CCN
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Critical Care Nurse. 2005;25: 14-23
Copyright © 2005 by the American Association of Critical-Care Nurses.
This Article
Right arrow Full Text (PDF)
Right arrow Respond to This Article
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Right arrow Take the CE Test
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Burns, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Burns, S. M.


Cover Article
CE Article

Mechanical Ventilation of Patients With Acute Respiratory Distress Syndrome and Patients Requiring Weaning

The Evidence Guiding Practice

Suzanne M. Burns, RN, MSN, RRT, ACNP, CCRN


Suzanne M. Burns is a professor of nursing and an advanced practice nurse in the medical intensive care unit at the University of Virginia in Charlottesville.

To purchase reprints, contact The InnoVision Group, 101 Columbia, Aliso Viejo, CA 92656. Phone, (800) 809-2273 or (949) 362-2050 (ext 532); fax, (949) 362-2049; e-mail, reprints{at}aacn.org.

* This article has been designated for CE credit. A closed-book, multiple-choice examination follows this article, which tests your knowledge of the following objectives:

  1. Identify lung-protective strategies in acute respiratory distress syndrome (ARDS)
  2. Describe the benefits of low-tidal-volume ventilation in ARDS
  3. Discuss evidence-based guidelines of mechanical ventilation in ARDS


Mechanical ventilation is one of the most commonly used technologies in critical care. Despite the prevalence of ventilators, care planning is heavily influenced by anecdote and clinical preference. A vast array of ventilator modes and mode options exist, and claims of what works and what does not abound. Critical care nurses’ knowledge and understanding of mechanical ventilation are central to ensuring patients’ safe passage from the acute stage of ventilation to weaning. Of key importance is the use of evidence that may improve patients’ outcomes. To that end, in this article, I discuss the science related to mechanical ventilation in patients with acute respiratory distress syndrome (ARDS) and in patients who require weaning.


   The Acute Stage of Ventilation: Supplying Ventilation to the Lungs in Patients With ARDS
 Top
 The Acute Stage of...
 The Weaning Stage of...
 Conclusions and Summary
 References
 
The acute stage of ventilation is described as that stage at which the patients require a high level of ventilatory support and their hemodynamic status is often unstable.15 A variety of volume and pressure modes of ventilation are used in an effort to improve oxygenation, ventilation, and acid-base status. The results of recent research in patients with ARDS are dramatically affecting how we use mechanical ventilation in such patients and how clinical end points of mechanical ventilation are selected. The concept of "lung-protective strategies," which include low-tidal-volume ventilation, positive end-expiratory pressure (PEEP), and prone positioning of patients, has emerged along with a renewed interest in the potential efficacy of high-frequency oscillation. A discussion focused on the evidence related to the use of such therapies follows.

Are Volume or Pressure Modes Better for Patients With ARDS?
Investigators611 have shown that animals with induced ARDS, treated with mechanical ventilation with "traditional" (ie, large) ventilator volumes experience more lung injury than do similar animals treated with mechanical ventilation with lower ventilator volumes.6,7 In these animals, plateau pressures of 35 cm H2O or greater for 72 hours resulted in alveolar fractures and increased alveolar flooding.811 The term volutrauma was coined to describe injuries due to the large traditional volumes, although questions remained about whether the tidal volumes or the resultant distending (plateau) pressures were actually responsible for the lung injury. Because the potential for volutrauma in humans was recognized, recommendations for the use of smaller tidal volumes began to emerge12,13 and studies in humans followed.1416

In a study by Hickling et al,14 a total of 53 patients with ARDS were treated with mechanical ventilation at low volumes (7 mL/kg) in an attempt to maintain peak airway pressures less than 30 cm H2O. Hospital mortality for the patients was significantly lower than the mean mortality predicted on the basis of on Acute Physiology and Chronic Health Evaluation II scores. After this study, the ARDS Network16 reported on the results of a randomized controlled trial designed to compare clinical outcomes of patients with ARDS who were assigned to low-volume (6 mL/kg) versus traditional-volume (12 mL/kg) ventilation. The study was stopped after a preliminary analysis of 861 patients indicated that mortality in the low-tidal-volume group was significantly lower than that in the control group (31.0% vs 39.8%, P=.007). Of interest, the plateau pressures when the tidal volume of 6 mL/kg was used were in the range of 26 to 30 cm H2O.16 This pressure was far lower than the plateau pressure (<35 cm H2O) that had been suggested as potentially lung protective in the animal studies.

