Beta Blocker Use in Cardiac Surgery and Association With Postoperative Course

NCT ID: NCT04769752

Last Updated: 2024-02-16

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1789 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-30

Study Completion Date

2023-12-22

Brief Summary

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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.

Detailed Description

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Conditions

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Cardiac Surgery With Cardiopulmonary Bypass

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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No beta-blocker

Patient do no treat with beta-blocker before the surgery

collection of the allocated treatment

Intervention Type OTHER

collection of the allocated treatment

collection of medical complications

Intervention Type OTHER

collection of medical complications

Beta blocker

Patient treat with beta-blocker in accordance to international guidelines

collection of the allocated treatment

Intervention Type OTHER

collection of the allocated treatment

collection of medical complications

Intervention Type OTHER

collection of medical complications

Beta blocker2

Patient treat with beta-blocker without respect of international guidelines

No interventions assigned to this group

Interventions

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collection of the allocated treatment

collection of the allocated treatment

Intervention Type OTHER

collection of medical complications

collection of medical complications

Intervention Type OTHER

Eligibility Criteria

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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
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Centre Hospitalier Universitaire Dijon

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Chu Dijon Bourogne

Dijon, , France

Site Status

Countries

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France

References

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Guinot PG, Fischer MO, Nguyen M, Berthoud V, Decros JB, Besch G, Bouhemad B. Maintenance of beta-blockers and cardiac surgery-related outcomes: a prospective propensity-matched multicentre analysis. Br J Anaesth. 2024 Aug;133(2):288-295. doi: 10.1016/j.bja.2024.04.018. Epub 2024 May 23.

Reference Type DERIVED
PMID: 38789363 (View on PubMed)

Other Identifiers

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Guinot 2021

Identifier Type: -

Identifier Source: org_study_id

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