Skip to content

Intraoperative Hypocapnia in PROVHILO and PROBESE

Associations of Intraoperative Hypocapnia With Patient Demographics, Ventilation Characteristics and Outcomes--Statistical Analysis Plan for an Individual Patient Data Analysis of PROVHILO and PROBESE

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05550181
Acronym
iHypoPRO
Enrollment
2793
Registered
2022-09-22
Start date
2022-11-29
Completion date
2023-03-31
Last updated
2023-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intraoperative Complications, Mechanical Ventilation Complication, Postoperative Complications, Pulmonary Complication, Surgery

Keywords

Postoperative Complications, Intraoperative Complications, Hypocapnia, Mechanical Ventilation

Brief summary

To gain a better understanding of the epidemiology of intraoperative hypocapnia, in particular the associations of intraoperative hypocapnia with patient demographics, ventilator characteristics, and perioperative complications we will perform an individual patient-level meta-analysis of two recent randomized clinical trials of intraoperative ventilation, the 'PROtective Ventilation using High versus LOw PEEP trial' (PROVHILO), and the 'Protective intraoperative ventilation with higher versus lower levels of positive end-expiratory pressure in obese patients trial' (PROBESE).

Detailed description

Lung-protective intraoperative ventilation (LPV) has the potential to improve the outcome of surgery patients through a reduction in postoperative pulmonary complications. Use of intraoperative ventilation strategies that use a low tidal volume could result in intraoperative hypercapnia. However, hypocapnia remains surprisingly common during intraoperative ventilation, possibly meaning that anesthesiologists continue to use high, if not too high respiratory rates or tidal volumes. Previous studies suggested associations between intraoperative derangement of end-tidal carbon dioxide (etCO2) and postoperative outcomes. Indeed, two studies in highly selected patient groups showed associations of intraoperative hypocapnia with prolonged length of hospital stay, in patients undergoing pancreaticoduodenectomy, and in patients undergoing hysterectomy. To gain a better understanding of the epidemiology of intraoperative hypocapnia, in particular the associations of intraoperative hypocapnia with patient demographics, ventilator characteristics, and perioperative complications we will perform an individual patient-level meta-analysis of two recent randomized clinical trials of intraoperative ventilation; PROVHILO and PROBESE.

Interventions

BEHAVIORALintraoperative mechanical ventilation with hypocapnia (etCO2 < 35 mm Hg)

A patient is considered 'hypocapnic' if the etCO2 was \< 35 mm Hg at any point during surgery, from start of the study till end of the study and classified as 'without hypocapnia' otherwise. In case of a missing value immediately before extubation, we will use the values as reported in the last hour of surgery.

Sponsors

Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
CollaboratorOTHER
Hospital Israelita Albert Einstein
CollaboratorOTHER
University Hospital Carl Gustav Carus
CollaboratorOTHER
Hospital Clínico Universitario de Valencia
CollaboratorOTHER
NMC Specialty Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Planned for major (abdominal) surgery. * At risk for postoperative pulmonary complications.

Exclusion criteria

* Planned thoracic surgery or neurosurgery. * Unscheduled surgery (i.e., urgent, or emergent surgeries) were excluded because these patients may have had metabolic abnormalities at the moment of surgery, i.e., metabolic acidosis, for which the anesthesiologist may have adjusted the intraoperative ventilator settings. This may have led to a 'compensatory' low etCO2. * Patients with etCO2 recordings are missing from the study databases.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of postoperative pulmonary complicationsUntil day seven or hospital discharge, whichever comes firstComposite of predefined and collected postoperative pulmonary complications. Postoperative pulmonary complications included mild, moderate, and severe respiratory failure; acute respiratory distress syndrome; bronchospasm; new pulmonary infiltrate; pulmonary infection; aspiration pneumonitis; pleural effusions; atelectasis; cardiopulmonary edema; and pneumothorax.

Secondary

MeasureTime frameDescription
Incidence of intensive care unit admissionUntil hospital discharge, death or 100 days, whichever comes firstIncidence of intensive care unit admission during hospital stay
Incidence of extrapulmonary pulmonary complicationsUntil day seven or hospital discharge, whichever comes first
Incidence of intraoperative complicationsIntraoperativelyDefined as intraoperative hypotension, arrhythmias; or need for rescue for desaturations; or need for vasoactive drugs.
Incidence of in-hospital mortalityFrom date of randomization until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 100 days
Incidence of major postoperative complicationsUntil day seven or hospital discharge, whichever comes firstCollapsed composite of complications developing within the first seven postoperative combining severe postoperative pulmonary complications, sepsis, septic shock and/or acute kidney injury
Incidence of 7-day mortalityMortality during the first seven days of hospitalizationUntil day seven or hospital discharge, whichever comes first

Countries

Brazil, Germany, Italy, Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026