But, the ARDS Network’s study16 has been criticized. For example, some have noted that volumes between 6 and 12 mL/kg (ie, 7, 8, 9, 10, and 11 mL/kg) were not tested, yet those volumes may be more reflective of common practice patterns. Others contended that the "control" group assignment of 12 mL/kg was excessively high and that the principle of scientific equipoise (ie, that genuine uncertainty exists about what treatment is best) may have been violated. Rubenfeld et al17 and Weinert et al18 subsequently examined practice patterns in the selection of tidal volume at academic institutions where clinicians were aware of the results of the ARDS Network’s study. Their results17,18 indicated that commonly selected tidal volumes were not in the range of 6 mL/kg but were rather in a higher range, findings that somewhat dispelled the validity of the concerns.

Regardless, questions persist about the effect of tidal volumes from 7 to 11 mL/kg and about the use of pressure modes to control plateau pressures in patients with ARDS.19,20 Because pressure modes of ventilation have characteristics that make them attractive for use in patients with noncompliant lungs, many wonder if pressure-targeted ventilation might be a comparable substitute for volume-targeted ventilation in patients with ARDS. Some of the characteristics of pressure-targeted ventilation are discussed next.

The decelerating flow pattern associated with pressure modes is thought to provide better gas distribution than volume ventilation does.2123 In addition, plateau pressure can be reliably limited by using pressure modes. Although some might assume that using pressure ventilation in patients with stiff lungs (in order to ensure a low plateau pressure) might result in outcomes similar to those found in the ARDS Network’s trial, much remains to be determined. For example, volumes delivered with pressure ventilation are affected by compliance (lung and chest wall) and resistance. Using a plateau pressure to ensure lung protection may not ensure volumes comparable to the tidal volume of 6 mL/kg used in the ARDS Network’s study.

The superiority of selected "new" pressure modes, such as pressure-release ventilation, for use in ARDS also has not been established. Randomized controlled trials comparing the modes with low-volume targeted ventilation will be necessary before the new pressure modes can be widely endorsed.

To date, the study by the ARDS Network,16 in which tidal volumes of 6 mL/kg were used, is the only study that has demonstrated a change in mortality. Until the effects of other modes of mechanical ventilation on the outcomes of patients with ARDS are clarified, the use of low-volume targeted ventilation rather than pressure-targeted ventilation is the suggested ventilatory strategy for protecting the lungs of these patients.

What About PEEP Levels?
In a randomized controlled trial of patients with ARDS, Amato et al24 studied outcomes associated with different levels of PEEP. The optimal level was determined by measuring lung compliance at increasing levels of PEEP. A level just above the lower inflection point (that level that resulted in an increase in compliance with a given level of PEEP) was selected as the lung recruitment PEEP for the intervention group. Findings of the study suggested that levels of PEEP of about 14 to 16 cm H2O (ie, higher than levels generally selected) were necessary to prevent derecruitment (lung closure).

Unfortunately, measurement of the inflection point at the bedside is technically difficult, and this method is unlikely to be widely used in clinical practice. Although the results of Amato et al24 suggest that PEEP levels of 14 to 16 cm H2O are required to open the lung in patients with ARDS, definitive methods for determining the appropriate level of required PEEP are unknown.

In the ARDS Network study,16 an algorithmic approach was used to assign levels of PEEP. Unfortunately, auto-PEEP (occult PEEP due to inadequate expiratory time) also occurred in many of the patients (eg, those with high respiratory rates and high minute volumes), making accurate assessment of the total level of PEEP difficult. Some have suggested that the auto-PEEP may have recruited the lung, perhaps contributing to the beneficial outcomes described by the investigators.25

How best to apply PEEP to recruit the lung and prevent derecruitment is not yet clear. Regardless, an understanding of these concepts is helpful for focusing clinical interventions.

Recruiting the Lungs and Keeping Them Open (Preventing Derecruitment)
In patients with ARDS, noncompliant lungs tend to collapse, and once collapsed, high inflation pressures are necessary to reopen the lungs. Knowledge of how the lungs in patients with ARDS inflate during mechanical ventilation is essential to our understanding of recruitment.

Computed tomography scans of patients with ARDS have improved our understanding of the alveolar filling patterns associated with ARDS.26,27 Once thought to be homogeneous, the pattern of alveolar filling in ARDS is actually heterogeneous. Some areas of the lung are open and others are closed. In the areas of aerated lung, the entire brunt of a tidal volume breath is experienced by the compliant (and open) lung tissue. Unfortunately, this small area of the lung (also called "baby lung") is at increased risk of injury from overdistention and the shear forces of repetitive opening and closing with tidal breathing. The stress on the lungs from the tidal breath may be an important mechanism associated with volutrauma.

