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Individualized vs Low PEEP in One Lung Ventilation

Primary Purpose

One-Lung Ventilation, Obesity, Lung Diseases

Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
One-lung ventilation with individualized PEEP
One-lung ventilation with low PEEP
Sponsored by
Dionne Peacher
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for One-Lung Ventilation

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subject undergoing elective pulmonary lobectomy requiring one-lung ventilation
  2. Body-mass index ≥ 30 kg/m2
  3. Age ≥ 18 years and ≤ 80 years

Exclusion Criteria:

  1. Age ≤ 18 year or ≥ 80 years
  2. Moderate or severe cardiac valvular disease
  3. Left ventricular ejection fraction < 30%
  4. Moderate or severe right ventricular systolic dysfunction
  5. Severe pulmonary hypertension
  6. Presence of pulmonary bullae or blebs on preoperative chest imaging studies (e.g., radiograph, computed tomograph)
  7. Emergency surgery
  8. Previous history of lung surgery on the non-operative lung
  9. Pregnancy
  10. Incarceration
  11. Mental incapacitation
  12. Patient refusal
  13. Non-English speaking

Sites / Locations

  • University of Iowa Hospitals and Clinics

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Individualized PEEP

Low PEEP

Arm Description

Individualized PEEP will be identified by performing a decremental PEEP protocol which will determine the level of PEEP that correlates with maximal lung compliance in each subject. Subjects will receive one-lung ventilation with individualized PEEP

Subjects will receive One-lung ventilation with low PEEP (5 cmH2O)

Outcomes

Primary Outcome Measures

Cerebral oximetry
Cerebral oximetry (a measure of oxygen levels in the brain) as measured by near-infrared spectroscopy (noninvasive monitor applied to the forehead)

Secondary Outcome Measures

Arterial blood oxygen tension (PaO2)
A measure of oxygen level in arterial blood
Venous blood oxygen tension (PvO2)
A measure of oxygen level in venous blood
Venous blood oxygen saturation (SvO2)
A measure of oxygen saturation in venous blood
Cardiac output
A measure of blood flow throughout the body
Phenylephrine dose
Total dose of phenylephrine (medication used to raise blood pressure)

Full Information

First Posted
June 2, 2018
Last Updated
July 1, 2021
Sponsor
Dionne Peacher
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1. Study Identification

Unique Protocol Identification Number
NCT03569774
Brief Title
Individualized vs Low PEEP in One Lung Ventilation
Official Title
The Effect of Individualized PEEP Compared to Low PEEP on Tissue Oxygenation During One Lung Ventilation in Obese Patients Undergoing Thoracic Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Withdrawn
Why Stopped
No subjects enrolled
Study Start Date
August 14, 2018 (Actual)
Primary Completion Date
May 19, 2021 (Actual)
Study Completion Date
May 19, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Dionne Peacher

