Effects of Different Ventilation Patterns on Lung Injury

January 5, 2020 updated by: Dongxue Li, Sixth Affiliated Hospital, Sun Yat-sen University

Effects of Different Ventilation Modes on Intraoperative Lung Injury and Postoperative Pulmonary Complications in Elderly Patients Undergoing Laparoscopic Colorectal Cancer Resection

In 1967, the term "respirator lung" was coined to describe the diffuse alveolar infiltrates and hyaline membranes that were found on postmortem examination of patients who had undergone mechanical ventilation.This mechanical ventilation can aggravate damaged lungs and damage normal lungs. In recent years, Various ventilation strategies have been used to minimize lung injury, including low tide volume, higher PEEPs, recruitment maneuvers and high-frequency oscillatory ventilation. which have been proved to reduce the occurrence of lung injury.

In 2012,Needham et al. proposed a kind of lung protective mechanical ventilation, and their study showed that limited volume and pressure ventilation could significantly improve the 2-year survival rate of patients with acute lung injury.Volume controlled ventilation is the most commonly used method in clinical surgery at present.Volume controlled ventilation(VCV) is a time-cycled, volume targeted ventilation mode, ensures adequate gas exchange. Nevertheless, during VCV, airway pressure is not controlled.Pressure controlled ventilation(PCV) can ensure airway pressure,however minute ventilation is not guaranteed.Pressure controlled ventilation-volume guarantee(PCV-VG) is an innovative mode of ventilation utilizes a decelerating flow and constant pressure. Ventilator parameters are automatically changed with each patient breath to offer the target VT without increasing airway pressures. So PCV-VG has the advantages of both VCV and PCV to preserve the target minute ventilation whilst producing a low incidence of barotrauma pressure-targeted ventilation.

Current studies on PCV-VG mainly focus on thoracic surgery, bariatric surgery and urological surgery, and the research indicators mainly focus on changes in airway pressure and intraoperative oxygenation index.The age of patients undergoing laparoscopic colorectal cancer resection is generally higher, the cardiopulmonary reserve function is decreased, and the influence of intraoperative pneumoperitoneum pressure and low head position increases the incidence of intraoperative and postoperative pulmonary complications.Whether PCV-VG can reduce the incidence of intraoperative lung injury and postoperative pulmonary complications in elderly patients undergoing laparoscopic colorectal cancer resection, and thereby improve postoperative recovery of these patients is still unclear.

Study Overview

Detailed Description

One hundred patients undergoing elective laparoscopic colorectal cancer resection (age > 65 years old, body mass index(BMI)18-30 kg/m2, American society of anesthesiologists(ASA )grading Ⅰ - Ⅲ ) will be randomly assigned to volume control ventilation(VCV)group and pressure controlled ventilation-volume guarantee(PCV-VG)group.General anesthesia combined with epidural anesthesia will be used to both groups.

Ventilation settings in both groups are VT 8 mL/kg,inspiratory/expiratory (I/E) ratio 1:2,inspired oxygen concentration (FIO2) 0.5 with air,2.0 L/min of inspiratory fresh gas flow,positive end-expiratory pressure (PEEP) 0 millimeter of mercury (mmHg),respiratory rate (RR) was adjusted to maintain an end tidal CO2 pressure (ETCO2) of 35 -45 mmHg.

In operation dates will be collected at the following time points: preanesthesia, 1 hour after pneumoperitoneum,2 hours after pneumoperitoneum ,30 minutes after admission to post-anaesthesia care unit (PACU) .The dates collected or calculated are the following:1)peak airway pressure,plate airway pressure, mean inspiratory pressure, dynamic compliance, RR,Exhaled VT andETCO2,2) Arterial blood gas analysis: arterial partial pressure of oxygen (PaO2), arterial partial pressure of carbon dioxide (PaCO2),power of hydrogen(PH), and oxygen saturation (SaO2),3) Oxygenation index (OI) calculation; PaO2/FIO2, 4) Ratio of physiologic dead-space over tidal volume(Vd/VT) (expressed in %) was calculated with Bohr's formula ; Vd/VT = (PaCO2 - ETCO2)/PaCO2,5) Hemodynamics: heart rate, mean arterial pressure (MAP),and central venous pressure (CVP),6) lung injury markers :Interleukin 6(IL6),Interleukin 8(IL8),Clara cell protein 16(CC16),Solution advanced glycation end products receptor(SRAGE),tumor necrosis factor α(TNFα) .