The closed lung parenchyma of patients with ARDS cannot be recruited without applying a critical opening pressure (ie, a pressure high enough to open closed alveoli). Further, once opened, the lung tissue is at risk of closing again (derecruitment) if optimal levels of PEEP or other strategies are not applied. Thus the concepts of lung recruitment and derecruitment are integrally related.

The use of PEEP levels from 14 to 16 cm H2O, as described by Amato et al,24 is suggested as one way to open the lungs. Another method is to provide periodic episodes of super-high levels of PEEP. Referred to as 40/40 or 60/60 maneuvers (eg, 40 cm H2O of PEEP for 40 seconds), these techniques have been used in a number of studies, but they are associated with a risk of barotrauma.24,2729

Once the Lungs Are Opened, How Are They Kept Open?
Unfortunately, it is unclear how to select a level of PEEP to stabilize ventilation once a recruitment maneuver is completed.3032 Although monitoring the effects of the selected settings on oxygenation and ventilation is a generally accepted way of deciding if the settings are preventing derecruitment over time, oxygenation may not be the best indicator. Oxygenation, traditionally used to assess the adequacy of PEEP, is unreliable because the increase in oxygenation may be the result of either recruitment or redistribution of blood flow to aerated areas of the lung (thus decreasing the shunt and improving oxygenation). Identification of a PEEP level that recruits lung and prevents repetitive opening injury associated with tidal breathing is thus an elusive clinical goal.

Investigators have used computed tomography to compare lung recruitment when different ventilatory maneuvers are used.27,33 Although this method is accurate, it is impractical for use in most clinical settings and widespread use of it is unlikely. Theoretically, another way to assess recruitment is to increase the level of PEEP and monitor the difference between the plateau pressure and the PEEP level. If the addition of PEEP results in recruitment of lung, the plateau pressure should not change; however, if PEEP is adding to alveolar overdistention, the plateau pressure will increase.

Although we have learned much about the effectiveness of PEEP in treating ARDS, much remains to be elucidated. To date, definitive methods of applying PEEP to ensure lung protection and to prevent derecruitment have not been clearly identified. Regardless, arbitrary selection of a PEEP level is unlikely to accomplish the goal.

Other Ways to Recruit the Lungs: What About High-Frequency Oscillation and Prone Positioning of Patients?
Unlike traditional ventilatory modes, high-frequency oscillation does not require bulk movement of volume in and out of the lungs; rather, a bias flow of gases is provided and an oscillator disperses the gases throughout the lung at very high frequencies in what has been called "augmented dispersion." The lungs are recruited and a mean airway pressure sufficient to cause a chest vibration (or "wiggle") is maintained.34 Although some think that this mode of ventilation may recruit the lungs and prevent tidal stress (damage due to tidal volume and repetitive opening of the stiff alveoli), to date only a single randomized controlled trial has been completed. The Multicenter Oscillatory Ventilation for Acute Respiratory Distress Syndrome Trial34 was designed to test the safety and efficacy of a specific ventilator for high-frequency oscillation. The results indicated a positive but non-significant trend in 30-day mortality in patients receiving mechanical ventilation with high-frequency oscillation. Unfortunately, the tidal volumes in the control group were not maintained in the "protective" range, a situation that makes it difficult to interpret the results. An additional concern is that patients generally require heavy sedation and often require paralytic agents to ensure compliance with high-frequency oscillation.

Prone positioning is useful in recruiting lung tissue. Studies in animal models and patients with ARDS in the prone position have revealed a number of responsible mechanisms.3545 Blood flow and gas distribution in the lungs are affected by gravity. When patients are supine, the alveoli in the dependent parts of the lungs (ie, the back) fill with fluid and collapse. When patients are turned to the prone position, the effect of gravity is reversed and lung tissue is recruited.35 In addition, pleural pressures are more uniform in the dorsal than in the ventral position, so lung recruitment is enhanced.3641 The third mechanism is a mechanical one. With prone positioning, the heart rests against the sternum (rather than against the lungs) and the abdomen moves away from the lungs.38,4244 As much as a third of the posterior part of the lungs may be recruited when patients are prone.42 Last, the anterior part of the chest, normally the most mobile part of the chest, is slightly restricted when patients are prone. Consequently, when the lungs are ventilated in a patient who is prone, the air is redistributed more evenly throughout the chest, including the dependent regions.45

The effect of prone positioning of patients on outcomes in ARDS is as yet unclear. Although our understanding of how prone positioning improves lung recruitment is fairly good, to date the only randomized controlled trial of prone positioning in patients with ARDS did not show a change in mortality.46 Patients in the study were maintained in a prone position for at least 6 hours a day for 10 days. The study was done before the results of the ARDS study on ventilation with low lung volumes were published,27 however, so volumes were not controlled. Of interest, in the sickest cohort of patients in the study, patients with a ratio of PaO2 to fraction of inspired oxygen of less than 88 (a ratio <200 is defined as ARDS), those assigned to the prone position had a better 10-day survival rate than did those who remained supine.

