Pain after gynecological laparoscopic surgery
Conditions
Interventions
Modeling group:None
validation group:None
High risk group:The frequency of telephone follow-up was increased, twice a day after discharge until 7 days after surgery, and the application of analgesic drugs was increased
Low risk group :According to the current postoperative routine follow-up procedure
control group:According to the current postoperative routine follow-up procedure
Sponsors
The First Affiliated Hospital of Zhejiang University School of Medicine
Eligibility
Sex/Gender
Female
Age
60 Years to 80 Years
Inclusion criteria
Inclusion criteria: ? The patient was = 60 years old with basic communication and understanding ability; ? met the diagnosis of benign ovarian fallopian tube lesion; ? expected operation time of =1 hour; ? patient and family gave informed consent to participate in the study.
Exclusion criteria
Exclusion criteria: ? Abnormal cognitive function; ? unable to communicate accurately in language; ? history of allergy to analgesic drugs used in this study; ? had psychiatric disorders.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| numerical rating scale; | — |
Secondary
| Measure | Time frame |
|---|---|
| Pittsburgh sleep quality index;pain catastrophizing scale;pain sensitivity questionnaire;hospital anxiety and depression scale;brief pain inventory; | — |
Countries
CHINA
Contacts
Public ContactJIN JIAOJIAO
The First Affiliated Hospital of Zhejiang University School of Medicine
Outcome results
None listed