Investigators will collect the following dates according to following-up after surgery: the incidence of postoperation pulmonary complications(PPC) based on PPC scale within seven days , incidence of pneumonia within seven days after surgery,incidence of atelectasis within seven days after surgery,length of hospital days after surgery, the incidence of postoperative unplanned admission to ICU, the incidence of operation complications within 7 days after surgery, the incidence of postoperative systematic complications within 7 days after surgery.

Study Type

Interventional

Enrollment (Anticipated)

100

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

    • Guangdong
      • Guangzhou, Guangdong, China, 510655
        • Recruiting
        • Six Affiliated Hospital, Sun Yat-sen University
        • Contact:
        • Contact:
          • Sanqing Jin, MD
          • Phone Number: 13719366863

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

65 years and older (Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. scheduled for Laparoscopic colorectal cancer resection
  2. age >65 years
  3. body mass index(BMI) 18-30kg / m2
  4. ASA gradingⅠ-Ⅲ

Exclusion Criteria:

  1. history of lung surgery
  2. severe restrictive or obstructive pulmonary disease (preoperative lung function test: forced vital capacity(FVC)< 50% predictive value of FVC,forced expiratory volume at one second(FEV1)< 50% predictive value of FEV1
  3. Acute respiratory failure, pulmonary infection, ALI/ARDS, and acute stage of asthmaAcute respiratory failure, pulmonary infection, acute lung injury(ALI),acute respiratory distress syndrome(ARDS), and acute stage of asthma (bronchodilators were needed for treatment) were found within 1 month before surgery
  4. Patients at risk of preoperative reflux aspiration
  5. Preoperative positive pressure ventilation (as obstructive sleep apnea hypopnea syndrome patients) or long-term home oxygen therapy were performed
  6. Serious heart, liver and kidney diseases: heart function class more than 3, severe arrhythmia (sinus bradycardia (ventricular rate < 60 times/min), atrial fibrillation, atrial flutter, atrioventricular block, frequent premature ventricular and polyphyly ventricular early, early to R on T, ventricular fibrillation and ventricular flutter), acute coronary syndrome, liver failure, kidney failure
  7. Neuromuscular diseases affect respiratory function, such as Parkinson's disease, myasthenia gravis and cerebral infarction affect normal breathing
  8. Mental illness, speech impairment, hearing impairment
  9. Contraindications for spinal anesthesia puncture
  10. Refuse to participate in this study or participate in other studies -

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Triple

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: pressure-controlled ventilation-volume guaranteed
patients will be allocated to pressure-controlled ventilation volume guaranteed in operation
patients will be allocated to pressure-controlled ventilation-volume guaranteed in operation
Placebo Comparator: volume controlled ventilation
patients will be allocated to volume controlled ventilation in operation
patients will be allocated to pressure-controlled ventilation volume guaranteed in operation

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
occurrence rate of Oxygenation index≤300mmHg
Time Frame: 10minutes before anesthesia,1 hour after pneumoperitoneum,2 hour after pneumoperitoneum,30 minutes after after extubation
Oxygenation index(OI)=PaO2/FiO2
10minutes before anesthesia,1 hour after pneumoperitoneum,2 hour after pneumoperitoneum,30 minutes after after extubation