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of the prospective crossover study is to investigate the effect of individualized positive end-expiratory pressure (PEEP) on measures of tissue oxygenation, compared with low PEEP.
Detailed Description
During surgery on the lung, ventilation of one lung at a time is often necessary. During thoracic surgery requiring one-lung ventilation (OLV), hypoxemia (reduced oxygen tension in blood) can present a clinical challenge. Due to multiple factors, the likelihood of hypoxemia during OLV in obese patients is increased. Atelectasis (collapse of the lung airspaces) contributes to hypoxemia and can be mitigated by application of recruitment maneuvers and positive end-expiratory pressure (PEEP). A recruitment maneuver is a breath given in a mechanically ventilated patient that helps to open up collapsed air spaces, and PEEP is application of a continuous amount of positive pressure that helps keep the air spaces open at the end of an exhaled breath. Adjusting the level of PEEP to each individual patient's optimal lung compliance (individualized PEEP) improves blood oxygen levels compared to application of standard low PEEP (5 cmH2O); however, higher levels of PEEP required to achieve optimal lung compliance could increase intrathoracic pressures to a level that impedes normal circulation. This could negatively affect blood flow (cardiac output) and delivery of oxgyen to vital organs. Evidence addressing OLV in obese patients is lacking. The purpose of this study is to compare brain oxygen levels (cerebral oxygen saturation) and measures of blood flow and gas exchange during OLV with individualized PEEP vs low standard PEEP in obese patients undergoing thoracic surgery. To our knowledge, there is no previous study that compares oxygen delivery to vital organs (such as the brain) during OLV using individualized PEEP versus standard low PEEP, in an obese patient population. In this study, subjects undergoing OLV during surgery to remove a portion of the lung (lobectomy) will undergo a process to determine their individualized PEEP and then two 20-minute experimental periods-- one period with OLV with low PEEP and one period with OLV with individualized PEEP. Measurements of cerebral oxygen saturation, blood oxygen levels, cardiac output, and blood pressure medication dose will be measuring before and after these experimental periods during surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
One-Lung Ventilation, Obesity, Lung Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Model Description
Mechanical ventilation with individualized PEEP will be compared to mechanical ventilating with low PEEP during lung isolation in each subject. Each subject will receive one PEEP level then will receive the second PEEP level. The order in which each subject receives the PEEP level will be randomized.
Masking
Participant
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Individualized PEEP
Arm Type
Experimental
Arm Description
Individualized PEEP will be identified by performing a decremental PEEP protocol which will determine the level of PEEP that correlates with maximal lung compliance in each subject. Subjects will receive one-lung ventilation with individualized PEEP
Arm Title
Low PEEP
Arm Type
Active Comparator
Arm Description
Subjects will receive One-lung ventilation with low PEEP (5 cmH2O)
Intervention Type
Procedure
Intervention Name(s)
One-lung ventilation with individualized PEEP
Intervention Description
During one-lung ventilation for lung resection surgery, PEEP will be applied. After a subject's individualized PEEP (PEEP that corresponds to maximum lung compliance) is determined, the subject will receive one-lung ventilation with individualized PEEP.
Intervention Type
Procedure
Intervention Name(s)
One-lung ventilation with low PEEP
Intervention Description
Subjects will receive one-lung ventilation with low PEEP (5 cmH2O)
Primary Outcome Measure Information:
Title
Cerebral oximetry
Description
Cerebral oximetry (a measure of oxygen levels in the brain) as measured by near-infrared spectroscopy (noninvasive monitor applied to the forehead)
Time Frame
Change from baseline cerebral oximetry at the end of each intraoperative 20 minute experimental period. All measurements are made during the 4-6 hour surgery.
Secondary Outcome Measure Information:
Title
Arterial blood oxygen tension (PaO2)
Description
A measure of oxygen level in arterial blood
Time Frame
Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery.
Title
Venous blood oxygen tension (PvO2)
Description
A measure of oxygen level in venous blood
Time Frame
Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery.
Title
Venous blood oxygen saturation (SvO2)
Description
A measure of oxygen saturation in venous blood
Time Frame
Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery.