Perhaps the most important fact associated with positioning patients prone is that it is a relatively safe intervention compared with other techniques (albeit a time- and effort-intensive one) that recruits lung and assists with drainage of secretions.47,48 Although studies are needed to definitively determine the importance of prone positioning in the management of ARDS, the use of this position may be less risky than use of some of the other recruitment maneuvers described.

What Ventilation, Oxygenation, and Acid-Base Thresholds Should Be Used With Protective Ventilatory Strategies?
Use of low-volume ventilation may result in significant hypercarbia.7,14,15,4953 In the past, ventilator settings were adjusted to attain eucarbia and a normal pH. Because the goal is to protect the lung, such an end point may not be possible. Instead, the goal should be to ensure that volutrauma does not occur. Because low-volume ventilation results in decreased alveolar ventilation, hypercarbia is expected. Called "permissive hypercarbia," the goal for acid-base status is to maintain a reasonable pH (approximately 7.25).7,14,15,4953 Bicarbonate infusions may be used if necessary in patients whose pH is lower and thought to be potentially harmful.1416,49 Although it is generally tolerated well in most patients, permissive hypercarbia is not appropriate for all patients. Examples include patients with elevated intracranial pressures and patients with some cardiac conditions.5153


   The Weaning Stage of Mechanical Ventilation
 Top
 The Acute Stage of...
 The Weaning Stage of...
 Conclusions and Summary
 References
 
The weaning stage of mechanical ventilation is described as that time when the patient’s physiological status is stable and progressive liberation from mechanical ventilation is possible.15 Various mechanical ventilatory modes and methods are used to ensure an expeditious process. Recent research on weaning has elucidated the importance of approaches in which protocols and comprehensive multidisciplinary processes of care delivery are used.

Mechanical Ventilation in the Weaning Stage: What Works?
To date, no mode of weaning has been shown to be superior to the others, yet how the various methods of weaning are used does seem to make a difference in clinical outcomes. In randomized controlled trials by Brochard et al54 and Esteban et al,55 patients were selected on the basis of entry criteria that established the subjects’ readiness to be weaned. If patients met the readiness criteria, they were assigned to a 2-hour spontaneous breathing trial during which they were monitored for signs of intolerance to the trial. If signs of intolerance emerged, the weaning trial was classified as a "failure" and the patient was randomly assigned to a weaning protocol. In the study by Esteban et al,55 patients who successfully sustained the 2-hour trial were extubated; the reintubation rate was 20%.

The protocol methods to which patients were randomly assigned included pressure-support ventilation, intermittent mandatory ventilation, and spontaneous breathing trials. Although Brochard et al54 found that pressure-support ventilation resulted in faster weaning and Esteban et al55 found that spontaneous breathing trials once per day were superior, both groups of investigators used similar protocols for assessing weaning readiness, advancing weaning trials, and defining success (tolerance) or failure (intolerance). The results of those 2 studies54,55 stimulated interest in testing the efficacy and safety of weaning protocols.

In studies by Ely et al56 and Kollef et al,57 patients were randomly assigned either to a weaning protocol managed by a nurse and respiratory therapist or to a traditional weaning plan designed by a physician. Compared with weaning according to the physician’s plan, weaning via the protocol resulted in significantly shorter durations of mechanical ventilation in both studies and a significantly shorter stay in the intensive care unit (ICU) in the study by Kollef et al.57

The usefulness of protocols in decreasing variation in processes of care is not restricted to weaning trials. The use of sedatives in patients receiving mechanical ventilation has been associated with prolonged duration of mechanical ventilation and prolonged stays in the ICU and hospital.57 In randomized controlled trials, the algorithmic management of sedation58 and use of a protocol to wean patients off infusions of sedatives59 resulted in significantly shorter duration of mechanical ventilation and shorter stays in the ICU and in the hospital.

