The effects of nitric oxide on coagulation and inflammation in ex vivo models of extracorporeal membrane oxygenation and cardiopulmonary bypass

Author:

Malfertheiner Maximilian V.12ORCID,Garrett Ashlen13,Passmore Margaret13ORCID,Haymet Andrew B.13ORCID,Webb Richard I.4,Von Bahr Viktor15,Millar Jonathan E.1,Schneider Bailey A.13,Obonyo Nchafatso G.1367ORCID,Black Debra1,Bouquet Mahe1,Bartnikowski Nicole13,Suen Jacky Y.13,Fraser John F.13

Affiliation:

1. The Critical Care Research Group The Prince Charles Hospital Brisbane Queensland Australia

2. The Department of Internal Medicine II, Cardiology and Pneumology University Medical Center Regensburg Regensburg Germany

3. The Faculty of Medicine The University of Queensland, Saint Lucia Brisbane Queensland Australia

4. The Centre for Microscopy and Microanalysis The University of Queensland, Saint Lucia Brisbane Queensland Australia

5. The Department of Physiology and Pharmacology, The Section for Anesthesiology and Intensive Care Medicine The Karolinska Institutet Stockholm Sweden

6. Initiative to Develop African Research Leaders (IDeAL) KEMRI‐Wellcome Trust Research Programme Kilifi Kenya

7. Wellcome Trust Centre for Global Health Research, Imperial College London London UK

Abstract

AbstractBackgroundExtracorporeal life support (ECLS) has extensive applications in managing patients with acute cardiac and pulmonary failure. Two primary modalities of ECLS, cardiopulmonary bypass (CPB) and extracorporeal membrane oxygenation (ECMO), include several similarities in their composition, complications, and patient outcomes. Both CPB and ECMO pose a high risk of thrombus formation and platelet activation due to the large surface area of the devices and bleeding due to system anticoagulation. Therefore, novel methods of anticoagulation are needed to reduce the morbidity and mortality associated with extracorporeal support. Nitric oxide (NO) has potent antiplatelet properties and presents a promising alternative or addition to anticoagulation with heparin during extracorporeal support.MethodsWe developed two ex vivo models of CPB and ECMO to investigate NO effects on anticoagulation and inflammation in these systems.ResultsSole addition of NO as an anticoagulant was not successful in preventing thrombus formation in the ex vivo setups, therefore a combination of low‐level heparin with NO was used. Antiplatelet effects were observed in the ex vivo ECMO model when NO was delivered at 80 ppm. Platelet count was preserved after 480 min when NO was delivered at 30 ppm.ConclusionCombined delivery of NO and heparin did not improve haemocompatibility in either ex vivo model of CPB and ECMO. Anti‐inflammatory effects of NO in ECMO systems have to be evaluated further.

Funder

Mallinckrodt Pharmaceuticals

Publisher

Wiley

Subject

Biomedical Engineering,General Medicine,Biomaterials,Medicine (miscellaneous),Bioengineering

Reference22 articles.

1. Extracorporeal Life Support Organization.ECLS Registry Report.2021[cited 2021 Oct 2]. Available from:https://www.elso.org/Registry/Statistics/InternationalSummary.aspx

2. The inflammatory response to extracorporeal membrane oxygenation (ECMO): a review of the pathophysiology

3. The evolution of cardiopulmonary bypass: lessons to be learned

4. STS/SCA/AmSECT clinical practice guidelines: anticoagulation during cardiopulmonary bypass;Shore‐Lesserson L;J Extra Corpor Technol,2018

5. Bleeding after Cardiopulmonary Bypass

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