Postcardiotomy Venoarterial Extracorporeal Membrane Oxygenation
NCT ID: NCT03508505
Last Updated: 2020-03-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
1000 participants
OBSERVATIONAL
2018-01-01
2020-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Data on the real benefit of VA-ECMO after cardiac surgery is limited and often derived from heterogeneous patient populations, which prevent conclusive results on the benefits of VA-ECMO in this setting. This issue will be investigated in the present retrospective European multicenter study.
In this setting, veno-arterial extracorporeal oxygenation (VA-ECMO) is the only means to provide cardiopulmonary support to recovery or as bridge to transplantation.
Data on the real benefit of VA-ECMO after cardiac surgery is limited and often derived from heterogeneous populations of patients who underwent different cardiac procedures. Patients with cardiac low-output after surgery for aortic dissection or valve surgery are expected to have different baseline characteristics (such as age and comorbidities) and underlying cardiac disease than patients undergoing isolated coronary surgery. Furthermore, available studies included patients operated two decades ago and this does not provide an exact measure of the benefits of this treatment strategy.
The possible benefits of using VA-ECMO after adult cardiac surgery will be investigated in this retrospective European multicenter study.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Optimal ECMO Flow in the Critical Phase of Cardiogenic Shock to Optimize Peripheral Organ Perfusion and Myocardial Stress
NCT06936839
Vaso-inotropic Score and ECMO-VA Support in Post-cardiotomy Cardiogenic Shock.
NCT05412303
PRecision Ecmo in CardIogenic Shock Evaluation
NCT05748860
Early Preventive Left Ventricle Unloading After VA-ECMO for Refractory Cardiogenic Shock
NCT07027202
Comparison of a New Semi-invasive Monitoring System With Transpulmonary Thermodilution in Cardiac Surgery Patients
NCT02312505
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Data on the real benefit of VA-ECMO after cardiac surgery is limited and often derived from heterogeneous and small size series of patients who underwent different cardiac surgery procedures. Patients with cardiac low-output after surgery for aortic dissection or valve surgery are expected to have different baseline characteristics (such as age and comorbidities) and underlying cardiac disease than patients undergoing isolated coronary surgery. Furthermore, available studies included patients operated two decades ago and, in view of the development of perfusion technology and perioperative care, this does not provide an exact measure of the current benefits of this treatment strategy. Importantly, the role of intra-aortic balloon pump, left ventricular venting, duration of VA-ECMO and hospital experience should be evaluated. The investigators sought to investigate these issues in a large multicenter study.
Patients and methods Patients who were treated with VA-ECMO for cardiac low-output after adult cardiac surgery (other than heart transplantation and/or implantation of a left ventricular assist device) in 21 centers of cardiac surgery from January 2010 to December 2017.
Eligibility criteria
* Patients aged \> 18 years;
* Patients who required VA-ECMO after elective, urgent or emergency adult cardiac surgery such as coronary surgery, heart valve surgery and/or aortic root surgery because of postoperative low-cardiac output syndrome and/or acute respiratory failure.
Exclusion criteria
* Patients aged \< 18 years;
* Any VA-ECMO implanted before index surgical procedure;
* Patients who underwent postoperatively veno-venous ECMO;
* Patients who required VA-ECMO after heart transplantation;
* Patients who required VA-ECMO after any left ventricular assist device.
Definition criteria Definition criteria and units of measurements are reported beside each baseline, operative and postoperative variables in the electronic datasheet.
