inserted between the endotracheal tube and the Y-piece of the ventilator. Airway pressure (Paw) was measured with a differential pressure transducer (SDX 001, ± 70 cm H2O; Sensym, Santa Clara, CA).
Esophageal pressure (Pes) was recorded with a balloon catheter connected to a differential pressure transducer (Validyne MP 45, ± 50 cm H2O). Gastric pressure (Pga) was similarly recorded in four patients. The position and the validity of the Pes and Pga measurements were checked by analyzing the shape of both curves, using the occlusion technique, and, as previously described, after the drinking of water and by gently pushing on the patient's abdomen (17, 18).
All signals were sampled and digitized at 200 Hz, and data were
entered into a microcomputer. VT, respiratory rate (RR), and minute
ventilation (
E) were obtained from the flow signal. The WOB per
breath was computed from Pes/VT loops, and was expressed as WOB
per liter of ventilation (WOB/L, in J/L), or as power of breathing (WOB/
min, J/min). The inspiratory WOB per breath was computed according to the following principles: Work per breath was calculated from a
Campbell diagram, by computing the area under the inspiratory Pes/
VT curve on the one hand and under the static Pes/VT curve of the
chest wall on the other hand (19). The Pes values at zero-flow points
were considered as the beginning and end of expiration. The theoretical value for chest wall compliance, which is 4% of the predicted value
of the vital capacity (VC) per centimeter of water, was used to trace
the static Pes/VT curve for the chest wall (19). Some degree of error in
estimating chest wall compliance probably occurs in some patients
when estimation is based on this theoretical value. This error, however, is the same when different periods of breathing are compared,
and therefore does not invalidate comparisons. The relaxation curve
of the chest wall was superimposed on the complete diagram, assuming that the end-expiratory elastic recoil pressure of the chest wall was
equivalent to the Pes level at the beginning of inspiratory effort. The
beginning of the sharp negative deflection of the Pes curve was taken
as the onset of effort. Any difference between this initial Pes level and
the zero-flow point indicated the presence of intrinsic positive end-
expiratory pressure (this difference was referred to as PEEPi) (8, 20-
22). Separate calculations of the resistive WOB and elastic WOB were
also made, and were expressed per liter of ventilation (rWOB/L and
eWOB/L, respectively). These latter calculations were made with
transpulmonary pressure (PTP) measurements, calculated as Paw minus Pes, and with measurements of volume.
Because the static chest wall line is displaced from the zero-flow point, the presence of PEEPi increases the area enclosed in the Campbell diagram, and increases the calculated WOB. When no expiratory abdominal activity is detected, PEEPi implies that the inspiratory muscles must generate sufficient force to counteract the opposing positive recoil pressure generated by dynamic hyperinflation before inspiratory flow begins, and it therefore acts as an inspiratory threshold load. In the four patients with recordings of Pga, we checked the absence of an increase in Pga during expiration as previously described (23). In four patients, however, such recordings were not obtained. For these patients we calculated WOB by using the two possible extreme assumptions about expiratory muscle activity, to see whether this influenced the results in terms of net effect on WOB. We first calculated inspiratory WOB by assuming that all PEEPi was due to dynamic hyperinflation (i.e., with no expiratory muscle activity), and then also calculated inspiratory WOB without taking into account the PEEPi, assuming that the entire PEEPi value (and its subsequent change) could be due to expiratory abdominal muscle activity and was not part of the inspiratory work. We refer to this second calculation, with lower values of WOB, as WOBlow.
WOB/min (in J/min) was obtained by multiplying the mean work
per breath by RR. Power divided by
E yielded WOB/L (in J/L). Ten
to 30 breaths were used to compute average values, depending on
breath-to-breath variability.
Because measurements of WOB do not take into account inspiratory efforts that are unable to trigger the ventilator, analysis of desynchronization also included measurements of the pressure-time product per breath (PTP/b) and per minute (PTP/min) for the inspiratory muscles. For assisted breaths, PTP/b was calculated from the beginning of the inspiratory deflection to the end of inspiratory flow relative to the Pes tracing, assuming that elastance of the chest wall was
linear within the range of VT. The static chest wall line was used as the
reference for the area calculation. For ineffective efforts, we considered a horizontal line as the reference for the calculation, since virtually no variation in volume was detected. PTP/min was calculated as
PTP/b multiplied by RR. In this way, a distinction was made between
the ventilator respiratory rate (RR) and the patient respiratory rate
(RRp). The percentage of ineffective inspiratory efforts was therefore
calculated as (1
RR/RRp) × 100 (24).
