Analysis of Risk Factors for Death After Blunt Traumatic Rupture of the Thoracic Aorta
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Purpose
Aortic injuries after blunt thoracic trauma are compared to the great incidence of accidents relatively rare, but potentially serious leading to death at scene in most of the cases. The study was undertaken to delineate mortality and its risk factors on three different levels (pre-hospital, in-hospital and overall). Between 1990 and 2003, all consecutive patients and victims with traumatic aortic rupture were retrospectively analyzed by reviewing hospital and autopsy records.
| Condition |
|---|
|
Aortic Rupture |
| Study Type: | Observational |
| Study Design: | Observational Model: Case-Only Time Perspective: Retrospective |
| Official Title: | Analysis of Risk Factors for Death After Blunt Traumatic Rupture of the Thoracic Aorta |
| Enrollment: | 85 |
| Study Start Date: | January 1990 |
| Study Completion Date: | December 2003 |
| Primary Completion Date: | December 2003 (Final data collection date for primary outcome measure) |
During the study period of 14 years (January 1990 to December 2003), all consecutive cases with traumatic rupture of the thoracic aorta being reported in the greater area of Zurich with about one million inhabitants were included in the present study. Related to the final outcome, patient data were drawn either from medical reports from the University Hospital of Zurich, which is a tertiary care teaching hospital and level I trauma center for the eastern part of Switzerland, or from autopsy reports from the Institute of Forensic Medicine of the University of Zurich, respectively. The latter group includes all patients, who died on the scene, in a assigning primary care hospital or on the way to the University Hospital of Zurich. In Switzerland, the criteria used for performing a full autopsy after a blunt traumatic death include all cases in which the events leading to the death are unclear or in which the cause of death is the result of suicide or extrinsic harm. Both, deaths at the scene and in-hospital deaths were included in the study.
Eligibility| Ages Eligible for Study: | 16 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Probability Sample |
Hospitalized patients Patients who died at the scene
Inclusion criteria:
- During the study period of 14 years (January 1990 to December 2003), all consecutive cases with traumatic rupture of the thoracic aorta being reported in the greater area of Zurich with about one million inhabitants were included in the present study
Exclusion criteria:
- Non-traumatic aortic rupture
- Non-traumatic aortic dissection
Contacts and Locations| Switzerland | |
| University Hospital Zurich, Division of Internal Medicine | |
| Zurich, ZH, Switzerland, 8091 | |
| Principal Investigator: | Daniel Franzen, MD | University Hospital Zurich, Division of Internal Medicine |
More Information
No publications provided
| Responsible Party: | University of Zurich |
| ClinicalTrials.gov Identifier: | NCT01632774 History of Changes |
| Other Study ID Numbers: | TAR |
| Study First Received: | June 28, 2012 |
| Last Updated: | July 2, 2012 |
| Health Authority: | Switzerland: Laws and standards |
Additional relevant MeSH terms:
|
Aortic Rupture Rupture Aneurysm, Ruptured Aneurysm Vascular Diseases |
Cardiovascular Diseases Aortic Aneurysm Aortic Diseases Wounds and Injuries |
ClinicalTrials.gov processed this record on May 22, 2013