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Clinical Trials/NCT04769752
NCT04769752CompletedNot Applicable

Use and Prescription of Beta-blockers Before Cardiac Surgery With Cardiopulmopnary Bypass: Multicenter Observational Analysis of Practices and Its Association With Postoperative Morbidity-mortality.

Centre Hospitalier Universitaire Dijon1 site in 1 country1,789 target enrollmentStarted: June 2020Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
1,789
Locations
1
Primary Endpoint
Number of patients treated with beta-blocker in accordance with international guidelines

Study Overview

Brief Summary

The objective of this study is to describe in a cohort of cardiac surgery patients the use of beta-blockers before surgery and their maintenance or withdraw according to international recommendations in order to compare patients who receive a beta-blocker with maintenance during the surgical period (international recommendation) to those for whom prescription and maintenance are not respected. Patients are treated according to standard practice and this protocol does not change patient management. No additional information or data is required by the study other than the data usually collected in the patient record (drug treatment, medical history, operating data, postoperative data, complications, length of stay).

The objectives of this research are :

  • To evaluate the proportion of patients receiving beta-blocker treatment prior to cardiac surgery.
  • To evaluate the proportion of patients receiving beta-blocker treatment before cardiac surgery and complying with international recommendations for its maintenance/stop in perioperative cardiac surgery.
  • To evaluate the incidence of complications and length of hospital stay in patients receiving beta-blockers based on compliance or non-compliance with recommendations.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Major patient ≥ 18 years
  • Patient operated cardiac surgery with cardiopulmonary bypass
  • Patients who have given oral consent to participate after full information

Exclusion Criteria

  • Off pump cardiac surgery

Outcomes

Primary Outcomes

Number of patients treated with beta-blocker in accordance with international guidelines

Time Frame: 7 days

Number of patients treated with beta-blocker in accordance with international guidelines

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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