1day before and 1-5days after operation
The Safety and Efficacy of the Enhanced Recovery After Surgery(ERAS)Applied on Cardiac Surgery With Cardiopulmonary Bypass
Brief Summary
This study evaluates the enhanced recovery after surgery (ERAS) concept over conventional postoperative care in patients with heart valve disease undergoing cardiac surgery with cardiopulmonary bypass. Half of participants will adherence to the ERAS, while the other half will under the conventional postoperative care.
Intervention / Treatment
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ERAS group (PROCEDURE)After operation use Ropivacaine 100mg infiltrating intercostal wound and self-controlled intravenous analgesia pump is applicable(Sufentanil 0.05ug/kg·h combine with Ketamine 40ug/kg·h).
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Conventional control group (PROCEDURE)Intravenous infusion of flucloxacillin sodium 1g before the operation
Condition or Disease
- Valvular Heart Disease
Phase
Study Design
Study type: | INTERVENTIONAL |
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Status: | Completed |
Study results: | No Results Available |
Age: | 18 Years to 70 Years |
Enrollment: | 226 (ACTUAL) |
Funded by: | Other |
Allocation: | Randomized |
Primary Purpose: | Treatment |
MaskingQUADRUPLE:
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Clinical Trial Dates
Start date: | Jul 01, 2015 | ACTUAL |
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Primary Completion: | Nov 01, 2016 | ACTUAL |
Completion Date: | May 01, 2017 | ACTUAL |
Study First Posted: | Jun 24, 2015 | ESTIMATED |
Results First Posted: | Aug 31, 2020 | |
Last Updated: | May 31, 2017 |
Sponsors / Collaborators
Lead Sponsor:
Xiangya Hospital of Central South University
Lead sponsor is responsible party
Responsible Party:
N/A
Location
Enhanced recovery after surgery (ERAS) or fast-track surgery is a perioperative and postoperative care concept initiated in the early 1990s aiming to reduce the length of hospital stays following elective abdominal surgery. The success of ERAS depends highly on multidisciplinary teamwork and patient compliance.
This study intends to compare the Enhanced Recovery After Surgery (ERAS) concept applied to patients with heart valve disease undergoing cardiac surgery with cardiopulmonary bypass under traditional perioperative management of patients, committed to reducing patient's physical and psychological stress by surgical trauma, achieve the purpose of fast recovery, in order to establish an effective perioperative management during cardiopulmonary bypass surgery, improve patients' satisfaction and to accelerate postoperative rehabilitation safely.
This study intends to compare the Enhanced Recovery After Surgery (ERAS) concept applied to patients with heart valve disease undergoing cardiac surgery with cardiopulmonary bypass under traditional perioperative management of patients, committed to reducing patient's physical and psychological stress by surgical trauma, achieve the purpose of fast recovery, in order to establish an effective perioperative management during cardiopulmonary bypass surgery, improve patients' satisfaction and to accelerate postoperative rehabilitation safely.
Participant Groups
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Perioperative management follows the Enhanced Recovery after Surgery(ERAS) program
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Perioperative management follows the conventional program
Eligibility Criteria
Sex: | All |
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Minimum Age: | 18 |
Maximum Age: | 70 |
Age Groups: | Adult / Older Adult |
Healthy Volunteers: | Yes |
Inclusion Criteria:
* Heart function grade II - III (Using the cardiac function classification method formulated by American Heart Disease Institute)
* The in - hospital was treated with extracorporeal circulation operation and general anesthesia.
* Had a good cognition, and signed the informed consent.
* Aged between 18 and 70.
* The age, clinical examination and other generally situation of the two groups of patients had no statistical significance.
Exclusion Criteria:
* Combined with other blood coagulation dysfunction, serious brain, liver and kidney dysfunction, endocrine system diseases and serious infectious disease.
* Patients with severe mental disorders cannot cooperate with the treatment.
* Emergency operation
* Have taboo of Echocardiography and pulmonary catheterization by echocardiography.
* Patients have been fitted with a pacemaker.
* Allergic to erythropoietin.
* Suspected or had alcohol, drug abuse history.
* Spinal deformity or paravertebral lesions.
* Heart function grade II - III (Using the cardiac function classification method formulated by American Heart Disease Institute)
* The in - hospital was treated with extracorporeal circulation operation and general anesthesia.
* Had a good cognition, and signed the informed consent.
* Aged between 18 and 70.
* The age, clinical examination and other generally situation of the two groups of patients had no statistical significance.
Exclusion Criteria:
* Combined with other blood coagulation dysfunction, serious brain, liver and kidney dysfunction, endocrine system diseases and serious infectious disease.
* Patients with severe mental disorders cannot cooperate with the treatment.
* Emergency operation
* Have taboo of Echocardiography and pulmonary catheterization by echocardiography.
* Patients have been fitted with a pacemaker.
* Allergic to erythropoietin.
* Suspected or had alcohol, drug abuse history.
* Spinal deformity or paravertebral lesions.
Primary Outcomes
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The postoperative hospital time From pre-surgery to discharge, up to 4 weeks
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Length of ICU stay From entering the ICU to roll out, up to 4 weeks
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The time of readiness to discharge From pre-surgery to discharge, up to 4 weeks
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The length of hospital stay From pre-surgery to discharge, up to 8 weeks
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Hospitalization cost When the patient is discharged
Secondary Outcomes
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Perioperative major adverse events From pre-surgery to discharge, up to 4 weeks
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Vasoactive drugs Support Hours From the start of drugs to stop them, up to 4 weeks
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Postoperative tracheal tube time From the end of surgery to the removal of tracheal tube, up to 4 weeks
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Duration of mechanical ventilation after surgery From the end of surgery to the recovery of spontaneous breathing, up to 4 weeks
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Time to first bowel movement From the end of surgery to first exhaust, up to 2 weeks
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Postoperative time to first exhaust From the end of surgery to first exhaust, up to 2 weeks
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1day before and 1-5days after operation
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1day before and 1-5days after operation
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1day before and 1-5days after operation
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1day before and 1-5days after operation
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1day before and 1-5days after operation
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1day before and 1-5days after operation
Other Outcomes
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Questions to the participants' health Six month
More Details
NCT Number: | NCT02479581 |
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Acronym: | ERAS |
Other IDs: | liman20150516 |
Study URL: | https://clinicaltrials.gov/study/NCT02479581 |
Last updated: Sep 29, 2023