ambulatory surgery
Conditions
Interventions
Group 1: Patients operated in AQS1-participating practices and clinics in Germany.
Data basis is the patient information and information from the physician section of the AQA1 (see details under prim
Sponsors
Leiter Fachbereich SchmerztherapieKlinik für Anästhesiologie und IntensivmedizinUniversitätsklinikum Jena
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Operation in the period 01.01.2004 - 31.12.2021 age >= 18 years
Exclusion criteria
Exclusion criteria: none
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complaints due to wound pain until day 3 after surgery. | — |
Secondary
| Measure | Time frame |
|---|---|
| Additional variables from the patient section of the AQS1: o adequate supply of pain medication in the recovery room o effects of head, throat and muscular pain after surgery o effect of wound pain after day 3 after surgery o adequate supply of pain medication at home o overall rating of the surgery Data from the physician section of the AQS1: complaints in the recovery room (wound, muscle, neck, and head pain). In addition, there is a detailed presentation of demographic (e.g., age, gender, ASA) and procedure-associated variables (type of anesthesia, medication, duration of surgery) as well as postoperative complications. | — |
Countries
Germany
Contacts
Public ContactPhilipp Baumbach
Klinik für Anästhesiologie und IntensivmedizinUniversitätsklinikum Jena
Outcome results
None listed