Occlusion pressure (P0.1) was also determined, using the slope of airway pressure-versus-time curves at the beginning of the inspiratory effort, during triggering of the ventilator demand valve, as previously described (25).
Protocol
Three series of measurements were repeated on the day before and 6 h
after tracheotomy, at three different PS levels. PS was initially set at
the same level as used before tracheotomy (baseline pressure support:
PS-B), and was also reduced (PS
5) and increased (PS+5) by 5 cm
H2O in a randomized order; recordings were made at the end of each
15-min period under each PS condition. Because some patients exhibited respiratory distress while breathing spontaneously without respiratory assistance, this ventilatory modality was not studied in our patients. One may consider, however, that the low level of PS to which
the patients were subjected was close to that of spontaneous unassisted breathing (8.5 ± 3.9 cm H2O). External PEEP and FIO2 were
kept constant during all measurements. FIO2 was chosen at a level sufficient to obtain more than 90% arterial oxyhemoglobin saturation.
The trigger pressure threshold for ventilation was fixed at 1 cm H2O
and kept constant before and after tracheotomy. Different ventilators
were used in the study, but measurements for a given patient were
made with the same ventilator.
Tracheotomy was performed surgically and with the patient under
general anesthesia produced with Propofol (Zeneca Pharma, Cergy,
France) and Fentanyl (Janssen, Boulogne-Billancourt, France). The
initial dosages were respectively 2 mg/kg and 2 × 10
3 mg/kg, with intravenous administration. The same drugs were readministered at half
the initial dosage every 15 min during the procedure. The inner cannula diameter was kept similar to that of the ETT, and was 8 mm in
seven of the patients and 7 mm in one. Resolution of anesthesia was
complete in all patients at the time of the second set of measurements
(usually 6 h after the end of the tracheotomy procedure).
In Vitro Measurements
Removed ETTs were kept after tracheotomy for the purpose of bench testing. Their flow-impeding characteristics were compared in vitro with those of unused ETTs and to tracheotomy tubes of the same inner diameter. The same transducers and acquisition system were used as in the patient study. Six sets of measurements were made during phasic ventilation of a lung model connected to a ventilator via the different cannulas. In this model, the resistance to airflow was entirely due to the cannula or to the tube. For a given used ETT, VT and RR were chosen to resemble the values observed during the clinical measurements at the three different PS levels, before and after tracheotomy, and a sinusoidal flow was chosen. The same breathing pattern was used for comparing the resistive work induced by the used tube with that induced by a new, clean tube and by a new tracheotomy cannula. A Veolar ventilator (Hamilton Medical, Bonaduz AG, Switzerland) was used for these measurements. The total work exerted by the lung model, including the cannula, was calculated by plotting the volume signal versus the airway pressure signal, and was then partitioned into its resistive and its elastic components. The resistive work of breathing (rWOB) was averaged for each PS assistance level and expressed in J/L.
Statistical Analysis
Data are expressed as mean ± SD. Because each level of PS before
tracheotomy corresponded to the same level after tracheotomy, paired comparisons were made. Values were compared through Wilcoxon's nonparametric test for small samples. A value of p
0.05 was considered significant.
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RESULTS |
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Characteristics of the Patients
During a 10-mo period, eight patients were included and completed the study. Detailed clinical data and outcome are shown in Table 1. The mean duration of tracheal intubation before tracheotomy was 31 ± 19 d. During the same period, two additional patients were included but could not complete the study because of local hemorrhage following the tracheotomy procedure.
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Clinical Results
The main findings for WOB are presented in Figure 1 and Table 2. A significant reduction in WOB/L was observed at PS-B
and PS
5, and a near-significant reduction was observed at
PS+5 (p = 0.05).
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Comparisons between WOBlow values obtained before and
after tracheotomy are shown in Table 2. A significant reduction was similarly observed for PS-B and PS
5.
Resistive and elastic work decreased significantly at PS-B
and PS
5 (Table 2).
A significant reduction in P0.1 was observed for all levels
of PS (Figure 2, Table 2). The measurements of PEEPi also indicated a significant reduction for all PS levels (Figure 3, Table 2). No variation in expiratory abdominal activity, as
judged by analysis of the shape of the Pga curve, was observed
in the four patients on whom this measurement was made.
