Cervical Spondylosis
Conditions
Interventions
Experimental group:Implement the ERAS scheme
Control group:conventional care
Sponsors
Xinqiao Hospital, Army Medical University
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Aged >= 18 years; 2. Inpatient cases, male or female; 3. Diagnosed with cervical degenerative disease; 4. Those who meet the indications for ACDF surgery and receive ACDF surgery for the first time; 5. Sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Pregnant and breastfeeding women, or female patients with reproductive plans during the study period; 2. Patients with cognitive impairment, kidney, liver or intestinal disease; 3. Patients diagnosed with tumor, infection, deformity; 4. Patients with allergies or contraindications to any of the pathway care elements; 5. Other chronic pain patients receiving chronic opioids or gabapentin and pregabalin at the same time (not related to surgical indications); 6. Patients whose primary or preferred language is not Chinese.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 40-item questionnaire as a measure of quality of recovery; | — |
Secondary
| Measure | Time frame |
|---|---|
| Numerical Rating Scale (pain measurement);Length of stay;Cost;Blood biochemistry;90-day readmission and reoperation; | — |
Countries
China
Contacts
Public ContactHuang Bo
Xinqiao Hospital, Army Medical University
Outcome results
None listed