ST Elevation Myocardial Infarction
Conditions
Brief summary
This is a before and after observational study of a therapeutic strategy to treat patients with confirmed ST-segment myocardial infarction (STEMI) with remote ischemic conditioning (RIC) before undergoing primary percutaneous coronary intervention (PCI). RIC is the purposeful application of brief, intermittent cycles of limb occlusion by inflation/deflation of a pneumatic cuff. The autoRIC device is an automatic RIC delivery device (the autoRIC® Device; CellAegis Devices Inc, Toronto, ON) that has received clearance from Health Canada for this use under the direction of a health care professional. Paramedics in the Peel and Halton regional emergency services and the Emergency department (ED) staff of Brampton Civic Hospital and Mississauga Hospital will treat patients experiencing STEMI with autoRIC, and study data will be collected from existing patient records. The 'before' group will include up to 900 patients who were treated before autoRIC implementation in the services and hospitals. These patients would have had a STEMI and undergone PCI, but did not receive the autoRIC device. The 'after' group will include up to 900 eligible patients who have had RIC treatment with the autoRIC device at the two participating sites following implementation in the services and hospitals. The primary analyses will compare the short-term and long-term outcomes of eligible patients who have received completed primary PCI for STEMI in the time period before the implementation and following the implementation of this RIC strategy. In addition, a health economic analysis will be conducted to determine the cost-effectiveness of the therapeutic strategy to treat STEMI patients with RIC prior to PCI.
Interventions
DEVICEautoRIC
Application of the autoRIC device
Sponsors
Sunnybrook Health Sciences Centre
Trillium Health Centre
Peel Regional Paramedic Service
Halton Region Paramedic Services
CellAegis US, Inc.
William Osler Health System
Study design
Allocation
NON_RANDOMIZED
Intervention model
SEQUENTIAL
Primary purpose
OTHER
Masking
NONE
Intervention model description
Before and after phase study
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* 18 years of age and older; * patients diagnosed with STEMI in the prehospital environment by responding paramedics from Peel Regional Paramedic Services or Halton Emergency Medical Service and transported to the PCI laboratory of Brampton Civic Hospital or Trillium Health Partners; * walk-in patients diagnosed with STEMI in the ED of either of these two facilities.
Exclusion criteria
* left-bundle branch block; * Lymphedema on either arm * PICC Line on either arm * AV fistula or no palpable pulse on either arm; * patient has a known bleeding disorder or known abnormality of blood flow to the left arm; * patient has peripheral nerve injury, abnormal nerve supply, peripheral neuropathy or pre- existing traumatic injury to the limb to be treated (left-arm).
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| 90-day MACCE | Within 90 days of PCI | Major adverse cardiovascular and cerebrovascular events (MACCE) in-hospital and within 90 days of PCI. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| 30, 60 and 180-day MACCE | Within 30, 60 and 180 days of admission | MACCE within 30, 60 and 180 days post hospital admission |
| LOS | Time from hospital admission to hospital discharge, up to 180 days of admission | Index hospitalization length of stay (LOS) |
| Cardiovascular-related death | Time from hospital admission to hospital discharge, up to 180 days of admission | Death due to cardiovascular related events |
| 30, 60, and 180-day cardiovascular-related readmission | 30, 60 and 180 days after index hospitalization | Hospital readmission within 30, 60, and 180 days of index hospitalization, due to cardiovascular events. |
| Infarct size | Time from hospital admission to hospital discharge, up to 180 days of admission | Size of infarct as measured by peak troponin level during index event admission |
Countries
Canada
Outcome results
None listed