There was only a trend toward a reduction in RR and
E,
whatever the PS level (Table 2).
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With regard to the analysis of synchronization, one patient (Patient 1) had ineffective inspiratory efforts at more than 2/min at all three PS levels before tracheotomy (Table 3). The percentage of ineffective inspiratory efforts increased when the PS level was increased. The PTP/b related to ineffective inspiratory efforts was similar whatever the PS level before tracheotomy, whereas the PTP/min for ineffective inspiratory efforts, expressed as a percentage of the PTP/min for effective efforts, was much higher for the PS+5 level. After tracheotomy, a reduction was observed in all of these parameters. Some mild levels of desynchronization (ineffective inspiratory efforts at less than 3/min) were observed in two other patients for PS+5 before tracheotomy, but disappeared after tracheotomy.
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In Vitro Results
The mean values of rWOB measured with the different tubes and cannulas are shown in Table 4. The lower values were observed for the tracheotomy tubes and the higher for the removed ETTs. The mean percentage reduction in rWOB with tracheotomy tubes was 21% versus new ETTs at the PS-B level. The mean reduction from tracheotomy tubes to removed ETTs amounted to 43% at the same PS level. There was significant extra work induced by the removed ETTs, with an increase in rWOB of 28% over the work with the new ETTs.
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DISCUSSION |
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Tracheotomy is widely performed in intensive care units. Little is known, however, about its effects on weaning from and the duration of mechanical ventilation. This study was the first to evaluate, in the clinical environment, the effects of tracheotomy on parameters that may have a major influence on the issue of discontinuation of mechanical ventilation. It mainly demonstrated a significant reduction in WOB and in P0.1. Part of this reduction resulted from substantial extra work imposed by used ETTs that had been left in place for prolonged periods.
It is important to determine the mechanisms by which WOB can be reduced after tracheotomy. WOB can be represented as the sum of resistive work (applied to the lungs and mainly to artificial and natural airways) and elastic work (applied to the lungs and the chest wall). A diminution in the resistive component of WOB was the first factor explaining the overall reduction in WOB with tracheotomy. Such a reduction can be due to the following factors:
/
r4 (where K is a constant,
the flow, and r the radius of the tube). In the case of a turbulent stream, the decrease in
pressure is K' ·
2/D5 (where K' is a constant and D is the
effective diameter). It should be pointed out that obstruction of the ETT was never clinically suspected in any patient before tracheotomy. Such data are in accordance with
the findings in a previous study by Wright and coworkers,
in which an augmentation in ETT resistance was found with in vivo as compared with in vitro measurements (27),
and are also in accordance with the findings in a recent
study by Villafane and coworkers in our group (28). In the
latter study, this phenomenon was explained by a permanent deposit of secretions on the inner wall of the ETT.
We also observed a reduction in the eWOB, which could
have resulted from a change in PEEPi, contributing to the total reduction in WOB. The amount of PEEPi depends on RR
and on
E in patients with obstructive disease, but these latter
parameters, although slightly decreased, were not significantly
modified after tracheotomy. It is therefore more likely that
the diminution in PEEPi observed after tracheotomy was related to a diminution in expiratory resistance of the airway, as
discussed earlier. Our patients could also have displayed a
change in expiratory abdominal activity after tracheotomy. Indeed, this pattern of ventilation has been shown as a possible cause of PEEPi (23). Unfortunately, no systematic recording of Pga was done, and we therefore cannot formally address this point for all patients. In the four patients for whom recordings of Pga were available, however, this pattern of breathing was not observed. Moreover, we calculated WOBlow for the other
patients and then substituted the calculated values for the
measured values for the overall comparison of WOB before
and after tracheotomy. This was an extreme assumption in
which we considered that all measured PEEPi values would
have been positive owing to active expiration. A significant reduction was again observed for PS-B and PS
5, indicating a
benefit in terms of inspiratory effort.
Additionally, a significant effect of the anesthesic drugs
used for the tracheotomy procedure might explain a decrease
in WOB, although this is unlikely in view of the short half-life of elimination of fentanyl and propofol and because the patients were perfectly awake at the time of the study. More importantly, we observed a diminution in WOB expressed in J/L,
with no significant change in
E, which can hardly be explained by a diminution of central inspiratory drive alone.
