Conventional versus minimally invasive extra-corporeal circulation in patients undergoing cardiac surgery: A randomized controlled trial (COMICS)

Author:

Angelini Gianni D1ORCID,Reeves Barnaby C1,Culliford Lucy A1,Maishman Rachel1,Rogers Chris A1,Anastasiadis Kyriakos2,Antonitsis Polychronis2,Argiriadou Helena2,Carrel Thierry3,Keller Dorothée3,Liebold Andreas4,Ashkaniani Fatma4,El-Essawi Aschraf5,Breitenbach Ingo6,Lloyd Clinton7,Bennett Mark7,Cale Alex8,Gunaydin Serdar9ORCID,Gunertem Eren9ORCID,Oueida Farouk10,Yassin Ibrahim M10,Serrick Cyril11,Murkin John M12,Rao Vivek11,Moscarelli Marco13ORCID,Condello Ignazzo13ORCID,Punjabi Prakash14ORCID,Rajakaruna Cha15,Deliopoulos Apostolos16,Bone Daniel15,Lansdown William15,Moorjani Narain17,Dennis Sarah17

Affiliation:

1. Bristol Medical School, University of Bristol, Bristol, UK

2. Aristotle University of Thessaloniki School of Medicine, Thessaloniki, Greece

3. University Hospital Bern, Bern, Switzerland

4. Universitätsklinikum Ulm, Ulm, Germany

5. Universitätsmedizin Göttingen, Göttingen, Germany

6. Klinikum Braunschweig, Braunschweig, Germany

7. University Hospitals Plymouth NHS Trust, Plymouth, UK

8. Hull University Teaching Hospitals NHS Trust, Hull, UK

9. Numune Training and Research Hospital in Ankara, Ankara, Turkey

10. Saud Al-Babtain Cardiac Centre, Dammam, Saudi Arabia

11. University Health Network, Toronto, ON, Canada

12. University of Western Ontario, London, ON, Canada

13. Anthea Hospital Bari, Italy

14. Imperial College Healthcare, London, UK

15. University Hospitals Bristol NHS Foundation Trust, Bristol, UK

16. AHEPA University Hospital, Thessaloniki, Greece

17. Royal Papworth Hospital, Cambridge, UK

Abstract

Introduction The trial hypothesized that minimally invasive extra-corporeal circulation (MiECC) reduces the risk of serious adverse events (SAEs) after cardiac surgery operations requiring extra-corporeal circulation without circulatory arrest. Methods This is a multicentre, international randomized controlled trial across fourteen cardiac surgery centres including patients aged ≥18 and <85 years undergoing elective or urgent isolated coronary artery bypass grafting (CABG), isolated aortic valve replacement (AVR) surgery, or CABG + AVR surgery. Participants were randomized to MiECC or conventional extra-corporeal circulation (CECC), stratified by centre and operation. The primary outcome was a composite of 12 post-operative SAEs up to 30 days after surgery, the risk of which MiECC was hypothesized to reduce. Secondary outcomes comprised: other SAEs; all-cause mortality; transfusion of blood products; time to discharge from intensive care and hospital; health-related quality-of-life. Analyses were performed on a modified intention-to-treat basis. Results The trial terminated early due to the COVID-19 pandemic; 1071 participants (896 isolated CABG, 97 isolated AVR, 69 CABG + AVR) with median age 66 years and median EuroSCORE II 1.24 were randomized (535 to MiECC, 536 to CECC). Twenty-six participants withdrew after randomization, 22 before and four after intervention. Fifty of 517 (9.7%) randomized to MiECC and 69/522 (13.2%) randomized to CECC group experienced the primary outcome (risk ratio = 0.732, 95% confidence interval (95% CI) = 0.556 to 0.962, p = 0.025). The risk of any SAE not contributing to the primary outcome was similarly reduced (risk ratio = 0.791, 95% CI 0.530 to 1.179, p = 0.250). Conclusions MiECC reduces the relative risk of primary outcome events by about 25%. The risk of other SAEs was similarly reduced. Because the trial terminated early without achieving the target sample size, these potential benefits of MiECC are uncertain.

Funder

Bristol NIHR BRC

Medtronic Europe

British Heart Foundation

Maquet Europe

Publisher

SAGE Publications

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