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

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04533698
Acronym
Volu-CABG
Enrollment
265
Registered
2020-08-31
Start date
2009-01-01
Completion date
2024-06-30
Last updated
2025-04-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Resternotomy

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.

Interventions

OTHERAssessment of reason for resternotomy

No intervention is performed. Reasons for resternotomy (coagulation, fluid balance and other) are retrospectively assessed.

OTHERAssessment of reason for avoidance of resternotomy

No intervention is performed. Reasons for avoidance resternotomy (coagulation, fluid balance and other) are retrospectively assessed.

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria

* None.

Design outcomes

Primary

MeasureTime frameDescription
Resternotomy7 daysResternotomy yes or no after elective or emergency aortocoronary bypass

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 5, 2026