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Work of Breathing and Mechanical Ventilation in Acute Lung Injury (WOBALI)

Primary Purpose

Acute Lung Injury

Status
Withdrawn
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Volume Control Ventilation
Pressure Control Ventilation
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Acute Lung Injury focused on measuring Mechanical Ventilation

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Both medical and surgical patients undergoing mechanical ventilatory support who meet criteria for Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS) as defined by the European-American Consensus Conference,
  • Mechanical ventilation via an endotracheal or tracheotomy tube,
  • PaO2/FiO2 < 300 mmHg with bilateral infiltrates on chest radiogram,
  • Clinical management with lung protective ventilation (Tidal volume < 8 mL/kg).

Exclusion Criteria:

  • Patients receiving "comfort care",
  • High cervical spinal cord injury or other neuromuscular disease,
  • Prisoners,
  • Pregnancy,
  • Less than 18 years of age,
  • Facial fractures and coagulopathies,
  • Patients placed on psychiatric hold.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Lung-Protective Ventilation

    Arm Description

    Lung-Protective Ventilation comparing volume vs. pressure control

    Outcomes

    Primary Outcome Measures

    proinflammatory cytokine expression in plasma

    Secondary Outcome Measures

    work of breathing

    Full Information

    First Posted
    August 16, 2009
    Last Updated
    March 3, 2015
    Sponsor
    University of California, San Francisco
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00961168
    Brief Title
    Work of Breathing and Mechanical Ventilation in Acute Lung Injury
    Acronym
    WOBALI
    Official Title
    Prospective Study on the Effects of Artificial Breathing Patterns on Work of Breathing in Patients With Acute Lung Injury.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Budgetary restrictions
    Study Start Date
    September 2009 (undefined)
    Primary Completion Date
    September 2012 (Anticipated)
    Study Completion Date
    September 2013 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University of California, San Francisco

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The primary goal of this study is to measure changes in biological markers of inflammation in critically-ill patients with acute lung injury (ALI) or acute respiratory distress syndrome (ARDS) while they are treated with different styles of lung-protective, artificial breathing assistance. Secondary goals are to measure the breathing effort of patients using different artificial breathing patterns from the breathing machine. The primary hypothesis is that volume-targeted artificial patterns will produce less inflammation. The secondary hypothesis is that volume-targeted artificial patterns will increase breathing effort compared to pressure-targeted artificial patterns.
    Detailed Description
    Ventilator-induced lung injury contributes to the progression of ALI/ARDS,1 and is thought to occur partly from the unequal distribution of a super-normal tidal volume to normal areas of the lung.2 Alveolar overdistension causes alveolar-capillary membrane damage,3 increased-permeability pulmonary edema4 and hyaline membrane formation.5 Therefore, it is recommended that tidal volume should be reduced to 6-7 mL/kg, and that the peak alveolar pressure, or the end-inspiratory plateau pressure (PPLAT), should be limited to < 30 cm H2O.6 The National Heart Lung and Blood Institute's ARDS Network demonstrated a 22% reduction in mortality using a "lung-protective" (low tidal volume) ventilation strategy in patients with ALI/ARDS.7 High tidal volume ventilation causes a rapid and substantial increase plasma levels of proinflammatory mediators which decrease in response to lung protective ventilation.8,9 A consequence of lung-protective ventilation is dyspnea and increased work of breathing.10 Our recent study11 on work of breathing during lung-protective ventilation found that inspiratory pleural pressure changes were extraordinarily high, averaging 15-17 cm H2O. Whereas tidal volume was well controlled during volume ventilation, in contrast, it exceeded target levels in 40% of patients during pressure control ventilation. High tidal volume-high negative pressure ventilation causes acute lung injury in animal models.12,13 Thus ventilator-induced lung injury results from excessive stress across lung tissue created by high transpulmonary (airway-pleural).pressure.14 This suggests the possibility that despite pressure control ventilation being set with a low positive airway pressure, "occult" high tidal volume-high transpulmonary pressure ventilation still may occur.11 However, during spontaneous breathing diaphragmatic contractions cause ventilation to be distributed preferentially to dorsal:caudal aspects of the lungs.15 Therefore, high transpulmonary pressures created by large negative swings in pleural pressure theoretically may not cause regional lung over-distension and ventilator-induced lung injury if tidal ventilation is preferentially distributed to dorsocaudal lung regions. However, a study16 examining the effects of diaphragmatic breathing during Pressure Control Ventilation found that dorsocaudal distribution of tidal volume was not necessarily improved compared to passive ventilation, as the amount of tidal ventilation distributed to areas of high ventilation/perfusion was unaltered. Regardless, during a recent conference on respiratory controversies in the critical care setting, it was noted that the effects of ventilator modes such as volume control, pressure control and airway pressure-release ventilation on proinflammatory cytokine expression during lung-protective ventilation has not been studied in humans.17 Thus it is unknown whether or not differences in transpulmonary pressure and tidal volume between these modes has a direct impact on lung inflammation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Acute Lung Injury
    Keywords
    Mechanical Ventilation

