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The Application of Enhanced Recovery After Surgery (ERAS) for Cardiovascular Surgery in Adult

Not Applicable
Not yet recruiting
Conditions
Enhanced Recovery After Surgery
Cardiac Surgery
Interventions
Procedure: ERAS
Registration Number
NCT05914090
Lead Sponsor
Yan Fuxia
Brief Summary

Among adults, patients undergoing elective extracorporeal circulation for cardiac surgery are included in the ERAS strategy intervention plan, which mainly includes preoperative education, preoperative oral intake of multidimensional carbohydrate beverages, multimodal analgesia, blood protection strategies, correction of perioperative hypoalbuminemia, early removal of tracheal intubation, maintenance of blood sugar at reasonable levels, and targeted liquid therapy. The traditional plan group follows the current clinical diagnosis and treatment routine. By comparing the differences in the incidence of major postoperative outcomes (MACCE events, major pulmonary complications, and acute kidney injury) between the intervention group and the non intervention group, as well as comparing other adverse events (including but not limited to pneumonia, massive bleeding, postoperative arrhythmia, incision infection, postoperative nausea, vomiting, and delirium), all cause secondary intubation, and all cause secondary surgery between the two groups, and recording hospitalization time, ICU stay time The removal time of tracheal intubation and drainage tube, as well as the pain score during hospitalization and the total amount of opioid drug use (converted to equivalent dose morphine), hospitalization cost, postoperative recovery quality QoR15 scale score, and patient satisfaction score, were recorded to explore whether the ERAS regimen can reduce the incidence of major postoperative adverse events, improve patient prognosis, and accelerate postoperative recovery compared to traditional regimens.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
3600
Inclusion Criteria
  • Patients aged 18 to 80 years
  • Patients awaiting elective cardiac surgery with cardiopulmonary bypass (CPB)
Exclusion Criteria
  • American Society of Anesthesiologists (ASA) class is above class V
  • Patients with cardiac assist device or mechanical ventilation
  • The ejection fraction of patients is less than 30%
  • Patients with morbid obesity
  • Patients with severe obstructive sleep apnea-hypopnea syndrome (OSAHS)
  • Patients with severe pulmonary disease, including severe chronic obstructive pulmonary disease (COPD) or respiratory failure
  • Patients with severe liver or renal dysfunction, including severe acute or chronic renal dysfunction need renal replacement therapy, and acute or chronic liver failure need artificial liver therapy
  • Patients with long-term opioid or sedative utilization
  • Patients with a history of alcohol or cigarette abuse
  • Patients with long-term hormone therapy
  • An international normalized ratio > 2.0
  • Patients with severe malnutrition
  • Mental or legal disability
  • Current enrollment in another clinical trial
  • Patients' refusal or low adherence

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Intervention groupERAS-
Primary Outcome Measures
NameTimeMethod
Composite outcomesduring hospitalization, an average of 1 week, assessed up to 30 days

The composite outcomes include the major adverse cardiac and cerebrovascular events (MACCE), major postoperative pulmonary complication (PPCs), and acute kidney injury (AKI).

Secondary Outcome Measures
NameTimeMethod
cumulative opioid dosageduring hospitalization, an average of 1 week, assessed up to 30 days

Total perioperative consumption of opioid analgesics

the quality of recovery score (QoR)-15 after surgeryAt 24 hour after surgery
length of hospital stayFrom the date of admission until the date of discharging, assessed up to 30 days

From the date of admission until the date of discharging

time to extubationThe time from the end of operation to the removal of tracheal intubation, assessed up to 30 days

The time from the end of operation to the removal of tracheal intubation

the duration of intensive care unit (ICU) stayTime from ICU admission to ICU discharge, assessed up to 30 days

Time from ICU admission to ICU discharge

overall medical costsduring hospitalization, an average of 1 week, assessed up to 30 days

Total cost of patients during hospitalization

satisfaction scorethe day before discharge, assessed up to 30 days

A satisfaction rating using a 0-10 number scale (0=unsatisfactory, 10=satisfactory)

time to drainage removalThe time from the end of operation to the removal of drainage tube, assessed up to 30 days

The time from the end of operation to the removal of drainage tube

the rate of other complicationsduring hospitalization, an average of 1 week, assessed up to 30 days

The rate of other complications include delium, pneumonia, pneumothorax, hematorrhea and so on

the rate of reintubation for any causeduring hospitalization, an average of 1 week, assessed up to 30 days

The rate of reintubation for any cause

the outcomes of long-term prognosis by telephone follow-upwithin 30 days, 3 months, and 1 year

the outcomes of prognosis

Trial Locations

Locations (1)

Fuwai hospital

🇨🇳

China, Beijing, China

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