Effects of Intracoronary Alteplase on Microvascular Function in Acute Myocardial Infarction.


Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
04 02 2020
Historique:
entrez: 29 1 2020
pubmed: 29 1 2020
medline: 15 12 2020
Statut: ppublish

Résumé

Background Impaired microcirculatory reperfusion worsens prognosis following acute ST-segment-elevation myocardial infarction. In the T-TIME (A Trial of Low-Dose Adjunctive Alteplase During Primary PCI) trial, microvascular obstruction on cardiovascular magnetic resonance imaging did not differ with adjunctive, low-dose, intracoronary alteplase (10 or 20 mg) versus placebo during primary percutaneous coronary intervention. We evaluated the effects of intracoronary alteplase, during primary percutaneous coronary intervention, on the index of microcirculatory resistance, coronary flow reserve, and resistive reserve ratio. Methods and Results A prespecified physiology substudy of the T-TIME trial. From 2016 to 2017, patients with ST-segment-elevation myocardial infarction ≤6 hours from symptom onset were randomized in a double-blind study to receive alteplase 20 mg, alteplase 10 mg, or placebo infused into the culprit artery postreperfusion, but prestenting. Index of microcirculatory resistance, coronary flow reserve, and resistive reserve ratio were measured after percutaneous coronary intervention. Cardiovascular magnetic resonance was performed at 2 to 7 days and 3 months. Analyses in relation to ischemic time (<2, 2-4, and ≥4 hours) were prespecified. One hundred forty-four patients (mean age, 59±11 years; 80% male) were prospectively enrolled, representing 33% of the overall population (n=440). Overall, index of microcirculatory resistance (median, 29.5; interquartile range, 17.0-55.0), coronary flow reserve(1.4 [1.1-2.0]), and resistive reserve ratio (1.7 [1.3-2.3]) at the end of percutaneous coronary intervention did not differ between treatment groups. Interactions were observed between ischemic time and alteplase for coronary flow reserve (

Identifiants

pubmed: 31986989
doi: 10.1161/JAHA.119.014066
pmc: PMC7033872
doi:

Substances chimiques

Fibrinolytic Agents 0
Tissue Plasminogen Activator EC 3.4.21.68

Banques de données

ClinicalTrials.gov
['NCT02257294']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e014066

Subventions

Organisme : British Heart Foundation
ID : PG/11/2/28474
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/14/64/31043
Pays : United Kingdom
Organisme : British Heart Foundation
ID : PG/11/55/28999
Pays : United Kingdom
Organisme : British Heart Foundation
ID : FS/16/74/32573
Pays : United Kingdom
Organisme : British Heart Foundation
ID : RE/18/6/34217
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_15113
Pays : United Kingdom
Organisme : Department of Health
ID : 12/170/4
Pays : United Kingdom
Organisme : Medical Research Council
ID : MC_PC_12037
Pays : United Kingdom
Organisme : Chief Scientist Office
ID : SCD/01
Pays : United Kingdom

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Auteurs

Annette M Maznyczka (AM)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Peter J McCartney (PJ)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Keith G Oldroyd (KG)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Mitchell Lindsay (M)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Margaret McEntegart (M)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Hany Eteiba (H)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Paul Rocchiccioli (P)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Richard Good (R)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Aadil Shaukat (A)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Keith Robertson (K)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Vivek Kodoth (V)

Leeds University and Leeds Teaching Hospitals NHS Trust Leeds United Kingdom.

John P Greenwood (JP)

Leeds University and Leeds Teaching Hospitals NHS Trust Leeds United Kingdom.

James M Cotton (JM)

Wolverhampton University Hospital NHS Trust Wolverhampton United Kingdom.

Stuart Hood (S)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Stuart Watkins (S)

West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Peter W Macfarlane (PW)

Electrocardiology Group Royal Infirmary Glasgow United Kingdom.

Julie Kennedy (J)

Electrocardiology Group Royal Infirmary Glasgow United Kingdom.

R Campbell Tait (RC)

Department of Haematology Royal Infirmary Glasgow United Kingdom.

Paul Welsh (P)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.

Naveed Sattar (N)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.

Damien Collison (D)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
West of Scotland Heart and Lung Centre Golden Jubilee National Hospital, Clydebank Glasgow United Kingdom.

Lynsey Gillespie (L)

Project Management Unit Greater Glasgow and Clyde Health Board Glasgow United Kingdom.

Alex McConnachie (A)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.
Robertson Centre for Biostatistics Institute of Health and Wellbeing, University of Glasgow Glasgow United Kingdom.

Colin Berry (C)

British Heart Foundation Glasgow Cardiovascular Research Centre Institute of Cardiovascular and Medical Sciences University of Glasgow Glasgow United Kingdom.

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Classifications MeSH