Daily remote ischaemic conditioning following acute myocardial infarction: a randomised controlled trial

Autor: Jayanth R. Arnold, Gerry P McCann, Leong L. Ng, N J Samani, Kamal Chitkara, Florence Y. Lai, Glenn Rodrigo, A P Vanezis, Radek Debiec, Jamal N Khan, John G Coghlan, Simon Hetherington, Sheraz A Nazir
Rok vydání: 2018
Předmět:
Male
medicine.medical_specialty
medicine.drug_class
Ischemia
heart failure
Context (language use)
030204 cardiovascular system & hematology
ventricular remodelling
law.invention
03 medical and health sciences
Ventricular Dysfunction
Left

0302 clinical medicine
Percutaneous Coronary Intervention
Postoperative Complications
Randomized controlled trial
law
Internal medicine
Natriuretic Peptide
Brain

Outcome Assessment
Health Care

Natriuretic peptide
Medicine
Humans
remote ischaemic conditioning
030212 general & internal medicine
Myocardial infarction
cardiovascular diseases
Heart Failure and Cardiomyopathies
Aged
Ejection fraction
business.industry
Hemodynamic Monitoring
Stroke Volume
Middle Aged
medicine.disease
primary percutaneous coronary intervention
Peptide Fragments
Clinical trial
ST elevation myocardial infarction
Heart failure
Ischemic Preconditioning
Myocardial

Cardiology
cardiovascular system
Female
Cardiology and Cardiovascular Medicine
business
Zdroj: Heart
ISSN: 1468-201X
Popis: BackgroundRemote ischaemic conditioning (rIC) is a cardioprotective tool which has shown promise in preclinical and clinical trials in the context of acute ischaemia. Repeated rIC post myocardial infarction may provide additional benefits which have not previously been tested clinically.MethodsThe trial assessed the role of daily rIC in enhancing left ventricular ejection fraction (LVEF) recovery in patients with impaired LVEF (ResultsThe treatment and control groups were well matched at baseline including for mean LVEF (42.8% vs 44.3% respectively, p=0.952). There was no difference in the improvement in LVEF over 4 months between the treatment and control groups (4.8%±7.8% vs 4.6%±5.9% respectively, p=0.924). No differences were seen in the secondary outcome measures including changes in infarct size and left ventricular end-diastolic and systolic volumes, major adverse cardiac and cerebral event, mean Kansas City Cardiomyopathy Questionnaire score and change in N-terminal pro-brain natriuretic peptide levels.ConclusionsDaily rIC starting on day 3 and continued for 4 weeks following successful P-PCI for STEMI did not improve LVEF as assessed by CMR after 4 months when compared with a matched control group.Trial registration numberNCT0166461.
Databáze: OpenAIRE