Also, our results were consistent with the flow-impeding characteristics of the cannula as assessed in vitro.
We also observed a significant reduction in P0.1 after tracheotomy. P0.1 was first presented as an index of central respiratory drive (29, 30). It has also been proposed as a predictor of successful weaning from ventilation (9, 12, 14). Two factors may explain the diminution in P0.1. The first is the modification of the mechanical characteristics of the respiratory system that occurs with tracheotomy, reducing hyperinflation and resistances. The second factor is the diminution of the inspiratory central drive in response to this modification and, although it is less likely for the reasons discussed earlier, to the anesthesic agents used for tracheotomy.
In three patients, and especially in one, we observed an improved synchrony with the ventilator after tracheotomy. This could have been related to a reduction in the resistive load and in PEEPi. In accord with previous findings by others, this patient showed a higher rate of desynchronization when higher levels of PS were employed (24, 31, 32).
The effect of tracheotomy on the duration of mechanical ventilation is unknown. To date, only one study has prospectively evaluated the effect of tracheotomy in a small group of trauma patients, suggesting a benefit in favor of early tracheotomy as compared with prolonged translaryngeal intubation (2). Several other reasons, however, are often mentioned for the decision to perform tracheotomy on medical patients, and these reasons have to be balanced against the risk of the procedure (4). Improved patient comfort has been reported in one study, resulting from a facilitation of communication, mobility, oral alimentation, and suctioning of secretions (2). No other benefit, such as a reduction in the risk of laryngeal or tracheal injury or a reduction in the risk of nosocomial pneumonia, could be demonstrated. Tracheotomy is thus frequently performed during weaning from mechanical ventilation without strong arguments, substantiated by clinical studies, to support it. Accordingly, in a review of the literature, Heffner promoted an anticipatory approach in which tracheotomy would be performed after at least 7 d of intubation, when extubation appeared to be distant, and when it was likely to produce an important benefit (3). Our results also indirectly suggest that detecting and/or preventing insidious ETT obstruction may offer an alternative to tracheotomy in some patients.
In summary, the present study contributes physiologic information about the respiratory benefit of tracheotomy, and also emphasizes the importance of the insidious obstruction of ETTs. This may justify the development of methods to detect and quantify this complication (33, 34). It can also justify the evaluation of devices designed to remove obstructions from ETTs (35), and could argue against the current practice of keeping the same ETT in place for a prolonged period. In tracheotomized patients, changing the tracheotomy cannula is easily performed in a systematic fashion, which can be considered another advantage of this technique.
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Footnotes |
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Correspondence and requests for reprints should be addressed to L. Brochard, Service de Réanimation Médicale, Hôpital Henri Mondor, Avenue du Maréchal De Lattre de Tassigny, 94010 Créteil, France. E-mail: laurent.brochard{at}hmn.ap-hop-paris.fr
(Received in original form July 10, 1997 and in revised form June 5, 1998).
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References |
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|
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1.
El Naggar, M., S. Sadagopan, H. Levine, H. Kantor, and V. J. Collins.
1976.
Factors influencing choice between tracheostomy and prolonged translaryngeal intubation in acute respiratory failure: a prospective study.
Anesth. Analg.
55:
195-201
2. Astrachan, D. I., J. C. Kirchner, and W. J. Goodwin Jr.. 1988. Prolonged intubations vs. tracheotomy: complications, practical and psychological considerations. Laryngoscope 98: 1165-1169 [Medline].
3. Heffner, J. E.. 1993. Timing of tracheotomy in mechanically ventilated patients. Am. Rev. Respir. Dis. 147: 768-771 [Medline].
4. Stock, M. C., C. G. Woodward, B. A. Shapira, R. D. Cane, V. Lewis, and B. Pecaro. 1986. Perioperative complications of elective tracheostomy in critically ill patients. Crit. Care Med. 14: 861-863 [Medline].
5. Stauffer, J. L., D. E. Olson, and T. L. E. Petty. 1981. Complications and consequences of endotracheal intubation and tracheotomy: a prospective study of 150 critically ill adult patients. Am. J. Med. 70: 65-76 [Medline].
6. Lessard, M. R., and L. J. Brochard. 1996. Weaning from ventilatory support. Clin. Chest Med. 17: 475-489 [Medline].
7. Henning, R. J., H. Shubin, and M. H. Weil. 1977. The measurement of the work of breathing for the clinical assessment of ventilator dependence. Crit. Care Med. 5: 264-268 [Medline].
