- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03960853
Effects of Different Ventilation Patterns on Lung Injury
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
Status
Conditions
Intervention / Treatment
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
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: Dongxue Li
- Phone Number: 008615802037417
- Email: liguoqing2010@126.com
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510655
- Recruiting
- Six Affiliated Hospital, Sun Yat-sen University
-
Contact:
- Dongxue Li
- Phone Number: 08615802037417
- Email: liguoqing2010@126.com
-
Contact:
- Sanqing Jin, MD
- Phone Number: 13719366863
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- scheduled for Laparoscopic colorectal cancer resection
- age >65 years
- body mass index(BMI) 18-30kg / m2
- ASA gradingⅠ-Ⅲ
Exclusion Criteria:
- history of lung surgery
- 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
- 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
- Patients at risk of preoperative reflux aspiration
- Preoperative positive pressure ventilation (as obstructive sleep apnea hypopnea syndrome patients) or long-term home oxygen therapy were performed
- 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
- Neuromuscular diseases affect respiratory function, such as Parkinson's disease, myasthenia gravis and cerebral infarction affect normal breathing
- Mental illness, speech impairment, hearing impairment
- Contraindications for spinal anesthesia puncture
- Refuse to participate in this study or participate in other studies -
Study Plan
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
Investigators
- Principal Investigator: Dongxue Li, Sixth Affiliated Hospital, Sun Yat-sen University
Publications and helpful links
General Publications
- Slutsky AS, Ranieri VM. Ventilator-induced lung injury. N Engl J Med. 2013 Nov 28;369(22):2126-36. doi: 10.1056/NEJMra1208707. No abstract available. Erratum In: N Engl J Med. 2014 Apr 24;370(17):1668-9.
- Kalmar AF, Foubert L, Hendrickx JF, Mottrie A, Absalom A, Mortier EP, Struys MM. Influence of steep Trendelenburg position and CO(2) pneumoperitoneum on cardiovascular, cerebrovascular, and respiratory homeostasis during robotic prostatectomy. Br J Anaesth. 2010 Apr;104(4):433-9. doi: 10.1093/bja/aeq018. Epub 2010 Feb 18.
- Dion JM, McKee C, Tobias JD, Sohner P, Herz D, Teich S, Rice J, Barry ND, Michalsky M. Ventilation during laparoscopic-assisted bariatric surgery: volume-controlled, pressure-controlled or volume-guaranteed pressure-regulated modes. Int J Clin Exp Med. 2014 Aug 15;7(8):2242-7. eCollection 2014.
- Respirator lung syndrome. Minn Med. 1967 Nov;50(11):1693-705. No abstract available.
- Needham DM, Colantuoni E, Mendez-Tellez PA, Dinglas VD, Sevransky JE, Dennison Himmelfarb CR, Desai SV, Shanholtz C, Brower RG, Pronovost PJ. Lung protective mechanical ventilation and two year survival in patients with acute lung injury: prospective cohort study. BMJ. 2012 Apr 5;344:e2124. doi: 10.1136/bmj.e2124.
- Ball L, Dameri M, Pelosi P. Modes of mechanical ventilation for the operating room. Best Pract Res Clin Anaesthesiol. 2015 Sep;29(3):285-99. doi: 10.1016/j.bpa.2015.08.003. Epub 2015 Sep 2.
- Mahmoud K, Ammar A, Kasemy Z. Comparison Between Pressure-Regulated Volume-Controlled and Volume-Controlled Ventilation on Oxygenation Parameters, Airway Pressures, and Immune Modulation During Thoracic Surgery. J Cardiothorac Vasc Anesth. 2017 Oct;31(5):1760-1766. doi: 10.1053/j.jvca.2017.03.026. Epub 2017 Mar 22.
- Choi EM, Na S, Choi SH, An J, Rha KH, Oh YJ. Comparison of volume-controlled and pressure-controlled ventilation in steep Trendelenburg position for robot-assisted laparoscopic radical prostatectomy. J Clin Anesth. 2011 May;23(3):183-8. doi: 10.1016/j.jclinane.2010.08.006. Epub 2011 Mar 4.
- Tran D, Rajwani K, Berlin DA. Pulmonary effects of aging. Curr Opin Anaesthesiol. 2018 Feb;31(1):19-23. doi: 10.1097/ACO.0000000000000546.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2019ZSLYEC-184
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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