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Clinical Trials/NCT04533698
NCT04533698
Completed
N/A

Impact of Fluid Resuscitation Protocol on the Incidence of Reoperation for Bleeding After Emergency Cardiopulmonary Bypass Grafting

University Hospital, Basel, Switzerland0 sites265 target enrollmentJanuary 1, 2009
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ConditionsResternotomy

Overview

Phase
N/A
Intervention
Not specified
Conditions
Resternotomy
Sponsor
University Hospital, Basel, Switzerland
Enrollment
265
Primary Endpoint
Resternotomy
Status
Completed
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

This is a retrospective data analysis of patients that underwent elective or emergency cardiopulmonary bypass. Resternotomy due to bleeding is frequent after sternotomy. Also due to implementation of Argipressin into clinical practice fluid resuscitation protocol has changed to more vasopressors and less fluid within the past five years. The investigators want to explore the influence of volume resuscitation protocol on incidence of rethoracotomy during the past twenty years.

Registry
clinicaltrials.gov
Start Date
January 1, 2009
End Date
June 30, 2024
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Sponsor
University Hospital, Basel, Switzerland
Responsible Party
Principal Investigator
Principal Investigator

Alexa Hollinger

Principal Investigator

University Hospital, Basel, Switzerland

Eligibility Criteria

Inclusion Criteria

  • •All patients that underwent elective or emergency aortocoronary bypass at the University Hospital Basel between 2009 and 2020.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Resternotomy

Time Frame: 7 days

Resternotomy yes or no after elective or emergency aortocoronary bypass

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