preoperative evaluation
Conditions
Interventions
Group 1: Once the indication for surgery has been established, patients are given access to pre-operative screening software. This replaces the paper-based pre-operative questioning. The software is a
Sponsors
Klinik für Anästhesiologie, Operative Intensivmedizin und Schmerzmedizin
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: o ASA classification I-IV o Patients from the following departments: Clinic for Urology and Urosurgery, Clinic for Gynaecology, Surgical Clinic: Rectal Centre, Bariatric Surgery o Signed declaration of consent for participation in the study)
Exclusion criteria
Exclusion criteria: o Emergency interventions o < 18 years of age o Mental impairment that does not allow the patient to understand the nature, scope and significance of the research project
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of the study is user satisfaction with the implemented solution. This will be recorded in writing for doctors and patients using standardised questionnaires directly after the premedication consultation. In addition, a further written survey of doctors will be carried out using a standardised questionnaire after the end of the study period. | — |
Secondary
| Measure | Time frame |
|---|---|
| o Duration of processing by the patient o Completeness of the information provided for a planned anaesthesiological procedure o Change in contact time between doctors and patients in the premedication discussion These endpoints are read out from the resulting care data after the end of the study period. | — |
Countries
Germany
Contacts
Public ContactDavid Ghezel-Ahmadi
Klinik für Anästhesiologie, Operative Intensivmedizin und Schmerzmedizin
Outcome results
None listed