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2.1. Objective:
• Primary Objective: To compare outcomes of patients with extremity injuries presenting with or without pre-hospital tourniquet placement.
2.2. Study Outcome Measures
This is a prospective, observational study. All patients who present to the participating ED's who meet inclusion/exclusion criteria will be identified by the treating trauma surgeons. Data collected will include basic patient demographics, data regarding the patient's injuries, data regarding tourniquet use, and data regarding outcomes. Please see the attached data collection tool for specifics (Appendix 12.1). Data will be collected prospectively in an observational manner using the data collection tool. Data collected on individual collection sheets will be de-identified. We plan to complete the data collection and analysis by 01\01\2021.
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| pre-hospital tourniquet placement | Other | patients with extremity injuries presenting with or without pre-hospital tourniquet placement. |
| Measure | Description | Time Frame |
|---|---|---|
| Incidence of arrival in shock | (Systolic Blood Pressure <90 mmHg (Millimeter of mercury)) | First 24 hours . |
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Inclusion Criteria:
≥ 18 y/o Patients with extremity injuries
Exclusion Criteria:
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All patients who present to the participating ED's who meet inclusion/exclusion criteria will be identified by the treating trauma surgeons.
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| Name | Affiliation | Role |
|---|---|---|
| Michael Truitt, M.D. | The Methodist Hospital Research Institute | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Methodist Dallas Medical Center | Dallas | Texas | 75203 | United States |
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