Postoperative pulmonary complications (PPCs) are a major cause of morbidity and mortality in surgical patients. National estimates suggest 1,062,000 PPCs per year, with 46,200 deaths, and 4.8 million additional days of hospitalization. The objective of the study is to develop and implement perioperative strategies to eliminate PPCs in abdominal surgery, the field with the largest absolute number of PPCs. We will conduct a randomized controlled pragmatic trial in 750 studied participants. The effectiveness of an individualized perioperative anesthesia-centered bundle will be compared to the usual anesthetic care in patients receiving open abdominal surgery. At the end of this project, the investigators expect to change clinical practice by establishing a new and clinically feasible anesthesia-centered strategy to reduce perioperative lung morbidity. The research will be conducted across 14 US academic centers, and will be funded by the National Institute of Health.
Postoperative pulmonary complications (PPCs) are a major cause of morbidity and mortality in surgical patients. National estimates suggest 1,062,000 PPCs per year, with 46,200 deaths, and 4.8 million additional days of hospitalization. Abdominal surgery is the field with the largest absolute number of PPCs. The long-term goal is to develop and implement perioperative strategies to eliminate PPCs. Whereas PPCs are as significant and lethal as cardiac complications, research in the field has received much less attention, and strategies to minimize PPCs are regrettably limited. Recently, the investigators and others have suggested a crucial role of anesthesia related interventions such as ventilatory strategies, and administration and reversal of neuromuscular blocking agents in reducing PPCs. These findings are consistent with the beneficial effects of lung protective ventilation during the adult respiratory distress syndrome (ARDS). While surgical patients differ substantially from ARDS patients as most have no or limited lung injury at the start of surgery, intraoperative anesthetic and abdominal surgery interventions result in lung derecruitment and predispose to or produce direct and indirect, potentially multiple-hit, lung injury. Thus, effective anesthetic strategies aiming at early lung protection in this group of patients are greatly needed. Indeed, the current lack of evidence results in wide and unexplained variability in anesthetic practices creating a major public health issue as some practices within usual care appear to be suboptimal and even potentially injurious. The investigators hypothesize that an anesthesia-centered bundle, based on recent findings and focused on perioperative lung protection, will minimize multiple and synergistic factors responsible for the multiple-hit perioperative pulmonary dysfunction and result in decreased incidence and severity of PPCs. Founded on strong preliminary data, we will leverage a network of US academic centers to study this hypothesis in two aims: Aim 1. To compare the number and severity of PPCs in participants receiving an individualized perioperative anesthesia-centered bundle to those in participants receiving usual anesthetic care during open abdominal surgery. For this, the investigators propose to conduct a prospective multicenter randomized controlled pragmatic trial with a blinded assessor in a total of 750 studied participants. The bundle will consist of optimal mechanical ventilation comprising individualized positive end-expiratory pressure to maximize respiratory system compliance and minimize driving pressures, individualized use of neuromuscular blocking agents and their reversal, and postoperative lung expansion and early mobilization; Aim 2. To assess the effect of the proposed bundle on plasma levels of lung injury biomarkers. The investigators theorize that our intervention will minimize overinflation and atelectasis reducing plasma levels of biomarkers of lung inflammatory, epithelial, and endothelial injury. Such mechanistic insights will facilitate bundle dissemination and support adoption as it has for lung protective ventilation for ARDS. At the end of this project, the investigators expect to change clinical practice by establishing a new and clinically feasible anesthesia-centered strategy to reduce perioperative lung morbidity.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
794
Brochure and video about relevance of postoperative pulmonary complications, postoperative mobilization and use of incentive spirometry.
PEEP will be set by maximizing respiratory system compliance along a decremental PEEP titration following an incremental recruitment maneuver.
Administration of neuromuscular blocking agents and their reversal will be done based on established protocol.
Participants will be encouraged to adhere to incentive spirometry to be started 2 hours after surgery and maintained until participant freely ambulates. Supervision will be provided 3 times/day for continuous education and management of barriers to optimal performance.
