Chu Dijon Bourogne
Dijon, 21000, France
NCT Number: NCT04769752
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.
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Notify Me18 year and older
All sexes
Observational
Dijon, 21000, France
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
collection of the allocated treatment
collection of medical complications
Time frame: 7 days
Number of patients treated with beta-blocker in accordance with international guidelines
Centre Hospitalier Universitaire Dijon
Other
Use and Prescription of Beta-blockers Before Cardiac Surgery With Cardiopulmopnary Bypass: Multicenter Observational Analysis of Practices and Its Association With Postoperative Morbidity-mortality.
Acronym: BLOCK
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