The use of protocols is linked to improved outcomes. However, the results of a study by Ely et al60 suggest that protocols must be applied carefully. Ely et al sought to implement a protocol for weaning in surgical units that involved spontaneous breathing trials. The protocol had been previously tested in a study of patients in a medical ICU and coronary care unit.56 Components of the protocol included a weaning readiness screening, a spontaneous breathing trial, and end points for stopping the trial. Educational sessions were used to update clinicians about the study, and respiratory care practitioners implemented the protocol. The spontaneous breathing trials were implemented only 10% of the time initially, but implementation increased to 30% with additional educational sessions. One of the major reasons for the lack of compliance with the protocol was that the protocol was not managed by any specific person (as it had been during the original study).60

Other methods of improving weaning outcomes for patients treated with mechanical ventilation include systematic comprehensive initiatives in which multiple evidence-based interventions are applied together in a single approach.6168 The interventions include clinical pathways, methods for evaluating progress, specific elements of care (eg, deep vein prophylaxis, nutrition, mobility) and protocols for weaning trials. Two prospective system initiatives indicate the effectiveness of the more comprehensive approaches.

Smyrnios et al67 designed a large-scale multidisciplinary approach to care of patients receiving mechanical ventilation in a medical ICU, a surgical ICU, and a coronary care unit. The initiative consisted of using a weaning algorithm and a nurse clinician to ensure compliance with the processes of care. Duration of mechanical ventilation, length of stay in the ICU, and length of stay in the hospital all improved significantly when the care initiative was used. Financial gains also occurred; however, mortality was not affected.

In another study,68 all adult patients in 5 critical care units (medical ICU, coronary care unit, thoracic-cardiovascular ICU, surgical-trauma ICU, and neurological ICU) who required mechanical ventilation for more than 3 consecutive days were managed and monitored by 4 advanced practice nurses for 1 year. The process consisted of an evidence-based clinical pathway, protocols for weaning trials and sedation management, and a standardized weaning assessment tool (Burns Wean Assessment Program). Results of the intervention were compared with outcomes prospectively collected before implementation of the approach. The findings included significant reductions in duration of mechanical ventilation, lengths of stay in the ICU and hospital, and mortality in the managed group. The beneficial outcomes were attributed to the management and monitoring of the process by the advanced practice nurses and the systematic multidisciplinary evidence-based approach to care of the patients.


   Conclusions and Summary
 Top
 The Acute Stage of...
 The Weaning Stage of...
 Conclusions and Summary
 References
 
To achieve the best outcomes, we must have an in-depth understanding of the evidence related to appropriate use of mechanical ventilation in patients with ARDS and in patients who require weaning. We have learned much from studies conducted in such patients, yet many questions about how best to apply the therapy remain unanswered. Low-volume lung ventilation is associated with decreased mortality as applied in the ARDS Network’s study.16 Until additional studies of other modes (pressure modes and high-frequency oscillation) indicate comparable outcomes, use of low-volume ventilation in patients with ARDS should be encouraged. Unfortunately, questions still abound related to how we might best recruit the lungs and keep them open (eg, optimal levels of PEEP, prone positioning).

In the area of weaning, evidence indicates that it is not the mode used but rather the method, specifically the use of protocols, that results in improved clinical outcomes. Further, outcomes are likely to be improved by multidisciplinary system initiatives that provide systematic evidence-based care.


   References
 Top
 The Acute Stage of...
 The Weaning Stage of...
 Conclusions and Summary
 References
 