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Occurrence rate of pulmonary complications
Time Frame: Day 0 to 7 after surgery
Pulmonary complications were assessed using the Postoperation Pulmonary complication ( PPC) scale,The scale is divided into four grades, with 0 indicating no pulmonary complications and 1 to 4 indicating increasingly severe pulmonary complications.
Day 0 to 7 after surgery
incidence of pneumonia
Time Frame: Day 0 to 7 after surgery
record the occurrence rate of pneumonia after surgery
Day 0 to 7 after surgery
incidence of pulmonary atelectasis
Time Frame: Day 0 to 7 after surgery
record the occurrence rate of pulmonary atelectasis after surgery
Day 0 to 7 after surgery
peak airway pressure
Time Frame: through mechanical ventilation,average of 3 hours
Peak airway Pressure(Ppeak, cm H2O)
through mechanical ventilation,average of 3 hours
Plateau airway pressure
Time Frame: through mechanical ventilation,average of 3 hours
Plateau airway pressure(Pplat, cm H2O)
through mechanical ventilation,average of 3 hours
Static lung compliance
Time Frame: through mechanical ventilation,average of 3 hours
Static lung compliance (Csta, ml/cm H2O) = Vt/ (Pplat-PEEP)
through mechanical ventilation,average of 3 hours
Dynamic lung compliance
Time Frame: through mechanical ventilation,average of 3 hours
Dynamic lung compliance (Cdyn , ml/cm H2O)= Vt/ (Ppeak-PEEP)
through mechanical ventilation,average of 3 hours
Arterial partial pressure of oxygen
Time Frame: 10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
Arterial partial pressure of oxygen (PaO2, mmHg)
10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
assessing change of Alveolar-arterial oxygen tension difference
Time Frame: 10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
Alveolar-arterial oxygen tension difference (mmHg)
10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
assessing change of Respiratory index
Time Frame: 10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
Fraction of inspired oxygen (FiO2); Respiratory index (RI) =Ratio of alveolar-arterial oxygen tension difference to FiO2
10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
assessing change of Alveolar dead space fraction
Time Frame: 10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum,30 minutes after extubation
Arterial carbon dioxide partial pressure (PaCO2); partial pressure of carbon dioxide in endexpiratory gas (PetCO2); Alveolar dead space fraction (Vd/Vt)=(PaCO2-PetCO2)/ PaCO2;
10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum,30 minutes after extubation
assessing change of lactic acid
Time Frame: 10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
lactate ( LAC), mmol/L
10 minutes before anesthesia, 1 hour after pneumoperitoneum, 2 hours after pneumoperitoneum, 30 minutes after extubation
assessing change of Advanced glycation end products receptor
Time Frame: 10 minutes before anesthesia,30 minutes after extubation
Advanced glycation end products receptor (RAGE, pg/ml)
10 minutes before anesthesia,30 minutes after extubation
assessing change of Tumor Necrosis Factor alpha
Time Frame: 10 minutes before anesthesia,30 minutes after extubation
Tumor Necrosis Factor alpha (TNF-α, pg/ml)
10 minutes before anesthesia,30 minutes after extubation
assessing change of Interleukin 6
Time Frame: 10 minutes before anesthesia,30 minutes after extubation
Interleukin 6 (IL-6, pg/ml)
10 minutes before anesthesia,30 minutes after extubation
assessing change of Interleukin 8
Time Frame: 10 minutes before anesthesia,30 minutes after extubation
Interleukin 8 (IL-8, pg/ml)
10 minutes before anesthesia,30 minutes after extubation
assessing change of Clara cell protein 16,
Time Frame: 10 minutes before anesthesia,30 minutes after extubation
Clara cell protein 16,
10 minutes before anesthesia,30 minutes after extubation
The occurrence rate of hypoxemia in PACU
Time Frame: 30 minutes after extubation
The occurrence rate of hypoxemia (SPO2<90% or PaO2<60 mmHg) in PACU
30 minutes after extubation
Occurrence rate of operation complications
Time Frame: within 7 days after operation
abdominal abscess, anastomotic fistula, bleeding and the incidence of reoperation within 7 days
within 7 days after operation
Occurrence rate of Systemic complications
Time Frame: within 7 days after surgery
Systemic complications including sepsis and septic shock
within 7 days after surgery
Antibiotic dosages
Time Frame: within 7 days after surgery
record the Antibiotic dosages within 7 days after surgery
within 7 days after surgery
incidence of Unplanned admission to ICU
Time Frame: within 30 days after surgery
Unplanned admission to ICU within 30 days after surgery
within 30 days after surgery
Length of ICU stay within 30 days after surgery
Time Frame: within 30 days after surgery
Length of ICU stay within 30 days after surgery
within 30 days after surgery
Length of hospital stay within 30 days after surgery
Time Frame: within 30 days after surgery
Length of hospital stay within 30 days after surgery
within 30 days after surgery
Death from any cause
Time Frame: within 30 days after surgery
Death from any cause 30 days after surgery
within 30 days after surgery
The occurrence rate of hypoxemia after surgery
Time Frame: within 7 days after surgery
The occurrence rate of hypoxemia (SPO2<90% or PaO2<60 mmHg) after surgery
within 7 days after surgery

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Dongxue Li, Sixth Affiliated Hospital, Sun Yat-sen University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 1, 2019

Primary Completion (Anticipated)

December 31, 2021

Study Completion (Anticipated)

December 31, 2021

Study Registration Dates

First Submitted

May 19, 2019

First Submitted That Met QC Criteria

May 21, 2019

First Posted (Actual)

May 23, 2019

Study Record Updates

Last Update Posted (Actual)

January 7, 2020

Last Update Submitted That Met QC Criteria

January 5, 2020

Last Verified

June 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 2019ZSLYEC-184

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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