Title
Cardiac output
Description
A measure of blood flow throughout the body
Time Frame
Measured at baseline, and then at the end of each 20 minute intraoperative experimental period. All measurements are made during the 4-6 hour surgery.
Title
Phenylephrine dose
Description
Total dose of phenylephrine (medication used to raise blood pressure)
Time Frame
Total dose of phenylephrine administered during each intraoperative 20 minute experimental period. All measurements are made during the 4-6 hour surgery.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Subject undergoing elective pulmonary lobectomy requiring one-lung ventilation Body-mass index ≥ 30 kg/m2 Age ≥ 18 years and ≤ 80 years Exclusion Criteria: Age ≤ 18 year or ≥ 80 years Moderate or severe cardiac valvular disease Left ventricular ejection fraction < 30% Moderate or severe right ventricular systolic dysfunction Severe pulmonary hypertension Presence of pulmonary bullae or blebs on preoperative chest imaging studies (e.g., radiograph, computed tomograph) Emergency surgery Previous history of lung surgery on the non-operative lung Pregnancy Incarceration Mental incapacitation Patient refusal Non-English speaking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dionne Peacher, MD
Organizational Affiliation
University of Iowa
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Iowa Hospitals and Clinics
City
Iowa City
State/Province
Iowa
ZIP/Postal Code
52242
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
All of the individual participant data collected during the trial, after deidentification will be shared with researchers who provide a methodologically sound proposal, to achieve aims in the approved proposal. IPD will be available for sharing immediately after publication and ending 5 years following article publication.
IPD Sharing Time Frame
IPD will be available for sharing immediately after publication and ending 5 years following article publication.
IPD Sharing Access Criteria
IPD will be accessible to researchers who provide a methodologically sound proposal, to achieve aims in the approved proposal
Citations:
PubMed Identifier
29361458
Citation
Campos JH, Feider A. Hypoxia During One-Lung Ventilation-A Review and Update. J Cardiothorac Vasc Anesth. 2018 Oct;32(5):2330-2338. doi: 10.1053/j.jvca.2017.12.026. Epub 2017 Dec 19. No abstract available.
Results Reference
background
PubMed Identifier
19417615
Citation
Karzai W, Schwarzkopf K. Hypoxemia during one-lung ventilation: prediction, prevention, and treatment. Anesthesiology. 2009 Jun;110(6):1402-11. doi: 10.1097/ALN.0b013e31819fb15d.
Results Reference
background
PubMed Identifier
24557111
Citation
Ferrando C, Mugarra A, Gutierrez A, Carbonell JA, Garcia M, Soro M, Tusman G, Belda FJ. Setting individualized positive end-expiratory pressure level with a positive end-expiratory pressure decrement trial after a recruitment maneuver improves oxygenation and lung mechanics during one-lung ventilation. Anesth Analg. 2014 Mar;118(3):657-65. doi: 10.1213/ANE.0000000000000105.
Results Reference
background
PubMed Identifier
22226331
Citation
de Matos GF, Stanzani F, Passos RH, Fontana MF, Albaladejo R, Caserta RE, Santos DC, Borges JB, Amato MB, Barbas CS. How large is the lung recruitability in early acute respiratory distress syndrome: a prospective case series of patients monitored by computed tomography. Crit Care. 2012 Jan 8;16(1):R4. doi: 10.1186/cc10602.
Results Reference
background
PubMed Identifier
16690982
Citation
Borges JB, Okamoto VN, Matos GF, Caramez MP, Arantes PR, Barros F, Souza CE, Victorino JA, Kacmarek RM, Barbas CS, Carvalho CR, Amato MB. Reversibility of lung collapse and hypoxemia in early acute respiratory distress syndrome. Am J Respir Crit Care Med. 2006 Aug 1;174(3):268-78. doi: 10.1164/rccm.200506-976OC. Epub 2006 May 11.
Results Reference
background
PubMed Identifier
28973363
Citation
Writing Group for the Alveolar Recruitment for Acute Respiratory Distress Syndrome Trial (ART) Investigators; Cavalcanti AB, Suzumura EA, Laranjeira LN, Paisani DM, Damiani LP, Guimaraes HP, Romano ER, Regenga MM, Taniguchi LNT, Teixeira C, Pinheiro de Oliveira R, Machado FR, Diaz-Quijano FA, Filho MSA, Maia IS, Caser EB, Filho WO, Borges MC, Martins PA, Matsui M, Ospina-Tascon GA, Giancursi TS, Giraldo-Ramirez ND, Vieira SRR, Assef MDGPL, Hasan MS, Szczeklik W, Rios F, Amato MBP, Berwanger O, Ribeiro de Carvalho CR. Effect of Lung Recruitment and Titrated Positive End-Expiratory Pressure (PEEP) vs Low PEEP on Mortality in Patients With Acute Respiratory Distress Syndrome: A Randomized Clinical Trial. JAMA. 2017 Oct 10;318(14):1335-1345. doi: 10.1001/jama.2017.14171.
Results Reference
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Individualized vs Low PEEP in One Lung Ventilation

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