Outcomes
1. Hospital death
2. Late death
3. Stroke
4. Tracheostomy
5. Gastrointestinal complications
6. Deep sternal wound infection
7. Vascular access site infection
8. Blood stream infection
9. Peripheral vascular injury
10. Major lower limb amputation
11. New onset dialysis
12. Peak postoperative serum creatinine level
13. Nadir postoperative pH during VA-ECMO
14. Peak postoperative arterial lactate level
15. Nadir postoperative hemoglobin level
16. Chest drainage output 24 h after surgery
17. Number of red blood cells units transfused intra- and postoperatively
18. Reoperation for intrathoracic bleeding
19. Reoperation for peripheral cannulation-related bleeding
20. Intensive care unit length of stay
21. Death on VA-ECMO
Analysis of clinical results
The aim of this registry is to perform a number of analysis evaluating:
1. Early and late survival of postcardiotomy VA-ECMO;
2. Predictors and causes of in-hospital death after successful weaning from postcardiotomy VA-ECMO;
3. Comparative analysis of peripheral versus central postcardiotomy VA-ECMO;
4. VA-ECMO plus intra-aortic baloon pump vs. isolated VA-ECMO;
5. Determinants of outcome after prolonged postcardiotomy VA-ECMO (\>5 days).
Publication of results The results of these studies will be submitted for publication to international, peer-reviewed journals in the fields of critical care, cardiology or cardiac surgery.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Venoarterial extracorporeal oxygenation
Veno-arterial extracorporeal oxygenation (VA-ECMO) is inserted in the acute setting in case of cardiac low output after adult cardiac surgery in order to provide cardiopulmonary support to recovery or as bridge to transplantation.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Patients who underwent postoperatively veno-venous ECMO;
* Patients who required VA-ECMO after heart transplantation;
* Patients who required VA-ECMO after any left ventricular assist device.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Karolinska Institutet
OTHER
Ospedali Riuniti Trieste
OTHER
Universitätsklinikum Hamburg-Eppendorf
OTHER
University of Burgundy
OTHER
CHU de Reims
OTHER
Rennes University Hospital
OTHER
Henri Mondor University Hospital
OTHER
Glenfield Hospital
OTHER
IRCCS Azienda Ospedaliero-Universitaria di Bologna
OTHER
University Hospital Muenster
OTHER
Institute for Clinical and Experimental Medicine
OTHER_GOV
Medical University of Vienna
OTHER
University Hospital, Udine, Italy
OTHER
Golden Jubilee National Hospital
OTHER_GOV
Heinrich-Heine University, Duesseldorf
OTHER
Helsinki University Central Hospital
OTHER
Helios Research Center
OTHER
Sahlgrenska University Hospital
OTHER
Lund University Hospital
OTHER
Prince Sultan Cardiac Center, Adult Cardiology Department.
OTHER
Turku University Hospital
OTHER_GOV
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Heart Center, Turku University Hospital
Turku, , Finland
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Biancari F, Perrotti A, Ruggieri VG, Mariscalco G, Dalen M, Dell'Aquila AM, Jonsson K, Ragnarsson S, Di Perna D, Bounader K, Gatti G, Juvonen T, Alkhamees K, Yusuff H, Loforte A, Lechiancole A, Chocron S, Pol M, Spadaccio C, Pettinari M, De Keyzer D, Fiore A, Welp H. Five-year survival after post-cardiotomy veno-arterial extracorporeal membrane oxygenation. Eur Heart J Acute Cardiovasc Care. 2021 Aug 24;10(6):595-601. doi: 10.1093/ehjacc/zuaa039.
Mariscalco G, Fiore A, Ragnarsson S, El-Dean Z, Jonsson K, Dalen M, Fux T, Ruggieri VG, Gatti G, Juvonen T, Zipfel S, Dell'Aquila AM, Perrotti A, Bounader K, Settembre N, Loforte A, Livi U, Pol M, Spadaccio C, Pettinari M, Reichart D, Alkhamees K, Welp H, Maselli D, Lichtenberg A, Biancari F; PC-ECMO group. Venoarterial Extracorporeal Membrane Oxygenation After Surgical Repair of Type A Aortic Dissection. Am J Cardiol. 2020 Jun 15;125(12):1901-1905. doi: 10.1016/j.amjcard.2020.03.012. Epub 2020 Mar 31.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
T3/2018
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.