The Effect of Advanced Improvement Program (ERAS) on Postoperative Outcomes in Patients Undergoing Open Heart Surgery
- Conditions
- Enhanced Recovery After SurgeryOpen Heart Surgery
- Interventions
- Other: ERAS (Enhanced Recovery After Surgery ) are evaluatedOther: ERAS are not evaluated
- Registration Number
- NCT03799965
- Lead Sponsor
- Kocaeli Derince Education and Research Hospital
- Brief Summary
Investigation of the effect of Enhanced Recovery After Surgery (ERAS) program on postoperative results of patients operated for open heart surgery.
- Detailed Description
The ERAS protocol, also known as evidence based "fast-track surgery" (FTS), is an evidence based combination of findings regarding suggestions for patient care on various levels of the perioperative period, which work in synergy for accelerating the postoperative recovery period. It has been used sucessfully for many surgical disciplines, primarily colorectal surgery, since it was first reported in 1997. However, there is a significant insufficiency of this patient oriented rehabilitation program regarding cardiovascular surgeries. This study is to compare the postoperative follow up periods of patients with ERAS protocol and patients with standard protocol who were both operated for cardiac surgery.
Following approval of the local ethics committee, 210 patients who are operated for elective cardiac surgery are enrolled in this prospective randomized clinical trial. The patients who are not applied the ERAS protocol are evaluated in the control group (n=51). The findings regarding the patients under ERAS protocol are evaluated based on evidence. Our primary is to compare the durations of stay in the intensive care unit and in hospital; our secondary is to compare the incidences of complications of the groups. The demographic data, operative measurements, complication rates, the amounts of perioperative bleeding and drainage and the duration of stay in the intensive care unit and hospital are recorded.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 210
- over 18 years old;
- Patients undergoing elective open heart surgery (cardiopulmonarybiasis, aortic and mitral valve replacement);
- ASA III ;
- Patients with informed consent for the study.
- Patients who refuse to participate in the study;
- Patients under emergency conditions.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description ERAS protocol are evaluated ERAS (Enhanced Recovery After Surgery ) are evaluated * It is to compare the durations of stay in the intensive care unit and in hospital * It is to compare the incidences of complications of the groups ERAS protocol are not evaluated ERAS are not evaluated * It is to compare the durations of stay in the intensive care unit and in hospital * It is to compare the incidences of complications of the groups
- Primary Outcome Measures
Name Time Method complications 24 hours compare the incidences of complications
durations of stay 24 hours compare the durations of stay in the intensive care unit and in hospital
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Emine yurt
🇹🇷Kocaeli, Derince, Turkey