Attachment style Pain therapy after thoracosurgical operations
Conditions
Interventions
Group 1: Postoperative patients after thoracic surgery of all types:
1st postoperative day: Individual pain management and the quality of pain therapy measured with QUIPS (quality improvement in post
Sponsors
Schmerzzentrum der Klinik für Anästhesiologie und Operative Intensivmedizin, Uniklinik Köln
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: - patients who were scheduled for a thoracic operation - Minimum age 18 years - written informed consent - consent of the patient after detailed explanation about the planned study
Exclusion criteria
Exclusion criteria: - patients younger than 18 years - no written informed consent - no anesthesiological admittance for the planned operation due to concomitant diseases
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary endpoint of this observational study is the intensity of pain measured with Numeric Rating Scale (NRS) and QUIPS questionnaire on first and tenth postoperative day and 6 months after operation. | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary endpoints (measured on first and 10th postoperative day and after 6 months) are the satisfaction with the pain therapy (measured with QUIPS questionnaire), the opioid consumption, mortality, morbidity, use of nicotine and alcohol, side effects of the pain therapy and perioperative complications. | — |
Countries
Germany
Contacts
Public ContactJohannes Löser
Schmerzzentrum der Klinik für Anästhesiologie und Operative Intensivmedizin der Uniklinik Köln
Outcome results
None listed