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Conventional versus minimally invasive extra-corporeal circulation in patients undergoing cardiac surgery: A randomized controlled trial (COMICS).
Angelini, Gianni D; Reeves, Barnaby C; Culliford, Lucy A; Maishman, Rachel; Rogers, Chris A; Anastasiadis, Kyriakos; Antonitsis, Polychronis; Argiriadou, Helena; Carrel, Thierry; Keller, Dorothée; Liebold, Andreas; Ashkaniani, Fatma; El-Essawi, Aschraf; Breitenbach, Ingo; Lloyd, Clinton; Bennett, Mark; Cale, Alex; Gunaydin, Serdar; Gunertem, Eren; Oueida, Farouk; Yassin, Ibrahim M; Serrick, Cyril; Murkin, John M; Rao, Vivek; Moscarelli, Marco; Condello, Ignazzo; Punjabi, Prakash; Rajakaruna, Cha; Deliopoulos, Apostolos; Bone, Daniel; Lansdown, William; Moorjani, Narain; Dennis, Sarah.
Afiliación
  • Angelini GD; Bristol Medical School, University of Bristol, Bristol, UK.
  • Reeves BC; Bristol Medical School, University of Bristol, Bristol, UK.
  • Culliford LA; Bristol Medical School, University of Bristol, Bristol, UK.
  • Maishman R; Bristol Medical School, University of Bristol, Bristol, UK.
  • Rogers CA; Bristol Medical School, University of Bristol, Bristol, UK.
  • Anastasiadis K; Aristotle University of Thessaloniki School of Medicine, Thessaloniki, Greece.
  • Antonitsis P; Aristotle University of Thessaloniki School of Medicine, Thessaloniki, Greece.
  • Argiriadou H; Aristotle University of Thessaloniki School of Medicine, Thessaloniki, Greece.
  • Carrel T; University Hospital Bern, Bern, Switzerland.
  • Keller D; University Hospital Bern, Bern, Switzerland.
  • Liebold A; Universitätsklinikum Ulm, Ulm, Germany.
  • Ashkaniani F; Universitätsklinikum Ulm, Ulm, Germany.
  • El-Essawi A; Universitätsmedizin Göttingen, Göttingen, Germany.
  • Breitenbach I; Klinikum Braunschweig, Braunschweig, Germany.
  • Lloyd C; University Hospitals Plymouth NHS Trust, Plymouth, UK.
  • Bennett M; University Hospitals Plymouth NHS Trust, Plymouth, UK.
  • Cale A; Hull University Teaching Hospitals NHS Trust, Hull, UK.
  • Gunaydin S; Numune Training and Research Hospital in Ankara, Ankara, Turkey.
  • Gunertem E; Numune Training and Research Hospital in Ankara, Ankara, Turkey.
  • Oueida F; Saud Al-Babtain Cardiac Centre, Dammam, Saudi Arabia.
  • Yassin IM; Saud Al-Babtain Cardiac Centre, Dammam, Saudi Arabia.
  • Serrick C; University Health Network, Toronto, ON, Canada.
  • Murkin JM; University of Western Ontario, London, ON, Canada.
  • Rao V; University Health Network, Toronto, ON, Canada.
  • Moscarelli M; Anthea Hospital Bari, Italy.
  • Condello I; Anthea Hospital Bari, Italy.
  • Punjabi P; Imperial College Healthcare, London, UK.
  • Rajakaruna C; University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Deliopoulos A; AHEPA University Hospital, Thessaloniki, Greece.
  • Bone D; University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Lansdown W; University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Moorjani N; Royal Papworth Hospital, Cambridge, UK.
  • Dennis S; Royal Papworth Hospital, Cambridge, UK.
Perfusion ; : 2676591241258054, 2024 Jun 04.
Article en En | MEDLINE | ID: mdl-38832503
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.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Perfusion Asunto de la revista: CARDIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Perfusion Asunto de la revista: CARDIOLOGIA Año: 2024 Tipo del documento: Article País de afiliación: Reino Unido