    7. Study Design

    Primary Purpose
    Supportive Care
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Lung-Protective Ventilation
    Arm Type
    Experimental
    Arm Description
    Lung-Protective Ventilation comparing volume vs. pressure control
    Intervention Type
    Other
    Intervention Name(s)
    Volume Control Ventilation
    Other Intervention Name(s)
    Volume Assist/Control
    Intervention Description
    Mechanical ventilation at a constant tidal volume of 6 mL/kg.
    Intervention Type
    Other
    Intervention Name(s)
    Pressure Control Ventilation
    Other Intervention Name(s)
    Pressure Assist/Control
    Intervention Description
    Mechanical ventilation at a constant airway pressure of 25-30 cm H2O
    Primary Outcome Measure Information:
    Title
    proinflammatory cytokine expression in plasma
    Time Frame
    2 hours
    Secondary Outcome Measure Information:
    Title
    work of breathing
    Time Frame
    2 hours

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    85 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Both medical and surgical patients undergoing mechanical ventilatory support who meet criteria for Acute Lung Injury (ALI) or Acute Respiratory Distress Syndrome (ARDS) as defined by the European-American Consensus Conference, Mechanical ventilation via an endotracheal or tracheotomy tube, PaO2/FiO2 < 300 mmHg with bilateral infiltrates on chest radiogram, Clinical management with lung protective ventilation (Tidal volume < 8 mL/kg). Exclusion Criteria: Patients receiving "comfort care", High cervical spinal cord injury or other neuromuscular disease, Prisoners, Pregnancy, Less than 18 years of age, Facial fractures and coagulopathies, Patients placed on psychiatric hold.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Mitchell Cohen, MD
    Organizational Affiliation
    University of California, San Francisco
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    Citation
    1. Dreyfus D, Sauman G. Ventilation induced injury. In: Principles and Practice of Mechanical Ventilation. Tobin M J. Editor. New York: McGraw Hill Publishers; 1994: 793-811.
    Results Reference
    background
    PubMed Identifier
    2193041
    Citation
    Hickling KG. Ventilatory management of ARDS: can it affect the outcome? Intensive Care Med. 1990;16(4):219-26. doi: 10.1007/BF01705155.
    Results Reference
    background
    PubMed Identifier
    1506359
    Citation
    Fu Z, Costello ML, Tsukimoto K, Prediletto R, Elliott AR, Mathieu-Costello O, West JB. High lung volume increases stress failure in pulmonary capillaries. J Appl Physiol (1985). 1992 Jul;73(1):123-33. doi: 10.1152/jappl.1992.73.1.123.
    Results Reference
    background
    PubMed Identifier
    2228868
    Citation
    Carlton DP, Cummings JJ, Scheerer RG, Poulain FR, Bland RD. Lung overexpansion increases pulmonary microvascular protein permeability in young lambs. J Appl Physiol (1985). 1990 Aug;69(2):577-83. doi: 10.1152/jappl.1990.69.2.577.
    Results Reference
    background
    PubMed Identifier
    6754260
    Citation
    Lachmann B, Jonson B, Lindroth M, Robertson B. Modes of artificial ventilation in severe respiratory distress syndrome. Lung function and morphology in rabbits after wash-out of alveolar surfactant. Crit Care Med. 1982 Nov;10(11):724-32. doi: 10.1097/00003246-198211000-00005. No abstract available.
    Results Reference
    background
    Citation
    6. Tuxen DV. Permisive hypercapnia. In: Principles and Practice of Mechanical Ventilation. Tobin M J. Editor. New York: McGraw Hill Publishers; 1994: 371-392.