  1. Burns SM, Clochesy J, Goodnough-Hanneman SK, Ingersoll GE, Knebel AR, Shekleton ME. Weaning from long-term mechanical ventilation. Am J Crit Care. 1995;4:4–22.
  2. Knebel AR, Shekleton ME, Burns SM, Clochesy JM, Goodnough-Hanneman SK, Ingersoll GL. Weaning from mechanical ventilation: concept development. Am J Crit Care. 1994;3:416–420.
  3. Goodnough-Hanneman SK, Ingersoll GL, Knebel AR, Shekleton ME, Burns SM, Clochesy JM. Weaning from short-term mechanical ventilation: a review. Am J Crit Care. 1994;3:421–443.
  4. Burns SM, Ryan B, Burns JE. The weaning continuum: use of Apache III, BWAP, TISS, and WI scores to establish stages of weaning. Crit Care Med. 2000;28:2259–2267.[Medline]
  5. Knebel A, Shekleton MD, Burns S, Clochesy JM, Hanneman SK. Weaning from mechanical ventilatory support: refinement of a model. Am J Crit Care. 1998;7:149–152.
  6. Dreyfuss D, Basset G, Soler P, Saumon G. Intermittent positive-end expiratory pressure hyperventilation with high inflation pressures produces pulmonary microvascular injury in rats. Am Rev Respir Dis. 1985;132:880–884.[Medline]
  7. Tremblay L, Valenza F, Ribeiro SP, Li J, Slutsky AS. Injurious ventilatory strategies increases cytokines and c-fos m-RNA expression in an isolated rat lung model. J Clin Invest. 1997;99:944–952.[Medline]
  8. Dreyfuss D, Saumon G. The role of tidal volume, FRC and end-inspiratory volume in the development of pulmonary edema following mechanical ventilation. Am Rev Respir Dis. 1993;148:1194–1203.[Medline]
  9. Dreyfus D, Saumon G. Ventilator induced lung injury. Am J Respir Crit Care Med. 1998;157:294–323.
  10. Dreyfuss D, Soler P, Bassett G, Saumon G. High inflation pressure pulmonary edema. Am Rev Respir Dis. 1988;137:1159–1164.[Medline]
  11. Fu Z, Costello ML, Tsukimoto K, et al. High lung volume increases stresss failure in pulmonary capillaries. J Appl Physiol. 1992;73:123–133.[Abstract/Free Full Text]
  12. Slutsky AS. Consensus conference on mechanical ventilation—January 28–30, 1993 at Northbrook, Illinois, USA: part 1. European Society of Intensive Care Medicine, the ACCP and the SCCM. [published correction appears in Intensive Care Med. 1994;20:378]. Intensive Care Med. 1994;20:64–79.[Medline]
  13. Slutsky AS. Consensus Conference on Mechanical Ventilation—January 28–30, 1993 at Northbrook, Illinois, USA: part 2. Intensive Care Med. 1994;20:150–162.[Medline]
  14. Hickling KG, Henderson SJ, Jackson R. Low mortality associated with low volume pressure-limited ventilation with permissive hypercapnia in severe adult respiratory distress syndrome. Intensive Care Med. 1990;16:372–377.[Medline]
  15. Hickling K. Low volume ventilation with permissive hypercapnia in the adult respiratory distress syndrome. Clin Intensive Care. 1992;3:67–78.[Medline]
  16. The Acute Respiratory Distress Syndrome Network. Ventilation with lower tidal volumes as compared with traditional tidal volumes for acute lung injury and the acute respiratory distress syndrome. N Engl J Med. 2000;342:1301–1307[Abstract/Free Full Text]
  17. Rubenfeld G, Caldwell E, Hudson L. Publication of study results does not increase use of lung protective ventilation patients with acute lung injury [abstract]. Am J Respir Crit Care Med. 2001;163:A295.
  18. Weinert CR, Gross CR, Marinelli WA. Impact of randomized trial results on acute lung injury ventilator therapy in teaching hospitals. Am J Respir Crit Care Med. 2003;167:1304–1309.[Abstract/Free Full Text]
  19. Stewart TE, Meade MO, Cook DJ, et al. Evaluation of a ventilation strategy to prevent barotrauma in patients at high risk for acute respiratory distress syndrome: Pressure-and Volume-Limited Ventilation Strategy Group. N Engl J Med. 1998;338:355–361.[Abstract/Free Full Text]
  20. Rappaport SH, Shpiner R, Yoshihara G, et al. Randomized, prospective trial of pressure-limited versus volume-controlled ventilation in severe respiratory failure. Crit Care Med. 1994;22:22–32.[Medline]
  21. MacIntyre NR. Respiratory function during pressure support ventilation. Chest. 1986;89:677–683.[Abstract/Free Full Text]
  22. Brochard L, Pluskwa F, Lemaire F. Improved efficacy of spontaneous breathing with inspiratory pressure support. Am Rev Respir Dis. 1987;136:411–415.[Medline]
  23. Davis K, Branson RD, Campbell RS, Porembka DT. Comparison of volume control and pressure control ventilation: is flow waveform the difference? J Trauma. 1996;41:808–814.[Medline]
  24. Amato MBP, Barbas CSV, Medeiros DM, et al. Effect of a protective-ventilation strategy on mortality in the acute respiratory distress syndrome. N Engl J Med. 1998;338:347–354.[Abstract/Free Full Text]
