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Clinical Trials/NCT04884841
NCT04884841
Recruiting
Not Applicable

Development and Validation of Models to Predict Postoperative Complications for Patients With Cardiac Surgery

China National Center for Cardiovascular Diseases1 site in 1 country70,000 target enrollmentJanuary 1, 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Surgery--Complications
Sponsor
China National Center for Cardiovascular Diseases
Enrollment
70000
Locations
1
Primary Endpoint
postoperative complications: ECMO
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

Patients undergoing cardiac surgery is routinely performed in clinical scenarios, highly postoperative morbidities and long-term mortality should be modified. A simple risk prediction model incorporating risk factors can help guide clinical decision making, patient counseling and treatment planning.

Detailed Description

Patients undergoing cardiac surgery is routinely performed in clinical scenarios, highly postoperative morbidities and long-term mortality should be modified.A nomogram is a pictorial representation of a scoring model that possesses a simple user interface and shows favorable predictive performance. By integrating a patient's diverse determinant variables, a nomogram can provide a personalized probability for quantitative predictions of the incidence of an outcome of interest.Therefore, we conducted a retrospective study to assess the incidence, risk factors and outcomes associated with major complications patients undergoing cardiac surgery.

Registry
clinicaltrials.gov
Start Date
January 1, 2012
End Date
December 12, 2025
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
China National Center for Cardiovascular Diseases
Responsible Party
Principal Investigator
Principal Investigator

Yuefu Wang

Principal Investigator, Clinical Professor

China National Center for Cardiovascular Diseases

Eligibility Criteria

Inclusion Criteria

  • Age more than 18 years Undergoing Cardiovascular surgery

Exclusion Criteria

  • Missing primary outcomes or variables

Outcomes

Primary Outcomes

postoperative complications: ECMO

Time Frame: 30 days

patients with ECMO

postoperative complications: acute kidney injury

Time Frame: 30 dyas

Diagnosed acute kidney injury (KDIGO)

postoperative complications: Infection

Time Frame: 30 days

Diagnosed infection

postoperative complications: delirium

Time Frame: 30 days

Diagnosed delirium (CAM,CAM-ICU)

postoperative complications: MACCE

Time Frame: 30 days, as follow up

Diagnosed MACCE

postoperative complications: Chronic Kidney disease

Time Frame: 30 days, as follow up

Diagnosed Chronic Kidney disease

postoperative complications: major bleeding

Time Frame: 30 days

Diagnosed major bleeding

postoperative complications: postoperative pulmonary complications

Time Frame: 30 days

Diagnosed postoperative pulmonary complications

postoperative complications: IABP

Time Frame: 30 days

patients with IABP

Length of ICU stay

Time Frame: Through study completion, an average of 30 days

Number of days the patient stays in the intensive care unit

Ventilation time

Time Frame: Through study completion, an average of 7 days

Number of hours the patient with mechanical ventilation

Secondary Outcomes

  • Total hospital costs(Through study completion, an average of 30 days)
  • ICU costs(Through study completion, an average of 30 days)
  • Length of hospital stay(Through study completion, an average of 30 days)
  • Length of postoperative hospital stay(Through study completion, an average of 30 days)

Study Sites (1)

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