Patient Outcome of Cardiac Surgery During the COVID-19 Pandemic
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- STATUS
- Recruiting
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- participants needed
- 350
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- sponsor
- Nantes University Hospital
Summary
This study will describe the recovery process of patients undergoing cardiac surgery during the covid-19 pandemic. This will focus on hemodynamic failure and organ dysfunction after surgery.
Capturing real-world data and sharing international experience will inform the management of this complex group of patients who undergo surgery throughout the COVID-19 pandemic, improving their clinical care.
This investigator-led, non-commercial, non-interventional does not collect any patient identifiable information.
Description
Performing cardiac surgery in the context of SARS-CoV2 infection is potentially at risk of marked post-operative hemodynamic failure (shock) due to the inflammatory reaction generated by the surgery and the extracorporeal circulation associated with the viral infection. In addition, in the absence of infection, 30-50% of patients will experience acute post-operative respiratory failure due to the combined effects of extracorporeal circulation and general anesthesia. The pulmonary tropism of the virus therefore is susceptible to increase in post-operative respiratory impairment.
Thus, the infection is likely to favor the occurrence of post-operative shock but also to aggravate respiratory failure and other post-operative organ failures.
Therefore, the investigators designed an observational study that aims at comparing two groups of patients:
- Cardiac or thoracic surgery patients with a negative Covid-19 PCR pre-operatively and in the 5 following days
- Cardiac or thoracic surgery patients with a positive Covid-19 PCR in the 5 days before or after surgery
Details
Condition | Patients Undergoing Cardiac or Thoracic Surgery |
---|---|
Age | 18years - 100years |
Treatment | No intervention |
Clinical Study Identifier | NCT04389463 |
Sponsor | Nantes University Hospital |
Last Modified on | 16 February 2024 |
How to participate?
Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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