Effect of Intravascular Cooling on Microvascular Obstruction (MVO) in Conscious Patients with ST-Elevation Myocardial Infarction Undergoing Primary PCI: Results from the COOL AMI EU Pilot Study.
Adult
Aged
Anterior Wall Myocardial Infarction
/ diagnostic imaging
Consciousness
Coronary Circulation
Europe
Feasibility Studies
Female
Humans
Hypothermia, Induced
/ adverse effects
Male
Microcirculation
Middle Aged
No-Reflow Phenomenon
/ diagnostic imaging
Percutaneous Coronary Intervention
/ adverse effects
Pilot Projects
Risk Factors
ST Elevation Myocardial Infarction
/ diagnostic imaging
Stroke Volume
Time Factors
Treatment Outcome
Ventricular Function, Left
Cardiac magnetic resonance
Hypothermia
Microvascular obstruction (MVO)
PPCI
STEMI
Journal
Cardiovascular revascularization medicine : including molecular interventions
ISSN: 1878-0938
Titre abrégé: Cardiovasc Revasc Med
Pays: United States
ID NLM: 101238551
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
19
06
2018
revised:
07
09
2018
accepted:
19
09
2018
pubmed:
12
11
2018
medline:
1
7
2020
entrez:
12
11
2018
Statut:
ppublish
Résumé
COOL AMI EU pilot was a multi-center, randomized controlled trial to assess feasibility and safety of rapid intravascular therapeutic hypothermia (TH) in conscious patients with anterior ST-elevation myocardial infarction (STEMI) undergoing primary PCI (PPCI). We report the effect of hypothermia upon microvascular obstruction (MVO). Conscious patients with anterior STEMI and symptom duration <6 h were recruited and randomized to PPCI + TH or PPCI alone. TH was induced using the ZOLL® Proteus™ intravascular temperature management system and rapid infusion of 1 L of cold normal saline, with a target temperature of 32 °C. MVO was measured by cardiac magnetic resonance (CMR) at 4 to 6 days post-MI. MVO larger than 3.9% of LV was considered as extensive MVO. 50 patients were randomized; mean age was 58 years, and 86% were men. At reperfusion, mean intravascular temperature for the TH group was 33.6 ± 1 °C. The presence of MVO was high and not different in both groups (74% vs. 77%, p = 0.79). The proportion of patients with extensive MVO was 11% in the TH group and 23% in the control group (OR 0.4 95%CI 0.07-2.35, p = 0.30). Patients with extensive MVO showed reduced EF at 4-6 days (34% versus 43%, p = 0.01). The percentage of patients with EF <35% at 30 days was 6% in the TH group versus 24% in the control group (p = 0.19). In the COOL-AMI Pilot Trial, the presence of MVO in both test groups was high and extensive MVO was related with reduced LVEF. The efficacy of therapeutic hypothermia (TH) in MVO reduction should be tested in a pivotal trial.
Identifiants
pubmed: 30414797
pii: S1553-8389(18)30416-0
doi: 10.1016/j.carrev.2018.09.014
pii:
doi:
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM
Pagination
799-804Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2018. Published by Elsevier Inc.