Participants will be encouraged to adhere to prescription of early ambulation.
University of California - San Francisco
San Francisco, California, United States
Stanford University
Stanford, California, United States
University of Colorado, Anschutz Medical Campus
Aurora, Colorado, United States
South Florida Veterans Affairs Foundation for Research and Education, Inc.
Miami, Florida, United States
Northwestern University
Evanston, Illinois, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
Brigham and Women's Hospital
Boston, Massachusetts, United States
Beth Israel Deaconess Hospital
Boston, Massachusetts, United States
Univerisity of Massachusetts Amherst Center
Worcester, Massachusetts, United States
Mayo Clinic
Rochester, Minnesota, United States
...and 6 more locations
Number and Severity of Postoperative Pulmonary Complications Between Participant Groups
The distribution of the number and severity of accumulated post-operative pulmonary complications (PPCs) between the control and intervention groups during the first 7 days after surgery.
Time frame: Postoperative Days 0 through 7
Number of Participants With Grade 1 and 2 Postoperative Pulmonary Complications
Individual grade 3 and 4 postoperative pulmonary complications within 7 days after the day of the surgery.
Time frame: Postoperative Days 0 through 7
Number of Participants With Grade 3 and 4 Postoperative Pulmonary Complications
Individual grade 3 and 4 postoperative pulmonary complications within 7, 30, and 90 days after the day of the surgery.
Time frame: Postoperative Days 7, 30, and 90
Number of Participants With Hypoxemia by Postoperative Day 7
Presence of any hypoxemia (as defined in PPC grade 1 and 2) within 7 days after the day of the surgery.
Time frame: Postoperative Days 0 through 7
Number of Participants With Atelectasis by Postoperative Day 7
Presence of atelectasis (radiological confirmation + either temperature \>37.5°C or abnormal lung symptoms/signs) by day 7 after the date of surgery.
Time frame: Days 0 through 7 after the day of surgery
Number of Participants With Pneumonia (Suspected and Proved) by Postoperative Day 7
Incidence of suspected (radiological evidence without bacteriological confirmation) and proved (radiological evidence and documentation of pathological organism) pneumonia by day 7 after the date of surgery.
Time frame: Days 0 through 7
Number of Participants With Ventilatory Dependence or Failure by Postoperative Day 7
Number of participants with ventilatory dependence (Grade 3, non-invasive or invasive ventilation \< 48h) or failure (Grade 4, postoperative non-invasive or invasive ventilation dependence ≥ 48h) by day 7 after the date of surgery.
Time frame: Days 0 through 7
Length of Postoperative Oxygen Support
Number of time (hours or days) spent in the postoperative oxygen therapy or other respiratory support
Time frame: Up to 7 days post-surgery
Number of Participants With Both Intraoperative Hypoxemia and Rescue Recruitment Maneuvers
The incidence of both intraoperative hypoxemia (SpO2 \< 85%) and rescue recruitment maneuvers during surgery. Received unplanned RM or PEEP titrations or adjustments during surgery for oxygenation or ventilation rescue.
Time frame: Day 0
Number of Participants With Intraoperative Cardiovascular Events
Number of participants with hypotension, bradycardia, tachycardia, arrhythmias, new ST-segment changes and cardiac arrest
Time frame: Day 0
Length of Hospital Stay
Number of days the participant has spent in the hospital since the day of the surgery.
Time frame: Days 0 through 7, 30, and 90
Number of Participants With Other Hospital Readmission(s) After Initial Discharge
The number of participants with hospital readmission(s), other than to the Intensive Care Unit, if admitted.
Time frame: After the date of discharge to day 90
Number of Participants With Any Major Extrapulmonary Complications
Number of participants with arrhythmia, paralytic ileus, surgical site infection, infection (source uncertain), acute renal failure, and systemic inflammatory response syndrome.
Time frame: Days 0 to 7
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