  25. de Durante G, del Turco M, Rustichini L, et al. ARDSNet lower tidal volume ventilatory strategy may generate intrinsic positive end-expiratory pressure in patients with acute respiratory distress syndrome. Am J Respir Crit Care Med. 2002;165:1271–1274.[Abstract/Free Full Text]
  26. Gattinoni L, Presenti A, Torresin A, et al. Adult respiratory distress syndrome profiles by computed tomography. J Thorac Imaging. 1986;1:25–30.[Medline]
  27. The ARDS Clinical Trials Network; National Heart, Lung and Blood Institute; National Institutes of Health. Effects of recruitment maneuvers in patients with acute lung injury and acute respiratory distress syndrome ventilated with high positive end-expiratory pressure. Crit Care Med. 2003;31:2592–2597.[Medline]
  28. Fujino Y, Goddon S, Dolhnikoff M, Hess D, Amato MB, Kacmarek RM. Repetitive high-pressure recruitment maneuvers required to maximally recruit lung in a sheep model of acute respiratory distress syndrome. Crit Care Med. 2001;29:1579–1586.[Medline]
  29. Foti G, Cereda M, Sparacino ME, et al. Effects of periodic lung recruitment maneuvers on gas exchange and respiratory mechanics in mechanically ventilated acute respiratory distress syndrome (ARDS) patients. Intensive Care Med. 2000;26:501–507.[Medline]
  30. Marini JJ. Recruitment maneuvers to achieve an "open lung": whether and how? Crit Care Med. 2001;29:1647–1648.[Medline]
  31. Lachmann B. Open up the lung and keep the lung open. Intensive Care Med. 1992;18:319–321.[Medline]
  32. Amato MBP, Barbas CSV, Medeiros DM, et al. Beneficial effects of the "open lung approach" with low distending pressures in acute respiratory distress syndrome. Am J Respir Crit Care Med. 1995;152:1835–1846.[Abstract]
  33. Gattinoni L, Pesanti A, Avalli L, Rossi F, Bombino M. Pressure volume curve of total respiratory system in acute respiratory failure: computed tomographic scan study. Am Rev Respir Dis. 1987;136:730–736.[Medline]
  34. Derdak S, Mehta A, Stewart TE, et al. High-frequency oscillatory ventilation for acute respiratory distress syndrome in adults. Am J Respir Crit Care Med. 2002;166:801–808.[Abstract/Free Full Text]
  35. Messerole E, Peine P, Wittkopp S, Marini JJ, Albert RK. The pragmatics of prone positioning. Am J Respir Crit Care Med. 2002;165:1359–1363.[Free Full Text]
  36. Pappert D, Rossaint R, Slama K, Gruning T, Falke KJ. Influence of positioning on ventilation-perfusion relationships in severe adult respiratory distress syndrome. Chest. 1994;106:1511–1516.[Abstract/Free Full Text]
  37. Gattinoni L, Pelosi P, Vitale G, Presenti A, D’Andrea L, Mascheront D. Body position changes redistribute lung computer tomographic density in patients with acute respiratory failure. Anesthesiology. 1991;74:15–25.[Medline]
  38. Pelosi P, Turbiolo D, Mascheroni D, et al. Effects of the prone position on respiratory mechanics and gas exchange during acute lung injury. Am J Respir Crit Care Med. 1998;157:387–389.
  39. Wiener CM, Kirk W, Albert RK. The prone position reverses the gravitational distribution of perfusion in dog lungs with oleic acid-induced injury. J Appl Physiol. 1990;68:1386–1392.[Abstract/Free Full Text]
  40. Lamm WJE, Graham MM, Albert RK. Mechanism by which the prone position improves oxygenation in acute lung injury. Am J Respir Crit Care Med. 1994;150:184–193.[Abstract]
  41. Beck KC, Vettermann J, Rehder K. Gas exchange in dogs in the prone and supine positions. J Appl Physiol. 1992;72:2292–2297.[Abstract/Free Full Text]
  42. Albert RK, Hubmayr RD. The prone position eliminates compression of the lungs by the heart. Am J Respir Crit Care Med. 2000;161:1660–1665.[Abstract/Free Full Text]
  43. Hoffman EA. Effect of body orientation on regional lung expansion: a computed tomographic approach. J Appl Physiol. 1985; 59:468–480.[Abstract/Free Full Text]
  44. Wiener CM, McKenna WJ, Myers MJ, Lavendar JP, Hughes JM. Left lower lobe ventilation is reduced in patients with cardiomegaly in the supine but not the prone position. Am Rev Respir Dis. 1990;141:150–155.[Medline]
  45. Albert RK. Editorial: for every thing (turn...turn...turn..). Am J Respir Crit Care Med. 1997;155:393–394.[Medline]
  46. Gattinoni L, Tognoni G, Pesenti A, et al. Effect of prone positioning on the survival of patients with acute respiratory failure. N Engl J Med. 2001;345:568–573.[Abstract/Free Full Text]
