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  3. Individualized Flow-Controlled versus Pressure-Controlled Ventilation in Cardiac Surgery: A Randomized Controlled Trial.
 

Individualized Flow-Controlled versus Pressure-Controlled Ventilation in Cardiac Surgery: A Randomized Controlled Trial.

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BORIS DOI
10.48620/92461
Publisher DOI
10.1097/ALN.0000000000005851
PubMed ID
41247873
Description
Background
Patients undergoing on-pump cardiac surgery are at high risk for perioperative lung injury and a hyper-inflammatory state associated with postoperative complications. We investigated the hypothesis that Flow-Controlled Ventilation (FCV) reduces the inflammatory stimulus compared to conventional Pressure-Controlled Ventilation (PCV) in this patient cohort. FCV has the unique feature of controlling airway flows during inspiration and expiration and the potential to reduce mechanical power of invasive ventilation.
Methods
In this single-center randomized controlled trial, 140 adult patients undergoing cardiac surgery with cardiopulmonary bypass were allocated 1:1 to FCV or PCV from Aug 10, 2020, to Nov 16, 2022. Participants received perioperatively either individualized FCV with a compliance-guided positive end-expiratory pressure (PEEP) and a compliance-guided driving pressure (ΔP) or PCV with a compliance-guided PEEP and ΔP for tidal volumes of 6-8 ml/kg predicted body weight. Postoperative plasmatic interleukin 8 (IL-8) levels six hours after cardiopulmonary bypass were defined as the primary endpoint. Explorative secondary outcomes included incidences of postoperative pulmonary and extrapulmonary complications, and hospital length of stay.
Results
Median postoperative IL-8 levels did not differ significantly between FCV and PCV (FCV 3.08 vs. PCV 3.60, beta coefficient 0.08 pg/ml, 95% CI -0.17 to 0.33; P = 0.573). ΔP values and tidal volumes were higher in the FCV group, but FCV yielded lower respiratory rates and minute volumes required for normocapnia. As a result, the FCV approach reduced the perioperatively applied mechanical power by 55%. After FCV, incidences of single postoperative pulmonary complications (e.g. confirmed pneumonia, moderate and severe hypoxemia) and any postoperative extrapulmonary complication were lower, and the hospital stay shorter.
Conclusions
FCV did not reduce plasmatic IL-8 levels at the predefined timepoint six hours after cardiopulmonary bypass. However, the reduction of mechanical power during individualized FCV application and the findings of the explorative secondary study outcomes justify future trials.
Date of Publication
2026-03-01
Publication Type
Article
Subject(s)
600 Technology > 610 Medicine & health
Language(s)
en
Contributor(s)
Becker, Simon
Kurz, Christian T
Schnitzler, Romina
Geppert, Johannes
Wichelhaus, Lisa-Marie
Denz, Robin
Poepping, Jonas
Rembecki, Martin
Berres, Dinah Maria
Strauch, Justus T
Bates, Declan G
Erdoes, Gabor
Clinic and Policlinic for Anaesthesiology and Pain Therapy
Clinic and Policlinic for Anaesthesiology and Pain Therapy - Partial Clinic Insel
Timmesfeld, Nina
Zahn, Peter K
Additional Credits
Clinic and Policlinic for Anaesthesiology and Pain Therapy
Series
Anesthesiology
Publisher
Lippincott, Williams & Wilkins
ISSN
1528-1175
0003-3022
Access(Rights)
open.access
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