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The Effect of Remote Ischemic Conditioning and Glyceryl Trinitrate on Perioperative Myocardial Injury in Cardiac Bypass Surgery Patients: Rationale and Design of the ERIC-GTN Study.
Hamarneh, Ashraf; Sivaraman, Vivek; Bulluck, Heerajnarain; Shanahan, Hilary; Kyle, Bonnie; Ramlall, Manish; Chung, Robin; Jarvis, Claire; Xenou, Maria; Ariti, Cono; Cordery, Roger; Yellon, Derek M; Hausenloy, Derek J.
Afiliação
  • Hamarneh A; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Sivaraman V; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Bulluck H; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Shanahan H; The Heart Hospital, London, United Kingdom.
  • Kyle B; The Heart Hospital, London, United Kingdom.
  • Ramlall M; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Chung R; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Jarvis C; The Heart Hospital, London, United Kingdom.
  • Xenou M; The Heart Hospital, London, United Kingdom.
  • Ariti C; Nuffield Trust, London, United Kingdom.
  • Cordery R; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Yellon DM; The Hatter Cardiovascular Institute University College London, London, United Kingdom.
  • Hausenloy DJ; The National Institute of Health Research, University College London Hospitals Biomedical Research Centre, London, United Kingdom.
Clin Cardiol ; 38(11): 641-6, 2015 Nov.
Article em En | MEDLINE | ID: mdl-26412308
ABSTRACT
Remote ischemic conditioning (RIC) using transient limb ischemia/reperfusion has been reported to reduce perioperative myocardial injury in patients undergoing coronary artery bypass grafting and/or valve surgery. The role of intravenous glyceryl trinitrate (GTN) therapy administered during cardiac surgery as a cardioprotective agent and whether it interferes with RIC cardioprotection is not clear and is investigated in the ERIC-GTN trial ( http//www.clinicaltrials.gov NCT01864252). The ERIC-GTN trial is a single-site, double-blind, randomized, placebo-controlled study. Consenting adult patients (age > 18 years) undergoing elective coronary artery bypass grafting ± valve surgery with blood cardioplegia will be eligible for inclusion. Two hundred sixty patients will be randomized to 1 of 4 treatment groups following anesthetic induction (1) RIC alone, a RIC protocol comprising three 5-minute cycles of simultaneous upper-arm and thigh cuff inflation/deflation followed by an intravenous (IV) placebo infusion; (2) GTN alone, a simulated sham RIC protocol followed by an IV GTN infusion; (3) RIC + GTN, a RIC protocol followed by an IV GTN infusion; and (4) neither RIC nor GTN, a sham RIC protocol followed by IV placebo infusion. The primary endpoint will be perioperative myocardial injury as quantified by the 72-hour area-under-the-curve serum high-sensitivity troponin T. The ERIC-GTN trial will determine whether intraoperative GTN therapy is cardioprotective during cardiac surgery and whether it affects RIC cardioprotection.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coxa da Perna / Vasodilatadores / Traumatismo por Reperfusão Miocárdica / Ponte de Artéria Coronária / Nitroglicerina / Precondicionamento Isquêmico / Extremidade Superior Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Coxa da Perna / Vasodilatadores / Traumatismo por Reperfusão Miocárdica / Ponte de Artéria Coronária / Nitroglicerina / Precondicionamento Isquêmico / Extremidade Superior Idioma: En Ano de publicação: 2015 Tipo de documento: Article