Factors Affect Outcomes in Cardiovascular Surgery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Coronary Artery Disease, Valvular Diseases, Vascular Diseases. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Factors That Affect the Outcomes of Cardiothoracic and Vascular Surgery
Overview
Identify factors that contribute to perioperative morbidity and mortality in patients undergoing cardiac surgery that involves cardiopulmonary bypass. Identify factors that affect perioperative morbidity and mortality in patients undergoing cardiac surgery.
Detailed description
Identify factors that affect perioperative morbidity and mortality in patients undergoing cardiac surgery.
Here are some examples, but may not limited the following factors:
1. demographic data 2. perioperative medications 3. comorbidity
Primary outcome measures
- all cause mortality [Time frame: 12 years]
Eligibility criteria
Inclusion criteria
Patients greater than or equal to 18 years old that underwent cardiovascular surgery at UC Davis Medical Center from 01/01/2001 to 07/15/2013.
Patients will only be included that underwent cardiovascular surgeries with or without cardiopulmonary bypass.
Exclusion criteria
Patients that did not undergo cardiovascular surgeries and age< 18 years old will be excluded from the study.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- University of California Davis Health System — Sacramento
Identifiers
NCT: NCT01932411 · 483753