8. Fleury, B., D. Murciano, C. Talamo, M. Aubier, R. Pariente, J. Milic, and Emili. 1985. Work of breathing in patients with chronic obstructive pulmonary disease in acute respiratory failure. Am. Rev. Respir. Dis. 131: 822-827 [Medline].
9. Sassoon, C. S. H., T. T. Te, C. K. Mahutte, and R. W. Light. 1987. Airway occlusion pressure: an important indicator for successful weaning in patients with chronic obstructive pulmonary disease. Am. Rev. Respir. Dis. 135: 107-113 [Medline].
10.
Fiastro, J. F.,
M. P. Habib,
B. Y. Shon, and
S. C. Campbell.
1988.
Comparison of standard weaning parameters and the mechanical work of
breathing in mechanically ventilated patient.
Chest
94:
232-238
11. Lewis, W. D., W. Chwais, P. N. Benotti, K. Lakshman, C. O'Donnell, G. L. Blackburn, and B. Bistrian. 1988. Bedside assessment of the work of breathing. Crit. Care Med. 16: 117-122 [Medline].
12. Murciano, D., J. Boczkowski, Y. Lecocguic, J. Milic, Emili, R. Pariente, and M. Aubier. 1988. Tracheal occlusion pressure: a simple index to monitor respiratory muscle fatigue during acute respiratory failure in patients with chronic obstructive pulmonary disease. Ann. Intern. Med. 108: 800-805 .
13. Brochard, L., A. Harf, H. Lorino, and F. Lemaire. 1989. Inspiratory pressure support prevents diaphragmatic fatigue during weaning from mechanical ventilation. Am. Rev. Respir. Dis. 139: 513-521 [Medline].
14. Fernandez, R., J. Cabrera, N. Calaf, and S. Benito. 1990. P0.1/PIMax: an index for assessing respiratory capacity in acute respiratory failure. Intensive Care Med. 16: 175-179 [Medline].
15. Shikora, S. A., B. R. Bistrian, B. C. Borlase, G. L. Blackburn, M. D. Stone, and P. N. Benotti. 1990. Work of breathing: reliable predictor of weaning and extubation. Crit. Care Med. 18: 157-162 [Medline].
16.
Plummer, A. L., and
D. R. Gracey.
1989.
Consensus conference on artificial airways in patients receiving mechanical ventilation.
Chest
96:
178-180
17. Baydur, A., P. K. Behrakis, W. A. Zin, M. J. Jaeger, and J. Milic-Emili. 1982. A simple method for assessing the validity of the esophageal balloon technique. Am. Rev. Respir. Dis. 126: 788-791 [Medline].
18. Diehl, J. L., F. Lofaso, P. Deleuze, T. Similowski, F. Lemaire, and L. Brochard. 1994. Clinically relevant diaphragmatic dysfunction after cardiac operations. J. Thorac. Cardiovasc. Surg. 10: 487-498 .
19. Roussos, C., and E. J. M. Campbell. 1986. Respiratory muscle energetics. In P. T. Macklem and J. Mead, editors. Handbook of Physiology, Sect. 3, Vol. 3: Respiration. American Physiological Society, Bethesda, MD. 481-509.
20. Pepe, P. E., and J. J. Marini. 1982. Occult positive end-expiratory pressure in mechanically ventilated patients with airflow obstruction: the auto-PEEP effect. Am. Rev. Respir. Dis. 126: 166-169 [Medline].
21. Rossi, A., S. B. Gottfried, L. Zocchi, B. S. Higgs, S. Lennox, P. M. A. Calverley, P. Begin, A. Grassino, and J. Milic-Emili. 1985. Measurement of static compliance of the total respiratory system in patients with acute respiratory failure during mechanical ventilation: the effect of intrinsic positive end expiratory pressure. Am. Rev. Respir. Dis. 131: 672-677 [Medline].
22. Petrof, B. J., M. Legaré, P. Goldberg, J. Milic-Emili, and S. B. Gottfried. 1990. Continuous positive airway pressure reduces work of breathing and dyspnea during weaning from mechanical ventilation in severe chronic obstructive pulmonary disease (COPD). Am. Rev. Respir. Dis. 141: 281-289 [Medline].
23. Lessard, M. R., F. Lofaso, and L. Brochard. 1995. Expiratory muscle activity increases intrinsic positive end-expiratory pressure independently of dynamic hyperinflation in mechanically ventilated patients. Am. J. Respir. Crit. Care Med. 151: 562-569 [Abstract].
24.
Fabry, B.,
J. Guttmann,
L. Eberhard,
T. Bauer,
C. Haberthür, and
G. Wolff.
1995.
An analysis of desynchronization between the spontaneously breathing patient and ventilator during inspiratory pressure support.
Chest
107:
1387-1394
25. Conti, G., G. Cinnella, E. Barboni, F. Lemaire, A. Harf, and L. Brochard. 1996. Estimation of occlusion pressure during assisted ventilation in patients with intrinsic PEEP. Am. J. Respir. Crit. Care Med. 154: 907-912 [Abstract].
26.
Habib, M. P..
1989.
Physiological implications of artificial airways.
Chest
96:
180-184
27. Wright, P. E., J. J. Marini, and G. R. Bernard. 1989. In vitro versus in vivo comparison of endotracheal tube airflow resistance. Am. Rev. Respir. Dis. 140: 10-16 [Medline].
28. Villafane, M., G. Cinnella, F. Lofaso, D. Isabey, A. Harf, F. Lemaire, and L. Brochard. 1996. Gradual reduction of endotracheal tube diameter during mechanical ventilation via different humidification devices. Anesthesiology 85: 1341-1349 [Medline].
29. Whitelaw, W. A., J. P. Derenne, J. Milic, and Emili. 1975. Occlusion pressure as a measure of respiratory center's output in conscious man. Respir. Physiol. 23: 181-199 [Medline].
30. Aubier, M., D. Murciano, M. Fournier, J. Milic, Emili, R. Pariente, and J. P. Derenne. 1980. Central respiratory drive in acute respiratory failure patients with chronic obstructive pulmonary disease. Am. Rev. Respir. Dis. 122: 191-199 [Medline].
31. Nava, S., C. Bruschi, F. Rubini, A. Palo, G. Iotti, and A. Braschi. 1995. Respiratory response and inspiratory effort during pressure support ventilation in COPD patients. Intensive Care Med. 21: 871-879 [Medline].
32. Leung, P., A. Jubran, and M. Tobin. 1997. Comparison of assisted ventilator modes on triggering, patient effort and dyspnea. Am. J. Respir. Crit. Care Med. 155: 1940-1948 [Abstract].
33. Lofaso, F., B. Louis, L. Brochard, A. Harf, and D. Isabey. 1992. Use of the Blasius resistance formula to estimate in vivo the effective diameter of endotracheal tubes. Am. Rev. Respir. Dis. 146: 974-979 [Medline].
34. Van Surell, C., B. Louis, F. Lofaso, L. Beydon, L. Brochard, A. Harf, J. J. Fredberg, and D. Isabey. 1994. Acoustic method to estimate the longitudinal area profile of endotracheal tubes. Am. J. Respir. Crit. Care Med. 149: 28-33 [Abstract].
35. Conti, G., R. Rocco, R. A. De Blasi, A. Luppa, M. Antonelli, M. Buffi, and A. Gasparetto. 1994. A new device to remove obstruction from endotracheal tubes during mechanical ventilation in critically ill patients. Intensive Care Med. 20: 573-576 [Medline].