  47. Douglas WW, Rehder K, Beynen FM, Sessler AD, Marsh HM. Improved oxygenation in patients with acute respiratory failure: the prone position. Am Rev Respir Dis. 1977;115:559–567.[Medline]
  48. Curley MAQ. Prone positioning of patients with acute respiratory distress syndrome: a systematic review. Am J Crit Care. 1999;8: 397–405.
  49. Menitove SM, Golring RA. Combined ventilator and bicarbonate strategy in the management of status asthmaticus. Am J Med. 1983;74:889–901.
  50. Darioli R, Perret C. Mechanical controlled hypoventilation in status asthmaticus. Am Rev Respir Dis. 1984;129:385–387.[Medline]
  51. Tuxen D. Permissive hypercapnia. In: Tobin MJ, ed. Principles and Practice of Mechanical Ventilation. New York, NY: McGraw Hill; 1994:371–392.
  52. Bidani A, Tzouanakis AE, Cardenas VJ, Zwischenberger JB. Permissive hypercapnia in acute respiratory failure. JAMA. 1994;272:957–962.[Abstract/Free Full Text]
  53. Bellomo R, Mclaughlin P, Tai E, Parkin G. Asthma requiring mechanical ventilation: a low morbidity approach. Chest. 1994;105: 891–896.[Abstract/Free Full Text]
  54. Brochard L, Ranes A, Benito S, et al. Comparison of three methods of gradual withdrawal from ventilatory support during weaning from mechanical ventilators. Am J Respir Crit Care Med. 1994;150:896–903.[Abstract]
  55. Esteban A, Frutos F, Tobin MJ, et al. A comparison of four methods of weaning patients from mechanical ventilation: Spanish Lung Failure Collaborative Group. N Engl J Med. 1995;332:345–350.[Abstract/Free Full Text]
  56. Ely EW, Baker AM, Dunagan DP, et al. Effect on the duration of mechanical ventilation of identifying patients capable of breathing spontaneously. N Engl J Med. 1996;335:1964–1969.
  57. Kollef MH, Shapiro SD, Silver P, et al. A randomized, controlled trial of protocol-directed versus physician-directed weaning from mechanical ventilation. Crit Care Med. 1997;25:567–574.[Medline]
  58. Brook AD, Ahrens TS, Schaff R, et al. Effect of a nursing-implemented sedation protocol on the duration of mechanical ventilation. Crit Care Med. 1999;27:2609–2615.[Medline]
  59. Kress JP, Pohlman AS, O’Connor MF, Hall JB. Daily interruption of sedative infusions in critically ill patients undergoing mechanical ventilation. N Engl J Med. 2000;342:1471–1477.[Abstract/Free Full Text]
  60. Ely EW, Bennett PA, Bowton DL, Murphy SM, Florance AM, Haponick EF. Large-scale implementation of a respiratory therapist-driven protocol for ventilator weaning. Am J Respir Crit Care Med. 1999;159:439–436.[Abstract/Free Full Text]
  61. Cohen IL, Bari N, Strosberg MA, et al. Reduction of duration and cost of mechanical ventilation in an intensive care unit by use of a ventilatory management team. Crit Care Med. 1991;19:1278–1284.[Medline]
  62. Rudy FB, Daly BJ, Douglas S, Montenegro HD, Song R, Dyer MA. Patient outcomes for the chronically critically ill: special care unit versus intensive care unit. Nurs Res. 1995;44:324–331.[Medline]
  63. Kite-Powell D, Sauban D, Ideno KT, et al. Optimizing outcomes in ventilator-dependent patients: challenging critical care practice. Crit Care Nurs Q. 1996;19:77–90.[Medline]
  64. Burns SM, Marshall M, Burns JD, et al. Design, testing and results of an outcomes managed approach to patients requiring prolonged ventilation. Am J Crit Care. 1998;7:45–57.
  65. Henneman E, Dracup K, Ganz T, Molayeme O, Cooper C. Effect of a collaborattive weaning plan on patient outcome in the critical care setting. Crit Care Med. 2001;29:297–303.[Medline]
  66. Henneman E, Dracup K, Ganz T, Molayeme O, Cooper CB. Using a collaborative weaning plan to decrease duration of mechanical ventilation and length of stay in the intensive care unit patients receiving long-term mechanical ventilation. Am J Crit Care. 2002;11:132–140.[Abstract/Free Full Text]
  67. Smyrnios NA, Connolly A, Wilson MM, et al. Effects of a multifaceted, multidisciplinary, hospital-wide quality improvement program on weaning from mechanical ventilation. Crit Care Med. 2002;30:1224–1230.[Medline]
  68. Burns SM, Earven D, Fisher C, et al. Implementation of an institutional program to improve clinical and financial outcomes of patients requiring mechanical ventilation: one year outcomes and lessons learned. Crit Care Med. 2003;31:2752–2763.[Medline]




This Article
Right arrow Full Text (PDF)
Right arrow Respond to This Article
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Right arrow Take the CE Test
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Burns, S. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Burns, S. M.


HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS