Skip to content

Prognostic Factors of Patients Undergoing Redo Cardiac Surgery

Prognostic Factors of Patients Undergoing Redo Cardiac Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03925376
Enrollment
1200
Registered
2019-04-24
Start date
2019-04-21
Completion date
2024-12-31
Last updated
2019-04-24

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

Conditions

Redo Cardiac Surgery

Keywords

Redo cardiac surgery, Outcome

Brief summary

This study aims to investigate the prognostic significance of baseline characteristics for patients undergoing redo cardiac surgery.

Detailed description

Redo cardiac surgery is associated with an increased risk of postoperative morbidity and mortality. Patients undergoing redo cardiac surgery are becoming increasingly complex due to multiple comorbidities, adherence of mediastinal structures to the undersurface of the sternum as well as the spatial location of patent bypass grafts relative to the route of entry. Association estimates between baseline characteristics and outcomes in those cohort are imprecise. The aim of this study is to identify prognostic factors associated with redo cardiac surgery which may help physicians predict clinical outcomes and guide their treatment decision.

Interventions

PROCEDURERedo cardiac surgery

Redo cardiac surgery is technically challenging due to scarring of tissues resulting in loss of tissue planes, adhesions, multiple comorbid factors and risk of injury during re-entry.Suggested techniques in coronary artery surgery with a left internal mammary artery include routing the graft through a slit in the pericardium to minimize the possibility of adherence to the sternal table.

Sponsors

Shanghai Zhongshan Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Patients undergoing redo cardiac surgery

Exclusion criteria

* Age \<18 years; * Patients with a DNR order or do not escalate care order.

Design outcomes

Primary

MeasureTime frameDescription
28-day mortality28 daysDeath from any cause at 28 days

Secondary

MeasureTime frameDescription
60- and 90-day mortality60 days and 90 daysDeath from any cause at 60- and 90-days

Other

MeasureTime frameDescription
Length of stay in the ICUup to 90 daysthe length of stay in the ICU
Length of stay in the hospitalup to 90 daysthe length of stay in the hospital
Percentage of participants with adverse eventsup to 90 daysAdverse events includes haemorrhage; need for intraoperative/postoperative intra-aortic balloon pumping (IABP); prolonged intubation; acute kidney injury or need for continuous renal replacement therapy (CRRT); poor neurological outcome; infection events

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026