    Results Reference
    background
    PubMed Identifier
    10793162
    Citation
    Acute Respiratory Distress Syndrome Network; Brower RG, Matthay MA, Morris A, Schoenfeld D, Thompson BT, Wheeler A. 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 May 4;342(18):1301-8. doi: 10.1056/NEJM200005043421801.
    Results Reference
    background
    PubMed Identifier
    10404912
    Citation
    Ranieri VM, Suter PM, Tortorella C, De Tullio R, Dayer JM, Brienza A, Bruno F, Slutsky AS. Effect of mechanical ventilation on inflammatory mediators in patients with acute respiratory distress syndrome: a randomized controlled trial. JAMA. 1999 Jul 7;282(1):54-61. doi: 10.1001/jama.282.1.54.
    Results Reference
    background
    PubMed Identifier
    12122519
    Citation
    Stuber F, Wrigge H, Schroeder S, Wetegrove S, Zinserling J, Hoeft A, Putensen C. Kinetic and reversibility of mechanical ventilation-associated pulmonary and systemic inflammatory response in patients with acute lung injury. Intensive Care Med. 2002 Jul;28(7):834-41. doi: 10.1007/s00134-002-1321-7. Epub 2002 Jun 15.
    Results Reference
    background
    PubMed Identifier
    8087364
    Citation
    Tuxen DV. Permissive hypercapnic ventilation. Am J Respir Crit Care Med. 1994 Sep;150(3):870-4. doi: 10.1164/ajrccm.150.3.8087364. No abstract available.
    Results Reference
    background
    PubMed Identifier
    16318643
    Citation
    Kallet RH, Campbell AR, Dicker RA, Katz JA, Mackersie RC. Work of breathing during lung-protective ventilation in patients with acute lung injury and acute respiratory distress syndrome: a comparison between volume and pressure-regulated breathing modes. Respir Care. 2005 Dec;50(12):1623-31.
    Results Reference
    background
    PubMed Identifier
    3057957
    Citation
    Dreyfuss D, Soler P, Basset G, Saumon G. High inflation pressure pulmonary edema. Respective effects of high airway pressure, high tidal volume, and positive end-expiratory pressure. Am Rev Respir Dis. 1988 May;137(5):1159-64. doi: 10.1164/ajrccm/137.5.1159.
    Results Reference
    background
    PubMed Identifier
    3230208
    Citation
    Mascheroni D, Kolobow T, Fumagalli R, Moretti MP, Chen V, Buckhold D. Acute respiratory failure following pharmacologically induced hyperventilation: an experimental animal study. Intensive Care Med. 1988;15(1):8-14. doi: 10.1007/BF00255628.
    Results Reference
    background
    PubMed Identifier
    15812622
    Citation
    Gattinoni L, Pesenti A. The concept of "baby lung". Intensive Care Med. 2005 Jun;31(6):776-84. doi: 10.1007/s00134-005-2627-z. Epub 2005 Apr 6.
    Results Reference
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    PubMed Identifier
    4604401
    Citation
    Froese AB, Bryan AC. Effects of anesthesia and paralysis on diaphragmatic mechanics in man. Anesthesiology. 1974 Sep;41(3):242-55. doi: 10.1097/00000542-197409000-00006. No abstract available.
    Results Reference
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    PubMed Identifier
    17417979
    Citation
    Myers TR, MacIntyre NR. Respiratory controversies in the critical care setting. Does airway pressure release ventilation offer important new advantages in mechanical ventilator support? Respir Care. 2007 Apr;52(4):452-8; discussion 458-60.
    Results Reference
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    Work of Breathing and Mechanical Ventilation in Acute Lung Injury

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