Postoperative fatigue syndrome
Conditions
Interventions
group Pectoralis-intercostal-rectus sheath (PIRS) Plane Block:Ultrasound-guided bilateral Pectoralis-intercostal-rectus sheath (PIRS) Plane Block (0.25% Ropivacaine)
Control group:Injecting equal amount of normal saline
Sponsors
Xuzhou Central Hospital
Eligibility
Sex/Gender
All
Age
65 Years to 80 Years
Inclusion criteria
Inclusion criteria: Elderly patients undergoing elective Off-Punmp coronary artery bypass grafting, age 65-80 years, BMI 18-30 kg/m2, ASA class II or III.
Exclusion criteria
Exclusion criteria: (1) preoperative diagnosis of fatigue syndrome; (2) allergy to local anesthetics; (3) history of psychiatric illness; (4) history of chronic pain; (5) preoperative use of nonsteroidal anti-inflammatory drugs or opioid analgesics; (6) surgical cancellation; (7) change of surgical approach; (8) patient death; (9) patient or family request for withdrawal.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the incidence of postoperative fatigue syndrome (POFS) ; | — |
Secondary
| Measure | Time frame |
|---|---|
| the incidence of POFS at week 8 postoperatively; postoperative pain;postoperative opioid consumption;;length of ICU stay;length of hospital stay;the incidence of adverse events; | — |
Countries
China
Contacts
Public ContactWang Liwei
Xuzhou Central Hospital
Outcome results
None listed