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Registry for the Improvement of Postoperative OutcomeS in Cardiac and Thoracic surgEry (RIPOSTE)

C

CMC Ambroise Paré

Status

Enrolling

Conditions

Postoperative Complications
Death
Cardiac Complication
Heart Diseases

Treatments

Procedure: Cardiothoracic surgery

Study type

Observational

Funder types

Other

Identifiers

NCT03209674
RIPOSTE

Details and patient eligibility

About

The registry for the improvement of postoperative outcomes in cardiac and thoracic surgery aims to prospectively collect data in order to test the association between various preoperative and per-operative variables ; and several postoperative outcomes such as mortality, shock, redo surgery, sepsis and extracorporeal life-support.

Full description

Cardiac and thoracic surgery is plagued by severe morbidity and mortality. Understanding and being able to predict postoperative outcomes may allow to better fit peri-operative care of cardio-thoracic patients.

RIPOSTE database aims to prospectively collect baseline characteristics and per-operative information in order to test associations with the incidence of postoperative outcomes.

Baseline characteristics include: age, EuroSCORE 2 and its components (age, gender, New York Heart Association (NYHA) functional class, angina symptoms, insulin-dependent diabetes mellitus, extracardiac arteriopathy, chronic pulmonary dysfunction, neurological or musculoskeletal dysfunction severely affecting mobility, previous cardiac surgery, renal function with creatinin clearance, active endocarditis, critical preoperative state, left ventricle ejection fraction, recent myocardial infarction, pulmonary artery systolic pressure, procedure urgency and weight of the procedure (coronary artery bypass graft, valve surgery and/or thoracic aorta)) weight, height, preoperative biology and preoperative echocardiography parameters when measured.

Peroperative information include: cardiac bypass duration, type of procedure, implanted device, valve size.

Postoperative outcomes include: death, postoperative shock, mediastinitis, length of stay in intensive care unit, overall length of stay, blood transfusion.

Enrollment

8,000 estimated patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • all patients eligible for cardiac or thoracic surgery

Exclusion criteria

  • non applicable

Trial contacts and locations

1

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Central trial contact

Lee S Nguyen, MD; Alain Brusset, MD

Data sourced from clinicaltrials.gov

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