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

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journal contribution
posted on 2019-09-04, 13:42 authored by AP Vanezis, JR Arnold, G Rodrigo, FY Lai, R Debiec, S Nazir, JN Khan, LL Ng, K Chitkara, JG Coghlan, SL Hetherington, GP McCann, NJ Samani
BACKGROUND: Remote 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. METHODS: The trial assessed the role of daily rIC in enhancing left ventricular ejection fraction (LVEF) recovery in patients with impaired LVEF (<45%) after ST segment elevation myocardial infarction (STEMI) treated with primary percutaneous coronary intervention (P-PCI). Patients were recruited from four UK hospitals and randomised to receive either 4 weeks of daily rIC or sham conditioning using the autoRIC Device (CellAegis) starting on day 3 post P-PCI. The primary endpoint was the improvement in LVEF over 4 months assessed by cardiac MRI (CMR). Seventy-three patients (38 cases, 35 controls) completed the study. RESULTS: The 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. CONCLUSIONS: Daily 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 NUMBER: NCT0166461.

Funding

This research received financial support from the NIHR Leicester Cardiovascular Biomedical Research Unit and the Masonic Charitable Foundation.

History

Citation

Heart, 2018, 104 (23), pp. 1955-1962

Author affiliation

/Organisation/COLLEGE OF LIFE SCIENCES/School of Medicine/Department of Cardiovascular Sciences

Version

  • VoR (Version of Record)

Published in

Heart

Publisher

BMJ Publishing Group with British Cardiovascular Society

eissn

1468-201X

Acceptance date

2018-04-23

Copyright date

2018

Available date

2019-09-04

Publisher version

https://heart.bmj.com/content/104/23/1955

Notes

The original data to all the results outlined in the manuscript can be provided in raw format on request in an anonymised form.

Language

en

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