Catheter-related infections in regional analgesia
Conditions
Interventions
Group 1: Patients with presumably normal immune function
Group 2: Immunosuppressed patients
Group 3: Patients with presumably normal immune function and perioperative antibiotic prophylaxis
Group 4: P
Sponsors
Universitätsklinikum des Saarlandes
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: All cases documented in the German Network for Safety in Regional Anesthesia and Acute Pain Therapy registry with a regional analgesic catheter placement (01.01.2007 until the day of data readout)
Exclusion criteria
Exclusion criteria: Implausible data entries
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Time to infection | — |
Secondary
| Measure | Time frame |
|---|---|
| Degree of infection No infection: no signs of infection Mild infection: presence of 2 symptoms out of redness, swelling, and pain. Moderate infection: mild infection plus 2 criteria: increased C-reactive protein, leukocytosis, fever, or pus at the punctured site. Severe infection: necessity of surgical intervention such as incisions or revisions. | — |
Countries
Germany
Contacts
Public ContactLukas Martin Müller-Wirtz
Universitätsklinikum des Saarlandes
Outcome results
None listed