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H. H. O'Connor, K. J. Kirby, N. Terrin, N. S. Hill, and A. C. White Decannulation Following Tracheostomy for Prolonged Mechanical Ventilation J Intensive Care Med, May 1, 2009; 24(3): 187 - 194. [Abstract] [PDF] |
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D. P. Veelo, D. A. Dongelmans, P. Middelhoek, J. C. Korevaar, and M. J. Schultz Adaptive Support Ventilation with Percutaneous Dilatational Tracheotomy: A Clinical Study Anesth. Analg., September 1, 2008; 107(3): 938 - 940. [Abstract] [Full Text] [PDF] |
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U. Schmidt, D. Hess, J. Kwo, S. Lagambina, E. Gettings, F. Khandwala, L. M. Bigatello, and H. T. Stelfox Tracheostomy Tube Malposition in Patients Admitted to a Respiratory Acute Care Unit Following Prolonged Ventilation Chest, August 1, 2008; 134(2): 288 - 294. [Abstract] [Full Text] [PDF] |
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P. B. Rahmanian, D. H. Adams, J. G. Castillo, J. Chikwe, and F. Filsoufi Tracheostomy is Not a Risk Factor for Deep Sternal Wound Infection After Cardiac Surgery Ann. Thorac. Surg., December 1, 2007; 84(6): 1984 - 1991. [Abstract] [Full Text] [PDF] |
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P. De Leyn, L. Bedert, M. Delcroix, P. Depuydt, G. Lauwers, Y. Sokolov, A. Van Meerhaeghe, and P. Van Schil Tracheotomy: clinical review and guidelines Eur. J. Cardiothorac. Surg., September 1, 2007; 32(3): 412 - 421. [Abstract] [Full Text] [PDF] |
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J-M. Boles, J. Bion, A. Connors, M. Herridge, B. Marsh, C. Melot, R. Pearl, H. Silverman, M. Stanchina, A. Vieillard-Baron, et al. Weaning from mechanical ventilation Eur. Respir. J., May 1, 2007; 29(5): 1033 - 1056. [Abstract] [Full Text] [PDF] |
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H. Prigent, D. Orlikowski, M. B. Blumen, K. Leroux, L. Legrand, M. Lejaille, L. Falaize, M. Ruquet, J-C. Raphael, and F. Lofaso Characteristics of tracheostomy phonation valves. Eur. Respir. J., May 1, 2006; 27(5): 992 - 996. [Abstract] [Full Text] [PDF] |
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S. Rana, S. Pendem, M. S. Pogodzinski, R. D. Hubmayr, and O. Gajic Tracheostomy in Critically Ill Patients Mayo Clin. Proc., December 1, 2005; 80(12): 1632 - 1638. [Abstract] [PDF] |
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F. Blot, C. Melot, and for the Commission d'Epidemiologie et de Recherche Indications, Timing, and Techniques of Tracheostomy in 152 French ICUs Chest, April 1, 2005; 127(4): 1347 - 1352. [Abstract] [Full Text] [PDF] |
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F. Lellouche, S. Taille, S. M. Maggiore, S. Qader, E. L'Her, N. Deye, and L. Brochard Influence of Ambient and Ventilator Output Temperatures on Performance of Heated-Wire Humidifiers Am. J. Respir. Crit. Care Med., November 15, 2004; 170(10): 1073 - 1079. [Abstract] [Full Text] [PDF] |
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M. H. Kollef Tracheostomy for Respiratory Failure: We Need More Answers Chest, January 1, 2004; 125(1): 7 - 9. [Full Text] [PDF] |
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I. de Chazal and R. D. Hubmayr Novel aspects of pulmonary mechanics in intensive care Br. J. Anaesth., July 1, 2003; 91(1): 81 - 91. [Full Text] [PDF] |
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D. Chiumello, P. Pelosi, E. Calvi, L.M. Bigatello, and L. Gattinoni Different modes of assisted ventilation in patients with acute respiratory failure Eur. Respir. J., October 1, 2002; 20(4): 925 - 933. [Abstract] [Full Text] [PDF] |
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V. Moscovici da Cruz, S.E. Demarzo, J.B.B. Sobrinho, M.B.P. Amato, L.P. Kowalski, and D. Deheinzelin Effects of tracheotomy on respiratory mechanics in spontaneously breathing patients Eur. Respir. J., July 1, 2002; 20(1): 112 - 117. [Abstract] [Full Text] [PDF] |
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N. R. MacIntyre Evidence-Based Guidelines for Weaning and Discontinuing Ventilatory Support : A Collective Task Force Facilitated by the American College of Chest Physicians; the American Association for Respiratory Care; and the American College of Critical Care Medicine Chest, December 1, 2001; 120 (2009): 375S - 396S. [Abstract] [Full Text] [PDF] |
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J. E. Heffner The Role of Tracheotomy in Weaning Chest, December 1, 2001; 120 (2009): 477S - 481S. [Abstract] [Full Text] [PDF] |
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D. Chiumello, P. Pelosi, M. Croci, L.M. Bigatello, and L. Gattinoni The effects of pressurization rate on breathing pattern, work of breathing, gas exchange and patient comfort in pressure support ventilation Eur. Respir. J., July 1, 2001; 18(1): 107 - 114. [Abstract] [Full Text] [PDF] |
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